VAERS Reports AS 7144B

VAERS 2711496

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

kritisch

Staat: MI
Alter: 68,0
Geschlecht: M
Eingang: 08.11.2023
Impfdatum: 13.09.2022
Beginn: 13.06.2023
Tage bis Beginn: 273,0
Dosis: 5
Route/Site: - / -

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

Acute respiratory failure Chest X-ray abnormal Computerised tomogram abdomen abnormal Computerised tomogram thorax abnormal Cough Dyspnoea Dyspnoea exertional Hypercapnia Hypoxia Pancreatic disorder Positive airway pressure therapy Rhinorrhoea Sick relative

Symptomtext

Admission Date: 6/13/2023 Discharge Date: 6/17/2023 DETAILS OF HOSPITAL STAY: Clinical Narrative: Patient is a 69 y.o. male patient who presented on 6/14/2023 with shortness of breath and exertional dyspnea that started on 6/13. He has hx of severe COPD/lives on 5L/uses Trilogy, GERD, hypertension, OSA, lung cancer s/p chemo/resection in close surveillance, diabetes mellitus. His wife has had a cold for a few weeks, and a few days ago, he started having cough, nasal drainage. He began having dyspnea that responded to his inhalers on the day prior to admission, but on 6/14, met with no improvement so came in. In the ED, he was quite distressed, given steroids multiple breathing treatments with little relief but finally improved when placed on Bipap. CXR without acute findings, however with mass in RUL similar to prior. CT C/A/P obtained as his pulmonologist wanted one this month for surveillance of his NSCC, and to better elucidate cause of his acute on chronic respiratory failure. This showed stable changes in RUL, no evidence for metastatic disease in chest, abd or pelvis. There was some note of mild pancreatic fat stranding, though had no abdominal pain or nausea. He requires admission for further evaluation and management of Acute on chronic respiratory failure with hypoxia and hypercapnea.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: GERD (gastroesophageal reflux disease) Lung nodule Lymphadenopathy, hilar Left Adrenal Nodule 1.2 cm biopsy negative for malignancy FDG avidity Tobacco abuse, in remission Pulmonary air trapping Diffusion capacity of lung (dl), decreased OSA (obstructive sleep apnea) Squamous cell lung cancer, left upper lobe of the lung s/p extended wedge 11/2/2017 Stage 1A (T1A N0 Mx) Squamous cell lung cancer, right upper lobe s/p lobectomy, Stage 1 Mediastinal adenopathy Malignant neoplasm of hilus of right lung (HCC) Anemia History of DVT (deep vein thrombosis) Chemotherapy-induced peripheral neuropathy Chronic respiratory failure with hypoxia and hypercapnia (HCC) Morbid obesity with BMI of 40.0-44.9, adult (HCC) Hypertension Hyperlipidemia Peripheral eosinophilia Gross hematuria Essential tremor Recurrent non-small cell lung cancer (NSCLC) (HCC) Steroid dependent (HCC) Pancreatic abnormality COVID-19 COPD, severe (HCC) Type 2 diabetes mellitus with diabetic polyneuropathy, without long-term current use of insulin (HCC) Dyspnea, steroid-responsive
Andere Medikamente: acetaminophen (TYLENOL) 325 MG tablet albuterol (PROVENTIL) (2.5 mg/3 mL) 0.083 % nebulization albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler alendronate (FOSAMAX) 70 MG tablet arformoterol (BROVANA)
Allergien: Darvon [Propoxyphene
Vorherige Impfungen: -

VAERS 2664951

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge AS7144B

kritisch

Staat: -
Alter: 57,0
Geschlecht: F
Eingang: 02.08.2023
Impfdatum: 09.09.2022
Beginn: 26.03.2023
Tage bis Beginn: 198,0
Dosis: 5
Route/Site: IM / LA

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

Acute respiratory failure Hypertension

Symptomtext

J96.01 ACUTE HYPOXEMIC RESPIRATORY FAILURE 3/26/2023 HTN (HYPERTENSION)

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

VAERS 2644706

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

kritisch

Staat: -
Alter: 60,0
Geschlecht: M
Eingang: 13.06.2023
Impfdatum: 17.09.2022
Beginn: 06.12.2022
Tage bis Beginn: 80,0
Dosis: 5
Route/Site: IM / LA

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

Acute respiratory failure

Symptomtext

ACUTE HYPOXEMIC RESPIRATORY FAILURE

Weitere VAERSDATA-Felder

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

VAERS 2607865

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

kritisch

Staat: -
Alter: 88,0
Geschlecht: M
Eingang: 31.03.2023
Impfdatum: 07.09.2022
Beginn: 08.03.2023
Tage bis Beginn: 182,0
Dosis: 1
Route/Site: - / -

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

Abdominal pain Acute respiratory failure Anticoagulant therapy Asthenia Atelectasis Computerised tomogram abdomen abnormal Condition aggravated Death Dehydration Diarrhoea COVID-19 Cardio-respiratory arrest Chest X-ray abnormal Chronic obstructive pulmonary disease Colitis ischaemic Dyspnoea Hypotension Hypoxia

Symptomtext

Perpetual Assessment: Patient is a 88 y.o. male h/o COPD (3L NC), CHF, CAD who presented from home on 3/8/2023 with sob, abd pain, diarrhea and weakness who was positive for COVID in the ED. Assessment and Plan Cardiorespiratory Arrest - Developed this in ER, due to below - Code status confirmed to be DNR CCA, DNI with patient and family prior to arrest. Patient expired at 1545. COPD Exacerbation Acute on Chronic respiratory failure Possible Sepsis/Pneumonia - Possible early pneumonia seen on CXR (atelectasis vs infiltrate) - Hypoxic 70's on presentation, placed on Non-rebreather with improvement - Given iv steroids, iv fluids with improvement in hemodynamics Diarrhea Dehydration - Most likely ischemic colitis given hypotension on presentation to ER - CT A/P showed concern by "bowel obstruction" and general surgery team was consulted by ER MD Medication Reconciliation: Reviewed DVT Prophylaxis: Lovenox Code Status: DNR CCA, DNI (confirmed with patient and family) Expected date of discharge: patient deceased in ER

Weitere VAERSDATA-Felder

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

VAERS 2607416

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

kritisch

Staat: WI
Alter: 97,0
Geschlecht: M
Eingang: 31.03.2023
Impfdatum: 07.09.2022
Beginn: 27.01.2023
Tage bis Beginn: 142,0
Dosis: 5
Route/Site: UN / UN

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

Atelectasis Biliary dilatation COVID-19 Cardio-respiratory arrest Chest X-ray abnormal Chest pain Cholecystectomy Cholecystitis Cholelithiasis Death Gallbladder disorder General physical health deterioration Jaundice SARS-CoV-2 test positive Ultrasound biliary tract Ultrasound liver Ultrasound pancreas

Symptomtext

On 1/27/2023, patient presented to the emergency department for evaluation of jaundice and chest pain. He had a positive COVID-19 NAA test but notably he did not have any COVID symptoms; His chest x-ray showed minimal plate-like atelectasis in the right lung base but there was no evidence of active pulmonary disease. Patient had an ultrasound of the liver/gallbladder/pancreas which showed that his gallbladder was distended with multiple gallstones and the common bile duct was slightly distended. He was diagnosed with cholecystitis and COVID-19 and admitted to the hospital for further treatment. Patient had a cholecystectomy on 1/29/2023. Postoperatively, the patient?s condition deteriorated. He coded and then died on 1/29/2023 while an inpatient at the hospital. Web Report received from the hospital indicated COVID-19 as a cause of death. Submitter does not have access to further medical information on this case. If more information is needed, please contact the admitting hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardio-respiratory arrest
Hospital-Tage: 2,0
Labordaten: 1/27/2023 - positive COVID-19 NAA test; Chest x-ray showed minimal plate-like atelectasis in the right lung base but there was no evidence of active pulmonary disease; Ultrasound of the liver/gallbladder/pancreas showed that gallbladder was distended with multiple gallstones and the common bile duct was slightly distended.
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Hypertension, Chronic renal failure stage 3a, Benign prostatic hyperplasia, Generalized osteoarthrosis, Macular degeneration (senile) of retina right eye.
Andere Medikamente: Unknown
Allergien: Unknown
Vorherige Impfungen: -

VAERS 2562207

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

kritisch

Staat: -
Alter: 84,0
Geschlecht: M
Eingang: 18.01.2023
Impfdatum: 07.09.2022
Beginn: 19.12.2022
Tage bis Beginn: 103,0
Dosis: 1
Route/Site: - / -

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

Acute respiratory failure Aortic aneurysm Benign prostatic hyperplasia Blood sodium decreased Body temperature increased C-reactive protein increased COVID-19 pneumonia Chest X-ray abnormal Computerised tomogram thorax abnormal Cough Dyspnoea Full blood count Gastrooesophageal reflux disease Hyperlipidaemia Hypertension Hyponatraemia Hypoxia Metabolic function test

Symptomtext

Patient is a pleasant 84-year-old male who presents to the emergency department today for chief complaint of shortness of breath. He reports his symptoms have been ongoing for approximately 1 week. He reports he was taken to home COVID test both of which have been negative. He presented to urgent care this morning for evaluation at which time he was prompted to come to the emergency department as he was found to be hypoxic. He reports that he normally walks approximately 2 miles per day, on his normal route he is noted that he is becoming increasingly dyspneic when normally he would not be. He does endorse a dry cough, that is elicited with deep inspiration. He denies any fever or chills. He denies any current pulmonary dysfunction, denies any smoking history. Patient states that he is fully vaccinated for COVID-19. Denies any chest pain, palpitations, fever/chills, abdominal pain, nausea/vomiting, diarrhea/constipation ED work-up: Chest x-ray shows multifocal pneumonia with both lungs, with positive COVID-19 swab. Does meet sepsis criteria. CT of the chest shows no acute PE, but does note new 9 mm nodule in the left upper lung which is concerning for malignancy and is new from previous CT in 2006. CBC and metabolic panel significant for WBC of 18.68, CRP 120, sodium 129. Patient is hemodynamically stable at this time. He is on 2 L nasal cannula with O2 saturation of approximately 93%. He does have a T-max of 100.9 degrees while in the ED. He was given 6 mg IV Decadron. He is admitted under the hospitalist service for further work-up and continuation of care Clinical Summary Patient did not qualify for remdesivir but did receive steroids. Patient never required intubation, only NC and will be discharged home with oxygen. Patient was noted to have a left upper lobe nodule and an ascending aortic aneurysm and patient is instructed to follow up with PCP. Patient will be discharged with dexamethasone for a total of 10 days. Patient did not require oxygen based on the 6 minute walk test prior to discharge. Discharge diagnosis Acute hypoxic respiratory failure Sepsis, secondary to COVID-19 pneumonitis 9 mm left upper lobe nodule Hyponatremia Hypertension Hyperlipidemia GERD BPH OSA

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 7,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2507192

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

kritisch

Staat: WI
Alter: 85,0
Geschlecht: M
Eingang: 14.11.2022
Impfdatum: 09.11.2022
Beginn: 13.11.2022
Tage bis Beginn: 4,0
Dosis: 5
Route/Site: IM / LA

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

Death

Symptomtext

expired

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Hospitalized, brain mass that is cancerous, signed onto hospice
Vorgeschichte: dementia, neoplasm of unspecified behavior of brain, History of Covid 19, pruritus, hypokalemia, peptic ulcer, benign prostatic hyperplasia without lower urinary tract symptoms, alcohol abuse, in remission, major depressive disorder, recurrent, borderline personality disorder, recurrent, insomnia, HTN, chronic obstructive pulmonary disease, gastro esophageal reflux disease without esophagitis, irritable bowel syndrome with diarrhea, dorsalgia
Andere Medikamente: Acetaminophen Tablet 325 MG Give 1 tablet by mouth every 4 hours as needed for Pain or Elevated, tropine Sulfate Solution 1 % Give 1 drop sublingually every 4 hours as needed for secretions 1-2 drops under tongue, Bisacodyl Suppository 10 M
Allergien: Lisinopril, Aricept
Vorherige Impfungen: -

VAERS 2481878

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

kritisch

Staat: GA
Alter: 63,0
Geschlecht: M
Eingang: 18.10.2022
Impfdatum: 16.09.2022
Beginn: 18.09.2022
Tage bis Beginn: 2,0
Dosis: 4
Route/Site: SYR / -

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

Death Unresponsive to stimuli

Symptomtext

The patient got an annual Flucelvax Quad shot and a Moderna Bivalent Booster on 9-16-22. He was fine on Friday and Saturday but was found unresponsive on Sunday, 9-18. He was taken to the hospital and died later that day.

Weitere VAERSDATA-Felder

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

VAERS 2480456

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

kritisch

Staat: WI
Alter: 64,0
Geschlecht: M
Eingang: 17.10.2022
Impfdatum: 14.10.2022
Beginn: 16.10.2022
Tage bis Beginn: 2,0
Dosis: 5
Route/Site: IM / RA

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

Death Malaise Pallor Unresponsive to stimuli

Symptomtext

death: At 1745 staff alerted writer to come into resident's room because he was not doing well. resident's vitals as follows; Temp 97.3, BP 114/71, HR 141, RR 42, O2 saturation 35%. Resident was ashen in color and was unresponsive. Hospice was called. The DON was updated on resident's change in condition and a confidential message was left for the professional guardian,

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: n/a
Vorgeschichte: ANOREXIA (R63.0) ANXIETY DISORDER, UNSPECIFIED (F41.9) ATHEROSCLEROTIC HEART DISEASE OF NATIVE CORONARY ARTERY WITHOUT ANGINA PECTORIS (I25.10) CHRONIC OBSTRUCTIVE PULMONARY DISEASE, UNSPECIFIED (J44.9) COVID-19 (U07.1) DEMENTIA IN OTHER DISEASES CLASSIFIED ELSEWHERE, UNSPECIFIED SEVERITY, WITHOUT BEHAVIORAL DISTURBANCE, PSYCHOTIC DISTURBANCE, MOOD DISTURBANCE, AND ANXIETY (F02.80) DYSPHAGIA, OROPHARYNGEAL PHASE (R13.12) LONG TERM (CURRENT) USE OF ANTICOAGULANTS (Z79.01) MAJOR DEPRESSIVE DISORDER, SINGLE EPISODE, UNSPECIFIED (F32.9) OTHER FRONTOTEMPORAL NEUROCOGNITIVE DISORDER (G31.09) PERSONAL HISTORY OF COVID-19 (Z86.16) PERSONAL HISTORY OF MALIGNANT NEOPLASM OF LARYNX (Z85.21) PERSONAL HISTORY OF PULMONARY EMBOLISM (Z86.711) SCHIZOPHRENIA, UNSPECIFIED (F20.9) UNSPECIFIED DEMENTIA, UNSPECIFIED SEVERITY, WITHOUT BEHAVIORAL DISTURBANCE, PSYCHOTIC DISTURBANCE, MOOD DISTURBANCE, AND ANXIETY (F03.90) UNSPECIFIED LACK OF COORDINATION (R27.9) UNSPECIFIED PSYCHOSIS NOT DUE TO A SUBSTANCE OR KNOWN PHYSIOLOGICAL CONDITION (F29) WEAKNESS (R53.1)
Andere Medikamente: Acetaminophen Suppository 650 MG Insert 1 suppository rectally every 4 hours as needed for Pain/Temp Acetaminophen Tablet 325 MG Give 2 tablet by mouth every 4 hours as needed for General Discomfort or Elevated Temp
Allergien: tree nuts
Vorherige Impfungen: -

VAERS 2696081

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

schwer

Staat: AL
Alter: 37,0
Geschlecht: M
Eingang: 14.10.2023
Impfdatum: 10.09.2022
Beginn: 01.10.2022
Tage bis Beginn: 21,0
Dosis: 4
Route/Site: SYR / AR

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

Cardiac function test Cardiac monitoring Dyspnoea Echocardiogram Myocarditis Palpitations

Symptomtext

Myocarditis. Shortness of breath, palpitations. Wore a heart sensor for 2 weeks until symptoms started to subside (took 3 months).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: -
Labordaten: Wore a Vital Connect sensor for 2 weeks to monitor myocarditis. I had some tests done to my heart at clinic . Also had an echocardiogram done.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2691678

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

schwer

Staat: AZ
Alter: 77,0
Geschlecht: M
Eingang: 05.10.2023
Impfdatum: 12.10.2022
Beginn: 27.09.2023
Tage bis Beginn: 350,0
Dosis: 5
Route/Site: IM / LA

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

Anticoagulant therapy Atelectasis COVID-19 Chest X-ray abnormal Cough Infusion Intensive care Pneumonitis Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive Tachypnoea

Symptomtext

no vaccine adverse event, but patient presented to the ED on 9/27/23 complaining of cough, congestion, runny nose x 2 days. Tested COVID + in the ED. Upon ED discharge 9/27/23 he was informed that he was ineligible for Paxlovid due to his anticoagulant use. Advised to return for remdesivir treatment if he chose. Patient returned to the ED ~ 3 hours later for remedesivir infusion. He was stable prior to the infusion, but during the infusion became tachypenic. Patient admitted to the ICU for observation.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 2,0
Labordaten: 9/27/23: CXR showed bibasilar atelectasis/pneumonitis.
Aktuelle Erkrankungen: unknown
Vorgeschichte: memory loss or impairment folate deficiency stool incontinence incontinence of urine subdural hygroma iron deficiency anemia benign prostatic hyperplasia chronic back pain generalized weakness recurrent falls unsteady gait hyperlipidemia impaired fasting glucose hearing disorder osteoarthritis of shoulder primary osteoarthritis of both knees ischemic dilated cardiomyopathy drug eluting coronary stent placement coronary artery disease, non-occlusive
Andere Medikamente: unknown
Allergien: NKDA documented in medical record
Vorherige Impfungen: -

VAERS 2636208

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge AS7144B

schwer

Staat: -
Alter: 85,0
Geschlecht: F
Eingang: 24.05.2023
Impfdatum: 14.09.2022
Beginn: 11.11.2022
Tage bis Beginn: 58,0
Dosis: 5
Route/Site: IM / LA

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

Atrial fibrillation Cardiac failure acute Cardiac pacemaker replacement Hypotension Left ventricular failure Syncope

Symptomtext

I95.9 HYPOTENSION 12/7/2022 ATRIAL FIBRILLATION, PERMANENT I95.9 HYPOTENSION 12/7/2022 AICD BATTERY REPLACEMENT I95.9 HYPOTENSION 12/7/2022 HYPOTENSION I95.9 HYPOTENSION 12/7/2022 SYSTOLIC HEART FAILURE, ACUTE ON CHRONIC I95.9 HYPOTENSION 12/7/2022 SYNCOPE

Weitere VAERSDATA-Felder

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

VAERS 2595766

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

schwer

Staat: WA
Alter: 31,0
Geschlecht: M
Eingang: 13.03.2023
Impfdatum: 07.09.2022
Beginn: 14.02.2023
Tage bis Beginn: 160,0
Dosis: 4
Route/Site: IM / LA

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

Loss of consciousness Syncope

Symptomtext

I had a random fainting event out of nowhere, I lost consciousness for about 20 seconds and came back to. I have an appointment in April for a follow up/ check up.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Scalp psoriasis
Andere Medikamente: Probiotic supplement; niacinamide; MSM powder
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2593857

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

schwer

Staat: NJ
Alter: 75,0
Geschlecht: M
Eingang: 09.03.2023
Impfdatum: 07.09.2022
Beginn: 26.02.2023
Tage bis Beginn: 172,0
Dosis: 5
Route/Site: IM / LA

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

Blood test Cold sweat Echocardiogram Electrocardiogram Syncope X-ray

Symptomtext

I experienced fainting and going into a cold sweat.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: EKG, X-Ray, Blood Test, Echocardiography
Aktuelle Erkrankungen: N/A
Vorgeschichte: Persistent Obstructive Pulmonary Disease
Andere Medikamente: Simvastatin; thyroxine; dutasteride; metoprolol; escitalopram
Allergien: N/A
Vorherige Impfungen: -

VAERS 2579622

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

schwer

Staat: MO
Alter: 90,0
Geschlecht: M
Eingang: 10.02.2023
Impfdatum: 07.09.2022
Beginn: 31.01.2023
Tage bis Beginn: 146,0
Dosis: 3
Route/Site: IM / LA

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

Asthenia Intensive care Syncope

Symptomtext

Case developed weakness with syncope at home, beginning 01/30/2023. It occurred again 01/31/2023 when case was transported via ambulance to a local Hospital where he remains in ICU.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: -
Labordaten: unknown
Aktuelle Erkrankungen: unknown
Vorgeschichte: difficulty communicating verbally
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2541942

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7144B

schwer

Staat: MA
Alter: 76,0
Geschlecht: F
Eingang: 23.12.2022
Impfdatum: 13.09.2022
Beginn: 13.10.2022
Tage bis Beginn: 30,0
Dosis: 5
Route/Site: IM / LA

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

Condition aggravated Guillain-Barre syndrome

Symptomtext

Flare up of GB

Weitere VAERSDATA-Felder

Praegender Schweregrund: Guillain-Barre syndrome
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: For the past three years I have residual side effects of Guillian Barre. Approximately one month after receiving booster and flu shot the same day, I had a flare up of GB
Andere Medikamente: Flu shot
Allergien: -
Vorherige Impfungen: -

VAERS 2535150

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

schwer

Staat: NC
Alter: 62,0
Geschlecht: M
Eingang: 16.12.2022
Impfdatum: 12.09.2022
Beginn: 23.11.2022
Tage bis Beginn: 72,0
Dosis: 4
Route/Site: SC / LA

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

Deep vein thrombosis Ultrasound Doppler abnormal

Symptomtext

DVT right calf

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: -
Labordaten: Ultrasound confirmation
Aktuelle Erkrankungen: None
Vorgeschichte: High cholesterol, controlled with meds. High blood pressure, controlled with meds
Andere Medikamente: atorvastatin 20 MG tablet nebivoloL 10 MG tablet tadalafiL 10 MG tablet cetirizine 10 MG tablet
Allergien: -
Vorherige Impfungen: -

VAERS 2533646

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7144B

schwer

Staat: -
Alter: 66,0
Geschlecht: F
Eingang: 16.12.2022
Impfdatum: 12.09.2022
Beginn: 23.09.2022
Tage bis Beginn: 11,0
Dosis: UNK
Route/Site: OT / -

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

Angiogram Blood pressure measurement Blood test Electrocardiogram Heart rate Hypertension Magnetic resonance imaging Syncope

Symptomtext

fainted this time/feeling lightheaded/razing heartbeat/ heart started to raze agai/nauseas; blood pressure going up/180 over 120 blood pressure; This spontaneous case was reported by a consumer and describes the occurrence of SYNCOPE (fainted this time/feeling lightheaded/razing heartbeat/ heart started to raze agai/nauseas) in a 66-year-old female patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. AS7144B) for COVID-19 prophylaxis. The occurrence of additional non-serious events is detailed below. Previously administered products included for COVID-19 prophylaxis: Moderna COVID-19 Vaccine (1st dose 4 21 2021 lot #040b21a) on 21-Apr-2021, Moderna COVID-19 Vaccine (2nd-027c21a) on 19-May-2021, Moderna COVID-19 Vaccine (1st booster lot #939903) on 22-Nov-2021 and Moderna COVID-19 Vaccine (2nd booster 4 lot #005m21a) on 28-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. Concurrent medical conditions included Blood pressure high (since 7 years ago). On 12-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 23-Sep-2022, the patient experienced SYNCOPE (fainted this time/feeling lightheaded/razing heartbeat/ heart started to raze agai/nauseas) (seriousness criterion medically significant) and HYPERTENSION (blood pressure going up/180 over 120 blood pressure). At the time of the report, SYNCOPE (fainted this time/feeling lightheaded/razing heartbeat/ heart started to raze agai/nauseas) and HYPERTENSION (blood pressure going up/180 over 120 blood pressure) had not resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, Angiogram: blood works, EKG, MRI, MRA, checked balance, fluid in the ear, heart monitor for 2 days & for 30 days, had an episode on the 21st heart started to raze again, echocardiogram ALL NEGATIVE, all results came back normal. On an unknown date, Blood pressure measurement: blood pressure going up/180 over 120 blood pressure. On an unknown date, Blood test: had blood work EKG all negative back to her MD and cardiologist 180 over 120 blood pressure which never happened before // blood works, EKG, MRI, MRA, checked balance, fluid in the ear, heart monitor for 2 days & for 30 days, had an episode on the 21st heart started to raze again, echocardiogram ALL NEGATIVE, all results came back normal. On an unknown date, Electrocardiogram: EKG, MRI, MRA, checked balance, fluid in the ear, heart monitor for 2 days & for 30 days, had an episode on the 21st heart started to raze again, echocardiogram ALL NEGATIVE, all results came back normal and Negative. On an unknown date, Heart rate: razing heartbeat/ heart started to raze again. On an unknown date, Magnetic resonance imaging: blood works, EKG, MRI, MRA, checked balance, fluid in the ear, heart monitor for 2 days & for 30 days, had an episode on the 21st heart started to raze again, echocardiogram ALL NEGATIVE, all results came back normal. 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 medication information was provided. No treatment medications were provided The patient was wondering of the side effects of the Moderna bivalent. She received the booster in Sep 12 2022, did not have any reaction 24hours after, on Sep 23 razing heartbeat feeling lightheaded and nauseas and blood pressure going up she did not faint this time. She went up in the ER, run multiple tests and they came up negative refer to a cardiologist. On the 7th Dec 2022 at night all of the symptoms started to happen again and fainted this time, went to the ER. Company comment: This spontaneous case concerns a 66-years-old female patient, with past medical history of Blood pressure high (for 7 years ago), (medically significant) who experienced the unexpected serious events of Syncope and Hypertension that occurred 12 days after the fifth dose of mRNA-1273 bivalent BA.4/BA.5 vaccination. Patient had received 1st dose, 2nd dose ,1st booster and 2nd booster with mRNA1273 vaccine were received in accordance with recommended schedule. The investigation of Magnetic resonance imaging, blood works, EKG, MRI, MRA, checked balance, fluid in the ear, heart monitor for 2 days & for 30 days, all were negative and within the normal limits. No further information on detailed clinical course, concomitant medications and treatment of the events was available in the report. Outcome of the events were not resolved. The past medical history of Blood pressure high remains a confounder. The benefit-risk relationship of mRNA-1273 Vaccine bivalent BA.4/BA.5 is not affected by this report. Event seriousness assessed as per medical judgement.; Sender's Comments: This spontaneous case concerns a 66-years-old female patient, with past medical history of Blood pressure high (for 7 years ago), (medically significant) who experienced the unexpected serious events of Syncope and Hypertension that occurred 12 days after the fifth dose of mRNA-1273 bivalent BA.4/BA.5 vaccination. Patient had received 1st dose, 2nd dose ,1st booster and 2nd booster with mRNA1273 vaccine were received in accordance with recommended schedule. The investigation of Magnetic resonance imaging, blood works, EKG, MRI, MRA, checked balance, fluid in the ear, heart monitor for 2 days & for 30 days, all were negative and within the normal limits. No further information on detailed clinical course, concomitant medications and treatment of the events was available in the report. Outcome of the events were not resolved. The past medical history of Blood pressure high remains a confounder. The benefit-risk relationship of mRNA-1273 Vaccine bivalent BA.4/BA.5 is not affected by this report. Event seriousness assessed as per medical judgement.

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Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Test Name: MRA; Result Unstructured Data: blood works, EKG, MRI, MRA, checked balance, fluid in the ear, heart monitor for 2 days & for 30 days, had an episode on the 21st heart started to raze again, echocardiogram ALL NEGATIVE, all results came back normal; Test Name: Blood pressure; Result Unstructured Data: blood pressure going up/180 over 120 blood pressure; Test Name: Blood work; Result Unstructured Data: had blood work EKG all negative back to her MD and cardiologist 180 over 120 blood pressure which never happened before // blood works, EKG, MRI, MRA, checked balance, fluid in the ear, heart monitor for 2 days & for 30 days, had an episode on the 21st heart started to raze again, echocardiogram ALL NEGATIVE, all results came back normal; Comments: 180 over 120 blood pressure which never happened // ALL normal blood works, EKG, MRI, MRA, checked balance, fluid in the ear, heart monitor for 2 days & for 30 days, had an episode on the 21st heart started to raze again but the results were also normal; Test Name: EKG; Result Unstructured Data: EKG, MRI, MRA, checked balance, fluid in the ear, heart monitor for 2 days & for 30 days, had an episode on the 21st heart started to raze again, echocardiogram ALL NEGATIVE, all results came back normal; Test Name: EKG; Test Result: Negative ; Test Name: Heart rate; Result Unstructured Data: razing heartbeat/ heart started to raze again; Test Name: MRI; Result Unstructured Data: blood works, EKG, MRI, MRA, checked balance, fluid in the ear, heart monitor for 2 days & for 30 days, had an episode on the 21st heart started to raze again, echocardiogram ALL NEGATIVE, all results came back normal
Aktuelle Erkrankungen: Blood pressure high (since 7 years ago)
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2491217

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

schwer

Staat: MI
Alter: 85,0
Geschlecht: M
Eingang: 15.12.2022
Impfdatum: 23.09.2022
Beginn: 23.11.2022
Tage bis Beginn: 61,0
Dosis: 4
Route/Site: - / -

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

Acute kidney injury Bladder catheterisation Bradycardia Cardiac pacemaker insertion Chest X-ray abnormal Anaemia Asthenia Atrioventricular block second degree Blood thyroid stimulating hormone normal COVID-19 Condition aggravated Coronary artery bypass Coronary artery disease Diastolic dysfunction Dyspnoea Echocardiogram normal Electrocardiogram abnormal Hypoxia

Symptomtext

Discharge Provider: MD Primary Care Provider at Discharge: MD Admission Date: 11/23/2022 Discharge Date: 12/09/2022 COVID positive Date: 12/7/2022 Per hospital summary: "Pt is an 85-year-old male with PMH of recent COVID-19 infection, aortic stenosis status post replacement, pAFib, dementia, CAD status post CABG x3, ILD, HFpEF who presented on 11/23 with shortness of breath. Chest x-ray was suspicious for pulmonary edema versus pneumonia. He was started on empiric Rocephin and doxycycline for CAP coverage. He was transferred to the intensive care unit after developing symptomatic bradycardia that required transvenous pacing. His clinical status improved after permanent pacemaker procedure on 11/25. Developed worsening shortness of breath secondary to fluid overload. Symptoms improved with Lasix. Developed AKI while on the Lasix. Nephrology was consulted. Urology consulted for hematuria. Foley was placed and hematuria resolved. Plan was to transition to a rehab given patient was medically optimized. However developed significant orthostatic hypotension which started on 12/01/2022 and worsening renal function likely from overdiuresis. Midodrine was added the patient continued to have significant orthostatic hypotension limiting therapy. Hospice was consulted for informational meeting. Consults: EP Critical care Nephrology Palliative Urology " Interim hospital course: Patient coming in with shortness of breath, initially treated for community-acquired pneumonia transfer to the intensive care unit initially for symptomatic bradycardia other required pacing, ultimately patient underwent pacemaker placement 11-25 developed fluid overload and improved with Lasix administration subsequently developing Aki which also improved prior to discharge. Urology was consulted for hematuria, Foley catheter was placed with resolution patient initial plan was transition to rehab however on further goals of care after worsening hypotension on 12/01 and midodrine initiation goals of care were further discussed and patient was open to hospice informational meeting. Discussion had with Hospice and decision was made to transition to home hospice with discharge on 12/09/2022 in medically stable condition. Patient to follow-up in enroll in Hospice on return home. Previous VAERS submitted 906617

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Praegender Schweregrund: Intensive care
Hospital-Tage: 16,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Interstitial lung disease Asbestosis Diaphragmatic hernia without obstruction or gangrene Allergic rhinitis, unspecified Hypoxia CAD in native artery Mediastinal lymphadenopathy Aortic stenosis Cardiomyopathy CHF (congestive heart failure) AAA (abdominal aortic aneurysm) PAF (paroxysmal atrial fibrillation) AV block, Mobitz 1 Ascending aorta dilatation Presence of prosthetic heart valve Presence of aortocoronary bypass graft Chronic diastolic (congestive) heart failure Bradycardia, unspecified Bradycardia Cardiac pacemaker in situ Barrett's esophagus without dysplasia Anemia, unspecified Unspecified dementia, mild, without behavioral disturbance, psychotic disturbance, mood disturbance, and anxiety BPH (benign prostatic hyperplasia) Gross hematuria Hyperlipidemia Hypothyroidism, unspecified Closed compression fracture of third lumbar vertebra Status post aortic valve replacement Elevated PSA Hiatal hernia Memory loss Severe muscle deconditioning Presbyopia Muscle weakness (generalized) Multiple comorbid conditions Advance care planning
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet aspirin 81 MG EC tablet calcium-vitamin D (OSCAL-500) 500-200 MG-UNIT TABS per tablet donepezil (ARICEPT) 5 MG tablet levothyroxine (SYNTHROID) 50 MCG tablet midodrine (PROAMATINE) 5 MG tablet Multiple
Allergien: NKA
Vorherige Impfungen: -

VAERS 2528816

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

schwer

Staat: NY
Alter: 64,0
Geschlecht: F
Eingang: 12.12.2022
Impfdatum: 22.09.2022
Beginn: 26.10.2022
Tage bis Beginn: 34,0
Dosis: 5
Route/Site: IM / RA

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

COVID-19 Injury Loss of consciousness Rib fracture SARS-CoV-2 test positive

Symptomtext

I tested positive for COVID-19 on 10/26/22. I had no COVID-19 symptoms. I went into the bathroom and passed out and hit the cabinet and broke 2 ribs. Since I had just tested positive for COVID-19, I did not go to the hospital right away. I waited until I was done taking the prescription of PAXLOVID and went in. When I went to the ER, the did a PCR test and tested positive. I am doing much better now.

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Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: 26OCT2022 COVID-19 test positive; 31OCT2022 PCR COVID-19 test positive; 16NOV2022 PCR COVID-19 test positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Diabetic; Multiple Sclerosis; Seasonal Asthma
Andere Medikamente: REBIF; oxybutynin; ezetimibe; levothyroxine; calcium; vitamin D; magnesium
Allergien: Penicillin; GANTRISIN; sulfa
Vorherige Impfungen: -

VAERS 2484181

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

schwer

Staat: FL
Alter: 83,0
Geschlecht: F
Eingang: 20.10.2022
Impfdatum: 07.09.2022
Beginn: 15.09.2022
Tage bis Beginn: 8,0
Dosis: 1
Route/Site: IM / LA

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

Anticoagulant therapy Atrial fibrillation Cardiac monitoring Echocardiogram normal Loss of consciousness

Symptomtext

I passed out on the plane, and they took me off. On the way to baggage claims, I passed out again in the wheelchair. I went to the emergency room, and they diagnosed me with A-fib. I was given an IV and medication was added. They did an echogram. I was there all evening until I checked myself out. I was no longer having symptoms when I left. I had an appointment to see my cardiologist and he put me on a blood thinner. I was told to wear a heart monitor for 14 days so currently I do not know if my condition has improved. I had a mini stroke about 5 years ago and so the doctor asked that I stay on blood thinners. I feel like I have recovered but it is unknown what can happen today or tomorrow.

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Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Echogram normal 09/2022
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: SYNTHROID; ramipril; atorvastatin; aspirin
Allergien: Mango; ragweed
Vorherige Impfungen: -

VAERS 2476321

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

schwer

Staat: MA
Alter: 41,0
Geschlecht: F
Eingang: 12.10.2022
Impfdatum: 02.09.2022
Beginn: 03.09.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: SYR / RA

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

Chills Hand fracture Headache Menstruation delayed Nausea Pain Presyncope Pyrexia X-ray

Symptomtext

09/03/22 ~2 AM (~8 hrs after shot): body aches, chills, fever (up to 102.1?F), oppressive headache. 09/03/22 ~9 AM (~14 hrs after shot): add to previous symptoms an episode (~30 min?) of near-fainting (felt like vasovagal syncope, but lowering head to the floor stopped me from passing out completely) and nausea. Contemplate an ER visit if temp nears 103, but it does not. Aches, fever, chills persist for ~3 days before resolving. 09/20/22 ~4 PM (2.5 weeks after shot): Right thumb fractures while using tools with that hand. There was no obvious impact event that caused this fracture. Cause is still unknown. *Thumb fracture is the event I sought medical care for.* 09/20/22: Period expected, but does not come until10/10 (3 weeks late).

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Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: x-rays on 09/22/22
Aktuelle Erkrankungen: none
Vorgeschichte: anxiety, depression, ibs, overweight, ocular migraine/migraine with aura, gerd, carpal tunnel syndrome, mild psoriasis, raynaud's phenomenon
Andere Medikamente: fluoxetine 40 mg (2 capsules daily), bupropion 100 mg sr 12 hr (1 tablet twice daily), norethindrone 0.35 mg (1 tablet daily), cetirizine 10 mg (1 tablet daily), famotidine 20 mg (1 tablet twice daily), melatonin 1 mg (2 tablets around bedt
Allergien: dust mites
Vorherige Impfungen: aches, fever, bad night sweats, 40yo, 05/2/21, Pfizer COVID (2nd dose)

VAERS 2468059

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

schwer

Staat: NY
Alter: 78,0
Geschlecht: M
Eingang: 04.10.2022
Impfdatum: 21.09.2022
Beginn: 01.09.2022
Tage bis Beginn: -
Dosis: 5
Route/Site: OT / -

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

Bell's palsy Blood pressure measurement Insomnia

Symptomtext

This spontaneous case was reported by a patient and describes the occurrence of BELL'S PALSY (Bells Palsy / droopy mouth on the left side/left side of patient face and left/couldn't close left eye / can blink left eye, but not as much as my right eye / The doctor gave him an eye patch) in a 78-year-old male patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. AS7144B) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included Bradycardia and Pacemaker insertion (cardiac). Concurrent medical conditions included Seizure (medication was lowered last year) and Blood pressure. Concomitant products included COLECALCIFEROL (VITAMIN D3) for an unknown indication. 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. In September 2022, the patient experienced BELL'S PALSY (Bells Palsy / droopy mouth on the left side/left side of patient face and left/couldn't close left eye / can blink left eye, but not as much as my right eye / The doctor gave him an eye patch) (seriousness criterion medically significant). On 24-Sep-2022, the patient experienced INSOMNIA (couldn't get much sleep last night). At the time of the report, BELL'S PALSY (Bells Palsy / droopy mouth on the left side/left side of patient face and left/couldn't close left eye / can blink left eye, but not as much as my right eye / The doctor gave him an eye patch) and INSOMNIA (couldn't get much sleep last night) had not resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, Blood pressure measurement: Blood pressure was 120/81 at the doctor's and 119/79 in the hospital. It was unknown if other vaccines given within 1 month prior to Moderna COVID-19 vaccine. Concomitant products included unspecified medications for seizure, blood pressure, water pill, and multivitamin for 50 plus. Dose Number one for Moderna, Lot number: 014M20A Dose was unknown, date administered was 20-Feb-2021. Dose Number twofor Moderna, Lot number: 006B21A Dose was unknown, date administered was 29-Mar-2021. Dose Number 1st booster for Moderna, Lot number: 034F21A Dose was unknown, date administered was 10-Nov-2021. Dose Number 2nd booster for Moderna, Lot number: 057M21A Dose was unknown, date administered was 27-Apr-2022. The patient's family was vegetarian. He listed the medications that he took, and he mentioned that the dosages of his blood pressure and seizure medications were lowered. On the last night and this morning of report, the left side of his face and left with unintelligible. He went to the emergency room. They have given him a medication to help with the problem. They thought It was Bell's Palsy. He had a droopy mouth on the left side. He could not close his left eye. The doctor gave him an eye patch. He could not get much sleep last night. On the day of this report he could close that eye and blink it a bit, but it was not as much as his right eye. On the patient's forehead wrinkles were there, so it indicated he did not have a stroke. The patient had a follow up with his physician on Wednesday 28-Sep-2022. They had tested him for Lyme's Disease. patient states that there is wrinkling of the forehead in the right side. company comment-This spontaneous case concerns a 78-year-old male patient with unspecified concomitant medications indicated for seizure and blood pressure, who experienced the expected, serious (medically significant) adverse event of special interest Bell's palsy in the context of having received mRNA-1273 .222 Bivalent (Original AND Omicron BA.4/BA.5) vaccine given as fifth dose in the COVID-19 vaccination series. Onset latency could not be determined as the exact onset date of the event was not provided. Patient presented to the emergency room with normal blood pressure, droopy mouth on the left side, and inability to close the left eye for which he was given an eye patch and unspecified medication. On follow-up, it was reported that patient can close that eye and blink it a bit, but not as much as his right eye. Wrinkling of the forehead was present. Patient was tested for Lyme disease with undisclosed result. Patient previously received 4 other doses of mRNA-1273 vaccines consisting of a 2-dose primary series, and 2 booster doses. Concurrent medical conditions of seizure and blood pressure control (as reported indications of unspecified concomitant medications) could be considered as risk factors since impaired immunity from stress brought on by medical conditions have been considered as triggers. The benefit-risk relationship of mRNA-1273 .222 Bivalent (Original AND Omicron BA.4/BA.5) is not affected by this report. This case was linked to MOD-2022-650861 (Patient Link). Sender's Comments: This spontaneous case concerns a 78-year-old male patient with unspecified concomitant medications indicated for seizure and blood pressure, who experienced the expected, serious (medically significant) adverse event of special interest Bell's palsy in the context of having received mRNA-1273 .222 Bivalent (Original AND Omicron BA.4/BA.5) vaccine given as fifth dose in the COVID-19 vaccination series. Onset latency could not be determined as the exact onset date of the event was not provided. Patient presented to the emergency room with normal blood pressure, droopy mouth on the left side, and inability to close the left eye for which he was given an eye patch and unspecified medication. On follow-up, it was reported that patient can close that eye and blink it a bit, but not as much as his right eye. Wrinkling of the forehead was present. Patient was tested for Lyme disease with undisclosed result. Patient previously received 4 other doses of mRNA-1273 vaccines consisting of a 2-dose primary series, and 2 booster doses. Concurrent medical conditions of seizure and blood pressure control (as reported indications of unspecified concomitant medications) could be considered as risk factors since impaired immunity from stress brought on by medical conditions have been considered as triggers. The benefit-risk relationship of mRNA-1273 .222 Bivalent (Original AND Omicron BA.4/BA.5) is not affected by this report.

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Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: Test Name: Blood pressure; Result Unstructured Data: Blood pressure was 120/81 at the doctor's; Test Name: Blood pressure; Result Unstructured Data: 119/79 in the hospital.
Aktuelle Erkrankungen: Blood pressure; Seizure (medication was lowered last year)
Vorgeschichte: Medical History/Concurrent Conditions: Bradycardia; Pacemaker insertion (cardiac)
Andere Medikamente: VITAMIN D3
Allergien: -
Vorherige Impfungen: -

VAERS 2463092

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

schwer

Staat: NJ
Alter: 45,0
Geschlecht: M
Eingang: 28.09.2022
Impfdatum: 23.09.2022
Beginn: 24.09.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

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

Altered state of consciousness Angiogram normal Anion gap increased Blood bicarbonate decreased Computerised tomogram normal Cyanosis Echocardiogram normal Ejection fraction normal Electrocardiogram normal Electroencephalogram abnormal Fibrin D dimer increased Hypopnoea Magnetic resonance imaging normal Oral discharge Postictal state Supine position Syncope Tongue injury

Symptomtext

26 hours after the vaccine

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Praegender Schweregrund: Syncope
Hospital-Tage: 4,0
Labordaten: 9/24/22 around 12pm; Patient was found supine on floor after witnessed collapse (by 8 year old). I found him blue, copious oral secretions, shallow ineffective breathing pattern. Altered consciousness regained with loss to time, place, person. Regained full AAO consciousness within 30 minutes while EMS there. Behavior appears post-ictal. Left side tongue laceration noted that he doesn?t recall origin. Bicarb low; anion gap elevated; d-dimer elevated. BP 220s/120s; HR 140s-150s on EMS initial vitals. CT negative; EKG Tropinins WNL; MRI, CT-A clear. Screening EEG shows abnormal haziness that could be due to poor sleep in the hospital- done on day 3 of hospital admission to telemetry. No arrhythmias noted. Echo EF 55-65. He has baseline HTN treated with lisinopril and hypothyroidism treated with synthroid.
Aktuelle Erkrankungen: None
Vorgeschichte: HTN, hypothyroid
Andere Medikamente: Lisinopril, synthroid, melatonin
Allergien: None
Vorherige Impfungen: -

VAERS 2461593

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7144B

schwer

Staat: CA
Alter: 55,0
Geschlecht: F
Eingang: 27.09.2022
Impfdatum: 10.09.2022
Beginn: 28.10.2021
Tage bis Beginn: -
Dosis: 5
Route/Site: OT / -

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

Blood pressure measurement COVID-19 immunisation Electrocardiogram Electrocardiogram T wave abnormal Fibrin D dimer Full blood count Interchange of vaccine products Metabolic function test Pulmonary oedema SARS-CoV-2 test Troponin

Symptomtext

Then she felt like there was fluid in her lungs/ The patient is still feeling sick after the vaccine/She also felt her breathing slowed down/She also developed a mild intermittent cough/horrible fatigue/felt tired/She is exhausted when she slept; Patient had received 2-dose primary series of Pfizer COVID-19 vaccine prior to mRNA-1273.222 vaccination; Patient had received 2-dose primary series of Pfizer COVID-19 vaccine prior to mRNA-1273.222 vaccination; This spontaneous case was reported by a patient and describes the occurrence of PULMONARY OEDEMA (Then she felt like there was fluid in her lungs/ The patient is still feeling sick after the vaccine/She also felt her breathing slowed down/She also developed a mild intermittent cough/horrible fatigue/felt tired/She is exhausted when she slept) in a 55-year-old female patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. AS7144B) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included Foot surgery in 2021. Previously administered products included for Product used for unknown indication: Pfizer (Dose 1, Lot number: EW0151) on 07-Apr-2021, Pfizer (Dose 2 and Lot number: EW0171) on 28-Apr-2021. Past adverse reactions to the above products included Fatigue with Pfizer; and No adverse event with Pfizer. Concurrent medical conditions included Sulfonamide allergy (sulfa), Heterozygous familial hypercholesterolaemia (Familial heterozygous hypocholesteremia) since 2015, Chronic migraine since 2014 and Lipid metabolism disorder (lipid disorder). Concomitant products included ESTRADIOL, LEVONORGESTREL (CLIMARA PRO) and ESTRADIOL, NORETHISTERONE ACETATE (ESTRADIOL AND NORETHINDRONE) for an unknown indication. On 10-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 28-Oct-2021, the patient experienced INTERCHANGE OF VACCINE PRODUCTS (Patient had received 2-dose primary series of Pfizer COVID-19 vaccine prior to mRNA-1273.222 vaccination) and COVID-19 IMMUNISATION (Patient had received 2-dose primary series of Pfizer COVID-19 vaccine prior to mRNA-1273.222 vaccination). In September 2022, the patient experienced PULMONARY OEDEMA (Then she felt like there was fluid in her lungs/ The patient is still feeling sick after the vaccine/She also felt her breathing slowed down/She also developed a mild intermittent cough/horrible fatigue/felt tired/She is exhausted when she slept) (seriousness criterion medically significant). At the time of the report, PULMONARY OEDEMA (Then she felt like there was fluid in her lungs/ The patient is still feeling sick after the vaccine/She also felt her breathing slowed down/She also developed a mild intermittent cough/horrible fatigue/felt tired/She is exhausted when she slept), INTERCHANGE OF VACCINE PRODUCTS (Patient had received 2-dose primary series of Pfizer COVID-19 vaccine prior to mRNA-1273.222 vaccination) and COVID-19 IMMUNISATION (Patient had received 2-dose primary series of Pfizer COVID-19 vaccine prior to mRNA-1273.222 vaccination) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): In September 2022, Blood pressure measurement: 72/42. In September 2022, Electrocardiogram: The cardiologist read the patient recent ECG and said that patient had a T-wave abnormality as well as further repolarization abnormality since the prior reading. The rate was faster than the previous record. and Normal. In September 2022, Fibrin D dimer: Normal. In September 2022, Full blood count: Normal. In September 2022, Metabolic function test: Normal. In September 2022, SARS-CoV-2 test: Normal. In September 2022, Troponin: Normal. On an unknown date, Electrocardiogram T wave abnormal: Abnormal. The patient received Moderna first booster on 28-Oct-2021 lot number was ??0F21A and Moderna second booster on 03-Apr-2022 lot number 066K21A. The patient had put HRT patch in the morning of vaccination. The patient linked the event fluid in lung was due to air quality. The patient reported that she had a lipid disorder and a T-wave abnormality, so patient had a previous ECG to compare it to. The patient reported that after the second Pfizer dose, patient also felt fatigue, but did not had the feeling in chest. The patient removed the hormone patch on 14-Sep-2022 because it kept falling off and then also started taking unspecified pills on 14-Sep-2022. The patient had 3 home tests with result provided as normal. Patient reported that she was exhausted when she slept and woke up really exhausted and fatigue was pretty bad. No other treatment information was provided. Company Comment: This is a spontaneous case, reported by a patient, concerning a 55-year-old female patient with no relevant medical history reported, who experienced the unexpected serious (medically significant) adverse event of special interest Pulmonary oedema, reported as fluid in the lungs, which occurred on the same month after receiving a dose of mRNA-1273.222 as the fifth dose of COVID-19 vaccine. Patient had received 2-dose primary series of Pfizer COVID-19 vaccine with adverse event of fatigue, approximately 16 months and 1 week prior to mRNA-1273.222 vaccination (Interchange of vaccine products and Revaccination with different COVID-19 vaccine). Patient also received 2 previous doses of Moderna COVID-19 vaccine as 3rd and 4th COVID-19 vaccines. It was reported that the patient had horrible fatigue, exhausted, slowed breathing, mild intermittent cough, feeling of fluid in the lungs and blood pressure of 72/42. Patient underwent ECG and cardiologist's reading revealed T-wave abnormality with faster rate and further repolarization abnormality compared to the previous ECG. No further details about the treatments were provided. Outcome of the event was unknown. The benefit-risk relationship of mRNA-1273.222 is not affected by this report.; Sender's Comments: This is a spontaneous case, reported by a patient, concerning a 55-year-old female patient with no relevant medical history reported, who experienced the unexpected serious (medically significant) adverse event of special interest Pulmonary oedema, reported as fluid in the lungs, which occurred on the same month after receiving a dose of mRNA-1273.222 as the fifth dose of COVID-19 vaccine. Patient had received 2-dose primary series of Pfizer COVID-19 vaccine with adverse event of fatigue, approximately 16 months and 1 week prior to mRNA-1273.222 vaccination (Interchange of vaccine products and Revaccination with different COVID-19 vaccine). Patient also received 2 previous doses of Moderna COVID-19 vaccine as 3rd and 4th COVID-19 vaccines. It was reported that the patient had horrible fatigue, exhausted, slowed breathing, mild intermittent cough, feeling of fluid in the lungs and blood pressure of 72/42. Patient underwent ECG and cardiologist's reading revealed T-wave abnormality with faster rate and further repolarization abnormality compared to the previous ECG. No further details about the treatments were provided. Outcome of the event was unknown. The benefit-risk relationship of mRNA-1273.222 is not affected by this report.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary oedema
Hospital-Tage: -
Labordaten: Test Date: 202209; Test Name: Blood pressure measurement; Result Unstructured Data: 72/42; Test Date: 202209; Test Name: ECG; Result Unstructured Data: The cardiologist read the patient recent ECG and said that patient had a T-wave abnormality as well as further repolarization abnormality since the prior reading. The rate was faster than the previous record.; Test Date: 202209; Test Name: ECG; Result Unstructured Data: Normal; Test Name: T-wave abnormality; Result Unstructured Data: Abnormal; Test Date: 202209; Test Name: d-dimer; Result Unstructured Data: Normal; Test Date: 202209; Test Name: CBC; Result Unstructured Data: Normal; Test Date: 202209; Test Name: chem panel; Result Unstructured Data: Normal; Test Date: 202209; Test Name: PCR COVID test; Result Unstructured Data: Normal; Test Date: 202209; Test Name: troponin; Result Unstructured Data: Normal
Aktuelle Erkrankungen: Chronic migraine; Heterozygous familial hypercholesterolaemia (Familial heterozygous hypocholesteremia); Lipid metabolism disorder (lipid disorder); Sulfonamide allergy (sulfa)
Vorgeschichte: Medical History/Concurrent Conditions: Foot surgery
Andere Medikamente: CLIMARA PRO; ESTRADIOL AND NORETHINDRONE
Allergien: -
Vorherige Impfungen: -

VAERS 2458562

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge as7144b

schwer

Staat: MA
Alter: 62,0
Geschlecht: F
Eingang: 24.09.2022
Impfdatum: 09.09.2022
Beginn: 18.09.2022
Tage bis Beginn: 9,0
Dosis: 3
Route/Site: IM / RA

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

Bell's palsy Chills Headache Injection site erythema Injection site swelling Pyrexia

Symptomtext

Site: Redness at Injection Site-Severe, Site: Swelling at Injection Site-Severe, Systemic: Bell's Palsy-Medium, Systemic: Chills-Mild, Systemic: Fever-Mild, Systemic: Headache-Mild

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2451279

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

schwer

Staat: AZ
Alter: 63,0
Geschlecht: F
Eingang: 20.09.2022
Impfdatum: 06.09.2022
Beginn: 18.09.2022
Tage bis Beginn: 12,0
Dosis: 5
Route/Site: IM / RA

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

Bell's palsy Dyskinesia Eyelid function disorder Facial paralysis Facial paresis Neurological examination abnormal Hypoaesthesia oral

Symptomtext

Bell's Palsy, left side, onset 12 days after bivalent booster

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: office visit 9/19/2022 with neuro exam confirming peripheral facial nerve palsy on the left
Aktuelle Erkrankungen: none, no recent viral illnesses
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2450635

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge as7144b

schwer

Staat: CT
Alter: 26,0
Geschlecht: M
Eingang: 18.09.2022
Impfdatum: 06.09.2022
Beginn: 06.09.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: UN / UN

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

Bell's palsy Eye swelling Hypoaesthesia Injection site bruising Nervous system disorder

Symptomtext

Site: Bruising at Injection Site-Mild, Systemic: Bell's Palsy-Medium, Systemic: Neurological Disorder (diagnosed by MD)-Mild, Systemic: Numbness (specify: facial area, extremities)-Mild, Additional Details: complianed about facial numbness of tongue cheek and eye swelling on one side. I, the pharmacist on duty advised the patient to seek medicall attention asap. he has not seen a doctor yet? but did complain of neurologocal deficiets

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2450596

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

schwer

Staat: NJ
Alter: 74,0
Geschlecht: F
Eingang: 18.09.2022
Impfdatum: 09.09.2022
Beginn: 09.09.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / RA

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

Dizziness Mobility decreased Presyncope

Symptomtext

Approx 18 hours after vaccination lightheadedness and dizziness. Almost passed out. Had to stay in bed for about 2 hours until reaction subsided.

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Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: arthritis, depression.
Vorgeschichte: -
Andere Medikamente: atorvastatin, sertraline, omeprazole, trazadone, clonazepam.
Allergien: none
Vorherige Impfungen: -

VAERS 2444633

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

schwer

Staat: NC
Alter: 19,0
Geschlecht: F
Eingang: 14.09.2022
Impfdatum: 10.09.2022
Beginn: 10.09.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Dizziness Flushing Hyperhidrosis Nausea Syncope Unresponsive to stimuli

Symptomtext

Systemic: Dizziness / Lightheadness-Severe, Systemic: Fainting / Unresponsive-Severe, Systemic: Flushed / Sweating-Medium, Systemic: Nausea-Medium

Weitere VAERSDATA-Felder

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

VAERS 2442860

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7144B

schwer

Staat: CA
Alter: 74,0
Geschlecht: F
Eingang: 13.09.2022
Impfdatum: 09.09.2022
Beginn: 10.09.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: SYR / LA

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

Asthenia Blood test normal Chest X-ray normal Cold sweat Computerised tomogram normal Diarrhoea Dizziness Dyspnoea Electrocardiogram normal Fatigue Headache Immunisation reaction Nausea Pain in extremity Pyrexia Syncope Urine analysis normal

Symptomtext

Starting in the morning on Saturday 09/10/2022, I had a headache, low grade fever, fatigue and a sore arm. The next day, the headache was worse and the fatigue was very pronounced and the arm was more sore. I developed COVID-19 arm this day. On Monday 09/12/2022, I woke up feeling better, but I quickly became short of breathe, had cold sweats, diarrhea, nausea and light headedness making me feel like I was going to pass out. So, I called the emergency number. I went to the hospital who ran an EKG, did a full blood chemistry panel, urine test, chest X-ray and CT scan. Everything came back looking okay. They were unsure what caused it but thought it was a syncopal reaction. I am still tired to this day and feel quite weak, and I still have the COVID-19 arm.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: EKG; Blood Chemistry Panel; Urine Test; Chest X-ray; CT scan : All came back normal
Aktuelle Erkrankungen: None
Vorgeschichte: High Blood Pressure
Andere Medikamente: Lisinopril; Low Dose Aspirin; CoQ10; Colace; Vitamin B12 Complex; Metamucil
Allergien: Sudafed
Vorherige Impfungen: Pneumonia vaccine (2013): a week after receiving the vaccine, I was hospitalized due to my heart stopping for a few seconds.

VAERS 2440841

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

schwer

Staat: MA
Alter: 65,0
Geschlecht: F
Eingang: 12.09.2022
Impfdatum: 08.09.2022
Beginn: 08.09.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / RA

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

Dizziness Fall Flushing Hyperhidrosis Loss of consciousness Syncope Unresponsive to stimuli

Symptomtext

Systemic: Dizziness / Lightheadness-Severe, Systemic: Fainting / Unresponsive-Severe, Systemic: Flushed / Sweating-Mild, Additional Details: Patient reported experiencing symptoms above approximately 8 hours post vaccination. She reports no prior adverse reactions to 4 COVID vaccines or flu shots received for many years. She also reports no history of diabetes or hypotension. Patient was home alone during reaction and lost consciousness alternating between partial and full loss resulting in a fall for about 2 hours until spouse returned home and helped her into bed. Patient reports feeling back to normal today after awakening.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2440727

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

schwer

Staat: FL
Alter: 79,0
Geschlecht: F
Eingang: 12.09.2022
Impfdatum: 09.09.2022
Beginn: 10.09.2022
Tage bis Beginn: 1,0
Dosis: 5
Route/Site: IM / LA

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

Chills Fatigue Head injury Hyperhidrosis Loss of consciousness Malaise Pyrexia Spinal column injury

Symptomtext

On 9/9/22 in the evening I got chills,low grade fever,sweats,fatigue. Woke up at 7am 9/10 feeling general malaise in a pool of sweat, went back to bed until 10:30am. Stood at the sink to brush my teeth felt I was losing consciousness,tried to lower myself to the floor but passed out was on floor don?t know how long but when conscious again called for help injured my head and coccyx

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Ca, vitamin D3, Neuriva plus,sugar bear hair multi vit, Claritin, iprattopium nasal spray,rosuvastatin,CoQ10 ,estrogen 1grm biweekly
Allergien: Flat fish,
Vorherige Impfungen: -

VAERS 2440444

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7144B

schwer

Staat: NH
Alter: 40,0
Geschlecht: M
Eingang: 12.09.2022
Impfdatum: 06.09.2022
Beginn: 06.09.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Dizziness Seizure

Symptomtext

Systemic: Seizure-Mild, Additional Details: Patient got lightheaded and then began seizing for less than 1 minute. Patient did not disclose that this had already happened to him with the covid vaccine previously. Administrator was notified after vaccine was given. 911 was called. EMTs came to check vitals (all normal after seizure). Patient said he did not want to go to hospital because this happened to him before and he was fine after.

Weitere VAERSDATA-Felder

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

VAERS 2438680

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7144B

schwer

Staat: CA
Alter: 21,0
Geschlecht: F
Eingang: 10.09.2022
Impfdatum: 06.09.2022
Beginn: 06.09.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: SYR / LA

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

Dizziness Fall Nausea Palpitations Syncope Tachycardia Unresponsive to stimuli

Symptomtext

Systemic: Dizziness/Lightheadedness-Mild, Systemic: Fainting/Unresponsive-Mild, Systemic: Nausea-Mild, Systemic: Tachycardia-Mild. Additional details: About 5-10 minutes after vaccine given, patient fainted and fell. She complained of nausea and heart racing. We called the EMTs. They took her to ER.

Weitere VAERSDATA-Felder

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

VAERS 2696691

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7144B

moderat

Staat: NY
Alter: 33,0
Geschlecht: M
Eingang: 16.10.2023
Impfdatum: 13.09.2022
Beginn: 16.07.2023
Tage bis Beginn: 306,0
Dosis: 4
Route/Site: SYR / LA

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

Blood test normal Cardiac flutter Chest discomfort Chest pain Dyspepsia Echocardiogram normal Electrocardiogram normal Palpitations

Symptomtext

Heart palpitations, instant racing heart when bending down. Chest pressure, chest pain, excessive heart burn that is intermittent after palpitation/heart flutter and episodes.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: EKG 8/5-8/19, Echocardiogram 8/30-31/2023, Blood test 07/21/2023 All tests were unremarkable.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Nine
Allergien: Nickel
Vorherige Impfungen: -

VAERS 2684520

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

moderat

Staat: -
Alter: 67,0
Geschlecht: F
Eingang: 21.09.2023
Impfdatum: 17.09.2022
Beginn: 24.08.2023
Tage bis Beginn: 341,0
Dosis: 1
Route/Site: - / -

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

Acidosis Acute kidney injury Asthenia Azotaemia Bladder dilatation Blood bicarbonate decreased Blood creatinine abnormal Blood creatinine increased Blood lactic acid Blood sodium decreased Blood urea increased COVID-19 COVID-19 pneumonia Chest X-ray abnormal Chills Chronic kidney disease Condition aggravated Cough

Symptomtext

Patient is a 68 y.o. female patient of doctor, DO with history of DM2, CKD, hypothyroid, HTN, HLD, depression, chronic pain, presented to Hospital with cough, weakness, chills, shortness of breath . Patient did not have any hypoxia during this hospitalization. Found to have dehydration and acute kidney injury on chronic kidney disease, given IV fluids, symptoms are improving. She has nausea and a headache but tolerating diet. Feels comfortable going home later this evening Assessment and plan Pneumonia due to COVID-19 URI symptoms resolved Positive for COVID-19 on 8/24/2023 CXR in the ED with bilateral lower lobe opacities Labs in the ED significant for COVID 19 positive, creatinine 3.57, BUN 104, bicarb 17, sodium 133, lactic acid 1.5 Received IV fluids, antibiotics discontinued Did not develop hypoxia AKI on CKD unknown stage Severe uremia Baseline creatinine around 1.1-1.3 Renal ultrasound showed nonobstructive right intrarenal calculi with otherwise unremarkable renal ultrasound with bladder mildly distended and otherwise unremarkable. Simple cyst measuring 2.2 x 2.7 x 2.3 cm on left kidney Creatinine on admission 3.57-- > 2.49 with HCO3 down to 16. Started bicarb gtt, acidosis resolved, back to NS Avoid nephrotoxic agents Serum creatinine continues to improve. Discontinue spironolactone Continue candesartan and hydrochlorothiazide at time of discharge Also on Jardiance for renal protection Follow-up BMP in 4 days after discharge Type 2 diabetes mellitus without long term insulin use Continue Jardiance Hypothyroidism Continue synthroid HTN Restart candesartan/hydrochlorthiazide at time of discharge Patient advised to check BP twice a day. Same place, same machine, same time. Maintain log and follow up with primary care physician in 1 week. Call primary care physician office if SBP consistently >180 or <90 HLD Continue statin Depression Continue bupropion and Latuda Chronic pain Continue gabapentin

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2674258

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7144B

moderat

Staat: -
Alter: 54,0
Geschlecht: F
Eingang: 21.08.2023
Impfdatum: 08.09.2022
Beginn: 19.04.2023
Tage bis Beginn: 223,0
Dosis: 3
Route/Site: IM / LA

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

Cardiac failure acute Hypervolaemia Left ventricular failure Pulmonary hypertension Transient ischaemic attack

Symptomtext

G45.9 TRANSIENT CEREBRAL ISCHEMIA 4/12/2023 DIASTOLIC HEART FAILURE, ACUTE ON CHRONIC G45.9 TRANSIENT CEREBRAL ISCHEMIA 4/12/2023 HYPERVOLEMIA G45.9 TRANSIENT CEREBRAL ISCHEMIA 4/12/2023 PULMONARY HTN

Weitere VAERSDATA-Felder

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

VAERS 2635421

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7144B

moderat

Staat: -
Alter: 63,0
Geschlecht: F
Eingang: 23.05.2023
Impfdatum: 07.09.2022
Beginn: 08.10.2022
Tage bis Beginn: 31,0
Dosis: 4
Route/Site: IM / LA

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

Hypotension

Symptomtext

PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE HYPOTENSION

Weitere VAERSDATA-Felder

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

VAERS 2631187

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

moderat

Staat: MO
Alter: 58,0
Geschlecht: M
Eingang: 12.05.2023
Impfdatum: 29.09.2022
Beginn: 31.01.2023
Tage bis Beginn: 124,0
Dosis: 5
Route/Site: IM / LA

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

Biopsy kidney Blood test Fluid retention General symptom Hypotonia Influenza Pneumonia Rest regimen

Symptomtext

Around March 2023, I went in for a kidney biopsy. At this time, I was diagnosed with Pneumonia and the Flu. I was in the hospital for a whole week. They treated the symptoms. I retained a lot of water. I shredded 20 liters of water the week I was in the hospital. I was on oxygen. I was on bed rest and moved around as much as I could. I did not have any surgeries or go into ICU. They were constantly drawing my blood. I was discharged to home oxygen, I had home occupational therapy and home physical therapy for 10 days. I was not steady on my feet and physical therapy helped get some of my muscle tone back. I followed up with Dr.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pneumonia
Hospital-Tage: 7,0
Labordaten: MAR2023 Blood work, too many to list
Aktuelle Erkrankungen: None
Vorgeschichte: Type 2 Diabetes
Andere Medikamente: Amlodipine; baby aspirin; atenolol; LEXAPRO; losartan; THER-M vitamin; KLOR-CON N20 potassium; 2 types of vitamin D; torsemide; simvastatin; HUMALOG; BASAGLAR KWIKPEN
Allergien: None
Vorherige Impfungen: -

VAERS 2631171

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

moderat

Staat: IA
Alter: 49,0
Geschlecht: F
Eingang: 12.05.2023
Impfdatum: 10.11.2022
Beginn: 20.02.2023
Tage bis Beginn: 102,0
Dosis: 4
Route/Site: SYR / LA

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

Bronchitis Dyspnoea exertional Fatigue Laboratory test abnormal Lung disorder Malaise Myalgia Oropharyngeal pain Peripheral swelling Upper respiratory tract infection

Symptomtext

My COVID-19 symptoms started on 02/20/2023 in the morning. I had a sore throat, lungs were bad condition. I am now diagnosed with Bronchitis. I went to my doctor's office on 02/21/2023 . My right arm to leg is swollen up my doctor said if it doesn't go down I will be getting more testing done but as of now its getting better. My doctor prescribed me with Prednisone, Arnuity inhaler, Benzonatate , Albuterol, Vitamin C .After running some tests my doctor as having upper respiratory infections. I still have exhaustion and muscles pain. My lungs are weak because I can't walk up the stairs I get shortness of breath.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea exertional
Hospital-Tage: -
Labordaten: 21FEB2023 Bronchitis Test - Positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Seasonal Allergies; High Cholesterol; Pre-Diabetes
Andere Medikamente: Atorvastatin; Metformin; Topiramate; Omeprazole
Allergien: Erythromycin; Seasonal Allergies
Vorherige Impfungen: All COVID-19 vaccines- Arm got red and swollen

VAERS 2621516

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

moderat

Staat: OH
Alter: 68,0
Geschlecht: F
Eingang: 26.04.2023
Impfdatum: 20.09.2022
Beginn: -
Tage bis Beginn: -
Dosis: 5
Route/Site: IM / LA

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

Hypertension Pain in extremity

Symptomtext

I had a sore arm after receiving the vaccine for about a day. My husband passed away on 07/05/2022. It was recommended that I see my doctor for a checkup after he passed away. I was diagnosed with hypertension on 10/02/2022. I am on medication to control the hypertension. It is not ideal, but it is better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Overweight
Andere Medikamente: Vitamin D; Multivitamin; Tylenol; Advil
Allergien: Norvasc
Vorherige Impfungen: -

VAERS 2619046

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

moderat

Staat: NY
Alter: 73,0
Geschlecht: M
Eingang: 21.04.2023
Impfdatum: 12.09.2022
Beginn: 10.12.2022
Tage bis Beginn: 89,0
Dosis: 5
Route/Site: IM / RA

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

COVID-19 Hypertension Nasopharyngitis Pain Pyrexia SARS-CoV-2 test positive Sinus headache

Symptomtext

In December 2022, I came down with COVID-19 after taking a test. I contacted my doctor who prescribed me Paxlovid. After taking the treatment, about 7-8 days later, I tested positive again for rebound COVID-19 after having a low-grade fever, body aches, sinus headache, and general cold-like symptoms. I informed my doctor again and was advised to just rest and let it run its course the second time around. Since then, I've recovered with no residual symptoms. About one month later, I was diagnosed with hypertension following my rebound COVID-19 infection.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: 10DEC2022 -- COVID-19 - Positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Hypothyroidism; High Cholesterol
Andere Medikamente: Levothyroxine; Rosuvastatin; Rocklatan; Dorzolamide Timolol; Multivitamin; Vitamin D3
Allergien: Ciprol
Vorherige Impfungen: -

VAERS 2617725

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

moderat

Staat: NY
Alter: 66,0
Geschlecht: M
Eingang: 19.04.2023
Impfdatum: 09.09.2022
Beginn: 07.10.2022
Tage bis Beginn: 28,0
Dosis: 5
Route/Site: SYR / LA

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

COVID-19 Condition aggravated Cough SARS-CoV-2 test positive

Symptomtext

10/7/2022 Started with a cough. Cough got worse 10/8. 10/9 Tested with an At Home COVID-19 test, positive. Went to Walk in clinic. Tested there with Rapid COVID-19 test, positive. Doctor recommended participant go to the Hospital. Proscribed Paxlovid but cautioned to consult with PCP due to possible medical interaction. At Hospital I received a one-time infusion of I believe Remdesivir. Release from hospital after infusion and had a pill for coughing proscribed. Over the next 10 days there was a few instances of mild fever hitting 99 degrees, cough diminished.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: 9Oct2022 At Home COVID-19 test, positive and Rapid COVID-19 test, both positive.
Aktuelle Erkrankungen: NA
Vorgeschichte: High Blood Pressure; Coronary Artery disease
Andere Medikamente: Clopidol; Metoprolol; Rosuvastatin; Potassium Chloride; Triamterene; Losartan; Azelastine Nasal Spray; Levocetirizine; Aspirin; Glucosamine; Coq 10
Allergien: NA
Vorherige Impfungen: -

VAERS 2610805

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

moderat

Staat: NH
Alter: 65,0
Geschlecht: M
Eingang: 06.04.2023
Impfdatum: 13.09.2022
Beginn: 20.09.2022
Tage bis Beginn: 7,0
Dosis: 5
Route/Site: IM / LA

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

Blood pressure systolic increased Condition aggravated Electrocardiogram normal Migraine

Symptomtext

Migraines went from a few a year to multiple per week continuing until present. Blood pressure went from normal to high (systolic formally 110?s, went up to 150?s).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: EKG - normal. Lab work pending.
Aktuelle Erkrankungen: None.
Vorgeschichte: Rare migraine headaches.
Andere Medikamente: Vitamin D, Niacinimide, AREDS-2, Fish Oil, Doxycycline (25mg)
Allergien: -
Vorherige Impfungen: -

VAERS 2604418

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

moderat

Staat: OH
Alter: 66,0
Geschlecht: F
Eingang: 27.03.2023
Impfdatum: 11.09.2022
Beginn: 09.02.2023
Tage bis Beginn: 151,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Dysgeusia Dyspnoea Fatigue Insomnia Malaise Oropharyngeal pain Pain Pharyngitis streptococcal Rhinorrhoea SARS-CoV-2 test positive Streptococcus test positive Vomiting

Symptomtext

On 2/9/2023, I had a runny nose and sore throat. I was on a cruise at the time. On 2/10/2023, I continued to get sicker with a very runny nose, body aches, and fatigue. I flew home that day. I was so out of breath that it took me an hour to walk from the plane to the shuttle at the airport, because I kept stopping on account of being out of breath. I threw up once that day. I woke up very sick the morning of 2/11/2023. I did a home antigen test, which immediately yielded a positive result. I then called my doctor, who prescribed me PAXLOVID, which I began taking on 2/12/2023. The runny nose, sore throat, and fatigue lasted for maybe ten days. The PAXLOVID left a foul taste in my mouth. I then felt better on 2/14/2023 and 2/15/2023, only to develop strep throat subsequently. I tested positive for strep throat on 2/25/2023. I had assumed that the symptoms of what I now know to be strep throat were just a continuation of the COVID-19. It took about twelve days for me to recover from the strep throat. On 2/25/2023, I was given a rapid test for COVID-19, and the result was negative. At the time of this writing, I'm doing fine, except I'm having trouble sleeping at night. I don't think it's COVID-19 related, but I do think that my illnesses may have thrown off my sleep cycle.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 11FEB2023 home antigen test, positive result; 25FEB2023 rapid antigen test, negative result; 25FEB2023 Streptococcus test, positive result
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetes, Type II; Prinzmetal Angina; Hypothyroidism
Andere Medikamente: Levothyroxine; bupropion; LEXAPRO; losartan; metoprolol succinate; metformin; amlodipine; baby aspirin; CRESTOR; PRILOSEC
Allergien: None
Vorherige Impfungen: -

VAERS 2603558

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

moderat

Staat: PA
Alter: 53,0
Geschlecht: F
Eingang: 24.03.2023
Impfdatum: 16.09.2022
Beginn: 17.01.2023
Tage bis Beginn: 123,0
Dosis: 3
Route/Site: IM / RA

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

Blood test normal Chest X-ray abnormal Chest discomfort Computerised tomogram normal Cough Dyspnoea Echocardiogram normal Electrocardiogram normal Headache Impaired work ability Pneumonia bacterial Pulmonary pain Pyrexia Respiratory tract congestion SARS-CoV-2 test negative

Symptomtext

I had a cough, congestion, headache, pain in my lung, chest heaviness, shortness of breath. I was at home and over the weekend was using over the counter medication trying to get relief. On Monday I had a fever of 101F, I called work they told me not to come in and my doctor called in a Medrol dose pack. I immediately started taking ibuprofen to get my fever down and taking the dose. By Tuesday, I wasn't getting any better, I went to the emergency room of the hospital I work at thinking I would just get a nebulizer treatment and go home. They ran PCR COVID-19 test, bloodwork, EKG. echocardiogram, chest x-ray, CT scan. The chest x-ray showed that I had a bacterial infection in my lung and I was admitted into the hospital. All other test were negative.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 3,0
Labordaten: 17JAN2023 PCR COVID-19 - negative; 17JAN2023 EKG - negative; 17JAN2023 Echocardiogram - negative; 17JAN2023 Bloodwork - negative; 17JAN2023 Chest x-ray - positive for a bacterial infection; 17JAN2023 CT scan - negative;
Aktuelle Erkrankungen: No
Vorgeschichte: Diabetes; Hypertension; Asthma
Andere Medikamente: Verapamil; Hydrochlorothiazide; Singulair; Metformin; Escitalopram; Multivitamin;
Allergien: Penicillin; Shellfish
Vorherige Impfungen: -

VAERS 2602382

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

moderat

Staat: TX
Alter: 59,0
Geschlecht: F
Eingang: 23.03.2023
Impfdatum: 20.09.2022
Beginn: 04.10.2022
Tage bis Beginn: 14,0
Dosis: 5
Route/Site: SYR / LA

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

Mobility decreased Pain in extremity Periarthritis

Symptomtext

I experienced soreness in my arm feels like I've been stabbed with a needle I now have frozen shoulder and I'm not able to move my arm up and down.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Ropinirole
Allergien: Betadine
Vorherige Impfungen: -

VAERS 2601792

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

moderat

Staat: MA
Alter: 61,0
Geschlecht: F
Eingang: 22.03.2023
Impfdatum: 12.09.2022
Beginn: 18.10.2022
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 Cardiac disorder Heart rate increased Hypertension Periarthritis Pyrexia SARS-CoV-2 test positive X-ray

Symptomtext

I really felt good the whole time. I felt good beside for 3 hours that I tested positive for COVID, which was October 18, 2023. I barely had a fever. Other than that, I felt good. I also developed a frozen shoulder. I had that for three months. It has since gone away. I did go get x-ray on January 8th. January 18, 2023, I started having weird heart problems. I had irregular heartbeat. I have also had high blood pressure. My heart rate would spike and my blood pressure. I haven't had any of those symptoms for a few weeks now.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: ZYRTEC; FLONASE
Allergien: N/A
Vorherige Impfungen: -

VAERS 2601789

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

moderat

Staat: GA
Alter: 80,0
Geschlecht: M
Eingang: 22.03.2023
Impfdatum: 16.09.2022
Beginn: 05.01.2023
Tage bis Beginn: 111,0
Dosis: 5
Route/Site: IM / LA

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

Blood glucose decreased COVID-19 Computerised tomogram normal Condition aggravated Feeling abnormal Pyrexia SARS-CoV-2 test negative SARS-CoV-2 test positive Urinary tract infection Urine analysis abnormal

Symptomtext

I had a high fever, I took a home COVID-19 that came back negative. I felt awful so my wife and I decided to go to the emergency room. Once in the emergency room they ran a PCR COVID-19 test that came back positive and ran a urinalysis test that came back positive for a UTI. My sugar dropped down while I was in the hospital to 32 and 33. I was given antibiotics to get rid of the UTI and they gave me glucose and ice cream to get my glucose numbers. I was sent home once my glucose levels were up to safe levels. I am currently taking medication for a possible staph infection that I may have gotten while in the hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: 5JAN2023 Home COVID-19 test - negative; 5JAN2023 Home PCR COVID-19 test - positive; 5JAN2023 Urinalysis test - positive; 5JAN2023 CT scan - negative
Aktuelle Erkrankungen: UTI
Vorgeschichte: Diabetes II
Andere Medikamente: Baby Aspirin
Allergien: No
Vorherige Impfungen: -

VAERS 2601761

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7144B

moderat

Staat: VA
Alter: 72,0
Geschlecht: F
Eingang: 22.03.2023
Impfdatum: -
Beginn: 21.02.2023
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Dyspnoea Influenza virus test negative Paranasal sinus discomfort Respiratory acidosis Respiratory tract congestion SARS-CoV-2 test positive Sinus congestion Sinus headache Sinusitis

Symptomtext

2/21/2023 I thought I had a sinus infection. I had head congestion and sinus pressure. On 2/22/23 I took an at home COVID test that was negative. I also took one on 2/23/23 that was negative. The night of 2/25/23 I got a really bad sinus headache. The next day I had an awful headache. My sinuses were so swollen, I could not breathe and was unable to open my sinuses up. That day, 2/26/23, I went to urgent care. I was tested for Flu and COVID. Flu was negative and COVID was positive. The doctor prescribed Paxlovid which I started taking that day. Within about 8 hours, my headache was gone. I took the Paxlovid for 5 days. After that , I felt like I was recovered. I took an at home COVID test on 3/7/23 and it was negative. Around 3/10/23 I began having congestion again. I tested positive for COVID on an at home COVID test. It was very mild sinus issues, not at all like the first time. I have recovered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 22FEB23- At Home COVID - Negative; 23FEB23- At Home COVID test - Negative; 26FEB23- Flu test - Negative; 26FEB23- COVID Test-Positive; 7MAR23 At Home COVID - Negative; 10MAR23-At Home COVID test - Positive
Aktuelle Erkrankungen: None
Vorgeschichte: Breast cancer, Lupus, Hypothyroidism
Andere Medikamente: Anastrozole, Plaquenil , Synthroid, Topiramate, Flonase, Vitamin D, One a Day Vitamin
Allergien: NSAIDs, Sulphur, Cephalosporins, Both kinds of Tetanus
Vorherige Impfungen: 2nd COVID (date uknown( felt a lump and later diagnosed with Breast Cancer

VAERS 2600403

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

moderat

Staat: NJ
Alter: 64,0
Geschlecht: F
Eingang: 21.03.2023
Impfdatum: 19.09.2022
Beginn: 18.03.2023
Tage bis Beginn: 180,0
Dosis: 5
Route/Site: IM / RA

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

COVID-19 Chills Cough Dizziness Headache Heart rate increased Oropharyngeal pain Pyrexia Rhinorrhoea SARS-CoV-2 test positive Tremor

Symptomtext

I had a sore throat, cough, running nose, headache, chills, fever of 101.3. Shakes, and high heart rate. I tested positive for COVID-19 at home. I talked to my doctor, and they said I could have Paxlovid but I decided not to take it. Now I am feeling dizzy.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: 03/19/2023, Positive, COVID-19 Test
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: B12; Vitamin D
Allergien: Walnuts; Pecans; Latex; Zithromycin; Eye Whites
Vorherige Impfungen: -

VAERS 2600047

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

moderat

Staat: LA
Alter: 72,0
Geschlecht: F
Eingang: 21.03.2023
Impfdatum: 19.09.2022
Beginn: 01.10.2022
Tage bis Beginn: 12,0
Dosis: 5
Route/Site: IM / LA

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

Blood cholesterol increased Blood test abnormal Cardiac stress test abnormal Cardiac valve disease Chest pain Computerised tomogram abnormal Echocardiogram Electrocardiogram abnormal Hypertension Scan with contrast abnormal

Symptomtext

I started experiencing mild chest pains that would occur throughout the day or wake me up at night. I went to the doctor, and they advised that I had high cholesterol and high blood pressure through a blood test on November 30, 2022. They ran heart test and referred me to a cardiologist who prescribed Rosuvastatin. The cardiologist ran more test, and they prescribed Amlodipine Desolate. My condition has improved. I rarely have the chest pain and my blood pressure is normal.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Stress Test-January 16, 2023-Abnormal Test results EKG-November 30, 2022-Diagnosed with high cholesterol and high blood pressure. December 29, 2022 Echocardiogram-January 2023 CT Scan with Contrast-January 23, 2023-Twisted Aorta Valve found-no surgery required
Aktuelle Erkrankungen: N/A
Vorgeschichte: Osteo Arthritis
Andere Medikamente: Tramadol; Hydrocodone; Xyzal; Fluticasone Propionate
Allergien: Anti inflammatorys; Pollen; Poison Ivy; Oak
Vorherige Impfungen: -

VAERS 2599485

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

moderat

Staat: OH
Alter: 71,0
Geschlecht: M
Eingang: 20.03.2023
Impfdatum: 17.09.2022
Beginn: 23.02.2023
Tage bis Beginn: 159,0
Dosis: 4
Route/Site: IM / LA

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

Blood test abnormal COVID-19 Feeling abnormal Pyrexia SARS-CoV-2 test positive Tremor White blood cell count increased

Symptomtext

On 02/23/2023, I felt weird in the morning. I took a home COVID-19 test later that morning. It was positive. I developed a fever about 102, I got the shakes and went to bed. I called Dr who said to alternate Ibuprofen and Advil and he prescribed Paxlovid. I had a couple of good days and then my fever returned. I went to see my doctor.. They ran blood tests and white blood was elevated. He gave me a prescription with an antibiotic. I have been fever free for 72 hours.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: 23FEB2023 COVID-19 Test - Positive; 06MAR2023 - Bloodwork- Elevated White Blood
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Cholesterol Medicine; Testosterone
Allergien: Lavender
Vorherige Impfungen: -

VAERS 2598598

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

moderat

Staat: MA
Alter: 74,0
Geschlecht: F
Eingang: 17.03.2023
Impfdatum: 14.09.2022
Beginn: 29.12.2022
Tage bis Beginn: 106,0
Dosis: 4
Route/Site: SYR / AR

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

Blood pressure increased COVID-19 Chest X-ray normal Cough Hypertension Laboratory test normal Rhinorrhoea SARS-CoV-2 test positive Wheezing

Symptomtext

I developed what felt like a cold cough and a runny nose, the of 29DEC2022 and 30DEC2022 I woke coughing and wheezing I took MUCINEX and felt better but the second time I wanted to be seen but it was a Friday night and I had to go to urgent care so I went 31DEC2022 a multi test was ran and the results were negative as was a chest x-ray. I was put on an albuterol inhaler and was told to continue MUCINEX and other fluids. Towards the end of the next week I was called by the Physician assistant regarding a report they wanted to see me about on 10JAN2023. At my exam I had wheezing and heavy coughing my blood pressure 224/100 it came down to 160/90 in about fifteen minutes. I was given FLOVENT, losartan and had me come back two days later and my medication was adjusted for my hypertension. I was seen on 12JAN2023, 18JAN2023, and on 25JAN23023. On 08FEB2023 my HBP was 140/80 and my medication was adjusted to losartan. 13FEB2023 my visit showed my HBP was stable.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: COVID-19 test positive.
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetes
Andere Medikamente: Metformin; vitamin D3; vitamin B12; magnesium; coQ10
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 2598570

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

moderat

Staat: NC
Alter: 74,0
Geschlecht: F
Eingang: 17.03.2023
Impfdatum: 04.09.2022
Beginn: 29.12.2022
Tage bis Beginn: 116,0
Dosis: 5
Route/Site: SYR / LA

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

Asthma COVID-19 Chest pain Condition aggravated Drainage Ear inflammation Eye inflammation Feeling abnormal Inflammation Oropharyngeal pain Respiratory disorder Respiratory tract congestion SARS-CoV-2 test positive Wheezing

Symptomtext

I tested positive for COVID-19 on 12/29/2022. I just had fever, but it wasn't particular highly. My temperature was 99.2 which is higher for me. Pulse was 65 and respirations were 16. My chest was hurting but I had 95% oxygen. I had congestion, drainage, and a sore throat. My heart was okay, but I was wheezing. I could feel asthma symptoms and I could feel like my airways were getting constricted. I can go from normal to bad asthma. I was prescribed PAXLOVID 300mg twice daily at urgent care. I also had prednisone 20mg twice daily for 7 days. I had a lot of inflammation around ears, eyes and throat from COVID-19. I felt so awful and I knew something was wrong. I woke up and said my throat hurt and felt deathly. My husband and our son also had COVID-19. We were all vaccinated as well. It wasn't so serious, but it was very spreadable. It took about another week or so to fully recover.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 29DEC2022 COVID-19 rapid test positive
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma; Hypertension; Hyperparathyroidism; MGUS; Obesity
Andere Medikamente: Amlodipine; carvedilol; olmesartan; rosuvastatin; albuterol inhaler; fluticasone; coQ10; CLARITIN nasal spray; azelastine HCI; multivitamin; lutein; guaifenesin; PROLIA shot; vitamin D
Allergien: Penicillin; GANTRISIN; BACTRIM
Vorherige Impfungen: -

VAERS 2598569

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

moderat

Staat: GA
Alter: 72,0
Geschlecht: F
Eingang: 17.03.2023
Impfdatum: 14.09.2022
Beginn: 05.02.2023
Tage bis Beginn: 144,0
Dosis: 5
Route/Site: SYR / RA

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

Abdominal pain Abdominal pain upper Aphonia Blood calcium decreased Cough Dehydration Diarrhoea Dysphagia Fatigue Feeding disorder Hypotension Influenza B virus test positive Pain Respiratory symptom SARS-CoV-2 test negative Urinary tract infection Vomiting

Symptomtext

I had severe diarrhea and vomiting for about 24 hours. I went to the ER while on a trip and got IV fluids there. The tested me for COVID-19 and the Flu and it was negative. They gave me fluids and medicine to slow down the symptoms. At the end of the 24 hour period I started coughing and respiratory symptoms. A week later we came back home, I couldn't eat, swallow, and lost my voice. I had deep achiness and went to the ER here locally. On February 13 I was admitted to the hospital and released on the 14th. I had low blood pressure, a UTI, low calcium and dehydration and a severe low cough. After I was discharged the weeks following, I was mostly treated for coughing with prescription cough medicine. The severe fatigue lasted for about four weeks now it's more periodic fatigue. I am very tired now. Also I am having abdominal pain and periodic stomach pains. The other symptoms of coughing all gone just fatigue. In the hospital while on the trip they didn't detect Influenza B, but they picked it up in my local HCF.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dehydration
Hospital-Tage: 2,0
Labordaten: 13FEB2023 COVID-19 test negative; 13FEB2023 Influenza test positive Influenza B
Aktuelle Erkrankungen: N/A
Vorgeschichte: Crohn's Disease
Andere Medikamente: SYNTHROID; calcium; vitamin D; omega 3
Allergien: Dairy products; penicillin
Vorherige Impfungen: -

VAERS 2598541

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

moderat

Staat: IN
Alter: 72,0
Geschlecht: M
Eingang: 17.03.2023
Impfdatum: 14.09.2022
Beginn: 11.02.2023
Tage bis Beginn: 150,0
Dosis: 5
Route/Site: SYR / AR

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

COVID-19 Cough Dyspnoea Fatigue Oropharyngeal pain Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

I had sore throat and the next day I took the test. I contacted my doctor after I took a home test and it came back as positive. I contacted my doctor via telephone. He prescribed me Paxlovid, the sore throat stopped in a couple of days. There were other symptoms with cough, congestion and fatigue. I am now having continuing shortness of breath and cough.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 13FEB2023 COVID-19 Home Test - Positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Finasteride; Eliquis; Metoprolol; Multivitamin; Prevacid
Allergien: N/A
Vorherige Impfungen: -

VAERS 2597620

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

moderat

Staat: FL
Alter: 75,0
Geschlecht: F
Eingang: 16.03.2023
Impfdatum: 08.09.2022
Beginn: 21.09.2022
Tage bis Beginn: 13,0
Dosis: 4
Route/Site: IM / LA

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

Atrial fibrillation Chest X-ray normal Computerised tomogram normal Condition aggravated Electrocardiogram ambulatory abnormal Full blood count normal Heart rate increased

Symptomtext

After 09/01/2021 I started experiencing an increased HR. I visited the ER in 10/2021 because my HR was about 160BPM I was put on a holter monitor for 3 day and I was diagnosed with Atrial Fibrillation . I was prescribed Eliquis and Metoprolol. I have had 13 episodes of AFIB since receiving the vaccination in 09/2021. I am currently scheduled for a Cardiac ablation.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: 10/23/2021 Chest x-ray - normal 10/23/2021 CBC - normal 10/23/2021 CT Scan - normal
Aktuelle Erkrankungen: None
Vorgeschichte: Gastritis; Gout; Atrial fibrillation; Indigestion; High Cholesterol; Chronic Asthma
Andere Medikamente: Metoprolol; Diltiazem; Valstatin; Albuterol Inhaler; Levothyroxine; Fluticasone nasal spray; Simpastatin; Rizatriptan; Eliquis
Allergien: None
Vorherige Impfungen: -

VAERS 2597032

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

moderat

Staat: TX
Alter: 67,0
Geschlecht: M
Eingang: 15.03.2023
Impfdatum: 12.09.2022
Beginn: 01.03.2023
Tage bis Beginn: 170,0
Dosis: 5
Route/Site: IM / AR

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

Abdominal pain Ageusia Asthenia COVID-19 Chest pain Cough Feeling abnormal Headache Influenza like illness Rhinorrhoea SARS-CoV-2 test positive Sinus disorder Somnolence Throat irritation

Symptomtext

3/1/2023 That night I began to have a scratchy, dry cough. The next day, I was really bad that morning. In addition to the scratchy dry cough, I was very weak all over and had a headache, nasal drainage, chest and abdominal pain from coughing so hard. I was so weak, I had to stay in bed all day. I self-medicated that night with Robitussin DM, Alka-Seltzer Cold and Flu tablets, Cold gel caps and had strong ginger tea. It felt like I had the flu. 3/3/23 when I woke up, I felt like I had taken too much medication and felt really bad. I had a bad headache and groggy. I had a temperature of around 100 degrees. At dinner, I noticed my taste buds had gone, no ability to taste anything. I took an at home COVID test and it was positive. I tried to find an Urgent Care that night and was unable to find a place to go to or someone to talk to. I reached an online conference with MD live. She told me I needed to get on Paxlovid. I went to the Emergency Room and was prescribed Paxlovid. I started on the Paxlovid on 3/4/23 for five days. I gradually got better and by the end of the five days, I felt a whole lot better and felt like it was working. I tested around 3/13/23 and tested negative for COVID. I have not fully recovered. I have a little bit of residual cough and sinus issues.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: At Home COVID test, positive and negative
Aktuelle Erkrankungen: No
Vorgeschichte: Diabetes Type 2, Hypertension
Andere Medikamente: Centrum Vitamins for Adults, Vitamin D3, Glipizide, Empagliflozin, Ozempic, Carvedilol, Atorvastatin
Allergien: None
Vorherige Impfungen: -

VAERS 2596964

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

moderat

Staat: RI
Alter: 71,0
Geschlecht: F
Eingang: 15.03.2023
Impfdatum: 11.09.2022
Beginn: 12.03.2023
Tage bis Beginn: 182,0
Dosis: 5
Route/Site: SYR / RA

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

Brain fog COVID-19 Cough Fatigue Feeling abnormal Mobility decreased Pain Pyrexia SARS-CoV-2 test positive

Symptomtext

I contracted COVID-19. I first started feeling a cough in addition I had a fever of 106. I am really exhausted; I almost did not get out of bed the whole day. I am now feeling sort of achy but not bad. Today I feel pretty bad. I called my doctor that evening when the cough began. The doctor told me I could chose to take PAXLOVID because of my age. I chose not to take it, because my symptoms are not dramatic. I am taking ADVIL occasionally I am having brain fog.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: 12MAR2023 COVID-19 at home test positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: VYVANSE
Allergien: N/A
Vorherige Impfungen: -

VAERS 2595588

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

moderat

Staat: IN
Alter: 56,0
Geschlecht: M
Eingang: 13.03.2023
Impfdatum: 09.09.2022
Beginn: 19.01.2023
Tage bis Beginn: 132,0
Dosis: 5
Route/Site: IM / RA

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

Abdominal discomfort Atrial fibrillation Back pain COVID-19 Chest pain SARS-CoV-2 test positive

Symptomtext

I had an upset stomach for a day after receiving the vaccine. I previously tested positive for COVID-19 on 01/19/2022 and again on 01/19/2023. I did not contact my doctor and I took over the counter medication to help with my symptoms. I took MUCINEX and TYLENOL to help with symptoms. I started feeling sharp pain in my chest and back. I went to the emergency room to be observed. I was diagnosed with AFIB. I am seeing a cardiologist. I am on medication that has stabilized my symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 19JAN2023 COVID-19 test positive; 19JAN2022 COVID-19 test positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Sleep Apnea
Andere Medikamente: Multivitamin
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 2595491

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144b

moderat

Staat: MI
Alter: 66,0
Geschlecht: M
Eingang: 13.03.2023
Impfdatum: 11.09.2022
Beginn: 15.11.2022
Tage bis Beginn: 65,0
Dosis: 5
Route/Site: IM / AR

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

Angioplasty Cardiac murmur Cardiac valve disease Catheterisation cardiac normal Congenital cardiovascular anomaly Dyspnoea Echocardiogram Echocardiogram abnormal Fatigue Headache Mitral valve prolapse

Symptomtext

I went in for my routine wellness exam, my doctor noticed I had a very promote heart murmur. At that time, I did not have any symptoms. Since that time, I have developed fatigue, headaches, shortness of breath. My doctor has ordered multiple test, to find out what could be causing the symptoms. The echocardiogram I had in November confirmed I have mitral valve prolapse. In December I had a TEE were it was discovered I had a congenital heart birth defect, and a heart catheterization that did come back negative. In January I had Angioplasty that show my valves are enlarged from working harder. I am now awaiting heart surgery to replace my valves.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 11/22 Echocardiogram - positive heart murmur; 12/22 TEE - positive genetic heart defect; 12/22 Heart catheterization - negative; 1/23 Angioplasty - positive showed they are enlarged.
Aktuelle Erkrankungen: No
Vorgeschichte: Heart Valve Disease
Andere Medikamente: Tylenol III; Dorzolamide; Latanoprost; Vitamin b complex; Flomax; Gabapentin; Tylenol
Allergien: No
Vorherige Impfungen: -

VAERS 2594868

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

moderat

Staat: CA
Alter: 73,0
Geschlecht: M
Eingang: 10.03.2023
Impfdatum: 08.09.2022
Beginn: 01.03.2023
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 abnormal COVID-19 Cardiac failure Chest X-ray abnormal Diuretic therapy Dyspnoea Fluid retention SARS-CoV-2 test positive

Symptomtext

I went to the hospital, because I had shortness of breath the night before. When I got to the hospital, I was put on an IV and underwent bloodwork. A routine COVID-19 test was done, and the result was positive. I was then admitted on COVID-19 precautions. They gave me one dose of IV remdesivir and treated me for heart failure. I was also given a diuretic to get rid of the fluid buildup. I was discharged the next day. After that, everything was fine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 1,0
Labordaten: 01MAR2023 - Bloodwork - Heart Failure; 01MAR2023 - COVID-19 Test - Positive Result; 01MAR2023 - Chest X-Ray - Heart Failure Detected
Aktuelle Erkrankungen: None
Vorgeschichte: Atrial Fibrillation; Hypertension
Andere Medikamente: Benecar; Bystolic; Magnesium; Vitamin D; Baby Aspirin
Allergien: Hydrochlorothiazide; Lipitor
Vorherige Impfungen: -

VAERS 2594786

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7144B

moderat

Staat: GA
Alter: 77,0
Geschlecht: F
Eingang: 10.03.2023
Impfdatum: 08.09.2022
Beginn: 01.01.2023
Tage bis Beginn: 115,0
Dosis: 5
Route/Site: IM / LA

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

Atrial fibrillation Cardiac stress test Chills Dyspnoea Echocardiogram Exposure to SARS-CoV-2 Feeling abnormal Heart rate increased Oropharyngeal pain Oxygen saturation decreased Pyrexia

Symptomtext

I started with a sore throat and the next day I had chills and fever and felt bad. I was exposed with my daughter, and she called me when she tested positive. I was having difficulty breathing and I then called ambulance. I was admitted to the hospital I was in a fib and had low oxygen level. They ran heart test because my heart rate was elevated. I was in the hospital for four days and was given Remdesivir in my IV three times which helped the oxygen levels. Because I was in a fib the doctor changed a bunch of my medication. I was discharged and I have to take oxygen if I do a lot of activities. I did follow up with my cardiologist and my lung doctor. A fib did resolve itself.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Echocardiogram; Chemically Stress Test
Aktuelle Erkrankungen: N/A
Vorgeschichte: COPD; Heart Disease; Sleep Apnea
Andere Medikamente: Carvedilol; Amlodipine; Potassium Chloride; Famotidine; Zetia; Atorvastatin; Magnesium Oxide; Lasix; Yupelri; Calcium Vitamin Pill; Multivitamin; Fish Oil
Allergien: Codeine; Morphine; Aloe; Demeriol
Vorherige Impfungen: -

VAERS 2594363

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

moderat

Staat: MD
Alter: 57,0
Geschlecht: M
Eingang: 10.03.2023
Impfdatum: 07.09.2022
Beginn: 28.01.2023
Tage bis Beginn: 143,0
Dosis: 5
Route/Site: UN / LA

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

Bronchospasm Cough Dyspnoea Oropharyngeal pain SARS-CoV-2 test negative Sneezing Streptococcus test negative Upper-airway cough syndrome

Symptomtext

On 1/28/23, I developed a sore throat. On 1/29/23, I developed severe nasal drip w/ frequent sneezing. On evening of 1/30/23, I had post-nasal drip/incessant coughing and difficulty breathing. I administered albuterol 108 (90 Base) MCzg/ACT inhaler to no effect. On 1/31/23, I visited an urgent care clinic, and was diagnosed with "Acute bronchospasm", and RX'ed benzonatate 100 mg capsule (3x daily as needed), prednisone 20 mg tablet (2x daily, 5 days), and promethazine-dextromethorphan 5ML syrup (4x daily as needed). Bronchial spasms stopped within 6 hours of treatment, and coughing and post-nasal drip gradually ceased after about 7 days of treatment.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 1/28/23 and 1/30/23, tested negative for COVID-19 using nasal swab home testing kits. 1/31/23 tested negative for strep due to possible exposure from niece (Rapid Strep A Antigen).
Aktuelle Erkrankungen: Seasonal "hay fever" allergies
Vorgeschichte: Seasonal "hay fever" allergies
Andere Medikamente: Sudafed (1/day), Benadryl (1/night), for seasonal allergies
Allergien: -
Vorherige Impfungen: -

VAERS 2594343

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

moderat

Staat: NJ
Alter: 40,0
Geschlecht: F
Eingang: 09.03.2023
Impfdatum: 06.09.2022
Beginn: 01.09.2022
Tage bis Beginn: -
Dosis: 4
Route/Site: SYR / UN

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

Erythema Food allergy Milk allergy Paraesthesia Pruritus SARS-CoV-2 test negative Urticaria

Symptomtext

After receiving my last dose of Moderna Bivalent, within the same month. I had hives all over body. It was red, tingling sensation, red, and itchy. On 11/19/2022 I went to my doctor who prescribed me steroids, levocetirizine, and EPIPEN. My doctor also did an allergy test which stated that I have allergic reaction to dairy products and specific vegetables. He referred me to an allergist. I went to the allergist on 12/19/2022. He repeated the same and it was ruled out that I had allergic reactions to dairy products and specific vegetables which they provided a list for. They advised me to follow the list. I also went to the dermatologist for the hives I was experiencing on 11/04/2022. She prescribed me with a steroid cream but it didn't help much. As this time I am just using the medication my doctor has provided and I am also trying to avoid dairy and vegetables. The steroid made my Thyroid levels up according to my doctor. As of now I am waiting for my annual check up so I can get my test repeated again to check for Thyroid level. I never had anything like before but it all started after getting my last Moderna Bivalent COVID-19 booster shot.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: 09MAR2023 COVID-19 test negative
Aktuelle Erkrankungen: N/A
Vorgeschichte: Glaucoma
Andere Medikamente: Multivitamins; latanoprost
Allergien: N/A
Vorherige Impfungen: -

VAERS 2593872

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

moderat

Staat: IL
Alter: 42,0
Geschlecht: F
Eingang: 09.03.2023
Impfdatum: 06.09.2022
Beginn: 03.02.2023
Tage bis Beginn: 150,0
Dosis: 4
Route/Site: IM / LA

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

Asthma COVID-19 Chest discomfort Condition aggravated Dyspnoea Dyspnoea exertional Exposure to SARS-CoV-2 Fatigue Imaging procedure Increased upper airway secretion Loss of personal independence in daily activities Malaise SARS-CoV-2 test positive Speech disorder Upper-airway cough syndrome

Symptomtext

It started with postnasal drip like a drippy throat. I had chest tightness due to asthma and those were the only symptoms I had. My whole family had COVID-19 prior to me getting these symptoms so I had been testing daily. I took a COVID-19 home test on 02/04/2023 and I called my provider who is an allergist. I was prescribed PAXLOVID by my primary care provider. My allergist prescribed PULMICORT 3 times a day and breathing treatments 3 times per day. I was also prescribed XOPENEX. I felt better a day after taking PAXLOVID. I had fatigue on and off and was not feeling well in general. The throat was better along with the postnasal drip. I still felt unwell, and the chest tightness returned after I was done with the course of PAXLOVID was completed. My symptoms became elevated, and I was having issues with exertion, talking and general activity. I was prescribed prednisone 40mg for 6 days. The dosage was reduced by 5 mg daily. I took another 2 weeks. The symptoms were slowly getting better. I was still taking the breathing treatments also. I returned to the doctor for a follow up and was cleared. My stamina is still not where it should be. I still have a little shortness of breath with exertion, but it is getting better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: COVID-19 home test 02/04/2023 positive. COVID-19 PCR test 02/03/2023 positive. Spirometry Lung test 03/02/2023 normal lung function. Improved from previous time. Pulsometer Imagery 03/02/2023-99% Oxygen level within normal range
Aktuelle Erkrankungen: N/A
Vorgeschichte: Asthma; Allergies; Hypothyroidism; High Cholesterol
Andere Medikamente: Levothyroxine; indapamide; montelukast; NASONEX; ASTELIN nasal spray; NUTRAFOL; magnesium; CHOLESTOFF; PEPCID; XYZAL
Allergien: Shellfish
Vorherige Impfungen: Flu vaccine, chills 3 years ago 39 years old. COVID-19 Dose 1-3, sore arm and muscle aches, Dose, sore arm, fever, headache, fat

VAERS 2593809

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

moderat

Staat: MA
Alter: 68,0
Geschlecht: F
Eingang: 09.03.2023
Impfdatum: 07.09.2022
Beginn: 07.10.2022
Tage bis Beginn: 30,0
Dosis: 5
Route/Site: IM / LA

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

Balance disorder Dysgraphia Dysstasia Extremity contracture Fall Mobility decreased Parkinson's disease

Symptomtext

In October of 2022, I was having problems getting up out of a chair. I was having problems rolling over in bed. I was having problems with my balance and had fallen twice. My toes were curling significantly in order to keep myself upright and my handwriting had changed completely. It was much smaller and very difficult to read. I went to see the doctor; he diagnosed me with Parkinson's disease. He prescribed Carbidopa-Levodopa. I'm reacting appropriately to the medication. Almost everything has gone back to normal. My handwriting is still not ideal but is legible. I am also still having some issues with balance, but other than that, everything has disappeared.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension; High Cholesterol
Andere Medikamente: Metoprolol; Atorvastatin; Vitamin D3; Aspirin; Calcium Carbonate
Allergien: Tetanus Shot
Vorherige Impfungen: Tetanus - 2013 - Numbness of head and face

VAERS 2593188

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

moderat

Staat: CA
Alter: 66,0
Geschlecht: F
Eingang: 08.03.2023
Impfdatum: 06.09.2022
Beginn: 08.02.2023
Tage bis Beginn: 155,0
Dosis: 5
Route/Site: IM / AR

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

Asthenia COVID-19 Cough Fatigue Headache Influenza like illness Middle insomnia Migraine SARS-CoV-2 test positive Somnolence

Symptomtext

I woke up at 1:30AM on February 8, 2023, with a terrible migraine. I took TYLENOL and went back to sleep. I had a terrible headache that entire day. The next day I still had a headache and was very fatigue. I tested for COVID-19, and it was positive. I made a telehealth visit with my physician and she prescribed me PAXLOVID. I took the first dose on February 9, 2023. I still had very low energy and my headache lasted several more days. I had flu like symptoms, a cough, and extreme tiredness. I slept a lot and continued to take TYLENOL and PAXLOVID. I felt better around February 16, 2023. I tested negative on February 17th, 2023. I quarantined for eleven days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: 09FEB2023 COVID-19 test positive; 17FEB2023 COVID-19 test negative
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Calcium; black cohosh; daily vitamin
Allergien: N/A
Vorherige Impfungen: -

VAERS 2593165

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

moderat

Staat: CT
Alter: 68,0
Geschlecht: F
Eingang: 08.03.2023
Impfdatum: 06.09.2022
Beginn: 25.02.2023
Tage bis Beginn: 172,0
Dosis: 5
Route/Site: IM / LA

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

Chest pain Chills Cough Oropharyngeal pain Pain Rhinorrhoea

Symptomtext

Chills, body ache, horrible runny nose, cough, sore throat, chest ache. Prescribe PAXLOVID.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Primary sclerosis; underactuated thyroid; Osteopenia; rheumatoid arthritis; Myotonia Gravis
Andere Medikamente: ARNUITY ELLIPTA inhaler; azelastine HCI 137; calcium; glucosamine; meloxicam; omeprazole; PREMARIN; CENTRUM; thyroxine; ursodiol; verapamil; vitamin D complex; ZYRTEC
Allergien: Sulfa drugs; gluten; adhesive
Vorherige Impfungen: -

VAERS 2593161

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

moderat

Staat: IL
Alter: 54,0
Geschlecht: F
Eingang: 08.03.2023
Impfdatum: 06.09.2022
Beginn: 08.12.2022
Tage bis Beginn: 93,0
Dosis: 5
Route/Site: IM / LA

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

Back pain Blood test Cardiac stress test Chest pain Computerised tomogram thorax normal Electrocardiogram normal X-ray normal

Symptomtext

Started having back pain after an hour realized it was chest pain on the left side of my chest. Went to the emergency room the next day, given an EKG, blood test and an X-ray with no findings. Went to my Cardiologist the next day and was given a Stress Test, EKG and a CT scan of heart, no findings. After a couple of days the pain went away.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: EKG negative, Blood test inconclusive; CT scan negative; Stress test inconclusive.
Aktuelle Erkrankungen: N/A
Vorgeschichte: Thoracic Outlet Syndrome
Andere Medikamente: ZYRTEC; dextroamphetamine; amitriptyline; multivitamin.
Allergien: Mango
Vorherige Impfungen: -

VAERS 2591969

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

moderat

Staat: NJ
Alter: 56,0
Geschlecht: M
Eingang: 06.03.2023
Impfdatum: 04.09.2022
Beginn: 05.01.2023
Tage bis Beginn: 123,0
Dosis: 5
Route/Site: IM / LA

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

Hypertension

Symptomtext

I went to the doctor for a physical. They checked my blood pressure and it was high. I was prescribed amlodipine. I never had high blood pressure before.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: Blood Pressure, 145/90, 01/2023
Aktuelle Erkrankungen: N/A
Vorgeschichte: GERD; Anxiety; Depression
Andere Medikamente: Lansoprazole; PRISTIQ; bupropion; PATADAY
Allergien: N/A
Vorherige Impfungen: -

VAERS 2591965

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

moderat

Staat: CA
Alter: 55,0
Geschlecht: F
Eingang: 06.03.2023
Impfdatum: 03.09.2022
Beginn: 01.10.2022
Tage bis Beginn: 28,0
Dosis: 5
Route/Site: SYR / UN

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

Chest pain Cough Respiratory tract congestion SARS-CoV-2 test negative

Symptomtext

I had my vaccination on 09/03/2022. I started to experience a lot of congestion coughing and chest pain in 10/2022. I tested COVID-19 negative 10/2022. I was informed to take cough medicine and FLONASE.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: COVID-19 negative 10/2022.
Aktuelle Erkrankungen: N/A
Vorgeschichte: Seasonal Allergies; Hypothyroidism; Depression; Anxiety; Joint Arthritis; Sleep Apnea
Andere Medikamente: SYNTHROID; trazodone; ZOLOFT; probiotic; vitamin D; estradiol
Allergien: Shellfish; calamine lotion; minocycline; pollen; dust; mold
Vorherige Impfungen: -

VAERS 2580027

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

moderat

Staat: GA
Alter: 70,0
Geschlecht: M
Eingang: 12.02.2023
Impfdatum: 04.09.2022
Beginn: 05.09.2022
Tage bis Beginn: 1,0
Dosis: 5
Route/Site: - / LA

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

Magnetic resonance imaging Moaning Mobility decreased Movement disorder Pain Skin warm Sleep disorder Vaccination site pain X-ray

Symptomtext

Soreness at vaccination site soon after vaccination.Soreness continued to develop over next 30 hours. Evening of 09/05/2022 soreness became ache and after bedtime (around 08.30) ache became more pronounced.Overnight sleep was interrupted on turning on to left arm and interruptions became more frequent as the night progressed. Next morning upper arm felt hot and as well as the ache there was now dull throbbing all of which continued to get worse along with restricted movement and after a few weeks as it was not improving I made an appointment with my PCP. I attended on 09/30/2022 when X-rays were taken and I was referred to a sports injury specialist who I saw on 11/09/2022. Pains and aches had continued to get worse

Weitere VAERSDATA-Felder

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

VAERS 2577352

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

moderat

Staat: NY
Alter: 73,0
Geschlecht: M
Eingang: 07.02.2023
Impfdatum: 12.09.2022
Beginn: 15.09.2022
Tage bis Beginn: 3,0
Dosis: UNK
Route/Site: SYR / LA

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

Abdominal distension Atrial fibrillation Barium double contrast Chronic obstructive pulmonary disease Computerised tomogram Computerised tomogram abdomen Constipation Cystoscopy Dry mouth Dyspnoea Faeces soft Magnetic resonance imaging Muscular weakness Pollakiuria Sleep disorder Ultrasound abdomen Ultrasound kidney Urodynamics measurement

Symptomtext

Frequency of urination: 40-50 times a day: still ongoing, but less frequent--12-15 times a day Severe constipation: lasting over 2-1/2 months; still ongoing with bloated stomach; liquid and very soft stool (unformed) owing to multiple laxatives Muscle weakness in thigh and calf; still ongoing Atrial fibrillation Extremely dry mouth--still ongoing, particularly at night COPD; breathing issues, particularly at night and mostly while lying down; less so sitting or standing up or during the day Waking up every 45 minutes to an hour at night due to dry mouth, unable to breathe, or a desperate urge to urinate

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Don't recall dates, but most tests were done October, November, and December 2022. They include CT scans of GI tracts, esophagus, stomach; MRI of prostrate; Barium contrast tests; Cystoscopy; Urodynamics. Had an ultrasound of kidney and bowels on2/7/23.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Crestor; Losartan; Metformin; Zetia; Cosopt; Zioptan; Vitamin D-3; CoQ10; Vitamin B-12
Allergien: None
Vorherige Impfungen: -

VAERS 2559502

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

moderat

Staat: IA
Alter: 52,0
Geschlecht: F
Eingang: 13.01.2023
Impfdatum: 13.10.2022
Beginn: 06.12.2022
Tage bis Beginn: 54,0
Dosis: 5
Route/Site: IM / RA

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

Dyspnoea Pulmonary function test Swelling

Symptomtext

On 12/06/2022 I started feeling shortness of breath and swollen extremities. I was referred 12/30/2022 to a Pulmonologist and was prescribed an inhaler. I also have an upcoming Cardiologist appointment on 01/20/2023.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 12/06/2022 Pulmonary Function test
Aktuelle Erkrankungen: None
Vorgeschichte: Hyperthyroid
Andere Medikamente: Levothyroxine; CLARITIN D; FLONASE
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 2548854

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

moderat

Staat: VA
Alter: 48,0
Geschlecht: F
Eingang: 03.01.2023
Impfdatum: 01.10.2022
Beginn: 19.11.2022
Tage bis Beginn: 49,0
Dosis: 4
Route/Site: SYR / AR

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

Asthma COVID-19 Condition aggravated Diarrhoea Eating disorder Fatigue Headache Irritable bowel syndrome Malaise Nausea Pain Pyrexia Respiratory tract congestion SARS-CoV-2 test positive Tongue blistering

Symptomtext

Starting 11/19/2022, I developed a strong headache and congestion. By 11/21/2022, I developed a fever of around 101, body aches, diarrhea, nausea and congestion. I tested myself that day for COVID-19 and it was positive. I contacted my doctor before I tested myself for COVID-19. I was prescribed PAXLOVID right away and started it that evening. It helped me feel better right away. For 3-4 days, I had mild symptoms and then felt better. I had lingering fatigue that lasted for about a week or so after the other symptoms resolved. I am still having lingering IBS symptoms that have yet to improve. Also, I have been having weird blistering of the tongue making it hard to eat certain things, and more frequent but mild asthma symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: At home COVID-19 test (11/21/2022): positive
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma; Diabetes; High Blood Pressure; Fibromyalgia
Andere Medikamente: Metformin ER; JARDIANCE; losartan; generic ZYRTEC; montelukast; duloxetine; SYMBICORT inhaler; women's multivitamin; famotidine
Allergien: Penicillin; dust; pollen
Vorherige Impfungen: -

VAERS 2535587

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

moderat

Staat: CT
Alter: 55,0
Geschlecht: F
Eingang: 16.12.2022
Impfdatum: 15.09.2022
Beginn: 30.09.2022
Tage bis Beginn: 15,0
Dosis: 4
Route/Site: SYR / LA

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

Arthralgia Gait disturbance Joint swelling Mobility decreased Pain Tendon disorder Tendon rupture X-ray

Symptomtext

Started having painful AC joint swelling and tenderness and aggravated by lifting arm and sideways extension and weight baring; Went to doctor and had an X-ray, no concrete findings; still sore and can't lift well, started Physical Therapy but it hasn't helped, Therapist believes that it may be a Tendon issue and if it doesn't clear up soon they'll have to give me an MRI if it doesn't get better by the new year; Also started having problems with Peroneal Tendon, making it hard to walk; went to urgent care and I was told it is a Tendon tear, am wearing a boot and going to start Physical Therapy.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: X-ray non conclusive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Asthma; Migraines; Depression; PTSD
Andere Medikamente: TRILEPTAL; lamotrigine; FETZIMA; vitamin D; multivitamin; SINGULAIR; albuterol inhaler; ibuprofen
Allergien: Penicillin; sulfa; lidocaine; acetaminophen; ABILIFY; REGLAN
Vorherige Impfungen: -

VAERS 2531221

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

moderat

Staat: CA
Alter: 77,0
Geschlecht: M
Eingang: 14.12.2022
Impfdatum: 12.09.2022
Beginn: 29.11.2022
Tage bis Beginn: 78,0
Dosis: 5
Route/Site: IM / LA

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

Arteriogram coronary abnormal Coronary artery disease Dizziness Dyspnoea

Symptomtext

dizziness and shortness of breath, follow-up visit with cardiologist, angiogram, diagnosed with coronary artery disease, angioplasty scheduled for 12/16/2022

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: glaucoma; elevated PSA; hypertension; hyperlipidemia
Andere Medikamente: Losartan 100 mg; Amlodipine 2.5mg; Rosuvastatin 20mg
Allergien: NKA
Vorherige Impfungen: -

VAERS 2531106

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

moderat

Staat: VA
Alter: 76,0
Geschlecht: F
Eingang: 14.12.2022
Impfdatum: 13.09.2022
Beginn: 26.10.2022
Tage bis Beginn: 43,0
Dosis: 5
Route/Site: IM / AR

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

Atrial fibrillation Cardiac ablation Cardiac monitoring abnormal Condition aggravated

Symptomtext

I hydrated very well the day before receiving the vaccine and had no trouble afterwards. On the morning of 10/26/2022 I was going into AFIB and went to the emergency room. I stayed there for 24 hours and discharged on 10/28/2022 with a heart monitor. On 11/22/2022 I had a heart ablation which was an outpatient procedure. I have a follow-up appointment with my cardiologist on 12/28/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Osteoporosis; AFIB; Chronic Sinusitis
Andere Medikamente: SYNTHROID; rosuvastatin; ELIQUIS; diltiazem; PROLIA; vitamin C; multivitamin; calcium D; ALIGN probiotic; sinus rinse
Allergien: Penicillin; BACTRIM
Vorherige Impfungen: -

VAERS 2530018

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

moderat

Staat: GA
Alter: 34,0
Geschlecht: M
Eingang: 13.12.2022
Impfdatum: 12.09.2022
Beginn: 23.09.2022
Tage bis Beginn: 11,0
Dosis: 4
Route/Site: SYR / RA

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

Arthralgia COVID-19 Cough Dyspnoea Headache Oropharyngeal pain Pain Pain in extremity Positive airway pressure therapy Pyrexia Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

Friday September 23 2022 at 9AM I woke up with a headache. light cough, body aches. sore throat and felt feverish. On Saturday nigh I took a COVID-19 test and the result was positive. My symptoms were lighter Saturday daytime but became worse at night and continued through Monday. Sunday I also experienced pain in the joints of my toes and in the arch of my foot. In addition to that I had labored breathing and used my C Pap at night. Monday September 26 2022 I had started to feel better in the early morning but a few hours later I had cough headache and sniffles. I was prescribed Molnutiravir by the urgent care clinic.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: COVID-19 test positive.
Aktuelle Erkrankungen: None
Vorgeschichte: Type 2 Diabetic; High Cholesterol; Migraines; Non Alcoholic Fatty Liver Disease; Sleep Apnea; Gurd
Andere Medikamente: Metformin; Multivitamin; Zyrtec; Vitamin E; Fish Oil; Cranberry; Calcium Phosphorous; Flonase
Allergien: Lactose Intolerant; Percocet; Meningococcal Vaccine; Rizatriptan; General Anasthia
Vorherige Impfungen: -

VAERS 2529053

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

moderat

Staat: VA
Alter: 79,0
Geschlecht: F
Eingang: 12.12.2022
Impfdatum: 06.09.2022
Beginn: 02.12.2022
Tage bis Beginn: 87,0
Dosis: 5
Route/Site: IM / LA

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

Cough Fatigue Heart rate increased Hypotension Influenza Influenza virus test positive Oropharyngeal pain Oxygen saturation decreased Pain Pyrexia

Symptomtext

I tested positive for the flu on 12/2/22. I had to go to the ER and had to stay overnight. I was prescribed metoprolol to slow down my heart because it was very rapid at the time. I also had low blood pressure and oxygen. I had a sore throat, fever, body aches, cough, and fatigue. I am starting to feel better, but not completely better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypotension
Hospital-Tage: -
Labordaten: 02DEC2022 flu test positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: LEVOXYL; estradiol; PROMETRIUM; pravastatin; amlodipine; glucosamine; hyaluronic acid; cinnamon; cranberry; bilberry; lutein; fish oil; vitamin C; selenium; coQ10; vitamin B complex; calcium citrate; magnesium; zinc; vitamin K2; vitamin D3
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 2527430

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

moderat

Staat: CO
Alter: 31,0
Geschlecht: F
Eingang: 08.12.2022
Impfdatum: 07.09.2022
Beginn: 14.11.2022
Tage bis Beginn: 68,0
Dosis: 4
Route/Site: IM / LA

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

Bronchial hyperreactivity COVID-19 Dyspnoea Dyspnoea exertional Exercise tolerance decreased Fatigue Lymphadenopathy Malaise Myalgia Nasal congestion Oropharyngeal discomfort Oropharyngeal pain Productive cough Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive Upper-airway cough syndrome

Symptomtext

I received the Moderna Bivalent booster on 9/7/2022. On 11/14/2022, I developed a runny nose. I was fatigued, but I didn't give it much thought, since it was late. On the morning of 11/15/2022, I woke with a very painful sore throat. I took a home antigen test that very quickly yielded a positive result. I took 2 more home antigen tests the same day just to make sure, and the results were positive both times. On 11/15/2022, which was at the height of my sore throat, I had a swollen lymph node on the right side of my neck; the swelling went down a few days later. Over 11/16/2022 and 11/17/2022, I continued to have fatigue and sore throat. I also developed muscle aches. I continued to have a runny nose. On about 11/17/2022, I began to have a cough, which was only slightly productive. The sore throat began to resolve at this point, but the cough and runny nose continued. I treated my symptoms with a version of DAYQUIL that did not have acetaminophen. I also took ADVIL for the sore throat and muscle aches. After I ran out of DAYQUIL, I switched to an ALKA-SELTZER cold medicine that had aspirin as an ingredient and included medicine for both daytime and nighttime in the same package. The medicines helped somewhat, but not completely. Around 11/20/2022 or 11/21/2022, the runny nose began to abate and was replaced primarily by nasal congestion. I also had continuing fatigue. During this time, I was frequently testing myself, as I work with immunocompromised people and I don't want to endanger them. Not only that, but it was around the end of November, and I didn't want to spread the virus to my family. Up until 11/24/2022, I continued to test positive. On 11/25/2022, I finally got a negative result. Even though the test result was negative, I still experienced significant fatigue, nasal congestion, and cough. Around 11/28/2022, I continued to have the nagging cough. Not only that, but I also had shortness of breath and exercise intolerance; climbing stairs was an ordeal. At this point, the congestion and postnasal drip were gone, but a tickling sensation in my throat made me cough. It was very uncomfortable, so I reached out to my doctor. She prescribed me benzonatate; unfortunately, it didn't really help much. It didn't completely get rid of the tickling sensation. Not only that, but it didn't provide long-lasting relief the way that it was supposed to. When I didn't get any relief from the benzonatate and I continued to have shortness of breath, I went to see the doctor again. She diagnosed me with reactive airway disease and prescribed me an albuterol inhaler. They helped somewhat, but not completely. At the time of this writing, I now no longer have to use the albuterol inhaler. However, I still experience shortness of breath whenever I climb the stairs and have to stop midway. This is unusual for me, because before I got sick, I frequently did mountain climbing. I think it's also worth mentioning that my doctor suspects that I had multiple viruses. I work with sick children who often suffer from viruses like RSV, strep throat, and flu A, so it's a possibility. However, we'll never know for certain, as there are no home tests for those conditions, and I wasn't tested for them, as I was staying at home and isolating after receiving my COVID-19 diagnosis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 11/15/2022-11/24/2022 home antigen tests positive results; 11/25/2022 home antigen test negative result.
Aktuelle Erkrankungen: None.
Vorgeschichte: None.
Andere Medikamente: Bupropion XR; cetirizine; vitamin D; MIRENA IUD.
Allergien: Sulfa drugs; seasonal allergies; carrots; almonds; pecans; walnuts; macadamia nuts; hazelnuts; chestnuts; brazil nuts; cherries; peaches; cantaloupe; soy sensitivity; TYLENOL.
Vorherige Impfungen: -

VAERS 2525489

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

moderat

Staat: NJ
Alter: 68,0
Geschlecht: F
Eingang: 07.12.2022
Impfdatum: 06.09.2022
Beginn: 11.11.2022
Tage bis Beginn: 66,0
Dosis: 5
Route/Site: IM / RA

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

Bed sharing Headache Hypoaesthesia Malaise Pain Paraesthesia Pruritus SARS-CoV-2 test positive

Symptomtext

I experienced an itchy, numb, tingly feeling in my right shoulder blade with each COVID-19 vaccine I have received, and it last a couple of weeks. On 11/11/2022 I began not feeling well with body aches, headache and it felt like a sinus infection. Later that day I test positive with a home test for COVID-19. I contacted my doctor on 11/12/2022 and was given the prescription PAXLOVID. Within three days I began to feel better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: 11NOV2022 COVID-19 test positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: PEPCID
Allergien: N/A
Vorherige Impfungen: -

VAERS 2522644

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

moderat

Staat: PA
Alter: 70,0
Geschlecht: M
Eingang: 04.12.2022
Impfdatum: 13.09.2022
Beginn: 26.09.2022
Tage bis Beginn: 13,0
Dosis: 5
Route/Site: IM / LA

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

Hypertension

Symptomtext

After 13 days I was found to have high blood pressure. I always have normal blood pressure. I had doctors visit 09/02/2022. BP was 120/64. I received vaccine on 09/13/2022. Next BP check was on 09/26/2022 and was 140/94. Since then the am checking BP quite often and is 130-150/85-90. No symptoms. There's no charge in my diet, no weight gain, I exercise 60-90 minutes regularly. No stress. Can't explain any other factors for high BP. So I believe covid booster could be responsible. I am a cardiologist. I don't have any symptoms. I have not started any BP medicine. I found a study regarding high BP after covid vaccine. I was wondering will this be permanent or temporary? Any suggestions/recommendation?

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Have myasthenia Gravis in rammison since 2015 History of high cholesterol more than 20 years
Vorgeschichte: Same as above
Andere Medikamente: I am on azathioprine for 7 years Atorvastatin for 20 years
Allergien: No
Vorherige Impfungen: -

VAERS 2499273

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

moderat

Staat: IN
Alter: 70,0
Geschlecht: M
Eingang: 04.11.2022
Impfdatum: 06.10.2022
Beginn: 01.11.2022
Tage bis Beginn: 26,0
Dosis: 1
Route/Site: SYR / LA

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

Arterial occlusive disease Arterial stent insertion Blood cholesterol normal Blood test normal Catheterisation cardiac abnormal Chest pain Dyspnoea Electrocardiogram Sleep disorder

Symptomtext

I woke up at about 3 in the morning on November 1 and had a pain across my upper chest. I got out of bed and walked around for a bit and it went away. I went back to bed and a minute later it came back. I got back up again and sat on the couch for 5 minutes then went back to bed. I woke up later that day and felt fine, and I did some work, ate dinner, and walked the river front with my wife. The same pain hit me at this point and I sat down and it went away. We walked another two blocks and it happened again. We continued to walk and my wife noticed I was really out of breath. When we got up the hill, after a short distance, the pain hit me again and I told my wife we may need to get help. My wife took me to the emergency room and they did some blood work and an EKG. After two hours, they determined they needed to transfer me to another hospital because they were concerned. When I got there, the heart specialist said they would need to do a catherization. They took me down about 10AM to their operation room and they did the catherization and found a blockage. It was a 90% blockage in one artery and inserted a stent. Everything went fine and they released me November 3 and they noted that I was fine and under no other restrictions. I was in perfect shape and health and I went for a walk later that evening. I just need to be careful with my right arm because of the catheterization insertion. Otherwise, I'm doing fine. They did note that my cholesterol was fine with the blood work. I did also talk to my neighbor earlier today and he noted that he had seen me a week prior to this event working in the yard and noticed that I was more out of breath than usual.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 2,0
Labordaten: Blood work indicated normal levels along with normal cholesterol; EKG; Catherization indicated 90% blockage in artery.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Chlorthalidone; potassium citrate; multivitamin
Allergien: None
Vorherige Impfungen: -

VAERS 2497779

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

moderat

Staat: VA
Alter: 30,0
Geschlecht: F
Eingang: 03.11.2022
Impfdatum: 11.09.2022
Beginn: 21.09.2022
Tage bis Beginn: 10,0
Dosis: 4
Route/Site: IM / LA

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

Condition aggravated Mechanical urticaria Urticaria

Symptomtext

10 days after vaccine I developed hives all over my body. I have had chronic hives since then (6 weeks, now) that I need to take daily antihistamines for to keep at bay. I have dermatographia as well which still occasionally worsens despite antihistamines.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: Sulfa medications.
Vorherige Impfungen: -

VAERS 2490085

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

moderat

Staat: AZ
Alter: 63,0
Geschlecht: F
Eingang: 26.10.2022
Impfdatum: 12.09.2022
Beginn: 19.10.2022
Tage bis Beginn: 37,0
Dosis: 5
Route/Site: SYR / LA

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

COVID-19 Chills Cough Dyspnoea Fatigue Headache Nasopharyngitis Pain Pyrexia Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

Cold symptoms 10/17-18. Headache, chills, fever, achy, runny nose, coughing, difficulty breathing, extreme fatigue - 10/19-10/20 Runny nose, extreme fatigue - 10/21-10/23

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Home covid test negative 10/17 Home covid test positive 10/19 Home covid test positive 10/24 Home covid test negative 10/25
Aktuelle Erkrankungen: none
Vorgeschichte: asthma, psoriatic arthritis, osteopoenia
Andere Medikamente: vitamin E, vitamin D, calcifood powder, allerplex, glucosamin chondrointin, zypan, ginko, magnesium, juice plus, bone complex, super eff, pure multivitamin, biost
Allergien: penicillin, keflex, cefzil, tetanus, squid, scungilli, bee stings
Vorherige Impfungen: -

VAERS 2488974

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

moderat

Staat: TX
Alter: 66,0
Geschlecht: M
Eingang: 25.10.2022
Impfdatum: 09.09.2022
Beginn: 21.09.2022
Tage bis Beginn: 12,0
Dosis: 5
Route/Site: SYR / LA

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

COVID-19 Cough Dyspnoea Exposure to SARS-CoV-2 Fatigue Headache Pain Pyrexia Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

Exposed to Covid on September 18th. Evening of the 21st had fever, coughing (lots), fatigue, bad headache, difficulty breathing, body pains, runny nose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Home COVID test turned deep purple the second exposed to the sample. Doctor visit was by phone. Doctor prescribed Paxlovid and inhalers.
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Wellbutrin, buspar, trazodone
Allergien: none
Vorherige Impfungen: -

VAERS 2484352

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

moderat

Staat: NC
Alter: 42,0
Geschlecht: F
Eingang: 20.10.2022
Impfdatum: 12.09.2022
Beginn: 06.10.2022
Tage bis Beginn: 24,0
Dosis: 1
Route/Site: SYR / LA

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

COVID-19 Migraine Oropharyngeal pain SARS-CoV-2 test positive

Symptomtext

I had my vaccination on 09/12/2022. I woke up 10/06/2022 with a sore throat and migraine. I had 2 COVID-19 negative tests on 10/06/2022. I tested COVID-19 positive on 10/07/2022. I contacted my doctor on 10/07/2022 and they prescribed PAXLOVID. I was also prescribed the antibodies infusion for 10/08/2022. 10/09/2022 I started the PAXLOVID till 10/14/2022 and taken off all my other prescriptions for 5 days until 10/14/2022. I resumed my regular medications 10/16/2022. On 10/18/2022 I started to feel worse again and restarted isolation.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: COVID-19 positive 10/07/2022
Aktuelle Erkrankungen: -
Vorgeschichte: Celiac; Migraines; Hip and Back Pain; Cushing's; PCOS; Hashimoto Disease
Andere Medikamente: BARIATRIC multivitamin; vitamin D; calcium; lisinopril; tizanidine; UBRELVY
Allergien: Celiac; bee stings; triptan
Vorherige Impfungen: -

VAERS 2483193

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

moderat

Staat: RI
Alter: 39,0
Geschlecht: M
Eingang: 19.10.2022
Impfdatum: 06.09.2022
Beginn: 01.09.2022
Tage bis Beginn: -
Dosis: 4
Route/Site: IM / LA

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

Balance disorder Dizziness Erythema Palpitations Pruritus

Symptomtext

1.5 weeks after the vaccination, my skin all over my body began to be severely itchy and has continued since. When scratching, my skin quickly turns red. This is consistent with my reaction to the Moderna COVID-19 booster taken last year, on 10/31/2021. I had 2.5 months of severe itching and then, it slowly subsided. Last year, I did not take my flu shot with my COVID booster as I did this year. For my current reaction, Zyrtec was suggested by my dermatologist to lessen the effects. Also, possibly unrelated to the booster: - Increased heart palpitations - Dizziness; off-balanced

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: 9/20/2022 dermatologist appointment with Dr. Urgent care twice in Sep for heart palpitations and dizziness/off-balanced As well as 10/19/2022 cardiologist appointment
Aktuelle Erkrankungen: Cold just prior to vaccination
Vorgeschichte: NA
Andere Medikamente: Vitamin D, 2000 IU daily
Allergien: NA
Vorherige Impfungen: Moderna COVID-19 booster (10/31/2021) - same itchiness

VAERS 2477106

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

moderat

Staat: -
Alter: 66,0
Geschlecht: F
Eingang: 13.10.2022
Impfdatum: 27.09.2022
Beginn: 27.09.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Atrial fibrillation Condition aggravated Tachycardia

Symptomtext

onset of rapid atrial fibrillation vs wide complex tachycardia, hospitalization

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: n/a
Vorgeschichte: atrial fib
Andere Medikamente: flecainaide, atorvastatin, eliquis, zetia, HCTZ, irbesartan , metoprolol, pantoprazol
Allergien: citalopram, amitryptiline, simvastatin, etomidate
Vorherige Impfungen: -

VAERS 2473246

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

moderat

Staat: FL
Alter: 81,0
Geschlecht: F
Eingang: 10.10.2022
Impfdatum: 08.10.2022
Beginn: 08.10.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / LA

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

Abdominal discomfort Abdominal pain Chills Diarrhoea Dysgeusia Eye pain Hypophagia Injection site pruritus Migraine Nausea Pruritus Swelling of eyelid Weight decreased

Symptomtext

Itching, Extreme Upset Stomach with very painful cramps repeatedly for hours, chills, nausea, metal taste in mouth, migraine headache, very sore eyes, eyelids and swelling there and underneath eyes, too, weight loss over 48 hours was 5 lbs., Still itches after 3 days (in left arm where it was given. The diarrhea was terrible-just barely made it to the bathroom, repeatedly over 30 hours. Did not know I was capable of having that much in my intestines when I ate little. The pains were like childbirth. Yesterday I could finally eat toast with jelly.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: None so far but have an appointment this Friday with a heart specialist and will let him know. Had already been referred to him about my BP Am better but not quite back to normal. Did not know what to check in next question.
Aktuelle Erkrankungen: -
Vorgeschichte: AFib, High BP Cholesterol
Andere Medikamente: Ramipril, Nebivolol, Livalo, Metformin, Seldenafil, Flecainide Acetate, Eliquis
Allergien: -
Vorherige Impfungen: -

VAERS 2470790

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

moderat

Staat: CO
Alter: 40,0
Geschlecht: F
Eingang: 06.10.2022
Impfdatum: 13.09.2022
Beginn: 13.09.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Hypoaesthesia Injection site bruising Injection site pain Paraesthesia

Symptomtext

Site: Bruising at Injection Site-Mild, Site: Pain at Injection Site-Mild, Additional Details: I was notified of this today 10/3/2022 by store corporate risk management. I'm not aware if patient notified us of this event prior. Patient experienced tingling and numbness in arm and palm after vaccination.

Weitere VAERSDATA-Felder

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

VAERS 2470772

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge as7144b

moderat

Staat: -
Alter: 75,0
Geschlecht: F
Eingang: 06.10.2022
Impfdatum: 01.10.2022
Beginn: 01.10.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / RA

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

Condition aggravated Pain in extremity

Symptomtext

patient called complaining of sore arm. she said shes been icing and using tylenol however it is not improving but not getting worse. recommended if the sore arm continues to go see a doctor but explained sore arm is common side effect with vaccine

Weitere VAERSDATA-Felder

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

VAERS 2468642

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

moderat

Staat: CT
Alter: 39,0
Geschlecht: M
Eingang: 04.10.2022
Impfdatum: 10.09.2022
Beginn: 22.09.2022
Tage bis Beginn: 12,0
Dosis: UNK
Route/Site: SYR / LA

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

Cardiac flutter Electrocardiogram normal Fatigue Limb discomfort Pain Palpitations

Symptomtext

The day after the injection, there was arm discomfort, fatigue, and body aches?none of which were terrible and were easily treated with Tylenol. Roughly 12 days after the booster, I began to have heart flutters. They occurred more often in the morning and evening, but were felt during the day. They were fairly regularly occurring during said time intervals leading up to my visit with Dr. I had been to a local Hospital affiliated Urgent Care clinic the day before I saw Dr. They have continued through 10/3, but are far less frequent. Heart palpitations were most prominent on the days of 9/22?9/25. There have been no palpitations today, 10/4. I have had no arm pain, chest pain, swelling of the extremities, or abnormal fatigue. I was given a halter monitor, fitted by a Hospital's cardiology department on Friday, 9/30. I have been wearing the monitor since then and will continue to wear it for 4 weeks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: No blood work was done. ECG in Urgent Care was normal. Heart in office visit was normal sounding with normal blood pressure.
Aktuelle Erkrankungen: Congestion with cough (COVID negative via PCR and 5 antigen tests done over the course of one week)
Vorgeschichte: Sarcoidosis
Andere Medikamente: Flinstone multivitamin, Vitamin D, Allegra (not Allegra D), Gabapentin, Flovent, Atorvastatin
Allergien: Mango, eggplant
Vorherige Impfungen: -

VAERS 2465199

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7144B

moderat

Staat: NJ
Alter: 77,0
Geschlecht: F
Eingang: 30.09.2022
Impfdatum: 16.09.2022
Beginn: 19.09.2022
Tage bis Beginn: 3,0
Dosis: UNK
Route/Site: OT / -

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

Chest X-ray Chest discomfort Condition aggravated Dyspnoea Heart rate Immunisation reaction Oxygen saturation Secretion discharge Suffocation feeling Tracheitis

Symptomtext

Adverse effect of the vaccine/COVID syndrome; Tracheitis; Heaviness in her chest; Mucous; Throat feels like it's suffocating/base of my throat can't close properly; Difficulty breathing/much worse/breathing was desperately worse/can't breathe properly; Difficulty breathing/can't breathe properly; This spontaneous case was reported by a patient and describes the occurrence of DYSPNOEA (Difficulty breathing/can't breathe properly), CONDITION AGGRAVATED (Difficulty breathing/much worse/breathing was desperately worse/can't breathe properly), IMMUNISATION REACTION (Adverse effect of the vaccine/COVID syndrome), TRACHEITIS (Tracheitis) and CHEST DISCOMFORT (Heaviness in her chest) in a 77-year-old female patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. AS7144B) for COVID-19 prophylaxis. The occurrence of additional non-serious events is detailed below. Concurrent medical conditions included Seasonal asthma (like weather related), Blood pressure high, Cholesterol, Penicillin allergy, Allergy to chemicals, Drug allergy and Seasonal allergy. Concomitant products included PREDNISONE and ALBUTEROL [SALBUTAMOL] for an unknown indication. On 16-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) 1 dosage form. On 19-Sep-2022, the patient experienced DYSPNOEA (Difficulty breathing/can't breathe properly). On 20-Sep-2022, the patient experienced CONDITION AGGRAVATED (Difficulty breathing/much worse/breathing was desperately worse/can't breathe properly). On an unknown date, the patient experienced IMMUNISATION REACTION (Adverse effect of the vaccine/COVID syndrome), TRACHEITIS (Tracheitis), CHEST DISCOMFORT (Heaviness in her chest), SECRETION DISCHARGE (Mucous) and SUFFOCATION FEELING (Throat feels like it's suffocating/base of my throat can't close properly). The patient was treated with PREDNISONE (intravenous) at an unspecified dose and frequency and PREDNISONE (oral) at an unspecified dose and frequency. At the time of the report, DYSPNOEA (Difficulty breathing/can't breathe properly) and CONDITION AGGRAVATED (Difficulty breathing/much worse/breathing was desperately worse/can't breathe properly) had not resolved and IMMUNISATION REACTION (Adverse effect of the vaccine/COVID syndrome), TRACHEITIS (Tracheitis), CHEST DISCOMFORT (Heaviness in her chest), SECRETION DISCHARGE (Mucous) and SUFFOCATION FEELING (Throat feels like it's suffocating/base of my throat can't close properly) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, Chest X-ray: Fine. On an unknown date, Heart rate: Fine. On an unknown date, Oxygen saturation: Fine. Patient did not ever have COVID positive test or diagnosis. Patient did not give other vaccines within 1 month prior to Moderna COVID-19 vaccine. Patient was on steroid inhalations. On 25-Mar-2021, patient received J and J vaccine dose 1 for COVID-19 vaccine, Lot number 1805031. On 11-Dec-2021, patient received Moderna 1st booster. The patient googled the website and looked for the side effects from the bivalent booster shot. Patient took the shot on 16-Sep-2022. By Monday, patient had difficulty breathing. By Tuesday, it was much worse. Patient called her physician, who put her on prednisone. Patient felt ok, but on Wednesday, patients breathing was desperately worse. Later, put patient on an antibiotic. By Friday, patient was at the hospital. Patient was seen in the emergency room and treated with IV prednisone and inhalation treatment. They told patient that had an adverse effect of the vaccine. They were treating it as a COVID syndrome. Patient did not have COVID, but breathing was not listed. It started out as tracheitis, but there was a heaviness in patient's chest. It came and went. Sometimes patient could breathe, but sometimes patient throat felt like it was suffocating. She had an appointment to see a pulmonologist. The patient stated the hospital told her she was fine on everything that patient's oxygen, heart rate, chest x-ray there was nothing could do for her. Patient just could breathe properly. The base of patient's throat felt like it did not close properly. This case was linked to US-MODERNATX, INC.-MOD-2022-650926 (E2B Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2022-650926:(Same Reporter)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Test Name: chest x-ray; Result Unstructured Data: Fine; Test Name: heart rate; Result Unstructured Data: Fine; Test Name: oxygen; Result Unstructured Data: Fine
Aktuelle Erkrankungen: Allergy to chemicals; Blood pressure high; Cholesterol; Drug allergy; Penicillin allergy; Seasonal allergy; Seasonal asthma (like weather related)
Vorgeschichte: -
Andere Medikamente: ALBUTEROL [SALBUTAMOL]
Allergien: -
Vorherige Impfungen: -

VAERS 2464601

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

moderat

Staat: FL
Alter: 60,0
Geschlecht: F
Eingang: 29.09.2022
Impfdatum: 06.09.2022
Beginn: 07.09.2022
Tage bis Beginn: 1,0
Dosis: 5
Route/Site: IM / LA

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

Chills Hypophagia Muscle spasms Sleep disorder Tremor

Symptomtext

I woke up at seven thirty in the morning and had a drink of water and almost immediately began cramping I tried to walk it off to coffee made it worse so I had to lay down on my side and most of the whole day I had this cramping I did not eat much throughout the day due to cramping I had to lay down and had a light dinner and felt slightly better in the middle of the night or around two or three AM I woke up with severe cramping to the point where my husband offered to take to ER hospital I said no as I thought I would feel better in the morning I had shaking chills as well throughout the night and the cramping eventually subside with one more bout of severe cramps that subside until I would drink or take a liquid or food into my body. The next morning I vacillated as to whether to see the doctor or not. My doctor put me on a BRAT diet to calm my system down and I was better in about five days total.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: No.
Aktuelle Erkrankungen: No.
Vorgeschichte: Hypothyroid.
Andere Medikamente: UNITHROID; FLONASE; ketoconazole shampoo
Allergien: Goat cheese.
Vorherige Impfungen: -

VAERS 2463456

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7144B

moderat

Staat: CA
Alter: 67,0
Geschlecht: F
Eingang: 28.09.2022
Impfdatum: 13.09.2022
Beginn: 14.09.2022
Tage bis Beginn: 1,0
Dosis: 5
Route/Site: IM / LA

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

Arthralgia Condition aggravated Myalgia Polymyalgia rheumatica

Symptomtext

I was in remission with Polymyalgia rheumatica and off prednisone for 3 months. Getting both vaccines at the same time cause my immune system revved up and cause a relapse of the condition. Really regret getting both shots at the same time. The information on the news was getting both at the same time is fine and it isn?t. They really should be spaced out.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: None, just contacted my rheumatologist and started back on prednisone, 5mgs. It?s somewhat managing the symptoms although I have days of joint and muscle pain.
Aktuelle Erkrankungen: None
Vorgeschichte: Polymyalgia Rheumatica
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2460737

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7144B

moderat

Staat: IN
Alter: 66,0
Geschlecht: F
Eingang: 26.09.2022
Impfdatum: 09.09.2022
Beginn: 10.09.2022
Tage bis Beginn: 1,0
Dosis: 5
Route/Site: IM / UN

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

Fatigue Laboratory test Mobility decreased Pyrexia

Symptomtext

The next day after the vaccine I had fever of 102, I stay in bed all day. The next day fever went down, I was tired for a couple of days and stay in bed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: Sept 2022 - Lab - Pending
Aktuelle Erkrankungen: N/A
Vorgeschichte: High Blood Pressure; Pre-Diabetes; Anemia; Shortness of Breath; Walking; Rheumatoid Arthritis; Glaucoma; COPD; Obesity
Andere Medikamente: Lovastatin ; Losartan
Allergien: N/A
Vorherige Impfungen: -

VAERS 2456717

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

moderat

Staat: CT
Alter: 57,0
Geschlecht: F
Eingang: 23.09.2022
Impfdatum: 18.09.2022
Beginn: 19.09.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Limb mass Mobility decreased Pain

Symptomtext

Large lump developed on inner left arm near elbow. The lump was painful and throbbing. Caused arm not to bend.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Codeine
Vorherige Impfungen: -

VAERS 2454321

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7144B

moderat

Staat: NY
Alter: 94,0
Geschlecht: F
Eingang: 22.09.2022
Impfdatum: 08.09.2022
Beginn: 08.09.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: OT / LA

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

Asthenia Balance disorder Chills Dyspnoea Fatigue Feeling abnormal Feeling cold Gait disturbance Head discomfort Headache Insomnia Loss of personal independence in daily activities Muscular weakness Tremor

Symptomtext

Difficulty walking; Balance was off; Legs are weak; Feels like dishwasher rag (no energy) / Weak; Shortness of breath / Pants breathing (shallow breathing and fast); She can't do normal household chores; She been going to bed earlier and sleeping later; had a headache in the morning; Felt bad; She was freezing could not get warm; Violently shaking; Pressure in her head (Headache) in the forehead area; Extremely fatigue / Completely exhausted / Completely wipe out; Chills; This spontaneous case was reported by a patient family member or friend and describes the occurrence of TREMOR (Violently shaking), HEAD DISCOMFORT (Pressure in her head (Headache) in the forehead area), GAIT DISTURBANCE (Difficulty walking), BALANCE DISORDER (Balance was off) and MUSCULAR WEAKNESS (Legs are weak) in a 94-year-old female patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. AS7144B) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Previously administered products included for Product used for unknown indication: Pfizer (1st dose, Lot number-EN6203) on 25-Feb-2021, Pfizer (2nd dose, Lot number: EN6208) on 18-Mar-2021, Pfizer (1st booster, Lot number: FF2589) on 15-Oct-2021, Pfizer (2nd booster and Lot number: FM0698) on 21-Apr-2022. Past adverse reactions to the above products included No adverse event with Pfizer, Pfizer, Pfizer and Pfizer. Concurrent medical conditions included Drug allergy (Extremely sensitive to medication (antihistamine)). Concomitant products included DIGOXIN, LEVOTHYROXINE, COLECALCIFEROL (VITAMIN D3), KRILL OIL, FAMOTIDINE (PEPCID [FAMOTIDINE]), CYANOCOBALAMIN (VITAMIN B12 [CYANOCOBALAMIN]), SUPER B COMPLEX WITH C and CRANBERRY [VACCINIUM MACROCARPON] for an unknown indication. On 08-Sep-2022, the patient received fifth dose of mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (Intramuscular) 1 dosage form. On 08-Sep-2022, the patient experienced TREMOR (Violently shaking), HEAD DISCOMFORT (Pressure in her head (Headache) in the forehead area), FEELING COLD (She was freezing could not get warm), FATIGUE (Extremely fatigue / Completely exhausted / Completely wipe out) and CHILLS (Chills). On 16-Sep-2022, the patient experienced FEELING ABNORMAL (Felt bad). On 18-Sep-2022, the patient experienced HEADACHE (had a headache in the morning). On an unknown date, the patient experienced GAIT DISTURBANCE (Difficulty walking), BALANCE DISORDER (Balance was off), MUSCULAR WEAKNESS (Legs are weak), ASTHENIA (Feels like dishwasher rag (no energy) / Weak), DYSPNOEA (Shortness of breath / Pants breathing (shallow breathing and fast)), LOSS OF PERSONAL INDEPENDENCE IN DAILY ACTIVITIES (She can't do normal household chores) and INSOMNIA (She been going to bed earlier and sleeping later). The patient was treated with PARACETAMOL (TYLENOL) at a dose of 500 mg as needed and IBUPROFEN (MOTRIN [IBUPROFEN]) for Headache, at an unspecified dose and frequency. At the time of the report, TREMOR (Violently shaking), HEAD DISCOMFORT (Pressure in her head (Headache) in the forehead area), GAIT DISTURBANCE (Difficulty walking), BALANCE DISORDER (Balance was off), MUSCULAR WEAKNESS (Legs are weak), ASTHENIA (Feels like dishwasher rag (no energy) / Weak), DYSPNOEA (Shortness of breath / Pants breathing (shallow breathing and fast)), FEELING ABNORMAL (Felt bad), LOSS OF PERSONAL INDEPENDENCE IN DAILY ACTIVITIES (She can't do normal household chores), FEELING COLD (She was freezing could not get warm), INSOMNIA (She been going to bed earlier and sleeping later) and CHILLS (Chills) outcome was unknown, FATIGUE (Extremely fatigue / Completely exhausted / Completely wipe out) had not resolved and HEADACHE (had a headache in the morning) was resolving. It was reported that patient never had COVID positive test. Patient daughter stated she did not really had medical issues. No other vaccine was given prior to Moderna COVID-19. She was freezing could not get war. She took Tylenol (500mg) twice, half hour apart a total 1000 mg. Patients daughter stated that she had to put a large hitting pad over her mother to try to get her warm. Then 4 blankets and bed spread. Patient felt weak on 15-Sep-2022. On 18-Sep-2022, she did not feel too bad, had a headache in the morning and Motrin did help. On 19-Sep-2022 she was completely exhausted. She went to lay down around 5 pm.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Drug allergy (Extremely sensitive to medication (antihistamine))
Vorgeschichte: -
Andere Medikamente: DIGOXIN; LEVOTHYROXINE; VITAMIN D3; KRILL OIL; PEPCID [FAMOTIDINE]; VITAMIN B12 [CYANOCOBALAMIN]; SUPER B COMPLEX WITH C; CRANBERRY [VACCINIUM MACROCARPON]
Allergien: -
Vorherige Impfungen: -

VAERS 2453015

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

moderat

Staat: IN
Alter: 23,0
Geschlecht: M
Eingang: 21.09.2022
Impfdatum: 09.09.2022
Beginn: 10.09.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: OT / -

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

Confusional state Disorientation Dizziness Dyspnoea Feeling abnormal Hypoaesthesia Loss of personal independence in daily activities Oxygen saturation Sensory disturbance

Symptomtext

This spontaneous case was reported by a patient and describes the occurrence of DIZZINESS (dizzy), DISORIENTATION (disoriented/He spoke in an online class and got really disoriented, had no idea of what he had said), CONFUSIONAL STATE (He would say something and be confused about it/percribing things slower), LOSS OF PERSONAL INDEPENDENCE IN DAILY ACTIVITIES (doesn't know if he is okay to drive) and SENSORY DISTURBANCE (feels sensory stuff in his hands /feet/ face /he is talking but he is not sure if he is making sense) in a 23-year-old male patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. AS7144B) for COVID-19 prophylaxis. The occurrence of additional non-serious events is detailed below. Previously administered products included for Product used for unknown indication: Pfizer vaccine (Dose Number: 1, Lot number: EW0150) on 03-Apr-2021, Pfizer vaccine (Dose Number: 2 and Lot number: EW0169) on 24-Apr-2021. Past adverse reactions to the above products included No adverse event with Pfizer vaccine and Pfizer vaccine. Concurrent medical conditions included Penicillin allergy, Allergic to cats, Reactive airways disease, Asthma and HIV infection. Concomitant products included EMTRICITABINE, TENOFOVIR DISOPROXIL FUMARATE (TRUVADA) for HIV infection. On 09-Sep-2022 at 10:00 AM, 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 10-Sep-2022, the patient experienced DIZZINESS (dizzy) and DISORIENTATION (disoriented/He spoke in an online class and got really disoriented, had no idea of what he had said). On an unknown date, the patient experienced CONFUSIONAL STATE (He would say something and be confused about it/percibing things slower), LOSS OF PERSONAL INDEPENDENCE IN DAILY ACTIVITIES (doesn't know if he is okay to drive), SENSORY DISTURBANCE (feels sensory stuff in his hands /feet/ face /he is talking but he is not sure if he is making sense), HYPOAESTHESIA (feels like numb), FEELING ABNORMAL (fingers in his feet feel weird) and DYSPNEA (his breathing felt a little like depressed). At the time of the report, DIZZINESS (dizzy), DISORIENTATION (disoriented/He spoke in an online class and got really disoriented, had no idea of what he had said), CONFUSIONAL STATE (He would say something and be confused about it/percibing things slower), LOSS OF PERSONAL INDEPENDENCE IN DAILY ACTIVITIES (doesn't know if he is okay to drive), SENSORY DISTURBANCE (feels sensory stuff in his hands /feet/ face /he is talking but he is not sure if he is making sense), HYPOAESTHESIA (feels like numb), FEELING ABNORMAL (fingers in his feet feel weird) and DYSPNEA (his breathing felt a little like depressed) had not resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, Oxygen saturation: 95-98 %. The patient received 2 doses of Novavax experimental vaccine on early 2021 before receiving the authorized vaccines. The patient received third dose of Moderna vaccine on 09-Dec-2021 as first booster. Lot number was 030H21B. The patient did not experience a similar event in the past. The patient did not seek any medical care. Treatment medication was not reported. This case was linked (Patient Link).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Test Name: blood oxygenation.
Aktuelle Erkrankungen: Allergic to cats; Asthma; HIV infection; Penicillin allergy; Reactive airways disease
Vorgeschichte: -
Andere Medikamente: TRUVADA
Allergien: -
Vorherige Impfungen: -

VAERS 2452219

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7144B

moderat

Staat: NY
Alter: 34,0
Geschlecht: F
Eingang: 20.09.2022
Impfdatum: 13.09.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: IM / LA

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

Angiogram pulmonary normal Bundle branch block left Chest pain Dyskinesia Echocardiogram abnormal Electrocardiogram abnormal Pain Pain in extremity Pain in jaw Scan myocardial perfusion normal Tachycardia Troponin normal

Symptomtext

Episode of exertional substernal chest pain radiating to jaw and left arm accompanied by tachycardia to 150s, all resolving with rest and returning with exertion lasting for 20 minutes.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 2,0
Labordaten: New left bundle branch block on EKG negative 1 and 3 hour troponins Echo showing septal dyskinesis CT angio showing no pulmonary vascular occlusions nuclear stress test showing no abnormalities
Aktuelle Erkrankungen: -
Vorgeschichte: L5-S1 lumbar disc herniation
Andere Medikamente: sertraline 50 mg
Allergien: cats, birch, white ash, mold
Vorherige Impfungen: -

VAERS 2450994

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

moderat

Staat: VA
Alter: 42,0
Geschlecht: F
Eingang: 19.09.2022
Impfdatum: 11.09.2022
Beginn: 11.09.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / LA

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

Hot flush Pharyngeal paraesthesia Rash Swollen tongue

Symptomtext

I experienced a rash on my left arm, my throat start tingling and my tongue swelled up and I start having hot flashes.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pharyngeal paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 2449715

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

moderat

Staat: NJ
Alter: 62,0
Geschlecht: F
Eingang: 17.09.2022
Impfdatum: 13.09.2022
Beginn: 13.09.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Arthralgia Back pain Chills Fatigue Hyperhidrosis Insomnia Mobility decreased Neck pain Pain in extremity Pyrexia Spinal pain

Symptomtext

I had the first two COVID shots and the first booster, all made by Pfizer. I had ZERO symptoms from those shots. I decided to get the second booster and pharmacy told me to take the Moderna Bivalent. In six hours I was feeling pain in my arm and back. It progressed down my spine and neck, both arm, and hips. I could barely move, even my hands. My legs could move, but I could not trun my body and it was agonizing. I had a fever, chills, and was soaked in sweat. I was literally thinking this was the end for me. I am a strong person and kept telling myself this will pass. The pain lasted two days and today is the fouth day and the pain is completely gone, but I am exhausted as I did not sleep and could not move. This was the worst suffering I ever had and will never take another vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Lexapro 10mg, 1X per day Vitamin D, 5000mg, 1X day
Allergien: None
Vorherige Impfungen: -

VAERS 2448553

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

moderat

Staat: IN
Alter: 36,0
Geschlecht: F
Eingang: 17.09.2022
Impfdatum: 10.09.2022
Beginn: 14.09.2022
Tage bis Beginn: 4,0
Dosis: N/A
Route/Site: IM / LA

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

Back pain Musculoskeletal chest pain Pyrexia SARS-CoV-2 test negative

Symptomtext

Excruciating back pain from ribs to should, pain around front ribs, fever. Taking Tylenol every 8 hours. 4 days with no improvement. Remains ingoing

Weitere VAERSDATA-Felder

Praegender Schweregrund: Musculoskeletal chest pain
Hospital-Tage: -
Labordaten: Negative at home covid tests 9/14/22, 9/17/22
Aktuelle Erkrankungen: Cold one week prior. Negative covid test
Vorgeschichte: Bipolar
Andere Medikamente: Wellbutrin, lamotragine, jolessa, ibprofen
Allergien: Nonw
Vorherige Impfungen: -

VAERS 2446303

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

moderat

Staat: DE
Alter: 32,0
Geschlecht: M
Eingang: 15.09.2022
Impfdatum: 03.09.2022
Beginn: 04.09.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

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

Induration Injection site induration Injection site pain Muscle tightness Muscular weakness Pain in extremity Swelling Tremor Urticaria

Symptomtext

Left arm had increasing pain starting from 9/4 from shoulder to elbow to hand with the peak on 9/6. Swelling and "welt" was also peaked on 9/6. There was a small decrease and drop on swelling/hardness by 9/6. Pain remained the same from 9/6. Pain is most prevalent in elbow area. Weakness remained in left arm and shoulder tension as well. Doctor appointment was made on 9/13 for morning of 9/14. Pain as of 9/15 remains at a 5/10 level right above elbow area.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: During 9/14 appointment, doctor noticed tremors in left arm as well as shoulder muscle hardness. Muscle relaxer was prescribed as well as heat and lidocane patches recommended. Instructions were to call back in a week or if pain got worse.
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetes Type 2
Andere Medikamente: Trulicity, Metformin, Glipizide, Losartan Potassium, Rosuvastatin
Allergien: Dust, Pollen, Animals
Vorherige Impfungen: -

VAERS 2444955

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS 7144B

moderat

Staat: NY
Alter: 70,0
Geschlecht: F
Eingang: 14.09.2022
Impfdatum: 08.09.2022
Beginn: 11.09.2022
Tage bis Beginn: 3,0
Dosis: 4
Route/Site: SYR / RA

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

Dyspnoea Headache

Symptomtext

Difficulty taking deep breath, excruciating headache

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Non
Aktuelle Erkrankungen: Cardiac ablation 4 weeks prior with pericarditis due to punctioning of heart wall.
Vorgeschichte: Pvc
Andere Medikamente: Rosuvastatin, Mybetriq, 81 mg aspirin, coq10
Allergien: None
Vorherige Impfungen: -

VAERS 2444639

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

moderat

Staat: OR
Alter: 49,0
Geschlecht: F
Eingang: 14.09.2022
Impfdatum: 08.09.2022
Beginn: 08.09.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: SYR / LA

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

Arthralgia Mobility decreased Pain in extremity

Symptomtext

Severe arm and shoulder pain beginning about 20-40 minutes following the injection. The pain was so severe I was unable to lift my arm for 36 hours. It lessened 48 hours later, but persists seven days after the vaccine, particularly after sleeping on the shoulder. It was so severe and surprising if a reaction that I mentioned it to my doctor at a routine appointment, and she said I should report it.

Weitere VAERSDATA-Felder

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

VAERS 2444009

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

moderat

Staat: FL
Alter: 68,0
Geschlecht: F
Eingang: 13.09.2022
Impfdatum: 09.09.2022
Beginn: 10.09.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Arthralgia Blood test Computerised tomogram thorax abnormal Dyspnoea Headache Mobility decreased Pyrexia Retching Scan with contrast abnormal Tremor Urine analysis Vomiting

Symptomtext

Fever, shakes, joint aches- all joints, headache, vomitting (mainly dry heaves), and inability to breathe. Had to call ambulance to get to hospital as I could not get up off the floor.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Blood and urine tests, CT scan with iodine. Only showed COPD.
Aktuelle Erkrankungen: None
Vorgeschichte: COPD, Heart attack 7/2016.
Andere Medikamente: Trelegy, ventolin as needed, atorvastatin 10 mg, metoprolol 25 mg., vitamin D3 50,000. QX/month, 81mg aspirin
Allergien: None known
Vorherige Impfungen: -

VAERS 2443456

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

moderat

Staat: MI
Alter: 67,0
Geschlecht: F
Eingang: 13.09.2022
Impfdatum: 10.09.2022
Beginn: 10.09.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: SYR / LA

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

Arthralgia Diarrhoea Fatigue Feeling cold Feeling hot Headache Heart rate increased Myalgia Tremor Vomiting

Symptomtext

Uncontrollable shaking, vomiting, diarrhea, chills alternating with feeling hot, joint and muscle aches, fatigue, fast heartbeat, bad headache. Shaking and vomiting stopped after a couple of hours, other symptoms have persisted for 3 days, but are improving. This did not happen with previous covid vaccines. Im wondering if it should not be given with the flu shot.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Clonazepam, Escitalopram. The high dose flu vaccine was administered at the same time as the bivalent vaccine , one in each arm.
Allergien: Zithromax. latex sensitivity
Vorherige Impfungen: -

VAERS 2442803

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7144B

moderat

Staat: PA
Alter: 39,0
Geschlecht: F
Eingang: 13.09.2022
Impfdatum: 11.09.2022
Beginn: 12.09.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: SYR / LA

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

Arthralgia Lymphadenopathy Mobility decreased Neck pain SARS-CoV-2 test negative Skin warm

Symptomtext

09/12/2022 at around 01:00AM I felt the pain in my neck and shoulder area. When I woke up I couldn't move my neck at all. At around 2:00PM I felt there was a lymph on my left shoulder blade it was hot to the touch. The pain was moderate. On 09/12/2022 I was able to have an appointment through video with my doctor. My doctor told me to take TYLENOL and hot pad on the lymph. She also told me if It gets worse to contact her immediately.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: COVID-19 Test- Negative
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Wellbutrin;
Allergien: Detour
Vorherige Impfungen: -

VAERS 2442791

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

moderat

Staat: NY
Alter: 44,0
Geschlecht: F
Eingang: 13.09.2022
Impfdatum: 10.09.2022
Beginn: 10.09.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Chest pain Electrocardiogram normal Painful respiration

Symptomtext

chest pain with deep inspiration while laying down that started the evening of the shot. Continued for 24 hours.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: EKG at 48hrs normal.
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: na
Allergien: none
Vorherige Impfungen: -

VAERS 2442726

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

moderat

Staat: MA
Alter: 31,0
Geschlecht: F
Eingang: 13.09.2022
Impfdatum: 12.09.2022
Beginn: 12.09.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Injected limb mobility decreased Pain in extremity

Symptomtext

4 hours following COVID vaccine administration to L shoulder, patients experienced moderate pain and restricted L arm range of motion.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: None to date
Aktuelle Erkrankungen: N/A
Vorgeschichte: asthma
Andere Medikamente: levonorgestrel-ethinyl estradiol 0.1-20 mg/mcg sertraline 50 mg
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2439932

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

moderat

Staat: OH
Alter: 33,0
Geschlecht: F
Eingang: 10.09.2022
Impfdatum: 08.09.2022
Beginn: 08.09.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Chest pain Dizziness Headache Pain in extremity Painful respiration

Symptomtext

Headache, dizziness, arm soreness all started around 6:15pm on the same day; and chest pain while taking deep breaths started 09/10/2022 morning.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: High blood pressure. Anxiety
Andere Medikamente: Sertraline. Hydrochlorothiazide. Amlodipine. Ibuprofen
Allergien: Naproxen
Vorherige Impfungen: Chills, fatigue, headache, muscle soreness, arm soreness after 1st dose of moderna Covid vaccine (04/23/2021)

VAERS 2428972

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS 7144B

moderat

Staat: CA
Alter: 69,0
Geschlecht: M
Eingang: 05.09.2022
Impfdatum: 03.09.2022
Beginn: 04.09.2022
Tage bis Beginn: 1,0
Dosis: 5
Route/Site: IM / LA

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

Chest pain Extra dose administered Pain Painful respiration

Symptomtext

Mild pericarditis. After having had very painful pericarditis about 10 hours after my first Moderna booster in November 2021 (see separate VAERS report just submitted Temporary Report 882509) which was successfully controlled with a maximum dose of Ibuprofen I took took 200 mg of Ibuprofen prophylactically about 6 hours after my second Moderna booster on April 15, 2022. I had no adverse reactions to that second booster. I did the same with this Moderna bivalent (i.e., 200 mg of Ibuprofen 6 hours after the vaccination). I had no problems during the night by started having chest pains at about 11:30 (about 16 hours after the vaccination). The pain was most severe when bending over and when breathing deeply. Taking 200 mg of Ibuprofen made symptoms go away in a couple of hours.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Daily men's over-50 multivitamin, fish oil capsule, 1000 IU vitamin D4, B50 B vitamins, 500 mg Vitamin C, 100 mg Pycnogenol. 200 mg Ibuprofen taken 6 hours after vaccination (over 12 hours before adverse event.)
Allergien: None
Vorherige Impfungen: Pericarditis about 12 hours after first Moderna booster in November 2021. See separate VAERS report (more severe than this reac

VAERS 2428686

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

moderat

Staat: TX
Alter: 39,0
Geschlecht: M
Eingang: 04.09.2022
Impfdatum: 02.09.2022
Beginn: 02.09.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Chest pain Lethargy Pain Vertigo

Symptomtext

Day 1: lethargy, body aches Day 2: lethargy, body aches, chest pain, severe vertigo.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Testosterone Thyroid
Allergien: None
Vorherige Impfungen: -

VAERS 2691598

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: AZ
Alter: 74,0
Geschlecht: F
Eingang: 05.10.2023
Impfdatum: 25.09.2022
Beginn: 30.09.2023
Tage bis Beginn: 370,0
Dosis: 4
Route/Site: IM / RA

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

Asthenia COVID-19 Cough Hypoxia Nausea Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

no adverse reaction to vaccine, but tested positive for COVID on 9/30/2023 upon presentation to the ED with symptoms of nausea, nonproductive coughing, rhinorrhea, congestion and generalized weakness. Admitted to the Adult Care unit x 2 days due to her age, weakness, and mild hypoxia.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Nausea
Hospital-Tage: 2,0
Labordaten: 9/30/2023: Emergency Department Course and Clinical Decision Making I reviewed her medical records. Given that the etiology for the patient's cough and generalized weakness was unclear from the patient's history of present illness, past medical history and physical exam findings alone, the appropriate laboratory and radiographic studies were obtained. I ordered a chest x-ray in order to assess the patient's heart size and mediastinum and to evaluate for any pulmonary infiltrates or effusions. I ordered a twelve-lead ECG in order to evaluate for any dysrhythmias or evidence of an acute ischemic cardiac injury. I ordered a CBC in order to assess the patient hemoglobin and hematocrit for anemia and to evaluate the white blood cell count as a marker of underlying infectious process. I ordered a cath urinalysis in order to evaluate for the presence of white blood cells, bacteria, leukocyte Estrace and/or nitrites to suggest an acute cystitis and to evaluate for microscopic hematuria to indicate a possible ureteral stone. Given my concern for SIRS and sepsis, I did order a lactic acid and 2 blood cultures. Lastly, I tested her for COVID-19.
Aktuelle Erkrankungen: unknown
Vorgeschichte: dysuria uncontrolled hypertension recurrent UTI hyperopia OU with astigmatism and presbyopia
Andere Medikamente: unknown
Allergien: lisinopril - unknown reaction
Vorherige Impfungen: -

VAERS 2677289

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: CA
Alter: -
Geschlecht: M
Eingang: 28.08.2023
Impfdatum: 09.09.2022
Beginn: -
Tage bis Beginn: -
Dosis: 6
Route/Site: - / -

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

Arthralgia Joint injury

Symptomtext

He was doing some balancing exercises and tweaked his ankle. His right ankle and pain was ongoing to this point.; He was doing some balancing exercises and tweaked his ankle. His right ankle and pain was ongoing to this point.; This spontaneous case was reported by a patient family member or friend and describes the occurrence of JOINT INJURY (He was doing some balancing exercises and tweaked his ankle. His right ankle and pain was ongoing to this point.) and ARTHRALGIA (He was doing some balancing exercises and tweaked his ankle. His right ankle and pain was ongoing to this point.) in an elderly male patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch nos. AS7144B and C23415) for COVID-19 prophylaxis. Concurrent medical conditions included Gout. Concomitant products included IBUPROFEN (ADVIL [IBUPROFEN]) for Gout. On 09-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-Aug-2023, received sixth dose of mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (unknown route) dosage was changed to 1 dosage form. On an unknown date, the patient experienced JOINT INJURY (He was doing some balancing exercises and tweaked his ankle. His right ankle and pain was ongoing to this point.) and ARTHRALGIA (He was doing some balancing exercises and tweaked his ankle. His right ankle and pain was ongoing to this point.). At the time of the report, JOINT INJURY (He was doing some balancing exercises and tweaked his ankle. His right ankle and pain was ongoing to this point.) and ARTHRALGIA (He was doing some balancing exercises and tweaked his ankle. His right ankle and pain was ongoing to this point.) had not resolved. Patient received his first dose of Moderna Covid-19 vaccine on 24-Jan-2021 (Lot number: 007M20A), second dose of Moderna Covid-19 vaccine on 27-Feb-2021 (lot number: 023M70A), third dose of Moderna Covid-19 vaccine on 23-Oct-2021 (lot number: 032F1A), Fourth dose of Moderna Covid-19 vaccine 13-Apr-2022 (lot number: 005M21A). It was reported that Prior to his most recent dose yesterday he noticed his ankle did not feel great. He was doing some balancing exercises and tweaked his ankle. His right ankle and pain was ongoing to this point. He has not taken medications or treatments for his symptoms but would like to know if he could take Advil or Aloprim.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Gout
Vorgeschichte: -
Andere Medikamente: ADVIL [IBUPROFEN]
Allergien: -
Vorherige Impfungen: -

VAERS 2462040

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: -
Alter: 67,0
Geschlecht: M
Eingang: 22.06.2023
Impfdatum: 09.09.2022
Beginn: 20.01.2023
Tage bis Beginn: 133,0
Dosis: 5
Route/Site: IM / RA

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

Angina pectoris Blood test normal Fatigue Loss of personal independence in daily activities

Symptomtext

ANGINA, UNSPECIFIED

Weitere VAERSDATA-Felder

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

VAERS 2626643

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: CA
Alter: 64,0
Geschlecht: M
Eingang: 04.05.2023
Impfdatum: 11.09.2022
Beginn: 14.03.2023
Tage bis Beginn: 184,0
Dosis: 5
Route/Site: IM / LA

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

COVID-19 Cough Exercise tolerance decreased Fatigue Pyrexia Respiratory tract irritation SARS-CoV-2 test positive

Symptomtext

My symptoms began as a cough and irritation in my chest. I had a low fever and a lot of fatigue. My fever lasted about a week. I tested positive on 3/16/2023. I had a rebound after 3 days of testing negative and now I have tested negative again. I feel better but I still have a lot of fatigue and I've lost my stamina for fitness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Multi Vitamin
Allergien: N/A
Vorherige Impfungen: -

VAERS 2620774

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: NJ
Alter: 61,0
Geschlecht: F
Eingang: 25.04.2023
Impfdatum: 19.09.2022
Beginn: 25.04.2023
Tage bis Beginn: 218,0
Dosis: 5
Route/Site: IM / LA

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

COVID-19 Chills Fatigue Feeling abnormal Influenza like illness SARS-CoV-2 test positive

Symptomtext

I was fine for 12 hours but then I didn't feel good for about 36 hours. I felt like I had the flu with chills and fatigue. I tested positive for COVID-19 on 03/23/2023. I contacted my doctor and got a prescription for Paxlovid. I tolerated the medication without any complications. As of today, I do not have any lingering COVID-19 symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: 23MAR2023 COVID-19 Test - Positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Heart Palpitations; Fasciculations and Cramps Syndrome
Andere Medikamente: Sertraline; Gabapentin
Allergien: N/A
Vorherige Impfungen: For all vaccines; I would be fine for 12 hours but then I didn't feel good for about 36 hours.

VAERS 2619974

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: FL
Alter: 77,0
Geschlecht: F
Eingang: 24.04.2023
Impfdatum: 12.09.2022
Beginn: 14.11.2022
Tage bis Beginn: 63,0
Dosis: 5
Route/Site: IM / LA

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

COVID-19 Computerised tomogram head normal Ear discomfort Fatigue Malaise Rhinorrhoea SARS-CoV-2 test positive Sinus congestion Sinusitis

Symptomtext

On about 11/14/2022, I was extremely tired and had general malaise. I took a home antigen test that day and got a negative result. I took it again about 11/15/2022 and got a positive result. I then underwent a PCR test that day, and it also yielded a positive result. I called my doctor and notified her of the situation. At that point, I didn't have a fever. The only symptoms I had were sinus congestion and runny nose. My doctor recommended that I take vitamin B3, vitamin C, and another supplement whose name escapes me. I continued to test positive for COVID-19 for two weeks afterwards. I finally tested negative around 12/5/2022. I went to an ENT on 3/8/2023, because I continued to have sinus congestion and fullness in the ear. The ENT diagnosed me with sinusitis and prescribed me amoxicillin/clavulanic acid, which I was to take for 21 days. This seems to have helped, because I feel fine now. On 4/13/2023, I underwent a CT scan of my sinuses, because my ENT wanted to see if my sinuses had cleared up or if I had a serious condition. The results indicated that my sinuses were clear.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 14NOV2022 - Home Antigen Test - Negative Result; 15NOV2022 - Home Antigen Test - Positive Result; 15NOV2022 - PCR Test - Positive Result; 05DEC2022 - Home Antigen Test - Negative Result; 13APR2023 - CT Scan of Sinuses - Clear Sinuses Indicated
Aktuelle Erkrankungen: None
Vorgeschichte: Rheumatoid Arthritis; Chronic Lymphocytic Leukemia
Andere Medikamente: Plaquenil; Doxycycline; Levothyroxine; Estradiol Vaginal Cream; Metronidazole Topical Cream; Fluticasone Nasal Spray; Calcium; Glucosamine Chondroitin; Hair, Skin, and Nails Vitamins with Biotin; Red Yeast Rice; Turmeric
Allergien: Hydrocodone
Vorherige Impfungen: -

VAERS 2616892

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: PA
Alter: 62,0
Geschlecht: F
Eingang: 18.04.2023
Impfdatum: 14.10.2022
Beginn: 23.03.2023
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 Cough Malaise Oropharyngeal pain SARS-CoV-2 test positive

Symptomtext

I was positive for COVID-19 on 23MAR2023, I had a sore throat and cough. I generally wasn't feeling well but the sore throat was really bad and severe, I don't remember that I had a fever. I took PAXLOVID that was prescribed by my doctor, I started to feel better about 2 weeks after.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: 23MAR2023 COVID-19 test positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Irritable Bowel Syndrome
Andere Medikamente: FLONASE; SYNTHROID; multivitamin; XYZAL
Allergien: Seasonal allergies
Vorherige Impfungen: -

VAERS 2612382

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: OH
Alter: 73,0
Geschlecht: F
Eingang: 10.04.2023
Impfdatum: 09.09.2022
Beginn: 26.12.2022
Tage bis Beginn: 108,0
Dosis: 5
Route/Site: SYR / LA

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

COVID-19 Cough Fatigue Malaise Pain Pyrexia SARS-CoV-2 test positive

Symptomtext

My COVID-19 infection symptoms started on 12/26/2022. I wasn't feeling well so I took a home COVID-19 test before going to work and it was negative. I had slight fever, felt achy and tired. Then I took another home test on 12/27/2022 which was positive. I had fever, tiredness, and cough. On 12/28/2022 my symptoms got worse. On 12/29/2022 symptoms stayed the same and I called my doctor's office where I did telehealth. They prescribed me PAXLOVID for 5 days. I also took TYLENOL for fever.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 27DEC2022 COVID-19 test positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: COPD
Andere Medikamente: Calcium; preservation; CENTRUM SILVER; zinc; vitamin; baby aspirin; CRESTOR; losartan; hydrochlorothiazide; carvedilol
Allergien: N/A
Vorherige Impfungen: 1st Shingles vaccine, I had body aches and tiredness. It really knocked me out for few days.

VAERS 2612319

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: OH
Alter: 69,0
Geschlecht: M
Eingang: 10.04.2023
Impfdatum: 15.09.2022
Beginn: 03.04.2023
Tage bis Beginn: 200,0
Dosis: 5
Route/Site: - / AR

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

Fatigue Influenza A virus test negative Influenza B virus test Insomnia Malaise Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test negative

Symptomtext

I was having a runny nose and congestion. That led to more congestion and some fatigue, but I am not sure that is not related and more to not sleeping will from being ill. I took three different COVID-19 Home Test's, and they were all negative. I also went into the pharmacy, and they tested me as well and it was negative as long as for influenza those were all negative as well. I did a telehealth anointment with my doctor, and they have me on OTC meds and using a Netti Pot as well.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID-19 Home Test; COVIDD-19 PCR; Influenza A and B
Aktuelle Erkrankungen: N/A
Vorgeschichte: Arrhythmic Heart-left branch bundle block
Andere Medikamente: Carvedilol; Quinapril; Hydrochlorothiazide; Multivitamin; Vitamin C
Allergien: Prednisone; Penicillin
Vorherige Impfungen: -

VAERS 2611887

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: NY
Alter: 64,0
Geschlecht: F
Eingang: 07.04.2023
Impfdatum: 07.09.2022
Beginn: 16.11.2022
Tage bis Beginn: 70,0
Dosis: 4
Route/Site: IM / LA

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

Ageusia Anosmia COVID-19 Oropharyngeal pain Pyrexia SARS-CoV-2 test positive

Symptomtext

I had a sore throat, fever for a day, loss sense of taste and smell. I tested myself day 1 and 2 for COVID-19 and tested negative. On day 3, I tested positive for COVID-19. I took Tylenol for my symptoms because my doctor said that my symptoms were so mild that I didn't need a prescription. It took at least 2 months for my smell to come back.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: Positive, COVID-19 Test, 11/18/2022
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Levothyroxine; Diethylpropion
Allergien: Sulfa Drugs
Vorherige Impfungen: -

VAERS 2610681

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: WI
Alter: 61,0
Geschlecht: F
Eingang: 06.04.2023
Impfdatum: 03.10.2022
Beginn: 24.11.2022
Tage bis Beginn: 52,0
Dosis: 5
Route/Site: IM / LA

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

COVID-19 Decreased appetite Dysgeusia Ear infection Gastrointestinal disorder Lung disorder Myalgia Paranasal sinus hypersecretion SARS-CoV-2 test positive Sinus disorder Weight decreased

Symptomtext

I was bothered by the flu vaccine. I got COVID in December 11, 2022. I experienced sinus, ear infection, nasal drainage, some muscle aches and everything tasty salty. I got tested for COVID on 12-11-2022. I did not take anti-viral medications and slept with my head elevated. I did not have an appetite. I tested negative the day after Christmas. My doctor put me on Doxycycline for one week and it took me awhile to get better since I also had GI symptoms. I also had some pleura in my lungs. I was losing half a pound of day. I dropped 30 pounds. I also have kidney cancer, stage 4, it is not genetic. Now I have been feeling bit better since mid March 2023.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myalgia
Hospital-Tage: -
Labordaten: 11DEC2022 COVID-19 Test-Positive
Aktuelle Erkrankungen: Kidney Cancer
Vorgeschichte: Obese; Type II Diabetic; History of Kidney Cancer
Andere Medikamente: Metformin; Gemfibrozil; Lisinopril; Amlodipine; Tomycine; Insulin; JARDIANCE; Nevola; Calcium with Vitamin D; D3; Multivitamin; B12; Ginger Tea
Allergien: Additives in Ranch Dressings; Lactose Intolerant; Latex; Dust Mites; Mold; Anti-Nausea Medication
Vorherige Impfungen: -

VAERS 2610663

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: MD
Alter: 64,0
Geschlecht: M
Eingang: 06.04.2023
Impfdatum: 07.09.2022
Beginn: 04.01.2023
Tage bis Beginn: 119,0
Dosis: 5
Route/Site: SYR / LA

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

COVID-19 Cardiac monitoring normal Electrocardiogram abnormal Heart rate increased Oropharyngeal pain SARS-CoV-2 test positive Sinus congestion

Symptomtext

First initial symptom was a rapid heartbeat, I knew it because my smart watch told me so. My heart rate was running 106 and 108 while inactive this was 11:00AM. I was just sitting still. I called my doctor via tele-medicine. I decided to take an at home COVID-19 test and it was positive. I also went to the urgent care for a PCR it was also positive. I had come in for an EKG. There was no concern other than the rate itself. The next day I had a sore throat and sines congestion. I was given PAXLOVID, which I took and my symptoms abated in a few days. My heart rate had been normal by the 7th. By the 11th I was testing negative. By that afternoon of the 12th, my heart was racing again it was in the mid 90's. I tested again on the 14th and I was positive again. I knew I had rebound. I was negative on the 21st. Since then my heart has popped up once or twice. on February 3rd, 5th, and the 19th, and March 5th. Since then I had no episodes. I actually wore a heart monitor for a week and everything came back normal.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: 04JAN2023 COVID-19 positive; 04JAN2023 EKG, irregular heart rate; 07FEB2023 EKG, normal; 07-14FEB Heart Monitor, normal
Aktuelle Erkrankungen: N/A
Vorgeschichte: High Blood Pressure
Andere Medikamente: Lisinopril; loratadine; fish oil
Allergien: N/A
Vorherige Impfungen: -

VAERS 2610647

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7144B

mild

Staat: CT
Alter: 73,0
Geschlecht: F
Eingang: 06.04.2023
Impfdatum: 12.04.2022
Beginn: 16.02.2023
Tage bis Beginn: 310,0
Dosis: 5
Route/Site: IM / LA

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

COVID-19 Cough Fatigue Pain Pyrexia SARS-CoV-2 test positive

Symptomtext

February 16, 2023 I was having a little cough and fatigue. The next day I took a home COVID-19 test because I woke up with a fever of 101.3, aches and pains. I contacted my doctor via a tele health appointment she prescribed me Paxlovid but I was unable to take the full dose. I took the medication for 5 days. I started feeling better and symptoms started to go away around two days of taking medication.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: FEB162023COVID-19home test- Positive
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma
Andere Medikamente: Famotidine; Rosuvastatin; Folic Acid; Asmanex; Aspirin; Acyclovir; Calcium; Vitamin D
Allergien: Sulfa Antibiotics; Cephalosporin; Acetazolamide; Levofloxacin; Nystatin; Magnesium Saliya; Prednisone; Valacyclovir; Cefadroxil; Sulfasalazine
Vorherige Impfungen: -

VAERS 2610436

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: AZ
Alter: 69,0
Geschlecht: M
Eingang: 05.04.2023
Impfdatum: 10.09.2022
Beginn: 01.03.2023
Tage bis Beginn: 172,0
Dosis: 4
Route/Site: SYR / RA

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

COVID-19 Cough Fatigue Headache Increased appetite Malaise Nasal discharge discolouration Nasopharyngitis Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

It started out with a cold little bit of a headache runny nose and a cough and then I got worse. Incredible runny nose with green stuff, fatigue and an increase in appetite, congestion, and headache. I was just really tired. My Dr. prescribed Paxlovid and I took Ibuprofen. I was sick over 2 weeks, no trouble breathing.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Covid-19 Positive test.
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Metoprolol; Losartan; Vitamin D-3, Fiber supplement
Allergien: Penicillin; Lamisil Oral
Vorherige Impfungen: -

VAERS 2609917

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: MA
Alter: 71,0
Geschlecht: F
Eingang: 05.04.2023
Impfdatum: 07.09.2022
Beginn: 01.10.2022
Tage bis Beginn: 24,0
Dosis: 5
Route/Site: IM / LA

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

Bronchitis viral COVID-19 Chest X-ray normal Cough Fatigue Feeling hot Hyperhidrosis Influenza like illness Nausea Pyrexia SARS-CoV-2 test positive Sleep disorder

Symptomtext

So the COVID-19 I was up every hour with coughing, a little fever and sweats, I would up and took a COVID-19 test and it was positive. I called my doctor and asked if she wanted me to take antiviral and she said yes. I took the antivirals for the next five days. I was fluish and fatigue. I was nausea on the first day but not the rest of the time. I was still fluish and fatigued that following week. I was still fatigued for two to three weeks afterwards. I had a bit of the rebound. The second health event, January 26th I was traveling, and I had a terrible wet cough. I was very warm I didn't get better rater three days. My doctor instructed me to go to urgent to ensure it was not pneumonia. They tested me and it was not pneumonia, but they thought it viral Bronchitis. I didn't take any medicine since there medication, so I had to wait for it to pass.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 26OCT2022 at home COVID-19 - Positive; 01FEB2023 Chest x-ray - Normal
Aktuelle Erkrankungen: N/A
Vorgeschichte: Cancer Remission
Andere Medikamente: Atorvastatin; Calcium
Allergien: Sceptor; Cipro; Sulfa drugs
Vorherige Impfungen: -

VAERS 2609094

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: PA
Alter: 67,0
Geschlecht: M
Eingang: 04.04.2023
Impfdatum: 07.09.2022
Beginn: 01.01.2023
Tage bis Beginn: 116,0
Dosis: 5
Route/Site: IM / LA

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

COVID-19 Cough Fatigue Pain Vaccine breakthrough infection

Symptomtext

I had a breakthrough case of Covid 19 with mild cough body aches fatigue I was prescribed Paxlovid.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: High Blood Pressure: Gout: Kidney Stones
Andere Medikamente: Metoprolol: Losartan+ hydrochlorothiazide: allopurinol: Vitamin D
Allergien: pennicilin
Vorherige Impfungen: -

VAERS 2607962

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: WI
Alter: 66,0
Geschlecht: F
Eingang: 01.04.2023
Impfdatum: 13.09.2022
Beginn: 05.01.2023
Tage bis Beginn: 114,0
Dosis: 5
Route/Site: SYR / LA

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

COVID-19 Cough Fatigue Malaise Respiratory tract congestion SARS-CoV-2 test negative SARS-CoV-2 test positive

Symptomtext

Tested positive for COVID with home test on 1/5/23. Husband tested positive on 1/2/23. I had a negative PCR test on 1/2/23, but some mild symptoms appeared 1/4/23. Temperature about 100. Fatigue, cough, congestion. Had Zoom visit with healthcare professional at PCP's practice on 1/5/23. Started Paxlovid 1/5/23 twice a day. Symptoms subsided within 2-3 days, but then recurred3-5 days after the 5-day Paxlovid regimen was completed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: PCR 1/2/23 negative. (no symptoms this date, but took test because husband tested positive on this date) Home test (iHealth Rapid Antigen) positive on 1/5/23
Aktuelle Erkrankungen: none
Vorgeschichte: osteoporosis
Andere Medikamente: Alendronate Sodium 70 mg once a week Vitamin D3 50 mcg/2000iu daily
Allergien: none
Vorherige Impfungen: -

VAERS 2607507

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: PA
Alter: 70,0
Geschlecht: F
Eingang: 31.03.2023
Impfdatum: 29.09.2022
Beginn: 15.10.2022
Tage bis Beginn: 16,0
Dosis: 5
Route/Site: IM / AR

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

Blood test normal Computerised tomogram normal Dizziness Dysarthria Electrocardiogram normal Electroencephalogram normal Incoherent SARS-CoV-2 test negative Transient ischaemic attack

Symptomtext

I got woozy and my speech got slurred. When I was talking, I wasn't making since. I had my First TIAA at 11:00AM and the second one was at 02:00PM on day 10/15/2022. I was in the emergency room for 29 hours. I have to take Aspirin 88mg , Lipitor 40MG .

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: 1,0
Labordaten: 15OCT22 CAT Scan-Normal; EKG-Normal; EEG-Normal; Blood Work-Normal; COVED- 19 Test -Negative
Aktuelle Erkrankungen: Diverticulitis
Vorgeschichte: Diverticulitis
Andere Medikamente: Multi-vitamin; Vitamin-D3 Calcium
Allergien: Banana
Vorherige Impfungen: -

VAERS 2607439

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: CO
Alter: 66,0
Geschlecht: M
Eingang: 31.03.2023
Impfdatum: 09.09.2022
Beginn: 07.03.2023
Tage bis Beginn: 179,0
Dosis: 3
Route/Site: SYR / LA

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

Abdominal discomfort Ageusia Anosmia Autoscopy Blood test COVID-19 Decreased appetite Dysgeusia Fatigue Gait disturbance Musculoskeletal stiffness Oropharyngeal pain Productive cough Sinusitis Thirst Weight decreased

Symptomtext

It started out as a sore throat the night before and became like a sinus infection the next day. I was feeling extremely tired and I felt like I was not in my body. I was stiff all over, hard to walk around. Lack of appetite and I was very thirsty. It gave my mouth a metallic taste and I had a sick feeling in my stomach. I lost my sense of smell and taste. I was extremely tired. Once I started the PAXLOVID I slowly started getting my sense of smell and taste back. I've lost about 13 pounds since I had COVID-19. I was also coughing up a lot of phlegm.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Blood test
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma; Sleep Apnea; Permanent Kidney damage; Hypothyroidism
Andere Medikamente: SINGULAIR; levothyroxine; lisinopril; amlodipine; ADVAIR; albuterol; vitamin D; vitamin B-6; PEPCID; FLONASE
Allergien: Hydrocodone
Vorherige Impfungen: -

VAERS 2607415

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: NY
Alter: 58,0
Geschlecht: F
Eingang: 31.03.2023
Impfdatum: 09.09.2022
Beginn: 26.01.2023
Tage bis Beginn: 139,0
Dosis: 5
Route/Site: IM / RA

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

COVID-19 Cough Dysgeusia Eczema Exercise tolerance decreased Fatigue Pyrexia SARS-CoV-2 test positive Sleep disorder

Symptomtext

I started with a sudden consistent dry cough. I took a home test the next day it was positive, and I called the doctor. I was told to take Nyquil and Dayquil. The cough was really bad it was keeping me awake. I had fatigue and five days in I had a really bad eczema outbreak. It was on my chest back, and stomach. I ran a fever on and off the entire time. It was up to 102. It took almost 10 days to be relieved of symptoms. I suffered from fatigued the entire month. I did develop a metallic taste in my mouth during that month. I'm still a little bit tired, I cant work out like I used to. It is significantly better I don't have to take naps like before after working.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 27JAN2023 COVID-19 Test - Positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: B12; Multivitamins; Zinc; Probiotic
Allergien: N/A
Vorherige Impfungen: -

VAERS 2607374

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: NY
Alter: 77,0
Geschlecht: M
Eingang: 31.03.2023
Impfdatum: 04.09.2022
Beginn: 16.02.2023
Tage bis Beginn: 165,0
Dosis: 4
Route/Site: IM / LA

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

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

Symptomtext

On 02/16/2023, midday, I had congestion, lots of aches and pains, I felt lousy. I had no fever and a little cough. That evening, I tested positive for COVID-19. I called my doctor for a telehealth visit. He prescribed Paxlovid. I start Paxlovid on 02/17/2023. I took it for 5 days. Symptoms went away rapidly. Five days later, on 02/22/2023, I tested negative. Symptoms came back and I was testing positive again with mild symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: 16FEB2023 - COVID-19 Test- Positive; 22FEB2023 - COVID-19 Test- Negative; 27FEB2023 - COVID-19 Test- Positive; 06Mar2023- COVID-19 Test- Negative
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Lisinopril; Sinvastatin
Allergien: N/A
Vorherige Impfungen: -

VAERS 2606888

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7144B

mild

Staat: FL
Alter: 68,0
Geschlecht: F
Eingang: 30.03.2023
Impfdatum: 12.09.2022
Beginn: 04.11.2022
Tage bis Beginn: 53,0
Dosis: 4
Route/Site: IM / RA

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

COVID-19 Fatigue Nausea Oropharyngeal pain Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

After the shot I had nausea and fatigue for 2 days. Months after I had a sore throat, fatigue, and sniffles. I saw the doctor on a cruise, and he tested me COVID-19 and it came back positive.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID-19 Test, 11/04/2022, Positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Type 2 Diabetes
Andere Medikamente: Crestor; Zetia; CoQ10; Loratadine; D3; Biotin; Invokamet; B6; Zyrtec; Centrum Silver; Super Complex; Baby Aspirin; Magnesium
Allergien: Fish Oil; Sea Food
Vorherige Impfungen: All COVID-19 Vaccines, Nauseous and Fatigue

VAERS 2606600

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: NJ
Alter: 67,0
Geschlecht: F
Eingang: 30.03.2023
Impfdatum: 15.09.2022
Beginn: 24.02.2023
Tage bis Beginn: 162,0
Dosis: 5
Route/Site: IM / RA

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

Blood glucose decreased COVID-19 Cough Heart rate increased Heart rate irregular Oropharyngeal pain Pulmonary congestion Pyrexia Sinus congestion Upper respiratory tract infection Vaccine breakthrough infection

Symptomtext

I had a breakthrough case of Covid 19 what started out like an upper respiratory infection with fever and sore throat coughing and sinus congestion. I had an irregular heartbeat or rapid heartbeat with low blood sugar. Lung congestion as well.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetes; Asthma; Congestive Heart Failure; Thyroid
Andere Medikamente: Levoxyl; metformin; vitamin B complex; fish oil; vitamin D; cranberry; fiber; losartan; ezetimibe; trimethoprim; rosuvastatin; ALLEGRA; PAXLOVID; Z-PAK; MUCINEX; benzonatate; albuterol inhaler.
Allergien: Iodine; ROCEPHIN; LEVAQUIN
Vorherige Impfungen: -

VAERS 2604885

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: NC
Alter: 68,0
Geschlecht: F
Eingang: 28.03.2023
Impfdatum: 26.09.2022
Beginn: 01.01.2023
Tage bis Beginn: 97,0
Dosis: 5
Route/Site: IM / LA

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

COVID-19 Chills Oropharyngeal pain Pain SARS-CoV-2 test positive

Symptomtext

I started having a sore throat, achiness, then having chills. I used a home COVID-19 test that came back immediately. I called my doctor to let them know I was positive, they called in a prescription of the PAXLOVID that I started taking immediately. It took three days for me to start feeling better, the only thing was the taste of the medication. I did quarantine for a full ten days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: 00JAN2023 home COVID-19 test, positive
Aktuelle Erkrankungen: No
Vorgeschichte: Diabetes; High Blood Pressure; High Cholesterol; Allergies; Acid Reflux; Depression
Andere Medikamente: Metformin; JANUVIA; losartan potassium; omeprazole; bupropion; vitamin D3; montelukast; lovastatin; meloxicam; fluticasone; loratadine; probiotic
Allergien: Lisinopril; yeast sensitivity
Vorherige Impfungen: -

VAERS 2604798

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: MI
Alter: 82,0
Geschlecht: M
Eingang: 28.03.2023
Impfdatum: 08.09.2022
Beginn: 15.02.2023
Tage bis Beginn: 160,0
Dosis: 5
Route/Site: IM / AR

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

Blood thyroid stimulating hormone abnormal Brain fog COVID-19 Fatigue Hallucination Listless SARS-CoV-2 test positive

Symptomtext

I started getting super tired, fuzzy in the brain, listless. I took two home COVID-19 test. I thought the I had messed up the first one so I took a second one, both tests came back positive. I called my doctor, he prescribed the PAXLOVID. I think I was not taking the medication correctly. I kept getting work halfway through the medication. On February 20, 2023, I called the EMS to come take me to the emergency room. My heart rate was 180 upon arrival of the EMS. I cannot remember all tests that were run. I was hallucinating at one time during my stay in the hospital. I am on the road to recovery; I have a follow up appointment with my primary care physician and a heart doctor May.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: 9,0
Labordaten: 15FEB2023 home COVID-19 test positive; 20FEB2023 PCR COVID-19 positive; 20FEB2023 TSH test, abnormal thyroid
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Atorvastatin; valsartan; verapamil; NIASPAN; ZETIA; tamsulosin; metoprolol
Allergien: No
Vorherige Impfungen: -

VAERS 2604206

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: VA
Alter: 33,0
Geschlecht: F
Eingang: 27.03.2023
Impfdatum: 23.09.2022
Beginn: 17.12.2022
Tage bis Beginn: 85,0
Dosis: 4
Route/Site: IM / AR

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

COVID-19 Exposure during pregnancy Exposure to SARS-CoV-2 Glucose tolerance test abnormal Illness Influenza Malaise Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

My husband had developed symptoms consistent with COVID-19. He took a home antigen test on about 12/15/2022, and the result was positive. My son then tested positive on about 12/16/2022. I took a home antigen test on 12/17/2022 and got a positive result. I didn't really have any symptoms of COVID-19 other than maybe a runny nose. I had had a runny nose throughout my pregnancy, though, so I didn't give it much thought. I contacted my midwife, who had me start taking 81 mg of aspirin, zinc, vitamin D, and vitamin C on a daily basis. I was told that I was to take the aspirin until the 36th week of pregnancy, and at the time of this writing, I am still taking it. I was told that I should take the zinc, vitamin D, and vitamin C during my illness, though, and I took those for a month. I am still pregnant, and my baby is due on 6/2/2023. During my pregnancy, I had COVID-19 in December 2022 and influenza A in January 2023. During my bout with influenza A, I took TamiFlu. I was sick for five to seven days. I also took Cepacol cough drops, Mucinex, Zyrtec, and acetaminophen during this time. Whenever I have gone for check-ups, the baby has always appeared healthy, and I have never had complications during my pregnancy. However, I did fail a one-hour glucose test, but I did pass a three-hour glucose test. This is my second pregnancy, and I never failed any glucose tests during my first pregnancy. My midwife has had me undergo increased surveillance. After the regular 20th week ultrasound, they are going to have me do an ultrasound every six weeks afterwards. Starting at the 36th week, I'm going to undergo a nonstress test every week until the baby arrives.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: 17DEC2022 - Home Antigen Test - Positive Result
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Prenatal Vitamins
Allergien: Seasonal Allergies; Cat Dander
Vorherige Impfungen: -

VAERS 2604090

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: MA
Alter: 75,0
Geschlecht: F
Eingang: 27.03.2023
Impfdatum: 21.09.2022
Beginn: 25.01.2023
Tage bis Beginn: 126,0
Dosis: 5
Route/Site: IM / LA

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

COVID-19 Headache Respiratory symptom Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive Sluggishness Symptom recurrence Wheezing

Symptomtext

I just had a running nose. I had a temperature of 99.9. I had upper respiratory symptoms of congestion, wheezing and headache. I did a at home test, and I was positive for COVID-19. I had these symptoms a couple of days, then I contacted my doctor. They prescribed Paxlovid, I started feeling relief after a few days and soon after, I thought I was good for a while. The symptoms did return on 02/04/2023, I was testing positive still. I feel fine now, I still feel sluggish.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: JAN2023 COVID-19 Test - Positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: High Blood Pressure
Andere Medikamente: Hydrochlorothiazide; Losartan; Multivitamins
Allergien: N/A
Vorherige Impfungen: -

VAERS 2603859

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144 B

mild

Staat: IL
Alter: 67,0
Geschlecht: F
Eingang: 26.03.2023
Impfdatum: 13.09.2022
Beginn: 16.01.2023
Tage bis Beginn: 125,0
Dosis: 1
Route/Site: IM / RA

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

COVID-19 Fatigue Influenza like illness SARS-CoV-2 test Vaccine breakthrough infection

Symptomtext

NOTHING AT THE TIME. BREAKTHROUGH COVID IN JAN 2023. FLU LIKE SYMPTOMS FOR A DAY OR TWO. TIREDNESS.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID TEST
Aktuelle Erkrankungen: NONE
Vorgeschichte: NONE
Andere Medikamente: RALOXIPHENE, VITAMIND3, calcium +D, zinc
Allergien: NONE
Vorherige Impfungen: -

VAERS 2603484

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: OH
Alter: 63,0
Geschlecht: F
Eingang: 24.03.2023
Impfdatum: 19.09.2022
Beginn: 11.03.2023
Tage bis Beginn: 173,0
Dosis: 5
Route/Site: IM / LA

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

COVID-19 Diarrhoea Dry mouth Headache Pain Paranasal sinus discomfort Pulmonary congestion SARS-CoV-2 test positive Stomatitis

Symptomtext

I had a headache, sinus pressure, congestion in my lungs, dry mouth, mouth sores, aches, diarrhea, but no fever. I took a COVID-19 test on 03/12/2023 which came back positive almost immediately. I called my doctor days later and was prescribed Paxlovid. I picked up the prescription but decided not to take as I began feeling better around day 4 or so after testing positive. Before picking up Paxlovid, I was taking Mucinex, Tylenol, and Nyquil to aid my recovery which is why I opted out taking the Paxlovid prescription. As of now, I'm making a recovery and treating my symptoms with Mucinex; I still haven't fully regained my voice, but still getting better slowly.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: 12MAR2023 -- COVID-19 Test - Positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Estrogen; Progesterone; Multivitamin; Vitamin D; Vitamin C; Turmeric; Glucosamine
Allergien: N/A
Vorherige Impfungen: -

VAERS 2602412

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: OH
Alter: 47,0
Geschlecht: F
Eingang: 23.03.2023
Impfdatum: 15.09.2022
Beginn: 05.03.2023
Tage bis Beginn: 171,0
Dosis: 5
Route/Site: IM / LA

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

Blood test abnormal Eye pain Herpes zoster Visual impairment

Symptomtext

It felt like a drilling pain in my eye socket that no pain killer could take away. When I went outside, I felt like I was being blinded even with sunglasses on. I made an appointment with my primary care physician who gave me steroids to help dim the pain and sent me to the neurologist. He ran a blood test to for the shingles virus, that did come back positive. I was given pain medication; I was also given the medication acyclovir to combat the shingles virus that I am currently taking now. My vision is getting better, but the rest is taking it's time to heal.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Eye pain
Hospital-Tage: -
Labordaten: 8MAR2023 Bloodwork, positive for shingles
Aktuelle Erkrankungen: No
Vorgeschichte: Asthma
Andere Medikamente: Vitamin C; biotin; magnesium; folic acid; vitamin D; FLEXERIL; ZOLOFT; XYZAL
Allergien: BACTRIM; TOPAMAX
Vorherige Impfungen: -

VAERS 2602314

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: IA
Alter: 73,0
Geschlecht: F
Eingang: 23.03.2023
Impfdatum: 21.09.2022
Beginn: 28.12.2022
Tage bis Beginn: 98,0
Dosis: 5
Route/Site: SYR / LA

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

COVID-19 Cough Nasal congestion Pyrexia SARS-CoV-2 test positive

Symptomtext

I tested positive on December 28, 2022 experienced stuffy nose, fever of 102.5, coughing, was taking over medication for symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: Covid test
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 2602252

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: TX
Alter: 63,0
Geschlecht: F
Eingang: 23.03.2023
Impfdatum: 16.09.2022
Beginn: 17.01.2023
Tage bis Beginn: 123,0
Dosis: 5
Route/Site: SYR / -

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

Cough Fatigue Nasal congestion Nasopharyngitis SARS-CoV-2 test negative Secretion discharge Viral infection

Symptomtext

I was diagnosed with a viral cold my symptoms were coughing, stuffy nose, mucus, no fever, tiredness, I had 2 negative Covid tests. I was taking TYLENOL and saline nasal spray for my symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Post liver transplant
Andere Medikamente: PROGRAF; CELLCEPT; CRESTOR; COLACE; aspirin; alendronate sodium; PEPCID AC; magnesium lactate; ferrous fumarate; COMBIGAN; TRAVATAN; BENADRYL
Allergien: N/A
Vorherige Impfungen: -

VAERS 2601809

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: GA
Alter: 78,0
Geschlecht: F
Eingang: 22.03.2023
Impfdatum: 16.09.2022
Beginn: 07.01.2023
Tage bis Beginn: 113,0
Dosis: 5
Route/Site: IM / -

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

COVID-19 Feeling abnormal Headache Pyrexia SARS-CoV-2 test positive

Symptomtext

I started feeling bad on January 7, 2023, was tired just wanted to lay around, I had a headache. I started to get a fever on the 9th of January so I took a home COVID-19 test that came back positive very fast. I called my doctor's office to let them know I had tested positive. My doctor called in a prescription of molnupiravir antiviral medication that I started taking that evening. By Thursday I was feeling better and gradually everyday it just kept getting better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: 9JAN2023 home COVID-19 test positive
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: TYLENOL
Allergien: No
Vorherige Impfungen: -

VAERS 2601771

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: CA
Alter: 61,0
Geschlecht: M
Eingang: 22.03.2023
Impfdatum: 20.09.2022
Beginn: 05.01.2023
Tage bis Beginn: 107,0
Dosis: 5
Route/Site: IM / LA

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

Cough Oropharyngeal pain Pyrexia SARS-CoV-2 test positive

Symptomtext

I had cough, a sore throat, and fever of 38 degrees Celsius.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: 05JAN2023 COVID-19 At Home Test - Negative; 07JAN2023 COVID-19 At Home Test - Negative; 08JAN2023 COVID-19 At Home Test - Positive; 15JAN2023 COVID-19 At Home Test - Negative
Aktuelle Erkrankungen: N/A
Vorgeschichte: Depression; Anxiety; Enlarged Prostate
Andere Medikamente: Tamsulosin; Alprazolam; Duloxetine; Beet Root; Finasteride; Vitamin D3; Centrum Silver Multivitamin; Cranberry; CoQ10; Lycopene; Vitamin B Complex
Allergien: N/A
Vorherige Impfungen: -

VAERS 2600414

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: IL
Alter: 61,0
Geschlecht: F
Eingang: 21.03.2023
Impfdatum: 17.09.2022
Beginn: 27.01.2023
Tage bis Beginn: 132,0
Dosis: 5
Route/Site: IM / LA

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

Ageusia Anosmia COVID-19 Myalgia Pyrexia SARS-CoV-2 test positive Sinus disorder Vomiting

Symptomtext

I thought I had a sinus infection that is why I went to the doctor. My fever was 103.0 I was throwing up my muscles was hurting. I lost my taste and smell.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myalgia
Hospital-Tage: -
Labordaten: 28JAN2023 COVID-19 Test -Positive
Aktuelle Erkrankungen: Asthma
Vorgeschichte: Asthma
Andere Medikamente: Bupropion; Pantoprazole; Spiriva
Allergien: Pantoprazole; levofloxacin; cefadroxil; hydrocodone; hydromorphone; sulfa; doxycycline
Vorherige Impfungen: -

VAERS 2600092

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: KS
Alter: 67,0
Geschlecht: M
Eingang: 21.03.2023
Impfdatum: 19.09.2022
Beginn: 05.03.2023
Tage bis Beginn: 167,0
Dosis: 5
Route/Site: IM / RA

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

COVID-19 Cough Fatigue Influenza A virus test negative Influenza B virus test Malaise Respiration abnormal Respiratory tract congestion SARS-CoV-2 test positive Somnolence

Symptomtext

I was on a cruise, had just landed from a connecting flight. When I departed, I was so fatigued my wife needed to push me in a wheelchair to the car. We came home very late so we went straight home I thought I might get better with some rest, but I started getting congestion, a cough, I did not run a fever. On 03/11/23 I went to a local urgent care to find get treatment for what was going on. I was tested for COVID-19 test that came back positive and Influenza A and B that came back negative. I was prescribed inhalers to help with my breathing, but I was too far into being sick to get PAXLOVID. I still have a bit of a cough and I still need a nap in the afternoons. I am getting better, but I am not quite there.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 11MAR2023 PCR COVID-19 test positive; 11MAR2023 Influenza A and B negative
Aktuelle Erkrankungen: No
Vorgeschichte: Hypertension
Andere Medikamente: Lisinopril; amlodipine; gabapentin; atorvastatin; hydroxyurea; iron; vitamin C
Allergien: No
Vorherige Impfungen: -

VAERS 2599892

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7144B

mild

Staat: IN
Alter: 68,0
Geschlecht: M
Eingang: 20.03.2023
Impfdatum: 13.09.2022
Beginn: 09.03.2023
Tage bis Beginn: 177,0
Dosis: 1
Route/Site: IM / -

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

COVID-19 Cough Fatigue Headache Nasal congestion Pain Pyrexia Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

COVID - low grade fever for 2 days, achy 2 days, tired 6 days, runny nose 5 days, headache 1 day. Occasional cough continues and stuffy nose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Covid test - 2 positive tests on 3/9/23
Aktuelle Erkrankungen: none
Vorgeschichte: HTN, BPH,
Andere Medikamente: diltiazem, rosuvastatin, hydrochlorothiazide, tadalafil, multi-vitamin, vitamin C, ibuprofen, citrizine
Allergien: sulfa, penicillin, shellfish
Vorherige Impfungen: -

VAERS 2599891

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7144B

mild

Staat: IN
Alter: 67,0
Geschlecht: F
Eingang: 20.03.2023
Impfdatum: 14.09.2022
Beginn: 06.03.2023
Tage bis Beginn: 173,0
Dosis: 1
Route/Site: IM / -

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

COVID-19 Cough Fatigue Malaise Pain Pyrexia SARS-CoV-2 test positive

Symptomtext

COVID positive. Cough, tired, aches, low fever for one day. Was ill for 3 days, cough for 2 weeks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Covid + test twice on 3/7/23
Aktuelle Erkrankungen: none
Vorgeschichte: HTN, GERD, incontinence
Andere Medikamente: Verapamil, atenolol, tolterodine, multi-vitamin, vitamin-D, calcium, biotin, omeprazole, acetominiphin
Allergien: oxybutinin
Vorherige Impfungen: -

VAERS 2599691

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: SC
Alter: 68,0
Geschlecht: M
Eingang: 20.03.2023
Impfdatum: 17.09.2022
Beginn: 27.02.2023
Tage bis Beginn: 163,0
Dosis: 5
Route/Site: IM / LA

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

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

Symptomtext

Started feeling congested and feverish and was coughing a lot. On 02/27/2023 took home COVID-19 test and it was positive. Called doctor and was prescribed PAXLOVID. Tested negative on 03/07/2023.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: 27FEB2023 home COVID-19 test positive; 03MAR2023 home COVID-19 test negative.
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Multivitamin; turmeric.
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2599588

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: MA
Alter: 77,0
Geschlecht: F
Eingang: 20.03.2023
Impfdatum: 07.09.2022
Beginn: 04.02.2023
Tage bis Beginn: 150,0
Dosis: 5
Route/Site: SYR / LA

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

COVID-19 Influenza like illness Oropharyngeal pain Pain Pyrexia SARS-CoV-2 test positive

Symptomtext

I was positive for COVID-19 on 04FEB2023, I had a sore throat, I had fever and body aches and general flu like symptoms. I contacted my doctor and prescribed me PAXLOVID, I started feeling better about 48 hours after taking the medication.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: 04FEB2023 COVID-19 test positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Low thyroid
Andere Medikamente: Levothyroxine
Allergien: N/A
Vorherige Impfungen: -

VAERS 2599551

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: VA
Alter: 64,0
Geschlecht: F
Eingang: 20.03.2023
Impfdatum: 03.09.2022
Beginn: 05.01.2023
Tage bis Beginn: 124,0
Dosis: 4
Route/Site: IM / LA

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

Diarrhoea Hepatic cyst Laboratory test Magnetic resonance imaging abnormal Pancreatic cyst Pancreatic enlargement Pancreatic mass Renal cyst Ultrasound pancreas abnormal

Symptomtext

I discovered through neurologist lab work. Pancreas enlarged with a mass. I went to my primary care physician, and they sent me for an ultrasound, and it also showed a mass. I went in for an MRI on January 20, 2023. The recommendation was to monitor it. I went to my gastroenterologist, and they will complete an endoscopy on April 06, 2023. I have diarrhea off and on but no other symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: Ultrasound, mass discovered January 16, 2023, MRI January 20, 2023, Cyst on the pancreas, liver and right kidney
Aktuelle Erkrankungen: N/A
Vorgeschichte: Epilepsy
Andere Medikamente: Divalproex sodium; spironolactone; RESTASIS; R lipoic acid; zinc; multivitamin; inflammation balance; plant sterols; vitamin B-complex; calcium
Allergien: KEPPRA; sulfa drugs; nickel
Vorherige Impfungen: -

VAERS 2599468

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: OK
Alter: 67,0
Geschlecht: F
Eingang: 20.03.2023
Impfdatum: 07.09.2022
Beginn: 07.02.2023
Tage bis Beginn: 153,0
Dosis: 4
Route/Site: IM / AR

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

COVID-19 Fatigue Influenza virus test Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

I was really fatigued and that was the major symptom I fought with, along with a runny nose. My husband had tested positive for COVID-19 so I took a COVID-19 home test and it was positive. I went into get a test and that was positive, and my health care provider put me on PAXLOVID. About three days after starting that medication I was much better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID-19 home test; COVID-19 PCR test; Influenza test
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Multivitamin; vitamin D; calcium; atorvastatin
Allergien: N/A
Vorherige Impfungen: -

VAERS 2598709

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7144B

mild

Staat: WA
Alter: 66,0
Geschlecht: M
Eingang: 17.03.2023
Impfdatum: 14.09.2022
Beginn: 03.02.2023
Tage bis Beginn: 142,0
Dosis: 5
Route/Site: IM / LA

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

COVID-19 Cough Headache Nasal congestion SARS-CoV-2 test positive Throat irritation

Symptomtext

I had a stuffing nose, cough, scratchy throat, and headache. I tested positive for COVID-19 and called my doctor. My doctor prescribed me Albuterol Benzonatate, and Flonase.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: COVID-19 Test, 02/10/2023, Positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Bronchitis
Andere Medikamente: Metoprolol; Pantoprazole; Losartan; Hydrocodone; Eliquis; Rosuvastatin; Tamsulosin; Furosemide; Super B Complex; Zyrtec; Flonase; D3; Multivitamin
Allergien: NSAIDS
Vorherige Impfungen: -

VAERS 2598554

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: FL
Alter: 65,0
Geschlecht: F
Eingang: 17.03.2023
Impfdatum: 15.09.2022
Beginn: 21.12.2022
Tage bis Beginn: 97,0
Dosis: 5
Route/Site: SYR / LA

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

Dizziness Facial bones fracture Fall Magnetic resonance imaging abnormal Magnetic resonance imaging spinal abnormal Spinal fracture

Symptomtext

On 09/15/2022 I received my Covid-19 vaccine. On 12/21/2022 I was feeling dizzy and fell and broke my nose and went to the emergency room. I was recommended for physical therapy.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: MRI- broken nose and vertebra
Aktuelle Erkrankungen: N/A
Vorgeschichte: High Blood Pressure
Andere Medikamente: Fluoxetine; Rosuvastatin; Olmesartan Medox/hctz; Aspirin
Allergien: Sulfa; Pollen
Vorherige Impfungen: -

VAERS 2598549

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: IN
Alter: 71,0
Geschlecht: F
Eingang: 17.03.2023
Impfdatum: 14.09.2022
Beginn: 18.02.2023
Tage bis Beginn: 157,0
Dosis: 5
Route/Site: SYR / AR

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

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

Symptomtext

I had severe chills and sore throat and the next day on 02/19/2023, I took the test, It was positive. I contacted my doctor via telephone. On that next day I had a slight fever, cough and fatigue. It left a metallic taste that was unpleasant. He prescribed me Paxlovid. About three days or so I felt better after it is taking the Paxlovid.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: 19FEB2023 COVID-19 at Home Test - Positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Levoxyl; Calcium; Baby Aspirin; Vitamin D; Vitamin C
Allergien: N/A
Vorherige Impfungen: -

VAERS 2598268

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: TX
Alter: 61,0
Geschlecht: F
Eingang: 16.03.2023
Impfdatum: 10.09.2022
Beginn: 29.01.2023
Tage bis Beginn: 141,0
Dosis: 5
Route/Site: IM / LA

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

Ageusia Anosmia Asthenia Balance disorder Blood test normal COVID-19 Chest X-ray normal Cough Dizziness Electrocardiogram normal Pyrexia SARS-CoV-2 test positive

Symptomtext

I had a cough, fever of 102.6, lost my balance, and dizzy. I tested positive for COVID-19. I called my doctor, and she didn't get back to me until 3 days. Three days after taking PAXLOVID, I lost my smell and taste. I had to go to the ER because I felt so weak. When I got to the ER, they EKG, chest x-ray, and blood work. Everything came back normal.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: COVID-19 test, 01/29/2023, positive, EKG, Chest X-ray, Blood work, normal, 02/03/2023
Aktuelle Erkrankungen: N/A
Vorgeschichte: Type 2 Diabetes; High Cholesterol; Hypertension
Andere Medikamente: Aspirin; XIGDUO XR; lisinopril; carvedilol
Allergien: CELEBREX
Vorherige Impfungen: -

VAERS 2597702

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: IL
Alter: 65,0
Geschlecht: M
Eingang: 16.03.2023
Impfdatum: 14.09.2022
Beginn: 09.03.2023
Tage bis Beginn: 176,0
Dosis: 5
Route/Site: SYR / LA

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

Ageusia Anosmia COVID-19 Chills Cough Fatigue Feeling hot Oropharyngeal pain Pyrexia Respiratory tract congestion SARS-CoV-2 test positive Sinus congestion Sinus pain Throat irritation

Symptomtext

3/9/23 that evening I had sinus congestion and pain, a little bit of a sore throat and then chills in the middle of the night. I felt like I had fever and it broke. The next morning, I still felt warm like I had a fever. It was a couple of degrees above normal. I was more congested, and throat was more sore. I took an at home COVID test and it was positive. I called the doctor. We discussed PAXLOVID and he thought because of the interaction with the medication I am on and because I am in good shape, a marathon runner, it wasn't necessary. I took TYLENOL to bring down fever and it was down by the next morning 3/11/23. I had severe fatigue on 3/10 and 3/11. My congestion started to clear. My sore throat became a lot worse. On 3/12/23 I lost about 80% of my sense of smell and taste. On 3/13/23 pretty much all symptoms were gone, except a scratchy throat and a little bit of a cough. My blood oxygen was running 97-99. My fever remained down. My sense of taste and smell have not returned. I am still tired, but not exhausted. I have not recovered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: COVID at home tests, negative and positive
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension; Atrial Fibrillation
Andere Medikamente: Diltiazem; triamterene; telmisartan; low dose aspirin; vitamin D3; vitamin B-12; magnesium
Allergien: None
Vorherige Impfungen: -

VAERS 2597657

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: NY
Alter: 69,0
Geschlecht: F
Eingang: 16.03.2023
Impfdatum: 14.09.2022
Beginn: 31.01.2023
Tage bis Beginn: 139,0
Dosis: 5
Route/Site: IM / RA

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

COVID-19 Chills Feeling abnormal Headache Influenza virus test negative Oropharyngeal pain Pyrexia Respiratory syncytial virus test negative Respiratory tract congestion SARS-CoV-2 test negative SARS-CoV-2 test positive Sneezing

Symptomtext

1/31/2023 I felt off in the afternoon. Overnight, I woke up with a sore throat and feeling worse. I got up the next morning, I tested with an at home COVID test and it was negative. I was congested like I was getting a cold. I felt worse throughout the day and night. I was sneezing, congested, and started running a fever, chills and had a constant headache. On 2/2/23 I took another at home COVID test and it was positive. I had an appointment with my doctor. They took 2 rapid COVID tests that were negative. I had a flu and RSV test that were both negative. I also had a PCR test that came back the next day positive for COVID. My doctor prescribed PAXLOVID which I began taking on 2/2/23 that night. I was pretty sick on that night and did not feel good. 2/3/23 in the evening and into the next day, I began feeling better. After finishing the PAXLOVID, I had a negative at home COVID test. On 2/11/23 in the afternoon, I was not feeling good, really tired and felt off. I suspected I was having a rebound of COVID. I did not feel good overnight. On 2/12/23 I tested positive with an at home COVID test. I called my doctor's office to let her know I had a lot worse symptoms. I ran a fever over 100, chills, very bad head congestion, very fatigued, a little tightness in my chest and a dry cough, but never a chest cold. I lost my sense of taste. I also had a constant headache. I tested with an at home COVID test about a week later and the test was negative. My symptoms were gone except for still feeling pretty tired. I did not feel like myself again until around 2/22/23 or 2/23/23. I have recovered with those symptoms. I have noticed an issue with my voice has a little bit of hoarseness that I did not have before having COVID.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: At home COVID tests, negative and positive; PCR COVID test, positive; COVID rapid tests, negative; RSV, negative; FLU, negative.
Aktuelle Erkrankungen: None
Vorgeschichte: Colitis; Hashimoto's; Arthritis (? type)
Andere Medikamente: Levothyroxine; TYLENOL
Allergien: Sulfa drugs; penicillin; gluten sensitivity; latex sensitivity
Vorherige Impfungen: Fever, chills for about 24 hours after COVID 19 vaccines, but was better with each vaccine. Shingles, several years ago, got chi

VAERS 2597641

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: CA
Alter: 74,0
Geschlecht: M
Eingang: 16.03.2023
Impfdatum: 07.09.2022
Beginn: 11.02.2023
Tage bis Beginn: 157,0
Dosis: 5
Route/Site: ID / AR

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

Malaise Myalgia Prostatic operation Pyrexia Tenderness Urine abnormality

Symptomtext

I had the onset of 99.8-degree fever, headache, myalgias, malaise, cloudy urine, and suprapubic tenderness. Those symptoms lasted about three days. I took levofloxacin 250mg twice a day for one week. Symptoms improved the next day but worsened again the following day before gradually clearing. I contacted medical advice two days after onset of symptoms. They recommended going to the emergency room, but I declined. Two weeks later, I had a post void residual measured which was normal. On October 11, 2022, I had a prostate procedure for B Benign Prostatic Hyperplasia, so I do not think this was vaccine related.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Hyperlipidemia; Benign Prostatic Hyperplasia; Urinary Retention; Vitamin D Deficiency; Bladder Stones; Prediabetes; History of Non-Melanoma Skin Cancer; Irritable Bowel Syndrome; Colon Polyp Adenomatous
Andere Medikamente: Atorvastatin; tamsulosin; finasteride; vitamin D; PROZAC
Allergien: None
Vorherige Impfungen: 01/15/2021 Moderna COVID-19 dose 1: Age 72, low grade fever, myalgias, and malaise; 02/17/2021 Moderna COVID-19 dose 2: Age: 72,

VAERS 2597057

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7144B

mild

Staat: MN
Alter: 43,0
Geschlecht: F
Eingang: 15.03.2023
Impfdatum: 08.09.2022
Beginn: 27.12.2022
Tage bis Beginn: 110,0
Dosis: 4
Route/Site: IM / LA

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

Brain fog COVID-19 Chills Cough Oropharyngeal pain Pain Respiratory tract congestion SARS-CoV-2 test

Symptomtext

I got COVID-19 later December I had sore throat, chills, brain fog, cough, congestion and body aches. I tested after a few days and then did a video call with a doctor and was given Paxlovid and within 24 hours I started to recover. About 7 days later I started to fully recover.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: COVID-19 Test
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Spironolactone; Mirana IUD; Daily Multivitamin
Allergien: Caffeine;Tetracyclene
Vorherige Impfungen: -

VAERS 2597010

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: IN
Alter: 71,0
Geschlecht: M
Eingang: 15.03.2023
Impfdatum: 13.09.2022
Beginn: 07.02.2023
Tage bis Beginn: 147,0
Dosis: 5
Route/Site: IM / LA

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

COVID-19 Cough Pain Pyrexia SARS-CoV-2 test positive

Symptomtext

It started off with a dry, hacking cough for a couple days. My wife and I took a home COVID-19 test which came back positive on 02/08/2023. Days later, it progressed to aches, pains, and a high-grade fever for one day that broke pretty fast. Later that evening, the pain got progressively worse so I went to urgent care. The nurse checked me over and prescribed me molnupiravir 4 tablets twice a day for 5 days. I tested again about three days after finishing the prescription and finally tested negative. Now, I'm doing perfectly well and better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: 08FEB2023 COVID-19 test positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Lisinopril; atorvastatin; vitamin C; zinc; vitamin D3; probiotic
Allergien: N/A
Vorherige Impfungen: -

VAERS 2597006

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: CA
Alter: 65,0
Geschlecht: M
Eingang: 15.03.2023
Impfdatum: 13.09.2022
Beginn: 17.02.2023
Tage bis Beginn: 157,0
Dosis: 5
Route/Site: IM / LA

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

Body temperature increased COVID-19 Cough Dysphagia Malaise Oesophageal obstruction Oropharyngeal pain SARS-CoV-2 test positive Sensation of foreign body

Symptomtext

On 2/17/2023, my girlfriend told me she had a sore throat. I then decided to take a home antigen test, and I got a positive result. I couldn't believe it, so I tested myself five times over 2/17/2023 and 2/18/2023. I had varying results; three were positive and two were negative. I later noticed that the two negative tests were from the same company, had the same lot number, and were due to expire in a couple of days. During this time, I had no symptoms. On the afternoon of 2/19/2023, I began to develop a sore throat and a general malaise. On 2/20/2023, my symptoms worsened, and I had a temperature of 100.6. On 2/21/2023, I was prescribed PAXLOVID, which I began taking that day at noon. This was the worst day as far as symptoms go, because my throat was so sore that I couldn't swallow. It felt like there was a painful lump in my throat. My temperature that day was 102. Later that day, I coughed my pill up when I took my second dose of the PAXLOVID. It was like there was an obstruction in my esophagus, and I repeatedly had to try swallowing the pill. Also, when I drank water, it didn't seem to go down. It just sat, and I would cough it up. The following days were a little better. By the time 2/25/2023 rolled around, I finished my last dose of PAXLOVID. By 2/27/2023, I felt much better, so I decided to test myself. I tested myself on 2/27/2023 and, and I got a positive result. On 3/1/2023, I tested myself again and got a positive result. On 3/10/2023, I finally got a negative result for the first time. I tested again on 3/12/2023, I tested and got a positive result. I then tested again on 3/14/2023 and got a negative result. At the time of this writing, I have a minor residual cough. Other than that, I feel fine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: 17FEB2023, 18FEB2023 home antigen tests positive results; 10MAR2023 home antigen test negative result; 12MAR2023 home antigen test positive result; 14MAR2023 home antigen test negative result
Aktuelle Erkrankungen: None
Vorgeschichte: Rosacea
Andere Medikamente: Multivitamin; metronidazole skin cream; melatonin; ibuprofen; fluticasone
Allergien: None
Vorherige Impfungen: -

VAERS 2596998

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: TN
Alter: 75,0
Geschlecht: M
Eingang: 15.03.2023
Impfdatum: 13.09.2022
Beginn: 24.02.2022
Tage bis Beginn: -
Dosis: 5
Route/Site: IM / LA

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

COVID-19 Fatigue Odynophagia Oropharyngeal discomfort Oropharyngeal pain SARS-CoV-2 test positive Sleep disorder

Symptomtext

I had a lot of fatigue, and I had a mild fever with the highest being 100 degrees. I had a very bad sore throat which was very uncomfortable for 3 or 4 days. When I ate or swallowed it hurt worst. On February 25, 2023, I tested I received a positive result on a COVID-19 home test. The doctor called in the prescription for Paxlovid which I began taking on Tuesday evening. I was slowly starting to feel better. I still had a lot of fatigue and disrupted sleep, but the fever had died down. Thru the 7th of March I received positive COVID-19 home test. I was slowly getting better but still testing positive for some time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID-19 home test-Positive-February 25, 2023
Aktuelle Erkrankungen: N/A
Vorgeschichte: High Cholesterol; GERD; High Blood Pressure
Andere Medikamente: Rosuvastatin; Losartan; Vitamin B Complex; Famotidine
Allergien: N/A
Vorherige Impfungen: -

VAERS 2596952

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: OR
Alter: 42,0
Geschlecht: F
Eingang: 15.03.2023
Impfdatum: 13.09.2022
Beginn: 27.02.2023
Tage bis Beginn: 167,0
Dosis: 4
Route/Site: IM / AR

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

COVID-19 Cough Fatigue Pain Pyrexia SARS-CoV-2 test positive Sinus congestion

Symptomtext

I started having a dry cough. I had a low-grade fever the first day with body aches. Then I got a high fever on March 1, 2023, of 101.5 degrees. I was very fatigue at this point and decided to call the nurse line because the Tylenol and Advil weren't working anymore. I tested mostly negative on March 7, 2023. I experienced sinus congestion up until March 12th and am still experiencing fatigue.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 28FEB2023 - COVID-19 Test- Positive; 07MAR2023 - COVID-19 Test - Negative
Aktuelle Erkrankungen: N/A
Vorgeschichte: Bipolar 2 Disorder
Andere Medikamente: Methylphenidate; Lamotrigine; Estradiol; Progesterone
Allergien: N/A
Vorherige Impfungen: -

VAERS 2596894

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: MI
Alter: 69,0
Geschlecht: F
Eingang: 15.03.2023
Impfdatum: 13.09.2022
Beginn: 03.03.2023
Tage bis Beginn: 171,0
Dosis: 5
Route/Site: SYR / RA

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

COVID-19 Cough Dysphonia Fatigue Oropharyngeal pain Pyrexia Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

I was positive for COVID-19 on 03MAR2023, I was feeling tired, sore throat, mild cough an a runny nose. I was also congested, my voice was rough and for one day I had a mild fever. I was prescribed paxlovid, I started to feel better the next day after taking the medication.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 03MAR2023 COVID-19- Test- Positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: High Blood Pressure; High Cholesterol; Low Thyroid
Andere Medikamente: Crestor; Lisinopril; Amlodipine; Levothyroxine; Vitamin D5000; Fish oil; Vitamin B; Multi Mineral; Estradiol patch; Progesterone; Vitamin E; Milk Thistle
Allergien: Hydrocodone; Atorvastatin
Vorherige Impfungen: -

VAERS 2596166

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: PA
Alter: 71,0
Geschlecht: F
Eingang: 14.03.2023
Impfdatum: 09.09.2022
Beginn: 21.02.2023
Tage bis Beginn: 165,0
Dosis: 5
Route/Site: SYR / LA

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

Back pain COVID-19 Cough Malaise Nasal congestion Oropharyngeal pain SARS-CoV-2 test positive

Symptomtext

On 09/09/2022 I received my Covid-19 vaccine. On 02/21/2023 I had back pain, heart burn, sore throat, cough, nasal congestion. After reaching out to my doctor I was diagnosed with Covid-19 and prescribed PAXLOVID. Symptoms lasted approx. two weeks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Back pain
Hospital-Tage: -
Labordaten: Covid 19 at home testing
Aktuelle Erkrankungen: N/A
Vorgeschichte: Sjogren's Syndrome
Andere Medikamente: RESTASIS; fenofibrate; losartan; vitamin D; CENTRUM SILVER; glucosamine; biotin; krill oil
Allergien: Amoxicillin
Vorherige Impfungen: -

VAERS 2596095

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: AL
Alter: 66,0
Geschlecht: F
Eingang: 14.03.2023
Impfdatum: 12.09.2022
Beginn: 25.01.2023
Tage bis Beginn: 135,0
Dosis: 5
Route/Site: SYR / LA

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

COVID-19 Cough Headache Nasal congestion Pain SARS-CoV-2 test positive

Symptomtext

I had first had symptoms on January 25th of 2023. I had a headache at first, the next day I felt body ache, nasal congestion and cough. I was away, I went to a clinic for testing COVID-19 on January 27th I tested positive. Tylenol and keeping down liquids helped me I needed no other medications.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: High Cholesterol; Acid Reflux
Andere Medikamente: Omeprazole; Atorvastatin; CoQ10; Vitamin E
Allergien: Penicillin
Vorherige Impfungen: Tetanus Vaccine as a child. I had an anaphylactic reaction; 6 years old;; Dates Unkown

VAERS 2596017

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: OH
Alter: 30,0
Geschlecht: M
Eingang: 14.03.2023
Impfdatum: 10.09.2022
Beginn: 23.02.2023
Tage bis Beginn: 166,0
Dosis: 4
Route/Site: SYR / LA

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

COVID-19 Heart rate increased Oropharyngeal pain Pyrexia SARS-CoV-2 test positive

Symptomtext

It began at eight PM 23FEB2023 with a sore throat, the next morning the sore throat continued and I also noted a fever, in the evening around five PM I noted my heart rate was120BPM for several hours at that point I scheduled a telehealth appointment and after describing my symptoms to the provider it was recommended to monitor and stay hydrated the following day 25FEB2023 all major symptoms self revolved.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: COVID-19 test positive.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2595712

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: CA
Alter: 60,0
Geschlecht: F
Eingang: 13.03.2023
Impfdatum: 09.09.2022
Beginn: 16.01.2023
Tage bis Beginn: 129,0
Dosis: 5
Route/Site: IM / LA

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

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

Symptomtext

It started with a severe cough, fever, muscle aches, and congestion. I went to the urgent care clinic and got diagnosed with COVID-19. I was given Paxlovid and Tessalon Perles. I also got OTC Mucinex and Mucinex DM. I got better, and then I got sick again. I had a rebound. I called my PCP and was given another prescription for Paxlovid. At this time, I was also taking Emergen-C, a separate supplement of 1000mg of vitamin C, Xycam, and Flonase nasal spray. The second round of Paxlovid pretty much knocked out my symptoms. At the time of this writing, I feel that I have recovered as much as I am going to from COVID-19, but my energy levels aren't what they were before I got sick.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: 20JAN2023 -Clinical Rapid Antigen Test - Positive Result; 26JAN2023 - Home Antigen Test - Negative Result; 28JAN2023 - Home Antigen Test - Positive Result
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Lipitor; Multivitamin; Milk Thistle; CoQ10; Fiber Supplement; Cetirizine
Allergien: Mild Latex Allergy
Vorherige Impfungen: -

VAERS 2595667

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: CA
Alter: 45,0
Geschlecht: F
Eingang: 13.03.2023
Impfdatum: 09.09.2022
Beginn: 07.02.2023
Tage bis Beginn: 151,0
Dosis: 5
Route/Site: SYR / LA

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

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

Symptomtext

I tested positive for COVID-19 on 02/13/2023. I had a cough, sore throat, headache. I called the provider the next day and prescribed PAXLOVID for 5 days. I tested negative for COVID-19 on 02/20/2023.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: 13FEB2023 COVID-19 test positive; 20FEB2023 COVID-19 test negative
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: ZYRTEC; vitamin C; magnesium
Allergien: Seasonal allergies; fruits; vegetables
Vorherige Impfungen: -

VAERS 2595662

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: PA
Alter: 64,0
Geschlecht: F
Eingang: 13.03.2023
Impfdatum: 10.09.2022
Beginn: 23.02.2023
Tage bis Beginn: 166,0
Dosis: 5
Route/Site: SYR / LA

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

Arthralgia Bone pain COVID-19 Headache Malaise Myalgia Oropharyngeal pain Pain of skin SARS-CoV-2 test positive

Symptomtext

2/23/2023 I woke up with a sore throat. I tested with an at home COVID test which was positive. Later in the day I got a headache. My bones, joints, skin and muscles all hurt. On a scale of 1-10, it was an 8?-9. I called my PCP and he refused to give me PAXLOVID because it was experimental. I called my immunologist. He prescribed PAXLOIVD, the kidney dose and began taking it that evening. By the next day, I felt crappy and still hurting a bit. By 2/25/23, I felt pretty normal. Since 2/28/23, I have tested negative for COVID.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: At home COVID tests, negative and positive
Aktuelle Erkrankungen: None
Vorgeschichte: Thyroid cancer; urticaria autoimmune disease; Asthma; Spinal Stenosis; Osteoarthritis
Andere Medikamente: Meloxicam; CELLCEPT; levothyroxine; gabapentin; ZYRTEC; VALTREX; estradiol; amitriptyline; WELLBUTRIN; vitamin D-3; probiotic; vitamin B-12; NP thyroid; FLEXERIL
Allergien: Sensitivities to penicillin; sulfa drugs; PERCOCET; walnuts; brazil nuts; macadamia nuts; bee stings
Vorherige Impfungen: -

VAERS 2595656

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: IL
Alter: 66,0
Geschlecht: F
Eingang: 13.03.2023
Impfdatum: 09.09.2022
Beginn: 25.02.2023
Tage bis Beginn: 169,0
Dosis: 5
Route/Site: IM / LA

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

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

Symptomtext

The symptoms of COVID-19 included headache, body aches, sore throat, and a cough. The symptoms lasted about two days. I contacted my doctor. She prescribed Paxlovid. I also took Mucinex, Tylenol, and Airborne. After the first two days, I just felt very fatigued.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 02/25/2022 At Home COVID-19 Test - Positive
Aktuelle Erkrankungen: None
Vorgeschichte: Hyperthyroidism; Gastric Reflux
Andere Medikamente: Methimazole; Omeprazole; Estradiol; Vitamin B12; Multivitamin; Vitamin D3; Metamucil; MiraLAX; Calcium
Allergien: Dust Mites; Trees; Dogs
Vorherige Impfungen: -

VAERS 2595648

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: TN
Alter: 41,0
Geschlecht: F
Eingang: 13.03.2023
Impfdatum: 10.09.2022
Beginn: 21.12.2022
Tage bis Beginn: 102,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Cough Pain Pyrexia Rhinorrhoea SARS-CoV-2 test positive Vertigo

Symptomtext

On 12/21/2022, I woke up with aches and pains. I had a fever, cough, and runny nose as well. I also ended up developing vertigo. I tested myself for COVID-19 and it was positive. I informed my doctor of my positive status but did not seek medical attention. I treated my symptoms with over-the-counter medication. My symptoms last around 5 or 6 days, with the exception of the vertigo which lasted around 45 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: 21DEC2022 - At Home COVID-19 Test - Positive
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma; GERD
Andere Medikamente: Multivitamin; Singulair; Cymbalta; Advair; Birth Control; Omeprazole
Allergien: None
Vorherige Impfungen: -

VAERS 2595526

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: NJ
Alter: 67,0
Geschlecht: M
Eingang: 13.03.2023
Impfdatum: 08.09.2022
Beginn: 19.12.2022
Tage bis Beginn: 102,0
Dosis: 5
Route/Site: IM / LA

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

Asthenia COVID-19 Cough Malaise Pain Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

I started feeling ill on Monday 12/19 and on 12/20 did a home COVID-19 test which was positive. Symptoms were cough and congestion but no fever, lack of energy body aches and within 5-6 days I started to recover. I did contact my doctor which prescribed PAXLOVID on the 12/23. The cough did linger for a month and a half.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: COVID-19
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Simvastatin; multivitamin; vitamin D
Allergien: LEVAQUIN; seasonal allergies
Vorherige Impfungen: -

VAERS 2595523

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: NC
Alter: 68,0
Geschlecht: M
Eingang: 13.03.2023
Impfdatum: 04.09.2022
Beginn: 08.03.2023
Tage bis Beginn: 185,0
Dosis: 5
Route/Site: IM / RA

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

Biopsy lymph gland Computerised tomogram abdomen abnormal Fatigue Lymphadenopathy

Symptomtext

I went into the hospital on 03/08/2023, while in the hospital it was discovered that I had several enlarged nodes in my abdomen when they did a CT scan. They did a biopsy to find out if the nodes are cancerous. I was feeling a bit fatigued but not too much. I am awaiting the result of the biopsy, to see where we are to proceed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 03/08/2023 CT scan, positive several enlarged nodes; biopsy, currently awaiting results.
Aktuelle Erkrankungen: No
Vorgeschichte: Hypothyroid; Sleep Disorder
Andere Medikamente: Levothyroxine; FLOMAX; acyclovir; pravastatin; gabapentin: bupropion; coQ10; CENTRUM SILVER
Allergien: No
Vorherige Impfungen: -

VAERS 2594860

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: PA
Alter: 81,0
Geschlecht: M
Eingang: 10.03.2023
Impfdatum: 08.09.2022
Beginn: 16.02.2023
Tage bis Beginn: 161,0
Dosis: 5
Route/Site: IM / LA

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

COVID-19 Chest X-ray normal Malaise Oropharyngeal pain Pyrexia SARS-CoV-2 test positive

Symptomtext

Started having a fever and sore throat. Took a home COVID-19 test and was positive. Doctor prescribed PAXLOVID, took full course. Took another COVID-19 test and was negative. Felt fine for a week then started feeling symptoms again and tested positive for COVID-19. Had a chest X-ray and it was clear. Rested and tested negative a week later.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: Home COVID-19 test, positive; Home COVID-19 test, negative; Chest X-ray, clear.
Aktuelle Erkrankungen: N/A
Vorgeschichte: Hypertension; High Cholesterol; Insomnia; Visual Migraines; Nocturnal Epilepsy.
Andere Medikamente: KEPPRA; atenolol; lisinopril; NEXIUM; hydrochlorothiazide; lamotrigine; zolpidem; magnesium; multivitamin; aspirin; melatonin; LIPITOR.
Allergien: N/A
Vorherige Impfungen: -

VAERS 2594648

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: IL
Alter: 71,0
Geschlecht: M
Eingang: 10.03.2023
Impfdatum: 06.09.2022
Beginn: 22.02.2023
Tage bis Beginn: 169,0
Dosis: 5
Route/Site: IM / RA

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

COVID-19 Exposure to SARS-CoV-2 Fatigue Nasopharyngitis Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

On 02/22/2023, in the morning, I had a slight runny nose and I felt tired. I had common cold symptoms. My wife was getting over COVID-19, so I did an antigen home test and it was positive. I texted the physician the next day. The next day, they called in Paxlovid, which I began on the afternoon of 02/24/2023. I took Paxlovid through 03/01/2023. I tested negative 02/28/2023.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 22FEB2023 - COVID-19 Test- Positive; 28FEB2023 - COVID-19 Test- Negative
Aktuelle Erkrankungen: N/A
Vorgeschichte: Thyroid Issue in Remission
Andere Medikamente: Turmeric; Biotin
Allergien: N/A
Vorherige Impfungen: -

VAERS 2594644

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: VA
Alter: 41,0
Geschlecht: F
Eingang: 10.03.2023
Impfdatum: 06.09.2022
Beginn: 29.09.2022
Tage bis Beginn: 23,0
Dosis: 4
Route/Site: IM / LA

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

Blood cholesterol abnormal COVID-19 Exposure to SARS-CoV-2 Malaise No adverse event SARS-CoV-2 test positive Thyroid function test abnormal

Symptomtext

I did not have an adverse reaction to the vaccine. I exposed to COVID-19 at my child's day care center. I tested positive for COVID-19 on 09/29/2022. I did not contact my doctor and my symptoms were very mild. My doctor's office requires her patients to come to the office to get the prescription for PAXLOVID. I did not want to do that. I took over the counter medication to help with my symptoms. As of today, my thyroid and cholesterol levels have changed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: 29SEPT2022 COVID-19 test positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: High Cholesterol; Hypothyroidism
Andere Medikamente: SYNTHROID; statin
Allergien: N/A
Vorherige Impfungen: -

VAERS 2593973

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: NY
Alter: 72,0
Geschlecht: M
Eingang: 09.03.2023
Impfdatum: 06.09.2022
Beginn: 19.12.2022
Tage bis Beginn: 104,0
Dosis: 5
Route/Site: IM / LA

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

COVID-19 Cough Fatigue Oropharyngeal pain Pyrexia Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

I got COVID-19 I had a home test and it was positive. I had sore throat, cough, congestion, mild fever, fatigue. It took 5-6 days I felt better every day and after a week I was negative.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 19DEC2022 COVID-19 test positive; 25DEC2022 COVID-19 test positive; 26DEC2022 COVID-19 test negative
Aktuelle Erkrankungen: N/A
Vorgeschichte: Liver Cirrhosis Disease
Andere Medikamente: Nadolol; lactulose; rifaximin; avian; vitamin D; famotidine
Allergien: N/A
Vorherige Impfungen: -

VAERS 2593927

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: GA
Alter: 74,0
Geschlecht: M
Eingang: 09.03.2023
Impfdatum: 07.09.2022
Beginn: 02.02.2023
Tage bis Beginn: 148,0
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 Fatigue Malaise Pain Pyrexia SARS-CoV-2 test positive

Symptomtext

I went on a camping trip with a friend. We did not test for COVID-19 before taking the trip. It was a 7- or 8-hour drive. My friend and I stayed the night in a hotel during the trip. Sometime during the night, my friend developed symptoms. He tested the next morning and was positive for COVID-19. We drove back in separate vehicles. I alerted my doctor of my exposure to COVID-19. The exposure occurred on 01/30/2023. My very minor symptoms began to show on 02/02/2023. My doctor immediately called in a prescription for PAXLOVID. I had a fever of 101 degrees, but that subsided as soon as I began taking the PAXLOVID. I had a little bit of fatigue and achiness for around 24 hours. The day after my symptoms began, I was able to take my normal neighborhood walk. The last time I had a physical, my kidney function was a little bit off, so I took an altered dosage of PAXLOVID. Before I was done with the five days of PAXLOVID, I was feeling fine and well enough to hike. Three days later, I had a slight fever return and was still testing positive. I called my doctor who advised that I take another round of PAXLOVID. My symptoms improved almost immediately after taking the PAXLOVID. I didn't test negative until around 2 or 3 days after finishing the PAXLOVID.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 02FEB2022 at home COVID-19 test positive; 04FEB2022 at home COVID-19 test positive; 06FEB2022 at home COVID-19 test positive; 07FEB2022 at home COVID-19 test positive; 08FEB2022 at home COVID-19 test positive; 09FEB2022 at home COVID-19 test positive; 017FEB2022 at home COVID-19 test negative; 018FEB2022 at home COVID-19 test negative
Aktuelle Erkrankungen: None
Vorgeschichte: Hypopituitarism; High Blood Pressure; High Cholesterol
Andere Medikamente: PRESERVISION; hydrocortisone; vitamin D; multivitamin; aspirin; levothyroxine; tamsulosin hydrochloride; atorvastatin; calcium; olmesartan medoxomil; diltiazem hydrochloride; vitamin B12 with B6 folate and biotin; mometasone; WIXELA inhaler
Allergien: None
Vorherige Impfungen: -

VAERS 2593901

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: MN
Alter: 71,0
Geschlecht: M
Eingang: 09.03.2023
Impfdatum: 07.09.2022
Beginn: 17.02.2023
Tage bis Beginn: 163,0
Dosis: 5
Route/Site: SYR / RA

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

COVID-19 Nasopharyngitis Oropharyngeal pain Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

I had a minor sore throat and that was the first symptom I had. That was on day 1 and I sprayed some chloraseptic mouth wash in my throat. After that, my throat didn't hurt. The next day, I had the sniffles and the day after that was when I actually had a cold. Runny nose, no fever. On Sunday evening of that week, I took a quick view at home COVID-19 test and I was positive. That Monday, I was able to see a physician. My doctor wasn't available but someone else at the clinic was, and they prescribed PAXLOVID. I took that for 5 days and I would say probably on the 3rd day, my cold symptoms were gone. I also did the 5 days of isolation then wore my mask for 5 days after that.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: 19FEB2023 at home COVID-19 test positive
Aktuelle Erkrankungen: None
Vorgeschichte: COPD; Hypertension; High Cholesterol; Obesity
Andere Medikamente: Tolterodine tartrate; alprazolam; hydrochlorothiazide; ADVAIR; SPIRIVA; PEPCID AC
Allergien: None
Vorherige Impfungen: -

VAERS 2593854

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: NY
Alter: 74,0
Geschlecht: F
Eingang: 09.03.2023
Impfdatum: 07.09.2022
Beginn: 18.02.2023
Tage bis Beginn: 164,0
Dosis: 5
Route/Site: IM / LA

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

COVID-19 Fatigue Nasal congestion Nasopharyngitis Rhinorrhoea SARS-CoV-2 test positive Sneezing

Symptomtext

On 02/18/2023 in the evening, I had early head cold symptoms. I was stuffy. The next morning, I knew it was coming. My nose was running and I was sneezing. The next day, it was no better and I decided to test for COVID-19. I tested positive. I had fatigue. I called my doctor's office. They wanted to put me on PAXLOVID, which I did. Cold symptoms and fatigue stayed, and then subsided. I am better now. I tested again 03/05/2023 and tested negative.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 20FEB2023 COVID-19 test positive; 05Mar2023 COVID-19 test negative
Aktuelle Erkrankungen: N/A
Vorgeschichte: Irritable Bowel Syndrome; Chronic Kidney Disease; Lupus
Andere Medikamente: CITRUCEL; acetaminophen; multivitamin; calcium with vitamin D3; amlodipine; omeprazole; torsemide; simvastatin; hydroxychloroquine; probiotic
Allergien: N/A
Vorherige Impfungen: -

VAERS 2593279

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: MI
Alter: 64,0
Geschlecht: F
Eingang: 08.03.2023
Impfdatum: 06.09.2022
Beginn: 23.01.2023
Tage bis Beginn: 139,0
Dosis: 5
Route/Site: - / RA

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

Asthenia COVID-19 Chills Cough Exercise tolerance decreased Fatigue Pain Pyrexia Rhinorrhoea SARS-CoV-2 test positive Sneezing

Symptomtext

After receiving my 5th dose of Moderna I contacted COVID-19 infection. My COVID-19 infection started on 01/23/2023 not sure what time of the day. I was sneezing, had a runny nose, fever, chills, fatigue, cough, and body aches. My energy levels became very slow. I tested with a home COVID-19 test on 01/26/2023 which was positive. I did a telehealth with a doctor on the same day and he prescribed me with PAXLOVID for 5 days. After 3 days of finishing the PAXLOVID I had a relapse on 02/02/2023. I had same symptoms except fever. We took over the counter medications such as TYLENOL and other cold medications. After COVID-19 infection my energy level and exercise tolerance is not the same.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: 26JAN2023 COVID-19 test positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Breast Cancer; Radiation Therapy; Heart Surgery; Asthma; Hodgkin's
Andere Medikamente: Warfarin; SYNTHROID; rosuvastatin; inhaler
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 2593269

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: MA
Alter: 67,0
Geschlecht: M
Eingang: 08.03.2023
Impfdatum: 06.09.2022
Beginn: 15.02.2023
Tage bis Beginn: 162,0
Dosis: 5
Route/Site: SYR / LA

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

COVID-19 Cough Headache Pyrexia SARS-CoV-2 test positive Sinus congestion

Symptomtext

I had a bad headache and was starting to get sinus congestion and a cough. I was feeling a little feverish. I took an at home COVID-19 test and it tested positive. After that, I was able to get the telehealth appointment around 08:40 that morning. After going through the meeting with the PA, she prescribed Paxlovid for me. I started to take the Paxlovid that day around 10:00AM and took the 5 day regimen every 12 hours. After the end of the first dose before the 2nd dose, the symptoms had subsided. For the 5 days of Paxlovid, I felt a little brain fog and had a metallic taste in my mouth. I didn't feel too bad, just lousy. I quarantined by myself for 5 days. Other than those 2 symptoms from the Paxlovid, I was fine. On the 5th day, I did test again and came back negative and I've been negative since. It was a pretty mild encounter with COVID-19. Took a couple weeks to feel fully myself again between the infection and the strong medication.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: 15FEB2023 At Home COVID-19 Test - Positive; 20FEB2023 At Home COVID-19 Test - Negative; 21FEB2023 At Home COVID-19 Test - Negative; 22FEB2023 At Home COVID-19 Test - Negative
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Losartan; Amlodipine; Atorvastatin
Allergien: None
Vorherige Impfungen: -

VAERS 2593266

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7144B

mild

Staat: TX
Alter: 80,0
Geschlecht: M
Eingang: 08.03.2023
Impfdatum: 06.09.2022
Beginn: 20.09.2022
Tage bis Beginn: 14,0
Dosis: 5
Route/Site: IM / LA

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

Cough Fatigue Respiratory tract congestion Somnolence

Symptomtext

Fatigue, Sleepy coughing Congestion

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Paxlovid: decongestant: Ente cover: Amoxicillin
Allergien: Shrimp Allergy
Vorherige Impfungen: -

VAERS 2593265

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: MD
Alter: 78,0
Geschlecht: M
Eingang: 08.03.2023
Impfdatum: 06.09.2022
Beginn: 24.12.2022
Tage bis Beginn: 109,0
Dosis: 5
Route/Site: IM / RA

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

Asthenia COVID-19 Cough Fatigue Hypersomnia Malaise Rhinorrhoea SARS-CoV-2 test positive Sneezing

Symptomtext

12/24/2022 I was feeling a little bit under the weather. I tested positive with a home COVID test on 12/25/2022. I was sneezing, coughing, runny nose and felt very tired. I began to sleep a lot more. I had no energy. I called the doctor on 12/26/22 and was prescribed PAXLOVID. I tested negative for COVID. After completing the PAXLOVID, I tested positive for COVID again. I was quite fatigued for around three weeks. I did not test negative again until 2 weeks and 5 days after testing positive the first time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID at home tests, 2 positive and 2 negative
Aktuelle Erkrankungen: None
Vorgeschichte: Knee issues; past eye issues
Andere Medikamente: Levothyroxine; montelukast; armodafinil; atorvastatin; escitalopram; omeprazole; BREO ELLIPTA; super papaya enzyme plus; D-mannose; ALLER-FEX; pygeum extract; ginger root; resveratrol; pumpkin seed oil; acetyl L-carnitine; phosphatidyl seri
Allergien: None
Vorherige Impfungen: -

VAERS 2593212

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: GA
Alter: 43,0
Geschlecht: F
Eingang: 08.03.2023
Impfdatum: 06.09.2022
Beginn: 23.02.2023
Tage bis Beginn: 170,0
Dosis: 4
Route/Site: IM / AR

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

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

Symptomtext

I had minor body aches for a day after receiving the vaccine. On 02/23/2023, I had a sore throat. I tested positive for COVID-19 on 02/24/2023. I contacted my primary care doctor, and they did not prescribe anything for me. I took TYLENOL, ADVIL, SUDAFED, AFRIN and MUCINEX to help with my symptoms. As of today, I continue to feel fatigued.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 24FEB2023 COVID-19 test positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Hashimoto's Disease; Thyroiditis
Andere Medikamente: N/A
Allergien: Seasonal allergies
Vorherige Impfungen: -

VAERS 2593123

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: CT
Alter: 70,0
Geschlecht: M
Eingang: 08.03.2023
Impfdatum: 06.09.2022
Beginn: 23.02.2023
Tage bis Beginn: 170,0
Dosis: 5
Route/Site: IM / LA

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

COVID-19 Chills Cough Fatigue Gastrointestinal disorder Headache Hypersensitivity Influenza like illness Oropharyngeal pain Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

I had some digestive issues and had some symptoms of an allergy that grew into sore throat, cough, headache, runny knows and chills This felt like a bad case of flu. Took an At Home COVID-19 Test, positive. Televisit with doctor on 2/25. Doctor Proscribed Paxlovid. The next day, Symptoms greatly abated. Did not take Paxlovid as symptoms abated by themselves. Over the next week, the symptoms got better and got worse up and down. Mostly Felt great deal of fatigue. Congestion lingers.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: 24Feb2023 At Home COVID-19 Test, positive
Aktuelle Erkrankungen: No
Vorgeschichte: Prediabetic; Glaucoma; Gurd
Andere Medikamente: Rosuvastatin; Eyedrops; Ambigram; Latanoprost; Aspirin; Vitamin B12; Ethoxzolamide; Glucosamine; Metformin; Omeprazole
Allergien: No
Vorherige Impfungen: -

VAERS 2593114

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7144B

mild

Staat: FL
Alter: 69,0
Geschlecht: M
Eingang: 08.03.2023
Impfdatum: 01.03.2023
Beginn: 04.03.2023
Tage bis Beginn: 3,0
Dosis: 5
Route/Site: IM / RA

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

COVID-19 Cough Eye irritation Pain SARS-CoV-2 test positive Sleep disorder Throat irritation

Symptomtext

I woke up in the middle of the night with a scratchy throat. By the next morning whole body aches, burning behind the eyes, cough. I called my provider and let them know about my symptoms and that I had COVID-19. Provider said to keep taking my OTC medications. I will retest for COVID-19 tomorrow 03/09/2023.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: 05MARCH2023- COVID-19 Test - Positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Pacemaker
Andere Medikamente: Simvastatin; Aspirin; Vitamin D
Allergien: Morphine
Vorherige Impfungen: -

VAERS 2593112

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: MI
Alter: 71,0
Geschlecht: F
Eingang: 08.03.2023
Impfdatum: 07.09.2022
Beginn: 01.11.2022
Tage bis Beginn: 55,0
Dosis: 5
Route/Site: IM / RA

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

Arthralgia COVID-19 Joint stiffness Osteoarthritis SARS-CoV-2 test positive

Symptomtext

I did not have an adverse event after receiving the vaccine. I tested positive for COVID-19 in November 2022. I contacted my doctor to give an update. I was offered PAXLOVID but declined because I felt my symptoms were mild. I rested a lot and isolated. In December 2022, I noticed an ache and stiffness in my right knee. The pain progressed in January 2023. A few weeks later, the pain was so paid I was waking up in the middle of the night. I had tried ibuprofen to help with the pain, but it wasn't helping. I got a prescription for a higher dose of ibuprofen. At this point, it is determined that I have osteoarthritis in my right knee.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: NOV2022 COVID-19 test positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Diabetic; High Blood Pressure; Rapid Heart Rate
Andere Medikamente: PRILOSEC; metformin
Allergien: N/A
Vorherige Impfungen: Dose 1; I had a COVID-19 right arm, very painful

VAERS 2593093

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7144B

mild

Staat: NY
Alter: 57,0
Geschlecht: F
Eingang: 08.03.2023
Impfdatum: 06.09.2022
Beginn: 21.02.2023
Tage bis Beginn: 168,0
Dosis: 5
Route/Site: IM / LA

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

COVID-19 Chills Cough Headache Infection Oropharyngeal pain Pain Pyrexia Respiratory tract congestion SARS-CoV-2 test positive Sneezing

Symptomtext

I experienced a breakthrough case of COVID-19 with sneezing, headaches, sore throat, sore ears, fever and chills, body aches, congestion and coughing.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: COVID-19- Positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Vascular arthritis
Andere Medikamente: Atorvastatin; Fluoxetine; Bupropion; Tylenol; Advil; Vitamin D
Allergien: Codeine
Vorherige Impfungen: -

VAERS 2592363

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: PA
Alter: 32,0
Geschlecht: M
Eingang: 07.03.2023
Impfdatum: 02.09.2022
Beginn: 17.01.2023
Tage bis Beginn: 137,0
Dosis: 4
Route/Site: SYR / LA

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

Chills Diarrhoea Fatigue Headache Pain Rhinorrhoea

Symptomtext

Started Tuesday night 17JAN2023 with chills aches fatigue just really a runny nose but on Thursday 19JAN2023 diarrhea and in the evening a headache and I had until Friday 20JAN2023 and the headache was persistent so I went into urgent care and was told to take plenty of fluids and EXCEDRIN. I was feeling better by the end of the weekend 22JAN2023 had mostly recovered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Red yeast rice supplement
Allergien: Amoxicillin
Vorherige Impfungen: -

VAERS 2591923

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: OH
Alter: 49,0
Geschlecht: F
Eingang: 06.03.2023
Impfdatum: 03.09.2022
Beginn: 13.02.2023
Tage bis Beginn: 163,0
Dosis: 5
Route/Site: IM / LA

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

COVID-19 Cough Fatigue Oropharyngeal pain Pain Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

I noticed a sore throat that lasted 3 days. After that I developed body aches, cough and congestion lasting about 3 days. 2/19 Took and At Home COVID-19 test, positive. Televisit with doctor who proscribed Paxlovid. Symptoms stayed the same for about 2 days after starting Paxlovid, and then things began to improve but still have lingering fatigue.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 19Feb2023 At Home COVID-19 test, positive
Aktuelle Erkrankungen: No
Vorgeschichte: Epstein-Barr virus
Andere Medikamente: Sythroid; fluoxetine; Singulair; Valtrex; Omeprazole; Bactrim; Xyzal; Nasal Spray; Multivitamin; Fish Oil; Calcium; Allegra; Quercetin
Allergien: Penicillin; Cipro; Soolantra
Vorherige Impfungen: -

VAERS 2591898

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: CA
Alter: 75,0
Geschlecht: M
Eingang: 06.03.2023
Impfdatum: 02.09.2022
Beginn: 11.02.2023
Tage bis Beginn: 162,0
Dosis: 5
Route/Site: IM / LA

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

COVID-19 Chronic sinusitis Cough Diarrhoea Fatigue Pyrexia SARS-CoV-2 test negative SARS-CoV-2 test positive

Symptomtext

On the morning of 2/11/2023, I developed fatigue, cough, fever, and diarrhea. I got a PCR test on the afternoon of 2/11/2023 and 2/12/2023, and they both yielded positive results. I began taking PAXLOVID on 2/11/2023. I was doing better the next day and was afebrile on the third day. I took a home antigen test on 2/8/2023, 2/10/2023, 2/11/2023, 2/12/2023, and 2/14/2023, and the results on all of them were negative. During the first week, I had fatigue and had to take naps. During the second week, I felt better. At the time of this writing, I'm okay, though I have a residual cough with a little bit of catarrh. I don't know if it's the result of the COVID-19 or my chronic sinusitis, but I suspect the prior.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: 11FEB2023, 12FEB2023 PCR tests, positive Results; 8FEB2023, 10FEB2023, 11FEB2023, 12FEB2023, 14FEB2023, home antigen tests, negative results
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension; Obstructive Sleep Apnea; Chronic Sinusitis; Retained Kidney Stone (Non-Problematic); Polyp in Maxillary Sinus; Diverticulosis; Benign Prostatic Hyperplasia; Benign Polyp in Colon; Atrial Premature Beat; Lumbar Disk Degeneration; Common Migraine; Bilateral Age-Related Cataracts; Posterior Vitreous Detachment (Both Eyes); Bradycardia with Resting Pulse of About 37; Osteopenia
Andere Medikamente: Lisinopril; multivitamin; vitamin D; vitamin K; magnesium citrate
Allergien: Ciprofloxacin; gentamicin; mefloquine; atovaquone/proguanil
Vorherige Impfungen: -

VAERS 2591837

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: IL
Alter: 71,0
Geschlecht: F
Eingang: 06.03.2023
Impfdatum: 02.09.2022
Beginn: 14.12.2022
Tage bis Beginn: 103,0
Dosis: 5
Route/Site: SYR / LA

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

Bronchitis COVID-19 Chest X-ray normal Cough Headache Influenza A virus test negative Influenza B virus test SARS-CoV-2 test positive

Symptomtext

Started symptoms on 12/14/2022 and on 12/16/2022 went to a clinic and tested positive for COVID-19. Diagnosed with acute bronchitis. I didn't not get rid of the cough until the end of January. I also still have headaches, but they are much less frequent.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: 12/16/2022 COVID-19 test positive, 12/16/2022 Flu A negative, 12/16/2022 Flu B negative, 12/16/2022 Chest X-ray negative
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Aspirin
Vorherige Impfungen: -

VAERS 2591813

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: MI
Alter: 84,0
Geschlecht: F
Eingang: 06.03.2023
Impfdatum: 18.09.2022
Beginn: 25.02.2023
Tage bis Beginn: 160,0
Dosis: 5
Route/Site: - / -

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

Atrial flutter Blood iron decreased Blood zinc decreased COVID-19 Chest X-ray abnormal Echocardiogram abnormal Fatigue Headache Hypochromic anaemia Hypoxia Liver function test normal Oropharyngeal pain Pulmonary congestion Transferrin saturation decreased

Symptomtext

Discharge Provider: MD Primary Care Provider: MD Admission Date: 2/25/2023 Discharge Date: Mar 3, 2023 PRESENTING PROBLEM: Hypoxia COVID-19 HOSPITAL COURSE: 84 year old female presented with complaints of sore throat, headache and fatigue and also exertional hypoxia. She was found to have covid infection and was hypoxemic requiring nasal cannula. CXR shows pulmonary congestion. She was started on remdesevir and decadron. Her LFTs remained normal the entire duration of her stay.Her hypoxia improved from requiring 3 liters down to 1 liter. Transition to Home consulted, patient enrolled and pulmo rehab for follow up and home med respectively . During her hospital stay she was found to have anemia. Indices indicative of microcytic hypochromic Iron and iron sat , Zinc all were low and were repleted. On day of discharge she was noted to be in atrial flutter in varying conductance She is known to heart facility, started on NOAC ( after questionable history of CVA perhaps bleed was ruled out ) , and cardizem. Her heart rate controlled, with Highest heart rate up to 98 on ambulation . Echo showed no pericardial effusion , mild pulmonary HTN ( also known and following with Pulmonary service, her EF 50% ) Discharged on 3/3/2023 hemodynamically stable, tolerating meals and ambulation . Zio patch on discharge

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Praegender Schweregrund: Fatigue
Hospital-Tage: 6,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Acquired hypothyroidism Dyslipidemia Atrial fibrillation Anxiety with depression Coronary artery disease involving coronary bypass graft of native heart without angina pectoris Essential hypertension Mitral regurgitation History of CVA (cerebrovascular accident) Swelling of right lower extremity Advanced care planning/counseling discussion Pulmonary hypertension Pre-operative examination for internal medicine Hypoxia COVID-19 Anemia
Andere Medikamente: acetaminophen (TYLENOL) 650 MG extended release tablet ALPRAZolam (XANAX) 0.25 MG tablet aspirin 81 MG EC tablet B Complex-Biotin-FA (B COMPLETE) TABS Biotin 1000 MCG CHEW Calcium Carbonate-Vit D-Min (CALCIUM 600+D3 PLUS MINERALS) 600-800 M
Allergien: Contrast Dye [Ivp Dye, Iodine Containing] Metoprolol Alendronate [Bisphosphonates]GI Upset Atenolol Cozaar [Losartan]Itching DoxycyclineHeadache EzetimibeOther Hctz LevaquinHeadache No Known Iodine AllergyOther Sulfa DrugsItching
Vorherige Impfungen: -

VAERS 2587177

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: FL
Alter: 77,0
Geschlecht: F
Eingang: 24.02.2023
Impfdatum: 09.09.2022
Beginn: 25.11.2022
Tage bis Beginn: 77,0
Dosis: 5
Route/Site: OT / -

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

COVID-19 Fatigue

Symptomtext

patient got COVID-19; patient is tired all the time; This spontaneous case was reported by a patient and describes the occurrence of COVID-19 (patient got COVID-19) and FATIGUE (patient is tired all the time) in a 77-year-old female patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. AS7144B) for COVID-19 prophylaxis. It was reported that patient had not received any other vaccines in the 4 weeks prior to COVID-19 vaccine. Concurrent medical conditions included Hypertension and Overweight. Concomitant products included LOSARTAN, CHARCOAL, ACTIVATED (CARBOTURAL), HYDROCHLOROTHIAZIDE, AMLODIPINE and POTASSIUM for an unknown indication. On 09-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 25-Nov-2022, the patient experienced COVID-19 (patient got COVID-19) and FATIGUE (patient is tired all the time). In December 2022, COVID-19 (patient got COVID-19) had resolved with sequelae. At the time of the report, FATIGUE (patient is tired all the time) had not resolved. 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. It was reported that patient received first dose of Moderna COVID-19 Vaccine on 22-Feb-2021 batch number 001A21A, second dose on 22-Mar-2021 batch number 047A21A, first booster on 25-Oct-2021 batch number 012521D and second booster on 30-Mar-2022 batch number 0B6L21A. It was reported that patient experienced headache and nausea during 24 hours after dose 2. On 25-Nov-2022 patient got COVID-19 even after getting the Moderna shots, and it lasted approximately for 16 days till Dec 2022 and patient was currently tired all the time. Treatment medications were not provided. This case was linked to US-MODERNATX, INC.-MOD-2023-712228 (Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2023-712228:Bivalent case

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Hypertension; Overweight
Vorgeschichte: Comments: It was reported that patient had not received any other vaccines in the 4 weeks prior to COVID-19 vaccine.
Andere Medikamente: LOSARTAN; CARBOTURAL; HYDROCHLOROTHIAZIDE; AMLODIPINE; POTASSIUM
Allergien: -
Vorherige Impfungen: -

VAERS 2582615

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: VA
Alter: 70,0
Geschlecht: M
Eingang: 16.02.2023
Impfdatum: 08.09.2022
Beginn: -
Tage bis Beginn: -
Dosis: 5
Route/Site: OT / -

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

Blood pressure measurement Heart rate Pain in extremity Rash macular Tongue erythema

Symptomtext

Red dots on the top and bottom of his tongue; red round, blotchy dots the size of a large pin-head on random places on his body/his forehead and looked as if bleeding; every single shot, he had a sore arm for 3 days; This spontaneous case was reported by a patient and describes the occurrence of TONGUE ERYTHEMA (Red dots on the top and bottom of his tongue), PAIN IN EXTREMITY (every single shot, he had a sore arm for 3 days) and RASH MACULAR (red round, blotchy dots the size of a large pin-head on random places on his body/his forehead and looked as if bleeding) 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. AS7144B) for COVID-19 prophylaxis. Concurrent medical conditions included Blood pressure. Concomitant products included METOPROLOL and LOSARTAN for Blood pressure high, SERTRALINE HYDROCHLORIDE (ZOLOFT), BUSPIRONE HYDROCHLORIDE (BUSPAR), CLONAZEPAM, RABEPRAZOLE SODIUM (ACIPHEX), TAMSULOSIN HYDROCHLORIDE (FLOMAX RELIEF), CABERGOLINE, SILDENAFIL CITRATE (VIAGRA) and FLUTICASONE PROPIONATE (FLONASE [FLUTICASONE PROPIONATE]) for an unknown indication. On 08-Sep-2022, the patient received fifth dose of mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (Intramuscular) 1 dosage form. On an unknown date, the patient experienced TONGUE ERYTHEMA (Red dots on the top and bottom of his tongue), PAIN IN EXTREMITY (every single shot, he had a sore arm for 3 days) and RASH MACULAR (red round, blotchy dots the size of a large pin-head on random places on his body/his forehead and looked as if bleeding). At the time of the report, TONGUE ERYTHEMA (Red dots on the top and bottom of his tongue) and RASH MACULAR (red round, blotchy dots the size of a large pin-head on random places on his body/his forehead and looked as if bleeding) outcome was unknown and PAIN IN EXTREMITY (every single shot, he had a sore arm for 3 days) had resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 26-Nov-2022, Blood pressure measurement: 190/100 mmHg. On an unknown date, Heart rate: 50. 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. It was reported that after Dose 5 patient went to a dentist on 9FEB2023. The dentist noted red dots on the top and bottom of patient's tongue. However, the patient does not remember after which shot, but he had red round, blotchy dots the size of a large pinhead on random places on his body. On the day of report it was on his forehead and looked as if bleeding. Patient further reported that the red dots come and go, and they are usually under the skin. Patient's high blood pressure was controlled by medications. Amlodipine was added 6 weeks ago. A week after Metoprolol was discontinued because of low heart rate and his blood pressure was a little off on 26NOV2022 and ER doctor added Amlodipine. Patient was enquiring that if anyone else experienced these reactions. Treatment medication information was not provided. This case was linked to MOD-2021-377198 (Patient Link).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: Test Date: 20221126; Test Name: Blood pressure; Test Name: HR; Result Unstructured Data: 50
Aktuelle Erkrankungen: Blood pressure
Vorgeschichte: -
Andere Medikamente: ZOLOFT; BUSPAR; CLONAZEPAM; METOPROLOL; LOSARTAN; ACIPHEX; FLOMAX RELIEF; CABERGOLINE; VIAGRA; FLONASE [FLUTICASONE PROPIONATE]
Allergien: -
Vorherige Impfungen: -

VAERS 2582249

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: OH
Alter: 62,0
Geschlecht: F
Eingang: 15.02.2023
Impfdatum: 22.09.2022
Beginn: 27.01.2023
Tage bis Beginn: 127,0
Dosis: 4
Route/Site: SYR / LA

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

COVID-19 Cough Fatigue Pyrexia Respiratory tract congestion SARS-CoV-2 test positive Sinus disorder Taste disorder Throat irritation

Symptomtext

Congestion; fatigue; sinus issues; scratchy throat. I thought I had a cold, then after a few days the cough and the 101 fever came in. The fever only lasted one day on 101 and it went down to 99 for the next 2 days. I called the doctor and was prescribed PAXLOVID. The temperature went away after 24 hours. The cough also became sporadic. I still have this taste in the back of my mouth that tastes like reflux with acid, however I have not lost any taste at all. The biggest symptom I had was the exhaustion. It is better now but it is still lingering after weeks.

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Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 5 COVID home test with positive result
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetic
Andere Medikamente: Gabapentin; metformin; WELLBUTRIN; turmeric; levothyroxine; solifenacin; CBD; atorvastatin
Allergien: None
Vorherige Impfungen: -

VAERS 2567827

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: VA
Alter: 53,0
Geschlecht: M
Eingang: 25.01.2023
Impfdatum: 25.10.2022
Beginn: 20.01.2023
Tage bis Beginn: 87,0
Dosis: 5
Route/Site: SYR / LA

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

COVID-19 Chills Cough Fatigue Headache Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

I had a runny nose, stuffy headache, fatigue, chills and cough. I tested with a at home test and at the doctor. I was prescribed PAXLOVID. I have seen improvement 48 hours after starting the medication.

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Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: 22JAN2023 COVID-19 test positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Diabetes
Andere Medikamente: TRUVADA; lisinopril; rosuvastatin; JANUMET; JARDIANCE; glipizide; RYBELSUS
Allergien: N/A
Vorherige Impfungen: -

VAERS 2550834

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: TN
Alter: 26,0
Geschlecht: M
Eingang: 05.01.2023
Impfdatum: 03.09.2022
Beginn: 13.09.2022
Tage bis Beginn: 10,0
Dosis: 4
Route/Site: IM / LA

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

Angioedema Chronic spontaneous urticaria Dermatitis contact Hypersensitivity Mechanical urticaria Pruritus Urticaria

Symptomtext

10 days after vaccination, hives and itching began. Initially diagnosed as contact dermatitis (confined to waistline) and treated with Benadryl and a steroidal topical cream. Within 48 hours, progressed to severe full-body hives and itching, with dermatographia and intermittent angioedema. Went to clinic and diagnosed with an allergic reaction; given a course of oral steroids and a steroid injection (administered in buttock). Relief lasted ~3 days. Saw allergist, who diagnosed idiopathic urticaria and prescribed treatment of 4 Allegra per day. 2 Tagamet per day were added to the Allegra regimen, because symptoms persisted. Then, Singulair was added to the regimen when symptoms continued to persist. A second round of oral steroids was prescribed approximately 6 weeks after the initial Allergist visit (7 weeks after symptom onset). The allergist revised the diagnosis to Chronic Idiopathic Urticaria at that point. Approximately 8 weeks after symptom onset, the first Xolair injection was administered. These injections will continue monthly. Patient continues to take Allegra and has been unable to wean off Tagamet or Singulair; two Xolair injections have been administered thus far. A link between the urticaria and the COVID and flu vaccines was not confirmed, although the allergist indicated that it could be related, in theory.

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Praegender Schweregrund: Chronic spontaneous urticaria
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Concussion, ankle sprain
Vorgeschichte: Celiac Disease, Hashimoto?s Thyroiditis, Postural Orthostatic Tachycardia Syndrome
Andere Medikamente: Propranolol, Levothyroxine, Vyvanse, focalin, lisinopril, Dymista, glycopyrrolate, Xyzal, Pataday, multivitamin, Vitamin D, fish oil, probiotic
Allergien: Bactrim, penicillins, cephalosporins
Vorherige Impfungen: -

VAERS 2546977

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7144B

mild

Staat: CA
Alter: 40,0
Geschlecht: F
Eingang: 30.12.2022
Impfdatum: 15.01.2021
Beginn: 09.12.2022
Tage bis Beginn: 693,0
Dosis: 5
Route/Site: IM / LA

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

COVID-19 Chemotherapy Computerised tomogram thorax normal Malaise Nasal congestion Oxygen saturation decreased

Symptomtext

Patient was seen and examined. She was getting chemotherapy today with taxol and incidentally noted to have O2 desat to lowest of 89% for a brief second then comes back up to ~93. Her Heme/Onc physician was concerned for PE and asked that she be evaluated in ER. She was never symptomatic. In ER CTPE was negative and no other acute cardiopulmonary issues were identified. She had COVID19 about 3 weeks ago with mild symptoms and remains with nasal congestion.

Weitere VAERSDATA-Felder

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

VAERS 2546618

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7144B

mild

Staat: IL
Alter: 62,0
Geschlecht: M
Eingang: 30.12.2022
Impfdatum: 03.09.2022
Beginn: -
Tage bis Beginn: -
Dosis: 5
Route/Site: OT / -

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

Vaccination site pain

Symptomtext

He had only a sore arm after each shot; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION SITE PAIN (He had only a sore arm after each shot) in a 62-year-old male patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. AS7144B) for COVID-19 prophylaxis. No Medical History information was reported. On 03-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 an unknown date, the patient experienced VACCINATION SITE PAIN (He had only a sore arm after each shot). At the time of the report, VACCINATION SITE PAIN (He had only a sore arm after each shot) had resolved. Not Provided Concomitant product use was not provided by the reporter. Dosage text was reported as Bivalent Booster. Treatment information was not provided. This case was linked to MOD-2022-692275 (Patient Link).

Weitere VAERSDATA-Felder

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

VAERS 2544729

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: PA
Alter: 49,0
Geschlecht: F
Eingang: 28.12.2022
Impfdatum: 27.09.2022
Beginn: 18.12.2022
Tage bis Beginn: 82,0
Dosis: 4
Route/Site: IM / LA

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

Asthenia COVID-19 Cough Nasal congestion Pyrexia SARS-CoV-2 test positive

Symptomtext

On the 18th I had a stuffy nose and was very weak. I had a slight fever around 99.4 to 99.6 for 3 days. I completed an at home COVID-19 test on 12/20/2022 and I took another PCR test on December 21, 2022, at the pharmacy. I was prescribed molnupiravir and started to take it on December 21st. I was feeling better by day 4 but still had a stuffy nose and a dry cough. I recovered after 4 days. I am still testing positive as recent as yesterday.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: COVID-19 home test 12/20/2022, COVID 19-PCR test 12/21/2022
Aktuelle Erkrankungen: N/A
Vorgeschichte: Asthma; Hypertension
Andere Medikamente: Amlodipine; atenolol; DAYPRO; multivitamin
Allergien: N/A
Vorherige Impfungen: -

VAERS 2543599

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: CT
Alter: 67,0
Geschlecht: F
Eingang: 27.12.2022
Impfdatum: 13.09.2022
Beginn: 06.12.2022
Tage bis Beginn: 84,0
Dosis: 5
Route/Site: - / -

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

COVID-19 Cough Fatigue Headache Influenza virus test negative Nausea SARS-CoV-2 test positive Sinus congestion Throat irritation

Symptomtext

Fatigue, scratchy throat, headache, sinus congestion, cough, mild nausea.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: SARS-CoV-2 RNA (COVID-19) test was positive on 12/20/2022 Influenza A and B tests were negative
Aktuelle Erkrankungen: -
Vorgeschichte: Diabetes, Hypothyroidism
Andere Medikamente: Synthroid, Pravastatin, Wellbutrin, Omeprazole, Gabapentin, Zyrtec, Metformin, Multi Vitamin
Allergien: -
Vorherige Impfungen: -

VAERS 2542006

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: IA
Alter: 54,0
Geschlecht: F
Eingang: 23.12.2022
Impfdatum: 22.09.2022
Beginn: 13.12.2022
Tage bis Beginn: 82,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Fatigue Impaired work ability Oropharyngeal pain Paranasal sinus discomfort Pyrexia Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

12/13/2022 in the evening I noticed head congestion, fatigue, and sore throat. 12/14 tested with an at home COVID-19 test positive. Saw Dr. that day, prescribed PAXLOVID and treat symptomatically. Symptoms were worse on 12/14, fever 102. Symptoms tapered off the next couple of days. Felt much better by 12/17. Returned to work 12/19. 12/19 was last dose of PAXLOVID. 12/21 symptoms of congestion, fatigue, and sinus pressure returned and are being treated symptomatically. 12/22 tested positive on at home Covid-19 test. This is where participant was at time of reporting.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 12/14 tested with an at home COVID-19 test positive. 12/22 tested positive on at home Covid-19 test.
Aktuelle Erkrankungen: No
Vorgeschichte: Asthma
Andere Medikamente: ADVAIR; omeprazole; montelukast; loratadine; probiotic; hydrochlorothiazide/lisinopril; FLONASE
Allergien: No
Vorherige Impfungen: -

VAERS 2510272

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7144B

mild

Staat: PA
Alter: 77,0
Geschlecht: F
Eingang: 22.12.2022
Impfdatum: 21.09.2022
Beginn: 01.11.2022
Tage bis Beginn: 41,0
Dosis: 5
Route/Site: OT / -

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

COVID-19 Chills Cough Oropharyngeal pain Pyrexia SARS-CoV-2 test SARS-CoV-2 test positive

Symptomtext

I had minor chills, mild fever never over 100, a little coughing, and sore throat. I tested positive for COVID-19 at home. I spoke to my doctor, and he prescribed me PAXLOVID. I started feeling better after a few days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: 11/11/2022, positive, COVID-19 test
Aktuelle Erkrankungen: N/A
Vorgeschichte: Guttate Psoriasis
Andere Medikamente: Multivitamin; D3; clonazepam; simvastatin; baby aspirin
Allergien: N/A
Vorherige Impfungen: -

VAERS 2510272

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: PA
Alter: 77,0
Geschlecht: F
Eingang: 22.12.2022
Impfdatum: 21.09.2022
Beginn: 01.11.2022
Tage bis Beginn: 41,0
Dosis: 5
Route/Site: IM / RA

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

COVID-19 Chills Cough Oropharyngeal pain Pyrexia SARS-CoV-2 test SARS-CoV-2 test positive

Symptomtext

I had minor chills, mild fever never over 100, a little coughing, and sore throat. I tested positive for COVID-19 at home. I spoke to my doctor, and he prescribed me PAXLOVID. I started feeling better after a few days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: 11/11/2022, positive, COVID-19 test
Aktuelle Erkrankungen: N/A
Vorgeschichte: Guttate Psoriasis
Andere Medikamente: Multivitamin; D3; clonazepam; simvastatin; baby aspirin
Allergien: N/A
Vorherige Impfungen: -

VAERS 2536779

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: TX
Alter: 53,0
Geschlecht: F
Eingang: 19.12.2022
Impfdatum: 16.09.2022
Beginn: 05.11.2022
Tage bis Beginn: 50,0
Dosis: 5
Route/Site: IM / LA

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

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

Symptomtext

I tested positive on 11/07/2022 for COVID-19. I had a sore throat, cough and fatigue. Also had a very low fever for one day. I then tested positive again on 11/19/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 07NOV2022 COVID-19 positive, 19NOV2022 COVID-19 positive, 23NOV2022 COVID-19 negative
Aktuelle Erkrankungen: N/A
Vorgeschichte: High Blood Pressure, High Triglyceride
Andere Medikamente: Fenofibrate; BYSTOLIC, vitamin C; vitamin D; multivitamin
Allergien: N/A
Vorherige Impfungen: -

VAERS 2536030

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7144B

mild

Staat: IN
Alter: 63,0
Geschlecht: M
Eingang: 17.12.2022
Impfdatum: 03.09.2022
Beginn: 15.10.2022
Tage bis Beginn: 42,0
Dosis: 5
Route/Site: SYR / LA

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

COVID-19 Chills Fatigue Irritability Oropharyngeal pain Pyrexia SARS-CoV-2 test positive Somnolence

Symptomtext

Started getting chills and a sore throat. After a couple of hours got very tired/sleepy and a fever. Also, got very irritated.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Used home COVID test on 10/16/22 and it was positive. I did not phone the doctor or go to the doctor.
Aktuelle Erkrankungen: None
Vorgeschichte: Had non-Hodgkin lymphoma in 2020, now in remission
Andere Medikamente: Synthroid, Fenofibrare, Ezetimibe tablets
Allergien: None
Vorherige Impfungen: -

VAERS 2535413

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: CA
Alter: 65,0
Geschlecht: M
Eingang: 16.12.2022
Impfdatum: 15.09.2022
Beginn: 21.11.2022
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 Cough Pyrexia Rhinorrhoea SARS-CoV-2 test positive Sneezing

Symptomtext

I was sneezing, nose running, little cough, tired, and small fever. I tested positive for COVID-19 at home. I had a telehealth visit and was prescribed PAXLOVID. I was feeling better by the 24th. I was testing positive for about 2 weeks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: 11/22/2022, positive, COVID-19 test
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Lisinopril; atorvastatin; omeprazole; aspirin; vitamin C; fish oil
Allergien: N/A
Vorherige Impfungen: COVID-19, sick for a day, 1st dose, Moderna

VAERS 2533324

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: PA
Alter: 64,0
Geschlecht: F
Eingang: 15.12.2022
Impfdatum: 13.09.2022
Beginn: 06.10.2022
Tage bis Beginn: 23,0
Dosis: 5
Route/Site: IM / LA

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

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

Symptomtext

Started with symptoms 12/04/2022 sore throat and nasal congestions; telehealth visit suggested over counter meds and quarantined.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: At home Covid test results were positive.
Aktuelle Erkrankungen: No
Vorgeschichte: Diabetes; high blood pressure
Andere Medikamente: Multivitamins; D3; B12; metformin; simvastatin; OZEMPIC; losartan; amlodipine; glipizide
Allergien: No
Vorherige Impfungen: -

VAERS 2533149

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: MA
Alter: 42,0
Geschlecht: M
Eingang: 15.12.2022
Impfdatum: 10.09.2022
Beginn: 20.10.2022
Tage bis Beginn: 40,0
Dosis: 4
Route/Site: IM / LA

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

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

Symptomtext

Our kid had cough and cold symptom, so we tested him, and he was negative. My wife had the same symptoms she tested negative as well. All this happened days before me. I had a slight cough and a headache. I tested positive for COVID-19 on October 22, and I called my primary care doctor. The doctor gave me PAXLOVID after checking the COVID-19 results. I was better within a few days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: At home test COVID-19
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: CONCERTA
Allergien: N/A
Vorherige Impfungen: -

VAERS 2531480

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: WA
Alter: 50,0
Geschlecht: F
Eingang: 14.12.2022
Impfdatum: 10.09.2022
Beginn: 25.10.2022
Tage bis Beginn: 45,0
Dosis: 5
Route/Site: IM / LA

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

Blood test COVID-19 Chest X-ray Decreased appetite Dizziness Fatigue Feeling abnormal Hyperhidrosis Laryngitis Malaise Nasal congestion Nasopharyngitis Oropharyngeal pain Respiratory symptom Respiratory tract congestion Rhinorrhoea SARS-CoV-2 antibody test positive SARS-CoV-2 test negative

Symptomtext

I received the Moderna Bivalent booster for COVID-19 on 9/10/2022. On 10/25/2022, I was on a cruise ship when I began to get the sniffles. On 10/27/2022, my sniffles got worse, so I took a home antigen test, which yielded a negative result. I felt like I was cycling through cold symptoms. I developed nasal congestion, sore throat, laryngitis, and congestion in the upper chest and laryngeal area. I took another home antigen test on 11/4/2022 and got a strongly positive result. I notified the cruise medical center. They came to my room and conducted a PCR test. In comparison with previous PCR tests I had received, their swabbing wasn't very thorough, since I could barely even feel the swab. Two hours later, they called me and let me know that the PCR result was negative and that I did not have to mask or self-isolate. I wasn't happy about this, because I was certain that I did have COVID-19. I had to eat, though, so I masked when I left the room to get food and then brought the food back to my room. I self-isolated as much as possible. On 11/5/2022, I wasn't feeling well, so I went to the ship's clinic. They did not perform another PCR test, but they did do blood work, a chest X-ray, and an oral swab to test for strep throat. They told me that I had tested positive for Streptococcus pyogenes, which I found strange, since I did not have classic strep throat symptoms. They prescribed me 300 mg of cefdinir, which I began taking on 11/7/2022; I was to take one pill twice a day. They also put me on an intravenous antibiotic, ceftriaxone sodium, on 11/5/2022 and 11/6/2022. I felt a little better after I started the antibiotics, but not much. I continued to have the symptoms of an upper respiratory infection, which included laryngitis, nasal congestion, and upper respiratory congestion. I measured my blood oxygen level, which remained in the normal range. I also ran a low-grade fever of 99-100 for a couple of days. During this time, I lost my appetite. I had a lot of post-nasal drip, which was just out of control. On 11/13/2022, the cruise ended, and my symptoms were about the same as before. I was still very congested and even wheezed a little. On 11/9/2022 and 11/12/2022, I had taken home antigen tests that had both yielded negative results. On 11/14/2022, I still had no appetite, plus I was dizzy and sweaty, so I went to an urgent care. My vitals were taken, and everything was normal. My lungs were clear, but the doctor thought it would be a good idea to switch out the antibiotics. I was prescribed an amoxicillin/AUGMENTIN combination, prednisone, and an albuterol inhaler. I started the medications that day, and I felt significantly better on 11/15/2022, though I still had respiratory congestion. I flew home on 11/18/2022. I continued to feel fatigued; the nasal congestion was gone, but I still had post-nasal drip and upper chest congestion. On 11/30/2022, I went to my workplace health center. They told me that my lungs sounded clear. They wondered if I had some acid reflux that could have aggravated the other symptoms. They prescribed me PRILOSEC and advised me to sleep with my head raised. I didn't feel noticeably better until 12/10/2022. Ever since then, I have continued to feel better, though I still have mild congestion and post-nasal drip. I also feel less fatigued. More than anything, I feel like I have been battling a drawn-out virus for the past 2 months.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: 10/27/2022, 11/9/2022, 11/12/2022 home antigen tests negative results; 11/4/2022 home antigen test positive result; 11/4/2022 PCR test negative result; 11/5/2022 blood work, chest X-ray, and Strep rapid test Streptococcus pyogenes diagnosed.
Aktuelle Erkrankungen: None.
Vorgeschichte: Hypertension; Pre-Diabetes; Peripheral Neuropathy of Unknown Cause (Feet and Calves Affected); History of Rectal Fistula.
Andere Medikamente: Losartan; MIRENA intrauterine device; ADVIL; NERVIVE PM nerve relief; ALLEGRA; sinus clear.
Allergien: Milk; CYMBALTA; COMPAZINE; CIPRO.
Vorherige Impfungen: -

VAERS 2531323

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: TX
Alter: 68,0
Geschlecht: F
Eingang: 14.12.2022
Impfdatum: 12.09.2022
Beginn: 11.12.2022
Tage bis Beginn: 90,0
Dosis: 5
Route/Site: IM / AR

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

COVID-19 Chills Fatigue Headache Myalgia Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

On 12/11/2022 it started with a frontal headache, chills, and muscle aches. That resolved within around 16 hours and then I developed congestion, mostly in the head. Within a couple of days that moved on into the bronchi and was accompanied with some pretty severe fatigue. I tested myself for COVID-19 on 12/12/2022 and it was positive. I saw my doctor, who prescribed PAXLOVID. Since beginning the medication, I've been getting better every day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: 12DEC2022 at home COVID-19 test positive
Aktuelle Erkrankungen: None
Vorgeschichte: Rheumatoid Arthritis
Andere Medikamente: NP thyroid
Allergien: None
Vorherige Impfungen: -

VAERS 2531085

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: GA
Alter: 73,0
Geschlecht: F
Eingang: 14.12.2022
Impfdatum: 13.09.2022
Beginn: 25.11.2022
Tage bis Beginn: 73,0
Dosis: 5
Route/Site: IM / LA

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

Blood test normal COVID-19 Chest X-ray normal Chest discomfort Cough Pyrexia SARS-CoV-2 test positive

Symptomtext

I tested positive for COVID-19 the day after the November holiday. I tested because my son was showing symptoms and tested positive three days prior. I started to develop symptoms of a high fever, bad cough and chest tightness. I went to the ER since I was feeling this way and I was given a prescription for PAXLOVID. I started taking it on 11/26/2022. Within 24 hours of taking PAXLOVID I noticed that my symptoms were going away.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: COVID-19; blood draw; chest x-ray. Everything came back normal.
Aktuelle Erkrankungen: None
Vorgeschichte: Tricuspid and Mitral valve from Rheumatic fever; high blood pressure
Andere Medikamente: Losartan; multivitamin over age of 50
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 2530943

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: VA
Alter: 33,0
Geschlecht: F
Eingang: 14.12.2022
Impfdatum: 10.09.2022
Beginn: 28.11.2022
Tage bis Beginn: 79,0
Dosis: 4
Route/Site: SYR / LA

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

COVID-19 Chills Fatigue Feeling abnormal Malaise Nasopharyngitis Pain Productive cough Pyrexia Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

Starting in the afternoon of 11/28/2022, I just started feeling very fatigued and malaise. Then, when I woke up the next day, I felt achy and tired but also felt like I was coming down with something. I took an at home COVID-19 test which was negative. That evening, I felt worse. Wednesday morning, 11/30/2022, I woke up feeling terrible, had a fever of 101 and had chills and felt super achy. I was coughing and had phlegm. I had chest congestion and I took an at home COVID-19 test that day which was positive. Due to my previous history of heart surgery, I wanted to get PAXLOVID for safety. So, I went to urgent care to get prescribed PAXLOVID. I started it that day. I felt a lot better the next day and I no longer had a fever. I continued to gradually get better day by day, The malaise and achy feeling were the symptoms that lingered the most. Then, I finished PAXLOVID on 12/04/2022 and honestly I felt 100% better at that point. On 12/07/2022, I started to feel congested again. Then, I continued having the cold symptoms through the weekend: runny nose and feeling a lot of phlegm in the back of my throat that I needed to clear. I felt malaise and achy again. Yesterday, 12/13/2022, I finally felt I was improving again. Today, I feel a little better but still have phlegm. Today would be the first day I have not taken a decongestant.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: At home COVID-19 test (11/29/2022): negative; At home COVID-19 test (11/30/2022): positive
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: IUD (KYLEENA); vitamin D; melatonin
Allergien: None
Vorherige Impfungen: -

VAERS 2530935

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: MA
Alter: 36,0
Geschlecht: F
Eingang: 14.12.2022
Impfdatum: 12.09.2022
Beginn: 08.12.2022
Tage bis Beginn: 87,0
Dosis: 4
Route/Site: IM / LA

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

Abortion spontaneous Chills Exposure during pregnancy

Symptomtext

After receiving the vaccine, I had chills that lasted one day. I was eight weeks pregnant, and I had a miscarriage on 12/08/2022. My due date was on 07/06/2023.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Albuterol inhaler
Allergien: N/A
Vorherige Impfungen: -

VAERS 2529935

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: TX
Alter: 70,0
Geschlecht: F
Eingang: 13.12.2022
Impfdatum: 02.09.2022
Beginn: 04.12.2022
Tage bis Beginn: 93,0
Dosis: 5
Route/Site: IM / LA

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

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

Symptomtext

My back started hurting really bad and I couldn't figure out why. Then, I developed a sore throat, runny nose, sneezing, and coughing. I took an at home test 12/5/22 and tested positive. I contacted my doctor, and he prescribed 5 days' worth Paxlovid, Prednisone, and Azithromycin. I am feeling much better now.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Back pain
Hospital-Tage: -
Labordaten: 05DEC2022 COVID-19 Test - Positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Ankylosing Spondylitis
Andere Medikamente: Vitamin D3; Vitamin B12; Indomethacin ER; Gabapentin; Tizanidine; Levothyroxine; Tramadol
Allergien: Codeine; Benzocaine
Vorherige Impfungen: -

VAERS 2529281

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: VA
Alter: 77,0
Geschlecht: M
Eingang: 12.12.2022
Impfdatum: 10.09.2022
Beginn: 16.09.2022
Tage bis Beginn: 6,0
Dosis: 5
Route/Site: - / -

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

COVID-19 Cough Echocardiogram normal Fatigue Magnetic resonance imaging normal Pyrexia SARS-CoV-2 test positive

Symptomtext

Right after my vaccination I got a dry cough, fatigue, and felt feverish. When it got to Friday, I tested myself for COVID-19 and it was negative. I went in to get tested at 4pm and it was positive for COVID-19. They prescribed me an antiviral. I developed TGA on 11/20/2022 for 2 hours. They took me to the doctor, and they did an MRI and echocardiogram. Everything was normal

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID-19 Test, 09/16/2022, Positive; MRI, Echocardiogram, Normal, 11/30/2022
Aktuelle Erkrankungen: N/A
Vorgeschichte: Gerd; A-Fib; High Blood Pressure; High Cholesterol
Andere Medikamente: Bystolic; Simvastatin; Chlorthalidone; Nexium; Eliquis
Allergien: Shellfish; Codeine
Vorherige Impfungen: I have a fever and a cough after every flu and COVID-19 for a couple days

VAERS 2529002

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7144B

mild

Staat: IN
Alter: 66,0
Geschlecht: F
Eingang: 12.12.2022
Impfdatum: 03.09.2022
Beginn: 18.10.2022
Tage bis Beginn: 45,0
Dosis: 5
Route/Site: SYR / LA

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

COVID-19 Exposure to SARS-CoV-2 Fatigue Nausea SARS-CoV-2 test positive Somnolence

Symptomtext

One the first day I started feeling very tired and sleepy, then I started feeling a little nauseous. I took a COVID test because my husband got sick with COVID 2 days prior. I tested positive and called my doctor?s office. Since I am 66 years old, have asthma and was recovering from surgery performed on 10/13/22 my doctor prescribed me Paxlovid 150.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma
Andere Medikamente: sdexamfetamine 40 MG capsule Commonly known as: VYVANSE acyclovir 800 MG tablet Commonly known as: ZOVIRAX ezetimibe 10 mg tablet Commonly known as: ZETIA albuterol 90 mcg/actuation inhaler fluticasone propion-salmeteroL 115-21 mcg/
Allergien: Wheat
Vorherige Impfungen: -

VAERS 2528865

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: OH
Alter: 73,0
Geschlecht: F
Eingang: 12.12.2022
Impfdatum: 09.09.2022
Beginn: 02.11.2022
Tage bis Beginn: 54,0
Dosis: 5
Route/Site: IM / LA

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

COVID-19 Chills Oropharyngeal pain Pyrexia Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

I tested positive for COVID-19 on 11/02/22. I had congestion, chills, and a fever of 101. After a day and a half, I developed a sore throat and still had a fever. I called my doctor, and they prescribed molnupiravir. It is an alternative to PAXLOVID. I was unable to take PAXLOVID because of some other medications I take. I was better after 6 days, but it took 10 days before I tested negative. I started having some congestion a few days ago.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: 02NOV2022 COVID-19 test positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Hypothyroidism; Premature Ventricular Contractions
Andere Medikamente: Atenolol; flecainide; levothyroxine; vitamin D3
Allergien: CIPRO
Vorherige Impfungen: -

VAERS 2527749

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: TX
Alter: 58,0
Geschlecht: F
Eingang: 09.12.2022
Impfdatum: 08.09.2022
Beginn: 30.10.2022
Tage bis Beginn: 52,0
Dosis: 5
Route/Site: IM / LA

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

Ageusia Anosmia COVID-19 Cough Diarrhoea Fatigue Feeling abnormal Headache Nausea Paranasal sinus hypersecretion SARS-CoV-2 test positive Throat irritation

Symptomtext

10/30/2022 I had a scratchy throat. 10/31 I woke up with a headache, brain fog, scratchy throat, fatigue, loss sense of smell and taste, nausea, and diarrhea. Tested on an at home COVID-19 test, positive. Tele visit with doctor. Doctor prescribed albuterol inhaler, Z-PAK, PAXLOVID, BROMFED cough medication. By 5th day, November 5th symptoms were very reduced. After PAXLOVID, I felt better. Once PAXLOVID was out, symptoms returned and got worse. This is when the doctor proscribed the Z-PAK. Symptoms gradually improved until November 19th when I felt better. Still lingering headache, sinus and nasal drainage, with occasional nausea.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: At home COVID-19 test positive 10/31
Aktuelle Erkrankungen: No
Vorgeschichte: Cervical Spinal Stenosis; Type 2 Diabetes
Andere Medikamente: CRESTOR; fenofibrate; aspirin; valaciclovir; metformin; chromium (III) picolinate; collagen; alpha lipoic acid; ZYRTEC; LYRICA; OZEMPIC
Allergien: Sulfa; eggs; cedar; mesquite; pine; mold
Vorherige Impfungen: First shingles shot caused arm to have a baseball sized welt that itched and felt like it was on fire. Age 54 or 55 Shingrix sec

VAERS 2526786

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: MA
Alter: 70,0
Geschlecht: M
Eingang: 08.12.2022
Impfdatum: 08.09.2022
Beginn: 27.11.2022
Tage bis Beginn: 80,0
Dosis: 5
Route/Site: IM / LA

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

COVID-19 Cough Fatigue Malaise Pain in extremity Pyrexia Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

After receiving the vaccine, I had a sore arm for two or three days and fatigue for one day. I started to not feel well on 11/27/2022 with a cough, fever and congestion. On 11/28/2022, I tested positive for COVID-19, and I started taking PAXLOVID. I was sick for about eight days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 28NOV2022 COVID-19 test positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: High Blood Pressure; High Cholesterol
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 2526656

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: CT
Alter: 79,0
Geschlecht: M
Eingang: 08.12.2022
Impfdatum: 02.09.2022
Beginn: 05.12.2022
Tage bis Beginn: 94,0
Dosis: 5
Route/Site: IM / LA

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

Cough Diarrhoea Fatigue Headache

Symptomtext

I experienced having a very bad cough, headache, diarrhea and tiredness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Mild hypertension
Andere Medikamente: Lisinopril; tadalafil
Allergien: N/A
Vorherige Impfungen: -

VAERS 2525442

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: TX
Alter: 80,0
Geschlecht: M
Eingang: 07.12.2022
Impfdatum: 06.09.2022
Beginn: 04.11.2022
Tage bis Beginn: 59,0
Dosis: 5
Route/Site: IM / UN

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

Fatigue Rhinorrhoea SARS-CoV-2 test

Symptomtext

I had a little sniffle with a temperature of 99.3. Very tired.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: At home rapid COVID-19 test
Aktuelle Erkrankungen: Common cold
Vorgeschichte: Neutropenia; Testicular hypofunction; Arthritis; GERD
Andere Medikamente: Men's multivitamin; BENEFIBER; clonidine; pegfilgrastim; iron supplement; fish oil; MERIVA; vitamin C
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2525435

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: TX
Alter: 36,0
Geschlecht: M
Eingang: 07.12.2022
Impfdatum: 04.09.2022
Beginn: 26.11.2022
Tage bis Beginn: 83,0
Dosis: 4
Route/Site: IM / RA

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

Fatigue Productive cough Pyrexia Respiratory tract congestion SARS-CoV-2 test negative

Symptomtext

I had chest congestion, productive cough, fatigue, and a fever. I did not test positive for COVID-19, and I took several tests. I was not prescribed medications. I am feeling better now, but I am still dealing with a cough.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 27NOV2022 COVID-19 test negative; 28NOV2022 COVID-19 test negative; 28NOV2022 flu test negative
Aktuelle Erkrankungen: N/A
Vorgeschichte: High Blood Pressure
Andere Medikamente: ZYRTEC; buspirone; vitamin D
Allergien: N/A
Vorherige Impfungen: -

VAERS 2524296

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: PA
Alter: 49,0
Geschlecht: M
Eingang: 06.12.2022
Impfdatum: 03.09.2022
Beginn: 26.11.2022
Tage bis Beginn: 84,0
Dosis: 4
Route/Site: IM / AR

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

COVID-19 Headache Pyrexia SARS-CoV-2 test positive Sinus congestion Sneezing

Symptomtext

I had quite a bit of sneezing with headache. I also had sinus congestion. I tested myself on November 27, 2022, and that test was positive. The sneezing increased and I developed a low-grade fever. I contacted my doctor who prescribed Paxlovid. I started the medication on Monday the 28th. My symptoms improved after about 36 hours. I felt 95% better but I took another test on Wednesday and Friday and I am still testing positive. I have completed 4 or 5 test so far. My symptoms are not gone but I am much better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: COVID-19 Binax Home Test-November 27, 2022-Positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: Moderna-2,3, & 4-Fatigue, Arm Pain with swelling and itching after Dose 2.

VAERS 2523727

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: MO
Alter: 32,0
Geschlecht: F
Eingang: 05.12.2022
Impfdatum: 04.09.2022
Beginn: 01.09.2022
Tage bis Beginn: -
Dosis: N/A
Route/Site: IM / RA

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

Arthralgia Pain in extremity Weight decreased

Symptomtext

Onset of severe joint paint in both feet and right knee in September 2022 as well as unexplained weight loss, saw primary care doctor in late October 2022 and have been referred to rheumatologist for evaluation for possible rheumatoid arthritis (long wait to get in, scheduled for January 2023)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: None yet
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma
Andere Medikamente: Prenatal vitamin, sunflower lecithin, Vitamin D 2000IU
Allergien: None
Vorherige Impfungen: -

VAERS 2511281

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7144B

mild

Staat: PA
Alter: 76,0
Geschlecht: M
Eingang: 18.11.2022
Impfdatum: 12.09.2022
Beginn: 12.09.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: OT / -

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

Accidental underdose Vaccination site pain

Symptomtext

sore arm; Administration error: only half dose given of bivalent vaccine; This spontaneous case was reported by a patient and describes the occurrence of VACCINATION SITE PAIN (sore arm) and ACCIDENTAL UNDERDOSE (Administration error: only half dose given of bivalent vaccine) in a 76-year-old male patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. AS7144B) for COVID-19 prophylaxis. Concurrent medical conditions included Coronary artery disease, Hypertension, Sleep apnea and Drug allergy (ophthalmic drops for pupils dilatation). Concomitant products included APIXABAN (ELIQUIS), LATANOPROST, SPIRONOLACTONE, LOSARTAN POTASSIUM, CHLORTALIDONE (CHLORTHALIDONE) and ATORVASTATIN for an unknown indication. On 12-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 12-Sep-2022, the patient experienced VACCINATION SITE PAIN (sore arm) and ACCIDENTAL UNDERDOSE (Administration error: only half dose given of bivalent vaccine). On 12-Sep-2022, VACCINATION SITE PAIN (sore arm) had resolved. At the time of the report, ACCIDENTAL UNDERDOSE (Administration error: only half dose given of bivalent vaccine) outcome was unknown. No treatment medication was reported. The patient received the 1st dose of Moderna vaccine on 02-Mar-2021, second dose of vaccine on 30-Mar-2021, first booster dose on 25-Oct-2021, second booster dose on 01-Apr-2022 with batch numbers 12A21A, 021B21A, 27C21A and 002M21A respectively.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Vaccination site pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Coronary artery disease; Drug allergy (ophthalmic drops for pupils dilatation); Hypertension; Sleep apnea
Vorgeschichte: -
Andere Medikamente: ELIQUIS; LATANOPROST; SPIRONOLACTONE; LOSARTAN POTASSIUM; CHLORTHALIDONE; ATORVASTATIN
Allergien: -
Vorherige Impfungen: -

VAERS 2511275

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7144B

mild

Staat: PA
Alter: 74,0
Geschlecht: F
Eingang: 18.11.2022
Impfdatum: 12.09.2022
Beginn: 12.09.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: OT / -

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

Accidental underdose Pain in extremity

Symptomtext

Sore arm; Administration error, half of a dose administered of Moderna bivalent; This spontaneous case was reported by a patient family member or friend and describes the occurrence of PAIN IN EXTREMITY (Sore arm) and ACCIDENTAL UNDERDOSE (Administration error, half of a dose administered of Moderna bivalent) in a 74-year-old female patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. AS7144B) for COVID-19 vaccination. Patient had no allergies. It was reported that patient never had COVID positive test or diagnosis. No other vaccines given within 1 month prior to Moderna COVID-19 vaccine. Concurrent medical conditions included High cholesterol (No improvement or worsening.), Seizures (No improvement or worsening.) and Epilepsy (No improvement or worsening.). Concomitant products included PRAVASTATIN, SERTRALINE and LEVETIRACETAM for an unknown indication. On 12-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 12-Sep-2022, the patient experienced PAIN IN EXTREMITY (Sore arm) and ACCIDENTAL UNDERDOSE (Administration error, half of a dose administered of Moderna bivalent). At the time of the report, PAIN IN EXTREMITY (Sore arm) had resolved and ACCIDENTAL UNDERDOSE (Administration error, half of a dose administered of Moderna bivalent) outcome was unknown. No medical care took by the patient. First dose of Moderna COVID-19 Vaccine was administered on 02-Mar-2021; lot number: 012A21A; expiration date: 17-Aug-2021. Second dose on 30-Mar-2021; lot number: 021B21A. First booster on 25-Oct-2021; lot number: 27C21A. Second booster on 01-Apr-2022; lot number: 002M21A. No treatment medication details was reported. This case was linked to MOD-2022-672848 (Patient Link).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Epilepsy (No improvement or worsening.); High cholesterol (No improvement or worsening.); Seizures (No improvement or worsening.)
Vorgeschichte: Comments: Patient had no allergies. It was reported that patient never had COVID positive test or diagnosis. No other vaccines given within 1 month prior to Moderna COVID-19 vaccine.
Andere Medikamente: PRAVASTATIN; SERTRALINE; LEVETIRACETAM
Allergien: -
Vorherige Impfungen: -

VAERS 2507127

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: PA
Alter: 59,0
Geschlecht: M
Eingang: 14.11.2022
Impfdatum: 08.09.2022
Beginn: 13.09.2022
Tage bis Beginn: 5,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Oropharyngeal pain Rhinorrhoea SARS-CoV-2 test positive Throat irritation

Symptomtext

Not really an adverse event, but I had Mild COVID several days after vaccine per below.... 09/08 - received my second booster (Moderna Bivalent) 09/11 - Attended Concert 09/13 - Evening. Symptoms noticed. Runny nose Scratchy throat. 09/14 - Took an at Home COVID test at 8 am and tested positive. 09-14 - Scheduled and did a Facetime call with my family Doctor and went over symptoms and Options. Decided not to take Paxlovid, unless symptoms worsened. 09/14 - 09/17 - Mild symptoms of running nose and sore throat diminished. I was never congested or had mucus in chest, no trouble breathing. 09/18 - Feeling totally fine by 09/18, no real symptoms, occasional need to blow nose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: 09/14 - Took an at home COVID test at 8 am and tested positive for COVID 09/17 - Took an at home COVID test: Tested positive for COVID 09/19 -Took an at home COVID test: Tested positive for COVID 09/23 -Took an at home COVID test: Tested NEGATIVE for COVID
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: 5 mg Crestor, Daily multi vitamin
Allergien: None
Vorherige Impfungen: -

VAERS 2506031

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge as7144b

mild

Staat: IL
Alter: 72,0
Geschlecht: M
Eingang: 11.11.2022
Impfdatum: 26.09.2022
Beginn: -
Tage bis Beginn: -
Dosis: 5
Route/Site: IM / RA

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

Impaired driving ability Limb injury Pain in extremity

Symptomtext

Patient called to say his left arm was injured after a vaccination. I looked in the file & it was Fluad. I asked him when he first started experiencing symptoms & he said about a week after. I asked if he could be more specific because we use this for documentation purposes & he repeated "about a week, it could have been 9 days it could have been 3 days." I asked him if he saw a doctor or if they did any imaging/scans or anything to confirm the injury & he said he did go to the Dr. & they told him to keep moving the arm & the pain should go away. I don't know when or where he went. I forgot to ask that. He said he's still in pain & mentioned it's hard to turn his steering wheel when driving. I did recommend if he's still in pain to see the Dr. again as they may be able to give a more definitive answer or at least refer to PT or something.

Weitere VAERSDATA-Felder

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

VAERS 2503283

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: PA
Alter: 70,0
Geschlecht: F
Eingang: 09.11.2022
Impfdatum: 06.09.2022
Beginn: 03.10.2022
Tage bis Beginn: 27,0
Dosis: 1
Route/Site: IM / LA

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

COVID-19 Cough Fatigue Headache Lethargy Pain in extremity SARS-CoV-2 test positive

Symptomtext

I had a sore arm, headache and tired after receiving the vaccine. I tested positive for COVID-19 with a home test on 10/03/2022. I did not have symptoms prior to testing. I contacted my doctor and was given prescription for PAXLOVID. I gradually started to feel better. Sixteen days later, I tested negative for COVID-19. I had a cough. Felt lethargic and had a headache. As of today, I still feel tired.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 03OCT2022 COVID-19 test positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: CIDP
Andere Medikamente: N/A
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 2499934

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: VA
Alter: 26,0
Geschlecht: F
Eingang: 05.11.2022
Impfdatum: 11.09.2022
Beginn: 24.09.2022
Tage bis Beginn: 13,0
Dosis: 4
Route/Site: - / LA

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

Chronic spontaneous urticaria Pruritus Sleep disorder Urticaria

Symptomtext

-I got the booster on 9/11 - Started having symptoms overnight on 9/23. I was woken up by intensely itchy feet and hands -On 9/26 I started getting hives as well -Every evening around 8 or 9 pm I get hives and get super itchy, my feet start to itch too -The symptoms are worse at night and are still waking me up in the night if I don't take antihistamines -Dr. diagnosed this as chronic spontaneous urticaria

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chronic spontaneous urticaria
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Postural Orthostatic Tachycardia Syndrome, Central Sensitization Syndrome
Andere Medikamente: Glycopyrrolate 2mg tablets, 4 per day Midodrine 5 mg, 3x a day Propranolol 20 mg, 1x day Viibryd 40 mg Seasonique Spironolactone 100mg One A Day Women?s Petites Vitamin B12
Allergien: Amoxicillin as a baby
Vorherige Impfungen: -

VAERS 2499866

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: CA
Alter: 69,0
Geschlecht: F
Eingang: 05.11.2022
Impfdatum: 09.09.2022
Beginn: 11.09.2022
Tage bis Beginn: 2,0
Dosis: N/A
Route/Site: IM / LA

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

Pruritus Rash

Symptomtext

Systemic: mild rash on shoulder, upper back, and chest. and pt took benadryl herself-Medium, Additional Details: Rash developed after one hour recevived vaccine and took Benadryl and apply hydrocortisone topicall herself. itch and rash getting better but not resolved even till today. pt called md but md did not answer her call today.

Weitere VAERSDATA-Felder

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

VAERS 2495091

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7144B

mild

Staat: MA
Alter: 62,0
Geschlecht: F
Eingang: 01.11.2022
Impfdatum: 22.09.2022
Beginn: 22.09.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Exfoliative rash Irritability Rash Rash erythematous Rash papular Rash pruritic Rash vesicular Scar Urticaria

Symptomtext

Within 30-40 minutes of the booster shot, small hives started breaking out on my arms and hands - then spread to other parts of the body and face over several days. Some were more flat-like (small raised bump) and red spots - which itched and caused irritability. Others were blistery and scaly and painful. Some large, some very small. They slowly faded or healed over 3 weeks or so. I tried Allegra, but didn't do much. I then took Benadryl at night to get some sleep. I have a few scars. No fever. I've never reacted this way to any other vaccine before. I called the Pharmacy RX and reported the reaction to the tech. A nurse then called and asked several question for her report. She then asked me to fill out this form. I also reported the reaction on my CDC weekly checkin texts. This reaction was notable ODD because with all the other Covid vaccines/boosters I had a sore arm, more flu like symptoms or headaches for a day or two and then all better. This time, NO other symptoms, not even a sore arm - Just hives.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Exfoliative rash
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Mild arthritis - knees and shoulders Bone spur/impingement issues with shoulder Fibromyalgia since 1986 Neuropathy from severe shingles
Andere Medikamente: Celecoxib 200 mg/ day for arthritis and fibromyalgia; Flonase spray for seasonal allergies, prn CBD oil/tinctures under tongue approximately 40-60 mg/day Probiotics and vitamins occasionally
Allergien: Penicillin Gabapentin
Vorherige Impfungen: -

VAERS 2491206

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: SC
Alter: 71,0
Geschlecht: M
Eingang: 27.10.2022
Impfdatum: 14.09.2022
Beginn: 21.10.2022
Tage bis Beginn: 37,0
Dosis: 1
Route/Site: IM / RA

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

COVID-19 Chest discomfort Fatigue Feeling abnormal Oropharyngeal pain SARS-CoV-2 test positive

Symptomtext

On the evening of the 21st I had sore throat and tightness in chest. On October of 22 went to urgent care and tested positive for COVID-19. They prescribed PAXLOVID and I began taking it around noon on the 22nd. On the 22nd I also began having fatigue and brain fog. After beginning PAXLOVID I haven't noticed significant improvements in my symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID-19 test
Aktuelle Erkrankungen: No
Vorgeschichte: Recurrent Melanoma and skin cancer; recurrent upper respiratory infections
Andere Medikamente: Atorvastatin; ezetimibe; CELEBREX; FLOMAX; baby aspirin; nicotinamide; acitretin
Allergien: None
Vorherige Impfungen: -

VAERS 2490651

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7144B

mild

Staat: NY
Alter: 67,0
Geschlecht: F
Eingang: 26.10.2022
Impfdatum: 21.09.2022
Beginn: 24.09.2022
Tage bis Beginn: 3,0
Dosis: 5
Route/Site: IM / RA

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

Computerised tomogram head normal Fatigue Feeding disorder Fluid intake reduced Headache Influenza virus test negative Neck pain Respiratory syncytial virus test negative SARS-CoV-2 test negative

Symptomtext

Extreme unrelenting headache and neck pain. Inability to eat and drink. Extreme fatigue.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: I was tested for Covid-19, flu and RSV 2 days in a row, at a hospital, and was negative for all. I had a CT scan to see if I had a brain bleed. Negative.
Aktuelle Erkrankungen: none
Vorgeschichte: IBS
Andere Medikamente: Levothyroxine 25 mcg. Centrum Silver Vit. D Famotidine Align Probiotic Pravastatin CO-Q 10 Loratidine 10mg.
Allergien: NKAnone
Vorherige Impfungen: -

VAERS 2489885

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: MI
Alter: 75,0
Geschlecht: M
Eingang: 26.10.2022
Impfdatum: 13.09.2022
Beginn: 18.10.2022
Tage bis Beginn: 35,0
Dosis: 1
Route/Site: SYR / LA

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

COVID-19 Fatigue Headache Nasopharyngitis Rhinorrhoea SARS-CoV-2 test positive Sinus congestion

Symptomtext

My symptoms started with sinus congestion and runny nose. I thought I had a head cold. I tested positive for COVID-19 on October 20, 2022. I called my doctor. They called me back and asked me a lot of questions. I sent a copy of the test result to them through the portal. They said it was too late for the antiviral medication. They recommended molnupiravir. I took four pills twice a day for 5 days. I took another COVID-19 test this past Monday and still tested positive. I still have a headache, congestion, runny nose, and exhaustion. This morning, I tested positive again.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 10/20/2022 at home COVID-19 test positive; 10/24/2022 at home COVID-19 test positive; 10/26/2022 at home COVID-19 test positive.
Aktuelle Erkrankungen: None
Vorgeschichte: High Blood Pressure; High Cholesterol
Andere Medikamente: Aspirin; hydrochlorothiazide; lisinopril; multivitamin; pravastatin; tamsulosin; tolterodine; METAMUCIL; melatonin
Allergien: None
Vorherige Impfungen: -

VAERS 2488248

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: PA
Alter: 46,0
Geschlecht: M
Eingang: 25.10.2022
Impfdatum: 01.09.2022
Beginn: 18.10.2022
Tage bis Beginn: 47,0
Dosis: 1
Route/Site: SYR / -

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

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

Symptomtext

I began with a very light cough on Tuesday evening, October 18. On Wednesday, I woke up and felt a high fever (101.5) and extreme fatigue. I also had a more severe cough and sore throat. I tested positive for COVID 19 on Wednnesday, October 19, 2022. I received Monlupiravir on Wednesday, as well. The sore throat resolved almost immediately. However, the cough remained. The most severe symptom was the extreme fatigue. I had a fever from Wednesday through Saturday. On Sunday, I began to feel a little bit better. On Tuesday morning, although I didn't feel much better, I did test negative.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: At home tests on Wednesday, Friday, Sunday and Monday were positive. (10/19, 10/21, 10/23, 10/24) At home test on Tuesday morning (10/25) was negative
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2487461

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: FL
Alter: 68,0
Geschlecht: F
Eingang: 24.10.2022
Impfdatum: 09.09.2022
Beginn: 04.10.2022
Tage bis Beginn: 25,0
Dosis: 1
Route/Site: IM / RA

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

COVID-19 Decreased appetite Fatigue SARS-CoV-2 test positive Thirst

Symptomtext

Patient was double vaccinated, and triple boosted. She has no risk factors. 3-4 days after attending a class reunion, Patient contracted a moderate case of Covid infection. The symptoms include sudden moderate to severe fatigue and lack of appetite and thirst. She was positive via covid home test for 10 days. She still has significant fatigue. Pulse Ox was always good 95 to 100 and she had little or no fever.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: Recovering from a broken bone in the left hand Occurred on July 30th, 2022.
Vorgeschichte: Motion sickness ~25 BMI No chronic diseases
Andere Medikamente: Acetaminophen, Spironolactone
Allergien: sensitive to narcotics
Vorherige Impfungen: -

VAERS 2487444

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: PA
Alter: 33,0
Geschlecht: F
Eingang: 24.10.2022
Impfdatum: 18.10.2022
Beginn: 20.10.2022
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / RA

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

Arthralgia Asthenia Back pain Impaired work ability Loss of personal independence in daily activities Neuralgia Pain Pain in extremity Sciatica

Symptomtext

Sciatic nerve pain along the right lower back, hip, and leg. Unable to work, lift leg or pick up my young children without severe pain and weakness. Symptoms started 10/20 and continue to worsen. Saw PCP 10/23 and started prednisone 10/23.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Ulcerative colitis
Andere Medikamente: Prenatal with DHA, Zyrtec, zoloft
Allergien: Strawberry
Vorherige Impfungen: -

VAERS 2485682

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge AS7144B

mild

Staat: NY
Alter: 73,0
Geschlecht: M
Eingang: 21.10.2022
Impfdatum: 10.09.2022
Beginn: 27.09.2022
Tage bis Beginn: 17,0
Dosis: 5
Route/Site: SYR / LA

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

COVID-19 Cough Oropharyngeal pain Pyrexia Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

I tested positive for Covid 19 on September 27, 2022 and I experienced sore throat, fever, coughing, and congestion also a fever of 102.7. I was prescribed Paxlovid for my symptoms. I also was taking Advil as well which helped reduce my fever.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: Home Covid testing
Aktuelle Erkrankungen: N/A
Vorgeschichte: Hypertension
Andere Medikamente: Ramipril; Amlodipine; Antibiotics; Focalin;
Allergien: N/A
Vorherige Impfungen: -

VAERS 2485574

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: FL
Alter: 41,0
Geschlecht: F
Eingang: 21.10.2022
Impfdatum: 03.09.2022
Beginn: 15.10.2022
Tage bis Beginn: 42,0
Dosis: 5
Route/Site: SYR / LA

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

COVID-19 Chills Fatigue Headache Influenza like illness SARS-CoV-2 test positive Sinus congestion

Symptomtext

I started with flu like symptoms and took a COVID-19 test. I had sinus congestion, head ache and chills. I was prescribed Paxlovid and on my last dose today. Symptoms today are almost gone minus some lingering fatigue.

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Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: COVID-19 test - positive
Aktuelle Erkrankungen: No
Vorgeschichte: Chronic cancer syndrome
Andere Medikamente: Synthroid
Allergien: Sulfur; Erythromycin; Penicillin; Dye contrast
Vorherige Impfungen: -

VAERS 2484509

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: VA
Alter: 39,0
Geschlecht: F
Eingang: 20.10.2022
Impfdatum: 07.09.2022
Beginn: 09.10.2022
Tage bis Beginn: 32,0
Dosis: 3
Route/Site: - / LA

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

Computerised tomogram normal Dizziness Headache Hyperacusis Pain Photophobia Vertigo

Symptomtext

On October 9th came down with severe headache that has not gone away. Symptoms include vertigo, dizziness, pain. Seen primary care doctor, seen at urgent care 10/10/2022, Emergency Department on 10/10/2022 and 10/14/2022. Seen by Dr on 10/12/22 Neurology. Headache has not gone away. Light and sound sensitive. Treated with imitrex 25-100mg/day, cyclobenzaprin 5mg, zofran 4mg, propranolol 40mg, butalbital, acetaminophen, caffeine, magnesium, compozine and toredol at hospital.

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Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: CT scan at Hospital on 10/10/2022 (normal) MRI with and without contrast scheduled for 10/27/2022
Aktuelle Erkrankungen: Cold
Vorgeschichte: Depression, seasonal in full remission; postpartum depression, in full remission;
Andere Medikamente: Fluoxetine 40mg Flonase Vitamin D 5,000 units daily
Allergien: Meclizine; monistat; omnicef
Vorherige Impfungen: -

VAERS 2483644

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7144B

mild

Staat: NY
Alter: 60,0
Geschlecht: M
Eingang: 20.10.2022
Impfdatum: 12.09.2022
Beginn: 12.09.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: OT / -

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

Bedridden Body temperature Dizziness Fatigue Headache Musculoskeletal stiffness Myalgia Pyrexia Vertigo

Symptomtext

Constant Vertigo began within a few hours after Bivalent Booster/Felt like everything was constantly spinning around head; Constant Dizziness began within a few hours after Bivalent Booster; Muscle Stiffness after Bivalent Booster; In bed for 2 weeks after Bivalent Booster; Body Aches after Bivalent Booster; Fever greater than 100 F after Bivalent Booster; Headaches after Bivalent Booster; Constant Fatigue began within a few hours after Bivalent Booster; This spontaneous case was reported by a patient and describes the occurrence of VERTIGO (Constant Vertigo began within a few hours after Bivalent Booster/Felt like everything was constantly spinning around head), DIZZINESS (Constant Dizziness began within a few hours after Bivalent Booster), MUSCULOSKELETAL STIFFNESS (Muscle Stiffness after Bivalent Booster), BEDRIDDEN (In bed for 2 weeks after Bivalent Booster) and MYALGIA (Body Aches after Bivalent Booster) in a 60-year-old male patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. AS7144B) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 12-Sep-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 12-Sep-2022, the patient experienced VERTIGO (Constant Vertigo began within a few hours after Bivalent Booster/Felt like everything was constantly spinning around head), DIZZINESS (Constant Dizziness began within a few hours after Bivalent Booster), MUSCULOSKELETAL STIFFNESS (Muscle Stiffness after Bivalent Booster), BEDRIDDEN (In bed for 2 weeks after Bivalent Booster), MYALGIA (Body Aches after Bivalent Booster), PYREXIA (Fever greater than 100 F after Bivalent Booster), HEADACHE (Headaches after Bivalent Booster) and FATIGUE (Constant Fatigue began within a few hours after Bivalent Booster). On 26-Sep-2022, VERTIGO (Constant Vertigo began within a few hours after Bivalent Booster/Felt like everything was constantly spinning around head), DIZZINESS (Constant Dizziness began within a few hours after Bivalent Booster), MUSCULOSKELETAL STIFFNESS (Muscle Stiffness after Bivalent Booster), BEDRIDDEN (In bed for 2 weeks after Bivalent Booster), MYALGIA (Body Aches after Bivalent Booster), PYREXIA (Fever greater than 100 F after Bivalent Booster), HEADACHE (Headaches after Bivalent Booster) and FATIGUE (Constant Fatigue began within a few hours after Bivalent Booster) had resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 12-Sep-2022, Body temperature: greater than 100 F. No Concomitant medications were provided. It was reported that patient received 3 Monovalent and 1 Bivalent Moderna COVID-19 vaccine. Patent received first dose of Moderna COVID-19 vaccine on 23 FEB 2021 with Lot 014M20A and Exp. Date as unknown. Patent received second dose of Moderna COVID-19 vaccine on 23 MAR 2021 with Lot 006B21A and Exp. Date as unknown. Patient received first Monovalent Booster dose of Moderna COVID-19 vaccine on 03 NOV 2021 with Lot 033B21A and Exp. Date as unknown. No treatment medications were provided. This case was linked to MOD-2022-660540, MOD-2021-374714 (Patient Link).

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Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: Test Date: 20220912; Test Name: Fever greater than 100 F after Bivalent Booster; Result Unstructured Data: greater than 100 F
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2483151

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: IL
Alter: 69,0
Geschlecht: F
Eingang: 19.10.2022
Impfdatum: 06.09.2022
Beginn: 26.09.2022
Tage bis Beginn: 20,0
Dosis: 1
Route/Site: SYR / LA

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

COVID-19 Cough Dysphonia Feeling abnormal Insomnia Nasopharyngitis Oropharyngeal pain Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

I felt like I had a very congested head cold, never ran a fever nor did I have a sore throat. I started coughing and currently still have the lingering cough. The cough is now making my throat sore. I took the PAXLOVID as well as OTC medication. I started feeling better around this time last week, but then over the weekend I started feeling crappy. I'm not testing positive for COVID-19 anymore and the doctor feels I could have caught a virus and not a rebound case. My voice is raspy currently. I feel worse today than I did when I had COVID-19 from coughing so much and not sleeping.

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Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: COVID-19 test, positive
Aktuelle Erkrankungen: I had a really bad spider bite and I was on declining pack of steroids
Vorgeschichte: Undisclosed autoimmune illness; Breast cancer survivor
Andere Medikamente: Lisinopril; letrozole; levothyroxine; ZOLOFT; multivitamin; calcium; 4 day of steroid pack methylprednisolone
Allergien: Sulfur
Vorherige Impfungen: -

VAERS 2482891

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: NY
Alter: 76,0
Geschlecht: M
Eingang: 19.10.2022
Impfdatum: 13.09.2022
Beginn: 14.10.2022
Tage bis Beginn: 31,0
Dosis: 5
Route/Site: IM / LA

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

COVID-19 Cough Fatigue Pyrexia SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

I had started getting a cough late in the evening. The next day I had a fever, and I took a COIVD-19 home test and it was positive. The day beforehand my wife had been in the hospital and when she was admitted to the hospital, she tested positive for COVID-19. She was not showing any symptoms and I had only tested because she was positive and then I had started with the cough. I have been very fatigued and am just tired. I am still coughing but the fever is now gone. I did want to report that I have had a breakthrough case of after being vaccinated.

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Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Home COIVD-19 Test
Aktuelle Erkrankungen: N/A
Vorgeschichte: Chronic Kidney Disease; Severe Aortic Valve Stenosis; High Blood Pressure; High Cholesterol; Gout; High Potassium
Andere Medikamente: Losartan; Amlodipine; Carvedilol ER; Terazosin; Crestor; Zetia; Allopurinol; Kayexalate; Vitamin B12; Vitamin D3; Biotin
Allergien: N/A
Vorherige Impfungen: -

VAERS 2482882

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: NY
Alter: 43,0
Geschlecht: M
Eingang: 19.10.2022
Impfdatum: 09.09.2022
Beginn: 12.10.2022
Tage bis Beginn: 33,0
Dosis: 1
Route/Site: IM / LA

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

COVID-19 Chills Feeling abnormal Headache Pain SARS-CoV-2 test positive

Symptomtext

A month after getting vaccine on October 12th began having achiness, chills, brain fog, and slight headache. Never had fever. Tested positive for COVID-19 on at home test October 13th. Still having same symptoms. Doctor ordered PAXLOVID and began taking that evening. Took TYLENOL as needed for achiness. Symptoms resolved fully by 10/17/2022.

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Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Positive at home COVID-19 test, positive PCR COVID-19 test.
Aktuelle Erkrankungen: Had some sort of non-COVID-19 bug on around August 21st
Vorgeschichte: Diabetes type 2, high cholesterol, porifera EPP
Andere Medikamente: Metformin; omeprazole; JANUVIA; enalapril; atorvastatin; LANTUS; TRULICITY
Allergien: None
Vorherige Impfungen: -

VAERS 2481731

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: PA
Alter: 42,0
Geschlecht: F
Eingang: 18.10.2022
Impfdatum: 16.09.2022
Beginn: 16.09.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: SYR / LA

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

Alanine aminotransferase normal Anion gap Aspartate aminotransferase normal Basophil count normal Basophil percentage Blood albumin normal Blood alkaline phosphatase normal Blood bilirubin normal Blood calcium normal Blood chloride normal Blood creatinine normal Blood glucose normal Blood potassium normal Blood sodium Blood test abnormal Blood thyroid stimulating hormone decreased Blood urea normal Carbon dioxide normal

Symptomtext

I almost immediately experienced dizziness and nausea. I figured it was from not really eating breakfast before. The dizziness and nausea continued to the point where I messaged my doctor through the patient portal a week later. She suggested I try meclizine, and if that didn't help to call for an appointment. The meclizine seemed to stop the nausea, dizziness, and at this point also sweating. Then a week after having relief, I had a dentist appointment. Being tipped back in the chair set it all off again. My doctor ordered bloodwork, and my thyroid had swung very hyper. I am currently awaiting an appointment with endocrinology. My Hashi's had been well controlled on medication for several years to this point.

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Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: All labs drawn on 10-7-2022 CBC with differential WBC 10.1 RBC 4.74 Hemoglobin 14.0 Hematocrit 41.8 MCV 88.2 MCH 29.5 MCHC 33.4 Platelet count 555 MPV 7.3 RDW 14.0 Neutrophils 64.2 Lymphocytes 24.6 Monocytes 6.8 Eosinophils 3.4 Basophils 1.0 Absolute Neutrophils 6.5 Absolute Lymphocytes 2.5 Absolute Monocytes 0.7 Absolute Eosinophils 0.3 Absolute Basophils 0.1 TSH 0.31 T4 Free 0.80 T3 Free 3.8 Comprehensive metabolic panel Sodium 14.0 Potassium 4.4 Chloride 104 CO2 25 Urea Nitrogen, Blood 12 Creatinine 0.91 Glucose 99 Calcium 10.0 Ast 17 Alt 19 Alk Phosphatase 120 Total Protein 7.2 Serum Albumin 4.1 Total Bilirubin 0.6 Anion Gap 11.0 eGFR 81
Aktuelle Erkrankungen: -
Vorgeschichte: asthma, ADHD, environmental allergies, Ehlers-Danlos hypermobility type, Hashimoto's thyroiditis, arthritis, eczema, elevated WBC and platelet count of unknown origin
Andere Medikamente: Cyclobenzaprine, NP thyroid, Vyvanse, Diclofenac, Xyzal, Singulair, Clonidine, Vitamin D3, Vitamin C, B12 injections
Allergien: environmental allergies to pretty much everything allergists test for on a typical allergy panel, gabapentin, gluten
Vorherige Impfungen: -

VAERS 2481094

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7144B

mild

Staat: MA
Alter: 64,0
Geschlecht: F
Eingang: 18.10.2022
Impfdatum: 07.09.2022
Beginn: 01.09.2022
Tage bis Beginn: -
Dosis: 5
Route/Site: OT / -

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

Myalgia

Symptomtext

Had considerable body aches; This spontaneous case was reported by a patient and describes the occurrence of MYALGIA (Had considerable body aches) in a 64-year-old female patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. AS7144B) for COVID-19 prophylaxis. Co-suspect product included non-company product INFLUENZA VACCINE (FLU [INFLUENZA VACCINE]) for an unknown indication. Patient had never tested COVID-19 positive. Previously administered products included for Product used for unknown indication: Shingles vaccine (With 2nd dose of vaccine) and Shingles vaccine (With 2nd dose of vaccine). Past adverse reactions to the above products included Myalgia with Shingles vaccine; and Shivering with Shingles vaccine. Concurrent medical conditions included Drug allergy (Sudafed allergic, cause Tachycardia). Concomitant products included NADOLOL for an unknown indication. On 07-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) .5 milliliter and dose of INFLUENZA VACCINE (FLU [INFLUENZA VACCINE]) (unknown route) 1 dosage form. In September 2022, after starting mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)), the patient experienced MYALGIA (Had considerable body aches). The patient was treated with IBUPROFEN at an unspecified dose and frequency. At the time of the report, MYALGIA (Had considerable body aches) had resolved. Patient received 0.5 mL of first dose of Moderna COVID-19 vaccine on 25-Mar-2021, Lot Number 002B21A. Patient received 0.5 mL of second dose of Moderna COVID-19 vaccine on 27-Apr-2021, Lot Number 009C21A. Patient received 0.25 mL of third dose of Moderna COVID-19 vaccine on 05-Nov-2021, Lot number 033F21A. Patient received 0.25 mL of fourth dose of Moderna COVID-19 vaccine on 11-Apr-2022, Lot number 005M21A. It was reported that the Body aches persisted for 18-24 hours. This case was linked to US-MODERNATX, INC.-MOD-2022-658071, US-MODERNATX, INC.-MOD-2022-658065, US-MODERNATX, INC.-MOD-2022-658064, US-MODERNATX, INC.-MOD-2022-658061 (E2B Linked Report). This case was linked to MOD-2022-658188, MOD-2022-658148 (Patient Link).; Sender's Comments: US-MODERNATX, INC.-MOD-2022-658071:Husband Dose 5 US-MODERNATX, INC.-MOD-2022-658065:Husband Dose 4 US-MODERNATX, INC.-MOD-2022-658064:Husband Dose 2-3 US-MODERNATX, INC.-MOD-2022-658061:Husband Dose 1

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Praegender Schweregrund: Myalgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Drug allergy (Sudafed allergic, cause Tachycardia)
Vorgeschichte: Comments: Patient had never tested COVID-19 positive.
Andere Medikamente: NADOLOL
Allergien: -
Vorherige Impfungen: -

VAERS 2478843

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: WA
Alter: 42,0
Geschlecht: F
Eingang: 14.10.2022
Impfdatum: 02.09.2022
Beginn: 01.10.2022
Tage bis Beginn: 29,0
Dosis: 4
Route/Site: UN / LA

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

Abdominal pain Appendicectomy Appendicitis Blood test Chills Computerised tomogram Decreased appetite Laparoscopic surgery Pyrexia SARS-CoV-2 test Streptococcus test Urine analysis Vomiting

Symptomtext

Appendicitis: felt sharp abdominal pain, vomiting, loss of appetite, fever and severe chills. Started Saturday Oct 1st upon waking (7:30am), continued through Sunday to ER visit and diagnosis (Oct 2nd @ 6:30pm). Had laparoscopic surgery to remove appendix (8:30pm) and an overnight hospital stay to recover. Released to return home Monday Oct 3rd at 5pm.

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Praegender Schweregrund: Abdominal pain
Hospital-Tage: 1,0
Labordaten: Oct 2: blood work, urinalysis, CT scan, COVID & strep tests (for admission) Oct 3: blood work Oct 7: blood work, urinalysis, CT scan Oct 11: blood work
Aktuelle Erkrankungen: none
Vorgeschichte: chronic constipation, chronic fatigue
Andere Medikamente: none
Allergien: penicillin
Vorherige Impfungen: -

VAERS 2477099

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7144B

mild

Staat: IN
Alter: 79,0
Geschlecht: F
Eingang: 13.10.2022
Impfdatum: 11.10.2022
Beginn: 11.10.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: SYR / LA

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

Arthralgia Fatigue Headache Lethargy Myalgia

Symptomtext

Muscle aches / Joint pain and soreness. Headache Fatigue/ lethargic

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Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: -
Andere Medikamente: Multi Vitamins Atorvastatin 20 MG every 3rd day. Propranolol 10MG for essential tremors Cetirizine 10 MG E every other day Omeprazole once daily
Allergien: None
Vorherige Impfungen: -

VAERS 2476597

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7144B

mild

Staat: TX
Alter: 67,0
Geschlecht: M
Eingang: 12.10.2022
Impfdatum: 03.09.2022
Beginn: 19.09.2022
Tage bis Beginn: 16,0
Dosis: 4
Route/Site: OT / -

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

Anti-thyroid antibody Blood thyroid stimulating hormone Body temperature Chest X-ray Influenza virus test Lipase Myalgia Oropharyngeal discomfort Pyrexia Red blood cell sedimentation rate SARS-CoV-2 test Streptococcus test Thyroiditis Thyroxine free Ultrasound scan Urine analysis

Symptomtext

throat discomfort; body aches; Thyroiditis after Bivalent booster / Ultrasound of Neck showed Thyroiditis after Bivalent booster; Fever 101F after Bivalent booster / Still runs low fever despite drinking enough water, after Bivalent booster; This spontaneous case was reported by a nurse and describes the occurrence of THYROIDITIS (Thyroiditis after Bivalent booster / Ultrasound of Neck showed Thyroiditis after Bivalent booster), OROPHARYNGEAL DISCOMFORT (throat discomfort), PYREXIA (Fever 101F after Bivalent booster / Still runs low fever despite drinking enough water, after Bivalent booster) and MYALGIA (body aches) 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. AS7144B) for COVID-19 vaccination. No known allergy. The patient's past medical history included Neck pain and Wide excision of melanoma (Patient had melanoma removed from arms several years ago). Concurrent medical conditions included Enlarged prostate, Hyperlipidemia, Anxiety disorder and Malignant melanoma (malignant melanoma 2017, basal and squamous cell) since 2017. Concomitant products included ESCITALOPRAM OXALATE for Anxiety disorder, SIMVASTATIN for Hyperlipidemia, VITAMIN D3, CURCUMA LONGA (TURMERIC [CURCUMA LONGA]) and PROBIOTIC [BIFIDOBACTERIUM BIFIDUM;BIFIDOBACTERIUM LACTIS;BIFIDOBACTERIUM LONGUM;LACTOBACILLUS ACIDOPHILUS;LACTOBACILLUS RHAMNOSUS] for an unknown indication. On 03-Sep-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 19-Sep-2022, the patient experienced THYROIDITIS (Thyroiditis after Bivalent booster / Ultrasound of Neck showed Thyroiditis after Bivalent booster) and PYREXIA (Fever 101F after Bivalent booster / Still runs low fever despite drinking enough water, after Bivalent booster). On 20-Sep-2022, the patient experienced OROPHARYNGEAL DISCOMFORT (throat discomfort) and MYALGIA (body aches). The patient was treated with AMOXICILLIN at an unspecified dose and frequency; PARACETAMOL (TYLENOL) at an unspecified dose and frequency; ACETAMINOPHEN at a dose of every evening; ZINC at a dose of 3 days; FLUTICASONE PROPIONATE (FLONASE ALLERGY RELIEF) at a dose of nasal spray; FLUTICASONE PROPIONATE, SALMETEROL XINAFOATE (ADVAIR) at a dose of inhaler; ATENOLOL on 05-Oct-2022 at an unspecified dose and frequency; METHIMAZOLE on 05-Oct-2022 at an unspecified dose and frequency and PREDNISONE on 05-Oct-2022 at an unspecified dose and frequency. On 05-Oct-2022, PYREXIA (Fever 101F after Bivalent booster / Still runs low fever despite drinking enough water, after Bivalent booster) had resolved. At the time of the report, THYROIDITIS (Thyroiditis after Bivalent booster / Ultrasound of Neck showed Thyroiditis after Bivalent booster), OROPHARYNGEAL DISCOMFORT (throat discomfort) and MYALGIA (body aches) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 19-Sep-2022, Body temperature: Fever of 101 F. On 19-Sep-2022, SARS-CoV-2 test: (Negative) Covid Negative. On 21-Sep-2022, SARS-CoV-2 test: (Negative) Negative. On 29-Sep-2022, Influenza virus test: (Negative) Negative. On 29-Sep-2022, SARS-CoV-2 test: (Negative) Negative. On 29-Sep-2022, Streptococcus test: (Negative) Negative. On 04-Oct-2022, Anti-thyroid antibody: 12.50. On 04-Oct-2022, Blood thyroid stimulating hormone: 0.006. On 04-Oct-2022, Chest X-ray: (Negative) Negative. On 04-Oct-2022, Lipase: 53. On 04-Oct-2022, Red blood cell sedimentation rate: 31. On 04-Oct-2022, Thyroxine free: 4.29. On 04-Oct-2022, Ultrasound scan: Ultrasound of Neck showed Thyroiditis. On 05-Oct-2022, Anti-thyroid antibody: 18 and 14.10. On 05-Oct-2022, Blood thyroid stimulating hormone: 0.006 and Less than 1. On 05-Oct-2022, Thyroxine free: 4.65. On an unknown date, Urine analysis: (Negative) Negative. 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. It was reported that all previous shots were Moderna COVID-19 vaccines. First dose: On 12JAN2021 (Lot 037K20A & MFG Exp. Date: unknown). 2nd shot: On 08FEB2021 (Lot 043L20A & MFG Exp. Date: unknown). First booster on 22NOV2021 (Lot 069F21A & MFG Exp. Date: unknown). All Moderna COVID-19 vaccines given intramuscular on arm. It was reported that patient had Negative COVID Test after Bivalent booster. Patient had symptoms as saturated bedding with sweat on 5Oct2022. Most recent FOLLOW-UP information incorporated above includes: On 10-Oct-2022: Follow-up received contains no new information On 11-Oct-2022: Significant live follow up received contains Dose details, Patient information, Medical history, Concomitant medications, Additional events, lab test, event details and Case narrative updated. Treatment drug added.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myalgia
Hospital-Tage: -
Labordaten: Test Date: 20221005; Test Name: thyroglobulin antibodies; Result Unstructured Data: 18; Test Date: 20221004; Test Name: Thyroid peroxidase AB; Result Unstructured Data: 12.50; Test Date: 20221005; Test Name: Thyroid peroxidase AB; Result Unstructured Data: 14.10; Test Date: 20221004; Test Name: Thyroid-stimulating hormone Test; Result Unstructured Data: 0.006; Test Date: 20221005; Test Name: Thyroid-stimulating hormone Test; Result Unstructured Data: 0.006; Test Date: 20221005; Test Name: Thyrotropin Binding Inhibtory Immunoglobulin; Result Unstructured Data: Less than 1; Test Date: 20220919; Test Name: Body temperature; Result Unstructured Data: Fever of 101 F; Test Date: 20221004; Test Name: chest X-ray; Test Result: Negative ; Result Unstructured Data: Negative; Test Date: 20220929; Test Name: Influenza A&B; Test Result: Negative ; Result Unstructured Data: Negative; Test Date: 20221004; Test Name: Lipase; Result Unstructured Data: 53; Test Date: 20221004; Test Name: erythrocyte sedimentation rate; Result Unstructured Data: 31; Test Date: 20220919; Test Name: COVID; Test Result: Negative ; Result Unstructured Data: Covid Negative; Comments: Abbott Binax; Test Date: 20220921; Test Name: COVID; Test Result: Negative ; Result Unstructured Data: Negative; Comments: Abbott Binax; Test Date: 20220929; Test Name: Covid antigen (Quidel); Test Result: Negative ; Result Unstructured Data: Negative; Test Date: 20220929; Test Name: A Strep; Test Result: Negative ; Result Unstructured Data: Negative; Test Date: 20221004; Test Name: Free T4; Result Unstructured Data: 4.29; Test Date: 20221005; Test Name: Free T4; Result Unstructured Data: 4.65; Test Date: 20221004; Test Name: Ultrasound of neck; Result Unstructured Data: Ultrasound of Neck showed Thyroiditis; Test Name: Urinalysis; Test Result: Negative ; Result Unstructured Data: Negative
Aktuelle Erkrankungen: Anxiety disorder; Enlarged prostate; Hyperlipidemia; Malignant melanoma (Skin cancer history, malignant melanoma 2017, basal and squamous cell)
Vorgeschichte: Medical History/Concurrent Conditions: Neck pain; Wide excision of melanoma (Patient had melanoma removed from arms several years ago); Comments: No known allergy
Andere Medikamente: SIMVASTATIN; VITAMIN D3; ESCITALOPRAM OXALATE; TURMERIC [CURCUMA LONGA]; PROBIOTIC [BIFIDOBACTERIUM BIFIDUM;BIFIDOBACTERIUM LACTIS;BIFIDOBACTERIUM LONGUM;LACTOBACILLUS ACIDO
Allergien: -
Vorherige Impfungen: -

VAERS 2475721

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: CA
Alter: 73,0
Geschlecht: F
Eingang: 11.10.2022
Impfdatum: 12.09.2022
Beginn: 04.10.2022
Tage bis Beginn: 22,0
Dosis: 5
Route/Site: IM / LA

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

COVID-19 Discomfort Fatigue Feeling abnormal Headache Insomnia Nasal congestion Nasopharyngitis Pain Pyrexia SARS-CoV-2 test positive Sleep disorder Throat irritation Upper respiratory tract congestion

Symptomtext

I received my dose of the Bivalent Moderna booster on 9/12/2022. On the afternoon of 10/04/2022, I began to get a scratchy throat. At first, I didn't think much of it. As the evening progressed, though, I felt sure that I was coming down with something. When I went to bed that night, I had difficulty sleeping, because I was uncomfortable and beginning to feel achy. On the morning of 10/05/2022, I felt pretty sure I had something. I took the home test for COVID-19 and immediately got a positive result. I spoke to my doctor by telehealth about treatment options. Since I'm on PLAVIX, PAXLOVID wasn't an option. I also opted not to get monoclonal antibodies. I had body aches, fever, upper respiratory congestion, and a headache 10/5/2022-10/7/2022. I took TYLENOL and NYQUIL, which helped with the fever, headaches, and inability to sleep. On 10/8/2022, I had a fever that reached 102.6, and it lasted only about an hour. Afterwards, it began to gradually taper off. Aside from the fever, nasal congestion, and fatigue, all of the other symptoms were gone at this point. On 10/9/2022 and 10/10/2022, I was very fatigued and felt like I had the remnants of a cold. At the time of this writing, I still feel tired, but the fatigue has lessened. Today I was able to work out to a tai chi video. I also still have a little bit of the nasal congestion remaining.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 10/5/2022 home COVID-19 test positive result.
Aktuelle Erkrankungen: None.
Vorgeschichte: Stroke Survivor; Osteopenia; Osteoarthritis.
Andere Medikamente: PLAVIX; LIPITOR; calcium; vitamin D; AREDS 2 vitamins for eyes.
Allergien: None.
Vorherige Impfungen: After receiving each of the Moderna vaccines for COVID-19, I felt ill for a couple of days. I had body aches, mild fever, fatigu

VAERS 2475696

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: MA
Alter: 38,0
Geschlecht: F
Eingang: 11.10.2022
Impfdatum: 06.09.2022
Beginn: 05.10.2022
Tage bis Beginn: 29,0
Dosis: 4
Route/Site: IM / RA

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

Abdominal pain Back pain Blood urine present C-reactive protein normal Computerised tomogram normal Differential white blood cell count normal Full blood count normal Injection site rash Laboratory test normal Lipase normal Rash pruritic Sleep disorder Ultrasound scan normal Urine analysis abnormal Vomiting

Symptomtext

I developed a rash at the injection site about 8 hours after the shot. It impeded my sleeping for a little bit. I also got some small itching bumps about 72 hours afterwards and lasted for about a week. That resolved, then 10/5/22, I woke up with severe back pain and abdominal pain in all four quadrants. I took Celebrex after several hours and that helped a little. Then, I took Pepto-Bismol and that made me throw up immediately. That made me feel better to where I was able to eat and drink a little. I was also at altitude and took Acetazolamide. On the evening 10/5/22, I was pain free without medication and went to bed. I woke up 4:30AM on 10/6/22, with severe abdominal pain and back pain and vomited. I then took Celebrex and had some relief. I had a telehealth appointment and they told me to go to the hospital. They ran a bunch of tests and discharged me with pain meds. I have a follow up with my doctor soon. I stopped taking Acetazolamide morning of 10/8/22 because I was back at sea level.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain
Hospital-Tage: -
Labordaten: CT Scan - 10/6/22 - Normal; Ultrasound - 10/6/22 - Normal; Urinalysis - 10/6/22 - Found a small amount of blood; CBS Differential - 10/6/22 - Normal; CHEM 13 - 10/6/22 - Normal; CRP-I - 10/6/22 - Normal; Lipase - 10/6/22 - Normal
Aktuelle Erkrankungen: Mild Rectal Bleeding
Vorgeschichte: Asthma; Polycystic Ovary Syndrome; Low Iron
Andere Medikamente: Flovent; Budesonide; Iron; Stool Softener; Lactase; Flynd; Denta 5000 Plus
Allergien: Resin; Gold Sodium Thiosulfate; Neomycin; Potassium Dichromate: Environmental Allergies
Vorherige Impfungen: -

VAERS 2475278

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: NY
Alter: 41,0
Geschlecht: M
Eingang: 11.10.2022
Impfdatum: 03.09.2022
Beginn: 03.09.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: SYR / LA

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

Asthenia COVID-19 Chills Fatigue Malaise Oropharyngeal pain Pyrexia Respiratory tract congestion SARS-CoV-2 test positive Secretion discharge Vaccine breakthrough infection

Symptomtext

The night after receiving my Moderna Bivalent booster I felt a little sick. This was not unusual. I had received 3 previous Pfizer shots (2 in original series plus 1 booster), all of which resulted in some amount of fever and/or chills and/or fatigue that lasted a day or two but then dissipated completely. This Moderna shot did not have a particularly acute reaction in the first few days, but I was very fatigued. Unlike with the first 3 Pfizer shots, the fatigue persisted for several weeks and never totally lifted. I do suffer from chronic fatigue syndrome, but I have a baseline energy level that has remained rather consistent for a while -- it was markedly lower for the month following my Moderna booster. Then, on Oct 6, about a month after my Moderna booster, I developed a breakthrough covid infection. I would describe my symptoms as mild to moderate: low fever that went away, sore throat, mucus and congestion, fatigue (though not noticeably more tired than energy level since booster).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Home antigen covid-19 tests positive on Oct 6, Oct 8, Oct 11.
Aktuelle Erkrankungen: -
Vorgeschichte: CFIDS, IBS, arthritis, osteoporosis, respiratory allergies
Andere Medikamente: VIT D3, VIT E, Tylenol
Allergien: -
Vorherige Impfungen: -

VAERS 2471958

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: TX
Alter: 67,0
Geschlecht: M
Eingang: 07.10.2022
Impfdatum: 03.09.2022
Beginn: 19.09.2022
Tage bis Beginn: 16,0
Dosis: 4
Route/Site: IM / UN

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

Anti-thyroid antibody Asthenia Blood thyroid stimulating hormone Blood triglycerides Chest X-ray Cough Full blood count Influenza A virus test negative Influenza B virus test Lipase Metabolic function test Oropharyngeal pain Pyrexia Red blood cell sedimentation rate SARS-CoV-2 test negative Streptococcus test negative Thyroiditis Thyroxine free

Symptomtext

Received Moderna Bivalent Booster on 9/3/2022. Symptoms began on 9/19/2022 (fever, weakness, sore throat, dry cough). Treated initially with Amoxicillin. Symptoms did not improve on Amoxicillin. Daily fevers as high as 101.7. Diagnosed with thyroiditis on 10/4/2022. Currently treated with Prednisone, methimazole and atenolol. I reported event to Moderna and this is the number we received "Private".

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: 9/30/2022 Influenza A&B, Covid antigen, Strep Group A screen (all negative) 10/4/2022 thyroid ultrasound, CXR, TSH and Free T4, Lipase, Thyroid Peroxidase antibody, Sedimentation Rate, CMP, CBC, Urinalysis 10/5/2022 thyroid antibodies TPO and TG, CMP, TSH and Free T4
Aktuelle Erkrankungen: seasonal allergies?
Vorgeschichte: Enlarged prostate, hyperlipidemia, history of melanoma, basal cell carcinoma, squamous cell carcinoma
Andere Medikamente: escitalopram, simvastatin, D3, probiotic, turmeric
Allergien: nka
Vorherige Impfungen: -

VAERS 2471322

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7144B

mild

Staat: NJ
Alter: 70,0
Geschlecht: F
Eingang: 07.10.2022
Impfdatum: 15.09.2022
Beginn: 15.09.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / LA

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

Vaccination site pain Vaccination site swelling

Symptomtext

Developed swelling about 4 inches further down in their inner arm; Tenderness about 4 inches further down and in their inner arm; This spontaneous case was reported by a nurse and describes the occurrence of VACCINATION SITE SWELLING (Developed swelling about 4 inches further down in their inner arm) and VACCINATION SITE PAIN (Tenderness about 4 inches further down and in their inner arm) in a 70-year-old female patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. AS7144B) for COVID-19 prophylaxis. Co-suspect product included non-company product INFLUENZA VACCINE INACT SPLIT 4V (FLUZONE HIGH DOSE QUADRIVALENT) for an unknown indication. Concurrent medical conditions included Hypertension. Concomitant products included LOSARTAN for Hypertension. On 15-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) 1 dosage form and dose of INFLUENZA VACCINE INACT SPLIT 4V (FLUZONE HIGH DOSE QUADRIVALENT) (unknown route) 1 dosage form. On 15-Sep-2022, the patient experienced VACCINATION SITE SWELLING (Developed swelling about 4 inches further down in their inner arm) and VACCINATION SITE PAIN (Tenderness about 4 inches further down and in their inner arm). The patient was treated with NAPROXEN SODIUM (ALEVE) at an unspecified dose and frequency. At the time of the report, VACCINATION SITE SWELLING (Developed swelling about 4 inches further down in their inner arm) and VACCINATION SITE PAIN (Tenderness about 4 inches further down and in their inner arm) had resolved. 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. The patient had a location reaction to one of the vaccines. The patient had received Flu shot: Fluzone Highdose along with Moderna COVID bivalent on 15-Sep-2022 on the upper left arm. Then not right away but later that day she developed swelling and tenderness about 4 inches further down and in their inner arm. Patient mentioned that it did go away. Patient took Aleve after the reaction and it helped.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Vaccination site pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Hypertension
Vorgeschichte: -
Andere Medikamente: LOSARTAN
Allergien: -
Vorherige Impfungen: -

VAERS 2470679

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: PA
Alter: 31,0
Geschlecht: F
Eingang: 06.10.2022
Impfdatum: 04.10.2022
Beginn: 05.10.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: SYR / RA

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

Rash Urticaria

Symptomtext

RASH AND HIVES AROUND TORSO AND THIGHS

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: NONE
Vorgeschichte: -
Andere Medikamente: LAMOTRIGENE
Allergien: CEPHALOSPORINS, MIRENA
Vorherige Impfungen: -

VAERS 2470116

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7144B

mild

Staat: NJ
Alter: 67,0
Geschlecht: F
Eingang: 05.10.2022
Impfdatum: 06.09.2022
Beginn: 26.09.2022
Tage bis Beginn: 20,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Exposure to SARS-CoV-2 Headache Nasal congestion Pain Pyrexia SARS-CoV-2 test positive

Symptomtext

I was exposed to covid on 09/26/2022. I was exposed to someone around 09/22/2022 because this person tested positive on this day. I experienced headaches, and the following day I had a rapid test and it was positive, had low grade fever, stuffy nose and head, just general achiness. I did a PCR test on 09/25/2022 but this rest came back negative. On the Antigen test when I took it was positive. The doctor I saw did another PCR test which came back positive. The doctor also prescribed Paxlovid which helped my symptoms. I have no symptoms today.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: COVID test; positive PCR test; positive
Aktuelle Erkrankungen: None
Vorgeschichte: Hypothyroidism due Thyroidectomy due to thyroid cancer
Andere Medikamente: Ibuprofen
Allergien: None
Vorherige Impfungen: After my first and second COVID-19 vaccine I had some mild symptoms of achiness and sore arm

VAERS 2469783

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7144B

mild

Staat: NC
Alter: 77,0
Geschlecht: M
Eingang: 05.10.2022
Impfdatum: 07.09.2022
Beginn: 08.09.2022
Tage bis Beginn: 1,0
Dosis: 5
Route/Site: SYR / LA

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

Arthralgia Arthritis Blood test abnormal Glucose tolerance impaired

Symptomtext

It was a arthritis episode in my left hip. It started aching so I went to the hospital and they ran blood tests and informed me that I was prediabetic. They are waiting a year until retesting.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: Bloodwork- prediabetic
Aktuelle Erkrankungen: No
Vorgeschichte: Acid reflux
Andere Medikamente: Omeprazole; Daily vitamins
Allergien: No
Vorherige Impfungen: -

VAERS 2469747

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: IL
Alter: 56,0
Geschlecht: F
Eingang: 05.10.2022
Impfdatum: 13.09.2022
Beginn: 16.09.2022
Tage bis Beginn: 3,0
Dosis: 6
Route/Site: IM / LA

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

Biopsy skin Herpes zoster Rash

Symptomtext

I noticed a rash on my face on 9/15 it got progressively got worse and on 9/16 I saw my doctor and he dx Shingles I was prescribed valacyclovir and topical hydrocortisone and steroids I also noticed a rash on my leg for which I went to see a Dermatologist on 9/22 and he prescribed another round of steroids. I am immunosuppressed prescribed steroids on the 9/22/2022. It is slowly improving but the rash on my leg continues to bother me. I again saw a Dermatologist to confirm that it was Shingles and not another skin condition. Saw a dermatologist on 10/03 again and he currently paused valacyclovir.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: Skin biopsy
Aktuelle Erkrankungen: None
Vorgeschichte: Hypothyroid; Interstitial Lung Disease
Andere Medikamente: SYNTHROID; losartan; atorvastatin; omeprazole; mycophenolate mofetil
Allergien: None
Vorherige Impfungen: -

VAERS 2451028

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7144B

mild

Staat: FL
Alter: 75,0
Geschlecht: F
Eingang: 04.10.2022
Impfdatum: 16.09.2022
Beginn: 16.09.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: OT / LA

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

Incorrect route of product administration Injection site erythema Injection site pain Injection site swelling Injection site warmth Pain Product administered at inappropriate site Rash erythematous Vaccination site erythema Vaccination site pain Vaccination site swelling Vaccination site warmth Skin warm Swelling Tenderness

Symptomtext

Error: Wrong Route (SC, IM, etc.)-

Weitere VAERSDATA-Felder

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

VAERS 2451028

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: FL
Alter: 75,0
Geschlecht: F
Eingang: 04.10.2022
Impfdatum: 16.09.2022
Beginn: 16.09.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / RA

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

Incorrect route of product administration Injection site erythema Injection site pain Injection site swelling Injection site warmth Pain Product administered at inappropriate site Rash erythematous Vaccination site erythema Vaccination site pain Vaccination site swelling Vaccination site warmth Skin warm Swelling Tenderness

Symptomtext

Error: Wrong Route (SC, IM, etc.)-

Weitere VAERSDATA-Felder

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

VAERS 2467183

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: OH
Alter: 80,0
Geschlecht: F
Eingang: 03.10.2022
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

Asthenia Dizziness Fall Head injury Hypersomnia Wound secretion

Symptomtext

PER PATIENT SHE WAS WEAK, DIZZY AND FEELING FAINT. STATES SHE FELL THE DAY AFTER THE VACCINE AND HIT HER HEAD. SITE ON TEMPLE OOZING. SLEPT MANY HOURS WHICH IS UNUSUAL FOR HER

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: NONE KNOWN
Vorgeschichte: NONE KNOWN
Andere Medikamente: UNKNOWN
Allergien: SULFA, WAS ILL FOR 2 DAYS AFTER HIGH DOSE FLU SHOT
Vorherige Impfungen: HIGH DOSE FLU

VAERS 2467134

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: OH
Alter: 52,0
Geschlecht: F
Eingang: 03.10.2022
Impfdatum: 29.09.2022
Beginn: 29.09.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Injection site bruising Injection site erythema Injection site pain Limb discomfort Pain in extremity Peripheral swelling

Symptomtext

Her arm had a red spot where the injection was, then it turned into a large bruise. She says her whole arm is sore and feels heavy. The soreness is all the way from her shoulder to her fingers and it is not improving. It is also swollen. She has tried ibuprofen and tylenol for the pain. She noticed swelling went down after the medication.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site bruising
Hospital-Tage: -
Labordaten: NA
Aktuelle Erkrankungen: NA
Vorgeschichte: -
Andere Medikamente: Omeprazole, spirolactone, one-a-day women's vitamins, welbutrin, gabapentin.
Allergien: Penicillin (reaction is hives)
Vorherige Impfungen: -

VAERS 2467075

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge as7144b

mild

Staat: TX
Alter: 62,0
Geschlecht: M
Eingang: 03.10.2022
Impfdatum: 12.09.2022
Beginn: 28.09.2022
Tage bis Beginn: 16,0
Dosis: 5
Route/Site: SYR / RA

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

Cellulitis Injection site erythema

Symptomtext

Site: Redness at Injection Site-Severe, Additional Details: Cellulitis

Weitere VAERSDATA-Felder

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

VAERS 2466698

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: WA
Alter: 34,0
Geschlecht: F
Eingang: 01.10.2022
Impfdatum: 30.09.2022
Beginn: 30.09.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / RA

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

Axillary pain Diarrhoea Injection site erythema Injection site swelling

Symptomtext

Injection site redness approximately nickel sized. Redness began 09/30/2022. Injection site swelling approximately nickel sized in diameter at time of reporting 10/01/2022 . Swelling began 09/30/2022. Pain in right arm pit as of Saturday 10/01/2022. Diarrhea. Began 10/01/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Axillary pain
Hospital-Tage: -
Labordaten: None as of 10/01/2022
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2465624

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: WA
Alter: 49,0
Geschlecht: F
Eingang: 30.09.2022
Impfdatum: 08.09.2022
Beginn: 16.09.2022
Tage bis Beginn: 8,0
Dosis: 4
Route/Site: IM / RA

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

Arthralgia Limb immobilisation Pain in extremity Tenosynovitis X-ray normal

Symptomtext

I started having some pain in my wrist and in my thumb. It happened one morning. It started to get better then got worse again. I went to the urgent care center on 09/28/2022. The diagnosed me Tenosynovitis. The put me in an immobilizing splint for my thumb and wrist for 2 weeks. I was advised to not use my thumb and wrist. They prescribed Meloxicam for pain. I was also advised to take Prilosec to protect my stomach. It is still throbbing but the less I move the better I feel.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: X-Ray 9-28-2022-normal
Aktuelle Erkrankungen: N/A
Vorgeschichte: Depression; Anxiety; Low Level Hypertension; ADHD
Andere Medikamente: Progesterone; Hydrochlorothiazide; Lexapro; Magnesium Calcium , Vitamin D; Tylenol
Allergien: Celexa; Sulfa; Propranolol; Lisinopril; Macrobid
Vorherige Impfungen: -

VAERS 2464900

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge as7144b

mild

Staat: MA
Alter: 44,0
Geschlecht: M
Eingang: 29.09.2022
Impfdatum: 04.09.2022
Beginn: 20.09.2022
Tage bis Beginn: 16,0
Dosis: 4
Route/Site: IM / RA

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

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

Symptomtext

positive for COVID on 9/20 cough, congestion, runny nose, body aches negative for COVID on 9/27

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: rapid antigen test positive for COVID 9/20
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: lexipro vitamin D metamucil
Allergien: none
Vorherige Impfungen: -

VAERS 2464598

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: CA
Alter: 68,0
Geschlecht: F
Eingang: 29.09.2022
Impfdatum: 07.09.2022
Beginn: 09.09.2022
Tage bis Beginn: 2,0
Dosis: 4
Route/Site: IM / RA

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

Arthralgia Depression Fatigue Headache Hypersomnia Immunisation reaction

Symptomtext

Very tired for several weeks, just exhausted then depression. Joint pain. Headaches on and off. No treatment. Still experiencing being tired but exhaustion and sleeping all the time plus depression has lifted.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: None. Last time physician stated let's just blame it on the vaccine.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Crestor and Fosamax
Allergien: None
Vorherige Impfungen: -

VAERS 2464553

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge as7144b

mild

Staat: OK
Alter: 74,0
Geschlecht: M
Eingang: 29.09.2022
Impfdatum: 20.09.2022
Beginn: 20.09.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / RA

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

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

Weitere VAERSDATA-Felder

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

VAERS 2463454

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: NV
Alter: 69,0
Geschlecht: F
Eingang: 28.09.2022
Impfdatum: 07.09.2022
Beginn: 20.09.2022
Tage bis Beginn: 13,0
Dosis: 5
Route/Site: IM / LA

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

COVID-19 Headache Oropharyngeal pain Pain in extremity Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

Tested positive for COVID on 9/20/2022 experienced minor symptoms. Mild headache, sore throat and arm, and light chest congestion. I took MUCINEX and it resolved quickly.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Atorvastatin; doxycycline hyclate
Allergien: None
Vorherige Impfungen: -

VAERS 2463207

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge As7144b

mild

Staat: NY
Alter: 42,0
Geschlecht: F
Eingang: 28.09.2022
Impfdatum: 25.09.2022
Beginn: 25.09.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Headache Intervertebral disc protrusion Myalgia Pain Pyrexia Spinal pain

Symptomtext

Intense muscle aches starting within hours. Fever 101 for 2 days, but the most intense side effect is a headache that has lasted Sunday night through Wednesday (now) and ongoing with no sign of improvement. This headache is so intense I cannot shake it. The body/muscle aches are intense too - every previous injury has been ?re-activated? - multiple herniated discs in neck & back are currently in intense pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Frequent bronchitis/pneumonia
Andere Medikamente: None
Allergien: Penicillin, aspirin, NSAIDs
Vorherige Impfungen: All previous covid vaccines, all previous vaccines as infant

VAERS 2462730

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7144B

mild

Staat: IA
Alter: 78,0
Geschlecht: F
Eingang: 28.09.2022
Impfdatum: 21.09.2022
Beginn: 21.09.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: OT / LA

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

Body temperature Chills Erythema Hyperhidrosis Pyrexia Rash macular Vaccination site bruising

Symptomtext

She had a bruise in the site of injection (left arm); Her neck and the top of her chest was red; Her neck and the top of her chest was red and blotchy; She woke up sweating; Fever of 100 degree F; Chills; This spontaneous case was reported by a patient and describes the occurrence of VACCINATION SITE BRUISING (She had a bruise in the site of injection (left arm)), ERYTHEMA (Her neck and the top of her chest was red), HYPERHIDROSIS (She woke up sweating), PYREXIA (Fever of 100 degree F) and CHILLS (Chills) in a 78-year-old female patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. AS7144B) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Co-suspect product included non-company product INFLUENZA VACCINE (FLU [INFLUENZA VACCINE]) for an unknown indication. Concurrent medical conditions included Drug allergy (Morphine), Drug allergy (Estrace), Ragweed allergy and Borderline diabetes (Several years, status: controlled). Concomitant products included VITAMINS NOS, FAMOTIDINE, MONTELUKAST, FENOFIBRATE, LISINOPRIL and ESCITALOPRAM for an unknown indication. 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)) (Intramuscular) 1 dosage form and dose of INFLUENZA VACCINE (FLU [INFLUENZA VACCINE]) (unknown route) 1 dosage form. On 21-Sep-2022, the patient experienced HYPERHIDROSIS (She woke up sweating), PYREXIA (Fever of 100 degree F) and CHILLS (Chills). On 23-Sep-2022, the patient experienced VACCINATION SITE BRUISING (She had a bruise in the site of injection (left arm)), ERYTHEMA (Her neck and the top of her chest was red) and RASH MACULAR (Her neck and the top of her chest was red and blotchy). The patient was treated with PARACETAMOL (TYLENOL) for Fever and Chills, at an unspecified dose and frequency. On 22-Sep-2022, HYPERHIDROSIS (She woke up sweating), PYREXIA (Fever of 100 degree F) and CHILLS (Chills) had resolved. At the time of the report, VACCINATION SITE BRUISING (She had a bruise in the site of injection (left arm)), ERYTHEMA (Her neck and the top of her chest was red) and RASH MACULAR (Her neck and the top of her chest was red and blotchy) had not resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 21-Sep-2022, Body temperature: 100 degree Fahrenheit. 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 received first dose of moderna vaccine on 02-Feb-2021 with lot number 011M20A Patient received second dose of moderna vaccine on 02-Mar-2021 with lot number 029A21A. Patient received first booster dose of moderna vaccine on 27-Oct-2021 with lot number 091D21A and expiration date of 12-Feb-2022 Patient received second booster dose of moderna vaccine on 07-Apr-2022. After previous shots everything was fine and patient did not experience any symptoms, but after bivalent booster patient experience symptoms. On 21-Sep-2022, during the night patient experienced fever of 100 degree F, chills and took Tylenol and went to bed but after a while patient woke up sweating. Next morning patient felt fine On 23-Sep-2022, the patient noticed that neck and the top of her chest was red and blotchy and had a bruise in the site of injection (left arm), these symptoms were still ongoing.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Test Date: 20220921; Test Name: Fever; Result Unstructured Data: 100 degree Fahrenheit
Aktuelle Erkrankungen: Borderline diabetes (Several years, status: controlled); Drug allergy (Morphine); Drug allergy (Estrace); Ragweed allergy
Vorgeschichte: -
Andere Medikamente: VITAMINS NOS; FAMOTIDINE; MONTELUKAST; FENOFIBRATE; LISINOPRIL; ESCITALOPRAM
Allergien: -
Vorherige Impfungen: -

VAERS 2462018

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: MA
Alter: 52,0
Geschlecht: F
Eingang: 27.09.2022
Impfdatum: 11.09.2022
Beginn: 12.09.2022
Tage bis Beginn: 1,0
Dosis: 5
Route/Site: IM / LA

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

Arthralgia Arthritis reactive Gait inability Swelling Ultrasound Doppler X-ray limb

Symptomtext

Reactive arthritis and joint pain and swelling. Unable to walk for 2 days/

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: X-ray of left knee 9/13/22, ultrasound of left leg 9/13/22
Aktuelle Erkrankungen: none
Vorgeschichte: cervical radiculopathy eczema
Andere Medikamente: Citalopram Gabapentin Biotin Probiotics
Allergien: Latex
Vorherige Impfungen: -

VAERS 2461594

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: AZ
Alter: 42,0
Geschlecht: F
Eingang: 27.09.2022
Impfdatum: 22.09.2022
Beginn: 23.09.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: OT / LA

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

Arthralgia

Symptomtext

Very achy /joints are achy/ dull ache; This spontaneous case was reported by a patient and describes the occurrence of ARTHRALGIA (Very achy /joints are achy/ dull ache) in a 42-year-old female patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. AS7144B) for COVID-19 vaccination. Co-suspect product included non-company product INFLUENZA VACCINE (FLU VACCINE VII) for Flu vaccination. Patient does not have allergy to medications, food or other products. On 22-Sep-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) .5 milliliter and dose of INFLUENZA VACCINE (FLU VACCINE VII) (unknown route) 1 dosage form. On 23-Sep-2022 at 7:00 AM, after starting mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)), the patient experienced ARTHRALGIA (Very achy /joints are achy/ dull ache). At the time of the report, ARTHRALGIA (Very achy /joints are achy/ dull ache) had not resolved. Concomitant product use was not provider by the reporter. On 08-MAR-2021, patient received First dose 0.5 mL of Moderna COVID-19 Vaccine with batch number 041L20A. On 05-APR-2021, patient received Second dose 0.5mL of Moderna COVID-19 Vaccine with batch number 041L20A. On 18-NOV-2021, patient received Third dose (First booster) dose of Moderna COVID-19 Vaccine with batch number 034F21A. Patient's symptoms were reported as stable. No treatment information was reported. This case was linked to MOD-2022-650279 (Patient Link).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: Patient does not have allergy to medications, food or other products.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2460239

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: PA
Alter: 42,0
Geschlecht: F
Eingang: 25.09.2022
Impfdatum: 09.09.2022
Beginn: 10.09.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

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

Arthralgia Hypoaesthesia Sensory disturbance Sensory loss

Symptomtext

I've had the first three shots with no side effects or issues. My last shot was in October of 2021. I woke up the next morning with loss of feeling in my left thumb and index finger as well as a region on the side of my forearm near my thumb. I also had more shoulder pain that normal with past shots... with the sensation that my shoulder and neck were "pulled" or "pinched" as with an injury but I hadn't recently been injured. I did have a lower back issue in April that I am in physical therapy for to increase range of motion, but no recent injury to that area. I wrote it off as a weird reaction but not something that was cause for immediate concern. When I didn't regain feeling a week later I called my doctor (who I've not yet met as he's newer to the office) to see if they had a recommendation. They recommended the emergency room which seemed excessive to me almost a week later with a couple of numb fingers and no extreme signs of distress. (SEPT 13-14). I had a scheduled an appointment with my asthma doctor on sept 18 and spoke to him about the event. He called an associate in neurology who recommended that I might want to see a neurologist or at least my pcp to get the process started, My asthma doctor also recommended I fill out this form to see if others have similar experiences. with the bivalent vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: Sept 13 Call to PCP who recommended emergency. Sept 18 appointment with who called a neurologist and Moderna to investigate similar reports and get recommendations September 27th...I have a PCP appointment (my yearly physical) where I intend to bring this up to them to get additional tests.
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma
Andere Medikamente: Vitamin B12, One a day vitamins, and clairtin for seasonal allergies.
Allergien: Penicillin, erythromycin, Zithromax, Bactrim, cechlor
Vorherige Impfungen: -

VAERS 2459766

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: TX
Alter: 24,0
Geschlecht: M
Eingang: 24.09.2022
Impfdatum: 11.09.2022
Beginn: 19.09.2022
Tage bis Beginn: 8,0
Dosis: N/A
Route/Site: IM / LA

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

Fatigue Headache Impaired work ability Influenza virus test negative SARS-CoV-2 test negative

Symptomtext

I did not have any adverse side effects in the short term after taking these vaccines (short term here is from the time of the shots which was 9/11/2022 to about 3-4 days later). However, starting 9/19/2022, I started experiencing a moderate to severe headaches. They would come in waves and were sometimes quite debilitating. I would have to stop working and lie down quite often. I tested negative for COVID (PCR at drive through) and the flu, so I chalked it up to the vaccine. The symptoms only very recently resolved, on 9/23/2022, and still feeling a bit of fatigue (though this might be unrelated). This was adverse for me because never have I had side effects nearly two weeks after a COVID vaccine let alone any sort of vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Asthma
Andere Medikamente: Singulair/Rescue Inhaler (Proair)
Allergien: -
Vorherige Impfungen: -

VAERS 2455972

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge as7144b

mild

Staat: -
Alter: 82,0
Geschlecht: F
Eingang: 23.09.2022
Impfdatum: 12.09.2022
Beginn: 13.09.2022
Tage bis Beginn: 1,0
Dosis: 5
Route/Site: - / LA

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

Extra dose administered Injection site bruising Injection site erythema Injection site swelling Injection site warmth

Symptomtext

Pt reported and presented with large red bubble at injection site. Area was from Left Deltoid to an inch or two above the left elbow. Area was warm and red and bruising was present

Weitere VAERSDATA-Felder

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

VAERS 2455636

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7144B

mild

Staat: CT
Alter: 66,0
Geschlecht: F
Eingang: 23.09.2022
Impfdatum: 14.09.2022
Beginn: 15.09.2022
Tage bis Beginn: 1,0
Dosis: 5
Route/Site: OT / LA

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

Cough Eye swelling Joint swelling Lip swelling Pain in extremity Rash Swelling face Urticaria

Symptomtext

Forehead is totally swollen and it hurts; woke up with a swollen bottom lip/lip swelling got worse on Monday and the patient went to see her Physician.; swelling above her right eye/left eye is swollen and almost shut.; patient has an asthma cough; swelling on both wrists/Swelling was so bad the patient could not bend her wrists/Patients wrists continued to swell.; Hives on both wrists/broke out in hives/hives on her wrists/welts on her waist which are getting better/My face and neck have hives; Rash under both of her arms; Sore arm; This spontaneous case was reported by a patient and describes the occurrence of JOINT SWELLING (swelling on both wrists/Swelling was so bad the patient could not bend her wrists/Patients wrists continued to swell.), LIP SWELLING (woke up with a swollen bottom lip/lip swelling got worse on Monday and the patient went to see her Physician.), EYE SWELLING (swelling above her right eye/left eye is swollen and almost shut.), COUGH (patient has an asthma cough) and SWELLING FACE (Forehead is totally swollen and it hurts) in a 66-year-old female patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. AS7144B) for COVID-19 prophylaxis. The occurrence of additional non-serious events is detailed below. Concurrent medical conditions included Asthma. Concomitant products included FAMOTIDINE, ATORVASTATIN, ESCITALOPRAM and ASPIRIN [ACETYLSALICYLIC ACID] for an unknown indication. On 14-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 15-Sep-2022, the patient experienced PAIN IN EXTREMITY (Sore arm). On 17-Sep-2022, the patient experienced JOINT SWELLING (swelling on both wrists/Swelling was so bad the patient could not bend her wrists/Patients wrists continued to swell.), URTICARIA (Hives on both wrists/broke out in hives/hives on her wrists/welts on her waist which are getting better/My face and neck have hives) and RASH (Rash under both of her arms). On 18-Sep-2022, the patient experienced LIP SWELLING (woke up with a swollen bottom lip/lip swelling got worse on Monday and the patient went to see her Physician.), EYE SWELLING (swelling above her right eye/left eye is swollen and almost shut.) and COUGH (patient has an asthma cough). On 21-Sep-2022, the patient experienced SWELLING FACE (Forehead is totally swollen and it hurts). The patient was treated with PREDNISONE on 17-Sep-2022 at a dose of taper; DIPHENHYDRAMINE HYDROCHLORIDE (BENADRYL [DIPHENHYDRAMINE HYDROCHLORIDE]) at a dose of 25 milligram; FAMOTIDINE (PEPCID [FAMOTIDINE]) at a dose of 20 milligram; HYDROXYZINE at an unspecified dose and frequency and DIPHENHYDRAMINE at a dose of 25 milligram. At the time of the report, JOINT SWELLING (swelling on both wrists/Swelling was so bad the patient could not bend her wrists/Patients wrists continued to swell.), LIP SWELLING (woke up with a swollen bottom lip/lip swelling got worse on Monday and the patient went to see her Physician.), EYE SWELLING (swelling above her right eye/left eye is swollen and almost shut.), COUGH (patient has an asthma cough), SWELLING FACE (Forehead is totally swollen and it hurts), URTICARIA (Hives on both wrists/broke out in hives/hives on her wrists/welts on her waist which are getting better/My face and neck have hives), RASH (Rash under both of her arms) and PAIN IN EXTREMITY (Sore arm) outcome was unknown. The patient's first primary series Moderna Covid-19 vaccine was on 6-FEB-202. Lot number was 011M20A the patient did not remember which arm that she received the vaccine in. The patient was a little tired. The patients' second Moderna Covid-19 vaccine was on 28-MAR-2021. Lot number was 003A21A expirarion date was not available. Patient did not remember which arm that she received the vaccine. The patient got tired and had a sore throat. Slept for a while. The patient's first booster dose was 22-OCT-2021. Lot number was 026D21A expiration date was not reported. The patient does not remember which arm she received the vaccine in. Patient had no adverse reactions. The patient received second booster dose on 31-MAR-2022. Lot number 041D21A expiration date was not provided. The patient did not remember which arm she received the vaccine. Patient had no adverse reactions. Hives and swelling on both wrists. Swelling was so bad the patient could not bend her wrists. The patient went to the walk-in clinic on Saturday 17-SEP-2022 where she was given a Prednisone taper and told to take 25mg of Benadryl along with 20mg of Pepcid. On Sunday the patient woke up with a swollen bottom lip and hives on her wrists and face. Patient's wrists continued to swell. Patient had swelling above her right eye. Patient has an asthma cough. Patient had welts on her waist which are getting better. The patient went back to the walk-in clinic and was told to continue taking Prednisone and take Hydroxyzine instead of Benadryl. The lip swelling got worse on Monday and the patient went to see her Physician. The Doctor sent her to the Emergency Room. The patient was given IV Steroids and Diphenhydramine and was kept overnight for observation. In the last 4 hours on 21-SEP-2022 patients left eye is swollen and almost shut. Face and neck had hives. Forehead was totally swollen, and it hurt. The patient was referred to a dermatologist and she will see the Dermatologist on 22-Sep-2022. This case was linked to MOD-2022-648652, MOD-2022-648680 (Patient Link).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Asthma
Vorgeschichte: -
Andere Medikamente: FAMOTIDINE; ATORVASTATIN; ESCITALOPRAM; ASPIRIN [ACETYLSALICYLIC ACID]
Allergien: -
Vorherige Impfungen: -

VAERS 2454460

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: AZ
Alter: 83,0
Geschlecht: F
Eingang: 22.09.2022
Impfdatum: 14.09.2022
Beginn: 14.09.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Arthralgia Injection site bruising Injection site swelling

Symptomtext

Site: Bruising at Injection Site-Medium, Site: Swelling at Injection Site-Severe, Systemic: Joint Pain-Severe

Weitere VAERSDATA-Felder

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

VAERS 2453019

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7144B

mild

Staat: MI
Alter: 74,0
Geschlecht: M
Eingang: 21.09.2022
Impfdatum: 09.09.2022
Beginn: 10.09.2022
Tage bis Beginn: 1,0
Dosis: 5
Route/Site: OT / RA

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

Feeling hot Influenza like illness Injection site muscle weakness Pyrexia Vaccination site movement impairment

Symptomtext

Can't raise my right arm; I have no strength in my right arm at all; I had flu-like symptoms; Was hot; I think I had a fever; This spontaneous case was reported by a patient and describes the occurrence of VACCINATION SITE MOVEMENT IMPAIRMENT (Can't raise my right arm), INJECTION SITE MUSCLE WEAKNESS (I have no strength in my right arm at all), INFLUENZA LIKE ILLNESS (I had flu-like symptoms), FEELING HOT (Was hot) and PYREXIA (I think I had a fever) 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. AS7144B) for COVID-19 prophylaxis. No medical history reported. It was unknown if the patient ever had COVID positive test or diagnosis. Concomitant products included INFLUENZA VACCINE (FLU [INFLUENZA VACCINE]) for an unknown indication. On 09-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 10-Sep-2022, the patient experienced INFLUENZA LIKE ILLNESS (I had flu-like symptoms), FEELING HOT (Was hot) and PYREXIA (I think I had a fever). On 14-Sep-2022, the patient experienced VACCINATION SITE MOVEMENT IMPAIRMENT (Can't raise my right arm) and INJECTION SITE MUSCLE WEAKNESS (I have no strength in my right arm at all). The patient was treated with PARACETAMOL (TYLENOL) on 10-Sep-2022 at an unspecified dose and frequency. At the time of the report, VACCINATION SITE MOVEMENT IMPAIRMENT (Can't raise my right arm) and INJECTION SITE MUSCLE WEAKNESS (I have no strength in my right arm at all) had not resolved and INFLUENZA LIKE ILLNESS (I had flu-like symptoms), FEELING HOT (Was hot) and PYREXIA (I think I had a fever) had resolved. On an unknown date the patient received first dose of Moderna vaccine, full dose with unknown lot number. On an unknown date the patient received second dose of Moderna vaccine, full dose with unknown lot number. On an unknown date the patient received first booster of Moderna vaccine, booster dose with unknown lot number. On an unknown date the patient received second booster of Moderna vaccine, booster dose with unknown lot number. Patient reported no side effects from the previously administered four doses of Moderna vaccines.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site muscle weakness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: No medical history reported. It was unknown if the patient ever had COVID positive test or diagnosis.
Andere Medikamente: FLU [INFLUENZA VACCINE]
Allergien: -
Vorherige Impfungen: -

VAERS 2452170

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: LA
Alter: 36,0
Geschlecht: F
Eingang: 20.09.2022
Impfdatum: 03.09.2022
Beginn: 13.09.2022
Tage bis Beginn: 10,0
Dosis: 5
Route/Site: SYR / RA

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

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

Symptomtext

On 09/03/2022 I had my vaccination. I woke up on 09/13/2022 with a cough congestion and some general fatigue. I took a at home COVID-19 test and it was negative. On 09/14/2022 I went to urgent care and tested COVID-19 Positive. I started Plaxovid on 09/14/2022. I am still having some chest congestion and cough on 09/20/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 09/14/2022 COVID-19 Positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Obese
Andere Medikamente: Trazadone; Multivitamin
Allergien: Penicillin; Cherries; Red Dye #40
Vorherige Impfungen: -

VAERS 2452161

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: CT
Alter: 63,0
Geschlecht: F
Eingang: 20.09.2022
Impfdatum: 09.09.2022
Beginn: 11.09.2022
Tage bis Beginn: 2,0
Dosis: 5
Route/Site: IM / LA

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

Dizziness Fatigue Impaired work ability Injection site erythema

Symptomtext

Received Moderna Bivalent Vaccine (Covid Vax #5 for me), on Friday, September 9. On Sunday, September 11, I I experienced a large red spot on my arm, located below the injection site which lasted up to 4 days until it started to fade. From Sunday, September 11 to Friday September 16, I experienced unexplained dizziness, light-headed feeling and fatigue to which I was unable to work.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: Was prescribe Bactin antibiotic from Walk in Clinic on Monday, September 12 for potential infection, and Prednisone (in which I did not take). Called HCP and instructed me to stop the antibiotic after only taken three pills.
Aktuelle Erkrankungen: None
Vorgeschichte: High-cholesterol
Andere Medikamente: Ritalin, Premarin, crestor, metformin
Allergien: None
Vorherige Impfungen: -

VAERS 2451972

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: TX
Alter: 53,0
Geschlecht: F
Eingang: 20.09.2022
Impfdatum: 11.09.2022
Beginn: 14.09.2022
Tage bis Beginn: 3,0
Dosis: 4
Route/Site: SYR / LA

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

Urticaria

Symptomtext

I started getting small hives on my legs, torso and face- consulted my doctor who I had seen earlier in the week for a poison ivy infection. New hives looked very different from area affected by poison ivy. Dr. changed my morning antihistamine from Allegra to Levocetirizine to help as well as prescribing a steroid cream for the spots on my face. Steroid cream did help the spots on my face. However, I am now 8 days post injection and new small hives are still appearing all over my body.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Urticaria
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Was experiencing poison ivy outbreak at time of vaccination
Vorgeschichte: High Blood Pressure
Andere Medikamente: Benadryl , Allegra, Flonase, lisinopril, probiotic, estroven
Allergien: Zpac
Vorherige Impfungen: -

VAERS 2451480

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: TX
Alter: 67,0
Geschlecht: M
Eingang: 19.09.2022
Impfdatum: 16.09.2022
Beginn: 17.09.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Asthenia Diarrhoea Fatigue Influenza like illness Pain in extremity

Symptomtext

Flu like symptoms, diarrhea, weakness/tired and sore arm.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: Heart Atrial Fibrillation, High Blood Pressure High Cholesterol
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: Sore arm

VAERS 2451297

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: MS
Alter: 68,0
Geschlecht: F
Eingang: 19.09.2022
Impfdatum: 16.09.2022
Beginn: 17.09.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / -

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

Injection site urticaria Pyrexia Urticaria

Symptomtext

Patient came in and spoke with RPh. Patient awoke feeling feverish. She then noticed a welp on arm at the injection site. On 9/19/2022 at 5 P.M. the reaction site measured 4 inches long by 2 & 1/2 inches in diamter. Patient stated she did not have any reaction to her previous Moderna primary series or her additional booster dose. She did not have any breathing issues or any other involvement except at the local site. Patient is going to take Benadryl tonight and if doesn't see improvement she will see her physician tomorrow for followup.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site urticaria
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension
Andere Medikamente: Lisinopril-HCTZ 20/12.5 1 daily
Allergien: No allergies listed
Vorherige Impfungen: -

VAERS 2451038

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7144B

mild

Staat: SC
Alter: 70,0
Geschlecht: M
Eingang: 19.09.2022
Impfdatum: 10.09.2022
Beginn: 17.09.2022
Tage bis Beginn: 7,0
Dosis: 5
Route/Site: IM / LA

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

Dizziness Electrocardiogram abnormal Ventricular extrasystoles

Symptomtext

On 9/17/22 I experienced dizziness. EKG on Watch showed numerous premature ventricular contractions (I am a physician). PVCs resolved within 30 minutes. Dizziness resolved by late afternoon.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension, hyper cholesterolemia
Andere Medikamente: Lisinopril, Lovastatin, Oxybutinin, Ampicillin, Clarythromycin, Nexium
Allergien: Yellow fever vaccine
Vorherige Impfungen: Yellow fever vaccine in 1981- airway constriction

VAERS 2450965

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: GA
Alter: 64,0
Geschlecht: F
Eingang: 19.09.2022
Impfdatum: 16.09.2022
Beginn: 16.09.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Immunisation reaction Injection site erythema Injection site pruritus Injection site swelling Pruritus

Symptomtext

PATIENT REPORTED IMMEDIATE ITCHING AROUND THE ARM AND CHEST. SPORADICALLY CHANGED TO DIFFERENT BODY AREAS. 24 HOURS AFTERWARDS PATIENT REPORTED "COVID ARM" RED, ITCHY, LIGHTLY RAISED INJECTION SITE AREA.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: NO OTHER ILLNESSES
Vorgeschichte: GIANT CELL ARTERITIS - CHRONIC CONDITION AND COMPLEX REGIONAL PAIN SYNDROME
Andere Medikamente: PROGESTERONE E4M 75MG AND VIVELLE 0.0375MCG
Allergien: BLUBERRIES
Vorherige Impfungen: -

VAERS 2450921

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7144B

mild

Staat: MD
Alter: 66,0
Geschlecht: F
Eingang: 19.09.2022
Impfdatum: 12.09.2022
Beginn: 14.09.2022
Tage bis Beginn: 2,0
Dosis: 5
Route/Site: IM / LA

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

Blood test normal Diarrhoea Diarrhoea haemorrhagic Gastrointestinal pain Rectal haemorrhage Urine analysis normal

Symptomtext

At 11:30PM on the 14th of September I started with extreme intestinal cramping followed by explosive diarrhea at 4AM the diarrhea turned bloody and ran out of diarrhea it but the blood sporadically continued until stopping at 9PM September 15 2022. At 8AM on the 15th of September 2022 my Primary care physician instructed me to go to the emergency room, I was examined and given fluids, blood work and urine tests were given which resulted in a hospital admission for observation. Colonoscopy recommended.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: Blood and Urine analysis. Colonoscopy recommended.
Aktuelle Erkrankungen: No.
Vorgeschichte: Brain Tumor; Neuro Fibromatosis; IBS;
Andere Medikamente: Zyrtec; Vitamin B 12; Vitamin D 3; Treser Vision; Co Q 10; Turmeric;
Allergien: Antibiotics; Dilantin; Shrimp; Dust mites; Tres; Grass ; Weeds; Mold;
Vorherige Impfungen: -

VAERS 2450832

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7144B

mild

Staat: CT
Alter: 49,0
Geschlecht: F
Eingang: 19.09.2022
Impfdatum: 16.09.2022
Beginn: 17.09.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: - / -

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

Fatigue Lethargy

Symptomtext

Extreme fatigue. Could be because of having flu shot and covid booster at same time, but the lethargy I've been feeling is unusual

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Taking Nurtec (every other day) - calcium, fish oil, acidophilus, glucosamine chondrointin
Allergien: Celery, penicillin
Vorherige Impfungen: -

VAERS 2450804

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge as7144b

mild

Staat: OH
Alter: 72,0
Geschlecht: F
Eingang: 19.09.2022
Impfdatum: 06.09.2022
Beginn: 07.09.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Contusion Injection site bruising Injection site erythema Injection site pain Injection site swelling Myasthenia gravis Pain

Symptomtext

Site: Bruising at Injection Site-Severe, Site: Pain at Injection Site-Medium, Site: Redness at Injection Site-Medium, Site: Swelling at Injection Site-Severe, Systemic: Body Aches Generalized-Severe, Additional Details: patient suffers from myasthenia gravis. adverse of the vaccine are still showing on day 8 after injection. patient visited her neurologist who informed her she may need infusions as it may be leading up to an episode. patients arm was still heavily bruised, although she said it was starting to feel better.

Weitere VAERSDATA-Felder

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

VAERS 2450798

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: OH
Alter: 75,0
Geschlecht: F
Eingang: 19.09.2022
Impfdatum: 15.09.2022
Beginn: 15.09.2022
Tage bis Beginn: 0,0
Dosis: N/A
Route/Site: IM / RA

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

Injection site bruising Injection site discolouration Injection site haemorrhage

Symptomtext

Site: Bruising at Injection Site-Mild, Additional Details: gave the COVID bivalent booster to patient. After taking out the needle, she did a normal and expected amount of bleeding. Once I stopped the bleeding after a few seconds, a bruise formed in the area. It got purple right around the injection site. Patient experienced no pain during and after the vaccination. She stated she bruises very easily. Bumping a table causes a bruise at home. Monitored patient for 15 minutes and followed up later, no adverse effects and she feels fine.

Weitere VAERSDATA-Felder

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

VAERS 2450651

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge as7144b

mild

Staat: FL
Alter: 63,0
Geschlecht: M
Eingang: 18.09.2022
Impfdatum: 09.09.2022
Beginn: 13.09.2022
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: IM / LA

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

Feeling abnormal Influenza like illness Malaise

Symptomtext

feeling of unwell, not self, felling flu like symptoms a few weeks after administration

Weitere VAERSDATA-Felder

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

VAERS 2450586

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: OH
Alter: 39,0
Geschlecht: M
Eingang: 18.09.2022
Impfdatum: 12.09.2022
Beginn: 12.09.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Injection site pain Injection site swelling

Symptomtext

Site: Pain at Injection Site-Severe, Site: Swelling at Injection Site-Severe

Weitere VAERSDATA-Felder

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

VAERS 2450523

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: MD
Alter: 73,0
Geschlecht: F
Eingang: 17.09.2022
Impfdatum: 12.09.2022
Beginn: 16.09.2022
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: IM / LA

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

Injection site erythema Injection site pruritus

Symptomtext

The patient called the pharmacy to report that around 8pm around 8pm she noticed redness and itchiness at the injection site. She is using Benadryl for the itchiness. She is monitoring the redness and will go to urgent care if it worsens or does not resolve within the next several days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: -
Andere Medikamente: -
Allergien: None
Vorherige Impfungen: -

VAERS 2449980

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: RI
Alter: 32,0
Geschlecht: M
Eingang: 17.09.2022
Impfdatum: 15.09.2022
Beginn: 15.09.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Chills Pain

Symptomtext

Full body aches starting 11 hours after vaccine and lasting a total of 36 hours. Chills starting at 11 hour and lasting for about 24 hours

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: Moderna 2nd dose

VAERS 2449877

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7144B

mild

Staat: NJ
Alter: 76,0
Geschlecht: M
Eingang: 17.09.2022
Impfdatum: 08.09.2022
Beginn: 08.09.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: OT / LA

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

Body temperature Cough Pain in extremity Pyrexia SARS-CoV-2 test

Symptomtext

developed a slight cough; 99.6 degree Fahrenheit fever; sore arm for 2 days; This spontaneous case was reported by a patient and describes the occurrence of COUGH (developed a slight cough), PYREXIA (99.6 degree Fahrenheit fever) and PAIN IN EXTREMITY (sore arm for 2 days) in a 76-year-old male patient who received mRNA-1273 BIVALENT (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. AS7144B) for COVID-19 prophylaxis. Patient had no allergies Patient never had COVID positive test or diagnosis Patient had no medical history relating to mentioned adverse event and both Acute and Chronic illnesses at the time of vaccination. On 08-Sep-2022, the patient received fifth dose of mRNA-1273 BIVALENT (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (unknown route) 1 dosage form. On 08-Sep-2022, the patient experienced PAIN IN EXTREMITY (sore arm for 2 days). On 13-Sep-2022, after starting mRNA-1273 BIVALENT (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)), the patient experienced COUGH (developed a slight cough) and PYREXIA (99.6 degree Fahrenheit fever). On 09-Sep-2022, PAIN IN EXTREMITY (sore arm for 2 days) had resolved. At the time of the report, COUGH (developed a slight cough) and PYREXIA (99.6 degree Fahrenheit fever) had not resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 13-Sep-2022, Body temperature: 99.6 degree Fahrenheit. In September 2022, SARS-CoV-2 test: (Negative) Negative and (Negative) Negative. No concomitant drug was reported. No other vaccines were given within 1 month prior to Moderna COVID-19 vaccine. On an unknow date patient received first dose of Moderna vaccine. On an unknow date patient received second dose of Moderna vaccine. On an unknown date patient received first booster dose of Moderna vaccine. On 31-Mar-2022 patient received second booster dose of Moderna vaccine (batch number: 046L21A). It was reported that patient had no side effects for the other Moderna vaccines. The adverse event did not cause patient to seek medical care. It was reported that new symptoms appeared and adverse event outcome was reported as ongoing. No treatment drug was reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: Test Date: 20220913; Test Name: Body temperature; Result Unstructured Data: 99.6 degree Fahrenheit; Test Date: 202209; Test Name: COVID-19 test; Test Result: Negative ; Result Unstructured Data: Negative; Test Date: 202209; Test Name: COVID-19 test; Test Result: Negative ; Result Unstructured Data: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: Patient had no allergies Patient never had COVID positive test or diagnosis Patient had no medical history relating to mentioned adverse event and both Acute and Chronic illnesses at the time of vaccination.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2449813

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7144B

mild

Staat: IL
Alter: 66,0
Geschlecht: M
Eingang: 17.09.2022
Impfdatum: 09.09.2022
Beginn: 09.09.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: OT / -

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

Body temperature Chills Headache Oropharyngeal pain Pain in extremity Pyrexia

Symptomtext

sore throat; arm was pretty sore; chills; fever of 101.7?F; headache; This spontaneous case was reported by a patient and describes the occurrence of OROPHARYNGEAL PAIN (sore throat), PAIN IN EXTREMITY (arm was pretty sore), CHILLS (chills), PYREXIA (fever of 101.7?F) and HEADACHE (headache) in a 66-year-old male patient who received mRNA-1273 BIVALENT (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. AS7144B) for COVID-19 vaccination. The patient's past medical history included COVID-19 (he was hospitalized) in March 2020, Hospitalization (due to COVID-19) in 2020, Meralgia paresthetica in 2014, Aortic valve insufficiency in 2018, Obstructive sleep apnoea syndrome (before COVID) and Cardiac catheterization. Concurrent medical conditions included Allergy to chemicals (Allergy to contrast dyes), Allergy to intravenous contrast media (Allergy to kidney IVP), Allergy to antibiotic (Allergy to Levaquin), Allergy to antibiotic (Allergy to Tetracycline), Seafood allergy (Allergy to certain sea food), Allergic reaction to bee sting (Allergy to bee stings), Fruit allergy (Allergy to certain melons), Restrictive pulmonary disease (Moderate restrictive lung disorder post COVID-19 sometimes worse because had periodic episodes) since 2020, Disease obstructive lung (post COVID-19, sometimes worse because he had periodic episodes) since 2020, Ankylosing spondylitis (Recent change in status such as improvement or worsening: improving) since 2016, Asthma (moderate persistent without complications, since 30 years ago, worse), Supraventricular tachycardia (aggravated with COVID but currently improving) since 2012, Sensory polyneuropathy (post COVID, still symptoms from this) since 2020, Neuropathy (occipital neuropathy, caused by COVID, still symptoms) since 2020, Hypothyroidism since 2014 and Chronic cough (after COVID, still symptoms) since 2020. Concomitant products included FLUTICASONE PROPIONATE, SALMETEROL XINAFOATE (ADVAIR), TIOTROPIUM BROMIDE (SPIRIVA [TIOTROPIUM BROMIDE]), ALBUTEROL [SALBUTAMOL], LEVOTHYROXINE, POTASSIUM CITRATE, ACETYLSALICYLIC ACID (ASPIRINE), FUROSEMIDE, MAGNESIUM GLUCONATE, VERAPAMIL, VITAMIN D [VITAMIN D NOS], ATORVASTATIN, OXYGEN and IPRATROPIUM BROMIDE for an unknown indication. On 09-Sep-2022, the patient received fifth dose of mRNA-1273 BIVALENT (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (unknown route) 1 dosage form. On 09-Sep-2022, the patient experienced OROPHARYNGEAL PAIN (sore throat), PAIN IN EXTREMITY (arm was pretty sore), CHILLS (chills), PYREXIA (fever of 101.7?F) and HEADACHE (headache). On 10-Sep-2022, OROPHARYNGEAL PAIN (sore throat), PAIN IN EXTREMITY (arm was pretty sore), CHILLS (chills), PYREXIA (fever of 101.7?F) and HEADACHE (headache) had resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, Body temperature: 101.7?F. In 17 or 18-February-2021, the patient received first dose of MODERNA COVID-19 VACCINE, (Intramuscular) 1 dosage form. On 17-Mar-2021, received second dose of MODERNA COVID-19 VACCINE, (unknown route) dosage was changed to 1 dosage form with the batch no 044A21A and Expiration date as 31-Aug-2021. On 04-Nov-2021, received third dose, 1st booster dose of MODERNA COVID-19 VACCINE,(unknown route) dosage was changed to 1 dosage form with the batch no 019F21A and Expiration date as20-Jan-2022. On 11-Apr-2022, received fourth dose of MODERNA COVID-19 VACCINE,(unknown route) dosage was changed to 1 dosage form with the batch no 028K21A. No treatment was given for symptoms. This case was linked to MOD-2021-045362 (Patient Link).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Test Name: Fever; Result Unstructured Data: 101.7?F
Aktuelle Erkrankungen: Allergic reaction to bee sting (Allergy to bee stings); Allergy to antibiotic (Allergy to Tetracycline); Allergy to antibiotic (Allergy to Levaquin); Allergy to chemicals (Allergy to contrast dyes); Allergy to intravenous contrast media (Allergy to kidney IVP); Ankylosing spondylitis (Recent change in status such as improvement or worsening: improving); Asthma (moderate persistent without complications, since 30 years ago, worse); Chronic cough (after COVID, still symptoms); Disease obstructive lung (post COVID-19, sometimes worse because he had periodic episodes); Fruit allergy (Allergy to certain melons); Hypothyroidism; Neuropathy (occipital neuropathy, caused by COVID, still symptoms); Restrictive pulmonary disease (Moderate restrictive lung disorder post COVID-19 sometimes worse because had periodic episodes); Seafood allergy (Allergy to certain sea food); Sensory polyneuropathy (post COVID, still symptoms from this); Supraventricular tachycardia (aggravated with COVID but currently improving)
Vorgeschichte: Medical History/Concurrent Conditions: Aortic valve insufficiency; Cardiac catheterization; COVID-19 (he was hospitalized); Hospitalization (due to COVID-19); Meralgia paresthetica; Obstructive sleep apnoea syndrome (before COVID)
Andere Medikamente: ADVAIR; SPIRIVA [TIOTROPIUM BROMIDE]; ALBUTEROL [SALBUTAMOL]; LEVOTHYROXINE; POTASSIUM CITRATE; ASPIRINE; FUROSEMIDE; MAGNESIUM GLUCONATE; VERAPAMIL; VITAMIN D [VITAMIN D NOS]; ATORVASTATIN; OXYGEN; IPRATROPIUM BROMIDE
Allergien: -
Vorherige Impfungen: -

VAERS 2449758

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7144B

mild

Staat: MI
Alter: 81,0
Geschlecht: M
Eingang: 17.09.2022
Impfdatum: 06.09.2022
Beginn: 07.09.2022
Tage bis Beginn: 1,0
Dosis: 5
Route/Site: OT / -

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

Body temperature Chills Pain in extremity Pyrexia SARS-CoV-2 test

Symptomtext

fever of 100.5; chills; Arm was hurting very badly; This spontaneous case was reported by a patient and describes the occurrence of PAIN IN EXTREMITY (Arm was hurting very badly), PYREXIA (fever of 100.5) and CHILLS (chills) in an 81-year-old male patient who received mRNA-1273 BIVALENT (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. AS7144B) for COVID-19 prophylaxis. No Medical History information was reported. On 06-Sep-2022, the patient received fifth dose of mRNA-1273 BIVALENT (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (Intramuscular) 1 dosage form. On 07-Sep-2022, the patient experienced PAIN IN EXTREMITY (Arm was hurting very badly). On 08-Sep-2022 at 5:00 AM, the patient experienced PYREXIA (fever of 100.5) and CHILLS (chills). The patient was treated with PARACETAMOL (TYLENOL) ongoing from 08-Sep-2022 at an unspecified dose and frequency. At the time of the report, PAIN IN EXTREMITY (Arm was hurting very badly) and CHILLS (chills) outcome was unknown and PYREXIA (fever of 100.5) had not resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 08-Sep-2022, Body temperature: 100.5. On 08-Sep-2022, SARS-CoV-2 test: (Negative) Negative. Patient received 4 doses of the Moderna COVID-19 vaccine by intramuscular injection on 6FEB2021 (lot number 023M20A), On 26MAR2021 (lot number 018B21A), On 29OCT2021 (lot number 014F21A), and On 4APR2022 (lot number 048L21A). No concomitant medications were reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Test Date: 20220908; Test Name: Body temperature; Result Unstructured Data: 100.5; Test Date: 20220908; Test Name: rapid home covid test; Test Result: Negative ; Result Unstructured Data: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2448554

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: CA
Alter: 72,0
Geschlecht: F
Eingang: 17.09.2022
Impfdatum: 14.09.2022
Beginn: 15.09.2022
Tage bis Beginn: 1,0
Dosis: 5
Route/Site: IM / LA

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

Abnormal dreams Anxiety Headache Pain Pyrexia

Symptomtext

First the usual head ache, fever and achy body. I also had disturbing dreams for 2 nights and woke up with intense anxiety the morning after, and some the second morning.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: Not test, I got the new covid vaccination
Aktuelle Erkrankungen: None
Vorgeschichte: Slightly high cholesterol
Andere Medikamente: No over the counter or prescription taken at this time or any time.
Allergien: No allergies, bloody nose with aspirin
Vorherige Impfungen: -

VAERS 2448447

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: PA
Alter: 37,0
Geschlecht: F
Eingang: 17.09.2022
Impfdatum: 16.09.2022
Beginn: 16.09.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Asthenia Chills Fatigue Feeling hot Headache Hyperhidrosis Lymphadenopathy Nausea Pain Pyrexia

Symptomtext

Fatigue, Weakness, Fever, swollen lymph nodes (swollen in neck), Nausea, Body Aches, Chills, Sweating, body always felt hot and over heated , headache Used Motrin and Tylenol to help the symptoms

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma, MTHFR mutation, primary left vena cava, GERD
Andere Medikamente: Daily Multi vitamin, Iron Supplements, B Complex Pill, Fish Oil Tab, Sigulair, Allegra, Baby Aspirin, Trelegy Inhaler, Dupiexnt Injection bi weekly, Spirivia Inhaler, Protonix Tablet
Allergien: Sulfa Drug Allergy
Vorherige Impfungen: Moderna Covid, 36 years old

VAERS 2448439

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: MA
Alter: 54,0
Geschlecht: M
Eingang: 17.09.2022
Impfdatum: 10.09.2022
Beginn: 11.09.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

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

Axillary mass Axillary pain Fatigue Injection site pain Injection site swelling Lethargy Lymphadenopathy

Symptomtext

Site: Pain at Injection Site-Severe, Site: Swelling at Injection Site-Severe, Systemic: Exhaustion / Lethargy-Medium, Systemic: pain/bubble under armpit of left arm-Severe, Systemic: Lymph Node Swelling-Severe, Additional Details: Patient is reporting pain, tenderness, and raised bubble type reaction under armpit of left arm that began 1 day after injection. There is also a tennis ball sized swollen area on side of chest close to armpit area that began 2 days after injection. Patient notified his PCP and will monitor for development or resolution of symptoms.

Weitere VAERSDATA-Felder

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

VAERS 2448067

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: TX
Alter: 55,0
Geschlecht: M
Eingang: 16.09.2022
Impfdatum: 13.09.2022
Beginn: 14.09.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

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

Chills Hyperhidrosis Injection site hypoaesthesia Injection site pain Pain Pyrexia Somnolence

Symptomtext

severe aches,high grade fever,chills,sweating over the course of 48 hours after which symptoms subsided. Also pain and numbness in left arm deltoid where vaccine administered "DEAD ARM"...Symptoms subsided after @48hours when first noticed but a residual "grogginess"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: NONE
Vorgeschichte: asthma...high blood pressure
Andere Medikamente: valclavocyir lisinopril
Allergien: NONE
Vorherige Impfungen: -

VAERS 2447953

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge as7144b

mild

Staat: PA
Alter: 74,0
Geschlecht: F
Eingang: 16.09.2022
Impfdatum: 14.09.2022
Beginn: 14.09.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / LA

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

Diarrhoea Headache Pyrexia

Symptomtext

fever,diarrhea, headache

Weitere VAERSDATA-Felder

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

VAERS 2447621

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge as7144b

mild

Staat: CT
Alter: 63,0
Geschlecht: F
Eingang: 16.09.2022
Impfdatum: 09.09.2022
Beginn: 11.09.2022
Tage bis Beginn: 2,0
Dosis: 5
Route/Site: IM / LA

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

Injection site erythema Injection site swelling Rash

Symptomtext

Site: Redness at Injection Site-Mild, Site: Swelling at Injection Site-Mild, Systemic: Allergic: Rash Generalized-Mild

Weitere VAERSDATA-Felder

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

VAERS 2447609

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: FL
Alter: 63,0
Geschlecht: F
Eingang: 16.09.2022
Impfdatum: 13.09.2022
Beginn: 13.09.2022
Tage bis Beginn: 0,0
Dosis: N/A
Route/Site: IM / LA

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

Asthenia Decreased appetite Dizziness Feeding disorder Feeling abnormal Headache Myalgia Nausea Pyrexia Retching Sleep disorder

Symptomtext

After about 6 hours, I felt weak and began having muscle aches all over. I developed a headache, had no appetite and felt feverish, but did not take my temperature. The nausea began around 10pm and lasted until the morning of 9/15/2022 (32 hours). Dry heaves and dizziness were experienced on 9/14/2022. I felt bad for a day and a half, unable to sleep or eat. I was surprised to have severe side effects after having no adverse effects from two Janssen shots in 2021 and the Pfizer booster in May 2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: None
Vorgeschichte: Heart failure; high blood pressure
Andere Medikamente: Valsartan; Furosemide; Carvedilol; Spironolactone; Vit D; Aspirin
Allergien: None
Vorherige Impfungen: -

VAERS 2446412

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7144B

mild

Staat: CA
Alter: 51,0
Geschlecht: F
Eingang: 15.09.2022
Impfdatum: 09.09.2022
Beginn: 10.09.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

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

Abdominal pain upper Diarrhoea Eructation Flatulence Gastritis Influenza virus test Nausea Pain SARS-CoV-2 test

Symptomtext

The morning of 9/10 I woke up feeling achy, extremely nauseated and diarrhea twice. I started taking Zofram to avoid vomiting. I experienced really bad upper stomach cramps and pain with a lot of gas and burping. It continued the next day and I went to the urgent care on 9/11 because the pain and gas was constant. Doctor advised that vaccine had caused inflammation in my stomach lining. She provided medication there at the urgent care and we waited 15 minutes and we saw that the medication was helping. She advised that I buy Gas-X and tums and she gave me a prescription for Omeprazole. I went back to the urgent care on 9/14 and advised doctor that I still had stomach pain and burping but its not as constant nor as severe but comes on randomly. As of 9/15 I feel better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain upper
Hospital-Tage: -
Labordaten: COVID test and Flu Test
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: Each COVID vaccine I had typical arm soreness and headaches

VAERS 2445041

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: MI
Alter: 76,0
Geschlecht: F
Eingang: 14.09.2022
Impfdatum: 12.09.2022
Beginn: 14.09.2022
Tage bis Beginn: 2,0
Dosis: 4
Route/Site: IM / LA

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

Injection site pruritus Injection site rash Injection site reaction Injection site warmth Rash erythematous

Symptomtext

At site, slightly itchy, warm to touch, red rash around site

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pruritus
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: None
Vorgeschichte: back issues spinal stenosis. gastric reflux
Andere Medikamente: 300 mg gabapentin (1/day), Vitamin D3 50 mcg (1/day), calcium 600 mg (2/day) , L-thyroxine 112 mcg (1/day), Venlafaxine 37.5 mg (1/day), omeprazole 20 mg (1/day), 1 baby aspirin per day, Aller-tec 1 per day, acid controller 1 per day.
Allergien: None
Vorherige Impfungen: -

VAERS 2445020

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: CA
Alter: 73,0
Geschlecht: F
Eingang: 14.09.2022
Impfdatum: 09.09.2022
Beginn: 10.09.2022
Tage bis Beginn: 1,0
Dosis: 5
Route/Site: IM / RA

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

Extra dose administered Injection site erythema Injection site pain Injection site pruritus Injection site swelling Injection site warmth

Symptomtext

Arm swollen from injection site to elbow. Red, hot, painful, at same time, itchy. Tried benadryl 2 days after didn't help. took3+ days until it resolved. Didn't happen with any of the other injections, although I had some usual pain at injection site previously. Ist booster sent me to bed with chills, fever and aching legs. Gone by next day. (probably should have reported that one!)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: bronchiectasis
Andere Medikamente: none at time
Allergien: gluten, lactose
Vorherige Impfungen: See previous explanation Was also a moderna booster (but was full strength for some immunity issues.

VAERS 2444974

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: NV
Alter: 76,0
Geschlecht: F
Eingang: 14.09.2022
Impfdatum: 12.09.2022
Beginn: 12.09.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / LA

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

Fatigue Headache Pain

Symptomtext

Afternoon of the shot: mild body aches, fatigue, headache. Next day - 9/13: body aches gone. Still fatigue, worse headache. Went to bed 4:30pm. Woke up nearly every hour. Got up at 7:30am the next morning (9/14). Feeling back to normal.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: Trip to hospital for dizziness. No cause found.
Vorgeschichte: Difficulty breathing due to several months of taking amiodarone several years ago.
Andere Medikamente: None.
Allergien: Amiodarone
Vorherige Impfungen: About 5 hrs. after receiving flu shot, suddenly became extremely tired. Went to bed. Slept 24 hrs. nonstop. Age approx. 52, don'

VAERS 2442945

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: TX
Alter: 37,0
Geschlecht: F
Eingang: 13.09.2022
Impfdatum: 12.09.2022
Beginn: 12.09.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Arthralgia Headache Myalgia Pain in extremity

Symptomtext

headache severe muscle pain and joint pain severe pain on the injection arm

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: sulfur; ragweed; cedar
Vorherige Impfungen: first Mondera booster

VAERS 2442910

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: TX
Alter: 30,0
Geschlecht: F
Eingang: 13.09.2022
Impfdatum: 08.09.2022
Beginn: 09.09.2022
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: SYR / LA

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

Cough Diarrhoea Dizziness Dry throat Fatigue Injection site inflammation Myalgia Nausea Oropharyngeal pain Productive cough Throat irritation

Symptomtext

I woke up approximately 7-8 hours after vaccination (September 9th) with extreme fatigue, dizziness, nausea, diarrhea, muscle soreness, and injection site inflammation (this was on both arms, but was far more pronounced on my left arm where I got my COVID booster shot). After 24 hours only fatigue, dizziness, and muscle soreness remained. The fatigue and muscle soreness are still ongoing, but at a significantly lower level than on the 9th. On the evening of September 12th (about 4 days after vaccination) my throat felt dry and scratchy, and I had a slight dry cough. On the morning of September 13th I woke up with a wetter, phlegmy cough and occasional sharp pain in my upper respiratory track/throat.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 2440762

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7144B

mild

Staat: FL
Alter: 65,0
Geschlecht: F
Eingang: 12.09.2022
Impfdatum: 06.09.2022
Beginn: 06.09.2022
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 Immunisation reaction Infection Injection site erythema Injection site pain Injection site swelling Injection site warmth Pain

Symptomtext

I received my fifth dose of my Moderna vaccine at the same time as receiving my flu shot. I had the soreness that I always have, but suddenly the injection site on my left arm got really red and swollen and hot and then it spread down to the top of my elbow and up toward my armpit and my left breast. I was in a lot of pain for a few days. I had a telehealth appointment where my doctor indicated that I either had an infection from the person not cleaning the area properly or a reaction to the vaccine. He put me on prednisone and Cephalexin on 09/09/2022. From 09/09/2022 to 09/11/2022 I noticed during that time that my blood pressure would get high, and thing were worse when I laid down. There were two nights where I would wake up and when I got up, I was in a lot of pain. As of today, my swelling has gone away, and I have a bit of tenderness but only in the localized area of the injection and it is very light.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma; High Cholesterol; Hypothyroid
Andere Medikamente: Atorvastatin; Advair Inhaler; Levothyroxine; Estradiol vaginal cream; Multivitamin with iron; Turmeric; Calcium with Magnesium; Glucosamine: Vitamin D3; Wall zinc; Biotin; Probiotics
Allergien: Codeine; Opioids; Lactose Intolerance
Vorherige Impfungen: -

VAERS 2440742

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: PA
Alter: 46,0
Geschlecht: F
Eingang: 12.09.2022
Impfdatum: 08.09.2022
Beginn: 09.09.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: SYR / LA

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

Asthenia Diarrhoea Fatigue Headache Loss of personal independence in daily activities Nausea Vomiting

Symptomtext

Extreme nausea, headache, and fatigue, persisting from 30 hour post-injection until ~90 hours post-injection. This was accompanied by intermittent diarrhea and vomiting. The level of nausea and headache were debilitating and required full cessation of all ordinary life activities.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: None. No medical attention was sought; symptoms were handled by rest and hydration.
Aktuelle Erkrankungen: None.
Vorgeschichte: None.
Andere Medikamente: None
Allergien: None known.
Vorherige Impfungen: -

VAERS 2440659

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: GA
Alter: 24,0
Geschlecht: F
Eingang: 12.09.2022
Impfdatum: 09.09.2022
Beginn: 09.09.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Hypersensitivity Urticaria

Symptomtext

Allergic Reaction; Broke out in hives.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Urticaria
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2440120

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: NY
Alter: 35,0
Geschlecht: F
Eingang: 11.09.2022
Impfdatum: 08.09.2022
Beginn: 09.09.2022
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: IM / LA

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

Injection site erythema Injection site nodule Injection site pruritus Injection site swelling

Symptomtext

Nodules developed under the skin at both injection sites They both turned bright red with the bump and itched a little. The COVID shot had a bigger nodule than the flu. I?m worried it could mean the shots did not make into the muscle and the vaccine built up in my tissue. They are still there but have not grown in size

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Hepatitis C, treated and cured Severe acid reflux
Andere Medikamente: Omeprazole 40mg daily Famotidine 20mg daily Calcium 600mg daily Vitmain D3 20mcg daily
Allergien: N/A
Vorherige Impfungen: Same reaction to two Pfizer COVID vaccines received in March 2021. The nodule was bigger that time and the redness was all down

VAERS 2440101

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: AL
Alter: 41,0
Geschlecht: F
Eingang: 11.09.2022
Impfdatum: 09.09.2022
Beginn: 09.09.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Arthralgia Fatigue Myalgia Pain of skin Pyrexia

Symptomtext

Starting 2 hours after vaccine, mild fever, severe fatigue, and severe joint, muscle, and skin pain lasting 36 hours. Tylenol 1000mg used every 6 hours provided only mild relief. After 36 hours mild fever is still present but pain is now mild to moderate and fatigue is moderate.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Ehlers Danlos syndrome, Mast cell activation syndrome, Neurocardiogenic syncope, Pelvic congestion syndrome, polycystic ovarian syndrome
Andere Medikamente: Pindolol, midodrine, duloxetine, pregabalin, progesterone, Claritin, Montelukast, cromolyn sodium, quercetin, turmeric.
Allergien: Sulfa, gluten, latex, whooping cough vaccine
Vorherige Impfungen: April 2021, age 40, Johnson and Johnson vaccine, severe bodyaches, fever, fatigue

VAERS 2440089

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge As7144b

mild

Staat: OH
Alter: 48,0
Geschlecht: F
Eingang: 11.09.2022
Impfdatum: 09.09.2022
Beginn: 10.09.2022
Tage bis Beginn: 1,0
Dosis: N/A
Route/Site: IM / RA

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

Injection site erythema Injection site pain Injection site rash Injection site swelling Pruritus

Symptomtext

Rash and red swelling of right arm below injection site. Very itchy. Injection site painful. Worse 2 days later.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Omeprezole, pravastatin, Qvar inhaler
Allergien: Sulfa drugs
Vorherige Impfungen: -

VAERS 2439486

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7144B

mild

Staat: MD
Alter: 57,0
Geschlecht: F
Eingang: 10.09.2022
Impfdatum: 07.09.2022
Beginn: 07.09.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Hypoaesthesia Injection site pain

Symptomtext

Site: Pain at Injection Site-Mild, Systemic: mild numbness on face-Mild, Systemic: Numbness (specify: facial area, extremities)-Mild, Additional Details: facial numbness on left side (side of vaccination).

Weitere VAERSDATA-Felder

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

VAERS 2438717

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge As7144b

mild

Staat: CT
Alter: 53,0
Geschlecht: F
Eingang: 10.09.2022
Impfdatum: 06.09.2022
Beginn: 07.09.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: SYR / LA

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

Diarrhoea

Symptomtext

Severe watery diarrhea for beginning day 2 after vaccine and continues into day 4.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Alopecia Ibs
Andere Medikamente: Lexapro 10mg Estradiol patch .025mg
Allergien: None
Vorherige Impfungen: -

VAERS 2436347

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: IL
Alter: 35,0
Geschlecht: M
Eingang: 09.09.2022
Impfdatum: 07.09.2022
Beginn: 08.09.2022
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: IM / -

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

Axillary pain Fatigue Flushing Headache Injection site pain Lymphadenitis Oedema peripheral Skin warm Sluggishness

Symptomtext

Arm soreness around injection site was more pronounced than typical. The day following the vaccination significant swelling and soreness/tenderness in the Patient's left armpit (same arm as the injection). It seems that the lymph node in the armpit is inflamed. Swelling is especially noticeable when compared to the unaffected side. No swelling, tenderness, or inflammation noticed in the armpit area on Patient's right side (non-injection arm). Other symptoms noticed that day include: sluggishness, tiredness, headache, and skin feeling flush/warm (temperature taken with no elevated temperature reading).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Axillary pain
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Vitamin A 10,000 IU (1 dose per day)
Allergien: -
Vorherige Impfungen: -

VAERS 2433389

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge as7144b

mild

Staat: TX
Alter: 76,0
Geschlecht: M
Eingang: 08.09.2022
Impfdatum: 04.09.2022
Beginn: 04.09.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: SYR / LA

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

Injection site erythema Injection site swelling

Symptomtext

Site: Redness at Injection Site-Mild, Site: Swelling at Injection Site-Mild, Additional Details: Patient felt okay no symptoms but injection site swole up and had a bubble around it. the injection site was red and swollen. Patient waited 15 min and was given an ice pack. the swelling was reduced but still a bump at injection site. patient felt fine no different then before and went home after 15 minutes.

Weitere VAERSDATA-Felder

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

VAERS 2433388

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge as7144b

mild

Staat: CT
Alter: 57,0
Geschlecht: M
Eingang: 08.09.2022
Impfdatum: 04.09.2022
Beginn: 04.09.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dry throat Fatigue Flushing Hyperhidrosis Lethargy

Symptomtext

Systemic: Exhaustion / Lethargy-Mild, Systemic: Flushed / Sweating-Mild, Additional Details: pt said his throat felt dry, but had no issues swallowing or breathing.

Weitere VAERSDATA-Felder

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

VAERS 2431841

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: SC
Alter: 29,0
Geschlecht: F
Eingang: 07.09.2022
Impfdatum: 03.09.2022
Beginn: 05.09.2022
Tage bis Beginn: 2,0
Dosis: UNK
Route/Site: SYR / LA

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

Chills Pruritus Rash Rash erythematous Rash macular

Symptomtext

Night of injection I had chills around 12 am but next day fine. On the second day I started getting itchy on my right arm, I thought a mosquito had bit me. Went to check and noticed both arms were covered in red blotches. Went to store to get hydrocortisone cream and Benadryl. Got home and noticed more red spots on my legs and lower back. I?m currently on day 3. I have also taken Zyrtec and Claritin.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Rheumatoid Athritis
Andere Medikamente: Had hep B vaccine (dose 1) placed the day before 9/2/22. Take Aleve daily.
Allergien: Coconut
Vorherige Impfungen: -

VAERS 2430075

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

mild

Staat: TX
Alter: 26,0
Geschlecht: F
Eingang: 06.09.2022
Impfdatum: 04.09.2022
Beginn: 05.09.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: SYR / RA

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

Injection site erythema Injection site swelling Pyrexia

Symptomtext

Recurring fever of 100-101?F lasting at least two days. Injection site swollen and red.

Weitere VAERSDATA-Felder

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

VAERS 2428842

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge As7144b

mild

Staat: IL
Alter: 37,0
Geschlecht: F
Eingang: 04.09.2022
Impfdatum: 02.09.2022
Beginn: 03.09.2022
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: - / -

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

Chills Nausea Pain Vomiting

Symptomtext

Approximately 12 hours after the vaccine was administered I experienced severe aches- so severe that extra strength ibuprofen and Tylenol did nothing for. I also experienced severe nausea and vomiting that lasted for 6 hours. It is now almost 48 hours post vaccine and I am still very achey and am experiencing chills.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: No prior illness
Vorgeschichte: None
Andere Medikamente: Pristiq, trazadone, xyzal
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 2428704

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge As7144b

mild

Staat: CO
Alter: 38,0
Geschlecht: M
Eingang: 04.09.2022
Impfdatum: 03.09.2022
Beginn: 04.09.2022
Tage bis Beginn: 1,0
Dosis: N/A
Route/Site: IM / RA

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

Headache Tinnitus

Symptomtext

Bad constant tinnitus/ringing in ears and extreme headache.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma (extremely mild)
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2698684

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: NY
Alter: 48,0
Geschlecht: M
Eingang: 19.10.2023
Impfdatum: 03.09.2022
Beginn: 01.10.2022
Tage bis Beginn: 28,0
Dosis: 4
Route/Site: - / -

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

Vitiligo

Symptomtext

Vitiligo; This spontaneous case was reported by a patient and describes the occurrence of VITILIGO (Vitiligo) in a 48-year-old male patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. AS7144B) for COVID-19 prophylaxis. The patient had never been tested positive for COVID-19. The patient no acute illness at the time of vaccination or up to one month before. The patient no chronic illness. Previously administered products included for COVID-19 prophylaxis: MODERNA COVID-19 VACCINE (First Dose LOT: 04A21A) on 12-Mar-2021, Moderna Covid-19 Vaccine (Second dose LOT:036B21A) on 09-Apr-2021 and Moderna Covid-19 Vaccine (Third Dose LOT:065FC21A) on 20-Nov-2021. Past adverse reactions to the above products included No adverse event with MODERNA COVID-19 VACCINE, Moderna Covid-19 Vaccine and Moderna Covid-19 Vaccine. Concurrent medical conditions included Drug allergy (sulfa drugs). On 03-Sep-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. In October 2022, the patient experienced VITILIGO (Vitiligo). At the time of the report, VITILIGO (Vitiligo) had not resolved. For mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (Unknown), the reporter considered VITILIGO (Vitiligo) to have an unknown relationship. It was reported that the patient always wore masks. The patient had not experienced similar events in the past. No concomitant medication was reported. Due to the event the patient visited the dermatologist on 01-Nov-2022. No treatment information was reported. Most recent FOLLOW-UP information incorporated above includes: On 16-Oct-2023: Significant follow-up received. Reporter details updated. Patient details updated. Current condition added. Previous doses batch number updated. Suspect administration date was updated. Reporter causality updated.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Vitiligo
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Drug allergy (sulfa drugs)
Vorgeschichte: Comments: The patient had never been tested positive for COVID-19. The patient no acute illness at the time of vaccination or up to one month before. The patient no chronic illness.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2695236

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: FL
Alter: 74,0
Geschlecht: M
Eingang: 12.10.2023
Impfdatum: 07.09.2022
Beginn: 01.02.2023
Tage bis Beginn: 147,0
Dosis: 5
Route/Site: - / LA

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

COVID-19 Rhinorrhoea SARS-CoV-2 test

Symptomtext

the patient had a very mild case of COVID-19, the patient tested positive and had the sniffles for one day; the patient had a very mild case of COVID-19, the patient tested positive and had the sniffles for one day; This spontaneous case was reported by a patient and describes the occurrence of RHINORRHOEA (the patient had a very mild case of COVID-19, the patient tested positive and had the sniffles for one day) and COVID-19 (the patient had a very mild case of COVID-19, the patient tested positive and had the sniffles for one day) in an elderly male patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. AS7144B) for COVID-19 prophylaxis. No Medical History information was reported. On 07-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. In February 2023, the patient experienced RHINORRHOEA (the patient had a very mild case of COVID-19, the patient tested positive and had the sniffles for one day) and COVID-19 (the patient had a very mild case of COVID-19, the patient tested positive and had the sniffles for one day). At the time of the report, RHINORRHOEA (the patient had a very mild case of COVID-19, the patient tested positive and had the sniffles for one day) and COVID-19 (the patient had a very mild case of COVID-19, the patient tested positive and had the sniffles for one day) had resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): In February 2023, SARS-CoV-2 test: Positive. 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 medication was reported. Reportedly, the patient received his first Moderna COVID-19 vaccine on 15-Jan-2021 with lot number 026L20A. Patient received in his left arm. The patient had no adverse reactions or side effects to 1st dose. The patient received his second Moderna COVID-19 vaccine on 02-Feb-2021 with lot number 029K20A. Patient received in his left arm. The patient had no adverse reactions or side effects to 2nd dose. The patient received his first booster dose of Moderna COVID-19 vaccine on 24-Aug-2021 with lot number 002F21A. Patient received in his left arm. The patient had no adverse reactions or side effects to first booster dose. The patient received his second booster dose of Moderna COVID-19 vaccine on 03-Mar-2022 with lot number 045L21A. Patient received in his left arm. The patient had no adverse reactions or side effects to second booster dose. The patient received his third booster dose of Moderna COVID-19 vaccine on 07-Sep-2022 with lot number AS7144B. Patient received in his left arm. The patient had no adverse reactions or side effects to third booster dose. In Feb-2023 the patient had a very mild case of COVID-19, the patient tested positive and had the sniffles for one day. No treatment information was provided. This case was linked to US-MODERNATX, INC.-MOD-2023-744661 (Patient Link).

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 202302; Test Name: COVID-19 Virus Test; Test Result: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2666401

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: NV
Alter: 76,0
Geschlecht: F
Eingang: 04.08.2023
Impfdatum: 22.09.2022
Beginn: -
Tage bis Beginn: -
Dosis: 5
Route/Site: OT / -

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

Atrial fibrillation COVID-19

Symptomtext

afib; COVID-19; This spontaneous case was reported by a patient and describes the occurrence of ATRIAL FIBRILLATION (afib) and COVID-19 (COVID-19) 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. AS7144B) for COVID-19 prophylaxis. No Medical History information was reported. On 22-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 an unknown date, the patient experienced ATRIAL FIBRILLATION (afib) (seriousness criteria hospitalization and medically significant) and COVID-19 (COVID-19) (seriousness criterion hospitalization). At the time of the report, ATRIAL FIBRILLATION (afib) had not resolved and COVID-19 (COVID-19) 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 medication was reported. Patient also received the Moderna COVID-19 Vaccine. It was reported that patient had been to the hospital 4 times with COVID-19 and afib in the past 8 weeks. No diagnosis of myocarditis or pericarditis. Hospital kept changing medications. No information on treatment. Company comment: This spontaneous case concerns a 76-year-old female patient with no medical history reported, who experienced Serious, unexpected (due to Hospitalization, Medically Significant criteria) AESI of atrial fibrillation and serious (hospitalization criteria) unexpected event of COVID-19. A dose of mRNA-1273 Vaccine was administered as fifth dose in COVID 19 vaccination series. Previous vaccinations were not reported. The patient assisted to the hospital 4 times in 8 weeks due to the events. Medication was indicated (details not provided). At the time of the latest report, atrial fibrillation had not resolved; and the outcome of COVID-19 was unknown. The benefit-risk relationship of mRNA-1273 is not affected by this report.

Weitere VAERSDATA-Felder

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

VAERS 2651714

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: -
Alter: 75,0
Geschlecht: M
Eingang: 30.06.2023
Impfdatum: 27.09.2022
Beginn: 27.06.2023
Tage bis Beginn: 273,0
Dosis: 5
Route/Site: OT / -

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

Expired product administered No adverse event Product storage error

Symptomtext

Vaccine was initially stored in the refrigerator on 25 May 2023, vaccine was expired on 08 Jun 2023 and administer on 27 Jun 2023; No adverse event; Patient received an expired dose from lot number 043H22A; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient received an expired dose from lot number 043H22A), PRODUCT STORAGE ERROR (Vaccine was initially stored in the refrigerator on 25 May 2023, vaccine was expired on 08 Jun 2023 and administer on 27 Jun 2023) and NO ADVERSE EVENT (No adverse event) in a 75-year-old male patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch nos. 043H22A and AS7144B) for COVID-19 prophylaxis. No Medical History information was reported. 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 27-Jun-2023, received sixth 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 27-Jun-2023, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient received an expired dose from lot number 043H22A). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine was initially stored in the refrigerator on 25 May 2023, vaccine was expired on 08 Jun 2023 and administer on 27 Jun 2023) and NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient received an expired dose from lot number 043H22A), PRODUCT STORAGE ERROR (Vaccine was initially stored in the refrigerator on 25 May 2023, vaccine was expired on 08 Jun 2023 and administer on 27 Jun 2023) 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 (Patient received an expired dose from lot number 043H22A) and PRODUCT STORAGE ERROR (Vaccine was initially stored in the refrigerator on 25 May 2023, vaccine was expired on 08 Jun 2023 and administer on 27 Jun 2023). Concomitant medication not reported. The vial did not undergo any temperature excursions. Vial size was 2.5 ml Treatment medication not reported. This case was linked to US-MODERNATX, INC.-MOD-2023-730860 (E2B Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2023-730860:same reporter with diffrent patient

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2651713

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: -
Alter: 77,0
Geschlecht: F
Eingang: 30.06.2023
Impfdatum: 27.09.2022
Beginn: 27.06.2023
Tage bis Beginn: 273,0
Dosis: 5
Route/Site: OT / -

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

Expired product administered No adverse event Product storage error

Symptomtext

Vaccine was initially stored in the refrigerator on 25 May 2023, vaccine was expired on 08 Jun 2023 and administer on 27 Jun 2023; No adverse event; Patient received an expired dose from lot number 043H22A; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient received an expired dose from lot number 043H22A), PRODUCT STORAGE ERROR (Vaccine was initially stored in the refrigerator on 25 May 2023, vaccine was expired on 08 Jun 2023 and administer on 27 Jun 2023) and NO ADVERSE EVENT (No adverse event) in a 77-year-old female patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch nos. 043H22A and AS7144B) for COVID-19 prophylaxis. No Medical History information was reported. 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 27-Jun-2023, received sixth 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 27-Jun-2023, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient received an expired dose from lot number 043H22A). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine was initially stored in the refrigerator on 25 May 2023, vaccine was expired on 08 Jun 2023 and administer on 27 Jun 2023) and NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient received an expired dose from lot number 043H22A), PRODUCT STORAGE ERROR (Vaccine was initially stored in the refrigerator on 25 May 2023, vaccine was expired on 08 Jun 2023 and administer on 27 Jun 2023) 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 (Patient received an expired dose from lot number 043H22A) and PRODUCT STORAGE ERROR (Vaccine was initially stored in the refrigerator on 25 May 2023, vaccine was expired on 08 Jun 2023 and administer on 27 Jun 2023). Concomitant medication not reported. The vial did not undergo any temperature excursions. Vial size was 2.5 ml Treatment medication not reported. This case was linked to US-MODERNATX, INC.-MOD-2023-730851 (E2B Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2023-730851:same reporter with diffrent patient

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2641594

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: MA
Alter: 54,0
Geschlecht: M
Eingang: 06.06.2023
Impfdatum: 08.09.2022
Beginn: 12.09.2022
Tage bis Beginn: 4,0
Dosis: 5
Route/Site: SYR / AR

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

Acoustic stimulation tests Tinnitus

Symptomtext

Persistent tinnitus symptoms started 4 days later in the morning of Monday, Sep 12, 2022 and have continued through the present date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acoustic stimulation tests
Hospital-Tage: -
Labordaten: Audiology test and evaluation by ear doctor on Sep 20, 2022 Audiology test on April 3, 2023 Evaluation by hearing doctor on June 5, 2023
Aktuelle Erkrankungen: -
Vorgeschichte: IBS-C due to FODMAP foods
Andere Medikamente: Budesonide in nasal rinse, multivitamins and various vitamin supplements, zinc, vitamins B, C, D, K2, Biotin, CBD oil, pumpkin seed oil, flax see oil, oil of oregano, beta-sitosterol, probiotic supplement, turmeric, ginger.
Allergien: -
Vorherige Impfungen: -

VAERS 2638485

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: GA
Alter: 69,0
Geschlecht: F
Eingang: 30.05.2023
Impfdatum: 14.09.2022
Beginn: 01.03.2023
Tage bis Beginn: 168,0
Dosis: 5
Route/Site: IM / LA

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

Computerised tomogram normal Magnetic resonance imaging abnormal Scan with contrast abnormal Sleep disorder Thyroid mass Tinnitus

Symptomtext

I early March 2023, I started hearing my heartbeat in my ears. It was especially loud at night when I was trying to sleep, I could move my pillow around to get the heartbeat blocked out so that I could sleep. Then I started to be able to her my heartbeat throughout the day. I made an appointment with PCP to see if we could find out what was going on. she ordered a CT scan with contrast that came back normal, she then ordered an MRI with contrast that came back normal. She did find a nodule on my thyroid; I have been referred to a doctor for that. I was advised to go home to see if the heartbeat coming through my ears so loudly will calm down. It has been about month since I seen my PCP, I am still hearing my heartbeat in m ears.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Computerised tomogram normal
Hospital-Tage: -
Labordaten: 00MAR2023 CT scan with contrast - normal; 00APR2023 MRI with contrast - positive for a nodule on thyroid
Aktuelle Erkrankungen: No
Vorgeschichte: Hyperlipidemia; Hypertension; Vertigo occasionally
Andere Medikamente: Pravastatin; Zetia; Lisinopril; Omeprazole; Multivitamin; Fish Oil; Calcium; Vitamin D; Baby Aspirin
Allergien: Tetanus; Mold Spores; Pancake Mix in the box
Vorherige Impfungen: Tetanus, extremely high fever, red swollen arm.

VAERS 2622297

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144-B

gering

Staat: CA
Alter: 68,0
Geschlecht: F
Eingang: 27.04.2023
Impfdatum: 02.09.2022
Beginn: 09.04.2023
Tage bis Beginn: 219,0
Dosis: 5
Route/Site: SYR / RA

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

COVID-19 Nasopharyngitis Oropharyngeal discomfort Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

I had my vaccination on 09/07/2022. On 04/09/2023 I started to have problems with my throat and had to keep clearing it. The next morning I felt worse and I tested COVID-19 Negative. I started to have more cold like symptoms. On 04/12/2023 I tested COVID-19 Positive. I was prescribed Paxlovid. I still have a little bit of congestion but I feel fine on 04/27/2023.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: 04/09/2023 test COVID-19 - Negative 04/12/2023 test - COVID-19 Positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Hypertension
Andere Medikamente: Losartan
Allergien: N/A
Vorherige Impfungen: -

VAERS 2615002

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: MA
Alter: -
Geschlecht: F
Eingang: 14.04.2023
Impfdatum: 12.09.2022
Beginn: 01.02.2023
Tage bis Beginn: 142,0
Dosis: UNK
Route/Site: OT / -

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

COVID-19 Decreased appetite Hypersomnia

Symptomtext

Slept a bit more than usual; Ate a bit less than usual; We were both infected with COVID-19 in February; This spontaneous case was reported by a consumer and describes the occurrence of HYPERSOMNIA (Slept a bit more than usual), DECREASED APPETITE (Ate a bit less than usual) and COVID-19 (We were both infected with COVID-19 in February) in a 5-month-old female patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. AS7144B) for COVID-19 prophylaxis. MEDICAL HISTORY (Parent): The mother's past medical history included COVID-19 (PCR positive) on 22-May-2022. Previously administered products included for COVID-19 prophylaxis: Janssen (Lot number: 203A21A) on 10-Apr-2021 and MODERNA COVID-19 VACCINE (Batch number: 067F21A; Intramuscular injection 0.25ml) on 19-Nov-2021. Past adverse reactions to the above products included No adverse event with Janssen and MODERNA COVID-19 VACCINE. Concurrent medical conditions included Hypertension (worsening) since 01-Jan-2007. MEDICAL HISTORY (Patient): The patient's past medical history included Foetal exposure during pregnancy. Concomitant products included PRENATAL VITAMINS [ASCORBIC ACID;BETACAROTENE;CALCIUM SULFATE;COLECALCIFEROL;CYANOCOBALAMIN;FERROUS FUMARATE;FOLIC ACID;NICOTINAMIDE;PYRIDOXINE HYDROCHLORIDE;RETINOL ACETATE;RIBOFLAVIN;THIAMINE MONONITRATE;TOCOPHERYL ACETATE;ZINC OXIDE] from 01-Jan-2022 to an unknown date and LABETALOL for an unknown indication. On 12-Sep-2022, the patient received dose of mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (Transplacental) .5 milliliter. In February 2023, the patient experienced HYPERSOMNIA (Slept a bit more than usual), DECREASED APPETITE (Ate a bit less than usual) and COVID-19 (We were both infected with COVID-19 in February). At the time of the report, HYPERSOMNIA (Slept a bit more than usual), DECREASED APPETITE (Ate a bit less than usual) and COVID-19 (We were both infected with COVID-19 in February) had resolved. No concomitant and treatment medications were reported. Mother reported that both herself and the baby were doing well and had a clean bill of health. Her daughter would be turning 6 months in Mar (20-26), 2023. Both were infected with COVID-19 in February. However, they were both mild cases. The baby had a slight fever for 2 days, slept a bit more than usual and ate a bit less than usual for a few days before returning to her healthy self. Mother was taking labetalol and prenatal vitamins daily and is still taking. Mother's pre-pregnancy weight was 155 pounds. Company comment-This spontaneous case concerns an 5-month-old female infant, with past history of foetal exposure during pregnancy reported, who experienced non serious unexpected AESI of Hypersomnia that occurred about 4-5 months after a booster dose of mRNA-1273.222 vaccination. It was reported that both mother and baby were infected with Covid-19, both mild cases. Baby had a slight fever for 2 days, slept a bit more than usual and ate a bit less than usual for a few days before returning to her healthy self. The benefit-risk relationship of mRNA-1273.222 vaccine is not affected by this report. This case was linked to US-MODERNATX, INC.-MOD-2022-646081, US-MODERNATX, INC.-MOD-2023-715204 (Parent-Child Link). See case US-MODERNATX, INC.-MOD-2023-715204,US-MODERNATX, INC.-MOD-2022-646081 for details regarding the child case.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Foetal exposure during pregnancy
Andere Medikamente: PRENATAL VITAMINS [ASCORBIC ACID;BETACAROTENE;CALCIUM SULFATE;COLECALCIFEROL;CYANOCOBALAMIN;FERROUS ; LABETALOL
Allergien: -
Vorherige Impfungen: -

VAERS 2614851

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: IL
Alter: 70,0
Geschlecht: F
Eingang: 13.04.2023
Impfdatum: 07.09.2022
Beginn: 09.12.2022
Tage bis Beginn: 93,0
Dosis: 5
Route/Site: IM / LA

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

Atelectasis COVID-19 Chest X-ray abnormal Influenza like illness Nasopharyngitis Productive cough Respiratory disorder SARS-CoV-2 test positive

Symptomtext

On 12/9/22, I had Flu like symptoms and that lasted for a couple days. I tested for COVID-19, and it was negative. I had a friend call me and tell me she tested positive on 12/14/22. I took another test and was positive. I had no symptoms at all, but I was testing positive. On 12/26/22, I came down with a bad cold that kept getting worse, so I went in to see urgent care. They prescribed azithromycin and benzonatate. I did not take the benzonatate because I wanted to cough up all the Phlegm. I was still not better, so I called my PCP, and they renewed my montelukast and albuterol. I still wasn't getting better, so I had to go back to urgent care on 3/15/23. They said because of all the respiratory issues I was having, that I was having a hyperactive Immune response. I was prescribed a nebulizer and prednisone. They also did a chest x-ray and it showed Minimal Bibasilar Atelectasis Changes.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Atelectasis
Hospital-Tage: -
Labordaten: 09DEC2022 COVID-19 test negative; 12DEC2022 COVID-19 test negative; 14DEC2023 COVID-19 test positive; 15MAR2023 X-Ray, Minimal Bibasilar Atelectasis Changes
Aktuelle Erkrankungen: N/A
Vorgeschichte: High Blood Pressure
Andere Medikamente: ADVIL; amlodipine; chlorthalidone; anastrozole
Allergien: Penicillin; feathers; mold; seasonal allergies
Vorherige Impfungen: -

VAERS 2614609

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: NE
Alter: 77,0
Geschlecht: M
Eingang: 13.04.2023
Impfdatum: 09.09.2022
Beginn: 14.02.2023
Tage bis Beginn: 158,0
Dosis: 5
Route/Site: IM / LA

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

COVID-19 SARS-CoV-2 test positive

Symptomtext

I had contracted COVID-19 and tested positive on Valentine's Day, 02/14/2023. I contacted my doctor the next morning and was prescribed Paxlovid for treatment and began the regime that same day. After a couple of days of treatment, I'm doing much better with no residual symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: 14FEB2023 -- COVID-19 Test - Positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Type 2 Diabetes
Andere Medikamente: Tamsulosin; Omeprazole; Atorvastatin; Metformin; Valsartan; Potassium Citrate; Aspirin; Centrum; Align Probiotic
Allergien: N/A
Vorherige Impfungen: -

VAERS 2611556

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: NY
Alter: 79,0
Geschlecht: M
Eingang: 07.04.2023
Impfdatum: 10.09.2022
Beginn: 01.01.2023
Tage bis Beginn: 113,0
Dosis: 5
Route/Site: IM / LA

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

COVID-19 SARS-CoV-2 test positive

Symptomtext

I did not have an adverse event after receiving the vaccine. I tested positive for COVID-19 in 01/2023. I contacted a provider and got a prescription remdesivir. I tolerated the medication without any complications. As of today, I am feeling better with no lingering COVID-19 symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: JAN2023 COVID-19 test positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: AFIB; Asthma
Andere Medikamente: N/A
Allergien: Contrast iodine
Vorherige Impfungen: -

VAERS 2611392

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: VA
Alter: 67,0
Geschlecht: M
Eingang: 07.04.2023
Impfdatum: 10.09.2022
Beginn: 28.03.2023
Tage bis Beginn: 199,0
Dosis: 5
Route/Site: IM / LA

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

COVID-19 Exposure to SARS-CoV-2 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 from my wife after she returned home from vacation. I tested positive for COVID-19 on 03/28/2023. I contacted my provider and got a prescription for PAXLOVID. I tolerated the medication without any complications. I tested positive for COVID-19 on 04/06/2023. I feel like my symptoms are milder with the rebound.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: 28MAR2023 COVID-19 test positive; 06APR2023 rebound COVID-19 test positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 2609236

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge as7144b

gering

Staat: PA
Alter: 69,0
Geschlecht: F
Eingang: 04.04.2023
Impfdatum: 01.09.2022
Beginn: 03.01.2023
Tage bis Beginn: 124,0
Dosis: 5
Route/Site: IM / LA

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

COVID-19 Influenza like illness SARS-CoV-2 test positive

Symptomtext

positive test for COVID-19, Paxlovid, moderate flu-like symptoms for about a week

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Rapid home test, 1/3/23, negative test 1/9/23
Aktuelle Erkrankungen: none
Vorgeschichte: hypertension
Andere Medikamente: Lisinopril, calcium, multivitamin, iron, Vitamin D, Vitamin C
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2607395

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: TX
Alter: 73,0
Geschlecht: M
Eingang: 31.03.2023
Impfdatum: 07.09.2022
Beginn: 27.09.2022
Tage bis Beginn: 20,0
Dosis: 5
Route/Site: IM / LA

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

Cardiac disorder Cardiac pacemaker insertion Cardiac stress test Catheterisation cardiac normal Echocardiogram abnormal

Symptomtext

I went in for a doctor's appointment. They did an echocardiogram and a stress test. I was advised that my heart had weakened. I believe it was about 305. They completed a catherization and did not find anything treatable. The put me on Carvedilol and Entresto and the cardiologist referred me to an electrophysiologist. I had a pacemaker implanted on March 22, 2023. I am still recovering. I saw my doctor for a check up on Wednesday the 29th and everything looked okay.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardiac disorder
Hospital-Tage: 1,0
Labordaten: Echocardiogram 09/20/2022-Heart weakened. Stress Test-09-22-2022-Results Unknown Heart Cath erization-10/18/2022
Aktuelle Erkrankungen: N/A
Vorgeschichte: Heart Failure diagnosed 4 years ago; Splenectomy; High Blood Pressure; Type 2 Diabetes; Prostate Cancer; Weak Kidney;
Andere Medikamente: Prasugrel; Amlodipine; Allopurinol; Wellbutrin; 1 A Day Senior Vitamin; Fish Oil; Prednisone
Allergien: N/A
Vorherige Impfungen: Moderna Dose 1-4-felt like fever soreness and flu like symptoms for 24 hours-age 72

VAERS 2606760

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: CA
Alter: 61,0
Geschlecht: F
Eingang: 30.03.2023
Impfdatum: 28.09.2022
Beginn: 01.10.2022
Tage bis Beginn: 3,0
Dosis: 5
Route/Site: SYR / LA

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

Lymphadenopathy Lymphoedema Muscle twitching Sleep disorder

Symptomtext

There are some lymph nodes in the groin area and they have been swollen and fluid filled ever since October 2022. They don't hurt at all. They don't change, and they're squishy and palpable and they were never like that before. Because of my back issues, I'm not really sure what it's related to. But they've been around ever since the vaccine. My doctor has ordered an ultrasound and we'll go on from there. Another strange thing that has happened recently has been a strange twitch in my leg when I go to bed. It happens for an hour or two sometimes and I've lost some sleep to that. I did some research online and the symptoms seem to be in relation to something specific called periodic limb movement disorder (PLMD). It is an uncontrollable need to twitch your legs. It comes in regular intervals for 20 to 25 seconds. It's not diagnosed officially as I've just tried to look into symptoms, but it's been disruptive and annoying when trying to sleep at night. I've done some changes such as less coffee, alcohol, and less screen time at night. I've also been using magnesium butter which is cream for my leg and some meditation. It's helped a bit, but it does come back from time to time. I'm not sure if that's a nervous system disorder, but I also need to get this checked out soon. I need to check with the swollen lymph nodes first and see if it's serious enough to see a specialist. Then we'll go on from there.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Lymphadenopathy
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Chronic back pain episode a few days prior vaccination
Vorgeschichte: Chronic lower back pain; Hypertension
Andere Medikamente: Hydrochlorothiazide; Lisinopril; Imvexxy; Centrum Women's Multivitamin; Raw Calcium Capsule (Magnesium, Calcium, Vitamin D3); Vitamin B Complex; Glucosamine Chondroitin; Biotin
Allergien: None
Vorherige Impfungen: -

VAERS 2603314

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: PA
Alter: 26,0
Geschlecht: F
Eingang: 24.03.2023
Impfdatum: 16.09.2022
Beginn: 04.03.2023
Tage bis Beginn: 169,0
Dosis: 4
Route/Site: - / AR

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

Iliotibial band syndrome X-ray normal

Symptomtext

I had trouble with my left knee and I went to see an Orthopedic Doctor to see why. I was told it was the IT band and PT was recommended to stretch the IT band area.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Iliotibial band syndrome
Hospital-Tage: -
Labordaten: X-ray nothing noted on the so stretching of the ligament or IT band was recommended.
Aktuelle Erkrankungen: None
Vorgeschichte: Hashimoto thyroiditis
Andere Medikamente: Levothyroxine; Iron: Prenatal vitamin
Allergien: Adhesive tape
Vorherige Impfungen: -

VAERS 2602337

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: IN
Alter: 76,0
Geschlecht: M
Eingang: 23.03.2023
Impfdatum: 20.09.2022
Beginn: 19.03.2023
Tage bis Beginn: 180,0
Dosis: 5
Route/Site: IM / AR

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

COVID-19 Dysphonia Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

Began having raspiness and runny nose on 03/19/2023. Symptoms continued so I tested on 03/20/2023 testing positive. Did telehealth visit on 03/21/2023. Was prescribed Paxlovid but was unable to take it due to possible drug interaction. Began different antiviral on 03/22/2023 in the evening. Symptoms have been very mild and I have had no symptoms at all today 03/23/2023

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: At home covid-19 test - positive
Aktuelle Erkrankungen: TAVR valve replacement
Vorgeschichte: Diabetes, Hypertension, COPD, Arthritis, GERD, Glaucoma, Hyperlipidemia
Andere Medikamente: 81 MG Aspirin, Celebrex 600, Lisinopril, Metformin 500MG, Protonix 40MG; Alegra 180MG; B complex; Multivitamin, Monolukast 10MG, Pravastatin 20 MG, Flomax, Gabapentin 300 MG,
Allergien: Iodine, Sulfa
Vorherige Impfungen: -

VAERS 2602328

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: CA
Alter: 70,0
Geschlecht: F
Eingang: 23.03.2023
Impfdatum: 04.09.2022
Beginn: 29.12.2022
Tage bis Beginn: 116,0
Dosis: 5
Route/Site: IM / 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 positive Wheezing

Symptomtext

My husband and I spent time with some friends over the holidays. One of the friends tested positive for COVID-19, and we stayed to help take care of them. At this point, I had never had COVID-19 before, though my husband had been infected one month earlier. I began having upper respiratory symptoms (cough, runny nose, slight wheeziness) about 12/29/2022. I took a home antigen test that day and got a positive result. I called my doctor, who prescribed Paxlovid, which I began taking that day. Within 48 hours I began to feel better. My cough began to improve. I never really had a fever. I think I got better at one point and then had a slight rebound in which I had runny nose, though I didn't test myself at that point. I isolated for about ten days. I took a home antigen test in the middle of February 2023 and got a negative result. Before I got COVID-19, I would use two different respiratory inhalers. One inhaler is budesonide formoterol, and the other is Ventolin, which I almost never use. While I was taking the Paxlovid, my doctor advised me not to take budesonide formoterol, but ever I finished my Paxlovid round, I have been using the budesonide formoterol. Originally, I was on two puffs twice a day, but I am currently on one puff twice a day. I would like to add that I used a pulse oximeter during my time with COVID=19, and my oxygen levels were normal.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: 29DEC2022 - Home Antigen Test - Positive Result; FEB2023 - Home Antigen Test - Negative Result
Aktuelle Erkrankungen: None
Vorgeschichte: High Cholesterol; Osteoporosis; Insomnia
Andere Medikamente: Crestor; Celexa; Glucosamine; MSM; Centrum Silver; Rutin Supplement; Turmeric; Vitamin D; TUMS; Viviscal Pro Supplement; Ativan (As Needed); Prolia Injection
Allergien: Ezetimibe
Vorherige Impfungen: With a previous COVID-19 vaccine dose, I had a rash on my breast. With another of COVID-19 vaccine, I had a rash around the inje

VAERS 2602269

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: MI
Alter: 76,0
Geschlecht: M
Eingang: 23.03.2023
Impfdatum: 18.09.2022
Beginn: 18.09.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / LA

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

Burning sensation

Symptomtext

After I went to bed, it was pronounced burning in my feet. Lasted a short time and went a way.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Burning sensation
Hospital-Tage: -
Labordaten: No
Aktuelle Erkrankungen: No
Vorgeschichte: COPD; Intrinsic heart disease
Andere Medikamente: MASTER multivitamin; prostate pill; glucosamine with MSN; fish oil; vitamin E; turmeric omeprazole; fluoxetine; simvastatin; metoprolol; inhaler
Allergien: No
Vorherige Impfungen: -

VAERS 2601853

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: CT
Alter: 57,0
Geschlecht: F
Eingang: 22.03.2023
Impfdatum: 18.09.2022
Beginn: 10.02.2023
Tage bis Beginn: 145,0
Dosis: 4
Route/Site: SYR / LA

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

Benign neoplasm of thyroid gland Neck mass Thyroid mass Ultrasound thyroid abnormal

Symptomtext

On are about 10FEB2023 or a day or two before I noticed out of the blue something strange on my neck quite a large lump and I visited my doctor who saw it himself we understood it to be on my thyroid and a thyroid ultrasound was ordered for 22FEB2023. The imaging showed a very large nodule on my thyroid as well as three smaller ones on the other side not noticed or seen before, the radiology report looked very benign but why they appeared is unknown.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Benign neoplasm of thyroid gland
Hospital-Tage: -
Labordaten: Thyroid ultrasound shows benign growth.
Aktuelle Erkrankungen: None
Vorgeschichte: High Cholesterol
Andere Medikamente: Anastrozole
Allergien: CIPRO; DIMETAPP
Vorherige Impfungen: -

VAERS 2600250

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: VA
Alter: 71,0
Geschlecht: F
Eingang: 21.03.2023
Impfdatum: 19.09.2022
Beginn: 19.01.2023
Tage bis Beginn: 122,0
Dosis: 4
Route/Site: SYR / LA

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

Biopsy endometrium abnormal Endometrial cancer Hysterectomy

Symptomtext

I was diagnosed with endometrial cancer and a complete hysterectomy.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Biopsy endometrium abnormal
Hospital-Tage: -
Labordaten: Biopsy result was cancer.
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension; High cholesterol
Andere Medikamente: Fenofibrate; hydrochlorothiazide; cholestyramine; CELEBREX; vitamin D; ZYRTEC generic
Allergien: Statin drugs
Vorherige Impfungen: -

VAERS 2598566

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: PA
Alter: 70,0
Geschlecht: F
Eingang: 17.03.2023
Impfdatum: 11.09.2022
Beginn: 19.12.2022
Tage bis Beginn: 99,0
Dosis: 5
Route/Site: IM / LA

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

Anticoagulant therapy Atrial fibrillation Blood test normal Cardiac monitoring Echocardiogram Electrocardiogram abnormal Heart rate increased

Symptomtext

12/19/2022 that evening I got up after eating dinner and I started having a very rapid heartbeat. It felt like someone was dribbling a basketball in my chest. I went to the emergency room. I had an EKG, bloodwork, was on a heart monitor and had an Echocardiogram. My heart rhythm was back to normal. I was diagnosed with atrial defibrillation. I stayed overnight so they could monitor my situation. I was seen by a lot of doctors. I saw a cardiologist that day and my heart rhythm was still normal. I was prescribed ELIQUIS and metoprolol which I am still taking. I was discharged home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anticoagulant therapy
Hospital-Tage: 1,0
Labordaten: EKG, atrial defibrillation; Echocardiogram, unsure of results; Bloodwork, normal
Aktuelle Erkrankungen: None
Vorgeschichte: Mitral valve prolapse; Hypothyroidism; Seasonal allergies; Atherosclerosis; Moderate Aortic regurgitation; Osteopenia; Colon polyp
Andere Medikamente: Levothyroxine; FLONASE; atorvastatin; saline solution; STATIN GUARD (coQ10); ONE A DAY women's 50 plus vitamin; CITRACAL plus vitamin D; AMLACTIN; REFRESH plus eye drops
Allergien: Gentamicin
Vorherige Impfungen: -

VAERS 2597791

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: CT
Alter: 69,0
Geschlecht: M
Eingang: 16.03.2023
Impfdatum: 14.09.2022
Beginn: 18.02.2023
Tage bis Beginn: 157,0
Dosis: 5
Route/Site: IM / LA

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

COVID-19 Cough Pulmonary congestion Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

I had developed runny nose, lung congestion and coughing. I tested positive for COVID-19 on 02/18/2023. I called my provider and the provider prescribed PAXLOVID. I continued with congestion for 3 days. I then returned to normal.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: 18FEB2023 COVID-19 positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Myasthenia Gravis; High Blood Pressure; High Cholesterol
Andere Medikamente: ZETIA; trandolapril; WELCHOL; MESTINON; NIASPAN; folic acid; vitamin D; CENTRUM SILVER; alpha lipoic acid
Allergien: Azathioprine; statin
Vorherige Impfungen: -

VAERS 2597632

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: CT
Alter: 74,0
Geschlecht: M
Eingang: 16.03.2023
Impfdatum: 14.09.2022
Beginn: 11.02.2023
Tage bis Beginn: 150,0
Dosis: 5
Route/Site: SYR / UN

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

COVID-19 Cough SARS-CoV-2 test positive

Symptomtext

I were positive for COVID-19 on 11FEB2023, I had a cough that's all. I was prescribed PAXLOVID, I started to lose the cough very fast about a day or 2. I did have a rebound of COVID and I was prescribed steroids.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: 11FEB2023 COVID-19 test positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Aortic Valve
Andere Medikamente: Amlodipine; aspirin; atorvastatin; LYRICA
Allergien: N/A
Vorherige Impfungen: -

VAERS 2597078

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7144B

gering

Staat: MO
Alter: 57,0
Geschlecht: F
Eingang: 15.03.2023
Impfdatum: 13.09.2022
Beginn: 01.10.2022
Tage bis Beginn: 18,0
Dosis: 5
Route/Site: - / RA

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

Neoplasm malignant

Symptomtext

I was diagnosed with Cancer on January 2023

Weitere VAERSDATA-Felder

Praegender Schweregrund: Neoplasm malignant
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Levothyrox; Atorvastatin; Bupropion; Escitalopram; Tantoprazole; Estradiol
Allergien: N/A
Vorherige Impfungen: -

VAERS 2596491

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: TX
Alter: 76,0
Geschlecht: M
Eingang: 14.03.2023
Impfdatum: 09.09.2022
Beginn: 01.11.2022
Tage bis Beginn: 53,0
Dosis: 5
Route/Site: IM / LA

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

Electrocardiogram ambulatory abnormal Heart rate irregular

Symptomtext

In November 2022, my wife and I were monitoring our blood pressure on our automatic blood pressure machine. It indicated that I had an irregular heartbeat. I scheduled an appointment with my doctor to discuss what he thought about it. He had me wear a Holter heart monitor for two weeks. The results did show I have an irregular heartbeat, but I am not in Afib. I was given a small dose of Metoprolol to take daily to help with the irregular heartbeat.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Electrocardiogram ambulatory abnormal
Hospital-Tage: -
Labordaten: 11/22 Holter monitor - positive for irregular heartbeat
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Valsartan; Amlodipine; Atorvastatin
Allergien: No
Vorherige Impfungen: -

VAERS 2596193

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: CA
Alter: 77,0
Geschlecht: F
Eingang: 14.03.2023
Impfdatum: 12.09.2022
Beginn: 17.02.2023
Tage bis Beginn: 158,0
Dosis: 5
Route/Site: IM / AR

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

Ageusia COVID-19 Feeling abnormal Feeling cold Nasopharyngitis SARS-CoV-2 test positive

Symptomtext

2/17/23 I woke up and felt horrible with a very bad cold and was freezing. I had a negative COVID test. On 2/18/23 I had a positive COVID test and still felt horrible. I called my doctor's office and she prescribed PAXLOVID. I started taking it that day and took it for the 5 days. On 3/3/23 I spoke to my doctor's office and discussed the positive results I continued to have even though I felt better. On 3/6/2023, I tested negative. By then I had lost my sense of taste, but I did feel better. I still do not have my sense of taste.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Ageusia
Hospital-Tage: -
Labordaten: At home COVID test, negative and positive
Aktuelle Erkrankungen: None
Vorgeschichte: Sleep Apnea
Andere Medikamente: Levothyroxine; lovastatin; ALLERCLEAR; mega D3 and MK7; coQ10
Allergien: Penicillin; hay fever
Vorherige Impfungen: Fever after every COVID vaccine. October of 2021 I had fever with the Flu shot for the first time. It was the only time.

VAERS 2596131

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: AZ
Alter: 37,0
Geschlecht: M
Eingang: 14.03.2023
Impfdatum: 12.09.2022
Beginn: 07.03.2023
Tage bis Beginn: 176,0
Dosis: 4
Route/Site: IM / LA

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

Angiogram Imaging procedure abnormal Retinal artery occlusion Visual impairment

Symptomtext

On 3/7/2023, I had blocked vision in the left eye. On 3/9/2023, I went to my optometrist, who told me to go to a specialist. On 3/10/2023, I went to an ophthalmologist. I was examined. When I went to ophthalmologist, my vision was already starting to improve, but I was diagnosed with branch retinal artery occlusion. My vision is still improving, and the ophthalmologist doesn't recommend any treatment and suggests that I continue going to my PCP. The ophthalmologist said that my vision should keep improving and that I should recover my vision completely. I have been taking anastrozole for infertility for a couple of months now, though I don't know if it is in any way related to my health event. At the time of this writing, I feel that I have recovered about 95%.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Angiogram
Hospital-Tage: -
Labordaten: 09MAR2023 - Retinal Image - Branch Retinal Artery Occlusion Suspected; 10MAR2023 - Retinal Image, Fluorescein Angiography - Branch Retinal Artery Occlusion Confirmed
Aktuelle Erkrankungen: None
Vorgeschichte: Anxiety
Andere Medikamente: Multivitamin
Allergien: None
Vorherige Impfungen: -

VAERS 2596120

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: MA
Alter: 67,0
Geschlecht: F
Eingang: 14.03.2023
Impfdatum: 09.09.2022
Beginn: 05.12.2022
Tage bis Beginn: 87,0
Dosis: 5
Route/Site: IM / LA

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

Bronchitis COVID-19 Cough Nasopharyngitis Productive cough Respiratory tract congestion Respiratory tract infection Rhinorrhoea SARS-CoV-2 test positive Secretion discharge Sputum discoloured Upper-airway cough syndrome

Symptomtext

12/5/2022 I had a runny nose, coughing, a lot of junky stuff in the chest. I tested positive for COVID with an at home test and I also had a PCR test which was positive. By 12/7/22 I was getting better. My doctor told me even though I was getting better that I should take PAXLOVID. I took it and finished the course. 12/21/22, I had the majority of all the symptoms again, but did not test positive for COVID. The illness was much worse and lasted longer. I had green junk from my chest and symptoms of a cold. All my symptoms were in my head and chest. The uncontrollable coughing was the worst. I was treated with MUCINEX and a Z PAK. This illness was really bad and was not COVID. It lasted into January, 2023. I recovered for a period of time until 3/7/2023. I got another respiratory infection, different from the previous one. I had uncontrollable coughing fits the mucous was thin from my sinuses and a lot of postnasal drip. I sounded so bad with my cough, I went to the doctor and was diagnosed with Bronchitis. I am taking albuterol inhaler which seems to help. I have not recovered, but am on the mend.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bronchitis
Hospital-Tage: -
Labordaten: At home COVID tests, negative and positive
Aktuelle Erkrankungen: None
Vorgeschichte: Rheumatoid Arthritis; Obesity
Andere Medikamente: Citalopram; WELLBUTRIN; metoprolol; COLACE; vitamin D; vitamin B3; vitamin B12; lorazepam; methotrexate; folic acid
Allergien: Sodium pentothal; NOVOCAIN; caffeine
Vorherige Impfungen: -

VAERS 2596109

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: WV
Alter: 81,0
Geschlecht: M
Eingang: 14.03.2023
Impfdatum: 08.09.2022
Beginn: 01.12.2022
Tage bis Beginn: 84,0
Dosis: 5
Route/Site: IM / AR

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

Chemotherapy Laboratory test abnormal Lung neoplasm malignant

Symptomtext

I am still doing chemotherapy until they can go in and surgically remove all the cancer. I went for my annual checkup, and they discovered the cancer in my lungs.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chemotherapy
Hospital-Tage: -
Labordaten: Lab Analyst
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Lisinopril; ONE A DAY multivitamin; calcium
Allergien: N/A
Vorherige Impfungen: -

VAERS 2595727

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: AZ
Alter: 69,0
Geschlecht: F
Eingang: 13.03.2023
Impfdatum: 10.09.2022
Beginn: 28.02.2023
Tage bis Beginn: 171,0
Dosis: 5
Route/Site: SYR / RA

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

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

Symptomtext

I had my vaccination on 09/10/2022. On 02/28/2023 I had a dry cough and I had extreme lethargy. I tested COVID-19 positive on 02/28/2023 with an at home COVID-19 test. I was prescribed PAXLOVD. I did get rebound COVID-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID-19 positive 02/28/2023.
Aktuelle Erkrankungen: N/A
Vorgeschichte: Polymyalgia Rheumatica
Andere Medikamente: Prednisone; levothyroxine; FOSAMAX
Allergien: Codeine; MSG
Vorherige Impfungen: -

VAERS 2595555

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: VA
Alter: 37,0
Geschlecht: F
Eingang: 13.03.2023
Impfdatum: 07.09.2022
Beginn: 18.12.2022
Tage bis Beginn: 102,0
Dosis: 4
Route/Site: IM / LA

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

Cannabinoid hyperemesis syndrome Gastrointestinal disorder Paranoia

Symptomtext

I experienced cannabinoid hyperemesis syndrome, intestinal issues and paranoia.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cannabinoid hyperemesis syndrome
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Premature degenerative disc disease; Ehlers-Danlos syndrome
Andere Medikamente: Metoprolol; metformin; lamotrigine
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 2595537

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: MI
Alter: 73,0
Geschlecht: F
Eingang: 13.03.2023
Impfdatum: 07.09.2022
Beginn: 03.03.2023
Tage bis Beginn: 177,0
Dosis: 5
Route/Site: IM / LA

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

Atrial fibrillation Blood test Chest X-ray Echocardiogram Electrocardiogram Heart rate increased

Symptomtext

This isnt something brand new, but I was having elevated heart rate that was about 160 which last about 45min before calling 911. When EMS arrived, they did an EKG, and I was in atrofibe.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Atrial fibrillation
Hospital-Tage: -
Labordaten: EKG(EMT); EKG(triage); bloodwork; cheat x-ray; echocardiogram
Aktuelle Erkrankungen: No
Vorgeschichte: Hypothyroid; Hypertension; Arthritis
Andere Medikamente: Synthroid; Lipitor; Norvasc; Trazadone; Melatonin Magnesium supplement; Biotin; Probiotic capsule; Multivitamin w/iron
Allergien: No
Vorherige Impfungen: -

VAERS 2594842

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: WA
Alter: 34,0
Geschlecht: M
Eingang: 10.03.2023
Impfdatum: 06.09.2022
Beginn: 02.01.2023
Tage bis Beginn: 118,0
Dosis: 4
Route/Site: IM / RA

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

COVID-19 Deafness SARS-CoV-2 test positive

Symptomtext

I contracted COVID-19 and began to experience hearing difficulty/loss so I consulted my doctor. She put me on PAXLOVID, I consulted a ENT afterwards for further help and I was prescribed prednisone, it hasn't resolved fully and I currently have a second option ENT for more aggressive approach to resolve.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: 02JAN23 COVID-19 at home test, positive
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma
Andere Medikamente: WIXELA; daily multivitamin; collagen supplement; vitamin D; fish oil
Allergien: None
Vorherige Impfungen: OCT 2020 first flu vaccine, triggered a cycle of shortness of breathe and tightness in the chest. I was 32 at the time.

VAERS 2593939

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: FL
Alter: 69,0
Geschlecht: M
Eingang: 09.03.2023
Impfdatum: 07.09.2022
Beginn: 04.01.2023
Tage bis Beginn: 119,0
Dosis: 5
Route/Site: IM / RA

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

COVID-19 Cough SARS-CoV-2 test positive

Symptomtext

Back on 11/25/2022 had a dry cough that lasted or weeks. I went to the clinic on 01/04/2023 tested for COVID-19 and it came back positive. The Provider prescribed Benzonatate for my cough and I took it for 10 days. Also prescribed Paxlovid for 5 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: 04JAN2023 - COVID-19 Test - Positive 10JAN2023 - COVID-19 Test - Negative
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Atorvastatin; Aspirin; Clopidogrel; Metformin; Valsartan
Allergien: N/A
Vorherige Impfungen: -

VAERS 2593815

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: OH
Alter: 59,0
Geschlecht: F
Eingang: 09.03.2023
Impfdatum: 07.09.2022
Beginn: 25.10.2022
Tage bis Beginn: 48,0
Dosis: 5
Route/Site: IM / AR

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

Fall Knee arthroplasty Knee operation Patella fracture Walking aid user

Symptomtext

I did not have an adverse reaction to the vaccine. In October 2022 I had to have both knees replaced. During physical therapy I fell and broke kneecap which required an additional surgery. As of today, I continue to take physical therapy to learn to walk without a walker.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fall
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 2593092

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: DC
Alter: 46,0
Geschlecht: M
Eingang: 08.03.2023
Impfdatum: 06.09.2022
Beginn: 01.01.2023
Tage bis Beginn: 117,0
Dosis: 4
Route/Site: IM / LA

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

Arthritis

Symptomtext

I did not have an adverse reaction to the vaccine. I developed symptoms of arthritis in January 2023. I went to my doctor in February 2023 and diagnosed with inflammatory arthritis. As of today, I am working with my doctor to find a medication that will help with the inflammation.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthritis
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Hypertension
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 2592240

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: MA
Alter: 41,0
Geschlecht: F
Eingang: 06.03.2023
Impfdatum: 04.09.2022
Beginn: 19.01.2023
Tage bis Beginn: 137,0
Dosis: 4
Route/Site: IM / RA

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

Biopsy breast abnormal Breast cancer female Breast conserving surgery Gene mutation identification test negative Invasive ductal breast carcinoma Magnetic resonance imaging breast abnormal Mammogram abnormal

Symptomtext

I was having 6-month mammograms to keep an eye on a spot I found in 2021. When I went for my mammogram on January 6, 2023, the doctor found a new spot within the last 6 months. The spot was biopsied January 18th, 2023, and the next day it was confirmed that it was Invasive Ductal Carcinoma. I had genetic testing done and all the tests were negative so it's not because of a genetic mutation. I had a Lumpectomy surgery on February 23, 2023, and I will be having radiation and chemotherapy starting this month. Surgery confirmed that I am stage 1A.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Biopsy breast abnormal
Hospital-Tage: 1,0
Labordaten: 25JAN2023 Genetic testing, negative; 18JAN2023 Biopsy, Carcinoma; 09FEB2023 MRI, confirmed diagnosis
Aktuelle Erkrankungen: N/A
Vorgeschichte: Asthma; High Cholesterol; Depression; CVA
Andere Medikamente: LEXAPRO; TRILEPTAL; amitriptyline; SYNTHROID; pravastatin
Allergien: PERCOCET
Vorherige Impfungen: -

VAERS 2591784

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: NJ
Alter: 54,0
Geschlecht: F
Eingang: 06.03.2023
Impfdatum: 04.09.2022
Beginn: 20.11.2022
Tage bis Beginn: 77,0
Dosis: 5
Route/Site: SYR / RA

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

Angiogram Angiogram cerebral abnormal Anticoagulant therapy Arteriogram carotid abnormal Blood test abnormal COVID-19 Carotid artery dissection Computerised tomogram neck Magnetic resonance imaging abnormal Magnetic resonance imaging head abnormal Tinnitus

Symptomtext

11/20/22 I was hearing a whooshing sound in my left ear, like your heartbeat. I went to see an ENT, had testing and had an appointment already scheduled with a Neurologist who did more testing. I had an MRI of the brain, MRA and MRI of the neck, Ultrasound of the Carotid and found an aneurysm. My diagnosis was a dissecting aneurysm of the left cervical ICA just below the base of the skull, 10mm x 7mm. After the results, my brother-in-law who is a Neurologist told me to go the ER. I ended up testing positive for COVID on 12/11/22. On 12/16/22 I went to the ER and spent 3 days in the hospital. The same tests were run, MRI and MRA and confirmed the diagnosis. They determined it was acute rather than chronic. I was started on PLAVIX and aspirin and sent home. I have continued to have testing and have an appointment with the Neurologist this week. I did have a follow up MRI that showed no change.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Angiogram
Hospital-Tage: 3,0
Labordaten: MRI of the brain, MRA of the Brain, MRI of the neck, MRA of neck, CT of the neck. Ultrasound of the Carotid. All test revealed dissecting aneurysm of the left cervical ICA. Bloodwork, abnormal, unknown. CTA of chest, abdomen and pelvis, unknown result.
Aktuelle Erkrankungen: No
Vorgeschichte: Pre Diabetic; Hypothyroid; Possibly Rheumatoid Arthritis; IBS; Migraines; Environmental allergies.
Andere Medikamente: Levothyroxine; EMGALITY; ZYRTEC; FLONASE; multivitamin; vitamin D; melatonin; apple cider vinegar gummies
Allergien: Sulfa; HLA
Vorherige Impfungen: -

VAERS 2589311

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge as7144b

gering

Staat: NY
Alter: 80,0
Geschlecht: M
Eingang: 01.03.2023
Impfdatum: 03.02.2023
Beginn: 03.02.2023
Tage bis Beginn: 0,0
Dosis: 6
Route/Site: IM / LA

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

Inappropriate schedule of product administration

Symptomtext

Error: Dose in Series Given Too Early-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Inappropriate schedule of product administration
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2589298

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge as7144b

gering

Staat: NY
Alter: 78,0
Geschlecht: F
Eingang: 01.03.2023
Impfdatum: 03.02.2023
Beginn: 03.02.2023
Tage bis Beginn: 0,0
Dosis: 6
Route/Site: IM / LA

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

Inappropriate schedule of product administration

Symptomtext

Error: Dose in Series Given Too Early-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Inappropriate schedule of product administration
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2570624

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: OH
Alter: 58,0
Geschlecht: F
Eingang: 30.01.2023
Impfdatum: 28.10.2022
Beginn: 23.01.2023
Tage bis Beginn: 87,0
Dosis: 5
Route/Site: SYR / LA

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

Breast mass Mammogram abnormal

Symptomtext

I had a mammogram 23JAN2023 it was noted that a small 4mm lump was detected in my left breast. A follow up ultrasound and views will be completed on 10FEB2023.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Breast mass
Hospital-Tage: -
Labordaten: Mammogram 23JAN20233 4mm lump detected.
Aktuelle Erkrankungen: None
Vorgeschichte: Hypothyroidism; Osteoporosis; Migraines
Andere Medikamente: Levothyroxine; sertraline; sumatriptan; ACTONEL
Allergien: None
Vorherige Impfungen: -

VAERS 2562415

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: WA
Alter: 46,0
Geschlecht: M
Eingang: 18.01.2023
Impfdatum: 21.09.2022
Beginn: 21.09.2022
Tage bis Beginn: 0,0
Dosis: N/A
Route/Site: IM / LA

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

Underdose

Symptomtext

Patient was given Moderna Bivalent Booster 0.25mcg, was to be given 0.5mcg. Wrong dose given.

Weitere VAERSDATA-Felder

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

VAERS 2562411

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: WA
Alter: 58,0
Geschlecht: F
Eingang: 18.01.2023
Impfdatum: 21.09.2022
Beginn: 21.09.2022
Tage bis Beginn: 0,0
Dosis: N/A
Route/Site: IM / RA

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

Underdose

Symptomtext

Moderna Bivalent Booster 0.25mcg was given to patient and was to receive a full dose 0.5mcg. Wrong dose given.

Weitere VAERSDATA-Felder

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

VAERS 2562408

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: WA
Alter: 32,0
Geschlecht: F
Eingang: 18.01.2023
Impfdatum: 21.09.2022
Beginn: 21.09.2022
Tage bis Beginn: 0,0
Dosis: N/A
Route/Site: IM / RA

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

Underdose

Symptomtext

Patient was given Moderna Bivalent Booster but was only given half the dose. Wrong dose given.

Weitere VAERSDATA-Felder

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

VAERS 2562349

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge as7144b

gering

Staat: OH
Alter: 60,0
Geschlecht: F
Eingang: 18.01.2023
Impfdatum: 14.09.2022
Beginn: 13.10.2022
Tage bis Beginn: 29,0
Dosis: 5
Route/Site: IM / LA

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

Arterial disorder IIIrd nerve disorder

Symptomtext

ocular nerve and artery issues that is ongoing

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arterial disorder
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Kidney disease with transplant, adrenal insufficiency, fmd, ibs, acid reflux, migraines, post menopausal, hypertension, high cholesterol,
Andere Medikamente: carvedilol, bactrim, astagrafxl, hydralazine, zetia, myfortic, prednisone, vitamin d3, pepcid, aspirin, prenatal, estrace
Allergien: meperidine hcl, novacaine, metronidazole, omeprazole, cipro, amoxicillin, rabdprazole sodium, esomeprazole magnesium, paroxetine hcl, nitrofurantoin, levoflaxacin, nystatin, nifedipine, doxycycline,
Vorherige Impfungen: -

VAERS 2560280

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: NJ
Alter: 70,0
Geschlecht: F
Eingang: 15.01.2023
Impfdatum: 14.09.2022
Beginn: 19.09.2022
Tage bis Beginn: 5,0
Dosis: 3
Route/Site: IM / LA

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

Ageusia Anosmia

Symptomtext

Total loss of smell and taste. I previously had 2 Covid19 Moderna vaccines and 3 Covid19 Moderna Bivalent vaccines, starting 02/12/2021. And spaced over time with most recent on 09/14/2022. After 2nd Covid19 Moderna vaccine, I started to loose my sense of smell and taste. After each vaccine this became worse with greater loss of smell and taste. The most recent vaccine on 09/14/2022 has left me with no smell or taste.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Ageusia
Hospital-Tage: -
Labordaten: Office visit with ENT Specialist, Dr. on 12/12/2022. She said there's currently nothing that can be done, not enough research on this issue. She advised smelling Essential Oils to try and retrain my olfactory cells. I have been doing this for 1 week with no improvement at all.
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: Covid 19 Moderna vaccines

VAERS 2558755

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: WA
Alter: 69,0
Geschlecht: F
Eingang: 12.01.2023
Impfdatum: 22.09.2022
Beginn: 22.09.2022
Tage bis Beginn: 0,0
Dosis: N/A
Route/Site: IM / LA

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

Incorrect dose administered

Symptomtext

Patient was given only half dose of Moderna Bivalent.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2558750

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: WA
Alter: 77,0
Geschlecht: M
Eingang: 12.01.2023
Impfdatum: 21.09.2022
Beginn: 21.09.2022
Tage bis Beginn: 0,0
Dosis: N/A
Route/Site: IM / LA

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

Incorrect dose administered

Symptomtext

Moderna Bivalent Booster was given to patient but was only given half the dose not full dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2558683

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: WA
Alter: 43,0
Geschlecht: F
Eingang: 12.01.2023
Impfdatum: 12.09.2022
Beginn: 12.09.2022
Tage bis Beginn: 0,0
Dosis: N/A
Route/Site: IM / LA

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

Incorrect dose administered

Symptomtext

Wrong dose of Moderna given. Half dose given of Bivalent.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2550125

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: PA
Alter: 75,0
Geschlecht: F
Eingang: 04.01.2023
Impfdatum: 02.10.2022
Beginn: 07.12.2022
Tage bis Beginn: 66,0
Dosis: 5
Route/Site: IM / LA

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

SARS-CoV-2 test negative Unevaluable event

Symptomtext

None stated.

Weitere VAERSDATA-Felder

Praegender Schweregrund: SARS-CoV-2 test negative
Hospital-Tage: -
Labordaten: COVID-19 test, negative
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: ALLEGRA
Allergien: Cephalosporins; shellfish
Vorherige Impfungen: COVID-19, 1st dose, felt sick

VAERS 2542377

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: PA
Alter: 63,0
Geschlecht: F
Eingang: 23.12.2022
Impfdatum: 12.09.2022
Beginn: 31.10.2022
Tage bis Beginn: 49,0
Dosis: 5
Route/Site: IM / RA

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

COVID-19 SARS-CoV-2 test positive

Symptomtext

I was infected with Covid seven weeks after my 5th vaccine. CDC called me and instructed me to fill out this form.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Received Prednisone po (Medrol dose pack) and Flovent PRN
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2539140

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge As7144b

gering

Staat: PA
Alter: 67,0
Geschlecht: F
Eingang: 21.12.2022
Impfdatum: 16.09.2022
Beginn: 01.12.2022
Tage bis Beginn: 76,0
Dosis: 5
Route/Site: IM / LA

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

COVID-19 Computerised tomogram Full blood count Influenza virus test Laboratory test SARS-CoV-2 test positive Scan with contrast

Symptomtext

Got covid less than three months post vaxx

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Covid and flu test; ct with contrast for pe; cbc, chemistries
Aktuelle Erkrankungen: Recovering from shoulder surgery, recovery from 10/5/21 phizer vax that created left wrist osteoarthritis surge/swelling
Vorgeschichte: Osteo arthritis
Andere Medikamente: Vitamin d, losartan 50, omega 3, curcumin, topical arnica, tylenol
Allergien: Cayenne
Vorherige Impfungen: Osteo arthritis surge

VAERS 2536621

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: PA
Alter: 75,0
Geschlecht: F
Eingang: 19.12.2022
Impfdatum: 26.09.2022
Beginn: 26.09.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

No adverse event Underdose

Symptomtext

No adverse reactions. Patient notified. Patient given 0.25mL of Moderna Bivalent booster dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2536617

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: PA
Alter: 74,0
Geschlecht: F
Eingang: 19.12.2022
Impfdatum: 26.09.2022
Beginn: 26.09.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

No adverse event Underdose

Symptomtext

No adverse reaction. Patient notified. Patient given Moderna Bivalent booster dose 0.25mL.

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2536614

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: PA
Alter: 59,0
Geschlecht: M
Eingang: 19.12.2022
Impfdatum: 26.09.2022
Beginn: 26.09.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

No adverse event Underdose

Symptomtext

No adverse reaction. Patient was notified. Patient was given Moderna Bivalent Booster 0.25mL dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2536609

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: PA
Alter: 67,0
Geschlecht: M
Eingang: 19.12.2022
Impfdatum: 26.09.2022
Beginn: 26.09.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Incorrect dose administered No adverse event

Symptomtext

No adverse reaction. Patient notified, Vaccine given was Moderna bivalent, patient was given 0.25mL of Moderna Bivalent booster dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2533217

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: OH
Alter: 64,0
Geschlecht: F
Eingang: 15.12.2022
Impfdatum: 09.09.2022
Beginn: 19.11.2022
Tage bis Beginn: 71,0
Dosis: 5
Route/Site: SYR / UN

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

Cough Respiratory syncytial virus infection SARS-CoV-2 test negative Sinusitis Throat irritation

Symptomtext

My RSV symptoms started on 11/19/2022 in the morning around 8:00AM. I had a scratchy throat. On 11/20/2022 I developed cough. I had no infection. I took MUCINEX MD. I went to the doctor's office on 11/21/2022. My doctor prescribed me with albuterol and TESSALON PERLES. I took the medications for a week and half. It took 2 weeks for me to recover from Sinus infection.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cough
Hospital-Tage: -
Labordaten: 15DEC2022 COVID-19 test negative
Aktuelle Erkrankungen: None
Vorgeschichte: Type 2 Diabetics; Hypothyroid; Cholesterol; High Blood Pressure: Non-Alcoholic Fatty Liver Disease
Andere Medikamente: Metformin; magnesium; pravastatin; lisinopril; LEXAPRO; CRESTOR; gabapentin; vitamin B12
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 2531197

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: CA
Alter: 70,0
Geschlecht: M
Eingang: 14.12.2022
Impfdatum: 13.09.2022
Beginn: 21.11.2022
Tage bis Beginn: 69,0
Dosis: 5
Route/Site: IM / LA

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

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

Symptomtext

I received the Moderna Bivalent booster for COVID-19 on 9/13/2022. On 11/21/2022, I developed a cough. On 11/22/2022, I took a home antigen test and got a positive result. I isolated. The only symptom I had was the cough. It did not worsen. Instead, it went away after about 2 days. On 11/23/2022, I spoke to my doctor, who prescribed Paxlovid. Even though my symptoms vanished quickly, I took the full course of Paxlovid. I was asymptomatic after the cough went away, but I continued to test positive until 11/29/2022. On 12/8/2022, I tested positive again. I was asymptomatic, though. I have continued to test regularly ever since. On the night of 12/13/2022, I developed a bit of a runny nose. When I tested myself on the morning of 12/14/2022, I still got a positive result. At the time of this writing, I still have a bit of a runny nose, but it's not as runny as it was on 12/13/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: 11/22/2022-11/28/2022--Home Antigen Tests--Positive Results; 11/29/2022--Home Antigen Test--Negative Result; 12/8/2022-12/14/2022--Home Antigen Tests--Positive Results.
Aktuelle Erkrankungen: None.
Vorgeschichte: None.
Andere Medikamente: Atorvastatin; Vitamin D; Heliocare Advanced Nicotinamide B3 Supplement.
Allergien: None.
Vorherige Impfungen: -

VAERS 2531194

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: VA
Alter: 35,0
Geschlecht: F
Eingang: 14.12.2022
Impfdatum: 09.09.2022
Beginn: 14.11.2022
Tage bis Beginn: 66,0
Dosis: 4
Route/Site: IM / -

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

Bed rest Cervix cerclage procedure Cervix disorder Exposure during pregnancy Ultrasound scan vagina abnormal

Symptomtext

I was diagnosed with cervical insufficiencies on November 14, 2022, and it was treated with Progesterone vaginal suppositories and a cerclage surgical procedure with bedrest for the remainder of the pregnancy. My due date is March 11, 2023. Due to my clinical details, I have a delivery date scheduled for February 25, 2022. The ultrasound was completed on November 14. They said the surgical procedure was successful, but I am still required to be on bedrest.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bed rest
Hospital-Tage: -
Labordaten: Transvaginal Ultrasound-November 14. 2022-Diagnosed with cervical insufficiencies
Aktuelle Erkrankungen: N/A
Vorgeschichte: Hyperthyroidism; ADHD
Andere Medikamente: Levothyroxine; Aspirin; Coline Nutritional Supplement; Prenatal Vitamin; Probiotic; Flaxseed Oil; Fish Oil; Vitamin D
Allergien: N/A
Vorherige Impfungen: -

VAERS 2531166

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: TX
Alter: 48,0
Geschlecht: F
Eingang: 14.12.2022
Impfdatum: 13.09.2022
Beginn: 17.11.2022
Tage bis Beginn: 65,0
Dosis: 4
Route/Site: IM / RA

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

Sinusitis Upper respiratory tract infection

Symptomtext

Sinus infection, upper respiratory infection. 1st round of treatment was a Z-pack. Second round of treatment was 10 days of Cefdinir 300MG 2 times per day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Sinusitis
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma
Andere Medikamente: Singular, Alegra, Albuterol
Allergien: N/A
Vorherige Impfungen: After second Moderna Vaccine in 2021, contracted Delta Variant, also required same antibiotics for sinus and upper respiratory i

VAERS 2528883

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: AR
Alter: 82,0
Geschlecht: F
Eingang: 12.12.2022
Impfdatum: 08.09.2022
Beginn: 08.12.2022
Tage bis Beginn: 91,0
Dosis: 5
Route/Site: IM / LA

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

COVID-19 SARS-CoV-2 test positive

Symptomtext

hospitalized with covid; fully vaccinated with 3 boosters

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: positive covid antigen 12/8/22
Aktuelle Erkrankungen: unknown
Vorgeschichte: Hypertension and Other (UTI, falls, dementia)
Andere Medikamente: unknown
Allergien: aspirin
Vorherige Impfungen: -

VAERS 2527452

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: PA
Alter: 83,0
Geschlecht: M
Eingang: 09.12.2022
Impfdatum: 07.09.2022
Beginn: 25.11.2022
Tage bis Beginn: 79,0
Dosis: 5
Route/Site: SYR / UN

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

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

Symptomtext

Tested positive for COVID-19 with following symptoms: Congestion (severe)

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: FloFlex home test for COVID-19
Aktuelle Erkrankungen: Skin rash (severe)
Vorgeschichte: Skin rash
Andere Medikamente: Triamcinolone Acetonide skin cream
Allergien: None known
Vorherige Impfungen: Skin rash (severe)

VAERS 2526158

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: OR
Alter: 43,0
Geschlecht: M
Eingang: 07.12.2022
Impfdatum: 06.09.2022
Beginn: 18.11.2022
Tage bis Beginn: 73,0
Dosis: 4
Route/Site: IM / LA

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

Sinusitis

Symptomtext

Sinus infection treated by 5-day course of Azithromycin.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Sinusitis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2526155

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: WA
Alter: 81,0
Geschlecht: M
Eingang: 07.12.2022
Impfdatum: 12.09.2022
Beginn: 12.09.2022
Tage bis Beginn: 0,0
Dosis: N/A
Route/Site: IM / RA

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

Underdose

Symptomtext

Patient was underdosed at 0.25mcg

Weitere VAERSDATA-Felder

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

VAERS 2525840

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: WA
Alter: 77,0
Geschlecht: F
Eingang: 07.12.2022
Impfdatum: 12.09.2022
Beginn: 12.09.2022
Tage bis Beginn: 0,0
Dosis: N/A
Route/Site: IM / LA

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

Underdose

Symptomtext

Pt was underdosed at 25 mcg. No ill effects occurred, pt was given a full dose on 11/8/22 following guidance from CDC.

Weitere VAERSDATA-Felder

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

VAERS 2523093

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: IN
Alter: 61,0
Geschlecht: F
Eingang: 05.12.2022
Impfdatum: 05.12.2022
Beginn: 05.12.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Extra dose administered Wrong patient

Symptomtext

I was given the patient's chart and it was the wrong chart. I thought I was drawing up a Covid Moderna Bivalent for the patient I had been talking to previously in the waiting room. So I drew up the Covid-19 Moderna Bivalent injection and called out her name and she got out of her seat and followed me into the exam room. I asked her about her health issues and wrote that on her chart. I then told her what I was giving her and she said why was she getting another one. I explained that the antibodies wear off after a few months and this particular one was manufactured to be effective against the newer strains and she ok to give. She then asked why she is not getting the other vaccines talked about with the front office and I told her I would go check on that. Then I gave her a copy of her Immunization Registry record and she stated,"This is not my name." At that time I repeated, "This is not your name?" and she said no, it is not! I asked her why she got up in the waiting room when I called out the name and she said "I must have misunderstood you." So, at that time I asked her to wait in the exam room while I went to get the correct chart. I then received her correct chart and drew up the correct immunizations and took them into her room and administered them to her after explaining that I had given her the wrong shot the first time. She asked if it would hurt her and I explained to her that it would not hurt, but she might have a more robust reaction since she had already had a bivalent Covid booster injection given to her in Sept 22

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: eosinophilic asthma
Andere Medikamente: none
Allergien: None
Vorherige Impfungen: -

VAERS 2509567

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge as7144b

gering

Staat: MI
Alter: 65,0
Geschlecht: F
Eingang: 16.11.2022
Impfdatum: 14.09.2022
Beginn: 01.09.2022
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / LA

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

Incorrect product formulation administered No adverse event Wrong product administered

Symptomtext

Patient received wrong Moderna vaccine. She is a bone marrow transplant patient. She was due for the 3 dose original Moderna. She had no adverse events. I have left a message to speak with her cancer doctor. Based on the guidelines, patient needs the original Moderna now and would then follow up in two months with the bivalent booster. I discussed this with the patient. I am waiting to speak with her doctor to discuss the action plan

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2508935

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: OH
Alter: 44,0
Geschlecht: M
Eingang: 15.11.2022
Impfdatum: 23.09.2022
Beginn: 24.09.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

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

Electrocardiogram ambulatory Heart rate irregular Lymphadenopathy

Symptomtext

Irregular/abnormal heartbeat which was not present prior to vaccination. (Unresolved) Extremely enlarge lymph node under arm that lasted more than one month. (Mostly resolved)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Electrocardiogram ambulatory
Hospital-Tage: -
Labordaten: 24-hour Holter Monitor for Heart (result received 11/15/2022) Further testing and bloodwork scheduled.
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: Doxycycline
Vorherige Impfungen: -

VAERS 2501067

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: WA
Alter: 51,0
Geschlecht: F
Eingang: 07.11.2022
Impfdatum: 07.11.2022
Beginn: 07.11.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / LA

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

Interchange of vaccine products

Symptomtext

Patient requested Pfizer Bivalent 12+; Moderna Bivalent 12+ was administered. No symptoms or signs that were outside of normal for this patient were observed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Interchange of vaccine products
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none known
Allergien: none
Vorherige Impfungen: -

VAERS 2499980

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: -
Alter: 11,0
Geschlecht: M
Eingang: 05.11.2022
Impfdatum: 26.10.2022
Beginn: 01.10.2022
Tage bis Beginn: -
Dosis: N/A
Route/Site: IM / LA

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

Incorrect dose administered

Symptomtext

Wrong dose size given. .5 ml given instead of .25 ml

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2497629

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge As7144B

gering

Staat: MI
Alter: 46,0
Geschlecht: M
Eingang: 03.11.2022
Impfdatum: 21.10.2022
Beginn: 21.10.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

Vaccine administered the day after the 30 day shelf life of being refrigerated. The patient reports no adverse reactions. Pt was Notified and offered a repeat dose and declined at this time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: no
Vorgeschichte: No diagnosis available.
Andere Medikamente: No medications taken
Allergien: NKA
Vorherige Impfungen: -

VAERS 2496776

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge As7144B

gering

Staat: MI
Alter: 50,0
Geschlecht: M
Eingang: 02.11.2022
Impfdatum: 21.10.2022
Beginn: 21.10.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Expired product administered No adverse event

Symptomtext

Expired dose given 12 hours after expiration. Vaccine never left out long the 1 minutes to draw up the dose. No complaint of any adverse reactions form the patient. Patientt notified and offered to repeat the dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: NO reported illnesses
Vorgeschichte: severe obstructive sleep apnea, fatty liver, chicken pox, primary insomnia, essential hypertension, facial twitching, class one obesity, former smoker, crohn's disease, HO of TIA and hyper cholesterolemia, PVD, Vit D decencies, asthma, type 2 DM, tenia versa color.
Andere Medikamente: selenium sulfide 2.5% lotion. meloxicam 7.5 mg tab. acetaminophen 325 mg tab, Lisinopril 40 mg tab, systane 0.4% - 0.3% eye drops
Allergien: NKA
Vorherige Impfungen: -

VAERS 2496561

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: MI
Alter: 61,0
Geschlecht: M
Eingang: 02.11.2022
Impfdatum: 24.10.2022
Beginn: 24.10.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Pt given Bivalent Booster 3 days post 30 day storage date which was 10/20/22. Moderna has been contacted. Pt was contacted and informed per Moderna Vaccine provided protection necessary against Covid. But per Provider discretion can offer another dose. Pt declined. Pt denies any s/e or symptoms currently.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: COPD, PVD, Hyperplasia, Anxiety, Depression
Vorgeschichte: COPD, PVD, Hyperplasia, Anxiety, Depression
Andere Medikamente: Albuterol, Buspirone, Cobivent, Cyclobenziprine, Epi-pen, Flonase, Incruse, Lasix, Miralax, Nortriptyline, Omeprazole, Tamosulosin, Topiramate, Trintellix, Ventolin
Allergien: Methyprednisone, Sulfa, Triaminolone
Vorherige Impfungen: -

VAERS 2496511

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: MI
Alter: 68,0
Geschlecht: M
Eingang: 02.11.2022
Impfdatum: 24.10.2022
Beginn: 24.10.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Product storage error

Symptomtext

Booster dose given 3 days post 30 day refrigerator storage shelf life. Refrigerator shelf life was to end at end of day on 10/20/22. Vaccine given on 10/24/22.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: Chronic Hepatitis C; Cirrhosis; Hypertension; Tobacco Use; Type II Diabetes; Elevated Ammonia levels,
Vorgeschichte: Chronic Hepatitis C; Cirrhosis; Hypertension; Tobacco Use; Type II Diabetes.
Andere Medikamente: Tylenol; Baby ASA; Basaglar; Benzotropine; Clonidine; Colace; Debox; Vitamin B; Fluphenazine; Lactulose; Lisinopril; Lorazepam; Metoprolol; Nifedipine; Potassium; Trimiteren/HCTZ; Vitamin D3.
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2494587

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7144B

gering

Staat: MI
Alter: 53,0
Geschlecht: M
Eingang: 01.11.2022
Impfdatum: 21.10.2022
Beginn: 21.10.2022
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

Symptomtext

No adverse event; Vaccine administered after the 30 day beyond use date; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine administered after the 30 day beyond use date) and NO ADVERSE EVENT (No adverse event) in a 53-year-old male patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. AS7144B) for COVID-19 vaccination. 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) 1 dosage form. On 21-Oct-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine administered after the 30 day beyond use date). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine administered after the 30 day beyond use date) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Vaccine administered after the 30 day beyond use date). No concomitant medications were reported. It was reported that patient received vaccine from opened individual vials of vial size 2.5 ml. The vial was initially stored in the refrigerator on 20-Sep-2022. The vial did not undergo any temperature excursions. Patient was administered the vaccine as Second booster dose. No treatment details were reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2494586

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7144B

gering

Staat: MI
Alter: 46,0
Geschlecht: M
Eingang: 01.11.2022
Impfdatum: 21.10.2022
Beginn: 21.10.2022
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

patient was administered vaccine after the 30 day beyond use date; No adverse event; patient was administered vaccine after the 30 day beyond use date; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (patient was administered vaccine after the 30 day beyond use date), PRODUCT STORAGE ERROR (patient was administered vaccine after the 30 day beyond use date) and NO ADVERSE EVENT (No adverse event) in a 46-year-old male patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. AS7144B) for COVID-19 vaccination. 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) 1 dosage form. On 21-Oct-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (patient was administered vaccine after the 30 day beyond use date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (patient was administered vaccine after the 30 day beyond use date) and NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (patient was administered vaccine after the 30 day beyond use date), PRODUCT STORAGE ERROR (patient was administered vaccine after the 30 day beyond use date) 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 (patient was administered vaccine after the 30 day beyond use date) and PRODUCT STORAGE ERROR (patient was administered vaccine after the 30 day beyond use date). No concomitant medications were reported. Individual vial was opened. Vial size was reported as 2.5 ml. The vial was initially stored in the refrigerator on 20-Sep-2022. The vial did not undergo any temperature excursions. No treatment medications were reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2493645

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7144B

gering

Staat: MI
Alter: 50,0
Geschlecht: M
Eingang: 31.10.2022
Impfdatum: 21.10.2022
Beginn: 21.10.2022
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

Patient was administered vaccine after the 30 day beyond use date; No adverse event; Patient was administered vaccine after the 30 day beyond use date; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient was administered vaccine after the 30 day beyond use date), PRODUCT STORAGE ERROR (Patient was administered vaccine after the 30 day beyond use date) and NO ADVERSE EVENT (No adverse event) in a 50-year-old male patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. AS7144B) for COVID-19 vaccination. 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) 1 dosage form. On 21-Oct-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient was administered vaccine after the 30 day beyond use date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Patient was administered vaccine after the 30 day beyond use date) and NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient was administered vaccine after the 30 day beyond use date), PRODUCT STORAGE ERROR (Patient was administered vaccine after the 30 day beyond use date) 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 (Patient was administered vaccine after the 30 day beyond use date) and PRODUCT STORAGE ERROR (Patient was administered vaccine after the 30 day beyond use date). No concomitant medications were reported. Individual vials or unbroken cartons was opened individual vials. Vial size was 2.5ml. The vial was initially stored in the refrigerator was 20-Sep-2022. The vial did not undergo any temperature excursions. No treatment medications were reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2493644

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7144B

gering

Staat: MI
Alter: 63,0
Geschlecht: M
Eingang: 31.10.2022
Impfdatum: 21.10.2022
Beginn: 21.10.2022
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

patients were administered the vaccine after the 30-day beyond use date; No adverse event; administered after the 30 day beyond use date; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (administered after the 30 day beyond use date), PRODUCT STORAGE ERROR (patients were administered the vaccine after the 30-day beyond use date) and NO ADVERSE EVENT (No adverse event) in a 63-year-old male patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. AS7144B) for COVID-19 vaccination. 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) 1 dosage form. On 21-Oct-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (administered after the 30 day beyond use date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (patients were administered the vaccine after the 30-day beyond use date) and NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (administered after the 30 day beyond use date), PRODUCT STORAGE ERROR (patients were administered the vaccine after the 30-day beyond use date) 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 (administered after the 30 day beyond use date) and PRODUCT STORAGE ERROR (patients were administered the vaccine after the 30-day beyond use date). No concomitant medications were reported. The vial size was 2.5mL. The vial was initially stored in the refrigerator on 20-Sep-2022. The vial did not undergo any temperature excursions. No treatment medications were reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2493642

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7144B

gering

Staat: MI
Alter: 61,0
Geschlecht: M
Eingang: 31.10.2022
Impfdatum: 24.10.2022
Beginn: 24.10.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: OT / -

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

Expired product administered No adverse event Product storage error

Symptomtext

Doses were administered >12 hours post puncture,Dose administered after 30-day Use By Date; No adverse event; Doses were administered >12 hours post puncture,Dose administered after 30-day Use By Date; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Doses were administered >12 hours post puncture,Dose administered after 30-day Use By Date), PRODUCT STORAGE ERROR (Doses were administered >12 hours post puncture,Dose administered after 30-day Use By Date) and NO ADVERSE EVENT (No adverse event) in a 61-year-old male patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. AS7144B) for COVID-19 prophylaxis. No Medical History information was reported. On 24-Oct-2022 at 9:33 AM, 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 24-Oct-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Doses were administered >12 hours post puncture. Dose administered after 30-day Use By Date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Doses were administered >12 hours post puncture. Dose administered after 30-day Use By Date) and NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Doses were administered >12 hours post puncture. Dose administered after 30-day Use By Date), PRODUCT STORAGE ERROR (Doses were administered >12 hours post puncture,Dose administered after 30-day Use By Date) 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 (Doses were administered >12 hours post puncture. Dose administered after 30-day Use By Date) and PRODUCT STORAGE ERROR (Doses were administered >12 hours post puncture. Dose administered after 30-day Use By Date). No concomitant medications were reported. The doses were administered post 12 hours of puncture. Visuals were first thawed on 20-Sep-2022. The vial size was 2.5 mL The vial was initially stored in the refrigerator on 20-Sep-2022. The vial was first punctured on 17-Oct-2022 at 9AM. The vial was stored in fridge post puncture. The vial did not undergo any temperature excursions. The vial was exposed to room temperature for less than a minute. No treatment medications were reported. This case was linked to US-MODERNATX, INC.-MOD-2022-665349 (E2B Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2022-665349:Patient 1

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2493080

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: MI
Alter: 58,0
Geschlecht: F
Eingang: 28.10.2022
Impfdatum: 21.10.2022
Beginn: 21.10.2022
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

Symptomtext

No adverse event; administered after the 30 day beyond use date; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (administered after the 30 day beyond use date) and NO ADVERSE EVENT (No adverse event) in a 58-year-old female patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. AS7144B) for COVID-19 vaccination. 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) 1 dosage form. On 21-Oct-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (administered after the 30 day beyond use date). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (administered after the 30 day beyond use date) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (administered after the 30 day beyond use date). No concomitant drug were reported. It was reported that HCP was transferred to excursions line to discussed HCP mentioned that 5 patients were administered the vaccine after the 30-day beyond use date. It is the same lot number as the previous case however the date of thaw and administration are different. 5 patients were administered the vaccine after 30-day BUD. vial was opened individual vials Vial size was reported as 2.5ml On 20-Sep-2022, the vial was initially stored in the refrigerator. The vial did not undergo any temperature excursion. Vaccines administered were first boosters for some and second booster for other patients.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2493076

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: MI
Alter: 68,0
Geschlecht: M
Eingang: 28.10.2022
Impfdatum: 24.10.2022
Beginn: 24.10.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / -

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

Expired product administered No adverse event

Symptomtext

No adverse event; Doses were administered >12 hours post puncture,Dose administered after 30-day Use By Date; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Doses were administered >12 hours post puncture,Dose administered after 30-day Use By Date) and NO ADVERSE EVENT (No adverse event) in a 68-year-old male patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. AS7144B) for COVID-19 prophylaxis. No Medical History information was reported. On 24-Oct-2022, the patient received third dose of mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (unknown route) 1 dosage form. On 24-Oct-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Doses were administered >12 hours post puncture,Dose administered after 30-day Use By Date). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Doses were administered >12 hours post puncture,Dose administered after 30-day Use By Date) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Doses were administered >12 hours post puncture,Dose administered after 30-day Use By Date). No concomitant medications were reported. It was reported that the vials were first thawed on 20-Sep-2022. Total 2 patient's were administered with the Bivalent vaccine. It was reported that opened individual vials with vial size 2.5 ml The vial was initially stored in the refrigerator on 20-Sep-2022. The vial was first punctured on 17-Oct-2022 at 9:33 AM. The vial was stored in the fridge post punctured. The vial did not undergo any temperature excursions. Total amount of time the vial was exposed to Room temperature range was less than a minute. No treatment details were reported. This case was linked to MOD-2022-665346 (E2B Linked Report).; Sender's Comments: MOD-2022-665346:Patient 1

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2491205

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: NY
Alter: 53,0
Geschlecht: M
Eingang: 27.10.2022
Impfdatum: 26.10.2022
Beginn: 26.10.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / RA

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

Inappropriate schedule of product administration No adverse event

Symptomtext

Patient received a second Moderna Bivalent booster 1 month and 12 days after his first bivalent booster. This was a clerical oversight, staff has been retrained. Patient was monitored and shows no adverse reaction.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Inappropriate schedule of product administration
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None known
Vorgeschichte: None known
Andere Medikamente: -
Allergien: None known
Vorherige Impfungen: -

VAERS 2490638

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7144B

gering

Staat: VA
Alter: 62,0
Geschlecht: M
Eingang: 27.10.2022
Impfdatum: 09.03.2021
Beginn: 10.09.2022
Tage bis Beginn: 550,0
Dosis: 3
Route/Site: - / -

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

COVID-19 COVID-19 immunisation

Symptomtext

REVACCINATION WITH DIFFERENT COVID-19 VACCINE; REBOUND COVID INFECTION; This spontaneous report received from a patient via other manufacturer (Pfizer) concerned a 64 year old male. The patient's height, and weight were not reported. The patient's concurrent conditions included: sleep apnea, penicillin allergy, and drug allergy (quinine). The patient received covid-19 vaccine ad26.cov2.s (dose number in series 1) (suspension for injection, route of admin not reported, batch number: 1805029 expiry: UNKNOWN) dose was not reported, 1 total, administered on 09-MAR-2021 in right arm for covid-19 prophylaxis. Age at time of vaccination 62 years old. Concomitant medications included acetylsalicylic acid, allopurinol, carvedilol, ergocalciferol, hydrochlorothiazide, krill oil, lisinopril, magnesium, rabeprazole, rosuvastatin, tamsulosin, testosterone, ubidecarenone, and vitamin b complex. It was unknown whether patient had any adverse event following vaccination with covid-19 vaccine ad26.cov2.s (dose number in series 1). The patient additionally received two doses of non-company suspect vaccine included: Moderna covid-19 vaccine (elasomeran) (dose number in series 2) (form of admin, and route of admin were not reported, batch number: 939906 expiry: UNKNOWN) dose was not reported, second dose administered on 23-OCT-2021 and (form of admin, and route of admin were not reported, batch number: 065K21A expiry: UNKNOWN) dose was not reported, third dose administered on 04-APR-2022 in right arm for covid-19 prophylaxis. It was unknown whether patient had any adverse event following vaccination with two doses of Moderna covid-19 vaccine (elasomeran) (dose number in series 2). The patient additionally received fourth dose of non-company suspect vaccine included: Moderna covid-19 vaccine (elasomeran) (dose number in series 3) (form of admin, and route of admin were not reported, batch number: AS7144B expiry: UNKNOWN) dose was not reported, administered on 10-SEP-2022 14:00 in right arm for covid-19 prophylaxis. Patient was revaccinated with different covid-19 vaccine (dose number in series 3). On an unspecified date in 2022, the patient experienced covid-19 (dose number in series 3). The patient received non-company co-suspect drug Paxlovid (form of administration, route of administration, batch number, and expiry were not reported) dose was not reported, administered from 08-OCT-2022 to 14-OCT-2022 for treatment of COVID-19. On 11-OCT-2022, Patient experienced rebound covid infection. The action taken with covid-19 vaccine ad26.cov2.s, elasomeran, and elasomeran was not applicable. The patient was recovering from rebound covid infection, and the outcome of revaccination with different covid-19 vaccine was not reported. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Drug allergy (quinine); Penicillin allergy; Sleep apnea
Vorgeschichte: -
Andere Medikamente: LISINOPRIL; HYDROCHLOROTHIAZIDE; TESTOSTERONE; RABEPRAZOLE; CARVEDILOL; ALLOPURINOL; MAGNESIUM; VITAMIN D [ERGOCALCIFEROL]; KRILL OIL; COQ10 [UBIDECARENONE]; ASPRIN; ROSUVASTATIN; TAMSULOSIN; VITAMIN B COMPLEX
Allergien: -
Vorherige Impfungen: -

VAERS 2490144

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge as7144b

gering

Staat: IL
Alter: 71,0
Geschlecht: F
Eingang: 26.10.2022
Impfdatum: 26.09.2022
Beginn: -
Tage bis Beginn: -
Dosis: 5
Route/Site: IM / RA

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

Incorrect route of product administration Injury

Symptomtext

I took the call from the patient & she proceeded to say that she "by no means" wanted to complain about her experience but she got a vaccine from a pharmacist on 9/26/22 who "doesn't know how to give vaccines." She said the vaccine was given way too high on her arm & her husbands was given way too high also, but he is fine & she is injured. She said she went to the Dr & the Dr confirmed it was high based on her pointing to where it was given & referred her to physical therapy which she now is going to. I explained that when errors like this are reported to us, we follow a procedure of filling out a VAERS report & internal incident report to document the incident. She immediately objected saying she didn't want to be part of ANY reporting or give any more information. Patient refused to give which arm or which vaccine was involved & didn't want to be contacted so I don't have any other information. The clinical pharmacy specialist & privacy specialist from our company confirmed that we still have to report this information despite her objections & despite their being a lack of information as she wouldn't give any more necessary information.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect route of product administration
Hospital-Tage: -
Labordaten: unknown
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2487800

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: NC
Alter: -
Geschlecht: U
Eingang: 25.10.2022
Impfdatum: 18.10.2022
Beginn: 18.10.2022
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

No adverse event; Patient was inadvertently administered on 18Oct2022 with bivalent booster dose which was beyond the 30 day use by date.; This vial was removed from the freezer to the refrigerator on 9/2/22.; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient was inadvertently administered on 18Oct2022 with bivalent booster dose which was beyond the 30 day use by date.), PRODUCT STORAGE ERROR (This vial was removed from the freezer to the refrigerator on 9/2/22.) and NO ADVERSE EVENT (No adverse event) 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. AS7144B) for COVID-19 vaccination. No Medical History information was reported. On 18-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) 1 dosage form. On 18-Oct-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient was inadvertently administered on 18Oct2022 with bivalent booster dose which was beyond the 30 day use by date.) and PRODUCT STORAGE ERROR (This vial was removed from the freezer to the refrigerator on 9/2/22.). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient was inadvertently administered on 18Oct2022 with bivalent booster dose which was beyond the 30 day use by date.), PRODUCT STORAGE ERROR (This vial was removed from the freezer to the refrigerator on 9/2/22.) 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 (Patient was inadvertently administered on 18Oct2022 with bivalent booster dose which was beyond the 30 day use by date.) and PRODUCT STORAGE ERROR (This vial was removed from the freezer to the refrigerator on 9/2/22.). No Concomitant medication was reported. It was reported that vial was removed from the freezer to the refrigerator on 9/2/22. No treatment information was provided. This case was linked to US-MODERNATX, INC.-MOD-2022-661812 (E2B Linked Report). Most recent FOLLOW-UP information incorporated above includes: On 20-Oct-2022: Non-Significant Followup received.; Sender's Comments: US-MODERNATX, INC.-MOD-2022-661812:Bivalent Case

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2483635

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: OH
Alter: 69,0
Geschlecht: M
Eingang: 20.10.2022
Impfdatum: 15.09.2022
Beginn: 01.10.2022
Tage bis Beginn: 16,0
Dosis: 5
Route/Site: OT / -

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

Erythema Itching scar Pustule Scratch

Symptomtext

itchiness on the BCG/TB vaccination scar; Small pustules; Scratching it made it worse; Redness; This spontaneous case was reported by a patient and describes the occurrence of ITCHING SCAR (itchiness on the BCG/TB vaccination scar), PUSTULE (Small pustules), SCRATCH (Scratching it made it worse) and ERYTHEMA (Redness) in a 69-year-old male patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. AS7144B) for COVID-19 vaccination. Co-suspect product included non-company product INFLUENZA VACCINE for an unknown indication. Concomitant products included LEVOTHYROXINE, FLUVASTATIN, HYDROCHLOROTHIAZIDE, LOSARTAN POTASSIUM (LOSARTAN HCTZ), ATENOLOL, PAROXETINE, VITAMIN D NOS and MULTIVITAMINS [VITAMINS NOS] for an unknown indication. On 15-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 an unknown date, the patient started INFLUENZA VACCINE (unknown route) at an unspecified dose. In October 2022, the patient experienced ITCHING SCAR (itchiness on the BCG/TB vaccination scar), PUSTULE (Small pustules), SCRATCH (Scratching it made it worse) and ERYTHEMA (Redness). At the time of the report, ITCHING SCAR (itchiness on the BCG/TB vaccination scar), PUSTULE (Small pustules), SCRATCH (Scratching it made it worse) and ERYTHEMA (Redness) had not resolved. The patient received moderna dose 1 on apr-2021, dose 2 was received 6 weeks after dose 1, first booster dose and second booster dose on apr-2022. The patient had never tested COVID positive or diagnosis. Patient had no allergies. The adverse event did not cause patient to seek medical care. The patient never had experienced a similar event in the past. It was reported that symptoms were improved. Treatment medication included topical cream. This case was linked to MOD-2022-660219, MOD-2022-660211 (Patient Link).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Erythema
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: LEVOTHYROXINE; FLUVASTATIN; LOSARTAN HCTZ; ATENOLOL; PAROXETINE; VITAMIN D NOS; MULTIVITAMINS [VITAMINS NOS]
Allergien: -
Vorherige Impfungen: -

VAERS 2482884

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: TX
Alter: 48,0
Geschlecht: F
Eingang: 19.10.2022
Impfdatum: 06.09.2022
Beginn: 10.10.2022
Tage bis Beginn: 34,0
Dosis: 1
Route/Site: SYR / LA

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

Basal cell carcinoma Biopsy skin abnormal Swelling

Symptomtext

I went to the Dermatologist to get my skin checked out and I asked her to look at an unfamiliar bump at the side of my nose. She biopsied the pump. I've never had any medical event prior to this. I have radiation starting next week.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Basal cell carcinoma
Hospital-Tage: -
Labordaten: Skin biopsy, Basil cell carcinoma.
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Birth control
Allergien: No
Vorherige Impfungen: -

VAERS 2482826

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: PA
Alter: 35,0
Geschlecht: F
Eingang: 19.10.2022
Impfdatum: 07.09.2022
Beginn: 14.09.2022
Tage bis Beginn: 7,0
Dosis: 1
Route/Site: IM / LA

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

Back disorder X-ray normal

Symptomtext

One week after receiving vaccine, I was standing at kitchen sink washing dishes and felt my back just go out. Saw an orthopedist two days later. X-rays where performed and they came back normal. Ortho doctor prescribed FLEXERIL, steroid pack, and physical therapy. After 1.5 weeks of prescribed therapy symptoms mostly resolved. I am still in PT and have follow up with ortho doctor on Friday. I experienced an almost exact event following my first dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Back disorder
Hospital-Tage: -
Labordaten: X-ray was negative
Aktuelle Erkrankungen: No
Vorgeschichte: Obesity
Andere Medikamente: Prenatal vitamin; ZOLOFT
Allergien: Penicillin; sulfa
Vorherige Impfungen: COVID-19 DEC 19, 2020 Pfizer-BioNTech

VAERS 2481666

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: -
Alter: 49,0
Geschlecht: F
Eingang: 18.10.2022
Impfdatum: 10.09.2022
Beginn: 13.09.2022
Tage bis Beginn: 3,0
Dosis: 4
Route/Site: - / -

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

Tinnitus

Symptomtext

Persistent bilateral tinnitus

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tinnitus
Hospital-Tage: -
Labordaten: ENT eval
Aktuelle Erkrankungen: -
Vorgeschichte: HTN, Lumbar facet arthrosis, GERD, history gastric bypass, vitamin D deficiency, Prediabetes
Andere Medikamente: Metformin, Metoprolol, Omeprazole, Tizanidine, Spironolactone, vitamin D
Allergien: adhesive tape, estrogen, Lisinopril, Amlodipine, asparagus, strawberries
Vorherige Impfungen: -

VAERS 2478348

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: OH
Alter: 85,0
Geschlecht: F
Eingang: 14.10.2022
Impfdatum: 12.10.2022
Beginn: 12.10.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / RA

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

Extra dose administered Interchange of vaccine products

Symptomtext

PATIENT RECEIVED A SECOND DOSE OF BI-VALENT VACCINE. FIRST BI-VALENT VACCINE (PFIZER LOT GH9694) WAS GIVEN ON 9/14/22. MODERNA BI-VALENT VACCINE WAS THEN GIVEN ON 10-12-22 (MODERNA LOT AS7144B)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2478347

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: OH
Alter: 69,0
Geschlecht: F
Eingang: 14.10.2022
Impfdatum: 12.10.2022
Beginn: 12.10.2022
Tage bis Beginn: 0,0
Dosis: 6
Route/Site: IM / RA

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

Extra dose administered Interchange of vaccine products

Symptomtext

PATIENT RECEIVED A SECOND DOSE OF BI-VALENT VACCINE. FIRST BI-VALENT VACCINE (PFIZER LOT GH9694) WAS GIVEN ON 9/14/22. MODERNA BI-VALENT VACCINE WAS THEN GIVEN ON 10-12-22 (MODERNA LOT AS7144B)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2478346

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: OH
Alter: 81,0
Geschlecht: F
Eingang: 14.10.2022
Impfdatum: 12.10.2022
Beginn: 12.10.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / RA

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

Extra dose administered Interchange of vaccine products

Symptomtext

PATIENT RECEIVED A SECOND DOSE OF BI-VALENT VACCINE. FIRST BI-VALENT VACCINE (PFIZER LOT GH9694) WAS GIVEN ON 9/14/22. MODERNA BI-VALENT VACCINE WAS THEN GIVEN ON 10-12-22 (MODERNA LOT AS7144B)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2475031

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7144B

gering

Staat: TX
Alter: -
Geschlecht: U
Eingang: 12.10.2022
Impfdatum: 17.09.2022
Beginn: 17.09.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / -

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

Circumstance or information capable of leading to medication error No adverse event

Symptomtext

No adverse event; Not sure if the patient received Bivalent or Monovalent Booster; This spontaneous case was reported by a nurse and describes the occurrence of CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR (Not sure if the patient received Bivalent or Monovalent Booster) and NO ADVERSE EVENT (No adverse event) 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. AS7144B) for COVID-19 vaccination. No Medical History information was reported. On 17-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) 1 dosage form. On 17-Sep-2022, the patient experienced CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR (Not sure if the patient received Bivalent or Monovalent Booster). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR (Not sure if the patient received Bivalent or Monovalent Booster) 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 CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR (Not sure if the patient received Bivalent or Monovalent Booster). No concomitant medication were reported. The reporter (nurse) mentioned that a MD recorded the lot number on the patient chart and vaccination card for a booster shot. The reporter mentioned that because of the date, she was sure that the shot was Bivalent but did not have proof. The reporter mentioned that they are not sure if this shot was bivalent or monovalent No treatment information was provided by the reporter.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Circumstance or information capable of leading to medication error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2472557

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: NJ
Alter: 80,0
Geschlecht: M
Eingang: 08.10.2022
Impfdatum: 09.09.2022
Beginn: 15.09.2022
Tage bis Beginn: 6,0
Dosis: 1
Route/Site: IM / RA

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

Abnormal dreams Blood pressure decreased Electrocardiogram Heart rate decreased Labile blood pressure Nervousness Sleep disorder

Symptomtext

it is important to note that I also received the Fluzone high dose bivalent immunization, lot # UJ875AA at the same time as the Moderna bivalent vaccine in the opposite arm a few days, estimate 5, after the injection, i began having very vivid dreams, 18 days later i felt shaky and discovered that my blood pressure dropped to in the low 100 and heartrate into the forties, i was seen by my cardiologist, on September 21, that would have been 3 weeks after the immunization, my heart rate was 43 in his office. the nebivolol was discontinued and I was started on hydrochlorothiazide, the blood pressure has been a bit labile, but the heart rate rose into the 70s. I continue to have very vivid, upsetting dreams which awaken me, about 2-3 times a week.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abnormal dreams
Hospital-Tage: -
Labordaten: ECG done on 9/21, HR 46, PR 162, QRS 136 (there is a long history of RBBB) QTc 399
Aktuelle Erkrankungen: renal lithiasis requiring surgical therapy, benign prostatic hypertrophy, new opnset essential hypertension
Vorgeschichte: extensive arterial calcifications with mild aortic stenosis
Andere Medikamente: rosuvastatin 10 mg, tamsulosin 0.8, nebivolol 2.5 mg, niacin 2,000 mg, cetirizine 10 mg, multi-vitamin, trunature prostate plus health complex- all once a day
Allergien: none
Vorherige Impfungen: -

VAERS 2470825

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: MO
Alter: 61,0
Geschlecht: F
Eingang: 06.10.2022
Impfdatum: 07.09.2022
Beginn: 27.09.2022
Tage bis Beginn: 20,0
Dosis: 5
Route/Site: IM / AR

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

COVID-19 SARS-CoV-2 test positive

Symptomtext

I did not have an adverse reaction to the vaccine. This time of year, I have seasonal allergies every year. I had to be tested for COVID-19 prior to a medical procedure. I went home and took a home test and it was positive on 09/27/2022. I went to the next level and had a NATT test and it confirmed COVID-19 positive on 09/27/2022. My symptoms felt more like allergies, so I would never think I had COVID-19. I did not obtain a prescription due to my liver cirrhosis. As of today, I continue to test positive.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Home test and a NATT test was positive for COVID-19 on 09/27/2022.
Aktuelle Erkrankungen: N/A
Vorgeschichte: Liver cirrhosis
Andere Medikamente: Metformin; Atorvastatin; Losartan; Prilosec
Allergien: Opioid derived drugs.
Vorherige Impfungen: -

VAERS 2470169

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: TX
Alter: 54,0
Geschlecht: M
Eingang: 05.10.2022
Impfdatum: 04.09.2022
Beginn: 14.09.2022
Tage bis Beginn: 10,0
Dosis: 5
Route/Site: IM / LA

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

Visual impairment

Symptomtext

My vision has been stable for 30+ years. It had changed (for the better) in August with my left eye. Starting around mid-September, the left eye seemed to change again. I went to see the doctor and it had changed again (needing a weaker prescription) but could never be made sharp like previously. I adjusted the glasses and it appears like my vision is changing again. The ophthalmologist had no reason for the vision changing and changing rapidly or the lack of sharpness. I started using lubricating eye drops and updated glasses. Based on the continued poor vision in my left eye, will see the ophthalmologist again next week. At this point, I don't know if this is related to the vaccine as I have had others with nothing like this before but it was recommended by the CDC call I got to report this.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Visual impairment
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: sulfa
Vorherige Impfungen: -

VAERS 2469001

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge as7144b

gering

Staat: DC
Alter: 36,0
Geschlecht: M
Eingang: 04.10.2022
Impfdatum: 09.09.2022
Beginn: 09.09.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Wrong product administered

Symptomtext

Error: Wrong Vaccine/Product Administered-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Wrong product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2468678

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: MD
Alter: 41,0
Geschlecht: M
Eingang: 04.10.2022
Impfdatum: 09.09.2022
Beginn: 09.09.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Syringe issue

Symptomtext

Error: Leaking from Syringe-

Weitere VAERSDATA-Felder

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

VAERS 2468473

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: IL
Alter: 45,0
Geschlecht: M
Eingang: 04.10.2022
Impfdatum: 08.09.2022
Beginn: 08.09.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Wrong product administered

Symptomtext

Error: Wrong Vaccine/Product Administered-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Wrong product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2468468

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: NC
Alter: 22,0
Geschlecht: M
Eingang: 04.10.2022
Impfdatum: 08.09.2022
Beginn: 08.09.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Wrong product administered

Symptomtext

Error: Wrong Vaccine/Product Administered-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Wrong product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2468463

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: MD
Alter: 24,0
Geschlecht: F
Eingang: 04.10.2022
Impfdatum: 08.09.2022
Beginn: 08.09.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Wrong product administered

Symptomtext

Error: Wrong Vaccine/Product Administered-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Wrong product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2468455

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: UT
Alter: 68,0
Geschlecht: M
Eingang: 04.10.2022
Impfdatum: 10.09.2022
Beginn: 10.09.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Incorrect dose administered

Symptomtext

Error: Wrong Dose of Vaccine - Too High-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2468453

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge as7144b

gering

Staat: MO
Alter: 67,0
Geschlecht: F
Eingang: 04.10.2022
Impfdatum: 13.09.2022
Beginn: 13.09.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Incorrect product formulation administered

Symptomtext

Error: Wrong Vaccine Formulation (ex. Prevnar 13 v. Prevnar 23)-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2468450

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge as7144b

gering

Staat: MO
Alter: 62,0
Geschlecht: M
Eingang: 04.10.2022
Impfdatum: 13.09.2022
Beginn: 13.09.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Incorrect product formulation administered

Symptomtext

Error: Wrong Vaccine Formulation (ex. Prevnar 13 v. Prevnar 23)-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2468448

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge as7144b

gering

Staat: MO
Alter: 74,0
Geschlecht: F
Eingang: 04.10.2022
Impfdatum: 13.09.2022
Beginn: 13.09.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Incorrect product formulation administered

Symptomtext

Error: Wrong Vaccine Formulation (ex. Prevnar 13 v. Prevnar 23)-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2468446

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge as7144b

gering

Staat: MO
Alter: 75,0
Geschlecht: M
Eingang: 04.10.2022
Impfdatum: 13.09.2022
Beginn: 13.09.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Incorrect product formulation administered

Symptomtext

Error: Wrong Vaccine Formulation (ex. Prevnar 13 v. Prevnar 23)-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2468444

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge as7144b

gering

Staat: MO
Alter: 32,0
Geschlecht: M
Eingang: 04.10.2022
Impfdatum: 13.09.2022
Beginn: 13.09.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Incorrect product formulation administered

Symptomtext

Error: Wrong Vaccine Formulation (ex. Prevnar 13 v. Prevnar 23)-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2468441

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge as7144b

gering

Staat: MO
Alter: 35,0
Geschlecht: M
Eingang: 04.10.2022
Impfdatum: 13.09.2022
Beginn: 13.09.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Incorrect product formulation administered

Symptomtext

Error: Wrong Vaccine Formulation (ex. Prevnar 13 v. Prevnar 23)-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2468439

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge as7144b

gering

Staat: MO
Alter: 19,0
Geschlecht: M
Eingang: 04.10.2022
Impfdatum: 13.09.2022
Beginn: 13.09.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Wrong product administered

Symptomtext

Error: Wrong Vaccine/Product Administered-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Wrong product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2454444

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge as7144b

gering

Staat: GA
Alter: 28,0
Geschlecht: F
Eingang: 04.10.2022
Impfdatum: 12.09.2022
Beginn: 12.09.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Unevaluable event Wrong product administered

Symptomtext

Error: Wrong Vaccine/Product Administered-

Weitere VAERSDATA-Felder

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

VAERS 2467150

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: MA
Alter: 54,0
Geschlecht: F
Eingang: 03.10.2022
Impfdatum: 02.09.2022
Beginn: 17.09.2022
Tage bis Beginn: 15,0
Dosis: 5
Route/Site: IM / LA

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

Blood test Electrocardiogram Full blood count Heart rate increased Heart rate irregular Thyroid function test

Symptomtext

I had very fast irregular hear beat it felt very scrambled up it eventually slowed but felt very irregular so I went to the ER at a local hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Blood test
Hospital-Tage: -
Labordaten: I had EKG, CBC blood profile and thyroid test.
Aktuelle Erkrankungen: No.
Vorgeschichte: Migraine headaches; Depression.
Andere Medikamente: Vitamin B12.
Allergien: CIPRO; cephalosporin.
Vorherige Impfungen: -

VAERS 2466915

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7144B

gering

Staat: NY
Alter: 68,0
Geschlecht: M
Eingang: 02.10.2022
Impfdatum: 21.09.2022
Beginn: 21.09.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / LA

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

Incorrect product formulation administered

Symptomtext

Client with appointment for Moderna Bivalent Booster received 0.25 at 1145am and returned to clinic 2pm for second 0.25 dosage of Moderna Bivalent Booster. Client tolerated well

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2466912

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7144B

gering

Staat: NY
Alter: 43,0
Geschlecht: M
Eingang: 02.10.2022
Impfdatum: 21.09.2022
Beginn: 21.09.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Underdose

Symptomtext

Patient with scheduled appointment for Moderna booster bivalent. Patient received 0.25 at 1205 pm which is half the recommended amount. Patient was called and returned to clinic at approximately 330pm and received the another 0.25 Moderna bivalent vaccine booster and tolerated well.

Weitere VAERSDATA-Felder

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

VAERS 2463778

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: CA
Alter: 74,0
Geschlecht: F
Eingang: 28.09.2022
Impfdatum: 19.09.2022
Beginn: 19.09.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / RA

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

Circumstance or information capable of leading to medication error

Symptomtext

The vaccine was injected into my RIGHT ARM. The official record says left. I tried to contact the pharmacy records and was hung up on, disconnected, etc. There is no way to contact them to change it. Further, the location of the injection in the store was strewn with medical waste. I told the pharmacist not to kneel down on the floor because of it. I was not given any information afterwards (no aftercare, no info about adverse affects) and was not told to stay on site / sit for at least 15 minutes. They also almost lost my vax card.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Circumstance or information capable of leading to medication error
Hospital-Tage: -
Labordaten: Mistake on my record. should be RIGHT ARM. If there were a reaction from the vaccine, they would not be able to justify that it was from the vaccine.
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: sulfa drugs
Vorherige Impfungen: -

VAERS 2461929

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: PA
Alter: 69,0
Geschlecht: F
Eingang: 27.09.2022
Impfdatum: 21.09.2022
Beginn: 21.09.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Underdose

Symptomtext

PATIENT RECEIVED 0.25ML INSTEAD OF 0.5ML

Weitere VAERSDATA-Felder

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

VAERS 2461924

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: PA
Alter: 77,0
Geschlecht: F
Eingang: 27.09.2022
Impfdatum: 21.09.2022
Beginn: 21.09.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Underdose

Symptomtext

PATIENT RECEIVED 0.25ML INSTEAD OF 0.5ML

Weitere VAERSDATA-Felder

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

VAERS 2461885

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: PA
Alter: 80,0
Geschlecht: F
Eingang: 27.09.2022
Impfdatum: 27.09.2022
Beginn: 27.09.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Underdose

Symptomtext

PATIENT RECEIVED 0.25ML INSTEAD OF 0.5ML

Weitere VAERSDATA-Felder

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

VAERS 2461880

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: PA
Alter: 81,0
Geschlecht: F
Eingang: 27.09.2022
Impfdatum: 27.09.2022
Beginn: 27.09.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / RA

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

Underdose

Symptomtext

patient received 0.25ml instead of 0.5ml of Moderna Bivalent Booster Dose

Weitere VAERSDATA-Felder

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

VAERS 2461874

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144b

gering

Staat: PA
Alter: 48,0
Geschlecht: F
Eingang: 27.09.2022
Impfdatum: 27.09.2022
Beginn: 27.09.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Incorrect dose administered Underdose

Symptomtext

Patient received 0.25ml instead of 0.5ml of Moderna Bivalent booster dose

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2460706

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: -
Alter: 76,0
Geschlecht: M
Eingang: 26.09.2022
Impfdatum: 20.09.2022
Beginn: 20.09.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Incorrect dose administered Incorrect product formulation administered

Symptomtext

On the above-listed date, a vaccination clinic was held for staff to receive the COVID-19 booster vaccination. On this day we had Bivalent Moderna Booster dosed vials on hand to be given to those requesting the booster dose. At the time of the clinic, the vaccinator was operating on incorrect information that the Moderna Booster vaccination for the Bivalent vaccine was 0.25 mls rather than the new dosage of 0.5mls. The error was not noticed until the end of the clinic. Immediately the error was communicated to those affected. All patients requesting so were vaccinated with the remaining 0.25 mls within 24 hours in line with the FDA and CDC recommendations for this specific error. Two patients were contacted but requested the full dosage of the booster vaccine in the coming weeks. Three patients were contacted and chose not to be vaccinated further. There were no reactions noted upon follow-up. All patients were advised to communicate with their primary care doctors and follow up with them should there be any adverse reactions. The entire department debriefed and confirmed all new information and rehabilitated the draw-up and delivery of SOPS for all vaccinations in the future. This error was taken very seriously and all means of ensuring this is to not happen in the future were implemented.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2460705

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: -
Alter: 52,0
Geschlecht: M
Eingang: 26.09.2022
Impfdatum: 20.09.2022
Beginn: 20.09.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Incorrect dose administered Incorrect product formulation administered

Symptomtext

On the above-listed date, a vaccination clinic was held for staff to receive the COVID-19 booster vaccination. On this day we had Bivalent Moderna Booster dosed vials on hand to be given to those requesting the booster dose. At the time of the clinic, the vaccinator was operating on incorrect information that the Moderna Booster vaccination for the Bivalent vaccine was 0.25 mls rather than the new dosage of 0.5mls. The error was not noticed until the end of the clinic. Immediately the error was communicated to those affected. All patients requesting so were vaccinated with the remaining 0.25 mls within 24 hours in line with the FDA and CDC recommendations for this specific error. Two patients were contacted but requested the full dosage of the booster vaccine in the coming weeks. Three patients were contacted and chose not to be vaccinated further. There were no reactions noted upon follow-up. All patients were advised to communicate with their primary care doctors and follow up with them should there be any adverse reactions. The entire department debriefed and confirmed all new information and rehabilitated the draw-up and delivery of for all vaccinations in the future. This error was taken very seriously and all means of ensuring this is to not happen in the future were implemented.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2460701

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: -
Alter: 58,0
Geschlecht: M
Eingang: 26.09.2022
Impfdatum: 20.09.2022
Beginn: 20.09.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Underdose

Symptomtext

On the above-listed date, a vaccination clinic was held for staff to receive the COVID-19 booster vaccination. On this day we had Bivalent Moderna Booster dosed vials on hand to be given to those requesting the booster dose. At the time of the clinic, the vaccinator was operating on incorrect information that the Moderna Booster vaccination for the Bivalent vaccine was 0.25 mls rather than the new dosage of 0.5mls. The error was not noticed until the end of the clinic. Immediately the error was communicated to those affected. All patients requesting so were vaccinated with the remaining 0.25 mls within 24 hours in line with the FDA and CDC recommendations for this specific error. Two patients were contacted but requested the full dosage of the booster vaccine in the coming weeks. Three patients were contacted and chose not to be vaccinated further. There were no reactions noted upon follow-up. All patients were advised to communicate with their primary care doctors and follow up with them should there be any adverse reactions. The entire department debriefed and confirmed all new information and rehabilitated the draw-up and delivery of SOPS for all vaccinations in the future. This error was taken very seriously and all means of ensuring this is to not happen in the future were implemented.

Weitere VAERSDATA-Felder

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

VAERS 2460697

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: -
Alter: 54,0
Geschlecht: M
Eingang: 26.09.2022
Impfdatum: 20.09.2022
Beginn: 20.09.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Underdose

Symptomtext

On the above-listed date, a vaccination clinic was held for staff to receive the COVID-19 booster vaccination. On this day we had Bivalent Moderna Booster dosed vials on hand to be given to those requesting the booster dose. At the time of the clinic, the vaccinator was operating on incorrect information that the Moderna Booster vaccination for the Bivalent vaccine was 0.25 mls rather than the new dosage of 0.5mls. The error was not noticed until the end of the clinic. Immediately the error was communicated to those affected. All patients requesting so were vaccinated with the remaining 0.25 mls within 24 hours in line with the FDA and CDC recommendations for this specific error. Two patients were contacted but requested the full dosage of the booster vaccine in the coming weeks. Three patients were contacted and chose not to be vaccinated further. There were no reactions noted upon follow-up. All patients were advised to communicate with their primary care doctors and follow up with them should there be any adverse reactions. The entire department debriefed and confirmed all new information and rehabilitated the draw-up and delivery of SOPS for all vaccinations in the future. This error was taken very seriously and all means of ensuring this is to not happen in the future were implemented.

Weitere VAERSDATA-Felder

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

VAERS 2460691

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: -
Alter: 73,0
Geschlecht: F
Eingang: 26.09.2022
Impfdatum: 20.09.2022
Beginn: 20.09.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Underdose

Symptomtext

On the above-listed date, a vaccination clinic was held for staff to receive the COVID-19 booster vaccination. On this day we had Bivalent Moderna Booster dosed vials on hand to be given to those requesting the booster dose. At the time of the clinic, the vaccinator was operating on incorrect information that the Moderna Booster vaccination for the Bivalent vaccine was 0.25 mls rather than the new dosage of 0.5mls. The error was not noticed until the end of the clinic. Immediately the error was communicated to those affected. All patients requesting so were vaccinated with the remaining 0.25 mls within 24 hours in line with the FDA and CDC recommendations for this specific error. Two patients were contacted but requested the full dosage of the booster vaccine in the coming weeks. Three patients were contacted and chose not to be vaccinated further. There were no reactions noted upon follow-up. All patients were advised to communicate with their primary care doctors and follow up with them should there be any adverse reactions. The entire department debriefed and confirmed all new information and rehabilitated the draw-up and delivery for all vaccinations in the future. This error was taken very seriously and all means of ensuring this is to not happen in the future were implemented.

Weitere VAERSDATA-Felder

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

VAERS 2460686

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: -
Alter: 47,0
Geschlecht: F
Eingang: 26.09.2022
Impfdatum: 20.09.2022
Beginn: 20.09.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Underdose

Symptomtext

On the above-listed date, a vaccination clinic was held for staff to receive the COVID-19 booster vaccination. On this day we had Bivalent Moderna Booster dosed vials on hand to be given to those requesting the booster dose. At the time of the clinic, the vaccinator was operating on incorrect information that the Moderna Booster vaccination for the Bivalent vaccine was 0.25 mls rather than the new dosage of 0.5mls. The error was not noticed until the end of the clinic. Immediately the error was communicated to those affected. All patients requesting so were vaccinated with the remaining 0.25 mls within 24 hours in line with the FDA and CDC recommendations for this specific error. Two patients were contacted but requested the full dosage of the booster vaccine in the coming weeks. Three patients were contacted and chose not to be vaccinated further. There were no reactions noted upon follow-up. All patients were advised to communicate with their primary care doctors and follow up with them should there be any adverse reactions. The entire department debriefed and confirmed all new information and rehabilitated the draw-up and delivery of SOPS for all vaccinations in the future. This error was taken very seriously and all means of ensuring this is to not happen in the future were implemented.

Weitere VAERSDATA-Felder

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

VAERS 2460683

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: -
Alter: 62,0
Geschlecht: M
Eingang: 26.09.2022
Impfdatum: 20.09.2022
Beginn: 20.09.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Underdose

Symptomtext

On the above-listed date, a vaccination clinic was held for staff to receive the COVID-19 booster vaccination. On this day we had Bivalent Moderna Booster dosed vials on hand to be given to those requesting the booster dose. At the time of the clinic, the vaccinator was operating on incorrect information that the Moderna Booster vaccination for the Bivalent vaccine was 0.25 mls rather than the new dosage of 0.5mls. The error was not noticed until the end of the clinic. Immediately the error was communicated to those affected. All patients requesting so were vaccinated with the remaining 0.25 mls within 24 hours in line with the FDA and CDC recommendations for this specific error. Two patients were contacted but requested the full dosage of the booster vaccine in the coming weeks. Three patients were contacted and chose not to be vaccinated further. There were no reactions noted upon follow-up. All patients were advised to communicate with their primary care doctors and follow up with them should there be any adverse reactions. The entire department debriefed and confirmed all new information and rehabilitated the draw-up and delivery of SOPS for all vaccinations in the future. This error was taken very seriously and all means of ensuring this is to not happen in the future were implemented.

Weitere VAERSDATA-Felder

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

VAERS 2460677

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: -
Alter: 61,0
Geschlecht: F
Eingang: 26.09.2022
Impfdatum: 20.09.2022
Beginn: 20.09.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: - / LA

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

Underdose

Symptomtext

On the above-listed date, a vaccination clinic was held for staff to receive the COVID-19 booster vaccination. On this day we had Bivalent Moderna Booster dosed vials on hand to be given to those requesting the booster dose. At the time of the clinic, the vaccinator was operating on incorrect information that the Moderna Booster vaccination for the Bivalent vaccine was 0.25 mls rather than the new dosage of 0.5mls. The error was not noticed until the end of the clinic. Immediately the error was communicated to those affected. All patients requesting so were vaccinated with the remaining 0.25 mls within 24 hours in line with the FDA and CDC recommendations for this specific error. Two patients were contacted but requested the full dosage of the booster vaccine in the coming weeks. Three patients were contacted and chose not to be vaccinated further. There were no reactions noted upon follow-up. All patients were advised to communicate with their primary care doctors and follow up with them should there be any adverse reactions. The entire department debriefed and confirmed all new information and rehabilitated the draw-up and delivery of or all vaccinations in the future. This error was taken very seriously and all means of ensuring this is to not happen in the future were implemented.

Weitere VAERSDATA-Felder

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

VAERS 2460671

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: -
Alter: 37,0
Geschlecht: M
Eingang: 26.09.2022
Impfdatum: 20.09.2022
Beginn: 20.09.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Underdose

Symptomtext

On the above-listed date, a vaccination clinic was held for staff to receive the COVID-19 booster vaccination. On this day we had Bivalent Moderna Booster dosed vials on hand to be given to those requesting the booster dose. At the time of the clinic, the vaccinator was operating on incorrect information that the Moderna Booster vaccination for the Bivalent vaccine was 0.25 mls rather than the new dosage of 0.5mls. The error was not noticed until the end of the clinic. Immediately the error was communicated to those affected. All patients requesting so were vaccinated with the remaining 0.25 mls within 24 hours in line with the FDA and CDC recommendations for this specific error. Two patients were contacted but requested the full dosage of the booster vaccine in the coming weeks. Three patients were contacted and chose not to be vaccinated further. There were no reactions noted upon follow-up. All patients were advised to communicate with their primary care doctors and follow up with them should there be any adverse reactions. The entire department debriefed and confirmed all new information and rehabilitated the draw-up and delivery of SOPS for all vaccinations in the future. This error was taken very seriously and all means of ensuring this is to not happen in the future were implemented.

Weitere VAERSDATA-Felder

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

VAERS 2460665

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: -
Alter: 27,0
Geschlecht: M
Eingang: 26.09.2022
Impfdatum: 20.09.2022
Beginn: 20.09.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Underdose

Symptomtext

On the above-listed date, a vaccination clinic was held for staff to receive the COVID-19 booster vaccination. On this day we had Bivalent Moderna Booster dosed vials on hand to be given to those requesting the booster dose. At the time of the clinic, the vaccinator was operating on incorrect information that the Moderna Booster vaccination for the Bivalent vaccine was 0.25 mgs rather than the new dosage of 0.5mgs. The error was not noticed until the end of the clinic. Immediately the error was communicated to those affected. All patients requesting so were vaccinated with the remaining 0.25 mgs within 24 hours in line with the FDA and CDC recommendations for this specific error. Two patients were contacted but requested the full dosage of the booster vaccine in the coming weeks. Three patients were contacted and chose not to be vaccinated further. There were no reactions noted upon follow-up. All patients were advised to communicate with their primary care doctors and follow up with them should there be any adverse reactions. The entire department debriefed and confirmed all new information and rehabilitated the draw-up and delivery of SOPS for all vaccinations in the future. This error was taken very seriously and all means of ensuring this is to not happen in the future were implemented.

Weitere VAERSDATA-Felder

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

VAERS 2460466

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: VA
Alter: 49,0
Geschlecht: M
Eingang: 26.09.2022
Impfdatum: 08.09.2022
Beginn: 12.09.2022
Tage bis Beginn: 4,0
Dosis: 4
Route/Site: IM / LA

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

Tinnitus

Symptomtext

Persistent tinnitus, primarily but not exclusively left-sided.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tinnitus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None diagnosed.
Vorgeschichte: Undiagnosed vascular issue: high APTT, high Beta 2 Glycoprotein 1 IGA.
Andere Medikamente: Vitamin D supplement (2000 IU), low-dose aspirin, Digestive Advantage gummies
Allergien: Erythromycin
Vorherige Impfungen: -

VAERS 2459726

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: -
Alter: 66,0
Geschlecht: M
Eingang: 24.09.2022
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: ja

Wrong product administered

Symptomtext

Administered covid bivalent instead of flu shot patient has not received bivalent vaccine yet so communicated the incident to them.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Wrong product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Unknown
Allergien: Unknown
Vorherige Impfungen: -

VAERS 2455980

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: RI
Alter: 37,0
Geschlecht: F
Eingang: 23.09.2022
Impfdatum: 04.09.2022
Beginn: 18.09.2022
Tage bis Beginn: 14,0
Dosis: 4
Route/Site: IM / LA

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

Dermatomyositis Herpes zoster

Symptomtext

2 weeks later developed Shingles, c7/t1 dermatomes

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dermatomyositis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Migraine
Vorgeschichte: None
Andere Medikamente: Emgality SQ q1mo migraine prophylaxis Eletriptan prn migraine
Allergien: Nkda
Vorherige Impfungen: -

VAERS 2455575

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: NJ
Alter: 34,0
Geschlecht: M
Eingang: 23.09.2022
Impfdatum: 03.09.2022
Beginn: 18.09.2022
Tage bis Beginn: 15,0
Dosis: 4
Route/Site: OT / -

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

COVID-19 SARS-CoV-2 test

Symptomtext

This spontaneous case was reported by a pharmacist and describes the occurrence of COVID-19 (COVID-19) in a 34-year-old male patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. AS7144B) for COVID-19 prophylaxis. The patient had no medical history, concomitant disease or risk factor. On 03-Sep-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 18-Sep-2022, the patient experienced COVID-19 (COVID-19). At the time of the report, COVID-19 (COVID-19) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 18-Sep-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 did not provide any causality assessments. No concomitant medications were reported. Patient tested positive for COVID-19 on 18-Sep-2022 after having received omicron-specific booster on 03-Sep-2022. It was unknown if the patient experienced any additional symptoms/events. No treatment drugs were reported. Company comment: This spontaneous case concerns a 34-year-old male patient with no reported medical history, who experienced unexpected, non-serious AESI Covid-19 (with positive Sars-CoV test), which occurred 15 days after vaccination of a fourth dose of mRNA-1273.222. No further information was provided. The outcome of the events was reported as unknown. The benefit-risk relationship of mRNA-1273 vaccine is not affected by this report. Reporter did not allow further contact. Sender's Comments: This spontaneous case concerns a 34-year-old male patient with no reported medical history, who experienced unexpected, non-serious AESI Covid-19 (with positive Sars-CoV test), which occurred 15 days after vaccination of a fourth dose of mRNA-1273.222. No further information was provided. The outcome of the events was reported as unknown. The benefit-risk relationship of mRNA-1273 vaccine is not affected by this report.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 20220918; Test Name: COVID-19 test; Test Result: Positive; Result Unstructured Data: Positive.
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: The patient had no medical history, concomitant disease or risk factor.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2455245

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: MA
Alter: 50,0
Geschlecht: M
Eingang: 22.09.2022
Impfdatum: 12.09.2022
Beginn: 14.09.2022
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / LA

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

Herpes zoster

Symptomtext

Developed shingles 2-3 days after receiving booster

Weitere VAERSDATA-Felder

Praegender Schweregrund: Herpes zoster
Hospital-Tage: -
Labordaten: Visual diagnosis on 9/21/22
Aktuelle Erkrankungen: None
Vorgeschichte: Acid reflux
Andere Medikamente: Omeprazole
Allergien: None
Vorherige Impfungen: -

VAERS 2453859

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: IA
Alter: 17,0
Geschlecht: F
Eingang: 21.09.2022
Impfdatum: 16.09.2022
Beginn: 16.09.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

No adverse event Product administered to patient of inappropriate age

Symptomtext

Administered vaccine to patient under the age of 18. No significant adverse effects noted.

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2452001

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: WI
Alter: 86,0
Geschlecht: F
Eingang: 20.09.2022
Impfdatum: 19.09.2022
Beginn: 19.09.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Pulse abnormal Somnolence Unresponsive to stimuli

Symptomtext

Unable to awaken, became unresponsive to verbal stimuli, pulse weak. Sent to ER, recovered completely, kept for observation over night.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulse abnormal
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: no
Vorgeschichte: -
Andere Medikamente: no
Allergien: no
Vorherige Impfungen: -

VAERS 2451837

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7144B

gering

Staat: KY
Alter: 52,0
Geschlecht: F
Eingang: 20.09.2022
Impfdatum: 06.09.2022
Beginn: 06.09.2022
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 Product administered at inappropriate site

Symptomtext

No adverse event; Bivalent vaccine was administered to a patient a little lower than the deltoid muscle.; This spontaneous case was reported by a pharmacist and describes the occurrence of PRODUCT ADMINISTERED AT INAPPROPRIATE SITE (Bivalent vaccine was administered to a patient a little lower than the deltoid muscle.) and NO ADVERSE EVENT (No adverse event) in a 52-year-old female patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. AS7144B) for COVID-19 vaccination. No Medical History information was reported. On 06-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) 1 dosage form. On 06-Sep-2022, the patient experienced PRODUCT ADMINISTERED AT INAPPROPRIATE SITE (Bivalent vaccine was administered to a patient a little lower than the deltoid muscle.). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, PRODUCT ADMINISTERED AT INAPPROPRIATE SITE (Bivalent vaccine was administered to a patient a little lower than the deltoid muscle.) 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 PRODUCT ADMINISTERED AT INAPPROPRIATE SITE (Bivalent vaccine was administered to a patient a little lower than the deltoid muscle.). No concomitant medications was reported. No treatment medications was reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2451032

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7144B

gering

Staat: TX
Alter: 24,0
Geschlecht: M
Eingang: 19.09.2022
Impfdatum: 09.09.2022
Beginn: 16.09.2022
Tage bis Beginn: 7,0
Dosis: 5
Route/Site: SYR / RA

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

COVID-19 Impaired work ability Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

I tested about 9:15 in the morning COVID-19 home test for work and I immediately left work, all I had was a sniffle and called the nurse at my university around 9:30 in the morning and we went over the COVID-19 recommendations and they advised me to go home and isolate which I did and on the 17th I saw a telehealth physician to go over symptoms and they prescribed me Paxlovid and a inhaler as needed and I am at home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID-19 home test 9/16/22 Positive
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma
Andere Medikamente: Prozac; Concerti; Descovy
Allergien: Penicillin; Zoloft; Peanut; Shrimp
Vorherige Impfungen: COVID-19 fatigue with all vaccines

VAERS 2449875

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7144B

gering

Staat: OH
Alter: -
Geschlecht: U
Eingang: 17.09.2022
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: UNK
Route/Site: OT / -

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

Accidental underdose No adverse event

Symptomtext

Patient was administered 0.25mL of Moderna COVID-19 Vaccine, Bivalent, instead of 0.5mL; No adverse event; This spontaneous case was reported by a nurse and describes the occurrence of ACCIDENTAL UNDERDOSE (Patient was administered 0.25mL of Moderna COVID-19 Vaccine, Bivalent, instead of 0.5mL) and NO ADVERSE EVENT (No adverse event) in an adult patient of an unknown gender who received mRNA-1273 BIVALENT (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. AS7144B) for COVID-19 prophylaxis. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 BIVALENT (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (unknown route) .25 milliliter. On an unknown date, the patient experienced ACCIDENTAL UNDERDOSE (Patient was administered 0.25mL of Moderna COVID-19 Vaccine, Bivalent, instead of 0.5mL) and NO ADVERSE EVENT (No adverse event). At the time of the report, ACCIDENTAL UNDERDOSE (Patient was administered 0.25mL of Moderna COVID-19 Vaccine, Bivalent, instead of 0.5mL) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 BIVALENT (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 ACCIDENTAL UNDERDOSE (Patient was administered 0.25mL of Moderna COVID-19 Vaccine, Bivalent, instead of 0.5mL). No concomitant medications were reported. No treatment medications were reported.

Weitere VAERSDATA-Felder

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

VAERS 2449873

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7144B

gering

Staat: OH
Alter: -
Geschlecht: U
Eingang: 17.09.2022
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: UNK
Route/Site: OT / -

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

Accidental underdose No adverse event

Symptomtext

Patient was administered 0.25mL of Moderna Covid-19 Vaccine, Bivalent, instead of 0.5mL.; No adverse event; This spontaneous case was reported by a nurse and describes the occurrence of ACCIDENTAL UNDERDOSE (Patient was administered 0.25mL of Moderna Covid-19 Vaccine, Bivalent, instead of 0.5mL.) and NO ADVERSE EVENT (No adverse event) in an adult patient of an unknown gender who received mRNA-1273 BIVALENT (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. AS7144B) for COVID-19 prophylaxis. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 BIVALENT (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (unknown route) .25 milliliter. On an unknown date, the patient experienced ACCIDENTAL UNDERDOSE (Patient was administered 0.25mL of Moderna Covid-19 Vaccine, Bivalent, instead of 0.5mL.) and NO ADVERSE EVENT (No adverse event). At the time of the report, ACCIDENTAL UNDERDOSE (Patient was administered 0.25mL of Moderna Covid-19 Vaccine, Bivalent, instead of 0.5mL.) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 BIVALENT (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 ACCIDENTAL UNDERDOSE (Patient was administered 0.25mL of Moderna Covid-19 Vaccine, Bivalent, instead of 0.5mL.). No concomitant medications were reported. No treatment details were reported. This case was linked to US-MODERNATX, INC.-MOD-2022-644874 (E2B Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2022-644874:

Weitere VAERSDATA-Felder

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

VAERS 2447897

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: IA
Alter: 60,0
Geschlecht: F
Eingang: 16.09.2022
Impfdatum: 14.09.2022
Beginn: 14.09.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Incorrect dose administered

Symptomtext

Patient received a dose of 0.25ml on 9/14/22 but will be coming back next week to receive a full dose of 0.5ml.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2447875

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144b

gering

Staat: IA
Alter: 56,0
Geschlecht: F
Eingang: 16.09.2022
Impfdatum: 14.09.2022
Beginn: 14.09.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Underdose

Symptomtext

Patient was given 0.25ml on 9/14/22, and came back on 9/16/22 for a full dose of 0.5ml

Weitere VAERSDATA-Felder

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

VAERS 2447872

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: IA
Alter: 62,0
Geschlecht: F
Eingang: 16.09.2022
Impfdatum: 14.09.2022
Beginn: 14.09.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Incorrect dose administered

Symptomtext

Patient was given 0.25ml on 9/14/22. Returned on 9/16/22 for the full 0.5ml dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2447870

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: IA
Alter: 82,0
Geschlecht: F
Eingang: 16.09.2022
Impfdatum: 14.09.2022
Beginn: 14.09.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Underdose

Symptomtext

Patient received dose of 0.25ml on 9/14/22. Came back on 9/16/22 and received 0.5ml, full dose.

Weitere VAERSDATA-Felder

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

VAERS 2447865

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: IA
Alter: 70,0
Geschlecht: F
Eingang: 16.09.2022
Impfdatum: 14.09.2022
Beginn: 14.09.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Incorrect dose administered

Symptomtext

Patient was given 0.25ml on 9/14/22, and came back to receive the full dose on 9/16/22 of 0.5ml.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2447860

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: IA
Alter: 74,0
Geschlecht: M
Eingang: 16.09.2022
Impfdatum: 14.09.2022
Beginn: 14.09.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / -

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

Underdose

Symptomtext

Patient was given the dose of 0.25ml on 9/14/22. They returned and received a full dose of 0.5ml on 9/16/22.

Weitere VAERSDATA-Felder

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

VAERS 2447855

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: IA
Alter: 58,0
Geschlecht: F
Eingang: 16.09.2022
Impfdatum: 14.09.2022
Beginn: 14.09.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Underdose

Symptomtext

Patient only received 0.25ml for a dose. Patient returned on 9-16-22 and received the full 0.5ml dose.

Weitere VAERSDATA-Felder

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

VAERS 2444984

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: IA
Alter: 38,0
Geschlecht: F
Eingang: 14.09.2022
Impfdatum: 12.09.2022
Beginn: 12.09.2022
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

Symptomtext

patient given 0.25ml (half) of required 0.5ml dose

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2440913

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: NC
Alter: 54,0
Geschlecht: M
Eingang: 12.09.2022
Impfdatum: 09.09.2022
Beginn: 09.09.2022
Tage bis Beginn: 0,0
Dosis: N/A
Route/Site: IM / UN

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

Incorrect product formulation administered

Symptomtext

The client received the Moderna Bivalent booster dose preparation instead of the Moderna Vaccine authorized for the primary vaccination series. The patient was called and advised of the CDC recommendation to repeat the dose immediately. The patient agreed and returned to the clinic for revaccination. 0.5mL Moderna Primary series (LOT # 017822A preparation administered without incident

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: NA
Aktuelle Erkrankungen: none reported
Vorgeschichte: none reported
Andere Medikamente: unknown
Allergien: unknown -- none reported
Vorherige Impfungen: -

VAERS 2440774

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: IN
Alter: 76,0
Geschlecht: F
Eingang: 12.09.2022
Impfdatum: 12.09.2022
Beginn: 12.09.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Device connection issue Syringe issue Underdose

Symptomtext

The needle came detached from the syringe during injection and the vaccine went all over my chest, the patients arm and face. It was determined patient did not receive the dose and we redid the dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Device connection issue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2440668

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: IL
Alter: 48,0
Geschlecht: F
Eingang: 12.09.2022
Impfdatum: 10.09.2022
Beginn: 12.09.2022
Tage bis Beginn: 2,0
Dosis: 4
Route/Site: IM / LA

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

Dysgeusia

Symptomtext

Metallic taste in mouth.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dysgeusia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: NA
Vorgeschichte: Fibromyalgia
Andere Medikamente: Vitamin D3 1000 Multivitamin plus iron Trazadone 100mg Desvenlafaxine 150mg Valacyclovir 500mg
Allergien: Sulfa drugs
Vorherige Impfungen: -

VAERS 2440445

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge as7144b

gering

Staat: IN
Alter: 79,0
Geschlecht: M
Eingang: 12.09.2022
Impfdatum: 08.09.2022
Beginn: 08.09.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RL

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

Syringe issue

Symptomtext

Error: Leaking from Syringe-

Weitere VAERSDATA-Felder

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

VAERS 2440111

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7144B

gering

Staat: NY
Alter: 42,0
Geschlecht: F
Eingang: 11.09.2022
Impfdatum: 07.09.2022
Beginn: 07.09.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Incorrect product formulation administered

Symptomtext

Error: Wrong Vaccine Formulation (ex. Prevnar 13 v. Prevnar 23)-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2440110

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7144B

gering

Staat: NY
Alter: 50,0
Geschlecht: M
Eingang: 11.09.2022
Impfdatum: 07.09.2022
Beginn: 07.09.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Product preparation issue

Symptomtext

Error: Wrong Vaccine Formulation (ex. Prevnar 13 v. Prevnar 23)-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product preparation issue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2440075

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7144B

gering

Staat: TX
Alter: 72,0
Geschlecht: M
Eingang: 11.09.2022
Impfdatum: 10.09.2022
Beginn: 10.09.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: - / LA

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

Urinary incontinence

Symptomtext

lack of bladder control

Weitere VAERSDATA-Felder

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

VAERS 2438752

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge AS7144B

gering

Staat: IN
Alter: 59,0
Geschlecht: M
Eingang: 10.09.2022
Impfdatum: 04.09.2022
Beginn: 07.09.2022
Tage bis Beginn: 3,0
Dosis: 4
Route/Site: IM / LA

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

Fluid retention

Symptomtext

the same day I received my vaccination, and the following day, I road my bicycle long distance, each day a multi-hour workout. By mid-week my left knee felt like it was accumulating fluid (limited range of motion). I assumed that I'd injured the knee. The next day I experience the same symptom with my right knee. A few days later my left knee is feeling better (greater range of movement), while my right knee continues to have a limited range of movment.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fluid retention
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Atorvastatin 40mg one per day, Lisinopril 20mg one per day, Chlorthalidone 25mg one per day, Ezetimibe 10mg one per day
Allergien: none
Vorherige Impfungen: -

VAERS 2438718

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AS7144B

gering

Staat: VA
Alter: 46,0
Geschlecht: M
Eingang: 10.09.2022
Impfdatum: 06.09.2022
Beginn: 06.09.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / LA

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

Syringe issue

Symptomtext

Error: Leak from syringe.

Weitere VAERSDATA-Felder

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

VAERS 2438682

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge as7144b

gering

Staat: NC
Alter: 26,0
Geschlecht: F
Eingang: 10.09.2022
Impfdatum: 06.09.2022
Beginn: 06.09.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Inappropriate schedule of product administration

Symptomtext

Error: Dose in Series Given Too Early-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Inappropriate schedule of product administration
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -