VAERS Reports 071 F21A

VAERS 2689419

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

kritisch

Staat: -
Alter: 66,0
Geschlecht: M
Eingang: 02.10.2023
Impfdatum: 05.11.2021
Beginn: 30.08.2023
Tage bis Beginn: 663,0
Dosis: 2
Route/Site: - / -

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

Acute respiratory failure Aortic aneurysm Aortic aneurysm repair Aortic dilatation Arterial repair Blood creatinine Blood culture negative Blood lactic acid Body temperature increased Brain natriuretic peptide increased C-reactive protein increased COVID-19 pneumonia Chronic kidney disease Chronic obstructive pulmonary disease Computerised tomogram thorax abnormal Condition aggravated Diabetes mellitus inadequate control Diarrhoea

Symptomtext

Patient is a 68 y.o. male patient of MD with history of Cancer, GERD, depression, HTn, OSA, COPD presented to Hospital with shortness of breath . Sepsis, Acute hypoxic respiratory failure d/t COVID-19 pneumonia, COPD exacerbation OSA Elevated D dimer P/w SOB, HA, N/V/D.vaccination unknown on arrival temp 99 increased to 101.5 , HR 10, RR 26, BP 133/61, satting 88% on RA< increased to 93% 2L Initial CBC w WBC 4., repeat LA 1.1 Troponin normal, BNP 641, D Dimer 1.0, CRP 43.8 CT Chest : no PE, emphysema and fibrosis, nodular opacity in RML possible round pneumonia , cannot exclude nodule Solumedrol given in ER Blood Cx NGTD Decadron 6mg daily for 10 days Continue cefdinir, Zithromax and home inhalers Follow up with pcp Renal Cell Carcinoma S/p partial nephrectomy in 201 Follows with urology at hospital AAA S/p repair endovascualr infrarenal aorta/iliac artery at hospital On admit CT has dilated of the aortic arch 3.6 cm, descending thoracic aorta 3 cm Will need vascular follow up CKD stage 3 a Creatinine over last year 1.3-1.46 At baseline on admit, 1.35 Nicotine dependence Current 1 PPD smoker Discussed and encouraged smoking cessation, >3min total time spent Nodular opacity in lung Most Likely pneumonia, follow up CT in 3 months recommended. Alternatively PET-CT could also be considered. T2DM - uncontrolled A1C: 7.8 continue oral meds F/u with pcp

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2674176

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

kritisch

Staat: -
Alter: 73,0
Geschlecht: F
Eingang: 21.08.2023
Impfdatum: 28.10.2021
Beginn: 30.12.2022
Tage bis Beginn: 428,0
Dosis: 3
Route/Site: IM / LA

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

Acute respiratory failure Ischaemic stroke Symptom recurrence

Symptomtext

ACUTE STROKE DUE TO ISCHEMIA, UNSPECIFIED TYPE AND ARTERY ACUTE HYPOXEMIC RESPIRATORY FAILURE 2/7/2023 -- RECURRENCE OF HOSPITALIZATION WITH SAME SYMPTOMS

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

VAERS 2647300

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

kritisch

Staat: MN
Alter: 78,0
Geschlecht: M
Eingang: 20.06.2023
Impfdatum: 05.11.2021
Beginn: 08.04.2023
Tage bis Beginn: 519,0
Dosis: N/A
Route/Site: UN / UN

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

Acute respiratory failure Asthenia COVID-19 COVID-19 pneumonia Hypophagia Mobility decreased SARS-CoV-2 test positive

Symptomtext

The patient has a history of COPD. He was brought to the ED by EMS on 4/8/23 for evaluation of weakness. Patient lives independently, and reported that he was too weak to get out of his chair and was not able to eat or drink anything for the past three days. Per EMS, O2 sats were in the high 80's. Notably, a rapid COVID PCR test resulted positive in the ED. Ultimately, the patient was admitted 4/8/23 - 4/13/23. Discharge diagnoses included severe COVID-19, COVID pneumonia, and acute hypoxemic respiratory failure due to COVID. During admission, the patient required up to 5L supplemental O2, however was able to be weaned down back to his baseline oxygen needs. He was treated with dexamethasone during admission. Of note, the patient has received the primary COVID vaccine series and one booster.

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

VAERS 2639065

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

kritisch

Staat: -
Alter: 71,0
Geschlecht: F
Eingang: 31.05.2023
Impfdatum: 30.10.2021
Beginn: 16.10.2022
Tage bis Beginn: 351,0
Dosis: 3
Route/Site: IM / LA

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

Acute respiratory failure

Symptomtext

ACUTE RESPIRATORY FAILURE ACUTE HYPOXEMIC RESPIRATORY FAILURE

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

VAERS 2587889

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

kritisch

Staat: MI
Alter: 81,0
Geschlecht: F
Eingang: 01.03.2023
Impfdatum: 27.10.2021
Beginn: 21.02.2023
Tage bis Beginn: 482,0
Dosis: 3
Route/Site: - / -

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

Acute respiratory failure COVID-19 Dyspnoea Hypoxia Pneumonia Computerised tomogram thorax normal Cough Resuscitation Pneumonia bacterial Positive airway pressure therapy SARS-CoV-2 test positive Sepsis Superinfection

Symptomtext

Discharge summary "Patient with Chronic respiratory failure with hypoxia (Home oxygen @ 6 L/m) due to Severe pan lobular emphysema and COPD. Patient had a recent COVID-19 virus infection and after discharge from the hospital developed increased shortness of breath. On presentation had evidence of Acute on chronic respiratory failure with hypoxia as well as signs of Sepsis. These appear due to a Right lower lobe pneumonia suspected to be a superimposed bacterial pneumonia. She has been started on CEFTRIAXONE and continues her dose of prophylaxis AZITHROMYCIN. She initially needed BiPAP but has been weaned down to supplemental oxygen per nasal cannula @ 6-7 L. "

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 6,0
Labordaten: Positive COVID PCR test on 2/08/23 and 2/21/23.
Aktuelle Erkrankungen: -
Vorgeschichte: (Principal) RESOLVED: Acute on chronic respiratory failure with hypoxia Gastroesophageal reflux disease with esophagitis. COVID-19 virus infection Right lower lobe pneumonia RESOLVED: Sepsis COPD (chronic obstructive pulmonary disease) Chronic respiratory failure with hypoxia Severe pan lobular emphysema Normocytic anemia Essential hypertension.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2587889

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

kritisch

Staat: MI
Alter: 81,0
Geschlecht: F
Eingang: 01.03.2023
Impfdatum: 27.10.2021
Beginn: 21.02.2023
Tage bis Beginn: 482,0
Dosis: 3
Route/Site: UN / UN

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

Acute respiratory failure COVID-19 Dyspnoea Hypoxia Pneumonia Computerised tomogram thorax normal Cough Resuscitation Pneumonia bacterial Positive airway pressure therapy SARS-CoV-2 test positive Sepsis Superinfection

Symptomtext

Discharge summary "Patient with Chronic respiratory failure with hypoxia (Home oxygen @ 6 L/m) due to Severe pan lobular emphysema and COPD. Patient had a recent COVID-19 virus infection and after discharge from the hospital developed increased shortness of breath. On presentation had evidence of Acute on chronic respiratory failure with hypoxia as well as signs of Sepsis. These appear due to a Right lower lobe pneumonia suspected to be a superimposed bacterial pneumonia. She has been started on CEFTRIAXONE and continues her dose of prophylaxis AZITHROMYCIN. She initially needed BiPAP but has been weaned down to supplemental oxygen per nasal cannula @ 6-7 L. "

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 6,0
Labordaten: Positive COVID PCR test on 2/08/23 and 2/21/23.
Aktuelle Erkrankungen: -
Vorgeschichte: (Principal) RESOLVED: Acute on chronic respiratory failure with hypoxia Gastroesophageal reflux disease with esophagitis. COVID-19 virus infection Right lower lobe pneumonia RESOLVED: Sepsis COPD (chronic obstructive pulmonary disease) Chronic respiratory failure with hypoxia Severe pan lobular emphysema Normocytic anemia Essential hypertension.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2579679

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

kritisch

Staat: MD
Alter: 49,0
Geschlecht: M
Eingang: 10.02.2023
Impfdatum: 10.03.2022
Beginn: 11.07.2022
Tage bis Beginn: 123,0
Dosis: 2
Route/Site: SYR / UN

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

Abdominal pain upper COVID-19 Chest X-ray normal Colectomy Cough Death Fatigue Feeling abnormal Ileostomy Intestinal obstruction Neoplasm Pancreatectomy SARS-CoV-2 test positive Sleep disorder Small cell carcinoma Surgery Tumour rupture

Symptomtext

My brother had his last COVID 19 shot in March 2022. By May/June he began feeling bad. Tired, fatigued. On 11 July 2022 he woke up in severe pain in the stomach and called my mom. She took him to the ER and they said he had a blockage in his intestine and sent him to his kidney hospital. The doctors operated the next morning and found a tumor mass that had ruptured. A few days later found out it was small cell cancer; which the doctors were in shock as it is extremely rare to find small cell cancer in the colon. Medical care was horrible after that and no one would give us any answers. During the surgery the cancer had spread to his pancreas which they removed with half of his colon. He had an illiotamy. The doctors never called in hospice or even told us a prognosis. They sent him home and he was back in the hospital in a few days. He went back to the hospital 3 times before he passed 5 weeks later on 16 Aug 2022. The last visit to the ER; about 5 days before he passed. He tested positive for COVID. The isolated him and did not allow him to go to dialysis. They sent him home and of course listed COVID as one of the causes of death.

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Praegender Schweregrund: Death
Hospital-Tage: 10,0
Labordaten: Limited i would say. The doctor were not forth coming with giving us any information or prognosis. Even though we begged them to tell us. Additionally cancer does not run in our family. and this just popped out of no where. One of the times my brother was in the hospital he was coughing and the doctor wasn't going to do anything. They finally sent him for chest xray but said he was fine.
Aktuelle Erkrankungen: Prior to his vaccinations: His health as follows: Juvenile diabetic since the age of 8. Insulin dependent. In 2008 he was a recipient of a kidney and pancreas transplant and did well health wise. in 2014 the transplanted kidney failed. He went back on dialysis. In early 2019 he received a second transplant kidney; however, this kidney had the CMV/BTK virus. He had some flare ups with the CMV virus and was in the hospital a few times in 2020 and 2021 for dehydration and cold symptoms from the virus. He received the first set of dosages of the COVID 19 Moderan vaccine on 2 Oct 2021 and 31 Oct 2021. He received a 3rd shot of Moderna on 3/13/2022.
Vorgeschichte: My brother had juvenile diabetes from the age of 8; and then end stage kidney failure since late 2021. As well what was previous mentioned; transplant kidney and pancreas in 2008; 2nd kidney in 2019, and the 2019 kidney failing in 2021.
Andere Medikamente: I'm actually reporting this information on my brother who passed away; believed to be from the vaccine on Aug 16, 2022. The address and phone number listed are mine. My brother resided in Private and this is where he received his medical c
Allergien: None
Vorherige Impfungen: -

VAERS 2578107

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071f21a

kritisch

Staat: SC
Alter: 68,0
Geschlecht: F
Eingang: 08.02.2023
Impfdatum: 28.10.2021
Beginn: 13.11.2021
Tage bis Beginn: 16,0
Dosis: UNK
Route/Site: IM / LA

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

Cerebrovascular accident Computerised tomogram head abnormal Echocardiogram Electrocardiogram Implantable cardiac monitor insertion Intensive care Laboratory test Magnetic resonance imaging head Thrombosis

Symptomtext

I had the booster on Oct, 28 and suffered a stroke on Nov. 13. Following transportation by ambulance to hospital, they did a CT scan of brain and determined a stroke from clot. TPA was administered by IV. Following 3 days in ICU, I came with a good prognsis.

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Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 3,0
Labordaten: Vascular Lab 11/13-11/15 2021 EKG 11/13-11/15 MRI of brain/brain stem 11/13-11/15 Physical/Occupational/Speech Therapy 11/13-11/15 CT head 11/13 Insertion of Heart Rhythm Monitor 11/15/2021 Heart Ultrasound 11/15/2021 TPA injection 11/13/2021 3 days ICU Medical Center
Aktuelle Erkrankungen: No illnesses at the time
Vorgeschichte: HIgh blood pressure
Andere Medikamente: Lipitor Ditropan XL Avapro Calcium Vitamin D baby aspirin Estrace (1/2) daily multivitamin
Allergien: penicillin
Vorherige Impfungen: -

VAERS 2549133

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

kritisch

Staat: SD
Alter: 61,0
Geschlecht: M
Eingang: 03.01.2023
Impfdatum: 09.11.2021
Beginn: 30.09.2022
Tage bis Beginn: 325,0
Dosis: 3
Route/Site: SYR / LA

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

COVID-19 Condition aggravated Death General physical health deterioration Pyrexia SARS-CoV-2 test positive Seizure Vaccine breakthrough infection Vomiting

Symptomtext

This is an instance of breakthrough COVID-19 after which death occurred. The individual was vaccinated with the Moderna product on 02/10/2021, 03/10/2021, and 1/09/2021. The individual tested positive for COVID-19 on 09/30/2022 at the residential facility at which they were a resident. They were seen in emergency department later in the day on 09/30/2022 with chief complaints of vomiting and fever. Symptom onset was thought to be 09/30/2022. They were given fluids , IV bebtelivomab, and acetaminophen . They were not hospitalized but were discharged back to residential facility. They were then seen in a clinic for 10/12/2022 for a "well adult exam." After that, their condition then deteriorated with increased seizure activity and fevers. They died on 10/17/2022.

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Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Dandy-Walker Malformation, Seizure Disorder (not specified), Anemia, Acute renal failure, history of deep vein thrombosis, Vagal nerve stimulator device in place The individual was a resident of a residential facility for persons who have developmental disabilities. The name of the facility is indicated in the Address portion of this form.
Andere Medikamente: -
Allergien: Clotrimazole (reaction: rash) Lotrimin (reaction: rash)
Vorherige Impfungen: -

VAERS 2495183

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

kritisch

Staat: MI
Alter: 66,0
Geschlecht: M
Eingang: 01.11.2022
Impfdatum: 21.05.2022
Beginn: 23.10.2022
Tage bis Beginn: 155,0
Dosis: 3
Route/Site: - / -

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

Acute respiratory failure Anticoagulant therapy COVID-19 Circulatory collapse Condition aggravated Hypotension Imaging procedure abnormal Obstructive sleep apnoea syndrome Pulmonary embolism Renal mass Respiratory failure SARS-CoV-2 test positive Shock Thrombectomy

Symptomtext

"Patient with 4 COVID vaccines who admitted with positive COVID test and pulmonary embolism for hospital admission. Provider d/c note: ""66 YO male presented with passive pulmonary embolism causing respiratory failure and circulatory failure. Found to have covid, though likely incidental given course and imaging findings. Treated with tpa and subsequent thrombectomy with resolution of respiratory failure. Patient noted to have concerning right renal mass on imaging, will need Urology evaluation for nephrectomy. Pulmonary consulted, likely safe for surgery in 1 month. Problem list: Acute respiratory failure with hypoxia - pulmonary embolism, COVID, OSA -resolved, off supplemental O2 -home BiPAP settings when sleeping Acute pulmonary embolism -s/p tpa 10/23, mechanical thrombectomy 10/24 -apixaban x 6 months Circulatory shock, resolved (due to pulmonary embolism) Right renal mass -Referred for Urology evaluation, concern for RCC -Requires a month of anticoagulation before nephrectomy is safe and anticoagulation can be held temporarily Diabetes mellitus type 2 in morbidly obese, Body mass index is 49.02 kg/m?. -sliding scale Humalog -resume metformin/ozempic on discharge Hypertension -valsartan/hydrochlorothiazide remain held with relative hypotension -reassess with PCP """

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 5,0
Labordaten: COVID Detected PCR on 10/23/2022
Aktuelle Erkrankungen: -
Vorgeschichte: Cardiovascular Essential hypertension Acute massive pulmonary embolism (HCC) Digestive BENIGN NEOPLASM OF COLON (211.3) Endocrine Controlled type 2 diabetes mellitus without complication, without long-term current use of insulin (HCC) Integumentary Actinic keratosis Psychological Binge eating disorder Respiratory OSA (obstructive sleep apnea) Urinary AKI (acute kidney injury) (HCC) Renal mass Other Morbid obesity with body mass index (BMI) of 50.0 to 59.9 in adult (HCC) History of kidney stones Shock circulatory (HCC)
Andere Medikamente: -
Allergien: Ace Inhibitors
Vorherige Impfungen: -

VAERS 2465583

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

kritisch

Staat: TX
Alter: 78,0
Geschlecht: F
Eingang: 30.09.2022
Impfdatum: 03.11.2021
Beginn: 20.09.2022
Tage bis Beginn: 321,0
Dosis: 3
Route/Site: IM / AR

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

Atrial fibrillation COVID-19 Chest X-ray normal Computerised tomogram head normal Condition aggravated Death General physical health deterioration Inappropriate schedule of product administration Mental status changes Pneumonia Pyrexia SARS-CoV-2 test positive Tachypnoea Urinary tract infection

Symptomtext

Moderna COVID-19 Vaccine EUA: COVID-19 case resulting in Hospitalization/Death. Rec'd Moderna vaccine on 1/16/2021, 2/19/21 and 11/03/21. Presented to ED with c/o AMS. Recently d/c after being admitted for PNA and UTI. On arrival to ER: febrile & tachypneic in AFib w/RVR, improved with IV Cardizem. Workup in the ER revealed COVID positive, CT head and chest x-ray no acute findings. Placed on Airvo and HFNC. Cont'd to deteriorate despite aggressive care. Transitioned to inpatient hospice and expired on 9/20/22. TX'd w/cefepime, decadron, remdesivir, zosyn, ceftriaxone, and vancomycin.

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Praegender Schweregrund: Death
Hospital-Tage: 20,0
Labordaten: covid + 8/31/22 - This sample was analyzed using the Roche LIAT SARS assay platform using PCR or equivalent Nucleic Acid Amplification (NAA) technology.
Aktuelle Erkrankungen: PNA and UTI
Vorgeschichte: advanced dementia, Parkinson's disease, chronic AFib, nonischemic cardiomyopathy status post pacemaker, BPH with
Andere Medikamente: amantadine, carbidopa/levodopa, dabigatran, ropinirole,
Allergien: Milk
Vorherige Impfungen: -

VAERS 2438757

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

kritisch

Staat: KY
Alter: 76,0
Geschlecht: M
Eingang: 10.09.2022
Impfdatum: 06.11.2021
Beginn: 16.08.2022
Tage bis Beginn: 283,0
Dosis: 3
Route/Site: - / -

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

Acute kidney injury Acute left ventricular failure Acute myocardial infarction Anticoagulation drug level above therapeutic Atrial fibrillation Bladder catheterisation COVID-19 Cardiac assistance device user Cardiac failure congestive Cardiac stress test abnormal Cardioversion Catheterisation cardiac abnormal Coronary artery disease Culture urine positive Dyspnoea Echocardiogram Ejection fraction decreased Enterococcus test positive

Symptomtext

Patient ID: MRN: Name: Age: 77 y.o. Birthday: Admit Date: 8/16/2022 8:55 PM Discharge Date: 8/24/2022 Unit: Admitting Physician: Discharge Physician: MD Discharge Diagnosis: Principal Problem: SOB (shortness of breath) Active Problems: Paroxysmal atrial fibrillation Supratherapeutic INR SVT (supraventricular tachycardia) Elevated troponin Acute combined systolic (congestive) and diastolic (congestive) heart failure Positive cardiac stress test AKI (acute kidney injury) Gross hematuria Hyperlipidemia HTN (hypertension) Type 2 diabetes mellitus with hyperglycemia, without long-term current use of insulin Hospital Course: Patient is a 77 y.o. male admitted with sob / covid 19 / paroxysmal afib / acute on chronic systolic and diastolic hf / uti / trop elevation determined to be type 2 mi. Seen by cards. Also concern for svt nonsustained. lhc performed. Moderate cad, no intervention. Tee / tte performed, ef 30-35%. Cardioverted to nsr. Started on amio / cardiac meds. aki developed after diuresis. Improving back to baseline. Restarting small dose acei. Will delay aldactone, but chf meds need titrating up outpatient with close monitoring of renal function. Uti grew e faecalis, started on amoxicillin and will finish this op. Not treated for covid 19 as symptoms unrelated to this. Nephrology assisted with case given aki and need for contrast. Urology also assisted, give gross hematuria briefly. Foley left in place. Removal op with urology. Life vest prior to dc. Close f/u op No new Assessment & Plan notes have been filed under this hospital service since the last note was generated. Service: Hospitalist Physical Exam on the Date of Discharge: Vitals: Blood pressure 100/63, pulse 107, temperature 97.7 ?F (36.5 ?C), temperature source Oral, resp. rate 14, height 6' (182.9 cm), weight 80.2 kg (176 lb 11.2 oz), SpO2 99 %. General Appearance: alert, NAD Lungs: normal effort Heart: S1 S2 heard Consults: IP CONSULT TO CARDIOLOGY IP CONSULT TO HEART FAILURE NURSE IP CONSULT TO DIETARY IP CONSULT TO CARDIAC REHAB IP CONSULT TO SOCIAL WORK IP CONSULT TO CARDIOLOGY IP CONSULT TO UROLOGY Disposition: home Discharge Condition: fair

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

VAERS 2433306

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 071F21A

kritisch

Staat: KY
Alter: 71,0
Geschlecht: M
Eingang: 08.09.2022
Impfdatum: 08.07.2021
Beginn: 12.08.2022
Tage bis Beginn: 400,0
Dosis: 2
Route/Site: - / -

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

Acute respiratory failure Anticoagulant therapy COVID-19 COVID-19 pneumonia Chest X-ray abnormal Diabetes mellitus Essential hypertension Respiratory failure

Symptomtext

Patient ID: 72 y.o. Admit Date: 8/12/2022 Discharge Date: 8/14/2022 Discharge Diagnosis: Principal Problem: Acute hypoxemic respiratory failure due to COVID-19 Active Problems: DM (diabetes mellitus) Long-term (current) use of anticoagulants Essential hypertension H/O mitral valve replacement with mechanical valve Hospital Course: 72 year old vaccinated male was admitted for respiratory failure from Covid-19 pneumonia. He has been on Remdesivir with steroids and has improved. He will be discharged home today after receiving the 3rd dose of Remdesivir. Patient educated on appropriate level of care post-discharge. Follow up with Primary Care Doctor in 5-7 days. Physical Exam on the day of discharge: Last Recorded Vital Signs: Temp: 98.1 ?F (36.7 ?C) Heart Rate (Monitor): 60 Pulse: 63 BP: 119/61 Respirations: 18 SpO2: 99 % O2 Flow Rate (l/min): 3 l/min General Appearance: no distress Eyes: PERRLA ENT: moist mucus membranes, no adenopathy Lungs: clear to auscultation bilaterally Heart: regular rate and rhythm Abdomen: soft, non-tender Skin: No rashes or lesions Extremities: full ROM Neuro: alert Consults: None Significant Diagnostic Studies: CXR Operations: nonr Disposition: Home Discharge Condition: Fair

Weitere VAERSDATA-Felder

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

VAERS 2431177

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

kritisch

Staat: KY
Alter: 79,0
Geschlecht: M
Eingang: 07.09.2022
Impfdatum: 06.11.2021
Beginn: 08.08.2022
Tage bis Beginn: 275,0
Dosis: 3
Route/Site: - / -

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

Acute left ventricular failure Acute myocardial infarction COVID-19 Chest X-ray Chronic kidney disease Echocardiogram Polyuria Renal impairment SARS-CoV-2 test positive Type 2 diabetes mellitus Ventricular hypokinesia

Symptomtext

Patient ID: 80 y.o. Admit Date: 8/8/2022 Discharge Date: 8/11/2022 Discharge Diagnosis: Principal Problem: Acute systolic heart failure Active Problems: NSTEMI (non-ST elevated myocardial infarction) COVID-19 virus infection Type 2 diabetes mellitus with stage 3 chronic kidney disease, with long-term current use of insulin Stage 3a chronic kidney disease Hospital Course: 80 year old male with dementia was admitted for CHF and MI. He also tested (+) for Covid-19 infection but did not require Remdesivir therapy. Cardiology saw him and started him on Amiodarone. TTE show moderate global hypokinesis of the left ventricle with 30-35% LVEF. He was also diuresed. Renal function remained stable. He will be discharged home today for follow up with cardiology. Patient educated on appropriate level of care post-discharge. Physical Exam on the day of discharge: Last Recorded Vital Signs: Temp: 97.4 ?F (36.3 ?C) Heart Rate (Monitor): 87 Pulse: 77 BP: 115/74 Respirations: 18 SpO2: 99 % O2 Flow Rate (l/min): 0 l/min General Appearance: no distress Eyes: PERRLA ENT: moist mucus membranes, no adenopathy Lungs: clear to auscultation bilaterally Heart: regular rate and rhythm Abdomen: soft, non-tender Skin: No rashes or lesions Extremities: full ROM Neuro: alert Consults: IP CONSULT TO HEART FAILURE NURSE IP CONSULT TO DIETARY IP CONSULT TO SOCIAL WORK IP CONSULT TO CARDIOLOGY IP CONSULT TO HEART FAILURE NURSE Significant Diagnostic Studies: TTE, CXR Operations: none Disposition: Home with HH Discharge Condition: Fair

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

VAERS 2425137

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

kritisch

Staat: LA
Alter: 63,0
Geschlecht: F
Eingang: 31.08.2022
Impfdatum: 29.11.2021
Beginn: 12.07.2022
Tage bis Beginn: 225,0
Dosis: 3
Route/Site: - / -

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

Acute myocardial infarction Anticoagulant therapy COVID-19 Catheterisation cardiac Chest pain Electrocardiogram abnormal Hypertension Percutaneous coronary intervention SARS-CoV-2 test positive Stent placement Superficial vein thrombosis Tobacco abuse Ventricular tachycardia

Symptomtext

Physician discharge summary: Admit date: 7/12/2022. Discharge date: 7/16/2022. Hospital course: Patient came in with chest pain. EKG confirmed inferior lateral MI. Patient taken emergently to the cath lab for LHC with left groin access where she received PCI to RCA with plans for staged PCI to LAD as an outpatient. Will require aspirin and Brilinta at discharge. Also started on statin, BB, ACEI. Of note, patient was already positive for COVID-19 when she came in. Pulmonology consulted for management. During her stay, she developed ventricular tachycardia requiring amiodarone. She also developed superficial thrombosis to right forearm requiring Lovenox. Patient is going home on Eliquis for this. Nursing staff confirmed with pharmacy and insurance that Eliquis will be covered 100%. Patient is now stable and cleared for discharge by hospitalist, as well as, pulmonology. Patient consult with doctor in 2 weeks for follow-up on medications and plans for future PCI of LAD. Discharge condition: Good.

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Praegender Schweregrund: Acute myocardial infarction
Hospital-Tage: -
Labordaten: LHC, stent placed; ECHO.
Aktuelle Erkrankungen: -
Vorgeschichte: STEMI (ST elevation myocardial infarction), HTN (hypertension), tobacco abuse, COVID-19, superficial thrombosis, VT
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2420876

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

kritisch

Staat: TN
Alter: 91,0
Geschlecht: M
Eingang: 26.08.2022
Impfdatum: 08.11.2021
Beginn: 10.08.2022
Tage bis Beginn: 275,0
Dosis: 3
Route/Site: IM / -

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

COVID-19 Death SARS-CoV-2 test positive

Symptomtext

Covid vaccine x 3. Positive covid on 8/10/2022. Admitted to the Medical Center on 08/18/22. DC'd home on 8/21/22. Readmitted on 8/21/2022 and expired on 8/24/22.

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

VAERS 2408485

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

kritisch

Staat: NY
Alter: 40,0
Geschlecht: F
Eingang: 11.08.2022
Impfdatum: 12.11.2021
Beginn: 12.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Acute pulmonary oedema Autopsy Cardiac arrest Death Endotracheal intubation Feeling abnormal Haemorrhage Pulmonary haemorrhage Resuscitation Toxicologic test normal Unresponsive to stimuli

Symptomtext

Significant other reported that patient started feeling poorly after the booster on 11/12. On 11/13 she was last seen at 1300. Found unresponsive and asystolic at 1650. No response to CPR, no shockable rhythm. No response to epinephrine. ED provider noted that ET tube was placed with large amounts of hemorrhage into the tube. TOD 1749. Autopsy revealed acute hemorrhagic pulmonary edema as the cause of death. No evidence of adverse vaccine reaction after 1st 2 doses.

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Praegender Schweregrund: Cardiac arrest
Hospital-Tage: -
Labordaten: Coroner reported negative toxicology screens post-mortem, including prescribed medications. No evidence of anaphylaxis.
Aktuelle Erkrankungen: Documented as of 11/14/2021 Alcoholic ketoacidosis Hypokalemia elevated lactic acid Gastritis Moderate calorie-protein malnutrition Acute alcoholic pancreatitis Hx of bulimia nervosa Chronic alcohol abuse 10 pack-year history of smoking (0.5 pack per day/20 years)
Vorgeschichte: Alcohol withdrawal syndrome hypercalcemia, hypochloremia, hypokalemia marijuana use
Andere Medikamente: Loperimide Effexor-XR Robaxin Gabapentin Carafate Atarax Naproxen Clonidine Protonix muti-vitamin - Theragran Zofran Oxycodone
Allergien: NKA
Vorherige Impfungen: -

VAERS 2366455

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

kritisch

Staat: SD
Alter: 90,0
Geschlecht: M
Eingang: 12.07.2022
Impfdatum: 04.02.2021
Beginn: 15.10.2021
Tage bis Beginn: 253,0
Dosis: 3
Route/Site: SYR / LA

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

COVID-19 COVID-19 pneumonia Death SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

This is an instance of breakthrough COVID-19 after which death occurred. The individual also died 6 days after receipt of third dose of the Moderna product. The positive test occurred after receipt of second dose but before the third. The individual was vaccinated with the Moderna product on 01/07/2021, 02/04/2021, and 11/01/2021. They tested positive for COVID-19 on 10/15/2021 at the assisted living facility at which they were a resident. They were hospitalized related to this illness 10/17/2021-10/20/2021 in an out-of-state hospital. They experienced complications of COVID-19 pneumonia. They died on 11/06/2021.

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Praegender Schweregrund: Death
Hospital-Tage: 3,0
Labordaten: Positive COVID-19 PCR test on 10/15/2021 despite being vaccinated.
Aktuelle Erkrankungen: -
Vorgeschichte: Congestive Heart Failure, COPD, past history of prostate cancer, Type II Diabetes, Gout, Hyperlipidemia, Hypertension, past history of myocardial infarction, hypothyroidism, diverticulosis The individual was a resident of the assisted living facility indicated in the Address portion of this form.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2317283

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

kritisch

Staat: IL
Alter: 77,0
Geschlecht: F
Eingang: 13.06.2022
Impfdatum: 07.11.2021
Beginn: 28.05.2022
Tage bis Beginn: 202,0
Dosis: 3
Route/Site: IM / LA

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

Acute respiratory failure Angiogram pulmonary abnormal Blood culture negative Blood gases Blood pH normal Brain natriuretic peptide increased Bronchoalveolar lavage normal Bronchoscopy C-reactive protein increased COVID-19 Carbon dioxide decreased Chronic obstructive pulmonary disease Condition aggravated Diaphragmatic disorder Endotracheal intubation Full blood count normal Fungal test positive Haemoglobin decreased

Symptomtext

Patient received moderna vaccine on 3/9/21, 4/9/21 and 11/10/21. Presented to ER on 5/28/22. Found to be COVID positive. admitted to hospital for acute on chronic hypoxic respiratory failure. On initial presentation, patient was saturating at 83% on home oxygen 3LNC. Patient continued to desaturation and oxygen requirements increased to high flow nasal cannula. Patient received a dose of solu-medrol and duoneb. CBC was unremarkable, hemoglobin of 8.3 (baseline 8-9), CRP 28.4, negative procal, blood cultures showed no growth. Sputum cultures showed normal respiratory flora and a light growth of yeast. Negative strep and legionella. BNP 141, negative troponin, ABG: pH(7.41, pCO2(39), pO2(55), CO2(26). CTA showed no PE, multifocal pneumonia. Patient was admitted to unit for treatment for acute on chronic hypoxic respiratory failure. Patient continued all other home therapies for COPD and started on antibiotics and steroids. During patients hospital course, her respiratory status began to decline and pulmonology was consulted. Pulmonology was consulted and patient was intubated on 6/1 and transferred to ICU. Patient received therapeutic bronchoscope with BAL, started on solu-medrol 62.5 mcg bid, continued on duonebs scheduled mucomyst and vest therapy. BAL cultures were negative. Patient was extubated on 6/2/2022. Patient was able to return to home oxygen baseline (3LNC). Pulmonology provided recommendations, which included the use of Vest PT, duonebs, prednisone taper, mucomyst, nasal hypertonic, flutter valve, albuterol, mucinex, trelegy, and mucinex. Patient was approached during admission for the possibility needing BIPAP/AVAPs nightly. Patient declined the recommendation, due to not being able to sleep. Pulmonolgy was contacted in regards to recommendation and stated that BIPAP/AVAPs would be beneficial for the patient, but did not qualify due to the results of ABGs during hospital admission. Patients respiratory status was stable and patient remained stable on home oxygen of 3L NC. Discharged on 6/6/22

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 9,0
Labordaten: 5/28/22 COVID19: positive 5/28/22 chest: Marked improvement in aeration of the left lung compared to the March 22, 2022 exam. Minimal persistent opacities present at the lateral left mid lung zone. Improved aeration of the right lung base as well with improved delineation of the right hemidiaphragmatic silhouette compared to prior.
Aktuelle Erkrankungen: -
Vorgeschichte: Breast cancer R Breast ? Bronchitis ? CKD (chronic kidney disease) ? COPD (chronic obstructive pulmonary disease) ? Elevated cholesterol ? Fluid retention ? HTN (hypertension) ? Neuropathy BLE ? Noncompliance with CPAP treatment ? Otitis media ? Oxygen dependent 4-6L home O2 ? Pharyngitis ? Rheumatoid arteritis RA ? Sinusitis ? Sleep apnea NON-COMPLIANT WITH CPAP T2Dm
Andere Medikamente: insulin detemir 100 UNIT/ML Sopn Commonly known as: LEVEMIR 20 Units by Subcutaneous route every morning albuterol 108 (90 Base) MCG/ACT Aers Commonly known as: PROVENTIL HFA, VENTOLIN HFA INHALE 2 PUFFS FOUR TIMES DAILY AS NEEDED amLODI
Allergien: Erthyromycin, pineapple, shllfish, sulfa, levofloxacin, clinda
Vorherige Impfungen: -

VAERS 2246360

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

kritisch

Staat: IL
Alter: 49,0
Geschlecht: M
Eingang: 21.04.2022
Impfdatum: 06.11.2021
Beginn: 17.03.2022
Tage bis Beginn: 131,0
Dosis: 3
Route/Site: IM / LA

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

Acute cardiac event Cardiac arrest Cardioversion Cough Implantable defibrillator insertion Interchange of vaccine products Laboratory test normal Pulse absent Resuscitation SARS-CoV-2 test negative Ventricular fibrillation

Symptomtext

slight intermittent dry cough a week prior to Cardiac event Sudden Cardiac arrest (pulseless ventricular fibrillation) CPR administered, 3 defibrillations by EMS Transport to Medical Center where substantial additional treatment provided Implant of Boston Scientific S-ICD (subcutaneous defibrillator) Discharge from hospital and recovering well

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Praegender Schweregrund: Cardiac arrest
Hospital-Tage: 8,0
Labordaten: At hospital admission tested negative for Covid19 (also negative for numerous other infections) Numerous tests during course of treatment..contact Medical Center for detailed test and results
Aktuelle Erkrankungen: None
Vorgeschichte: Mild Allergies (trees/grass/mold/ragweed)
Andere Medikamente: None
Allergien: Peanuts
Vorherige Impfungen: fainted, 35 years old, 2/23/2007, multiple vaccinations

VAERS 2233724

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

kritisch

Staat: -
Alter: 89,0
Geschlecht: M
Eingang: 14.04.2022
Impfdatum: 06.11.2021
Beginn: 17.12.2021
Tage bis Beginn: 41,0
Dosis: 2
Route/Site: - / -

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

Acute kidney injury COVID-19 COVID-19 pneumonia Cardiac arrest Death Endotracheal intubation Intensive care Life support Resuscitation SARS-CoV-2 test positive Unresponsive to stimuli

Symptomtext

pt had a positive COVID test on 12/17/21 in Senior Living facility; transferred to hospital on 12/20/21 with COVID pneumonia and ARF; O2 supplementation; given Remdesivir, but family requested it to be stopped early; ABX; O2 demands increased; ICU; made some improvement; became unresponsive; intubated; vasopressors started; pt experienced cardiac arrest; CPR with ACLS protocol performed without success; pt died in the hospital

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Praegender Schweregrund: Cardiac arrest
Hospital-Tage: 9,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Atrial Fibrillation, COPD, HTN, Parkinson's disease; lymphoma on treatment
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2218399

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

kritisch

Staat: TN
Alter: 62,0
Geschlecht: F
Eingang: 06.04.2022
Impfdatum: 03.11.2021
Beginn: 22.11.2021
Tage bis Beginn: 19,0
Dosis: 3
Route/Site: IM / LA

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

Anticoagulant therapy Pulmonary embolism

Symptomtext

Left lower pulmonary embolism. Will be on anticoagulants for the remainder of my life.

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Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 2,0
Labordaten: Hospitalized
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension - controlled with medication low potassium - controlled with medication GERD - controlled with medication
Andere Medikamente: Triamterene/HCTZ 37.5/25 Ramipril 10 mg Metoprolol succ 100 mg Pantoprazole sod 40 mg Atorvastatin 20 mg Potassium 20 meq twice daily OTC multivitamin OTC Vitamin D
Allergien: Hydrocodone makes me itch.
Vorherige Impfungen: -

VAERS 2218071

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

kritisch

Staat: -
Alter: 65,0
Geschlecht: M
Eingang: 06.04.2022
Impfdatum: 07.07.2021
Beginn: 29.11.2021
Tage bis Beginn: 145,0
Dosis: 1
Route/Site: IM / LA

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

COVID-19 Pulmonary embolism SARS-CoV-2 test positive

Symptomtext

Received the Janssen vaccine on 7/7/2021 Moderna vaccine received 2/19/2022 after the adverse event on 11/29/2021 COVID 19 positive on 11/29/2021 Hospitalized with COVID 19 and bilateral upper and lower pulmonary emboli

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

VAERS 2148190

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

kritisch

Staat: KY
Alter: 88,0
Geschlecht: M
Eingang: 28.02.2022
Impfdatum: 10.10.2021
Beginn: 10.02.2022
Tage bis Beginn: 123,0
Dosis: 3
Route/Site: IM / LA

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

Acute kidney injury Acute respiratory failure Anaemia Atrial fibrillation Cardiac failure acute Cardiac failure congestive Condition aggravated Constipation Deep vein thrombosis Dialysis Haematoma Hypercapnia Hypotension Leukocytosis Positive airway pressure therapy Procalcitonin Respiratory failure Transfusion

Symptomtext

Admitted with a/c hypoxic resp failure, a/c dCHF, AKI. Prolonged hospitalization. Re-initiated dialysis during admission, this will be continued on discharge. He is to have dialysis tomorrow and this has been set up. He is requiring BiPAP qHS and PRN and this is available and ready for patient at SNF. He will have to have a sleep study. Pulmonary and renal followed patient. IVC filter placed during admission. Leukocytosis peaked at 22, has been on IV steroids. He has completed abx. Procal and WBC have trended down during admission. He is on midodrine for low BPs. He is medically stable for discharge to SNF. Needs close f/u with pulmonary. * Acute on chronic respiratory failure with hypoxia and hypercapnia Remains stable. BiPAP qHS and PRN. Completed abx. Pulmonary following. IS and acapella. A/c dCHF - dialysis. Negative fluid balance. Weight down. AKI - continue dialysis. Nephrology following. Has chair time already. DVT with recent hematoma - s/p IVC filter earlier this admission. Anemia - stable. No indication for transfusion at this point but has received blood transfusions during admission. AFib - continue tele and current medications. Constipation - continue lactulose. AME - multiple issues as above. Resolved.

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 16,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: PAF, CHF, HTN, AVM of small bowel,
Andere Medikamente: unable to ascertain
Allergien: nka
Vorherige Impfungen: -

VAERS 2078806

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

kritisch

Staat: MI
Alter: 84,0
Geschlecht: M
Eingang: 01.02.2022
Impfdatum: 19.11.2021
Beginn: 19.01.2022
Tage bis Beginn: 61,0
Dosis: 3
Route/Site: IM / AR

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

Acute respiratory failure Anaemia Angioplasty Anticoagulant therapy Asymptomatic COVID-19 COVID-19 COVID-19 pneumonia Cellulitis Computerised tomogram thorax abnormal Hypoxia Impaired healing Inappropriate schedule of product administration Magnetic resonance imaging Renal impairment SARS-CoV-2 test positive Toe amputation Toxic encephalopathy Vascular operation

Symptomtext

Hospitalized 01/19/2022-still currently admitted; COVID-19 positive 01/19/2022; fully vaccinated plus booster ASSESSMENT / PLAN: COVID Acute hypoxic respiratory failure secondary to above COVID positive 1/19 Asymptomatic; per facility have not noted any symptoms either CT thorax does not show findings of COVID Decadron 6mg daily Remdesivir contraindicated due to renal function Supplemental O2 PRN; currently on 3L, wean as able Admitted with COVID-19 pneumonia and acute hypoxic respiratory failure. On 3 L by nasal cannula. Started on Decadron. Unlikely to benefit from Remdesivir. Wean off O2 as able. CT thorax does not show findings of COVID however the patient is wheezing and hypoxic. He also has right lower extremity cellulitis and nonhealing 2nd toe amputation. Had a recent angioplasty of the right lower extremity with vascular surgery. Will start the patient on vancomycin and Zosyn. Heparin drip in place of Xarelto for now. MRI to rule out osteomyelitis. Vascular surgery consult. Consider podiatry consult pending MRI findings. The patient also has acute encephalopathy likely toxic metabolic in the setting of cellulitis and COVID. Monitor for now. Patient has acute on chronic anemia. 01/23/22 notes: COVID pnuemonia. Acute hypoxic respiratory failure secondary to above -resolved COVID positive 1/19 Asymptomatic; per facility have not noted any symptoms either CT thorax does not show findings of COVID on room air now. Will stop decadron in case that is causing agitation. 01/31/2022 notes: Acute hypoxic respiratory failure resolved COVID-19 pneumonia resolved Currently on room air Disposition: awaiting placement to skilled nursing facility

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 13,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Non-pressure chronic ulcer of other part of right foot with fat layer exposed (HCC) Acute respiratory failure with hypoxia CHF (congestive heart failure) ( Chronic anticoagulation Atrial fibrillation Obesity Tobacco abuse, in remission OSA (obstructive sleep apnea) Hypothyroidism Type 2 diabetes mellitus with diabetic neuropathy, without long-term current use of insulin Chronic diarrhea of unknown origin Peripheral sensory neuropathy Hyperlipidemia Essential hypertension Vasomotor rhinitis Claudication Peripheral vascular disease DOE (dyspnea on exertion) Vitamin B12 deficiency Spinal stenosis of lumbar region without neurogenic claudication Hiatal hernia Osteoarthritis of left knee History of total bilateral knee replacement Unspecified inflammatory spondylopathy, lumbosacral region
Andere Medikamente: apixaban (ELIQUIS) 2.5 MG tablet aspirin 81 MG chewable tablet bisacodyl (DULCOLAX) 10 MG suppository Blood Glucose Monitoring Suppl MISC collagenase ointment cyanocobalamin (B-12) 1000 MCG/ML injection Elastic Bandages & Supports (JOBST RE
Allergien: Atorvastatin Ezetimibe
Vorherige Impfungen: -

VAERS 2075564

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21a

kritisch

Staat: KY
Alter: 79,0
Geschlecht: F
Eingang: 31.01.2022
Impfdatum: 01.11.2021
Beginn: 30.01.2022
Tage bis Beginn: 90,0
Dosis: 2
Route/Site: IM / LA

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

Anticoagulant therapy Arrhythmia COVID-19 COVID-19 pneumonia Chronic kidney disease Condition aggravated Death Fibrin D dimer increased Haemoglobin decreased Hypertension Positive airway pressure therapy Renal impairment Torsade de pointes Ultrasound Doppler normal Ventricular fibrillation

Symptomtext

Patient expired as a result of pneumonia due to Covid-19 virus.

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Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: HFNC 95% wean as tolerated. Alternating with BiPap. remdesivir stopped per ID after 3 doses due to worsening renal function, Solu Medrol 40 q8, heparin SC, s/p sarilumab. V fib, Patient developed sudden onset of arrhythmia with very brief torsade de point that degenerated into V. Fib, Patient indicated multiple times that she wishes to remain DO NOT RESUSCITATE/DO NOT INTUBATE. No resuscitation efforts attempted. She showed no recovery from her fatal arrhythmia. Patient was declared deceased at 10:32 AM. HTN, home meds. CKD, nephrology following. D dimer elevated, US BLE no DVT, no CTA due to renal function. heparin SC. She was previously on heparin drip and this was stopped due to a drop in hemoglobin.
Aktuelle Erkrankungen: PAF, Essential hypertension, pulmonary hypertension, hyperkalemia
Vorgeschichte: PAF, Essential hypertension, pulmonary hypertension
Andere Medikamente: levothyroxine 50mcg, albuterol 90mcg, metoprolol 25mg, diltiazem 30 mg, aspirin 81mg, duloxetine 30mg, pantoprazole 40mg, Macitentan 10 mg, tiotropium bromide, nystatin powder
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 2055498

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071f21a

kritisch

Staat: NY
Alter: 27,0
Geschlecht: F
Eingang: 21.01.2022
Impfdatum: 18.11.2021
Beginn: 18.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Anticoagulant therapy Antiphospholipid syndrome Blood test Cerebral infarction Cerebrovascular accident Coagulopathy Feeling abnormal Impaired work ability Magnetic resonance imaging head abnormal Malaise Thrombosis Transient ischaemic attack

Symptomtext

I was dx with clotting disease, Antiphospholipid syndrome following the first two Moderna vaccines. I had complete opposite issue prior with bleeding before vaccinations. After booster shot, I was very ill for 48 hours following. Did not feel like myself since booster. Had multiple small strokes 1 month after Booster shot on 12/25/21 at 9:30 in the morning. Had to go to emergency room. MRI confirmed brain infarct in multiple areas of left hemisphere of frontal and parietal lobes. Had TIA about a week later, and was admitted to hospital for two nights. I am now on blood thinners because of the clots. Having to take shots every 12 hours. I have been out of work every since the morning when this all started. I have brain fog and issues that prevent me from working right now.

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Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 3,0
Labordaten: 2 MRIs, 12/30/2021 and 01/04/2021 - both showing brain infarct from strokes. A TON of blood work I have done all of the time, almost every three days to make sure my blood doesn?t get too thick and have another stroke.
Aktuelle Erkrankungen: NONE.
Vorgeschichte: Idiopathic thrombocytopenia purpura and Von Willbrands Disease
Andere Medikamente: Wellbutrin 300mg Womens Multivitamin Magnesium 300mg
Allergien: Compazine and gabapentin
Vorherige Impfungen: -

VAERS 2039535

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

kritisch

Staat: -
Alter: 61,0
Geschlecht: F
Eingang: 17.01.2022
Impfdatum: 03.11.2021
Beginn: 02.12.2021
Tage bis Beginn: 29,0
Dosis: UNK
Route/Site: - / -

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

Acute myocardial infarction

Symptomtext

NSTEMI . ED Visit to hospital admission. This visit was within 6 weeks of receiving the COVID vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute myocardial infarction
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2014296

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

kritisch

Staat: NJ
Alter: 72,0
Geschlecht: F
Eingang: 07.01.2022
Impfdatum: 01.10.2021
Beginn: 30.12.2021
Tage bis Beginn: 90,0
Dosis: 3
Route/Site: IM / -

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

COVID-19 Death SARS-CoV-2 test positive Underdose

Symptomtext

Covid #1 given on 2/15/2021, #2 on 3/15/2021 and boosted on 10/31/2021. Boosted was with 0.25 mL and not 0.5, which would have been more appropriate for an immunocompromised patient. Booster dose given at Pharmacy. Patient admitted to hospital on 12/30/2021 and expired on 1/6/2022 Tested positive for Covid-19 on admission

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Praegender Schweregrund: Death
Hospital-Tage: 7,0
Labordaten: Covid-19 Positive 12/30/2021
Aktuelle Erkrankungen: -
Vorgeschichte: non alcoholic liver cirrhosis, pancytopenia, GI bleed
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1963208

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

kritisch

Staat: NH
Alter: 38,0
Geschlecht: F
Eingang: 20.12.2021
Impfdatum: 20.11.2021
Beginn: 09.12.2021
Tage bis Beginn: 19,0
Dosis: 3
Route/Site: SYR / LA

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

Computerised tomogram Electrocardiogram Pulmonary embolism

Symptomtext

Multiple subsegmental pulmonary emboli (left lung, distal region)

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Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: -
Labordaten: CT Scan and EKG (12/9/21)
Aktuelle Erkrankungen: None
Vorgeschichte: Protein S Deficiency (clotting disorder)
Andere Medikamente: Femara (for fertility); daily vitamin; magnesium (200mg)
Allergien: Tree nut allergy
Vorherige Impfungen: -

VAERS 1951973

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

kritisch

Staat: ND
Alter: 40,0
Geschlecht: F
Eingang: 15.12.2021
Impfdatum: 04.11.2021
Beginn: 06.11.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: - / RA

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

Angiogram pulmonary abnormal Anticoagulant therapy Back pain Blood test C-reactive protein increased Chest pain Dyspnoea Electrocardiogram Fibrin D dimer increased Influenza virus test Metabolic function test Pulmonary embolism Pulmonary thrombosis SARS-CoV-2 test Troponin increased Ultrasound scan X-ray

Symptomtext

Day 2 (Saturday) following vaccination I became short of breath with pain in my chest and back. Was seen 4 days after vaccination (Monday, November 8th) and after subsequent testing, discovered a Pulmonary Embolism. Monday, November 8th I went into a walk-in clinic. Testing was done to include Covid-19, influenza, as well as blood work to include troponin and metabolic panel, x-ray and EKG completed. Troponin was elevated and was advised to be admitted to local hospital for further testing. Following admittance to hospital, further bloodwork drawn as well as troponin testing, which leveled out. D-dimer and C-reactive protein came back elevated. Ultrasound testing was done on legs and a CTA chest scan. CT showed multiple clots in lungs. Was put on a heparin drip until release the following day. Am currently on xarelto to help break up clots. No clotting issues prior, no travel, no surgery, no immobility, no birth control used and no smoking.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1924852

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

kritisch

Staat: KS
Alter: 90,0
Geschlecht: M
Eingang: 06.12.2021
Impfdatum: 09.11.2021
Beginn: 03.12.2021
Tage bis Beginn: 24,0
Dosis: 3
Route/Site: IM / LA

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

Arrhythmia Back pain Blood albumin decreased Blood alkaline phosphatase increased Blood calcium decreased Blood creatine phosphokinase Blood creatinine increased Blood glucose increased Blood lactic acid decreased Blood urea increased Carbon dioxide decreased Death Differential white blood cell count Fall Full blood count abnormal Haematocrit decreased Haemoglobin decreased International normalised ratio normal

Symptomtext

No immediate adverse events or signs/symptoms post vaccination. On 12/03/2021 at approximately 1420 Patient was found on the floor by staff from a fall incident he was complaining of pain to neck and back and due to personal hx of cervical fractures EMS notified for transport to ER. Poor oxygenation noted and oxygen applied via nasal cannula while awaiting EMS transport to Hospital ER. At approximately 1700 Nursing Home received word that all scans/x-rays were normal and resident would be returning to Nursing Home. Some time after this notification while resident was still in the ER he developed a cardiac dysrhythmia which he succumbed to.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: 12/03/2021: CBCD, CMP, PT/INR, CPK, Lactic Acid, Troponin, MRSA PCR Nasal Swab, Covid Antigen, Abnormal Lab Values - CBCD: WBC 11.9, RBC 3.88, Hgb 11.1, Hematocrit 35.3, MCHC 31.4, Neutrophils % 93, Lymphocytes % 2, Monocytes % 3 Abnormal Lab Values - CMP: Carbon Dioxide 20.0, Glucose 236, BUN 52, Creatinine 2.0, Albumin 3.0, Total Calcium 7.9, Alkaline Phosphatase 157 Abnormal Lab Values - PT/INR: INR 1.1 Abnormal Lab Values - Lactic Acid: 2.3 Abnormal Lab Values - MRSA PCR (Nasal): Positive
Aktuelle Erkrankungen: See Question 12 - no illnesses prior to vaccination
Vorgeschichte: ALZHEIMER'S DISEASE WITH BEHAVIORAL DISTURBANCES, ATHEROSCLEROTIC HEART DISEASE, ESSENTIAL (PRIMARY) HYPERTENSION, HYPOTHYROIDISM, HYPERLIPIDEMIA, HYPOKALEMIA, MAJOR DEPRESSIVE DISORDER, GENERALIZED ANXIETY DISORDER, HEART FAILURE, GASTRO-ESOPHAGEAL REFLUX DISEASE, CHRONIC KIDNEY DISEASE, UNSPECIFIED ATRIAL FIBRILLATION, TYPE 2 DIABETES MELLITUS, HX MALIGNANT NEOPLASM OF PROSTATE, HYPERPARATHYROIDISM
Andere Medikamente: Aspirin 81 mg daily, Atorvastatin Calcium Tablet 40 MG Daily, Calcium Tablet 1000 MG daily, Cetirizine HCl Tablet 10 MG daily, Cholecalciferol Tablet 25 MCG (1000 UT) daily, Cinacalcet HCl Tablet 30 MG daily, Donepezil HCl Tablet 10 MG dail
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 1885630

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

kritisch

Staat: -
Alter: 88,0
Geschlecht: F
Eingang: 19.11.2021
Impfdatum: 27.10.2021
Beginn: 10.11.2021
Tage bis Beginn: 14,0
Dosis: UNK
Route/Site: - / -

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

Cerebrovascular accident

Symptomtext

I63.9 - CVA (cerebral vascular accident) I63.9 - Cerebrovascular accident (CVA), unspecified mechanism

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

VAERS 1857987

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

kritisch

Staat: WI
Alter: 50,0
Geschlecht: M
Eingang: 11.11.2021
Impfdatum: 01.11.2021
Beginn: 02.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Death Headache Malaise Myocardial infarction Pain in extremity Resuscitation Syncope Pulmonary embolism

Symptomtext

CLIENT COMPLAINED OF RIGHT CALF PAIN THAT STARTED 11/2/21 NIGHT, HE TOLD HIS DOCTOR HE HAD A BLOOD CLOT LAST YEAR PER MEDICAL RECORD. CLIENT WAS WALKING IN TO SEE HIS DOCTOR WHEN HE COLLAPSED AFTER CPR AND 4 ROUNDS OF EPINEPHRINE CLIENT TIME OF DEATH 11:34 A.M.

Weitere VAERSDATA-Felder

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

VAERS 1850618

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

kritisch

Staat: CA
Alter: 68,0
Geschlecht: F
Eingang: 08.11.2021
Impfdatum: 27.10.2021
Beginn: 27.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Angiogram Laboratory test Myocardial infarction

Symptomtext

I was transported by ambulance on October 27, 2021. I had a heart attack had to have an angiogram done to ensure no damage. I'm scheduled to go have cardio rehab.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
Hospital-Tage: 1,0
Labordaten: Angiogram Lab Work
Aktuelle Erkrankungen: No
Vorgeschichte: Stents in heart (2007)
Andere Medikamente: Lisinopril Levothyroxine Rosuvastatin Gabapentin
Allergien: Penicillin Amoxicillin
Vorherige Impfungen: -

VAERS 1850464

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

kritisch

Staat: KY
Alter: 56,0
Geschlecht: F
Eingang: 08.11.2021
Impfdatum: 05.11.2021
Beginn: 06.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Death

Symptomtext

Pt was found deceased at home on 11/06/2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Hyperlipidemia Hypertension Varicose Veins
Andere Medikamente: Metoprolol Succ ER 50 MG Tab Take 1 by mouth at bedtime Vitamin D2 1.25mg Take 1 by mouth weekly Meloxicam 15mg Tablet Take 1 by mouth daily Pravastatin Sodium 20 MG Tab Take 1 by mouth daily Tramadol HCL 50 MG Tablet 1-2 by mouth twice to
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2672783

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071f21a

schwer

Staat: FL
Alter: 63,0
Geschlecht: F
Eingang: 17.08.2023
Impfdatum: 01.09.2022
Beginn: 01.10.2022
Tage bis Beginn: 30,0
Dosis: 3
Route/Site: SYR / LA

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

Catheterisation cardiac normal Chest pain Dyspnoea Ejection fraction decreased Fatigue Heart rate irregular Magnetic resonance imaging abnormal Magnetic resonance imaging heart Myocarditis Pericardial effusion

Symptomtext

Symptoms: chest pain, shortness of breath, fatigue, irregular heart beat beginning October 2022, worsening steadily. Diagnosis: Myocarditis diagnosed after cardiac catheterization (March 2023) showed no blockages and cardiac perfusion MRI (April 2023) showed edema in heart wall, reduced ejection fraction. Treatment: rest, no alcohol or caffeine, no strenuous activity or heavy meals Followup MRI scheduled for 8-30-2023.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: -
Labordaten: Myocarditis diagnosed after cardiac catheterization (March 2023) showed no blockages and cardiac perfusion MRI (April 2023) showed edema in heart wall, reduced ejection fraction. Followup MRI scheduled for 8-30-2023.
Aktuelle Erkrankungen: none
Vorgeschichte: lupus (SLE), hypothyroidism
Andere Medikamente: plaquenil, liothyronine, HRT(estrogen-biest compound + testosterone gel)
Allergien: sulfa; mercury products; levaquin; tuna
Vorherige Impfungen: -

VAERS 2466635

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

schwer

Staat: KY
Alter: 70,0
Geschlecht: M
Eingang: 01.10.2022
Impfdatum: 06.11.2021
Beginn: 26.09.2022
Tage bis Beginn: 324,0
Dosis: 3
Route/Site: IM / RA

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

Asthenia Atrioventricular block first degree COVID-19 Cardiac stress test abnormal Cardiac telemetry Catheterisation cardiac abnormal Coronary artery occlusion Cough Dyspnoea Echocardiogram abnormal Ejection fraction decreased Electrocardiogram abnormal Fall Malaise Percutaneous coronary intervention Presyncope SARS-CoV-2 test positive Troponin increased

Symptomtext

To ED with shortness of breath, cough, malaise, generalized weakness worsening over a few days and fall. Felt he may pass out. No chest pain. COVID-19 (+) in ED. Elevated troponin. EKG - SR with first degree AV Block. Cardiology Consult. Abnormal stress test, heart catheterization with 80% ostial RCA with PCI. EF 25-30% per ECHO. Admitted. IV Remdesivir. Telemetry. IV Lasix.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: 4,0
Labordaten: Left heart catheterization with 80% ostial RCA with PCI. EF 25-30% per ECHO.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2466126

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

schwer

Staat: NJ
Alter: 42,0
Geschlecht: F
Eingang: 30.09.2022
Impfdatum: 07.11.2021
Beginn: 08.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Chills Fatigue Nausea Pain Pain in jaw Pyrexia Syncope Vomiting

Symptomtext

Fever, chills, body aches, nausea, vomiting, extreme fatigue and fainting at 12am. I now have extreme jaw pain.

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Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Birth control
Allergien: None
Vorherige Impfungen: -

VAERS 2317305

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

schwer

Staat: IL
Alter: 67,0
Geschlecht: F
Eingang: 13.06.2022
Impfdatum: 19.11.2021
Beginn: 02.06.2022
Tage bis Beginn: 195,0
Dosis: 3
Route/Site: IM / -

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

Acute kidney injury Agitation Blood creatinine increased COVID-19 Cardiac failure congestive Chest X-ray abnormal Chronic kidney disease Condition aggravated Hypophagia Inflammation Pulmonary oedema SARS-CoV-2 test positive

Symptomtext

Patient received moderna vaccine on 4/28/21, 5/26/21 and 11/19/21. Presented to ER on 6/2/22 and found to be covid positive. The patient came to the emergency room again on June 2nd with a concern about acute congestive heart failure, but the major problem seems to be acute kidney injury on top of chronic kidney disease and a COVID-19 infection. *** her creatinine baseline used to be 1.9, and after discharge she was a little higher, but now this hospitalization started going above 4. The patient was seen by Nephrology. She was hydrated. Her p.o. intake was poor. Yesterday, she became more agitated requiring a dose of Haldol. Today, she is much better. She does have reasonably good output. She received monoclonal antibodies for COVID infection. She is currently on Decadron. She has 2 more days left. Discharged on 6/9/22

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary oedema
Hospital-Tage: 7,0
Labordaten: 6/2/22 COVID19: positive. 6/2/22 chest xray: Interstitial prominence suggesting interstitial edema or inflammation.
Aktuelle Erkrankungen: -
Vorgeschichte: CAD (coronary artery disease), CKD (chronic kidney disease), stage III (HCC), Diabetes mellitus (HCC), Hypertension, Personal history of noncompliance with medical treatment, presenting hazards to health, Secondary hyperparathyroidism (HCC) (3/30/2022), Third nerve palsy, Thyroid disease, Unspecified transient cerebral ischemia, and Unspecified viral hepatitis without mention of hepatic coma.
Andere Medikamente: amLODIPine 10 MG Tabs Commonly known as: NORVASC 10 mg, Oral, DAILY aspirin EC 81 MG Tbec 81 mg, Oral, DAILY atorvastatin 40 MG Tabs Commonly known as: LIPITOR 40 mg, Oral, EVERY MORNING calcitRIOL 0.5 MCG Caps Commonly known as: ROCA
Allergien: penicillins
Vorherige Impfungen: -

VAERS 2317171

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

schwer

Staat: FL
Alter: 53,0
Geschlecht: M
Eingang: 13.06.2022
Impfdatum: 04.11.2021
Beginn: 22.04.2022
Tage bis Beginn: 169,0
Dosis: 2
Route/Site: SYR / RA

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

Anticoagulant therapy Chest X-ray Electrocardiogram Hypertension Thrombosis Ultrasound scan

Symptomtext

Diagnosed with high blood pressure and prescribed Lisinopril 10mg on 04/22/2022. Diagnosed with blood clots and prescribed Eliquis 5mg (2X daily) on 05/16/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: Blood pressure check on 04/22/2022 and 05/20/2022 at Clinic. Chest x-ray and EKG on 05/20/2022 at Clinic. Sonogram on 05/16/2022 at Medical Center. Sonogram on 05/31/2022 at Surgeons office.
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 2152549

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

schwer

Staat: VA
Alter: 66,0
Geschlecht: M
Eingang: 02.03.2022
Impfdatum: 08.02.2022
Beginn: 14.02.2022
Tage bis Beginn: 6,0
Dosis: 4
Route/Site: IM / LA

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

Pain in extremity Thrombosis Ultrasound scan

Symptomtext

On 02/14/2022 I noticed midday there was a pain in my left calf. It stayed the same for 24 hours told my wife who is a nurse and she said I need to meet with my doctor that afternoon. He immediately realized it was blood clot by the way my calf looked, and the pain in my toes. He asked me to immediately go get a ultrasound but I couldn't do until Thursday. I went to a local hospital on Thursday and they confirmed blood clot was there. Then doctor prescribed Xarelto to be taken 2 times a day for 21 days, then once daily after that. I need to meet with hematologist in a couple of days to find out long term aspects of all this.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: Ultrasound.
Aktuelle Erkrankungen: None
Vorgeschichte: Rheumatoid arthritis
Andere Medikamente: Orencia infusion; Lipitor 20mg daily; Vitamin D3; Potassium citrate; Doxycycline 40mg daily; Prednisone 5mg (as needed); Zyrtec; Tylenol (as needed); Advil (as needed)
Allergien: None
Vorherige Impfungen: -

VAERS 1893669

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071f21a

schwer

Staat: TN
Alter: 29,0
Geschlecht: M
Eingang: 13.02.2022
Impfdatum: 17.11.2021
Beginn: 18.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Chest pain Injection site pain Palpitations Chest X-ray normal Chest discomfort Electrocardiogram Nausea Haemoptysis Investigation Pericarditis Rash

Symptomtext

Patient describes left sided chest pain/pressure without radiation that is worse when he leans forward. Patient has nausea, but no vomiting. Patient rates pain 6 out of 10. Pain is refractory to ibuprofen. Patient is prescribed ibuprofen 600mg every 6 hours and colchicine 0.6 mg twice daily. Patient is instructed to follow up with cardiology as outpatient.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: -
Labordaten: EKG : (Sinus 90, normal axis, normal interval, possible right ventricular conduction delay, PR depression in the inferior leads, possible PR depression versus ST elevation in the precordial leads although this is difficult to ascertain due to wandering baseline) Chest x ray is within normal limits.
Aktuelle Erkrankungen: none documented
Vorgeschichte: bipolar depression
Andere Medikamente: none documented
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 2083306

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071f21a

schwer

Staat: MO
Alter: 63,0
Geschlecht: M
Eingang: 02.02.2022
Impfdatum: 29.11.2021
Beginn: 01.12.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / -

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

Bell's palsy Extraocular muscle paresis Eyelid disorder Facial paresis Flushing Hypoaesthesia Hypoaesthesia eye Hypoaesthesia oral Laboratory test normal Magnetic resonance imaging head Muscular weakness Neurological examination normal

Symptomtext

did get vaccine nov 1 st 2021 vaccine moderna , then second vaccine nov 30th , then december 2nd developed eye weakness co bilateral lower extremity numbness only in feet -started 1st of october then developed flushing in face and the progressed to numbness on top of head and eyes and into mouth co face and head numbness and face muscles feel weak seeing dr then after second vaccine moderna, 2 days after developed facial weakness and inability to open eye-suspected bells palsy vs guillane barre , scheduled for spinal tap next week and testing for tick borne illness and myasthenia gravis denies generalized muscle weakness in other parts of body was started on mestinon for MG

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: lab work done and normal 1/26/22 MRI brain 12/21 and normal neurology consult
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: magnesium, vitamin C, omega
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2076423

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

schwer

Staat: NY
Alter: 46,0
Geschlecht: M
Eingang: 31.01.2022
Impfdatum: 10.11.2021
Beginn: 13.11.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: IM / LA

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

Brain natriuretic peptide C-reactive protein Dyspnoea Electrocardiogram Hypoxia Malaise Myocarditis Pyrexia Tachycardia Troponin increased

Symptomtext

Tachycardia, fever, malaise, progressed to dyspnea, hypoxia, AMS, myocarditis with confirmed EKG changes, elevated troponins, CRP and BNP also developed superimposed PNA.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Psychiatric issues.
Andere Medikamente: Clozapine; Gabapentin; Lorazepam; Olanzapine; Zydis; Divalproex.
Allergien: NKDA.
Vorherige Impfungen: -

VAERS 2071587

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071f21a

schwer

Staat: WI
Alter: 60,0
Geschlecht: M
Eingang: 28.01.2022
Impfdatum: 25.01.2022
Beginn: 25.01.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / AR

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

Dizziness Fatigue Lethargy Pyrexia Syncope Unresponsive to stimuli

Symptomtext

Systemic: Dizziness / Lightheadness-Severe, Systemic: Exhaustion / Lethargy-Severe, Systemic: Fainting / Unresponsive-Severe, Systemic: Fever-Severe

Weitere VAERSDATA-Felder

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

VAERS 2057714

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

schwer

Staat: NY
Alter: 58,0
Geschlecht: F
Eingang: 22.01.2022
Impfdatum: 05.11.2021
Beginn: 12.11.2021
Tage bis Beginn: 7,0
Dosis: UNK
Route/Site: SYR / LA

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

Bell's palsy Corneal abrasion Ear pain Eye pain Eyelid function disorder Facial paralysis Neck pain Pain Punctal plug insertion Vaccination complication

Symptomtext

11/12/2021: 3:30 PM: severe inner ear pain, pain radiating into neck approx 5:00 PM: visited urgent care; diagnosed with ear infection; prescribed amoxycillin 11/13/2021: Morning: awoke with paralysis to left side of face; went to emergency room, diagnosed with Bell's Palsy; prescribed Prednisone 20mg/ 3x daily for 7 days and Valtrex 1G, 3x/day for 10 days; adiviseds to stop Amoxycillin as there was no ear infection present 11/15/2021: Experienced severe pain in left eye; went to ophthalmologist; diagnosed with 5 corneal abrasions on left eye due to inability to close eye because of Bell's Palsy; prescribed Ofloxacin Ophhalmic Solution 0.3%. 11/15/2021: Office visit Dr. (filling in for pcp); diagnosed with Bell's Palsy. 11/17/2021: Follow up visit to Ophthalmologist; punctal plug inserted; prescribed artificial tears and moisturinzing gel for eye at night 11/29/2021 : Office visit, Dr., neurologist diagnosed Bell's Palsy: "This is most likely Bell's Palsy secondary to vaccine booster"stated in doctor's Clinical Notes. 12/1/2021: Visit to Opthalmologist: follow-up 1/12/2022: Visit to Ophthalmologist : follow-up In addition; I have been receiving physical therapy 2z weekly

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: MRI of brain ordered by neurologist; pending
Aktuelle Erkrankungen: NONE
Vorgeschichte: NONE
Andere Medikamente: NONE
Allergien: Nitrofurantoin
Vorherige Impfungen: -

VAERS 1989556

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

schwer

Staat: ME
Alter: 68,0
Geschlecht: M
Eingang: 29.12.2021
Impfdatum: 29.12.2021
Beginn: 29.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Abdominal pain lower Hyperhidrosis Injection site pain Somnolence Speech disorder Syncope Tremor

Symptomtext

Patient previously received Janssen lot #1805022 and chose to boost with Moderna. 12/29/2021 at approximately 15:50 RN administered vaccine in left deltoid. Patient complained 3 minutes after receiving Moderna booster in left deltoid that he was experiencing left arm pain at injection site, patient was A&Ox3, patient was in wheelchair and was escorted to observation, no complaints at that time. Approximately 5 minutes later RN heard "I need a nurse" coming from observation. RN went to observation and found patient sitting upright in wheelchair, appeared drowsy and non-verbal. RN instructed the Guard in observation to call 911. RN asked patient's wife and daughter about patient's medical HX. Wife stated to RN that her father has diabetes, COPD, and a pacemaker. Patient then became coherent and told RN that his left arm was hurting where he had rotator cuff issues. Patient then had a syncope episode and was tremoring and diaphoretic. Patient again become coherent and told RN he was experiencing lower abdominal pain. Patient then had another syncopal episode. Each episode lasting approximately 5-10 seconds. Patient become coherent again, Fire and Rescue and EMT arrived and assessed patient. Patient was able to converse with EMT's and was placed on stretcher and left via ambulance from Mall and transported to Hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: COPD, Diabetes, Pacemaker
Andere Medikamente: Unknown
Allergien: Lyrica
Vorherige Impfungen: -

VAERS 1924627

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

schwer

Staat: CA
Alter: 69,0
Geschlecht: F
Eingang: 09.12.2021
Impfdatum: 03.12.2021
Beginn: 04.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Acute left ventricular failure Arteriogram coronary normal Brain natriuretic peptide increased Cardiac imaging procedure abnormal Catheterisation cardiac normal Chest pain Dyspnoea Echocardiogram abnormal Ejection fraction decreased Left ventricular dysfunction Influenza like illness Laboratory test Myocardial oedema Myocarditis Nausea Right ventricular dysfunction Troponin T increased Ventricular hypokinesia

Symptomtext

Chest pain, shortness of breath, nausea, vomiting starting the day following the vaccination. Found to have new onset acute systolic heart failure with ejection fraction of 22%. A cardiac catheterization was pursued revealing normal coronary arteries. Cardiac MRI confirmed the suspected diagnosis of myocarditis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: 5,0
Labordaten: Troponin T 1231 BNP 2308 Echocardiogram: Moderately reduced left ventricular function at 33% with mildly reduced right ventricular function Coronary Angiogram: Normal coronary arteries Cardiac MRI: Severely reduced left ventricular systolic function EF 22% with asymmetric mid ventricular severe hypokinesis. Appearance of diffuse myocardial edema with lateral LV wall involvement. Reduced right ventricular function.
Aktuelle Erkrankungen: No acute illnesses
Vorgeschichte: Prior gastric bypass Depression Osteoarthritis Hypothyroidism
Andere Medikamente: LevoTHYROxine 100 mcg Tablet Mirabegron (MYRBETRIQ) 50 mg ER 24 hr Tablet ER Tablet Paroxetine (PAXIL) 40 mg tablet Pregabalin (LYRICA) 150 mg capsule Trazodone (DESYREL) 100 mg Tablet
Allergien: NSAIDS previously caused GI ulcer
Vorherige Impfungen: -

VAERS 1916845

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

schwer

Staat: CA
Alter: 60,0
Geschlecht: M
Eingang: 02.12.2021
Impfdatum: 27.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / UN

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

Autonomic nervous system imbalance Blood pressure orthostatic Brain natriuretic peptide increased Bundle branch block right C-reactive protein increased Chest X-ray abnormal Chest discomfort Chest pain Chills Dizziness Dizziness exertional Electrocardiogram abnormal Fibrin D dimer normal Hypotension Influenza like illness Left atrial enlargement Left ventricular hypertrophy Lung infiltration

Symptomtext

This 60 yo received his Moderna booster together with a flu vaccine on 10/27/21. Within 24 hours he developed flu like symptoms including low grade fever, chills, body aches which resolved within 24-48 hours but within 2-3 days he developed dizziness described as light-headedness especially with exertion. He initially suspected this was related but would just go away, but persisted and did not resolve. He checked his blood pressures and noticed his SBP was in the 80's to 90's on 11/8 and 11/9 and he also felt some tightness in his chest with exertion and almost had LOC while walking on 11/9 which prompted him to go to Palomar ER 11/10. Studies there showed an ECG with RBBB but o/w normal, negative Troponin x 2 and negative D-dimer with borderline BNP of 134 and CRP elevated of 3.24 with mild normocytic anemia. CXR was read as showing bibasilar and perihilar infiltrates but no pulmonary vascular congestion or interstitial edema. He has held his amlodipine and he feels much better the last few days though still has light-headedness with exertion like going up stairs, though no longer has chest tightness. repeat labs here showed persistent mild anemia with now elevated Platelets and ferritin though CRP is lower. Repeat BNP, d-dimer and troponin is pending today. ECG still shows RBBB but is o/w normal. CXR here is normal.60 yo male with unusual persistent symptoms of orthostatic hypotension, dizziness and atypical chest pain, which is now improved, which started within 2-3 days of receiving his Moderna booster and flu vaccine together on 10/27/2021. He also was found to have mildly abnormal CXR, elevated CRP and BNP at Palomar med center 11/10 and took Azithromcyin x 5 days and feels better but Platelets are higher now and ferritin very high (likely from acute phase reaction) though CRP is lower but he still has orthostatic blood pressure despite stopping his amlodipine he was previously on. Will repeat BNP and d-dimer and troponin today but will likely need some cardiac work up so will consult with cardiology for most efficient and effective work up to rule out cardiac cause addendum: Please see full Peer to Peer note by cardiology. It is suspected patient likely has a form of autonomic dysfunction secondary to COVID vaccination. This should resolve with time but may take 8 weeks per cardiology however, they agree with proceeding with ASAP echo to r/o cardiac dysfunction or other underlying conditions. Also, patient is on Propranolol from psychiatry, 2 tabs bid. I explained this to patient and recommended lower dose to 1 tablet twice a day and monitor BP and pulse and to notify me of any new symptoms or worsening. will repeat labs in the following week.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: see above. Main findings were initial abnormal CXR with possible fluid that resolved on repeat within a few days. elevated CRP, platelets and ferritin which eventually started coming down though ferritin still elevted bu coming down and felt to be due to acute phase reaction. orthostatc hypotension. Echo showed mild LVH andmild LA enlargement he is improving but not quite back to baseline yet and still not all the way back on amlodipine givne low BP but improving
Aktuelle Erkrankungen: Depression with anxiety, elevated fasting glucose, hypertension
Vorgeschichte: as above, depression with anxiety, elevated fasting glucose and hypertension
Andere Medikamente: Atorvastatin 10mg per day, HCTZ 25mg per day,Imipramine 150mg daily, Propranolol 20mg 2 tabs in am and 2in pm, Venlafaxine 150mg daily, amlodipinei 5mg daily
Allergien: None
Vorherige Impfungen: -

VAERS 1913532

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

schwer

Staat: MD
Alter: 22,0
Geschlecht: M
Eingang: 01.12.2021
Impfdatum: 01.12.2021
Beginn: 01.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Seizure Skin laceration Syncope

Symptomtext

Patient had received his booster Moderna shot. After about ten minutes, he tried to get up from his chair. He slumped and fainted, and he seized for about five seconds before coming to. He did cut his nose (we're not entirely sure how). I had him lie on the floor with his feet elevated because he stated he felt lightheaded. Paramedics were called, and they took over.

Weitere VAERSDATA-Felder

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

VAERS 1902138

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

schwer

Staat: VT
Alter: 59,0
Geschlecht: M
Eingang: 26.11.2021
Impfdatum: 28.10.2021
Beginn: 18.11.2021
Tage bis Beginn: 21,0
Dosis: 3
Route/Site: IM / UN

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

Chest X-ray Echocardiogram Laboratory test Pericarditis

Symptomtext

Pericarditis

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Praegender Schweregrund: Pericarditis
Hospital-Tage: -
Labordaten: Chest X-ray, Echocardiogram, Labs Date: 11/18/21
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Erythromycin derivatives
Vorherige Impfungen: -

VAERS 1889041

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

schwer

Staat: MN
Alter: 33,0
Geschlecht: F
Eingang: 21.11.2021
Impfdatum: 03.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Chest pain Dyspnoea Exercise tolerance decreased Fatigue Headache Loss of personal independence in daily activities Mobility decreased Pain Palpitations Pyrexia Syncope

Symptomtext

Fever of 103 deg for 36 hours, then fever of 100-101 deg for 36 hours, body aches, headache, joint hypermobility, syncope. After 72 hours, fever subsided and then the following symptoms continued for 2 weeks after dose 2 and 3 weeks after dose 3: fatigue, headache, chest pain, heart palpitations, activity intolerance, shortness of breath, exercise intolerance.

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Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: mast cell activation syndrome postural orthostatic tachycardia syndrome
Andere Medikamente: -
Allergien: amoxicillin
Vorherige Impfungen: developed POTS after HPV vaccines in 2007

VAERS 1874391

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

schwer

Staat: IL
Alter: 57,0
Geschlecht: F
Eingang: 16.11.2021
Impfdatum: 15.11.2021
Beginn: 15.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Fall Headache Hyperhidrosis Syncope Vomiting

Symptomtext

Patient received a booster of Moderna without any incidence. Aproximately 20 minutes post vaccination patient stated felt dizzy and lightheaded. Had patient sit in chair and gave a cup of water. Did eat about 4-5 hours prior to incident. Patient stated had a headache and did vomit not long before feeling dizzy. After another 5-10minutes stated felt worse and was getting up from chair when patient had syncopal episode and fell down. LOC about 30sec or less. Was verbal and moving everything after, no tremors/shaking/incontinence noted during or after. Patient recalled everything after. Did have some diaphoresis and HR 100-120 until EMS arrived 5 minutes later.

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Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: unknown, transferred to hospital by EMS
Aktuelle Erkrankungen: unknown
Vorgeschichte: -
Andere Medikamente: unknown
Allergien: PCN, Peaches, Benadryl
Vorherige Impfungen: -

VAERS 1873844

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071f21a

schwer

Staat: CO
Alter: 23,0
Geschlecht: M
Eingang: 16.11.2021
Impfdatum: 16.11.2021
Beginn: 16.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Disorientation Loss of consciousness Pallor Seizure Tremor

Symptomtext

patient passed out less than 5 minutes after receiving the moderna booster vaccine (0.25mL) and the influenza vaccine (flulaval quadrivalent). He had received the first two moderna shots in the past and had no issues. They were both administered in the left deltoid muscle. After I administered both vaccines a couple minutes later, the patient lost all color in face and began to seize (no history of seizures in the past). His arms began to shake, he made a loud moan, and starting moving his head around. Patient was sitting in a chair at the time and so I lowered him slowly and safely to the floor and laid him on his left side supporting his head. He lost consciousness for about 30 seconds (thats how long the seizure lasted) and afterwards regained consciousness. Was alert and able to answer questions correctly, but expressed that he didnt know what had occurred but that he felt disoriented. Two to three minutes went by and he began to seize again for the next 30 seconds. paramedics were called. no injury to the patient. trasnferred to the hospital to get checked out. documented accordingly in VAERS report and in patients chart. Patient should not receive another moderna vaccine or another flulaval vaccine in the future.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: N/A. Paramedics called to transfer patient to hospital to get checked out.
Aktuelle Erkrankungen: NONE
Vorgeschichte: NONE. hx of syncope with vaccines. hasnt happened in years.
Andere Medikamente: NONE
Allergien: NONE
Vorherige Impfungen: hx of syncope after a vaccine a few years ago.

VAERS 1873408

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071f21a

schwer

Staat: NJ
Alter: 18,0
Geschlecht: F
Eingang: 16.11.2021
Impfdatum: 11.11.2021
Beginn: 11.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Seizure

Symptomtext

Systemic: Seizure-Mild, Additional Details: Pt convulsive for about few seconds, still response, and alert

Weitere VAERSDATA-Felder

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

VAERS 1873073

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

schwer

Staat: MA
Alter: 36,0
Geschlecht: M
Eingang: 16.11.2021
Impfdatum: 01.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / RA

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

Deep vein thrombosis Dysstasia Pain in extremity Ultrasound scan abnormal

Symptomtext

Three days following administration of my COVID booster (11/4/21), I began feeling mild pain in my left calf. Over the course of the next 10 days, the pain began to worsen and got to the point where I could no longer stand on the leg. On the morning of 11/14/21 I went to the local Medical Center Emergency Room for treatment. Following physical examination and ultrasound, I was diagnosed with deep vein thrombosis in my left popliteal vein. I was prescribed Eliquis and told to stay off of my feet as much as possible and am awaiting a follow-up visit with my nephrologist to discuss continued treatment.

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Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: -
Labordaten: Ultrasound of left leg (11/14/21)
Aktuelle Erkrankungen: None
Vorgeschichte: Autosomal dominant polycystic kidney disease, Type I Arnold-Chiari Malformation, eosinophilic esophagitis
Andere Medikamente: Lisinopril, Jynarque, amlodipine besylate, esomeprazole magnesium
Allergien: None
Vorherige Impfungen: -

VAERS 1869433

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071f21a

schwer

Staat: CA
Alter: 65,0
Geschlecht: M
Eingang: 15.11.2021
Impfdatum: 29.10.2021
Beginn: 06.11.2021
Tage bis Beginn: 8,0
Dosis: 3
Route/Site: SYR / RA

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

Bell's palsy Computerised tomogram head normal Facial paralysis

Symptomtext

Bell's Palsy. Complete paralysis of right face. No improvement over first week

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Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: CT Head - negative
Aktuelle Erkrankungen: None
Vorgeschichte: Possible hypertension, untreated.
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1868416

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

schwer

Staat: NY
Alter: 61,0
Geschlecht: F
Eingang: 14.11.2021
Impfdatum: 09.11.2021
Beginn: 10.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / RA

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

Abdominal pain Arthralgia Asthenia Chills Dysstasia Gait inability Headache Hyperhidrosis Insomnia Mobility decreased Pain Seizure Vaccination site pain

Symptomtext

Several hours after shot extreme body/joint aches and headache. Took ibuprofen symptoms waned. Later in evening some chills and sweat. Went to bed. at an unknown time I experienced total incapacitation, and what I would describe as an ACID trip. Bright yellow colors followed by shivering and convulsions. Turning to the colors of a electric stove burner getting redder and redder and sweating. Severe vaccine site pain upon every movement whether moving arm or not. If I had been able I probably would have called 911. (I live alone) Around 3:30 am I began to "wake" up and become coherent symptoms gone by 4:30 am unable to sleep, unable to get out of bed. unable to walk/stand. Finally fell into fitful sleep at about 6:30 AM got up at around 12:30 PM severe abdominal muscle pain from convulsions. Took Ibuprofen. rested on couch all day. Ate very little as unable to fend for myself. Went to bed. Still very weak the next morning (Thursday). Felt better as the day went on and back to normal on Friday.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: rectal bleeding unknown cause
Vorgeschichte: none
Andere Medikamente: ibuprofen earlier in the day for body aches
Allergien: sensitive to eggs and peppers
Vorherige Impfungen: -

VAERS 1867778

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071f21a

schwer

Staat: SC
Alter: 33,0
Geschlecht: M
Eingang: 13.11.2021
Impfdatum: 13.11.2021
Beginn: 13.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Confusional state Dizziness Seizure Syncope Unresponsive to stimuli

Symptomtext

Systemic: Confusion-Severe, Systemic: Dizziness / Lightheadness-Medium, Systemic: Fainting / Unresponsive-Medium, Systemic: Seizure-Medium

Weitere VAERSDATA-Felder

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

VAERS 1864828

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

schwer

Staat: OH
Alter: 51,0
Geschlecht: F
Eingang: 12.11.2021
Impfdatum: 03.11.2021
Beginn: 03.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Activated partial thromboplastin time Blood glucose Computerised tomogram Computerised tomogram head Electrocardiogram Facial paralysis Full blood count Hypoaesthesia Hypoaesthesia oral Impaired work ability Metabolic function test Troponin

Symptomtext

40 min after receiving the vaccine, I began to have left upper lip numbness which then spread to the entire left side of my face and tongue. I had a slight left facial droop. I also had numbness to my left hand including the first 4 fingers. I went to the emergency room and they did a CT/CTA to rule out a stroke and it was negative. They drew blood work and this also was negative. The symptoms lasted until the next morning. I missed work that day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: -
Labordaten: CT Brain, CTA neck with IV contrast, EKG, blood glucose, CBC, BMP, PT, APTT, troponin T
Aktuelle Erkrankungen: None
Vorgeschichte: Exercise induced asthma
Andere Medikamente: None
Allergien: PCN, Morphine
Vorherige Impfungen: fever, chills, body aches after 2nd vaccine

VAERS 1864781

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

schwer

Staat: OK
Alter: 59,0
Geschlecht: F
Eingang: 12.11.2021
Impfdatum: 30.10.2021
Beginn: 08.11.2021
Tage bis Beginn: 9,0
Dosis: 3
Route/Site: SYR / LA

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

Blindness transient Blindness unilateral C-reactive protein normal Computerised tomogram head Computerised tomogram normal Condition aggravated Pain Photopsia Pyrexia Red blood cell sedimentation rate normal Sensitive skin Thrombosis Ultrasound Doppler normal

Symptomtext

On 11/8 at 1pm, I was in the store speaking with an employee. I lost ALL vision in right eye for approx 5-10 minutes. When vision returned, I immediately drove to eye doctor who examined my eye, did eye scan/picture, and sent me to my PCP. It was their opinion that I had a small clot that caused visual loss. CT was completed and is normal. Carotid Doppler is also normal. So far, no known cause. This happened 9 days post vaccination. On 10/31, I developed a low fever, body aches & skin sensitivity. I also had a momentary pinpoint flash in my right eye and for just a few seconds. I didn?t have concern until complete loss on 11/8.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: Head CT - normal Carotid Doppler - normal Blood work for CRP & ESR levels - normal
Aktuelle Erkrankungen: None
Vorgeschichte: High blood pressure
Andere Medikamente: Hydrochlorthiazide 25mg/1 per day
Allergien: Cantaloupe, avacado
Vorherige Impfungen: Normal body aches, low fever for 24 hours

VAERS 1864729

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071f21a

schwer

Staat: OH
Alter: 74,0
Geschlecht: F
Eingang: 12.11.2021
Impfdatum: 09.11.2021
Beginn: 09.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Blood pressure decreased Dyspnoea Intensive care Malaise

Symptomtext

patient received booster dose of 0.25 ml moderna and experienced a drop in blood pressure (60/36) and was admitted to intensive care unit with difficulty breathing from 11-09 to 11-11, reported feeling better but slightly under the weather. as of 11-12 patient is reporting feeling almost back to normal.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: morphine, Penicillin, sulfa, tricyclic antidepressants
Vorherige Impfungen: -

VAERS 1861250

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

schwer

Staat: NY
Alter: 59,0
Geschlecht: M
Eingang: 11.11.2021
Impfdatum: 10.11.2021
Beginn: 10.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Dizziness Headache Loss of consciousness Syncope Unresponsive to stimuli

Symptomtext

Patient was immunized with J&J on 4/7/21. He had syncope & hospitalization with first dose. His doctor advised him to get the booster but to get Moderna. We administered Moderna and asked him to wait 30 minutes for observation. At 10 minutes post vaccination he said he was a little light headed. We gave him juice and water and we kept him chatting and joking for 15 more minutes. He seemed fine but then grasped his head and said he had a crushing headache. He then slumped over unconscious. He was breathing and had a pulse but was unresponsive. EMS was called. When they arrived they said the patient was known to them and had a seizure disorder (which his family denies). The patient was conscious when the EMS took him to the hospital. We have not received an update yet

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: unknown
Aktuelle Erkrankungen: We know that he had syncope with the J&J vaccine that was administered on April 7, 2021. He was hospitalized afterwards. He spoke to his physician who advised him to get the booster but told him to get Moderna. I have no official records but I know that he told me he is a diabetic
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: syncope, 59, 04/7/21, Janssen

VAERS 1857379

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

schwer

Staat: MO
Alter: 24,0
Geschlecht: F
Eingang: 10.11.2021
Impfdatum: 09.11.2021
Beginn: 09.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Flushing Hyperhidrosis Syncope Unresponsive to stimuli

Symptomtext

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

Weitere VAERSDATA-Felder

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

VAERS 1849444

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

schwer

Staat: CT
Alter: 57,0
Geschlecht: F
Eingang: 07.11.2021
Impfdatum: 27.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Anxiety Blood test normal Chest X-ray normal Chills Electrocardiogram normal Headache Hypertension Hypotension Nausea Psychogenic movement disorder Pyrexia Retching Syncope Tremor Vomiting

Symptomtext

I originally received the J&J vaccine in March 2021 and had no side effects. My family is traveling to in December so my husband and I went to receive our booster shots. Moderna was available and we went to a local pharmacy to get that booster The following day I experienced the usual reported side effects - headache, nausea, vomiting/dry heaves, fever (101.4) and chills. Then I started to experience extremely high blood pressure (while I had fainted twice in the previous week because my BP was too low - around 70/50 it was then presenting at 200+/100+),extreme anxiety, uncontrollable shaking (my doctor told me it was called psychogenic movement disorder as a result of extremely high anxiety. If these had been reported side effects, I may not have gone to the emergency room, as at the time I was unemployed.At the time I was admitted my BP was 208/108.

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Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Chest xray to see if I had an enlarged heart of if there were blockages; extensive blood work to see if there was, among other things, an issue with my kidney function; an EKG to see if I was having a heart attack and other physical tests to see if I was having a stroke.. They found nothing abnormal and determined that these symptoms were as a result of the COVID booster.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Vitamin D Escitalopram 10mg Atorvastatn 10 mg
Allergien: None
Vorherige Impfungen: -

VAERS 1848937

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

schwer

Staat: MD
Alter: 82,0
Geschlecht: F
Eingang: 06.11.2021
Impfdatum: 28.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: - / -

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

Headache Loss of consciousness Nausea Photophobia Vomiting

Symptomtext

Worst headache imaginable where I felt as if Atlas were pressing the world against my forehead Extreme nausea and vomiting Passing out Extreme sensitivity to light Called emergency services emergency services came and sat me up, checked all my vital signs, I signed a form because I refused to go to the hospital Day # 8: eating causes nausea and bad headache still

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Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Pre-diabetes
Andere Medikamente: Synthroid 75 mg. Lanoxin 125 mcg. Lipitor 10 mg. Aspirin 325 mg. Vitamin D
Allergien: Topical neosporin. Topical Bacitracin. Topical. Silvadene Salmon. Eggs. Strawberries
Vorherige Impfungen: -

VAERS 1840665

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21a

schwer

Staat: VA
Alter: 18,0
Geschlecht: F
Eingang: 03.11.2021
Impfdatum: 30.10.2021
Beginn: 31.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Abdominal pain upper Anxiety Asthenia Autoscopy Disorientation Dizziness Gastrointestinal tube insertion Gastrointestinal tube removal Insomnia Limb discomfort Loss of consciousness Malaise Nausea Pain Pain in extremity Pyrexia Spinal pain Staring

Symptomtext

About 10 minutes after recieving the vaccine, I felt dizzy and weak, but assuming this was due to the normal histamine and blood flow reactions I have when confronted with new things in or near my body, I thought everything was fine. That night, however, I felt very anxious but oddly giddy. I couldn't sleep, even though I tried everything to make myself fall asleep. It was a sort of out of body experience, as I normally would have become frustrated and gotten up to do something, but I just laid there and stared at the wall. Around 3, maybe 3:30 AM, my limbs started to feel extremely heavy and achy. This feeling traveled to my whole body, and I started to feel like the aches were radiating from my spine. After about 30 more minutes, I became extremely disoriented, and it felt like the room was spinning. My vision was very blurry, and was fading in and out from black. At around 5 AM, I got up to use the restroom, but passed out for maybe 5 seconds, after a few steps. When I woke up, I was very nauseous. I was trying not to vomit, because I had an tube in, but it was the most intense feeling of nausea that I think I've ever felt, and I ended up vomiting forcefully (it was only bile, but a lot of it. I should also mention that I hardly ever vomit, as my gag reflex does not work very well). Because my tube came out when I vomited, we had to call the ambulance, but oddly, I felt almost completely better after vomiting-- the only symptom that remained was slight dizziness and stomach pain from my tube being vomited up. However, at the ER, I had a fever of 101.3 F, and moving was beginning to increase my stomach pain. The nurse pulled my tube out (it had been dangling out of my mouth and nose), and gave me Zofran (I do not remember the specific dosage). By around 6:30 AM, my fever had decreased to 99 F. I was discharged from the ER shortly after 7 AM. By Monday (November 1) evening, my symptoms were entirely gone (although I felt sick from my tube being forcefully removed when I vomited, and had just a few residual aches). Currently, I feel like I have recovered other than my tube being out (therefore I'm unable to receive all the nutrients I need). We are working on getting an appointment for a replacement tube.

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Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Psychogenic Non-Epileptic Seizures, Amplified Musculoskeletal Pain Syndrome, Mast Cell Activation.
Vorgeschichte: Chronic Dysautonomia, Small Fiber Neuropathy, Gastroparesis, Postural Orthostatic Tachacardia Syndrome, Narcolepsy,
Andere Medikamente: Pregabalin, Modafinil, Famotidine, Low Dose Naltrexone, Desvenlafaxine Extended Release, Fludrocortisone, Salt Stick Vitassium Buffered Electrolyte Salts, High Potency Vitamin D-3, Neuropathy] [-Lido] Cream" -- Topical Application, Peptide
Allergien: Topical & Local Anesthetics, Skin Adhesives/Adhesive Bandages, Dairy
Vorherige Impfungen: Age 17-- Pfizer COVID Vaccine First Dose (3/24/21) and Pfizer COVID Vaccine Second Dose (4/15/21): Both of these vaccines caused

VAERS 1840575

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071f21a

schwer

Staat: SC
Alter: 52,0
Geschlecht: F
Eingang: 03.11.2021
Impfdatum: 27.10.2021
Beginn: 02.11.2021
Tage bis Beginn: 6,0
Dosis: 3
Route/Site: - / LA

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

Dyskinesia Seizure like phenomena

Symptomtext

Patient random jerks in full body, arm, face, and legs. Patient says it is similar to a seizure.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure like phenomena
Hospital-Tage: -
Labordaten: They are going to doctor soon.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1839620

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

schwer

Staat: FL
Alter: 35,0
Geschlecht: F
Eingang: 03.11.2021
Impfdatum: 02.11.2021
Beginn: 02.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Confusional state Muscle rigidity Mydriasis Seizure Syncope Unresponsive to stimuli Vomiting

Symptomtext

Systemic: Fainting/Unresponsive-Medium, Systemic: Seizure-Medium, Systemic: Vomiting-Mild, Additional Details: Approximately 5 minutes after 0.5mL Moderna was given, patient's pupils fully dilated and arm muscles rigid. She came to but did not know where she was. EMS called; patient declined to be taken to hospital.

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

VAERS 1837001

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

schwer

Staat: CA
Alter: 31,0
Geschlecht: M
Eingang: 02.11.2021
Impfdatum: 30.10.2021
Beginn: 30.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Chills Dizziness Dyspnoea Flushing Hyperhidrosis Nausea Seizure Syncope Tremor Unresponsive to stimuli Vomiting

Symptomtext

Systemic: Allergic: Difficulty Breathing-Medium, Systemic: Chills-Medium, Systemic: Dizziness / Lightheadness-Medium, Systemic: Fainting / Unresponsive-Medium, Systemic: Flushed / Sweating-Medium, Systemic: Nausea-Medium, Systemic: Seizure-Medium, Systemic: Shakiness-Medium, Additional Details: Nurse RN gave patient 0.5 ml second dose Moderna vaccine on 10/30/21. Patient was originally afebrile, alert, and oriented. He reported feeling slightly nauseous after receiving vaccine and after few minutes, patient presented with syncope episode and signs of seizure. EMS came after he came to and patient was okay after vomiting a few times. He left store after about 30 minutes.

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

VAERS 1832375

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

schwer

Staat: CA
Alter: 54,0
Geschlecht: F
Eingang: 31.10.2021
Impfdatum: 29.10.2021
Beginn: 30.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Activated partial thromboplastin time Computerised tomogram Computerised tomogram head Differential white blood cell count normal Disorientation Dysstasia Ear haemorrhage Electrocardiogram Extra dose administered Full blood count normal Metabolic function test Mouth injury Skin laceration Syncope

Symptomtext

This was a booster, 8 months out from second dose of the Moderna vaccine. At about 12 hours after injection, I got up to get Tylenol. I was having trouble standing up and was very disorientated. My husband came to help me find the Tylenol. I turned to return to bed and then my husband heard me hit the floor (concrete floors in our bedroom). When he turned me over, I was limp, my eyes were open, but not focused on anything. Then I started coming to. I had split my chin open and had blood coming out of my ear. I didn't know what day it was nor when he told me, could I retain the information, and kept asking. I don't remember hitting the floor. He said I was face down with my arms at my side. I received stitches in my chin and mouth, had a scan of my head and an EKG of my heart. They found no fractures or broken bones. The brain scan came back fine as well.

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Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Tests the hospital did included: ECG, CT Facial Bones WO Contrast, CT Head wO Contrast, CT IAC WO Contrast, CBC with Auto Diff (some values out of range, but mostly normal), Comprehensive Metabolic Panel, APTT (out of range), Laceration repair X2
Aktuelle Erkrankungen: -
Vorgeschichte: hypothyroidism
Andere Medikamente: Synthroid 50 mg., Adapalene gel, Clindamycin Phospahate and Benzoyl Peroxide Gel, ibuprophen, Tylenal
Allergien: penicillin (not life threatening), latex, pollen, react sometimes to high histamine foods
Vorherige Impfungen: -

VAERS 1829547

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071f21a

schwer

Staat: AR
Alter: 65,0
Geschlecht: F
Eingang: 29.10.2021
Impfdatum: 29.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Feeling hot Loss of consciousness Presyncope

Symptomtext

patient had been given a moderma booster 0.25 ml IM into right arm. I turned and was getting left arm ready and was giving Fluzone Hd into LA when patient suddenly said that she was hot and something was wrong.. Patient started fanning herself. I got a cold compress to apply to forehead. Her husband came in to see what was going on. She started to go in and out of consciousness. Paramedics were called during this time. An eppi pen administered. Pearamedics arrived within 10 minutes. The accessed her . She continued to lose consciousness while being moniter and finally came back. Her husband transported her to hiopital ER for follow up. When I talked to the husband later in day she was home and recovered. Drs told husband they thought she a vegal response.

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Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: unknown
Vorgeschichte: none
Andere Medikamente: unknown
Allergien: none
Vorherige Impfungen: -

VAERS 1826444

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

schwer

Staat: MO
Alter: 42,0
Geschlecht: F
Eingang: 28.10.2021
Impfdatum: 26.10.2021
Beginn: 27.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Chills Dizziness Pyrexia Syncope

Symptomtext

Fainted three times the morning after vaccine (between 6:45-7:15 am); slight fever and chills following fainting episodes. I drank water, took ibuprofen and went back to bed. Then I got up at 2 pm, no further fainting or dizziness.

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

VAERS 2624422

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: WV
Alter: 70,0
Geschlecht: M
Eingang: 01.05.2023
Impfdatum: 05.03.2021
Beginn: 02.04.2021
Tage bis Beginn: 28,0
Dosis: 3
Route/Site: SYR / LA

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

Acoustic stimulation tests Asthenia Balance disorder Blood test Computerised tomogram Dizziness Gait inability Hyperhidrosis Magnetic resonance imaging Malaise Mobility decreased Tinnitus Vertigo Vomiting

Symptomtext

Dizziness, vertigo, vomiting, tinnitus, heartbeat in ear, unbalanced, breaking out in a sweat, so sick can?t hold my head up, so weak can?t walk.

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Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: Multiple Blood work, multiple CT scans, hearing tests, mri
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetic, black lung
Andere Medikamente: Aspirin, lisinopril, janumet, vascepa, tamsulosin, atorvastatin, finasteride, omega 3, breo Elliot?s, triamciolone, cetinizine
Allergien: Iv p dye
Vorherige Impfungen: -

VAERS 2595784

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: IL
Alter: 40,0
Geschlecht: F
Eingang: 13.03.2023
Impfdatum: 01.11.2021
Beginn: 01.07.2022
Tage bis Beginn: 242,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Asthenia Back pain C-reactive protein increased Dysstasia Electromyogram normal Magnetic resonance imaging head normal Magnetic resonance imaging spinal normal Mobility decreased Muscle disorder Muscular weakness Musculoskeletal pain Musculoskeletal stiffness Myalgia Neck pain Pain in extremity Red blood cell sedimentation rate increased Sensory disturbance

Symptomtext

I started with neck pain and upper back pain that developed overnight. Every morning, I felt like I had done manual labor the day before. Beginning at the end of August or beginning of September, I started noticing pain in both of my hips and glutes. By the end of September, the pain, stiffness, and weakness spread to the upper half of my thighs. It made it more difficult to rise from a seated position. By early November, the muscle issues had spread to my shoulders and upper half of upper arms. It made it difficult to raise my arms. By December, I began having Tendonitis issues in my left elbow and my left thumb. In January, I began having Tendonitis issues in my right elbow. The Tendonitis issues prevent me from putting my hands behind my back. Beginning in February, I began having pain in my hands in the morning that eases up throughout the day. It feels more joint related that muscle related. Beginning in March, I began having an unusual sensation in my left knee and lower half of my quad. It felt like a swollen knee and tugging sensation in my quad when my knee was bent, but I did not experience pain. On March 11, I began feeling pain in that knee. All the muscle symptoms seem to get worse overnight and are at their worst first thing in the morning and after periods of inactivity. It has been treated with Celebrex with minimal improvement. I?ve taken Ibuprofen with minimal improvement. I?ve also taken Prednisone with a great amount of improvement while on a short high dose regiment and moderate to minimal improvement on extended lower doses.

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Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: 09/28/2022 C-Reactive Protein - 1.10mg/dl; 02/04/2023 RBC Sedimentation Rate - 38mm/hour; 02/04/2023 Vitamin B12 - 1012pg/ml; 02/10/2023 C-Reactive Protein 44mg/liter; 02/10/2023 RBC Sedimentation Rate - 77mm/hour; 02/14/2023 RBC Sedimentation Rate - 55mm/hour; 12/12/2022 MRI Lumbar Spine - Normal; 12/21/2022 MRI Thoracic and Cervical Spine - Results didn't show cause for symptoms; 01/17/2023 EMG of Lower Extremities - Normal; 01/20/2023 MRI Brain - Results didn't show cause for symptoms
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension; Sleep Apnea; Insulin Resistance; Migraines; Obesity
Andere Medikamente: Emgality; Depo Provera; Losartan; Metformin; Metoprolol; Pantoprazole; Vitamin B Complex; Calcium Plus Vitamin D; Multivitamin
Allergien: Seasonal; Dust; Mold; Grass Pollen; Augmentin; Nickel; Latex; Adhesive Tape
Vorherige Impfungen: 12/19/2020 Pfizer Dose 1 COVID-19: Age - 40, Experienced extreme pain and swelling at injection site and extreme fatigue for tw

VAERS 2554576

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: NY
Alter: 53,0
Geschlecht: M
Eingang: 09.01.2023
Impfdatum: 11.10.2022
Beginn: 21.10.2022
Tage bis Beginn: 10,0
Dosis: 3
Route/Site: IM / LA

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

Bundle branch block right COVID-19 Cardiomyopathy Chest X-ray abnormal Chest pain Echocardiogram abnormal Electrocardiogram abnormal Left ventricle outflow tract obstruction Lung disorder SARS-CoV-2 test positive Sinus rhythm Troponin normal

Symptomtext

10/21/2022-Presents to ED, c/o Cp x 2 days. EKG NSR R BBB. 02 Sat WNL. Trop 0.017. Covid + test. CXR-mod increased pulm markings, may r/t mod bronchitis/developing pulm infection. Relief with nitro. 10/22 /2022-Trop0.019 EKG- no change. No SOB or cough, remdesivir held. Solumedrol. 10/24/2022-echo showed CMP with LVOT obs, gradient in 60-70's. unchanged from previous. Start BB. VSS 10/25/2022- Known LV OT, lw dose metoprolol, follow with cardio, D/C home.

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Praegender Schweregrund: Chest pain
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Chronic Hep C, COPD, CAD, GERD, opioid dependence,Type 2 DM, HX MI, CVA, ICD in place
Andere Medikamente: -
Allergien: Methadone, PCN
Vorherige Impfungen: -

VAERS 2496442

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: TX
Alter: 63,0
Geschlecht: M
Eingang: 02.11.2022
Impfdatum: 01.11.2021
Beginn: 05.04.2022
Tage bis Beginn: 155,0
Dosis: 3
Route/Site: IM / AR

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

Anticoagulant therapy Balance disorder Computerised tomogram Discomfort Fall Full blood count Gait disturbance Limbal swelling Magnetic resonance imaging Mobility decreased

Symptomtext

In April I woke up and could not move my whole right side was heavy and I could not move it. I tried to get out of bed and fell on the floor. Once I got up and tried to walk it would throw me off balance. Sometimes I would fall sometimes I would just lean over and wait until I would regain my strength. I went to see my doctor four days later. He put me on PLAVIX, my right side extremities are still a little bigger than the left side. I am awaiting on an appointment to see a Neurologist.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: CT Scan; MRI scan; complete blood panel
Aktuelle Erkrankungen: No
Vorgeschichte: High Blood Pressure
Andere Medikamente: COREG; amlodipine; baby aspirin
Allergien: Statin medication
Vorherige Impfungen: -

VAERS 2492531

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: IA
Alter: 76,0
Geschlecht: M
Eingang: 28.10.2022
Impfdatum: 21.10.2021
Beginn: 25.09.2022
Tage bis Beginn: 339,0
Dosis: 3
Route/Site: IM / AR

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

COVID-19 Cough Deafness Dyspnoea Pulmonary congestion Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive Secretion discharge Sinus congestion

Symptomtext

On 9/25/2022, I had a cough, chest congestion, and sinus congestion, runny nose, and some trouble breathing. On 9/25/2022, I took a COVID-19 home test and it was positive. I gave it 3 weeks to run its course. After 3 weeks I was not better. I continued to have the same symptoms. Around 10/12/2022, I went to see my doctor. I have a history of pneumonia. I did not have pneumonia yet, so the doctor prescribed an antibiotic and a steroid, prednisone. It's started to see improvement in about a week. As of today, 10/28/22 I still have congestion, lots of mucous, a little bit of hearing loss, but no loss of taste and smell.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 9/25/2022 COVID-19 home test positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: None
Andere Medikamente: N/A
Allergien: None
Vorherige Impfungen: -

VAERS 2436257

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: MN
Alter: 90,0
Geschlecht: F
Eingang: 09.09.2022
Impfdatum: 27.01.2021
Beginn: 19.08.2022
Tage bis Beginn: 569,0
Dosis: 3
Route/Site: - / -

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

COVID-19 Chest pain Cough Dyspnoea SARS-CoV-2 test positive

Symptomtext

CHEST PAINT, COUGH, SOB, COVID EXACERBATION

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Praegender Schweregrund: Chest pain
Hospital-Tage: 5,0
Labordaten: POSITIVE COVID TEST 8/18/2022
Aktuelle Erkrankungen: -
Vorgeschichte: Anemia Arthritis Follicular Thyroid Cancer Gout High Cholesterol Hypertension Small Bowel Obstruction Hyperlipidemia Insomnia Degenerative Disc Disease Primary Osteoarthritis Involving Multiple Joints Hypocalcemia Hypoparathyroidism Purpura, Nonthrombocytopenic Follicular Adenoma Prediabetes Pneumonia E-coli Uti Chronic Colitis
Andere Medikamente: Allopurinol (Zyloprim) 100 Mg Oral Tablet Atorvastatin (Lipitor) 20 Mg Oral Tablet Calcitriol (Rocaltrol) 0.25 Mcg Oral Capsule Diltiazem (Dilt-xr) 240 Mg Oral Cdcr Levothyroxine (Synthroid) 100 Mcg Oral Tablet Lisinopril-hydrochlorothiazid
Allergien: -
Vorherige Impfungen: -

VAERS 2416777

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: KY
Alter: 76,0
Geschlecht: M
Eingang: 09.09.2022
Impfdatum: 14.11.2021
Beginn: 21.08.2022
Tage bis Beginn: 280,0
Dosis: 3
Route/Site: IM / LA

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

Alcoholism Asymptomatic COVID-19 Blood sodium decreased Computerised tomogram thorax Condition aggravated Essential hypertension Hyponatraemia Mental status changes Metabolic encephalopathy Procalcitonin increased SARS-CoV-2 test positive Systemic inflammatory response syndrome Type 2 diabetes mellitus Unevaluable event

Symptomtext

Admitted to hospital

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Praegender Schweregrund: Condition aggravated
Hospital-Tage: 8,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2433305

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: KY
Alter: 77,0
Geschlecht: F
Eingang: 08.09.2022
Impfdatum: 04.11.2021
Beginn: 12.08.2022
Tage bis Beginn: 281,0
Dosis: 3
Route/Site: - / -

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

Blood sodium decreased COVID-19 Chest X-ray Emphysema Hypertension Hyponatraemia

Symptomtext

Patient ID: Admit Date: 8/12/2022 Discharge Date: 8/14/2022 Discharge Diagnosis: Principal Problem: Hyponatremia Active Problems: COVID-19 virus infection Pulmonary emphysema HTN (hypertension) Hospital Course: 78 year old vaccinated female was admitted for hyponatremia and Covid-19 infection. She received 3 doses of Remdesivir during the hospital stay. Hyzaar was switched to Cozaar. Na has improve to 134 from 120. She is discharged home today in stable condition. Patient educated on appropriate level of care post-discharge. Follow up with Primary Care Doctor in 5-7 days. Physical Exam on the day of discharge: Last Recorded Vital Signs: Temp: 98.2 ?F (36.8 ?C) Heart Rate (Monitor): 78 Pulse: 84 BP: 110/61 Respirations: 18 SpO2: 96 % O2 Flow Rate (l/min): 2 l/min General Appearance: no distress Eyes: PERRLA ENT: moist mucus membranes, no adenopathy Lungs: clear to auscultation bilaterally Heart: regular rate and rhythm Abdomen: soft, non-tender Skin: No rashes or lesions Extremities: full ROM Neuro: alert, normal strength and tone Consults: IP CONSULT TO NEPHROLOGY IP CONSULT TO SOCIAL WORK Significant Diagnostic Studies: CXR Operations: none Disposition: Home Discharge Condition: Fair

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

VAERS 2428526

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: KY
Alter: 73,0
Geschlecht: M
Eingang: 03.09.2022
Impfdatum: 17.11.2021
Beginn: 31.07.2022
Tage bis Beginn: 256,0
Dosis: 1
Route/Site: - / -

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

Benign prostatic hyperplasia Bladder catheterisation COVID-19 Chronic obstructive pulmonary disease Condition aggravated Culture urine positive Essential hypertension Gastric ulcer Hyperammonaemia Lower urinary tract symptoms Pseudomonas test positive SARS-CoV-2 test positive Sepsis Urinary tract infection Urinary tract obstruction

Symptomtext

Patient ID: 74 y.o. Admit Date: 7/31/2022 Discharge Date: 8/5/22 Principal Dx/ Final Dx: Sepsis Relevant Inpt Dx: Principal Problem: Sepsis Active Problems: Chronic systolic CHF (congestive heart failure) Pulmonary emphysema S/P AKA (above knee amputation) bilateral HTN (hypertension) Type 2 diabetes mellitus with hyperglycemia, with long-term current use of insulin Atrial fibrillation HPI: Hospital Course: This 74 year old man with bilateral AKA was admitted with sepsis. He had uti due to chronic foley catheter. Urine culture grew pseudomonas. He will complete 10 days or iv cefepime as unable to find oral medication based on sensitivities. He had midline placed and this should be removed when antibiotics are done. Follow up with pcp. His sepsis syndrome is resolved He tested positive for covid but did not require treatment for this Consults: IP CONSULT TO SEPSIS NURSE NAVIGATOR IP CONSULT TO SOCIAL WORK IP CONSULT TO WOUND CARE IP CONSULT TO IV THERAPY Disposition: home Discharge Condition: fair Discharge Medications: Current Discharge Medication List START taking these medications Details Lactobacillus rhamnosus GG (CULTURELLE) 15 billion cell sprinkle capsule Take 1 Capsule by mouth Twice a day for 14 days. Qty: 28 Capsule, Refills: 0 Associated Diagnoses: Sepsis due to Pseudomonas species without acute organ dysfunction NS (sodium chloride 0.9%) mini-bag 100 mL with cefepime (MAXIPIME) 2 g Administer 2 g intravenously Every 8 hours for 10 days. Indications: sepsis Qty: 30 Each, Refills: 0 Associated Diagnoses: Urinary tract infection without hematuria, site unspecified CONTINUE these medications which have CHANGED Details magnesium oxide (MAG-OX) 400 mg tablet Take 1 Tablet by mouth Twice a day for 7 days. Qty: 14 Tablet, Refills: 0 Associated Diagnoses: Hypomagnesemia !! oxybutynin chloride (DITROPAN XL) 15 mg ER tablet Take 1 Tablet by mouth Once Daily. Qty: 90 Tablet, Refills: 3 Associated Diagnoses: BPH with obstruction/lower urinary tract symptoms !! - Potential duplicate medications found. Please discuss with provider. CONTINUE these medications which have NOT CHANGED Details !! oxybutynin chloride (DITROPAN-XL) 10 mg ER tablet Take 10 mg by mouth Once Daily. sennosides-docusate sodium (SENOKOT-S) 8.6-50 mg Take 1 Tablet by mouth At bedtime as needed. lactulose (CHRONULAC) 20 gram/30 mL solution Take 30 mL by mouth Twice a day. Qty: 1000 mL, Refills: 0 Associated Diagnoses: Hyperammonemia metoprolol (LOPRESSOR) 25 mg tablet Take 1 Tablet by mouth Twice a day for 30 days. Qty: 60 Tablet, Refills: 0 Associated Diagnoses: Primary hypertension pantoprazole (PROTONIX) 40 mg DR tablet Take 1 Tablet by mouth Once Daily for 30 days. Qty: 30 Tablet, Refills: 0 Associated Diagnoses: Gastric ulcer, unspecified chronicity, unspecified whether gastric ulcer hemorrhage or perforation present furosemide (LASIX) 40 mg tablet Take 1 Tablet by mouth Once Daily. Indications: fluid in the lungs due to chronic heart failure Qty: 90 Tablet, Refills: 3 insulin detemir U-100 (LEVEMIR U-100 INSULIN) 100 unit/mL injection Administer 25 Units subcutaneously At bedtime. Qty: 10 mL, Refills: 0 Associated Diagnoses: S/P AKA (above knee amputation) bilateral !! insulin aspart U-100 (NOVOLOG) 100 unit/mL injection Administer 0.1 mL subcutaneously Before meals. Qty: 10 mL, Refills: 0 Associated Diagnoses: S/P AKA (above knee amputation) bilateral !! insulin aspart U-100 (NOVOLOG) 100 unit/mL injection SCALE 2 Blood Sugars: 101-150 - None 151-200 - 2 Units 201-250 - 4 Units 251-300 - 6 Units 301-350 - 8 Units Greater than 350 - 10 Units Qty: 10 mL, Refills: 0 Associated Diagnoses: S/P AKA (above knee amputation) bilateral ipratropium-albuteroL (DUO-NEB) 0.5 mg-3 mg(2.5 mg base)/3 mL nebulizer solution Take 3 mL by nebulization Every 4 hours. Qty: 180 Each, Refills: 0 Associated Diagnoses: COPD with acute exacerbation albuterol (PROVENTIL) 2.5 mg /3 mL (0.083 %) nebulization Take 1 Vial by nebulization Every 6 hours. Indications: chronic obstructive pulmonary disease tiotropium bromide 1.25 mcg/actuation Mist Take 2 Sprays by inhalation Daily. Calcium-Cholecalciferol, D3, 250-125 mg-unit Tab Take 1 Tablet by mouth Daily. Indications: prevention of a low amount of calcium in the blood Famotidine 40 mg tablet Take 20 mg by mouth Twice a day. Indications: gastroesophageal reflux disease acetaminophen (TYLENOL) 325 mg tablet Take 2 Tabs by mouth Every 6 hours as needed for Fever, temp greater than or equal to 100.5F (for oral temperature (or equivalent) of 100.5 degrees Fahrenheit or greater). Indications: pain Qty: 0 Tablet, Refills: 0 tamsulosin (FLOMAX) 0.4 mg capsule Take 0.4 mg by mouth Daily. Indications: enlarged prostate apixaban (ELIQUIS) 5 mg tablet Take 5 mg by mouth Twice a day. Indications: a flutter methocarbamoL (ROBAXIN) 500 mg tablet Take 500 mg by mouth Three times a day as needed for Other (muscle spasm). Indications: muscle spasm RT OXYGEN PER DELIVERY DEVICE 4 L/min by Nasal Cannula route RT Continuous. Indications: COPD/SOB menthol-zinc oxide (CALMOSEPTINE) 0.44-20.625 % ointment 1 Dose by Topical route Every 3 days. and PRN Indications: a wound ferrous sulfate 325 mg (65 mg iron) DR tablet Take 325 mg by mouth Daily. Indications: anemia from inadequate iron Budesonide-Formoterol (SYMBICORT 160-4.5 MCG) 160-4.5 mcg/Actuation inhaler Take 2 Puffs by inhalation Twice a day. Indications: COPD with Chronic Bronchitis polyethylene glycol 3350 (MIRALAX) 17 gram packet Take 17 g by mouth Daily as needed for Constipation. Indications: constipation nystatin (NYSTOP) powder 1 Applicator by Topical route Twice a day. Indications: skin infection due to a Candida yeast !! - Potential duplicate medications found. Please discuss with provider. Antibiotics - Dx and expected end date: Cefepime iv to complete 10 days treatment Lines/ Catheters and expected date of removal: Mid line Remove when antibiotics are complete

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

VAERS 2426422

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: -
Alter: 59,0
Geschlecht: F
Eingang: 01.09.2022
Impfdatum: 29.10.2021
Beginn: 17.07.2022
Tage bis Beginn: 261,0
Dosis: 3
Route/Site: - / -

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

Asymptomatic COVID-19 Cardiac stress test normal Cardiac telemetry normal Catheterisation cardiac abnormal Chest X-ray normal Chest pain Dyspnoea Echocardiogram normal Ejection fraction Nausea Neck pain Pain SARS-CoV-2 test positive Sinusitis Troponin normal

Symptomtext

Age: 60 y.o. Admit Date: 7/18/2022 9:33 AM Discharge Date: 7/19/2022 Admitting Physician: Discharge Physician: Discharge Diagnosis: Principal Problem: Atypical chest pain Active Problems: Morbid obesity with BMI of 45.0-49.9, adult Coronary artery disease involving native coronary artery of native heart with angina pectoris COVID-19 HPI: Patient is a 60 y.o. female who presents to ED with c/o CP that started as she was getting ready for work. Had sharp pain that radiated into L arm and neck. Associated with nausea and shortness of breath. Was initially severe but improved to dull ache. Other symptoms resolved. Has known h/o CAD on LHC in 2019 but did not need stent. Initial trop negative, admitted for further cardiac evaluation. COVID +, she was treated for a sinus infection 6 days ago, denies any current symptoms. Pt had NM stress test- which is negative - pt is stable for DC Hospital Course: Atypical chest pain Description of the Problem/Progression: New Plan: Admit. R/o MI with serial labs. Telemetry. Echo. Cardiology consulted. - no cardiac issue - pt is stable for DC from cardiac sten point stress test - negative COVID-19- carrier- asymptomatioc Description of the Problem/Progression: Likely incidental, ?contributing to symptoms Plan: Isolation. Not hypoxic and CXR clear, does not need treatment. Check COVID labs. Coronary artery disease involving native coronary artery of native heart with angina pectoris Description of the Problem/Progression: chronic Morbid obesity with BMI of 45.0-49.9, adult Description of the Problem/Progression: chronic DC home -f/u with PCP as oitpatient Physical Exam on the Date of Discharge: Constitutional: Appearance: She is well-developed. HENT: Head: Normocephalic. Eyes: Pupils: Pupils are equal, round, and reactive to light. Cardiovascular: Rate and Rhythm: Normal rate and regular rhythm. Pulmonary: Effort: Pulmonary effort is normal. Breath sounds: Normal breath sounds. Abdominal: General: Bowel sounds are normal. Palpations: Abdomen is soft. Musculoskeletal: General: Normal range of motion. Cervical back: Neck supple. Skin: General: Skin is warm and dry. Neurological: Mental Status: She is alert and oriented to person, place, and time. Consults: CONSULT TO CARDIOLOGY Significant Diagnostic Studies: Conclusion The LV EF is calculated at 75% Fixed anteoapical defect Possible breast attenutaion Low risk Stress test Disposition: home Discharge Condition: good Discharge Medications and Orders: Current Discharge Medication List CONTINUE these medications which have NOT CHANGED Details busPIRone (BUSPAR) 5 mg tablet Take 1 Tablet by mouth Twice a day. Qty: 180 Tablet, Refills: 1 Associated Diagnoses: Anxiety and depression Levothyroxine 125 mcg Cap Take 125 mcg by mouth Once Daily. THYROID Qty: 90 Capsule, Refills: 3 Associated Diagnoses: Hypothyroidism due to acquired atrophy of thyroid buPROPion (WELLBUTRIN) 75 mg tablet Take 1 Tablet by mouth Once Daily. Qty: 90 Tablet, Refills: 1 Associated Diagnoses: Reactive depression fluticasone propionate (FLONASE ALLERGY RELIEF) 50 mcg/Actuation nasal spray Spray 2 Sprays in nose Once Daily. Qty: 3 Each, Refills: 3 Associated Diagnoses: Seasonal allergies levocetirizine (XYZAL) 5 mg tablet Take 5 mg by mouth Once Daily. Qty: 90 Tablet, Refills: 1 Associated Diagnoses: Seasonal allergies semaglutide (OZEMPIC) 0.25 mg/0.2 mL (2 mg/1.5 mL) sub-Q injection Administer 0.4 mL (0.5 mg total) subcutaneously Every week Qty: 12 Each, Refills: 1 Associated Diagnoses: Insulin resistance; Class 3 severe obesity due to excess calories with serious comorbidity and body mass index (BMI) of 45.0 to 49.9 in adult cyclobenzaprine (FLEXERIL) 10 mg tablet Take 1 Tablet by mouth At bedtime. Qty: 90 Tablet, Refills: 3 Associated Diagnoses: Degenerative disc disease, cervical; Cervical radicular pain amitriptyline (ELAVIL) 50 mg tablet Take 1 Tablet by mouth At bedtime. Indications: 50 mg at bedtime Qty: 90 Tablet, Refills: 3 Associated Diagnoses: Other insomnia; Intractable chronic migraine without aura and without status migrainosus; Neck pain metoprolol (LOPRESSOR) 25 mg tablet Take 1 Tablet by mouth Once Daily. Qty: 90 Tablet, Refills: 3 Associated Diagnoses: Essential hypertension albuterol (VENTOLIN HFA) 90 mcg/Actuation inhaler Take 2 Puffs by inhalation Every 4 hours as needed. Qty: 3 Each, Refills: 1 Associated Diagnoses: Moderate persistent asthma with exacerbation potassium chloride (KLOR-CON) 20 mEq tablet Take 1 Tablet by mouth Once Daily. Qty: 90 Tablet, Refills: 1 Associated Diagnoses: Hypokalemia DULoxetine (CYMBALTA) 60 mg DR capsule Take 2 Caps by mouth Once Daily. DEPRESSION Qty: 180 Capsule, Refills: 3 Associated Diagnoses: Chronic pain syndrome; Reactive depression torsemide (DEMADEX) 20 mg tablet Take 20 mg by mouth Daily as needed. aspirin 81 mg chewable tablet Take 81 mg by mouth Daily. valacyclovir HCl (VALTREX PO) Take by mouth As needed. LORATADINE (CLARITIN PO) 10 mg Daily. STOP taking these medications predniSONE (DELTASONE) 20 mg tablet Comments: Reason for Stopping: cefdinir (OMNICEF) 300 mg capsule Comments: Reason for Stopping: fluconazole (DIFLUCAN) 100 mg tablet Comments: Reason for Stopping: predniSONE (DELTASONE) 20 mg tablet Comments:

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

VAERS 2425336

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071f21a

moderat

Staat: LA
Alter: 76,0
Geschlecht: M
Eingang: 31.08.2022
Impfdatum: 29.10.2021
Beginn: 14.07.2022
Tage bis Beginn: 258,0
Dosis: 2
Route/Site: - / -

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

Asthenia Blood magnesium normal COVID-19 Condition aggravated Loss of personal independence in daily activities Metabolic function test normal SARS-CoV-2 test positive Urine analysis normal

Symptomtext

Hospitalist Discharge Summary 76 y.o. Admit Date: 7/14/2022 Discharge Date: 7/25/2022 Principal Dx/ Final Dx: COVID-19 virus infection Relevant Inpt Dx: Principal Problem: COVID-19 virus infection Active Problems: Generalized weakness Parkinson disease Follow-up Recommendations: #1 please take medication as prescribed #2 please keep follow-up appointments HPI: As per Dr's Note: "Patient is a 76 y.o. male with Parkinson's who came to the ER due to worsening generalized weakness. He usually moves around with a walker but now feels weaker than usual. He required full assistance in the ER. UA (-) for infection. Mg and BMP are normal. He tested (+) for Covid-19 infection, He had received the Covid-19 vaccine. He has been admitted." Hospital Course: Patient presented with generalized weakness. He was found to have COVID-19 infection. He was started on Remdecivir and he completed the full treatment. He was also evaluated by neurology for weakness due to underlying history of Parkinson disease. He was seen by physical therapy and they recommended placement which was arranged with the help of social services. Patient was recommended to follow-up with the neurology as an outpatient. Unresolved issues requiring follow up (w/ labs or studies): None @HOSPDCED@ Consults: IP CONSULT TO NEUROLOGY IP CONSULT TO SOCIAL WORK IP CONSULT TO WOUND CARE Significant Diagnostic Studies: Positive COVID-19 test Operations: None Wound care recs: None Disposition: SNF Discharge Condition: good

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

VAERS 2379455

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: NY
Alter: 72,0
Geschlecht: F
Eingang: 22.07.2022
Impfdatum: 21.02.2021
Beginn: 21.02.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Asthenia Balance disorder Fatigue Gait disturbance Headache Hemiparesis Loss of personal independence in daily activities Mobility decreased Muscular weakness Visual impairment

Symptomtext

02/24/2021 = dose #1 within 30 minutes of receiving first dose I had a severe , throbbing headache that lasted 6 days with no relief from Tylenol (only treatment tried), extreme weakness resulting in being in bed x 4 days and needing assistance to get out of bed to use bathroom facilitiy, unable to function with daily ADL's, vision disturbance, extreme fatigue lasting 2 weeks, balance/walking issues that still exist today, weakness to right leg/foot. On 6 different occassions after the headaches landed me back in bed for roughly 36 hours. The headache was in less severity but lasted until approximately 1 month ago (06/2022). 03/25/2021 = dose #2 = same experience as after dose #1. 11/03/2021 = booster #1 or dose #3 = same as above, but bed time was 3 days. 05/20/2022 = fourthe dose or booster #2 = same as booster #1 above.

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Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: MS; HTN
Andere Medikamente: Copaxone 40 mg; Cardia XT; HCTZ; Pravastatin; ASA; Omeprozole; Botin; Vit. D3; Calcium;
Allergien: Toprol; Bactrim; Macrobid
Vorherige Impfungen: -

VAERS 2373976

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: MI
Alter: 93,0
Geschlecht: M
Eingang: 19.07.2022
Impfdatum: 30.11.2021
Beginn: 05.07.2022
Tage bis Beginn: 217,0
Dosis: 3
Route/Site: - / -

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

Asthenia Atypical pneumonia COVID-19 Cerebral small vessel ischaemic disease Chest X-ray abnormal Computerised tomogram head abnormal Encephalopathy Exposure to SARS-CoV-2 Full blood count abnormal Hypoacusis Leukocytosis Liver function test Metabolic function test abnormal Renal function test Renal impairment SARS-CoV-2 test positive Scan with contrast abnormal X-ray normal

Symptomtext

Discharge Provider: Primary Care Provider: Admission Date: 7/5/2022 Discharge Date: Jul 12, 2022 PRESENTING PROBLEM: Weakness [R53.1] COVID-19 [U07.1] Acute encephalopathy [G93.40] HOSPITAL COURSE: 94 y.o. male with known BPH, symptomatic bradycardia s/p pacemaker, CKD, HTN who presented on 07/05/2022 with acute encephalopathy from Assisted Living Facility. At baseline patient is oriented to 4, still his own decision maker, hard of hearing. COVID infection going around his facility, developed worsening weakness that started last week June 28. Patient tested positive at facility the day that patient was sent to emergency department. There was a plan hospice meeting by family on 07/06 but facility unable to take care of patient hence sent here to Hospital. In ED, pt VSS. CXR showing atypical pneumonia. CBC showing mild leukocytosis. CMP showing stable renal dysfunction. Pt had right femur and pelvic x-ray unremarkable. CT head w/o contrast showing no acute process, old ischemic changes and possible NPH. Patient was given a course of Remdesivir with liver and renal function monitored. Patient had shown improvement of his metabolic encephalopathy after the 1st 48 hours of stay. Was then was able to evaluate and patient started on soft diet. Hospice meeting with health hospice and 2nd hospice occurred. Patient met hospice criteria. Planned to sign up for hospice with Hospice. He was made comfort measures inpatient. Placement was arranged on 7/12/22.

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Praegender Schweregrund: Atypical pneumonia
Hospital-Tage: 7,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Dysphagia BPH with urinary obstruction Benign essential HTN CKD (chronic kidney disease), stage III (HCC) Cardiac pacemaker in situ Weakness Acute encephalopathy
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet aspirin 81 MG chewable tablet bisacodyl (DULCOLAX) 10 MG suppository Calcium Carbonate-Vitamin D3 600-400 MG-UNIT TABS Cholecalciferol (VITAMIN D3) 250 MCG (10000 UT) CAPS finasteride (PROSCAR) 5 M
Allergien: None
Vorherige Impfungen: -

VAERS 2327096

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: KY
Alter: 85,0
Geschlecht: F
Eingang: 22.06.2022
Impfdatum: 06.11.2021
Beginn: 14.03.2022
Tage bis Beginn: 128,0
Dosis: 3
Route/Site: IM / LA

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

Acute kidney injury Ammonia increased Anticoagulant therapy COVID-19 COVID-19 pneumonia Encephalopathy Fibrin D dimer increased Haemoglobin decreased Laboratory test normal Pancytopenia Platelet count decreased Respiratory failure

Symptomtext

85 year old vaccinated female was admitted for Covid-19 pneumonia and associated respiratory failure. She received Remdesivir therapy. Her condition did not improve initially. D dimer remains severely elevated and she required anticoagulation. Work up for thrombosis have been repeatedly consistently (-). She also became encephalopathic and required Lactulose therapy due to rise in ammonia level. She developed GI bleed from the anticoagulation and it was stopped. Hgb remains stable at 10.6 today. Plt still low at 69,000. She also suffered from AKI but it resolved. Pancytopenia is from the combination of recent Covid-19 infection and underlying fatty liver causing cirrhosis. She will finally be able to discharge to hospital today on O2.

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Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 15,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: CHF, Cirrhosis, AKI, hiatal hernia, Thrombocytopenia
Andere Medikamente: unable to ascertain
Allergien: NKA
Vorherige Impfungen: -

VAERS 2325510

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: MN
Alter: 78,0
Geschlecht: M
Eingang: 21.06.2022
Impfdatum: 03.11.2021
Beginn: 20.06.2022
Tage bis Beginn: 229,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Dyspnoea SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Patient presents to the ED for evaluation of SOB and subsequently tested positive for COVID-19 on 6/20/22 via PCR. This meets criteria for vaccine breakthrough case review.

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

VAERS 2315942

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: OH
Alter: 33,0
Geschlecht: F
Eingang: 10.06.2022
Impfdatum: 12.02.2021
Beginn: 14.04.2021
Tage bis Beginn: 61,0
Dosis: 3
Route/Site: IM / LA

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

Antinuclear antibody negative Cardiac monitoring Coronavirus infection Differential white blood cell count normal Full blood count abnormal Mean platelet volume increased Palpitations Petechiae Red blood cell sedimentation rate normal

Symptomtext

-Heart palpitations about beginning of April 2021. -Recurring petechial rash on face (always left cheek) documented photos on Aug 14 2021, then it briefly went away and recurred August 30, 2021. Most recent episode started June 8, 2022. Nonblanchable, non raised, not itchy. Looks just like broken capillaries all over my cheek.

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Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: -4/13/2021 wore zio patch for heart monitoring without any significant incidence. -8/20/2021 saw dermatologis for the petechial rash. Ruled out eczema, and ran Sed Rate , ANA, and a CBC w diff (all WNL aside an elevated MPV). I believe this rash is related to the vaccine because the first two incidences were shortly after getting my first two series and this most recent rash has occurred just after my first time being infected with coronavirus.
Aktuelle Erkrankungen: None
Vorgeschichte: Epilepsy
Andere Medikamente: Topamax, clonazepam, Flonase, Claritin, mirena IUD, naturemade womens multivitamin, allergy immunotherapy
Allergien: Seasonal allergies
Vorherige Impfungen: -

VAERS 2315533

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071f21a

moderat

Staat: IA
Alter: 62,0
Geschlecht: F
Eingang: 10.06.2022
Impfdatum: 23.11.2021
Beginn: 27.11.2021
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: IM / LA

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

Tremor

Symptomtext

leg tremor

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: vitamin d.b12, atorvastatin, lenothyroxine
Allergien: -
Vorherige Impfungen: -

VAERS 2301635

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: MD
Alter: 66,0
Geschlecht: F
Eingang: 29.05.2022
Impfdatum: 27.10.2021
Beginn: 27.10.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: SYR / LA

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

Arthralgia Bipolar disorder Condition aggravated Crying Injection site pain Injection site swelling Loss of personal independence in daily activities Magnetic resonance imaging abnormal Pain Periarthritis Rotator cuff syndrome Screaming Sleep disorder X-ray limb

Symptomtext

I had an appt with my Pharmacists for my shots as listed above with the date and time listed above. They had a female of whom I had no knowledge of her name, position or qualifications that gave me my shots. I was taken in a back office that was dark and sat in a chair against the wall. I slouch and she was standing over me and used a swab and did the shots. Within 24 hours the biceps of both arms had swelled to approximately a 2 1/2 inch radius and approximately 1/4 inch high. I put ice on both areas until the swelling went down approximately 2-4 hours later. The biceps stayed sore throughout the month of November and most of December, 2021, when both shoulders started having a "cutting" pain when I moved my arms and/or shoulders a certain way.. I sleep on my side and have a bed that raises or lowers at the top. I have it raised to approximately a 15 degree angle. I could not sleep well; my shoulder pain would either keep me awake and I'd toss and turn all night. It was starting to hurt when I raised my arms, put them forward or to the side. When hanging at my sides they throb. It was extremely painful to wipe myself after using the toilet. It hurts to pull down i.e. a shirt. It hurts to pull up i.e. my underwear. It takes about 15 minutes just to put on a bra, in a way that hurts the least. The pain was getting worse and worse i.e. if 8 was pretty bad mine was a 12-13 or higher. I started getting up at 5:00 am or 6:00 am, drink my coffee, get on my computer and go back to bed around 10:00 am or 11:00 am. I would sleep until it was time to feed my cats at 4:15 p.m. I sometimes went back to bed and just stayed in bed until the next morning. This continued this way through January and by then I was in so much pain and could not function properly I literally begged my doctor to let me get MRI's in both shoulders. On February 17th, 2022 I met with Dr . He did a physical exam of my arms/shoulders, what I could/could not do, how much pain, etc. He prescribed Physical Therapy 2-3 times per week for as long as needed (they have a Physical Therapy on site). I am trying my best however due to pain, I am sometimes not able to move and cancel my appointment. I recently (5/27/2022) started trying hydrotherapy at Recreation Center/Indoor Pools and hot tub. My next PT appointment is 6/01/2022. As of today 5/29/2022 I would rate my current pain in both shoulders as an 8, however not consistently- sometimes its higher. I have never ever had this much pain in my entire life. It feels as though I am being stabbed with a knife and then the skin sliced open. I have basically stopped the screaming/crying phase- I just bite the bullet I've had the pain for so long and I think to myself "maybe if I ignore it, it will go away". This has been a mess especially with my Bipolar Disorder and trying to stay emotionally stable.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: CRA MRN: 144911CR Acc: 19030017 12/08/21 XRAY Shoulder Min. 2 Views Right Shoulder NOTE: Dr (Primary Care) was told BOTH SHOULDERS WERE IN PAIN On February 07,2022 I had an MRI done on both shoulders. On February 08/2022 the results came back as follows: Diagnosis of Adhesive Capsulitis of Left Shoulder Diagnosis of Adhesive Capsulitis of Right Shoulder Diagnosis of Impingement syndrome of Left Shoulder Diagnosis of Rotor Cuff Tear, Right Diagnosis of Shoulder pain, Left Diagnosis of Shoulder pain, Right Orthopaedic Dr MRI'S MRI scan of arm joint (73221-RT) MRI'S MRI scan of arm joint (73321-LT) NOTE: Due to existing pacemaker Adventist is the closest facility that will do an MRI with a pacemaker.
Aktuelle Erkrankungen: Pulmonologist/check breathing & Vascular Dr./ck veins in leg
Vorgeschichte: Bipolar Dirorder, Pacemaker, Current smoker /quitting
Andere Medikamente: see list below
Allergien: Nicotine patch, gum
Vorherige Impfungen: -

VAERS 2298805

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: IL
Alter: 66,0
Geschlecht: F
Eingang: 27.05.2022
Impfdatum: 12.11.2021
Beginn: 01.03.2022
Tage bis Beginn: 109,0
Dosis: 3
Route/Site: IM / LA

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

Anticoagulant therapy Atrial fibrillation COVID-19 Chest discomfort Dyspnoea Electrocardiogram Electrocardiogram ambulatory abnormal Heart rate increased Magnetic resonance imaging heart SARS-CoV-2 test positive

Symptomtext

Started tightness in my chest, short of breath, and rapid heartbeat. Saw my Dr a few days later and had an EKG. Still experienced same symptoms. NP ordered halter monitor on 3/4 which I wore for 48hrs. Results showed I was in AFIB NP rx'd Elaquis. Saw Dr. on 4/25 and rx'd Metaprolol. Going for an angiogram in June. Tested positive for Covid on 5/27

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: EKG, Cardiac MRI,
Aktuelle Erkrankungen: None
Vorgeschichte: COPD, Lupus, Hypothryoid, gastric reflux, restless leg syn, osteoporosis, back pain
Andere Medikamente: Levothyroxin, Wixila, Spuriva, Preventol, Gabapentin, alindranate, Psyclobenzaprine, Iron, Omeprozal
Allergien: Penicillin, susinocoline
Vorherige Impfungen: -

VAERS 2283118

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: MA
Alter: 76,0
Geschlecht: F
Eingang: 18.05.2022
Impfdatum: 22.10.2021
Beginn: 01.11.2021
Tage bis Beginn: 10,0
Dosis: 3
Route/Site: IM / AR

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

Blood test Condition aggravated Echocardiogram abnormal Pericardial drainage Pericardial effusion

Symptomtext

Due to my Pericardial Effusion my cardiologist has been monitoring me twice a year for 18 years. After receiving the 3rd dose of moderna my cardiologist began to express concern about the size of the effusion. I had an echo cardiogram with him 11/01/2021 and from that point on he wanted to see me monthly which is very unusual. After multiple months of monthly echocardiograms my cardiologist decided that he wanted me to undergo a pericardiocentesis to address the size of my effusion. That was done on 3/30/2022. Since then, the effusion has returned somewhat and my doctor wants to continue monitoring. He also ordered a blood test to inquire the level of my antigen load because he would prefer me to hold off on getting any more Covid vaccines unless it is absolutely necessary. I am awaiting the results from that blood test.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 1,0
Labordaten: Echocardiogram-multiple-first one on 11/01/2021-monthly following that. Blood test to find antigen load-5/18/2022-waiting on results Blood work-April 2021-results and purpose unknown
Aktuelle Erkrankungen: None
Vorgeschichte: Pericardial Effusion
Andere Medikamente: None.
Allergien: Atropine
Vorherige Impfungen: -

VAERS 2268700

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: NY
Alter: 79,0
Geschlecht: F
Eingang: 10.05.2022
Impfdatum: 05.11.2021
Beginn: 07.12.2021
Tage bis Beginn: 32,0
Dosis: 3
Route/Site: IM / LA

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

Anticoagulant therapy Blood test abnormal C-reactive protein increased COVID-19 COVID-19 pneumonia Chest X-ray abnormal Chest pain Computerised tomogram thorax abnormal Dyspnoea exertional Fibrin D dimer increased Leukocytosis Lung infiltration Lung opacity Malaise Oxygen saturation decreased SARS-CoV-2 test positive Tachypnoea Wheezing

Symptomtext

12/7 - In ER with chest pain. Patient was tachypnic O2 sat 94% RA, desat to 80s ambulating. RR 33, HR101. WBC 30.1, D dimer 270. Temp WNL. Covid + with CXR showing bibasilar patchy infiltrates. CT showed no PE, airspace opacities mostly groundglass. Admitted for Covid 19/chest pain r/o ACS. Monoclonal A, decadron, Lovenox, fluids given. 12/8 - chest pain resolved. Sat WNL on room air. 12/9 - Discharged 12/10- Returns to ED worsening Covid symptoms-O2 sat in 70s. In 90s on 2LNC. Significant wheezing heard on inspiration and exportation. Treated with O2, Decadron, fluids. Admit to inpatient for Covid pneum. Baricitinib,Doxycycline, Remdisivir ordered. WBC trending down-29.2. Vitals WNL. Lovenox,decadron continued.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 7,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: COPD; GERD; HTN; Diabetes II; Obesity;, Anxiety
Andere Medikamente: -
Allergien: Aspirin; Ibuprofen; Sulfonamide antibiotics; Insect venom
Vorherige Impfungen: -

VAERS 2266002

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: WI
Alter: 68,0
Geschlecht: M
Eingang: 06.05.2022
Impfdatum: 29.10.2021
Beginn: 22.11.2021
Tage bis Beginn: 24,0
Dosis: 3
Route/Site: IM / LA

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

Atelectasis Chest X-ray abnormal Computerised tomogram normal Cough Dyspnoea Fatigue Headache Pulmonary fibrosis Wheezing

Symptomtext

I had a nagging dry cough. When I would take a deep breath, it would trigger a cough. It never produced any expectorant. I was more pronounced when sitting in my recliner. I presented itself less when I was sitting upright. There was also a wheeze that went along with. I used saline rinses, Afrin nose spray and gargled with hot salt water. Nothing seemed to work. The doctor listened to it and indicated that I was suffering from fatigue, cough and shortness of breath. I was also experiencing headaches. She completed a chest x-ray and CT scan. She indicated that a shadow showed up showing patchy area of atelectasis or scarring bilaterally. Asymptomatic prominent in the right hilum when compared to the left. A CT scan was done and there was no pneumonia. I sucked in a dose of chlorine gas as a teenager which caused me issues with breathing for a couple of weeks to they contributed the scarring to the event that happened. I was treated with prednisone and an antibiotic. The cough went away and then returned. I still have the cough but it is not as bad.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Chest X-ray CT scan
Aktuelle Erkrankungen: None
Vorgeschichte: Polio
Andere Medikamente: Celecoxib Clonidine Diltiazem CD Finasteride Fluticasone Propionate Triamterene hctz Sildenafil Losartan Lovastatin Metformin XR Multi Mineral-Multi Vitamin Nortriptyline Potassium Chloride
Allergien: None
Vorherige Impfungen: -

VAERS 2264816

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: WA
Alter: 64,0
Geschlecht: M
Eingang: 05.05.2022
Impfdatum: 03.11.2021
Beginn: 20.04.2022
Tage bis Beginn: 168,0
Dosis: 3
Route/Site: IM / AR

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

COVID-19 Chest discomfort Chest pain Chills Cough Diarrhoea Fatigue Myalgia Oropharyngeal pain Pyrexia Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

I contracted COVID-19 4/20/22 with symptoms of cough, chest pain/tightness which was very short lived, chills, fatigue, sore throat, congestion, slight diarrhea, myalgia, and felt feverish. I was prescribed molnupiravir 4/21/22 and my symptoms resolved after the 5th day with only a lingering cough, which has resolved.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: COVID-19 rapid nasal swap was positive 4/21/22
Aktuelle Erkrankungen: No
Vorgeschichte: Arrhythmia Atrial flutter Mild depression Gout
Andere Medikamente: Bupropion daily Eliquis daily Allopurinol daily Metoprolol daily Amiodaron daily
Allergien: No
Vorherige Impfungen: -

VAERS 2263538

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: MA
Alter: 61,0
Geschlecht: M
Eingang: 04.05.2022
Impfdatum: 01.11.2021
Beginn: 15.04.2022
Tage bis Beginn: 165,0
Dosis: 3
Route/Site: IM / LA

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

Blood test COVID-19 Chest X-ray Cough Dyspnoea Fatigue Influenza virus test negative Nasopharyngitis Oropharyngeal pain Pain Rhinorrhoea SARS-CoV-2 test positive Sneezing

Symptomtext

I started getting symptoms of sore throat. I took an at home COVID-19 test on 4/16/2022 that was negative. My symptoms progressed on 4/17/2022 when it felt like a head cold with sneezing and runny nose. I took a COVID-19 home test on 4/19/2022 due to feeling worse. I had achiness, tiredness, fatigue, trouble breathing, and cough. On 4/20/2022, when I would cough, it would hurt. I was notified that my neighbor had COVID as well. I contacted my doctor and did a visit and they did blood work and retested which was positive for COVID and negative for flu. I received a chest x-ray as well. I was prescribed Paxlovid and a steroid inhaler.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: COVID-19 tests, flu test, blood work, chest x-ray.
Aktuelle Erkrankungen: None
Vorgeschichte: CAD, HTN, Lymphocytic colitis
Andere Medikamente: Atorvastatin, Metoprolol, HCTZ/Lisinopril, Aspirin 81mg
Allergien: None
Vorherige Impfungen: -

VAERS 2258948

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: CT
Alter: 44,0
Geschlecht: F
Eingang: 29.04.2022
Impfdatum: 28.10.2021
Beginn: 05.02.2022
Tage bis Beginn: 100,0
Dosis: 3
Route/Site: SYR / AR

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

Balance disorder Blood test normal Gait disturbance Hypoaesthesia Magnetic resonance imaging spinal normal Paraesthesia Sensory loss

Symptomtext

02:05 2022 Morning, months after my vaccine, I began to feel numbness creeping up from my feet to my lower leg, within a 24 hour period it was from my belly button down that I had numbness. There was no pain however there was a lack of sensation in my lower body. I set up an appointment with my Ortho specialist, they stated that after the exam there was nothing that seemed to be wrong, however he did give me a prescription for PT and I have been doing that since. I have been working with two PT specialists and at times I do feel a difference, however I still notice that it will come and go with the loss of sensation in my toes and lower leg. I have gone to the ER and I had blood work, lumbar and thoracic spine MRI and ruled out any issues. I am still currently feeling loss of sensation in my toes and lower legs at times that are worse. I have also felt in my upper torso area I have noticed a different sensation in my skin in my upper chest area and back as well. I was having difficulty with walking and balance due to severity of loss of sensations.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Bloodwork: normal within range for myself. MRI of Spine: nothing noticeably wrong.
Aktuelle Erkrankungen: N/A
Vorgeschichte: Rheumatoid Arthritis; Brain Tumor
Andere Medikamente: Multivitamin daily; Zyrtec for allergies
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2238751

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: WI
Alter: 40,0
Geschlecht: F
Eingang: 18.04.2022
Impfdatum: 14.11.2021
Beginn: 19.02.2022
Tage bis Beginn: 97,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Cough Diarrhoea Dyspnoea Dyspnoea exertional Fatigue Headache Oropharyngeal pain SARS-CoV-2 test positive

Symptomtext

I started getting symptoms of diarrhea, fatigue, headache, cough, and sore throat. The fatigue continued and then I also started getting shortness of breath on exertion. I took an at home COVID-19 test which was positive. A couple of days later, I did a rapid and PCR test that was negative at the doctors office.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: COVID-19 tests
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: Flu shot, dizziness.

VAERS 2226569

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 071F21A

moderat

Staat: TN
Alter: 59,0
Geschlecht: M
Eingang: 11.04.2022
Impfdatum: 01.11.2021
Beginn: 01.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dyspnoea

Symptomtext

I have had severe shortness of breath and has not gotten better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: No
Vorgeschichte: Diabetic Type 2, Lung Cancer
Andere Medikamente: Fibrate, Meloxicam, Haloperidol, Pioglitazone HCL, Lisinopril, Hydrochlorothiazide, Fish Oil, Multivitamin, Low Dose Aspirin, Amlodipine Besylate
Allergien: Tide Soap
Vorherige Impfungen: -

VAERS 2225362

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: WA
Alter: 48,0
Geschlecht: M
Eingang: 09.04.2022
Impfdatum: 03.11.2021
Beginn: 22.11.2021
Tage bis Beginn: 19,0
Dosis: 3
Route/Site: IM / LA

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

Migraine

Symptomtext

Migraine every few weeks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: No tests. Just Dr
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: Ampicillin
Vorherige Impfungen: -

VAERS 2223193

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: OH
Alter: 50,0
Geschlecht: M
Eingang: 08.04.2022
Impfdatum: 26.03.2021
Beginn: 31.10.2021
Tage bis Beginn: 219,0
Dosis: 3
Route/Site: IM / LA

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

Asymptomatic COVID-19 Hypertension SARS-CoV-2 test positive Small intestinal obstruction Umbilical hernia Urinary tract infection

Symptomtext

Moderna COVID vaccines received on 2/26/2021 and 3/26/2021 Hospitalized at Hospital on 10/31/2021 Diagnosis: Positive COVID 19 with rapid but repeat PCR test was negative, partial small bowel obstruction, Acute UTI, Hypertension, Umbilical Hernia Treatment related to bowel obstruction, removed COVID restrictions due to negative PCR test, rapid likely false positive since asymptomatic and vaccinated per report

Weitere VAERSDATA-Felder

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

VAERS 2204965

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: PA
Alter: 54,0
Geschlecht: M
Eingang: 29.03.2022
Impfdatum: 30.11.2021
Beginn: 29.11.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / LA

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

Cardiac discomfort Dyspnoea Tachycardia

Symptomtext

Shortness of breath with tachycardia lasting 6 weeks plus. Felt that heart had not enough room to beat properly.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: None. I have no insurance.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: second vaccine dose given on 01/12/2021 Pfizer. Giving me shortness of breath with tachycardia. Lasted about 4 weeks.

VAERS 2196693

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: SC
Alter: 69,0
Geschlecht: F
Eingang: 24.03.2022
Impfdatum: 04.03.2022
Beginn: 14.03.2022
Tage bis Beginn: 10,0
Dosis: 3
Route/Site: SC / LA

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

Balance disorder C-reactive protein normal Full blood count normal Hypoaesthesia Hypoaesthesia oral Metabolic function test Muscle spasms Paraesthesia Paraesthesia oral

Symptomtext

3/14/22Numbness/tingling LE bilaterally with severe muscle spasms at times. Feeling off balance at times. 3/17 /22 as above with lip and facial numbness/tingling bilaterally. 3/21/22 as above with numbness/tingling fingertips and thumb bilaterally.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: CBC with diff ;03/22/2022 CMP ;03/22/2022 C Reactive Protein ;03/22/2022 All results WNL
Aktuelle Erkrankungen: None
Vorgeschichte: Osteoporosis MVP
Andere Medikamente: Vitamin B complex Vitamin C 1000mg/day CoQ10 200 mg/day Vitamin D3 250mcg/day Calcium 1000mg/day AZO cranberry Perservision AREDS2 Biotin 10000mcg/day Probiotic
Allergien: PCN Erythromycin HCTZ Flu Vaccine
Vorherige Impfungen: Flu Unsure of dates Diaphoretic, tachycardia, extreme pallor, blacking out within hours of vaccine. No problems with other vacci

VAERS 2187530

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: -
Alter: 90,0
Geschlecht: F
Eingang: 18.03.2022
Impfdatum: 30.10.2021
Beginn: 11.11.2021
Tage bis Beginn: 12,0
Dosis: 3
Route/Site: IM / UN

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

Cardiac failure Pneumonia

Symptomtext

Patient hospitalized for heart failure and pneumonia of both lungs within 6 weeks of receiving covid vaccination booster.

Weitere VAERSDATA-Felder

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

VAERS 2182464

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: OH
Alter: 51,0
Geschlecht: F
Eingang: 16.03.2022
Impfdatum: 26.02.2021
Beginn: 27.02.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Echocardiogram abnormal Electrocardiogram ambulatory abnormal Left ventricular dysfunction Mitral valve incompetence Pericardial effusion Pulmonary valve incompetence Supraventricular tachycardia Tachycardia

Symptomtext

Adverse reaction started 24 hrs after first vaccine, tachycardia. Intermittent symptoms of tachycardia have continued every since. After second vaccine, symptoms of tachycardia kept me awake 3 of 7 nights per week. After third vaccine (booster), I developed cardiac SVT's and sought medical attention.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Supraventricular tachycardia
Hospital-Tage: -
Labordaten: Echo Cardiogram - 12/9/2021 Left ventricular ejection fraction is estimated at 65%. Normal systolic. LV function: Mild diastolic LV dysfunction. E'e 8.7, Trace mitral and pulmonic regurgitation, Trivial pericardial effusion Holter Monitor - 1/18/2022 Patient was in regular sinus rhythm throughout most of the recording. Occasional short runs of nonsustained supraventricular tachycardia (4-5) beat runs). Also some periods of sinus tachycardia. No ventricular arrhythmias were noted.
Aktuelle Erkrankungen: None
Vorgeschichte: Past History of Kidney Stones, mild cardiac arrhythmia (skip beats)
Andere Medikamente: Inderal 20 mg bid, Urocit-K 1080 mcg, Vitamin D3 1000 IU
Allergien: NKDA, Milk
Vorherige Impfungen: -

VAERS 2179780

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: SC
Alter: 66,0
Geschlecht: F
Eingang: 15.03.2022
Impfdatum: 05.11.2021
Beginn: 07.11.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

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

Feeling abnormal Injury Pain Pneumonia Pyrexia Road traffic accident

Symptomtext

About 2 days after the vaccine, I started hurting and had a low grade fever. I felt bad for 2 weeks. In December, I had a lung infection that lasted until Feb. During that time also I was in a car accident. I had a doctors appointment to get seen about the lung infection and was on my way when I had a car accident. I was put in the hospital for 4 days and then was transferred to a skilled nursing facility. While there, I was treated for the lung infection. Since, I had injuries and was on pain meds, I don't remember exactly what all I was given for the lung infection but know that I took an Inhaler.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pneumonia
Hospital-Tage: 4,0
Labordaten: Unknown
Aktuelle Erkrankungen: None
Vorgeschichte: Cancer history; history of lung issues
Andere Medikamente: Calcium Supplement; Vitamin D
Allergien: Tetracycline; Codeine; Lisinopril; Shellfish
Vorherige Impfungen: -

VAERS 2157880

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: CT
Alter: 76,0
Geschlecht: M
Eingang: 04.03.2022
Impfdatum: 04.11.2021
Beginn: 14.02.2022
Tage bis Beginn: 102,0
Dosis: 3
Route/Site: SYR / LA

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

Asthenia COVID-19 Chest pain Fatigue Headache Illness Mobility decreased Musculoskeletal chest pain Oropharyngeal pain Pneumonia Pyrexia SARS-CoV-2 test negative SARS-CoV-2 test positive Sinusitis X-ray

Symptomtext

About the 13th of February I had a sore throat. I noticed that I had a fever too. The next day my sore throat got really bad, and I started having pain in my chest and ribs. I equated that with pneumonia because I had it before in the past. When I went to the doctor it was confirmed that I had pneumonia and also covid. I was prescribed some medication for the pneumonia for 10 days. I am just now starting to feel better, but I am still very weak. I feel like I have a sinus infection. I had a really bad headache that was more like a head cold. I was sick but not deathly sick. I was on my back in bed for a week because it was too exhausting to get up and move around.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Covid test- negative (around February 14, 2022) x-ray- showed pneumonia (February 15, 2022) Covid test- positive (February 15, 2022)
Aktuelle Erkrankungen: None
Vorgeschichte: Cardiovascular Disease High Blood Pressure
Andere Medikamente: I don't want to add them at this time.
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2137128

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: OH
Alter: 51,0
Geschlecht: F
Eingang: 24.02.2022
Impfdatum: 29.10.2021
Beginn: 31.12.2021
Tage bis Beginn: 63,0
Dosis: 3
Route/Site: IM / LA

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

Blood test Cellulitis Chest X-ray Chills Hyperhidrosis Localised infection Malaise Pain Pneumonia Pyrexia SARS-CoV-2 test negative White blood cell count increased

Symptomtext

sudden onset of Shaking chills, fever 102.7 oral, body aches, feeling of malaise. Tylenol and motrin taken for fever and pain; started wed 12/29/21 w low grade temp and bodyaches; woke in the night soaking wet; then two days later (12/31/2021) developed sudden onset of above symptoms; sent to ED at advice from doctor. at ED-Covid swab done and negative, blood drawn, found to have a high white blood cell count, given IV fluids; treated for early pneumonia-given prescription for antibiotics, 1/2/22 developed leg infection (cellulitis), given a shot of antibiotics by PCP, started on second antibiotic

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pneumonia
Hospital-Tage: -
Labordaten: Covid swab-negative blood work-high white blood cell count chest xray done after seeing PCP, 1/3/2022 more blood work done; leg checked for blood clot and abcess
Aktuelle Erkrankungen: none
Vorgeschichte: partial posterior tibialis tendon tear
Andere Medikamente: none
Allergien: erthyromycin
Vorherige Impfungen: -

VAERS 2119299

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: NY
Alter: 61,0
Geschlecht: F
Eingang: 17.02.2022
Impfdatum: 16.11.2021
Beginn: 16.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Biopsy lymph gland Fatigue Impaired work ability Lymphadenopathy Mobility decreased Pain Pain in extremity Pyrexia Ultrasound thyroid

Symptomtext

The initial event started the night of the vaccine with sore arm, tired, achy ,fever and lasted about 36 hours. Swollen lymph nodes on left side (neck) for two weeks, I could not lift my arm (24 hours). Unable to go to work for 2 days. By the third day, felt fatigue and tired but able to work. Thyroid nodules was biopsied because it was so swollen and painful. Took Tylenol for the pain, warm compresses to get relief.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: Radiology: Thyroid Ultrasound 01/18/2022, nodule in neck doubled in size, left side. On 02/01/2022 lymph node biopsy - benign.
Aktuelle Erkrankungen: None
Vorgeschichte: Thyroid nodules for about 10 years.
Andere Medikamente: NAC L-Glutathione K2D3 10,000 Vitamin C
Allergien: Sulfur
Vorherige Impfungen: -

VAERS 2114151

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071f21A

moderat

Staat: MI
Alter: 48,0
Geschlecht: M
Eingang: 15.02.2022
Impfdatum: 28.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Carpal tunnel syndrome Electromyogram abnormal Hypoaesthesia Paraesthesia

Symptomtext

My hands went numb whenever I wasn't using them, especially when sleeping. I am woken up several times a night with numb hands and tingling fingers. This got slightly better about 2 weeks after my booster but it has not improved since and is still very substantial.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: EMG 2 Limbs 12/29/2021 Tested positive in both hands for moderate to severe carpal tunnel They recommend surgery on both hands but I am still working with insurance to get it approved.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Omeprazole 20mg Lisinopril 20mg Atorvastatin 40mg Escitalopram 20mg Testosterone Cyp 1 ml Multivitamin
Allergien: None
Vorherige Impfungen: -

VAERS 2112967

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: CA
Alter: 51,0
Geschlecht: F
Eingang: 15.02.2022
Impfdatum: 06.11.2021
Beginn: 06.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Head discomfort Headache Hypertension Hypoaesthesia Impaired work ability Magnetic resonance imaging head Migraine Myalgia Paraesthesia Pyrexia

Symptomtext

I want to say that I received my first vaccine on January 2021, started having headaches for three weeks. Then I got second vaccine in February I also had headaches. On the third vaccine I got a fever on November 06, 2021 with more intense headaches. Last week I was not able to work 02/02/2022 to 02/04/2022, had disability note. I had MRI on 02/12/2022 I have migraine headaches, really bad. I had an MRI came back normal. I am under medication to suppress the migraines. I also have muscle aches and pain. I also took OTC Ibuprofen as pain mediation. I start having a bad headache on 01/22/2022, left side of my head feels very very high pressure and tingling sensation and numbness to the inside of my nose, only my left side and I started worrying. I went to ER stayed there 3 hours and then released me. On January 26, 2022, with the same symptoms of my migraines and high blood pressure. On the 01/26/2021, my blood pressure was 107/90. I was not able to leave my work on 01/28/2022 due to a meeting and I told my supervisor I had to go again to the ER. On 01/30/2022 I went again to the ER due to my migraine headaches and took labs, was given IV and I stayed there for 5 hours and then the nurse told me that your PCP needs to see you. On 01/31/2022 I was put IV and I was sent to the neurologist and I will give you a week off from work. On 02/10/2022 I went to see a neurologist and that is when they start me on medication for my migraines. I got an MRI on 02/12/2022 of the brain. MRI did not show any abnormal findings.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: MRI brain was normal, labs were performed
Aktuelle Erkrankungen: I had a very bad muscular pain.
Vorgeschichte: Hypothyroidism, Fibromyalgia diagnosed on 06/2021. I also had a treatment with my PCP, under treatment.
Andere Medikamente: None reported
Allergien: Shrimp
Vorherige Impfungen: -

VAERS 2110483

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: KY
Alter: 19,0
Geschlecht: F
Eingang: 14.02.2022
Impfdatum: 10.02.2022
Beginn: 10.02.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Headache Tremor

Symptomtext

1330 EMPLOYEE RECEIVED THE COVID VACCINE. EMPLOYEE SAT IN EMPLOYEE HEALTH OFFICE FOR APPROX 15 MINUTES AFTER INJECTION. EMPLOYEE RETURNED WITHIN 5 MINUTES OF LEAVING AND STATED SHE WAS SHAKING AND HAD A SEVERE HEADACHE. EMPLOYEE WAS ESCORTED OUT TO ER AND WAS SEEN BY A PROVIDER. EMPLOYEE WAS GIVEN IBUPROFEN AND DISCHARGED FROM THE ER WITH A DIAGNOSIS OF HEADACHE-UNSPECIFIED. EMPLOYEE RETURNED BACK TO WORK.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: NA
Aktuelle Erkrankungen: NA
Vorgeschichte: PHOTOPHOBIA, CONGENITAL KIDNEY DISEASE
Andere Medikamente: NO MEDICATION
Allergien: NO KNOWN ALLERGIES
Vorherige Impfungen: -

VAERS 2098669

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: CA
Alter: 49,0
Geschlecht: F
Eingang: 09.02.2022
Impfdatum: 01.10.2021
Beginn: 14.01.2022
Tage bis Beginn: 105,0
Dosis: 3
Route/Site: SYR / LA

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

Angina pectoris Arthralgia Back pain Blood test Chest X-ray Chest pain Computerised tomogram thorax Electrocardiogram Fibrin D dimer Musculoskeletal pain Pleurisy

Symptomtext

01/14/22: Severe chest and heart pain when resting and worse with breathing, back/spine pain, shoulder blade and shoulder pain. Medic visit, ekg OK. 01/14/22: Symptoms not subsiding, visit to ER. Chest Xray OK, standard blood panel OK. Diagnosed with Costocondritis. Giving NSAID and muscle relaxer and lidocaine patch. Symptoms wax and wane for days w/heart pals, irregular beats etc. 01/27/22 Severe pain returns especially when leaning. 01/28/22 sent for spine xray and D Dimer (stat); prescription for Tramadol in case of severe pain returning. 01/29/22 Called in AM by Dr to go to ER ASAP due to "very high" D Dimer. ER 2nd D Dimer also positive high, Chest X-Ray ok but atelectasis noted, CT chest scan for P/E no findings. ER Dr notes "sticky" rib, and poss "inflammation" or "autoimmune" or "pleurisy" causing symptoms. Notes unusual activity on heart monitor and gives referral to see cardiologist. Cardiologist pending for 02/14/22...

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: See Above/Same as above
Aktuelle Erkrankungen: None
Vorgeschichte: Reynaud's Disease
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: Influenza: SIRVA (all various dates years past)

VAERS 2071639

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: IL
Alter: 52,0
Geschlecht: F
Eingang: 28.01.2022
Impfdatum: 08.12.2021
Beginn: 11.12.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / -

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

Blood test normal Chest discomfort Chest pain Computerised tomogram normal Condition aggravated Rash Sensation of foreign body Swollen tongue Throat irritation Urine analysis normal Urticaria

Symptomtext

Sept 7, 2021 - Had a hive on my neck thought it was a bug bite, went away the next day. Dec. 11, 2021 - had a severe pain in my chest, tight feeling, throat lump feeling, went to ER, ran bloodwork, CT, urine, I was told I was fine. Dec. 19, 2021 - Hives, welts, rashes on various body parts, contacted the doctor ; Dec. 23, 2021. Dec. 23, 2021 - Swelling of tounge, tickle in throat, was taken to ER and give Bendryl, Predazone, Pepcid AC. Present - Continues - typically once a week have a hive or rash in various locations. Went on a low histamine diet, take Benadryl and/or Pepcid AC when needed. I have photos of each rash/hive from Sept.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: All seems to look normal according to the Doctors.
Aktuelle Erkrankungen: Unknown hives, swelling of tounge
Vorgeschichte: None
Andere Medikamente: None
Allergien: Unknown, Augmenten, Latex.
Vorherige Impfungen: -

VAERS 2054199

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: NJ
Alter: 57,0
Geschlecht: F
Eingang: 21.01.2022
Impfdatum: 01.11.2021
Beginn: 01.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Fatigue Full blood count Gingival bleeding Herpes zoster Hypoaesthesia Influenza like illness Lymphadenopathy Malaise Mobility decreased Nausea Paraesthesia Pyrexia Rash

Symptomtext

She got her vaccine, within 24 hours she started with fever, which reached about 100.3, felt ill. Then, she felt horrible body aches, like flu-like and had to crawl to the bathroom. That passed and had extreme fatigue and glands felt swollen. She felt that she was tolerating it and even a couple of weeks felt the extreme fatigue and not feeling right. Then 2 weeks after that broke out with shingles on the left femoral nerve. Was told to go to the ER, but she didn't due to active COVID patient's in the ER. This was a Friday, and by Monday the rash was severe and could not lift her leg. The Dr. called in Valtrex for the rash. Due to the pain she saw another doctor and told her to alternate Tylenol and Ibuprofen. She is 6 weeks off of the medicine and still has some residual nerve issue, can feel some of the tingling and numbness and has markings where the rash was. The worse of it took about 3-4 weeks to subside. First 10 days were horrible. Had a urinalysis done that was negative. She then after taking the medicine brushed her teeth and was bleeding. She gets the flu shot every year. After the COVID vaccines she had nausea and felt like she was going to pass out about 5-6 hours after it. Worse reactions than what she would get with the flu vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: CBC which came back normal.
Aktuelle Erkrankungen: 2 1/2 weeks prior she got her flu shot.
Vorgeschichte: PTSD.
Andere Medikamente: Multivitamin; Vitamin D; Xanax; Acid blocker (TUMS type).
Allergien: None.
Vorherige Impfungen: -

VAERS 2044261

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: RI
Alter: 92,0
Geschlecht: M
Eingang: 18.01.2022
Impfdatum: 27.10.2021
Beginn: 14.11.2021
Tage bis Beginn: 18,0
Dosis: 3
Route/Site: IM / -

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

Anticoagulant therapy Antiplatelet therapy Carotid artery stenosis Computerised tomogram normal Condition aggravated Dysarthria Hemiparesis Transient ischaemic attack

Symptomtext

He presented with garbled speech and left-sided weakness, the provider notified, and the patient was sent to ER. Hospital records indicate the patient's symptoms resolved prior to the EMS arriving; however, the patient was transported for evaluation. His presentation was consistent with a TIA. He was continued on dual antiplatelet therapy with aspirin and Plavix.2. Bilateral carotid artery stenosis was noted. The patient has a history of symptomatic carotid stenosis, hyperlipidemia, hypertension, Carotid artery syndrome, and ischemic stroke. V

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 3,0
Labordaten: CT was negative for abnormality; however, his aorta was blocked significantly. surgical intervention was recommended and scheduled. He was admitted.
Aktuelle Erkrankungen: Symptomatic Carotid Stenosis
Vorgeschichte: Stroke Obesity Essential Hypertension TIA Peripheral vertigo Type II diabetes
Andere Medikamente: -
Allergien: Simvastatin
Vorherige Impfungen: -

VAERS 2043552

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: NY
Alter: 75,0
Geschlecht: F
Eingang: 18.01.2022
Impfdatum: 25.10.2021
Beginn: 31.12.2021
Tage bis Beginn: 67,0
Dosis: UNK
Route/Site: IM / LA

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

Asthenia Blood test COVID-19 Chills Ear pain Feeding disorder Headache Hypersomnia Lethargy Nausea SARS-CoV-2 antibody test SARS-CoV-2 test negative Taste disorder Tremor Vaccine breakthrough infection

Symptomtext

1st vaccine- 1/14/2021?.. 2nd dose 2/11/2021?. Booster dose. 10/25/2021 I had a breakthrough case from December 31, 2021 thru January 6, 2022 Symptoms: severe headache first night, severe stabbing pain in right ear for four days, lethargic and weak for first three days which I slept day and night. Chills, shaking uncontrollably fir one hour- no fever. Unable to eat due to sleeping and nausea, contacted my PA on day 3 1/2 and was ordered to take, ampicillin 850mgm BID for ten days and a round of steroids for 6 days. I lost 9 pounds in the first four days. My PA sent me to a tent testing site on day 5 and came back negative- I then took a take at home rapid test which also came back negative. When I was able to eat on day 5 my taste was ?weird? ?blueberries tasted like perfume, carrot soup tasted like liquid mashed potatoes but the spice ( ginger) burned my throat and I could not taste the ginger. I had no sore throat during the whole time. It took seven days for my food to taste normal. I went to see my PA on day 12 and because of my symptoms and two negative tests she had me get an IGG titer bloodwork for COVID antibodies?? she called is less than 24 hours to tell me I had had COVID. I had my two initial vaccines and my booster and I am very strict with masks and sanitizers

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: I
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: 1c Metoprolol succ ER 25mg O.D. Magnesium oxide.500 mgm OD 1c Levothyroxine 62.5 mcg O.D. Zinc 50 mgm OD vitamin D 5,000 U Monday- Friday. Hair formula 1 cap BID ASA 81mg OD.
Allergien: -
Vorherige Impfungen: -

VAERS 2025242

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: MN
Alter: 85,0
Geschlecht: M
Eingang: 11.01.2022
Impfdatum: 11.11.2021
Beginn: 08.01.2022
Tage bis Beginn: 58,0
Dosis: 3
Route/Site: IM / LA

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

Anticoagulant therapy COVID-19 Cardiac failure Hypoxia Laboratory test Pneumonia X-ray

Symptomtext

Hospitalized on 1/8/22 for Heart Failure and COVID with hypoxia and pneumonia. TX includes O2, decadron, holding lisinopril, labs, PT/OT, lovenox

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pneumonia
Hospital-Tage: -
Labordaten: xray, labs
Aktuelle Erkrankungen: -
Vorgeschichte: Colon Cancer, COPD, HTN, HLD, Lyng Cancer, Lung Disease, Mental Health Disorder, urinary retention
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2019770

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: FL
Alter: 38,0
Geschlecht: M
Eingang: 09.01.2022
Impfdatum: 05.01.2022
Beginn: 06.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Chest pain Tachycardia

Symptomtext

Tachycardia HR in. the 140s-150s, midsternal chest discomfort

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Depression
Andere Medikamente: Wellbutrin XL 300 mg
Allergien: Lamictal
Vorherige Impfungen: -

VAERS 2010877

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: CT
Alter: 66,0
Geschlecht: M
Eingang: 06.01.2022
Impfdatum: 01.11.2021
Beginn: 24.12.2021
Tage bis Beginn: 53,0
Dosis: 3
Route/Site: IM / RA

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

COVID-19 Chest pain Cough Headache Influenza like illness Malaise Nasal congestion Pain Pyrexia SARS-CoV-2 test positive Sinus disorder

Symptomtext

Covid symptoms started on 12/24/2021 and felt like I had the flu. Symptoms were nasal congestion, coughing, body aches, and a slight fever. They lasted several days. I tested positive on 12/24/21. I started taking zpak 2 days ago. I also had chest pain, sinus issues, and a headache.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Covid
Aktuelle Erkrankungen: None
Vorgeschichte: High Blood Pressure and Type 2 Diabetes.
Andere Medikamente: High Blood Pressure and Diabetes Medications
Allergien: None
Vorherige Impfungen: -

VAERS 1998818

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: NC
Alter: 40,0
Geschlecht: F
Eingang: 03.01.2022
Impfdatum: 25.10.2021
Beginn: 03.11.2021
Tage bis Beginn: 9,0
Dosis: 1
Route/Site: SYR / LA

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

Migraine Parosmia Taste disorder

Symptomtext

At two (2) week mark, patient began experiencing daily migraine headaches. Pain became severe. Daily pain lasted approximately 2 weeks. When migraines subsided, patient noticed that smell and taste were "off". Had experienced loss of smell and taste with COVID infection but this was different. Now many foods are described as tasting like petroleum jelly. Many smells are described as burning oil. Rancid or rotten items are described as sweet smelling. Smell and taste so bad that has almost induced vomiting.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: COVID positive in September.
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 1997391

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: PA
Alter: 53,0
Geschlecht: F
Eingang: 01.01.2022
Impfdatum: 31.12.2021
Beginn: 31.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Back pain Condition aggravated Pain

Symptomtext

Body aches, especially to should and hip sockets, lower back, ankles and wrists.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Fibromyalgia, hand pain, right shoulder pain
Andere Medikamente: Valsartan, meloxicam, synthroid, pramipexole, hydrochlorothiazide, bupropion, zinc, K2 + D3, L-Lysine, calcium citrate
Allergien: Sulfa
Vorherige Impfungen: Dizziness

VAERS 1988679

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: FL
Alter: 49,0
Geschlecht: F
Eingang: 29.12.2021
Impfdatum: 03.11.2021
Beginn: 08.11.2021
Tage bis Beginn: 5,0
Dosis: 3
Route/Site: SYR / RA

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

Blood test Chest pain Electrocardiogram Inflammation Lymphadenopathy Pruritus Rash Rash macular Urticaria

Symptomtext

right after getting the booster shot my lymph node under right arms started to swell but went down after about four days. and after that I got a rash or it was itchy under my right arm and a day later I was broke out in hives. My hands and arms were very itchy. I contacted my doctor that gave me a five day course of prednisone that did help the itching but I still had big red spots all over my body, and then I started to get streaks on my sides and my whole body felt like it was inflamed. And it has now progressed to where the itching really isn't so bad but now I'm getting really strong chest pains that I even had to go the the ER for. My primary doctor also did test for thyroid issues and recommended I see an allergist that recommended I stay on antihistamines. My chest feels like it might explode.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Battery of blood test at ER, EKG, blood test for thyroid issues at primary doctor
Aktuelle Erkrankungen: None
Vorgeschichte: Herpes
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1988447

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071f21a

moderat

Staat: MO
Alter: 50,0
Geschlecht: F
Eingang: 29.12.2021
Impfdatum: 12.11.2021
Beginn: 13.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Injection site erythema Injection site pain Mobility decreased

Symptomtext

Site: Pain at Injection Site-Severe, Site: Redness at Injection Site-Medium, Systemic: patient cannot lift arm above shoulder-Severe, Systemic: Joint Pain-Severe, Additional Details: Patient visited a doctor and received a steroid pack, but still no better

Weitere VAERSDATA-Felder

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

VAERS 1984670

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: VA
Alter: 45,0
Geschlecht: F
Eingang: 28.12.2021
Impfdatum: 19.11.2021
Beginn: 19.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Asthenia Injected limb mobility decreased Pain Pain in extremity

Symptomtext

Recipient states that approximately 2 hours or less after vaccination her left arm began to hurt. As of today she states radiating pain, weakness, and inability of full use of left arm. I advised her to not receive 2nd dose of COVID vaccine and to see PCP.

Weitere VAERSDATA-Felder

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

VAERS 1963255

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: KS
Alter: 80,0
Geschlecht: M
Eingang: 20.12.2021
Impfdatum: 09.11.2021
Beginn: 14.12.2021
Tage bis Beginn: 35,0
Dosis: 3
Route/Site: IM / RA

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

Atrial fibrillation Chest pain Condition aggravated Confusional state Delusion Enterococcus test positive Hallucination Hypokalaemia Mental status changes Pseudomonas test positive Sepsis Staphylococcus test positive Troponin increased Urinary retention Urinary tract infection Wound Wound infection staphylococcal

Symptomtext

No immediate adverse events or signs/symptoms post vaccination. On 12/14/21 resident c/o chest pain and was sent to Hospital ER for further evaluation. He was subsequently admitted to hospital where he remains to trend Troponin levels after slight elevation noted. Prior to this resident began exhibiting a change in mental status with hallucinations and delusions which started around 12/08/2021. He has been on several antibiotics for COPD exacerbation, UTI, chronic abscess to coccyx bone in the time frame of 1 month prior to vaccination to current date. He was admitted to acute care at Hospital on 12/14/21 for chest pain, elevated troponin (0.06), hypokalemia, and confusion. He was started on IV antibiotics for UTI infection and deep coccyx wound. Troponin again elevated in subsequent lab collection (0.11 from 0.05). Post admission diagnoses UTI with Sepsis, Chest pain with history of coronary artery disease, Stage 3 pressure ulcer of coccyx, Congestive Heart Failure - stable. Follow-up progress notes from 12/16/21 indicate UTI treated with IV Invanz, coccyx wound treated with IV vancomycin, improvement of hallucinations/confusion, Atrial fibrillation with RVR, hypokalemia, urinary retention. Transitioned to skilled care at Hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: COPD Exacerbation, Chronic Bullous Pemphigoid, Moisture-associated skin damage to buttocks.
Vorgeschichte: Benign Prostatic Hyperplasia With Lower Urinary Tract Symptoms, Bullous Pemphigoid, Chronic Kidney Disease, Congestive Heart Failure, Coronary Artery Disease, Chronic Obstructive Pulmonary Disease, Depressive Disorder, Gastro-Esophageal Reflux Disease Without Esophagitis, Hyperlipidemia, Hypokalemia, Xerosis Cutis, Personal History Methicillin Resistant Staphylococcus Aureus Infection, Neuromuscular Dysfunction Of Bladder WOTJ Urinary Retention, Osteoarthritis, Macular Degeneration, Heart Failure, Personal History Of Urinary Tract Infection, Hallucinations - Onset 12/08/2021.
Andere Medikamente: Influenza (Seasonal) Fluzone High-Dose Quadrivalent (lot UJ765AB); Acetaminophen Tablet 650 mg by mouth every 4 hours as needed Albuterol Sulfate HFA Aerosol Solution 108 (90 Base) MCG/ACT 2 puff inhale every 1 hours as needed Aspirin 81
Allergien: Codeine, Bactrim, Latex, Tape
Vorherige Impfungen: -

VAERS 1959329

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: -
Alter: 31,0
Geschlecht: F
Eingang: 17.12.2021
Impfdatum: 05.11.2021
Beginn: 03.12.2021
Tage bis Beginn: 28,0
Dosis: 1
Route/Site: SYR / RA

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

Hypoaesthesia Insomnia Pain in extremity Paraesthesia

Symptomtext

11-5-21 I GOT MY BOOSTER SHOT IN MY ARM ON 12-3-21 I STARTED TO GET A NUMBING FEELING IN MY RIGHT HAND TO WHERE LIKEIT IS ASLEEP ITS NOT A REALLY GOOD FEELING IT HURTS AND I CANT SLEEP BARELY AT NIGHT CUZ IT WILL START TO GO NUMB THIS STARTED AFTER MY BOOSTER SHOT

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: NONE JUST GOT THE BOOSTER SHOT
Aktuelle Erkrankungen: no
Vorgeschichte: no
Andere Medikamente: no
Allergien: penicillin, coconut,cinnomon and bees
Vorherige Impfungen: -

VAERS 1959114

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: PA
Alter: 62,0
Geschlecht: M
Eingang: 17.12.2021
Impfdatum: 16.12.2021
Beginn: 17.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Paraesthesia

Symptomtext

pts wife reported pt was experiencing a "pins and needles" sensation that was moving around his neck and head

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: aldactone 25mg
Allergien: nkda
Vorherige Impfungen: -

VAERS 1959076

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: CA
Alter: 59,0
Geschlecht: M
Eingang: 17.12.2021
Impfdatum: 11.11.2021
Beginn: 01.12.2021
Tage bis Beginn: 20,0
Dosis: 3
Route/Site: IM / LA

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

Asthma Chills Condition aggravated Cough Dyspnoea Feeling abnormal Musculoskeletal chest pain Nasopharyngitis Pain Pyrexia SARS-CoV-2 test

Symptomtext

The first day, I had chills and then on the 2nd day, I started getting body aches. Then that went away in about a day or two. Then a few days later, I thought I had a fever or something like that, I just felt warm. I didn't measure temperature or anything. All I know is that I remember feeling odd. Towards the end of November, I started coughing. I started coughing continuously every day more so. The last 4 days, maybe because of the cold, the area around my rib cage is sore. I started using albuterol because of the asthma starting yesterday because I was experiencing shortness of breath when I am coughing. The coughing has almost subsided, but the pain is all around still there. Denied assistant in person at the doctor because they required a COVID test before coming because of the cough.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: None, Scheduled COVID test 12/17/2021
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1952082

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: NY
Alter: 60,0
Geschlecht: F
Eingang: 15.12.2021
Impfdatum: 02.12.2021
Beginn: 02.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Abdominal pain upper Cough Dyspnoea Fatigue Illness Malaise Myalgia Pyrexia

Symptomtext

I received my Moderna booster shot on Thursday, Dec 2 2021. I started to feel ill by 11:00 pm that evening. I was pretty sick with symptoms (low-grade fever, muscle aches, fatigue, stomach pain) that lasted throughout Friday and Saturday. Saturday morning, I experienced a new symptom; I had trouble breathing where I could not process oxygen. At one point, my oxygen level was an 86. I experienced this breathing issue for about an hour. On Sunday I no longer had fever nor fatigue, but around 4pm started coughing. I still have an intermittent cough as of today Dec 15 but every day, I cough less. I felt perfectly fine prior to receiving the booster. My symptoms were similar to what I had experienced with receiving the first 2 vaccines except the breathing issue processing oxygen. I was taking deep breaths to try and compensate for the fact I could not process oxygen well. This was alarming hence why I am filling out this form.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: N/A.
Aktuelle Erkrankungen: None
Vorgeschichte: Dysautonomia
Andere Medikamente: Synthroid; Metoprolol; Multivitamin; Vitamin D; Vitamin B12; Biotin
Allergien: Erythromycin
Vorherige Impfungen: Already noted previously on this form.

VAERS 1952038

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: NC
Alter: 38,0
Geschlecht: F
Eingang: 15.12.2021
Impfdatum: 06.11.2021
Beginn: 08.11.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: SYR / LA

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

Blood test Dyspnoea Echocardiogram Electrocardiogram Electrocardiogram ambulatory Exercise tolerance decreased Tachycardia

Symptomtext

Tachycardia since 11/8/2021 and feeling winded with any physical movement. Unable to exercise after 1 month.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: PCP visit with blood workup and EKG on 11/12/2021 Cardiologist visit with ECHO, holter monitor, and blood workup. On 11/17/2021 and 11/18/2021
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Allergic to diflucan
Vorherige Impfungen: -

VAERS 1948196

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: MN
Alter: 43,0
Geschlecht: F
Eingang: 14.12.2021
Impfdatum: 02.11.2021
Beginn: 26.11.2021
Tage bis Beginn: 24,0
Dosis: UNK
Route/Site: - / LA

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

Ageusia Anosmia Condition aggravated Ear pain Fatigue Glossodynia Lymphadenopathy Nasal congestion Odynophagia Pain in jaw Sialoadenitis

Symptomtext

About 2.5 weeks after receiving the booster shot while (unknowingly) simultaneously having COVID, I has about 2 days of stuffy sinuses and experiencing intermittent severe pain when swallowing, ear, jaw and tongue hurting on right side, with a swollen gland. On 12/3 this pain became constant, I went to see an ENT doctor on 12/6 who diagnosed with sialadenitis (infected salivary gland) on my right side. I was treated with a course of metylPREDNISolone 4 mg tablets (started 12/7, finished 12/12) and Clindamycin HC 300 mg capsule, of which I took 12 of 21 doses before discontinuing per my ENT doctor's instruction because of GI upset (started evening of 12/6, last dose mid-day 12/10). The symptoms of my sialadenitis (severe pain when swallowing, ear, jaw and tongue hurting on right side, swollen gland) are completely gone.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: I had a mild case of COVID (did not realize it was COVID, felt like my typical stuffy nose from allergies that had started 10.30.2021) when I received my booster shot. I had checked with pharmacy and they said since I didn't have a fever I could come in and get booster. The next two days after booster (11.3 and 11.4) my head stuffiness was worse, felt fatigued, but also wasn't sure if simply side effects from booster and I was otherwise staying home. At the end of week (Friday, 11.5.2021) I lost my taste and smell, took a rapid antigen COVID test that came back positive.
Vorgeschichte: exercise and cold-induced asthma
Andere Medikamente: multi-vitamins with minerals tablet (aka Women's One-A-Day), cholecalciferol 2,000 unit tablet (aka Vitamin D), Vitamin C, lactobacillus combination no. 4.3 billion cell cap (aka probiotic), Omega-3-DHA-EPA-Fish Oil 1,200 mg, ipratropium 4
Allergien: Amoxicillin-Pot Clavulanate, soy, lactose intolerance,
Vorherige Impfungen: -

VAERS 1944551

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: VA
Alter: 61,0
Geschlecht: F
Eingang: 13.12.2021
Impfdatum: 26.10.2021
Beginn: 27.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Blood cholesterol Blood glucose Blood thyroid stimulating hormone decreased Fatigue Glycosylated haemoglobin Injected limb mobility decreased Malaise Migraine Pain Pyrexia

Symptomtext

10/27/2021 the very next day, I woke up feeling really, sick. My left arm- I could not lift it up. I could not get my shirt on and off. I had a little bit of a migraine. I took the Ubrelvy to stop it from getting worse. I only take that on a as needed bases. My temperature was 100.2 very low-grade fever for most of the day. I drank lots of water and ate a plant-based breakfast, oatmeal, and took it easy and tele-worked. The next day,10/28/2021, my temperature came down to 99.8 in the morning and then went back to normal. My arm was not as sore. I was able to lift my shirt on and off. When I woke up on 10/28/2021I could tell I felt a little bit better, but I kept having the extreme exhaustion. and fatigue. and just a little bit of the aches, but not as bad as 10/27/2021. On 11/23/2021- I went to get my physical and to tell my NP, I was having extreme exhaustion and fatigue since I had the vaccination. I also told her that I was having blood vessels rupturing and bursting on my arms and on my legs. The blood vessels in my arms and legs started bursting since after the 1st Dose and Dose2 of Moderna. I started to have more of the blood vessels bursting on both my arms and legs after the 3rd dose of the Moderna. The blood test showed my thyroid was going toward hyperthyroid. I have always had hypothyroid, Hashimoto for 13 or 14 years, since 2009. I have not recovered from the AEs. I still have extreme exhaustion and fatigue and I am still having my blood vessels bursting.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: 11/23/2021 fasting blood test - everything came back normal Blood count, Thyroid went up 1.0, Cholesterol, A-1C Glucose, Physical The blood test showed my thyroid was going toward hyperthyroid. I have always had hypothyroid, Hashimoto for 13 or 14 years, since 2009. The doctor changed the dosage of Synthroid, (the generic) from 50 mcg to 25 mcg.
Aktuelle Erkrankungen: I was very healthy 10/25/2021 and 10/26/2021
Vorgeschichte: History of chronic migraine and migraine with aura Gastritis GERD Hypothyroid - Hashimoto I was taking Synthroid .05 mcg they changed it on 11/23/2021
Andere Medikamente: Wixela Advair for Asthma; Nexium 24 hour; Carafate; Citricale Calcium J; Atorvastatin 20mg; Singulair 10mg; Carafate at bedtime; Protonix 40 mg at bedtime; Wixela Advair for asthma one puff before bedtime. Fall 2019, I started taking migrai
Allergien: Erythromycin; Iodine contrast - Anaphylactic
Vorherige Impfungen: -

VAERS 1933320

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: MD
Alter: 48,0
Geschlecht: F
Eingang: 08.12.2021
Impfdatum: 06.11.2021
Beginn: 16.11.2021
Tage bis Beginn: 10,0
Dosis: 3
Route/Site: IM / LA

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

Blood test normal Cardiac stress test normal Chest X-ray normal Computerised tomogram abdomen normal Computerised tomogram thorax normal Cough Dyspnoea Electrocardiogram normal Fibrin D dimer increased Lung disorder Pulmonary function test decreased Urticaria

Symptomtext

On November 16, 2021 at 6:00 a.m., I broke out in full blown hives all over my body. I took a Benadryl and then Allegra. I have had continued hives, shortness of breath ( with a lung function of 44 % in the small bronchioles), and coughing. I have had two separate emergency room visits on November 19 and on November 30th. I saw my internist on November 24th and she prescribed Allegra, Protonix, Pepcid AC, and Albuterol inhaler. I saw a pulmonologist on December 2nd who prescribed a short term course of prednisone ( 40 mg daily for 5 days) and the Duo Inhaler. I saw an allergist on December 8th who had switched my DUO inhaler to the QVAR inhaler. No one seems to know what is causing my reaction. I saw my internist, Dr. for my regular physical on November 12th-I had no breathing problems, hives, coughing at that visit. I was fine before November 16th and only took Synthroid and a multivamin. My world changed on November 16 th and is unexplained to everyone that I have seen. Folks are only treating my symptoms, but I am discouraged with my shortness of breath on lung exhalation. Have other folks had a reaction to the Moderna Booster? I am currently taking Protonix, Allegra, Albuterol inhaler, Qvar inhaler and Pepcid AC whereby I formerly have not had any breathing issues. Please help!

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 1,0
Labordaten: Normal chest x-rays- 2, Normal CT scans of Abdomen and lungs, normal EKG, normal stress test. High d-dimer test.Normal bloodwork. I have bloodwork from two different ER visits.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Synthroid 175 mcg. and a multivitamin
Allergien: Bee sting Possible Lexapro allergy
Vorherige Impfungen: -

VAERS 1932687

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: OH
Alter: 25,0
Geschlecht: F
Eingang: 08.12.2021
Impfdatum: 16.11.2021
Beginn: 18.11.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

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

Blood magnesium Blood thyroid stimulating hormone Chest X-ray Dyspnoea exertional Echocardiogram Electrocardiogram Electrocardiogram ambulatory Full blood count Laboratory test Metabolic function test Palpitations Tachycardia Troponin

Symptomtext

Palpitations and tachycardia at rest, dyspnea on minimal exertion. No specific treatment. Improving on own

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea exertional
Hospital-Tage: -
Labordaten: 11/28 - EKG, CXR, labs (CBC, CMP, Troponin X 2, BNP, D-dimer) 12/01 - EKG, labs (Mag, TSH, CMP) 12/08 - Echo, Holter monitor
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Birth control
Allergien: -
Vorherige Impfungen: -

VAERS 1927877

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: MO
Alter: 48,0
Geschlecht: F
Eingang: 07.12.2021
Impfdatum: 06.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 11,0
Dosis: 3
Route/Site: OT / -

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

Hypertension Urticaria

Symptomtext

Patient has high blood pressure because of the hives; Patient broke up in bad hives; This spontaneous case was reported by a consumer and describes the occurrence of URTICARIA (Patient broke up in bad hives) and HYPERTENSION (Patient has high blood pressure because of the hives) in a 48-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 071F21A) for COVID-19 vaccination. Concomitant products included LEVOTHYROXINE for an unknown indication. On 06-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 17-Nov-2021, the patient experienced URTICARIA (Patient broke up in bad hives). On an unknown date, the patient experienced HYPERTENSION (Patient has high blood pressure because of the hives). The patient was treated with CETIRIZINE HYDROCHLORIDE (ZYRTEC [CETIRIZINE HYDROCHLORIDE]) at an unspecified dose and frequency; PREDNISONE at an unspecified dose and frequency and PEPSIN at an unspecified dose and frequency. At the time of the report, URTICARIA (Patient broke up in bad hives) and HYPERTENSION (Patient has high blood pressure because of the hives) outcome was unknown. concomitant medication included levothyroxine used for thyroids

Weitere VAERSDATA-Felder

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

VAERS 1913173

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: MI
Alter: 63,0
Geschlecht: M
Eingang: 01.12.2021
Impfdatum: 05.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Paraesthesia

Symptomtext

Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)-

Weitere VAERSDATA-Felder

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

VAERS 1909516

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: MA
Alter: 38,0
Geschlecht: F
Eingang: 30.11.2021
Impfdatum: 29.10.2021
Beginn: 01.11.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: IM / LA

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

Condition aggravated Dyspepsia

Symptomtext

Following the Moderna booster shot (I received the Johnson & Johnson vaccine on 4/11/21), I began to experience severe heartburn during and after strenuous exercise. The symptoms have persisted after I made dietary adjustments and took a 2-week course of over-the-counter omeprazole. Typically I might experience heartburn once a month or every other month, but never this often and never this severe.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: I have an appointment on 12/20/21 during which I will discuss the symptoms with my doctor.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: CBD as a sleep aid
Allergien: None
Vorherige Impfungen: -

VAERS 1905863

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: GA
Alter: 58,0
Geschlecht: F
Eingang: 29.11.2021
Impfdatum: 18.11.2021
Beginn: 18.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Feeling abnormal Lip swelling Paraesthesia oral

Symptomtext

Approximately 5 minutes after vaccine patient stated she was "feeling weird". She then began to say her lips were "tingling". At this time 50 of diphenhydramine was given to the patient. Minor swelling was noted to her upper lip. Patient was taken to the ED for monitoring.

Weitere VAERSDATA-Felder

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

VAERS 1897401

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: NC
Alter: 63,0
Geschlecht: F
Eingang: 24.11.2021
Impfdatum: 12.11.2021
Beginn: 12.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Asthenia Dizziness Dyspnoea Headache Pain

Symptomtext

Systemic: Allergic: Difficulty Breathing-Mild, Systemic: Body Aches Generalized-Mild, Systemic: Dizziness / Lightheadness-Medium, Systemic: Headache-Severe, Systemic: Weakness-Mild

Weitere VAERSDATA-Felder

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

VAERS 1890640

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: FL
Alter: 48,0
Geschlecht: F
Eingang: 22.11.2021
Impfdatum: 08.11.2021
Beginn: 08.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

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

Chills Feeling hot Headache Injection site bruising Pain Paraesthesia Pyrexia Sleep disorder Urticaria

Symptomtext

Started with low fever/body ache/and slight HA evening of shot (9pm), went to bed. Woke up with fever/chills took Tylenol approx 12 am and went back to bed. Woke up off and on with HA worsening, but by 8 am I took Topirimate (regular med I take for migraines), pantoprozole, and another Tylenol and went back to bed. Woke up with full on Migraine and tried to tuff it out. Around noon had to take an Ubrelvy (abortive migraine medicine). I noticed around the same time that the left side of my face was hot and itchy. I asked my husband if I had hives on my face and he said yes. I got up and looked and I did have raised welts along my left cheek, chin, and throat area. About an hour later I ended up taking a benedryl because it was getting worse. That made me sleepy so I went back to bed. Later I woke up and my migraine was not as severe. I took another benedryl and Tylenol and went back to bed. By Wednesday morning the hives were down to two smaller (approx some sized welts) still on my left chin/cheek area. My migraine was gone and I just had a lingering HA /body aches, and alternating fever and chills throughout the day. I noticed Wednesday that my injection site had a huge bruise (half dollar sized) over the area. That bruise is still lingering after 2 weeks. It has been very prominent on my arm, and has been shocking to see. I have picks of the hives from Wednesday morning and various shots of my bruise over the past two weeks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: No tests performed as I did not go to urgent care. I work with physicians and am friends with physicians who saw my hives. Since they were responding to benedryl I did not go to urgent care. I regret not going, as they were not formally documented. I have pics to verify, and a physician willing to make a statement if needed to document.
Aktuelle Erkrankungen: IBS, migraines, reflux, multiple joint arthritis
Vorgeschichte: Same as above
Andere Medikamente: Nothing that morning
Allergien: Sentra/sulfa (anaphylaxis), erythromycin, various insect venom (anaphylaxis), various cosmetics (swelling), pet dander, seasonal allergies
Vorherige Impfungen: Seasonal Flu shot(approx 1997 or 1998) 24 or 25 years old ?, had hives/urticaria all over body, treated with steroids and allerg

VAERS 1888351

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: MO
Alter: 91,0
Geschlecht: M
Eingang: 20.11.2021
Impfdatum: 16.11.2021
Beginn: 20.11.2021
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: IM / LA

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

Injected limb mobility decreased Injection site bruising Injection site discomfort Injection site erythema Injection site oedema Injection site swelling Injection site warmth Pain

Symptomtext

Upon assessment the deltoid region (approx size of an orange in diameter) is with edema, erythema, and is feverish to touch. There is a small dime size bruise in the center of the erythema and Veteran reports slight left upper extremity discomfort with ROM. Cool compress applied, PRN medication management as ordered

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: Prilosec, omeprazole, Tamiflu
Vorherige Impfungen: -

VAERS 1886101

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071f21A

moderat

Staat: MI
Alter: 36,0
Geschlecht: M
Eingang: 19.11.2021
Impfdatum: 04.11.2021
Beginn: 19.11.2021
Tage bis Beginn: 15,0
Dosis: 3
Route/Site: IM / LA

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

Chills Condition aggravated Extra dose administered Headache Hyperhidrosis Interchange of vaccine products Joint contracture Lymph node palpable Lymphadenopathy Muscle rigidity Nausea Pyrexia Sleep disorder

Symptomtext

I started to have fever and chills about 6-7 hours after receiving the Moderna booster. I went to sleep in the evening and woke in the middle of the night with severe chills, sweating, headache, nausea, and a feeling of rigidity in the muscles of my forearms and wrists, with involuntary contraction of my hands. I wasn't in a condition to check my temperature with a thermometer. I took two aspirin, drank some cold water, and the chills improved and the muscle rigidity and hand contraction went away. I continued to have chills, headache and nausea return every 4-6 hours, into the next day, which I alleviated with 1-2 aspirin during each interval. By the next afternoon, about a day after receiving the booster, I was feeling subjectively much better and measured my temperature with an oral thermometer: it was 102 Fahrenheit. Two days subsequently, I noticed a palpable left axillary lymph node, which persisted for another 2-3 days. Altogether, these symptoms were similar but to a worse degree than what I experienced after the second dose of the Pfizer vaccine nine months earlier. However, the fever seemed higher and came on faster; the muscle rigidity/hand contraction, and axillary lymphadenopathy were new symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1881153

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21a

moderat

Staat: OK
Alter: 31,0
Geschlecht: F
Eingang: 18.11.2021
Impfdatum: 10.11.2021
Beginn: 11.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Eye movement disorder Eye pain Headache Migraine Myalgia Nausea Pain Photophobia Pyrexia

Symptomtext

Overwhelming body aches and muscle pain, migraine, fever, nausea. Awoke exactly 12 hours after administration with symptoms. Symptoms made it difficult to move or open eyes due to light sensitivity and pain. Eventually took ibuprofen which helped alleviate headache. Symptoms abated after 24 hours

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Daily standard adult multivitamin
Allergien: Sulfa drugs
Vorherige Impfungen: -

VAERS 1870234

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: VA
Alter: 70,0
Geschlecht: F
Eingang: 15.11.2021
Impfdatum: 29.10.2021
Beginn: 01.11.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: SYR / LA

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

Arthralgia Chest pain Laboratory test Myalgia Pain

Symptomtext

I have been having since I got my second shot, back in March, body aches and joint aches/muscle pain. I thought I just needed to exercise more. I got the booster shot and 4-5 days later, I got chest pains - brief in duration - 2 to 3 minutes. They would go away and come back anytime during the day. It didn't wake me up at night. I went to the doctor on the 11th of November for all of these symptoms and she ordered lab work and I got that done on the same day. No treatment yet. I haven't had any in several days (chest pains). I had the flu shot after this vaccine on the following Friday. I had that on the 5th of November. I had it had Pharmacy injection in right arm.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Waiting for results of lab work - I'm waiting to talk to her Tuesday or Wednesday.
Aktuelle Erkrankungen: No
Vorgeschichte: Low back pain Eczema
Andere Medikamente: Verapamil SR 120mg once a da Potassium Chloride - 20mg a day HCTZ - 25mg once a day Levothyroxine - 112mcg once a day Omeprazole 20mg once a day Gabapentin 100mg once a day at night OTC Vit D3 - 100mcg
Allergien: Contact Dermatitis - something in my flower bed but don't know what - I get blisters and stuff like that Hives but don't know what it is EKG leaves - when they do the sticky things on it - if they are there longer then a quick rhythm strip then I'll break out on a rash wherever they are Cephalexin
Vorherige Impfungen: -

VAERS 1869731

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: AZ
Alter: 47,0
Geschlecht: M
Eingang: 15.11.2021
Impfdatum: 02.11.2021
Beginn: 02.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Arthralgia Blood pressure increased Chest X-ray Computerised tomogram head normal Condition aggravated Feeling abnormal Headache Heart rate abnormal Ocular discomfort Pyrexia

Symptomtext

When I received the injection within 10 second felt increased pressure behind my left eye. From me taking blood pressure medication I kind of knew that wasn't a good sign. When I got home, I got home checked my BP it was 155/90. I checked my BP the next morning it was 148/87 and had pounding headache, aching joints, and fever. I went to the ER my vitals were taking hours later 136/85 resting heart rate 122 which is around 80,85). They took my vitals one more time in the waiting room it was about the same. When I got to the room, I received saline drops and they continued to monitor me. Since the ER I have continued to monitor my BP, it has increased which isn't normal. On 11/14/2021 my BP 148/85 108 beats per mins and on 11/15/2021 BP 135/77 with 75 beats per min. I'm following up with my doctor to help lower my blood pressure very concerned I might have a stroke or some issue. I have not felt quite right since the vaccine struggling with my BP and heart rate.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 1,0
Labordaten: CT Scan of brain rule out canal bleeds Chest X-ray
Aktuelle Erkrankungen: No
Vorgeschichte: Diabetes Blood pressure under control since 2016 or 2017
Andere Medikamente: Metformin Losartan
Allergien: No
Vorherige Impfungen: -

VAERS 1869643

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071f21A

moderat

Staat: TN
Alter: 45,0
Geschlecht: F
Eingang: 15.11.2021
Impfdatum: 12.11.2021
Beginn: 13.11.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Abdominal pain Migraine Nausea Vomiting

Symptomtext

Systemic: Abdominal Pain-Medium, Systemic: Headache-Severe, Systemic: Nausea-Medium, Systemic: Vomiting-Severe, Additional Details: started vomiting and having non stop migraine when she woke up saturday after getting shot sunday, vomits any time she takes medicine, has had continuous headache, no relief with tylenol/ibuprofen/or sumatriptan

Weitere VAERSDATA-Felder

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

VAERS 1868128

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: WI
Alter: 57,0
Geschlecht: F
Eingang: 14.11.2021
Impfdatum: 13.11.2021
Beginn: 13.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Feeling abnormal Feeling drunk Hypertension

Symptomtext

Systemic: Hypertension-Mild, Additional Details: Pt reported feeling "weird, almost like drunk" within 15 min after immunization (pt had both flu shot and moderna booster). Measured BP and HR twice with a ~10 min-interval and HR was normal but BP reading was in the 170s/100s range both times. Pt felt good enough to go to car with family to see MD. Called pt after a couple of hours to check up on her. Pt went to see MD and was released to home. BP was ~140/90 in the office and was going down. Pt stated that she felt fine now. Pt will follow up.

Weitere VAERSDATA-Felder

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

VAERS 1864944

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: MI
Alter: 94,0
Geschlecht: F
Eingang: 12.11.2021
Impfdatum: 30.10.2021
Beginn: 31.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Chills Dyspnoea Injection site pain Injection site swelling Injection site warmth Pyrexia

Symptomtext

Slight swelling, tenderness, and warmth at injection site. Chills. Slight fever. Breathing issues

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Checked vital signs - vital signs all good. Given nebulizer treatment. Breathing improved.
Aktuelle Erkrankungen: -
Vorgeschichte: Acute breathing issues
Andere Medikamente: Ipratrotium Bromide, Albuterol, Synthroide 88mcg , Plavix 75mg, Losartan 25mg, Lasix 40 mg, Bayer aspirin 81mg, Metoprolol 25 mg, Potassium Cloride 10mg
Allergien: -
Vorherige Impfungen: -

VAERS 1861820

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: VA
Alter: 78,0
Geschlecht: F
Eingang: 11.11.2021
Impfdatum: 11.11.2021
Beginn: 11.11.2021
Tage bis Beginn: 0,0
Dosis: 7+
Route/Site: IM / LA

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

Paraesthesia Throat tightness

Symptomtext

Patient complained of tingling of the ears and throat tightness

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: None taken
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Unknown
Andere Medikamente: Unknown
Allergien: None listed
Vorherige Impfungen: -

VAERS 1860528

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: WI
Alter: 24,0
Geschlecht: F
Eingang: 11.11.2021
Impfdatum: 10.11.2021
Beginn: 10.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Paraesthesia

Symptomtext

Systemic: Tingling (specify: facial area, extemities)-Mild, Additional Details: 15 minutes after immunization, patient reported that she had tingling on the arm and in the fingers after injection. Pt said the tingling got better. I let pt know that it could be temporary due to nerve irratation, which should go away in a couple of days; however, it could also be nerve damage that may last longer and have a more severe impact. Pt will watch out closely for a few days and contact doctor if it gets worse or does not go away after 2-3 days. I will follow up 11/11 and/or 11/12.

Weitere VAERSDATA-Felder

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

VAERS 1860148

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: CT
Alter: 57,0
Geschlecht: F
Eingang: 11.11.2021
Impfdatum: 27.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: OT / -

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

Anxiety Blood pressure measurement Blood test Chills Hypertension Nausea Pain Pyrexia Tremor Vaccination complication Vomiting

Symptomtext

Blood pressure went incredibly high 208/108; Shaking uncontrollably; Aches; Extremely high anxiety; Emergency said it was probably side effects from the vaccine; Fever; Chills; Nausea; Vomiting; This spontaneous case was reported by a consumer and describes the occurrence of HYPERTENSION (Blood pressure went incredibly high 208/108) in a 57-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 071F21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 27-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 28-Oct-2021, the patient experienced HYPERTENSION (Blood pressure went incredibly high 208/108) (seriousness criterion medically significant), TREMOR (Shaking uncontrollably), PAIN (Aches), ANXIETY (Extremely high anxiety), VACCINATION COMPLICATION (Emergency said it was probably side effects from the vaccine), PYREXIA (Fever), CHILLS (Chills), NAUSEA (Nausea) and VOMITING (Vomiting). At the time of the report, HYPERTENSION (Blood pressure went incredibly high 208/108), TREMOR (Shaking uncontrollably), PAIN (Aches), ANXIETY (Extremely high anxiety), VACCINATION COMPLICATION (Emergency said it was probably side effects from the vaccine), PYREXIA (Fever), CHILLS (Chills), NAUSEA (Nausea) and VOMITING (Vomiting) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 28-Oct-2021, Blood pressure measurement: 208/108 (High) Blood pressure 208/108 incredibly high.. On 28-Oct-2021, Blood test: normal (normal) blood test normal.. Concomitant product was not provided by the reporter. Treatment information was not provided. Company comment: This case concerns a 57-year-old, female patient with no previous relevant medical history reported, who experienced the unexpected event of hypertension. The event occurred 1 day after the third dose of mRNA-1273 Moderna vaccine. The rechallenge was not applicable since the event happened after the third dose. The benefit-risk relationship of mRNA-1273 Moderna vaccine is not affected by this report.; Sender's Comments: This case concerns a 57-year-old, female patient with no previous relevant medical history reported, who experienced the unexpected event of hypertension. The event occurred 1 day after the third dose of mRNA-1273 Moderna vaccine. The rechallenge was not applicable since the event happened after the third dose. The benefit-risk relationship of mRNA-1273 Moderna vaccine is not affected by this report.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: Test Date: 20211028; Test Name: Blood Pressure; Result Unstructured Data: Blood pressure 208/108 incredibly high.; Test Date: 20211028; Test Name: Blood test; Result Unstructured Data: blood test normal.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1858327

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071f21A

moderat

Staat: CA
Alter: 88,0
Geschlecht: F
Eingang: 10.11.2021
Impfdatum: 29.10.2021
Beginn: 05.11.2021
Tage bis Beginn: 7,0
Dosis: UNK
Route/Site: SYR / LA

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

Bed rest Condition aggravated Ear discomfort Fatigue Headache Meniere's disease Nasal congestion Pain Tinnitus

Symptomtext

That evening I began having a bad headache and body aches. Was exhausted needed bed rest for 2 days. Felt better, then one week later began getting a headache and nasal congestion - then next morning my ears were affected - Pressure and headache, sounds of a million bees buzzing. The Moderna booster shot had affected my under control Menieres disease. Felt like I had a bad cold but pressure on ears did not cease. Began taking cold medication for relief another 2 days in bed and slowly the sounds are less and the pressure is now only on my right ear.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: Nothing
Vorgeschichte: A form of Menieres disease over 20 years, under control until about 7 days later when I began having the headaches that I had the first weekend following the booster shot. That night it affected my ears - with the sounds of a million bees humming and pressurel- Had to stay in bed for a couple days. It is very slowly getting better.
Andere Medikamente: Tirosint, Hyzaar, Klor-Con , Spironolactone, Eliquis, Metoprolol. Atorvastatin, Fluticasone nasal spray, Tylenol, Vitamin E
Allergien: Steroids, Pennecillin
Vorherige Impfungen: -

VAERS 1847413

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21a

moderat

Staat: CA
Alter: 28,0
Geschlecht: M
Eingang: 05.11.2021
Impfdatum: 02.11.2021
Beginn: 02.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Chest pain Chills Dyspnoea Headache Heart rate irregular Immediate post-injection reaction Insomnia Pyrexia

Symptomtext

Vaccine was administered at 1430 Headache was noticed immediately. I kept myself hydrated with water. At 1830, I started getting chest pains and shortness of breath. I put on a pulse ox, sat still for five minutes and my pulse was fluctuating after that. It was irregular for hours. To treat sob, I used my inhaler and kept my head elevated. I couldn?t sleep at night. Around 100 on 11/3/2021, I started experiencing a mild fever and chills. I wasn?t able to sleep so I treated myself with Theraflu. Fever and chills went away by 11/3. Today (11/5/2021), I was still experiencing chest pains.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Asthma
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1846715

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: FL
Alter: 71,0
Geschlecht: M
Eingang: 05.11.2021
Impfdatum: 29.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Injury Joint injury Paraesthesia Product administration error

Symptomtext

Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)-

Weitere VAERSDATA-Felder

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

VAERS 1846081

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21a

moderat

Staat: AZ
Alter: 70,0
Geschlecht: F
Eingang: 05.11.2021
Impfdatum: 04.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Chills Ear discomfort Extra dose administered Headache Heart rate increased Pain Pain in extremity Pyrexia Tremor

Symptomtext

101 Fever with chills and shakes, heart rate around 100bpm, body and head ache, pain down whole left arm, Bruit in left ear.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Bisoprolol Fumirate, Crestor, Xanax
Allergien: Penicillin, Wheat
Vorherige Impfungen: Moderna, 2/2021, 3/2021 age 69 Same symptoms

VAERS 1843171

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: OH
Alter: 71,0
Geschlecht: F
Eingang: 04.11.2021
Impfdatum: 04.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / RA

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

Extra dose administered Hypoaesthesia Pain in extremity Paraesthesia

Symptomtext

patient report that after 5 mins after getting the shot she started to have pain and tingling in her right arm down to fingers...stayed at the pharmacy an additional 5 mins and was told to move arm around...slight numbness at her temple going down to cheek bones...

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: no
Aktuelle Erkrankungen: no
Vorgeschichte: no
Andere Medikamente: no
Allergien: percincix
Vorherige Impfungen: H1N1 vaccine back in Jan 2010

VAERS 1842660

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071f21a

moderat

Staat: CA
Alter: 48,0
Geschlecht: M
Eingang: 04.11.2021
Impfdatum: 01.11.2021
Beginn: 02.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / AR

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

Arthralgia Injected limb mobility decreased Injection site pain

Symptomtext

Site: Pain at Injection Site-Severe, Systemic: Joint Pain-Severe, Additional Details: patient called to report that he is having pain in his arm that got the covid shot and is having difficult lifting and moving it. patient claims the shot was given too high into the joint and states he has pictures. patient said he will be going to the doctor tomorrow to get checked out

Weitere VAERSDATA-Felder

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

VAERS 1837122

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: NJ
Alter: 24,0
Geschlecht: F
Eingang: 02.11.2021
Impfdatum: 02.11.2021
Beginn: 02.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Dizziness Hypertension Nausea Tachycardia Tremor Visual impairment

Symptomtext

AFTER WAITING 15MIN, PATIENT WAS ABOUT TO LEAVE THEM EXPIERENCED NAUSEA/DIZZINESS ALONG WITH SEEING DARK SPOTS. PT WAS ALSO TACHYCARDIC WITH HIGH BLOOD PRESSURE. 911 WAS CALLED AS PT BEGAN TO SHAKE. PARAMEDICS CAME AND PT WENT TO HOSPITAL. PT DID NOT LOSE CONSCIOUSNESS OR HAVE DIFFICULTY BBREATHING.

Weitere VAERSDATA-Felder

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

VAERS 1836770

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071f21a

moderat

Staat: NY
Alter: 55,0
Geschlecht: F
Eingang: 02.11.2021
Impfdatum: 01.11.2021
Beginn: 02.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: - / LA

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

Dizziness Dyspnoea Limb discomfort Nausea Vomiting

Symptomtext

dizziness, nausea, shortness of breath, vomiting, arm heavy

Weitere VAERSDATA-Felder

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

VAERS 1833283

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071f21a

moderat

Staat: OH
Alter: 28,0
Geschlecht: F
Eingang: 01.11.2021
Impfdatum: 29.10.2021
Beginn: 30.10.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / RA

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

Chest discomfort Dyspnoea Injection site pain Pain in extremity Palpitations

Symptomtext

Site: Pain at Injection Site-Medium, Additional Details: Pt is complaining of a sore arm, racing heart, chest tightness and some shortness of breath. Was vaccinated 3 days ago; I didn't ask when the symptoms started. I did advise her to call her MD. I will call her on my next day to work to see if she was seen. I assume they will want to and that is the option I selected.

Weitere VAERSDATA-Felder

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

VAERS 1832960

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: CT
Alter: 66,0
Geschlecht: F
Eingang: 01.11.2021
Impfdatum: 30.10.2021
Beginn: 30.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Headache Heart rate increased Immediate post-injection reaction Malaise Pain Palpitations

Symptomtext

Immediately after the shot I felt light headed and my pulse quickened considerably. A nurse took my blood pressure which was normal but said my pulse was over 80 which is high for me (usually 62). Later that night I started to not feel well. During the night my heart and pulse were racing, I had a headache and my body felt like I fell down a flight of stairs. This continued all day the day following the vaccine. Today, Nov. 1 I have recovered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Resedronate, Vitamin D
Allergien: None
Vorherige Impfungen: -

VAERS 1831706

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: VA
Alter: 53,0
Geschlecht: F
Eingang: 30.10.2021
Impfdatum: 29.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Chest X-ray Dyspnoea Electrocardiogram Hypertension Neck pain

Symptomtext

Pain in neck and side, difficulty breathing, and high blood pressure

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: ECG and chest X-ray
Aktuelle Erkrankungen: -
Vorgeschichte: High blood pressure, high cholesterol, reflux, arthritis
Andere Medikamente: Losartan, Prevacid, Atoravastatin, hormone replacement, Montelukast, Zyrtec, probiotic, stool softener, fiber gummy
Allergien: Amoxicillin
Vorherige Impfungen: -

VAERS 1831682

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071f21a

moderat

Staat: FL
Alter: 29,0
Geschlecht: M
Eingang: 30.10.2021
Impfdatum: 30.10.2021
Beginn: 30.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Dizziness Fatigue Flushing Hyperhidrosis Hypersensitivity Hypertension Immediate post-injection reaction Injection site swelling Lethargy Nausea Tremor Vomiting

Symptomtext

Site: Swelling at Injection Site-Mild, Systemic: Dizziness / Lightheadness-Medium, Systemic: Exhaustion / Lethargy-Medium, Systemic: Flushed / Sweating-Mild, Systemic: Hypertension-Medium, Systemic: Nausea-Severe, Systemic: Shakiness-Medium, Systemic: Vomiting-Severe, Additional Details: immediatley after recieving first dose, patient beganing showing signs of allergic reaction. Patient began vomiting and feeling nauseaus immediately after.

Weitere VAERSDATA-Felder

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

VAERS 1831559

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: MI
Alter: 45,0
Geschlecht: F
Eingang: 30.10.2021
Impfdatum: 26.10.2021
Beginn: 26.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Fatigue Impaired work ability Injected limb mobility decreased Injection site erythema Injection site induration Injection site pain Injection site swelling Injection site warmth Mobility decreased Pain Sleep disorder

Symptomtext

Light-headed, tiredness, impaired work ability, mobility decreased, injected limb mobility decreased, pain upon movement, sleep disturbed, Injection site pain, redness, swelling, induration and warmth.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Asthma, Depression, Anxiety, Bursitis and arthritis in both hips
Andere Medikamente: Inhalers, Claritin, Nasal spray, SAME, Pepcid
Allergien: Animal dander, Seasonal, Environmental
Vorherige Impfungen: Influenza like illness, Injection site pain, bruising, swelling, redness, induration

VAERS 1829455

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: SC
Alter: 56,0
Geschlecht: F
Eingang: 29.10.2021
Impfdatum: 23.10.2021
Beginn: 23.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Blood magnesium normal Blood thyroid stimulating hormone Electrocardiogram Electrocardiogram abnormal Fibrin D dimer increased Full blood count normal Heart rate decreased Immediate post-injection reaction Metabolic function test Pain in extremity Palpitations Troponin Ventricular extrasystoles

Symptomtext

On the day of my third (booster) Moderna shot, my arm began hurting almost immediately after the injection, which was of no concern, as this happened with the first two doses. About three hours later, I noticed heart palpitations, which are abnormal for me. I lay down to rest, then the palpitations began again not long after I got up a couple of hours later. My husband and I both felt my pulse and talked about whether I should go to the ER, but decided to wait until the next day to see if the problem would go away. The next morning, I felt fine until I had been up for a few hours and the palpitations began again. I called the local Urgent Care clinic to ask what I should do, and they suggested starting directly at the Emergency Room based on my symptoms, so I went to the ER at around 1:30pm. An EKG taken soon after my arrival indicated abnormalities, so I was admitted and taken back to a patient cubicle where numerous tests began. I was given 4 BAYER aspirin, then when the symptoms abated I was released around 5:30pm. Once I began moving around again, the palpitations started up, but they abated after I took a 10mg dose of Propanolol prescribed at the ER. The next day, I started the day with a beta blocker, and palpitations began again after around 9 hours, so I took another one before bed. The day after that (the fourth day after my vaccine), I did not take a beta blocker until palpitations began around 2pm, then I swam laps. That night, my pulse registered an alarming 36 BPM, and I thought about returning to the ER, but decided against it, as I had an appointment with my primary care physician to discuss the ER visit and subsequent concerns. At that visit on October 27, my doctor decided to refer me to a cardiologist, and my appointment with that provider is scheduled for November 3rd. I have stopped taking the beta blockers, and I continue to have low heart rates beginning mid day, alternating with palpitations throughout the day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: Basic Metabolic Panel, Complete Blood Count, Magnesium and TSH all normal; D-dimer and Troponin slightly elevated; ECG and EKG noting Supraventricular bigeminy
Aktuelle Erkrankungen: No
Vorgeschichte: hypothyroidism
Andere Medikamente: Synthroid 75 mcg; Vitamin D 25mcg
Allergien: No
Vorherige Impfungen: -

VAERS 1829016

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: PA
Alter: 54,0
Geschlecht: F
Eingang: 29.10.2021
Impfdatum: 25.10.2021
Beginn: 25.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / RA

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

Dyspnoea Fatigue Headache Injection site pain Injection site warmth

Symptomtext

breathing issues bad enough to use my inhaler 3 times in 24hrs, fatigue, headaches and pain and hot at injection site: motrin, rest and ice

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: allergy related asthma, hypertension and allergies
Andere Medikamente: none
Allergien: oxycodone, percocet, morphiene, slight reaction to tramadol
Vorherige Impfungen: -

VAERS 1821729

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: NY
Alter: 72,0
Geschlecht: F
Eingang: 27.10.2021
Impfdatum: 24.10.2021
Beginn: 24.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Chills Diarrhoea Fatigue Nausea Pain Pyrexia Tremor

Symptomtext

Had a fever of 101 the nights following each of my first two previous Moderna vaccines, as well as soreness at the site of the injection. All was resolved in about 24 hours. The reaction to this 3rd dose was MUCH greater, even with 100 mg/Tylenol every 6 hours. The vaccine was administered at 2:30 pm. last Sunday. By midnight I had a fever of 102 with tremendous chills, and shakes so bad I could hardly walk or hold a cup of water. I also had nausea and diarrhea so was up all night. The next morning my fever was down to 100, and I was mostly just tired with minor body aches. Fever was gone by the afternoon. I slept well that night and was fine by the next day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Losartan 50 mg daily
Allergien: None
Vorherige Impfungen: As described earlier, I had soreness at the vaccination site for 48 hours after my first two Moderna vaccines, and a fever of 10

VAERS 1816330

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

moderat

Staat: CT
Alter: 74,0
Geschlecht: M
Eingang: 25.10.2021
Impfdatum: 23.10.2021
Beginn: 24.10.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: SYR / LA

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

Balance disorder Chills Decreased appetite Fatigue Lethargy Pyrexia Tremor

Symptomtext

SEVERE SHAKES AND CHILLS, BALANCE PROBLEMS FOR AND HOUR OR TWO. 101.1F FEVER. TIREDNESS THE NEXT DAY. LOSS OF APPETITE. LETHARGY.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: MODERNA 3RD VACCINATION
Aktuelle Erkrankungen: NONE
Vorgeschichte: HEART DISEASE, 3 STENTS, COUGH ASTHMA, GERD
Andere Medikamente: atorvastatin 20 mg tablet, Brilinta 90 mg tablet, metoprolol succinate 25 mg 24 hr tablet, vit A/vit C/vit E/zinc/copper (PRESERVISION AREDS ORAL), esomeprazole 40 mg DR capsule, aspirin 81 mg EC tablet
Allergien: Pollen Extracts, Environmental
Vorherige Impfungen: SAME SYMPTOMS WHEN I GO THE 2ND MODERNA SHOT. NO BAD SYMPTOMS AFTER THE FIRST MODERNA SHOT

VAERS 2710477

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: -
Alter: 70,0
Geschlecht: F
Eingang: 06.11.2023
Impfdatum: 17.02.2021
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

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

Chills Decreased appetite Pyrexia

Symptomtext

Loss of appetite; High fever; chills; This spontaneous case was reported by a consumer and describes the occurrence of DECREASED APPETITE (Loss of appetite), PYREXIA (High fever) and CHILLS (chills) in a 70-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 044A21A and 071F21A) for COVID-19 prophylaxis. Concurrent medical conditions included Type 2 diabetes mellitus, Irritable bowel syndrome, Blood pressure high, Mitral regurgitation and Drug allergy (codeine, Miralax, magnesium citrate.). On 17-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 17-Mar-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On an unknown date, the patient experienced DECREASED APPETITE (Loss of appetite), PYREXIA (High fever) and CHILLS (chills). At the time of the report, DECREASED APPETITE (Loss of appetite), PYREXIA (High fever) and CHILLS (chills) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant and treatment medications were not reported. The patient had received all Moderna COVID-19 vaccines so far and her reactions have been high fever, chills, loss of appetite. She would only have to stay at home for a couple of days after which she was able to return to work. With one of the doses, her fever went to 104F. This case was linked to US-MODERNATX, INC.-MOD-2023-747880 (E2B Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2023-747880:Same patient (Different vaccine)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Blood pressure high; Drug allergy (codeine, Miralax, magnesium citrate.); Irritable bowel syndrome; Mitral regurgitation; Type 2 diabetes mellitus
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2580013

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: NJ
Alter: 58,0
Geschlecht: M
Eingang: 12.02.2023
Impfdatum: 05.08.2022
Beginn: 20.01.2023
Tage bis Beginn: 168,0
Dosis: 3
Route/Site: SYR / RA

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

Back pain Blister Burning sensation Pain in extremity Pruritus

Symptomtext

01/20/2023 Itching and burning started on left side of lower back. Pain and burning started from left lower back to left inner thigh and left side of stomach up to umbilical. After 4-5 days blister appear from back to left inner thigh with burning and severe. Contacted doctor.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Back pain
Hospital-Tage: -
Labordaten: Tab. Valtrex 1gm Elocon 0.1% cream
Aktuelle Erkrankungen: none
Vorgeschichte: Angioplasty
Andere Medikamente: tab. Amlodepin 10mg Tab. Lisinopril 20mg Tab. Coreg 12.5mg Tab. Aspirin 81mg Tab. Atorvastatin 10mg
Allergien: none
Vorherige Impfungen: -

VAERS 2569876

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: FL
Alter: 51,0
Geschlecht: F
Eingang: 27.01.2023
Impfdatum: 05.11.2021
Beginn: 10.01.2022
Tage bis Beginn: 66,0
Dosis: 3
Route/Site: SYR / LA

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

Contusion Pruritus Rash

Symptomtext

A terrible rash that traveled my entire body, starting from my neck, all the way down my legs, arms, stomach , breasts, and finally ending on my back. The rash lasted six months had to go to the doctor and was put on prednisone. It helped for a short time and then had to use Cortizone topicals to relieve itch until it went away . The rash was so bad. That bruising started happening. It was a very difficult six months.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Zoloft
Allergien: None
Vorherige Impfungen: -

VAERS 2561139

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071f21a

mild

Staat: MA
Alter: 69,0
Geschlecht: F
Eingang: 16.01.2023
Impfdatum: 27.10.2021
Beginn: 27.06.2022
Tage bis Beginn: 243,0
Dosis: 3
Route/Site: IM / RA

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

Allergy to chemicals Blood test COVID-19 Dermatitis contact Eczema Rash SARS-CoV-2 test positive Skin test positive

Symptomtext

Mild rash on legs and arms became extreme after testing positive for Covid on July 17, 2022. The rash spread to my neck and face. After seeing three dermatologists and an allergist I was diagnosed with Eczema and contact dermatitis. I had never experienced this type of rash everything changed after I got covid.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: Patch testing determined I was allergic to Decyl glucoside, Formaldehyde, Nickle Sulfate Hexahydrate and Potassium Dichromate. Blood tests too many to list.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Nortriptylene, Vitamin D, Silver Centrum Vitamin, Acyclovir
Allergien: Amtriptyline, Cyclobenaprine, Formaldehyde, Nickel Sulfate Hexahydrate, Decyl gluside and Potassium Dichromate
Vorherige Impfungen: -

VAERS 2524378

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: CA
Alter: 49,0
Geschlecht: F
Eingang: 06.12.2022
Impfdatum: 29.11.2021
Beginn: 14.07.2022
Tage bis Beginn: 227,0
Dosis: 3
Route/Site: IM / LA

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

Asthenia COVID-19 Chemotherapy Cough Eye irritation Headache Malaise Nausea Oropharyngeal pain Pain Productive cough Pyrexia Quarantine SARS-CoV-2 test positive Secretion discharge Vomiting

Symptomtext

I got my Moderna booster for COVID-19 on 11/29/2021. On 7/14/2022, I developed body aches. I thought that maybe the body aches were caused by the chemotherapy I was receiving for my breast cancer, but then on 7/15/2022, I also developed fever with the body aches. My eyes burned, and I had to put a wet cloth over them to soothe them. On 7/16/2022 and 7/17/2022, I had nausea and vomiting. I had absolutely no energy at all. My mother put a trash can next to my bed for me to vomit into, but I didn't even have the energy to turn toward the can to throw up into it. On 7/16/2022, I took ibuprofen to treat my fever, and it helped me get to sleep. On 7/17/2022, I didn't have any fever when I woke up and I felt a little better. My mother fixed me some vegetable soup, which I was able to eat. However, a short time later, I threw it up. When the night came, my fever returned and I had to take some ibuprofen to treat it. The ibuprofen only worked for about 2 hours at the most, and whenever it wore off, the fever spiked again. I went to sleep shortly thereafter and I was able to sleep through the night. On the morning of 7/18/2022, I had some fruit for breakfast and took some more ibuprofen. I felt better that day, because the fever was gone, but I still had some headache and body aches. On 7/19/2022 and 7/20/2022, I developed a productive cough, which produced a lot of mucus. On 7/19/2022, I took a home antigen test and got a positive result. On 7/20/2022, I then took a PCR test at the clinic, which ultimately also yielded a positive result. I was supposed to go to my regular chemotherapy appointment on 7/20/2022, but I was too sick and weak from having COVID-19 to be able to withstand it. When I tested positive, I was not prescribed any antivirals or any other medications to treat it, but I don't know why. The cough lasted until about 7/21/2022, but the headache lasted for about a week longer. Before I got sick, I almost never had headaches, but this headache was severe and long-lasting. I treated my cough with hot tea with ginger and lemon, which helped soothe my sore throat and helped me go to sleep. I followed the CDC's isolation guidelines, and I came out of isolation after about 10 days. I began to feel better around 7/28/2022 and 7/29/2022, because I then no longer had a fever, nausea, vomiting, or headache. At the time of this writing, I still occasionally get headaches, though they are not nearly as strong as they were when I had COVID-19.

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Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: 7/19/2022 home antigen test positive result; 7/20/2022 PCR test positive result.
Aktuelle Erkrankungen: None.
Vorgeschichte: Breast Cancer (Left Breast).
Andere Medikamente: Cetirizine.
Allergien: Morphine sensitivity.
Vorherige Impfungen: I once had flu-like symptoms shortly after getting the flu vaccine. Before that, I had never had the flu. After the shot, I ende

VAERS 2511662

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: MN
Alter: 40,0
Geschlecht: M
Eingang: 18.11.2022
Impfdatum: 15.11.2021
Beginn: 31.08.2022
Tage bis Beginn: 289,0
Dosis: 3
Route/Site: IM / LA

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

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

Symptomtext

I test pretty regularly for COVID-19 and I had an upcoming event and wanted to make sure I was able to attend. I tested positive for COVID-19 but I did not have symptoms at that time. A few days later I started having more cold like symptoms coughing and sore throat. I had major fatigue and was so tired and was worn out.

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Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID-19 home test
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Losartan; amlodipine; metoprolol
Allergien: N/A
Vorherige Impfungen: -

VAERS 2507308

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: CA
Alter: 63,0
Geschlecht: M
Eingang: 14.11.2022
Impfdatum: 03.11.2021
Beginn: 28.08.2022
Tage bis Beginn: 298,0
Dosis: 2
Route/Site: IM / LA

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

Blood test Herpes zoster Pain

Symptomtext

On 8/28/2022 I had shingles. I went to the emergency room. They went away with treatment, valacyclovir and gabapentin. They gave me a morphine drip while I was in the emergency room for the pain.

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Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: Blood work
Aktuelle Erkrankungen: N/A
Vorgeschichte: HIV Positive; Osteoporosis
Andere Medikamente: TRIUMEQ; vitamin D; ROGAINE
Allergien: Cat dander; chlorhexidine
Vorherige Impfungen: -

VAERS 2499347

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071f21a

mild

Staat: SC
Alter: 67,0
Geschlecht: F
Eingang: 04.11.2022
Impfdatum: 26.02.2021
Beginn: 26.02.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / RA

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

Alopecia Arthralgia Immune-mediated adverse reaction Lichen sclerosus

Symptomtext

My last dose was bivalent but this site does not allow for multiple vaccinations/dates to be the potential source of the problem. I am having signs of over active immune functions with autoimmune symptoms of hair loss, lichen sclerosus, joint pain and the like. The hair loss worsened with time. I have no way of knowing if its related to my covid vaccinations but thought I should report it.

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Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: graves disease Please note I had covid vaccinations on 2/21, 3/21, with boosters on 11/21, 4/22 and 9/311/22. I am having signs of excessive autoimmune activity with hair loss, lichen sclerosus, joint pain, and sciatica. While there is no way to know for sure if it is related to the vaccinations, I felt I should report it to VSafe who suggested I file a report.
Andere Medikamente: synthroid, pravastatin, D3, tumeric, b complex, omega 3's, estradiol
Allergien: latex, demerol, augmentin
Vorherige Impfungen: -

VAERS 2480484

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071f21a

mild

Staat: AZ
Alter: 61,0
Geschlecht: F
Eingang: 17.10.2022
Impfdatum: 01.11.2021
Beginn: 02.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Dizziness Vertigo

Symptomtext

vertigo, dizziness

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Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Breast cancer remission, copd asthma
Andere Medikamente: advil
Allergien: keflex, ppd test, skin glue
Vorherige Impfungen: -

VAERS 2459845

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: SC
Alter: 30,0
Geschlecht: F
Eingang: 24.09.2022
Impfdatum: 17.11.2021
Beginn: 01.02.2022
Tage bis Beginn: 76,0
Dosis: 1
Route/Site: IM / LA

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

Abnormal menstrual clots Headache Heavy menstrual bleeding Menstrual disorder

Symptomtext

After the Moderna vaccine, I have been having extreme menstrual issues. My cycle is normally very light and since getting the shot, I have been bleeding heavily with large clots. I also only bleed 5 days and now I am bleeding a month straight. I have to wear two long pads at one time and I have to change it every hour because its full. Another side effect that I have not is extreme headaches, where I use to not have any.

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Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: I went to the doctor , Dr. in Aug 23', about this issues after dealing with it for so long and I was given Provera to try to stop my bleeding and regulate my periods, but it was unsuccessful.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2396412

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: MI
Alter: 77,0
Geschlecht: F
Eingang: 29.07.2022
Impfdatum: 28.10.2021
Beginn: 24.07.2022
Tage bis Beginn: 269,0
Dosis: 3
Route/Site: IM / -

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

COVID-19 Cough Dizziness Nausea SARS-CoV-2 test positive

Symptomtext

Symptoms = cough, dizziness, nausea, tested positive for COVID, lives in extended living facility, s/p hospital stay 5 days earlier, discharged back to facility. Now back to Emer. dept. hospital for Covid-19. Tested positive on 7/24. May have been tested on 6/30 at the facility.

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Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: SARS-CoV-2 (COVID-19) by Nucleic Acid Amplification, POC- detected on 7/24/22.
Aktuelle Erkrankungen: -
Vorgeschichte: chronic A fib, Hx aortic valve replacement, type 2 diabetes, htn, s/p knee replacement, S/P TAVR, obesity, CHF, acute on chronic kidney disease, COPD, CAD
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2316393

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: -
Alter: 49,0
Geschlecht: F
Eingang: 11.06.2022
Impfdatum: 15.03.2021
Beginn: 29.10.2021
Tage bis Beginn: 228,0
Dosis: 2
Route/Site: OT / RA

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

Blood test COVID-19 Feeling abnormal Interchange of vaccine products Pain in extremity SARS-CoV-2 test

Symptomtext

COVID-19/ lethargic/very tired/headaches; Interchange of vaccine products; Arm was Sore; Felt Funky; This spontaneous case was reported by a consumer and describes the occurrence of COVID-19 (COVID-19/ lethargic/very tired/headaches), PAIN IN EXTREMITY (Arm was Sore), FEELING ABNORMAL (Felt Funky) and INTERCHANGE OF VACCINE PRODUCTS (Interchange of vaccine products) in a 49-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 071F21A) for Prophylactic vaccination. Co-suspect product included non-company product COVID-19 VACCINE NRVV AD26 (JNJ 78436735) (JANSSEN COVID-19 VACCINE) for Prophylactic vaccination. The patient was not breastfeeding at the time of this report. The patient was left handed. The patient was not aware of being around anybody that had covid-19 prior to coming down with it and was not really sure where she picked it up. The patient did not think she got COVID-19 prior to being vaccinated. The patient had no history of diabetes, hypertension, heart disease, auto-immune disorder or immunosuppressive disorder etc. The patient had no illness at the time of vaccination and no past history of similar events. Patient had no allergy to vaccine drug or food, had no pre-existing acute illness 30 days prior to vaccination, and no history of hospitalization in last 30 days. The patient had no other suspected causes including co-administered vaccines / risk factors. The patient's past medical history included Injection site pain on 15-Mar-2021, Sickness in 2021, Chills in 2021, Fever in 2021, Headache in 2021, Photosensitivity in 2021, Vaccination failure in 2021 and Exposure to SARS-CoV-2 (Upon returning from travel, the patient's son had cold symptoms. The patient's son and herself were tested and both came back positive) in January 2022. Previously administered products included for Prophylactic vaccination: influenza vaccine (It was reported that regularly she got the flu vaccination over the years sometime had soreness in arm but not a big reaction.). Past adverse reactions to the above products included Pain in arm with influenza vaccine. Family history included Egg allergy (Patient's father was allergic to eggs and could not have any egg based vaccines.). Concurrent medical conditions included Allergy NOS, Depression (Started takin anti-depressant in 2019, continued taking through 2020 and 2021 decided to try hormone replacement therapy and had been effective.) and Sleep problem. Concomitant products included DIPHENHYDRAMINE HYDROCHLORIDE for Sleep problem, VITAMINS NOS (USANA AO PRO) for an unknown indication. On 15-Mar-2021, the patient received first dose of COVID-19 VACCINE NRVV AD26 (JNJ 78436735) (JANSSEN COVID-19 VACCINE) (unknown route) 1 dosage form. On 29-Oct-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. In 2021, the patient experienced PAIN IN EXTREMITY (Arm was Sore) and FEELING ABNORMAL (Felt Funky). On 29-Oct-2021, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced INTERCHANGE OF VACCINE PRODUCTS (Interchange of vaccine products). In January 2022, the patient experienced COVID-19 (COVID-19/ lethargic/very tired/headaches). At the time of the report, COVID-19 (COVID-19/ lethargic/very tired/headaches) had resolved and PAIN IN EXTREMITY (Arm was Sore), FEELING ABNORMAL (Felt Funky) and INTERCHANGE OF VACCINE PRODUCTS (Interchange of vaccine products) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): In 2021, Blood test: results not reported Results not reported. In January 2022, SARS-CoV-2 test: positive (Positive) positive. In 2022, SARS-CoV-2 test: negative (Negative) tested negative after few weeks.. The patient's additional concomitant medications included hormone replacement therapy drug for depression and Niva (ethinylestradiol/norethisterone, 1-5 MG-MCG). It was reported that patient was not aware of an issue with the vaccine temperature/storage/transport. For the side effects from dose 1 Janssen vaccine, the patient might have taken Motrin (Ibuprofen) or Aspirin (could not recall), over the counter and did not visit a physician. It was reported that after dose 2 vaccine, there was no fever or nothing big. In Oct-2021 or Nov-2021 she had annual physical, and blood work then, not related to any COVID or COVID symptoms. On Jan-2022 patient had first COVID test by PCR test and the symptoms included lethargic, very tired, headaches without cold symptoms. After a few weeks, it was resolved, patient tested negative again and had no symptoms. No treatment details were reported. Company comment: This spontaneous case concerns a 49-year-old female patient, with exposure to SARS-CoV-2 and with previous vaccination of COVID-19 VACCINE NRVV AD26 (JNJ 78436735), who experienced the non-serious, unexpected adverse event of special interest COVID-19. Other non-serious events were also reported immediately following vaccination. Interchange of vaccine products was specified as an additional event wherein the patient received the single dose COVID-19 vaccine of COVID-19 VACCINE NRVV AD26 (JNJ 78436735) 8 months prior to mRNA-1273. The COVID-19 infection occurred approximately 3 months after receiving the first dose of mRNA-1273 (dose 2 in series). The patient was exposed to her son who initially exhibited cold symptoms after a travel. She then presented with lethargy, tiredness and headaches. COVID-19 PCR testing was performed for her and her son, and results came back positive. Treatment details were not provided in the case although the infection was reported resolved after an unknown duration. The patient's exposure from a relative with positive travel history and eventual positive COVID-19 test, and primary vaccination with co-suspect COVID-19 VACCINE NRVV AD26 (JNJ 78436735) remain as confounders for contracting the infection. The benefit-risk relationship of mRNA-1273 Vaccine is not affected by this report. This case was linked to MOD-2022-581871.; Sender's Comments: This spontaneous case concerns a 49-year-old female patient, with exposure to SARS-CoV-2 and with previous vaccination of COVID-19 VACCINE NRVV AD26 (JNJ 78436735), who experienced the non-serious, unexpected adverse event of special interest COVID-19. Other non-serious events were also reported immediately following vaccination. Interchange of vaccine products was specified as an additional event wherein the patient received the single dose COVID-19 vaccine of COVID-19 VACCINE NRVV AD26 (JNJ 78436735) 8 months prior to mRNA-1273. The COVID-19 infection occurred approximately 3 months after receiving the first dose of mRNA-1273 (dose 2 in series). The patient was exposed to her son who initially exhibited cold symptoms after a travel. She then presented with lethargy, tiredness and headaches. COVID-19 PCR testing was performed for her and her son, and results came back positive. Treatment details were not provided in the case although the infection was reported resolved after an unknown duration. The patient's exposure from a relative with positive travel history and eventual positive COVID-19 test, and primary vaccination with co-suspect COVID-19 VACCINE NRVV AD26 (JNJ 78436735) remain as confounders for contracting the infection. The benefit-risk relationship of mRNA-1273 Vaccine is not affected by this report.

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Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: Test Date: 2021; Test Name: blood test; Result Unstructured Data: Results not reported; Test Date: 202201; Test Name: COVID-19 PCR test; Test Result: Positive ; Result Unstructured Data: positive; Test Date: 2022; Test Name: COVID-19 PCR test; Test Result: Negative ; Result Unstructured Data: tested negative after few weeks.
Aktuelle Erkrankungen: Allergy NOS; Depression (Started takin anti-depressant in 2019, continued taking through 2020 and 2021 decided to try hormone replacement therapy and had been effective.); Sleep problem
Vorgeschichte: Medical History/Concurrent Conditions: Chills; Egg allergy (Patient's father was allergic to eggs and could not have any egg based vaccines.); Exposure to SARS-CoV-2 (Upon returning from travel, the patient's son had cold symptoms. The patient's son and herself were tested and both came back positive); Fever; Headache; Injection site pain; Photosensitivity; Sickness; Vaccination failure; Comments: The patient was not breastfeeding at the time of this report. The patient was left handed. The patient was not aware of being around anybody that had covid-19 prior to coming down with it and was not really sure where she picked it up. The patient did not think she got COVID-19 prior to being vaccinated. The patient had no history of diabetes, hypertension, heart disease, auto-immune disorder or immunosuppressive disorder etc. The patient had no illness at the time of vaccination and no past history of similar events. Patient had no allergy to vaccine drug or food, had no pre-existing acute illness 30 days prior to vaccination, and no history of hospitalization in last 30 days. The patient had no other suspected causes including co-administered vaccines / risk factors.
Andere Medikamente: USANA AO PRO; DIPHENHYDRAMINE HYDROCHLORIDE
Allergien: -
Vorherige Impfungen: -

VAERS 2307963

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: OH
Alter: 62,0
Geschlecht: F
Eingang: 03.06.2022
Impfdatum: 22.11.2021
Beginn: 01.05.2022
Tage bis Beginn: 160,0
Dosis: 2
Route/Site: OT / RA

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

Asthenia COVID-19 Decreased appetite Interchange of vaccine products Nausea

Symptomtext

Patient received a dose of Janssen COVID-19 vaccine approximately 8 months prior to mRNA-1273 vaccination; Nausea; weakness; loss of appetite for food or drink; Nausea; weakness; loss of appetite for food or drink; Nausea; weakness; loss of appetite for food or drink; Initial COVID-19 infection prior to COVID-19 treatment; This spontaneous case was reported by a patient and describes the occurrence of COVID-19 (Initial COVID-19 infection prior to COVID-19 treatment), ASTHENIA (Nausea; weakness; loss of appetite for food or drink), DECREASED APPETITE (Nausea; weakness; loss of appetite for food or drink), NAUSEA (Nausea; weakness; loss of appetite for food or drink) and INTERCHANGE OF VACCINE PRODUCTS (Patient received a dose of Janssen COVID-19 vaccine approximately 8 months prior to mRNA-1273 vaccination) in a 62-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 071F21A) for COVID-19 vaccination. Co-suspect product included non-company product SULFAMETHOXAZOLE, TRIMETHOPRIM (BACTRIM) for an unknown indication. Previously administered products included for Product used for unknown indication: Janssen (Dose number: 1, batch/lot No: 1802068 and location of injection: right arm vaccine administration time: 02:00 PM) on 08-Mar-2021. Past adverse reactions to the above products included No adverse event with Janssen. Concurrent medical conditions included Cancer, Blood pressure high, High cholesterol, Drug allergy and Allergy to antibiotic. On 22-Nov-2021 at 1:00 PM, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 28-May-2022, the patient started SULFAMETHOXAZOLE, TRIMETHOPRIM (BACTRIM) (unknown route) at an unspecified dose. In May 2022, the patient experienced COVID-19 (Initial COVID-19 infection prior to COVID-19 treatment). On 28-May-2022 at 11:00 AM, the patient experienced ASTHENIA (Nausea; weakness; loss of appetite for food or drink), DECREASED APPETITE (Nausea; weakness; loss of appetite for food or drink) and NAUSEA (Nausea; weakness; loss of appetite for food or drink). On an unknown date, the patient experienced INTERCHANGE OF VACCINE PRODUCTS (Patient received a dose of Janssen COVID-19 vaccine approximately 8 months prior to mRNA-1273 vaccination). At the time of the report, COVID-19 (Initial COVID-19 infection prior to COVID-19 treatment) and INTERCHANGE OF VACCINE PRODUCTS (Patient received a dose of Janssen COVID-19 vaccine approximately 8 months prior to mRNA-1273 vaccination) outcome was unknown and ASTHENIA (Nausea; weakness; loss of appetite for food or drink), DECREASED APPETITE (Nausea; weakness; loss of appetite for food or drink) and NAUSEA (Nausea; weakness; loss of appetite for food or drink) was resolving. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. On 25-May-2022, the patient received co-suspect product Pfizer (active drug substance: COVID 19 Treatment) for treatment of COVID-19. Lot number reported was 300691085301 and date of last administration was 28-May-2022. The patient's treatment included change in antibiotic and nausea medicine. Company Comment: This is a spontaneous case concerning a 62-year-old female patient with relevant concurrent medical conditions of Cancer and High blood pressure and concomitant medication of Aurobino, who experienced the unexpected non-serious adverse event of special interest COVID-19, described as initial COVID-19 infection prior to COVID-19 treatment, which occurred approximately 6 months after receiving a dose of mRNA-1273 vaccine as second COVID-19 vaccination. Patient had received a dose of Janssen COVID-19 vaccine with no reported adverse event, approximately 8 months prior to mRNA-1273 vaccination (Interchange of vaccine products). Patient took a COVID-19 treatment for three days and noted nausea, weakness and loss of appetite. These symptoms occurred on the same day that the concomitant drug Aurobino started which had a active substance of Sulfamethoxazole/Bactrim, which is an anti-infective drug and may suggest onset of another infection, which can be considered confounders to the symptoms of nausea, weakness and loss of appetite. Patient's medication was changed and patient was given a medication for nausea. No further details about the diagnostic procedures were provided. Outcome of the event COVID-19 was unknown. The relevant concurrent medical conditions of Cancer remains as a confounder for the symptoms of nausea, weakness and loss of appetite, while the High blood pressure remains as a confounder for the symptom of nausea. The benefit-risk relationship of mRNA-1273 is not affected by this report.; Sender's Comments: This is a spontaneous case concerning a 62-year-old female patient with relevant concurrent medical conditions of Cancer and High blood pressure and concomitant medication of Aurobino, who experienced the unexpected non-serious adverse event of special interest COVID-19, described as initial COVID-19 infection prior to COVID-19 treatment, which occurred approximately 6 months after receiving a dose of mRNA-1273 vaccine as second COVID-19 vaccination. Patient had received a dose of Janssen COVID-19 vaccine with no reported adverse event, approximately 8 months prior to mRNA-1273 vaccination (Interchange of vaccine products). Patient took a COVID-19 treatment for three days and noted nausea, weakness and loss of appetite. These symptoms occurred on the same day that the concomitant drug Aurobino started which had a active substance of Sulfamethoxazole/Bactrim, which is an anti-infective drug and may suggest onset of another infection, which can be considered confounders to the symptoms of nausea, weakness and loss of appetite. Patient's medication was changed and patient was given a medication for nausea. No further details about the diagnostic procedures were provided. Outcome of the event COVID-19 was unknown. The relevant concurrent medical conditions of Cancer remains as a confounder for the symptoms of nausea, weakness and loss of appetite, while the High blood pressure remains as a confounder for the symptom of nausea. The benefit-risk relationship of mRNA-1273 is not affected by this report.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Nausea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Allergy to antibiotic; Blood pressure high; Cancer; Drug allergy; High cholesterol
Vorgeschichte: -
Andere Medikamente: BACTRIM
Allergien: -
Vorherige Impfungen: -

VAERS 2293113

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: CA
Alter: 70,0
Geschlecht: F
Eingang: 24.05.2022
Impfdatum: 21.11.2021
Beginn: 06.05.2022
Tage bis Beginn: 166,0
Dosis: 3
Route/Site: IM / RA

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

COVID-19 Cough Decreased appetite Fatigue Influenza like illness Myalgia Oropharyngeal pain Pain in extremity SARS-CoV-2 test positive Sinus disorder Upper-airway cough syndrome Vaccine breakthrough infection

Symptomtext

Breakthrough COVID-19 case: I started feeling achy in my arms. Like if I had done 50 push ups. Then I started to feel like I was getting the Flu or a Sinus infection. I had post nasal drip that was causing a sore throat and a wet cough. I did not have an appetite and I was tired. I took some Sudafed and an over the counter expectorant. It did work very well. On 05/10/2022, I decided to go to the pharmacy and test for COVID-19 and it came back negative. On 05/12/2022, I took a rapid test and it came back positive. The next day I went into a drive through test site and did a PCR test and it came back positive as well. On Friday 05/20/2022, I tested myself twice and they came back negative. I also went back to the drive through test site and tested negative again. My throat are still a tiny bit sore and my muscles are still sore.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: High Cholesterol
Andere Medikamente: Lipitor 5mg once daily, Multivitamin, Turmeric, Vitamin C, CoQ10, Biotin, Wellness Herbal Health, Cranberry Extract, Immune Enhancers, Vitamin D, Calcium
Allergien: -
Vorherige Impfungen: Dose 2 COVID-19 vaccine: Chilly for about 5 hours.

VAERS 2286776

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071f21a

mild

Staat: CA
Alter: 57,0
Geschlecht: M
Eingang: 20.05.2022
Impfdatum: 05.11.2021
Beginn: 06.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Injection site erythema Injection site pruritus Injection site swelling Pruritus Rash

Symptomtext

Site: Itching at Injection Site-Mild, Site: Redness at Injection Site-Mild, Site: Swelling at Injection Site-Mild, Systemic: Allergic: Itch (specify: facial area, extremeties)-Mild, Systemic: Allergic: Rash (specify: facial area, extremeties)-Mild

Weitere VAERSDATA-Felder

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

VAERS 2284996

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: PA
Alter: 70,0
Geschlecht: F
Eingang: 19.05.2022
Impfdatum: 08.11.2021
Beginn: 10.11.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: SYR / LA

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

Blood test normal Chills Ear discomfort Electrocardiogram normal Fatigue Head discomfort Heart rate increased

Symptomtext

Same day of vaccination for dose 3, I started having chills and fatigue. Two days after vaccination, I started feeling discomfort on the left side of my head and ear. Also, my heart rate would be abnormally high (upper 130's) with exertion/exercise. I was not associating it with my vaccine. In January 2022, I was still having discomfort on my left side of head and ear and heart rate was still elevated in upper 130's with exercise/exertion. I went in to see my PCP on 1-19-2022 and he ran some tests such as bloodwork and EKG. All of my bloodwork and EKG come back fine. He recommended increasing fluids for hydration. That had no impact on my symptoms at all. Symptoms had resolved by end of Feb 2022. I received my 4th vaccine on 4-27-2022 and the same symptoms came back. I am being scheduled for a cardiac stress test, date unknown.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Bloodwork; EKG on 1-19-2022 at Dr office.
Aktuelle Erkrankungen: None
Vorgeschichte: Dairy Sensitivity; Fibromyalgia; Glaucoma
Andere Medikamente: Gabapentin 900mg at hs, Lactaid capsules as needed
Allergien: Azithromycin; AZOPT; brimonidine; SIMBRINZA; tramadol
Vorherige Impfungen: -

VAERS 2268813

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: TX
Alter: 39,0
Geschlecht: F
Eingang: 10.05.2022
Impfdatum: 01.11.2021
Beginn: 02.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / UN

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

Fatigue Headache Pyrexia Tinnitus

Symptomtext

About 24 hours and I had fever and headache. After 3 days, fever was gone and 7 days the headache was gone. I then started getting ringing in my ear and fatigue. It lasted about 1 and 2 months and fatigue started to get so strong.

Weitere VAERSDATA-Felder

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

VAERS 2267873

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: OH
Alter: 48,0
Geschlecht: F
Eingang: 09.05.2022
Impfdatum: 03.11.2021
Beginn: 03.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Aphonia Arthralgia Asthma COVID-19 Cough Diarrhoea Disorientation Feeling abnormal Headache Heart rate abnormal Injection site swelling Pyrexia SARS-CoV-2 test positive Vaccine breakthrough infection Vomiting Weight decreased

Symptomtext

I woke up really disoriented and felt weird. I ran to the bathroom and I started vomiting and had diarrhea at the same time. I also was running a fever of 101.6. I contacted my doctor and was told to increase fluids. I was taking TYLENOL and MOTRIN for the fever. The vomiting was the one time, but the diarrhea lasted a few days. I also experienced severe headaches that concentrated on the top of my head. I also had a softball size swelling at the injection site that lasted for a few weeks. I experienced these symptoms for about a month before they subsided and during this time, I ended up losing a total of 8 pounds. I did also end up having a breakthrough COVID-19 case on 01/20/2022. I experienced fever, headaches and breathing treatment. The cough was severe to the point I ended up losing my voice. That is when I got tested and it came back positive. I contacted my doctor and he prescribed steroids'. I had a reaction to steroids. I was taking MUCINEX and TYLENOL MOTRIN. These symptoms last about a month. I still experience heart rate issues, asthma and joint pain. I had been referred to see a Rheumatologist.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Pulmicort 0.5mg every 12hours Albuterol 2.5mg every 4 hours as needed Trazodone 50mg once daily Ventolin 90mcg 2 puffs every 4 hours as needed Singulair 10mg once daily Protonix 40mg once daily Pravachol 10mg once daily Zoloft 50mg once da
Allergien: Steroids' Penicillin Sulfa
Vorherige Impfungen: Flu shot: red at injection site.

VAERS 2267520

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: AZ
Alter: 36,0
Geschlecht: F
Eingang: 09.05.2022
Impfdatum: 05.11.2021
Beginn: 26.04.2022
Tage bis Beginn: 172,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Diarrhoea Fatigue Headache Heart rate increased Hypoacusis Inflammation Malaise Myalgia Oropharyngeal pain Pain Pyrexia Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

I contracted COVID-19 4/26/2022 with symptoms of headache, fatigue, diarrhea, widespread inflammation and pain, myalgia, fever of 100.9, elevated heart rate, congestion, muted sense of hearing due to fluid/head congestion, sore throat, and I was ill for 10 days. I went to the Clinic on day 5 of illness and was not prescribed any medication after I tested positive for COVID-19 that day. I still have minor runny nose, but all other symptoms have resolved.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: COVID-19 rapid nasal swab 5/1/2022 positive
Aktuelle Erkrankungen: No
Vorgeschichte: High cholesterol Insulin resistance Had thyroid removed Depression Anxiety
Andere Medikamente: Metformin Levothyroxine Atorvastatin Albuterol Lexapro Lithium
Allergien: No
Vorherige Impfungen: -

VAERS 2266057

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: HI
Alter: 57,0
Geschlecht: F
Eingang: 06.05.2022
Impfdatum: 24.11.2021
Beginn: 19.03.2022
Tage bis Beginn: 115,0
Dosis: 3
Route/Site: SYR / LA

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

Cough Fatigue Headache Oropharyngeal pain Paranasal sinus discomfort Sinus congestion

Symptomtext

On March 19th, 2022 I had headache, sore throat, sinus pressure and congestion, fatigue. I didn't get the infusion since I wasn't a candidate. It went into my lungs and developed an unproductive cough. Mucinex and vitamin c and d. This lasted 16 days before I tested negative. I went on a higher dose of advair for my asthma and albuterol. I was put on steroids for ten days. It finally got better on April 28th, 2022. The fatigue is still here.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma
Andere Medikamente: None
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 2264788

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: IL
Alter: 72,0
Geschlecht: M
Eingang: 05.05.2022
Impfdatum: 03.11.2021
Beginn: 19.04.2022
Tage bis Beginn: 167,0
Dosis: 3
Route/Site: SYR / LA

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

Body temperature increased COVID-19 Chills Cough Feeling abnormal Hypersomnia Nasopharyngitis Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

I started feeling sort of congested on Saturday evening the 16th it continued to Sunday felt more like a cold. On Monday I started to feel abnormal I slept longer than normal but started coughing and Monday evening I had heavy cough then Tuesday I had chills and took my temperature, and it was 100.1 later in the day it went up to 100.7. I took COVID home test, and it was positive, I contact my doctor's office and they were closed so I scheduled a telehealth appointment on Wednesday morning after taking a second home test to verify it was also positive. Explained my symptoms to my doctor and prescribed an antiviral treatment that I started taking that evening.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: COVID Home Test - Positive 04/19/2022
Aktuelle Erkrankungen: None
Vorgeschichte: Atrial Fibrillation
Andere Medikamente: Metoprolol; Xarelto; Lovastatin; Fish Oil; Vitamin D3; Vitamin E
Allergien: None
Vorherige Impfungen: -

VAERS 2263485

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: SC
Alter: 68,0
Geschlecht: F
Eingang: 04.05.2022
Impfdatum: 01.11.2021
Beginn: 16.04.2022
Tage bis Beginn: 166,0
Dosis: 3
Route/Site: SYR / LA

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

COVID-19 Cough Diarrhoea Gingival pain Immunisation reaction Pain Pyrexia Rhinorrhoea SARS-CoV-2 test positive Sinus pain Throat irritation Vaccine breakthrough infection

Symptomtext

5 1/2 months after vaccination on 4-15-2022, I started having a cough. The following day on 4-16, I had a fever of 100.0, body aches, a scratchy throat, runny nose and sinus pain. I went to go test and it was positive for COVID-19. Thru that night, I started having diarrhea. One week later, I started having gum pain so I went to my dentist and they stated I had COVID-19 sores in my mouth. I am reporting a breakthrough case of COVID-19 after being fully vaccinated.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: COVID-19 test at CVS - positive results
Aktuelle Erkrankungen: None
Vorgeschichte: Emphysema GERD Diverticula History LUL lung removal April 2021 due to Cancer Nodule Osteoarthritis
Andere Medikamente: Pantoprazole 20mg daily Zolpidem 12.5mg ER at hs Restasis 1 gtt each eye bid OTC Calcium 600mg daily Omega 3 1200mg daily Vitamin D 1000mg daily Magnesium 400mg daily Oxycodone apap 5/325mg as needed (usually 1.5 tabs daily) Advil 400mg as
Allergien: Pcn Keflex Phenothiazine
Vorherige Impfungen: -

VAERS 2263251

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: MA
Alter: 40,0
Geschlecht: F
Eingang: 04.05.2022
Impfdatum: 01.11.2021
Beginn: 22.04.2022
Tage bis Beginn: 172,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Chills Cough Decreased appetite Fatigue Headache Nasal congestion Nausea SARS-CoV-2 test positive

Symptomtext

Fell ill with COVID-19: onset of fatigue, chills, nausea, nasal congestion, cough, headache, lack of appetitie on Day 0; nausea intensified and required Rx for Zofran Days 3-7; return to work on Day 10; continued symptoms (currently Day 12) include fatigue, cough, nasal congestion, headache, nausea (reduced and no longer requiring Zofran), lack of appetite

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Home test on Day 1 (23 Apr 2022) - positive
Aktuelle Erkrankungen: none
Vorgeschichte: depression, anxiety
Andere Medikamente: Lexapro, Wellbutrin
Allergien: Sulfa drugs, adhesives (topical reaction)
Vorherige Impfungen: -

VAERS 2261734

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: CT
Alter: 81,0
Geschlecht: F
Eingang: 03.05.2022
Impfdatum: 30.10.2021
Beginn: 13.04.2022
Tage bis Beginn: 165,0
Dosis: 3
Route/Site: SYR / LA

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

COVID-19 Chills Fatigue Feeling abnormal Headache Pain Productive cough Pyrexia SARS-CoV-2 test positive

Symptomtext

I had achiness, chills slight fever for 2 days after the vaccine. With Covid I had headache, productive cough, chills, tiredness, brain fog that lasted 7 or 8 days. I was in bed for 3 days and on antiviral.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: At home COVID test - positive. Stayed positive for about 8 days.
Aktuelle Erkrankungen: No
Vorgeschichte: Asthma; high cholesterol
Andere Medikamente: Lipitor, Asmanex, Albuterol
Allergien: No
Vorherige Impfungen: -

VAERS 2260447

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: NY
Alter: 40,0
Geschlecht: F
Eingang: 02.05.2022
Impfdatum: 29.10.2021
Beginn: 11.01.2022
Tage bis Beginn: 74,0
Dosis: 3
Route/Site: SYR / AR

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

COVID-19 Chest discomfort Fatigue Gastrooesophageal reflux disease Headache Menstruation irregular SARS-CoV-2 test positive Ultrasound scan abnormal

Symptomtext

01/11/2022 Tested positive for COVID-19. I was having terrible reflux issues two days prior. It began with tightness in my chest and almost went to the ER. My throat hurt and I began to get a really bad headache that none of my meds were helping. The day after my test, I took dexamethasone that helped considerably. However, I continued to have fatigue and I was having terrible reflux issues continued. I was prescribed a stronger antacid that helped out as well. A week after COVID-19, I had a terrible menstrual cycle for about two months. Ultrasound done that showed no issues as well. My cycle is still having issues to this day. No more reflux, or headaches, or fatigue.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID-19 Test: Positive, Ultrasound: Came back normal.
Aktuelle Erkrankungen: N/A
Vorgeschichte: Asthma
Andere Medikamente: Birth Control, Gabapentin, Propranolol, Nortriptyline, Allergy Medicine Zyrtec, Symbicort
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2260359

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: CA
Alter: 74,0
Geschlecht: F
Eingang: 02.05.2022
Impfdatum: 27.10.2021
Beginn: 19.01.2022
Tage bis Beginn: 84,0
Dosis: 3
Route/Site: SYR / LA

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

Abdominal pain upper Blood test Computerised tomogram abnormal Diverticulitis Pain Sleep disorder Urine analysis

Symptomtext

The day before I had stomach pains not too severe but off and on during the day. Then I woke the next morning at 4:30am with severe pain. Eventually, I decided I needed to go to the emergency room. I was given a blood test, urinalyses and a CAT scan. The CAT scan is was showed that I had diverticulitis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain upper
Hospital-Tage: -
Labordaten: Blood test; Urinalyses; CAT Scan
Aktuelle Erkrankungen: None
Vorgeschichte: Postherpetic Neuralgia
Andere Medikamente: Gabapentin Nortriptyline Estradiol Lysine Flonase
Allergien: Amoxicillin
Vorherige Impfungen: -

VAERS 2258620

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: OH
Alter: 61,0
Geschlecht: F
Eingang: 29.04.2022
Impfdatum: 28.10.2021
Beginn: 20.04.2022
Tage bis Beginn: 174,0
Dosis: 3
Route/Site: IM / LA

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

Ear pain Headache Neck pain Oropharyngeal pain Pharyngeal swelling Streptococcus test negative

Symptomtext

Developed pain in right side of throat (inside throat and outside on R-side neck) and in right ear on 4/20/22. Also developed headache on 4/19/22 which persisted through 4/24/22. Went to Clinic employee walk-in clinic on 4/21/22 because inside of throat felt swollen. Both ears were clear and rapid strep test was negative. Advised to keep eye on it, gargle with salt water and use Tylenol or Motrin as needed. No ATB prescribed. By Friday, 4/22/22 the pain was subsiding on the right side of throat/neck and moved to left side of throat/neck. Headache persisted during this time. Throat was significantly improved by Monday, 4/25/22 and headache had resolved.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Ear pain
Hospital-Tage: -
Labordaten: 4/21/22 Rapid Strep Test at Clinic Employee walk-in clinic - test was negative for strep.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Prozac, AREDS-2 supplement, Vit B-12 500 mcg/daily
Allergien: None
Vorherige Impfungen: -

VAERS 2257382

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: IL
Alter: 35,0
Geschlecht: F
Eingang: 28.04.2022
Impfdatum: 03.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Rash pruritic

Symptomtext

So, it was like a rash that was itchy, it was on my back, stomach and chest, it was really itchy. I just took Benadryl over the counter, I would wash with cool water. I would take a Benadryl every 12 hours. It would get better and then come back. This lasted for about 30 day. By the first week of December it just completely disappeared. It was just gone. It wasn't bad enough where I would not do this again, it was annoying, but nothing to harsh.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash pruritic
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Vitamin D
Allergien: None
Vorherige Impfungen: -

VAERS 2254647

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: IL
Alter: 74,0
Geschlecht: F
Eingang: 27.04.2022
Impfdatum: 09.11.2021
Beginn: 10.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Fatigue Injection site rash Pain in extremity

Symptomtext

11/10/2021 I started to notice I had a rash developing midway of my upper arm between the injection site and elbow. After reaching out to my doctor, they stated that this has been occurring with patients that received Moderna vaccines and that it would go away after a few days which it did. My arm was very sore and I was also very fatigued. This all lasted around 3 days post vaccine and then the rash subsided. No reoccurring symptoms to report.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: Seasonal Allergies
Vorgeschichte: Mild Lupus; Fibromyalgia; Elevate Blood Pressure that is under control; Allergies
Andere Medikamente: Lisinopril; Azelastine; Xyzal; Qvar; Vitamin D; Aspirin Low Dosage; Estrace Cream; Patanol Drops
Allergien: Penicillin; Shellfish; Tree Nuts
Vorherige Impfungen: D-Tap Vaccine when I was very young cause me to have a fever, fatigue, and pain in my arm.

VAERS 2254540

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: SC
Alter: 66,0
Geschlecht: M
Eingang: 27.04.2022
Impfdatum: 30.10.2021
Beginn: 31.10.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / LA

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

Chills Fatigue Headache Pain

Symptomtext

10/31/2021 Most pronounced symptom I had was fatigue, followed by a headache then chills. This lasted about 24 hours. I also had a little it of achiness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Lipitor 20mg; Daily Vitamin
Allergien: Codeine; Sulfa
Vorherige Impfungen: -

VAERS 2249745

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: CA
Alter: 65,0
Geschlecht: F
Eingang: 24.04.2022
Impfdatum: 24.04.2021
Beginn: 24.04.2022
Tage bis Beginn: 365,0
Dosis: 3
Route/Site: IM / -

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

COVID-19 Face and mouth X-ray Feeling cold Headache Interchange of vaccine products Nasal discomfort Nasopharyngitis SARS-CoV-2 test positive Sinus disorder Somnolence

Symptomtext

1/22/22 - sudden onset headache after day with grandchildren and supper with son and daughter in law. COVID positive 1/23/22 after sleeping most of day. Basically like a cold for the next week, did the usual to prevent cold complications - Flonase and Q-var inhaler. 4/7/22 - ongoing sinus problems, ( nose burns because of coldness, causes headaches requiring Excedrin 1-2 times a day. No congestion, no fever, no sinus pressure, no sinus tenderness) Augmentin Rx x 10 days after video visit. Burning coldness quit after 2 doses, and resumed the day following completion of Augmentin on 4/15. MD appt 4/19 with Keflex ordered x 10 days. Burning coldness stopped after 2 doses, resumed 4/24.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: Sinus x-rays
Aktuelle Erkrankungen: Neuropathy
Vorgeschichte: Diabetes, Fibromyalgia
Andere Medikamente: Simvastatin, Metformin, Losartin, Amlodipine, Neurontin, Bcomplex, Centrum silver, Omega 3, Coq10, Bromelain, Vitamin D and eE, Alfalfa, Turmeric, kelp
Allergien: Bactrim
Vorherige Impfungen: -

VAERS 2247920

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: AZ
Alter: 23,0
Geschlecht: F
Eingang: 22.04.2022
Impfdatum: 06.11.2021
Beginn: 06.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Axillary pain Influenza like illness Lymph node pain Lymphadenopathy Pain in extremity Peripheral swelling Sleep disorder

Symptomtext

11/06/2021 I started experiencing around 2-3:00am in the morning I had a flu like symptoms except fever. My left arm was swollen and was very painful. I discover a pea size lymph node under my arm pit and it was hurting. It was uncomfortable I couldn't sleep on that side. After 3 months all my symptoms were gone but the pain from lymph node was still there. I went to see my doctor she checked me and said that a pea size lymph node which was swollen and she told me to monitor it. she told me to go back in 3 months if it didn't go away. I took Advil but it didn't help.

Weitere VAERSDATA-Felder

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

VAERS 2206942

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: TX
Alter: 53,0
Geschlecht: F
Eingang: 30.03.2022
Impfdatum: 06.11.2021
Beginn: 01.01.2022
Tage bis Beginn: 56,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Headache Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

I tested positive for COVID-19. I had a runny nose and headache. I received a steroid shot and I used Mucinex and Sudafed as treatment.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: I tested positive for COVID-19 on 01/06/2022.
Aktuelle Erkrankungen: None
Vorgeschichte: N/A
Andere Medikamente: Xigduo; Lisinopril; Atorvastatin; Tamoxifen
Allergien: Latex; Z-pak
Vorherige Impfungen: -

VAERS 2206714

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: OH
Alter: 50,0
Geschlecht: F
Eingang: 30.03.2022
Impfdatum: 02.11.2021
Beginn: 13.01.2022
Tage bis Beginn: 72,0
Dosis: 3
Route/Site: IM / RA

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

COVID-19 Fatigue Headache Increased upper airway secretion Oropharyngeal pain Pyrexia SARS-CoV-2 test positive

Symptomtext

I got COVID after Dose 3 started with low grad fever, sore throat with a lot of drainage, fatigue and headache symptoms lasted for a week a 1/2.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Rapid antigen test (results positive)
Aktuelle Erkrankungen: Allergy shots since November 2021
Vorgeschichte: Asthma
Andere Medikamente: Metoprolol, Flovent, Wellbutrin, Omeprazole, Trazadone
Allergien: Environmental allergies
Vorherige Impfungen: -

VAERS 2188319

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: AZ
Alter: 47,0
Geschlecht: M
Eingang: 18.03.2022
Impfdatum: 17.02.2021
Beginn: 04.03.2022
Tage bis Beginn: 380,0
Dosis: 3
Route/Site: IM / LA

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

Ageusia Anosmia COVID-19 Fatigue Headache Nausea Respiratory tract congestion SARS-CoV-2 RNA SARS-CoV-2 test positive Vomiting

Symptomtext

I was told to report that I caught Covid and suffered lengthy symptoms despite vaccination. Beginning around March 4, 2022, I began having extreme fatigue, chest congestion, and painful headache. I briefly also had nausea and vomited once (more like reflux vomit) that day. Covid confirmed on March 7, 2022. It is now March 18, 2022, and I am still suffering with fatigue cycles, chest congestion, headaches, and loss of taste and smell.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: March 7, 2022: SARS-CoV-2 RNA (Covid-19), Qualitative NAAT, positive.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Sertraline
Allergien: Sulfa antibiotics
Vorherige Impfungen: -

VAERS 2173332

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21a

mild

Staat: TN
Alter: 43,0
Geschlecht: M
Eingang: 11.03.2022
Impfdatum: 10.11.2021
Beginn: 15.11.2021
Tage bis Beginn: 5,0
Dosis: 3
Route/Site: SYR / LA

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

Rash

Symptomtext

After the booster shot, I did not feel any issue for a day or two. However, from 2nd or 3rd day onwards I started having rashes on my body and it is continuing till date (however the frequency and the amount of rashes reduced compared to the beginning). I am taking Zyrtec and that is helping with rashes.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Chron's
Vorgeschichte: None
Andere Medikamente: B12 Shot and Mesacol for Chron's
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2165999

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: GA
Alter: 82,0
Geschlecht: F
Eingang: 08.03.2022
Impfdatum: 28.10.2021
Beginn: 03.03.2022
Tage bis Beginn: 126,0
Dosis: 3
Route/Site: IM / LA

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

Back pain Blood test normal Intervertebral disc degeneration Spinal X-ray abnormal Spinal deformity

Symptomtext

03/03/2022 I have had back pain starting about a month back . Sought care from my doctor because it seemed worse after my booster shot. She took my blood work because it was my usual yearly appointment anyway. Also did an x-ray and found a continued degeneration of my disc and curvature. Nurse called with these results yesterday and suggested to get an MRI.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Back pain
Hospital-Tage: -
Labordaten: 3/3/2022 Blood Work (Normal) 3/3/2022 X-Ray (Curvature of the spine, Continued degeneration of spinal discs)
Aktuelle Erkrankungen: None
Vorgeschichte: Osteoarthritis
Andere Medikamente: Carvedilol, Ezetimibe, Glucosamine Chondroitin, A, B-12, D3, C, Zinc
Allergien: Codeine, Shellfish
Vorherige Impfungen: -

VAERS 2162594

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: VA
Alter: 26,0
Geschlecht: F
Eingang: 07.03.2022
Impfdatum: 27.10.2021
Beginn: 06.11.2021
Tage bis Beginn: 10,0
Dosis: 3
Route/Site: IM / LA

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

Urticaria

Symptomtext

I experienced the following symptoms after my booster shot: Hives Breakout (Primarily - abdomen, chest, back, both arms, and leg), and chest tightness. I took some anti allergy medication for treatment but it did not work or did not do much so I decided to visit a doctor for consultation and he diagnosed me with unspecified carinaria and was prescribed with Hydroxyzine Hydrochloride (25mg) . As of today 03/07/2022 I still experience some hives breakout on my chest, back and abdomen.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Urticaria
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Psoriasis
Vorgeschichte: None
Andere Medikamente: Nexplanon
Allergien: None
Vorherige Impfungen: -

VAERS 2162121

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: MD
Alter: 36,0
Geschlecht: F
Eingang: 06.03.2022
Impfdatum: 14.02.2022
Beginn: 15.02.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Chills Fatigue Feeling abnormal Full blood count Headache Injection site pain Metabolic function test Myalgia Nausea SARS-CoV-2 test

Symptomtext

I received the third dose of the Moderna Vaccine on 2/14/2022. Twenty four hours after vaccination, I began to experience side effects. Side effects included: headache, chills, muscle aches, nausea, tiredness, and pain at the site of injection. Nearly 3 weeks later, I am still experiencing the side effects. I experience chills and a headache everyday. Last week, I felt a pulsation to the right side of my head and then a mild headache came on. Sometimes the headache is on the left side of my head. I continue to experience joint and muscle pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: I went to the doctor. A CBC and BMP were done. Also, I had a COVID- 19 test. All tests were done on 2/22/2022.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Multivitamins
Allergien: No
Vorherige Impfungen: -

VAERS 2151041

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: TX
Alter: 66,0
Geschlecht: M
Eingang: 01.03.2022
Impfdatum: 31.10.2021
Beginn: 08.02.2022
Tage bis Beginn: 100,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Diarrhoea Infusion Respiratory tract congestion

Symptomtext

I had severe congestion and diarrhea. My wife was also ill. This prompted me to take the at home test and tested positive. I was advised to rest and drink a lot of water. I was checking my O2 levels also but was more concerned about my wife. We were sent to get an infusion on that Thursday after testing positive. The doctor did a video appointment with me prior to the appointment and set it up. I have completely recovered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: Infusion.
Aktuelle Erkrankungen: None
Vorgeschichte: Acid Reflux
Andere Medikamente: Pantoprazole, Rosuvastatin, fruits and vegetables caplet
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2148349

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: VA
Alter: 75,0
Geschlecht: F
Eingang: 28.02.2022
Impfdatum: 08.11.2021
Beginn: 08.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SC / LA

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

Injection site pain X-ray

Symptomtext

Left shoulder and upper arm pain, worsening over 3 month period.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: Primary Care Visit. Orthopedic Visit. X-Rays. Steroid Injection and Physical Therapy to begin.
Aktuelle Erkrankungen: none
Vorgeschichte: High cholesterol, mild glaucoma
Andere Medikamente: Cholesterol med, calcium, magnesium, biotin, PreserVision, vitamin C, glaucoma drops, Tylenol as needed, Claritin as needed
Allergien: codeine
Vorherige Impfungen: -

VAERS 2134554

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: AZ
Alter: 43,0
Geschlecht: F
Eingang: 23.02.2022
Impfdatum: 31.10.2021
Beginn: 20.01.2022
Tage bis Beginn: 81,0
Dosis: 3
Route/Site: IM / UN

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

Ageusia Anosmia Asthenia COVID-19 Cough Fatigue Feeling abnormal Headache Illness Impaired work ability Influenza like illness Malaise Oropharyngeal pain Pyrexia Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

Booster 10/31/2021 Moderna, breakthrough case of Covid-19. Started feeling unwell on 01/20/2022. Positive COVID-19 PCR on 01/21/2022. COVID acute sickness for about 10 days, feeling flu like symptoms, low energy, fever, loss of smell and taste, runny nose, sore throat and cough. While over the acute illness as of 02/23/2022, but still having symptoms. After a month later fatigue, bad headaches, and brain fog that impacted ability to work more than a couple of hours per day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: PCR test
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: No
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2129238

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: OH
Alter: 38,0
Geschlecht: M
Eingang: 21.02.2022
Impfdatum: 08.11.2021
Beginn: 02.02.2022
Tage bis Beginn: 86,0
Dosis: 3
Route/Site: IM / LA

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

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

Symptomtext

I tested positive for Covid-19. I had a severe sore throat. I was prescribed Magic Oral Suspension (CMP) mouthwash as treatment.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: I tested positive for Covid-19 on 02/05/2022.
Aktuelle Erkrankungen: None
Vorgeschichte: mild asthma
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2109440

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: VA
Alter: 75,0
Geschlecht: M
Eingang: 12.02.2022
Impfdatum: 25.10.2021
Beginn: 02.01.2022
Tage bis Beginn: 69,0
Dosis: 3
Route/Site: IM / LA

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

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

Symptomtext

Contracted COVID-19. Cold symptoms (including sore throat).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: PCR.
Aktuelle Erkrankungen: None
Vorgeschichte: High blood pressure (under control), high cholesterol (under control), obstructive sleep apnea (under control)
Andere Medikamente: Too long to list.
Allergien: Sulfa; Klonopin
Vorherige Impfungen: -

VAERS 2102165

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: FL
Alter: 73,0
Geschlecht: F
Eingang: 10.02.2022
Impfdatum: 09.11.2021
Beginn: 19.11.2021
Tage bis Beginn: 10,0
Dosis: 3
Route/Site: IM / LA

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

Influenza like illness Injection site swelling Rash Swelling

Symptomtext

Rash, swelling, flu like symptoms. Swollen injection site required icing.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site swelling
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Thyroid
Andere Medikamente: Levothyroxine; estrogen; estazolam; multivitamin
Allergien: None
Vorherige Impfungen: -

VAERS 2101858

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: MA
Alter: 65,0
Geschlecht: F
Eingang: 10.02.2022
Impfdatum: 04.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / -

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

Fatigue Immediate post-injection reaction Malaise Mouth ulceration Oral herpes Pain Rash Scar

Symptomtext

Immediate reaction feeling sore, achy and fatigue. Felt very ill for three days. Had rash on vaccination arm. Most troubling was the oral herpes infection that appeared on day three. Multiple sores that took weeks to heal. Scarring.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: About two weeks after the sores healed I had a new outbreak that lasted weeks . I was prescribed oral antivirals. I. The first outbreak I used topical antiviral
Aktuelle Erkrankungen: -
Vorgeschichte: High BP Autoimmune thyroidistis Arthritis Tinnitus High cholesterol
Andere Medikamente: Lisinopril Amlodipine Vitamins B-12, D Omega three
Allergien: Penicillin Tramadol Cyclosporine Cats Soy
Vorherige Impfungen: -

VAERS 2099689

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: NC
Alter: 56,0
Geschlecht: M
Eingang: 09.02.2022
Impfdatum: 06.11.2021
Beginn: 08.11.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: IM / RA

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

Pain Pain in extremity

Symptomtext

Over three months from the date of my second vaccination and my right arm is still extremely painful. It's difficult to lift my arm to the side without incurring severe pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: HTN, asthma, acid reflux, small fiber mialga, heart palpitations
Andere Medikamente: omneprazole, Breo Ellipta, Ventolin, Olmesartan, multivitamin, Flonase, Asteline, Claritan, Fish Oil,
Allergien: Amlodipine, topical iodine
Vorherige Impfungen: -

VAERS 2098764

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: LA
Alter: 44,0
Geschlecht: F
Eingang: 09.02.2022
Impfdatum: 02.11.2021
Beginn: 03.01.2022
Tage bis Beginn: 62,0
Dosis: 3
Route/Site: SYR / LA

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

COVID-19 Chest discomfort Diarrhoea Pyrexia SARS-CoV-2 test SARS-CoV-2 test negative SARS-CoV-2 test positive Sinus congestion Sinusitis

Symptomtext

01/03/2022 First PCR test was incoclusive. The week before I had sinus infection and your husband tested positive the day before so you went to Urgent Care in town. That was a negative rapid test. I did another PCR test 5 days after he tested positive and was negative. Then I did another test 01/04/2022 PCR and that came inclonclusive Then on the 5th I did at home test that came back positive. My symptoms were more severe than my husband and sons. I had sinus/chest congestion, GI diahhrea, fever that broke within 2 days. I did not need doctors care. I did do a tele-doc the week of the 17th because it turned into a sinus infection. They prescribed Augmentin and it cleared up within week

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: 1st Rapid test was 12/28/2021 Neg 2nd PCR 12/31/2021 Neg 3rd 01/04/2022 PCR inconclusive 4th 01/05/2022 Home test came back positive
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Claritin multi-vitamin Vitamin D
Allergien: None
Vorherige Impfungen: -

VAERS 2091632

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: NJ
Alter: 47,0
Geschlecht: F
Eingang: 05.02.2022
Impfdatum: 12.11.2021
Beginn: 22.11.2021
Tage bis Beginn: 10,0
Dosis: UNK
Route/Site: - / -

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

Pain in extremity

Symptomtext

I have received two Pfizer COVID 19 vaccinations in March of 2021 and a Moderna COVID 19 booster in November of 2021. I received the two Pfizer shots in my upper left arm and experience the expected soreness in my arm for about 2-3 days each time. However, after that time period, I continued to experience sharp pain in my arm and muscle weakness off/on for the next few months with an inability to move my left arm above my head or behind to my back without experiencing severe pain. When I received the Moderna booster, I asked to get in my right arm. I am now experiencing the same issue in the right arm with a sharp pain that comes and goes but is noticeable enough that it keeps me up at night. Meanwhile, almost a year after receipt of my original Pfizer vaccine the pain in my left arm is noticeably less. I read about Parsonage-Turner syndrome following COVID-19 Vaccination in two patients and thought to report my experience here as well, though I have no laboratory or imaging results to share/confirm.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: None. I was advised that while imaging can be useful in diagnosis that there is no approved treatment.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Iron 22mg daily D3 5000IU daily B12 5000ug 1Xwk B complex 50mg Biotin 5000ug
Allergien: None
Vorherige Impfungen: See previous description of similar experience with the Pfizer COVID-19 vaccine

VAERS 2088102

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: VA
Alter: 37,0
Geschlecht: F
Eingang: 04.02.2022
Impfdatum: 31.10.2021
Beginn: 31.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Erythema Pruritus

Symptomtext

Systemic: Allergic: Itch (specify: facial area, extremities)-Mild, Additional Details: Patient felt neck and face turn red.

Weitere VAERSDATA-Felder

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

VAERS 2085980

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: WY
Alter: 43,0
Geschlecht: M
Eingang: 03.02.2022
Impfdatum: 19.12.2021
Beginn: 26.12.2021
Tage bis Beginn: 7,0
Dosis: UNK
Route/Site: IM / LA

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

Rash Rash macular

Symptomtext

red dot rash on arms and legs

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: NO
Vorgeschichte: HYPERTENSION, DIABETES, HYPERLIPIDEMIA
Andere Medikamente: -
Allergien: PENICILLIN
Vorherige Impfungen: -

VAERS 2085179

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: MD
Alter: 55,0
Geschlecht: M
Eingang: 03.02.2022
Impfdatum: 27.10.2021
Beginn: 03.01.2022
Tage bis Beginn: 68,0
Dosis: 3
Route/Site: IM / RA

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

COVID-19 Fatigue Nasopharyngitis SARS-CoV-2 test negative SARS-CoV-2 test positive

Symptomtext

My wife works in the medical field and I believe she was exposed 12/29-12/30. The first test I took was January 6th and that PCR test was NEG. I had significant fatigue between January 2-4th. The following week on January 13th (Thursday) my symptoms subsided but I took another PCR Test at that one came back positive. I made an appt with my PCP just to let her know. I saw her before I got the test result and I wanted to be in touch with her in case it got worse. I drank a ton of water. Over the weekend symptoms turned into feeling like a head cold by that following Tuesday I believe by the 11th I felt fully well. On the 15th I took another PCR test and it was Negative.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Two PCR COVID tests. 1st one NEG. 2nd one POS, 3rd test on January 15th NEg
Aktuelle Erkrankungen: No
Vorgeschichte: Obesity
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2075475

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: NC
Alter: 57,0
Geschlecht: F
Eingang: 31.01.2022
Impfdatum: 03.11.2021
Beginn: 01.11.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / LA

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

Coating in mouth Oral lichen planus Oral mucosal blistering Oral mucosal erythema Oral pain

Symptomtext

Symptoms of oral blisters and sore, red areas with white striae in buccal mucosa began approximately 2 weeks after Moderna Booster in Nov. 2021. Diagnosed with Oral Lichen Planus in Jan. 2022 by local ENT physician. Treatment with topical Clobetasol Ointment is ongoing. If not resolved, plan is to treat with systemic steroids or Tacrolimus.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oral pain
Hospital-Tage: -
Labordaten: No tests have been performed yet. Biopsy may be performed at a later time when symptoms have resolved enough to tolerate.
Aktuelle Erkrankungen: None
Vorgeschichte: Hypothyroidism, Insomnia, Seasonal Allergies
Andere Medikamente: Levothyroxine, Trazodone, Loratadine
Allergien: None
Vorherige Impfungen: Fever, headache, sore arm mainly with second vaccine

VAERS 2072049

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: MI
Alter: 93,0
Geschlecht: M
Eingang: 28.01.2022
Impfdatum: 04.11.2021
Beginn: 27.01.2022
Tage bis Beginn: 84,0
Dosis: 3
Route/Site: - / -

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

Abdominal pain COVID-19 Decreased appetite Fatigue Headache SARS-CoV-2 test positive

Symptomtext

Patient presented to the ED on 1/27/22 with complaints of 3 weeks of fatigue, headache, abdominal pain, and decreased appetite. He tested positive for COVID on 1/27/22.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain
Hospital-Tage: 2,0
Labordaten: COVID PCR+ on 1/27/22
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2071162

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: NH
Alter: 75,0
Geschlecht: F
Eingang: 28.01.2022
Impfdatum: 03.11.2021
Beginn: 03.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: OT / LA

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

Inappropriate schedule of product administration Vaccination site pain

Symptomtext

Got a pain in left arm; got Pfizer as1st dose on 29-Jan-2021, then got the Moderna Covid-19 Vaccine as 2nd dose on 03-Nov-2021; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION SITE PAIN (Got a pain in left arm) and INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (got Pfizer as1st dose on 29-Jan-2021, then got the Moderna Covid-19 Vaccine as 2nd dose on 03-Nov-2021) in a 75-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 071F21A) for COVID-19 vaccination. Previously administered products included for Product used for unknown indication: Pfizer (1st dose) on 29-Jan-2021. Past adverse reactions to the above products included Allergic reaction with Pfizer. On 03-Nov-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 03-Nov-2021, the patient experienced INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (got Pfizer as1st dose on 29-Jan-2021, then got the Moderna Covid-19 Vaccine as 2nd dose on 03-Nov-2021). On an unknown date, the patient experienced VACCINATION SITE PAIN (Got a pain in left arm). On 03-Nov-2021, INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (got Pfizer as1st dose on 29-Jan-2021, then got the Moderna Covid-19 Vaccine as 2nd dose on 03-Nov-2021) had resolved. At the time of the report, VACCINATION SITE PAIN (Got a pain in left arm) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medications were not provided. Treatment information was not provided.

Weitere VAERSDATA-Felder

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

VAERS 2068762

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: MN
Alter: 31,0
Geschlecht: F
Eingang: 27.01.2022
Impfdatum: 05.11.2021
Beginn: 15.11.2021
Tage bis Beginn: 10,0
Dosis: 3
Route/Site: IM / RA

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

Arthralgia Exposure during pregnancy Joint swelling Mechanical urticaria Peripheral swelling Pruritus Rash SARS-CoV-2 test negative Urticaria

Symptomtext

On Monday November 15th patient experienced onset of pruritus around 6:00 p.m.. The following day Tuesday 11/16/2021 she developed welts on her chest which progressed to most of the skin surfaces over the course of 1-2 days. She also experienced joint pain and swelling in the wrists, finger joints, then also knees and ankles. The joints swelling was prominent in her wrists and hands such that she had removed her ring on her finger. She had to remove her watch. She could not close her hands for 3-4 days. The joint swelling resolved after around 1 week before she could go back to exercise. She has had persisting dermatographia some at least into January 27, 2022. She has a dermatitis type rash on the upper chest and upper back. Estimated 9 month due date is June 3, 2022. ( Estimated 9 weeks pregnant at time of vaccine and around 10-11 weeks pregnant at the time of the onset of the pruritus and then rash and joint swelling) She appears to have had an otherwise normal pregnancy and describes very strict avoidance of any gluten products with a known history of celiac disease.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: COVID test was performed and was negative.
Aktuelle Erkrankungen: N/A
Vorgeschichte: Celiac disease, Migraine HAs, TMJ joint disease, Postpartum anxiety/depression
Andere Medikamente: Prenatal vitamins
Allergien: Gluten (documented celiac disease) and Ibuprofen GI intolerance
Vorherige Impfungen: -

VAERS 2068615

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: OH
Alter: 45,0
Geschlecht: F
Eingang: 27.01.2022
Impfdatum: 08.12.2021
Beginn: 04.01.2022
Tage bis Beginn: 27,0
Dosis: 3
Route/Site: SYR / LA

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

Ageusia Anosmia COVID-19 Influenza virus test negative Pain in extremity SARS-CoV-2 test positive

Symptomtext

Participant has breakthrough case of COVID 01/04/2022. Mild sore arm. Still don't have my sense of smell or taste back entirely.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: Covid Test -Positive. Flu -Neg.
Aktuelle Erkrankungen: No
Vorgeschichte: Lymphocytic colitis
Andere Medikamente: Vitamin D, Fish Oil, Calcium, Sertraline 100mg 1x daily, Meloxicam
Allergien: Red dye, Monistat
Vorherige Impfungen: FLU vaccines with Thermasol caused allergic reaction. FLU vaccines without I am fine

VAERS 2066145

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: OR
Alter: 73,0
Geschlecht: F
Eingang: 26.01.2022
Impfdatum: 27.10.2021
Beginn: 30.12.2021
Tage bis Beginn: 64,0
Dosis: 3
Route/Site: IM / RA

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

Pain in extremity Peripheral swelling Phlebitis

Symptomtext

At the end of December, I noted that when I woke up in the morning that my left calf was painful. I walk on a daily basis: 2 miles a day. I proceeded to do that later in the morning. In the next morning, it was too painful to do my usual walk so I did 2 laps. By new year's I didn't walk because it was too painful. After new year's, I decided to push through the pain and go for a walk and could only do half of what I normally do. So because the leg was swollen and there was a lump on the outer portion of my left calf, I decided to call the doctor. After consulting with him, he said it was phlebitis. And he put me on Eliquis 10mg twice daily for one week, and he said to cut back to 5mg twice daily after that week and he said to check in with him after 3-4 months. It has slowly resolved and I would say it took 10 days until it really felt good enough to continue walking again. So now I continue to walk but only 1 ? miles daily because I do not want to aggravate it.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Hx of DVT, Inferior vena cava plication from historic reaction to hormone from birth control
Andere Medikamente: Chlorthalidone
Allergien: Sulfa Drugs; Contrast Dye; Seasonal allergies
Vorherige Impfungen: -

VAERS 2066017

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: CT
Alter: 34,0
Geschlecht: F
Eingang: 26.01.2022
Impfdatum: 02.11.2021
Beginn: 13.11.2021
Tage bis Beginn: 11,0
Dosis: 3
Route/Site: IM / LA

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

Allergy test Urticaria Urticaria chronic

Symptomtext

Developed spontaneous urticaria several days after injection, requiring daily Zyrtec for the unforeseeable future. I have never had reactions like this in the past. I now have chronic urticaria after the injection.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Urticaria
Hospital-Tage: -
Labordaten: Urgent care visit (11/15) Allergy panel (11/19) PCP visit (11/19) Allergy consultation & follow up (1/3/22 & 1/31/22)
Aktuelle Erkrankungen: N/A
Vorgeschichte: PTSD, depression
Andere Medikamente: Lexapro 10 mg daily
Allergien: N/A
Vorherige Impfungen: Large local reaction

VAERS 2060292

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: PA
Alter: 25,0
Geschlecht: M
Eingang: 24.01.2022
Impfdatum: 05.11.2021
Beginn: 23.11.2021
Tage bis Beginn: 18,0
Dosis: 3
Route/Site: IM / LA

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

Urticaria

Symptomtext

I break out in hives all over my body in small areas for a short period of time (15-30 minutes). Sometimes it is random, other times it is after contact with any sort of surface, material, or abrasion

Weitere VAERSDATA-Felder

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

VAERS 2057879

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: NY
Alter: 72,0
Geschlecht: M
Eingang: 23.01.2022
Impfdatum: 08.04.2021
Beginn: 16.04.2021
Tage bis Beginn: 8,0
Dosis: 3
Route/Site: SYR / LA

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

Appendicectomy Appendicitis Chills Computerised tomogram Dyspepsia Nausea X-ray

Symptomtext

Appendicitis. Removed Appendix on 04/17/2021. Chills, nausea Feeling of indigestion just below the center of the rib cage.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: They did a Cat scan and an Xray.
Aktuelle Erkrankungen: None
Vorgeschichte: Arrythmia
Andere Medikamente: None
Allergien: Vicodin
Vorherige Impfungen: -

VAERS 2043099

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: MI
Alter: 31,0
Geschlecht: F
Eingang: 18.01.2022
Impfdatum: 01.11.2021
Beginn: 14.11.2021
Tage bis Beginn: 13,0
Dosis: 3
Route/Site: SYR / LA

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

Chills Fatigue Pain in extremity Urticaria

Symptomtext

Initial reaction (same day) sore arm lasting about 3 days, heavy chills lasting about 7 hours, fatigue lasting about 24 hours. 14 days later, full body systemic hives lasting several days. hives erupted 11/14. initially treated with benadryl. Medical treatment sought 11/18. Given an injection of depo-medrol and a prednisone burst, advised to continue benadryl and add pepcid. Hives lasted approximately 1 week.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Hashimotos Thyroiditis, allergic rhinitis, epistaxis, unexplained uterine bleeding
Andere Medikamente: Levothyroxine, Zyrtec, Birth Control Pill, Singular, and multivitamin
Allergien: N/A
Vorherige Impfungen: -

VAERS 2042027

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: MA
Alter: 65,0
Geschlecht: M
Eingang: 18.01.2022
Impfdatum: 06.01.2022
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: OT / -

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

Hypoacusis Neck pain SARS-CoV-2 test

Symptomtext

Lost his hearing in a 90% for almost 5 hours/I couldn't hear anything/he hear himself with a squeaky voice, but patient wife mention could her Patient with regular normal voice; Lower back pain moved up to his neck; This spontaneous case was reported by a consumer and describes the occurrence of HYPOACUSIS (Lost his hearing in a 90% for almost 5 hours/I couldn't hear anything/he hear himself with a squeaky voice, but patient wife mention could her patient with regular normal voice) and NECK PAIN (Lower back pain moved up to his neck) in a 65-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 071F21A) for COVID-19 vaccination. Previously administered products included for COVID-19 vaccination: COVID-19 VACCINE NRVV AD26 (JNJ 78436735). Past adverse reactions to the above products included No adverse event with COVID-19 VACCINE NRVV AD26 (JNJ 78436735). Concurrent medical conditions included Low back pain (treated with painkiller). On 06-Jan-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On an unknown date, the patient experienced HYPOACUSIS (Lost his hearing in a 90% for almost 5 hours/I couldn't hear anything/he hear himself with a squeaky voice, but patient wife mention could her Patient with regular normal voice) and NECK PAIN (Lower back pain moved up to his neck). At the time of the report, HYPOACUSIS (Lost his hearing in a 90% for almost 5 hours/I couldn't hear anything/he hear himself with a squeaky voice, but patient wife mention could her Patient with regular normal voice) had resolved and NECK PAIN (Lower back pain moved up to his neck) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, SARS-CoV-2 test: negative (Negative) Negative. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter considered NECK PAIN (Lower back pain moved up to his neck) to be related. No further causality assessment was provided for HYPOACUSIS (Lost his hearing in a 90% for almost 5 hours/I couldn't hear anything/he hear himself with a squeaky voice, but patient wife mention could her Patient with regular normal voice). No concomitant product was provided. No treatment information was provided. The patient could hear himself with a squeaky voice, but patient wife mention she could hear the Patient with his regular normal voice. No expiration date available on vaccination card.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Neck pain
Hospital-Tage: -
Labordaten: Test Name: COVID-19 virus test; Test Result: Negative; Result Unstructured Data: Negative.
Aktuelle Erkrankungen: Low back pain (treated with painkiller.)
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2040468

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: MS
Alter: 25,0
Geschlecht: F
Eingang: 17.01.2022
Impfdatum: 27.12.2021
Beginn: 27.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Aphasia Computerised tomogram Dysphagia Eyelid ptosis Headache Hypoaesthesia Laboratory test

Symptomtext

Left eye droop (2hours) Unable to swallow or talk (30seconds intermediate for 4 hours) Both arms numb (2 days) Severe headache (14 days )

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: CT scan 01/06/2022 Lab work01/06/2022
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2038356

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071f21a

mild

Staat: VT
Alter: 83,0
Geschlecht: F
Eingang: 16.01.2022
Impfdatum: 23.12.2021
Beginn: 26.12.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / LA

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

Limb discomfort Pain in extremity Peripheral swelling

Symptomtext

First two COVID-19 vaccinations were Pfizer - patient complained that left arm was "lame" from the elbow down. They could not lift their arm and it "felt swollen" and heavy.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: none known of
Aktuelle Erkrankungen: none that they know of
Vorgeschichte: -
Andere Medikamente: flovent hfa Losartan simvastatin esomperazole famotidine nabumetone
Allergien: codeine penicillin sulfa
Vorherige Impfungen: -

VAERS 2031568

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: KS
Alter: 25,0
Geschlecht: M
Eingang: 13.01.2022
Impfdatum: 02.12.2021
Beginn: 15.12.2021
Tage bis Beginn: 13,0
Dosis: 3
Route/Site: SYR / RA

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

Urticaria

Symptomtext

Repeatedly breaking out into hives - Treated with antihistamine

Weitere VAERSDATA-Felder

Praegender Schweregrund: Urticaria
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: Ichthyosis
Andere Medikamente: N/A
Allergien: Amoxicillin
Vorherige Impfungen: -

VAERS 2027857

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071f21a

mild

Staat: NH
Alter: 40,0
Geschlecht: F
Eingang: 12.01.2022
Impfdatum: 02.12.2021
Beginn: 03.12.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: SYR / LA

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

Dysgeusia Ear discomfort Oropharyngeal pain Pruritus Sleep disorder Swollen tongue Throat irritation Urticaria

Symptomtext

About 36 hours after booster shot I woke up in the night with itchy legs. The itching disapeared by the morning. On the 11th day after the booster shot my head was extremely itchy during the evening hours, the itching was gone by the morning. The 12th day in the early evening (around 3pm) my wrists were itchy, I noticed I had a single hive. By later that evening around 6pm, my legs began to itch again, this time there were multiple hives. That evening when I was about to fall asleep I suddenly (within a matter of 5 mins or less) developed a soar throat and then the taste of chemicals in my mouth, my throat was starting to burn. I woke up several times throughout the night to burning in my throat and the taste of chemicals in my mouth and throat that I needed to try to cough out. The next morning was throat was raw and soar but the chemical taste was gone, the hives were still present and would appear and disapear in different places on my body throughout the day and were very itchy. On the 13th day my ears began to extremely burn and itch and their was pressure in my ears as well. My tongue felt swollen so I decided to call my dr. we tried OTC benadryl, allegra pepcid to no avail. after 21 days i went back to the dr and he prescribed me steroids and prescription strenght antihistamines. I am waiting to see if it helps

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: not yet
Aktuelle Erkrankungen: NA
Vorgeschichte: NA
Andere Medikamente: NA
Allergien: Sulfa allergy
Vorherige Impfungen: -

VAERS 2019703

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: NC
Alter: 61,0
Geschlecht: F
Eingang: 09.01.2022
Impfdatum: 16.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / RA

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

Chills Influenza like illness Insomnia Pain Pyrexia

Symptomtext

Began running a fever overnight. I had chills all night and didn't sleep well. I realized why in the morning when I took my temperature and it was 100.4. I was achy and felt like I had the flu all day. My fever went as high as 102.2 before I finally took Advil which brought it down to about 100 before it started going up again. By evening I was fever free and felt better the next day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Levothyroxin, multi-vitamin, vitamin D, Zinc, B Complex, Zyrtec
Allergien: None
Vorherige Impfungen: -

VAERS 2014186

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: FL
Alter: 55,0
Geschlecht: M
Eingang: 07.01.2022
Impfdatum: 21.12.2021
Beginn: 03.01.2022
Tage bis Beginn: 13,0
Dosis: 3
Route/Site: IM / RA

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

Balance disorder Dizziness Nausea Nystagmus SARS-CoV-2 test negative Vertigo Vestibular neuronitis

Symptomtext

Sudden acute vertigo presumably triggered by vestibular neuritis. Symptoms include nystagmus, dizziness, nausea and loss of balance. Symptoms are slowly subsiding at day 4.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: Negative COVID RAT on 01/05/2022
Aktuelle Erkrankungen: -
Vorgeschichte: GERD Nasal allergies
Andere Medikamente: Flonase Protonix
Allergien: -
Vorherige Impfungen: -

VAERS 2005901

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: FL
Alter: 65,0
Geschlecht: F
Eingang: 05.01.2022
Impfdatum: 10.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 7,0
Dosis: 3
Route/Site: ID / RA

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

Burning sensation Electromyogram normal Nerve conduction studies normal Pain in extremity Sensory disturbance Small fibre neuropathy

Symptomtext

Approximately a week after I received Moderna Covid booster, I started experience sharp pains in my both feet. The pain developed into small fiber neuropathy like symptoms (burning feet, pain everywhere in feet, unusual and bothersome sensations in feet). A trip to a podiatrist resulted in the doctor's suggestion that I get a NVC/EMG tests. Both tests gave NORMAL results, I have no preexisting conditions, and, unfortunately only now found out that my symptoms could've been caused by the Covid Vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: NVC/EMG NORMAL on 01/04/1922.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Vitamin B Complex, Lion"s Maine, Turkey Tail
Allergien: None
Vorherige Impfungen: -

VAERS 2001079

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: CT
Alter: 57,0
Geschlecht: M
Eingang: 04.01.2022
Impfdatum: 16.12.2021
Beginn: 17.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Fatigue Nausea

Symptomtext

Extreme nausea and fatigue for two days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: High blood pressure, high cholesterol, Hypogonadism
Andere Medikamente: Enalapril, Atorvastatin, Prilosec OTC, Low dose aspirin, multivitamin , Testosterone gel
Allergien: Sulfa based medication
Vorherige Impfungen: -

VAERS 1999098

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: NC
Alter: 46,0
Geschlecht: F
Eingang: 03.01.2022
Impfdatum: 30.10.2021
Beginn: 09.11.2021
Tage bis Beginn: 10,0
Dosis: 3
Route/Site: SYR / AR

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

Lip swelling Mechanical urticaria Peripheral swelling Pruritus Urticaria

Symptomtext

Hives/itch on whole body, swelling in hands, feet, lips. Began ~10 days after injection. Treatment was two 6-day courses of Prednisone, zyrtec, allegra, benadryl. Hives mostly resolved at 8 weeks, continued dermatographia.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mechanical urticaria
Hospital-Tage: -
Labordaten: Allergist appointment scheduled for 01/05/2022
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Zyrtec, Flonase, Prozac, Wellbutrin, Liothyronine
Allergien: Trees, grasses, dust, mold.
Vorherige Impfungen: "Covid Arm" after dose 1

VAERS 1998942

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: TX
Alter: 48,0
Geschlecht: F
Eingang: 03.01.2022
Impfdatum: 01.11.2021
Beginn: 11.11.2021
Tage bis Beginn: 10,0
Dosis: 3
Route/Site: IM / RA

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

Antinuclear antibody negative Back pain Blood pH Blood test normal C-reactive protein decreased Chlamydia test negative HIV antibody negative Laboratory test normal Neck pain Neisseria test negative Pruritus Rash Red blood cell sedimentation rate normal Treponema test negative Urine analysis normal Urticaria

Symptomtext

Woke up the morning of 11/11/21 with welts and itching on front torso. Throughout the day, it migrated to other areas of the body. The morning of 11/12 the welts had combined together on back of neck and lower back causing extreme pain. Tele-doc prescribed Prednisone pack. Rash continued and was present on every part of skin including scalp. Worse at night. PCP visit on 11/19/21 and confirmed hives. Ran several blood tests to rule out other causes - all results were negative. PCP prescribed 20mg prednisone/2xdaily for 5 days. 12/2/21 went to dermatologist. Hives confirmed. Reviewed any changes made within the past 2 months and doctor indicated cause was likely COVID vaccine booster. Dermatologist administered steroid shot and indicated me to take antihistamine twice daily (2 different types). As of today 1/3/21 - hives continue, though not as severe as first 2 weeks of onset.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Back pain
Hospital-Tage: -
Labordaten: All tests conducted 11/19/21: Antinuclear Antibodies (ANA) 11 panel with screen - negative C-reactive protein (CRP) - value .10 Chlamydia, Gonorrhoeae, Trichomonas - Not Detected Erythorocyte Sedimentation Rate Automated - <2 HIV 1/2 Ab Screen w/p24Ag - Nonreactive RPR - Nonreactive Urinalysis - negative, ph 6.5
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Tamoxifen 20mg/daily
Allergien: None
Vorherige Impfungen: -

VAERS 1998840

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: CT
Alter: 33,0
Geschlecht: F
Eingang: 03.01.2022
Impfdatum: 11.11.2021
Beginn: 22.11.2021
Tage bis Beginn: 11,0
Dosis: 3
Route/Site: IM / RA

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

Allergy test negative Full blood count normal Mechanical urticaria Metabolic function test normal Pruritus Red blood cell sedimentation rate normal Thyroid function test normal Urticaria

Symptomtext

Intensely itchy skin, hives and dermatographia. Started 10 days after booster on 11/22/21. Controlled with Allegra, Pepcid, Zyrtec but still unable to wean off antihistamines to date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mechanical urticaria
Hospital-Tage: -
Labordaten: Underwent extensive allergy testing to rule out other sources of allergic response, no other allergies noted. CBC, ESR, CMP, thyroid function labs all sent and normal.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1991718

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: NJ
Alter: 75,0
Geschlecht: F
Eingang: 30.12.2021
Impfdatum: 29.10.2021
Beginn: 01.11.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: OT / -

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

Cyst Pain Vaginal infection

Symptomtext

Vaginal Herpes; painful; Cyst; This spontaneous case was reported by a consumer and describes the occurrence of CYST (Cyst), VAGINAL INFECTION (Vaginal Herpes) and PAIN (painful) in a 75-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 071F21A) for COVID-19 vaccination. The patient's past medical history included Herpes infection (she had herpes sore in the past but never vaginal herpes.). Concurrent medical conditions included Drug allergy (Steroid allergy) and Sjogren's syndrome. On 29-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 08-Nov-2021, the patient experienced VAGINAL INFECTION (Vaginal Herpes). In November 2021, the patient experienced CYST (Cyst) and PAIN (painful). At the time of the report, CYST (Cyst) and VAGINAL INFECTION (Vaginal Herpes) had not resolved and PAIN (painful) outcome was unknown. The patient developed cyst which burst with sticky fluid in it and smell bad.first HCP visited and said it is not sure could be shingles. the patient think virus opened up her system and she was attacked No concomitant medications were reported No treatment information was provided

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Drug allergy (Steroid allergy); Sjogren's syndrome
Vorgeschichte: Medical History/Concurrent Conditions: Herpes infection (she had herpes sore in the past but never vaginal herpes.)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1985453

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071f21A

mild

Staat: MD
Alter: 81,0
Geschlecht: F
Eingang: 28.12.2021
Impfdatum: 01.11.2021
Beginn: 01.12.2021
Tage bis Beginn: 30,0
Dosis: UNK
Route/Site: - / -

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

Eye swelling Herpes zoster Lacrimation increased Rash Urticaria

Symptomtext

This was the booster shot. My mother developed a rash, hives and her eye drained and became swollen the next day. Each day after the booster became worse. On Saturday, December 4th, 2021, she went to Urgent Care and rushed to Hospital ER. She was diagnosed with SHINGLES.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Diabetes and Third Stage Kidney Disease, HBP, Breast cancer (treatment completed)
Vorgeschichte: HBP, Kidney Disease, Breast Cancer
Andere Medikamente: Spironolactone- 25 MG; Losartan- 50 MG; Furosemide- 40 MG; Atorvastatin Calcium Tablets- 20 MG; Metoprolol Succinate ER- 100 MG; Amlodipine Besylate- 10 MG; Lantus Glargine Injection- 100 units/ml and OTC- Extra Strength Tylenol- 650 MG
Allergien: Blood Thinners
Vorherige Impfungen: -

VAERS 1984757

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: KS
Alter: 71,0
Geschlecht: F
Eingang: 28.12.2021
Impfdatum: 26.03.2021
Beginn: 26.03.2021
Tage bis Beginn: 0,0
Dosis: N/A
Route/Site: SYR / LA

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

Balance disorder Dizziness Head injury Vertigo

Symptomtext

Slightly dizzy after injection 45 minutes after, Felt able to drive straight home. Rested on couch & more dizzy with veritigo up to 2 hours after resting.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: none. I hit my head on the pavement 12/27/2020. Since then medical exams & treatment. Results were loss of balance & further treatment.
Aktuelle Erkrankungen: none
Vorgeschichte: low thyroid, high cholesterol, low immunesystem, acid reflux, allergies--dust trees grass
Andere Medikamente: buproprion, duloxetine, lorazapam, lamotragine, synthroid, rovustatin, antihistamine, loratadine
Allergien: codeine
Vorherige Impfungen: -

VAERS 1982476

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: WI
Alter: 49,0
Geschlecht: F
Eingang: 27.12.2021
Impfdatum: 13.11.2021
Beginn: 14.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Aldolase normal Ammonia normal Arthralgia Back pain C-reactive protein normal Differential white blood cell count normal Full blood count normal Impaired driving ability Loss of personal independence in daily activities Metabolic function test Musculoskeletal stiffness Myalgia Pain Pain in extremity Polymyalgia rheumatica Prothrombin time normal Pyrexia Red blood cell sedimentation rate increased

Symptomtext

I received my Moderna booster on 11/13/2021 at about 3PM. On 11/14/2021 at about 9AM, I awoke with muscle pain in the upper body, as well as joint pain and stiffness that were also primarily in the upper body. I took a full dose of oxycontin and oxycodone, but they helped the pain only slightly. The pain was so intense that standing, bending, reaching, and turning my head were very difficult. My husband had to help me with basic tasks, such as dressing myself, retrieving items from cabinets, and getting into my vehicle. I was also unable to drive. I was unable to roll over in bed, and I couldn't sit up in bed without using a side rail to pull myself up. On top of all that, I also had a fever of 101.4. Aside from the fever, all of my symptoms continued on 11/15/2021. I then felt mildly better on 11/16/2021 and 11/17/2021, as the stiffness, joint pain, and muscle pain were less pronounced. Then on 11/18/2021, the pain returned to its previous intensity. It ranged between a 6 and 7 on a 1-10 scale. Oxycontin and oxycodone reduced the pain to a 4 or 5. I also began to have more pain in the lower back, hips, and thighs. On 12/10/2021, I underwent lab tests that included bloodwork for ESR, CRP, aldolase, ammonia levels, and CBC with differential were done. I also underwent a comprehensive metabolic panel and a prothrombin time test. When I got my test results on 12/18/2021, I learned my ESR levels were 43, but my CRP and aldolase levels were normal. The rest of the tests were also within my normal range. I was given a 5-day supply of 20 mg of prednisone. By 12/20/2021, I finally experienced some relief. When I saw my internist on 12/20/2021, I was diagnosed with polymyalgia rheumatica. She told me to continue taking 20 mg of prednisone daily and to return in about 4 weeks for follow-up tests and an office visit.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Heart Arrhythmias; Mitochondrial Disease; Asthma; Seizure Disorder; Gastroesophageal Reflux Disease (GERD); Gastric Ulcers; Dysautonomia; Insomnia; Chronic Pain (from Mitochondrial Disorder); Hashimoto's Disease; Gastroparesis; Dysmotility; Fatty Liver Disease
Andere Medikamente: Levocarnitine; Coenzyme Q10 (coQ10); vitamin B1; vitamin B2; vitamin E; vitamin D; vitamin B12; folate; Magnesium; Vitamin C; Nadolol; Omeprazole; Levothyroxine; Lamictal; Albuterol; Oxycodone; Oxycontin; Calcium; Trazodone; Acetyl L-carnit
Allergien: Doxycycline; Morphine; Erythromycin; Statins; Propofol; Lactated Ringers; Non-steroidal anti-inflammatory drugs (NSAIDs); Acetaminophen; Vicodin
Vorherige Impfungen: I experienced possible serum sickness from a tetanus shot in 1999.

VAERS 1975218

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: VA
Alter: 40,0
Geschlecht: F
Eingang: 23.12.2021
Impfdatum: 08.11.2021
Beginn: 12.12.2021
Tage bis Beginn: 34,0
Dosis: 3
Route/Site: SYR / LA

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

Arthralgia COVID-19 Chest discomfort Cough Fatigue Headache Myalgia Nasal congestion Rhinorrhoea SARS-CoV-2 test positive Sneezing

Symptomtext

I had a headache, muscle pain, joint pain, nasal congestion, runny nose, sneezing, coughing, chest discomfort, and fatigue. I found out I had COVID on December 16th. I had the anti body infusion on December 21st.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: At Home COVID Test- positive (December 2021) PCR COVID Test- positive (December 2021)
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma
Andere Medikamente: Zyrtec 10mg 1xday Nexium 40mg 1xday
Allergien: Tegaderm Cats Mites
Vorherige Impfungen: Covid Vaccine (2nd dose) -I had breathing problems and tachycardia. (April 9, 2021)

VAERS 1971964

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: GA
Alter: 39,0
Geschlecht: M
Eingang: 22.12.2021
Impfdatum: 22.12.2021
Beginn: 22.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Urticaria

Symptomtext

IM in left arm. Pt began having hives on right arm and chest per RN. Pt given benadryl 25 mg PO and Norco 5/325 PO.

Weitere VAERSDATA-Felder

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

VAERS 1964437

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: NJ
Alter: 47,0
Geschlecht: M
Eingang: 20.12.2021
Impfdatum: 08.11.2021
Beginn: 21.11.2021
Tage bis Beginn: 13,0
Dosis: UNK
Route/Site: IM / -

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

Urticaria

Symptomtext

Hives all over the body, treating with xyzal or zyrtec. Symptoms started Day 13 after booster shot

Weitere VAERSDATA-Felder

Praegender Schweregrund: Urticaria
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Crestor 10 MG
Allergien: No
Vorherige Impfungen: -

VAERS 1964016

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: FL
Alter: 31,0
Geschlecht: M
Eingang: 20.12.2021
Impfdatum: 01.12.2021
Beginn: 10.12.2021
Tage bis Beginn: 9,0
Dosis: 3
Route/Site: IM / LA

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

Eyelid function disorder Pruritus Rash Rash erythematous Rash pruritic Swelling face Swelling of eyelid Urticaria

Symptomtext

Started having itching on December 10th at around 1800, went to sleep and then woke up at 0400 on December 11th and noted to have hives all over my body including my face, took OTC Benadryl and the hives subsided but itching remained throughout the day. Supplemented with OTC Allegra later in the day and continued to monitor. Woke up on December 12th at 0233am and noted to have severe swelling on my face, left eyelid almost closed shut, right eyelid starting to swell up as well. Hives noted all over my body. Took another benadryl and slept again. Woke up at 9am with the symptoms unresolved. Informed my PCP and got prescribed and medrol dose pack. Started taking this on December 12th at noon. Over the next several hours the facial swelling subsided but the hives remained and appeared in various portions of my body intermittently. Over the next several days there was no more swelling/angioedema and the hives have gone away but still getting intermittent red rashes and still continue to itch. As of Dec 20th at 1700, still noted to have intermittent itching and rashes sporadically on my extremities / face and have been managing symptoms with OTC allegra and OTC famotidine.

Weitere VAERSDATA-Felder

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

VAERS 1963202

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: TX
Alter: 39,0
Geschlecht: F
Eingang: 20.12.2021
Impfdatum: 19.11.2021
Beginn: 30.11.2021
Tage bis Beginn: 11,0
Dosis: 3
Route/Site: SYR / LA

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

Ear swelling Rash Urticaria

Symptomtext

Severe Hives all over body that led to a trip to the emergency room on Wed, 12/1/2021. My ears swelled up to the point they were sticking out so far I looked like a monkey. I told the ER that I had recently had my Moderna booster, but they did not think that was the reason I was breaking out. Got an IV of Benadryl and steroids, and they urged me to get an appt with an allergist since we didn't know what had caused my reaction. By Friday I was still breaking out. Got an appt to see an allergist on Sat, 12/4/2021. When I went in to allergist and we went through a list of symptoms. After going through a laundry list of things that could have caused the out break, I told them about my booster. She immediately felt that was what caused the outbreak. I have been taking 3-4 Allegra a day for about 2 weeks, and using topical cream as needed. Some days I am ok, but other days my hives are quite bad.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Allegra
Allergien: None
Vorherige Impfungen: -

VAERS 1962454

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071f21a

mild

Staat: NY
Alter: 39,0
Geschlecht: F
Eingang: 19.12.2021
Impfdatum: 14.11.2021
Beginn: 24.11.2021
Tage bis Beginn: 10,0
Dosis: 3
Route/Site: - / LA

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

Erythema Feeling abnormal Musculoskeletal stiffness Pain Pain in extremity Pruritus Urticaria

Symptomtext

After I went to bed on Nov 24th, I noticed I was very itchy and my right leg ached. I was vaguely remembered something like that happening about a week after my first or second Moderna shot so I didn't think much of it. However on the 25th the itchiness continued. Eventually it became severe enough that I looked in the a mirror and was shocked at how red my skin was. The rash seemed to move around my body, coming and going. By evening it wasn't just red but raised welts and painful. I could even feel welts in my ear canals. The skin on the back of my head and neck felt weird and stiff. I went to urgent care the next day. The provider there didn't know what caused it and did not believe it is related to the vaccine, and gave me a steroid shot and prescriptions for oral steroids and antihistamines. By that evening the itchiness has spread to the palms of my hands and bottoms of my feet. However the sensation was less painful and itchy and I was able to sleep. The next day I didn't feel itchy, however my skin was very prone to getting red where touched. This continued even after I ran out of steroids after 10 days. I saw a dermatologist who was convinced it was from the vaccine, doesn't want me to get any more covid shots, and urged me to see an allergist. I will be seeing an allergist on 12/20/21. In preparation for this I stopped taking the antihistamine on 12/13 and the itching has become quite severe again but the welts are not as bad.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Diagnoses with strep (not tested for it though.)
Vorgeschichte: Pericardial cysts, right shoulder pain
Andere Medikamente: None
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1957838

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: FL
Alter: 38,0
Geschlecht: F
Eingang: 17.12.2021
Impfdatum: 28.10.2021
Beginn: 30.11.2021
Tage bis Beginn: 33,0
Dosis: 1
Route/Site: OT / -

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

Bedridden Body temperature Hypersensitivity Impaired work ability Lymph node pain Lymphadenopathy Neuropathy peripheral Pain Pyrexia

Symptomtext

Pain lymph node under left armpit; Swelling lymph node under left armpit; sensitivity for 4 days; Fever 103F; Left side neuropathy; With Neuropathy she could not go to work; Stayed in bed; Body aches; This spontaneous case was reported by a consumer and describes the occurrence of NEUROPATHY PERIPHERAL (Left side neuropathy) in a 38-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 071F21A and 071F21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 28-Oct-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 29-Nov-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 30-Nov-2021, the patient experienced NEUROPATHY PERIPHERAL (Left side neuropathy) (seriousness criterion medically significant), IMPAIRED WORK ABILITY (With Neuropathy she could not go to work), BEDRIDDEN (Stayed in bed), PAIN (Body aches), HYPERSENSITIVITY (sensitivity for 4 days) and PYREXIA (Fever 103F). On 04-Dec-2021, the patient experienced LYMPH NODE PAIN (Pain lymph node under left armpit) and LYMPHADENOPATHY (Swelling lymph node under left armpit). The patient was treated with IBUPROFEN for Fever, at an unspecified dose and frequency and PARACETAMOL (TYLENOL [PARACETAMOL]) for Fever, at an unspecified dose and frequency. On 03-Dec-2021, NEUROPATHY PERIPHERAL (Left side neuropathy), PAIN (Body aches), HYPERSENSITIVITY (sensitivity for 4 days) and PYREXIA (Fever 103F) had resolved. On 05-Dec-2021, IMPAIRED WORK ABILITY (With Neuropathy she could not go to work) and BEDRIDDEN (Stayed in bed) had resolved. On 06-Dec-2021, LYMPH NODE PAIN (Pain lymph node under left armpit) and LYMPHADENOPATHY (Swelling lymph node under left armpit) had resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 30-Nov-2021, Body temperature: 103 (High) Fever 103 F. Concomitant medication information was not provided by the reporter. It was reported that within 24 hours after second shot, on 30 Nov2021 she had left side neuropathy not diagnosed by MD, Fever 103F, body aches and sensitivity for 4 days. On Day 5 to 7 she had swelling and pain of lymph node under left armpit. With Neuropathy she could not go to work and stayed in bed. She did not see a doctor but reported her adverse reaction to a nurse practitioner at the clinic she normally visits. The ARNP told her to call Moderna and report her adverse reaction. Company Comment: This case concerns a 38-year-old female subject, with no medical history reported, who experienced the unexpected and serious event of Neuropathy peripheral. The event occurred 1 day after the second dose of mRNA-1273 vaccine. The rechallenge is not applicable, as no additional dosing will be given. The benefit-risk relationship of mRNA-1273 vaccine is not affected by this report. This case was linked to MOD-2021-405124 (Patient Link).; Sender's Comments: This case concerns a 38-year-old female subject, with no medical history reported, who experienced the unexpected and serious event of Neuropathy peripheral. The event occurred 1 day after the second dose of mRNA-1273 vaccine. The rechallenge is not applicable, as no additional dosing will be given. The benefit-risk relationship of mRNA-1273 vaccine is not affected by this report.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Lymph node pain
Hospital-Tage: -
Labordaten: Test Date: 20211130; Test Name: body temperature; Result Unstructured Data: Fever 103 F
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1954936

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: MA
Alter: 71,0
Geschlecht: F
Eingang: 16.12.2021
Impfdatum: 01.11.2021
Beginn: 14.11.2021
Tage bis Beginn: 13,0
Dosis: 3
Route/Site: SYR / LA

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

Blood test Rash pruritic

Symptomtext

Twelve days after the booster shot (third shot) I broke out in a rolling rash starting on the tops of my feet and the palms of my hands and the back of my elbows. It was very itchy and woke me in the nighttime. I would break out in different locations on my arms, back neck, scalp and mid-torso and occasionally on my thighs. Topical creams did not help. I contacted my physician who had me take Claritin once a day and Benadryl at night. Still the rash and itchiness did not subside. After seeing her I was put on a 5-day regimen of prednisone which did help. But for a week after completing that dosage I still needed to take the Claritin and for several days the Benadryl. Still I break out in red patches on my torso or neck, but there is no rash and no itchiness. It is as if my skin remembers the irritation and reacts.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash pruritic
Hospital-Tage: -
Labordaten: Lab blood work was done--results were normal
Aktuelle Erkrankungen: None
Vorgeschichte: arthritis, high cholesterol (take medication), thyroid (take medication)
Andere Medikamente: Synthroid Tab 75MCG, Lovastatin Tab40MG,Fluticasone spray 50mcg, D3 1,000IU, Calcium Gummies 500mg
Allergien: None
Vorherige Impfungen: Some soreness, tiredness and ashiness after first two covid shots and slight rash at shot site after second shot two weeks after

VAERS 1950926

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071f21a

mild

Staat: NY
Alter: 44,0
Geschlecht: F
Eingang: 15.12.2021
Impfdatum: 28.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Injection site erythema Injection site swelling

Symptomtext

Site: Redness at Injection Site-Medium, Site: Swelling at Injection Site-Mild

Weitere VAERSDATA-Felder

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

VAERS 1944073

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: NC
Alter: 66,0
Geschlecht: F
Eingang: 13.12.2021
Impfdatum: 01.11.2021
Beginn: 11.11.2021
Tage bis Beginn: 10,0
Dosis: 3
Route/Site: SYR / LA

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

Decreased appetite Headache Injection site pain Nausea Pyrexia Thirst

Symptomtext

Lasted continuously for 4 days after onset: symptoms included high fever, severe headache, thirst beyond normal, suppressed hunger, nausea, sore injection site, all of which gradually tapered off on the fourth day. Did not seek medical treatment, increased fluid intake & bed rest.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: Rhino allergies
Vorgeschichte: Severe 0steo Arthritis (early onset)
Andere Medikamente: Adderall, Methadone, Neurontin, metoclopramide, ClaratinD 24, estradiol, Montelukast, Duloxetine HCL DR.
Allergien: No
Vorherige Impfungen: -

VAERS 1943648

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: OH
Alter: 55,0
Geschlecht: F
Eingang: 13.12.2021
Impfdatum: 02.12.2021
Beginn: 03.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / -

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

Dysphonia Lymphadenopathy Nasal congestion Nausea Oropharyngeal pain Pain Pyrexia Throat tightness

Symptomtext

Patient stated within 24 hours throat felt tight, sore and she became hoarse. Patient also stated she felt nauseated, body aches and had a low-grade fever. Within the first 5 days, she also experienced nasal congestion and swollen lymph nodes under arms. She continues to have nasal congestion and swollen lymph nodes. Took OTC Benadryl, Motrin, Advil and Aleve.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Nausea
Hospital-Tage: -
Labordaten: States has PCP appointment scheduled for 12/14/2021.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Hormone patch
Allergien: Unknown
Vorherige Impfungen: -

VAERS 1942536

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: PA
Alter: 84,0
Geschlecht: M
Eingang: 12.12.2021
Impfdatum: 13.11.2021
Beginn: 13.11.2021
Tage bis Beginn: 0,0
Dosis: N/A
Route/Site: IM / LA

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

Chills Injection site erythema Injection site pruritus Injection site swelling Pyrexia

Symptomtext

ITCHING, REDNESS AND SWELLING OF INJECTION SITE; FEVER, CHILLS.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: OVER ACTIVE BLADDER, GLAUCOMA, ASTHMA
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1942405

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071f21a

mild

Staat: WI
Alter: 36,0
Geschlecht: F
Eingang: 11.12.2021
Impfdatum: 13.11.2021
Beginn: 25.11.2021
Tage bis Beginn: 12,0
Dosis: 3
Route/Site: IM / RA

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

Pruritus Urticaria

Symptomtext

Hives and itchy spots on chest, neck, face, arms and scalp

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: No illness but I am breastfeeding
Vorgeschichte: -
Andere Medikamente: Prenatal vitamin
Allergien: None
Vorherige Impfungen: -

VAERS 1936169

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: SC
Alter: 65,0
Geschlecht: M
Eingang: 09.12.2021
Impfdatum: 03.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 14,0
Dosis: 3
Route/Site: SYR / LA

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

Pruritus Urticaria

Symptomtext

Severe acute urticaria from groin to neck. Initial treatment at Urgent Care - Cortisone injection and 6 day Prednisolone. Daily Zyrtec. Benadryl as needed apply Sarna Anti-itch cream to affected areas to relieve itch. Apply diphehydramine gel if needed Primary Care physician added daily Pepcid tablet and advised to continue topical treatment as required. Referred to Allegy specialist. Allergy specialist recommended increasing Zyrtec to 2 tablets in morning and Pepcid 1 tablet at night with guidance to increase as high as 4 or each if required. As symptoms subside gradually wean off of Zyrtec and Pepcid. Follow up appointment on February 16, 2022

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Epilepsy, Elevated intraocular pressure,pre-hypertension
Andere Medikamente: Atorvastatin, Amoldopine, Carbamazepine, Alphagan, Xalatan
Allergien: None
Vorherige Impfungen: -

VAERS 1935615

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: TN
Alter: 54,0
Geschlecht: M
Eingang: 09.12.2021
Impfdatum: 30.10.2021
Beginn: 31.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Arthralgia Back pain Chills Decreased appetite Fatigue Headache Illness Injection site pain Pain Pain in extremity Pyrexia

Symptomtext

all symptoms started the morning after on 10/31/21 - fever 103, chills, severe hip pain , severe upper back pain, lower back pain that radiated into right knee, pain in both knees, pain in both hands especially knuckles/ fingers, pain at injection sight, very fatigued, no appetite. severe headache. Took ibuprofen for symptoms which slightly helped for just a couple of hours then fever was back and all other symptoms increased. There was little improvement with anything I did. This went on for just over 24 hours. The Fatigue continued for the rest of the week. I was more sick from the mandated shot then when I actually had covid.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: Covid September 24th start
Vorgeschichte: none
Andere Medikamente: none
Allergien: Vicodin
Vorherige Impfungen: flu shot about 8 years ago - had a rash

VAERS 1931759

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: FL
Alter: 38,0
Geschlecht: F
Eingang: 08.12.2021
Impfdatum: 28.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / -

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

Decreased appetite Fatigue Lymph node pain Lymphadenopathy

Symptomtext

Pain lymph node after first shot; Swelling lymph node after first shot; Loss of appetite after first shot; Fatigue after first shot; This spontaneous case was reported by a consumer and describes the occurrence of DECREASED APPETITE (Loss of appetite after first shot), LYMPH NODE PAIN (Pain lymph node after first shot), FATIGUE (Fatigue after first shot) and LYMPHADENOPATHY (Swelling lymph node after first shot) in a 38-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 071F21A) for COVID-19 vaccination. No Medical History information was reported. On 28-Oct-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 28-Oct-2021, the patient experienced DECREASED APPETITE (Loss of appetite after first shot) and FATIGUE (Fatigue after first shot). On 02-Nov-2021, the patient experienced LYMPH NODE PAIN (Pain lymph node after first shot) and LYMPHADENOPATHY (Swelling lymph node after first shot). On 01-Nov-2021, DECREASED APPETITE (Loss of appetite after first shot) and FATIGUE (Fatigue after first shot) had resolved. On 04-Nov-2021, LYMPH NODE PAIN (Pain lymph node after first shot) and LYMPHADENOPATHY (Swelling lymph node after first shot) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. No concomitant medications reported. No treatment information was provided. This case was linked to MOD-2021-405144 (Patient Link).

Weitere VAERSDATA-Felder

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

VAERS 1846237

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: GA
Alter: 55,0
Geschlecht: F
Eingang: 08.12.2021
Impfdatum: 03.11.2021
Beginn: 06.11.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / LA

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

Lip pain Lip swelling Oral herpes Urticaria

Symptomtext

This is an addendum to my Agency report filed at the Health Center on 11/4/2021. On 11/6/2021 I experienced hives and continued having swelling of my lips. I have not ever had lip fillers or injections. I continue to have intermittent lip swelling and hives several times a week. Each time I take Benedryl which relieves the symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Lip pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: overweight
Andere Medikamente: One A Day multivitamin; vitamin D
Allergien: no known allergies
Vorherige Impfungen: -

VAERS 1927752

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: OH
Alter: 74,0
Geschlecht: F
Eingang: 07.12.2021
Impfdatum: 29.11.2021
Beginn: 29.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / RA

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

Arthralgia Asthenia Body temperature Feeding disorder Pyrexia Somnolence

Symptomtext

Could not eat anything; Could not get off toilet because weak; Temperature of 100.6; Achy by the hip; In bed all day sleeping; This spontaneous case was reported by a consumer and describes the occurrence of SOMNOLENCE (In bed all day sleeping), FEEDING DISORDER (Could not eat anything), ASTHENIA (Could not get off toilet because weak), PYREXIA (Temperature of 100.6) and ARTHRALGIA (Achy by the hip) in a 74-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 071F21A) for COVID-19 vaccination. No medication history information was provided. Previously administered products included for Product used for unknown indication: Johnson and Johnson (Received the Johnson and Johnson regular dose for the primary series in April 2021.) until April 2021. Past adverse reactions to the above products included No adverse event with Johnson and Johnson. Concomitant products included ATENOLOL, AMLODIPINE, FOLIC ACID, LEVOTHYROXINE and SULFASALAZINE for an unknown indication. On 29-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 29-Nov-2021, the patient experienced SOMNOLENCE (In bed all day sleeping). On 30-Nov-2021, the patient experienced FEEDING DISORDER (Could not eat anything), ASTHENIA (Could not get off toilet because weak), PYREXIA (Temperature of 100.6) and ARTHRALGIA (Achy by the hip). At the time of the report, SOMNOLENCE (In bed all day sleeping), FEEDING DISORDER (Could not eat anything), ASTHENIA (Could not get off toilet because weak), PYREXIA (Temperature of 100.6) and ARTHRALGIA (Achy by the hip) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 30-Nov-2021, Body temperature: 100.6 (High) 100.6. No treatment medications were provided. Reporter stated that his daughter also received the vaccine, and did not have any symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: Test Date: 20211130; Test Name: Body temperature; Result Unstructured Data: 100.6
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: No medication history information was provided
Andere Medikamente: ATENOLOL; AMLODIPINE; FOLIC ACID; LEVOTHYROXINE; SULFASALAZINE
Allergien: -
Vorherige Impfungen: -

VAERS 1924739

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: TX
Alter: 45,0
Geschlecht: M
Eingang: 06.12.2021
Impfdatum: 13.11.2021
Beginn: 22.11.2021
Tage bis Beginn: 9,0
Dosis: 3
Route/Site: SYR / LA

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

Pruritus Rash Urticaria

Symptomtext

Full body hives. Started in torso and genitals and worked way through whole body. Did a round of steroids for 5 days. Rash is still present. Zyrtec seems to help relieve the hives and itching. Needs to be taken daily. Without it hives start again. Hives are still present as of 12/6/21. Booster Vaccine is the only thing different in all of lifestyle.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: High blood pressure
Andere Medikamente: Lisinopril, amlodipine
Allergien: None
Vorherige Impfungen: -

VAERS 1924518

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: NY
Alter: 47,0
Geschlecht: F
Eingang: 06.12.2021
Impfdatum: 09.11.2021
Beginn: 18.11.2021
Tage bis Beginn: 9,0
Dosis: 3
Route/Site: IM / LA

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

Dry skin Rash Rash papular

Symptomtext

Developed a rash on my back and neck, raised, dry, patchy areas slightly raised. Of note, as a healthcare provider several other colleagues also noted a similar rash 7-10 days after receiving booster MRNA vaccine. This is a minor inconvenience but fascinating and worth sharing in the event others note a rash.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: NA
Aktuelle Erkrankungen: NA
Vorgeschichte: Hypothyroid, migraines
Andere Medikamente: Tooamax, Armour Thyroid
Allergien: NA
Vorherige Impfungen: -

VAERS 2563180

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: -
Alter: 45,0
Geschlecht: F
Eingang: 04.12.2021
Impfdatum: 27.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Headache Pain Pyrexia

Symptomtext

Headache, Fever body ache Narrative:

Weitere VAERSDATA-Felder

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

VAERS 1919765

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: -
Alter: 61,0
Geschlecht: F
Eingang: 03.12.2021
Impfdatum: 24.11.2021
Beginn: 28.11.2021
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: OT / -

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

Headache Pain

Symptomtext

Achy; Headachy; This spontaneous case was reported by a consumer and describes the occurrence of PAIN (Achy) and HEADACHE (Headachy) in a 61-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 071F21A) for COVID-19 vaccination. No Medical History information was reported. On 24-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 28-Nov-2021, the patient experienced PAIN (Achy) and HEADACHE (Headachy). The patient was treated with PARACETAMOL (TYLENOL [PARACETAMOL]) for Adverse event, at an unspecified dose and frequency. At the time of the report, PAIN (Achy) and HEADACHE (Headachy) outcome was unknown. Patient also reports being on 2 or 3 daily regular medications before the vaccine. Patient reports similar late onset reactions from the second dose. This case was linked to MOD-2021-046491 (Patient Link).

Weitere VAERSDATA-Felder

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

VAERS 1919234

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: -
Alter: 80,0
Geschlecht: F
Eingang: 03.12.2021
Impfdatum: 10.03.2021
Beginn: 03.11.2021
Tage bis Beginn: 238,0
Dosis: 2
Route/Site: OT / -

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

Skin exfoliation Swelling face Urticaria

Symptomtext

This spontaneous report received from a patient concerned an 80 year old female. The patient's height, and weight were not reported. The patient's pre-existing medical conditions included: The patient had no known allergies and was not pregnant at the time of vaccination. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1805031 expiry: UNKNOWN) dose was not reported,1 total administered on 10-MAR-2021 for prophylactic vaccination (dose series 1). Non-company suspect vaccine included: MRNA 1273 (batch number: 071F21A expiry: UNKNOWN, form of admin, route of admin, and were not reported) dose was not reported, administered on 28-OCT-2021 for prophylactic vaccination (dose series 2). No concomitant medications were reported. On 03-NOV-2021 following vaccination with MRNA 1273, the patient experienced some hives which was getting worse and also had swollen face, scaly face, hives on face and arm and hives were causing very bad itching (dose series 2) for which patient applied water, Vaseline, cream and possibly milk. The action taken with covid-19 vaccine ad26.cov2.s and MRNA 1273 was not applicable. The patient had not recovered from hives on face and arm / hives causing bad itching, swollen face, and scaly face. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Urticaria
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: The patient had no known allergies.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1917984

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: SD
Alter: 32,0
Geschlecht: F
Eingang: 02.12.2021
Impfdatum: 03.11.2021
Beginn: 15.11.2021
Tage bis Beginn: 12,0
Dosis: 3
Route/Site: IM / LA

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

Mechanical urticaria Urticaria

Symptomtext

Urticaria and symptomatic dermatographism, intermittent, responds to Zyrtec, still happening now but seems to be improving

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mechanical urticaria
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1917123

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: GA
Alter: 49,0
Geschlecht: F
Eingang: 02.12.2021
Impfdatum: 27.10.2021
Beginn: 29.11.2021
Tage bis Beginn: 33,0
Dosis: 3
Route/Site: IM / RA

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

Arthralgia Back pain Bone pain Feeling abnormal Pain

Symptomtext

I have been having general aches and pains in my joints and bones. I do have some arthritis but this is totally different because I usually don't have pain like this. I started feeling odd a couple of days ago. Every time I get up from sitting my back would get to hurting. When I sit back down it would stop, but then I would still feel the aches. I do have bone spurs and so those would hurt too. When I had got home that day I just ended up going to bed because I was hurting so much. When I got up I took my steroid for my bone spurs. Since taking the steroid I have been feeling better. It has helped with some of the pain in my joints and bones. When I went to bed that first night I couldn't even move because it hurt. It is hard to rest or move after getting up. I am feeling better now than what I did on the original day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Citalopram 40mg 1xday Flonase 1xday Omeprazole 40mg 1xday Progesterone 100mg 1xday Zyrtec 10mg 1xday Multivitamin Glucosamine and Chondroitin 2xday Vitamin D Viviscal 2xday Estroven
Allergien: Levaquin Doxycycline
Vorherige Impfungen: -

VAERS 1916463

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: TX
Alter: 66,0
Geschlecht: F
Eingang: 02.12.2021
Impfdatum: 27.10.2021
Beginn: 27.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Fatigue Headache Pain in extremity

Symptomtext

I had extreme fatigue, headaches and tired and sore arm. It went away after a couple days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Thyroid, Cholesterol
Andere Medikamente: Atorvastatin, Levothyroxine
Allergien: Sulpha Drugs, Food Allergies
Vorherige Impfungen: -

VAERS 1914257

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: CA
Alter: 34,0
Geschlecht: F
Eingang: 01.12.2021
Impfdatum: 30.10.2021
Beginn: 13.11.2021
Tage bis Beginn: 14,0
Dosis: 3
Route/Site: IM / LA

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

Erythema Mechanical urticaria Pruritus Skin test positive Urticaria

Symptomtext

I developed Dermatographia on November 13 (two weeks after booster dose of Moderna). I have full body hives with itching and redness. The hives would appear, linger for around 30 minutes, disappear, and then start somewhere else. I began taking Benadryl regularly for itching. I went to a local urgent care on November 15 and was prescribed a 6 day pack of Methylprednisolone, once daily Pepcid, and Triamcinolone Acetonide topical cream. I was also told to continue Bendaryl use. The itching and hives continue unabated with momentary relief from Benadryl. The topical cream helped a little. I saw my primary care doctor on November 18 and she suggested Allegra instead of Benadryl. I tried that for one day but the itching was unbearable so I switched back to Benadryl. On November 23 I went to urgent care again and was given a steroid shot in the bum and told to try liquid Benadryl. At this point the slightest touch made me break out in hives within 2-3 mins. The hives and red marks continued to dissipate after 30 mins. On November 29 I saw a dermatologist and was diagnosed with Dermatographia. The prescribed regime at the moment is 2x daily Claritin - once in the morning and once in the evening. I'm still getting the hives but they are much less itchy. If the itching gets worse the dermatologist recommended x3 daily Claritin - two in the am and one in the evening.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mechanical urticaria
Hospital-Tage: -
Labordaten: Dermatographia is identified by a skin swipe test to see if the patient breaks out in hives when lines are lightly drawn on the skin. I did within 2 mins.
Aktuelle Erkrankungen: none
Vorgeschichte: two acute cases of ITP (2002; 2019); platelet counts currently normal
Andere Medikamente: Low-Osgestrel, Claritin-D
Allergien: sulpha, codein
Vorherige Impfungen: -

VAERS 1913513

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: TX
Alter: 69,0
Geschlecht: F
Eingang: 01.12.2021
Impfdatum: 30.10.2021
Beginn: 24.11.2021
Tage bis Beginn: 25,0
Dosis: 3
Route/Site: SYR / RA

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

Fatigue Urinary tract infection Urine analysis abnormal

Symptomtext

I had extreme fatigue. I went to the doctor on 11/26/2021. They said I had an urinary track infection. I was prescribed antibiotics for nitrofurantoin 100mg 2xday for 7 days.

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Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Urinalyses- found UTI (11/26/2021)
Aktuelle Erkrankungen: None
Vorgeschichte: I don't want to add them.
Andere Medikamente: Pramipexole 1.5mg 1xday Alendronate Sodium tablets 70mg 1xweek
Allergien: None
Vorherige Impfungen: -

VAERS 1909021

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: NC
Alter: 57,0
Geschlecht: F
Eingang: 30.11.2021
Impfdatum: 23.11.2021
Beginn: 24.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Injection site erythema Injection site pain Injection site swelling Pyrexia

Symptomtext

Site: Pain at Injection Site-Medium, Site: Redness at Injection Site-Medium, Site: Swelling at Injection Site-Medium, Systemic: Fever-Mild.

Weitere VAERSDATA-Felder

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

VAERS 1906133

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: IL
Alter: 31,0
Geschlecht: F
Eingang: 29.11.2021
Impfdatum: 24.11.2021
Beginn: 25.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Headache Induration Pain Pruritus

Symptomtext

gigantic wheel, hardness, itching, pain, extreme headache

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Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: previous NON covid upper respiratory infection approx 1 month prior.
Vorgeschichte: NONE
Andere Medikamente: OCP- Slynd
Allergien: Amoxicillin
Vorherige Impfungen: -

VAERS 1905501

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: OH
Alter: 93,0
Geschlecht: M
Eingang: 29.11.2021
Impfdatum: 16.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Balance disorder Gait disturbance Muscular weakness Pain in extremity

Symptomtext

Patient stated that beginning on 11/17/21 he began having a sore, achy arm all the way up to his neck that lasted 2-3 days. He also complained of losing his balance since that Wednesday. He states "his legs give out" and has to hold onto something at all times. It has been an ongoing issue since the day after his Covid Moderna Booster. He has not contacted his doctor about this issue. Encouraged him to contact doctor today. Patient saw his cardiologist on 11/18 and has another appoitment with his cardiologist on 11/29 for an echocardiogram.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Shortness of Breath, mild neuropathy
Andere Medikamente: Blood pressure medication, lipitor
Allergien: None
Vorherige Impfungen: -

VAERS 1905500

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: MD
Alter: 91,0
Geschlecht: M
Eingang: 29.11.2021
Impfdatum: 23.11.2021
Beginn: 24.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / RA

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

Asthenia Cough Influenza Pruritus Rash macular Rhinorrhoea Swelling face

Symptomtext

Flu symptoms (cough, runny nose, weak), itchy and red patches on back and face, swollen face

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Dutasteride,Lactobacillu,,Celecoxib,Preser Vision-Areds ,zinc,multivitamin,Sertraline
Allergien: -
Vorherige Impfungen: -

VAERS 1904389

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: GA
Alter: 64,0
Geschlecht: F
Eingang: 28.11.2021
Impfdatum: 06.11.2021
Beginn: 06.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Chills Fatigue Hyperhidrosis Nausea Pyrexia Vomiting

Symptomtext

Chills approximately after 6 hours, fever after 8 hours gradually increasing through the night to reach 104. Chills, sweats, vomiting lasting all night. Fever went down to 102.5 after 12 hours, subsiding after 24 hours. No medication taken to reduce the fever. Fatigue and nausea lasted 48 hours. It was the first time I had a flu shot combined with another shot, and I think it maybe why I had such a strong reaction. I did not have strong reactions to the 1st and 2nd Covid vaccines (both Moderna), ans I usually do not have a reaction to the flu shot except for a sore arm for a few days.

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Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: none
Vorgeschichte: anxiety and depression
Andere Medikamente: Lorazepam 1 mg twice a day Buproprion 300 mg QD loratadine 10mg QD
Allergien: none
Vorherige Impfungen: -

VAERS 1900033

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: ME
Alter: 35,0
Geschlecht: F
Eingang: 25.11.2021
Impfdatum: 22.11.2021
Beginn: 22.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Abdominal pain upper Exposure during pregnancy

Symptomtext

20 Weeks Pregnant. Felt constant cramping and aching on right side of lower stomach (felt like period cramps on right side ovary). Cramping and aching lasted 24 hours. Pain was moderate, never got severe, but definitely not something I was expecting.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain upper
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Hyperemesis/Morning Sickness
Vorgeschichte: -
Andere Medikamente: -
Allergien: Penicillin, Red Dye
Vorherige Impfungen: -

VAERS 1899978

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: CT
Alter: 54,0
Geschlecht: F
Eingang: 25.11.2021
Impfdatum: 04.11.2021
Beginn: 09.11.2021
Tage bis Beginn: 5,0
Dosis: 3
Route/Site: IM / LA

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

Rash

Symptomtext

Full body rash

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Anxiety, IBS, GERD
Andere Medikamente: Lorazepam, Levothyroxine, Pepcid, Multivitamin, Allegra
Allergien: Allergic to penicillin, sulfa and cephalosporins
Vorherige Impfungen: -

VAERS 1898172

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: AL
Alter: 88,0
Geschlecht: F
Eingang: 24.11.2021
Impfdatum: 19.11.2021
Beginn: 20.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / RA

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

Injection site erythema Injection site pruritus Injection site warmth Vaccination complication

Symptomtext

Patient came in stating she had an adverse reaction to a Covid immunization. She said she had some redness and itching at the injection site, as well as heat in the area. She said it was not painful and has resolved with the exception of the itching. She is contacting her prescriber for more information.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: penicillins
Vorherige Impfungen: -

VAERS 1897531

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: FL
Alter: 67,0
Geschlecht: F
Eingang: 24.11.2021
Impfdatum: 24.11.2021
Beginn: 24.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Abdominal pain upper

Symptomtext

PATIENT RECEIVED MODERNA VACCINE DOSE # 2 TO LEFT ARM AT 1:13PM, DIRECTED TO THE OBSERVATION AREA TO BE MONITORED FOR 15 MINUTES AND STARTED HAVING RIGHT UPPER QUADRANT ABD PAIN 10/10 AT 1:23. VITAL SIGNS OBTAINED, PATIENT WANTED TO GO TO URGENT CARE, PT TAKEN VIA WHEELCHAIR TO URGENT CARE.

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Praegender Schweregrund: Abdominal pain upper
Hospital-Tage: -
Labordaten: UNKNOWN AT THIS TIME
Aktuelle Erkrankungen: ADRENAL INSUFFIENCY
Vorgeschichte: -
Andere Medikamente: HYDROCORTISONE ALBUTEROL DIAZEPAM CYMBALTA PEPCID
Allergien: -
Vorherige Impfungen: -

VAERS 1892929

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: FL
Alter: 74,0
Geschlecht: F
Eingang: 23.11.2021
Impfdatum: 08.11.2021
Beginn: 09.11.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: OT / LA

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

Cheilitis Dysphagia Lip swelling Mood altered Oral discomfort Pyrexia

Symptomtext

top lip was swollen and really sore; lip was burning real bad.; lip was sore and it was hurting; lip was hurting, could not drink well cause the need to use a straw; fever of up to 102?F; fever of up to 102?F and was not talking; This spontaneous case was reported by a consumer and describes the occurrence of MOOD ALTERED (fever of up to 102?F and was not talking), LIP SWELLING (top lip was swollen and really sore), ORAL DISCOMFORT (lip was burning real bad.), CHEILITIS (lip was sore and it was hurting) and DYSPHAGIA (lip was hurting, could not drink well cause the need to use a straw) in a 74-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 071F21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concomitant products included BACLOFEN for Muscle stiffness, CITALOPRAM HYDROCHLORIDE (CITALOPRAM [CITALOPRAM HYDROCHLORIDE]), COLECALCIFEROL (VITAMIN D3), MAGNESIUM, ACETYLSALICYLIC ACID (ECOTRIN), PANTOPRAZOLE SODIUM SESQUIHYDRATE (PANTOPRAZOLE 40), AMLODIPINE BESYLATE, SIMVASTATIN, AMITRIPTYLINE and APIXABAN (ELIQUIS) for an unknown indication. On 08-Nov-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 09-Nov-2021, the patient experienced MOOD ALTERED (fever of up to 102?F and was not talking) and PYREXIA (fever of up to 102?F). On 11-Nov-2021, the patient experienced LIP SWELLING (top lip was swollen and really sore), ORAL DISCOMFORT (lip was burning real bad.), CHEILITIS (lip was sore and it was hurting) and DYSPHAGIA (lip was hurting, could not drink well cause the need to use a straw). The patient was treated with PARACETAMOL (TYLENOL [PARACETAMOL]) for Adverse event, at an unspecified dose and frequency. At the time of the report, MOOD ALTERED (fever of up to 102?F and was not talking) and PYREXIA (fever of up to 102?F) was resolving and LIP SWELLING (top lip was swollen and really sore), ORAL DISCOMFORT (lip was burning real bad.), CHEILITIS (lip was sore and it was hurting) and DYSPHAGIA (lip was hurting, could not drink well cause the need to use a straw) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 09-Nov-2021, Body temperature: 102 (High) fever of up to 102?F. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. Other concomitant medicine: torax delayed release DR 250mg for headache and isinopril 10mg for unknown indication Patient lip was really hurting and buring so care taker provide vaseline

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: Test Date: 20211109; Test Name: Fever; Result Unstructured Data: fever of up to 102?F
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: CITALOPRAM [CITALOPRAM HYDROCHLORIDE]; VITAMIN D3; MAGNESIUM; ECOTRIN; PANTOPRAZOLE 40; AMLODIPINE BESYLATE; SIMVASTATIN; AMITRIPTYLINE; ELIQUIS; BACLOFEN
Allergien: -
Vorherige Impfungen: -

VAERS 1891202

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071f21a

mild

Staat: WA
Alter: 69,0
Geschlecht: F
Eingang: 22.11.2021
Impfdatum: 01.11.2021
Beginn: 20.11.2021
Tage bis Beginn: 19,0
Dosis: 1
Route/Site: SYR / LA

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

Injection site erythema Injection site induration Injection site pain

Symptomtext

Hard red area at site of injection, very tender, still tender, no outcome yet

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: No
Vorgeschichte: Weak Aortic heart valve
Andere Medikamente: Lisinopril
Allergien: Clopidogrel
Vorherige Impfungen: -

VAERS 1889946

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: VA
Alter: 83,0
Geschlecht: M
Eingang: 22.11.2021
Impfdatum: 08.11.2021
Beginn: 20.11.2021
Tage bis Beginn: 12,0
Dosis: 3
Route/Site: - / -

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

Dizziness Fatigue Nausea

Symptomtext

Dizziness, nauseated, temp of 100.3, fatigue.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None.
Vorgeschichte: High blood pressure, high cholesterol, prostate cancer.
Andere Medikamente: -
Allergien: None.
Vorherige Impfungen: -

VAERS 1889929

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: VA
Alter: 79,0
Geschlecht: F
Eingang: 22.11.2021
Impfdatum: 08.11.2021
Beginn: 08.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / -

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

Chills Pyrexia

Symptomtext

Chills, low grade temp; took Tylenol.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None.
Vorgeschichte: Hypothyroidism.
Andere Medikamente: None.
Allergien: -
Vorherige Impfungen: -

VAERS 1888489

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: TX
Alter: 50,0
Geschlecht: F
Eingang: 21.11.2021
Impfdatum: 31.10.2021
Beginn: 31.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / RA

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

Arthralgia Movement disorder Muscle tightness Musculoskeletal stiffness Sciatica

Symptomtext

10 minutes after the shot my muscles begin to tighten up and my sciatic started hurting I couldn?t move my legs and now my muscles are stiff all my joints hurt.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Degenerative disc disease, sciatica.
Andere Medikamente: None
Allergien: Eggs, dairy, milk, licorice, cocoa, peanuts,. Mobic
Vorherige Impfungen: Influenza: anaphylactic and Hospitalization, MMR: skin bubbled, Varicella: skin bubbled

VAERS 1887661

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: TN
Alter: 33,0
Geschlecht: F
Eingang: 20.11.2021
Impfdatum: 05.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / RA

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

Culture throat Feeling abnormal Gingival bleeding Gingival blister Gingival pain Gingival swelling Mouth haemorrhage Mouth ulceration Oral discomfort Oral mucosal blistering Oral pain Oropharyngeal pain Pain in extremity Stomatitis Tongue blistering Viral test

Symptomtext

Her mouth was full of sores and blister, inside her mouth, lips and tongue; Her mouth was full of sores and blister, inside her mouth, lips and tongue; She feels she was scrooge/ She was really mad for these situation; Gums were swollen; Roof of her mouth was blistered and was very really painful/looked like raw meat; Mouth was sore, mouth was red/her mouth was full of sores; Throat hurt has gotten worse; Mouth was hurting really bad/ mouth was hurting so much that she does not want to talk anymore; Mouth was bleeding, it looked almost cut; Gums bleed when she brushed her teeth; Gums were hurting really bad; Gums were blistered; Discomfort in mouth; Sore arm; This spontaneous case was reported by a consumer and describes the occurrence of MOUTH HAEMORRHAGE (Mouth was bleeding, it looked almost cut), GINGIVAL BLEEDING (Gums bleed when she brushed her teeth), GINGIVAL PAIN (Gums were hurting really bad), GINGIVAL BLISTER (Gums were blistered) and GINGIVAL SWELLING (Gums were swollen) in a 33-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 071F21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concurrent medical conditions included Medullary cystic disease and Allergy to chemicals.Concomitant products included NALTREXONE for Medullary cystic disease, LORAZEPAM, QUETIAPINE, TIZANIDINE and MULTIVITAMIN [VITAMINS NOS] for an unknown indication. On 05-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 05-Nov-2021, the patient experienced GINGIVAL BLEEDING (Gums bleed when she brushed her teeth), GINGIVAL PAIN (Gums were hurting really bad), GINGIVAL BLISTER (Gums were blistered), ORAL DISCOMFORT (Discomfort in mouth) and PAIN IN EXTREMITY (Sore arm). On 06-Nov-2021, the patient experienced MOUTH HAEMORRHAGE (Mouth was bleeding, it looked almost cut), GINGIVAL SWELLING (Gums were swollen), ORAL MUCOSAL BLISTERING (Roof of her mouth was blistered and was very really painful/looked like raw meat), MOUTH ULCERATION (Mouth was sore, mouth was red/her mouth was full of sores), ORAL PAIN (Mouth was hurting really bad/ mouth was hurting so much that she does not want to talk anymore) and OROPHARYNGEAL PAIN (Throat hurt has gotten worse). On an unknown date, the patient experienced STOMATITIS (Her mouth was full of sores and blister, inside her mouth, lips and tongue), TONGUE BLISTERING (Her mouth was full of sores and blister, inside her mouth, lips and tongue) and FEELING ABNORMAL (She feels she was scrooge/ She was really mad for these situation). The patient was treated with IBUPROFEN (ADVIL [IBUPROFEN]) at an unspecified dose and frequency; IBUPROFEN at an unspecified dose and frequency; VALACICLOVIR HYDROCHLORIDE (VALACYCLOVIR HCL) (oral) ongoing from 08-Nov-2021 for Blistering of mouth, at a dose of 1 g three times a day and LIDOCAINE (oral) for Blistering of mouth, at an unspecified dose and frequency. At the time of the report, MOUTH HAEMORRHAGE (Mouth was bleeding, it looked almost cut), GINGIVAL BLEEDING (Gums bleed when she brushed her teeth), GINGIVAL PAIN (Gums were hurting really bad), GINGIVAL BLISTER (Gums were blistered), GINGIVAL SWELLING (Gums were swollen), ORAL MUCOSAL BLISTERING (Roof of her mouth was blistered and was very really painful/looked like raw meat), MOUTH ULCERATION (Mouth was sore, mouth was red/her mouth was full of sores), STOMATITIS (Her mouth was full of sores and blister, inside her mouth, lips and tongue), TONGUE BLISTERING (Her mouth was full of sores and blister, inside her mouth, lips and tongue), ORAL PAIN (Mouth was hurting really bad/ mouth was hurting so much that she does not want to talk anymore), ORAL DISCOMFORT (Discomfort in mouth), OROPHARYNGEAL PAIN (Throat hurt has gotten worse), FEELING ABNORMAL (She feels she was scrooge/ She was really mad for these situation) and PAIN IN EXTREMITY (Sore arm) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available):On 06-Nov-2021, Culture throat: (Negative) Negative. On 06-Nov-2021, Viral test: (Positive) Positive. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter considered MOUTH ULCERATION (Mouth was sore, mouth was red/her mouth was full of sores) and STOMATITIS (Her mouth was full of sores and blister, inside her mouth, lips and tongue) to be possibly related. No further causality assessments were provided for MOUTH HAEMORRHAGE (Mouth was bleeding, it looked almost cut), GINGIVAL BLEEDING (Gums bleed when she brushed her teeth), GINGIVAL PAIN (Gums were hurting really bad), GINGIVAL BLISTER (Gums were blistered), GINGIVAL SWELLING (Gums were swollen), ORAL MUCOSAL BLISTERING (Roof of her mouth was blistered and was very really painful/looked like raw meat), TONGUE BLISTERING (Her mouth was full of sores and blister, inside her mouth, lips and tongue), ORAL PAIN (Mouth was hurting really bad/ mouth was hurting so much that she does not want to talk anymore), ORAL DISCOMFORT (Discomfort in mouth), OROPHARYNGEAL PAIN (Throat hurt has gotten worse), FEELING ABNORMAL (She feels she was scrooge/ She was really mad for these situation) and PAIN IN EXTREMITY (Sore arm). Patient had initial doses of Pfizer vaccine and was administered booster dose of Moderna vaccine. On 05-Nov-2021, she noticed discomfort in her mouth. Woken up in the middle of the night from the sore arm, applied ice pack to the soreness. The reporter visited to a clinic on 06-Nov-2021, the doctor did strep throat swab and shingles swab which returned negative. The doctor did think it was oral thrush. A viral test (caller did not know which viral test it was for exactly) returned positive. Concomitant medications included for medullary cystic kidney disease, caller claimed normal kidney function, on low dose naltrexone when necessary for pain from the kidney disease. Following up with a psychiatrist, taking lorazepam 1mg when necessary, quetiapine 25mg every night, tizanidine 4 mg once daily, also a vitamin/folic acid and following up with a urologist, prescribed with progesterone cream. Dentist gave caller laser treatment over the blisters in her mouth and prescribed her with lidocaine mouthwash to use in conjunction with the magic mouthwash. Treatment include swishes onugard oil with water and Magic Mouthwash which was a numbing agent, to swish and spit when necessary. Most recent FOLLOW-UP information incorporated above includes:On 07-Nov-2021: Follow up received and it contains information about patient demographics and treatment medications were updated and new events added.On 09-Nov-2021: Follow up received and it contain information about concomitant medications and new events were added.On 11-Nov-2021: Follow up received and it contain newinformation about medical history, lab data and events.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Gingival pain
Hospital-Tage: -
Labordaten: Test Date: 20211106; Test Name: Strep throat swab and shingles swab; Test Result: Negative ; Result Unstructured Data: Negative; Test Date: 20211106; Test Name: Viral test; Test Result: Positive; Result Unstructured Data: Positive.
Aktuelle Erkrankungen: Allergy to chemicals; Medullary cystic disease.
Vorgeschichte: -
Andere Medikamente: NALTREXONE; LORAZEPAM; QUETIAPINE; TIZANIDINE; MULTIVITAMIN [VITAMINS NOS.]
Allergien: -
Vorherige Impfungen: -

VAERS 1872672

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: SC
Alter: 67,0
Geschlecht: M
Eingang: 19.11.2021
Impfdatum: 12.11.2021
Beginn: 13.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Cellulitis Infection Injection site pain Injection site swelling Erythema Extra dose administered Injection site cellulitis Injection site infection Peripheral swelling Skin warm

Symptomtext

Booster given in left arm above elbow. Next morning upon waking left lower arm swollen red and hot to touch. Redness continued to enlarge become darker as days passed requiring doctor visit 2 days post injection

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: 11/15/21 - office visit was diagnosed with an injection site infection/ cellulitis requiring Antibiotic treatment for 7 days
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension, Hyperlipidemia
Andere Medikamente: Lisinopril, Zocor
Allergien: None
Vorherige Impfungen: -

VAERS 1872672

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: SC
Alter: 67,0
Geschlecht: M
Eingang: 19.11.2021
Impfdatum: 12.11.2021
Beginn: 13.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SC / LA

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

Cellulitis Infection Injection site pain Injection site swelling Erythema Extra dose administered Injection site cellulitis Injection site infection Peripheral swelling Skin warm

Symptomtext

Booster given in left arm above elbow. Next morning upon waking left lower arm swollen red and hot to touch. Redness continued to enlarge become darker as days passed requiring doctor visit 2 days post injection

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: 11/15/21 - office visit was diagnosed with an injection site infection/ cellulitis requiring Antibiotic treatment for 7 days
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension, Hyperlipidemia
Andere Medikamente: Lisinopril, Zocor
Allergien: None
Vorherige Impfungen: -

VAERS 1879314

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: MO
Alter: 80,0
Geschlecht: F
Eingang: 18.11.2021
Impfdatum: 28.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / -

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

Discomfort Inappropriate schedule of product administration Pruritus Skin exfoliation Swelling face Urticaria

Symptomtext

hives which started getting worse/ hives on face and some on arm; face is swollen; its scaly; very bad itching; discomfort; Inappropriate schedule of vaccine administered; This spontaneous case was reported by a consumer and describes the occurrence of URTICARIA (hives which started getting worse/ hives on face and some on arm), SWELLING FACE (face is swollen), SKIN EXFOLIATION (its scaly), PRURITUS (very bad itching) and DISCOMFORT (discomfort) in an 80-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 071F21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Previously administered products included for an unreported indication: COVID-19 VACCINE JANSSEN (1st dose and lot # 1805031) on 10-Mar-2021. On 28-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 28-Oct-2021, the patient experienced INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Inappropriate schedule of vaccine administered). On 03-Nov-2021, the patient experienced URTICARIA (hives which started getting worse/ hives on face and some on arm), SWELLING FACE (face is swollen), SKIN EXFOLIATION (its scaly), PRURITUS (very bad itching) and DISCOMFORT (discomfort). The patient was treated with PARAFFIN (VASELINE [PARAFFIN]) (topical) in 2021 for Adverse event, at an unspecified dose and frequency. On 28-Oct-2021, INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Inappropriate schedule of vaccine administered) had resolved. At the time of the report, URTICARIA (hives which started getting worse/ hives on face and some on arm), SWELLING FACE (face is swollen), SKIN EXFOLIATION (its scaly) and PRURITUS (very bad itching) had not resolved and DISCOMFORT (discomfort) outcome was unknown. No concomitant medications were provided by the reporter. Treatment information include applying some water, cream, and possibly milk (agent could not capture for sure, asked consumer again and she said "yes"). Patient states there is no change in her diet and not allergic to anything that she knows of. Most recent FOLLOW-UP information incorporated above includes: On 11-Nov-2021: Follow-up received on 11-NOV-2021 include adverse event discomfort added.

Weitere VAERSDATA-Felder

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

VAERS 1877563

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: WI
Alter: 32,0
Geschlecht: F
Eingang: 17.11.2021
Impfdatum: 13.11.2021
Beginn: 15.11.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

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

Injection site erythema Injection site pain Injection site swelling Injection site warmth

Symptomtext

Red, warm, slightly swollen area of 2-3" in diameter that is painful to the touch. 4 days post vaccination- area is still slightly red and warm with minimal swelling.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: loratadine
Allergien: amoxicillin
Vorherige Impfungen: -

VAERS 1877275

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: MD
Alter: 47,0
Geschlecht: F
Eingang: 17.11.2021
Impfdatum: 29.10.2021
Beginn: 02.11.2021
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: IM / LA

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

Arthralgia Body temperature increased Erythema Extra dose administered Fatigue Joint swelling

Symptomtext

4 days after COVID-19 booster vaccination developed pain in left shoulder. Initially had some redness that resolved. "feels that joint is swollen". Patient notes that vaccination was given "higher" on shoulder than prior vaccination. Some low grade temperature, tired - resolved

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: nothing specific.
Vorgeschichte: Abnormal mammogram - seen on R breast mammo and U/S - R92.8 Adhesive capsulitis of shoulder, right shoulder - RV-12/17/2020 ( onset 12/2020 ) - M75.01 Ankle sprain, right ankle - ATFL high grade sprain/rupture - S93.401D Bladder pain syndrome - N30.10 Chronic fatigue syndrome - RV-12/17/2020 - R53.82 Chronic pain syndrome - #PainMedicine (percocet) - G89.4 Cytochrome p450 (CYP2C19) mutation - E88.89 Easy bruising - R23.3 Elevated hemoglobin A1c - A1c 6.3% (08/2021) - R73.09 Episodic Swelling of Right Cheek - RV-07/28/2021 ( onset 2019 ) - R22.0 Face pain - RV - 07/28/2021 - G50.1 Family history of breast cancer - mother, negative genetic testing - Z80.3 Generalized anxiety disorder - with insomnia - F41.1 History of struma ovarii tumors - #Follows w/ Gyn/Onc - Z85.43 History of tobacco smoking - 1/2-1PPD x 21 years ( onset 1989, resolved 2010 ) - Z87.891 Hyperlipidemia - E78.5 Hypertension - I10 Hypokalemia - E87.6 Inflammatory polyarthritis - #Rheumatology - M06.4 Intra-abdominal fluid collection - RV-03/18/2021 - R19.09 hx of struma ovarii s/p surgery 2010, TAH and B/L SO (no cervix or ovaries) 2011, mass resection 2014 Leg pain, right leg - RV-10/20/2021 ; poss steroid myopathy ( onset 2013 ) - M79.604 MCAS - MCAS/HATS - D89.49 Mast cell activation syndrome (MCAS) / Hereditary Alpha Tryptasemia Syndrome (HATS) Migraine headache(s) with aura - G43.109 Narcolepsy - on Modafinil - G47.419 Nausea - R11.0 Nonalcoholic fatty liver disease - K76.0 Overactive bladder - #Urology - N32.81 Patent foramen ovale - #OutsideMD - Q21.1 Pericarditis - resolved ( resolved 01/2021 ) - I30.9 Peritoneal adhesions - K66.0 Severe obesity - E66.01 Umbilical hernia - RV-03/18/2021 - K42.9 Ventricular premature beats - #Managed by cardiology - I49.3 Vitamin B12 deficiency - E53.8 Vitamin D deficiency - 18.6 ( onset 05/2019 ) - E55.9 Adverse effect of other vaccines and biological substances, initial encounter - RV-04/20/2021 - Resolved - T50.Z95D Cholelilthiasis - Resolved - K80.20 Pericarditis - Resolved - I30.9
Andere Medikamente: acetaminophen, 500 mg tabs, 2 tabs PO q8h as needed for pain alfuzosin, 10 mg ER 24 hr tabs, 1 tab PO qday as needed for urinary retention benzonatate, 100 - 200 mg PO tid as needed for cough Carafate, 100 mg/mL susp, 5 - 10 mL PO qd-qid as
Allergien: Ace Inhibitors (cough) Cymbalta (depression/brain zaps) Dilaudid (panic, anxiety) Gadolinium-Containing Contrast Media (hives) Wellbutrin (tinnitus) Zoloft (brain fog) Albuterol (panic, anxiety) Alprazolam (insomnia, brain fog) Amlodipine (tongue swelling) chlorthalidone (hypokalemia) Clindamycin (rash) Clonidine (low heart rate, dizziness) Diltiazem (headache) Hydrochlorothiazide (skin peeling) Lorazepam (insomnia, nausea) Losartan (dizziness, muscle cramps) Metoprolol (dizziness, nausea, anxiety) nifedipine (nauseous, dizzy) Oxycodone (dizziness, nausea) Trazodone (dizziness, headache) valsartan (headache, flushing)
Vorherige Impfungen: COVID J&J vaccine (04/06/2021) - fatigue x 1 month; influenza vaccines (hot swollen arm)

VAERS 1877195

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: IL
Alter: 54,0
Geschlecht: F
Eingang: 17.11.2021
Impfdatum: 13.11.2021
Beginn: 14.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Headache Lethargy Pain Pyrexia

Symptomtext

Fever, headache, body ache and lethargy for 3 days.

Weitere VAERSDATA-Felder

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

VAERS 1876762

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: CA
Alter: 32,0
Geschlecht: F
Eingang: 17.11.2021
Impfdatum: 30.10.2021
Beginn: 10.11.2021
Tage bis Beginn: 11,0
Dosis: 3
Route/Site: IM / LA

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

Eye swelling Myalgia Rash

Symptomtext

I experienced rashes on most of my upper body. My arms, back, chest and hands. I'm having muscle aches in both of my arms. The rash has moved to my face and my eyes are swollen. I went to Urgent Care and was told to continue taking Zyrtec.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myalgia
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Lutera Prenatal Vitamin Flo FE Iron Supplement Vitamin C 500mg Sunflower Lecithin
Allergien: None
Vorherige Impfungen: My second dose of Moderna, I experienced a light fever that was cured with Tylenol.

VAERS 1876659

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: TX
Alter: 35,0
Geschlecht: F
Eingang: 17.11.2021
Impfdatum: 01.11.2021
Beginn: 12.11.2021
Tage bis Beginn: 11,0
Dosis: 3
Route/Site: SYR / LA

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

Maternal exposure during breast feeding Rash Rash pruritic Scab Scratch Skin burning sensation Urticaria

Symptomtext

1Nov2021, 12 Nov saw the rash, it was itchy by my neck. 13Nov2021 burning rash like hives in the evening on scalp, 14nov it spread on neck, chest, breast and belly, and on right ear. Started scratching and scabbed edotgraphifism. Not on my arms or legs. 14Nov went to doctors, took antihistamine and took Zyrtec for 5 days, 16Nov saw a dermatologist, it could be the vaccine. The rash is starting to come back if I didn't take Zyrtec (5days). PT was breast feeding.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Can't remember Prenatal Vitamin D
Allergien: No
Vorherige Impfungen: -

VAERS 1876095

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: -
Alter: 63,0
Geschlecht: F
Eingang: 17.11.2021
Impfdatum: 26.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 3,0
Dosis: N/A
Route/Site: IM / LA

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

Burning sensation Dry skin Ear discomfort Rash Rash erythematous Rash pruritic Skin burning sensation

Symptomtext

A red, itchy rash appeared mainly in the center of my neck 3 days after vaccine; continued to be itchy/dry after almost one week, but appearance got better and no longer red; treated w/hydrocortisone cream (OTC) and resolved itself after ~10 days. Other symptoms included slight burning of skin along my chin, lower cheeks, ear lobes, and scalp, but no visible rash in those places. (These also resolved after ~10 days.)

Weitere VAERSDATA-Felder

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

VAERS 1873927

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: IL
Alter: 80,0
Geschlecht: M
Eingang: 16.11.2021
Impfdatum: 05.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Hypoaesthesia Pain in extremity

Symptomtext

Pt with ipsilateral pain and numbness in L arm since event

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: None
Vorherige Impfungen: -

VAERS 1873909

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: WA
Alter: 63,0
Geschlecht: F
Eingang: 16.11.2021
Impfdatum: 11.11.2021
Beginn: 11.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Chills Diarrhoea Fatigue Headache Hyperhidrosis Nausea

Symptomtext

Persistent diarrhea, nausea, fatigue, headache, chills, sweats onset with nausea immediately following vaccination. Diarrhea resolved the night of the vaccine (11/11/2021). Remainder of symptoms currently persisting.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma
Andere Medikamente: Albuterol
Allergien: Beestings
Vorherige Impfungen: -

VAERS 1873541

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: NY
Alter: 74,0
Geschlecht: F
Eingang: 16.11.2021
Impfdatum: 28.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / LA

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

Chills Disturbance in attention Extra dose administered Fatigue Feeling abnormal Feeling cold Feeling hot Headache Injection site pain

Symptomtext

5 hours after injection, felt chilled but warm forehead. no temperature elevation. headache. fatigue and unable to focus that lasted 6 days. injection site is still sensitive to the touch 2 weeks later. tylenol regular strength. chills and feeling warm were gone after 2 days. fatigue and mental "fogginess" lasted 6 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: high blood pressure, thyroid, copd
Andere Medikamente: montelukast, atorvastatin, diltiazem, levothyroxine, altrozalam, ipratropium bromide, proair, spireva, zyrtec, omega 3
Allergien: doxycycline, keflex, bactrim, losartan
Vorherige Impfungen: -

VAERS 1873338

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: MI
Alter: 39,0
Geschlecht: F
Eingang: 16.11.2021
Impfdatum: 01.11.2021
Beginn: 02.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Lymph node pain Lymphadenopathy

Symptomtext

PAINFUL SWOLLEN LYMP NODE- FOR THREE TO FOUR DAYS POST VACCINATION. CONTACTED CDC TO BETTER INFORM PATIENT ADVISED TO TAKE ANTI INFLAMATORY NSAID AND USE COOL CLEAN CLOTH TO THE SWOLLEN LYMP NODE UNDER THE ARM

Weitere VAERSDATA-Felder

Praegender Schweregrund: Lymph node pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: FIBROMYALGIA
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1873031

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: NY
Alter: 65,0
Geschlecht: F
Eingang: 16.11.2021
Impfdatum: 15.11.2021
Beginn: 16.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / RA

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

Fatigue Feeling abnormal Influenza Pain in extremity

Symptomtext

Flu symptoms, very sore arm. Foggy cognition, fatigue

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: COPD, OSTEOPOROSIS
Andere Medikamente: -
Allergien: Mold, Morphine
Vorherige Impfungen: -

VAERS 1870923

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: CO
Alter: 34,0
Geschlecht: F
Eingang: 15.11.2021
Impfdatum: 09.11.2021
Beginn: 10.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Chills Dark circles under eyes Eye haemorrhage Nausea Ocular icterus Pain Petechiae Scleral haemorrhage Skin discolouration Vomiting

Symptomtext

I woke up at 1:30 AM with severe chills, body aches, and some nausea, which was not unexpected. I took 2 ibuprofen and tried to go back to sleep. At 2:30 AM, I woke up immediately needing to vomit, but not able to get out of bed in time. I ended up vomiting over the side of my bed so forcefully that I couldn't breathe and felt like I was asphyxiating. This went on for about 5 minutes. I couldn't move off the couch for 36 hours after the first onset of symptoms. I ate saltines and drank mint tea for 48 hours. The worst part was that I vomited so forcefully that I burst blood vessels in my eyes and all over my face. I had dark skin under my mouth and eyes for 5 days and the whites of my eyes were extremely bloody. People at work thought I was unsafe at home because of my appearance. It is now 6 days later and I still have petechiae and yellow eyes.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: -
Vorgeschichte: Lactose intolerance, gluten intolerance, PTSD
Andere Medikamente: Sertraline, BuSpar, ibuprofen, cranberry, inositol
Allergien: -
Vorherige Impfungen: I felt flu-ish after my first and second Moderna doses, but nothing like this.

VAERS 1869654

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: MI
Alter: 54,0
Geschlecht: F
Eingang: 15.11.2021
Impfdatum: 08.11.2021
Beginn: 09.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Injection site mass Injection site vesicles Musculoskeletal discomfort Pain

Symptomtext

The day after the vaccine, I felt my arm and it was lumpy. I had two blisters above and beneath the site of the injection, fluid filled blisters. The dermatologist poked a needle in each of them and drained them. That resolved that. The very first day of my vaccine, I was sore and achy. It all went away except that I am having prolonged and lingering neck discomfort. It's not muscular, it's more nerve ending feeling. I can barely turn my neck right and left. It's interfering with sleep and it's very uncomfortable. No treatment except Motrin every now and then. I had my flu shot Monday, September 20th, I don't have the brand name or lot number. I am not sure which arm it was. I had it at Dr. office.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site mass
Hospital-Tage: -
Labordaten: No
Aktuelle Erkrankungen: Last week of September the 27th and the week following I had four COVID tests and a flu test and they were all negative. COVID like symptoms but it was some kind of virus
Vorgeschichte: Fluctuating High Blood Pressure that comes and goes
Andere Medikamente: Thyroid medicine NP Thyroid Zoloft
Allergien: Almonds Pitted Fruit Kiwi
Vorherige Impfungen: -

VAERS 1869440

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: MD
Alter: 68,0
Geschlecht: F
Eingang: 15.11.2021
Impfdatum: 27.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Gait disturbance

Symptomtext

Developed severe bilateral hip pain that is muscular, possibly skeletal, in nature. Trouble walking. Taking Tylonol for pain. 8/10 on the pain scale. Pain has decreased somewhat, but still taking Tylonol 3x daily to function. Has last going on 3 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: Range of motion test (during routine physical) 11/12/2021
Aktuelle Erkrankungen: None
Vorgeschichte: -
Andere Medikamente: -
Allergien: None
Vorherige Impfungen: -

VAERS 1868371

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge 071F21A

mild

Staat: AR
Alter: 39,0
Geschlecht: F
Eingang: 14.11.2021
Impfdatum: 26.10.2021
Beginn: 05.11.2021
Tage bis Beginn: 10,0
Dosis: 1
Route/Site: SYR / RA

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

Impaired work ability Pruritus Rash Urticaria

Symptomtext

On Friday, 11/5, my scalp began to itch around 10pm. On Saturday , 11/6, 6pm, I began to itch on my chest. I took a Benadryl and my issue improved. Sunday morning around 1am, I woke up to severe itching and took another Benadryl. Around 5am, the same morning, I noticed a rash under my arm. I began breaking out in hives on my face, waistline, sides, under arms, groin area. I consulted with a family friend (who is a nurse practitioner)via phone/pictures . She prescribed me Prednisone 60mg to be taken for three days, as well as Famotodine. I was unable to work for two days and went to my local doctor on Wednesday afternoon. He extended the prednisone for 5 days at a lower dose of 40mg. As well as continue the Famotodine and Zyrtec. It appears that I am still having some type of reaction and will follow up as needed.

Weitere VAERSDATA-Felder

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

VAERS 1867175

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: PA
Alter: 47,0
Geschlecht: F
Eingang: 13.11.2021
Impfdatum: 03.11.2021
Beginn: 03.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / -

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

Fatigue Interchange of vaccine products Nasal congestion Oropharyngeal discomfort Pain Rash pruritic Rhinorrhoea Throat irritation

Symptomtext

Drainage to throat; Nasal congestion; Nose was running like a faucet; Continuous rash over her body which is itching; Fatigue; Last night throat was burning really bad on one side; Body aches; 1st/2nd COVID19 vaccine doses were Pfizer; This spontaneous case was reported by a consumer and describes the occurrence of INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (1st/2nd COVID19 vaccine doses were Pfizer), THROAT IRRITATION (Last night throat was burning really bad on one side), OROPHARYNGEAL DISCOMFORT (Drainage to throat), NASAL CONGESTION (Nasal congestion) and RHINORRHOEA (Nose was running like a faucet) in a 47-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 071F21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Previously administered products included for Product used for unknown indication: Flu vaccine on 16-Oct-2021. Past adverse reactions to the above products included No adverse event with Flu vaccine. Concurrent medical conditions included Anxiety, Depression and Autoimmune disorder (undiagnosed autoimmune condition.). On 03-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 03-Nov-2021, the patient experienced INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (1st/2nd COVID19 vaccine doses were Pfizer). On 04-Nov-2021, the patient experienced THROAT IRRITATION (Last night throat was burning really bad on one side) and PAIN (Body aches). On an unknown date, the patient experienced OROPHARYNGEAL DISCOMFORT (Drainage to throat), NASAL CONGESTION (Nasal congestion), RHINORRHOEA (Nose was running like a faucet), RASH PRURITIC (Continuous rash over her body which is itching) and FATIGUE (Fatigue). The patient was treated with PARACETAMOL (TYLENOL [PARACETAMOL]) for Adverse event, at an unspecified dose and frequency and DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PARACETAMOL, PSEUDOEPHEDRINE HYDROCHLORIDE (DAYQUIL) for Adverse event, at an unspecified dose and frequency. On 03-Nov-2021, INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (1st/2nd COVID19 vaccine doses were Pfizer) had resolved. At the time of the report, THROAT IRRITATION (Last night throat was burning really bad on one side), RHINORRHOEA (Nose was running like a faucet), PAIN (Body aches) and FATIGUE (Fatigue) outcome was unknown and OROPHARYNGEAL DISCOMFORT (Drainage to throat), NASAL CONGESTION (Nasal congestion) and RASH PRURITIC (Continuous rash over her body which is itching) had not resolved. No concomitant products were reported. Most recent FOLLOW-UP information incorporated above includes: On 09-Nov-2021: Follow up received contains significant information, patient details, medical history and event details updated.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Anxiety; Autoimmune disorder (undiagnosed autoimmune condition.); Depression
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1866995

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: FL
Alter: 14,0
Geschlecht: M
Eingang: 13.11.2021
Impfdatum: 29.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / LA

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

Product administered to patient of inappropriate age Vaccination site pain

Symptomtext

Left arm sore at injection site/pain on left arm/pain in left arm were vaccine was injected; 14 year old son was given the Moderna covid19 vaccine an that it was the wrong vaccine; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION SITE PAIN and PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE in a 14-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 071F21A) for COVID-19 vaccination. Previously administered products included for Product used for unknown indication: INFLUENZA VACCINE. Past adverse reactions to the above products included Hand pain with INFLUENZA VACCINE. Concurrent medical conditions included Allergy to nuts, Crab, Pollen, Cat, Dog, and Improvement after treatment since April 2018. Concomitant products included VITAMIN D from 2019 to an unknown date, VITAMIN C from 2019 to an unknown date and MULTIVITAMIN for an unknown indication. On 29-Oct-2021 at 3:45 PM, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 29-Oct-2021, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE. On 29-Oct-2021 at 8:00 PM, the patient experienced VACCINATION SITE PAIN. On 29-Oct-2021, PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE had resolved. On 01-Nov-2021, VACCINATION SITE PAIN had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Reporter stated that patient was inadvertently given his first dose of the Moderna vaccine on 29 OCT 2021 instead of Pfizer's. Patient had treated his left arm pain with pack of ice. Treatment information was not provided by the reporter. Most recent FOLLOW-UP information incorporated above includes on 01-Nov-2021 the Follow up received contain significant information. Added reporter details, patient Date Of Birth, suspect product details, and events. On 04-Nov-2021 the Follow up received was non significant. On 04-Nov-2021 the Follow up received contain significant information, updated patient demographics, medical history, vaccination time, concomitant drugs, and event details.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Vaccination site pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Allergy to animal (Dog); Allergy to animal (Cat); Allergy to nuts; Food allergy (Crab); Pollen allergy; Soy allergy
Vorgeschichte: -
Andere Medikamente: VITAMIN D; VITAMIN C; MULTIVITAMIN
Allergien: -
Vorherige Impfungen: -

VAERS 1865591

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: OH
Alter: 43,0
Geschlecht: U
Eingang: 12.11.2021
Impfdatum: 09.11.2021
Beginn: 10.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Axillary pain Fatigue Feeling abnormal Lymph node pain Lymphadenopathy

Symptomtext

swollen lymphnode and pain under left arm pit. Tired, overall feeling bad. Lymphnode very painful.

Weitere VAERSDATA-Felder

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

VAERS 1865190

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: FL
Alter: 43,0
Geschlecht: F
Eingang: 12.11.2021
Impfdatum: 25.01.2021
Beginn: 23.02.2021
Tage bis Beginn: 29,0
Dosis: 3
Route/Site: IM / -

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

Erythema Eye swelling Pruritus Swollen tongue Wheezing

Symptomtext

First vax was mild itching to palms and feet as well as localized itching with mild wheezing- controlled with OTC allergy meds and combivent. Second shot was all over itching, moderate wheezing, tongue and eye swelling. OTC allergy meds were ineffective, took Benadryl and combivent. Booster shot- itching and redness to scalp, palms, soles of the feet and tip of the tongue with mild wheezing. OTC allergy meds were ineffective, took Benadryl and combivent.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma
Andere Medikamente: Fetzima, Lamotrigine, Glycopyrrolate, Rosuvastatin, Flonase, Zyrtec, Pepcid, Albuterol, Respimat Combivent and fire ant allergy shots
Allergien: Darvocet, TB skin test and Caramel Color
Vorherige Impfungen: -

VAERS 1864901

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: WV
Alter: 51,0
Geschlecht: F
Eingang: 12.11.2021
Impfdatum: 11.11.2021
Beginn: 11.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Asthenia Fatigue Headache Myalgia

Symptomtext

Headache, extreme muscle pain, weakness and fatigue.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetes htn gerd
Andere Medikamente: Ozempic,benazipril,protonix and dapsone
Allergien: Codeine pcn morphine restoril
Vorherige Impfungen: -

VAERS 1864440

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: CA
Alter: 70,0
Geschlecht: M
Eingang: 12.11.2021
Impfdatum: 27.10.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: OT / LA

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

Myalgia Pruritus Rash macular Scratch Swelling Urticaria Vaccination complication

Symptomtext

started getting hives/ different parts of his body started breaking out in hives; now he states he is getting itchiness, like in the side of his palm, his finger, his feet around different parts have itchiness,; He states he still has bumps where the hives were at, not as pronounced but he still sees them.; He states that when he took a shower it kind of made them show up more; blotches seemed stirred red; Caller states he scratches the different parts of his body and he doesn't see anything; little soreness where he had the shot when he had the booster shot; This spontaneous case was reported by a consumer and describes the occurrence of URTICARIA (started getting hives/ different parts of his body started breaking out in hives), PRURITUS (now he states he is getting itchiness, like in the side of his palm, his finger, his feet around different parts have itchiness,), SWELLING (He states he still has bumps where the hives were at, not as pronounced but he still sees them.), VACCINATION COMPLICATION (He states that when he took a shower it kind of made them show up more) and RASH MACULAR (blotches seemed stirred red) in a 70-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 071F21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 27-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced URTICARIA (started getting hives/ different parts of his body started breaking out in hives), PRURITUS (now he states he is getting itchiness, like in the side of his palm, his finger, his feet around different parts have itchiness,), SWELLING (He states he still has bumps where the hives were at, not as pronounced but he still sees them.), VACCINATION COMPLICATION (He states that when he took a shower it kind of made them show up more), RASH MACULAR (blotches seemed stirred red), SCRATCH (Caller states he scratches the different parts of his body and he doesn't see anything) and MYALGIA (little soreness where he had the shot when he had the booster shot). At the time of the report, URTICARIA (started getting hives/ different parts of his body started breaking out in hives), PRURITUS (now he states he is getting itchiness, like in the side of his palm, his finger, his feet around different parts have itchiness,), SWELLING (He states he still has bumps where the hives were at, not as pronounced but he still sees them.), VACCINATION COMPLICATION (He states that when he took a shower it kind of made them show up more), RASH MACULAR (blotches seemed stirred red), SCRATCH (Caller states he scratches the different parts of his body and he doesn't see anything) and MYALGIA (little soreness where he had the shot when he had the booster shot) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medications were not included. Treatment medications include Anti-histamines. This case was linked to MOD-2021-375381, MOD-2021-375384 (Patient Link).

Weitere VAERSDATA-Felder

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

VAERS 1863704

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: MN
Alter: 64,0
Geschlecht: M
Eingang: 12.11.2021
Impfdatum: 01.11.2021
Beginn: 01.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / LA

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

Musculoskeletal stiffness Myalgia Vaccination site erythema

Symptomtext

The patient looked at arm in the mirror and noticed a pinkish or reddish, 2x3" area in a teardrop shape near the injection site; Muscle aches; Stiffness in the arm; This spontaneous case was reported by a consumer and describes the occurrence of MUSCULOSKELETAL STIFFNESS (Stiffness in the arm), VACCINATION SITE ERYTHEMA (The patient looked at arm in the mirror and noticed a pinkish or reddish, 2x3" area in a teardrop shape near the injection site) and MYALGIA (Muscle aches) in a 64-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 071F21A) for COVID-19 vaccination. Concomitant products included CENTRUM SILVER PRO for an unknown indication. On 01-Nov-2021 at 11:00 AM, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .25 ml. On 01-Nov-2021 at 4:00 PM, the patient experienced MUSCULOSKELETAL STIFFNESS (Stiffness in the arm). On 02-Nov-2021 at 7:00 AM, the patient experienced MYALGIA (Muscle aches). On 04-Nov-2021 at 10:00 AM, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced VACCINATION SITE ERYTHEMA (The patient looked at arm in the mirror and noticed a pinkish or reddish, 2x3" area in a teardrop shape near the injection site). On 04-Nov-2021, MYALGIA (Muscle aches) had resolved. On 05-Nov-2021, MUSCULOSKELETAL STIFFNESS (Stiffness in the arm) had resolved. On 06-Nov-2021, VACCINATION SITE ERYTHEMA (The patient looked at arm in the mirror and noticed a pinkish or reddish, 2x3" area in a teardrop shape near the injection site) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter considered MUSCULOSKELETAL STIFFNESS (Stiffness in the arm), VACCINATION SITE ERYTHEMA (The patient looked at arm in the mirror and noticed a pinkish or reddish, 2x3" area in a teardrop shape near the injection site) and MYALGIA (Muscle aches) to be possibly related. The patient stated he had not taken any medications or treatments. This case was linked to MOD-2021-375541, MOD-2021-375520 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 08-Nov-2021: Follow up received includes concomitant medication added, updated outcome of all events and causality was updated.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myalgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: CENTRUM SILVER PRO
Allergien: -
Vorherige Impfungen: -

VAERS 1863571

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: WI
Alter: 66,0
Geschlecht: F
Eingang: 12.11.2021
Impfdatum: 25.10.2021
Beginn: 25.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / -

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

Balance disorder Chills Fatigue Headache Myalgia Pyrexia

Symptomtext

Balance problems; Fever after booster; Chills after booster; Headache after booster; Fatigue after booster; Body aches after booster; This spontaneous case was reported by a nurse and describes the occurrence of BALANCE DISORDER (Balance problems), PYREXIA (Fever after booster), CHILLS (Chills after booster), HEADACHE (Headache after booster) and FATIGUE (Fatigue after booster) in a 66-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 071F21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 25-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 25-Oct-2021, the patient experienced PYREXIA (Fever after booster), CHILLS (Chills after booster), HEADACHE (Headache after booster), FATIGUE (Fatigue after booster) and MYALGIA (Body aches after booster). On 01-Nov-2021, the patient experienced BALANCE DISORDER (Balance problems). On 27-Oct-2021, PYREXIA (Fever after booster), CHILLS (Chills after booster), HEADACHE (Headache after booster), FATIGUE (Fatigue after booster) and MYALGIA (Body aches after booster) had resolved. At the time of the report, BALANCE DISORDER (Balance problems) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No Concomitant medications were reported. No Treatment information was reported. This case was linked to MOD-2021-374915 (Patient Link).

Weitere VAERSDATA-Felder

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

VAERS 1861839

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: KS
Alter: 54,0
Geschlecht: F
Eingang: 11.11.2021
Impfdatum: 10.11.2021
Beginn: 10.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Injection site erythema Injection site haemorrhage Injection site induration Injection site pruritus Injection site warmth Injection site extravasation Pain in extremity Urticaria

Symptomtext

The tech put a circular Band-Aid on the site and injected through it. The injection was incredibly fast and felt like the needle was immediately pulled out. It was unusual. The Band-Aid began to come off immediately. I pressed it down and my fingers became wet with an odorless liquid. The tech said this sometime happened, dried the site and applied another round bandage. It came off after a few seconds, She left, returned with a strip Band-Aid, again dried the injection site and applied this Band-Aid. It stayed on. The site began itching soon after. 24-hours later the site blood remains and is red. The redness has spread for several inches and contains a hard hot welt about 3 inches long. I had no skin reactions to my first two injections. The arm is sore. This occurred with the previous injections.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site extravasation
Hospital-Tage: -
Labordaten: I called the pharmacy and informed the pharmacist about 24 hours after the shot. He said he would consult and call me back. He has not yet called.
Aktuelle Erkrankungen: None
Vorgeschichte: Arthritis
Andere Medikamente: Multivitamin
Allergien: None
Vorherige Impfungen: Brief muscle aches, mild chills and fever following second Moderna injection.

VAERS 1861631

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071f21a

mild

Staat: FL
Alter: 24,0
Geschlecht: F
Eingang: 11.11.2021
Impfdatum: 11.11.2021
Beginn: 11.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Pruritus Throat irritation Throat tightness

Symptomtext

Pt received second dose of Moderna vaccine at 0835. Pt reported tightness and itching of throat and face at 0853. Adverse event emergency protocol initiated. Oxygen saturation 90% on RA, Benadryl 25mg PO giiven, Pt transferred to in house Urgent care via wheelchair. was treated with 125mg solumedrol, benadrly 25mg IV, LR 500 ml IV, oxygen saturation up to 98% RA. patient monitored until patient stated improvement of symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: UNKNOWN
Vorgeschichte: Asthma ? Chronic pain of right knee 12/18/2020 ? Elevated blood pressure reading 11/12/2017 ? Heart murmur ? Pain of upper extremity 11/12/2017 ? Sleep apnea of newborn outgrew by age 3 FRACTURE SURGERY right arm ? TONSILLECTOMY 9/12/2019
Andere Medikamente: UNKNOWN
Allergien: HYDROCODONE SULFA
Vorherige Impfungen: RASH AFTER FIRST MODERNA DOSE

VAERS 1861613

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: SC
Alter: 36,0
Geschlecht: M
Eingang: 11.11.2021
Impfdatum: 08.11.2021
Beginn: 10.11.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Fear of falling Hyperacusis Tinnitus

Symptomtext

Tinnitus in left ear beginning at 1 PM on 11/10/21, very strong ringing sound for first 10 hours (until sleep), dissipated but present the next morning and day. Noise sensitivity in both ears beginning at 1 PM on 11/10/21, strong for first 10 hours (until sleep), dissipated but present the next morning and day. Dizziness approximately 20 hours after tinnitus (9 AM on 11/11/21), had to sit down multiple times because I felt like I would have fallen over. Faint ringing sound in both ears as of 6:30 PM on 11/11/21.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: Pineapple, Scallops
Vorherige Impfungen: -

VAERS 1860845

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: IL
Alter: 73,0
Geschlecht: F
Eingang: 11.11.2021
Impfdatum: 06.11.2021
Beginn: 06.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Lip swelling Pruritus Rash Rash erythematous

Symptomtext

Extremely itchy all over body since the evening after the shot. Swollen lip next morning and red rash under eyes following morning. Still itchy 5 days later. Taking Benedral. On 4th day after shot went to immediate care center and doctor prescribed prednizone 20 mg if itching becomes unbearable. Trying to wait so prednizone does not negate vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Lotamax, Lumigan and AlphaganP eye drops
Allergien: Sulfa
Vorherige Impfungen: Got Covid arm 5 days after 1st shot of Moderna

VAERS 1860184

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: VA
Alter: -
Geschlecht: F
Eingang: 11.11.2021
Impfdatum: 29.10.2021
Beginn: 01.11.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: OT / -

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

Pain in jaw

Symptomtext

she was having severe jaw pain and it lasted until today; This spontaneous case was reported by a consumer and describes the occurrence of PAIN IN JAW (she was having severe jaw pain and it lasted until today) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 071F21A) for COVID-19 vaccination. Previously administered products included for COVID-19 vaccination: PFIZER BIONTECH COVID-19 VACCINE (1st dose - 10Mar2021 with lot number EN6199 2nd dose - 31Mar2021 with lot number ER8732) from 10-Mar-2021 to 31-Mar-2021. Past adverse reactions to the above products included No adverse event with PFIZER BIONTECH COVID-19 VACCINE. Concurrent medical conditions included TMJ syndrome (She has a condition called TMJ and was wondering if the vaccine can trigger jaw pain.). On 29-Oct-2021 at 11:00 AM, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 01-Nov-2021, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced PAIN IN JAW (she was having severe jaw pain and it lasted until today). On 02-Nov-2021, PAIN IN JAW (she was having severe jaw pain and it lasted until today) had resolved. Concomitant information was not reported. Treatment information was not reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in jaw
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: TMJ syndrome (She has a condition called TMJ and was wondering if the vaccine can trigger jaw pain.)
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1858977

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: MO
Alter: 73,0
Geschlecht: F
Eingang: 10.11.2021
Impfdatum: 03.11.2021
Beginn: 03.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Chills Erythema Fatigue Headache Nausea Pain Peripheral swelling Pyrexia SARS-CoV-2 test negative

Symptomtext

Fever (100.7) Severe body aches lasting 2-3 days Chills lasting several hours Nausea Extreme fatigue Headache Swollen and red arm lasting 4-5 days

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: COVID rapid test (negative)
Aktuelle Erkrankungen: None
Vorgeschichte: Lupus Hashimoto?s thyroiditis Sick Sinus Syndrome Osteo and rheumatoid Arthritis
Andere Medikamente: Levothyroxine Metoprolol Wellbutrin Gabapentin Tramadol Excedrin Vit D3 B-Complex Biotin
Allergien: Compazine Morphine
Vorherige Impfungen: -

VAERS 1858369

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: IL
Alter: 71,0
Geschlecht: F
Eingang: 10.11.2021
Impfdatum: 09.11.2021
Beginn: 09.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Pruritus Rhinorrhoea Sleep disorder Urticaria

Symptomtext

I began to experience intense itching , runny nose, and patches of hives on both arms and legs, back and stomach area. My sleep pattern was disturbed to the point that I had to search the internet seeking relief. I then took 2 Allegra allergy tablets for the itch and used Hydrcortisone creme topically on the hive patches. After doing both, I got relief in about 3-4 hours.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: None as yet.
Aktuelle Erkrankungen: 2 week treatment for H pylori bacteria
Vorgeschichte: abdominal pain in lower right quadrant arthritis
Andere Medikamente: Metropolol Succ 50 mg x 2 Rosuvastatin Calcium 40 mg x 1 Pantoprazole Sod Dr 40 mg x 1 Oysco 500 + D x 1 Vitamin D3 50 mcg x 1 Centrum Silver Multivitamin for Women
Allergien: Penicillin (Hives reaction) Sulfa drugs (Unknown reaction) Shellfish (rapid heartbeat, immobility)
Vorherige Impfungen: -

VAERS 1858151

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: AZ
Alter: 64,0
Geschlecht: M
Eingang: 10.11.2021
Impfdatum: 09.11.2021
Beginn: 10.11.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: IM / LA

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

Dizziness

Symptomtext

Patient developed dizziness the day following Moderna booster dose.

Weitere VAERSDATA-Felder

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

VAERS 1857669

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: NM
Alter: 48,0
Geschlecht: F
Eingang: 10.11.2021
Impfdatum: 07.11.2021
Beginn: 09.11.2021
Tage bis Beginn: 2,0
Dosis: UNK
Route/Site: IM / LA

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

Fatigue Headache Injection site pain Injection site swelling Interchange of vaccine products Lymph node pain Lymphadenopathy Pain

Symptomtext

This was the Moderna Booster after the Janssen Vaccination on 3/17/2021. I have soreness and swelling at the injection site, as well as significant visible swelling and soreness/pain of the lymph nodes in my armpit. Also have slight headache, fatigue, and body soreness. The lymph nodes are my primary complaint.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: Headache (36h) and fatigue (about a week) after Janssen shot. DTAP caused digestive side effects

VAERS 1857645

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: TN
Alter: 58,0
Geschlecht: F
Eingang: 10.11.2021
Impfdatum: 06.11.2021
Beginn: 07.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Headache Hyperhidrosis Injection site erythema Injection site induration Injection site mass Injection site pain Injection site pruritus Injection site warmth Myalgia Nausea

Symptomtext

Covid injection #3 "booster": expected side effects 12 hours after injection: headache, muscle pain, sweating, nausea side effect day 3-current day 5 after injection: injection site pain, bright red, hard lump, heat, itching. 4 inch diameter area right deltoid

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: hypothyroid; hypertension, anxiety
Andere Medikamente: lisinopril-hydrochlorothiazide, l-thyroxine, D-3, B-complex, venlefaxine
Allergien: none
Vorherige Impfungen: -

VAERS 1857365

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: MN
Alter: 86,0
Geschlecht: M
Eingang: 10.11.2021
Impfdatum: 07.11.2021
Beginn: 07.11.2021
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-Medium, Site: Swelling at Injection Site-Medium

Weitere VAERSDATA-Felder

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

VAERS 1856697

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: FL
Alter: 82,0
Geschlecht: M
Eingang: 10.11.2021
Impfdatum: 01.11.2021
Beginn: 02.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: OT / -

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

Rash erythematous Rash pruritic

Symptomtext

On the inside of his elbow on both arms he has a red spot; red spot itches; This spontaneous case was reported by a consumer and describes the occurrence of RASH ERYTHEMATOUS (On the inside of his elbow on both arms he has a red spot) and RASH PRURITIC (red spot itches) in an 82-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 071F21A) for COVID-19 vaccination. No Medical History information was reported. On 01-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 02-Nov-2021, the patient experienced RASH ERYTHEMATOUS (On the inside of his elbow on both arms he has a red spot) and RASH PRURITIC (red spot itches). At the time of the report, RASH ERYTHEMATOUS (On the inside of his elbow on both arms he has a red spot) and RASH PRURITIC (red spot itches) outcome was unknown. no concomitant drugs were reported. no treatment drugs were reported

Weitere VAERSDATA-Felder

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

VAERS 1856659

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071f21a

mild

Staat: OH
Alter: 27,0
Geschlecht: F
Eingang: 10.11.2021
Impfdatum: 29.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / -

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

Chills Fatigue Genital ulceration Pain

Symptomtext

acute genital ulcers; Body aches; Fatigue; chills; This spontaneous case was reported by a pharmacist and describes the occurrence of GENITAL ULCERATION (acute genital ulcers), PAIN (Body aches), FATIGUE (Fatigue) and CHILLS (chills) in a 27-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 071f21a) for COVID-19 vaccination. Concurrent medical conditions included Immunocompromised and Rheumatoid arthritis. Concomitant products included RITUXIMAB (RITUXAN) from 06-Nov-2020 to 10-May-2021 for Rheumatoid arthritis, LEVOTHYROXINE SODIUM (SYNTHROID) and SPIRONOLACTONE for an unknown indication. On 29-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 29-Oct-2021, the patient experienced PAIN (Body aches), FATIGUE (Fatigue) and CHILLS (chills). On 01-Nov-2021, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced GENITAL ULCERATION (acute genital ulcers). The patient was treated with CLOBETASOL for Genital ulceration, at an unspecified dose and frequency. At the time of the report, GENITAL ULCERATION (acute genital ulcers), PAIN (Body aches), FATIGUE (Fatigue) and CHILLS (chills) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. The patient was wondering if she had severe reaction because the rituximab (Rituxan) infusion was not separated with the vaccine. The patient reported she did not produce antibodies, rheumatologist recommended to space out with infusion, rescheduled the infusion so she could get the 3rd dose of vaccine before her infusion. After developing, the acute genital ulcers after 3rd dose, the patient had not seen a doctor yet. The patient used leftover clobetasol cream from previous treatment. Treatment information for rest of the events were not reported by the reporter. This case was linked to MOD-2021-370939, MOD-2021-371163 (Patient Link).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Immunocompromised; Rheumatoid arthritis
Vorgeschichte: -
Andere Medikamente: SYNTHROID; SPIRONOLACTONE; RITUXAN
Allergien: -
Vorherige Impfungen: -

VAERS 1855770

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: CA
Alter: 43,0
Geschlecht: F
Eingang: 09.11.2021
Impfdatum: 07.11.2021
Beginn: 07.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Injection site erythema Injection site pain Injection site warmth

Symptomtext

Patient received their second moderna vaccine shot and reported "a red, warm and painful to the touch" reaction to their injection site. They didn't receive any treatment.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None reported
Andere Medikamente: Omeprazole, Levothyroxine, Vit D2 (Ergo) , Ibuprofen, Optivar,
Allergien: None
Vorherige Impfungen: -

VAERS 1855042

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: NH
Alter: 29,0
Geschlecht: F
Eingang: 09.11.2021
Impfdatum: 09.11.2021
Beginn: 09.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RL

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

Chest discomfort Painful respiration Throat tightness

Symptomtext

Symptoms started at 12:30pm today about 1.5 hours after administration. Started having tightness in throat and chest, with slight discomfort while breathing. Alerted Lead Medical Assistant and Clinical Coordinator, was given 50mg of Benadryl at 12:30pm and another 50mg at 4:30pm when slight tightness in throat started coming back with good effect.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Painful respiration
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma, pcos, anxiety, adhd/add
Andere Medikamente: Adderall XR 30mg, amitriptyline 25mg, bupropion 150mg XL, Zyrtec 10mg, singular 10mg
Allergien: Any triptan medication, seafood, shellfish, latex
Vorherige Impfungen: Both previous Moderna vaccines. Both reported to Clinical Coordinator of my office.

VAERS 1854887

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: TX
Alter: 70,0
Geschlecht: M
Eingang: 09.11.2021
Impfdatum: 02.11.2021
Beginn: 02.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Joint swelling Movement disorder Muscle spasms

Symptomtext

After receiving the 3rd Booster of Moderna 11/02/2021, patient started experiencing symptoms that evening of right knee pain (previous knee replacement 2+yrs), swelling, difficulty moving (lasting 2 days) and muscle spasms in the right knee. No noted primary visit/communications. Symptoms subsided.

Weitere VAERSDATA-Felder

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

VAERS 1854640

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: -
Alter: 42,0
Geschlecht: F
Eingang: 09.11.2021
Impfdatum: 06.11.2021
Beginn: 06.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Headache Injection site pain Nausea Pruritus

Symptomtext

itching (6hrs after injection- onset within 15min) pain at injection site (4 days) nausea (on 2nd day) headache (4 days)

Weitere VAERSDATA-Felder

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

VAERS 1854190

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: OH
Alter: 72,0
Geschlecht: F
Eingang: 09.11.2021
Impfdatum: 03.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: IM / RA

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

Bone pain Cough Diarrhoea Fatigue Headache Myalgia Pyrexia

Symptomtext

Fever, muscle and bone aches, headache, cough, fatique, diarrhea

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bone pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Losartan, duloxetine, Atorvastatin, omeprazole, zyrtec
Allergien: -
Vorherige Impfungen: -

VAERS 1850947

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071f21a

mild

Staat: TX
Alter: 66,0
Geschlecht: F
Eingang: 08.11.2021
Impfdatum: 05.11.2021
Beginn: 06.11.2021
Tage bis Beginn: 1,0
Dosis: N/A
Route/Site: IM / LA

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

Injection site bruising Injection site erythema Injection site pain Injection site swelling

Symptomtext

Site: Bruising at Injection Site-Mild, Site: Pain at Injection Site-Mild, Site: Redness at Injection Site-Mild, Site: Swelling at Injection Site-Mild

Weitere VAERSDATA-Felder

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

VAERS 1850134

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071f21a

mild

Staat: IL
Alter: 37,0
Geschlecht: F
Eingang: 08.11.2021
Impfdatum: 05.11.2021
Beginn: 06.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Injection site erythema Injection site pain Injection site warmth Vaccination site reaction

Symptomtext

Site: Redness at Injection Site-Mild, Additional Details: Patient said the following day, noticed a warm, red, achiness radiating upwards from injection site. symptoms common with Covid Arm, rph suggested using a cold compress and tylenol and to follow up with MD if symptoms get worse

Weitere VAERSDATA-Felder

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

VAERS 1850130

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071f21a

mild

Staat: TN
Alter: 33,0
Geschlecht: F
Eingang: 08.11.2021
Impfdatum: 05.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Gingival bleeding Injection site pain Mouth swelling Oral pain Stomatitis

Symptomtext

Site: Pain at Injection Site-Mild, Additional Details: pt states has developed mouth sores that are very painful. Her gum line is also bleeding. swelling and sores have worsened since getting the vaccine on 11/5 and pt to call her provider today if an on call available or going to the urgent care.

Weitere VAERSDATA-Felder

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

VAERS 1850127

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071f21a

mild

Staat: CA
Alter: 26,0
Geschlecht: M
Eingang: 08.11.2021
Impfdatum: 05.11.2021
Beginn: 06.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Injection site erythema

Symptomtext

Site: Redness at Injection Site-Mild

Weitere VAERSDATA-Felder

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

VAERS 1849601

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: FL
Alter: 21,0
Geschlecht: F
Eingang: 07.11.2021
Impfdatum: 05.11.2021
Beginn: 07.11.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Erythema Pain in extremity Peripheral swelling Rash erythematous Rash macular

Symptomtext

48 hours after injection: Found that both hands are swollen with both palms having a red, blotchy rash with pain in joints and redness. Received injection in left arm, rash/swelling/pain are more prevalent in left hand. Symptoms improve with OTC antihistamines and analgesics.

Weitere VAERSDATA-Felder

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

VAERS 1849134

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: NC
Alter: 38,0
Geschlecht: M
Eingang: 06.11.2021
Impfdatum: 03.11.2021
Beginn: 03.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

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

Chills Headache Hyperhidrosis Injection site pain Pain

Symptomtext

At approximately 10 pm on 11/03/2021, I began having body aches along with my left arm hurting at the injection site. At 5:00 am, I was awakened by severe chills that I couldn't get to stop. I took 2 Tylenol 500mg and went back to bed. Approximately 2 hours later, I was awakened by being drenched in sweat, severe body aches and a bad headache. At approximately 11 am, I took 2 Tylenol 500mg and went back to bed and slept on and off for the next 12 hours (taking 2 - Tylenol 500mg every 6 hours). At approximately 11 pm on 11/04/2021, my main symptoms began to dissipate. By 11 am, on 11/05/2021, all symptoms stopped except my left arm hurting at the injection site.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Wellbutrin, Modafinil
Allergien: Amoxicillin, Latex
Vorherige Impfungen: -

VAERS 1849109

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071f21a

mild

Staat: MO
Alter: 70,0
Geschlecht: F
Eingang: 06.11.2021
Impfdatum: 04.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: IM / LA

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

Erythema Rash Swelling

Symptomtext

rash, redness, and swelling

Weitere VAERSDATA-Felder

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

VAERS 1849068

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071f21a

mild

Staat: MD
Alter: 64,0
Geschlecht: F
Eingang: 06.11.2021
Impfdatum: 28.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Injection site bruising Injection site haemorrhage

Symptomtext

patient had bleeding after injection from injection site and also had bruising

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site bruising
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: n/a
Allergien: sulfa
Vorherige Impfungen: -

VAERS 1849056

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: TN
Alter: 65,0
Geschlecht: F
Eingang: 06.11.2021
Impfdatum: 26.10.2021
Beginn: 05.11.2021
Tage bis Beginn: 10,0
Dosis: 3
Route/Site: IM / RA

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

Blood glucose increased Chest X-ray normal Computerised tomogram head Dizziness Ear discomfort Extra dose administered Full blood count normal Laboratory test Magnetic resonance imaging normal Metabolic function test Nausea Vomiting

Symptomtext

Acute onset of dizziness, nausea, later vomiting. Started 0730 upon arising. Last vomiting was about 12:45 (5 hours of duration) with residual nausea. Went to the Emergency Department to rule out early signs of a stroke. Tests (lab, chest xray, CT Brain, MRI Brain) were all negative. I was discharged. Perhaps this series of symptoms started from irritation in nerves in ears (problem I had in 2015). I had my first stroke (Lucunar pin point in Left hippocampus) that resulted in amnesia (inability to form new memories for a few hours). THere were NO motor function changes and the only thing positive was the MRI. This stroke was 5.5 months after second Moderna.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: 11.5.2021 CBC, CMP, Chest Xray, CT Brain, MRI--basically all negative for a stroke. Glucose was elevated only on admission to the ED.
Aktuelle Erkrankungen: none
Vorgeschichte: Post-stroke (temporary memory only NO motor function was 9.10.2021) so meds changed around a couple times prior to my Moderna BOOSTER (1/2 dose). Otherwise, Osteoarthritis Left knee.
Andere Medikamente: Allergy shots (Day before). ASA 81 mg, Atorvastatin 10 mg, Vitamin D orally 20,000 units
Allergien: Sulfa-Hives. No foods.
Vorherige Impfungen: -

VAERS 1848832

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: OK
Alter: 52,0
Geschlecht: M
Eingang: 06.11.2021
Impfdatum: 04.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Dizziness Feeling abnormal Hallucination Lethargy Pyrexia Vertigo

Symptomtext

12 hours after recieving 2nd dose of COVID-19 vaccine, symptoms began to appear. I began to feel feverish and lethargic. By 30 hours after, I had a very high fever and began hallucinating. I felt as though I was leaving my body. I had taken Ibuprofen earlier and then took Tylenol along with meclizine to alleviate the vertigo and dizziness. I awoke this morning at 9am 11/6/21 feeling much better with no further side effects.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: vitamins
Allergien: none
Vorherige Impfungen: -

VAERS 1848267

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: MA
Alter: 66,0
Geschlecht: F
Eingang: 06.11.2021
Impfdatum: 26.10.2021
Beginn: 26.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / RA

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

Arthralgia Fatigue Headache Hyperhidrosis Myalgia Pyrexia Vaccination site pruritus

Symptomtext

sweating; Body ache; injection site right arm itches; Headache; pyrexia; all joints hurt; Tired; This spontaneous case was reported by a consumer and describes the occurrence of HYPERHIDROSIS (sweating), MYALGIA (Body ache), VACCINATION SITE PRURITUS (injection site right arm itches), HEADACHE (Headache) and PYREXIA (pyrexia) in a 66-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 071F21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 26-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 26-Oct-2021, the patient experienced MYALGIA (Body ache), VACCINATION SITE PRURITUS (injection site right arm itches), HEADACHE (Headache), PYREXIA (pyrexia), ARTHRALGIA (all joints hurt) and FATIGUE (Tired). On 27-Oct-2021, the patient experienced HYPERHIDROSIS (sweating). On 27-Oct-2021, PYREXIA (pyrexia) had resolved. At the time of the report, HYPERHIDROSIS (sweating), MYALGIA (Body ache), VACCINATION SITE PRURITUS (injection site right arm itches), HEADACHE (Headache), ARTHRALGIA (all joints hurt) and FATIGUE (Tired) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Concomitant medications were not provided. Treatment information was not provided. This case was linked to MOD-2021-367384, MOD-2021-367334 (Patient Link).

Weitere VAERSDATA-Felder

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

VAERS 1846884

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: NE
Alter: 66,0
Geschlecht: F
Eingang: 05.11.2021
Impfdatum: 28.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Chills Cough Erythema Pain in extremity Rhinorrhoea SARS-CoV-2 test negative Sinus pain

Symptomtext

I had a sore arm. I had a red spot. I had a running nose, cough, and chills. My arm was sore and red. On Tuesday, I had sinus pain. I called my provider. They wanted me to take a COVID-19 test, negative results. I am on day 7 and I still have the cough and running nose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: COVID-19 test
Aktuelle Erkrankungen: N/A
Vorgeschichte: Type 2 Diabetic
Andere Medikamente: Tylenol
Allergien: Penicillin Bacterium Telex Corn
Vorherige Impfungen: TB

VAERS 1846645

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: IL
Alter: 37,0
Geschlecht: M
Eingang: 05.11.2021
Impfdatum: 31.10.2021
Beginn: 01.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Pyrexia

Symptomtext

Unexplained fever of 104.8 within 12 hours in injection

Weitere VAERSDATA-Felder

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

VAERS 1845890

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: MA
Alter: 48,0
Geschlecht: M
Eingang: 05.11.2021
Impfdatum: 25.10.2021
Beginn: 26.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Chills Feeling abnormal Feeling cold Insomnia Pain in extremity

Symptomtext

First evening was fine, typical soreness in arm was only symptom. Next day was fine, feeling a little 'out of it', moderate soreness in arm continued. Second evening, extreme chills lasting the entire night (did not sleep at all). Felt I could not get warm despite plenty of heat and blankets used. Symptoms dissipated by morning. No further symptoms after that.

Weitere VAERSDATA-Felder

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

VAERS 1844552

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: CA
Alter: 42,0
Geschlecht: F
Eingang: 04.11.2021
Impfdatum: 30.10.2021
Beginn: 04.11.2021
Tage bis Beginn: 5,0
Dosis: 3
Route/Site: SYR / LA

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

Urticaria

Symptomtext

Broke out in hives all over my body. Taking Benadryl, went to urgent care and given Benadryl shot.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Urticaria
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Tilia Fe, Dymista
Allergien: -
Vorherige Impfungen: -

VAERS 1844069

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: VA
Alter: 24,0
Geschlecht: F
Eingang: 04.11.2021
Impfdatum: 03.11.2021
Beginn: 03.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Injection site erythema Injection site pain Injection site pruritus Injection site swelling Injection site warmth Rash

Symptomtext

Injection site red, swollen and warm to touch. Rash (small bumps) on whole body. Injection site sore and sometimes itchy.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: No.
Aktuelle Erkrankungen: None.
Vorgeschichte: None.
Andere Medikamente: (birth control), Topimax (headache meds), Ritzitriptan, Claritin, Flonase, Melatonin
Allergien: None.
Vorherige Impfungen: -

VAERS 1842848

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071f21a

mild

Staat: WA
Alter: 37,0
Geschlecht: M
Eingang: 04.11.2021
Impfdatum: 25.10.2021
Beginn: 01.11.2021
Tage bis Beginn: 7,0
Dosis: 1
Route/Site: SYR / LA

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

Arthralgia Injection site pruritus Injection site swelling

Symptomtext

Large raised spot at spot of injection. Has become very itchy, and should pain developing in both shoulders.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Gerd
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1841184

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: CA
Alter: 63,0
Geschlecht: M
Eingang: 03.11.2021
Impfdatum: 01.11.2021
Beginn: 02.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Asthenia Chills Decreased appetite Headache Myalgia Pyrexia

Symptomtext

fever (101.3) muscle aches chills weak head ache not hungry

Weitere VAERSDATA-Felder

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

VAERS 1839891

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: CT
Alter: 72,0
Geschlecht: F
Eingang: 03.11.2021
Impfdatum: 28.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Burning sensation Fatigue Pruritus Rash

Symptomtext

The day after receiving my third dose, I felt extremely fatigued. The following day I felt itching and burning on the right side of my face and neck. Later that evening, I saw breaking out on my arms and upper torso. From then on, it filled in very quickly with a heavy rash down my legs and badly on my back. Monday, I went to my Primary Care Physician, and was diagnosed that the rash was drug related. The only different thing I had done, was receive my vaccine. I received a prescription for prednisone and was told to continue taking Benadryl. As of today, the rash is still moderate on my back, legs, and arms. It has disappeared from my face and neck though.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: No tests were performed.
Aktuelle Erkrankungen: I was not experiencing any illness.
Vorgeschichte: Fifteen years ago, I had cancer, but I do not have any health conditions now.
Andere Medikamente: I was taking Gabapentin 1200mg. Ipratropium Bromide (nasal spray twice daily). Multivitamin Vitamin D3 Calcium Fish Oil
Allergien: I do not have any allergies.
Vorherige Impfungen: -

VAERS 1837690

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: NH
Alter: 35,0
Geschlecht: F
Eingang: 02.11.2021
Impfdatum: 01.11.2021
Beginn: 01.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Axillary pain Chills Headache Injection site erythema Pain Sleep disorder Urticaria

Symptomtext

Large 2 inch red welt at injection site that is causing pain into my armpit. Body aches and chills, mild headache and trouble sleeping night of injection

Weitere VAERSDATA-Felder

Praegender Schweregrund: Axillary pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: No
Vorgeschichte: Asthma
Andere Medikamente: Zyrtex and Singulair
Allergien: Gluten allergy
Vorherige Impfungen: -

VAERS 1837215

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: MO
Alter: 31,0
Geschlecht: F
Eingang: 02.11.2021
Impfdatum: 27.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

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

Axillary pain Lymphadenopathy

Symptomtext

Enlarged lymph nodes under left arm (front of armpit). Very tender in both armpits, on sides of breasts.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Axillary pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Mold toxicity
Andere Medikamente: Daily vitamin, Vitamin D 5K Omega Magnesium Glycinate Melatonin
Allergien: Augmentin allergy
Vorherige Impfungen: -

VAERS 1836941

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: VA
Alter: 74,0
Geschlecht: F
Eingang: 02.11.2021
Impfdatum: 27.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Arthralgia Extra dose administered Myalgia

Symptomtext

Note that this was my booster shot. I am still having MUCH more hip and knee joint pain than normal with my arthritis on the 6th day after my shot.. Additionally, I am having muscle pain in my leg. I did not have these side effects after the first two shots.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: none yet as of this date (11/02/2021)
Aktuelle Erkrankungen: No infections, but see item 12
Vorgeschichte: osteoarthritis, microscopic colitis, interstitial cystitis/painful bladder syndrome
Andere Medikamente: Amlodipine, benazepril, amitriptyline, multivitamin, vitamin D, fiber
Allergien: lots of antibiotics, including penicillin, sulfa drugs, tetracycline & others. No known food allergies
Vorherige Impfungen: Decades ago I fainted after a tetanus vacination.

VAERS 1834258

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: MI
Alter: 63,0
Geschlecht: F
Eingang: 01.11.2021
Impfdatum: 29.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Erythema Induration Peripheral swelling Pruritus

Symptomtext

Harding lump in arm, redness that has expanded up to about shoulder area, the area is also itchy, pt will follow up with her doctor

Weitere VAERSDATA-Felder

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

VAERS 1834228

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21a

mild

Staat: NC
Alter: 38,0
Geschlecht: F
Eingang: 01.11.2021
Impfdatum: 31.10.2021
Beginn: 31.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Pain Pain in extremity Pyrexia

Symptomtext

10 hours post vaccine sore arm, low grade fever, generalized aches and pains. Fever and aches still persist on day two

Weitere VAERSDATA-Felder

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

VAERS 1833815

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: NY
Alter: 62,0
Geschlecht: F
Eingang: 01.11.2021
Impfdatum: 29.10.2021
Beginn: 30.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Lymph node pain Lymphadenopathy

Symptomtext

swollen left armpit lymph nodes, sore, tender.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Lymph node pain
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: lidocaine and dental filling on October 5, 2021
Vorgeschichte: celiac, stage zero COPD, stage one emphysema, spinal scoliosis, obesity since quit smoking in 2006, osteoporosis
Andere Medikamente: none
Allergien: codeine and derivatives, gluten (celiac disease), dust allergy, perhaps seasonal allergy symptoms (runny nose + occasional sneezing)
Vorherige Impfungen: -

VAERS 1833751

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: OH
Alter: 67,0
Geschlecht: F
Eingang: 01.11.2021
Impfdatum: 01.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 28,0
Dosis: 3
Route/Site: SYR / LA

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

Dizziness Extra dose administered Fatigue Injection site erythema Injection site pruritus Injection site warmth Pain Pyrexia

Symptomtext

Typical fever, body aches, dizzy, exhausted, but as those resolved on day 3 itching began at firm reddened injection site, also hot to touch, irregular borders, no raised rash. Not a skin infection. Called my PCP for a large part of the winter this year as I was last year and got doses 11 & 2 at PHARMACY. Office told me to ice it. Pharmacy said apply hydrocortisone cream. MY CONCERN IS DOES THIS INCREASE MY CHANCES OF A SYSTEMIC ALLERGIC REACTION WITH MODERNA DOSING IF WE HAVE TO REPEAT COVID VAX IN FALL OF 2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension (treated), migraines with cyclical vomiting (treated), GERD (treated)
Andere Medikamente: Singular, atenolol, Zyrtec, lisinopril HCTZ, Effexor, Vit D, rosuvastatin, meloxicam (stopped prior to vax and began at 48 hrs post vax), esomeprazol OTC
Allergien: Ampicillin
Vorherige Impfungen: -

VAERS 1833438

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: NY
Alter: 26,0
Geschlecht: M
Eingang: 01.11.2021
Impfdatum: 28.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 1,0
Dosis: N/A
Route/Site: IM / RA

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

Chest discomfort Fatigue Headache Injection site pain Pyrexia

Symptomtext

Fever of 100.8 degrees, lowered to normal a day after appearing Headache, gone with fever Tightness/fatigue in chest, went away at approx. 3:00 PM on the same day Pain at injection site, persistent to the time of this report but severity has gone down dramatically

Weitere VAERSDATA-Felder

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

VAERS 1833398

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: NC
Alter: 69,0
Geschlecht: F
Eingang: 01.11.2021
Impfdatum: 28.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Diarrhoea Extra dose administered Headache Lethargy Nausea Vaccination site erythema Vaccination site mass

Symptomtext

Patient describes day after receiving vaccine developing a big red lump (~5" in diameter). She also developed nausea, a headache, extreme lethargy, and severe diarrhea.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Unknown
Andere Medikamente: Unknown
Allergien: Unknown
Vorherige Impfungen: -

VAERS 1833199

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: RI
Alter: 30,0
Geschlecht: M
Eingang: 01.11.2021
Impfdatum: 29.10.2021
Beginn: 30.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / RA

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

Chills Diarrhoea Extra dose administered Fatigue Feeling cold Headache Inappropriate schedule of product administration Injection site pain

Symptomtext

Moderna vaccine booster received within an hour after the flu vaccine (flu in left arm, Moderna in right) on Friday afternoon. Not sure which of the vaccines was the cause, or if it was the combination. Friday Evening through Sunday Morning - arm sore at the injection site. Took Motrin Saturday morning - diarrhea. Took Imodium AD Saturday afternoon - chills - wore sweats, a thermal shirt, and a fleece bathrobe/blanket in 60+deg weather, and was still cold Saturday and Sunday - headache (mild, nowhere near migraine level). Took Motrin Saturday and Sunday - tired. Took a few naps

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Asthma
Andere Medikamente: Montelucast, Caffiene, Fish Oil, Lactaid, Zyrtec, Multivitamin, Flu Shot (received about 30min before Moderna Booster)
Allergien: Bengay, Provolone, Almonds
Vorherige Impfungen: -

VAERS 1832381

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21a

mild

Staat: FL
Alter: 74,0
Geschlecht: F
Eingang: 31.10.2021
Impfdatum: 30.10.2021
Beginn: 30.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Chills Headache Nausea Pain Pain in extremity

Symptomtext

Body aches, very sore arm, headache, nausea, chills

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: COPD, HASHIMOTO'S HYPOTHYROIDISM, HIGH BLOOD PRESSURE, SCOLIOSIS LUMBAR SPINE, ARTHRITIS
Vorgeschichte: COPD, HASHIMOTO'S HYPOTHYROIDISM, HIGH BLOOD PRESSURE, SCOLIOSIS LUMBAR SPINE, ARTHRITIS
Andere Medikamente: Levothyroxyn, montelucast, valsartan, vitamins: D3, B12, multi vitamin.
Allergien: Daisies, bee stings, preventative shots for poison ivy.
Vorherige Impfungen: Had a terrible night. Body aches, very sore arm, headache, nausea. After dose #2 on 03/29/2021. Age 74. Moderna

VAERS 1832111

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: NC
Alter: 70,0
Geschlecht: F
Eingang: 31.10.2021
Impfdatum: 25.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: SYR / LA

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

Injection site pain Lymphadenopathy

Symptomtext

Swollen lymph nodes on left side under arm and groin occurred 3 days after vaccination. Other expected symptoms day 1-2, sore arm at injection site.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: None to date
Aktuelle Erkrankungen: None
Vorgeschichte: Low thyroid, osteoarthritis lower back
Andere Medikamente: Levothyroxine, lisinopril-hydrochlorothiazide, hydrochlorothiazide, pravastatin, estradiol topical, Tylenol, preparation-H.
Allergien: Cipro
Vorherige Impfungen: -

VAERS 1832047

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: FL
Alter: 76,0
Geschlecht: F
Eingang: 31.10.2021
Impfdatum: 27.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Injection site erythema Injection site inflammation Injection site pruritus

Symptomtext

REDNESS, INFLAMATION, ERYTHEMA, PRURITIS AT INJECTION SITE

Weitere VAERSDATA-Felder

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

VAERS 1831960

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: TN
Alter: 52,0
Geschlecht: M
Eingang: 31.10.2021
Impfdatum: 28.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Feeling cold Injection site pain Pain Pyrexia Submaxillary gland enlargement

Symptomtext

About 17-19 hours after I received my Moderna booster I developed chills, mild fever, soreness in injection location of left shoulder, followed by my left armpit being very swollen and body aches. It also felt like I could have diarrhea, but it was just regular bowels.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Paxil Klonopin Buspar Risperdal
Allergien: -
Vorherige Impfungen: About 12 hours after my 2nd Moderna vaccine I developed chills and body aches. 52 yrs old, 10/28/2021, Moderna vaccine booster.

VAERS 1831498

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21a

mild

Staat: FL
Alter: 90,0
Geschlecht: M
Eingang: 30.10.2021
Impfdatum: 25.10.2021
Beginn: 26.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Asthenia Blood test Chills Dizziness Feeling abnormal Infection Injection site bruising Injection site erythema Injection site pain Injection site swelling Pain

Symptomtext

Site: Bruising at Injection Site-Medium, Site: Pain at Injection Site-Medium, Site: Redness at Injection Site-Medium, Site: Swelling at Injection Site-Medium, Systemic: Body Aches Generalized-Medium, Systemic: Chills-Medium, Systemic: Dizziness / Lightheadness-Medium, Systemic: Weakness-Medium, Additional Details: Pt received booster vaccine monday 10/25, came next day with slight bruising/swelling. appeared to be injection site rxn confirmed by both rph. Told him to follow up with md if it gets worse. Wed called and said feeling better, then hours later called and felt worse. Went to md friday and they suspect an infection and given abx awaiting blood work to confirm

Weitere VAERSDATA-Felder

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

VAERS 1830009

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071f21a

mild

Staat: OK
Alter: 48,0
Geschlecht: F
Eingang: 29.10.2021
Impfdatum: 28.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Cold sweat Confusional state Injection site swelling Lymphadenopathy Pyrexia

Symptomtext

Mom called on 10/29 concerned about her daughter who received her moderna covid booster on 10/28. mom stated daughter is currently in chemotherapy and has developed several symptoms such as a fever of over 100* for 24 hours, cold sweats, swelling at the injection site, swollen lymph nodes, and confusion. I told mom to tell daughter to seek medical attention at either an urgent care or at the ER and to also inform her doctor of the reaction.

Weitere VAERSDATA-Felder

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

VAERS 1829657

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071f21a

mild

Staat: IL
Alter: 19,0
Geschlecht: F
Eingang: 29.10.2021
Impfdatum: 29.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Dizziness Injection site haemorrhage Pallor

Symptomtext

Patient received moderna vaccine and after removal of the needle, she began to bleed from the injection. She began to feel dizzy and lightheaded, face turned a bit white. We gave her water and gatorade and she began to feel better. We continued to monitor her for about 30 mins before she left

Weitere VAERSDATA-Felder

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

VAERS 1829404

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: NC
Alter: 68,0
Geschlecht: M
Eingang: 29.10.2021
Impfdatum: 27.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: - / LA

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

Chills Headache Injection site pain Pyrexia

Symptomtext

After the vaccine I had pain in the injection site, chilis, headache, and high temperature at 99.0.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Hypertension High cholesterol Bradycardia
Andere Medikamente: Rosuvastatin Amlodipine Metoprolol Tartrate Losartan Aspirin Loratadine Flonase
Allergien: Lactose-Intolerance Amoxicillin Levaquin
Vorherige Impfungen: With the second COVID-19 vaccine my side affects where similar to the side affects I had with the booster.

VAERS 1825815

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: IL
Alter: 25,0
Geschlecht: F
Eingang: 28.10.2021
Impfdatum: 27.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / RA

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

Injection site erythema Injection site induration Injection site swelling Injection site warmth

Symptomtext

Aprox 30 hours after third dose (booster), I developed a large, hard, bump, red in color and warm to the touch, approx 2-3 inches in diameter, on the upper arm underneath the injection site (not in lymph node under arm).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: -
Andere Medikamente: Sprintec, lysine (1000 mg), Valacyclovir as needed
Allergien: Codeine, monocycline
Vorherige Impfungen: -

VAERS 1825656

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: IL
Alter: 67,0
Geschlecht: F
Eingang: 28.10.2021
Impfdatum: 27.10.2021
Beginn: 27.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Fatigue Pain

Symptomtext

0.5ml administered as a third dose. Patient was contacted for a well-being check. reports body aches, fatigue. Patient agrees to continue with Tylenol as needed.

Weitere VAERSDATA-Felder

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

VAERS 1825449

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: IL
Alter: 67,0
Geschlecht: U
Eingang: 28.10.2021
Impfdatum: 27.10.2021
Beginn: 27.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Incorrect dose administered Injection site pain

Symptomtext

Third dose given as 0.5ml Patient denied any reaction. other than soreness at the injection site.

Weitere VAERSDATA-Felder

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

VAERS 1821940

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: MD
Alter: 64,0
Geschlecht: F
Eingang: 27.10.2021
Impfdatum: 27.10.2021
Beginn: 27.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Rash Urticaria

Symptomtext

Hives and rash noted after vaccination, monitored for 30min

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: unable to provide this information
Vorgeschichte: unable to provide this information
Andere Medikamente: unable to provide this infomation
Allergien: unable to provide this information
Vorherige Impfungen: -

VAERS 1821770

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: NY
Alter: 19,0
Geschlecht: F
Eingang: 27.10.2021
Impfdatum: 27.10.2021
Beginn: 27.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Feeling hot Hyperhidrosis Pallor

Symptomtext

Pt described feeling hot and feeling like she was going to faint/pass out. Pt appeared to be sweating around face/forehead, and was visibly pale. I advised her to lower her mask, so she could cool off, and offered a cold paper towel. There was visible paleness of her lips. She did NOT mention any difficulty breathing, tingling or nausea. When she looked slightly better, I offered her a water to drink. Her color started to come back, and she looked a lot better than she did when she first complained of symptoms. She said she was feeling better. I advised her to wait a few more minutes before leaving. She looked much better when leaving the store (and never did actually pass out).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: no
Vorgeschichte: asthma
Andere Medikamente: unknown
Allergien: no
Vorherige Impfungen: same reaction, unknown vaccine

VAERS 1819665

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

mild

Staat: IL
Alter: 74,0
Geschlecht: M
Eingang: 27.10.2021
Impfdatum: 25.10.2021
Beginn: 25.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Fatigue Incorrect dose administered Pyrexia

Symptomtext

Patient received wrong booster dose. Patient received 0.5mL dose instead of 0.25mL dose. 24 hours post vaccine administration, patient states "feeling a little feverish and tired that night I received the vaccine, but feeling better now."

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none noted
Vorgeschichte: Hx of Heart Disease
Andere Medikamente: None noted
Allergien: NKA
Vorherige Impfungen: -

VAERS 1814663

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21a

mild

Staat: MI
Alter: 64,0
Geschlecht: F
Eingang: 25.10.2021
Impfdatum: 23.10.2021
Beginn: 25.10.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: SYR / LA

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

Axillary pain Lymphadenopathy Sleep disorder

Symptomtext

Swollen Lymph notes in left arm pit. Woke up during the night from the pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Axillary pain
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: -
Andere Medikamente: Multiple vitamins-minerals, Armour Thyroid 60mg, Atorvastain 10MG, cymbalta 90mg
Allergien: none
Vorherige Impfungen: -

VAERS 2695800

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: -
Alter: -
Geschlecht: U
Eingang: 13.10.2023
Impfdatum: 30.10.2021
Beginn: 30.09.2022
Tage bis Beginn: 335,0
Dosis: 2
Route/Site: - / -

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

Blood test COVID-19 immunisation Hyponatraemia Suspected COVID-19

Symptomtext

HYPONATREMIA; SUSPECTED COVID-19 INFECTION; REVACCINATION WITH DIFFERENT COVID-19 VACCINE; This spontaneous report received from a patient via other manufacturer (pfizer) concerned a patient of unspecified age, sex, race and ethnic origin. The patient's height, and weight were not reported. The patient's concurrent conditions included: rheumatoid arthritis, diabetes insipidus (since 2015), hypothyroidism, and unspecified drug allergy. The patient received covid-19 vaccine ad26.cov2.s (dose number in series 1) (suspension for injection, route of admin not reported, batch number: 1805020, expiry: UNKNOWN) dose was not reported, 1 total administered on 30-OCT-2021 for covid-19 prophylaxis. It was unknown whether patient had any adverse events following vaccination with first dose of covid-19 vaccine ad26.cov2.s. (dose number in series 1). The patient received non-company suspect moderna covid-19 vaccine (elasomeran) (dose number in series 2) (form of admin and route of admin were not reported batch number: 071F21A, expiry: UNKNOWN) dose was not reported, administered on 14-MAY-2022 for covid-19 prophylaxis. It was unknown whether patient had any adverse events following vaccination moderna covid-19 vaccine (elasomeran) (dose number in series 2). The patient additionally received non-company suspect pfizer (tozinameran) (dose number in series 3) (form of admin and route of admin were not reported, batch number: UT7751KA, expiry: UNKNOWN) dose was not reported, administered on 30-SEP-2022 for covid-19 prophylaxis which was revaccination with different covid-19 vaccine (dose number in series 3). Concomitant medications included desmopressin, diphenhydramine, estradiol, guaifenesin, hydroxychloroquine, ibuprofen, levothyroxine, paracetamol, phenylephrine, and pseudoephedrine hydrochloride. On an unspecified date in 2023, the patient experienced suspected covid-19 infection (dose number in series 3). The patient administered non-company suspect drug (name unspecified) (form of admin, route of admin, batch number and expiry were not reported) dose was not reported, administered first dose on 02-OCT-2023 and last dose on 03-OCT-2023 for treatment of covid 19. On 03-OCT-2023 at 08:00, the patient experienced hyponatremia, and was hospitalized (date unspecified) (dose number in series 3). Duration of hospitalization was reported as 3 and discharge information were not reported. Laboratory data (dates unspecified) included: Blood test not reported. Treatment medications (dates unspecified) included: IV (intravenous) fluids, sodium tablet and fluid restricts. The action taken with covid-19 vaccine ad26.cov2.s, elasomeran, and tozinameran was not applicable. The patient recovered from hyponatremia on 04-OCT-2023, and the outcome of suspected covid-19 infection and revaccination with different covid-19 vaccine was not reported. This report was serious (Hospitalization Caused / Prolonged).; Sender's Comments: V0: 20231013890-hyponatremia. The event shows an incompatible temporal relationship. Therefore, this event is considered inconsistent with vaccine administration.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Blood test
Hospital-Tage: -
Labordaten: Test Name: BLOOD WORK; Result Unstructured Data: not reported
Aktuelle Erkrankungen: Diabetes insipidus (since 2015); Drug allergy; Hypothyroidism; Rheumatoid arthritis
Vorgeschichte: -
Andere Medikamente: IBUPROFEN; ACETAMINOPHEN; SUDAFED [PSEUDOEPHEDRINE HYDROCHLORIDE]; DIPHENHYDRAMINE; GUAIFENESIN; PHENYLEPHRINE; DESMOPRESSIN; LEVOTHYROXINE; ESTROGEN; HYDROXYCHLOROQUINE
Allergien: -
Vorherige Impfungen: -

VAERS 2670815

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: -
Alter: 61,0
Geschlecht: M
Eingang: 14.08.2023
Impfdatum: 20.12.2021
Beginn: 20.01.2023
Tage bis Beginn: 396,0
Dosis: 3
Route/Site: IM / RA

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

Obstructive sleep apnoea syndrome

Symptomtext

ADULT OBSTRUCTIVE SLEEP APNEA, SEVERE

Weitere VAERSDATA-Felder

Praegender Schweregrund: Obstructive sleep apnoea syndrome
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2646314

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: MI
Alter: 72,0
Geschlecht: F
Eingang: 16.06.2023
Impfdatum: 02.11.2021
Beginn: 08.02.2022
Tage bis Beginn: 98,0
Dosis: 3
Route/Site: - / -

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

COVID-19 SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Breakthrough case admission after 3 vaccines Moderna 2/6/21 lot# 031L20A; Moderna 3/6/21 lot# 030A21A; Moderna 11/2/21 lot# 071F21A

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID +
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2637353

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: -
Alter: 68,0
Geschlecht: F
Eingang: 26.05.2023
Impfdatum: 22.11.2021
Beginn: 13.02.2022
Tage bis Beginn: 83,0
Dosis: 3
Route/Site: IM / LA

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

Computerised tomogram thorax abnormal Drug withdrawal maintenance therapy Hypoxia

Symptomtext

R09.02 HYPOXIA 2/13/2022 ABNL CHEST CT SCAN R09.02 HYPOXIA 2/13/2022 LONG TERM METHADONE THERAPY FOR DRUG MAINTENANCE THERAPY

Weitere VAERSDATA-Felder

Praegender Schweregrund: Computerised tomogram thorax abnormal
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2631081

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: -
Alter: 75,0
Geschlecht: F
Eingang: 12.05.2023
Impfdatum: 28.10.2021
Beginn: 04.08.2022
Tage bis Beginn: 280,0
Dosis: 3
Route/Site: IM / LA

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

Acute myeloid leukaemia Obstructive sleep apnoea syndrome

Symptomtext

OBSTRUCTIVE SLEEP APNEA 8/4/2022 ACUTE MYELOID LEUKEMIA

Weitere VAERSDATA-Felder

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

VAERS 2623965

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: -
Alter: 31,0
Geschlecht: F
Eingang: 01.05.2023
Impfdatum: 29.12.2021
Beginn: 23.03.2022
Tage bis Beginn: 84,0
Dosis: 3
Route/Site: - / -

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

Hypoxia Symptom recurrence

Symptomtext

PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE HYPOXIA 3/24/2022 -- RECURRENCE OF SAME SYMPTOMS

Weitere VAERSDATA-Felder

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

VAERS 2616118

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: CT
Alter: 54,0
Geschlecht: F
Eingang: 17.04.2023
Impfdatum: 04.11.2021
Beginn: 18.01.2022
Tage bis Beginn: 75,0
Dosis: 3
Route/Site: IM / LA

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

Blood copper Blood folate Blood lactic acid Blood test abnormal C-reactive protein Contusion Full blood count abnormal HIV test Haemorrhage Hepatitis B virus test Hepatitis C virus test International normalised ratio Iron binding capacity total Laboratory test Liver function test increased Platelet count decreased Prothrombin time Serum ferritin

Symptomtext

On 1/18/22 had my annual physical and CBC showed platelets going from 274 to 80 , platelets continue to drop after monthly testing and was referred to a hematologist continue to have issues with low platelets, bleeding and bruising . Recent blood work now has liver functions high 1/20/23 and being followed with testing by gastroenterologists. I had no issues prior to the Covid vaccinations.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Blood copper
Hospital-Tage: -
Labordaten: Labs CBC 1/18/22, immature platelets 1/18/22, CBC 2/16/22, immature platelets 1/26/22, CBC 3/30/22, Ferritin, iron TIBC, PT/INR, Folate, HIV, Hep B and C, copper, C-reactive and Lactate7/28/22, Immature Platelets and CBC 9/30/22, Immature platelets and CBC 10/10/22, immature platelets and CBC 10/17/22, immature platelets and CBC 10/24/22, MDS panel, Flow, CBC 11/1/22, CBC and immature platelets 1/20/23, US 1/30/23 and liver functions, CBC and platelets 3/31/23
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Birth control pills, Vitamin C, Vitamin B12, multi-vitamin and Zertec
Allergien: Sulfa drugs
Vorherige Impfungen: -

VAERS 2609161

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: MO
Alter: 60,0
Geschlecht: M
Eingang: 04.04.2023
Impfdatum: 27.11.2021
Beginn: 15.03.2023
Tage bis Beginn: 473,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 SARS-CoV-2 test positive

Symptomtext

Unable to speak with case due to hospitalization. Case was admitted to Hospital, on 03/15/2023, tested positive for COVID 19 on 03/28/2023. On 03/30/2023 was discharged from Hospital and admitted to Hospital, where case is currently.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: unknown
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2574369

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: MI
Alter: 89,0
Geschlecht: M
Eingang: 02.02.2023
Impfdatum: 28.10.2021
Beginn: 06.05.2022
Tage bis Beginn: 190,0
Dosis: 3
Route/Site: - / -

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

COVID-19 SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Breakthrough case admission after 3 vaccines Moderna 3/6/21 Lot# 029A21A; Moderna 4/3/21 Lot# 045A21A; Moderna 10/28/21 Lot# 071F21A

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID+
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2567726

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: MI
Alter: 82,0
Geschlecht: M
Eingang: 25.01.2023
Impfdatum: 03.11.2021
Beginn: 20.12.2021
Tage bis Beginn: 47,0
Dosis: 3
Route/Site: - / -

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

COVID-19 SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Breakthrough case admission after 3 vaccines Moderna 2/3/21 Lot# 007M20A; Moderna 3/3/21 Lot# 023M20A; Moderna 11/3/21 Lot# 071F21A

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID +
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2529034

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: KY
Alter: 65,0
Geschlecht: F
Eingang: 12.12.2022
Impfdatum: 02.12.2021
Beginn: 04.12.2022
Tage bis Beginn: 367,0
Dosis: 2
Route/Site: IM / LA

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

Unevaluable event

Symptomtext

Admitted to hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Unevaluable event
Hospital-Tage: 6,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2528991

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071f21a

gering

Staat: KY
Alter: 82,0
Geschlecht: M
Eingang: 12.12.2022
Impfdatum: 29.10.2021
Beginn: 30.11.2022
Tage bis Beginn: 397,0
Dosis: 3
Route/Site: IM / LA

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

Unevaluable event

Symptomtext

Admitted to hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Unevaluable event
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2526748

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: OH
Alter: 44,0
Geschlecht: M
Eingang: 08.12.2022
Impfdatum: 03.12.2021
Beginn: 20.05.2022
Tage bis Beginn: 168,0
Dosis: 3
Route/Site: SYR / LA

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

Atrial fibrillation Blood albumin normal Blood calcium normal Blood chloride increased Blood creatinine normal Blood glucose normal Blood potassium normal Blood sodium normal Blood test normal Blood urea normal Carbon dioxide normal Chest X-ray normal Electrocardiogram abnormal Electrocardiogram ambulatory normal Electrocardiogram normal Full blood count normal Glomerular filtration rate normal Heart rate increased

Symptomtext

It was on May 20 2021 between four and five AM that my smart watch woke me up with high rate heart notification so I did one lead EKG on watch and indicated I was in atrial filiation I took six readings from my home to the hospital and the heart rate ranged form 116-143 BPMs. At the hospital blood work was done and all results were normal.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Atrial fibrillation
Hospital-Tage: -
Labordaten: Blood profile; Tropine level was low right at 7. ECG test was standard ranges. Prothrombin time was 11.7 seconds. Comprehensive metabolic panel; sodium 139; potassium 3.6; chloride 107; Co2 total was 23; BUN 18; Creatine 1.08; Albuin 4.2; Calcium 9.6; Glucose 105; Protien7.3; Estimated GFR value 83; CBC range normal; chests x-ray results normal. Lungs clear. Holter monitor prescribed for 24hrs AMB only.; No sustained atrial or ventricular arrhythmias noted.
Aktuelle Erkrankungen: None
Vorgeschichte: Kidney stones
Andere Medikamente: Hydrochlorothiazide; potassium pill; PROTONIX
Allergien: Erythromycin; doxycycline
Vorherige Impfungen: -

VAERS 2512959

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071f21a

gering

Staat: KY
Alter: 71,0
Geschlecht: F
Eingang: 21.11.2022
Impfdatum: 02.11.2021
Beginn: 13.11.2022
Tage bis Beginn: 376,0
Dosis: 3
Route/Site: IM / RA

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

Unevaluable event

Symptomtext

Admitted to hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Unevaluable event
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2502021

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071f21a

gering

Staat: KY
Alter: 84,0
Geschlecht: F
Eingang: 08.11.2022
Impfdatum: 04.12.2021
Beginn: 05.11.2022
Tage bis Beginn: 336,0
Dosis: 3
Route/Site: IM / RA

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

Unevaluable event

Symptomtext

Admitted to hospital

Weitere VAERSDATA-Felder

Praegender Schweregrund: Unevaluable event
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2501952

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071f21a

gering

Staat: KY
Alter: 74,0
Geschlecht: F
Eingang: 08.11.2022
Impfdatum: 10.03.2021
Beginn: 28.10.2022
Tage bis Beginn: 597,0
Dosis: 3
Route/Site: IM / RA

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

Unevaluable event

Symptomtext

Admitted to hospital

Weitere VAERSDATA-Felder

Praegender Schweregrund: Unevaluable event
Hospital-Tage: 11,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2501934

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071f21a

gering

Staat: KY
Alter: 83,0
Geschlecht: F
Eingang: 08.11.2022
Impfdatum: 05.03.2021
Beginn: 28.10.2022
Tage bis Beginn: 602,0
Dosis: 3
Route/Site: IM / RA

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

Unevaluable event

Symptomtext

Admitted to hospital

Weitere VAERSDATA-Felder

Praegender Schweregrund: Unevaluable event
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2486025

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071 F21A

gering

Staat: MA
Alter: 74,0
Geschlecht: F
Eingang: 22.10.2022
Impfdatum: 04.03.2021
Beginn: 15.04.2022
Tage bis Beginn: 407,0
Dosis: 2
Route/Site: - / -

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

COVID-19 COVID-19 immunisation SARS-CoV-2 test Vaccination failure

Symptomtext

REVACCINATION WITH DIFFERENT COVID-19 VACCINE; CONFIRMED CLINICAL VACCINATION FAILURE; CONFIRMED COVID-19 INFECTION; This spontaneous report received from a patient via (pfizer) concerned a 76 year old female. Initial information was processed along with additional information on 18-OCT-2022. The patient's height, and weight were not reported. The patient's past medical history included: two parathyroids removed, and concurrent conditions included: hypothyroid (after removal of thyroid (cancer)), gastroesophageal reflux disease, and osteopenia. The patient received covid-19 vaccine ad26.cov2.s (Dose number in series 1) (suspension for injection, route of admin not reported, batch number: 1805022 expiry: unknown) dose was not reported, 1 total, administered on 04-MAR-2021 on right arm for covid-19 prophylaxis. The patient received two doses of non-company suspect vaccine (Spikevax, moderna covid-19 vaccine) elasomeran (Dose number in series 2) (form of admin, route of admin were not reported, batch number: 071 F21A expiry: unknown) dose was not reported, administered on 27-OCT-2021 on right arm and third dose received (Dose number in series 3) (form of admin, route of admin were not reported, batch number: 005M21A expiry: UNKNOWN) dose was not reported, administered on 15-APR-2022 on right arm for covid-19 prophylaxis which was revaccination with different covid-19 vaccine (Dose number in series 3). Age at time of vaccination 74 years old. Concomitant medications included biotin, calcium, calcium carbonate/colecalciferol, fish oil, levothyroxine, omeprazole, and vitamins nos. On an unspecified date in 2022, the patient had covid-19 infection (Dose number in series 3). The patient received Nirmatrelvir/ritonavir (Paxlovid) (form of admin, route of admin and batch number were not reported, expiry: unknown) dose was not reported, administered from 24-SEP-2022 to 28-SEP-2022 for covid-19 treatment. On 03-OCT-2022 23:00 (5 days after end of paxlovid), the patient experienced return of Covid symptoms like runny nose, post nasal drip, sneezing, extreme congestion, cough, chills, fatigue, shortness of breath only upon exertion, The patient had positive Covid antigen test 7 days after end of Paxlovid (confirmed covid-19 infection (Dose number in series 3) and had confirmed clinical vaccination failure (Dose number in series 1). On 05-OCT-2022, Laboratory data included: COVID-19 antigen test Positive. Treatment medications (dates unspecified) included: ibuprofen, pseudoephedrine hydrochloride, dextromethorphan, and guaifenesin for covid-19. The action taken with covid-19 vaccine ad26.cov2.s and elasomeran was not applicable and with paxlovid treatment discontinued. The patient was recovering from confirmed covid-19 infection, and the outcome of confirmed clinical vaccination failure and revaccination with different covid-19 vaccine was not reported. This report was serious (Other Medically Important Condition). This report was associated with product quality complaint 90000255690.; Sender's Comments: V0: 20221030593-covid-19 vaccine ad26.cov2.s-confirmed clinical vaccination failure . The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There are other factors more likely to be associated with the event(s) than the drug. Specifically: SPECIAL SITUATIONS. Therefore, this event(s) is considered not related.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 20221005; Test Name: COVID-19 ANTIGEN TEST; Test Result: Positive
Aktuelle Erkrankungen: Gastrooesophageal reflux disease; Hypothyroidism (after removal of thyroid (cancer)); Osteopenia
Vorgeschichte: Medical History/Concurrent Conditions: Parathyroidectomy
Andere Medikamente: LEVOTHYROXINE; OMEPRAZOLE; CALCIUM; BIOTIN; OMEGA 3 FISH OIL [FISH OIL]; VITAMIN D 2000
Allergien: -
Vorherige Impfungen: -

VAERS 2451833

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: -
Alter: -
Geschlecht: U
Eingang: 20.09.2022
Impfdatum: 11.03.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: OT / LA

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

COVID-19 immunisation Interchange of vaccine products Suspected COVID-19

Symptomtext

interchange of vaccine products; Covid-19 Immunisation; Suspected covid-19 infection/runny nose, cough, and weakness; This spontaneous case was reported by a patient and describes the occurrence of SUSPECTED COVID-19 (Suspected covid-19 infection/runny nose, cough, and weakness), INTERCHANGE OF VACCINE PRODUCTS (interchange of vaccine products) and COVID-19 IMMUNISATION (Covid-19 Immunisation) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 005M51A and 071F21A) for COVID-19 prophylaxis. Co-suspect products included non-company products COVID-19 VACCINE NRVV AD26 (JNJ 78436735) (JANSSEN COVID-19 VACCINE) for COVID-19 prophylaxis and NIRMATRELVIR, RITONAVIR (PAXLOVID) for COVID-19 treatment. Concurrent medical conditions included Hypothyroidism and Drug allergy. On 11-Mar-2021, the patient received first dose of COVID-19 VACCINE NRVV AD26 (JNJ 78436735) (JANSSEN COVID-19 VACCINE) (unknown route) 1 dosage form. On 27-Oct-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 13-May-2022, received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 09-Jul-2022, the patient started NIRMATRELVIR, RITONAVIR (PAXLOVID) (unknown route) at an unspecified dose. In 2022, the patient experienced SUSPECTED COVID-19 (Suspected covid-19 infection/runny nose, cough, and weakness). On an unknown date, the patient experienced INTERCHANGE OF VACCINE PRODUCTS (interchange of vaccine products) and COVID-19 IMMUNISATION (Covid-19 Immunisation). At the time of the report, SUSPECTED COVID-19 (Suspected covid-19 infection/runny nose, cough, and weakness) had not resolved and INTERCHANGE OF VACCINE PRODUCTS (interchange of vaccine products) and COVID-19 IMMUNISATION (Covid-19 Immunisation) outcome was unknown. Not Provided No concomitant medications were reported. It was unknown whether patient had any adverse event following dose 1 and 2. On 16-Jul-2022, 2 days after completing Paxlovid, the patient experienced runny nose, cough, and weakness. Reporter assessed causality for event suspected COVID-19 with Janssen vaccine as possibly related. The patient was not taking any other medications/products with in 2 weeks of starting COVID-19 treatment. No treatment details were reported. Company Comment: This is a spontaneous case concerning a patient of unknown age and gender with no relevant medical history, who experienced the unexpected non-serious event of (AESI) Suspected Covid-19 and additional events of Covid-19 immunization and interchange of vaccine products. The events Covid-19 immunization and interchange of vaccine products occurred approximately 7 months after the after the first dose of Janssen Covid-19 Vaccine. It was reported event suspected covid-19 occurred approximately 2 months after the third dose of mRNA-1273 Vaccine. It was also reported patient took Paxlovid for 5 days, then after 2 days of completion of Paxlovid patient experienced the event Suspected covid-19. No further details on lab test results and further treatment received were reported. The benefit-risk relationship of mRNA-1273 Vaccine, is not affected by this report.; Sender's Comments: This is a spontaneous case concerning a patient of unknown age and gender with no relevant medical history, who experienced the unexpected non-serious event of (AESI) Suspected Covid-19 and additional events of Covid-19 immunization and interchange of vaccine products. The events Covid-19 immunization and interchange of vaccine products occurred approximately 7 months after the after the first dose of Janssen Covid-19 Vaccine. It was reported event suspected covid-19 occurred approximately 2 months after the third dose of mRNA-1273 Vaccine. It was also reported patient took Paxlovid for 5 days, then after 2 days of completion of Paxlovid patient experienced the event Suspected covid-19. No further details on lab test results and further treatment received were reported. The benefit-risk relationship of mRNA-1273 Vaccine, is not affected by this report.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 immunisation
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Drug allergy; Hypothyroidism
Vorgeschichte: -
Andere Medikamente: PAXLOVID
Allergien: -
Vorherige Impfungen: -

VAERS 2449611

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071f21a

gering

Staat: KY
Alter: 86,0
Geschlecht: F
Eingang: 17.09.2022
Impfdatum: 06.11.2021
Beginn: 12.09.2022
Tage bis Beginn: 310,0
Dosis: 3
Route/Site: IM / RA

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

Unevaluable event

Symptomtext

Admitted to hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Unevaluable event
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2442826

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071f21a

gering

Staat: KY
Alter: 75,0
Geschlecht: M
Eingang: 13.09.2022
Impfdatum: 29.10.2021
Beginn: 07.06.2022
Tage bis Beginn: 221,0
Dosis: 3
Route/Site: IM / LA

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

Unevaluable event

Symptomtext

Admitted to hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Unevaluable event
Hospital-Tage: 6,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2442818

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071f21a

gering

Staat: OH
Alter: 71,0
Geschlecht: F
Eingang: 13.09.2022
Impfdatum: 06.11.2021
Beginn: 15.06.2022
Tage bis Beginn: 221,0
Dosis: 3
Route/Site: IM / LA

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

Unevaluable event

Symptomtext

Admitted to hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Unevaluable event
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2438785

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: KY
Alter: 84,0
Geschlecht: M
Eingang: 10.09.2022
Impfdatum: 06.11.2021
Beginn: 17.08.2022
Tage bis Beginn: 284,0
Dosis: 3
Route/Site: - / -

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

Blood pressure abnormal Hypertensive encephalopathy Magnetic resonance imaging abnormal Metabolic encephalopathy

Symptomtext

Admit Date: 8/17/2022 Discharge Date: 8/20/22 Principal Dx/ Final Dx: Acute metabolic encephalopathy Relevant Inpt Dx: Principal Problem: Acute metabolic encephalopathy Active Problems: Rheumatoid arthritis involving both wrists with positive rheumatoid factor Essential hypertension HPI: Hospital Course: This 84 year old man was admitted with acute metabolic encephalopathy. It was felt to be hypertensive encephalopathy. His BP improved and he has been doing well. He is alert and conversant and ambulating in hall. MRI shows chronic changes but nothing acute Consults: IP CONSULT TO NEUROLOGY IP CONSULT TO SOCIAL WORK Disposition: home Discharge Condition: fair

Weitere VAERSDATA-Felder

Praegender Schweregrund: Blood pressure abnormal
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2438756

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071f21a

gering

Staat: LA
Alter: 75,0
Geschlecht: M
Eingang: 10.09.2022
Impfdatum: 29.10.2021
Beginn: 26.08.2022
Tage bis Beginn: 301,0
Dosis: 3
Route/Site: IM / RA

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

Extra dose administered

Symptomtext

Admitted to hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2425351

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: SC
Alter: 71,0
Geschlecht: M
Eingang: 31.08.2022
Impfdatum: 05.05.2022
Beginn: 20.08.2022
Tage bis Beginn: 107,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19

Symptomtext

Contracted COVID-19 - 8/22/2022

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: Hypertension
Andere Medikamente: Lisinopril/HCTZ 20/25mg, Docusate Sodium 100 mg, Centrum Silver Men 50+ multivitamin
Allergien: Codeine
Vorherige Impfungen: -

VAERS 2433332

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: -
Alter: 97,0
Geschlecht: M
Eingang: 17.08.2022
Impfdatum: 04.04.2022
Beginn: 08.06.2022
Tage bis Beginn: 65,0
Dosis: 3
Route/Site: IM / LA

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

Metabolic encephalopathy

Symptomtext

Narrative: Acute Metabolic Encephalopathy

Weitere VAERSDATA-Felder

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

VAERS 2408348

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: KY
Alter: 81,0
Geschlecht: F
Eingang: 11.08.2022
Impfdatum: 04.10.2021
Beginn: 18.05.2022
Tage bis Beginn: 226,0
Dosis: 2
Route/Site: IM / LA

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

COVID-19

Symptomtext

Admitted to the hospital with COVID-19.

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Praegender Schweregrund: COVID-19
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Arthritis, Burn of left hand, CAD (coronary artery disease), Community acquired pneumonia, Constipation, COPD, Dizziness, Epilepsy, Fall, Fatigue, Foot drop, Former smoker, Heart attack, CABG (06/09/2015), OTHER MEDICAL (6/3/14), Hyperlipidemia, Hypertension, Kidney disease, Lung disease, MRSA (methicillin resistant Staphylococcus aureus) infection (5/20/15), MRSA infection, MRSA infection, MRSA infection (07/20/2020), MRSA nasal colonization (7/16/2020), On home O2, Osteomyelitis, Osteoporosis, PAD (peripheral artery disease), PICC (peripherally inserted central catheter) in place (6/3/15), Seizure, and Seizures.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2401349

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: NJ
Alter: 70,0
Geschlecht: F
Eingang: 04.08.2022
Impfdatum: 26.02.2021
Beginn: 26.05.2022
Tage bis Beginn: 454,0
Dosis: 3
Route/Site: SYR / LA

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

COVID-19 Exposure to SARS-CoV-2 SARS-CoV-2 test positive

Symptomtext

On May 26, I tested positive for COVID. My great niece and nephew, who I care for tested positive on 5/21/22. My niece who was fully vaccinated and boosted with one shot tested positive on 5/24/22. My other great niece tested positive on the 24th also. My sister also tested positive on 5/26. The twin girls who are 3 were to young to be vaccinated. Their daycare center stopped requiring masks in March and stopped notifying parents in May when someone tested positive at the center. My 6 year old nephew was also vaccinated We always wore masks in public.

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Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: No
Vorgeschichte: Low platelet count but does not require treatment Seasonal allergies Mike asthma which does not require treatment
Andere Medikamente: Levothyroxine Fluticasone propionate nasal spray Zyrtec Centrum silver Citracal Womens propbiotic B-6
Allergien: None but I often have several side effects to medications so My doctors monitor what they give me.
Vorherige Impfungen: -

VAERS 2398865

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: -
Alter: -
Geschlecht: U
Eingang: 02.08.2022
Impfdatum: 11.03.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

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

Suspected COVID-19

Symptomtext

SUSPECTED COVID-19 INFECTION; This spontaneous report received from a patient via other manufacturer (Pfizer) concerned a patient of unspecified age and sex. The patient's height, and weight were not reported. The patient's concurrent conditions included: hypothyroidism, and drug allergy (Name of drug not reported), and other pre-existing medical conditions included: patient was not taking any other medications/products within 2 weeks of starting COVID-19 treatment. The patient initially received covid-19 vaccine ad26.cov2.s (dose number in series 1) (suspension for injection, route of admin not reported, batch number: 1805020 expiry: Unknown) dose was not reported, 1 total administered on 11-MAR-2021 in left arm for covid-19 prophylaxis. 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 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: 071F21A expiry: Unknown,) dose was not reported, administered on 27-OCT-2021 in left arm for covid-19 prophylaxis. It was unknown whether patient had any adverse event following vaccination Moderna covid-19 vaccine (elasomeran, dose number in series 2). The patient additionally received 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: 005M51A expiry: Unknown) dose was not reported, administered on 13-MAY-2022 in left arm for covid-19 prophylaxis. On an unspecified date in 2022, the patient experienced suspected covid-19 infection (dose number in series 3) The patient was prescribed with non-company suspect drug Paxlovid (form of admin and route of admin were not reported, batch number: unknown, expiry: Unknown) dose not reported, administered first dose on 09-JUL-2022 and last dose on 14-JUL-2022 for covid-19 treatment. No concomitant medications were reported. On 16-JUL-2022, 2 days after completing Paxlovid the patient experienced runny nose, cough, and weakness (dose number in series 3). The action taken with covid-19 vaccine ad26.cov2.s, elasomeran and elasomeran was not applicable and was discontinued for paxlovid. The patient had not recovered from suspected covid-19 infection. This report was non-serious.; Sender's Comments: V0: Medical assessment comment is not required as per standard procedure as case is assessed as non-serious.

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Praegender Schweregrund: Suspected COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Drug allergy (Name of drug not reported); Hypothyroidism
Vorgeschichte: Comments: patient was not taking any other medications/products within 2 weeks of starting COVID-19 treatment.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2335049

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: GA
Alter: 66,0
Geschlecht: F
Eingang: 25.06.2022
Impfdatum: 03.11.2021
Beginn: 31.05.2022
Tage bis Beginn: 209,0
Dosis: 3
Route/Site: OT / -

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

Expired product administered Product storage error

Symptomtext

Patient was inadvertently administed with the 11 days of expired vaccine that was initially stored in the refrigerator on 27 May 2022; Patient was inadvertently administed the vaccine 11 days after expiration date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient was inadvertently administed the vaccine 11 days after expiration date) and PRODUCT STORAGE ERROR (Patient was inadvertently administed with the 11 days of expired vaccine that was initially stored in the refrigerator on 27 May 2022) in a 67-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 033K21-2A and 071F21A) for COVID-19 prophylaxis. Previously administered products included for Product used for unknown indication: Pfizer (Primary series.) and Pfizer (Primary series.). Past adverse reactions to the above products included No adverse reaction with Pfizer and Pfizer. Concurrent medical conditions included Drug allergy (Benadryl). On 03-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 31-May-2022, received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 31-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient was inadvertently administed the vaccine 11 days after expiration date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Patient was inadvertently administed with the 11 days of expired vaccine that was initially stored in the refrigerator on 27 May 2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient was inadvertently administed the vaccine 11 days after expiration date) and PRODUCT STORAGE ERROR (Patient was inadvertently administed with the 11 days of expired vaccine that was initially stored in the refrigerator on 27 May 2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication were reported. It was unknown whether the patient had been diagnosed with/ tested positive for COVID 19. Acute and Chronic illness at the time of vaccination and up to one month before was reported as none. On 03-Nov-2021, patient received first booster dose of Moderna vaccine. On 31-May-2022, patient received second booster dose of Moderna vaccine (batch no. 033K21-2A) after expiration date. Number of doses/vials administered were reported as one vial. It was reported that the vial was initially stored in the refrigerator on 27May2022 and vial did not undergo any temperature excursions. It was unknown if AE cause patient to seek medical care (office visit, Urgent care, ER, hospitalized). Unknown if patient experienced a similar event in the past. No treatment medications were reported.

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Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Drug allergy (Benadryl)
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2325302

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 071F21A

gering

Staat: CA
Alter: 68,0
Geschlecht: F
Eingang: 21.06.2022
Impfdatum: 30.04.2022
Beginn: 06.06.2022
Tage bis Beginn: 37,0
Dosis: 4
Route/Site: - / LA

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

COVID-19 Drug ineffective SARS-CoV-2 test

Symptomtext

Covid dx 06Jun; Covid dx 06Jun; This is a spontaneous report received from contactable reporter(s) (Physician). The reporter is the patient. A 68-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 30Apr2022 at 12:00 as dose 4 (booster), single (Lot number: 071F21A) at the age of 68 years, in left arm for COVID-19 immunization; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown), as dose 2, single (Batch/Lot number: unknown) and as dose 3 (booster), single (Batch/Lot number: unknown) for COVID-19 immunization. The patient had no relevant medical history. The patient's concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 06Jun2022, outcome "unknown" and all described as "Covid dx 06Jun". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (06Jun2022) Covid diagnosed; (13Jun2022) Negative, notes: Day 8; (14Jun2022) Negative, notes: Day 9; (14Jun2022) Positive, notes: Day 10. Therapeutic measures were taken as a result of drug ineffective, covid-19; patient had received treatment with start of drug 06Jun2022 and date of last administration was 11Jun2022.; Sender's Comments: Based on the known safety profile and Limited information in the case report a casual association between LOE events and suspect drug BNT162B2 cannot be excluded.

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Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 20220606; Test Name: Covid; Result Unstructured Data: Test Result:Covid diagnosed; Test Date: 20220613; Test Name: Covid; Test Result: Negative ; Comments: Day 8; Test Date: 20220614; Test Name: Covid; Test Result: Negative ; Comments: Day 9; Test Date: 20220614; Test Name: Covid; Test Result: Positive ; Comments: Day 10
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: known allergies: None other medical history: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2317158

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: MI
Alter: 82,0
Geschlecht: M
Eingang: 13.06.2022
Impfdatum: 01.11.2021
Beginn: 09.06.2022
Tage bis Beginn: 220,0
Dosis: 2
Route/Site: - / -

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

COVID-19 SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

COVID vaccine breakthrough case

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Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID positive test 6/10/22
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2316377

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: -
Alter: 31,0
Geschlecht: F
Eingang: 11.06.2022
Impfdatum: 08.04.2021
Beginn: 01.05.2022
Tage bis Beginn: 388,0
Dosis: 2
Route/Site: - / -

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

COVID-19 SARS-CoV-2 test Vaccination failure

Symptomtext

CONFIRMED CLINICAL VACCINATION FAILURE; CONFIRMED COVID-19 INFECTION; This spontaneous report received from a patient via other manufacturer Pfizer concerned a 33 year old female. Initial information was processed with the additional information received on 07-JUN-2022. The patient's height, and weight were not reported. The patient's concurrent conditions included: asthma, depression, and sulfa drugs allergy, and other pre-existing medical conditions included: Patient was not pregnant at the time of reporting. The patient received covid-19 vaccine ad26.cov2.s (dose number in series 1) (suspension for injection, route of admin not reported, batch number: 1808982 expiry: UNKNOWN) dose was not reported, 1 total, administered on 08-APR-2021 in right arm for prophylactic vaccination. Age at time of vaccination 31 years old. The patient additionally received non-company suspect vaccine included: Moderna (spikevax) vaccine (elasomeran) (dose number in series 2) (form of admin, and route of admin were not reported, batch number: 071F21A expiry: UNKNOWN) dose was not reported, administered on 04-NOV-2021 in right arm for prophylactic vaccination. Concomitant medications included fluticasone propionate/salmeterol xinafoate, levosalbutamol, spironolactone, valaciclovir and decongestant cough suppressant/expectorant with nasal. On an unspecified date in MAY-2022, patient reported that symptoms never fully disappeared, still had a cough. On 18-MAY-2022, the patient was prescribed with Paxlovid (nirmatrelvir and ritonavir) for covid-19 treatment. Patient received last dose of Paxlovid on 22-MAY-2022. On 23-MAY-2022, patient had moderate shortness of breath in addition to cough but she tested negative. Laboratory data included: COVID-19 virus test Negative. Symptoms continued all week. On 27-MAY-2022, patient tested positive again, no change in symptoms (confirmed covid-19 infection (dose number in series 2), which led to confirmed clinical vaccination failure (dose number in series 1). Laboratory data included: COVID-19 virus test Positive. Patient was still experiencing same symptoms on 28-MAY-2022. Treatment medications (dates unspecified) included: methylprednisolone. The action taken with covid-19 vaccine ad26.cov2.s, and elasomeran was not applicable. The patient had not recovered from confirmed covid-19 infection, and the outcome of confirmed clinical vaccination failure was not reported. This report was serious (Other Medically Important Condition). This report was associated with product quality complaint.; Sender's Comments: V0-20220609449-Covid-19 vaccine ad26.cov2.s-Confirmed clinical vaccination failure. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There are other factors more likely to be associated with the event(s) than the drug. Specifically: SPECIAL SITUATIONS. Therefore, this event(s) is considered not related.

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Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 20220523; Test Name: COVID-19 VIRUS TEST; Test Result: Negative ; Test Date: 20220527; Test Name: COVID-19 VIRUS TEST; Test Result: Positive
Aktuelle Erkrankungen: Asthma; Depression; Drug allergy
Vorgeschichte: Comments: Patient was not pregnant at the time of reporting.
Andere Medikamente: VALACYCLOVIR [VALACICLOVIR]; SPIRONOLACTONE; ADVAIR; LEVALBUTEROL [LEVOSALBUTAMOL]
Allergien: -
Vorherige Impfungen: -

VAERS 2315007

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: ME
Alter: 73,0
Geschlecht: F
Eingang: 10.06.2022
Impfdatum: 27.10.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: OT / RA

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

COVID-19 SARS-CoV-2 test

Symptomtext

COVID-19; This spontaneous case was reported by a consumer and describes the occurrence of COVID-19 (COVID-19) in a 73-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 071F21A) for COVID-19 vaccination. Concurrent medical conditions included Allergy to antibiotic (Doxicylline). Concomitant products included CELECOXIB (CELEBREX), VITAMIN D3 and METOPROLOL for an unknown indication. On 27-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced COVID-19 (COVID-19). The patient was treated with NIRMATRELVIR, RITONAVIR (PAXLOVID) from 25-May-2022 to 29-May-2022 for COVID-19 treatment, at an unspecified dose and frequency. At the time of the report, COVID-19 (COVID-19) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 29-May-2022, SARS-CoV-2 test: negative (Negative) Negative. On 03-Jun-2022, SARS-CoV-2 test: positive (Positive) Positive. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. It was reported that patient was taking other medications/products within 2 weeks of starting COVID-19 treatment. It was reported that patient had previously received a COVID-19 Vaccine. It was reported that the patient had a rebound of Covid and had tested positive occurring 5 days after completing Paxlovid treatment. Patient had tested negative and feeling well after finishing Paxlovid. With device date as 04-Jun-2022. Company comment-This spontaneous case concerns a female patient aged 73 years with no relevant medical history reported, who experienced the unexpected non serious Covid 19 on an unknown date after receiving the 3rd dose of mRNA-1273 vaccine in the covid 19 vaccination series. It was reported that the patient was treated for covid infection with Paxlovid from 25th May 2022 to 29th May 2022 for 5 days. Patient reported feeling well after Paxlovid and was tested negative. Five days later patient had rebound covid with symptoms and a positive test. No further details on clinical course, other lab test results were reported. The current pandemic situation of COVID 19 may remain as confounder and elderly age of the patient as a risk factor to the event Covid-19.The benefit-risk relationship of mRNA-1273 Vaccine is not affected by this report. Event seriousness assessed per medical judgement.; Sender's Comments: This spontaneous case concerns a female patient aged 73 years with no relevant medical history reported, who experienced the unexpected non serious Covid 19 on an unknown date after receiving the 3rd dose of mRNA-1273 vaccine in the covid 19 vaccination series. It was reported that the patient was treated for covid infection with Paxlovid from 25th May 2022 to 29th May 2022 for 5 days. Patient reported feeling well after Paxlovid and was tested negative. Five days later patient had rebound covid with symptoms and a positive test. No further details on clinical course, other lab test results were reported. The current pandemic situation of COVID 19 may remain as confounder and elderly age of the patient as a risk factor to the event Covid-19.The benefit-risk relationship of mRNA-1273 Vaccine is not affected by this report. Event seriousness assessed per medical judgement.

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Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 20220529; Test Name: COVID-19 test; Test Result: Negative ; Result Unstructured Data: Negative; Test Date: 20220603; Test Name: COVID-19 test; Test Result: Positive ; Result Unstructured Data: Positive
Aktuelle Erkrankungen: Allergy to antibiotic (Doxicylline)
Vorgeschichte: -
Andere Medikamente: CELEBREX; VITAMIN D3; METOPROLOL
Allergien: -
Vorherige Impfungen: -

VAERS 2313634

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: -
Alter: 49,0
Geschlecht: F
Eingang: 09.06.2022
Impfdatum: 29.10.2021
Beginn: 23.04.2022
Tage bis Beginn: 176,0
Dosis: 2
Route/Site: OT / RA

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

Blood test COVID-19 Feeling abnormal Influenza A virus test Influenza B virus test Interchange of vaccine products SARS-CoV-2 test Sinus congestion

Symptomtext

Interchange of vaccine products; Feeling congested and having drainage in her sinus; Felt funky again; Patient took a test at home and tested positive straight away; This spontaneous case was reported by a consumer and describes the occurrence of FEELING ABNORMAL (Felt funky again), SINUS CONGESTION (Feeling congested and having drainage in her sinus), COVID-19 (Patient took a test at home and tested positive straight away) and INTERCHANGE OF VACCINE PRODUCTS (Interchange of vaccine products) in a 49-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 048L21A and 071F21A) for Prophylactic vaccination. Previously administered products included for Prophylactic vaccination: Janssen Covid-19 Vaccine (Dose on. 1, batch lot no. 1805020, right arm administered in afternoon.) on 15-Mar-2021, Janssen Covid-19 Vaccine (Dose on. 1, batch lot no. 1805020, right arm administered in afternoon, reaction duration 48 hours.) on 15-Mar-2021, Janssen Covid-19 Vaccine (Dose on. 1, batch lot no. 1805020, right arm administered in afternoon, reaction duration 48 hours.) on 15-Mar-2021, Janssen Covid-19 Vaccine (Dose on. 1, batch lot no. 1805020, right arm administered in afternoon, reaction duration 48 hours.) on 15-Mar-2021, Janssen Covid-19 Vaccine (Dose on. 1, batch lot no. 1805020, right arm administered in afternoon, reaction duration 48 hours.) on 15-Mar-2021, Janssen Covid-19 Vaccine (The vaccine really hurt and felt like being injected with poison (dose number in series 1).) on 15-Mar-2021 and Influenza vaccine (It was reported that regularly she got the flu vaccination over the years sometimes had soreness in arm but not a big reaction.). Past adverse reactions to the above products included Chills with Janssen Covid-19 Vaccine; Fever with Janssen Covid-19 Vaccine; Headache with Janssen Covid-19 Vaccine; Injection site pain with Janssen Covid-19 Vaccine; Pain in arm with Influenza vaccine; Photosensitivity reaction with Janssen Covid-19 Vaccine; and Sickness with Janssen Covid-19 Vaccine. Concurrent medical conditions included Allergy (Unspecified allergy) and Depression (Started taking anti-depressant in 2019. continued taking through 2020 and 2021. decided to try hormone replacement therapy and had been effective.). Concomitant products included ETHINYLESTRADIOL;NORETHISTERONE from 02-Apr-2022 to an unknown date for an unknown indication. On 29-Oct-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 02-Apr-2022 at 11:00 AM, received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 23-Apr-2022, the patient experienced COVID-19 (Patient took a test at home and tested positive straight away). On 04-May-2022, the patient experienced FEELING ABNORMAL (Felt funky again). On 04-May-2022 at 5:30 PM, the patient experienced SINUS CONGESTION (Feeling congested and having drainage in her sinus). On an unknown date, the patient experienced INTERCHANGE OF VACCINE PRODUCTS (Interchange of vaccine products). The patient was treated with NIRMATRELVIR, RITONAVIR (PAXLOVID) from 24-Apr-2022 to April 2022 for COVID-19 treatment, at a dose of 1 dosage form, morning and evening untill doses end.; FLUTICASONE PROPIONATE (FLONASE [FLUTICASONE PROPIONATE]) at an unspecified dose and frequency and DIPHENHYDRAMINE HYDROCHLORIDE (BENADRYL CHILDRENS) at a dose of at night to sleep. At the time of the report, FEELING ABNORMAL (Felt funky again) and SINUS CONGESTION (Feeling congested and having drainage in her sinus) had resolved, COVID-19 (Patient took a test at home and tested positive straight away) was resolving and INTERCHANGE OF VACCINE PRODUCTS (Interchange of vaccine products) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): In 2021, Blood test: not reported Not reported. In January 2022, SARS-CoV-2 test: positive (Positive) Positive. In April 2022, SARS-CoV-2 test: positive (Positive) at home COVID test Positive. On 23-Apr-2022, SARS-CoV-2 test: positive (Positive) Positive. On 05-May-2022, Influenza A virus test: negative (Negative) Negative. On 05-May-2022, Influenza B virus test: negative (Negative) Negative. In May 2022, SARS-CoV-2 test: positive (Positive) at home COVID test Positive. In 2022, SARS-CoV-2 test: negative (Negative) Tested negative after few weeks. It was reported by the reporter that on 21-Apr-2022 or 22-Apr-2022 patient felt like coming down with head cold, was tired, sleeping a lot. Patient felt doozy and lousy but did not have difficulty in breathing. it was more just congestion, headache and fatigue type symptoms. The patient took home test and tested positive. Patient received Paxlovid as treatment which helped the patient feel better everyday after treatment. Patient went to clinic on 5 May 2022 for an additional dose of Paxlovid. 2nd dose of Paxlovid was not advised. The patient was sent home and told to drink fluids and try to sleep, that helped. the patient felt better and the 2nd set of symptoms from the episode were mostly over. Patient recovered from sensitivity to light, sick, chills, headache and fever on Mar 2021. The patient was treated with ibuprofen or Aspirin over the counter and did not see any physician for dose number in series 1. The patient was not pregnant nor breastfeeding at the time of this report. The patient was left handed. The patient was not aware of being around anybody that had covid-19 prior to coming down with it and was not really sure where she picked it up. The patient did not think she got COVID-19 prior to being vaccinated. The patient had no history of diabetes, hypertension, heart disease, auto-immune disorder or immunosuppressive disorder etc. The patient had no illness at the time of vaccination and no past history of similar events. Patient had no allergy to vaccine drug or food, had no pre-existing acute illness 30 days prior to vaccination, and no history of hospitalization in last 30 days. The patient had no other suspected causes including co-administered vaccines / risk factors. The patient's father was allergic to eggs and could not have any egg-based vaccines. The patient experience soreness in arm when treated with influenza vaccine for prophylactic vaccination. It was reported that regularly she got the flu vaccination over the years sometime had soreness in arm but not a big reaction Company Comment: This is a spontaneous case concerning a 49-year-old female patient with no relevant medical history, who experienced the unexpected, non-serious adverse event of special interest of COVID-19, approximately 21 days after receiving the second dose of mRNA-1273 vaccine (third COVID-19 vaccine). The patient was treated with Nirmatrelvir/Ritonavir. The event was resolving at the time of the report. Interchange of vaccine products was also reported as the patient received other COVID-19 vaccine (Janssen) as first dose approximately 7 months prior to the first dose of mRNA-1273. The benefit-risk relationship of mRNA-1273 is not affected by this report. This case was linked to MOD-2022-582590 (Patient Link).; Sender's Comments: This is a spontaneous case concerning a 49-year-old female patient with no relevant medical history, who experienced the unexpected, non-serious adverse event of special interest of COVID-19, approximately 21 days after receiving the second dose of mRNA-1273 vaccine (third COVID-19 vaccine). The patient was treated with Nirmatrelvir/Ritonavir. The event was resolving at the time of the report. Interchange of vaccine products was also reported as the patient received other COVID-19 vaccine (Janssen) as first dose approximately 7 months prior to the first dose of mRNA-1273. The benefit-risk relationship of mRNA-1273 is not affected by this report.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Blood test
Hospital-Tage: -
Labordaten: Test Date: 2021; Test Name: Blood Test; Result Unstructured Data: Not reported; Test Date: 20220505; Test Name: Influenza A test; Test Result: Negative ; Result Unstructured Data: Negative; Test Date: 20220505; Test Name: Influenza B test; Test Result: Negative ; Result Unstructured Data: Negative; Test Date: 202201; Test Name: COVID-19 PCR test; Test Result: Positive ; Result Unstructured Data: Positive; Test Date: 202204; Test Name: COVID-19 PCR test; Test Result: Positive ; Result Unstructured Data: at home COVID test Positive; Test Date: 20220423; Test Name: COVID-19 PCR test; Test Result: Positive ; Result Unstructured Data: Positive; Test Date: 202205; Test Name: COVID-19 PCR test; Test Result: Positive ; Result Unstructured Data: at home COVID test Positive; Test Date: 2022; Test Name: COVID-19 PCR test; Test Result: Negative ; Result Unstructured Data: Tested negative after few weeks
Aktuelle Erkrankungen: Allergy (Unspecified allergy); Depression (Started taking anti-depressant in 2019. continued taking through 2020 and 2021. decided to try hormone replacement therapy and had been effective.)
Vorgeschichte: -
Andere Medikamente: ETHINYLESTRADIOL;NORETHISTERONE
Allergien: -
Vorherige Impfungen: -

VAERS 2309443

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: -
Alter: 33,0
Geschlecht: F
Eingang: 04.06.2022
Impfdatum: 04.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: OT / RA

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

COVID-19 Interchange of vaccine products SARS-CoV-2 test

Symptomtext

Symptoms never fully disappeared, still had a cough.On 27-May-2022 Patient tested positive again, no change in symptoms; Johnson & Johnson Dose Number: 1 on 08Apr2021; Moderna Dose Number: 2 on 04Nov2021; This spontaneous case was reported by a patient and describes the occurrence of COVID-19 (Symptoms never fully disappeared, still had a cough.On 27-May-2022 Patient tested positive again, no change in symptoms) and INTERCHANGE OF VACCINE PRODUCTS (Johnson & Johnson Dose Number: 1 on 08Apr2021; Moderna Dose Number: 2 on 04Nov2021) in a 33-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 071F21A) for COVID-19 vaccination. Previously administered products included for Product used for unknown indication: Johnson & Johnson's Janssen COVID-19 Vaccine (Dose Number: 1 Batch/Lot No: 1808982 Location of injection: Arm Right) on 08-Apr-2021; for Drug use for unknown indication: Sulfa (Sulfa drugs). Past adverse reactions to the above products included Allergy with Sulfa; and No adverse event with Johnson & Johnson's Janssen COVID-19 Vaccine. Concurrent medical conditions included Asthma and Depression. Concomitant products included VALACYCLOVIR [VALACICLOVIR] from 06-Oct-2010 to an unknown date, SPIRONOLACTONE from 25-Apr-2022 to an unknown date, FLUTICASONE PROPIONATE, SALMETEROL XINAFOATE (ADVAIR) from 01-Feb-2022 to 18-May-2022 and LEVALBUTEROL [LEVOSALBUTAMOL] from 15-Jan-2021 to an unknown date for an unknown indication. On 04-Nov-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 04-Nov-2021, the patient experienced INTERCHANGE OF VACCINE PRODUCTS (Johnson & Johnson Dose Number: 1 on 08Apr2021; Moderna Dose Number: 2 on 04Nov2021). In May 2022, the patient experienced COVID-19 (Symptoms never fully disappeared, still had a cough.On 27-May-2022 Patient tested positive again, no change in symptoms). The patient was treated with NIRMATRELVIR, RITONAVIR (PAXLOVID) from 18-May-2022 to 22-May-2022 for COVID-19, at an unspecified dose and frequency and METHYLPREDNISOLONE ACETATE (METHYLPREDNISOLONE [METHYLPREDNISOLONE ACETATE]) at an unspecified dose and frequency. At the time of the report, COVID-19 (Symptoms never fully disappeared, still had a cough.On 27-May-2022 Patient tested positive again, no change in symptoms) had not resolved and INTERCHANGE OF VACCINE PRODUCTS (Johnson & Johnson Dose Number: 1 on 08Apr2021; Moderna Dose Number: 2 on 04Nov2021) had resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 23-May-2022, SARS-CoV-2 test: negative (Negative) Negative. On 27-May-2022, SARS-CoV-2 test: positive (Positive) Positive. An unspecified 'Cough suppressant/expectorant with nasal decongestant' was reported as concomitant medication which was started on 17May2022. Patient was taking other medications/products within 2 weeks of starting COVID-19 treatment. Patient previously received a COVID-19 vaccine. Device Date was reported as 28May2022. Company Comment: This is a spontaneous case of interchange of vaccine products for this 33-year-old, female patient with relevant medical history of Asthma and Depression, and past drug history of administration of one dose of the Johnson & Johnson COVID-19 vaccine, who experienced the unexpected, non-serious AESI of COVID-19. The event occurred approximately 6 months after receiving a dose (second dose in COVID-19 vaccination series) of the mRNA-1273 vaccine. On an unspecified date, the patient experienced COVID-19 symptoms which included cough. She initially took an unspecified cough suppressant/expectorant with nasal decongestant. The following day, the patient took and completed a 5-day course of Paxlovid (nirmatrelvir, ritonavir) from 18May2022 to 22May2022. It was reported that after the last dose of Paxlovid, the symptoms never fully resolved and the patient still had a cough. One day after the last dose of Paxlovid, the patient also experienced moderate shortness of breath but she tested negative for SARS-CoV-2. It was reported that the symptoms continued all week. Five days after the last dose of Paxlovid, the patient tested positive for SARS-CoV-2. The patient was treated with methylprednisolone (unspecified dosage, frequency and duration). However, the event had not resolved at the time of the report. The medical history of Asthma and Depression, which are known risk factors for COVID-19, remain as confounders. The benefit-risk relationship of the mRNA-1273 vaccine is not affected by this report.; Sender's Comments: This is a spontaneous case of interchange of vaccine products for this 33-year-old, female patient with relevant medical history of Asthma and Depression, and past drug history of administration of one dose of the Johnson & Johnson COVID-19 vaccine, who experienced the unexpected, non-serious AESI of COVID-19. The event occurred approximately 6 months after receiving a dose (second dose in COVID-19 vaccination series) of the mRNA-1273 vaccine. On an unspecified date, the patient experienced COVID-19 symptoms which included cough. She initially took an unspecified cough suppressant/expectorant with nasal decongestant. The following day, the patient took and completed a 5-day course of Paxlovid (nirmatrelvir, ritonavir) from 18May2022 to 22May2022. It was reported that after the last dose of Paxlovid, the symptoms never fully resolved and the patient still had a cough. One day after the last dose of Paxlovid, the patient also experienced moderate shortness of breath but she tested negative for SARS-CoV-2. It was reported that the symptoms continued all week. Five days after the last dose of Paxlovid, the patient tested positive for SARS-CoV-2. The patient was treated with methylprednisolone (unspecified dosage, frequency and duration). However, the event had not resolved at the time of the report. The medical history of Asthma and Depression, which are known risk factors for COVID-19, remain as confounders. The benefit-risk relationship of the mRNA-1273 vaccine is not affected by this report.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 20220523; Test Name: COVID-19 test; Test Result: Negative ; Result Unstructured Data: Negative; Test Date: 20220527; Test Name: COVID-19 test; Test Result: Positive ; Result Unstructured Data: Positive
Aktuelle Erkrankungen: Asthma; Depression
Vorgeschichte: -
Andere Medikamente: VALACYCLOVIR [VALACICLOVIR]; SPIRONOLACTONE; ADVAIR; LEVALBUTEROL [LEVOSALBUTAMOL]
Allergien: -
Vorherige Impfungen: -

VAERS 2303045

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: -
Alter: 51,0
Geschlecht: M
Eingang: 31.05.2022
Impfdatum: 08.03.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: OT / RA

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

COVID-19 SARS-CoV-2 test

Symptomtext

Confirmed Covid-19 infection; This spontaneous case was reported by a patient and describes the occurrence of COVID-19 (Confirmed Covid-19 infection) in a 52-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 071F21A) for Prophylactic vaccination. Co-suspect product included non-company product COVID-19 VACCINE NRVV AD26 (JNJ 78436735) (JANSSEN COVID-19 VACCINE) for Prophylactic vaccination. Concurrent medical conditions included Allergy to nuts (Tree nut allergy). Concomitant products included PARACETAMOL (TYLENOL) and IBUPROFEN (ADVIL [IBUPROFEN]) for an unknown indication. On 08-Mar-2021, the patient received first dose of COVID-19 VACCINE NRVV AD26 (JNJ 78436735) (JANSSEN COVID-19 VACCINE) (unknown route) 1 dosage form. On 09-Nov-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced COVID-19 (Confirmed Covid-19 infection) (seriousness criterion medically significant). The patient was treated with RITONAVIR from 20-Apr-2022 to 25-Apr-2022 for COVID-19, at an unspecified dose and frequency. At the time of the report, COVID-19 (Confirmed Covid-19 infection) had not resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, SARS-CoV-2 test: negative (Negative) Negative and positive (Positive) Positive. Cocomitant medications included tissue rejuvenator. On unspecified date on 2022, the patient experienced confirmed clinical vaccination failure with dose number in series 1. It was reported that on unknown date patient was tested negative for covid-19 after 10 days. On 01-May-2022 stated that patient had more severe symptoms reoccurred ( coded to confirmed covid-19 infection) (dose numder in series 2). Patient reported that he assumed the symptoms were something else and infected patient's partner as he was no longer isolating and on unknown date patient was tested pasitive again on day 16. This report was associated wit product quality complaint: 90000231245. The reporter and Mfr. causality for Janssen Covid-19 vaccine for the events confirmed Covid-19 infection and confirmed clinical vaccination failure was reported as possible. Confirmed clinical vaccination failure event has a compatible/ suggestive temporal relationship, was labelled, and as unknown scientific plausibility. There are other factors more likely to be associated with the event(s) than the drug. Specifically: Special situations. Therefore, thus event(s) was considered not related. COMPANY COMMENT: This is an spontaneous case concerning a 52-years-old male patient with medical history of Allergy to nuts, Concomitant products included PARACETAMOL and IBUPROFEN, first dose of JANSSEN COVID-19 VACCINE on 08-Mar-2021, RITONAVIR from 20-Apr-2022 to 25-Apr-2022 for COVID-19 who experienced the unexpected event of COVID-19 (seriousness criterion medically significant) in the context of 2nd dose of mRNA-1273 vaccine. The benefit-risk relationship of mRNA-1273 vaccine is not affected by this report.; Sender's Comments: This is an spontaneous case concerning a 52-years-old male patient with medical history of Allergy to nuts, Concomitant products included PARACETAMOL and IBUPROFEN, first dose of JANSSEN COVID-19 VACCINE on 08-Mar-2021, RITONAVIR from 20-Apr-2022 to 25-Apr-2022 for COVID-19 who experienced the unexpected event of COVID-19 (seriousness criterion medically significant) in the context of 2nd dose of mRNA-1273 vaccine. The benefit-risk relationship of mRNA-1273 vaccine is not affected by this report.

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Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: COVID-19 virus test; Test Result: Negative ; Result Unstructured Data: Negative; Test Name: COVID-19 virus test; Test Result: Positive ; Result Unstructured Data: Positive
Aktuelle Erkrankungen: Allergy to nuts (Tree nut allergy)
Vorgeschichte: -
Andere Medikamente: TYLENOL; ADVIL [IBUPROFEN]
Allergien: -
Vorherige Impfungen: -

VAERS 2296520

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: MD
Alter: 74,0
Geschlecht: F
Eingang: 26.05.2022
Impfdatum: 29.10.2021
Beginn: 28.02.2022
Tage bis Beginn: 122,0
Dosis: 3
Route/Site: SYR / LA

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

COVID-19 SARS-CoV-2 test positive

Symptomtext

I tested positive for COVID 3 months after my 3rd vaccine.

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Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: High Blood Pressure, High Cholesterol, Pre-diabetic
Andere Medikamente: Losartan 50mg, atorvastatin 40mg, Metformin 1000mg, Aspirin 81mg, Fish Oil, Vitamin C, Vitamin B12, Zinc
Allergien: None
Vorherige Impfungen: -

VAERS 2286398

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: NY
Alter: 51,0
Geschlecht: M
Eingang: 20.05.2022
Impfdatum: 09.11.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: OT / -

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

COVID-19 SARS-CoV-2 test Vaccination failure

Symptomtext

CONFIRMED CLINICAL VACCINATION FAILURE; CONFIRMED COVID-19 INFECTION; This spontaneous report received from a patient via other manufacturer (Pfizer) concerned a 52 year old male. Initial information was processed along with additional information received on 16-MAY-2022. The patient's height, and weight were not reported. The patient's concurrent conditions included: tree nut allergy. The patient previously received covid-19 vaccine ad26.cov2.s 9 (Dose number in series 1) (suspension for injection, route of admin not reported, batch number: 1805022 and expiry: unknown) dose was not reported, 1 total, administered on 08-MAR-2021 in right arm for prophylactic vaccination. Age at time of vaccination 51 years old. Concomitant medications included ibuprofen (advil), paracetamol (Tylenol) and Hammer Nutrition Tissue Rejuvenator and Race Cap. On an unspecified date in 2022, the patient experienced confirmed clinical vaccination failure (Dose number in series 1). The patient received non-company suspect vaccine Moderna covid-19 vaccine (elasomeran) (Dose number in series 2) (form of admin, route of admin was not reported, batch number: 071F21A, expiry: unknown) dose was not reported, administered on 09-NOV-2021 in right arm for prophylactic vaccination. The patient reported that he tested negative for covid-19 after 10 days (date unspecified). Treatment medications for covid-19 included: ritonavir (Paxlovid) from 20-APR-2022 to 25-APR-2022. On 01-MAY-2022, patient reported more severe symptoms reoccurred (coded to confirmed covid-19 infection) (Dose number in series 2). Patient reported that he assumed the symptoms were something else and infected his partner as he was no longer isolating. Patient tested positive again on day 16 (date unspecified). The action taken with covid-19 vaccine ad26.cov2.s, and elasomeran was not applicable. The patient had not recovered from confirmed covid-19 infection, and the outcome of confirmed clinical vaccination failure was not reported. This report was serious (Other Medically Important Condition). This report was associated with product quality complaint: 90000231245; Sender's Comments: V0:20220530373-COVID-19 VACCINE Ad26.COV2.S-confirmed clinical vaccination failure The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There are other factors more likely to be associated with the event(s) than the drug. Specifically: SPECIAL SITUATIONS. Therefore, this event(s) is considered not related.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: COVID-19 virus test; Result Unstructured Data: positive; Test Name: COVID-19 virus test; Result Unstructured Data: negative
Aktuelle Erkrankungen: Allergy to nuts
Vorgeschichte: Comments: Unknown
Andere Medikamente: TYLENOL [PARACETAMOL]; ADVIL [IBUPROFEN]
Allergien: -
Vorherige Impfungen: -

VAERS 2286397

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: IN
Alter: 36,0
Geschlecht: F
Eingang: 20.05.2022
Impfdatum: 28.10.2021
Beginn: 24.04.2022
Tage bis Beginn: 178,0
Dosis: 2
Route/Site: OT / -

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

COVID-19 SARS-CoV-2 test Vaccination failure

Symptomtext

CONFIRMED CLINICAL VACCINATION FAILURE; CONFIRMED COVID-19 INFECTION; This spontaneous report received from a patient via other company (Pfizer) concerned a 36 year old female. Initial information was processed along with the additional information received on 13-MAY-2022 and 18-MAY-2022. The patient's height, and weight were not reported. The patient's past medical history included: drug allergy, and concurrent conditions included: asthma, migraines, and seasonal allergies. The patient was not pregnant at the time of reporting. On 11-NOV-2020, the patient received covid-19 vaccine ad26.cov2.s (dose number in series: 1) (suspension for injection, route of admin not reported, batch number: 4381412, expiry: unknown) dose was not reported, 1 total administered to right arm for prophylactic vaccination. The age at time of vaccination was 35 years old. On 28-OCT-2021, the patient received non-company suspect elasomeran (Moderna vaccine) (dose number in series: 2) (form of admin and route of admin were not reported, batch number: 071F21A, expiry: unknown) dose was not reported, administered to left arm for prophylactic vaccination. No concomitant medications were reported. On 24-APR-2022, the patient experienced onset of covid-19 symptoms (dose number in series: 2). On the same day, the patient began treatment with Paxlovid (batch number: FX2740) for covid-19. On 28-APR-2022, the patient tested negative on a home antigen test. On 29-APR-2022, the patient took the last dose of Paxlovid. On 04-MAY-2022, the patient had symptoms and this corresponds to day 11 from initial symptom onset and tested positive for covid-19 (unspecified test) which indicated confirmed covid-19 infection (dose number in series: 2) and confirmed clinical vaccination failure (dose number in series: 1). The action taken with covid-19 vaccine ad26.cov2.s, and elasomeran was not applicable. The patient had not recovered from confirmed covid-19 infection, and the outcome of confirmed clinical vaccination failure was not reported. This report was serious (Other Medically Important Condition). This report was associated with a product quality complaint: 90000230965. The suspected product quality complaint has been confirmed to be the reported allegation could not be confirmed. A manufacturing related root cause could not be identified based on the PQC evaluation/investigation performed.; Sender's Comments: V0:20220526665-covid-19 vaccine ad26.cov2.s-confirmed clinical vaccination failure.The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There are other factors more likely to be associated with the event(s) than the drug. Specifically: SPECIAL SITUATIONS. Therefore, this event(s) is considered not related.

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Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 20220428; Test Name: COVID-19 rapid POC test; Result Unstructured Data: negative; Test Date: 20220504; Test Name: COVID-19 virus test; Result Unstructured Data: positive
Aktuelle Erkrankungen: Asthma; Migraine; Seasonal allergy
Vorgeschichte: Medical History/Concurrent Conditions: Drug allergy; Comments: The patient was not pregnant at the time of reporting.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2285035

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: NY
Alter: 38,0
Geschlecht: F
Eingang: 19.05.2022
Impfdatum: 16.11.2021
Beginn: 24.04.2022
Tage bis Beginn: 159,0
Dosis: 3
Route/Site: IM / RA

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

COVID-19 Vaccine breakthrough infection

Symptomtext

Breakthrough Covid case. Took Paxlovid. Resolved in 5 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: Sulfa antibiotics
Vorherige Impfungen: -

VAERS 2278004

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: CT
Alter: 43,0
Geschlecht: F
Eingang: 16.05.2022
Impfdatum: 13.11.2021
Beginn: 29.04.2022
Tage bis Beginn: 167,0
Dosis: 3
Route/Site: OT / -

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

COVID-19

Symptomtext

Covid Relapse; This spontaneous case was reported by a consumer and describes the occurrence of COVID-19 (Covid Relapse) in a 43-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 071F21A) for COVID-19 vaccination. Co-suspect product included non-company product TOZINAMERAN (PFIZER BIONTECH COVID-19 VACCINE) for COVID-19 vaccination. Concurrent medical conditions included Hypertension, Asthma and ADHD. On 13-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 19-Apr-2022, the patient received dose of TOZINAMERAN (PFIZER BIONTECH COVID-19 VACCINE) (unknown route) 1 dosage form. On 24-Apr-2022, received dose of TOZINAMERAN (PFIZER BIONTECH COVID-19 VACCINE) (unknown route) dosage was changed to 1 dosage form. On 29-Apr-2022, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced COVID-19 (Covid Relapse). At the time of the report, COVID-19 (Covid Relapse) was resolving. Additional Past drug reported as no and reaction as allergy. No concomitant medications were reported. The patient was taking other unspecified medications/products within 2 weeks of starting COVID-19 treatment. Company comment: This spontaneous case concerns a 43-year-old, female patient with medical history of Hypertension and Asthma, who experienced the unexpected, non-serious AESI of COVID-19. The event occurred 167 days after administration of third dose of mRNA-1273. The patient was administered with two doses of Pfizer 5 days prior to the event, the interval between the two doses is 5 days. The events were conservatively considered as related since the temporal association cannot be assessed/excluded due to the limited information available. Details of concomitant medications, medical history, clinical course, treatment and outcome were not provided. The benefit-risk relationship of mRNA-1273 is not affected by this report.; Sender's Comments: This spontaneous case concerns a 43-year-old, female patient with medical history of Hypertension and Asthma, who experienced the unexpected, non-serious AESI of COVID-19. The event occurred 167 days after administration of third dose of mRNA-1273. The patient was administered with two doses of Pfizer 5 days prior to the event, the interval between the two doses is 5 days. The events were conservatively considered as related since the temporal association cannot be assessed/excluded due to the limited information available. Details of concomitant medications, medical history, clinical course, treatment and outcome were not provided. The benefit-risk relationship of mRNA-1273 is not affected by this report.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: ADHD; Asthma; Hypertension
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2275257

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: AZ
Alter: 49,0
Geschlecht: F
Eingang: 13.05.2022
Impfdatum: 15.03.2021
Beginn: 19.04.2022
Tage bis Beginn: 400,0
Dosis: 2
Route/Site: OT / -

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

Suspected COVID-19 Vaccination failure

Symptomtext

SUSPECTED CLINICAL VACCINATION FAILURE; SUSPECTED COVID-19 INFECTION; This spontaneous report received from a patient via Pfizer concerned a 50 year old female. The patient's height, and weight were not reported. The patient's past medical history included: unspecified allergy, and concurrent conditions included: depression, and other pre-existing medical conditions included: The patient was not pregnant at the time of report. The patient received covid-19 vaccine ad26.cov2.s (Dose number in series 1) (suspension for injection, route of admin not reported, batch number: 1805020 expiry: Unknown) dose was not reported, 1 total administered to right arm on 15-MAR-2021 for prophylactic vaccination. Age at time of vaccination 49 years old. The patient received additional mon-company suspect vaccine included: Moderna covid-19 vaccine (elasomeran) (Dose number in series 2) (form of admin, route of admin, and were not reported batch number: 071F21A expiry: Unknown (dose 1), batch number: 048L21A expiry: Unknown(dose 2)) dose was not reported, administered on 29-OCT-2021 (dose 1), and dose was not reported, administered on 02-APR-2022 11:00 (dose 2) both doses to right arm for prophylactic vaccination. Age at time of vaccination 49 years old. Concomitant medications included Niva (ethinylestradiol/norethisterone) (1-5 MG-MCG). On 19-APR-2022, the patient experienced symptoms (suspected covid-19 infection) (dose number in series 2) which led to suspected clinical vaccination failure (Dose number in series 1). On 24-APR-2022, (on day 5 after symptoms started) she started treatment with Paxolovid (ritonavir). The patient stated that it was very helpful to her, felt better every day after treatment. On 03-MAY-2022 she was feeling totally well (Dose number in series 2). On 04-MAY-2022 (At 05:30) she woke up feeling congested and having drainage in her sinuses and feeling under the weather (Dose number in series 2). The action taken with covid-19 vaccine ad26.cov2.s, and elasomeran was not applicable. The patient had not recovered from suspected covid-19 infection, and the outcome of suspected clinical vaccination failure was not reported. This report was serious (Other Medically Important Condition). This report was associated with product quality complaint.; Sender's Comments: V0: 20220518282-covid-19 vaccine ad26.cov2.s-suspected clinical vaccination failure . The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There are other factors more likely to be associated with the event(s) than the drug. Specifically: SPECIAL SITUATIONS. Therefore, this event(s) is considered not related.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Suspected COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Depression
Vorgeschichte: Medical History/Concurrent Conditions: Allergy; Comments: The patient was not pregnant at the time of report.
Andere Medikamente: ETHINYLESTRADIOL;NORETHINDRONE
Allergien: -
Vorherige Impfungen: -

VAERS 2264743

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: IL
Alter: 85,0
Geschlecht: F
Eingang: 05.05.2022
Impfdatum: 06.11.2021
Beginn: 29.04.2022
Tage bis Beginn: 174,0
Dosis: 3
Route/Site: IM / LA

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

Asymptomatic COVID-19 Fall Femoral neck fracture SARS-CoV-2 test positive

Symptomtext

Patient received moderna vaccine on 1/26/21, 2/23/21, and 11/6/21. COVID positive on 4/29/22. Presented to ER on 4/29/22 and admitted. She sustained a right femoral neck fracture after a mechanical fall at home and therefore admitted. She was also noted to be COVID-19 positive (asymptomatic) upon admission. Discharged on 5/3/22

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Praegender Schweregrund: Asymptomatic COVID-19
Hospital-Tage: 4,0
Labordaten: 4/29/22 COVID19: positive
Aktuelle Erkrankungen: -
Vorgeschichte: hypertension, hyperlipidemia, diabetes non-insulin dependent
Andere Medikamente: atorvastatin 80 MG Tabs Commonly known as: LIPITOR 80 mg, Oral, NIGHTLY CALTRATE 600+D PO 1 Tablet, Oral, DAILY fenofibrate 54 MG Tabs Commonly known as: LOFIBRA 54 mg, Oral, DAILY folic acid 400 MCG Tabs Commonly known as: FOLVITE 40
Allergien: none
Vorherige Impfungen: -

VAERS 2263015

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071f21a

gering

Staat: MA
Alter: 57,0
Geschlecht: F
Eingang: 04.05.2022
Impfdatum: 28.10.2021
Beginn: 28.10.2021
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 Low-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2261956

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: MA
Alter: 69,0
Geschlecht: M
Eingang: 03.05.2022
Impfdatum: 01.11.2021
Beginn: 29.03.2022
Tage bis Beginn: 148,0
Dosis: 3
Route/Site: SYR / LA

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

COVID-19 SARS-CoV-2 test positive

Symptomtext

None

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: PCR test Pos on 3/29/2022
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Atorvastatin 40 mg Hydrochlorothiazide 25 mg
Allergien: None
Vorherige Impfungen: -

VAERS 2261917

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: MI
Alter: 87,0
Geschlecht: M
Eingang: 03.05.2022
Impfdatum: 26.10.2021
Beginn: 01.04.2022
Tage bis Beginn: 157,0
Dosis: 3
Route/Site: - / -

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

COVID-19

Symptomtext

Covid-19.

Weitere VAERSDATA-Felder

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

VAERS 2261888

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: NY
Alter: 42,0
Geschlecht: F
Eingang: 03.05.2022
Impfdatum: 29.10.2021
Beginn: 19.04.2022
Tage bis Beginn: 172,0
Dosis: 3
Route/Site: SYR / LA

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

COVID-19 SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Breakthrough case of COVID-19: I took cold medicine for a few weeks, it was too late to receive antiviral medication. I had a tele visit with the doctor and took a PCR test and tested positive.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID-19 PCR (04/24/2022) - positive
Aktuelle Erkrankungen: No
Vorgeschichte: Thyroid; seasonal allergies
Andere Medikamente: Levothyroxine, Melatonin, Vitamin C, and Vitamin D.
Allergien: No
Vorherige Impfungen: -

VAERS 2260518

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: PA
Alter: 55,0
Geschlecht: F
Eingang: 02.05.2022
Impfdatum: 31.10.2021
Beginn: 26.04.2022
Tage bis Beginn: 177,0
Dosis: 3
Route/Site: SYR / LA

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

COVID-19 SARS-CoV-2 test positive

Symptomtext

Diagnosed with Covid-19

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: PCR Covid test
Aktuelle Erkrankungen: None
Vorgeschichte: CGD
Andere Medikamente: Bactrim, Itraconazole
Allergien: None
Vorherige Impfungen: -

VAERS 2259914

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071f21a

gering

Staat: NY
Alter: 67,0
Geschlecht: M
Eingang: 01.05.2022
Impfdatum: 05.11.2021
Beginn: 01.12.2021
Tage bis Beginn: 26,0
Dosis: 3
Route/Site: IM / LA

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

Magnetic resonance imaging Tinnitus Ultrasound Doppler

Symptomtext

Pulsatile Tinnitus

Weitere VAERSDATA-Felder

Praegender Schweregrund: Magnetic resonance imaging
Hospital-Tage: -
Labordaten: 2 MRIs, Doppler ultrasound
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Omeprozole, vitamin D
Allergien: -
Vorherige Impfungen: -

VAERS 2249989

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: PA
Alter: 78,0
Geschlecht: M
Eingang: 25.04.2022
Impfdatum: 29.10.2021
Beginn: 31.10.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: SYR / UN

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

Acoustic stimulation tests abnormal Deafness bilateral Hearing aid user Sudden hearing loss

Symptomtext

Sudden hearing loss in both ears. According to ENT and audiologist, the loss is almost profound. A hearing test from a year ago shows normal hearing. Hearing aids are now necessary

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acoustic stimulation tests abnormal
Hospital-Tage: -
Labordaten: ENT dr. examination and hearing tests
Aktuelle Erkrankungen: -
Vorgeschichte: MGUS abnormal protein
Andere Medikamente: D3 Eliquis 5 mg twice day Atenolol 50 mg Amlodipine 5 mg Duloxetine 30 mg Lisinipril 20 mg
Allergien: sulfa morphine
Vorherige Impfungen: -

VAERS 2249970

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: TX
Alter: 71,0
Geschlecht: M
Eingang: 25.04.2022
Impfdatum: 28.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Blood test COVID-19 Stomatitis White blood cell count decreased

Symptomtext

After each Covid vaccination (1/28/2021, 02/25/2021 and 10/28/2021) I suffered acute mouth sores (all reported on V-Safe). After actually getting Covid in Demeter 2021, the same mouth sores appeared, and continued on and off until now. A blood check last week indicated a very low WBC.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Blood test
Hospital-Tage: -
Labordaten: Blood count 4/20/2021 and 4/22/2021.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Atorvastatin 40mg Valsartan 160mg
Allergien: None
Vorherige Impfungen: As noted above, after each Covid vaccination, acute mouth sores (ulcers)

VAERS 2243648

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: VA
Alter: 63,0
Geschlecht: F
Eingang: 20.04.2022
Impfdatum: 30.10.2021
Beginn: 01.11.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: SYR / RA

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

Hyperhidrosis Night sweats

Symptomtext

I started having night sweats again like when I had menopause. I called the doctor and told them and told them I wanted to go back on the estradiol because I was getting up at night to change clothes 2-3 times because of all the sweat.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hyperhidrosis
Hospital-Tage: -
Labordaten: No
Aktuelle Erkrankungen: No
Vorgeschichte: High blood pressure; Depression
Andere Medikamente: Diltiazem 90mg; Potassium citrate ER; Aspirin; Losartan potassium; Omeprazole; Citalopram
Allergien: Ace inhibitors; Seasonal allergies
Vorherige Impfungen: -

VAERS 2243512

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: VA
Alter: 44,0
Geschlecht: F
Eingang: 20.04.2022
Impfdatum: 12.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 5,0
Dosis: 3
Route/Site: IM / LA

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

Alopecia Blood test normal Lymphadenopathy Mammogram normal

Symptomtext

I noticed hair loss that was gradual. It is noticeable now. I went to my dermatologist and suggested a medication. I also talked to my PCP about that. I have not been on the medication long enough to notice. I also have a swollen lymph node which is on both sides. This lasted for 6 weeks. I had a mammogram which did not indicate anything. I have also had blood work to check my hormone levels which was normal.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Alopecia
Hospital-Tage: -
Labordaten: Mammogram; blood work
Aktuelle Erkrankungen: None
Vorgeschichte: Leaky Heart Valve; PCOS; Migraines
Andere Medikamente: Wellbutrin 150 mg, Bystolic 5 mg, Klonopin .5mg, Lexapro 10mg, Metformin ER 1500mg, Topamax 100mg, Multivitamin, Famotidine, Zyrtec
Allergien: Aspirin; Ibuprofen; NSAIDS
Vorherige Impfungen: -

VAERS 2238609

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: MN
Alter: 78,0
Geschlecht: F
Eingang: 18.04.2022
Impfdatum: 06.11.2021
Beginn: 17.04.2022
Tage bis Beginn: 162,0
Dosis: 3
Route/Site: UN / UN

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

COVID-19 Vaccine breakthrough infection

Symptomtext

admission/hospitalization with breakthrough COVID

Weitere VAERSDATA-Felder

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

VAERS 2223205

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: OH
Alter: 86,0
Geschlecht: F
Eingang: 08.04.2022
Impfdatum: 26.02.2021
Beginn: 08.10.2021
Tage bis Beginn: 224,0
Dosis: 3
Route/Site: IM / RA

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

Adverse event

Symptomtext

Moderna COVID vaccines received on 1/29/2021 and 2/26/2021 Hospitalized at Hospital on 10/8/2021 for COVID-19 Additional Moderna Booster received on 12/30/2021 after the adverse event

Weitere VAERSDATA-Felder

Praegender Schweregrund: Adverse event
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2216682

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071f21a

gering

Staat: MI
Alter: 50,0
Geschlecht: F
Eingang: 05.04.2022
Impfdatum: 29.10.2021
Beginn: 28.03.2022
Tage bis Beginn: 150,0
Dosis: 3
Route/Site: SYR / RA

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

COVID-19 SARS-CoV-2 test positive

Symptomtext

3/28/22 tested positive covid

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Copd
Andere Medikamente: -
Allergien: Codeine and all opiates
Vorherige Impfungen: -

VAERS 2209345

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: TX
Alter: 26,0
Geschlecht: F
Eingang: 31.03.2022
Impfdatum: 30.10.2021
Beginn: 21.01.2022
Tage bis Beginn: 83,0
Dosis: 3
Route/Site: IM / RA

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

Loss of personal independence in daily activities Paranasal sinus discomfort SARS-CoV-2 test Sinusitis

Symptomtext

Sinus pressure that did not improve with OTC and was unable to return to class without a test or doctors note. I recently took a COVID test prior to this sinusitis. At the doctor was given a prescription nasal spray fluticasone propionate and advised to keep with OTC regimen. The nasal spray worked and took about a week to clear.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of personal independence in daily activities
Hospital-Tage: -
Labordaten: No Medical test or Labs.
Aktuelle Erkrankungen: None
Vorgeschichte: Seasonal and Environmental Allergies
Andere Medikamente: Depo, Chamomile
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2201399

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: AR
Alter: 76,0
Geschlecht: F
Eingang: 28.03.2022
Impfdatum: 30.10.2021
Beginn: 26.03.2022
Tage bis Beginn: 147,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 SARS-CoV-2 test positive

Symptomtext

hospitalized with covid; fully vaccinated with booster

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: 1,0
Labordaten: positive covid pcr 3/26/22
Aktuelle Erkrankungen: unknown
Vorgeschichte: HTN, chronic back pain/fibromyalgia
Andere Medikamente: unknown
Allergien: morphine
Vorherige Impfungen: -

VAERS 2196544

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: MD
Alter: 57,0
Geschlecht: F
Eingang: 24.03.2022
Impfdatum: 28.10.2021
Beginn: 26.12.2021
Tage bis Beginn: 59,0
Dosis: 3
Route/Site: SYR / -

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

COVID-19 SARS-CoV-2 test positive

Symptomtext

Breakthrough of COVID virus after all 3 doses of the vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID test.
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Premarin
Allergien: Sespin; Shellfish
Vorherige Impfungen: -

VAERS 2182579

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: -
Alter: 92,0
Geschlecht: F
Eingang: 16.03.2022
Impfdatum: 02.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: - / -

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

Unevaluable event

Symptomtext

Hospitalization following COVID vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Unevaluable event
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2180083

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: MD
Alter: 75,0
Geschlecht: F
Eingang: 15.03.2022
Impfdatum: 30.12.2021
Beginn: 19.01.2022
Tage bis Beginn: 20,0
Dosis: 4
Route/Site: IM / AR

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

Abscess management Biopsy Oral dysplasia Tongue abscess

Symptomtext

At the beginning of Jan I had a number of abscesses on my tongue for about 2 weeks and at the end of that time there was one last issue under my tongue that turned out to be epithelial dysplasia. I was referred to a oral surgeon who found more than one and removed these on Feb 17. I am currently fit and healthy and have recovered 3/15.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abscess management
Hospital-Tage: -
Labordaten: 01/31 Biopsy(epithelial dysplasia on tongue)
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension; Diabetes type 2; Low immunoglobin-G and low white blood cell count; aortic stenosis
Andere Medikamente: Human IVIG, Atenolol, Hydrochlorothiazide, Losartan potassium, Amlodipine, Aspirin 81mg, Tricor, Crestor, Janumet, Glimepiride, One A Day Women's, Fish oil, D3
Allergien: BIAXIN; adhesives
Vorherige Impfungen: -

VAERS 2177645

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: NY
Alter: 42,0
Geschlecht: F
Eingang: 14.03.2022
Impfdatum: 01.11.2021
Beginn: 01.01.2022
Tage bis Beginn: 61,0
Dosis: 3
Route/Site: SYR / -

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

Acoustic stimulation tests abnormal Tinnitus

Symptomtext

I started to get horrible tinnitus (loud high pitched ringing in my ears) in Dec 2021 - Jan 2022. Began getting debilitating migraines after my first Covid vaccine in April 2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acoustic stimulation tests abnormal
Hospital-Tage: -
Labordaten: Heating test 2/18/21.
Aktuelle Erkrankungen: Migraines
Vorgeschichte: Migraine
Andere Medikamente: Influenza (Seasonal) Afluria Quadrivalent
Allergien: None
Vorherige Impfungen: -

VAERS 2177474

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: CT
Alter: 66,0
Geschlecht: M
Eingang: 14.03.2022
Impfdatum: 17.11.2021
Beginn: 01.12.2021
Tage bis Beginn: 14,0
Dosis: 3
Route/Site: IM / LA

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

Atrial fibrillation Atrial flutter Cardiac murmur Cardiac operation Mitral valve prolapse

Symptomtext

12/30/2021 Heart murmur/ Atrial Flutter. Mitral Valve Prolapse and AFib. Open heart surgery 01/26/2021 Repaired still in AFib awaiting conversion.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Atrial fibrillation
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: -
Andere Medikamente: One a day for men 50 plus Baby aspirin Glucosamine-Chodroitin Culturelle Rovustatin
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2174800

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: -
Alter: 34,0
Geschlecht: F
Eingang: 12.03.2022
Impfdatum: 25.03.2021
Beginn: 05.11.2021
Tage bis Beginn: 225,0
Dosis: UNK
Route/Site: OT / -

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

Maternal exposure during pregnancy Premature rupture of membranes Suspected COVID-19

Symptomtext

Suspected COVID-19 infection; Premature rupture of membrane; Maternal exposure during pregnancy; This spontaneous prospective pregnancy case was reported by a consumer and describes the occurrence of PREMATURE RUPTURE OF MEMBRANES (Premature rupture of membrane), SUSPECTED COVID-19 (Suspected COVID-19 infection) and MATERNAL EXPOSURE DURING PREGNANCY (Maternal exposure during pregnancy) in a 35-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 071F21A) for COVID-19 vaccination. Co-suspect product included non-company product COVID-19 VACCINE NRVV AD26 (JNJ 78436735) (JANSSEN COVID-19 VACCINE) for COVID-19 immunisation. Concurrent medical conditions included Anxiety, Endometriosis, Hypothyroidism, Irritable bowel syndrome, GERD and Obsessive-compulsive disorder. Concomitant products included PRENATAL VITAMINS [ASCORBIC ACID;BIOTIN;MINERALS NOS;NICOTINIC ACID;RETINOL;TOCOPHEROL;VITAMIN B NOS;VITAMIN D NOS], RANITIDINE HYDROCHLORIDE (ZANTAC) from 01-May-2021 to 01-Jun-2021, LEVOTHYROXINE SODIUM (SYNTHROID) from 01-Mar-2021 to an unknown date, CALCIUM CARBONATE (TUMS CHEWIES) from 01-Apr-2021 to an unknown date, CETIRIZINE HYDROCHLORIDE (ZYRTEC ALLERGY) from 01-Mar-2021 to an unknown date, PANTOPRAZOLE from 01-Mar-2021 to an unknown date and FLUOXETINE from 01-Mar-2021 to an unknown date for an unknown indication. On 25-Mar-2021, the patient received dose of COVID-19 VACCINE NRVV AD26 (JNJ 78436735) (JANSSEN COVID-19 VACCINE) (unknown route) 1 dosage form. On 05-Nov-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. The patient's last menstrual period was on 18-Mar-2021 and the estimated date of delivery was 23-Dec-2021. On 05-Nov-2021, the patient experienced MATERNAL EXPOSURE DURING PREGNANCY (Maternal exposure during pregnancy). On 21-Dec-2021, the patient experienced PREMATURE RUPTURE OF MEMBRANES (Premature rupture of membrane). On an unknown date, the patient experienced SUSPECTED COVID-19 (Suspected COVID-19 infection). The patient received mRNA-1273 (Moderna COVID-19 Vaccine) beginning around the thirty-third week of the pregnancy and COVID-19 VACCINE NRVV AD26 (JNJ 78436735) (JANSSEN COVID-19 VACCINE) beginning around the first week of the pregnancy. The delivery occurred on an unknown date, which was reported as Unknown. For neonate 1, The outcome was reported as Unknown. On 05-Nov-2021, MATERNAL EXPOSURE DURING PREGNANCY (Maternal exposure during pregnancy) had resolved. At the time of the report, PREMATURE RUPTURE OF MEMBRANES (Premature rupture of membrane) and SUSPECTED COVID-19 (Suspected COVID-19 infection) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. No treatment information was provided. Company comment:This spontaneous case reported by another pharmaceutical company (Janssen) concerns a 35-year-old-female patient with no relevant medical history who experienced the unexpected, non-serious AESI of Suspected COVID-19 infection. The onset date of the event and test results are unknown. Non-serious events of Premature rupture of membrane and Maternal exposure during pregnancy were also reported to occurred 16 days after the first dose of mRNA-1273 vaccine (second dose in series for COVID-19 vaccination/First dose in series from Janssen). Interchange of vaccine products is also noted in this case and the patient received 1 dose of Janssen COVID-19 vaccine approximately 8 months prior to administration of mRNA-1273 vaccine. Clinical course and treatment details were not reported in the case. The benefit-risk relationship of mRNA-1273 in not affected by this report; Sender's Comments: This spontaneous case reported by another pharmaceutical company (Janssen) concerns a 35-year-old-female patient with no relevant medical history who experienced the unexpected, non-serious AESI of Suspected COVID-19 infection. The onset date of the event and test results are unknown. Non-serious events of Premature rupture of membrane and Maternal exposure during pregnancy were also reported to occurred 16 days after the first dose of mRNA-1273 vaccine (second dose in series for COVID-19 vaccination/First dose in series from Janssen). Interchange of vaccine products is also noted in this case and the patient received 1 dose of Janssen COVID-19 vaccine approximately 8 months prior to administration of mRNA-1273 vaccine. Clinical course and treatment details were not reported in the case. The benefit-risk relationship of mRNA-1273 in not affected by this report

Weitere VAERSDATA-Felder

Praegender Schweregrund: Maternal exposure during pregnancy
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Anxiety; Endometriosis; GERD; Hypothyroidism; Irritable bowel syndrome; Obsessive-compulsive disorder
Vorgeschichte: -
Andere Medikamente: PRENATAL VITAMINS [ASCORBIC ACID;BIOTIN;MINERALS NOS;NICOTINIC ACID;RETINOL;TOCOPHEROL;VITAMIN B NOS; ZANTAC; SYNTHROID; TUMS CHEWIES; ZYRTEC ALLERGY; PANTOPRAZOLE; FLUOXETINE
Allergien: -
Vorherige Impfungen: -

VAERS 2171652

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: NY
Alter: 41,0
Geschlecht: F
Eingang: 10.03.2022
Impfdatum: 06.11.2021
Beginn: 04.12.2021
Tage bis Beginn: 28,0
Dosis: 1
Route/Site: IM / LA

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

Joint range of motion decreased

Symptomtext

Patient called 3/08/22 that her left arm (administered vaccine) has mild and has decreased range of motion since first COVID vaccine. First dose 11/6/2021, then second dose 12/4/2021 did not mention soreness or ROA upon administration. She called pharmacy over 3 months later on 3/8/22 to discuss her symptoms and instructed to apply compress and take ibuprofen/acetaminophen. She came in person 3/10/21 and instructed to continue applying compress and medication. If Aes continue, contact primary for further studies or physical therapy.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Joint range of motion decreased
Hospital-Tage: -
Labordaten: NA
Aktuelle Erkrankungen: NA
Vorgeschichte: NA
Andere Medikamente: NA
Allergien: NONE
Vorherige Impfungen: -

VAERS 2165384

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: GA
Alter: 72,0
Geschlecht: F
Eingang: 08.03.2022
Impfdatum: 03.11.2021
Beginn: 01.11.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: SYR / LA

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

Anaemia Blood iron decreased Blood test abnormal Chronic kidney disease Infusion

Symptomtext

It wasn't a specific event, I went to the doctor for my annual physical checkup. she did bloodwork and said my iron was low. She had me take a more specific blood test and sent me for iron infusion and referred me to a hematologist. The hematologist said that I had anemia due to chronic kidney disease. I have a colonoscopy scheduled for next week to see if I have bleeding in the colon.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaemia
Hospital-Tage: -
Labordaten: bloodwork - anemia due to chronic kidney disease
Aktuelle Erkrankungen: None
Vorgeschichte: I have a benign brain tumor, high blood pressure, high cholesterol
Andere Medikamente: Lisinopril 30MG daily, Nexium MG daily, Atorvastatin 20MG M/W/F, Calcium 1200mg daily, Fish Oil 1290mg, D3 5000IU daily
Allergien: To my knowledge, sulfur
Vorherige Impfungen: -

VAERS 2157835

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: KY
Alter: 79,0
Geschlecht: F
Eingang: 04.03.2022
Impfdatum: 29.11.2021
Beginn: 26.02.2022
Tage bis Beginn: 89,0
Dosis: 3
Route/Site: IM / LA

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

Asymptomatic COVID-19

Symptomtext

not a true covid admission, asymptomatic and no treatment provided

Weitere VAERSDATA-Felder

Praegender Schweregrund: Asymptomatic COVID-19
Hospital-Tage: 8,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: PAF, Hypotension, rectal cancer, asthma, kidney disease
Andere Medikamente: unable to ascertain
Allergien: codeine, Ativan, erythromycin
Vorherige Impfungen: -

VAERS 2150886

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: OK
Alter: 74,0
Geschlecht: F
Eingang: 01.03.2022
Impfdatum: 30.10.2021
Beginn: 28.12.2021
Tage bis Beginn: 59,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 SARS-CoV-2 test positive

Symptomtext

Tested positive on 12/28. No fever but had bad cough and nasal congestion. Worst of symptoms lasted about a week, diminishing symptoms about another week.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: PCR test
Aktuelle Erkrankungen: none
Vorgeschichte: diabetic, depression
Andere Medikamente: too numerous to list
Allergien: to numerous to list
Vorherige Impfungen: -

VAERS 2201090

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: -
Alter: 72,0
Geschlecht: M
Eingang: 17.02.2022
Impfdatum: 11.11.2021
Beginn: 01.02.2022
Tage bis Beginn: 82,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19

Symptomtext

Narrative: COVID admission in fully vaccinated patient

Weitere VAERSDATA-Felder

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

VAERS 2116431

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: MD
Alter: 39,0
Geschlecht: F
Eingang: 16.02.2022
Impfdatum: 05.11.2021
Beginn: 07.12.2021
Tage bis Beginn: 32,0
Dosis: 3
Route/Site: IM / RA

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

Heavy menstrual bleeding

Symptomtext

Heavy menstrual cycle following a month after vaccination and month of vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Heavy menstrual bleeding
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: Asthma
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2116003

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: -
Alter: 84,0
Geschlecht: M
Eingang: 16.02.2022
Impfdatum: 05.01.2021
Beginn: 20.11.2021
Tage bis Beginn: 319,0
Dosis: 3
Route/Site: - / -

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

COVID-19 SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

event occurred after second vaccine; breakthrough case admission

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: 11/20/21 COIVD +
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2096467

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: KY
Alter: 47,0
Geschlecht: F
Eingang: 08.02.2022
Impfdatum: 01.11.2021
Beginn: 08.11.2021
Tage bis Beginn: 7,0
Dosis: 3
Route/Site: SYR / LA

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

Contraception Endometrial ablation Ultrasound scan vagina Vaginal haemorrhage

Symptomtext

On 11/08/2021--I started having heavy vaginal bleeding. It stopped on 01/07/2022, and it started right back the very next day, 01/08/2022 The doctor put me on a birth control pill, Sprintec, and utilized it like a dose pack, I started at 5 days, and 4 days, and decreased, etc. That did not help. She also put me on iron pills 324 mg, twice a day. Then she put me on Provera, 10 mg once a day, I took that for 2 weeks and that did not help. Then she put me on Provera 10mg, until I had the surgery. The heavy bleeding stopped on 01/21/2022, when I had surgery at outpatient surgery. I had a uterine ablation. I would say unknown at this point in time. I have a follow up appointment tomorrow, 02/09/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Contraception
Hospital-Tage: -
Labordaten: vaginal ultrasound on 12/18/2021
Aktuelle Erkrankungen: no
Vorgeschichte: no
Andere Medikamente: none
Allergien: no
Vorherige Impfungen: -

VAERS 2092891

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: -
Alter: 69,0
Geschlecht: M
Eingang: 07.02.2022
Impfdatum: 25.10.2021
Beginn: 17.11.2021
Tage bis Beginn: 23,0
Dosis: 3
Route/Site: - / -

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

Coronary artery bypass

Symptomtext

Coronary artery bypass grafting x4 on pump. Hospital admission within 6 weeks of receiving the COVID vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Coronary artery bypass
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2087481

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: -
Alter: 42,0
Geschlecht: F
Eingang: 04.02.2022
Impfdatum: 06.11.2021
Beginn: 30.12.2021
Tage bis Beginn: 54,0
Dosis: 2
Route/Site: OT / -

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

SARS-CoV-2 test Suspected COVID-19 Vaccination failure

Symptomtext

Vaccination failure; Suspected COVID-19 infection; This spontaneous case was reported by a consumer and describes the occurrence of SUSPECTED COVID-19 (Suspected COVID-19 infection) and VACCINATION FAILURE (Vaccination failure) in a 43-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 071F21A) for Prophylactic vaccination. Previously administered products included for Prophylactic vaccination: JANSSEN COVID-19 VACCINE (vaccinated to left arm, batch no 202A21A,Reaction started on 04 Jan 2022) on 09-Apr-2021, JANSSEN COVID-19 VACCINE (vaccinated to left arm, batch no 202A21A and Reaction started on 30 December 2021) on 09-Apr-2021. Past adverse reactions to the above products included Suspected COVID-19 with JANSSEN COVID-19 VACCINE; and Vaccination failure with JANSSEN COVID-19 VACCINE. On 06-Nov-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 30-Dec-2021, the patient experienced SUSPECTED COVID-19 (Suspected COVID-19 infection) (seriousness criterion medically significant). On 04-Jan-2022, the patient experienced VACCINATION FAILURE (Vaccination failure) (seriousness criterion medically significant). At the time of the report, SUSPECTED COVID-19 (Suspected COVID-19 infection) had not resolved and VACCINATION FAILURE (Vaccination failure) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 04-Jan-2022, SARS-CoV-2 test: positive (Positive) Positive. Concomitant medication were not reported. On 06 Nov 2021, patient received booster dose of Moderna vaccine. On 30 Dec 2021, the patient experienced symptoms of congestion, runny nose and sneezing (Suspected Covid 19 infection) and reported her illness was a mild case. Treatment medication were not reported. Company comment: This case concerns a 43-year-old female patient with unknown medical history who experienced the serious unexpected events of Suspected COVID-19 and Vaccination failure after the dose of mRNA-1273. The event of Suspected COVID-19 occurred approximately one month and twenty five days and the event of vaccination failure occurred about one month and thirty days after the booster dose of mRNA-1273. At the time of the report, outcome of Suspected COVID-19 was not recovered and the outcome of vaccination failure was unknown. Based on the current available information, the mRNA-1273 vaccine does not contain a virus capable of causing COVID-19 infection after vaccination, therefore, the causality for Suspected COVID-19 is not applicable. The benefit-risk relationship of the mRNA-1273 vaccine is not affected by this report. Event seriousness assessed as per Regulatory Authority reporting.; Sender's Comments: This case concerns a 43-year-old female patient with unknown medical history who experienced the serious unexpected events of Suspected COVID-19 and Vaccination failure after the dose of mRNA-1273. The event of Suspected COVID-19 occurred approximately one month and twenty five days and the event of vaccination failure occurred about one month and thirty days after the booster dose of mRNA-1273. At the time of the report, outcome of Suspected COVID-19 was not recovered and the outcome of vaccination failure was unknown. Based on the current available information, the mRNA-1273 vaccine does not contain a virus capable of causing COVID-19 infection after vaccination, therefore, the causality for Suspected COVID-19 is not applicable. The benefit-risk relationship of the mRNA-1273 vaccine is not affected by this report. Event seriousness assessed as per Regulatory Authority reporting.

Weitere VAERSDATA-Felder

Praegender Schweregrund: SARS-CoV-2 test
Hospital-Tage: -
Labordaten: Test Date: 20220104; Test Name: COVID-19 HOME TEST; Test Result: Positive ; Result Unstructured Data: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2082614

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge 071F21A

gering

Staat: NC
Alter: 57,0
Geschlecht: F
Eingang: 02.02.2022
Impfdatum: 02.02.2022
Beginn: 19.01.2022
Tage bis Beginn: -
Dosis: 1
Route/Site: IM / LA

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

COVID-19 SARS-CoV-2 test positive

Symptomtext

Tested positive for Covid on January 19, 2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Two positive rapid Covid tests on 1-19-2022 at work as well as positive PCR on 1-21-2022
Aktuelle Erkrankungen: na
Vorgeschichte: high blood pressure
Andere Medikamente: na
Allergien: na
Vorherige Impfungen: -

VAERS 2074622

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071f21a

gering

Staat: IL
Alter: 55,0
Geschlecht: M
Eingang: 29.01.2022
Impfdatum: 09.11.2021
Beginn: 19.12.2021
Tage bis Beginn: 40,0
Dosis: 4
Route/Site: SYR / LA

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

Blindness unilateral Blood test

Symptomtext

Lost vision in right eye.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Blindness unilateral
Hospital-Tage: -
Labordaten: Eye clinic 2/22/21 , blood work then steroid iv in hospital on 12/23,24th, and 25th back to clinic on the 1/24/ 22.
Aktuelle Erkrankungen: None.
Vorgeschichte: High blood pressure.
Andere Medikamente: Lisincpril/HCYZ;Sulfasalazine;Folic Acid;Hydrocod/Acetam; Sidenafil; Fluticasone Propionate;Excedrin Migraine; Ibuprofen.
Allergien: None.
Vorherige Impfungen: -

VAERS 2069379

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: OH
Alter: 25,0
Geschlecht: M
Eingang: 27.01.2022
Impfdatum: 28.12.2020
Beginn: 01.01.2021
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: - / -

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

COVID-19 SARS-CoV-2 test positive

Symptomtext

Tested positive for COVID

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: PCR
Aktuelle Erkrankungen: None
Vorgeschichte: NF1
Andere Medikamente: Zoloft Trazadone
Allergien: None
Vorherige Impfungen: -

VAERS 2069106

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: KY
Alter: 66,0
Geschlecht: M
Eingang: 27.01.2022
Impfdatum: 03.11.2021
Beginn: 23.01.2022
Tage bis Beginn: 81,0
Dosis: UNK
Route/Site: - / -

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

COVID-19 SARS-CoV-2 test positive

Symptomtext

Covid positive contact unknown. Up to date on Booster

Weitere VAERSDATA-Felder

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

VAERS 2068735

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: CA
Alter: 52,0
Geschlecht: F
Eingang: 27.01.2022
Impfdatum: 05.11.2021
Beginn: 06.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Lymphadenopathy

Symptomtext

Pt. states that after receiving the 3rd dose of Moderna 11/05/2021, started experiencing symptoms that evening of swelling in the Left armpit lymphnoid (lasting 18hrs). No noted Primary visit/communications.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Lymphadenopathy
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Multiple Sclerosis
Andere Medikamente: Gabapentin, Cyclobenzaprine
Allergien: Lyrica
Vorherige Impfungen: -

VAERS 2068677

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: MA
Alter: 86,0
Geschlecht: F
Eingang: 27.01.2022
Impfdatum: 03.11.2021
Beginn: 16.01.2022
Tage bis Beginn: 74,0
Dosis: UNK
Route/Site: - / -

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

Asymptomatic COVID-19 SARS-CoV-2 test positive

Symptomtext

Tested positive for Covid 19. Did not experience symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Asymptomatic COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2068525

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: NH
Alter: 52,0
Geschlecht: F
Eingang: 27.01.2022
Impfdatum: 03.11.2021
Beginn: 03.11.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Dyspepsia

Symptomtext

Pt immediately started experiencing problems with her digestive system. She relays them being "IBS symptoms" and has tried a probiotic for approx 20 days without symptoms improving. A referral to GI had been done.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspepsia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None.
Vorgeschichte: Hypothyroidism; GERD;Kidney donor; Malignant neoplasm of upper-outer; Quadrant of R breast, 2013; Asthma.
Andere Medikamente: Omeprazole.
Allergien: Cephalosporins;Cephalexin;Penicillins.
Vorherige Impfungen: -

VAERS 2066967

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: MI
Alter: 41,0
Geschlecht: F
Eingang: 26.01.2022
Impfdatum: 23.11.2021
Beginn: 01.12.2021
Tage bis Beginn: 8,0
Dosis: 3
Route/Site: IM / -

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

Angiogram pulmonary abnormal Iliac vein occlusion Ultrasound Doppler abnormal

Symptomtext

Ended up in hospital with bilateral PEs and iliac vein almost completely occluded from the groin down.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Angiogram pulmonary abnormal
Hospital-Tage: 4,0
Labordaten: CT angiogram and Doppler 12/2021
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension
Andere Medikamente: Metoprolol
Allergien: None
Vorherige Impfungen: -

VAERS 2065631

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: IL
Alter: 53,0
Geschlecht: F
Eingang: 26.01.2022
Impfdatum: 25.10.2021
Beginn: 20.12.2021
Tage bis Beginn: 56,0
Dosis: 3
Route/Site: IM / LA

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

Adnexa uteri mass Ovarian cyst Ultrasound pelvis abnormal Ultrasound scan vagina Ultrasound scan vagina abnormal

Symptomtext

I had a CT scan to evaluate known kidney stones 12/20/21. In addition to stones, the scan revealed a 3.2 cm "left adnexal lesion" which was diagnosed as an ovarian cyst on an ultrasound on 1/20/22. I can't imagine this is related to my booster shot, but I reported it and got a call requesting follow up of this, so I am dutifully reporting it.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Adnexa uteri mass
Hospital-Tage: -
Labordaten: Pelvic & transvaginal ultrasound 1/20/2022.
Aktuelle Erkrankungen: Hypoparathyroidism Hypocalcemia/hypocalciuria Kidney stones Hx Papillary Thyroid Cancer (thyroid removed 1/2020)
Vorgeschichte: as above Asthma (attacks rare and medications used prn, none used or needed in month of/before vaccination)
Andere Medikamente: levothyroxine, 150 mcg calcitriol, .25 mcg indapamide, 2.5 mg B Complex Vitamin Vitamin D3, 1000 iu Oscal-500
Allergien: fluoroquinolones (cipro, floxin) crab
Vorherige Impfungen: -

VAERS 2065484

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: KY
Alter: 27,0
Geschlecht: F
Eingang: 26.01.2022
Impfdatum: 01.11.2021
Beginn: 09.01.2022
Tage bis Beginn: 69,0
Dosis: UNK
Route/Site: - / -

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

COVID-19 Exposure to SARS-CoV-2 SARS-CoV-2 test positive

Symptomtext

Covid positive through household contact. Up to date on booster

Weitere VAERSDATA-Felder

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

VAERS 2062630

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071f21a

gering

Staat: MI
Alter: 92,0
Geschlecht: F
Eingang: 25.01.2022
Impfdatum: 04.11.2021
Beginn: 21.01.2022
Tage bis Beginn: 78,0
Dosis: 3
Route/Site: - / -

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

COVID-19 SARS-CoV-2 test positive

Symptomtext

positive covid test in fully vaccinated and boosted pt

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: HTN, CHF, obesity, Afib
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2055533

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: MT
Alter: 54,0
Geschlecht: F
Eingang: 21.01.2022
Impfdatum: 29.12.2020
Beginn: 27.12.2021
Tage bis Beginn: 363,0
Dosis: 3
Route/Site: IM / -

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

Biopsy thyroid gland Cytology abnormal Dysphagia Thyroid mass Ultrasound thyroid abnormal

Symptomtext

4.2cm left thyroid nodule found on ultrasound due to difficulty swallowing

Weitere VAERSDATA-Felder

Praegender Schweregrund: Biopsy thyroid gland
Hospital-Tage: -
Labordaten: Thyroid ultrasound 12/28/2021, US thyroid fine needle aspiration 01/04/2022. Total thyroidectomy scheduled for 02/18/2022 due to abnormal cytology
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Wellbutrin, Soma, Prempro
Allergien: NSAIDS
Vorherige Impfungen: -

VAERS 2034745

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: PA
Alter: 42,0
Geschlecht: F
Eingang: 14.01.2022
Impfdatum: 06.11.2021
Beginn: 30.12.2021
Tage bis Beginn: 54,0
Dosis: 2
Route/Site: OT / -

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

SARS-CoV-2 test Suspected COVID-19 Vaccination failure

Symptomtext

SUSPECTED CLINICAL VACCINATION FAILURE; SUSPECTED COVID-19 INFECTION; This spontaneous report received from a patient concerned a 43 year old white female of unspecified ethnicity. Initial information was processed along with the additional information received on 11-JAN-2022. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. On 09-APR-2021, the patient received covid-19 vaccine ad26.cov2.s (dose number in series: 1) (suspension for injection, route of admin not reported, batch number: 202A21A, and expiry: UNKNOWN) dose was not reported, 1 total, administered to left arm for prophylactic vaccination. No concomitant medications were reported. On 06-NOV-2021, the patient received booster dose of non-company suspect vaccine mrna 1273 (Moderna) (dose number in series: 2) (form of admin, route of admin not reported, batch number: 071F21A expiry: UNKNOWN) dose was not reported, administered for prophylactic vaccination. On 30-DEC-2021, following vaccination with covid-19 vaccine ad26.cov2.s, the patient experienced symptoms of congestion, runny nose, and sneezing (suspected covid-19 infection) and reported her illness is a mild case. On 04-JAN-2022, the patient experienced suspected clinical vaccination failure. Laboratory data included: COVID-19 antigen test (Home kit test) (NR: not provided) Positive (dose number in series: 1). The action taken with covid-19 vaccine ad26.cov2.s, and mrna 1273 (Moderna) was not applicable. The patient had not recovered from suspected covid-19 infection, and the outcome of suspected clinical vaccination failure was not reported. This report was serious (Other Medically Important Condition) This report was associated with product quality complaint number: 90000210214. The suspected product quality complaint has been confirmed to be the reported allegation was not confirmed and the root cause was determined to be not manufacturing related based on the PQC evaluation/investigation performed.; Sender's Comments: V0: 20220105417-covid-19 vaccine ad26.cov2.s-Suspected clinical vaccination failure . This event(s) is considered not related. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There are other factors more likely to be associated with the event(s) than the drug. Specifically: SPECIAL SITUATIONS

Weitere VAERSDATA-Felder

Praegender Schweregrund: SARS-CoV-2 test
Hospital-Tage: -
Labordaten: Test Date: 20220104; Test Name: COVID-19 antigen test; Result Unstructured Data: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2025367

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: IL
Alter: 80,0
Geschlecht: F
Eingang: 11.01.2022
Impfdatum: 22.11.2021
Beginn: 22.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / AR

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

Incorrect dose administered

Symptomtext

EXTRACTION OF THE MODERNA VACCINE FROM THE VIAL WAS NOT CONSISTENT WITH A MODERNA TECHNIQUE (I.E. MORE THAN 20 BOOSTER DOSES WERE DRAWN UP FROM THE VIAL).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2025359

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: IL
Alter: 81,0
Geschlecht: M
Eingang: 11.01.2022
Impfdatum: 22.11.2021
Beginn: 22.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / AR

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

Wrong technique in product usage process

Symptomtext

EXTRACTION OF THE MODERNA VACCINE FROM THE VIAL WAS NOT CONSISTENT WITH A MODERNA TECHNIQUE (I.E. MORE THAN 20 BOOSTER DOSES WERE DRAWN UP FROM THE VIAL).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Wrong technique in product usage process
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2025354

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: IL
Alter: 27,0
Geschlecht: F
Eingang: 11.01.2022
Impfdatum: 21.11.2021
Beginn: 21.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / AR

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

Wrong technique in product usage process

Symptomtext

EXTRACTION OF THE MODERNA VACCINE FROM THE VIAL WAS NOT CONSISTENT WITH A MODERNA TECHNIQUE (I.E. MORE THAN 20 BOOSTER DOSES WERE DRAWN UP FROM THE 15ML VIAL).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Wrong technique in product usage process
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2025346

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: IL
Alter: 78,0
Geschlecht: F
Eingang: 11.01.2022
Impfdatum: 19.11.2021
Beginn: 19.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / AR

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

Wrong technique in product usage process

Symptomtext

EXTRACTION OF THE MODERNA VACCINE FROM THE VIAL WAS NOT CONSISTENT WITH A MODERNA TECHNIQUE (I.E. MORE THAN 20 BOOSTER DOSES WERE DRAWN UP FROM THE 15ML VIAL).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Wrong technique in product usage process
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2014231

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: -
Alter: 83,0
Geschlecht: M
Eingang: 07.01.2022
Impfdatum: 25.10.2021
Beginn: 05.11.2021
Tage bis Beginn: 11,0
Dosis: 3
Route/Site: - / -

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

Carotid artery stenosis Surgery

Symptomtext

Bilateral carotid artery stenosis. Surgery and hospital admission. This visit was within 6 weeks of receiving the COVID vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Carotid artery stenosis
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2647052

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: NJ
Alter: 75,0
Geschlecht: F
Eingang: 05.01.2022
Impfdatum: 29.10.2021
Beginn: 05.11.2021
Tage bis Beginn: 7,0
Dosis: 3
Route/Site: SC / LA

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

Herpes virus infection Skin lesion

Symptomtext

I had a herpes sore on my left buttock. This was diagnosed by Dr.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Herpes virus infection
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: Type 2 Diabetes Sjogren's Syndrome , Acid Reflux
Andere Medikamente: ALLEGRA AMLODIPINE BESYLATE AMOXICILLIN ATORVASTATIN CALCIUM CEVIMELINE HCL CLOTRIMAZOLE CREAM CLOTRIMAZOLE-BETAMETHASONE CRM ESTRADIOL VAGINAL CREAM FAMOTIDINE FLUTICASONE PROP IPRATROPIUM BROMIDE MECLIZINE METFORMIN HCL ER PREGABALIN REST
Allergien: None
Vorherige Impfungen: -

VAERS 1999124

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: KY
Alter: 28,0
Geschlecht: F
Eingang: 03.01.2022
Impfdatum: 27.12.2021
Beginn: 27.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

C-reactive protein Eye swelling Full blood count Hordeolum Metabolic function test Swelling Swelling face

Symptomtext

ON THE NIGHT OF 12/27/21 EMPLOYEE REPORTED RIGHT EYE SWELLING. EMPLOYEE STATED IT CAME UP AS A STY. TUESDAY SWELLING MOVED INTO NOSE AND ON WEDNESDAY IT WAS THE WHOLE RIGHT SIDE OF FACE. EMPLOYEE WENT TO CARE CENTER AND ER AND WAS TREATED. EMPLOYEE RECEIVED A STERIOD SHOT IN THE ER AND WAS SENT HOME WITH AN ANTIBIOTIC EYE DROP, AZITHROMYCIN, CLINDAMYCIN, PEPCID AND WAS TO TAKE BENADRYL EVERY 4 HOURS. EMPLOYEE WAS DISCHARGED HOME. ON THURSDAY IMPROVEMENT WAS NOTED. ON FRIDAY EMPLOYEES ENTIRE FACE WAS SWOLLEN. EMPLOYEE BACK TO ER AND EMPLOYEE RECEIVED IV PEPCID, IV DECADRON, IV BENADRYL, AND WAS SENT HOME ON PREDISONE. ON SATURDAY IMPROVEMENT NOTED ON SUNDAY IMPROVEMENT NOTED. MONDAY 1/3/22 CONTINUES TO IMPROVE SL SWELLING IN NOSE IS NOTED.

Weitere VAERSDATA-Felder

Praegender Schweregrund: C-reactive protein
Hospital-Tage: -
Labordaten: CBC CMP CRP C4 COMPLETED ON 12/31/21
Aktuelle Erkrankungen: Bronchitis 7 days after taking 1 injection in November
Vorgeschichte: HTN, BORN WITH 1 KIDNEY, ANXIETY AND DEPRESSION
Andere Medikamente: lisinopril 10 mg daily lexapro 20 mg daily HCTZ 12.5 mg daily
Allergien: bactrim, Cipro, Cefzil
Vorherige Impfungen: -

VAERS 1997936

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071f21a

gering

Staat: NY
Alter: 46,0
Geschlecht: F
Eingang: 02.01.2022
Impfdatum: 02.11.2021
Beginn: 02.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Tinnitus

Symptomtext

Tinnitus- severe

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tinnitus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: NA
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1988938

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: OH
Alter: 51,0
Geschlecht: M
Eingang: 29.12.2021
Impfdatum: 08.12.2021
Beginn: 10.12.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

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

Herpes zoster

Symptomtext

shingles. started 72 hours after vaccine. treated with valcyclovir and gabapentin

Weitere VAERSDATA-Felder

Praegender Schweregrund: Herpes zoster
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: claritin
Allergien: none
Vorherige Impfungen: -

VAERS 1982083

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: VA
Alter: 14,0
Geschlecht: M
Eingang: 27.12.2021
Impfdatum: 22.12.2021
Beginn: 27.12.2021
Tage bis Beginn: 5,0
Dosis: 1
Route/Site: IM / RA

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

Product administered to patient of inappropriate age

Symptomtext

Patient received a dose of Moderna vaccine in error. We should not have administered as he is under the age of 18 and it is not approved for this age group. It was an error due to mom working here and dad coming in to get his first dose so son came and no one caught the fact that he wasn't proper age group.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product administered to patient of inappropriate age
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: PCN
Vorherige Impfungen: -

VAERS 1970528

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: IN
Alter: 52,0
Geschlecht: F
Eingang: 22.12.2021
Impfdatum: 01.11.2021
Beginn: 01.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / -

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

Accidental underdose Inappropriate schedule of product administration

Symptomtext

received booster instead of third shot; Inappropriate schedule of vaccine administered; This spontaneous case was reported by a consumer and describes the occurrence of ACCIDENTAL UNDERDOSE (received booster instead of third shot) and INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Inappropriate schedule of vaccine administered) in a 52-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 071F21A) for COVID-19 vaccination. Previously administered products included for Product used for unknown indication: J & J Vaccine (Lot number 1805025) in March 2020. Past adverse reactions to the above products included No adverse event with J & J Vaccine. Concurrent medical conditions included Immunocompromised (Autoimmune patient). On 01-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 01-Nov-2021, the patient experienced ACCIDENTAL UNDERDOSE (received booster instead of third shot) and INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Inappropriate schedule of vaccine administered). On 01-Nov-2021, ACCIDENTAL UNDERDOSE (received booster instead of third shot) and INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Inappropriate schedule of vaccine administered) had resolved. Symptoms: It was reported that the patient was immunocompromised and should have received full dose of vaccine instead of half dose. No concomitant medications were reported No treatment medications were reported

Weitere VAERSDATA-Felder

Praegender Schweregrund: Accidental underdose
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Immunocompromised (Autoimmune patient)
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1959378

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: CA
Alter: 21,0
Geschlecht: F
Eingang: 17.12.2021
Impfdatum: 13.12.2021
Beginn: 13.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Patient was administered a dose from a vial that was previously open and punctured 4 days before administration, Vial was punctured 12/09/2021 and doses was administer 12/13/2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: No
Allergien: No
Vorherige Impfungen: -

VAERS 1959366

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: CA
Alter: 35,0
Geschlecht: F
Eingang: 17.12.2021
Impfdatum: 13.12.2021
Beginn: 13.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Moderna vaccine was administered from a vial that was punctured 4 days prior to administration. Vial was always stored in the refrigerator and was never involved in any temperature excursions. But dose was administer from a vial that was opened 12/09/2021 and dose was administered 12/13/21.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: no
Vorgeschichte: no
Andere Medikamente: none
Allergien: no
Vorherige Impfungen: -

VAERS 1952142

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071f21A

gering

Staat: CT
Alter: 15,0
Geschlecht: F
Eingang: 15.12.2021
Impfdatum: 15.12.2021
Beginn: 15.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product administered to patient of inappropriate age

Symptomtext

Patient wanted the moderna vaccine. Before giving the shot I confirmed with the patient that she is getting maderna as requested. In the process of completing the paperwork I found out the patient is less that 18 and this shot is not approved for children under 18 yet.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product administered to patient of inappropriate age
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 1946790

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: KY
Alter: 66,0
Geschlecht: U
Eingang: 14.12.2021
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: OT / -

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

Expired product administered

Symptomtext

Doses administered to patients 18 hours after first vial puncture; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Doses administered to patients 18 hours after first vial puncture) in a 66-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 071F21A) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (Doses administered to patients 18 hours after first vial puncture). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Doses administered to patients 18 hours after first vial puncture) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant and treatment information were reported by the reporter

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1946789

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: KY
Alter: 69,0
Geschlecht: U
Eingang: 14.12.2021
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: OT / -

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

Expired product administered

Symptomtext

This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Doses administered to patients 18 hours after first vial puncture) in a 69-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 071F21A) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (Doses administered to patients 18 hours after first vial puncture). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Doses administered to patients 18 hours after first vial puncture) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was reported by the reporter. No treatment information was reported by the reporter.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1942113

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: VA
Alter: 63,0
Geschlecht: M
Eingang: 11.12.2021
Impfdatum: 28.10.2021
Beginn: 03.11.2021
Tage bis Beginn: 6,0
Dosis: 3
Route/Site: SYR / LA

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

Tinnitus

Symptomtext

Around the beginning of November, I started experiencing a low roaring sound in my ears (like a lawnmower), especially at night when it's very quiet. I initially thought that there was something running in my house i.e. roof wind turbines, heating system, plumbing, appliances, etc. However, I couldn't find anything making the same noise that I was hearing. I asked my wife many times if she heard anything, but she did not. I ordered some earplugs and started using them around the first week of November, but they didn't really help. So, I started wearing my Bluetooth earpiece to bed and playing music of ?midnight rain and thunderstorms?. That?s the only thing that really helped and I continue doing that to this day. On December 5, I requested an evaluation by my doctor. I am waiting for an appointment date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tinnitus
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: none
Vorgeschichte: Benign prostatic hyperplasia
Andere Medikamente: Alfusozin 10mg (daily), Vitamin D2 ER Tab 50000 (weekly), Latanaprost 0.005 (daily, left eye), Fluticasone 50mcg (as needed)
Allergien: none
Vorherige Impfungen: -

VAERS 1941804

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: IL
Alter: 72,0
Geschlecht: F
Eingang: 11.12.2021
Impfdatum: 10.11.2021
Beginn: 09.12.2021
Tage bis Beginn: 29,0
Dosis: 1
Route/Site: OT / LA

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

Expired product administered

Symptomtext

Patient received a dose of the Moderna COVID-19 vaccine more than 12 hours after it was punctured; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient received a dose of the Moderna COVID-19 vaccine more than 12 hours after it was punctured) in a 72-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 071F21A and 071F21A) for COVID-19 vaccination. No medical history was reported by the reporter. Concomitant products included HYDROCHLOROTHIAZIDE, METFORMIN, SIMVASTATIN and LISINOPRIL for an unknown indication. On 10-Nov-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 09-Dec-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 09-Dec-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient received a dose of the Moderna COVID-19 vaccine more than 12 hours after it was punctured). On 09-Dec-2021, EXPIRED PRODUCT ADMINISTERED (Patient received a dose of the Moderna COVID-19 vaccine more than 12 hours after it was punctured) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Total amount of time the vial was exposed to room temperature range (8? to 25?C= 46? to 77?F). .4 hours at room temperature No treatment medications were reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: No medical history was reported by the reporter.
Andere Medikamente: HYDROCHLOROTHIAZIDE; METFORMIN; SIMVASTATIN; LISINOPRIL
Allergien: -
Vorherige Impfungen: -

VAERS 1941795

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: KY
Alter: 20,0
Geschlecht: U
Eingang: 11.12.2021
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: OT / -

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

Expired product administered

Symptomtext

Doses administered to patients 18 hours after first vial puncture; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Doses administered to patients 18 hours after first vial puncture) in a 20-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 071F21A) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (Doses administered to patients 18 hours after first vial puncture). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Doses administered to patients 18 hours after first vial puncture) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant product use was provided by the reporter. No treatment medication was provided. The vial was stored in the refrigerator after the first puncture.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1941792

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: KY
Alter: 61,0
Geschlecht: U
Eingang: 11.12.2021
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: OT / -

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

Expired product administered

Symptomtext

Doses administered to patients 18 hours after first vial puncture; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Doses administered to patients 18 hours after first vial puncture) in a 61-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 071F21A) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (Doses administered to patients 18 hours after first vial puncture). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Doses administered to patients 18 hours after first vial puncture) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. No treatment medications were reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1941791

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: KY
Alter: 50,0
Geschlecht: U
Eingang: 11.12.2021
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: OT / -

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

Expired product administered

Symptomtext

Doses administered to patients 18 hours after first vial puncture; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Doses administered to patients 18 hours after first vial puncture) in a 50-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 071F21A) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (Doses administered to patients 18 hours after first vial puncture). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Doses administered to patients 18 hours after first vial puncture) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Vial had been punctured for 18 hours. The vial was stored in the refrigerator after the first puncture. No relevant concomitant medications were reported. Treatment medication was not provided by the reporter.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1941789

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: KY
Alter: 34,0
Geschlecht: U
Eingang: 11.12.2021
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: OT / -

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

Expired product administered

Symptomtext

Doses administered to patients 18 hours after first vial puncture; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Doses administered to patients 18 hours after first vial puncture) in a 34-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 071F21A) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (Doses administered to patients 18 hours after first vial puncture). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Doses administered to patients 18 hours after first vial puncture) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medication was not provided. Treatment information was not provided.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1936591

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: PA
Alter: 60,0
Geschlecht: F
Eingang: 09.12.2021
Impfdatum: 07.12.2021
Beginn: 08.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Feeling abnormal Muscular weakness

Symptomtext

Weakness in legs and an unsteady feeling.

Weitere VAERSDATA-Felder

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

VAERS 1936270

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: IL
Alter: 36,0
Geschlecht: F
Eingang: 09.12.2021
Impfdatum: 09.12.2021
Beginn: 09.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Underdose

Symptomtext

Pt. was scheduled for her first dose of Moderna vaccine. Vaccinator gave her a booster dose (1/2 dose) rather than first dose.

Weitere VAERSDATA-Felder

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

VAERS 1931315

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071f21a

gering

Staat: FL
Alter: 41,0
Geschlecht: F
Eingang: 08.12.2021
Impfdatum: 04.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: OT / -

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

Nerve injury Vaccination site discolouration Vaccination site induration

Symptomtext

the site is discolored/ injection area on the arm got hard and black; the injection area on the arm got hard and black; nerves in their hand are bad; This spontaneous case was reported by a consumer and describes the occurrence of NERVE INJURY (nerves in their hand are bad), VACCINATION SITE DISCOLOURATION (the site is discolored/ injection area on the arm got hard and black) and VACCINATION SITE INDURATION (the injection area on the arm got hard and black) in a 41-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 071f21a) for COVID-19 vaccination. No Medical History information was reported. On 04-Nov-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. In 2021, the patient experienced NERVE INJURY (nerves in their hand are bad). On 05-Nov-2021, the patient experienced VACCINATION SITE DISCOLOURATION (the site is discolored/ injection area on the arm got hard and black) and VACCINATION SITE INDURATION (the injection area on the arm got hard and black). The patient was treated with PARACETAMOL (TYLENOL [PARACETAMOL]) for Adverse event, at an unspecified dose and frequency. On 24-Nov-2021, VACCINATION SITE INDURATION (the injection area on the arm got hard and black) had resolved. At the time of the report, NERVE INJURY (nerves in their hand are bad) and VACCINATION SITE DISCOLOURATION (the site is discolored/ injection area on the arm got hard and black) had not resolved. mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was withdrawn on an unknown date. Patient went to the doctor on 2nd December 2021 and the doctor recommended them to not take the second dose. No concomitant medication were given.

Weitere VAERSDATA-Felder

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

VAERS 1924964

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: CA
Alter: 52,0
Geschlecht: F
Eingang: 06.12.2021
Impfdatum: 03.11.2021
Beginn: 24.11.2021
Tage bis Beginn: 21,0
Dosis: 3
Route/Site: IM / LA

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

HIV infection

Symptomtext

Pt. states that after receiving the 3rd dose of Moderna 11/03/2021, started experiencing symptoms 11/24/2021 of Tested Positive HIV factors while registering to donate Blood /later documents mailed with Negative results 11/30/2021. Also received the Influenza Vaccine 11/12/2021.

Weitere VAERSDATA-Felder

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

VAERS 1924819

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071f21a

gering

Staat: RI
Alter: 34,0
Geschlecht: M
Eingang: 06.12.2021
Impfdatum: 26.11.2021
Beginn: 04.12.2021
Tage bis Beginn: 8,0
Dosis: 3
Route/Site: - / -

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

Erythema multiforme

Symptomtext

erythema multiforme

Weitere VAERSDATA-Felder

Praegender Schweregrund: Erythema multiforme
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Cerebral Palsy
Andere Medikamente: Flonase, Loratadine
Allergien: Sulfa antbx, yellow food dye
Vorherige Impfungen: -

VAERS 1920466

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: NY
Alter: 56,0
Geschlecht: F
Eingang: 03.12.2021
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / LA

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

Asthenia Blood sodium decreased Somnolence

Symptomtext

I experienced low sodium since June and it makes me weak and sleepy.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Asthenia
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Diabetes, Hypertension, Depression, Anxiety
Andere Medikamente: Yes
Allergien: N/A
Vorherige Impfungen: -

VAERS 1915832

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: IA
Alter: 74,0
Geschlecht: F
Eingang: 02.12.2021
Impfdatum: 23.11.2021
Beginn: 23.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Wrong product administered

Symptomtext

came into the pharmacy on morning of 11/23/2021 inquiring about flu and covid shots. Since appointments are required at this site, they made appointments online and stopped back that afternoon during a rush time. I saw them waiting and remembered our conversation earlier about covid vaccines. Therefore, I pushed paperwork forward for booster shots after verifying eligibility and gave them to our nurse. After vaccinations, they were asked for their covid cards and it was then determined their appointments were made for flu shots. I immediately told them about the error and asked if they were experiencing any issues. I updated their covid cards to reflect booster doses given and will follow-up with them. They declined flu shots at that time because they wanted to space shots out. After they left, I contacted their doctor to alert them of the error.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Wrong product administered
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: -
Andere Medikamente: -
Allergien: NKA
Vorherige Impfungen: -

VAERS 1914260

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071f21a

gering

Staat: MD
Alter: 72,0
Geschlecht: U
Eingang: 01.12.2021
Impfdatum: 01.12.2021
Beginn: 01.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Inappropriate schedule of product administration

Symptomtext

Booster shot was given before 6 month date

Weitere VAERSDATA-Felder

Praegender Schweregrund: Inappropriate schedule of product administration
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1912687

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: IA
Alter: 79,0
Geschlecht: M
Eingang: 01.12.2021
Impfdatum: 23.11.2021
Beginn: 23.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Wrong product administered

Symptomtext

Patient came into the pharmacy for a scheduled flu shot. He had been in earlier that day and had talked to me about both the Covid vaccine and the flu shot. When they came in, the pharmacy was very busy and I recalled our conversation about the Covid vaccine booster. Therefore, I pushed the paperwork through for the Moderna booster instead of the flu shot. The shot was given and when the patients were asked for their Covid cards, the pharmacist then discovered that they were here for flu vaccines. I, the pharmacist, then came over and talked with pt about the mix-up. I confirmed that he was due for the booster vaccine, but was wanting to wait a couple weeks for it. I tried answering all of their questions that I could at the time and then made sure to document it after. Their provider was contacted that day to communicate the mistake.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Wrong product administered
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Diabetes, hypertension, high cholesterol
Andere Medikamente: -
Allergien: NKA
Vorherige Impfungen: -

VAERS 1911778

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 071F21A

gering

Staat: NC
Alter: 78,0
Geschlecht: F
Eingang: 01.12.2021
Impfdatum: 02.11.2021
Beginn: 22.11.2021
Tage bis Beginn: 20,0
Dosis: 3
Route/Site: OT / -

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

Alopecia

Symptomtext

My hair started falling out. It's gotten worse in last month, or so.; This spontaneous case was reported by a consumer and describes the occurrence of ALOPECIA (My hair started falling out. It's gotten worse in last month, or so.) in a 78-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 071F21A) for COVID-19 vaccination. No Medical History information was reported. On 02-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 22-Nov-2021, the patient experienced ALOPECIA (My hair started falling out. It's gotten worse in last month, or so.). At the time of the report, ALOPECIA (My hair started falling out. It's gotten worse in last month, or so.) outcome was unknown. No concomitant medications were reported. No treatment medications were reported. This case was linked to MOD-2021-395776, MOD-2021-395763, MOD-2021-395825 (Patient Link).

Weitere VAERSDATA-Felder

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