VAERS Reports #011J20A

VAERS 2589256

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

kritisch

Staat: MI
Alter: 72,0
Geschlecht: F
Eingang: 01.03.2023
Impfdatum: 08.02.2021
Beginn: 18.02.2023
Tage bis Beginn: 740,0
Dosis: 1
Route/Site: UN / UN

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

Acute kidney injury Blood creatinine increased COVID-19 Cerebrovascular accident Condition aggravated Culture urine negative Dehydration Depressed level of consciousness Fractional excretion of sodium Mental status changes Red blood cells urine positive Renal impairment SARS-CoV-2 test positive Urinary casts absent Urine analysis abnormal White blood cells urine positive

Symptomtext

Discharge summary "Nursing home resident with dementia and recent stroke sent to ER with altered mental status and new COVID positivity. ER evaluation noted obtundation and new rise in Cr to 7 from a prior of 1. She was admitted and given IVF for what was presumed to be severe dehydration and possible ACE toxicity; urine culture was negative. FENA was low suggestive of hypovolemia. However, despite aggressive fluid replacement her Cr did not improve; her UA was positive for WBC and RBC but not WBC cast. She required NC oxygen support. Her sensorium returned to baseline but her Cr did not improve. The possibility of COVID associated nephritis was considered and she was started on empiric decadron with prompt improvement of her renal function. She was discharged home to her SNF for further care. Creatinine improved to 3.7 at the time of discharge and she was making abundant urine. ACE was stopped as it was unclear how much this contributed to her AKI. Hydralazine was started for BP control."

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Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 3,0
Labordaten: COVID 19 PCR test positive on 2/20/2023
Aktuelle Erkrankungen: -
Vorgeschichte: Admission Diagnoses: UTI (urinary tract infection) [N39.0] Hyperglycemia [R73.9] Generalized weakness [R53.1] AKI (acute kidney injury) [N17.9] AMS (altered mental status) [R41.82] Altered mental status [R41.82] Discharge Diagnoses: Principal Problem: Acute metabolic encephalopathy Active Problems: AKI (acute kidney injury) COVID-19 virus infection Diabetes mellitus History of CVA (cerebrovascular accident) Parkinsonism Hypertension due to endocrine disorder Muscle weakness (generalized) Moderate late onset Alzheimer's dementia Nursing home resident Moderate vascular dementia with psychotic disturbance
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2560189

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011 J 20 A

kritisch

Staat: AK
Alter: 86,0
Geschlecht: F
Eingang: 14.01.2023
Impfdatum: 31.12.2020
Beginn: 09.01.2021
Tage bis Beginn: 9,0
Dosis: 2
Route/Site: SYR / UN

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

Arthralgia Cerebrovascular accident Dysstasia Loss of personal independence in daily activities Magnetic resonance imaging head abnormal Speech disorder Visual impairment

Symptomtext

Patient got the vaccine on 12/31/2020. Had very sore shoulders could hardly get up. Talked to her on the 9th and she said she could not see out of her eyes correctly. Could not text me anymore. She texted every day. My sister called on the 16 said mom was not taking correctly . She was having a stroke. Had to take her in 4 times before they would admit her. Did not give her an MRI until the next afternoon.

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Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 131,0
Labordaten: Testing showed huge stroke.
Aktuelle Erkrankungen: -
Vorgeschichte: reumatoid arthritis
Andere Medikamente: Blood pressure medication, rheumatoid arthritis medication, steroids
Allergien: -
Vorherige Impfungen: -

VAERS 2526865

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

kritisch

Staat: MI
Alter: 85,0
Geschlecht: M
Eingang: 08.12.2022
Impfdatum: 26.11.2021
Beginn: 17.11.2022
Tage bis Beginn: 356,0
Dosis: 1
Route/Site: - / -

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

Agitation Anticoagulant therapy Asymptomatic COVID-19 Cerebral hypoperfusion Cerebral infarction Cerebrovascular accident Condition aggravated Confusional state Embolism Hemiparesis Muscular weakness Perfusion brain scan abnormal SARS-CoV-2 test positive Treatment failure

Symptomtext

"Patient with 3 COVID vaccines who admitted and had COVID detected PCR found upon d/c planning. Asymptomatic for COVID found during routine testing for facilty placement. ""86 year old patient with a history of paroxysmal atrial fibrillation, Parkinson's disease, and mild cognitive impairment presented with L sided weakness with suspected CVA involving the left parasagittal frontal lobe as visualized on CT Cerebral perfusion, showing critical hypoperfusion, with subsequent weakness in his right upper and right lower extremities. Suspect thromboembolic based on the location and distribution of the infarct. Neurology was consulted. It was deemed Eliquis failure, for which Neurology recommended transition to Xarelto, which the patient tolerated without complication. ASA was discontinued due to risk of bleed/hemorrhagic conversion while already on anticoagulation given his history of atrial fibrillation. The patient also demonstrated recurring agitation and confusion, and attempts at initiating pharmacotherapy were made with some success. By discharge, the patient was on a regimen of Seroquel 25 mg in the morning, Seroquel 50 mg in the early evening, and PRN haldol oral solution for breakthrough agitation. The morning dose to be administered at the discretion of the family, depending on striking a balance of agitation prevention and interactivity. The patient was found to be COVID positive on PCR screen, however he was asymptomatic. He was discharged home with family in stable condition."""

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Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 13,0
Labordaten: COVID Detected PCR on 11/28/2022
Aktuelle Erkrankungen: -
Vorgeschichte: Cardiovascular Hypertension CAD (coronary artery disease) Giant cell arteritis Vascular headache Hyperlipidemia Carotid occlusion, right PAC (premature atrial contraction) PVC (premature ventricular contraction) Bilateral carotid artery disease A-fib Acute CVA (cerebrovascular accident) TIA (transient ischemic attack) Digestive GERD (gastroesophageal reflux disease) Endocrine Hypothyroidism Integumentary Skin cancer (melanoma) Psychological vascular plus parkinson's dementia Respiratory Asthma Urinary Urge incontinence of urine Stage 3 chronic kidney disease Acute cystitis Other Lumbar spondylosis Periodic limb movements of sleep Knee pain, left Tremor History of stroke of right MCA Dysarthria Radicular syndrome of left leg Status post lumbar surgery- Open L2-3 through L4-5 bilateral laminectomies with medial facetectomies on 2/17/15 Compression fracture of first lumbar vertebra Chronic pain of left knee History of digestive system disease History of colonic polyps Rubral tremor Prediabetes Parkinson's disease (*) Steroid dependence (*) - prednisone, for GCA Chronic gout due to renal impairment involving toe of right foot Urinary frequency Sepsis due to urinary tract infection Altered mental status, unspecified
Andere Medikamente: -
Allergien: Tamiflu, Lyrica
Vorherige Impfungen: -

VAERS 2263451

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

kritisch

Staat: MI
Alter: 67,0
Geschlecht: M
Eingang: 04.05.2022
Impfdatum: 08.02.2021
Beginn: 25.04.2022
Tage bis Beginn: 441,0
Dosis: 1
Route/Site: UN / UN

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

Acute respiratory failure COVID-19 Cerebral infarction Cough Delirium Delusion Dysphagia Haematuria Hemiplegia Hyperglycaemia Hypoxia Neuropsychiatric symptoms SARS-CoV-2 test positive Vascular dementia

Symptomtext

Provider discharge summary "Patient had been under hospice care at a local extended care facility due to history of Vascular dementia with behavior disturbance and Hemiplegia, Dysphagia as late effects of cerebral infarction developed Hypoxia. This appears due to a COVID-19 virus infection. He has been started on DECADRON and REMDESIVIR. He improved and was able to be weaned off supplemental oxygen. He completed his course of DECADRON in the hospital. The patient was medically stable for discharge on 4/29/22 but the facility where he had been residing initially refused to take the patient back and as such his hospital stay was inappropriately lengthened. Continuing medications for dementia: QUETIAPINE GABAPENTIN DIVALPROEX ESCITALOPRAM BUPROPION For history of stroke on ASPIRIN, CLOPIDOGREL,. For hyperglycemia on sliding scale but had not required much coverage. "

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 7,0
Labordaten: Positive COVID 19 PCR 4/25/22
Aktuelle Erkrankungen: -
Vorgeschichte: Tobacco abuse (Chronic) 7/11/2016 History of heavy alcohol consumption 7/11/2016 HTN, goal below 140/80 (Chronic) 7/11/2016 History of CVA with residual deficit (Chronic) 7/11/2016 Carotid artery stenosis/R ICA occlusion 7/13/2016 Dysphagia (Chronic) 7/19/2016 Hemiplegia as late effect of cerebral infarction (Chronic) 10/21/2016 Gastroesophageal reflux disease without esophagitis 11/3/2016 OSA (obstructive sleep apnea) 11/29/2016 Pigmented skin lesion 12/1/2016 Insomnia 3/9/2017 Mixed hyperlipidemia 3/9/2017 DNR (do not resuscitate) 11/2/2017 Irritability and anger 9/26/2018 Urge incontinence of urine 1/24/2019 Incontinence of feces 5/23/2019 Coagulation disorder (HCC) 9/5/2019 Peripheral polyneuropathy 11/20/2019 Type 2 diabetes mellitus with circulatory disorder, with long-term current use of insulin 1/14/2020 Uncircumcised male 2/25/2020 History of cigarette smoking 2/25/2020 Delusional disorder 5/26/2021 Vascular dementia with behavior disturbance (Chronic) 10/29/2021 Hematuria 11/26/2021 Cough 11/26/2021 Hospice care patient 1/26/2022 Delirium due to another medical condition, persistent, hyperactive 3/1/2022 COVID-19 virus infection 4/26/2022 Acute respiratory failure with hypoxia 5/4/2022
Andere Medikamente: acetaminophen 500 mg Oral every 4 hours PRN aspirin 81 mg Oral Daily bisacodyl 5 mg Oral DAILY PRN bupropion HCl 150 mg One bid Patient taking differently: Take 150 mg by mouth 2 (two) times daily. clopidogrel bisulfate 75 mg Oral Dai
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 1723124

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

kritisch

Staat: TN
Alter: 72,0
Geschlecht: M
Eingang: 02.05.2022
Impfdatum: 21.01.2021
Beginn: 26.07.2021
Tage bis Beginn: 186,0
Dosis: 1
Route/Site: IM / UN

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

Anticoagulant therapy C-reactive protein increased COVID-19 pneumonia Chest X-ray abnormal Computerised tomogram thorax abnormal Chest X-ray Chest tube insertion Computerised tomogram Computerised tomogram thorax Death Cough Culture negative Dyspnoea Laboratory test abnormal Leukocytosis Echocardiogram Ultrasound scan Malaise

Symptomtext

Presented to ED with covid like symptoms for the past 8 days including cough, fever, and dyspnea. Requiring HFNC 60% FIO2, given 1 dose of Decadron, along with 1 L IVF's. Initial labs significant for leukocytosis, marked elevation of CRP, and procalcitonin. Concern for bacterial superinfection in the setting of Covid PNA, started on Azithromycin and ceftaz. Started on dexamethasone. On 8/19/21 worsening respiratory effort and oxygenation, repeat chest CT demonstrated moderate bilateral pulmonary emboli, and placed on heparin infusion, Vancomycin restarted d/t concern for possible post viral staphylococcal PNA. Patient requested to be DNR/DNI and transition to comfort measures and transitioned to inpatient hospice.

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Praegender Schweregrund: Death
Hospital-Tage: 23,0
Labordaten: Cxray: consistent with Covid PNA 7/28/2021: CT chest shows 3CM L renal lesion 8/12/2021: CT guided Left Pleural collection asp Sputum culture x 2 negative
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2252564

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011j20a

kritisch

Staat: SD
Alter: 76,0
Geschlecht: M
Eingang: 26.04.2022
Impfdatum: 09.11.2021
Beginn: 21.03.2022
Tage bis Beginn: 132,0
Dosis: 1
Route/Site: SYR / LA

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

Acute respiratory failure Brain injury COVID-19 COVID-19 pneumonia Death Myocardial infarction SARS-CoV-2 test positive Septic shock Vaccine breakthrough infection

Symptomtext

This is an instance of breakthrough COVID-19 after which death occurred. The individual was vaccinated with the Moderna product on 01/05/2021, 02/02/2021, and 11/09/2021. They tested positive for COVID-19 on 03/21/2022. They were hospitalized 03/19/2022-03/26/2022 and discharged to a hospice facility on 03/26/2022. They remained in the hospice facility until their death on 03/28/2022. They had terminal metastatic lung cancer and were found to have had complications of acute hypoxemic respiratory failure, hypoxic ischemic brain injury, septic shock, COVID-19 pneumonia, and a Type II myocardial infarction.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 7,0
Labordaten: Positive COVID-19 test on 03/21/2022 despite being vaccinated and boosted.
Aktuelle Erkrankungen: -
Vorgeschichte: Metastatic Right Lung Cancer
Andere Medikamente: -
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 2095471

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

kritisch

Staat: MI
Alter: 75,0
Geschlecht: M
Eingang: 08.02.2022
Impfdatum: 27.08.2021
Beginn: 01.02.2022
Tage bis Beginn: 158,0
Dosis: 1
Route/Site: IM / AR

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

Acute respiratory failure Anticoagulant therapy Arterial catheterisation Asthenia Blood gases Breath sounds abnormal C-reactive protein COVID-19 COVID-19 pneumonia Central venous catheterisation Chest X-ray Decreased appetite Differential white blood cell count Dyspnoea Endotracheal intubation Fibrin D dimer Full blood count General physical condition abnormal

Symptomtext

Hospitalized 02/01/2022-still currently admitted; COVID-19 positive 02/01/2022; fully vaccinated plus booster HISTORY OF PRESENT ILLNESS: This is a 76-year-old male with a past medical history of O2 dependent chronic obstructive pulmonary disease on 2.5 L chronically, CML on Gleevec for at least the last 6 years, pulmonary hypertension, chronic kidney disease stage 3, history of pulmonary embolism in March 2019 for which he is on Eliquis. Patient presents with 2 week history of cough productive of clear sputum with red streaks, progressive shortness of breath. He has also had malaise and weakness. He checked his O2 sats this morning and it was in the 60s, he turned his oxygen up in came to the emergency department for evaluation. Patient denies any fevers. He has had diarrhea which is not any different for him since being on Gleevec, several loose stools a day. He denies any nausea or vomiting. No loss of taste or smell but states he is just not hungry. On arrival to the emergency department he was afebrile, blood pressure 113/54, breathing 24 breaths per minute heart rate 103, satting 74% on 2.5 L, now satting 91% on high-flow nasal cannula 60%, 50 L on exam he is ill appearing, conversational dyspnea with frequent wet cough. Lungs show crackles at the bases bilaterally coarse breath sounds in the mid fields. Heart was regular rate and rhythm. Abdomen nontender extremities showed no significant edema Pneumonia due to COVID-19 virus ASSESSMENT/PLAN: Acute on chronic hypoxemic respiratory failure secondary to COVID-19 pneumonia -symptom onset greater than 2 weeks, positive test 2 weeks ago per patient -continue supple oxygen up to and including intubation -prednisone 60 mg IV 2 times a day -patient is out of window for remdesivir due to symptom duration -daily labs including CMP, complete blood count with diff, CRP, D-dimer -incentive spirometry, deep breathing -pronation as tolerated -patient is on Gleevec, therefore immunosuppressed -will start antibiotics with Zosyn and vancomycin -check MRSA screen -patient is on Eliquis for VTE, given his acute illness, I will change it to a heparin drip tonight given we may have to perform procedures -Pepcid for GI prophylaxis 02/05/2022 notes: ASSESSMENT / PLAN: * Pneumonia due to COVID-19 virus Assessment & Plan Patient deteriorated to respiratory failure and was endotracheally intubated and placed on mechanical ventilation this morning. General surgery was consulted and kindly placed a triple-lumen central venous catheter and arterial line. Patient symptom onset greater than 2 weeks. Day 1 of mechanical ventilation. Patient on day 4/7 piperacillin tazobactam. Continue steroid therapy with Solu-Medrol will increase dose to 60 mg q.12 hours due to worsening respiratory status. Maintain negative fluid balance with Lasix 40 mg IV 2 times a day. Patient paralyzed(Day 1) and proned. Monitor ABGs q.4 hours. Daily chest x-ray. Resume unfractionated heparin therapy. Convert to Lovenox tonight. Consulted VICU for support and recommendations. Appreciate their input. Acute on chronic respiratory failure with hypoxemia (HCC) Assessment & Plan Patient required increase in his oxygen therapy to 100% by high-flow nasal cannula and had persistent hypoxemia on ABG so was endotracheally intubated and placed on the mechanical ventilator. 02/08/2022 notes: Assessment and Plan Acute on chronic respiratory failure with hypoxemia (HCC) Assessment & Plan Secondary to COVID-19 viral pneumonia on background of COPD/emphysema with chronic hypoxic respiratory failure (baseline 2.5 LPM) Admitted 2/1 Initially treated with HFNC, then intubated 2/5 Current support: FIO2 (%): 40 % Sedation: Deeply sedated, with NMB - Continue with lung protective ventilatory strategy - Wean FiO2 and PEEP as able, goal PaO2 55-80 and SpO2 88-95% - Continue with deep sedation, goal RASS -5, and NMB for now - Continue with prone positioning as long as FiO2 needs </= 60% and P/F ratio <150 - Avoid hypervolemia as possible, goal even to slightly positive fluid balance given renal dysfunction - Continue empiric zosyn, to complete 7 days of abx tx today (infectious studies thus far NGTD) * Pneumonia due to COVID-19 virus Assessment & Plan - Continue steroids for COVID related pneumonitis; will need 10 days minimum of steroid tx - Fluid balance as above - Therapeutic anticoagulation as below - Otherwise, management of acute hypoxic respiratory failure as above

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 7,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Elevated bilirubin Peripheral neuropathy Umbilical hernia History of malignant neoplasm of large intestine Osler-Vaquez disease (HCC) Allergic rhinitis Anemia Colon cancer (HCC) Familial polycythemia Hyperlipidemia Neuropathy of foot Cholelithiasis Calculus of gallbladder without cholecystitis without obstruction Headache, primary exertional Cough headache Adenosylcobalamin synthesis defect Dyslipidemia Inflammation of membranes covering brain and spinal cord Pulmonary hypertension (HCC) Temporary cerebral vascular dysfunction Abnormal MRI of the head Hx of colonic polyps Diverticulosis
Andere Medikamente: apixaban (ELIQUIS) 5 MG TABS imatinib (GLEEVEC) 400 MG tablet Respiratory Therapy Supplies (OXYGEN THERAPY)
Allergien: Albuterol Moderna
Vorherige Impfungen: -

VAERS 2038533

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

kritisch

Staat: CA
Alter: 54,0
Geschlecht: F
Eingang: 16.01.2022
Impfdatum: 19.03.2021
Beginn: 13.03.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: IM / LA

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

Blood test Computerised tomogram Echocardiogram Electrocardiogram Pulmonary embolism Ultrasound scan

Symptomtext

Had my second moderna civid vaccine on 3/2/22 Ended up in hospital with PE ( pulmonary embolism) on 3/13/21. hospital

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Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: -
Labordaten: Ct scan 3/13/21, blood, work 3/13, heparin 3/13/21 Blood work 3/27/21. Now on blood thinners Heart echo/3/14 /21in hospital, ultrasound 3/13 on legs none. EKG 3/13/21
Aktuelle Erkrankungen: None
Vorgeschichte: RA, asthma
Andere Medikamente: Hydroxychlorquin Cardia
Allergien: Cipro
Vorherige Impfungen: -

VAERS 2501570

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

kritisch

Staat: -
Alter: 99,0
Geschlecht: M
Eingang: 02.01.2022
Impfdatum: 05.01.2021
Beginn: 22.01.2021
Tage bis Beginn: 17,0
Dosis: 1
Route/Site: IM / RA

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

Death

Symptomtext

Narrative:

Weitere VAERSDATA-Felder

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

VAERS 2498947

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

kritisch

Staat: -
Alter: 85,0
Geschlecht: M
Eingang: 02.01.2022
Impfdatum: 04.01.2021
Beginn: 12.02.2021
Tage bis Beginn: 39,0
Dosis: 1
Route/Site: IM / LA

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

Acute respiratory failure Cardiac failure Death Lung adenocarcinoma Pleural effusion

Symptomtext

Narrative: Death not suspected to be related to COVID-19 vaccine administration. Patient was on Hospice care for Acute on chronic mixed respiratory failure with acute on chronic pleural effusions secondary to HFrEF/RVR and RLL adenocarcinoma.

Weitere VAERSDATA-Felder

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

VAERS 2498863

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

kritisch

Staat: -
Alter: 90,0
Geschlecht: M
Eingang: 02.01.2022
Impfdatum: 05.01.2021
Beginn: 19.01.2021
Tage bis Beginn: 14,0
Dosis: 1
Route/Site: IM / LA

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

Death

Symptomtext

Narrative: No documentation found in chart review indicating that death was related to COVID-19 vaccine administration

Weitere VAERSDATA-Felder

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

VAERS 1997722

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

kritisch

Staat: MI
Alter: 69,0
Geschlecht: F
Eingang: 02.01.2022
Impfdatum: 11.01.2021
Beginn: 08.05.2021
Tage bis Beginn: 117,0
Dosis: 2
Route/Site: IM / LA

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

Cerebrovascular accident

Symptomtext

Stroke

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Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 52,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Chronic Back pain, Arthritis, Hypothyroidism, Brain Tumor
Andere Medikamente: Lumigan, combigan, Oxycodone,, Vitamin D, Omerazole, levothyroxine
Allergien: PCN,Reglan, Supartz
Vorherige Impfungen: See VAERS report

VAERS 1963691

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011j20a

kritisch

Staat: CA
Alter: 61,0
Geschlecht: M
Eingang: 20.12.2021
Impfdatum: 07.01.2021
Beginn: 04.12.2021
Tage bis Beginn: 331,0
Dosis: 1
Route/Site: IM / LA

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

Acute respiratory failure COVID-19 Chest X-ray Cough Dyspnoea Hypoxia Malaise Pyrexia SARS-CoV-2 test positive

Symptomtext

presented to the ER on 12/4/2021 with shortness of breath, fever to 101 at home, hypoxic to 83% at home. Wife recovered from COVID-19. Has dry cough Patient was admitted for worsening shortness of breath after positive COVID-19 test, was found to have acute hypoxemic respiratory failure. Patient was treated with remdesivir and dexamethasone initially, chest x-ray showed potential consolidative process concern for bacteria superinfection as such levofloxacin was started. Patient initially required increasing oxygen supplementation up to 6 L however by day 5 of admission was improving in terms of oxygenation. On the day of discharge she was saturating mid 90s on 4 L nasal cannula and had experienced significant symptomatic improvement of symptoms. Patient finished 5 days of remdesivir and will continue 5 additional days of dexamethasone and levofloxacin as outpatient. Patient will follow up with primary care to ensure continued improvement and resolution of Covid symptoms and to wean off of oxygen as outpatient.

Weitere VAERSDATA-Felder

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

VAERS 1929245

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

kritisch

Staat: MI
Alter: 61,0
Geschlecht: F
Eingang: 07.12.2021
Impfdatum: 21.01.2021
Beginn: 08.11.2021
Tage bis Beginn: 291,0
Dosis: 1
Route/Site: - / -

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

Acute respiratory failure COVID-19 COVID-19 pneumonia Chest X-ray abnormal Chills Cough Death Endotracheal intubation Exposure to SARS-CoV-2 General physical health deterioration Hypotension Increased bronchial secretion Intensive care Pleural effusion Positive airway pressure therapy Productive cough Pyrexia Renal impairment

Symptomtext

COVID vaccinated patient admitted for COVID pneumonia who subsequently died. Provider discharge note: "62yo female with PMHx significant for HLD, CKD3, HLD, GERD, DM2 who presented to the ED with progressively worsening cough. She went to a funeral on 10/21 and later found out 8 people who were at the funeral had COVID. Later that day she also developed a cough which has got progressively more productive of white to tan secretions then developed shaking chills. She did receive the Moderna COVID vaccines in December and January 2021. Patient was admitted to the hospital for sepsis and acute on chronic respiratory failure 2/2 COVID-19 pneumonia. She initially was alternating between BiPAP and HFNC. She was treated with Remdesivir and decadron, as well as Rocephin and doxycycline for possible superimposed bacterial infection. Patient's respiratory status progressively worsened to the point where she became altered and required intubation in the ED. CCU was consulted for further management and patient was transferred to the CCU. The following day, patient noted to have decreased UOP, worsening kidney function, and increased secretions in ETT overnight. Febrile to 39.1C. Patient noted to have new left pleural effusion on CXR. Lasix 80mg IV TID ordered. Nephrology consulted. Patient on CRRT overnight. On 11/8, patient was noted to be hypotensive overnight requiring phenylephrine. Continue on CRRT. Patient's family was consulted for update on worsening status. They arrived at the ICU and made the decision to withdraw care. Pressors and paralytics were discontinued. Patient was extubated at 1427. Time of death was 1437."

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: -
Labordaten: Positive COVID test on 11/05/21.
Aktuelle Erkrankungen: -
Vorgeschichte: Essential hypertension Gastroesophageal reflux disease without esophagitis History of gout Mixed hyperlipidemia Peripheral polyneuropathy Osteoarthritis Rosacea Type 2 diabetes mellitus with diabetic polyneuropathy, without long-term current use of insulin (*) Stage 3b chronic kidney disease (*) Class 2 obesity in adult History of kidney stones Normocytic normochromic anemia
Andere Medikamente: Albuterol, Zyloprim, Norvasc, Lipitor, Flexeril, Voltaren gel, Jardiance, Amaryl, Cozaar, Metformin, Metrocream, Protonix, Klor-Con, Lyrica
Allergien: Sulfa antibiotics, succinylcholine
Vorherige Impfungen: -

VAERS 2564323

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

kritisch

Staat: -
Alter: 99,0
Geschlecht: M
Eingang: 03.12.2021
Impfdatum: 07.01.2021
Beginn: 17.01.2021
Tage bis Beginn: 10,0
Dosis: 1
Route/Site: IM / RA

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

Death

Symptomtext

Narrative: 98 y/o male received first dose of COVID-19 vaccine (Moderna) on 1/7/2021. Was in facility at the time, expired 1/17/2021.

Weitere VAERSDATA-Felder

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

VAERS 1873588

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 011J20A

kritisch

Staat: AR
Alter: 85,0
Geschlecht: M
Eingang: 16.11.2021
Impfdatum: 31.12.2020
Beginn: 03.11.2021
Tage bis Beginn: 307,0
Dosis: 1
Route/Site: - / -

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

Altered state of consciousness Bronchitis chronic COVID-19 COVID-19 pneumonia Chest X-ray abnormal Death Dyspnoea Emphysema General physical condition abnormal Hypoxia Lung infiltration Patient uncooperative Pneumonia aspiration SARS-CoV-2 test positive

Symptomtext

PT ADMITTED ON: 11/03/2021: The patient is admitted to the Palliative care service. HISTORY OF PRESENT ILLNESS: Patient is an 86-year-old man who had a change in level of consciousness and became dyspneic and hypoxic at the nursing home today. He is a resident at Nursing Home. He was sent to the emergency room where he has been found to certainly be hypoxic and has evidence of pneumonia on chest x-ray with a positive COVID test. The patient himself is unable to give the history. REVIEW OF SYSTEMS: The patient is unable to complete review of systems. PAST MEDICAL HISTORY: Patient is unable to cooperate. SOCIAL HISTORY: His sister has arrived today. Additional information for Item 18: (con't): EXPIRED DATE: 11/05/2021: The patient expired on 11/05/2021. ADMISSION DIAGNOSIS: COVID-19 virus infection. FINAL DIAGNOSES: 1. Pneumonia due to COVID-19 virus. 2. Chronic obstructive bronchitis with pulmonary emphysema. 3. Aspiration pneumonia. 4. Encounter for palliative care. HISTORY OF PRESENT ILLNESS: Patient is an 86-year-old man who presented to the hospital from a local nursing home with dyspnea. He was evaluated in the emergency room where he was found to have right-sided pneumonia or right-sided infiltrate on chest x-ray. He had a positive COVID test. He had changes of emphysema on his chest x-ray. His sister arrived in the emergency room and made it clear that she wants the care focused on his comfort. He looked very ill in the emergency room the night that I arrived and I just did not think it was fair to put the sisters through all the hospice procedures to get the patient admitted. I thought his death was imminent. HOSPITAL COURSE: The patient was admitted. He received IV morphine usually about once per shift for shortness of breath. He expired on the morning of 11/05/2021. The first morning after admission he actually was clinically improved and was able to say just a few words and on the morning of 11/05, he said just a few words. He expired that morning. Cause of death was COVID-19 pneumonia. His sister was counseled following this. No autopsy was desired.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 3,0
Labordaten: Coronavirus 19 dated 11/02/2021: Detected.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1865474

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

kritisch

Staat: OH
Alter: 85,0
Geschlecht: M
Eingang: 12.11.2021
Impfdatum: 20.01.2021
Beginn: 01.02.2021
Tage bis Beginn: 12,0
Dosis: 1
Route/Site: SYR / UN

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

Death Platelet count decreased Radiotherapy

Symptomtext

Event: Low Platelet count. Treatment: Received radiation therapy and blood infusions Outcome: Death

Weitere VAERSDATA-Felder

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

VAERS 1785202

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

kritisch

Staat: PR
Alter: 31,0
Geschlecht: M
Eingang: 14.10.2021
Impfdatum: 14.01.2021
Beginn: 30.08.2021
Tage bis Beginn: 228,0
Dosis: 1
Route/Site: IM / LA

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

Angiosarcoma Biopsy Death Dizziness Imaging procedure Laboratory test Photophobia Vertigo Vomiting

Symptomtext

Patient presented to medical clinic on 30AUG21 for evaluation of vertigo, photophobia, dizziness, vomiting. Patient was evaluated on 31AUG21 via Emergency Department, was later diagnosed with Angiosarcoma and passed away on 07OCT21.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Angiosarcoma
Hospital-Tage: 38,0
Labordaten: Multiple laboratory tests, imaging and biopsies performed during the period between 31AUG to 07OCT.
Aktuelle Erkrankungen: None
Vorgeschichte: Low Back Pain (reported 2019)
Andere Medikamente: unknown
Allergien: NKDA/NKA
Vorherige Impfungen: -

VAERS 1754078

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

kritisch

Staat: GA
Alter: 96,0
Geschlecht: M
Eingang: 01.10.2021
Impfdatum: 05.01.2021
Beginn: 15.04.2021
Tage bis Beginn: 100,0
Dosis: 1
Route/Site: SYR / UN

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

COVID-19 pneumonia Death

Symptomtext

Death due to COVID-19 PNEUMONIA

Weitere VAERSDATA-Felder

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

VAERS 1726200

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

kritisch

Staat: MI
Alter: 25,0
Geschlecht: M
Eingang: 23.09.2021
Impfdatum: 26.01.2021
Beginn: 16.09.2021
Tage bis Beginn: 233,0
Dosis: 1
Route/Site: - / UN

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

Blood glucose normal COVID-19 Cerebrovascular accident Cheilitis Chest pain Computerised tomogram thorax normal Cough Dyspnoea Echocardiogram abnormal Ejection fraction decreased Electrocardiogram abnormal Electroencephalogram normal Fatigue Hemiparesis Intensive care Intervertebral disc degeneration Laboratory test normal Magnetic resonance imaging head normal

Symptomtext

Hospitalized 9/1/2021; COVID-19 positive (9/16/2021); fully vaccinated Patient is a 26 y.o. male who presented with fatigue, fever and chest pain. Patient has a history of HTN, OSA, and obesity. Patient had onset fever, body aches and fatigue night of 9/14/2021. Patient took tylenol and motrin with continued symptoms. Cough and congestion started on 9/16/21 with increasing shortness of breath. Notified of recent work exposure for COVID and was found to be positive on 9/16. Patient is fully vaccinated with moderna in early 2021, with sister who was also vaccinated ended up intubated with COVID 1 month prior. Patient also reported rash onset 9/17 after recent exposure to son who had HFMD. Rash is found on face, hands, feet, and truck with sores to inner lips and sore throat. Increased shortness of breath, chest pain and cough on night of 9/17, in which prompted him to seek further care. Patient denies abdominal pain, nausea, vomiting or urinary symptoms. In the ED, patient was found to have unremarkable laboratory findings. EKG showed sinus tachycardia with normal tropinins. CT thorax completed without evidence of PE. Although no acute findings, patient was admitted to hospitalist service for COVID due to continued tachypnea and tachycardia for continued monitoring and symptomatic treatment. 9/19/2021 at 0304 I patient with acute stroke findings. Last known normal established das 0247 when RN administered tylenol. BP 145/96, glucose 131. Patient with obvious left side hemiparises, no facial asymmetry, protecting airway, led visual field defect. NIH 14. STAT imaging ordered at 0311. Nursing escorted patient down to CT. Neurology and recommended tPA if no bleed or other contraindication and transfer to neuro ICU barring large vessel occlusion. Radiology called backed, no bleed noted on CT head, normal perfusion Study, CT angio with some findings felt 2/2 poor timing of contrast. tPA ordered and administered. He is transferred in stable condition via ground to another facility on 9/19/21. Currently hospitalized, Patient stable now, awaiting discharge to inpatient rehab.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 5,0
Labordaten: Neurology note: -MRI brain without contrast - motion degraded exam, possible artifactual diffusion hyperintensity in the posterior right hippocampus. -MRV Brain - Moderately motion degraded exam, however the venous sinuses are patent -MRI C spine with contrast - No evidence of focal spinal cord signal abnormalities or abnormal enhancement. No significant spinal canal or neural foraminal narrowing -Repeat HCT 24hr post-tPA administration stable with no signs of bleed. -Echo - LVEF 55%, unclear visualization of LA due to suboptimal windows. -Repeat MRI Brain with and without contrast with no evidence of infarct, lesion or abnormal enhancement -EEG report with no epileptiform abnormalities noted. Normal study MRI Spine lumbar 9/20/21: 1. Motion degraded exam. 2. No significant spinal canal or neural foraminal narrowing. 3. No acute fracture or malalignment of the lumbar spine. 4. Minimal nonspecific facet joint fluid bilaterally at L4-L5. Findings may relate to degenerative changes, joint hypermobility, and/or altered biomechanics. Correlate for facet joint pain. MRI Spine thoracic 9/22/21: 1. Multilevel degenerative disc disease with extensive prominent epidural fat resulting in moderate spinal canal narrowing from T6-T7 through T10-T11. 2. No significant neural foraminal narrowing. 3. Unchanged minimal T1 and mild T2 superior endplate deformities. 4. Otherwise, no evidence of acute fracture or malalignment of the thoracic spine
Aktuelle Erkrankungen: Office visit with PCP on 9/16/2021: Patient presents to the office for the CC of cough and congestion x 2 days. Cough is dry. Mildly sob. Symptoms started with shaking chills and body aches yesterday and have since progressed. Nasal congestion and rhinorrhea. Sore throat. NVD. Weak. Fatigued. +exposure covid19 and HFM. Denies rash. Suspect underlying viral etiology. Recommend supportive care. APAP/IBU for pain/fever. Albuterol PRN. Push fluids. COVID19 test ordered.
Vorgeschichte: Past medical history obstructive sleep apnea, hypertension, morbid obesity, anxiety and depression, ADD
Andere Medikamente: albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler ascorbic acid (VITAMIN C) 1000 MG tablet betamethasone dipropionate 0.05 % cream cloNIDine (CATAPRES) 0.1 MG tablet dicyclomine (BENTYL) 20 MG tablet esci
Allergien: Zithromax
Vorherige Impfungen: -

VAERS 1689608

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

kritisch

Staat: FL
Alter: 88,0
Geschlecht: F
Eingang: 10.09.2021
Impfdatum: 26.01.2021
Beginn: 20.08.2021
Tage bis Beginn: 206,0
Dosis: 1
Route/Site: IM / -

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

Acute respiratory distress syndrome Acute respiratory failure COVID-19 COVID-19 pneumonia Chills Death Diarrhoea Dyspnoea General physical health deterioration Malaise Productive cough Pyrexia Respiratory tract congestion SARS-CoV-2 test positive Sepsis Vaccine breakthrough infection

Symptomtext

COVID-19 Breakthrough case. 8/20/21: Patient states he has had COVID like symptoms for almost 2 weeks now and had an outpatient positive COVID test 9 days ago on 8/11/2021. He states he has had symptoms of a productive cough, worsening shortness of breath, chest congestion, some diarrhea, subjective fevers and chills that have now resolved. He states at baseline he has some shortness of breath but since testing positive for COVID, SOB has been worse than his baseline. He states he had a Regeneron treatment 2 days ago but does not believe his symptoms are any better. Admitted 8/20/21. Note: previously received Moderna COVID-19 vaccines on 12/29/21 & 1/26/21. Diagnosed with ARDS, acute hypoxic respiratory failure, Covid-19 viral pneumonia and sepsis. Condition deteriorated and patient died on 8/29/21.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 11,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: atrial fibrillation (on Eliquis), diabetes mellitus, COPD, CKD (stage III), hypothyroidism and right eye blindness
Andere Medikamente: albuterol, apixaban, atorvastatin, azithromycin, cholecalciferol, cyanocobalamin, diltiazem, folic acid, levothyroxine, lisinopril, memantine, metoprolol succinate, artificial tears, prednisone
Allergien: nka
Vorherige Impfungen: -

VAERS 1689045

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

kritisch

Staat: GA
Alter: 86,0
Geschlecht: M
Eingang: 10.09.2021
Impfdatum: 18.02.2021
Beginn: 09.08.2021
Tage bis Beginn: 172,0
Dosis: 2
Route/Site: IM / LA

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

COVID-19 Death SARS-CoV-2 test positive

Symptomtext

Hospitalization (8/9/2021-8/18/2021) and death (8/18/2021) due to COVID-19

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 9,0
Labordaten: 08/13/2021 PCR+ COVID-19 test at Medical Center
Aktuelle Erkrankungen: -
Vorgeschichte: Chronic Lung Disease (asthma/emphysema/COPD), Diabetes Mellitus, Cardiovascular disease, Chronic Renal disease
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1685408

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

kritisch

Staat: FL
Alter: 66,0
Geschlecht: M
Eingang: 09.09.2021
Impfdatum: 04.02.2021
Beginn: 27.07.2021
Tage bis Beginn: 173,0
Dosis: 1
Route/Site: IM / -

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

Aphasia Asthenia Chest X-ray abnormal Confusional state Deep vein thrombosis Memory impairment Pulmonary congestion Pulmonary embolism SARS-CoV-2 test positive

Symptomtext

7/27/21: presents to the ED with confusion and generalized weakness. Son states pt has been forgetful, unable to verbalize, and has not been finishing sentences. Chest x-ray was read as: Mild pulmonary vascular congestion. admitted. Treated for PE/DVT. Not treated for any disease related to Covid. 8/27/21: discharged Note: previously vaccinated with Moderna COVID-19 vaccine: First Dose: 01/07/21 Lot Number O11J20A; Second Dose: 02/04/21 Lot Number 029K20A

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: -
Labordaten: Tested negative for Covid on 7/27/21 (admission) but then tested positive on 8/4/21.
Aktuelle Erkrankungen: -
Vorgeschichte: HTN, DM, HLD, and CAD with MI
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1591913

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

kritisch

Staat: FL
Alter: 81,0
Geschlecht: M
Eingang: 20.08.2021
Impfdatum: 09.02.2021
Beginn: 07.08.2021
Tage bis Beginn: 179,0
Dosis: 1
Route/Site: IM / -

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

Blood creatinine increased COVID-19 Cough Death SARS-CoV-2 test positive

Symptomtext

8/7/2021: Patient is a pleasant 82-year-old male c significant past medical history of CVA c left-sided deficits, P 80, hypertension, hyperlipidemia, diabetes, heart failure, carotid artery disease history of endarterectomy. Patient presents to Hospital from nursing home for slight cough. He did test positive for COVID on 8/7/2021 but is been satting well on room air. Chest x-ray is still in progress. Laboratory significant for a dramatic increase in creatinine. Creatinine of 3.42 on 08/07 which has increased from 1.84 2 days prior. 8/12/2021: patient to hospice 8/19/2021: patient expired

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 13,0
Labordaten: 8/7/2021: SARS CoV 2 PCR COVID-19 Positive
Aktuelle Erkrankungen: unknown
Vorgeschichte: CAD, HTN, DM, CVA (with residual left sided deficits)
Andere Medikamente: unknown
Allergien: heparin
Vorherige Impfungen: -

VAERS 1450549

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge 011J20A

kritisch

Staat: LA
Alter: 34,0
Geschlecht: F
Eingang: 06.07.2021
Impfdatum: 28.01.2021
Beginn: 30.06.2021
Tage bis Beginn: 153,0
Dosis: 1
Route/Site: IM / RA

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

Death Exposure during pregnancy Syncope

Symptomtext

As reported, the recipient/patient who is approximately 7 months pregnant, collapsed while in the shopping mall which resulted in death.

Weitere VAERSDATA-Felder

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

VAERS 1433476

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

kritisch

Staat: TN
Alter: 78,0
Geschlecht: F
Eingang: 29.06.2021
Impfdatum: 12.01.2021
Beginn: 19.03.2021
Tage bis Beginn: 66,0
Dosis: 1
Route/Site: IM / -

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

Acute respiratory distress syndrome Death Mechanical ventilation Pneumonia

Symptomtext

PNEMONIA, ARDS, VENT REQUIRED 4 DAYS DOD3/19/21

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: DM2, HTN, CAD, LUNG DISEASE, HX OF TIA
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1420707

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

kritisch

Staat: MT
Alter: 85,0
Geschlecht: F
Eingang: 23.06.2021
Impfdatum: 13.01.2021
Beginn: 14.01.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

COVID-19 Death Respiratory symptom SARS-CoV-2 test positive

Symptomtext

Patient presented to ER on 01/18/2021 and stated respiratory symptoms began on 01/14/2021. Positive Covid test that day. Patient was released from ER and admitted as inpatient to the hospital on 01/23/2021 and expired of Covid related symptoms on 02/02/2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 11,0
Labordaten: 01/18/2021
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Diabetes Type II Diastolic Dysfunction Hypertension Obesity Hyperlipidemia
Andere Medikamente: Flonase, Amlodipine, Atenolol, HCTZ, Losartan, Metformin, Simvastatin, Vitamin D3
Allergien: NKA
Vorherige Impfungen: -

VAERS 1382602

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

kritisch

Staat: AK
Alter: 68,0
Geschlecht: M
Eingang: 08.06.2021
Impfdatum: 05.02.2021
Beginn: 07.04.2021
Tage bis Beginn: 61,0
Dosis: 2
Route/Site: IM / RA

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

Cerebrovascular accident Death Mental status changes

Symptomtext

Altered mental status, stroke, death

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1316660

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011j20A

kritisch

Staat: NY
Alter: 62,0
Geschlecht: F
Eingang: 14.05.2021
Impfdatum: 03.02.2021
Beginn: 22.03.2021
Tage bis Beginn: 47,0
Dosis: 1
Route/Site: IM / LA

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

Abdominal pain Acute myocardial infarction Anaemia Colitis ischaemic Intestinal ischaemia Thrombocytosis

Symptomtext

Developed severe abdominal pain 3/22/2021. Hospitalized and dx w ISCHEMIC COLITIS, MESSENTERIC ISCHEMIA, TYPE II NSTEMI, ANEMIA and THROMBOCYTOSIS. Hospitalized 9 days

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute myocardial infarction
Hospital-Tage: 9,0
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: htn
Andere Medikamente: hctz/lis, crestor,mvi,vit d
Allergien: PCN Sulfa
Vorherige Impfungen: -

VAERS 1302329

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

kritisch

Staat: VA
Alter: 48,0
Geschlecht: F
Eingang: 10.05.2021
Impfdatum: 12.01.2021
Beginn: 20.01.2021
Tage bis Beginn: 8,0
Dosis: 1
Route/Site: IM / LA

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

Biopsy Computerised tomogram thorax Dyspnoea exertional Erythema induratum Granulomatous dermatitis Injection site rash Pruritus Pulmonary embolism Rash Rash papular Skin mass

Symptomtext

On 20 Jan 2021, 8 days after immunization developed bullseye rash on L upper arm at site of injection and nodular/papular dermatitits on anterior thiges bilaterally. Was seen by urgent care on 20 Jan 2021 and prescribed prednisone 20mg daily x 5 days. L upper arm lesion resolved after 3 days but anterior thigh lesions remained. She was seen by dermatology on 3 Feb 2021 and biopsy performed. Lesions described at that time as indurated erythematous to violaceous subcutaneous nodules. Seen in follow up at dermatology 9 Feb 2021 and had intralesional steroid injections. Seen by dermatology 16 Feb 2021 as treated lesions persisted, now lesions appeared on anterior thighs and patient c/o increased pruritus. She was treated with 1st and 2nd generation H1 blockers and a 2 week prednisone taper. Biopsy consistent with granulomatous dermatitis/panniculitis. Starting early Feb 2021, noted gradually worening symptoms of dyspnea on exertion. Seen by pulmonologist who ordered a chest CT and subsequently diagnosed with pulmonary embolus. She was started on abixiban daily. She was further evaluated by cardiology, hematology and rheumatology in March and April 2021. She had been on OCP at the time of diagnosis of the PE and this was changed to Nexaplan implant by Gyn. Workup with all specialists ongoing. Pulmonology recently added Fluticasone/Salmeterol inhaler which she finds has not improved her dyspnea.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: -
Labordaten: Biopsy of anterior thigh lesions consistent with granulomatous dermatitis/panniculitis. Chest CT c/w pulmonary embolus
Aktuelle Erkrankungen: -
Vorgeschichte: nonallergic rhinitis venom allergy endometriosis
Andere Medikamente: Fexofenadine 180mg daily, Cetirizine 10mg daily, Vit D, Calcium, OCP, EpiPen
Allergien: sulfa antibiotic: rash at age 9; Mirena IUD, rash within 2 weeks; Contact dermatitis: latex, adhesives from bandages, some cosmetics
Vorherige Impfungen: 15 Dec 2015, received varicella vaccine and 2 days later had large local swelling, redness at site of injection. Treated with ce

VAERS 1301825

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

kritisch

Staat: PA
Alter: 66,0
Geschlecht: F
Eingang: 10.05.2021
Impfdatum: 15.01.2021
Beginn: 01.02.2021
Tage bis Beginn: 17,0
Dosis: 1
Route/Site: OT / -

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

Cerebrovascular accident Encephalitis

Symptomtext

Stroke; Encephalitis; This spontaneous case was reported by a consumer (subsequently medically confirmed) and describes the occurrence of CEREBROVASCULAR ACCIDENT (Stroke) and ENCEPHALITIS (Encephalitis) in a 67-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 011J20A) for COVID-19 vaccination. Concurrent medical conditions included Blood disorder NOS (blood clotting disorder from 20 years). Concomitant products included ACETYLSALICYLIC ACID (BABY ASPIRIN) for an unknown indication. On 15-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 01-Feb-2021, the patient experienced CEREBROVASCULAR ACCIDENT (Stroke) (seriousness criterion medically significant) and ENCEPHALITIS (Encephalitis) (seriousness criterion medically significant). At the time of the report, CEREBROVASCULAR ACCIDENT (Stroke) and ENCEPHALITIS (Encephalitis) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. The patient reported that magnetic resonance imaging (MRI scan) performed months back detected encephalitis, stroke and stated as totally asymptomatic. The patient reported to be taking Clopidogrel (Plavix) to treat the event. Company Comment: Based on the current available information and temporal association between the use of the product and the start date of these events, a causal relationship cannot be excluded. This case was linked to MOD-2021-101992 (Patient Link).; Sender's Comments: Based on the current available information and temporal association between the use of the product and the start date of these events, a causal relationship cannot be excluded.

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Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Blood disorder NOS (blood clotting disorder from 20 years)
Vorgeschichte: -
Andere Medikamente: BABY ASPIRIN
Allergien: -
Vorherige Impfungen: -

VAERS 1249604

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

kritisch

Staat: PA
Alter: 18,0
Geschlecht: F
Eingang: 23.04.2021
Impfdatum: 31.12.2020
Beginn: 31.12.2020
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / -

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

Aphasia Cerebrovascular accident Gait inability

Symptomtext

Stroke/left side of the body; Can't talk; can't walk; This spontaneous case was reported by a non-health professional and describes the occurrence of CEREBROVASCULAR ACCIDENT (Stroke/left side of the body) in a 19-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 011J20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included No adverse event (no medical history reported). On 31-Dec-2020, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 31-Dec-2020, the patient experienced CEREBROVASCULAR ACCIDENT (Stroke/left side of the body) (seriousness criteria disability and medically significant), APHASIA (Can't talk) and GAIT INABILITY (can't walk). At the time of the report, CEREBROVASCULAR ACCIDENT (Stroke/left side of the body), APHASIA (Can't talk) and GAIT INABILITY (can't walk) outcome was unknown. Not Provided The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown Route) was unknown. There was no concomitant medications reported. No treatment medications were provided. Very limited information regarding these events has been provided at this time. Further information has been requested. Reporter did not allow further contact; Sender's Comments: Very limited information regarding these events has been provided at this time. Further information has been requested.

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Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: No adverse event (no medical history reported)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1211294

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011j20a

kritisch

Staat: FL
Alter: 41,0
Geschlecht: M
Eingang: 14.04.2021
Impfdatum: 27.01.2021
Beginn: 16.03.2021
Tage bis Beginn: 48,0
Dosis: 1
Route/Site: IM / LA

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

Blindness Cerebrovascular accident Computerised tomogram abdomen Computerised tomogram head abnormal Computerised tomogram pelvis

Symptomtext

I suffered a stroke on March 19, 2021 that effected my Occipital and Temporal Lobes on the right side of my brain. The primary symptom was almost total and complete blindness. Taken to emergency room, made a stroke alert, tPA cleared clot, spent 5 days at the hospital.

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Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 4,0
Labordaten: Multiple CT's March 16, 2021 Additional CT of brain w/o contrast March 17,2021 Ct abdomen and pelvis March 19,2021
Aktuelle Erkrankungen: N/A
Vorgeschichte: Hyperlipidemia, hypogonadism
Andere Medikamente: Crestor, Clomid, Multi-vitamin
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2189400

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

kritisch

Staat: LA
Alter: 80,0
Geschlecht: M
Eingang: 25.03.2021
Impfdatum: 17.02.2021
Beginn: 17.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Anticoagulant therapy Chest pain Chills Computerised tomogram thorax abnormal Decreased appetite Dyspnoea Fibrin D dimer increased Pleuritic pain Pulmonary embolism Pyrexia Ultrasound Doppler normal

Symptomtext

After receiving 2nd COVID on 2/17/21 - pt started with chills, fever, decreased appetite, increased shortness of breath and pleurtic pain. Left sided chest pain. Patient started on xarelto 3/2/21 - using oxygen continous. Will continue on xarelto and follow up in clinic 6/17/21.

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Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: -
Labordaten: 3/2/21 D-Dimer - 1.9 3/2/21 CT of chest - multiple pulmonary emboli 3/2/21 U/S BLE - negative for clots
Aktuelle Erkrankungen: none
Vorgeschichte: cervical disc disease, HTN, CAD, anxiety, depression, lumbar disc disease BPH, peripheral neuropathy, CKD St3, emphysema, pneumonia 2020, migraines
Andere Medikamente: acebutolol, aspirin, Zetia, isosorbide mono, plavix, alprazolam, finasteride, hydralazine, tramadol
Allergien: aldactone, demerol, keflex, lyrica, statins, vicodin, codeine, lisinopril, nubain, tetracycline
Vorherige Impfungen: -

VAERS 1114822

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

kritisch

Staat: LA
Alter: 51,0
Geschlecht: F
Eingang: 19.03.2021
Impfdatum: 30.12.2020
Beginn: 31.12.2020
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / -

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

COVID-19 Cough Death Dyspnoea Headache Myalgia Pyrexia SARS-CoV-2 test positive

Symptomtext

Diagnosed with COVID (confirmed with a positive COVID test) the say after her vaccine. Eventually died from complications of COVID. Because vaccine was administered prior to her illness, I am putting this in the VAERS system. Symptoms included SOB, coughing, muscle aches. headache, fever.

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Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: COVID test 12/31/2020
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: none
Vorherige Impfungen: -

VAERS 1116103

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

kritisch

Staat: -
Alter: 80,0
Geschlecht: M
Eingang: 18.03.2021
Impfdatum: 06.01.2021
Beginn: 17.02.2021
Tage bis Beginn: 42,0
Dosis: 1
Route/Site: IM / LA

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

Death

Symptomtext

Death Narrative:

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

VAERS 1116097

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

kritisch

Staat: -
Alter: 95,0
Geschlecht: M
Eingang: 18.03.2021
Impfdatum: 07.01.2021
Beginn: 21.01.2021
Tage bis Beginn: 14,0
Dosis: 1
Route/Site: IM / LA

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

Death

Symptomtext

Death Narrative:

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

VAERS 1110906

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

kritisch

Staat: TN
Alter: 78,0
Geschlecht: M
Eingang: 18.03.2021
Impfdatum: 19.12.2020
Beginn: 20.02.2021
Tage bis Beginn: 63,0
Dosis: 1
Route/Site: IM / AR

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

Computerised tomogram abnormal Dyspnoea Inappropriate schedule of product administration Lung opacity Palpitations Pulmonary embolism SARS-CoV-2 antibody test negative SARS-CoV-2 test negative

Symptomtext

78 year old man without prior DVT/PE history, who had first Moderna vaccine dose on 12/29/20 (lot 011J20A) and second Moderna vaccine dose on 02/02/21 (030L20A) (information from patient provided vaccination card) who presented to the ER on 02/20/21 with one week of subjective dyspnea and palpitations. Chest CT with bilateral pulmonary emboli. There were also groundglass opacities in the right upper lobe. Rapid test for COVID 19 on 02/20/21 was negative. Subsequent antibody testing for COVID19 on 03/01/20 (IgG, IgA. IgM) also interpreted as negative. The pulmonary embolus was considered to be unprovoked and an association with prior COVID19 vaccination is interpreted as possible but unproven. The patient was initiated on anticoagulation. Further workup for underlying thrombophilia hematological disorders is pending at this time however the current assessment remains as an unprovoked pulmonary embolus occurring 18 days after second Moderna vaccine dose. Current CT imaging without evidence of recurrent malignancy and there are no identifiable risk factors for pulmonary embolus. The physician submitting this report is a Hematologist Oncologist.

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Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: -
Labordaten: As above.
Aktuelle Erkrankungen: None
Vorgeschichte: Gastroesophageal reflux well controlled Prostate cancer s/p prostatectomy 2010 in remission since then
Andere Medikamente: Omeprazole
Allergien: None
Vorherige Impfungen: -

VAERS 1030447

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

kritisch

Staat: OH
Alter: 46,0
Geschlecht: F
Eingang: 18.03.2021
Impfdatum: 30.12.2020
Beginn: 03.02.2021
Tage bis Beginn: 35,0
Dosis: 1
Route/Site: OT / -

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

Arthralgia Back pain Burning sensation Chills Decreased appetite Body temperature Chest X-ray Computerised tomogram Dysstasia Groin pain Headache Imaging procedure Impaired work ability Gait disturbance Musculoskeletal chest pain Neck pain Pain in extremity Pain in jaw

Symptomtext

two pulmonary embolisms in right lung/Found old pulmonary embolism in left lung; pain moved up bilaterally to her arms, neck and jaw; pain in neck; pain moved up bilaterally to her arms, neck and jaw; wasn't able to ambulate independently; Rib pain; temperature of 101.8; significant decrease in appetite; unusual pain in her legs, hips and lower back; A spontaneous report was received from a nurse concerning a 46-year-old, female patient who received Moderna's COVID-19 vaccine (mRNA-1273) and experienced unusual pain in her legs, hips, lower back, pain in both arms, neck jaw and ribs, decrease in appetite, fever, and pulmonary embolism. The patient's medical history was not provided. Concomitant medications included levothyroxine, prednisone, tizanidine and apixaban. On 30-Dec-2020, prior to the onset of events, the patient received their first of two planned doses of mRNA-1273 (lot/batch 011J20A) intramuscularly for prophylaxis of COVID-19 infection and patient had a sore arm, muscle aches and slight headaches. On 25-Jan-2021, prior to the onset of events, the patient received their second of two planned doses of mRNA-1273 (lot/batch 026L20A) intramuscularly for prophylaxis of COVID-19 infection. On 03-Feb-2021 the patient started developing an unusual pain in her legs, hips, and lower back that eventually moved up to her arms, neck and jaw. She reported that she had a significant decrease in appetite that Saturday, 06-Feb-2021, and on 07-Feb-2021, she had a temperature of 101.8. She reported feeling like she had the flu. Patient reported having a COVID-19 test that came back negative. The pain continued to increase between Sunday night and Tuesday morning. Patient then developed pain in her ribs when she would lay down. She wasn't able to ambulate independently. On 09-Feb-2021, she went to the hospital. They did a chest X-ray and computed tomography (CT) scan. Those tests showed two new pulmonary embolisms in the right lung and an old pulmonary embolism in the left lung. Patient was hospitalized 09-FEb-2021 until 12-Feb-2021. She reported that her body was still inflamed. In her labs it showed her thyroid levels had doubled from her previously good thyroid levels checked in Oct 2020. Treatment information was not provided. The patient received both scheduled doses of mRNA-1273; therefore, action taken with mRNA-1273 in response to the events was not applicable. The outcomes of the events, pain in her legs, hips, lower back, neck, jaw bilateral arm pain, decrease in appetite, fever, pain in ribs and pulmonary embolism, were considered controlled with medication.; Reporter's Comments: Based on the current available information and temporal association between the use of the product and the start date of the event, a causal relationship cannot be excluded.

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Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 4,0
Labordaten: Test Date: 20210207; Test Name: temperature; Result Unstructured Data: 101.8; Test Date: 20210209; Test Name: chest x-ray; Result Unstructured Data: found two new pulmonary embolisms in the right lung and an old PE in the left lung; Test Date: 20210209; Test Name: ct scan; Result Unstructured Data: found two new pulmonary embolisms in the right lung and an old PE in the left lung; Test Date: 20210207; Test Name: covid-19; Test Result: Negative ; Result Unstructured Data: Negative; Test Date: 202102; Test Name: thyroid; Result Unstructured Data: thyroid levels had doubled from her previously good thyroid levels checked in Oct2020.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: No adverse event (No medical history reported.)
Andere Medikamente: LEVOTHYROXINE; PREDNISONE; TIZANIDINE; APIXABAN
Allergien: -
Vorherige Impfungen: -

VAERS 1105535

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

kritisch

Staat: NY
Alter: 63,0
Geschlecht: M
Eingang: 16.03.2021
Impfdatum: 05.01.2021
Beginn: 15.01.2021
Tage bis Beginn: 10,0
Dosis: 1
Route/Site: SYR / LA

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

Deep vein thrombosis Echocardiogram Magnetic resonance imaging Pulmonary embolism Scan with contrast Thrombosis Ultrasound scan

Symptomtext

Multiple blood clots in right leg (DVT) and multiple blood clots in lungs (PE)

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Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 4,0
Labordaten: Contrast dye MRI 1/23/1021 Ultrasound of legs 1/23/2021 Echocardiogram 1/23/2021
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Meloxocam Pantoprazole SOD DR 40 Mg daily Fexofenadine (Allegra) 180 Mg Daily Ambien 10 Mg as needed Fluticasone 50 MCC/ACT per nostril daily Fibercon 625 MG Daily Senna 8.6 mg daily Vitamin C 1000 MG Daily Multi Vitamin Daily
Allergien: Sulfa based
Vorherige Impfungen: -

VAERS 1079976

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

kritisch

Staat: NY
Alter: 44,0
Geschlecht: M
Eingang: 07.03.2021
Impfdatum: 23.12.2020
Beginn: 23.12.2020
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Cough Death Dysgeusia Exposure to SARS-CoV-2 Feeling abnormal Gastrointestinal tract irritation Headache Malaise Micturition urgency Pain Pollakiuria Resuscitation SARS-CoV-2 test negative Somnolence Syncope Upper respiratory tract infection

Symptomtext

12/23/20 (Moderna #1) - Malaise, cough on 12/24, went to walk-in on 12/25 c/o cough, malaise, rx'd Augmentin x14d, Rapid covid negative (and PCR resulted negative). 12/27 slept all day, 12/28 back to work. 1/12/21 metallic taste in mouth, severe GI sx, malaise, aches, headache. 1/14 seen at walk-in and covid swabbed Negative. 1/21/21 exposed to parents who found out they were covid + on 1/22/21. 1/25/21 (Moderna #2) - Continued with persistent cough and GI sx. Then also developed urinary frequency and urgency. Seen at urgent care 2/1 c/o cough, dx URI, rx'd augmenting. Woke up morning of 2/2/21 abruptly, stood up, said something was wrong, and collapsed. CPR attempted immediately, EMS brought him to ER where he was pronounced dead.

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Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: HTN
Andere Medikamente: After 1st vaccination (12/23/20): Triamterene/HCTZ, Losinopril, DayQuil, Mucinex, prescribed Augmentin 12/25/20 After 2nd (1/25/21): Addition of Zinc, Quercetin, Vitamin C, Augmentin rx'd 2/1/21
Allergien: None
Vorherige Impfungen: -

VAERS 1070038

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

kritisch

Staat: HI
Alter: 68,0
Geschlecht: M
Eingang: 03.03.2021
Impfdatum: 14.01.2021
Beginn: 22.01.2021
Tage bis Beginn: 8,0
Dosis: 1
Route/Site: IM / LA

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

Death

Symptomtext

Client passed away 8 days after being vaccinated. It is unknown if it occurred from the vaccine or other comorbidities.

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Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: Unknown
Aktuelle Erkrankungen: COPD
Vorgeschichte: COPD Vascular Disease Chronic Pain Opioid Dependence HTN
Andere Medikamente: Plavix Aspirin Lisinopril Diazepam Morphine Sulfate Lyrica Spiriva Respinate Proair Air
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 1049559

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

kritisch

Staat: MI
Alter: 50,0
Geschlecht: F
Eingang: 23.02.2021
Impfdatum: 06.01.2021
Beginn: 10.01.2021
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: IM / RA

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

Acute respiratory failure Computerised tomogram Hypoxia Mast cell degranulation test Phrenic nerve injury Pulmonary function test X-ray

Symptomtext

Acute Respiratory Failure with Hypoxia, Phrenic Nerve Dysfunction Right side

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 14,0
Labordaten: MAST cell, PFT, Sniff test, High Resolution CT scan
Aktuelle Erkrankungen: None
Vorgeschichte: HTN GERD
Andere Medikamente: Loratadine 10mg QD Omeprazole 20mg QD Triampterine/ HCTZ 37.5/25mg QD
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 1038250

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

kritisch

Staat: NY
Alter: 73,0
Geschlecht: F
Eingang: 18.02.2021
Impfdatum: 24.12.2020
Beginn: 25.12.2020
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: OT / -

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

Computerised tomogram Deep vein thrombosis Dyspnoea Fatigue Oxygen saturation Oxygen saturation decreased Pulmonary embolism Pyrexia SARS-CoV-2 test

Symptomtext

Sadle embolism in lungs; DVT in left leg; Slight fever; Extreme fatigue; Shortness of breath,struggling for every breath; Low o2 sat; A spontaneous report was received from a health care professional, who was a 73-year-old, female patient who received Moderna's COVID-19 Vaccine (mRNA-1273) and experienced shortness of breath, slight fever, extreme fatigue, left leg deep vein thrombosis (DVT), and saddle pulmonary embolism (PE). The patients' medical history was not provided. No concomitant medications list was provided. On 24 Dec 2020, prior to the onset of symptoms, patient received the first of two planned doses of mRNA-1273 (Batch number 011J20A) for the prophylaxis of COVID -19 infection. On 25 Dec 2020, patient experienced shortness of breath with low oxygen saturation levels. On 26 Dec 2020, the patient's oxygen saturation levels were down to 89% with slight fever and extreme fatigue. On 27 Dec 2020, patient's energy was back to normal. On 28 Dec 2020, the patient woke up in the morning with symptoms of almost could not breathe, could not walk across the room. The patient's vital signs included oxygen saturation 83%. The patient was struggling for every breath. The patient tested negative for COVID-19. On 30 Dec 2020, another COVID-19 test was negative. On 31 Dec 2020, patient's vital signs included oxygen saturation closer to 90%, and she reported getting better. Symptoms remained the same for about a week. On 08 Jan 2021, the patient experienced left ankle and foot swollen. The patient was seen by physician and then sent to emergency room where it was determined that the patient had DVT in the left leg. A computerized tomogram (CT) scan found clots in the left lung, or saddle PE. On 09 Jan 2021, the patient was discharged from the hospital. Treatment for the events experienced included intravenous heparin and blood thinners. Action taken with planned second dose of mRNA-1273 in response to the events was not provided. The event, extreme fatigue, was considered resolved on 27 Dec 2020. The outcome of the events, shortness of breath, slight fever, DVT and saddle PE were not provided. Follow-up received on 19 Jan 2021 included updated events (DVT and saddle PE), updated event details, treatment, and hospitalization details.; Reporter's Comments: This spontaneous report refers to a case of 73- year-old female patient who experienced serious event of pulmonary embolism and deep vein thrombosis and non-serious events of shortness of breath, oxygen saturation levels were down to 89% with slight fever and extreme fatigue the next day after administration of the first dose of mRNA-1273, lot # 011J20A, expiration date-unknown. Based on temporal information provided and the known safety profile of the vaccine and the absence of any other etiology factors, a causal association between the vents of shortness of breath, oxygen saturation levels were down to 89% with slight fever and extreme fatigue and the administration of mRNA-1273 vaccine cannot be excluded. Fever and fatigue are consistent with the known safety profile of mRNA-1273 vaccine. There is no enough information t clinically assess the causal association between the events of pulmonary embolism and deep vein thrombosis as the patient's medical history and list of concomitant medications were lacking. Main field defaults to ?possibly related'

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Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 2,0
Labordaten: Test Date: 20210108; Test Name: cat scan; Test Result: Positive ; Result Unstructured Data: Blood clots in both lungs, saddle embolism; Test Date: 20201225; Test Name: O2 sat; Result Unstructured Data: low; Test Date: 20201226; Test Name: O2 sat; Test Result: Inconclusive 89 %; Result Unstructured Data: Inconclusive; Test Date: 20201228; Test Name: O2 sat; Test Result: Inconclusive 83 %; Result Unstructured Data: Inconclusive; Test Date: 20201231; Test Name: O2 sat; Test Result: Inconclusive 90 %; Result Unstructured Data: Inconclusive; Test Date: 20201228; Test Name: covid-19 test; Test Result: Negative ; Result Unstructured Data: negative; Test Date: 20201230; Test Name: covid-19 test; Test Result: Negative ; Result Unstructured Data: negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: No adverse event (No reported medical history)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1036881

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

kritisch

Staat: AK
Alter: 70,0
Geschlecht: M
Eingang: 17.02.2021
Impfdatum: 11.01.2021
Beginn: 20.01.2021
Tage bis Beginn: 9,0
Dosis: 1
Route/Site: IM / LA

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

Myocardial infarction

Symptomtext

Myocardial Infarction

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Praegender Schweregrund: Myocardial infarction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Chronic cardiac conditions, chronic lung. Chronic smoker
Andere Medikamente: Multiple cardiac medications including anticoagulation; medications for chronic lung condition
Allergien: Penicillins
Vorherige Impfungen: -

VAERS 1020684

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

kritisch

Staat: MI
Alter: 73,0
Geschlecht: M
Eingang: 10.02.2021
Impfdatum: 13.01.2021
Beginn: 16.01.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: IM / RA

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

Anticonvulsant drug level decreased Blood pressure abnormal Death Heart rate abnormal Pneumonia Seizure

Symptomtext

Patient received vaccine at Public Health Clinic. Patient ended up having a seizure 3 days later and ended up in the hospital. Found to have right lobe pneumonia and low depakote level. Patient noted to have multiple seizures at hospital, issues with stabilizing HR and BP, and passed away on 1/20/21.

Weitere VAERSDATA-Felder

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

VAERS 1017660

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

kritisch

Staat: NY
Alter: 94,0
Geschlecht: M
Eingang: 09.02.2021
Impfdatum: 10.01.2021
Beginn: 26.01.2021
Tage bis Beginn: 16,0
Dosis: 1
Route/Site: IM / RA

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

COVID-19 COVID-19 pneumonia Death Respiratory failure

Symptomtext

Patient contracted COVID and was hospitalized. He later died- respiratory failure secondary to COVID-19 pneumonia. This was not related to a vaccine adverse event, but reporting based on requirements.

Weitere VAERSDATA-Felder

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

VAERS 1012604

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

kritisch

Staat: GA
Alter: 76,0
Geschlecht: M
Eingang: 08.02.2021
Impfdatum: 11.01.2021
Beginn: 05.02.2021
Tage bis Beginn: 25,0
Dosis: 1
Route/Site: IM / RA

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

Death

Symptomtext

Death

Weitere VAERSDATA-Felder

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

VAERS 1005276

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

kritisch

Staat: -
Alter: 75,0
Geschlecht: M
Eingang: 05.02.2021
Impfdatum: 15.01.2021
Beginn: 16.01.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Chemotherapy Chills Death Malaise Metastases to bone Metastases to liver Prostate cancer metastatic Prostatic specific antigen increased

Symptomtext

chills 1 day after vaccine administration; found dead by family 1/18/2021 Narrative: Per patient family report, patient said the next day after vaccination that he didn't feel well because of chills. Patient was found dead at home by his family on January 18th. He was a 74yo man with castrate resistant prostate cancer and liver and bone metastases with rising PSA, status post intravenous chemotherapy 1/7/21

Weitere VAERSDATA-Felder

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

VAERS 992571

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

kritisch

Staat: PA
Alter: 75,0
Geschlecht: M
Eingang: 01.02.2021
Impfdatum: 29.01.2021
Beginn: 30.01.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / RA

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

Condition aggravated Death Dyspnoea Unresponsive to stimuli

Symptomtext

Patient's wife called the physician's office with increasing SOB. MD advised that the patient go to the ED. While dressing, the patient became unresponsive, 911 called. Patient expired in ED.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: He stated he was experiencing some shortness of breath with cold and walking up the steps. The patient did report that they had some bloody stool early in the week but that had resolved.
Vorgeschichte: PMH: DM, HTN, Obesity, hyperlipidemia, Chronic kidney Disease, polyp?s removal. History of Angioedema secondary Ace Inhibitor
Andere Medikamente: unknown
Allergien: ACE inhibitor
Vorherige Impfungen: -

VAERS 991080

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

kritisch

Staat: MA
Alter: 69,0
Geschlecht: M
Eingang: 01.02.2021
Impfdatum: 28.12.2020
Beginn: 06.01.2021
Tage bis Beginn: 9,0
Dosis: 1
Route/Site: IM / LA

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

Sudden death

Symptomtext

Patient sudden death reported by family. No further details available at this time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Sudden death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Unknown
Andere Medikamente: Unknown
Allergien: Unknown
Vorherige Impfungen: -

VAERS 979081

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

kritisch

Staat: CA
Alter: 89,0
Geschlecht: M
Eingang: 27.01.2021
Impfdatum: 21.01.2021
Beginn: 22.01.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / RA

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

Death

Symptomtext

Patient found dead in home the next morning. May or may not be connected to vaccination. Instructed to report it from our medical director and director of nursing.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: None
Vorgeschichte: Acute systolic congestive heart failure, Atrial Fibrillation, Coronary Artery Disease, Left Ventricular Hypertrophy, Arteriosclerotic Heart Disease, Carotid Artery Stenosis, Ischemic Cardiomyopathy, Hypertension, Osteoarthritis, Myelodysplasia, COPD, Dyslipidemia, Malignant Neoplasm of Colon, Anemia
Andere Medikamente: Warfarin, Tamsulosin, Metoprolol, Vitamin D3, Lasix
Allergien: NKA
Vorherige Impfungen: -

VAERS 977319

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

kritisch

Staat: MI
Alter: 46,0
Geschlecht: M
Eingang: 27.01.2021
Impfdatum: 29.12.2020
Beginn: 25.01.2021
Tage bis Beginn: 27,0
Dosis: 1
Route/Site: IM / LA

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

Death

Symptomtext

Notified by patient's sister on 1/26/2021 that patient died in his sleep on 1/25/2021. She did not know cause of death.

Weitere VAERSDATA-Felder

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

VAERS 975020

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

kritisch

Staat: NY
Alter: 73,0
Geschlecht: F
Eingang: 26.01.2021
Impfdatum: 24.12.2020
Beginn: 28.12.2020
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: IM / RA

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

Chills Computerised tomogram thorax abnormal Cough Deep vein thrombosis Dyspnoea Erythema Joint swelling Lethargy Pain in extremity Peripheral swelling Pulmonary embolism Pyrexia SARS-CoV-2 antibody test negative SARS-CoV-2 test negative Ultrasound Doppler abnormal

Symptomtext

Had normal side effects the day after, 12/25/20 slight fever, lethargy, not even sore arm. on the 27th, felt fine. On 12/28/20, woke up not able to breath, oxygen saturation 83%, could not walk across the room without gasping for air, which lasted for about 2 days. Could not reach her PCP due to holidays, was convinced she had COVID. Went to drive-thru facility and got the COVID test on 12/28/20, negative on 12/29/20. Then made another APT, went back on 12/30/20 had negative test again. On 12/30/20 started feeling better, was not great but her 02 SAT's were about 90. Stayed that way until 1/8/21, had FU from lumpectomy with surgeon, when she got up her left ankle/foot were very swollen and red looking. Saw that Dr., and discussed the postop business and showed her the foot/leg told her to have it looked at. Her PCP was closed, she went to radiology Dept in Hospital and found DVT in her left leg. She was then told to go to the ER and ordered a CT scan, which showed pulmonary emboli in both lungs. Put on heparin IV right away, later transferred to another hospital where CV surgeon on staff. By that evening they decided that she was walking , talking and checking blood levels, kept her overnight and sent her home the next day. Needed to be on blood thinners, and saw pulmonologist. Has APT with hematologist this week. Pulm told her to call and report adverse reaction. Today, 1/26/21 her 02 SAT's are in the 99%, leg is still swollen, and is able to breath better. On Eliquis which will prevent new clots, but the others should be absorbed. Got 2nd dose on 1/21/21 and had only the classic side-effects for about 30 hours but was then fine. Had fever, chills, nausea, sore arm, cough, but then was fine. Same lot # as dose 2.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 1,0
Labordaten: Had venous doppler US on 1/8/21 which showed the DVT, CT scan of chest showed clots in the lungs, has saddle embolisms as well. Did a rapid COVID test which was also negative. Her PCP also did blood draw for antibodies which was negative. Is on Eliquis for the prevention of further blood clots. Saw Pulmonologist, and has APT with hematologist coming up.
Aktuelle Erkrankungen: Had lumpectomy on 11/17/20 that showed precancerous pathology report.
Vorgeschichte: High blood pressure, family history of Alpha1 anti-tripsin deficiency. She has single alliel form. Over time she gets short of breath, can go 2 flights of steps but not 3. Can play tennis but not doubles.
Andere Medikamente: Losartan, Vitamin D.
Allergien: None.
Vorherige Impfungen: -

VAERS 970495

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

kritisch

Staat: NC
Alter: 77,0
Geschlecht: F
Eingang: 25.01.2021
Impfdatum: 13.01.2021
Beginn: 16.01.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: IM / RA

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

Sudden cardiac death

Symptomtext

Patient expired three days after receiving first dose of Moderna COVID-19 vaccine. The death certificate states cause of death is sudden cardiac arrest.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Sudden cardiac death
Hospital-Tage: -
Labordaten: Unknown.
Aktuelle Erkrankungen: -
Vorgeschichte: Hypertension, Diabetes Type 2, cardiac disease.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 965256

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

kritisch

Staat: GA
Alter: 38,0
Geschlecht: M
Eingang: 22.01.2021
Impfdatum: 23.12.2020
Beginn: 19.01.2021
Tage bis Beginn: 27,0
Dosis: 1
Route/Site: IM / RA

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

Death

Symptomtext

Found deceased, presumed while exercising

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Hypertension Hyperlipidemia Obstructive Sleep Apnea Obese Hearing loss Degenerative Disc Lumbar
Andere Medikamente: Atorvastatin calcium 20mg daily
Allergien: NKDA
Vorherige Impfungen: -

VAERS 962940

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

kritisch

Staat: WI
Alter: 83,0
Geschlecht: M
Eingang: 22.01.2021
Impfdatum: 20.01.2021
Beginn: 20.01.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / -

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

Cardiac arrest Crepitations Death Dyspnoea Productive cough Cold sweat Pallor

Symptomtext

Patient began with a wet productive cough with crackles heard at 4 pm, at 5pm he went to dinner and still had cough, at 630 was administered his medications and he had cough, no shortness of breath and was in a good mood. By 7:45pm CNA found him in the lounge with labored breathing, 02 was at 85%. They gave him 4 liters o2, then a facemask at 5 liters which brought his o2 into the 90's. At that time called ambulance, patient arrived to ER around 9:20pm and passed away shortly after. Cardiac Arrest

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: None done when arrived at ER.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 962940

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

kritisch

Staat: WI
Alter: 83,0
Geschlecht: M
Eingang: 22.01.2021
Impfdatum: 20.01.2021
Beginn: 20.01.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / UN

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

Cardiac arrest Crepitations Death Dyspnoea Productive cough Cold sweat Pallor

Symptomtext

Patient began with a wet productive cough with crackles heard at 4 pm, at 5pm he went to dinner and still had cough, at 630 was administered his medications and he had cough, no shortness of breath and was in a good mood. By 7:45pm CNA found him in the lounge with labored breathing, 02 was at 85%. They gave him 4 liters o2, then a facemask at 5 liters which brought his o2 into the 90's. At that time called ambulance, patient arrived to ER around 9:20pm and passed away shortly after. Cardiac Arrest

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: None done when arrived at ER.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 963213

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

kritisch

Staat: CA
Alter: 30,0
Geschlecht: M
Eingang: 21.01.2021
Impfdatum: 18.01.2021
Beginn: 21.01.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: IM / LA

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

Acute myocardial infarction Catheterisation cardiac Chest pain Electrocardiogram ST segment elevation Myocarditis Troponin increased

Symptomtext

Patient had 4 hours of chest pain 3 days after vaccine. EKG showed STEMI. Troponin elevated at 4.8. Patient sent for cardiac catheterization and results pending. At this time suspect myocarditis, but STEMI not yet excluded

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute myocardial infarction
Hospital-Tage: -
Labordaten: 1/21/2021: Troponin 4.8 at 10:00. EKG showed inferior and lateral ST elevation
Aktuelle Erkrankungen: No
Vorgeschichte: None
Andere Medikamente: Daily Multivitamin
Allergien: None
Vorherige Impfungen: -

VAERS 957799

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

kritisch

Staat: VA
Alter: 81,0
Geschlecht: M
Eingang: 20.01.2021
Impfdatum: 14.01.2021
Beginn: 15.01.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / -

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

Asthenia Cardiac arrest Confusional state Death Electrocardiogram Full blood count normal Metabolic function test Troponin normal

Symptomtext

Presented to Urgent Care for weakness and confusion, transferred to ED, patient had a cardiac arrest and was unable to be resuscitated

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardiac arrest
Hospital-Tage: -
Labordaten: CBC - unremarkable CMP - stable known renal disease otherwise unremarkable Troponin normal EKG - non acute
Aktuelle Erkrankungen: -
Vorgeschichte: HTN AAA with endovascular stent ESRD COPD
Andere Medikamente: sotaloL (BETAPACE) 80 mg Tablet omeprazole (PRILOSEC) 20 mg Capsule, Delayed Release(E.C.) sevelamer carbonate (RENVELA) 800 mg Tablet polyethylene glycol 3350 (MIRALAX PO) acetaminophen (TYLENOL EXTRA STRENGTH PO) fluticasone propionate (F
Allergien: Lipitor
Vorherige Impfungen: -

VAERS 953348

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

kritisch

Staat: AR
Alter: 81,0
Geschlecht: M
Eingang: 18.01.2021
Impfdatum: 22.12.2020
Beginn: 24.12.2020
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / LA

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

Death

Symptomtext

Patient was living in a nursing home with positive cases when administered. His age and chronic condition was such that he did not have time after the vaccination to avoid exposure or develop immunity.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Chronic pain, high blood pressure
Andere Medikamente: Atorvastatin, Ibuprofen, Oxybutinin, Morphine Sulfate
Allergien: None
Vorherige Impfungen: -

VAERS 941811

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

kritisch

Staat: LA
Alter: 56,0
Geschlecht: F
Eingang: 13.01.2021
Impfdatum: 04.01.2021
Beginn: 11.01.2021
Tage bis Beginn: 7,0
Dosis: 1
Route/Site: IM / LA

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

Albumin urine present Bacterial test positive Chest X-ray abnormal Death Hypoxia Lung infiltration Pyrexia Respiratory distress Respiratory failure SARS-CoV-2 test negative Sepsis Urine leukocyte esterase positive White blood cell count normal White blood cells urine positive

Symptomtext

Resident began having fever on 1/11/21 @0600. VS= T-102 B/P- 100/57 P- 112 RR- 24 O2 Sat 92% on RA. MD called. Rapid COVID Test was negative. CBC,CMP, U/A were ordered as well as CXR. Resident's condition declined. At 3:00pm resident started having respiratory distress and hypoxia O2 Sat 89%. Supplemental O2/mask @ 5LPM. Neb TX, EKG, and Rocephin 1 GM ordered. Condition worsened. Resident sent to nearest ER for evaluation. Later in the evening the staff AT Medical Center called to inform staff that resident had expired @ 2230 as a result of Respiratory Failure and Sepsis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: CXR on 1/11/21: Suspicion of minimal infrahilar infiltrates bilaterally. U/A on 1/11/21: Leuk Esterase 3+, Albumin 2+, Few Bacteria, White cells 10 CBC on 1/11/21: WBC 8.9
Aktuelle Erkrankungen: NONE
Vorgeschichte: HUNTINGTON'S CHOREA, HTN, HLP, HYPOTHYROID, DEPRESSION, CONSTIPATION, AND DYSPHAGIA
Andere Medikamente: Haldol 2mg TWICE DAILY, DEPAKENE 750MG THREE TIMES
Allergien: NKDA & NO FOOD ALLERGIES
Vorherige Impfungen: -

VAERS 941743

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

kritisch

Staat: NY
Alter: 60,0
Geschlecht: F
Eingang: 13.01.2021
Impfdatum: 12.01.2021
Beginn: 13.01.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / RA

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

Death

Symptomtext

This person was found to be deceased on routine rounds during the night, 3am. No symptoms of reaction noted post vaccine. No injection site reaction. No reports of any allergic reaction.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Benign polycythemia, Type II DM, Anxiety, Epilepsy, Blepharitis (bilateral), cataract (not specified), Allergic rhinitis, constipation, scoliosis, osteoporosis, dyspahgia, urinary incontinence, Dermatitis, breast cancer (right breast lumpectomy), history of respiratory infection, DNR AND MOLST were in place at time of death
Andere Medikamente: Amitiza, Anastrozole, Calcium Carbonate, Levemir, Novolog, Docusate, Fiber Lax, Fluvoxamine Maleate, Gavilax, Glucerna, Ketoconazole, levetiracetam, loratadine, Selenium sulfide lotion, vimpat, vitamin D3, Prolia AS needed medications: fle
Allergien: No known drug or food allergies
Vorherige Impfungen: -

VAERS 963163

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

kritisch

Staat: -
Alter: 88,0
Geschlecht: M
Eingang: 12.01.2021
Impfdatum: 06.01.2021
Beginn: 08.01.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / LA

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

Death

Symptomtext

Narrative:

Weitere VAERSDATA-Felder

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

VAERS 937818

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

kritisch

Staat: OH
Alter: 63,0
Geschlecht: M
Eingang: 12.01.2021
Impfdatum: 07.01.2021
Beginn: 09.01.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / LA

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

Death

Symptomtext

This is being reported because of the incident occurring 2 days after the Moderna Covid-19 vaccination. It was reported that the patient expired on 1/9/21, 2 days after receiving the Moderna vaccine. Upon screening of patient prior to administration on 1/7/21, the patient completed paperwork answering NO to the following "Do you currently have any active infections or acute respiratory illness or fever."

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: HTN CAD Stemi with stent placement BPH
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 931558

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011j20a

kritisch

Staat: AR
Alter: 47,0
Geschlecht: F
Eingang: 09.01.2021
Impfdatum: 22.12.2020
Beginn: 30.12.2020
Tage bis Beginn: 8,0
Dosis: 1
Route/Site: IM / -

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

Cerebrovascular accident Computerised tomogram Hypercoagulation Injection site pruritus Injection site swelling Injection site warmth Laboratory test Magnetic resonance imaging brain Magnetic resonance imaging neck Scan with contrast

Symptomtext

7 day after site itching, hot swelling. Unsure if related 9 day after suffered CVA and have hyper coagulation

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 1,0
Labordaten: CT with contrast, MRI and MRA of head, MRI neck, expensive labwork
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 929391

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

kritisch

Staat: NY
Alter: 37,0
Geschlecht: F
Eingang: 08.01.2021
Impfdatum: 06.01.2021
Beginn: 06.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Acute respiratory failure Anaphylactic reaction Dysphagia Endotracheal intubation Heart rate increased Swelling of eyelid Vomiting

Symptomtext

1/6/21 Pt received vaccine and complained of difficulty swallowing and rapid heart rate. Pt received methylprednisolone 125mg IVP, diphenhydramine 25mg IVP, & famotidine 20mg IVP. Pt reported improvement and was discharged. Sent home on diphenhydramine and oral prednisone. 1/7/21 Pt unable to swallow her own secretions and experienced eyelid swelling. Pt vomitted. Pt received epinephrine and Benadryl X 1 dose each. Pt then transported to hospital via ambulance. Reason for admission - acute respiratory failure secondary to anaphylactic reaction. Decision was made to emergently intubate the patient for airway protection despite aggressive intervention. Pt successfully extubated 1/8/21. Plan to discharge home and start Medrol Dose Pack 1/9/21.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Bell's palsy Migraine Seizures Systemic lupus erythematosus
Andere Medikamente: Escitalopram 10mg 1 po Qday Gabapentin 300mg po three times a day
Allergien: Dilantin Ibuprofen Latex Morphine Penicillins Tegretol Valium
Vorherige Impfungen: -

VAERS 922669

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

kritisch

Staat: OH
Alter: 46,0
Geschlecht: F
Eingang: 06.01.2021
Impfdatum: 26.12.2020
Beginn: 04.01.2021
Tage bis Beginn: 9,0
Dosis: 1
Route/Site: IM / RA

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

Computerised tomogram thorax Deep vein thrombosis Pulmonary embolism Ultrasound Doppler

Symptomtext

Patient (myself) developed DVT/PE diagnosed on 1/4/2021

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: -
Labordaten: CT scan of chest. Doppler of Left Leg.
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma
Andere Medikamente: Metformin Birth Control Pills
Allergien: Aspirin Anaprox Sulfa
Vorherige Impfungen: -

VAERS 2567712

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: FL
Alter: 58,0
Geschlecht: F
Eingang: 25.01.2023
Impfdatum: 02.11.2021
Beginn: 11.01.2023
Tage bis Beginn: 435,0
Dosis: 1
Route/Site: IM / -

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

Adenocarcinoma COVID-19 Chest tube insertion Computerised tomogram thorax abnormal Cough Dyspnoea Intensive care Pericardial effusion Pericardial excision Pleural effusion Pleural fluid analysis abnormal Pyrexia SARS-CoV-2 test positive

Symptomtext

Pt recived the third Moderna vaccine on 11/2/21. She came to ER due to SOB, cough, and fever 102.6 on 1/10/23. She was tested positive COVID PCR on 1/10/23 and admitted for further evaluation. Next day, her CT chest demonstrated a large pericardial effusion with impending tamponade, so she was transferred to ICU unit, where cardiac window was performed on 1/12/23. She was also found out large pleural effusion and had PleurX catheter placed. She recieved 5 days of remodesivir and steroid. Both pericardial and pelural fluids showed adnocarcinoma. She was medically stable and discharged home on 1/15/23.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 6,0
Labordaten: SARS-CoV COVID19 PCR + pm 1/10/23
Aktuelle Erkrankungen: unknown
Vorgeschichte: stage IV triple negative breast cancer mets to brain
Andere Medikamente: -
Allergien: PCN, Cephalosporines, Keflex, Fluconazole, Sulfa
Vorherige Impfungen: -

VAERS 2483628

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: -
Alter: 70,0
Geschlecht: F
Eingang: 21.10.2022
Impfdatum: 06.01.2021
Beginn: 01.01.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: OT / -

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

Fatigue Feeling abnormal Myalgia Nausea Syncope Malaise Vomiting

Symptomtext

Feeling a little under the weather; Body ache after each vaccine but not really bad; Fatigue; Nausea; Vomiting; Faint 14 to 16 hours later after dose 1; This spontaneous case was reported by a patient and describes the occurrence of SYNCOPE (Faint 14 to 16 hours later after dose 1) in a 70-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 011J20A) for COVID-19 prophylaxis. The occurrence of additional non-serious events is detailed below. Concomitant products included ALENDRONATE SODIUM (ALENDRONATE) for an unknown indication. On 06-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. In January 2021, the patient experienced SYNCOPE (Faint 14 to 16 hours later after dose 1) (seriousness criterion medically significant). On an unknown date, the patient experienced MALAISE (Feeling a little under the weather), MYALGIA (Body ache after each vaccine but not really bad), FATIGUE (Fatigue), NAUSEA (Nausea) and VOMITING (Vomiting). The patient was treated with PARACETAMOL (TYLENOL) at an unspecified dose and frequency. At the time of the report, SYNCOPE (Faint 14 to 16 hours later after dose 1), MALAISE (Feeling a little under the weather), MYALGIA (Body ache after each vaccine but not really bad), FATIGUE (Fatigue), NAUSEA (Nausea) and VOMITING (Vomiting) outcome was unknown. mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) dosing remained unchanged. Patient took Tylenol once or twice after vaccine but nothing else. Company Comment: This is a spontaneous case, reported by a patient, concerning a 70-year-old female patient with no medical history reported, who experienced the unexpected serious (medically significant) event of Syncope, which occurred 14 to 16 hours after receiving the first dose of mRNA-1273 vaccine. It was reported that the patient also had fatigue, nausea, vomiting, a little bit of body ache, and feeling unwell. Patient took paracetamol once or twice after having the vaccine. No further details about the clinical course and diagnostic procedures were provided. Outcome of the events were unknown. The benefit-risk relationship of mRNA-1273 is not affected by this report. This case was linked to MOD-2022-659978, MOD-2022-659976, MOD-2022-659974 (Patient Link).; Sender's Comments: This is a spontaneous case, reported by a patient, concerning a 70-year-old female patient with no medical history reported, who experienced the unexpected serious (medically significant) event of Syncope, which occurred 14 to 16 hours after receiving the first dose of mRNA-1273 vaccine. It was reported that the patient also had fatigue, nausea, vomiting, a little bit of body ache, and feeling unwell. Patient took paracetamol once or twice after having the vaccine. No further details about the clinical course and diagnostic procedures were provided. Outcome of the events were unknown. The benefit-risk relationship of mRNA-1273 is not affected by this report.

Weitere VAERSDATA-Felder

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

VAERS 2468376

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: NY
Alter: 59,0
Geschlecht: F
Eingang: 04.10.2022
Impfdatum: 06.01.2021
Beginn: 06.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Guillain-Barre syndrome Immediate post-injection reaction Muscular weakness

Symptomtext

She got her vaccine, she immediately felt weakness in both legs, and the weakness was coming back and forth every 15-20 minutes apart. She was thinking that she could fall down because her legs were very weak. The weakness was immediately resolving, and did not allow her to fall down, and kept coming back and forth. She talked to the provider and it lasted for 6 months and gradually resolved. He diagnosed as a Guillain Barre Syndrome. She was then given exempt status from her doctor so she did not have to get further vaccines. She did not have any testing to determine the diagnosis or send her to any specialists.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Guillain-Barre syndrome
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: None.
Vorgeschichte: None.
Andere Medikamente: None.
Allergien: None.
Vorherige Impfungen: Tdap vaccine with very bad headache, high fever and some kind of facial swelling, but resolved in one day. This was 15 years ag

VAERS 2451807

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: GA
Alter: 55,0
Geschlecht: F
Eingang: 20.09.2022
Impfdatum: 31.12.2020
Beginn: 31.12.2020
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / LA

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

Anaphylactic reaction Blood pressure abnormal Blood pressure measurement Dyspnoea Fatigue Feeling hot Heart rate Heart rate increased

Symptomtext

A spontaneous report was received from a physical therapist concerning a 55-year-old, female patient, who received Moderna's COVID-19 vaccine (mRNA-1273) and experienced anaphylaxis, felt warm/feeling hot, breathing problem/dyspnea, tired for the next couple of days/fatigue, increased heart rate, abnormal blood pressure. The patient's medical history was not provided. No relevant concomitant medications were provided. On 31 Dec 2020, prior to the onset of the events, the patient received their first of two planned doses of mRNA-1273 (Lot number: 011J20A) intramuscularly in the left deltoid for prophylaxis of COVID-19 infection. On 31 Dec 2020, the patient developed anaphylaxis within seven to eight minutes after vaccination and was hospitalized. First, she felt warm and removed her sweater. Very rapidly, she had problems with breathing. She was discharged after six hours. She only had one rebound reaction. She was sent home after her heart rate and blood pressure were back to normal. She was tired for the next couple of days. Treatment medications included two epinephrine injection in the right thigh and IV diphenhydramine in the left arm. She reported that they gave her 15 litres of oxygen and another medication, which she cannot recall the name. Action taken with mRNA-1273 in response to the events was not applicable. The outcome of the reported events were considered as resolved. Reporter's Comments: Based on the current available information and temporal association between the use of the product and the start date of the events, a causal relationship cannot be excluded.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: Test Date: 20201231; Test Name: blood pressure; Result Unstructured Data: abnormal; Test Date: 20201231; Test Name: Heart rate; Result Unstructured Data: abnormal.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: No adverse event (no reported medical history)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2387006

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011j20a

schwer

Staat: FL
Alter: 74,0
Geschlecht: F
Eingang: 23.07.2022
Impfdatum: 06.01.2021
Beginn: 04.02.2021
Tage bis Beginn: 29,0
Dosis: 1
Route/Site: OT / -

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

Asthenia Atrophy Gait disturbance Muscle spasms Chest discomfort Dyspnoea Fatigue Sinusitis Syncope

Symptomtext

Patient is still building the strength; Both of her hips cramped; Difficult to walk; Left side almost atrophied; This spontaneous case was reported by a patient and describes the occurrence of MUSCLE SPASMS (Both of her hips cramped), GAIT DISTURBANCE (Difficult to walk), ASTHENIA (Patient is still building the strength) and ATROPHY (Left side almost atrophied) in a 74-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 028l20a and 011j20a) for COVID-19 prophylaxis. Previously administered products included for Flu vaccination: Flu Vaccine (flu vaccine in the fall but not too close to the COVID shots). Past adverse reactions to the above products included No adverse event with Flu Vaccine. Concurrent medical conditions included Drug allergy (codeine or SUDAFED made her heart race) and Seasonal allergy. On 06-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 03-Feb-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 04-Feb-2021, the patient experienced MUSCLE SPASMS (Both of her hips cramped) and GAIT DISTURBANCE (Difficult to walk). In 2021, the patient experienced ATROPHY (Left side almost atrophied). On an unknown date, the patient experienced ASTHENIA (Patient is still building the strength). The patient was treated with IBUPROFEN (ADVIL [IBUPROFEN]) at an unspecified dose and frequency; PARACETAMOL (TYLENOL) at an unspecified dose and frequency and DICLOFENAC (VOLTAREN [DICLOFENAC]) at an unspecified dose and frequency. At the time of the report, MUSCLE SPASMS (Both of her hips cramped) and ATROPHY (Left side almost atrophied) had resolved and GAIT DISTURBANCE (Difficult to walk) and ASTHENIA (Patient is still building the strength) was resolving. No concomitant product use was provided. The patient had never experienced a similar event in the past and she never had COVID positive test or diagnosis. Patient was not immunocompromised. Patient experienced reactions progressively more serious with each vaccination. The right hip cramp only lasted one day. The left hip had only subsided in the last month. After the 2nd shot the patient had contacted her doctor. For the hip it was difficult to get into physical therapy, however the patient worked with a trainer to regain strength on her left side as the left side almost atrophied which lasted almost a year and 4 months. Patient's symptoms had improved and was still building the strength.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Drug allergy (codeine or SUDAFED made her heart race); Seasonal allergy
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2262385

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: CA
Alter: 24,0
Geschlecht: F
Eingang: 03.05.2022
Impfdatum: 13.01.2021
Beginn: 15.01.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: SYR / LA

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

Chest discomfort Chest pain Dizziness Echocardiogram Electrocardiogram Fatigue Heart rate increased Laboratory test Loss of personal independence in daily activities Magnetic resonance imaging heart Nausea Pain Pericarditis Rash Syncope

Symptomtext

Chest pain (sharp stabbing pains, squeezing pain, pressure) Nausea Rash Dizziness Body Fatigue and pain Elevated heart rate Fainting I have been dealing with symptoms for over a year and finally received a diagnosis of chronic pericarditis this week. I have been suffering all of these symptoms, the chest pain and pressure impact my daily life and prevent me from my daily activities

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: -
Labordaten: EKG, ECHO, Cardiac MRI, Zio patch, multiple lab draws
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a prior to vaccine
Andere Medikamente: Levora
Allergien: Suprax
Vorherige Impfungen: -

VAERS 2255259

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A,

schwer

Staat: MO
Alter: 39,0
Geschlecht: F
Eingang: 27.04.2022
Impfdatum: 05.01.2021
Beginn: 25.01.2021
Tage bis Beginn: 20,0
Dosis: 1
Route/Site: IM / RA

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

Anticoagulant therapy Blood test Computerised tomogram Pulmonary thrombosis Rib excision Subclavian vein thrombosis Ultrasound scan Venogram

Symptomtext

Blood clot in subclavian vein, had a veinogram, placed on blood thinners, had to have first rib removed, blood clot in lung.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary thrombosis
Hospital-Tage: 7,0
Labordaten: Blood work , ultrasound, CT, Jan 31, 2021. veinogram Feb 1, 2021. surgery to remove 1st rib Mar 12,2021
Aktuelle Erkrankungen: NA
Vorgeschichte: -
Andere Medikamente: Thyroid medicine, zrytec
Allergien: PCN
Vorherige Impfungen: Was on blood thinners when 2nd dose was given

VAERS 2254549

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: FL
Alter: 67,0
Geschlecht: F
Eingang: 27.04.2022
Impfdatum: 27.01.2021
Beginn: 25.04.2022
Tage bis Beginn: 453,0
Dosis: UNK
Route/Site: - / -

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

COVID-19 Hypoxia Intensive care Positive airway pressure therapy SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Covid19 breakthrough. 1st vaccine received on 12/30/2020. 68 y/o female with PMHx of OSA, COPD, GERD, HTN, DM, Kidney stones, CHF, Dysphagia, complicated UTI with MDRO pseudomonas and ecoli presents from Inpatient rehab with Hypoxia requiring transfer to ICU on bipap at 80% FIO2. Pt treated with IV ABX, Remdesivir and steroids.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: -
Labordaten: SARS CoV2 PCR Covid19-Detected on 04/25/2022
Aktuelle Erkrankungen: -
Vorgeschichte: Kidney stones, OSA, GERD, DM, HTN, COPD, Anemia, MDRO Pseudomonas UTI, CHF, Dysphagia
Andere Medikamente: -
Allergien: Clindamycin, Shellfish, Spinach
Vorherige Impfungen: -

VAERS 2219935

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011j20a

schwer

Staat: FL
Alter: 71,0
Geschlecht: F
Eingang: 07.04.2022
Impfdatum: 28.12.2020
Beginn: 01.04.2022
Tage bis Beginn: 459,0
Dosis: 3
Route/Site: OT / -

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

Chills Concussion Headache Mass Nausea Pyrexia SARS-CoV-2 test Syncope

Symptomtext

Fever; Chills; Headache; Extreme nausea; Walk to the bathroom to try to throw up and feel better but she ended waking up on the bathroom floor; When she wash her head and find a lump; She think either she past out and hit her head, or slip and had a concussion, and has no memory; This spontaneous case was reported by a consumer and describes the occurrence of SYNCOPE (Walk to the bathroom to try to throw up and feel better but she ended waking up on the bathroom floor), MASS (When she wash her head and find a lump), CONCUSSION (She think either she past out and hit her head, or slip and had a concussion, and has no memory), PYREXIA (Fever) and CHILLS (Chills) in a 72-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 002m21a, 011j20a, 028l20a and 004f21a) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Patient had no medical history relating to mentioned AE and both acute and chronic illnesses at the time of vaccination. Concurrent medical conditions included Adhesive tape allergy (Adhesive types). On 28-Dec-2020, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 25-Jan-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 27-Aug-2021, received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 31-Mar-2022, received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 01-Apr-2022, the patient experienced SYNCOPE (Walk to the bathroom to try to throw up and feel better but she ended waking up on the bathroom floor), MASS (When she wash her head and find a lump) and CONCUSSION (She think either she past out and hit her head, or slip and had a concussion, and has no memory). On 01-Apr-2022 at 3:00 AM, the patient experienced NAUSEA (Extreme nausea). On an unknown date, the patient experienced PYREXIA (Fever), CHILLS (Chills) and HEADACHE (Headache). At the time of the report, SYNCOPE (Walk to the bathroom to try to throw up and feel better but she ended waking up on the bathroom floor), MASS (When she wash her head and find a lump), CONCUSSION (She think either she past out and hit her head, or slip and had a concussion, and has no memory), PYREXIA (Fever), CHILLS (Chills), NAUSEA (Extreme nausea) and HEADACHE (Headache) was resolving. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, SARS-CoV-2 test: no (Negative) Patient never had COVID positive test or diagnosis. No concomitant medication was provided. No treatment medication was provided. The first booster was on the 27-Aug-2021. After getting the second booster of the Moderna COVID-19 vaccine, patient experienced side effects that was considerate normal like fever, chills, headache and things like that and side effects that concern patient, like extreme nausea, at 3 am on the 01-Apr-2022, when walked to the bathroom to try to throw up and feel better but patient ended waking up on the bathroom floor and was soaking wet and even more concerning, when patient washed head, patient found a lump. Patient thinks either patient passed out and hit head or slip and had a concussion and had no memory of hitting head. Patient thinks that she could potentially have a brain bleed, but there were no symptoms of that. Patient was concerned that if there was ever need of booster, patient was not confident on getting it because that was very serious. Patient wanted to know if she should get booster in the future. Patient was recommended to get medical recommendation that would be proper to be done by health provider. Patient thinks Moderna is a sham and use to like Moderna but is going to call. AE did not cause patient to seek medical care (office visit, Urgent care, ER, hospitalized), AE outcome was unknown but symptoms were reported to be improved.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Test Name: COVID positive test; Test Result: Negative; Result Unstructured Data: Patient never had COVID positive test or diagnosis
Aktuelle Erkrankungen: Adhesive tape allergy (Adhesive types).
Vorgeschichte: Comments: Patient had no medical history relating to mentioned AE and both acute and chronic illnesses at the time of vaccination.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2104866

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: AL
Alter: 39,0
Geschlecht: F
Eingang: 11.02.2022
Impfdatum: 13.01.2021
Beginn: 13.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / -

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

Electrocardiogram Hypoglycaemia Hypotension Migraine Pain Pyrexia Syncope

Symptomtext

Intractable migraine, fever, hypotension, hypoglycemia, severe body pain, syncope

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: EKG, vital signs
Aktuelle Erkrankungen: none
Vorgeschichte: Type 1 diabetes, hypothyroidism
Andere Medikamente: Celexa, levothyroxine, insulin
Allergien: none
Vorherige Impfungen: -

VAERS 2095515

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: FL
Alter: 71,0
Geschlecht: F
Eingang: 11.02.2022
Impfdatum: 13.01.2021
Beginn: 06.12.2021
Tage bis Beginn: 327,0
Dosis: 1
Route/Site: OT / -

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

Asthenia Dysstasia Guillain-Barre syndrome

Symptomtext

Guillain Barre syndrome six weeks after booster dose; This spontaneous case was reported by a consumer and describes the occurrence of GUILLAIN-BARRE SYNDROME (Guillain Barre syndrome six weeks after booster dose) in a 71-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 939903, 028L20A and 011J20A) for COVID-19 vaccination. Concurrent medical conditions included Drug allergy, High cholesterol and Muscle spasms. Concomitant products included VALACICLOVIR HYDROCHLORIDE (VALTREX) for Cardiovascular event prophylaxis, INFLUENZA VACCINE (FLU) for Flu, ROSUVASTATIN CALCIUM (CRESTON) for High cholesterol, CYCLOBENZAPRINE HYDROCHLORIDE (FLEXERIL [CYCLOBENZAPRINE HYDROCHLORIDE]) for Muscle spasms, FAMOTIDINE (PEPCID AC) for Stomach discomfort. On 13-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 11-Feb-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 27-Oct-2021, received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 06-Dec-2021, the patient experienced GUILLAIN-BARRE SYNDROME (Guillain Barre syndrome six weeks after booster dose) (seriousness criteria hospitalization and medically significant). The patient was hospitalized from 06-Dec-2021 to 22-Dec-2021 due to GUILLAIN-BARRE SYNDROME. In January 2022, GUILLAIN-BARRE SYNDROME (Guillain Barre syndrome six weeks after booster dose) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Patient had no history of COVID-19. 6 weeks after the booster dose of Moderna vaccine, patient developed Guillain Barre syndrome. Patient was admitted to the hospital on 06-Dec-2021 and discharged on 22-Dec-2021. Patient has recovered at home. Patient believes she had already recovered since the middle of JAN-2022. Patient has not experienced a similar event in the past. Patient received the Flu vaccine with the booster at the same time. Patient had no information about the Flu vaccine. Treatment given for symptoms: Contact information from Medical Center provided with full medical history. Consent for Safety follow-up with patient, HCP and vaccine facilities was provided. Patient can also provide primary care doctor and a neurologist contact information. Company Comment: This is a spontaneous case concerning a 71-year-old, female patient with no medical history reported, who experienced the unexpected, serious (Hospitalized and Medically Significant), AESI event of Guillain-Barre syndrome. The event occurred 40 days after the third dose of mRNA-1273 vaccine. At the time of report, outcome of the event was Resolved. The benefit-risk relationship of mRNA-1273 vaccine is not affected by this report.; Sender's Comments: This is a spontaneous case concerning a 71-year-old, female patient with no medical history reported, who experienced the unexpected, serious (Hospitalized and Medically Significant), AESI event of Guillain-Barre syndrome. The event occurred 40 days after the third dose of mRNA-1273 vaccine. At the time of report, outcome of the event was Resolved. The benefit-risk relationship of mRNA-1273 vaccine is not affected by this report.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Guillain-Barre syndrome
Hospital-Tage: 17,0
Labordaten: -
Aktuelle Erkrankungen: Drug allergy; High cholesterol; Muscle spasms
Vorgeschichte: -
Andere Medikamente: CRESTON; FLEXERIL [CYCLOBENZAPRINE HYDROCHLORIDE]; VALTREX; PEPCID AC; FLU
Allergien: -
Vorherige Impfungen: -

VAERS 1858034

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: MA
Alter: 39,0
Geschlecht: F
Eingang: 01.02.2022
Impfdatum: 05.11.2021
Beginn: 08.11.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: IM / LA

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

Anxiety C-reactive protein increased Cardiac imaging procedure abnormal Chest discomfort Chest pain Cardiac stress test abnormal Ejection fraction decreased Electrocardiogram T wave inversion Chills Cough Ear pain Echocardiogram normal Ejection fraction normal Electrocardiogram abnormal Fatigue Headache Hyperhidrosis Left ventricular dilatation

Symptomtext

Patient received moderna vaccines on 12/30/20, 1/26/21, and lastly the booster on 11/5/21. Patient presented to Hospital on 11/8/21 with chest pain 3 days after receiving the moderna booster. EKG had some T wave inversions, troponin was 400. Patient was found to have myopericarditis on cardiac MRI. Patient was appropriately treated with colchicine and ibuprofen with outpatient cardiology follow up.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: 2,0
Labordaten: MRI cardiac non stress test on 11/8/21: 1. The left ventricular size is mildly dilated (LVEDV indexed is 83 ml/m2). The left ventricular ejection fraction is 51 % by Simpson's method. Global left ventricular function is low normal. There is hypokinesis of the left ventricular mid to distal inferior walls. The left ventricular mass is normal. 2. There is no resting first pass myocardial perfusion defect. There is mid-myocardial and subepicardial late gadolinium enhancement at basal to apical inferior, basal to mid inferolateral, and mid anterolateral segments of the left ventricle (5-segment). There is associated elevation in the global native T1-time, measured at 1372 msec (normal native T1-time is 1200 +/- 80 msec for 3T) and of the extracellular volume fraction of the affected segments, measured at 39% (normal extracellular volume fraction is 28-32%). There is consistent evidence of myocardial edema by T2 weighted imaging. There is focal thickening of pericardium with late gadolinium enhancement of the pericardium adjacent to the inferior, inferolateral and anterolateral walls. Collectively the above findings are consistent with an acute perimyocarditis (viral etiology likely) without full thickness involvement of the inferior and inferolateral walls with minimal reduction of systolic thickening. These findings are consistent with primarily edema of these segments with a reasonable likelihood of restoration of regional function. These above findings are not consistent with ischemic, or infiltrative etiologies. 3. The right ventricular size is normal. Global right ventricular function is mildly decreased with a right ventricular ejection fraction of 43%. There is no late gadolinium enhancement of the right ventricle. CONCLUSIONS: Overall, findings are consistent with acute perimyocarditis with mild reduction of global LV function.
Aktuelle Erkrankungen: N/A
Vorgeschichte: None
Andere Medikamente: caltrate
Allergien: NSAID, penicillins
Vorherige Impfungen: -

VAERS 1858034

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: MA
Alter: 39,0
Geschlecht: F
Eingang: 01.02.2022
Impfdatum: 05.11.2021
Beginn: 08.11.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: IM / LA

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

Anxiety C-reactive protein increased Cardiac imaging procedure abnormal Chest discomfort Chest pain Cardiac stress test abnormal Ejection fraction decreased Electrocardiogram T wave inversion Chills Cough Ear pain Echocardiogram normal Ejection fraction normal Electrocardiogram abnormal Fatigue Headache Hyperhidrosis Left ventricular dilatation

Symptomtext

Patient received moderna vaccines on 12/30/20, 1/26/21, and lastly the booster on 11/5/21. Patient presented to Hospital on 11/8/21 with chest pain 3 days after receiving the moderna booster. EKG had some T wave inversions, troponin was 400. Patient was found to have myopericarditis on cardiac MRI. Patient was appropriately treated with colchicine and ibuprofen with outpatient cardiology follow up.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: 2,0
Labordaten: MRI cardiac non stress test on 11/8/21: 1. The left ventricular size is mildly dilated (LVEDV indexed is 83 ml/m2). The left ventricular ejection fraction is 51 % by Simpson's method. Global left ventricular function is low normal. There is hypokinesis of the left ventricular mid to distal inferior walls. The left ventricular mass is normal. 2. There is no resting first pass myocardial perfusion defect. There is mid-myocardial and subepicardial late gadolinium enhancement at basal to apical inferior, basal to mid inferolateral, and mid anterolateral segments of the left ventricle (5-segment). There is associated elevation in the global native T1-time, measured at 1372 msec (normal native T1-time is 1200 +/- 80 msec for 3T) and of the extracellular volume fraction of the affected segments, measured at 39% (normal extracellular volume fraction is 28-32%). There is consistent evidence of myocardial edema by T2 weighted imaging. There is focal thickening of pericardium with late gadolinium enhancement of the pericardium adjacent to the inferior, inferolateral and anterolateral walls. Collectively the above findings are consistent with an acute perimyocarditis (viral etiology likely) without full thickness involvement of the inferior and inferolateral walls with minimal reduction of systolic thickening. These findings are consistent with primarily edema of these segments with a reasonable likelihood of restoration of regional function. These above findings are not consistent with ischemic, or infiltrative etiologies. 3. The right ventricular size is normal. Global right ventricular function is mildly decreased with a right ventricular ejection fraction of 43%. There is no late gadolinium enhancement of the right ventricle. CONCLUSIONS: Overall, findings are consistent with acute perimyocarditis with mild reduction of global LV function.
Aktuelle Erkrankungen: N/A
Vorgeschichte: None
Andere Medikamente: caltrate
Allergien: NSAID, penicillins
Vorherige Impfungen: -

VAERS 2054278

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: OH
Alter: 56,0
Geschlecht: F
Eingang: 21.01.2022
Impfdatum: 15.11.2021
Beginn: 04.01.2022
Tage bis Beginn: 50,0
Dosis: UNK
Route/Site: SYR / RA

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

Fibrin D dimer Thrombosis Ultrasound Doppler

Symptomtext

blood clot right calf

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: D-Dimer 1/4/22 Venus Doppler 1/5/22
Aktuelle Erkrankungen: None
Vorgeschichte: High cholesterol
Andere Medikamente: Multi vitamin, Zyrtec, Atorvastatin 40 mg, Doxycyc Mono 100 mg, Metronidazole Gel USP 1%, Probiotic
Allergien: None
Vorherige Impfungen: -

VAERS 2028844

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: MI
Alter: 47,0
Geschlecht: M
Eingang: 12.01.2022
Impfdatum: 26.01.2021
Beginn: 02.01.2022
Tage bis Beginn: 341,0
Dosis: 1
Route/Site: IM / AR

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

Abdominal pain upper Anticoagulant therapy COVID-19 CSF protein increased Condition aggravated Decreased appetite Deep vein thrombosis Demyelinating polyneuropathy Dysstasia Fatigue Head discomfort Hepatic lesion Hypoaesthesia oral Immunoglobulin therapy Inappropriate schedule of product administration Intranasal hypoaesthesia Lymphadenopathy Muscular weakness

Symptomtext

Hospitalized 1/2/2022-still currently admitted; transferred to hospital on 1/4/2022; COVID-19 positive 1/2/2022; fully vaccinated HISTORY OF PRESENT ILLNESS: Patient is a 47 y.o. male who presents as a transfer from Hospital. Past medical history of hodgkin's lymphoma, recent diagnosis of cecal adenocarcinoma, and GERD. Patient presented on 1/2/22 with complaint of lower extremity weakness. Patient states he got up during the early morning on 1/2/22 to use the bathroom. After sitting for a minute, he was unable to stand up from the toilet. He attempted to stand, but his legs were weak and buckled under him. Both legs were weak, but the right seemed to be notably more weak than the left. At that time he also noted his right upper lip and nasal fold felt numb. Prior to this weakness episode, patient he had been having some fatigue, stomach cramps, vomiting, lack of appetite, and head congestion. These symptoms all began on 12/29/21. Covid-19 -stable on RA -symptoms began 6 days ago -can hold on decadron. Start if any signs of clinical worsening -Mucinex PRN congestion -check CRP 1/11/2022 note: 1. New onset weakness Resolved. Appreciate neurology input. CSF shows a total protein of 88 which is mildly elevated from the baseline and less than 50 wbc's. Responded to 5 doses of IVIG for suspected AIDP. 2. Post lumbar puncture headache. Resolved with hydration. 3.COVID 19 Has been fully vaccinated. Stable on room air. Does not have any respiratory symptoms at this time. Will hold Decadron and remdesivir at this time. .4.Liver lesions concerning for metastatic liver disease. Appreciate input from Oncology. 5. Recent history of cecal adenocarcinoma. Status post resection in December. Appreciate input from Oncology.. 6. Lymphadenopathy versus carotid body tumor of right neck Appreciate input from Oncology. 7. Right calf tenderness Doppler shows right calf DVT in the right peroneal and tibial veins. Started on Lovenox therapeutic dose. Appreciate Heme input. Per notes appears to be waiting on Ultrasound 1/13/2022 and PET scan.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: 8,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Lower extremity weakness Muscle weakness of lower extremity Moderate protein-calorie malnutrition Hodgkin's Lymphoma about 30 years ago, GERD, recent cecal adenocarcinoma s/p resection on 12/14, not yet on chemotherapy treatment.
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet Multiple Vitamins-Minerals (ONE-A-DAY 50 PLUS PO) omeprazole (PRILOSEC) 20 MG delayed release capsule
Allergien: NKA
Vorherige Impfungen: -

VAERS 2525045

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: -
Alter: 59,0
Geschlecht: M
Eingang: 28.12.2021
Impfdatum: 06.05.2021
Beginn: 06.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Deep vein thrombosis Pain in extremity Peripheral swelling Ultrasound Doppler abnormal

Symptomtext

Developed left leg pain and swelling, was diagnosed by ultrasound with a DVT in the left lower extremity Narrative: The employee reports developing acute leg pain and swelling during an evening martial arts class. He was diagnosed that night by ultrasound with a DVT of the left lower extremity. Denies any history of prior DVT.

Weitere VAERSDATA-Felder

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

VAERS 1371353

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: VA
Alter: 62,0
Geschlecht: F
Eingang: 22.12.2021
Impfdatum: 04.01.2021
Beginn: 01.01.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: OT / RA

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

Antinuclear antibody increased Antinuclear antibody positive Arthralgia C-reactive protein Echocardiogram Atrial fibrillation Chest pain Dyspnoea Full blood count Metabolic function test Pericarditis Rash Red blood cell sedimentation rate Haemorrhagic stroke Heart rate Hemiplegia Product dose omission issue Rheumatoid factor

Symptomtext

Sjogrens syndrome; Chest pain; Shortness of breath; Pericarditis; A-Fib/ when she went into atrial fibrillation, her heart was beating really abnormal; A major hemorragic stroke; Had a major hemorragic stroke, which left her paralized in her left arm and left leg; Did not receive the second dose; Broke out in a rash; Joint pain, specially on her wrist; This spontaneous case was reported by a consumer and describes the occurrence of SJOGREN'S SYNDROME (Sjogrens syndrome), ATRIAL FIBRILLATION (A-Fib/ when she went into atrial fibrillation, her heart was beating really abnormal), HAEMORRHAGIC STROKE (A major hemorragic stroke), HEMIPLEGIA (Had a major hemorragic stroke, which left her paralized in her left arm and left leg), CHEST PAIN (Chest pain), DYSPNOEA (Shortness of breath) and PERICARDITIS (Pericarditis) in a 62-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 011J20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 04-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 04-Jan-2021, the patient experienced PRODUCT DOSE OMISSION ISSUE (Did not receive the second dose). In January 2021, the patient experienced RASH (Broke out in a rash) and ARTHRALGIA (Joint pain, specially on her wrist). On 07-May-2021, the patient experienced SJOGREN'S SYNDROME (Sjogrens syndrome) (seriousness criteria hospitalization and medically significant), CHEST PAIN (Chest pain) (seriousness criterion hospitalization), DYSPNOEA (Shortness of breath) (seriousness criterion hospitalization) and PERICARDITIS (Pericarditis) (seriousness criteria hospitalization and medically significant). In May 2021, the patient experienced ATRIAL FIBRILLATION (A-Fib/ when she went into atrial fibrillation, her heart was beating really abnormal) (seriousness criteria hospitalization and medically significant), HAEMORRHAGIC STROKE (A major hemorragic stroke) (seriousness criteria hospitalization and medically significant) and HEMIPLEGIA (Had a major hemorragic stroke, which left her paralized in her left arm and left leg) (seriousness criteria hospitalization and medically significant). The patient was hospitalized from 07-May-2021 to sometime in June 2021 due to ATRIAL FIBRILLATION, CHEST PAIN, DYSPNOEA, HAEMORRHAGIC STROKE, HEMIPLEGIA, PERICARDITIS and SJOGREN'S SYNDROME. The patient was treated with METOPROLOL for Adverse event, at an unspecified dose and frequency. On 04-Jan-2021, PRODUCT DOSE OMISSION ISSUE (Did not receive the second dose) had resolved. In June 2021, HAEMORRHAGIC STROKE (A major hemorragic stroke), CHEST PAIN (Chest pain), DYSPNOEA (Shortness of breath) and PERICARDITIS (Pericarditis) had resolved. At the time of the report, SJOGREN'S SYNDROME (Sjogrens syndrome), HEMIPLEGIA (Had a major hemorragic stroke, which left her paralized in her left arm and left leg), RASH (Broke out in a rash) and ARTHRALGIA (Joint pain, specially on her wrist) outcome was unknown and ATRIAL FIBRILLATION (A-Fib/ when she went into atrial fibrillation, her heart was beating really abnormal) had not resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): In May 2021, Echocardiogram: abnormal (abnormal) Fluid around her heart. In May 2021, Heart rate: ab (abnormal) heart was beating really abnormal. In May 2021, Rheumatoid factor: 100 (High) Very high. In June 2021, Echocardiogram: normal (normal) She was ok, no fluid. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter considered SJOGREN'S SYNDROME (Sjogrens syndrome) to be related. No further causality assessments were provided for ATRIAL FIBRILLATION (A-Fib/ when she went into atrial fibrillation, her heart was beating really abnormal), HAEMORRHAGIC STROKE (A major hemorragic stroke), HEMIPLEGIA (Had a major hemorragic stroke, which left her paralized in her left arm and left leg), CHEST PAIN (Chest pain), DYSPNOEA (Shortness of breath), PERICARDITIS (Pericarditis), PRODUCT DOSE OMISSION ISSUE (Did not receive the second dose), RASH (Broke out in a rash) and ARTHRALGIA (Joint pain, specially on her wrist). No concomitant medications were provided. Lab data included ECGs (electrocardiogram) and a bunch of autoinmune disease testing for lupus with unknown results. Doctor advised patient not to get the second dose, as doctor was afraid of having a worse reaction, so patient did not receive the second dose. The patient was in a wheelchair. Couldn't rule out Rheumatoid arthritis, but stated that patient had Sjogrens syndrome. Patient heart was beating really abnormal and that continued after patient came home, but they changed the medication and got better. Treatment medications also included unspecified antiinflamatory for pericarditis. Company comment This case concerns a 62-year-old female patient, with no reported medical history, who experienced the unexpected serious events of SJOGREN'S SYNDROME, ATRIAL FIBRILLATION, HAEMORRHAGIC STROKE, HEMIPLEGIA and the expected serious event of PERICARDITIS. The events occurred approximately 4 months after the administration of the first dose of mRNA-1273 vaccine. On 7May2021 she started having chest pain and was admitted in the hospital with pericarditis. They found she had an autoimmune disease and stated that she had Sjogrens syndrome. About a week after, she had a major hemorragic stroke, which left her paralized in her left arm and left leg. PRODUCT DOSE OMISSION ISSUE was considered as an additional event. The benefit-risk relationship of mRNA-1273 vaccine is not affected by this report.; Sender's Comments: This case concerns a 62-year-old female patient, with no reported medical history, who experienced the unexpected serious events of SJOGREN'S SYNDROME, ATRIAL FIBRILLATION, HAEMORRHAGIC STROKE, HEMIPLEGIA and the expected serious event of PERICARDITIS. The events occurred approximately 4 months after the administration of the first dose of mRNA-1273 vaccine. On 7May2021 she started having chest pain and was admitted in the hospital with pericarditis. They found she had an autoimmune disease and stated that she had Sjogrens syndrome. About a week after, she had a major hemorragic stroke, which left her paralized in her left arm and left leg. PRODUCT DOSE OMISSION ISSUE was considered as an additional event. The benefit-risk relationship of mRNA-1273 vaccine is not affected by this report.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: -
Labordaten: Test Date: 202105; Test Name: Ecocardiogram; Result Unstructured Data: Fluid around her heart; Test Date: 202106; Test Name: Ecocardiogram; Result Unstructured Data: She was ok, no fluid; Test Date: 202105; Test Name: Heart beat; Result Unstructured Data: heart was beating really abnormal; Test Date: 202105; Test Name: Rheumatoid factor; Result Unstructured Data: Very high
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1944472

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: MI
Alter: 81,0
Geschlecht: F
Eingang: 13.12.2021
Impfdatum: 29.12.2020
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: IM / LA

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

Anticoagulant therapy Balance disorder Computerised tomogram head abnormal Dysarthria Interchange of vaccine products Ischaemic stroke Magnetic resonance imaging head abnormal Walking aid user

Symptomtext

Moderna COVID-19 Vaccine EUA. On 01/10/2021 states she was feeling fine and when she answered the phone her son noted that she was slurring her speech. Her husband was home at the time and she was taken to the hospital. CT scan and MRI completed and showed an ischemic stroke. She states she still occasionally slurs her speech and sometimes loses her balance so she now walks with a cane. She is now on 2 medications for blood pressure and is also on plavix. She had mentioned to the physicians that she had received a dose of Moderna on 12/29/20. She went on to receive her second Moderna on 1/26/2021 and a booster of Pfizer on 12/10/2021 with no side effects to date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Ischaemic stroke
Hospital-Tage: 4,0
Labordaten: CT scan and MRI of brain
Aktuelle Erkrankungen: none
Vorgeschichte: hypertension
Andere Medikamente: Losartan
Allergien: nickel
Vorherige Impfungen: -

VAERS 1913063

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: MO
Alter: 63,0
Geschlecht: M
Eingang: 01.12.2021
Impfdatum: 10.02.2021
Beginn: 20.11.2021
Tage bis Beginn: 283,0
Dosis: 1
Route/Site: IM / -

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

Dyspnoea Endotracheal intubation Hypoxia Intensive care Mechanical ventilation

Symptomtext

Patient admitted to the hospital with shortness of breath and hypoxia. Received Regeneron infusion on 11/19/2021, but needed to be admitted for worsening symptoms on 11/20/2021. Patient ultimately needed to be intubated and is still currently intubated in the ICU at day #7 on the ventilator today.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Arthritis, CAD, chronic back pain, costochondritis, depression, foot fracture, tobacco abuse, hyperlipidemia, hypertension, leg pain, low back pain, melanoma, MRSA skin infection 2010, myocardial infarction, obesity, OSA, renal calculi, restrictive lung disease, TIA, UTI
Andere Medikamente: Albuterol HFA inhaler Amlodipine 5 mg daily Aspirin 81 mg daily Atorvastatin 40 mg daily Symbicort inhaler Chlorthalidone 25 mg daily Docusate Gabapentin 600 mg daily Isosorbide mononitrate 30 mg daily Losartan 100 mg daily Metoprolol XL 1
Allergien: None
Vorherige Impfungen: -

VAERS 1913063

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: MO
Alter: 63,0
Geschlecht: M
Eingang: 01.12.2021
Impfdatum: 10.02.2021
Beginn: 20.11.2021
Tage bis Beginn: 283,0
Dosis: 2
Route/Site: IM / -

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

Dyspnoea Endotracheal intubation Hypoxia Intensive care Mechanical ventilation

Symptomtext

Patient admitted to the hospital with shortness of breath and hypoxia. Received Regeneron infusion on 11/19/2021, but needed to be admitted for worsening symptoms on 11/20/2021. Patient ultimately needed to be intubated and is still currently intubated in the ICU at day #7 on the ventilator today.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Arthritis, CAD, chronic back pain, costochondritis, depression, foot fracture, tobacco abuse, hyperlipidemia, hypertension, leg pain, low back pain, melanoma, MRSA skin infection 2010, myocardial infarction, obesity, OSA, renal calculi, restrictive lung disease, TIA, UTI
Andere Medikamente: Albuterol HFA inhaler Amlodipine 5 mg daily Aspirin 81 mg daily Atorvastatin 40 mg daily Symbicort inhaler Chlorthalidone 25 mg daily Docusate Gabapentin 600 mg daily Isosorbide mononitrate 30 mg daily Losartan 100 mg daily Metoprolol XL 1
Allergien: None
Vorherige Impfungen: -

VAERS 1889556

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: GA
Alter: 59,0
Geschlecht: F
Eingang: 22.11.2021
Impfdatum: 23.12.2020
Beginn: 23.12.2020
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Confusional state Electrocardiogram Heart rate increased Immediate post-injection reaction Loss of consciousness Nausea Skin discolouration

Symptomtext

Immediately after received the vaccine, received experienced rapid heart rate, loss of conscious for 3 seconds, nausea, skin turned gray, confusion. The physician at side drove my car near to the ambulance. Physician, paramedics and medical staff assisted me inside ambulance. Electronic Blood pressure monitor in the ambulance marked BP 186/96 and HR 96. The paramedics performed several electrocardiograms. Paramedics inquired physician at site to complete an adverse event report. Physician states no report will be needed at this time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: No proof of EMT care provided. Physician at the vaccination clinic kept the electrocardiograms performed in the Ambulance.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1689564

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: MD
Alter: 23,0
Geschlecht: F
Eingang: 10.09.2021
Impfdatum: 25.01.2021
Beginn: 23.08.2021
Tage bis Beginn: 210,0
Dosis: 1
Route/Site: IM / RA

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

Asthma Electrocardiogram ST segment depression Electrocardiogram abnormal Pericarditis Ultrasound scan abnormal

Symptomtext

Pericarditis Asthma Pt developed pericarditis and asthma 8 months after vaccine, requiring medication and hospitalizations.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: 2,0
Labordaten: EKG: PR depression US: Hyperechoic pericardium
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 957061

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: OH
Alter: 39,0
Geschlecht: F
Eingang: 09.09.2021
Impfdatum: 23.12.2020
Beginn: 01.12.2020
Tage bis Beginn: -
Dosis: 1
Route/Site: IM / RA

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

Asthenia Blood test Computerised tomogram head normal Hypoaesthesia Lumbar puncture Condition aggravated Exposure to SARS-CoV-2 Facial paralysis Fatigue Guillain-Barre syndrome Dyspnoea Paraesthesia Paralysis Hyporeflexia Lumbar puncture abnormal Pain Rheumatoid arthritis

Symptomtext

This is a courtesy report as notes from hospital did not indicate a previous VARES had been completed. Regulatory authority rec'd faxes from hospital indicating pt was dx w/ Guillain-Barre syndrome "secondary to either COVID-19 vaccination or COVID-19 (she was not positive but family was)".

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: -
Labordaten: Unknown
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Unknown
Andere Medikamente: Unknown
Allergien: Unknown
Vorherige Impfungen: -

VAERS 957061

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: OH
Alter: 39,0
Geschlecht: F
Eingang: 09.09.2021
Impfdatum: 23.12.2020
Beginn: 01.12.2020
Tage bis Beginn: -
Dosis: 1
Route/Site: OT / -

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

Asthenia Blood test Computerised tomogram head normal Hypoaesthesia Lumbar puncture Condition aggravated Exposure to SARS-CoV-2 Facial paralysis Fatigue Guillain-Barre syndrome Dyspnoea Paraesthesia Paralysis Hyporeflexia Lumbar puncture abnormal Pain Rheumatoid arthritis

Symptomtext

This is a courtesy report as notes from hospital did not indicate a previous VARES had been completed. Regulatory authority rec'd faxes from hospital indicating pt was dx w/ Guillain-Barre syndrome "secondary to either COVID-19 vaccination or COVID-19 (she was not positive but family was)".

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: -
Labordaten: Unknown
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Unknown
Andere Medikamente: Unknown
Allergien: Unknown
Vorherige Impfungen: -

VAERS 1678173

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: CT
Alter: 49,0
Geschlecht: F
Eingang: 07.09.2021
Impfdatum: 23.12.2020
Beginn: 27.08.2021
Tage bis Beginn: 247,0
Dosis: 1
Route/Site: OT / -

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

Feeling hot Muscle spasms Myalgia Pain in extremity Peripheral swelling Thrombosis Ultrasound Doppler

Symptomtext

Confirmed a blood clot in the left leg; Like a "Charlie Horse"; left leg started to feel pain; Left leg swelled; Left leg got hot; Soreness on the left calf muscle/like a sore muscle; This spontaneous case was reported by a nurse and describes the occurrence of THROMBOSIS (Confirmed a blood clot in the left leg) in a 50-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 029L20A and 011J20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concurrent medical conditions included Drug allergy. On 23-Dec-2020, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 19-Jan-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 27-Aug-2021, the patient experienced MUSCLE SPASMS (Like a "Charlie Horse"), PAIN IN EXTREMITY (left leg started to feel pain), PERIPHERAL SWELLING (Left leg swelled), FEELING HOT (Left leg got hot) and MYALGIA (Soreness on the left calf muscle/like a sore muscle). On 28-Aug-2021, the patient experienced THROMBOSIS (Confirmed a blood clot in the left leg) (seriousness criterion medically significant). The patient was treated with RIVAROXABAN (XARELTO) for Clot blood, at an unspecified dose and frequency. At the time of the report, THROMBOSIS (Confirmed a blood clot in the left leg), MUSCLE SPASMS (Like a "Charlie Horse"), PAIN IN EXTREMITY (left leg started to feel pain), PERIPHERAL SWELLING (Left leg swelled), FEELING HOT (Left leg got hot) and MYALGIA (Soreness on the left calf muscle/like a sore muscle) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 28-Aug-2021, Ultrasound Doppler: abnormal (abnormal) Confirmed a blood clot in the left leg. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Relevant concomitant medication was reported as birth control pills. She went to see her physician on 28-Aug-2021, and her doctor performed a Doppler test and test confirmed a blood clot in the left leg. She was prescribed Xarelto and will need to take the medication for three months. Company comment: Based on the current available information and temporal association between the use of the product and the start date of the events, a causal relationship cannot be excluded. However, 7 months since the second dose and birth control pills as concomitant medication could be confounders for the events. Further information has been requested. This case was linked to MOD-2021-003812 (Patient Link).; Sender's Comments: Based on the current available information and temporal association between the use of the product and the start date of the events, a causal relationship cannot be excluded. However, 7 months since the second dose and birth control pills as concomitant medication could be confounders for the events. Further information has been requested.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: Test Date: 20210828; Test Name: Doppler test; Result Unstructured Data: Confirmed a blood clot in the left leg
Aktuelle Erkrankungen: Drug allergy
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1677281

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: NC
Alter: 78,0
Geschlecht: F
Eingang: 07.09.2021
Impfdatum: 11.01.2021
Beginn: 08.02.2021
Tage bis Beginn: 28,0
Dosis: 1
Route/Site: OT / LA

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

Arthralgia Body temperature Breast pain Breast tenderness Decreased appetite Diarrhoea Dizziness Dyspnoea Fatigue Feeling abnormal Gait disturbance Glossodynia Herpes zoster Mobility decreased Mouth swelling Mouth ulceration Musculoskeletal chest pain Ocular discomfort

Symptomtext

She faints, has to put her head down,; fast heartbeat; difficulty breathing; her arms are totally limp; diagnosed with shingles in her eye; silent migraine/silent migraine on the left side that later became more intense; joints in her hands a little less painful; still having pain/joints in her hands a little less painful/pain had diminished but was still evident; legs, specially the bottom half, were extremely swollen; left breast was extremely tender, it woke her up; rib cage hurt on the left and right side/rib cage was a little less painful; left breast was extremely painful, it woke her up; lump on her left thumb; diarrhea; cheek and cheek bones on the left side were "very very tender"; rash continued/rash was brighter; tongue was sore, heavily coated and swollen.; tongue was sore; The roof of her mouth ulcerated; The "normal dizziness after eating" increased for many days/"normal dizziness" continued to increase for several more days/ate and then became dizzy/dizziness was back; mouth was sore; pain on her teeth; rash on her upper torso and in the injection site; low appetite/ ate very little all day; pain at the site of injection; low fever (99.7? F); "very very tired"/tired; left side of her face was swollen; mouth and tongue were swollen/mouth and tongue were lumpy; back of her throat swollen/throat was swollen; mouth and tongue were lumpy/mouth and tongue were swollen; couldn't open her eyes; couldn't use her arms and legs/unable to walk/couldn't even attempt to walk; "It was like she was punched by the person who administered the vaccine"; "I knew that I was going to crash"/she "was crashing"/collapsed; This spontaneous case was reported by a consumer (subsequently medically confirmed) and describes the occurrence of SYNCOPE (She faints, has to put her head down,), TACHYCARDIA (fast heartbeat), MOUTH SWELLING (mouth and tongue were swollen/mouth and tongue were lumpy), HERPES ZOSTER (diagnosed with shingles in her eye) and GLOSSODYNIA (tongue was sore) in a 79-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 028L20A and 011J20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included Dental implantation (Tooth implant two years ago). Concurrent medical conditions included Rheumatoid arthritis, Allergy (allergic to some staff on Tooth implant.) and Faint (Faints after eating.). Concomitant products included PROBIOTICS NOS for an unknown indication. On 11-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 08-Feb-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 08-Feb-2021, the patient experienced OCULAR DISCOMFORT (couldn't open her eyes), MOBILITY DECREASED (couldn't use her arms and legs/unable to walk/couldn't even attempt to walk), FEELING ABNORMAL ("I knew that I was going to crash"/she "was crashing"/collapsed) and VACCINATION SITE DISCOMFORT ("It was like she was punched by the person who administered the vaccine"). On 09-Feb-2021, the patient experienced MOUTH SWELLING (mouth and tongue were swollen/mouth and tongue were lumpy), PHARYNGEAL SWELLING (back of her throat swollen/throat was swollen), SWELLING FACE (left side of her face was swollen), SWOLLEN TONGUE (mouth and tongue were lumpy/mouth and tongue were swollen), TOOTHACHE (pain on her teeth), DECREASED APPETITE (low appetite/ ate very little all day), VACCINATION SITE RASH (rash on her upper torso and in the injection site), VACCINATION SITE PAIN (pain at the site of injection), PYREXIA (low fever (99.7? F)) and FATIGUE ("very very tired"/tired). On 10-Feb-2021, the patient experienced GLOSSODYNIA (tongue was sore), TONGUE COATED (tongue was sore, heavily coated and swollen.), ORAL PAIN (mouth was sore), DIZZINESS (The "normal dizziness after eating" increased for many days/"normal dizziness" continued to increase for several more days/ate and then became dizzy/dizziness was back) and MOUTH ULCERATION (The roof of her mouth ulcerated). On 11-Feb-2021, the patient experienced TENDERNESS (cheek and cheek bones on the left side were "very very tender"), DIARRHOEA (diarrhea) and RASH (rash continued/rash was brighter). On 14-Feb-2021, the patient experienced SWELLING (lump on her left thumb). On 15-Mar-2021, the patient experienced BREAST PAIN (left breast was extremely painful, it woke her up), MUSCULOSKELETAL CHEST PAIN (rib cage hurt on the left and right side/rib cage was a little less painful) and BREAST TENDERNESS (left breast was extremely tender, it woke her up). On 22-Mar-2021, the patient experienced PERIPHERAL SWELLING (legs, specially the bottom half, were extremely swollen). On 31-Mar-2021, the patient experienced PAIN (still having pain/joints in her hands a little less painful/pain had diminished but was still evident). On 01-Apr-2021, the patient experienced TYPICAL AURA WITHOUT HEADACHE (silent migraine/silent migraine on the left side that later became more intense) and ARTHRALGIA (joints in her hands a little less painful). On 02-Apr-2021, the patient experienced HERPES ZOSTER (diagnosed with shingles in her eye). On an unknown date, the patient experienced SYNCOPE (She faints, has to put her head down,), TACHYCARDIA (fast heartbeat), DYSPNOEA (difficulty breathing) and GAIT DISTURBANCE (her arms are totally limp). On 08-Feb-2021, OCULAR DISCOMFORT (couldn't open her eyes), MOBILITY DECREASED (couldn't use her arms and legs/unable to walk/couldn't even attempt to walk), FEELING ABNORMAL ("I knew that I was going to crash"/she "was crashing"/collapsed) and VACCINATION SITE DISCOMFORT ("It was like she was punched by the person who administered the vaccine") had resolved. On 12-Feb-2021, VACCINATION SITE RASH (rash on her upper torso and in the injection site) had resolved. On 29-Mar-2021, PERIPHERAL SWELLING (legs, specially the bottom half, were extremely swollen) had resolved. At the time of the report, SYNCOPE (She faints, has to put her head down,), TACHYCARDIA (fast heartbeat), MOUTH SWELLING (mouth and tongue were swollen/mouth and tongue were lumpy), HERPES ZOSTER (diagnosed with shingles in her eye), GLOSSODYNIA (tongue was sore), PHARYNGEAL SWELLING (back of her throat swollen/throat was swollen), BREAST PAIN (left breast was extremely painful, it woke her up), SWELLING FACE (left side of her face was swollen), TYPICAL AURA WITHOUT HEADACHE (silent migraine/silent migraine on the left side that later became more intense), TONGUE COATED (tongue was sore, heavily coated and swollen.), MUSCULOSKELETAL CHEST PAIN (rib cage hurt on the left and right side/rib cage was a little less painful), TENDERNESS (cheek and cheek bones on the left side were "very very tender"), BREAST TENDERNESS (left breast was extremely tender, it woke her up), SWOLLEN TONGUE (mouth and tongue were lumpy/mouth and tongue were swollen), ORAL PAIN (mouth was sore), TOOTHACHE (pain on her teeth), DYSPNOEA (difficulty breathing), DIZZINESS (The "normal dizziness after eating" increased for many days/"normal dizziness" continued to increase for several more days/ate and then became dizzy/dizziness was back), SWELLING (lump on her left thumb), GAIT DISTURBANCE (her arms are totally limp), PAIN (still having pain/joints in her hands a little less painful/pain had diminished but was still evident), MOUTH ULCERATION (The roof of her mouth ulcerated), DECREASED APPETITE (low appetite/ ate very little all day), DIARRHOEA (diarrhea), RASH (rash continued/rash was brighter), ARTHRALGIA (joints in her hands a little less painful), VACCINATION SITE PAIN (pain at the site of injection), PYREXIA (low fever (99.7? F)) and FATIGUE ("very very tired"/tired) had resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, Body temperature: 99.7 (Inconclusive) 99.7 F. On an unknown date, Mammogram: abnormal (abnormal) false positive diagnose of breast cancer. Patient was allergic to some staffs (not specified) On 31-Mar-2021 she went to hospital as because of pain and took some test on rib cages,results were unknown Patient had seen heart specialist and did some tests, included heart monitor and said nothing was wrong. It was reported false positives for cancer with the vaccine. Company comment: Based on the current available information and temporal association between the use of the product and the start date of the events Event syncope was automatically upgraded as a serious event as per IME list. However, based on the information available and as per medical judgment it is classified as Non-serious., a causal relationship cannot be excluded. This case was linked to MOD-2021-297711 (Patient Link).; Sender's Comments: Based on the current available information and temporal association between the use of the product and the start date of the events Event syncope was automatically upgraded as a serious event as per IME list. However, based on the information available and as per medical judgment it is classified as Non-serious., a causal relationship cannot be excluded.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Test Name: Body temperature; Test Result: Inconclusive ; Result Unstructured Data: 99.7 F; Test Name: Mammogram; Result Unstructured Data: false positive diagnose of breast cancer
Aktuelle Erkrankungen: Allergy (allergic to some staff on Tooth implant.); Faint (Faints after eating.); Rheumatoid arthritis
Vorgeschichte: Medical History/Concurrent Conditions: Dental implantation (Tooth implant two years ago)
Andere Medikamente: PROBIOTICS NOS
Allergien: -
Vorherige Impfungen: -

VAERS 1624552

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: NC
Alter: 39,0
Geschlecht: F
Eingang: 23.08.2021
Impfdatum: 23.12.2020
Beginn: 24.12.2020
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / RA

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

Amnesia Bell's palsy Computerised tomogram head normal Confusional state Dizziness Electrocardiogram Fatigue Gait disturbance Hyperhidrosis Hypoaesthesia oral Influenza like illness Laboratory test Movement disorder Speech disorder

Symptomtext

I started having mild on paying around 1:00 AM. I woke up and took some Tylenol. I 24 hours after getting the injection I had flu like symptoms. 48 hours after the injection I was dizzy and a little confused. I took a couple of Benadryl and intermittently traded my owl just with Tylenol. I drink a lot of fluids and Gatorade to try to remain hydrated and rested as much as I could. I woke up on 12/25/20 and felt a little better. That evening, I started feeling a little confused but was tired from playing with my kids and their new toys at Christmas. Tell my husband I was just going to go to bed. I woke up on 1226, covered in sweat and had difficulty ambulating informing my words. I was concerned I may have had a stroke. I didn?t recognize my children and couldn?t recall their names. I went to the emergency room and was told this 100% could NOT be a vaccine reaction and I was withdrawing from adderall. I take a 10 mg dose daily and it?s not uncommon for me to skip that for weeks at a time, I tried to explain that but again, nobody was allowed to come in the facility with me and I was having difficulty speaking. My blood pressure was 190s/89 ish and they did a ct of my head that was overall, unimpressive and clear. The reaction ended with me having Bell?s palsy approximately 10 days after the vaccine and on the same side I received my injection in. In between onset of sx. And the Bell?s palsy, my lips would go numb, intermittently and sometimes my right arm and right leg would turn inward, intermittently (like decorticating posturing).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: Ct scan Labs EKG Vitals All were done on 12/26/2020
Aktuelle Erkrankungen: Likely Covid exposure or presumed Covid one month prior to vaccination, flu shot within one month of Covid vaccine
Vorgeschichte: Psoriasis, sjogren?s, psoriatic arthritis, past history of shingles, past history of oligohydramniosis, tardive dyskinesia with reglan, fainted with gardasil shot 2 and 3, anxiety, depression.
Andere Medikamente: Adderall xr 10 mg daily Multivitamin daily Macrobid daily Xanax prn
Allergien: Hornets, green beans, reglan, wellbutrin, bactrim
Vorherige Impfungen: -

VAERS 1599860

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: PR
Alter: 37,0
Geschlecht: F
Eingang: 21.08.2021
Impfdatum: 04.01.2021
Beginn: 02.02.2021
Tage bis Beginn: 29,0
Dosis: 1
Route/Site: OT / LA

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

Asthma Contusion Dyspnoea Feeling abnormal Haemoglobin Hypokinesia Platelet count Red blood cell count Spirometry Tachycardia Ultrasound Doppler Venous thrombosis

Symptomtext

Venous thrombosis; Bruise on right and left leg; Could not get up; Difficult breathing; Asthma; Severe tachycardia; Felt a little weird; This spontaneous case was reported by a nurse and describes the occurrence of VENOUS THROMBOSIS (Venous thrombosis), TACHYCARDIA (Severe tachycardia), FEELING ABNORMAL (Felt a little weird), HYPOKINESIA (Could not get up) and DYSPNOEA (Difficult breathing) in a 37-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 011M20A and 011J20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concurrent medical conditions included Thyroid disorder NOS and Migraine. Concomitant products included TOPIRAMATE (TOPAMAX) for Migraine, LEVOTHYROXINE SODIUM (SYNTHROID) for Thyroid disorder NOS. On 04-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 02-Feb-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 02-Feb-2021, the patient experienced TACHYCARDIA (Severe tachycardia) and FEELING ABNORMAL (Felt a little weird). On 03-Feb-2021, the patient experienced HYPOKINESIA (Could not get up), DYSPNOEA (Difficult breathing) and ASTHMA (Asthma). On 04-Feb-2021, the patient experienced CONTUSION (Bruise on right and left leg). On 01-Mar-2021, the patient experienced VENOUS THROMBOSIS (Venous thrombosis). At the time of the report, VENOUS THROMBOSIS (Venous thrombosis), TACHYCARDIA (Severe tachycardia), FEELING ABNORMAL (Felt a little weird), HYPOKINESIA (Could not get up), DYSPNOEA (Difficult breathing), ASTHMA (Asthma) and CONTUSION (Bruise on right and left leg) had not resolved. Not Provided DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 03-Feb-2021, Spirometry: abnormal (abnormal) Confirmed asthma. On 17-Mar-2021, Haemoglobin: low (Low) Low. On 17-Mar-2021, Red blood cell count: low (Low) Low. On 17-Mar-2021, Ultrasound Doppler: abnormal (abnormal) Venous thrombosis in her left leg. Had an arterial doppler of the right leg only because the clot was still there in the left leg.. On an unknown date, Platelet count: abnormal (abnormal) Platelet count was uncontrolled. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Treatment details included levalbuterol for asthma and 20 mg rivaroxaban for venous thrombosis. Concomitant medication also included the use of anticoagulant from 01 Mar 2021. The reporter stated the bruise on the right was super big, it didn't hurt. Two days later it kept getting bigger and got bigger and there was no way to control it. On 12 Apr 2021, another clot was found on right leg so now she had two clots one in left and one in right leg. Also her hemoglobin and red blood cells are still lowand the platelets are uncontrolled. This case was linked to US-MODERNATX, INC.-MOD-2021-059897 (E2B Linked Report). Most recent FOLLOW-UP information incorporated above includes: On 15-Apr-2021: As per the follow up received on 15 Apr 2021, the concomitant medication, platelet count details and an additional event details, i.e. a clot on right leg has been added. The outcome was also updated from unknown to not recovered as the reporter states that she still have the events previously reported.; Sender's Comments: US-MODERNATX, INC.-MOD-2021-059897:First Dose Case

Weitere VAERSDATA-Felder

Praegender Schweregrund: Venous thrombosis
Hospital-Tage: -
Labordaten: Test Date: 20210317; Test Name: Haemoglobin; Result Unstructured Data: Low; Test Name: Platelet count; Result Unstructured Data: Platelet count was uncontrolled; Test Date: 20210317; Test Name: Red boold cell count; Result Unstructured Data: Low; Test Date: 20210203; Test Name: spirometry; Result Unstructured Data: Confirmed asthma; Test Date: 20210317; Test Name: Arterial doppler / venous doppler; Result Unstructured Data: Venous thrombosis in her left leg. Had an arterial doppler of the right leg only because the clot was still there in the left leg.
Aktuelle Erkrankungen: Migraine; Thyroid disorder NOS
Vorgeschichte: -
Andere Medikamente: SYNTHROID; TOPAMAX
Allergien: -
Vorherige Impfungen: -

VAERS 1545442

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: NC
Alter: 54,0
Geschlecht: M
Eingang: 11.08.2021
Impfdatum: 29.01.2021
Beginn: 03.07.2021
Tage bis Beginn: 155,0
Dosis: 2
Route/Site: SYR / LA

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

Abdominal pain Acute kidney injury Anticoagulant therapy Biopsy prostate abnormal Bladder catheterisation Blood test Catheter placement Chest X-ray Chest pain Computerised tomogram Dyspepsia Prostatomegaly Thrombosis Urinary tract disorder

Symptomtext

1st event: March 15th -It felt like I had indigestion; I had pain in my chest. I went to URGENT CARE. She told me to go to ER when I said I had chest pain. Went to ER; They put me on a gurney. That was a blood clot and they treated me with ER - two days in patient hospital. IV fluids and they put me on Eliquis. They sent me home with Eliquis and said to take it for the next 6 months. 2nd event: in July -I had abdominal pains. I went to ER; I was having issues urinating. I felt all blocked up. My prostrate was blown up. I had acute Kidney failure. They had to drain my bladder. They admitted me for three days and I had IV catheter for a week. Put me on medication: Flomax. They still have me on Eliquis. I am still taking Flomax, too. I have had follow ups with doctors from the hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: 3,0
Labordaten: X-ray - chest; CAT scan; Hematologist did blood work on me - for first event. 2nd event: CAT scan - to check kidneys and bladder. Prostrate exam and a biopsy about a week later. Recommend I do some other surgery to help with my prostrate. We're waiting on that.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Nothing
Allergien: No
Vorherige Impfungen: -

VAERS 1490604

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011j20A

schwer

Staat: CT
Alter: 30,0
Geschlecht: F
Eingang: 21.07.2021
Impfdatum: 29.12.2020
Beginn: 30.05.2021
Tage bis Beginn: 152,0
Dosis: 1
Route/Site: IM / RA

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

Anticoagulant therapy Cerebral venous sinus thrombosis Computerised tomogram Diplopia Headache Magnetic resonance imaging head abnormal Visual impairment

Symptomtext

Headache, visual disturbances, double vision, went to the ED and had MRI showing the cerebral venous clot and I was on a heparin drip for 5 days before transitioning to oral Coumadin; 3 weeks later changed to Eliquis for 6 months

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebral venous sinus thrombosis
Hospital-Tage: 9,0
Labordaten: Mri 6/3/2021 also CT
Aktuelle Erkrankungen: None
Vorgeschichte: I developed a cerebral venous sinus thrombosis, needing blood thinners for 6months. I had no other risk factors other than being on birth control and getting the moderna vaccine. I?m concerned that the combination of these two things helped caused my clot.
Andere Medikamente: Birth control pills blisovi
Allergien: None
Vorherige Impfungen: -

VAERS 1489583

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: IN
Alter: 56,0
Geschlecht: F
Eingang: 21.07.2021
Impfdatum: 30.03.2021
Beginn: 30.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / LA

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

Anaphylactic reaction Blood pressure measurement Chest discomfort Headache Hypertension Myalgia Nausea Pyrexia Urticaria Vomiting

Symptomtext

Her blood pressure was also elevated 186/119; Headache; Anaphylactic reaction; Hives all over her body; Tightness in her chest; Fever; Nausea; Vomiting; Body aches; This spontaneous case was reported by a health care professional and describes the occurrence of ANAPHYLACTIC REACTION (Anaphylactic reaction) in a 56-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 011J20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concurrent medical conditions included Obesity. On 30-Mar-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 30-Mar-2021, the patient experienced ANAPHYLACTIC REACTION (Anaphylactic reaction) (seriousness criterion medically significant). 30-Mar-2021, the patient experienced URTICARIA (Hives all over her body), CHEST DISCOMFORT (Tightness in her chest), PYREXIA (Fever), NAUSEA (Nausea), VOMITING (Vomiting) and MYALGIA (Body aches). On an unknown date, the patient experienced HYPERTENSION (Her blood pressure was also elevated 186/119) and HEADACHE (Headache). At the time of the report, ANAPHYLACTIC REACTION (Anaphylactic reaction), URTICARIA (Hives all over her body), CHEST DISCOMFORT (Tightness in her chest), HYPERTENSION (Her blood pressure was also elevated 186/119), PYREXIA (Fever), NAUSEA (Nausea), VOMITING (Vomiting), MYALGIA (Body aches) and HEADACHE (Headache) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 30-Mar-2021, Blood pressure measurement: 186/119 (High) High. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter considered ANAPHYLACTIC REACTION (Anaphylactic reaction), URTICARIA (Hives all over her body), CHEST DISCOMFORT (Tightness in her chest), HYPERTENSION (Her blood pressure was also elevated 186/119), PYREXIA (Fever), NAUSEA (Nausea), VOMITING (Vomiting), MYALGIA (Body aches) and HEADACHE (Headache) to be related. Patient received treatment in the emergency department (unspecified). No concomitant medication was reported. Company Comment: Based on current available information and temporal association between the use of the product and the start date of the event, a causal relationship cannot be excluded. Most recent FOLLOW-UP information incorporated above includes: On 16-Jun-2021: Follow-up received on 16-JUN-2021 and included relevant medical history, outcome of events and Causality. On 16-Jul-2021: Follow-up received on 16-JUL-2021 and included events (anaphylactic reaction and hypertension); Sender's Comments: Based on current available information and temporal association between the use of the product and the start date of the event, a causal relationship cannot be excluded.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: Test Date: 20210330; Test Name: Blood pressure; Result Unstructured Data: High
Aktuelle Erkrankungen: Obesity
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1437909

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: OH
Alter: 49,0
Geschlecht: F
Eingang: 30.06.2021
Impfdatum: 27.01.2021
Beginn: 27.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Acidosis Angina unstable Aortic valve thickening Aortitis Atrioventricular block Bilevel positive airway pressure Biopsy artery Bladder catheterisation Blood gases Blood test normal Cardiac failure Cardiac pacemaker insertion Cardiac procedure complication Cardiac stress test abnormal Catheter placement Catheterisation cardiac abnormal Chest X-ray Chest discomfort

Symptomtext

ONSET OF S/S: Approximately a week or two later I noted that when I would walk into work from our employee parking lot/garage that I would have onset of chest pressure, shortness of breath and pain radiating down both arms and occasionally my neck when it was at it's worse. Initially, while I didn't feel like I was feeling stressed, I was concerned that I might be experiencing panic attacks. Dismissing it as that I shared with my Husband my concerns in late February. At that point in time, we were seeing a decrease in cases and so I was hopeful that maybe my mental state and anxieties might resolve. So I continued to dismiss the problem. Disease Progression: Unfortunately, the symptoms continued to progress. It progressed to happening when I was leaving work or when it was required that I go anywhere in an real rush (a frequent occurrence). By early April, we went for a family vacation. Almost every day as we walked into, around and out of the parks I would have to slow down and res to catch my breath and slow my heartrate which would spike up into the 140-160s. By the end of the week it was happening multiple times each day. It was always initiated by an increase in activity or exertion. We decided that it was not anxiety related and that she needed to see a doctor to pursue a diagnosis. 4/12/21: Due to already having an appointment set up with my OB/GYN prior to our vacation - that was the first appointment that I kept because I was hopeful or suspicious that my symptoms may really be menopausal in source. The hormone work-up did not reveal any abnormalities. However, at that time they did send in a referral to Dr., Cardiologist. 5/17/21: I met with Dr. at which an Echo and NM Stress test were ordered. 5/28/21: Echo & routine stress test were completed. Insurance would not cover an actual NM Stress test so the order was changed to routine. I failed the treadmill stress test within 4.42 minutes with the same symptoms I had been experiencing. Test was terminated due to worsening symptoms. , took approximately 10 minutes to recover. HR reached goal HR @ 157. At that time Dr. recommended starting a daily Aspirin tx and suggested that a possible heart cath may be needed. Dr. followed up these tests with a referral for a left heart cath, daily 81mg Aspirin and 12.5mg Metoprolol XR daily. During this almost 3 week time period my symptoms were getting increasingly worse and requiring less and less activity to instigate my symptoms. 6/15/21: Left heart catheterization procedure to evaluate the blood flow to the heart. Impression and plan per Dr. Impression: Severe ostial RCA and left main disease with preserved LV systolic function. Crescendo angina Plan: Findings were reviewed the patient and her family. Ostial coronary disease raise the concern whether she had some type of aortitis but clinically there is no history for this and no prior chest irradiation. Surgical intervention appears indicated as soon as possible and I have consulted Dr. In the interim, continue aspirin, metoprolol. Initiate statin therapy. (The remainder of the following record as documented by my husband and myself) They completed the procedure and it indicated two of the main blood vessels in her heart were constricted. The vessel on the right side was 95% restricted and the vessel on the left was 65-70% restricted. The doctors reported afterward that they had difficulty inserting the catheter. They also indicated that they found no build-up of plaque in other vessels or other reasons for the vessels to be restricted. They expressed surprise and confusion as to the cause of the damage to the vessels. They walked through the risk factors and indicated that she had none of the traditional risk factors. She never smoked. She is not diabetic. She is young and otherwise healthy. They told us that they see this type of damage to the heart from people who had radiation therapy from treatment of Hodgkin?s Lymphoma when they were young. They also indicated that this is something that can happen to Type 1 diabetics. They expressed that this was very unusual and they did not know why she had this condition. They felt there was a high risk of a heart attack due to the blockage and recommended that she be admitted to the hospital. The proposed a course of treatment was traditional bypass surgery. They felt due to the location and type of blockage that other procedures like a stent would not be feasible. It was at this point in the consult room when the doctor shared the information above that I express my first question about whether this could be related either to a Covid infection (she was never diagnosed or had any symptoms) or due to the vaccine. I asked this because the symptoms began after her second shot. Because of her job we followed the news on the virus and vaccines closely. Many reports indicated that the virus causes severe heart and lung damage. Recently there were reports of inflammation of the heart associated with people who had recently been vaccinated. When I proposed this connection, Dr said that the Myocarditis and Pericarditis reported to be associated with the vaccine did not present in this way. He expressed that he did not think it was related. Patient came out of the procedure and was admitted. Later that evening Dr. came in to discuss the upcoming heart procedure. He described the blockage and why it was critical that it be addressed. He also expressed surprise that she was having this issue and did not have any of the normal symptoms of heart disease. He described the surgery as a triple bypass to restore blood flow to the two sides of the heart affected by the blockage. He indicated he would take a vein from her arm and a vein from her leg and bypass the affected areas of the restricted vessels. It was not clear to me (we did not have any pictures or models to visualize the process) exactly how it would proceed but he said it is a very common procedure and of the bypass surgeries it is the easiest due to the location. He did not expect any issues and indicated it was a 99% success rate. In the conversation, he expressed multiple times that this was very unusual. I asked if it was possible it could be Covid or vaccine related. He did not believe it was related. 6/16/21 Wednesday patient spent the day being prepped for surgery. Vein mapping, ABG, CXR completed. 6/17/21 Thursday morning, she went into surgery. We received the updates with no indication of any issues. After surgery Dr. came in for the post op consult. He said that things did not go as planned. They harvested the veins in preparation. When they went in the ascending aorta was severely inflamed. He said that normal thickness is a millimeter and that it is flexible. Patient had a 6mm wall thickness and was very difficult to work with. This caused them to only bypass 2 vessels. He indicated he was concerned about attaching to the inflamed aorta and that it was very difficult to ensure the stitches went all the way through. He was worried about the efficacy of the connection. He also stated that the inflammation was unusual and that it was possible that if they had earlier diagnosed the inflammation as the cause of the restriction it might have been possible to avoid surgery and treating the inflammation would have cleared the restrictions on the vessels. I asked again if this might be related either to Covid or to the vaccine. This time he said that he did not know and that he would consult with others. He also reported that he took a small part of the aorta out and had sent it to the lab for testing. He did not indicate which tests they would do or what they were looking for specifically. Operative Findings - per Dr. notes in MyChart: 1. The entire ascending aorta was noted to be significantly inflamed and thickened. The thickness of the aorta was noted to be approximately 5 to 6 mm in thickness. Because of the thickened aortic leaflets very hard to place an aortic cannula, antegrade catheter and placement of the proximal graft. Initially the plan was to do 2 bypasses to the left system 1 to the left anterior descending artery using the internal mammary artery and vein to the first obtuse marginal branch using a saphenous vein. Because of the inflammatory condition of the aorta it was decided to place only 1 bypass using the left internal mammary artery to the left system. This was done to avoid any unnecessary manipulation of the ascending aorta. The above-mentioned findings are consistent with aortitis. 2. The left anterior descending artery was noted with approximately 2 mm in diameter. 3. The distal right coronary artery was noted to be approximately 2.5 mm in diameter but slightly inflamed. Patient made it to her ICU room (436) and late Thursday evening was extubated and went for a CT to see if they could see the inflammation. That night she had to go on Bipap to help her oxygenation. Per lab work - became very acidotic requiring Bipap post extubation that evening. 6/18/21: Friday, she continued Bipap to maintain oxygenation. She had a heart rate issue late in the morning and had to have a pace maker attached. Dr came back on Friday and said that he had talked to other doctors and they were going to refer patient to a Rheumatologist at OSU to evaluate if she has an autoimmune disease. 2 U RBCs for low Hgb. No s/s of active bleeding 6/19/21: Saturday went smoothly. She came off Bipap. She was able to get up and walk out to the hall. Chest Tubes, Cordis and foley removed. TR to SE6 stepdown unit. Restarted on beta blocker 6/20/21: Sunday She went to the bathroom and got cleaned up. The nurse changed the dressings on her incisions. 6/22/21: Echo completed. Ambulated in the hall. Discharged home.

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Praegender Schweregrund: Intensive care
Hospital-Tage: 7,0
Labordaten: Too many results to report. Will obtain from medical team and provide at a later date. Per the medical team all of my chemistries, hematology, cardiac work-up labs were all negative. Auto-Immune work up in progress.
Aktuelle Erkrankungen: none
Vorgeschichte: GERD
Andere Medikamente: Cymbalta, Nexium
Allergien: none
Vorherige Impfungen: -

VAERS 1427798

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: CA
Alter: 69,0
Geschlecht: F
Eingang: 25.06.2021
Impfdatum: 23.01.2021
Beginn: 24.01.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / RA

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

Cardiac monitoring Euphoric mood Laboratory test Loss of consciousness

Symptomtext

Felt high later in day and into night 2:30am got up to use restroom returning to bed passed out trying to into bed passed out again took things slow next day and stayed in bed and ate very little mon-wed getting better each day thur felt like I was going to pass out again called Dr and said sound like I was getting better if I pass out go straight to ER It took a good week to get back to normal

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Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: wore a heat monitor for a week everything ok blood tests were actually better a month later after the shot
Aktuelle Erkrankungen: none
Vorgeschichte: removal of thyroid yeast infection
Andere Medikamente: Synthroid 112 mg Fluzonazole 200 mg metamucil Nystatin cream calcium 500 mg VetD3 2000IU saline nasal mist refresh optive systan over night
Allergien: sulfa
Vorherige Impfungen: -

VAERS 1409512

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011j20a

schwer

Staat: KS
Alter: 40,0
Geschlecht: F
Eingang: 18.06.2021
Impfdatum: 11.01.2021
Beginn: 11.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / LA

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

Anaphylactic reaction Blood pressure measurement Dysgeusia Erythema Fatigue Feeling hot Headache Heart rate Heart rate irregular Irritability Nausea Oxygen saturation Pallor Pruritus Swelling face Urticaria Vaccination complication Vaccination site pruritus

Symptomtext

Heart rate irregular; vision was blurry; pale; face was itchy/itching all over body sporadic and not localized; Redness in face/blotchy red hot; metallic taste afte the vaccine was administered; anaphylatic reaction; warmness up the arm and into the neck after getting the vaccine; facial swelling; Hives; Irritable; didn't feel good/truck ran over her; Vaccination site warmth; itchiness at injection site; Fatigue; Headache; Nausea; This spontaneous case was reported by a nurse (subsequently medically confirmed) and describes the occurrence of ANAPHYLACTIC REACTION (anaphylatic reaction) in a 40-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 011j20a) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concurrent medical conditions included Sulfonamide allergy (developed hives and stomach upset when young adult) and Drug allergy (Erythromycin -developed hives when young adult). On 11-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intravenous) 1 dosage form. On 11-Jan-2021, the patient experienced ANAPHYLACTIC REACTION (anaphylatic reaction) (seriousness criterion medically significant), FEELING HOT (warmness up the arm and into the neck after getting the vaccine), SWELLING FACE (facial swelling), URTICARIA (Hives), IRRITABILITY (Irritable), VACCINATION COMPLICATION (didn't feel good/truck ran over her), PALLOR (pale), PRURITUS (face was itchy/itching all over body sporadic and not localized), ERYTHEMA (Redness in face/blotchy red hot), DYSGEUSIA (metallic taste afte the vaccine was administered), VACCINATION SITE WARMTH (Vaccination site warmth), VACCINATION SITE PRURITUS (itchiness at injection site), FATIGUE (Fatigue), HEADACHE (Headache) and NAUSEA (Nausea). On 15-Jan-2021, the patient experienced VISION BLURRED (vision was blurry). On an unknown date, the patient experienced HEART RATE IRREGULAR (Heart rate irregular). The patient was treated with ONDANSETRON (ZOFRAN [ONDANSETRON]) on 11-Jan-2021 for Nausea, at an unspecified dose and frequency; DIPHENHYDRAMINE HYDROCHLORIDE (BENADRYL ALLERGY [DIPHENHYDRAMINE HYDROCHLORIDE]) on 11-Jan-2021 for Nausea, at an unspecified dose and frequency; EPINEPHRINE on 11-Jan-2021 at an unspecified dose and frequency and PREDNISONE on 11-Jan-2021 at an unspecified dose and frequency. On 19-Jan-2021, ANAPHYLACTIC REACTION (anaphylatic reaction) had resolved. At the time of the report, FEELING HOT (warmness up the arm and into the neck after getting the vaccine), SWELLING FACE (facial swelling), URTICARIA (Hives), IRRITABILITY (Irritable), VACCINATION COMPLICATION (didn't feel good/truck ran over her), PALLOR (pale), PRURITUS (face was itchy/itching all over body sporadic and not localized), ERYTHEMA (Redness in face/blotchy red hot), VACCINATION SITE PRURITUS (itchiness at injection site), FATIGUE (Fatigue), HEADACHE (Headache) and NAUSEA (Nausea) had resolved, VISION BLURRED (vision was blurry) had not resolved and DYSGEUSIA (metallic taste afte the vaccine was administered), HEART RATE IRREGULAR (Heart rate irregular) and VACCINATION SITE WARMTH (Vaccination site warmth) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 11-Jan-2021, Blood pressure measurement (120-80 mmHg): 104/60 mmHg (Inconclusive) at 10:16 am and 164/90 mmHg (Inconclusive) at 10:25 am. On 11-Jan-2021, Heart rate: 129 (Inconclusive) at 10:16 am, 79 (Inconclusive) at 10:20 am and 125 (Inconclusive) at 10:25 am. On 11-Jan-2021, Oxygen saturation: 84 (Inconclusive) 84 and 97 (Inconclusive) 97. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intravenous) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intravenous), the reporter did not provide any causality assessments. The patient received the vaccine at 9:50 am on 11-Jan-2021 and returned to the room at 10:10 am with the symptoms. EMS was notified and Epi Pen administered at 10:16 am. The patient's oxygen saturation was initially 80% and the hands were very cold. The patient was transported to ER and was dismissed later on in the day. The signs and symptoms of anaphylactic reaction were reported as itching/pruritis, hives/uriticria, irregular heart rate/palpitations, nausea, difficulty breathing, swelling of upper airway, sensation of throat closing, angioedema, prickling/tingling sensation, feeling hot and flushing. Based on the current available information and temporal association between the use of the product and the start date of the events, a causal relationship cannot be excluded. Most recent FOLLOW-UP information incorporated above includes: On 26-Jan-2021: Additional event was updated. On 14-Apr-2021: The diagnosis, symptoms, patient information and vaccination site details were updated.; Sender's Comments: Based on the current available information and temporal association between the use of the product and the start date of the events, a causal relationship cannot be excluded.

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Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: Test Date: 20210111; Test Name: Blood pressure; Test Result: Inconclusive ; Result Unstructured Data: at 10:16 am; Test Date: 20210111; Test Name: Blood pressure; Test Result: Inconclusive ; Result Unstructured Data: at 10:25 am; Test Date: 20210111; Test Name: Pulse rate; Test Result: Inconclusive ; Result Unstructured Data: at 10:16 am; Test Date: 20210111; Test Name: Pulse rate; Test Result: Inconclusive ; Result Unstructured Data: at 10:20 am; Test Date: 20210111; Test Name: Pulse rate; Test Result: Inconclusive ; Result Unstructured Data: at 10:25 am; Test Date: 20210111; Test Name: O2 Saturation; Test Result: Inconclusive ; Result Unstructured Data: 84; Test Date: 20210111; Test Name: O2 Saturation; Test Result: Inconclusive ; Result Unstructured Data: 97
Aktuelle Erkrankungen: Drug allergy (Erythromycin -developed hives when young adult); Sulfonamide allergy (developed hives and stomach upset when young adult)
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1323329

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: NC
Alter: 34,0
Geschlecht: F
Eingang: 17.05.2021
Impfdatum: 05.01.2021
Beginn: 25.04.2021
Tage bis Beginn: 110,0
Dosis: 1
Route/Site: IM / LA

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

Blindness Blood test Breast pain Chills Cognitive disorder Computerised tomogram Confusional state Decreased appetite Dyskinesia Electrocardiogram Exposure during pregnancy Fatigue Feeling abnormal Formication Full blood count Headache Heart rate increased Hypoaesthesia

Symptomtext

-received vaccine while pregnant: normal pregnancy except for vision loss Feb 2nd -baby born on due date, no complications, healthy weight (6 lbs 15.8 oz) and baby is healthy SYMPTOMS 3 months post-vaccine, over a 3 week period beginning 4/25/21: -tingling and "crawling sensation" in arms, legs, left side of head, left ear -extreme headache, fatigue, jerking/convulsions, extreme muscle weakness -ER visit 5/9/21: CT, EKG, labs all normal -fever up to 102F, increased pulse -loss of appetite -numbness in extremities -nerve pain -breast pain -chills and night sweats -pronounced weakness -tongue ulcer -cognitive issues such as brain fog, confusion

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Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: 5/6/21: vit D, thyroid, vit B12, and A1c blood tests ALL NORMAL 5/9/21: CT scan, EKG, CBC and blood tests ALL NORMAL 5/11/21: CBC (WBCs slightly elevated) and blood test for Lyme's disease NEGATIVE 5/14/21: ultrasound of the right breast (no lump noted) 5/14/21: MRI (to rule out MS) no results yet
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: an over-the-counter prenatal vitamin
Allergien: no known allergies
Vorherige Impfungen: -

VAERS 1304129

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: NY
Alter: 58,0
Geschlecht: F
Eingang: 10.05.2021
Impfdatum: 31.01.2021
Beginn: 31.01.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Anaphylactic reaction

Symptomtext

Anaphylatic reaction after injection- treated in hospital

Weitere VAERSDATA-Felder

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

VAERS 916177

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: SD
Alter: 34,0
Geschlecht: F
Eingang: 10.05.2021
Impfdatum: 31.12.2020
Beginn: 31.12.2020
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / AR

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

Burning sensation COVID-19 Diarrhoea Dizziness Dyspnoea Feeling abnormal Heart rate increased Hypotension Immediate post-injection reaction Loss of consciousness Nausea Oral mucosal eruption Palpitations Rash Rash erythematous SARS-CoV-2 test negative SARS-CoV-2 test positive Tachycardia

Symptomtext

Immediately, felt nauseated and dizzy. I started throwing up about 30 minutes after vaccine. They gave me an IV and some Zofran. They monitored for me for an hour while I got two bags of IVs. I still felt nauseated when I left for lunch. I couldn't eat. I started throwing up again after lunch and I had two episodes of diarrhea. Felt short of breath (not wheezing) and face felt like it was burning. I rash and it was red and burning around my mouth and face. I felt really dizzy and light headed and they took me back to a treatment room. I felt like I was going to pass out. I couldn't stop throwing up at all - at that point. They put the vital signs machine on my - O2 was 84; I had low blood pressure; and I was really tachycardia - it was 135 - was very high. They gave epinephrine; Benadryl - 50 mg; solumedrol - 125 mg. I have an anaphylactic care plan in my chart because of my latex allergies. I think they gave me everything off of that. I started wheezing. I believe I passed out. When I came coherent again - I was in an ambulance with breathing mask and IVs. They took me to ER to monitor me. They monitored me for three hours - I don't believe they did an epi-drip but they were seeing if they needed to start one. I think they gave me a second epi-injection in the ambulance. They gave me steroids and told me to use my antihistamine (already had Zyrtec). They gave me a higher dose of prednisone - they dosed me to 20mg instead of my daily 5. Those helped with my symptoms. On the 4th, I had a negative result for COVID - my heart rate was still crazy - super high - felt like I was having palpitations . So On Tuesday, the 5th, when I went back to follow up, I had COVID. I was still feeling horrible and having all kinds of symptoms. They had tested me for COVID before coming into clinic - and I was positive. I took OTC stuff at home for COVID. I still have ongoing heart palpitations/ tachycardia. that I experience. I saw an allergy specialist after getting a doctor referral - he just said don't take the Moderna vaccine again. I still have to see a cardiologist . I have a repeat cardio/echogram tomorrow. They put me on Pepcid.

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Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Jan 4 - COVID - negative - Jan 5 - COVID -positive result on the 5th -
Aktuelle Erkrankungen: no
Vorgeschichte: asthma; rheumatoid arthritis
Andere Medikamente: Celebrex; Prednisone; Zyrtec
Allergien: Wasps; Latex; Compazine; Tubersol
Vorherige Impfungen: Tubersol - 2009 - what they use to inject you with - this was for PPD injection

VAERS 1295224

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: NH
Alter: 58,0
Geschlecht: M
Eingang: 07.05.2021
Impfdatum: 28.01.2021
Beginn: 04.05.2021
Tage bis Beginn: 96,0
Dosis: 1
Route/Site: IM / LA

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

Deep vein thrombosis Ultrasound scan abnormal

Symptomtext

LEFT LOWER EXTREMITY DEEP VENOUS THROMBOSIS

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Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: -
Labordaten: ULTRASOUND 05/06/21
Aktuelle Erkrankungen: INSOMNIA
Vorgeschichte: INSOMNIA
Andere Medikamente: AMBIEN
Allergien: REGLAN
Vorherige Impfungen: -

VAERS 1272205

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: MI
Alter: 68,0
Geschlecht: F
Eingang: 29.04.2021
Impfdatum: 01.01.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: OT / -

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

Thrombosis

Symptomtext

Blood clots; This spontaneous case was reported by a consumer and describes the occurrence of THROMBOSIS (Blood clots) in a 68-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 011J20A and 038K20A) for COVID-19 vaccination. No Medical History information was reported. On 01-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 05-Feb-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On an unknown date, the patient experienced THROMBOSIS (Blood clots) (seriousness criterion medically significant). At the time of the report, THROMBOSIS (Blood clots) outcome was unknown. Not Provided No concomitant medications were reported. The patient had no problems after her second dose. Treatment information was not provided. Action taken with mRNA-1273 in response to events was not applicable. Company comment: Based on the current available information and temporal association between the use of the product and the start date of the events, a causal relationship cannot be excluded.; Sender's Comments: Based on the current available information and temporal association between the use of the product and the start date of the events, a causal relationship cannot be excluded.

Weitere VAERSDATA-Felder

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

VAERS 2628148

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: KS
Alter: 68,0
Geschlecht: F
Eingang: 26.04.2021
Impfdatum: 30.12.2020
Beginn: 31.12.2020
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Anticoagulant therapy Arthralgia Back pain Blood cholesterol Brain fog Chest X-ray abnormal Computerised tomogram Computerised tomogram thorax abnormal Flank pain Gait disturbance Headache Impaired work ability Influenza virus test negative Insomnia Joint swelling Laboratory test Mobility decreased Muscle spasms

Symptomtext

12/31/20 Severe Brain Fog. Several events, but mainly administering wrong meds to wrong person at work. In 26 yrs. had never done that & wrote an med error due to vaccine. 1/3/21 Felt like I had been hit by a truck. Pain in rt side, back & shoulders. Not able to sleep. Called boss - had over 300 hrs of sick leave. 1/5/21 Saw Dr at clinic. 1/5/21 Dr - clinic - Had pneumonia in rt lung (X-ray) Possible blood clot - Lab - CT scan - 3 blood clots in rt. lung. Gave me muscle relaxer for back spasms & shot for pain. Returned to ER for 2 shots in stomach for blood clots. 1/6/21 Began taking Eliquis (blood thinners). 1/8/21 Back to clinic - pain - P.A. - pain pills. 1/9/21 Decided to sleep in recliner knew I could not make it out of bed. Was using ice & heat on my back & left knee was swollen. At 4:00 a.m. realized stuck in chair. Called daughter-in-law 1/10/21 to take me to ER. Saw PA. X-rays chest & Lft. (Knee (normal wear & tear). More pain pills & shot. Went to stay w/ my son & wife. Borrowed a walker and had to be assisted to bathroom. 1/12/21 Worse headache & neck pain. Requested trip to ER I held my head the 40 miles to hospital & my left knee was swollen double. Admitted to Medical Center. Had Covid & Flu test (both negative) Another CT scan. Gave me steroids and leg (knee) was fine by Wed. I was put on Oxygen and was sent home w/ 4 tanks. Remained on blood thinners. I remained w/ my son & wife for a few days. Still had some brain fog after arriving at my home. 4/9/21 I saw Dr. Tested my cholesterol as he took me off statin and putting me on another drug. I am continuing to take blood thinners. Plan to return 2 oxygen tanks. Will not take the 2nd vaccine. The County Health Nurse who gave me the vaccine refused to submit the reaction. She called me and my daughter in law called her when I went into the hospital. Later she told me my provider had to report it.

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Praegender Schweregrund: Pulmonary thrombosis
Hospital-Tage: 3,0
Labordaten: 1/5/21 Lab-X-ray-CT-scan 1/10/21 X-rays-Chest Lft knee 1/12/21 Covid & Flu test neg CT Scan
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Excedrine, Synthroid, Areds-Eye Multi-vitamin Statin & Effexor
Allergien: Penicillin, Codeine, Floride
Vorherige Impfungen: -

VAERS 1235495

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: MA
Alter: -
Geschlecht: F
Eingang: 21.04.2021
Impfdatum: 26.03.2021
Beginn: 27.03.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: OT / -

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

Blood phosphorus Chills Diarrhoea Dizziness Electrocardiogram Feeling abnormal Hyperhidrosis Hypotension Nausea Syncope Vomiting

Symptomtext

extreme dizziness; fainted; unable to get a reading because the pressure was so low; diarrhea; felt like I was hallucinating; sweating; shivering; vomiting; nausea; This spontaneous case was reported by a consumer and describes the occurrence of SYNCOPE (fainted) in a 40-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 011J20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included No adverse event (No reported medical history). On 26-Mar-2021 at 1:45 PM, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 27-Mar-2021, the patient experienced HYPOTENSION (unable to get a reading because the pressure was so low), DIARRHOEA (diarrhea), FEELING ABNORMAL (felt like I was hallucinating), HYPERHIDROSIS (sweating), CHILLS (shivering), VOMITING (vomiting) and NAUSEA (nausea). On 27-Mar-2021 at 1:30 AM, the patient experienced SYNCOPE (fainted) (seriousness criterion medically significant) and DIZZINESS (extreme dizziness). 27-Mar-2021 at 1:30 AM, the patient experienced LOSS OF CONSCIOUSNESS (lost consciousness) (seriousness criterion medically significant). At the time of the report, SYNCOPE (fainted), DIZZINESS (extreme dizziness), DIARRHOEA (diarrhea) and VOMITING (vomiting) had resolved and HYPOTENSION (unable to get a reading because the pressure was so low), FEELING ABNORMAL (felt like I was hallucinating), HYPERHIDROSIS (sweating), CHILLS (shivering) and NAUSEA (nausea) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 27-Mar-2021, Blood phosphorus: 0.6 mg/dl and 4.7 mg/dl. On 27-Mar-2021, Electrocardiogram: abnormal (abnormal) elongated heart rhythm (Arrhythmias) and normal normal. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Treatment for the events included IV fluids and oral phosphorus.; Sender's Comments: Based on the current available information and temporal association between the use of the product and the start date of the events, a causal relationship cannot be excluded.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Test Date: 20210327; Test Name: blood phosphorus; Test Result: Inconclusive ; Result Unstructured Data: 0.6; Test Date: 20210327; Test Name: blood phosphorus; Test Result: Inconclusive ; Result Unstructured Data: 4.7; Test Date: 20210327; Test Name: ECG; Result Unstructured Data: elongated heart rhythm (Arrhythmias); Test Date: 20210327; Test Name: ECG; Result Unstructured Data: normal
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: No adverse event (No reported medical history)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2635900

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: -
Alter: 55,0
Geschlecht: M
Eingang: 19.04.2021
Impfdatum: 02.02.2021
Beginn: 15.03.2021
Tage bis Beginn: 41,0
Dosis: 1
Route/Site: IM / RA

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

Thrombosis

Symptomtext

Blood clot developed in the posterior lower right leg Narrative:

Weitere VAERSDATA-Felder

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

VAERS 1229047

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: IA
Alter: 43,0
Geschlecht: F
Eingang: 19.04.2021
Impfdatum: 07.01.2021
Beginn: 18.01.2021
Tage bis Beginn: 11,0
Dosis: UNK
Route/Site: IM / AR

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

Anticoagulant therapy Antiphospholipid antibodies Antithrombin III Cerebral venous sinus thrombosis Computerised tomogram head Factor V Leiden mutation Headache Magnetic resonance imaging head Protein C Protein S Ultrasound Doppler Venogram

Symptomtext

Hospitalized with cerebral venous sinus thrombosis from 1/26/2021-1/29/2021. Presented with severe headache. Treatment included anticoagulation initially with heparin infusion, followed by oral anticoagulation with Eliquis. She required prescription medications for management of headache. Discharged home with ongoing headache.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebral venous sinus thrombosis
Hospital-Tage: 3,0
Labordaten: CT brain (1/26/21) MRI/MRV brain (1/26/21) Lower extremity duplex (1/26/21) Labs (antiphospholipid antibody panel, protein C and S, antithrombin III, Factor V Leiden)
Aktuelle Erkrankungen: None
Vorgeschichte: Endometriosis
Andere Medikamente: Oral contraceptive (Desogestrel/Ethinyl Estradiol 0.15/0.03 mg Tylenol PRN Ibuprofen PRN
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 1220980

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: GA
Alter: 78,0
Geschlecht: F
Eingang: 16.04.2021
Impfdatum: 11.01.2021
Beginn: 09.03.2021
Tage bis Beginn: 57,0
Dosis: 2
Route/Site: OT / LA

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

Pain in extremity Skin discolouration Swelling Thrombosis

Symptomtext

Blood clot; Left leg pain; Discoloration (blue-purple); Swelling; This spontaneous case was reported by an other health care professional and describes the occurrence of THROMBOSIS (Blood clot), PAIN IN EXTREMITY (Left leg pain), SKIN DISCOLOURATION (Discoloration (blue-purple)) and SWELLING (Swelling) in a 78-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 011J20A and 013L20A) for COVID-19 vaccination. The patient's past medical history included Clot blood in 2010. Concurrent medical conditions included Drug allergy (Dalaudid, Ambien and Demerol) and Hypertension. Concomitant products included DAPAGLIFLOZIN PROPANEDIOL MONOHYDRATE (FARXIGA), GLIMEPIRIDE (AMARYL), ACETYLCARNITINE HYDROCHLORIDE (NEUROTIN [ACETYLCARNITINE HYDROCHLORIDE]), COLECALCIFEROL (CALTRATE VITAMIN D DAILY), MINERALS NOS, VITAMINS NOS (CENTRUM A TO ZINC) and VITAMIN D NOS for an unknown indication. On 11-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On an unknown date, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 09-Mar-2021, the patient experienced PAIN IN EXTREMITY (Left leg pain) (seriousness criterion hospitalization), SKIN DISCOLOURATION (Discoloration (blue-purple)) (seriousness criterion hospitalization) and SWELLING (Swelling) (seriousness criterion hospitalization). On an unknown date, the patient experienced THROMBOSIS (Blood clot) (seriousness criterion hospitalization). At the time of the report, THROMBOSIS (Blood clot), PAIN IN EXTREMITY (Left leg pain), SKIN DISCOLOURATION (Discoloration (blue-purple)) and SWELLING (Swelling) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Patient was sent to hospital to remove clots. The patient stated that the clot was 2/3 size of thigh. The patient scheduled to have a second procedure in May to remove blockages from iliac. Action taken with mRNA-1273 was not applicable. Based on the current available information and temporal association between the use of the product and the onset date of the reported events, a causal relationship cannot be excluded. Prior medical history of blood clot is considered a significant risk factor.; Sender's Comments: Based on the current available information and temporal association between the use of the product and the onset date of the reported events, a causal relationship cannot be excluded. Prior medical history of blood clot is considered a significant risk factor.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Hypertension
Vorgeschichte: Medical History/Concurrent Conditions: Clot blood; Drug allergy (Dalaudid, Ambien and Demerol)
Andere Medikamente: FARXIGA; AMARYL; NEUROTIN [ACETYLCARNITINE HYDROCHLORIDE]; CALTRATE VITAMIN D DAILY; CENTRUM A TO ZINC; VITAMIN D NOS
Allergien: -
Vorherige Impfungen: -

VAERS 2046296

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: KS
Alter: 59,0
Geschlecht: F
Eingang: 15.04.2021
Impfdatum: 03.02.2021
Beginn: 11.04.2021
Tage bis Beginn: 67,0
Dosis: 1
Route/Site: IM / LA

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

Condition aggravated Nausea Photopsia Seizure

Symptomtext

Client phoned to report that she experienced a seizure occuring on 4/11/21 in the early evening. She was riding in the back seat of a vehicle and became nauseus and began seeing flashing lights. She was taken by her husband to the nearest ED where they stabilized her. She has never had seizure activity before. Does have occasional migraines which are accompanied by flashing lights. Client is scheduled for an MRI on 4/15/21. She has not had any seizure activity since the episode on 4/11/21 Vaccination Dates: Dose 1 on 1/6/21 Dose 2 on 2/3/21

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: MRI scheduled for 4/15/21
Aktuelle Erkrankungen: None
Vorgeschichte: Hyperthyroidism
Andere Medikamente: Zoloft, Methimazole, Tennolol; Clonazepam
Allergien: Cipro
Vorherige Impfungen: -

VAERS 1181614

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: GA
Alter: 78,0
Geschlecht: F
Eingang: 08.04.2021
Impfdatum: 11.01.2021
Beginn: 09.03.2021
Tage bis Beginn: 57,0
Dosis: 1
Route/Site: IM / LA

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

Pain in extremity Peripheral swelling Skin discolouration Thrombosis

Symptomtext

Moderna EUA Pt started having left leg pain, discoloration (blue-purple) and swelling on 3/9/2021. Pt went to the hospital and was later called to come back to the hospital because she had a blood clot. Pt was sent to clinic and had a procedure by to remove clots. Pt states that the clot was "2/3 size of thigh." Pt states that she is scheduled to have a second procedure in May to remove blockages from iliacs.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: See description above. Pt did not provide any specific lab results. States that her doctor was supposed to submit VAERS report.
Aktuelle Erkrankungen: -
Vorgeschichte: Hx of blood clots on left popliteal 2010 Hypertension but seems to have resolves
Andere Medikamente: Forsega Amaryl Neurotin Vitamins- Caltrate, Centrum, Vit D
Allergien: Demerol Dalaudid Ambien
Vorherige Impfungen: -

VAERS 1178260

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: PR
Alter: 37,0
Geschlecht: F
Eingang: 07.04.2021
Impfdatum: 04.01.2021
Beginn: 02.02.2021
Tage bis Beginn: 29,0
Dosis: 1
Route/Site: OT / LA

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

Asthenia Asthma Contusion Deep vein thrombosis Dyspnoea Fatigue Feeling abnormal Haemoglobin Red blood cell count Tachycardia Vaccination complication

Symptomtext

This spontaneous case was reported by a nurse (subsequently medically confirmed) and describes the occurrence of DEEP VEIN THROMBOSIS (Venous thrombosis in her left leg/clot was in left leg) in a 37-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 011M20A and 011J20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concomitant products included LEVOTHYROXINE SODIUM (SYNTHROID) and TOPIRAMATE (TOPAMAX) for an unknown indication. On 04-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 02-Feb-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 02-Feb-2021, the patient experienced TACHYCARDIA (Severe Tachycardia/ Still very tachycardia) and FEELING ABNORMAL (Felt a little weird). On 03-Feb-2021, the patient experienced DYSPNOEA (Difficulty breathing), FATIGUE (Could not get up), ASTHMA (Asthma) and ASTHENIA (Could not get up). On 04-Feb-2021, the patient experienced CONTUSION (Bruise on her right and left leg) and VACCINATION COMPLICATION (Had a reaction to the vaccine). On 01-Mar-2021, the patient experienced DEEP VEIN THROMBOSIS (Venous thrombosis in her left leg/clot was in left leg) (seriousness criterion medically significant). On an unknown date, the patient experienced HAEMOGLOBIN DECREASED (Hemoglobin decreased) and RED BLOOD CELL COUNT DECREASED (Red blood cells are low). At the time of the report, DEEP VEIN THROMBOSIS (Venous thrombosis in her left leg/clot was in left leg), TACHYCARDIA (Severe Tachycardia/ Still very tachycardia), DYSPNOEA (Difficulty breathing), FEELING ABNORMAL (Felt a little weird), FATIGUE (Could not get up), ASTHMA (Asthma), CONTUSION (Bruise on her right and left leg), ASTHENIA (Could not get up), VACCINATION COMPLICATION (Had a reaction to the vaccine), HAEMOGLOBIN DECREASED (Hemoglobin decreased) and RED BLOOD CELL COUNT DECREASED (Red blood cells are low) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): In March 2021, Haemoglobin: low gram per litre (Low) LOW. In March 2021, Red blood cell count: low cells per microlitre (Low) LOW. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Treatment informations reported were Levalbuterol tartrate and Rivaroxaba 20 mg This case was linked to MOD-2021-059897 (Patient Link).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: -
Labordaten: Test Date: 202103; Test Name: hemoglobin; Result Unstructured Data: LOW; Test Date: 202103; Test Name: Red blood test; Result Unstructured Data: LOW
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: No adverse event (No reported medical history.)
Andere Medikamente: SYNTHROID; TOPAMAX
Allergien: -
Vorherige Impfungen: -

VAERS 1176103

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: CA
Alter: 25,0
Geschlecht: F
Eingang: 07.04.2021
Impfdatum: 23.12.2020
Beginn: 01.03.2021
Tage bis Beginn: 68,0
Dosis: 2
Route/Site: SYR / RA

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

Computerised tomogram pelvis abnormal Peripheral artery thrombosis Scan with contrast abnormal Thrombosis Ultrasound abdomen abnormal

Symptomtext

Pelvic blood clot in right common iliac artery

Weitere VAERSDATA-Felder

Praegender Schweregrund: Peripheral artery thrombosis
Hospital-Tage: -
Labordaten: Ultra sound, CT scan with contrast
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Birth control - Nikki Trazodone Hydroxyzine Pam Sertraline
Allergien: None
Vorherige Impfungen: -

VAERS 1163187

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: NY
Alter: 72,0
Geschlecht: F
Eingang: 03.04.2021
Impfdatum: 18.01.2021
Beginn: 22.03.2021
Tage bis Beginn: 63,0
Dosis: 2
Route/Site: IM / UN

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

Angiogram pulmonary normal Borrelia test negative C-reactive protein increased Chest pain Electrocardiogram ST segment depression Neutrophil percentage increased Pericarditis Procalcitonin increased Pyrexia Troponin normal White blood cell count increased

Symptomtext

Pt presented to the ER on 3/22/21 c/o sudden chest pain and fever of 101.1. She was transferred to the hospital due to concern for possible acute MI. She was ultimately found to have idiopathic pericarditis after further work up and discharged home on colchicine 2 days later.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: 2,0
Labordaten: CTA chest neg for pulmonary emboli WBC 13.6 with 88% neutrophils CRP 118.9 Troponin <0.01 Lyme titer neg procalcitonin 2.77 ekg with diffuse ST segment depression
Aktuelle Erkrankungen: None
Vorgeschichte: Hx CAD 2013 stent to LAD, hyperlipidemia
Andere Medikamente: Asa 81mg daily, Famotidine 20mg bid, rosuvastatin 20mg daily, estridiol 0.01%
Allergien: nkda
Vorherige Impfungen: -

VAERS 1151059

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: NY
Alter: 71,0
Geschlecht: F
Eingang: 31.03.2021
Impfdatum: 19.01.2021
Beginn: 13.01.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: OT / LA

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

Erythema Feeling hot Illness Influenza like illness Injection site erythema Loss of consciousness Pain Pruritus Pyrexia Sensitive skin Vaccination site reaction

Symptomtext

warm to touch; Red cheeks; almost flu like symptoms; sick; knocked out; Fever of 102 F; delayed cutaneous hypersensitive arm; sore; itching; covid arm; red at injection site; A spontaneous report was received from a consumer concerning 71year old, female patient who received Moderna's COVID-19 vaccine (mRNA-1273) and developed redness/erythema , warm to touch/feeling hot, cutaneous hypersensitive arm/cutaneous sympoms, injection site was red/ vaccination site erythema, hot, sore/pain and itching/pruritus, like COVID arm/vaccination site reaction. After the second shot of vaccine she got sick/sickness, fever of 102 F/pyrexia, flu like symptoms/influenza like illness and was knocked out/loss of consciousness. The patient's medical history was not provided. Concomitant product use was not provided by the reporter. The patient received their first of two planned doses of mRNA-1273 (Batch number: 011J20A) on 19 Jan 2021. On 21 Feb 2021, approximately on the same day prior to the onset of the symptoms, the patient received their second of two planned doses of mRNA-1273 (Batch number: 013L20A) intramuscularly in the left arm for prophylaxis of COVID-19 infection. Consumer had reported that 12 days after receiving the first dose, patient experienced delayed cutaneous hypersensitive arm. Arm was red at injection site, which later spread to whole upper arm. The injection site was re, hot, sore, itchy like COVID arm. Which was resolved later, and she had taken diphenhydramine for it. After receiving her second dose of vaccine she got sick, fever of 102 F, knocked out, almost flu like symptoms. which lasted for couple of days and was resolved on 23 Feb 2021. For which she had taken acetaminophen for it. Also, she had red cheeks, warm to touch for last few days, almost 2 weeks after her 2nd dose of vaccine. Treatment for the event included diphenhydramine and acetaminophen. The patient received both scheduled doses of mRNA-1273 prior to the events; therefore, action taken with the drug in response to the events is not applicable. The outcome of the events, redness, warm to touch, cutaneous hypersensitive arm, injection site was red, hot, sore and itchy like COVID arm were considered resolved and for she got sick, fever of 102 F, knocked out and flu like symptoms was unknown.; Reporter's Comments: Based on the current available information and temporal association between the use of the product and the start date of the event, a causal relationship cannot be excluded.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: No adverse event (No reported medical history)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1137215

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: CA
Alter: -
Geschlecht: F
Eingang: 26.03.2021
Impfdatum: 12.01.2021
Beginn: 12.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / LA

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

Chest discomfort Dizziness Dyspnoea Injection site erythema Injection site reaction Loss of consciousness Nausea Pain Pyrexia

Symptomtext

passed out about 7 to 8 times; Pain on the right side of body; Dizziness; Felt like golf ball in right chest; Couldn't breathe; Nausea; Fever; Injection site redness; Outer part of the skin is bumpy; A spontaneous report was received from a consumer, a 46-year-old female patient, who was administered Moderna's COVID-19 vaccine (mRNA-1273) and experienced passed out about 7 to 8 times/loss of consciousness, pain on the right side of body/pain, dizziness, felt like golf ball in right chest/chest discomfort, couldn't breathe/dyspnea, nausea, fever/pyrexia, injection site redness/injection site erythema and outer part of the skin is bumpy/injection site reaction. The patient's medical history included was migraine. Product known to have been used by the patient, within two weeks prior to the event, included was ibuprofen for migraine. On 12 Jan 2021, the patient received their first of two planned doses of mRNA-1273 (Lot number: 011J20A) intramuscularly in her left arm for prophylaxis of COVID-19 infection. On 12 Jan 2021, the patient experienced feeling a lot of pain on the right side of her body and the shot was given on her left arm. Fever, nauseous, supper dizzy, passed out about 7 to 8 times, felt like she got a golf ball in her right chest, red on the injection site, the outer part of the skin is all bumpy, couldn't breathe. Treatment for the events included were ibuprofen and diclofenac injection. The Action taken with the second dose of mRNA-1273 in response to the event was not reported. The outcome of the events, passed out about 7 to 8 times/loss of consciousness, pain on the right side of body/pain, dizziness, felt like golf ball in right chest/chest discomfort, couldn't breathe/dyspnea, nausea, fever/pyrexia, injection site redness/injection site erythema and outer part of the skin is bumpy/injection site reaction were considered as unknown.; Reporter's Comments: Based on the current available information and temporal association between the use of the product and the start date of the events, a causal relationship cannot be excluded. Further information has been requested.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Migraine
Vorgeschichte: -
Andere Medikamente: ADVIL [IBUPROFEN]
Allergien: -
Vorherige Impfungen: -

VAERS 1116226

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: FL
Alter: -
Geschlecht: F
Eingang: 19.03.2021
Impfdatum: 05.01.2021
Beginn: 05.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / -

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

Bell's palsy Erythema Peripheral swelling

Symptomtext

Bell's palsy; Firm red swollen arm; Firm red swollen arm; A spontaneous report was received from a consumer concerning a female patient who received Moderna's COVID-19 vaccine (mRNA-1273) and developed firm red (erythema), swollen arm (peripheral swelling) and bell's palsy. The patient's medical history was not provided. No relevant concomitant medications were reported. On 05 Jan 2021, prior to the onset of the events, the patient received their first of two planned doses of mRNA-1273 (Batch number: 011J20A) for prophylaxis of COVID-19 infection. On 05 Jan 2021, the patient developed firm red swollen arm. On 22 Jan 2021, the patient experienced medically significant event of symptoms of bell's palsy. No treatment information was provided. Action taken with mRNA-1273 in response to the events developed firm red (erythema), swollen arm (peripheral swelling) and Bell's palsy was not reported. The outcome of the event firm red (erythema) and swollen arm (peripheral swelling) was resolved on an unspecified date. The outcome of the event bell's palsy was not reported.; Reporter's Comments: Based on the current available information and temporal association between the use of the product and the start date of the events, a causal relationship cannot be excluded. Further information has been requested.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: No adverse event (No recorded medical history)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1111333

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: CA
Alter: 72,0
Geschlecht: F
Eingang: 18.03.2021
Impfdatum: 17.02.2021
Beginn: 17.01.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: OT / -

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

Chills Erythema Injection site erythema Injection site induration Injection site pruritus Injection site swelling Loss of consciousness Myalgia Pruritus

Symptomtext

Blackout and Had to go to Bed; Red From Shoulder to elbow; Intense itching From Shoulder to elbow; Mild Chills; Hard to the Touch; Swollen Injection Site.; Injection Site was Very Red (Golf Ball Size); Intense Itching 2-4" across on injection site; Muscle pain; A spontaneous report was received from a consumer concerning a 72-year-old female patients, who received Moderna's Covid 19 vaccine(mRNA1273) experienced muscle pain, itching across on injection site, injection site was very red (golf ball size), hard to the touch and swollen injection site, mild chills, started blackout, itching and redness from shoulder to elbow. The patient's medical history was not provided. Concomitant product use was not provided by the reporter. On 17 Feb 2021, prior to the onset of the symptom, the patient received their first of two planned doses of mRNA-1273 (Batch Number: 011J20A) intramuscularly for prophylaxis of COVID-19 infection. On 19 Feb 2021, approximately 2 hours prior to the onset of symptoms, the patient received second of two planned doses of mRNA-1273 (Batch Number: 41L20A) intramuscularly in the left arm for prophylaxis of COVID-19 infection. On 17 Feb 2021, the patient experienced muscle pain. On 19 Feb 2021, after two hours of vaccination, the patient experienced intense itching 2-4" across on injection site. Eight hours post second shot patient's injection site was very red (Golf Ball Size), hard to the touch and swollen. 25 hours after the injection patient developed mild chills followed by blackout and had to go bed, intense itching and redness from shoulder to elbow. Treatment for the event included Hydrocortisone cream. Action taken with mRNA-1273 in response to the events was not provided. The outcome of the events mild chills, started blackout, intense itching and was reported recovering. The outcome of the events itching across on injection site, injection site was very red (golf ball size), hard to the touch and swollen injection site was reported recovered. The outcome of the events muscle pain, itching and redness from shoulder to elbow was not reported.; Reporter's Comments: Based on the information provided which includes a strong temporal association, and the known safety profile of the mRNA-1273 vaccine, a causal association between the reported events and the administration of vaccine cannot be excluded.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: No adverse event (No medical history provided.)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 908550

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: CT
Alter: 48,0
Geschlecht: F
Eingang: 17.03.2021
Impfdatum: 24.12.2020
Beginn: 24.12.2020
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Blood pressure increased Electrocardiogram Hyperhidrosis Palpitations Presyncope Sinus rhythm Tachycardia

Symptomtext

Pt received 1st dose of vaccine and waited at least 30 minutes in the observation area. As she was driving home, developed tachycardic, diaphoresis, sweating, and felt pre-syncopal. Pulled over at pharmacy where she was given benadryl and an ambulance was called to transport her to the ED. In the ED, received famotidine 20mg PO and methylprednisolone 125mg IV and fluids. She was observed for 2 hours and discharged home with a prescription for prednisone 20mg BID x 3 days. Patient received 2nd dose of vaccine on 1/21/21 (Moderna, lot #012L20A) after premedicating with 25mg benadryl. While she was sitting in the observation area after vaccination, she developed sudden onset palpitations, sweating, and increased blood pressure. She was send to the ED and observed for 90 minutes, after which she was discharged with a referral to an allergist.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: 12/24/20: ECG normal sinus rhythm
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: MVI, miralax
Allergien: none
Vorherige Impfungen: -

VAERS 1105534

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: PR
Alter: 37,0
Geschlecht: F
Eingang: 16.03.2021
Impfdatum: 02.02.2021
Beginn: 06.02.2021
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: IM / LA

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

Asthenia Deep vein thrombosis Dyspnoea Haematoma Migraine Pain in extremity Peripheral swelling Skin warm Tachycardia Ultrasound Doppler abnormal

Symptomtext

Tachycardia for couple of days after the vaccination. Shortness of breath since the moment of the first dose. Pain on both legs after first dose. Severe Migraines on the second dose of the vaccine that lasted for 3 weeks. Hematoma on the leg without pain, with swelling. Leg pain with warmth sensation.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: -
Labordaten: Doppler of lower extremities. DX: Deep Vein Thrombosis on the left leg with partial obstruction of the popliteal vein.
Aktuelle Erkrankungen: Mitral valve
Vorgeschichte: Thyroid
Andere Medikamente: Topamax, sintroid, Wellbutrin.
Allergien: Shellfish
Vorherige Impfungen: -

VAERS 1078510

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: -
Alter: 29,0
Geschlecht: F
Eingang: 06.03.2021
Impfdatum: 27.02.2021
Beginn: 28.02.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / RA

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

Syncope

Symptomtext

syncope episode with second vaccine dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: hypothyroidism
Andere Medikamente: levothyroxine
Allergien: penicillin, cephalosporin, clindamycin
Vorherige Impfungen: -

VAERS 1071494

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: LA
Alter: 59,0
Geschlecht: F
Eingang: 04.03.2021
Impfdatum: 11.02.2021
Beginn: 12.02.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: ID / LA

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

Eye contusion Eye swelling Face injury Loss of consciousness

Symptomtext

Passed out in the bathroom. Hit face. Do not believe she was out very long. Sustained a swollen and bruised right eye that eventually moved to the left.

Weitere VAERSDATA-Felder

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

VAERS 1057331

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: MO
Alter: 64,0
Geschlecht: F
Eingang: 26.02.2021
Impfdatum: 24.02.2021
Beginn: 26.02.2021
Tage bis Beginn: 2,0
Dosis: UNK
Route/Site: IM / LA

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

Erythema Paralysis Peripheral swelling Skin warm

Symptomtext

Lot # 011L20A- patient reported L arm reddness, swelling and warmth. Lot # 031L20A- patient reported L arm reddness, swelling and warmth, along with palsy of the L side of her face.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paralysis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: na
Vorgeschichte: na
Andere Medikamente: blood thinners
Allergien: Sulfa, codeine, demerol, morphine, valium
Vorherige Impfungen: -

VAERS 1056177

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: NY
Alter: 32,0
Geschlecht: F
Eingang: 26.02.2021
Impfdatum: 23.12.2020
Beginn: 23.12.2020
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / -

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

Blood test Exposure during pregnancy Facial paralysis Ultrasound foetal

Symptomtext

Bells palsy; Pregnancy; A spontaneous report was received from a physician, who was also a 32-year-old female patient who received Moderna's COVID-19 vaccine (mRNA- 1273) during pregnancy and the patient has been diagnosed with Bell's palsy after delivery. The patient's medical history included exercise induced asthma. Products known to have been used by the patient, within two weeks prior to the event, included ascorbic acid/betacarotene/calcium sulfate/colecalciferol/cyanocobalamin/ferrous fumarate/folic acid/nicotinamide/pyridoxine hydrochloride/retinol acetate/riboflavin/thiamine mononitrate/tocopheryl acetate/zinc oxide and omeprazole. On 23 DEC 2020, the patient received their first of two planned doses of mRNA-1273 (Batch number: 011J20A) for the prophylaxis of COVID-19 infection. On 20 JAN 2021, the patient received their second of two planned doses of mRNA-1273 (Batch number: 029L20A) for the prophylaxis of COVID-19 infection. On an unknown date, an ultrasound and quad screen (levels of alpha-fetoprotein (AFP), human chorionic gonadotropin (HCG), estriol and inhibin A in pregnant women's blood) were performed, and the results were normal. There were no complications during the pregnancy. On 01 Feb 2021, the patient delivered the baby. No other delivery or infant details were reported. On 10 Feb 2021, the patient was diagnosed with Bell's palsy. No treatment information was provided. The patient received both scheduled doses of mRNA-1273 prior to the events; therefore, action taken with the drug in response to the events is not applicable. The outcome of the reported event, Bell's Palsy, was unknown.; Reporter's Comments: Based on the current available information and temporal association between the use of the product and the start date of the event, a causal relationship cannot be excluded.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: -
Labordaten: Test Name: Quad Screen; Result Unstructured Data: Quad screen (levels of alpha-fetoprotein (AFP), human chorionic gonadotropin (HCG), estriol and inhibin A in pregnant women's blood.; Test Name: Ultrasound; Result Unstructured Data: Normal
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Exercise induced asthma
Andere Medikamente: PRENATAL VITAMINS [ASCORBIC ACID;BETACAROTENE;CALCIUM SULFATE;COLECALCIFEROL;CYANOCOBALAMIN;FERROUS ; OMEPRAZOLE
Allergien: -
Vorherige Impfungen: -

VAERS 1039887

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: MA
Alter: 22,0
Geschlecht: F
Eingang: 18.02.2021
Impfdatum: 05.02.2021
Beginn: 05.02.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: OT / LA

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

Abnormal sensation in eye Anaphylactic reaction Dyspnoea Obstructive airways disorder Rales Wheezing

Symptomtext

Anaphylactic reaction; Burning sensation in eyeballs; Wheezing; Rales; Airways were closing; Can't breathe; A spontaneous report was received from a consumer concerning a 22-year-old, female patient, who received Moderna's COVID-19 vaccine (mRNA-1273) and experienced an anaphylactic reaction, burning sensation in eyeballs/abnormal sensation in eye, wheezing, rales, airways were closing/obstructive airways disorder, and can't breathe/dyspnoea. The patient's medical history was not provided. No relevant concomitant medications were reported. On 05 Feb 2021, within 5 minutes prior to the onset of the event, the patient received their second of two planned doses of mRNA-1273 (Lot number: 011J20A) intramuscularly in the left arm for prophylaxis of COVID-19 infection. On 05 Feb 2021, within 5 minutes after receiving her second dose of vaccine, the patient reported a burning sensation in her eyeballs, followed by wheezing and rales in her lungs. She was given epinephrine and taken to the emergency room via an ambulance. She was given a second dose of epinephrine. Her airways were closing and she could not breathe. She was given a steroid, diphenhydramine, H2 antagonist and albuterol. Consent given for follow up calls. Action taken with mRNA-1273 in response to the event was not reported. The outcome of the events, anaphylactic reaction, burning sensation in eyeballs, wheezing, rales, airways were closing, and can't breathe, was not provided.; Reporter's Comments: Based on the current available information and temporal association between the use of the product and the onset date of the events, a causal relationship cannot be excluded.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: No adverse event (No medical history reported)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1038030

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: CA
Alter: -
Geschlecht: F
Eingang: 18.02.2021
Impfdatum: 26.01.2021
Beginn: 26.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / -

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

Angioedema Appendicitis Arthralgia Cardiac disorder Chills Fatigue Headache Loss of consciousness Mouth ulceration Nasal congestion Nausea Neuralgia Pain Pyrexia

Symptomtext

Appendicitis; Angioedema of the face; congestion; Joint pain; Nausea; Fatigue; fever; cardiac abnormalities; "blacked out"; Ulcers in/around the mouth; "zaps" all over her body and to her brain; overall body pain; Headaches; Chills; A spontaneous report was received from a healthcare professional concerning a 47-year-old female patient who received Moderna's COVID-19 vaccine (mRNA-1273) and experienced appendicitis, angioedema of the face, ulcer in/around the mouth, joint pain, zaps all over her body and to her brain, headaches, chills, nausea, fatigue, "blacked out" loss of consciousness, congestion, overall body pain, cardiac abnormalities. The patient's medical history included Covid-19. No relevant concomitant medications were reported. In March of 2020, the patient was first diagnosed with COVID-19. The patient reported she has since been considered a "long hauler" and has experienced various symptoms of the disease since that time. On 26 Jan 2021, the patient received their first of two planned doses of mRNA-1273 ([LOT# 011J20A]) intramuscularly for prophylaxis of COVID-19 infection. After receiving the first dose of the vaccine the patient initially experienced joint pain and "zaps" all over her body and to her brain, headaches, chills and overall body pain. On an unspecified date, after visiting her doctor, the patient was diagnosed with angioedema of the face. Treatment medication included 2 different unspecified antihistamines. Once that condition was remedied (date unspecified), the patient still experienced fatigue, nausea and congestion. On 28 Jan 2021 the patient experienced swelling of the mouth and ulcers in and around the mouth. On 29 Jan 2021, the patient experienced severe stomach pain and cramping as well as a fever that worsened through the night. Treatment included oxycodone hydrochloride. On the morning of 29 Jan 2021, the patient was still experiencing abdominal pain and began vomiting. The pain was so much that the patient "blacked out" and was transported to the Emergency Room (ER). At the ER the patient experienced unspecified cardiac abnormalities. While in the ER, the patient was diagnosed with appendicitis and subsequently underwent an appendectomy. On 30 Jan 2021, the patient was discharged from the ER and was still experienced nausea, fatigue and fever. Action taken with mRNA-1273 in response to the events was not reported. The event of appendicitis was considered recovered/resolved on 30 Jan 2021, the event of angioedema and "blacked out" were considered recovered/resolved (dates not reported). The events of nausea, fatigue, and fever were considered not recovered/not resolved. The event outcome for ulcers in/around the mouth, joint pain, "zaps" all over her body and to her brain, headaches, chills, congestion, overall body pain, and cardiac abnormalities was considered unknown.; Reporter's Comments: This case concerns a 47-year-old, female subject, with medical history of COVID-19 (Mar-2020), who experienced serious events of angioedema, LOC, and appendicitis. Based on the current available information and temporal association between the use of the product and the start date of the event, a causal relationship cannot be excluded. Based on the mechanism of action of mRNA-1273, the event of appendicitis is considered not related to the vaccine. Further information has been requested.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: COVID-19
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1036498

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: AK
Alter: 64,0
Geschlecht: F
Eingang: 17.02.2021
Impfdatum: 26.01.2021
Beginn: 26.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Blood test Cerebellar stroke Computerised tomogram abnormal Dizziness Magnetic resonance imaging abnormal Nausea Vomiting

Symptomtext

According to the information I have gathered, she became dizzy, nauseated, vomiting later in the day. This continued for nearly two weeks. She then presented to an emergency room and was diagnosed with a cerebellar stroke that likely started on the same day as her vaccine per that physicians report.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebellar stroke
Hospital-Tage: 4,0
Labordaten: 2/11/2021 was admitted to the hospital and received multiple blood tests, MRI's, CT Scans that resulted in the diagnosis of a cerebellar stroke that was approximately two weeks old.
Aktuelle Erkrankungen: unk
Vorgeschichte: anemia RA HTN cataracts DM2 Hypothyroid
Andere Medikamente: humira vitamin d restasis erythromycin opthalmic flonase folic acid lisinopril c hctz plaquenil synthroid methotrexate rybelsus zocor
Allergien: doxycycline compazine PCN phenergan
Vorherige Impfungen: -

VAERS 1029448

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: OH
Alter: 49,0
Geschlecht: F
Eingang: 14.02.2021
Impfdatum: 22.12.2020
Beginn: 04.01.2021
Tage bis Beginn: 13,0
Dosis: 1
Route/Site: SYR / LA

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

Abdominal pain upper Computerised tomogram Full blood count Headache Impaired work ability Syncope Vomiting

Symptomtext

12/22 Vaccination Unknown dates; around the holidays 1.5.2021 - missed 2 weeks of work. I started the propranolol. I ended up with extreme HA, vomiting, syncope, Stomach pain, couldn't keep anything down. Lasted for 2 weeks. *2nd shot - same symptoms

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: CT scan blood panel
Aktuelle Erkrankungen: n/a
Vorgeschichte: asthmatic, chronic kidney disease, hypertension, autonomic dysreflexia , seizure disorder, chronic migraines
Andere Medikamente: prednisone, keppra, lexapro, propranolol
Allergien: acetaminophen, advocare, albuterol, aspirin, adhesive tape, Augmentin, Bactrim, bee sting, zipro, CT Scan dye, Demerol, diaconate, diclofenac, Entex, flexural, ibuprofen, enteral, lamictal, latex, Mestinon, mobic, MRI dye, Mucinex, naproxen, Neurontin, oxycodone, paxel, peanuts robitussen, theroquil, shellfish, sulfa, tophorol, trazadone, Zoloft
Vorherige Impfungen: -

VAERS 1026794

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: HI
Alter: 81,0
Geschlecht: F
Eingang: 12.02.2021
Impfdatum: 15.01.2021
Beginn: 19.01.2021
Tage bis Beginn: 4,0
Dosis: UNK
Route/Site: IM / LA

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

Facial paralysis

Symptomtext

Left facial droop. Sent to Emergency Department via EMS 1/19/2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: 3,0
Labordaten: Contact Medical Center
Aktuelle Erkrankungen: DM, HTN, HYPERLIPIDEMIA, MILD COGNITIVE IMPAIRMENT, DEMENTIA, OBESITY
Vorgeschichte: DM, HTN, HYPERLIPIDEMIA, MILD COGNITIVE IMPAIRMENT, DEMENTIA, OBESITY
Andere Medikamente: AMMONIUM LACTATE 12 % LOTION; ARTIFICIAL TEARS (OR EQUIVALENT); ASPIRIN 81 MG TABS; CALCIUM 600 MG + D3 400 IU TABS; CORN STARCH POWDER TOPICAL; DONEPEZIL 5 MG TAB; FLUOCINONIDE 0.05 % CREAM; LANTUS SOLOSTAR 100 UNIT/ML SOPN; LISINOPRIL 2.5
Allergien: AMOXICILLIN (RASH)
Vorherige Impfungen: -

VAERS 1023933

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: WI
Alter: 67,0
Geschlecht: F
Eingang: 11.02.2021
Impfdatum: 08.01.2021
Beginn: 04.02.2021
Tage bis Beginn: 27,0
Dosis: 1
Route/Site: IM / LA

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

Bell's palsy Ear pain Swelling face

Symptomtext

Patient had Bells palsy with associated ear pain and facial swelling.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Influenza diagnosed on 2/3/21
Vorgeschichte: DM II, obesity, acid reflux, wide complex tachycardia, ruptured cerebral aneurysm, hyperlipidemia, hypertension, osteoarthritis,
Andere Medikamente: -
Allergien: azithromycin, honey bee venom, codeine
Vorherige Impfungen: -

VAERS 1021918

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: CA
Alter: 58,0
Geschlecht: F
Eingang: 11.02.2021
Impfdatum: 13.01.2021
Beginn: 21.01.2021
Tage bis Beginn: 8,0
Dosis: 1
Route/Site: OT / LA

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

Clumsiness Diarrhoea Dizziness Dysstasia Fall Fatigue Feeling abnormal Flushing Headache Injection site swelling Mass Nausea Pain Rash erythematous Syncope

Symptomtext

Flushed; Body aches; Red rashy spot; Fatigued; The site on my left arm got to a baseball size; Headaches; Felt like I would throw up; Ended up fainting/ went down for a second time; Diarrhea; Light headed; Discombobulated; A spontaneous report was received from a 58 year old, female patient who received Moderna's COVID-19 vaccine (mRNA-1273) and experienced diarrhea, felt that she would throw up, light headed, fainted, discombobulated, site on her left arm got to a baseball size, and in the middle was a red rashy spot, flushed, fatigued, had body aches and headaches. The patient's medical history included high blood pressure. Relevant concomitant medications included unknown blood pressure medication. On 13 Jan 2021, the patient received their first of two planned doses of mRNA-1273 (Lot: 011J20A) intramuscularly in left arm for prophylaxis of COVID-19 infection. On 21 Jan 2021, around three, the patient experienced diarrhea, she thought it was food poisoning. While on the "pot" with diarrhea she felt that she would throw up. She mentioned that she became lightheaded but did not throw up and ended up fainting. She fell off the pot and decided to lay down in her bed. She got lightheaded again and went down for a second time. She stated she had a difficult time getting up; she crawled to the bed. When she attempted to stand up, she could feel she was lightheaded again. The patient mentioned that maybe she was down 45 minutes before getting to lay on her bed. She felt discombobulated. She felt very clumsy when trying to dial her sister's number; she left a message on the machine and was struggling to get her words together. The site on her left arm got to a baseball size, and in the middle was a red rashy spot. On Friday evening, 26 Jan 2021, the patient stated she started feeling better. She mentioned that she was flushed, fatigued and had body aches. The patient stated she hasn't tried any treatments but took paracetamol for headaches and tried to rest. Action taken with mRNA-1273 in response to the events was not reported. The outcome of the events, diarrhea, felt that she would throw up, light headed, fainted, discombobulated, site on her left arm got to a baseball size, and in the middle was a red rashy spot, were resolving. The outcome of the events, headaches, flushed, fatigued and body aches, were unknown.; Reporter's Comments: This case concerns a 58 year old female patient with medical history of high blood pressure, who experienced a serious unexpected event of Syncope and NS unexpected events of diarrhea, nausea, dizziness, confusional state, injection site swelling, rash erythematous, flushing , fatigue, pain and headache. The events occurred approximately 8 days after first dose of the study medication administration. she only took paracetamol for headaches and tried to rest without any other treatment. Based on the current available information and temporal association between the use of the product and the start date of the event, a causal relationship cannot be excluded.

Weitere VAERSDATA-Felder

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

VAERS 1020367

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: GA
Alter: 61,0
Geschlecht: F
Eingang: 10.02.2021
Impfdatum: 13.01.2021
Beginn: 13.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Anaphylactic reaction Blood glucose increased

Symptomtext

Allergie to ASA-anaphylactic

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: elevated glicose
Aktuelle Erkrankungen: autoimmune disorder, high strep viral load, hx of scarlet feve
Vorgeschichte: autoimmune disorder, 4x cancer survivor
Andere Medikamente: naturethoid, omnicef, valcyclovir, clarithrpmycin, azithromyci
Allergien: ASA
Vorherige Impfungen: -

VAERS 1020253

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: NY
Alter: 37,0
Geschlecht: F
Eingang: 10.02.2021
Impfdatum: 09.02.2021
Beginn: 10.02.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Loss of consciousness

Symptomtext

Passed out approximately 24 hours after second dose of vaccine.

Weitere VAERSDATA-Felder

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

VAERS 1007463

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: VT
Alter: 38,0
Geschlecht: F
Eingang: 10.02.2021
Impfdatum: 06.01.2021
Beginn: 02.02.2021
Tage bis Beginn: 27,0
Dosis: UNK
Route/Site: IM / LA

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

Bell's palsy

Symptomtext

Bells Palsy, R side of face, onset 2/2/21

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: Lyme test pending but no known exposure
Aktuelle Erkrankungen: none
Vorgeschichte: seasonal allergies
Andere Medikamente: albuterol prn, fluticasone nasal spray prn
Allergien: seasonal allergies, NKDA
Vorherige Impfungen: -

VAERS 2670609

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: -
Alter: 35,0
Geschlecht: F
Eingang: 08.02.2021
Impfdatum: 04.01.2021
Beginn: 04.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Cough Headache Nausea Pain in extremity Respiratory tract congestion Syncope Vomiting Wheezing

Symptomtext

Headache, CoughWheeze, NauseaVomiting, Syncope, Congestion, Left arm pain Narrative: Other Relevant History:

Weitere VAERSDATA-Felder

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

VAERS 1006123

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: VA
Alter: 25,0
Geschlecht: F
Eingang: 05.02.2021
Impfdatum: 03.02.2021
Beginn: 03.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Fall Syncope

Symptomtext

Client fainted after COVID-19 vaccination completed. Client fell out of chair onto floor. EMS called and assessed patient's vitals, confirmed no injury or illness. Client reported this happened before after receiving shot. Client monitored x 30 min with no further issues. The initial VAERS report filled out by vaccinator . Given to me by clinic nurse lead. Attempted to fax but unable to get through due to fax busy.

Weitere VAERSDATA-Felder

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

VAERS 1005662

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: NY
Alter: 51,0
Geschlecht: F
Eingang: 05.02.2021
Impfdatum: 22.12.2020
Beginn: 06.01.2021
Tage bis Beginn: 15,0
Dosis: 1
Route/Site: IM / RA

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

Angiogram Computerised tomogram head Computerised tomogram neck Diplopia Hypertension IVth nerve paralysis Laboratory test

Symptomtext

On 1/6/2021 I had onset of High BP and Double Vision. Diagnosed with a 4th Cranial Nerve palsy on Left by Neurology and Ophthalmology.

Weitere VAERSDATA-Felder

Praegender Schweregrund: IVth nerve paralysis
Hospital-Tage: -
Labordaten: CT on 1/6/2021 of Head. CT with Contrast on 1/14/2021 of head and neck. Angiogram-Neck and Lyme test.
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: metoprolol
Allergien: nka
Vorherige Impfungen: -

VAERS 1005468

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011j20a

schwer

Staat: AZ
Alter: 49,0
Geschlecht: M
Eingang: 05.02.2021
Impfdatum: 30.12.2020
Beginn: 01.01.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / UN

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

COVID-19 Illness Mechanical ventilation Respiratory distress SARS-CoV-2 test positive

Symptomtext

Hospitalized with resp distress Jan1 , 2021 COVID-19 positive Severe illness, mechanical ventilation Remains hospitalized Feb 5, 2021

Weitere VAERSDATA-Felder

Praegender Schweregrund: Respiratory distress
Hospital-Tage: 36,0
Labordaten: no
Aktuelle Erkrankungen: Diabetes mellitus obesity
Vorgeschichte: diabetes obesity
Andere Medikamente: no
Allergien: no
Vorherige Impfungen: -

VAERS 2587507

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: -
Alter: 59,0
Geschlecht: F
Eingang: 04.02.2021
Impfdatum: 21.01.2021
Beginn: 21.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Arthralgia Chills Cough Dizziness Headache Myalgia Pyrexia Syncope Tooth fracture Wheezing

Symptomtext

Headache, Myalgia, Arthralgia, Fever, CoughWheeze, Syncope, Lightheaded , cough developed in 30 min lasted for 3 hrs . next morning muscle aches worse than usual, chills, chipped tooth due to chattering of lips Narrative:

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: shingles-flu like symptoms for 3 days: Anthrax-fever, myalgia

VAERS 1001912

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011j20a

schwer

Staat: PR
Alter: 34,0
Geschlecht: F
Eingang: 04.02.2021
Impfdatum: 20.02.2020
Beginn: 20.01.2021
Tage bis Beginn: 335,0
Dosis: UNK
Route/Site: IM / RA

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

Chills Dysphagia Dyspnoea Ear pain Eyelid ptosis Facial pain Facial paralysis Fatigue Headache Hypoaesthesia Nausea Neck pain Pain in jaw Peripheral swelling Pyrexia Swelling face

Symptomtext

After the fever of 40C, chills, tiredness, nausea, headache. Started to feel pain on the left side of my face. Next day the pain has spread to my neck and ear. On day number three they felt numb, day number four lots of pain on my jaw. Day number 5 I couldn't even swallow and had difficulty breathing. When I looked in the mirror the left side of my face was very swollen like a ball and my face looked like it was paralyzed. I went to the ER where I was seen, but it remains the same days afterwards. My cheek doesn't look the same, looks bigger and the eye is droopy, my neck and ear hurts, it is difficult to swallow. My left arm is numb and swollen.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: depression, epilepsy, asthma, gastritis, anxiety, hypoglycemia
Vorgeschichte: depression, epilepsy, asthma, gastritis, anxiety, hypoglycemia
Andere Medikamente: Prozac 20mg
Allergien: -
Vorherige Impfungen: -

VAERS 1001062

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: AR
Alter: 48,0
Geschlecht: F
Eingang: 04.02.2021
Impfdatum: 07.01.2021
Beginn: 07.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Anxiety Dizziness Hemiparesis Mydriasis Presyncope

Symptomtext

PT WAS APPREHENSIVE OF RECEIVING THE VACCINE AT THE TIME OF INJECTION. PT BEGAN TO COMPLAIN OF DIZZINESS AND LEFT-SIDED WEAKNESS. PUPIL WAS DILATED. BP 200/140. SENT TO ER. FINAL DIAGNOSIS OF VASOVAGAL RESPONSE.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: PANTOPRAZOLE 40MG DICLOFENAC 75MG METHOCARBAMOL HYDROCODONE/APAP
Allergien: NKDA
Vorherige Impfungen: -

VAERS 999433

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: HI
Alter: 39,0
Geschlecht: M
Eingang: 04.02.2021
Impfdatum: 24.12.2020
Beginn: 04.01.2021
Tage bis Beginn: 11,0
Dosis: 1
Route/Site: IM / LA

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

Depressed level of consciousness Headache Hypoacusis Hypoaesthesia Magnetic resonance imaging Syncope Tinnitus X-ray

Symptomtext

Faint, decrease level of consciousness, ringing in left ear, numbness of left side of body, decrease hearing in left ear and headaches

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Visited M, taken x-rays. Ached for MRI and audiology appointments.
Aktuelle Erkrankungen: N/a
Vorgeschichte: N/a
Andere Medikamente: N/a
Allergien: N/a
Vorherige Impfungen: -

VAERS 1001616

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: -
Alter: 38,0
Geschlecht: M
Eingang: 03.02.2021
Impfdatum: 29.12.2020
Beginn: 29.12.2020
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

COVID-19 Chills Cough Myalgia SARS-CoV-2 test positive Syncope Wheezing

Symptomtext

Myalgia, CoughWheeze, Syncope, Chills Narrative: covid tested positive 1/1/21. symptoms resolved 1/2/21.

Weitere VAERSDATA-Felder

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

VAERS 995964

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: CA
Alter: 56,0
Geschlecht: M
Eingang: 02.02.2021
Impfdatum: 14.01.2021
Beginn: 31.01.2021
Tage bis Beginn: 17,0
Dosis: 1
Route/Site: SYR / LA

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

Bell's palsy

Symptomtext

Bells Palsy occurred on 1-31-2021 after receiving the shot on 1-14-2021. No other issues or illness before or after getting the vaccine which would explain getting Bells Palsy. Have not been ill or seen doctor except for regular check-ups as necessary.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: Doctor visit on 2-2-2021.
Aktuelle Erkrankungen: None
Vorgeschichte: High Blood pressure Cholesterol
Andere Medikamente: Losartan Pot/Hydrochlor Othiazide Tab 100-25MG Atorvastatin Calcium Tab 40MG
Allergien: None
Vorherige Impfungen: -

VAERS 994477

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: WI
Alter: 49,0
Geschlecht: F
Eingang: 02.02.2021
Impfdatum: 28.01.2021
Beginn: 28.01.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Diarrhoea Flushing Impaired work ability Malaise Pain Presyncope

Symptomtext

Approximately 20 minutes after second vaccine, became orthostatic, flushed, and pre-syncopal. Given intravenous diphenhydramine, and sent home ~60 minutes later. Patient did take off work the next day, experiencing aches, malaise, and diarrhea.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Anxiety, DM2, obesity, GERD, hyperlipidemia, OSA, arthropathic psoriasis, Prinzmetal angina
Andere Medikamente: Glargine insulin 35 units daily, ferrous sulfate 325 mg daily, pantoprazole 40 mg daily, metformin XR 1,000 mg daily, levothyroxine 125 mcg daily, lisdexamfetamine 20 mg daily, empagliflozin 10 mg daily
Allergien: N/A
Vorherige Impfungen: -

VAERS 992774

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: CO
Alter: 92,0
Geschlecht: M
Eingang: 01.02.2021
Impfdatum: 19.01.2021
Beginn: 20.01.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Atelectasis Cardiac pacemaker adjustment Cellulitis Chest X-ray abnormal Computerised tomogram abdomen Distributive shock Echocardiogram Hypotension Lung consolidation Lung opacity Oedema peripheral Pleural effusion Pulmonary congestion Sepsis

Symptomtext

On 1/20/2021 the resident experienced hypotension while at dialysis and was not able to complete treatment prior to being transferred to the hospital. He also had congestion in lungs. The hospital notes indicate upon admission to the hospital he was being treated for # Shock - distributive - cover for sepsis, check u/s RLE, possible SIRS response after second COVID vaccine. MAP >55 and # ESRD. While in the hospital resident was treated for hypotension, right lower leg cellulitis and the rate of pacemaker was increased.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Distributive shock
Hospital-Tage: 8,0
Labordaten: CXR on 1/21 and 1/26/21 indicating worsening lung expansion and bilateral opacities that probably reflect components of atelectasis and consolidation. Small/moderate right pleural effusion is slightly more conspicuous and small left effusion, pulmonary vascular congestion. Echocardiogram, CT abdomen and pelvis and leg with edema
Aktuelle Erkrankungen: Resident is dialysis dependent. Was evaluated by NP for epistaxis in December and was seen in ER and treated with Tranexamic. Resident is oxygen dependent due to COPD. Resident had an unwitnessed fall on 1/9/2021.
Vorgeschichte: End Stage Renal Disease- dialysis dependent, renal cancer, Atherosclerotic heart disease, Type 2 diabetes, COPD, GERD, Atrial Fibrillation, cardiac pace maker, prostate cancer, history of covid positive -resulting in hospitalization and received convalescent plasma in May, 2020
Andere Medikamente: Aspirin Tablet 81 MG, Clopidogrel Bisulfate Tablet 75 MG, Colace Capsule 100 MG, Darbepoetin Alfa Solution Prefilled Syringe 25 MCG/0.42ML, Glucosamine-Chondroit-Vit C-Mn Tablet, Levothyroxine Sodium Tablet 88 MCG, Lyrica Capsule 50 MG, Mel
Allergien: Codeine, Lactose Intolerant, Cats, Pollen
Vorherige Impfungen: -

VAERS 990355

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: NY
Alter: 60,0
Geschlecht: M
Eingang: 01.02.2021
Impfdatum: 07.01.2021
Beginn: 11.01.2021
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: OT / RA

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

Deep vein thrombosis Ultrasound Doppler

Symptomtext

DVT blood clot; A spontaneous report was received from a 60-year-old male consumer who received Moderna's COVID-19 vaccine (mRNA-1273) and developed deep vein thrombosis (DVT) blood clot. The patient's medical history, as provided by the reporter, included factor V Leiden, enlarged prostate, DVT, pulmonary embolism and hypertension. Concomitant medications reported included valsartan, alfuzosin, and acetylsalicylic acid. On 07 Jan 2021, approximately four days prior to the onset of the events, the patient received their first of two planned doses of mRNA-1273 (Lot number: 011J20A) intramuscularly in the right arm for prophylaxis of COVID-19 infection. On 11 Jan 2021, the patient developed DVT blood clot and experienced leg pain so intense that he could not walk. A doppler exam showed the DVT was from the top of the calf to mid-thigh. Treatment for the event included a rivaroxaban starter pack with dose tapering. Action taken with mRNA-1273 in response to the event deep vein thrombosis (DVT) blood clot was not reported. The outcome of the event, DVT blood clot, was unknown.; Reporter's Comments: This case concerns a 60-year-old male patient with a relevant medical history of factor V Leiden, DVT, pulmonary embolism and hypertension who received their first of two planned doses of mRNA-1273 (Lot number: 011J20A) intramuscularly in the right arm for prophylaxis of COVID-19 infection. Patient experienced the medically significant unlisted event of Deep vein thrombosis approximately four days after administration of vaccine. Treatment for the event included rivaroxaban. Based on the temporal association between the use of the product and the event occurring after receiving the vaccine, a causal relationship cannot be excluded and the event of Deep vein thrombosis is possibly related to the product. Of note, the patient's underlying Factor V Leiden which predispose to developing abnormal blood clots, and prior medical history of DVT with pulmonary embolism are considered risk factors to the occurrence of the event.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: -
Labordaten: Test Date: 202101; Test Name: Doppler exam; Result Unstructured Data: lower extremity blood clot, top of calf to mid thigh
Aktuelle Erkrankungen: Enlarged prostate; Factor V Leiden thrombophilia; Hypertension
Vorgeschichte: Medical History/Concurrent Conditions: DVT (5 years ago); Pulmonary embolism (History of 4 PE's five years ago)
Andere Medikamente: VALSARTAN; ALFUZOSIN; BABY ASPIRIN
Allergien: -
Vorherige Impfungen: -

VAERS 988493

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: OR
Alter: 43,0
Geschlecht: F
Eingang: 30.01.2021
Impfdatum: 28.12.2020
Beginn: 28.12.2020
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Anaphylactic reaction Blood glucose normal Erythema Feeling jittery Flushing Palpitations Tongue disorder

Symptomtext

During the 15 minute observation following the 1st Moderna vaccine dose, the patient reported her tongue 'felt thick,' flushed skin, redness on face, neck, hands, BP=98/60, HR=100. Patient felt 'jittery' and 'heart racing.' Was transferred to ED for evaluation given that patient reported her tongue 'getting tighter.' In the ED, the patient was treated with diphenhydramine 25mg x 2 doses, methylprednisolone 125mg x 1 dose, famotidine 20mg x 1 dose, and NS IV fluids. Hypoglycemia was ruled out with CBG=87. The physician avoided treatment with epinephrine due to it being listed on her allergy list with a reaction of 'shortness of breath.' Symptoms resolved over the next 3 hours. The patient was discharged home with a new prescription of oral prednisone taper. Subsequent follow-up with her primary care provider, in consultation with an ID provider, recommended that this patient NOT get a 2nd dose. Covid-19 vaccine was added to her allergy list with a reaction of 'anaphylaxis.'

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: CBG = 87 (12/28/20)
Aktuelle Erkrankungen: -
Vorgeschichte: asthma, depression, bipolar disorder
Andere Medikamente: Albuterol MDI, Qvar, atomoxetine, buspirone, cholecalciferol, lamotrigine, Lithium carbonate, olanzapine
Allergien: Cinnamon (anaphylaxis), Iodinated contrast (hives), epinephrine (shortness of breath)
Vorherige Impfungen: -

VAERS 987080

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: PA
Alter: 80,0
Geschlecht: M
Eingang: 29.01.2021
Impfdatum: 04.01.2021
Beginn: 05.01.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / RA

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

Anti-muscle specific kinase antibody Asthenia CSF culture Dysphagia Endotracheal intubation Fungal disease carrier Guillain-Barre syndrome Helicobacter test negative Leukocytosis Lymphocyte count increased Magnetic resonance imaging abnormal Plasmapheresis Pneumonia Procalcitonin increased Protein total Radiculopathy Respiratory failure Sensory loss

Symptomtext

Client developed a mild covid infection 12/8/21 and recovered. He was admitted 12/25 with hypogycemia and mild weakness and sent home He was given his first dose of the Moderna vaccine 1/4/21 at approximately 9AM covid vaccine clinic He developed weakness the next day (1/5) prompting admission to a hospital and then transition to subacute rehabilitation briefly Work up at hospital revealed progressive respiratory failure and pneumonia requiring intubation and progressive ascending weakness and sensory loss without upper motor neuron changes. MRI : nerve root enhancement LP : protein 40, +/- 80 lymphocytes, cultures negative B 12 and B6 normal extensive CSF testing still pending campylobacter and Musk antibodies negative Neurology diagnosed likely AIDP (Guillain-Barre) and an EMG is planned for the near future. Neurology felt the cause of his GBS was likely his covid infection verses his Moderna vaccination He was treated with plasmapheresis. Client received dexamethasone, remdesivir, and zosyn and doxycycline when progressive leukocytosis and procalcitonin elevation was noted. Candida was cultured from tracheal aspirates but felt most likely d/t colonization with an option to treat further if he did not continue to improve. He is now extubated, unable to swallow and has profound weakness and distal sensory loss. He will transition to Acute rehab in the near future. Comorbidities:as described in the above section and... DM2, CKD3, HTN, DJD, BPH ( h/o prostate surgery), h/o Lumbar surgery and hernia repair, GERD, hypothyroidism, hyperlipidemia. Possible etiologies of his AIDP ( GBS) would include his recent covid infection, the Moderna Vaccine, or other undiagnosed infection. He got his flu shot 9/25 ( fluzone sanofi) so this is not likely to be the culprit

Weitere VAERSDATA-Felder

Praegender Schweregrund: Guillain-Barre syndrome
Hospital-Tage: 20,0
Labordaten: Work up at Hospital revealed progressive respiratory failure and pneumonia requiring intubation and progressive ascending weakness and sensory loss without upper motor neuron changes. MRI : nerve root enhancement LP : protein 40, +/- 80 lymphocytes, cultures negative B 12 and B6 normal extensive CSF testing still pending campylobacter and Musk antibodies negative Neurology diagnosed likely AIDP (Guillain-Barre) and an EMG is planned for the near future. His progression and physical exam were classic for GBS Neurology felt the cause of his GBS was likely his covid infection verses his Moderna vaccination He was treated with plasmapheresis.
Aktuelle Erkrankungen: COVID infection 12/8/21
Vorgeschichte: glaucoma, diabetes, hypothyroidism, hyperlipidemia, elevated PSA, BPH, Lumbar DDD, ED
Andere Medikamente: prilosec 20 bid flonase 50 mcg nasla spray qhs glipizide 5mg ac breakfast/supper lipitor 10 mg qhs dorzolamide/timolol/ eye drops bid OU latanprost eye drops 1 qhs OU senekot bid prn loratidine 10 mg daily synthroid 125 mcg daily ipratropi
Allergien: none
Vorherige Impfungen: -

VAERS 986414

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: CA
Alter: 61,0
Geschlecht: F
Eingang: 29.01.2021
Impfdatum: 15.01.2021
Beginn: 16.01.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Back pain Burning sensation Condition aggravated Electric shock sensation Hypoaesthesia Paraesthesia

Symptomtext

On January 16, the day after being vaccinated (1/15/21), I woke up with my arms, hands, legs and feet tingling and numb all over and it lasted on and off all day January 16 and on and off all day January 17 and has persisted every day until Monday, January 26 when the symptoms became worse. Instead of tingling in all extremities (with some numbness) the sensations changed to a pins and needles sensation with burning and random electrical shock sensations. I want to note that, yes, I have radiculopathies - however, I have never had them change so suddenly and increase in intensity so fast. Also, the pins and needles sensation with burning and random electrical shocks are brand new symptoms for me (my radiculopathies have not presented this way before). I reported these symptoms to my primary care provider today (1/29/21) and she instructed me to report my symptoms to VAERS and she is referring me to neurology. Note: I received my vaccination outside of my health care system and received it through the county because I could get the vaccination sooner that way. I did not report these symptoms sooner because they were not listed as a possible adverse effect of getting the COVID19 Moderna vaccination. However, as these symptoms have worsened over the past 2 weeks I have become concerned. I have not added any OTC medications or supplements to the ones listed prior. I have gone to a chiropractor twice during this time for relief of my back pain with no positive outcomes. Waiting to see the neurologist.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Electric shock sensation
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: none
Vorgeschichte: chronic low back pain, chronic pelvic pain, anxiety and depression, left bundle branch block, lumbar and cervical radiculopathy, erythromelalgia
Andere Medikamente: Nortriptyline, Ativan, Tylenol, multivitamin, Vit D, Vit K2, CoQ10, magnesium glycinate, fish oil, melatonin, probiotic, Vit B12, alpha lipoic acid, curcumin
Allergien: Gabapentin, steroids, mepivicaine, valium, klonapin, depakene, baclofen
Vorherige Impfungen: -

VAERS 984390

UNKNOWN MANUFACTURER · COVID19 (COVID19 (UNKNOWN)) · Charge 011J20A

schwer

Staat: GA
Alter: 32,0
Geschlecht: M
Eingang: 29.01.2021
Impfdatum: 28.12.2020
Beginn: 28.12.2020
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / LA

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

Hyperhidrosis Muscle twitching Pallor Presyncope

Symptomtext

Felt like might pass out; Proceeded to become limp, pale and sweaty; Proceeded to become limp, pale and sweaty; Hands rhythmically twitched back and forth; A spontaneous report was received from a nurse concerning a 32-year-old, male, patient who received Moderna's COVID-19 vaccine (mRNA-1273) and felt like he might pass out, became limp, pale, and sweaty, and hands rhythmically twitched back and forth. The patient's medical history included allergy to penicillin. No relevant concomitant product use was reported. On 28 Dec 2020, approximately three minutes prior to the onset of the events, the patient received their first of two planned doses of mRNA-1273 (Lot number: 011J20A) intramuscularly in the left arm for prophylaxis of COVID-19 infection. On 28 Dec 2020, the patient began to feel like he was going to pass out minutes after receiving the vaccine. He became more limp, pale, and sweaty and his hands rhythmically twitched back and forth. His eyes closed and he leaned back in his chair, but he remained upright. The nurse elevated his feet, fanned his face and upper body, and applied wet paper towels to the back of his neck. After approximately two minutes, the patient's level of consciousness returned to baseline and he felt better after five minutes. He remained seated and sipped water for 30 minutes. Action taken with mRNA-1273 in response to the events was not provided. The outcome of the events, felt like he might pass out, became limp, pale, and sweaty, and hands rhythmically twitched back and forth, was considered resolved on 28 Dec 2020.; Reporter's Comments: This case concerns a 32-year-old, male, patient, who experienced a serious unexpected event of presyncope and non-serious unexpected event of pallor, hyperhidrosis This case concerns a 32-year-old, male, patient, who experienced a serious unexpected event of presyncope and non-serious unexpected event of pallor, hyperhidrosis and muscle twitching. The event occurred 15 min after first dose of mRNA-1273, lot # 011J20A. Treatment included no medications, but feet elevation and wet towel on the back of his neck. Based on the current available information and temporal association between the use of the product and onset of the events a causal relationship cannot be excluded.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Allergy to antibiotic (Penicillin)
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 981919

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: NC
Alter: 67,0
Geschlecht: F
Eingang: 28.01.2021
Impfdatum: 26.01.2021
Beginn: 26.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Anaphylactic reaction Bronchospasm Cough Dyspnoea Pruritus Respiratory distress Throat irritation Wheezing

Symptomtext

On 01/26/21, 67 yo F with anemia, asthma, Afib (on rivaroxaban), fibromyalgia, DM2, HLD, and osteoarthritis was administered COVID-19 Moderna vaccine 0.5 mL in left deltoid (Lot #011J20A, Exp: 05/11/21). Pt has numerous documented allergies including iodine (hives, facial swelling), Shellfish Containing Products (Hives, facial swelling) and penicillin (edema). Pt initially tolerated injection without incident and was sent for post-injection observation. Within 10 minutes, pt developed acute SOB, increased WOB, wheezing, and cough. Pt also reported itching skin and scratchy throat. Provider notified and exam found pt in respiratory distress with increased work of breathing, bronchospasm and wheezing. Pt had no rash, lip swelling or vomiting. Vitals assessed as O2 sats >96%, BP 140-150s/60s, HR 70-80s. Pt was administered albuterol 2.5 mg via nebulization x 2, diphenhydramine 50 mg IM and epinephrine 0.3 mg IM. Pt was subsequently transported to ED. By time of arrival, pt's symptoms had significantly improved. Pt administered famotidine 20 mg IV and prednisone 60 mg PO and placed on continuous cardiac and pulse oximetry monitoring. After complete symptom resolution, pt was discharged in stable condition. Pt's allergy profile was updated to include Moderna Covid-19 Vaccine (eua) (rxn: Anaphylaxis; severity: High).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: anemia, asthma, Afib (on rivaroxaban), fibromyalgia, DM2, HLD, and osteoarthritis
Vorgeschichte: -
Andere Medikamente: Unknown
Allergien: Cefuroxime Itching High Glucosamine Swelling High Iodine Swelling High Shellfish Containing Products Swelling High Metoclopramide Other (Shakes, confusion) Medium Penicillins Rash, Medium Apixaban Rash Codeine Nausea
Vorherige Impfungen: -

VAERS 2658606

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: -
Alter: 44,0
Geschlecht: F
Eingang: 27.01.2021
Impfdatum: 14.01.2021
Beginn: 15.01.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Arthralgia Cough Dry throat Feeling cold Myalgia Pain Pain in extremity Syncope Wheezing

Symptomtext

Myalgia, Arthralgia, CoughWheeze, Syncope, Body pain,throat dry, sore left arm, feels cold, coughing Narrative:

Weitere VAERSDATA-Felder

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

VAERS 2657403

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: -
Alter: 59,0
Geschlecht: F
Eingang: 27.01.2021
Impfdatum: 21.01.2021
Beginn: 21.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Arthralgia Cough Diarrhoea Dizziness Fatigue Headache Injection site pain Myalgia Pain Pyrexia Syncope Wheezing

Symptomtext

Headache, Myalgia, Arthralgia, Fever, CoughWheeze, Diarrhea, Syncope, Lightheaded , headache, body ache, fatique, sore injection sit , Narrative:

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: yes Shingles- Bodyaches, chill, fever

VAERS 979188

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: CA
Alter: 56,0
Geschlecht: F
Eingang: 27.01.2021
Impfdatum: 24.01.2021
Beginn: 26.01.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / RA

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

Anaphylactic reaction Aphasia Arthralgia Blood pressure increased Cough Feeling abnormal Headache Pain in extremity Paraesthesia Pharyngeal swelling Swollen tongue Throat clearing

Symptomtext

I experienced the typical reactions of headache, achy joints , and sore arm on 01/25/2021 which continue today, however my anaphylactic event occurred yesterday 01/26/2021.. after my shower I was feeling odd my hands and feet were tingly and I could feel my b/p go up . I made a phone call trying relax but mid call I could not speak due to throat and tongue swelling and then development of a cough trying to clear my throat. I grabbed my sons epi pen but I was able to still get air so I didn?t use it. My husband transported me to the ER. They took my straight back took my vitals and administered Benadryl, Pepcid and Dexamethasone IM and worked well, they observed me for few hours and I was released. I have follow-up appt tomorrow with primary care,

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension
Andere Medikamente: Atenolol
Allergien: Penicillin Erythromycin Walnuts
Vorherige Impfungen: -

VAERS 974119

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: -
Alter: 29,0
Geschlecht: F
Eingang: 26.01.2021
Impfdatum: 22.12.2020
Beginn: 22.12.2020
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / LA

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

Abdominal discomfort Asthenia Blood pressure increased Blood pressure measurement Chest discomfort Dizziness Heart rate Hypoaesthesia Nausea Palpitations Presyncope Rash macular Tachycardia

Symptomtext

Dizziness; Blood pressure 140/98; Pulse 123; Nausea; Numbness to her body; Chest tightness; Abdominal discomfort; Felt like she was going to pass out; Developed blotchy skin to chest and neck area within minutes of injection; Heart racing; Weakness; A spontaneous report was received from a consumer concerning a 29-year-old, female patient who experienced numbness, chest tightness, abdominal discomfort [Abdominal discomfort], felt like she was going to pass out, blotchy skin to chest and neck area [Rash macular], racing heart [Palpitations], weakness [Asthenia], dizziness [Dizziness], blood pressure 140/98 [Increased blood pressure], pulse 123 [Tachycardia] and nausea [Nausea]. The patient's medical history included asthma and there were no known drug allergies. Additionally, it was noted that there was no history of anaphylaxis. Concomitant product use included cetirizine and ibuprofen. On 22-Dec-2020, a short time prior to the onset of the symptoms, the patient received their first of two planned doses of mRNA-1273 (Lot# 011J20A}) intramuscularly in the left arm for prophylaxis of COVID-19 infection. Following vaccination, the patient immediately developed numbness to her body, chest tightness and abdominal discomfort. She remained alert and oriented but voiced concern that she felt like she was going to pass out. She developed blotchy skin to the chest and neck area within minutes of injection. Her vital signs included blood pressure of 140/98 and a pulse of 123. She was given water to drink which she tolerated well. She continued with symptoms of nausea, blotchy skin, heart racing and weakness. Dizziness was also reported. She was taken to the Emergency Room. Treatment for the event included epinephrine, methylprednisolone sodium succinate, diphenhydramine and lorazepam. Action taken with mRNA-1273 in response to the events was not provided. The outcome of the events was reported as recovered.; Reporter's Comments: This case concerns a 29 year-old, female patient with medical history of asthma, who experienced events of numbness, chest tightness, abdominal discomfort, felt like she was going to pass out, blotchy skin to chest and neck area, racing heart, weakness, dizziness, nausea, blood pressure of 140/98 and pulse of 123. The events occurred immediately after the first and last dose of mRNA-1273 vaccine administration. The patient was taken to the Emergency Room and recovered after receiving epinephrine, methylprednisolone sodium succinate, diphenhydramine and lorazepam. Based on the current available information and temporal association between the use of the product and the start date of the events, a causal relationship cannot be excluded and the events are assessed as possibly related.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: Test Date: 20201222; Test Name: Blood pressure; Test Date: 20201222; Test Name: Pulse
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Asthma (No medical history reported)
Andere Medikamente: CETIRIZINE; IBUPROFEN
Allergien: -
Vorherige Impfungen: -

VAERS 974091

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: AL
Alter: 63,0
Geschlecht: F
Eingang: 26.01.2021
Impfdatum: 29.12.2020
Beginn: 29.12.2020
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / -

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

Abdominal pain Diarrhoea Dizziness Dysphagia Fatigue Loss of consciousness Pharyngeal swelling Sensation of foreign body

Symptomtext

Pt presented to clinic and reports 3-4 hours after receiving first injection she felt fatigue and noticed some swelling in her throat and a noticeable palpable lump with some difficult swallowing. This went away after a few hours. Pt woke up the next morning with abdominal pain and reports standing up and passing out. Pt states she had diarrhea throughout the day also with dizziness.

Weitere VAERSDATA-Felder

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

VAERS 2639433

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: -
Alter: 51,0
Geschlecht: F
Eingang: 22.01.2021
Impfdatum: 31.12.2020
Beginn: 07.01.2021
Tage bis Beginn: 7,0
Dosis: 1
Route/Site: IM / LA

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

Arthralgia Bell's palsy Ear pain Facial paralysis Headache Myalgia Pyrexia

Symptomtext

Headache, Myalgia, Arthralgia, Fever, left sided facial drop Narrative: 1/5/21 severe left ear pain and on 1/7/21 left facial drop went to ED dx with Bell's Palsy

Weitere VAERSDATA-Felder

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

VAERS 963815

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: FL
Alter: 68,0
Geschlecht: F
Eingang: 22.01.2021
Impfdatum: 04.01.2021
Beginn: 04.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / LA

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

Pain in extremity Syncope

Symptomtext

fainted; a little pain in arm; A spontaneous report was received from a consumer concerning a 68-years-old, female patient who received Moderna's COVID-19 vaccine (mRNA-1273) and experienced fainting and pain in her arm. The patient's medical history was not provided. Concomitant product use was not provided by the reporter. On 04 Jan 2021, at approximately 09:00am, prior to the onset of the events, the patient received their first of two planned doses of mRNA-1273 (Lot number: 011J20A) intramuscularly in the left deltoid prophylaxis of COVID-19 infection. On 04 Jan 2021, after receiving the vaccine, the patient felt a little pain in her arm. On 05 Jan 2021, at approximately 19:00 the patient fainted after standing up. She hit her head on the floor and had a small bump on her head. No treatment information was provided. Action taken with the second dose of mRNA-1273 in response to the event was not reported. The outcome of the events, fainting and pain in her arm, were considered unknown.; Reporter's Comments: This case concerns a 68-year-old female subject with who experienced a serious, unexpected event of fainting and pain her arm. Her medical history and con meds were not provided. The fainting event occurred 1 day after the first dose of the mRNA-1273 study medication administration, after patient stood up, fainted, and hit her head on the floor and sustained a small bump on her head. Treatment for this event was not provided. Very limited information regarding the fainting event has been provided at this time. Based on temporal association between the use of the product and the start date of the event, a causal relationship cannot be excluded.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: No adverse event (No reported medical history.)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2461718

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011j20a

schwer

Staat: -
Alter: -
Geschlecht: F
Eingang: 19.01.2021
Impfdatum: 19.01.2021
Beginn: 15.01.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: IM / LA

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

Anaphylactic reaction Arthralgia Cough Dizziness Headache Myalgia Palpitations Syncope Tachypnoea Wheezing

Symptomtext

Dizziness, Headache, Myalgia, Arthralgia, Anaphylaxis, Tachypnea, CoughWheeze, Palpitations, Syncope Narrative: Rapid onset of anaphylaxis (prior history) treated in ED with steroids, Benadryl and pepcid

Weitere VAERSDATA-Felder

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

VAERS 956558

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: NY
Alter: 75,0
Geschlecht: M
Eingang: 19.01.2021
Impfdatum: 30.12.2020
Beginn: 31.12.2020
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: IM / LA

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

Computerised tomogram head Fall Loss of consciousness

Symptomtext

Pt reported he fell and was found unconscious at home by family members after going to bed the night of receiving vaccine. Pt reports was unaware of incident.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Pt seen by primary medical provider, referred to have CT of head.
Aktuelle Erkrankungen: None reported.
Vorgeschichte: HTN.
Andere Medikamente: Amlodipine 2.5 mg 1 tab daily, Lisinopril 10 mg 1 tab daily.
Allergien: NKDA
Vorherige Impfungen: -

VAERS 953126

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011j20a

schwer

Staat: OH
Alter: 53,0
Geschlecht: F
Eingang: 18.01.2021
Impfdatum: 16.01.2021
Beginn: 17.01.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Altered state of consciousness Fall Feeling hot Hyperhidrosis Impaired work ability Musculoskeletal stiffness Nausea Pallor Syncope

Symptomtext

Moderna COVID-19 Vaccine EUA received on Saturday. Sunday morning in the middle of my sleep, I woke feeling hot and sweaty, slightly nauseated, and like I had to defecate. I stood up, felt like low blood pressure but wanted to get to the bathroom. I walked towards the door, opened the door and fainted, falling backwards. My spouse states I was pale,staring at the ceiling and kind of stiff in my arms and legs for about 3 minutes. He spoke to me, checked my pulse, covered me, poked my feet. As I came back to awareness I tried to speak and was unintelligible but then became more conscious. He tested me with questions to make sure I was ok. I defecated after that but did not vomit. I was tired the rest of the day and napped for several hours. I don't seem to have hurt anything in the fall. I am instructed to be off work Monday by my supervisor.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Covid-19 starting date 12/19/2020
Vorgeschichte: Rheumatoid Arthritis (under control), Hypothyroid, 5 past vasovagal incidents since 1987. May have passed out one other time.
Andere Medikamente: Levothyroxine, sertraline, calcium and vit D, Claritin, turmeric, zinc
Allergien: Sensitivity to wheat, red food dye #40
Vorherige Impfungen: -

VAERS 952677

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: NY
Alter: 60,0
Geschlecht: M
Eingang: 18.01.2021
Impfdatum: 07.01.2021
Beginn: 11.01.2021
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: IM / RA

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

Condition aggravated Deep vein thrombosis Gait disturbance Pain in extremity Ultrasound scan

Symptomtext

DVT in right leg 4 days after injection, severe pain in thigh/calf, difficulty walking Placed on Xarelto 15mg 2X daily for 21 days and then 20mg daily for 9 days. Next Doctor visit is 1/26/2021 at 9:00am Next scheduled Covid 19 vaccine is scheduled for 2/5/2021 at 7:15am

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: -
Labordaten: Sonogram on 1/14/2021
Aktuelle Erkrankungen: None
Vorgeschichte: High Blood Pressure BPH DVT on June 6, 2016
Andere Medikamente: Valsartan 160mg daily Alfuzosin 10mg daily Aspirin 81mg daily
Allergien: None
Vorherige Impfungen: -

VAERS 951211

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: NY
Alter: 30,0
Geschlecht: M
Eingang: 17.01.2021
Impfdatum: 16.01.2021
Beginn: 17.01.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: IM / LA

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

Asthenia Balance disorder Body temperature increased Fall Fatigue Gait disturbance Lethargy Syncope

Symptomtext

Around 11:15 am, Jan 17, 2021, while standing at the toilet, my son either lost his balance or fainted and fell to the floor. He was able to cushion his fall so that he did not have any broken bones, bleeding etc. He said he felt weak and tired. I had to help him up from the floor. He was able to assist me but it was like lifting a dead weight (he weighs about 150). He was able to walk to his bed with his arms around my neck holding him upright. He is very tired/lethargic and not himself. Temperature is 99.7F by mouth. He has rested since the incident. Giving him apple juice to keep him hydrated. I need to help him up to a sitting position before he can drink.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: None. We did not call a doctor or 911.
Aktuelle Erkrankungen: None
Vorgeschichte: elevated cholestoral
Andere Medikamente: lipitor, 10mg, qd; acidophilus chewable probiotic, qd; fiber gummy, qd; multiple vitamin, qd; fish oil, 15 ml, qd
Allergien: NKA
Vorherige Impfungen: -

VAERS 949578

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: OH
Alter: 32,0
Geschlecht: F
Eingang: 15.01.2021
Impfdatum: 08.01.2021
Beginn: 08.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Dizziness Electrocardiogram Fall Headache Laboratory test Pain in extremity Syncope Urine analysis

Symptomtext

Immediate slight dizziness, continued for 1.5 hours, slight headache. Then 1.5 hours post vaccination syncope, fall to floor. ER workup was clear immediately following event, no abnormal testing, labs and ekg all normal. 1 week post vaccine, no other symptoms aside from sore arm.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Orthostatic pressures- normal all blood work and urine labs normal EKG normal Blood pressures normal heart rate normal All following syncope.
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Daily in evening: 50 mg Zinc, 500mg Vitamin C, Women's Prenatal Multi Vitamin
Allergien: Benzoyl Peroxide (hives) Doxycycline (possible) PCN (possible)
Vorherige Impfungen: -

VAERS 946446

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: NY
Alter: 41,0
Geschlecht: F
Eingang: 15.01.2021
Impfdatum: 09.01.2021
Beginn: 09.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Electrocardiogram Feeling hot Palpitations Swollen tongue Syncope Tremor Vital signs measurement Vomiting

Symptomtext

Injection given IM in patient's L deltoid. EUA distributed to patient per CDC regulations. Lot # 011J20A Manufactured by Moderna Patient filled out COVID 19 Immunization Screening and Consent Form. Pt presented to clinic 1/9/2021 for first dose of Moderna COVID-19 vaccine. 10-12 mins post vaccine pt began to feel warm/dizzy. Pt experienced a brief episode of syncope, shortly after pt regained consciousness , and then experienced 1 episode of emesis Pt was alert, reported hx of vasovagal type sx's, She was given juice, took Midodrine, and given IV Sodium Chloride 0.9% VSS Pt then reported feeling fast heart rate, EKG done w/ NSR Pt began to experience body tremors, HR 109, BP WNL EpiPen administered at 10:58 a.m. per provider's order Pt reports subjective tongue swelling , Second dose of Epi given 11:08a.m. Pt transported to Hospital via ambulance

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: n/a
Vorgeschichte: History of vasovagal like symptoms
Andere Medikamente: n/a
Allergien: n/a
Vorherige Impfungen: -

VAERS 946300

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: MO
Alter: 28,0
Geschlecht: F
Eingang: 15.01.2021
Impfdatum: 23.12.2020
Beginn: 23.12.2020
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / AR

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

Epilepsy Seizure

Symptomtext

PLEASE NOTE: The patient verbally reported this event to me on 01/14/2021. The event occurred 12/23/2020. Seizure approximately 5-6 hours after receiving the vaccine. Repeat seizures approximately 30 and 54 hours post vaccination. Please note, the patient states she is a newly diagnosed epileptic. She claimed her neurologist recently adjusted her seizure medications as well prior to the vaccination.

Weitere VAERSDATA-Felder

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

VAERS 944637

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: OH
Alter: 37,0
Geschlecht: F
Eingang: 14.01.2021
Impfdatum: 31.12.2020
Beginn: 31.12.2020
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Hypoaesthesia oral Palpitations Paraesthesia oral Syncope Tachycardia

Symptomtext

Tachycardia, palpitations, lightheadedness/near syncope, and numbness/tingling to tongue and lips 10 minutes after receiving vaccine. All symptoms resolved in about 15 minutes with the exception of numbness/tingling to tongue and lips which lasted 3 hours. Symptoms resolved on their own without treatment/medication other than lying flat with feet up and drinking a bottle of water. I was assessed by medical professionals at the vaccine clinic which was located inside of the hospital. I consulted with an ED physician but did not require any additional treatment.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Vitamin D 2000 IU PO daily Spironolactone 50mg PO daily Pepcid 20mg PO daily Deplin 15mg PO daily Calcium Carbonate 750mg PO daily
Allergien: Amoxicillin
Vorherige Impfungen: -

VAERS 943945

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: NC
Alter: 43,0
Geschlecht: F
Eingang: 14.01.2021
Impfdatum: 12.01.2021
Beginn: 13.01.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Angiogram Asthenia Chest X-ray normal Computerised tomogram head normal Confusional state Electrocardiogram normal Feeling abnormal Fibrin D dimer increased Head injury Headache Laboratory test normal Loss of consciousness Pain in extremity

Symptomtext

I was fine the day of the vaccination. I started feeling bad overnight - got a headache and arm got sore. When I woke up in the morning to get ready for work I felt very weak. I walked into my bathroom and lost conciousness. I woke up on the floor and had hit my forehead on the tile floor. I was confused when I got up, and proceeded to get into the shower. I then passed out again in the shower and hit the back of my head against the shower wall. My husband found me as I woke up on the shower floor. He called my doctor and took me to the emergency department on doctors advice.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: on 1/13 /21 in the emergency department I had a chest X-ray, CT scan of my head, and a chest angiography to rule out pulmonary embolism due to a slightly elevated D-dimer blood test. All other lab tests were within normal limits (they checked me for anemia, checked electrolytes and CBC, did a urinalysis). All X-rays and scans were negative. They also completed an EKG in emergency department, which was normal but fast. My pulse rate was 100-108 while I was in emergency department. blood pressure and pulse ox were all normal.
Aktuelle Erkrankungen: I did have covid diagnosed on 12/30/20, but I had very mild symptoms and was completely recovered by the time I received the vaccination.
Vorgeschichte: none
Andere Medikamente: Ortho Cyclen oral contraceptive, fluticasone nasal spray, cetirizine 10mg tablets
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1416914

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011j20a

schwer

Staat: -
Alter: 30,0
Geschlecht: F
Eingang: 13.01.2021
Impfdatum: 07.01.2021
Beginn: 06.01.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: IM / LA

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

Arthralgia Dizziness Headache Myalgia Nausea Pyrexia Syncope Vomiting

Symptomtext

Dizziness, Headache, Myalgia, Arthralgia, Fever, NauseaVomiting & Syncope Narrative:

Weitere VAERSDATA-Felder

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

VAERS 941920

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: IA
Alter: 27,0
Geschlecht: F
Eingang: 13.01.2021
Impfdatum: 07.01.2021
Beginn: 09.01.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / RA

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

Bell's palsy Oral herpes

Symptomtext

Patient reported cold sores in her mouth on 1/9/2021 and then on 1/12/21 was seen in Dr. office and diagnosed with Bells Palsy. Patient was started on antivirals and prednisone.

Weitere VAERSDATA-Felder

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

VAERS 941476

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: FL
Alter: 45,0
Geschlecht: M
Eingang: 13.01.2021
Impfdatum: 28.12.2020
Beginn: 28.12.2020
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Angiogram Chills Computerised tomogram Hemianopia Intensive care Ischaemic stroke Magnetic resonance imaging Malaise Migraine Nausea Pyrexia

Symptomtext

Patient received vaccine in afternoon of 12/28. She works in ER as housekeeper 7pm-7am. The day she received the vaccine she became ill with fever chills and nausea and left work at 2am. On 12/31 she developed hemianopia. She went to ER and they did CT scan. She was told it was complex migraine. She left and came Home. On 1/1/21 her vision was back to normal. On 1/3 she suffered bilateral cerebellum ischemic stroke. She is currently in medical center. In Trauma.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 6,0
Labordaten: CT CT Angio MRI/MRA
Aktuelle Erkrankungen: -
Vorgeschichte: Diabetes Morbid obesity Hypertension Herpes
Andere Medikamente: Valacyclovir 1gm daily Spirinolactone 100mg TID Januva 100mg 1 daily Glimepiride 2mg BID Elmiron 100mg TID Lisinopril 20mg once daily Escitalopram 10mg once daily
Allergien: None
Vorherige Impfungen: -

VAERS 941437

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: NC
Alter: 39,0
Geschlecht: F
Eingang: 13.01.2021
Impfdatum: 29.12.2020
Beginn: 29.12.2020
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Loss of consciousness Syncope

Symptomtext

within 5-10 minutes of injection, felt light-headed and fainted, support was with her and we helped her to the floor until stretcher could be moved over to her, immediately came to, placed on stretcher, rested for 10-15 minutes, drank water, felt well and got up from stretcher, no issues

Weitere VAERSDATA-Felder

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

VAERS 940695

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: MO
Alter: 32,0
Geschlecht: F
Eingang: 13.01.2021
Impfdatum: 12.01.2021
Beginn: 12.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Anaphylactic reaction Dyspnoea Feeling hot Flushing Palpitations Throat tightness

Symptomtext

Client complained of feeling flushed, hot, heart racing and tight throat and difficulty breathing. Vitals taken and placed in supine position with feet elevated but complained of hard to breathe so sat up. Started yelling she couldn't breathe, encouraged her to calm down take deep breaths, able to take drinks of water, and talk. BP 144/80 Pulse: 119 No swelling noted and no blueness of lips or fingers. Calmed down after drank water but then started yelling again in about 2 minutes she couldn't breathe and she wanted EPI would I please give her EPI. Gave 0.5cc Epinephrine, this immediately helped she said still wanted 911 called noted no breathing issues or swallowing issues drinking water, also called 911 . Ambulance here at 1:45 and checked o2 sat reported 98% Vitals taken by ambulance but not reported to us. Called the patient this morning 01/13/2021, she reported she had another episode in the ambulance she felt she couldn't breathe and they gave her Benadryl 0.5cc and she said she never had another episode after she got to the hospital, she reported the ER DR. diagnosed her with anaphylactic reaction to the vaccine. She returned to work this morning no issues she reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: Unknown, she did not report any labs to us.
Aktuelle Erkrankungen: None reported
Vorgeschichte: None reported
Andere Medikamente: Celexa daily High caffeine tea
Allergien: None
Vorherige Impfungen: -

VAERS 932059

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: LA
Alter: 49,0
Geschlecht: M
Eingang: 13.01.2021
Impfdatum: 08.01.2021
Beginn: 09.01.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / -

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

Alanine aminotransferase normal Anion gap Arthralgia Aspartate aminotransferase normal Asthenia Balance disorder Diarrhoea Dizziness Electrocardiogram abnormal Blood albumin normal Blood alkaline phosphatase normal Blood bilirubin normal Blood calcium decreased Blood chloride normal Blood creatinine normal Blood glucose normal Blood potassium normal Blood sodium normal

Symptomtext

49 yo male was vaccinated 01/08/2021 and reported some dizziness. Saturday morning 01/09/2021 he woke up feeling weak, tired, and had significant nausea. The patient had an episode of vomiting x2 which made him weaker. The patient then had a near-syncopal event, which prompted his wife bringing him in for evaluation. He denies significant fever, chills, headache, cough or congestion. However, at the hospital he reports some joint pain, fevers and chills. Upon arriving at the ER, BP 126/72, p. 94, resp 18, temp 98.7, pulse ox 98%. HT 6'2", WT 208#, BMI 39.5. Physical exam was otherwise unremarkable. Workup: WBC 10.5, Hgb 15.6, Hct 45.6, Platelet 293,000, left shift w/93% neutrophils. Na 141, Potass 3.5, Chl 105, C

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: 1,0
Labordaten: Workup: WBC 10.5, Hgb 15.6, Hct 45.6, Platelet 293,000, left shift w/93% neutrophils. Na 141, Potass 3.5, Chl 105, CO2 28.1, gap 11.4, Gluc 128, BUN 19, Cr 1.11, protein 7.2, Alb 3.8
Aktuelle Erkrankungen: None known, on weight loss medication
Vorgeschichte: Hypertension, Kidney Stones, Hypogonadism,
Andere Medikamente: Amlodipine 5mg/day, Losartan 100mg/day, Naproxen 500mg bid pe
Allergien: NKDA
Vorherige Impfungen: -

VAERS 932059

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: LA
Alter: 49,0
Geschlecht: M
Eingang: 13.01.2021
Impfdatum: 08.01.2021
Beginn: 09.01.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Alanine aminotransferase normal Anion gap Arthralgia Aspartate aminotransferase normal Asthenia Balance disorder Diarrhoea Dizziness Electrocardiogram abnormal Blood albumin normal Blood alkaline phosphatase normal Blood bilirubin normal Blood calcium decreased Blood chloride normal Blood creatinine normal Blood glucose normal Blood potassium normal Blood sodium normal

Symptomtext

49 yo male was vaccinated 01/08/2021 and reported some dizziness. Saturday morning 01/09/2021 he woke up feeling weak, tired, and had significant nausea. The patient had an episode of vomiting x2 which made him weaker. The patient then had a near-syncopal event, which prompted his wife bringing him in for evaluation. He denies significant fever, chills, headache, cough or congestion. However, at the hospital he reports some joint pain, fevers and chills. Upon arriving at the ER, BP 126/72, p. 94, resp 18, temp 98.7, pulse ox 98%. HT 6'2", WT 208#, BMI 39.5. Physical exam was otherwise unremarkable. Workup: WBC 10.5, Hgb 15.6, Hct 45.6, Platelet 293,000, left shift w/93% neutrophils. Na 141, Potass 3.5, Chl 105, C

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: 1,0
Labordaten: Workup: WBC 10.5, Hgb 15.6, Hct 45.6, Platelet 293,000, left shift w/93% neutrophils. Na 141, Potass 3.5, Chl 105, CO2 28.1, gap 11.4, Gluc 128, BUN 19, Cr 1.11, protein 7.2, Alb 3.8
Aktuelle Erkrankungen: None known, on weight loss medication
Vorgeschichte: Hypertension, Kidney Stones, Hypogonadism,
Andere Medikamente: Amlodipine 5mg/day, Losartan 100mg/day, Naproxen 500mg bid pe
Allergien: NKDA
Vorherige Impfungen: -

VAERS 937571

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: MO
Alter: 50,0
Geschlecht: F
Eingang: 12.01.2021
Impfdatum: 28.12.2020
Beginn: 11.01.2021
Tage bis Beginn: 14,0
Dosis: 1
Route/Site: IM / LA

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

Bell's palsy

Symptomtext

Patient developed Bells Palsy.

Weitere VAERSDATA-Felder

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

VAERS 937128

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: FL
Alter: 68,0
Geschlecht: F
Eingang: 12.01.2021
Impfdatum: 04.01.2021
Beginn: 05.01.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Contusion Dizziness Fatigue Head injury Malaise Pain in extremity Syncope

Symptomtext

MODERNA COVID-19 Vaccine EUA I took the vaccine on Monday Jan 4 at around 9 AM. During the day only pain in the left arm. On Tuesday I felt tired all day long. At 7 PM, I took a Coke inside the fridge and I noticed and told my husband I was not feeling well. I put the coke in the glass, after I took the glass in my hand and then I fainted. Never in my life I have fainted before. I hit my head in the floor. Now I have some bruise in my face, mainly around my left eye. Feeling a little dizzy, I am in quarantine I and my husband are staying home all the time. I have my doctor scheduled for next Thursday.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Not done yet. I have my doctor scheduled for next Thursday. January 14.
Aktuelle Erkrankungen: No
Vorgeschichte: Left bundle blockage of the heart
Andere Medikamente: Ezetimibe 10 mg; Atenolol 2,5 mg; Atorvastatin 10 mg, Vitamin D and Aspirin low dose 81 mg
Allergien: No
Vorherige Impfungen: -

VAERS 935780

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: OH
Alter: 61,0
Geschlecht: F
Eingang: 11.01.2021
Impfdatum: 05.01.2021
Beginn: 05.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Abdominal pain upper Blood test Chest X-ray Computerised tomogram Contusion Dysstasia Electrocardiogram Eye contusion Fatigue Feeling of body temperature change Headache Loss of consciousness Malaise Memory impairment Poor quality sleep Sensation of foreign body Swelling face Swelling of eyelid

Symptomtext

Extremely tired went to bed at 8:30. At 11:00, tossed and turned until 12:16 a.m. Did not think she could stand up. Walked in the bathroom had pain in stomach, was very hot and freezing at the same time, was shaking. Head hurt was hurting so bad. Tried standing up from toilet, was passed out. Eye, half of face is bruised and swollen , eye shut for two days. More than forty minutes passed before she could call her husband. Does not remember anything because she was passed out. Husband came in and grabbed her, to get her back into bed. she could not stand. Went to ER at Hospital. Had CT scan, blood work , EKG, chest xray. Was still kind of out of it but was able to communicate with nurses. Face is still black and blue. Last night got up at 4:00 a.m. something was wrong with her throat. Felt like a walnut was in her throat. Went to doctor this morning. They said it was a reaction from the shot. Got an EpiPen, prednisone. Call them in 2 days to let them know how she's doing and also wear a heart monitor because they do not know how to take care of her, Has had vision blurriness in both eyes. Has not felt well at all.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Ct Scan, EKG, chest xray, bloodwork
Aktuelle Erkrankungen: no
Vorgeschichte: Thyroid
Andere Medikamente: Levothyroxyn, Lisinopril
Allergien: Penicillin, Amoxicillin, Sulfur, pineapple
Vorherige Impfungen: -

VAERS 934289

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: WV
Alter: 63,0
Geschlecht: F
Eingang: 11.01.2021
Impfdatum: 23.12.2020
Beginn: 02.01.2021
Tage bis Beginn: 10,0
Dosis: 1
Route/Site: IM / LA

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

Bell's palsy Eye pain Facial paralysis Full blood count normal Headache Hypoaesthesia oral

Symptomtext

JAN2-HEADACHE, JAN 3 RIGHT SIDE OF TONGUE BECAME NUMB, AND JAN 4 RIGHT SIDE OF MOUTH BECAME NUMB, RIGHT EYE PAIN WITH TEARING, NOTICABLE DROOPING RIGHT SIDE OF FACE, MINIMAL ACTIVE MOVEMENT, FLUIDS DRIBBLED OUT OF RIGHT SIDE OF MOUTH WHEN DRINKING LIQUIDS, EVALUATED BY PA ON 1/5, DIAGNOSED WITH BELL'S PALSY, STARTED ON VALACYCLOCIR 1 GM THREE TIMES A DAY AND PREDNISONE TAPER BEGINNING WITH 60 MG X 5 DAYS AND TAPERING DOWNWARD

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: CBC - NORMAL, LYME TITER - PENDING
Aktuelle Erkrankungen: NONE
Vorgeschichte: HTN, HASHIMOTOS THYROIDITIS, HYDRENITIS SUPPORATIVA, ARTHRITIS
Andere Medikamente: HCTZ, AMITRIPTYLINE, ELIQUIS, CYMBALTA, ESTRAGEN PATCH, PROAIR AS NEEDED, CINNAMON, NIAGEN, FIBER, MAGNESIUM, PROBIOTICS, QUNOL, SUNFLOWER LECITHIN, VITAMIN D3, ZINC
Allergien: DEMEROL, PERCOCET, WELLBUTRIN, CELEBREX, GABAPENTIN, NSAIDS
Vorherige Impfungen: -

VAERS 933771

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: NJ
Alter: 39,0
Geschlecht: F
Eingang: 11.01.2021
Impfdatum: 07.01.2021
Beginn: 07.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Bell's palsy Facial paralysis Paraesthesia oral

Symptomtext

1/7- RECEIVED VACCINE AND REPORTED HAVING TINGLING TO LIPS (A FEW HOURS LATER), TOOK BENADRYL AND REPORTED THAT TINGLING WENT AWAY. 1/8- REPORTED TINGLING TO LEFT OUTERLIP AND AND WENT TO ER AND DIAGNOSED WITH BELL PALSY / FACIAL PARALYSIS AFTER EVALUATION

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: 1/8 CT HEAD
Aktuelle Erkrankungen: None
Vorgeschichte: Cervicalgia ? DJD (degenerative joint disease) of cervical spine ? Obesity ? Paresthesia and pain of both upper extremities
Andere Medikamente: Unknown
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1395618

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011j20a

schwer

Staat: -
Alter: 34,0
Geschlecht: M
Eingang: 10.01.2021
Impfdatum: 29.12.2020
Beginn: 29.12.2020
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Condition aggravated Eye movement disorder Feeling abnormal Headache Nausea Pruritus Seizure Urticaria Vomiting

Symptomtext

Headache, Seizures, UrticariaPruritus & NauseaVomiting Narrative: NORMALLY HAVE SEIZURES EVERY EVENING, BUT THIS SEIZURE ABOUT 5.5 POST VACCINE WAS MUCH MORE SEVERE WITH "EYES ROLLING IN BACK OF HEAD" AND FELT "IN A DAZE". TOOK AN EXTRA DOSE OF CLONAZIPAM 1 MG

Weitere VAERSDATA-Felder

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

VAERS 932948

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: KS
Alter: 40,0
Geschlecht: M
Eingang: 10.01.2021
Impfdatum: 27.12.2020
Beginn: 28.12.2020
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Bell's palsy Computerised tomogram head Laboratory test normal

Symptomtext

Bells Palsy approximately 24 hours after vaccination. I presented to the ER for evaluation. I was treated with steroids and antivirals for 7 days. Symptoms ave still persisted to date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: Labs and CT scan of brain normal.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 990775

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011j20a

schwer

Staat: -
Alter: 34,0
Geschlecht: M
Eingang: 09.01.2021
Impfdatum: 29.12.2020
Beginn: 29.12.2020
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Eye movement disorder Feeling abnormal Headache Nausea Pruritus Seizure Urticaria Vomiting

Symptomtext

Headache, Seizures, UrticariaPruritus & NauseaVomiting Narrative: NORMALLY HAVE SEIZURES EVERY EVENING, BUT THIS SEIZURE ABOUT 5.5 HRS POST VACCINE WAS MUCH MORE SEVERE WITH "EYES ROLLING IN BACK OF HEAD" AND FELT "IN A DAZE". TOOK AN EXTRA DOSE OF CLONAZIPAM 1 MG

Weitere VAERSDATA-Felder

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

VAERS 981697

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011j20a

schwer

Staat: -
Alter: 33,0
Geschlecht: F
Eingang: 09.01.2021
Impfdatum: 30.12.2020
Beginn: 31.12.2020
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Arthralgia Cough Headache Myalgia Pyrexia Syncope Wheezing

Symptomtext

Headache, Myalgia, Arthralgia, Fever, CoughWheeze & Syncope Narrative:

Weitere VAERSDATA-Felder

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

VAERS 931174

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: CT
Alter: 28,0
Geschlecht: M
Eingang: 09.01.2021
Impfdatum: 28.12.2020
Beginn: 08.01.2021
Tage bis Beginn: 11,0
Dosis: 1
Route/Site: - / LA

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

Dizziness Palpitations Presyncope Vaccination site erythema Vaccination site swelling Vaccination site warmth

Symptomtext

11 days after initial vaccination: vaccination site became warm swollen and red. Physically felt lightheaded/dizzy with near syncope episode and heart palpitations. Took Zyrtec, Benadryl and went to emergency room.

Weitere VAERSDATA-Felder

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

VAERS 930613

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: AK
Alter: 37,0
Geschlecht: F
Eingang: 08.01.2021
Impfdatum: 08.01.2021
Beginn: 08.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Dizziness Hypersensitivity Presyncope Throat irritation Throat tightness

Symptomtext

Major allergic reaction, became lightheaded with a near syncopal episode. Patient complained of tightness and itchiness in her throat.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: Potatoes, bupropion, morphine,
Vorherige Impfungen: -

VAERS 930277

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: CA
Alter: 50,0
Geschlecht: M
Eingang: 08.01.2021
Impfdatum: 08.01.2021
Beginn: 08.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Presyncope

Symptomtext

patient described feeling lightheaded, near syncope, 'almost passed out' 15 minutes after vaccine administration

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 930005

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: AZ
Alter: 26,0
Geschlecht: F
Eingang: 08.01.2021
Impfdatum: 22.12.2020
Beginn: 22.12.2020
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Chest X-ray Computerised tomogram head Headache Hypoaesthesia Lumbar puncture Magnetic resonance imaging spinal Metabolic function test Paraesthesia Swollen tongue Syncope Urine analysis

Symptomtext

initial; swelling of tongue, tingling and numbness in legs, syncope. later; HA

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: 6,0
Labordaten: head CT, cxr, spinal mri, spinal tap, cmp/vitals/UA
Aktuelle Erkrankungen: none
Vorgeschichte: cholecystectomy one month prior to vaccination with chronic diarrhea since
Andere Medikamente: none
Allergien: cephalosporins, tramadol
Vorherige Impfungen: -

VAERS 929384

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: PR
Alter: 32,0
Geschlecht: M
Eingang: 08.01.2021
Impfdatum: 08.01.2021
Beginn: 08.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Blood glucose increased Dizziness Feeling hot Hyperhidrosis Musculoskeletal stiffness Posture abnormal Staring Syncope

Symptomtext

Fifteen minutes after vaccine administration, patient was sitting outside and had an episode of vasovagal syncope. He became diaphoretic, thousand yard stare, limbs stiff, and then slumped for less than 5 seconds while sitting. He was lowered to the ground and legs elevated, supplemental oxygen provided. He came to within 15 seconds of initial symptoms. He stated he felt hot and ?woozy.? Vital signs: BP 107/69, HR 88, SpO2: 99, Resp: 16, temp 98.8. Blood glucose 127. Patient states he was out in the sun the day prior and did not hydrate as he should have. Cool water was provided and he received 500mL of saline IV. Patient was monitored for 2 hours post episode and was released back to work feeling good without any further issues. Patient stated he had a previous sync opal episode upon receiving some anxiety producing news in the past and states that this episode felt similar.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: 01/08/2021: blood glucose: 127
Aktuelle Erkrankungen: Denies any.
Vorgeschichte: Denies any.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 928642

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: OH
Alter: 61,0
Geschlecht: F
Eingang: 08.01.2021
Impfdatum: 07.01.2021
Beginn: 07.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Anaphylactic reaction Dyspnoea Tachypnoea Use of accessory respiratory muscles Wheezing

Symptomtext

Patient was brought to the ED after receiving the Moderna vaccine for difficulty breathing. Per RN progress note: "Pt arrived via wheelchair from auditorium, pt had received her first COVID vaccine left deltoid, approx. 10 minutes later pt appeared to have an anaphylactic reaction, pt arrives wheezing and tachypneic, labored breathing with accessory muscle use." The patient was placed on supp oxygen and received epinephrine 0.5mg IM x1, Benadryl 50mg IV x1, hydrocortisone 200mg IV x1, lorazepam 1mg IV x1. Pt discharged after 6 hour observation with Rx's for EpiPen, prednison, Benadryl, and famotidine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Asthma, T2DM, diabetic neuropathy, HTN, depression
Andere Medikamente: Cymbalta, Breo Ellipta, Ventolin, carvedilol, amlodipine, lisinopril, dulaglutide
Allergien: N/A: According to medical record and the vaccine pre-screening questionnaire, pt does not have a history of severe allergies or anaphylaxis.
Vorherige Impfungen: -

VAERS 928461

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: FL
Alter: 67,0
Geschlecht: M
Eingang: 08.01.2021
Impfdatum: 29.12.2020
Beginn: 03.01.2021
Tage bis Beginn: 5,0
Dosis: 1
Route/Site: IM / LA

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

Anaphylactic reaction Computerised tomogram abnormal Eye swelling Intensive care Laboratory test Lip swelling Oedema Pharyngeal oedema Pruritus Rash Rash erythematous Rash papular Swelling face

Symptomtext

Anaphylactic reaction, Severe edema and raised red rash entire body, Severe itching ,Soft tissue edema of throat. Swelling of, eyes, lips, face. Multiple trips to ER, treated with steroids, Benadryl, prevacid. , CURRENTLY IN ICU ON EPINEPHRINE DRIP, STEROIDS, MULTIPLE MEDS

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: 5,0
Labordaten: Multiple labs, ct scan soft tissue edema of throat
Aktuelle Erkrankungen: none
Vorgeschichte: Diabetes
Andere Medikamente: Metformin, Lisinopril, Simvastatin, Ozempic , pantopazol
Allergien: Cephlasporin
Vorherige Impfungen: -

VAERS 918491

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: -
Alter: 40,0
Geschlecht: F
Eingang: 08.01.2021
Impfdatum: 30.12.2020
Beginn: 30.12.2020
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Abdominal pain Anaphylactic reaction Diarrhoea Headache Lacrimation increased Myalgia Nausea Muscle spasms Retching Vomiting

Symptomtext

approx 2-4 hours after receiving the vaccine, developed HA, myalgias, nausea, vomiting, diarrhea

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: treated for anaphylaxis
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 925765

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: OH
Alter: 30,0
Geschlecht: F
Eingang: 07.01.2021
Impfdatum: 30.12.2020
Beginn: 30.12.2020
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Facial paralysis Hypoaesthesia Paraesthesia

Symptomtext

Pt presented back to clinic on 1/7/21 and shared adverse event of numbness/tingling on right side of face and right leg (same side as vaccine was given). She was treated by PCP for potential bells palsy.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: Raynaud's syndrome (2016 note in EMR)
Andere Medikamente: unknown
Allergien: Latex
Vorherige Impfungen: -

VAERS 925159

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: VA
Alter: 28,0
Geschlecht: F
Eingang: 07.01.2021
Impfdatum: 06.01.2021
Beginn: 07.01.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / RA

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

Asthenia Back pain Chills Dehydration Dizziness Feeling hot Headache Heart rate increased Insomnia Loss of consciousness Migraine Neck pain Pyrexia

Symptomtext

Moderna COVID-19 Vaccine EUA. Around 7pm on 06Jan21, symptoms began with a headache, increased heart rate, inability to sleep/relax. On 07Jan21, Migraine headache, inability to sleep/relax, increased heart rate, passed out, lightheaded, back pain, neck pain, weak, fever, chills, hot, dehydrated (even with large consumption of water). Took two motrin and an hour nap, which severely decreased above symptoms but still experienced them.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: I did not receive any medical tests or seek medical attention.
Aktuelle Erkrankungen: NA
Vorgeschichte: NA
Andere Medikamente: Viorelle, multi vitamin, vitamin c, zinc/magnesium/d3 vitamin
Allergien: NA
Vorherige Impfungen: -

VAERS 924050

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: HI
Alter: 55,0
Geschlecht: F
Eingang: 07.01.2021
Impfdatum: 06.01.2021
Beginn: 06.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Anaphylactic reaction Dyspnoea Cough Pallor Respiratory distress

Symptomtext

Was notified by observational team leader (EMT) at 8:38 am. Patient appeared to be coughing, pale and in respiratory distress. Clinic Manager called 911 at 8:40 am. Observational team leader performed vital signs at 8:40 am (BP: 160/90, P: 108, R: 24). Physician on-site attended and assessed patient. Patient offered and declined epinephrine. Vital signs taken at 8:45 am (P: 82, R: 16). EMR arrived on-site at 8:47 am and transported patient to Hospital at 8:58 am.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Unknown
Vorgeschichte: -
Andere Medikamente: -
Allergien: Unknown
Vorherige Impfungen: -

VAERS 919646

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: OH
Alter: 64,0
Geschlecht: M
Eingang: 04.01.2021
Impfdatum: 29.12.2020
Beginn: 30.12.2020
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Blood thyroid stimulating hormone Chest X-ray Chills Choking sensation Dyspnoea Electrocardiogram Fatigue Full blood count Headache Loss of consciousness Metabolic function test Nausea Troponin I Urticaria

Symptomtext

Patient began having headache and fatigue 12/29. Early morning of 12/30 patient reported severe chills. Felt better during the day of 12/30 with only a headache. Night of 12/30 patient reported severe chills again and wanted to call the doctor in the morning, but the felt better on 12/31. The night of 12/31 patient again had chills, but less severe (rated 3/10 on scale). Night of 1/1 patient reported slight hive like rash that went away with warm Epsom salt bath. 1/3 0100 patient woke up with severe hives down back of legs and lower back. Got into a hot tub to soak and once the patient got out he was standing at the sink and passed out. His wife got him back to bed. Around 0700 on 1/3 patient woke up to urinate and he passed out again. He states both times he passed out felt the same stating "I felt like I was going to vomit and then all of a sudden I couldn?t breath, almost like I was choked out."

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Lab Tests (1/3/2021): CBC CMP TSH Troponin-l Diagnostic Studies (1/3/2021): Chest AP 1V Chest X-ray EKG
Aktuelle Erkrankungen: -
Vorgeschichte: Splenectomy. Cancer survivor.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 919640

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: TN
Alter: 26,0
Geschlecht: F
Eingang: 04.01.2021
Impfdatum: 26.12.2020
Beginn: 27.12.2020
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Blood test Chills Dehydration Dry mouth Hypotension Loss of consciousness Pain Pain in extremity Urine analysis

Symptomtext

got the shot around 11 am on 12/26 and my mouth became immediately parched. My arm was super sore as the day went on and around 4:30 am I woke up shivering with chills and aches and a mild temp of 99. Passed out and BP was extremely low. Parents called an ambulance and I went to Emergency room.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: blood work--dehydration urine test catscan on head where I fell tests on heart to determine why blood pressure was so low
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: jolessa (birth control)
Allergien: Zithromax medro dose pack
Vorherige Impfungen: -

VAERS 919624

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: PA
Alter: 29,0
Geschlecht: F
Eingang: 04.01.2021
Impfdatum: 29.12.2020
Beginn: 29.12.2020
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Asthenia Blood pressure decreased Chills Decreased appetite Dizziness Fatigue Headache Hot flush Lymphadenopathy Mobility decreased Nausea Pain in extremity Paraesthesia Speech disorder Syncope

Symptomtext

Around 10 or 11 pm, arm pain, chills, fatigue, headache, nausea, swollen lymph nodes, lightheadedness, fainted in tub. Next day, fatigue all day, couldn't talk, or eat. Went back to bed again. The following day hot flashes, weakness. went to ER. Felt like blood pressure was dropping, tingling in legs, difficulty lifting her head.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: no
Aktuelle Erkrankungen: no
Vorgeschichte: no
Andere Medikamente: no
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 919546

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: AL
Alter: 51,0
Geschlecht: F
Eingang: 04.01.2021
Impfdatum: 29.12.2020
Beginn: 01.01.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: IM / LA

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

Antinuclear antibody positive Antiphospholipid antibodies Aphasia Blood cholesterol increased Blood homocysteine Coagulation time Craniotomy Low density lipoprotein increased Mechanical ventilation Thrombotic stroke

Symptomtext

thrombotic stroke -necessitating hospitalization; and craniotomy; required mechanical ventilator for 2 days. Patient now extubated, breathing on her own. Patient remains hospitalized with marked deficits (aphasic)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombotic stroke
Hospital-Tage: 3,0
Labordaten: Total cholesterol- 465 LDL- 351 ANA (+) Labs pending- Lupus AC; antiphospholipid AB, homocysteine levels; hypercoagulability profile
Aktuelle Erkrankungen: PMH- Lupus; HTN; marked hyperlipidemia
Vorgeschichte: Lupus Hypertension Hyperlipidemia
Andere Medikamente: Plaquenil Fioricet Midrin
Allergien: None listed
Vorherige Impfungen: -

VAERS 919372

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: PA
Alter: 28,0
Geschlecht: F
Eingang: 04.01.2021
Impfdatum: 22.12.2020
Beginn: 31.12.2020
Tage bis Beginn: 9,0
Dosis: UNK
Route/Site: SYR / RA

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

Blood test Computerised tomogram Ear pain Eating disorder Eyelid function disorder Facial paralysis Headache

Symptomtext

Bell's Palsy on the right side of my face. ear ache, head ache all on the right side. droopiness of the right eye and right side of lips. inability to fully shut my eye., difficulty eating and drinking. Attempted to go to an urgent care on 1/02/2021, but they sent me to the ER. ER evaluated me and sent me home with antivirals and steroids. I was sent home with Prednisone and Acyclovir

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: -
Labordaten: CAT scan and blood work both on 01/02/2021
Aktuelle Erkrankungen: n/a
Vorgeschichte: migraines and asthma
Andere Medikamente: adderall xr meloxicam baclofen pristiq
Allergien: shellfish All nuts except almonds sulfa drugs lexapro penicillin amoxicillin
Vorherige Impfungen: -

VAERS 918081

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: NY
Alter: 26,0
Geschlecht: M
Eingang: 04.01.2021
Impfdatum: 30.12.2020
Beginn: 31.12.2020
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / RA

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

Chest X-ray Ear discomfort Haematology test normal Hypoaesthesia Injected limb mobility decreased Injection site pain Injection site reaction Joint stiffness Laboratory test normal Malaise Musculoskeletal stiffness Pain Pain in extremity Pallor Photophobia Presyncope Throat tightness Tinnitus

Symptomtext

I received the shot around 0730 on 12/30/2020. Went home and got ready for work. Around 12am 12/31/2020 my arm started to radiate at the injection site and was very tense. I placed a heat pack on the right harm but the pain did not dissipate. My arm continued to be in pain for the rest of the night. Around 0240 I ate dinner, had water and still had some arm pain. Around 0345 my arm started to flare up and sent pain sensations throughout my body. My right arm was increasingly discomforting, I could barely move it. The sensations spread to my legs, numbing them and my throat had felt as if it were closing up. I got up to get the attention of the nurse and was able to flag her down. She said I was pale as a ghost. My vision was very blurry, I could not hear anything because my ears had filled up and everything was muffled. My head had begun to ring and I was on the brink of fainting when a chair was given to me. My eyes had become extremely sensitive to the light, I was given water and spoken to about what had happened leading up to the event. I was greeted by the paramedics who drew my blood, placed an IV and transferred me to the Acute Care portion of the Emergency Department. My vitals were 76/49, 80/50, 90/56, 100/60 before being brought to the ER. On 1/1/2021 My thighs have been sore/tense, my knees and ankles have been stiff and just feeling sickly. On 1/2/2021 much of the same symptoms are present. The soreness in the muscles isn't as prevalent, however joints still are stiff On 1/3/2021, congestion and runny nose are still present, stiffness in ankles and now shins are prevalent.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: 12/31/2020 0500 Chemistry and Hematology Results were all within normal range Chest x-ray completed. Staff suggested follow up with cardiologist. 1000ml Lactated Ringers was given in to me in my left arm
Aktuelle Erkrankungen: Cough, Congestion, Runny nose
Vorgeschichte: Raynaud's
Andere Medikamente: Nutrilite Men's Pack ( Daily Vitamin)
Allergien: None
Vorherige Impfungen: -

VAERS 917882

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: NJ
Alter: 49,0
Geschlecht: F
Eingang: 03.01.2021
Impfdatum: 22.12.2020
Beginn: 22.12.2020
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Anaphylactic reaction Dizziness Dyspnoea Erythema Flushing Nausea Palpitations Respiratory distress SARS-CoV-2 test negative Swollen tongue Wheezing

Symptomtext

Patient is hospital employee who completed screening form for COVID-19 vaccine by answering "no" to all contraindication questions. Approx 10 minutes after receiving COVID-19 vaccine dose # 1, patient was still in vaccine clinic area and complained of dizziness, palpitations and flushing. I observed patient fanning herself with papers. She was escorted out of the immediate clinic room, and assessed by paramedics present as having an anaphylactic reaction. Epinephrine 0.3 mg IM and diphenhydramine 50 mg IV given in clinic, Rapid Response was called overhead and patient immediately transported down the hall to the Emergency Dept. In ED, pt was noted as having swollen tongue, large areas of erythema on face, arms and chest, shortness of breath, nausea, dizziness (per ED physician notes). Pt reported being hospitalized in ICU with COVID disease more than 3 months ago, including intubation (not treated at this hospital), and has been back at work since August 2020. ED physical exam noted bilateral wheezing and patient in acute distress. In ED, pt administered racemic epinephrine 2.25% 0.5 mL via neb, epinephrine 0.3 mg IM, diphenhydramine 50 mg IV, Solu-Medrol 125 mg IV, famotidine 20 mg IV and epinephrine 5 mg/250 mL IV drip (started at 0.118 mcg/kg/min). Acute symptoms reported to resolve in ED. COVID test was negative. ED physician discovered that pt had history of multiple medications, including previous anaphylactic reaction to radiocontrast dye requiring intubation (which was not disclosed on the vaccine screening form). Pt admitted to Telemetry floor for observation. Overnight course was unremarkable, and patient was discharged the following day with prescription for Prednisone taper and prescription for Epi-pen. Advised not to return for second dose of COVID vaccine. EMR updated to reflect possible anaphylactic reaction to Moderna COVID-19 vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: 1,0
Labordaten: COVID-19 antigen negative, BP 126/52, pulse 96 on admission to ED
Aktuelle Erkrankungen: none reported
Vorgeschichte: Past Medical History (as noted in H&P) ? Acquired hypothyroidism ? Anxiety ? Chronic deep vein thrombosis (DVT) of distal vein of lower extremity ? Chronic midline low back pain ? Complex regional pain syndrome I ? Essential hypertension ? Fibromyalgia ? Gastroesophageal reflux disease without esophagitis ? History of pseudoseizure ? Laryngospasm ? MDD (major depressive disorder) ? RSD (reflex sympathetic dystrophy)
Andere Medikamente: Biotin 1 mg PO daily, Levothyroxine 112 mcg PO daily, MVI tablet PO daily, Paroxetine 20 mg PO QHS
Allergien: cefuroxime (shortness of breath), gadolinium (anaphylaxis, March 2018), iodine (anaphylaxis), quinolones (shortness of breath, "paralyze"), gabapentin (hallucinations), vancomycin (itching)
Vorherige Impfungen: -

VAERS 917667

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

schwer

Staat: AL
Alter: 47,0
Geschlecht: F
Eingang: 03.01.2021
Impfdatum: 30.12.2020
Beginn: 31.12.2020
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Chills Pain Presyncope Pyrexia

Symptomtext

Most horrible fever, chills, body aches, near syncope.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Rheumatoid Arthritis, SAR
Andere Medikamente: Tylenol
Allergien: Betadine
Vorherige Impfungen: -

VAERS 2711122

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: AZ
Alter: 70,0
Geschlecht: F
Eingang: 07.11.2023
Impfdatum: 27.01.2021
Beginn: 01.01.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

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

Condition aggravated Headache Muscle spasms Pyrexia Tremor

Symptomtext

the shakes; fever which was worst on the second dose; headaches; Second dose was the worst; After all the doses of the vaccine her whole body was cramping; This spontaneous case was reported by a patient and describes the occurrence of MUSCLE SPASMS (After all the doses of the vaccine her whole body was cramping), TREMOR (the shakes), CONDITION AGGRAVATED (Second dose was the worst), PYREXIA (fever which was worst on the second dose) and HEADACHE (headaches) in a 70-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 011J20A and 002A21A) for COVID-19 prophylaxis. Previously administered products included for Product used for unknown indication: PNEUMOCOCCAL VACCINE. Past adverse reactions to the above products included No adverse event with PNEUMOCOCCAL VACCINE. On 27-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 24-Feb-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. In January 2021, the patient experienced MUSCLE SPASMS (After all the doses of the vaccine her whole body was cramping). In February 2021, the patient experienced CONDITION AGGRAVATED (Second dose was the worst). On an unknown date, the patient experienced TREMOR (the shakes), PYREXIA (fever which was worst on the second dose) and HEADACHE (headaches). The patient was treated with PARACETAMOL (TYLENOL) at an unspecified dose and frequency and IBUPROFEN at a dose of 200 milligram. In January 2021, MUSCLE SPASMS (After all the doses of the vaccine her whole body was cramping) had resolved. At the time of the report, TREMOR (the shakes), CONDITION AGGRAVATED (Second dose was the worst), PYREXIA (fever which was worst on the second dose) and HEADACHE (headaches) outcome was unknown. Not Provided mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) dosing remained unchanged. Patient has received hepatitis vaccines in the past. With the cramps it would prevent her from sewing. That lasted for 08-10 hrs. No concomitant medication was reported. This case was linked to MOD-2023-748279 (Patient Link).

Weitere VAERSDATA-Felder

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

VAERS 2640235

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: CA
Alter: 37,0
Geschlecht: F
Eingang: 02.06.2023
Impfdatum: 13.01.2021
Beginn: 29.01.2021
Tage bis Beginn: 16,0
Dosis: 1
Route/Site: IM / LA

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

Abnormal menstrual clots Aphasia Asthenia Blood iron Blood thyroid stimulating hormone Brain fog Full blood count Heavy menstrual bleeding Hypoaesthesia Laboratory test Lhermitte's sign Lipids Lumbar puncture Magnetic resonance imaging head Magnetic resonance imaging spinal Menstruation irregular Metabolic function test Multiple sclerosis

Symptomtext

Initially numbness and tingling in bilateral lower extremities, weakness, then Lhermitte's sign, then complete numbness in left side of body, intense brain fog, trouble forming sentences, heat sensitivity. Had a series of MRI's done and lumbar puncture. Diagnosed with Multiple Sclerosis on July 16, 2021. Had no previous signs or symptoms. Also has irregular, prolonged, heavy menstrual cycle with immense clotting.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: 02/20/21 Xray Cervical spine 03/03/21 MRI Cervical spine w/o contrast 04/16/21 CBC, CMP, Vitamin D 25 OH, T4 Total, Lipid Panel, TSH, Iron profile, Vitamin B12 05/06/21 MRI Brain w/ and w/o contrast 05/18/21 MRI Thoracic spine w/ and w/o contrast 07/09/21 MRI Brain w and w/o contrast 07/09/21 MRI Cervical spine w and w/o contrast 07/16/21 Labs and Spinal Tap
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2634935

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: FL
Alter: 93,0
Geschlecht: F
Eingang: 22.05.2023
Impfdatum: 09.01.1921
Beginn: 03.07.2022
Tage bis Beginn: 37.065,0
Dosis: 1
Route/Site: - / -

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

Alcohol use Blood pressure increased COVID-19 COVID-19 pneumonia Computerised tomogram abdomen abnormal Diverticulum Failure to thrive Glomerular filtration rate Leukocytosis Lumbar vertebral fracture Malnutrition Pancreatic atrophy Platelet count increased Renal function test normal SARS-CoV-2 test positive Spinal compression fracture Swallow study Tachycardia

Symptomtext

BREAKTHROUGH COVID: FULLY VACCINATED WITH BOOSTER. The patient presents with Failure to thrive.COVID PNA/URI w/ acute moderate protein calorie malnx, atrophied pancreas w/ chronic daily EtOH use w/o known SUD. VSS on RA with intermittent tachycardia and elevated BP. No BMs recorded since admission. Gross leukocytosis, elevated platelets. Renal indices WNL with GFR in 60s, troponin elevated-peak 76 COVID positive. UA negative. CT abdomen pelvis: Diverticulosis without diverticulitis, no acute inflammatory processes, chronic moderate T12-L3 compression fractures, severe diffuse pancreatic atrophy- on personal review mod stool in pelvis/sigmoid.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 4,0
Labordaten: SWALLOW STUDY : REQUIRED MODIFIED LIQUID DIET.
Aktuelle Erkrankungen: UNKNOWN
Vorgeschichte: HTN and COPD
Andere Medikamente: UNKNOWN
Allergien: CIPROFLOXACIN, CODINE
Vorherige Impfungen: -

VAERS 2625792

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: VA
Alter: 33,0
Geschlecht: F
Eingang: 03.05.2023
Impfdatum: 04.02.2021
Beginn: 14.02.2021
Tage bis Beginn: 10,0
Dosis: 1
Route/Site: - / -

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

Asthma Autonomic nervous system imbalance Chest discomfort Chest pain Dyspnoea Echocardiogram abnormal Left ventricular hypertrophy Palpitations Pulmonary function test abnormal Pulmonary hypertension Tricuspid valve incompetence

Symptomtext

Patient developed heart palpations since 02/14/2021, shortness of breath and increase in heart palpitation severity and length in Aug 2021. 2 ED visits Dec 2022 for chest tightness/ pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 1,0
Labordaten: Echo: Showed LVH tricuspid regurg and pulmonary htn PFTs showed asthma
Aktuelle Erkrankungen: None
Vorgeschichte: None at time of vaccination Currently patient with pulmonary hypertension, autonomic nervous system dysfunction, LVH and tricuspid regurg
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2610467

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: -
Alter: -
Geschlecht: M
Eingang: 06.04.2023
Impfdatum: 13.01.2021
Beginn: 01.05.2022
Tage bis Beginn: 473,0
Dosis: 5
Route/Site: OT / RA

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

Blood pressure measurement Blood triglycerides increased Hypotension Steal syndrome

Symptomtext

Low blood pressure after dialysis.; Steal syndrome in left hand/Patient developed complications with dialysis fistula that lead to circulation issues in left hand/no feeling to hand; This spontaneous case was reported by a patient and describes the occurrence of HYPOTENSION (Low blood pressure after dialysis.) and STEAL SYNDROME (Steal syndrome in left hand/Patient developed complications with dialysis fistula that lead to circulation issues in left hand/no feeling to hand) in an adult male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 011J20A, 028L20A, 088D21A, 083J21A and 016B22A) for COVID-19 prophylaxis. The patient's past medical history included Transcatheter aortic valve replacement (aortic valve replacement with a TAVR procedure), Dialysis and Fistula repair in July 2021. Concurrent medical conditions included Immunocompromised, Renal disease (Dialysis), Atrial fibrillation, Coronary artery disease, Hyperlipidemia, Hypertriglyceridemia, Prostate cancer and Diabetes. Concomitant products included METOPROLOL TARTRATE for Atrial fibrillation, ROSUVASTATIN CALCIUM (CRESTOR) for Coronary artery disease and Hypertriglyceridaemia, EICOSAPENTAENOIC ACID ETHYL ESTER (VASCEPA) for Diabetes, RANOLAZINE (RANEXA SR), APIXABAN (ELIQUIS), INSULIN LISPRO (HUMALOG), ESOMEPRAZOLE, COLECALCIFEROL (VITAMIN D3), CLOPIDOGREL, CALCITRIOL, SODIUM ZIRCONIUM CYCLOSILICATE (LOKELMA), CINACALCET, LEVOTHYROXINE SODIUM (SYNTHROID), LANTHANUM CARBONATE, METHOXY POLYETHYLENE GLYCOL-EPOETIN BETA (MIRCERA), SEVELAMER, FISH OIL, TOCOPHEROL, UBIDECARENONE (COENZYME Q10 PLUS) and INSULIN DETEMIR (LEVEMIR) for an unknown indication. On 13-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 10-Feb-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 31-Aug-2021, received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 23-Feb-2022, received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 25-Jul-2022, received fifth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. In 2021, the patient experienced STEAL SYNDROME (Steal syndrome in left hand/Patient developed complications with dialysis fistula that lead to circulation issues in left hand/no feeling to hand) (seriousness criterion medically significant). In May 2022, the patient experienced HYPOTENSION (Low blood pressure after dialysis.) (seriousness criterion hospitalization). At the time of the report, HYPOTENSION (Low blood pressure after dialysis.) and STEAL SYNDROME (Steal syndrome in left hand/Patient developed complications with dialysis fistula that lead to circulation issues in left hand/no feeling to hand) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): In May 2022, Blood pressure measurement: low blood pressure after dialysis. On an unknown date, Blood triglycerides increased: Increased. mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosing remained unchanged. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Patient had no Thyroid. In March or April of 2021 the patient developed Steal syndrome in his left hand.The patient has limited use of his left hand. The patient then developed complications with his dialysis fistula that lead to circulation issues in left hand. In July of 2021 the patient had a dialysis fistula repaired. In November of 2021 the patient had the dialysis fistula blocked off with a procedure at the hospital. No treatment information was reported. Company comment--This spontaneous case concerns an adult male patient of unknown age with relevant medical history of Immunocompromised status, Renal disease (on Dialysis), Atrial fibrillation, Coronary artery disease and Diabetes reported, who experienced the unexpected serious (Hospitalization) event of Hypotension ( reported as Low blood pressure after dialysis), unexpected serious (medically significant) event of Steal syndrome in the context of mRNA-1273 vaccination. Patient had received primary vaccination at an appropriate schedule, third dose after 6 months and fourth dose after 6 months subsequently. It was reported that about 1-2 months after second dose, patient developed Steal syndrome in his left hand with limited use of his left hand. Later developed complications with his dialysis fistula that lead to circulation issues in his left hand. He had a dialysis fistula repaired after 3 months, followed by dialysis fistula blocked off with a procedure at the hospital in the subsequent months. About three months after Dose 4, patient was hospitalized for low blood pressure after dialysis. No further information on detailed clinical course, investigations results, other treatment details was available in the report. Outcome of the events was unknown at the time of report. The relevant medical history remains as confounder to the events. The benefit-risk relationship of mRNA-1273 vaccine is not affected by this report. This case was linked to MOD-2023-718140 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 01-Apr-2023: Live Significant follow up received which contains new events, concomitant medications, patient age group and medical history were added, and Product details were updated.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypotension
Hospital-Tage: -
Labordaten: Test Date: 202205; Test Name: Blood pressure; Result Unstructured Data: low blood pressure after dialysis; Test Name: Triglycerides high; Result Unstructured Data: Increased
Aktuelle Erkrankungen: Atrial fibrillation; Coronary artery disease; Diabetes; Hyperlipidemia; Hypertriglyceridemia; Immunocompromised; Prostate cancer; Renal disease (Dialysis)
Vorgeschichte: Medical History/Concurrent Conditions: Dialysis; Fistula repair; Transcatheter aortic valve replacement (aortic valve replacement with a TAVR procedure)
Andere Medikamente: VASCEPA; RANEXA SR; ELIQUIS; HUMALOG; ESOMEPRAZOLE; CRESTOR; VITAMIN D3; CLOPIDOGREL; CALCITRIOL; LOKELMA; METOPROLOL TARTRATE; CINACALCET; SYNTHROID; LANTHANUM CARBONATE; MIRCERA; SEVELAMER; COENZYME Q10 PLUS; LEVEMIR
Allergien: -
Vorherige Impfungen: -

VAERS 2579593

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: GA
Alter: 53,0
Geschlecht: F
Eingang: 10.02.2023
Impfdatum: 08.01.2021
Beginn: 04.02.2021
Tage bis Beginn: 27,0
Dosis: 1
Route/Site: IM / -

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

Annuloplasty Cardiac murmur Cough Dyspnoea Fatigue Illness Malaise Respiratory symptom

Symptomtext

Patient started getting sick following the second injection in early March 2021. Patient having respiratory symptoms, Chronic Cough, Breathing problems, Chest related illnesses that continued every couple months per patient never going away. Was sent to Pulmonologist but no real progress in relief of symptoms then progressing last year to Chronic fatigue, gradually worsening up to the date patient found to have a RR+R with Grade 2-3/6 holosystolic murmur heard over the entire precordium and sent to cardiology in October 2022, within 3 months of murmur detection patient received surgical intervention in January of 2023 of Prosthetic Mitral heart valve (ANNULOPLASTY RING). See following pages sent through system.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 7,0
Labordaten: See following documents, uploaded after form.
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Vitamins
Allergien: Penicillin, Sulfa
Vorherige Impfungen: -

VAERS 2576390

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: NJ
Alter: 79,0
Geschlecht: F
Eingang: 06.02.2023
Impfdatum: 08.10.2022
Beginn: 01.11.2022
Tage bis Beginn: 24,0
Dosis: UNK
Route/Site: IM / LA

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

Burning sensation Laboratory test normal Nerve conduction studies Paraesthesia Quantitative sudomotor axon reflex test Small fibre neuropathy

Symptomtext

After receiving he October vaccine I developed tingling and burning in both feet. Have been diagnosed with small fiber neuropathy.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: All laboratory tests are normal. Have had nerve conduction study and Q-SART test.
Aktuelle Erkrankungen: None
Vorgeschichte: Restless Leg Syndrome
Andere Medikamente: Medipex, Vitamins, Calcium Citrate, probiotic
Allergien: None
Vorherige Impfungen: -

VAERS 2574229

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: OH
Alter: 24,0
Geschlecht: M
Eingang: 02.02.2023
Impfdatum: 24.12.2020
Beginn: 27.01.2021
Tage bis Beginn: 34,0
Dosis: 1
Route/Site: IM / RA

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

Angina pectoris Chest pain Chills Influenza like illness Malaise Pain Painful respiration

Symptomtext

Day 1 after 2nd dose - extremely ill with flu symptoms and chills Day 2 after 2nd dose - sharp, burning chest pain around heart Entire 1st years after 2nd dose - Pain (Sharp, burning) around heart that worsened with deep breaths and exercising

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: I don?t have a PCP. I am an ICU nurse and the doctors on my unit didn?t take my complaints seriously at the time, and were constantly encouraging me to get more boosters. I didn?t feel comfortable getting more while I was still experiencing adverse effects from the 2nd dose.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2554839

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: MI
Alter: 30,0
Geschlecht: F
Eingang: 10.01.2023
Impfdatum: 22.12.2020
Beginn: 23.11.2022
Tage bis Beginn: 701,0
Dosis: 1
Route/Site: - / -

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

COVID-19 Chest pain Pregnancy SARS-CoV-2 test positive

Symptomtext

11/23/22 presents to ed for "chest pain" "COVID" "34 weeks pregnancy". PMHx of "graves disease, anxiety disorder"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 11/23/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2486032

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: CA
Alter: 74,0
Geschlecht: F
Eingang: 26.10.2022
Impfdatum: 17.01.2021
Beginn: 01.10.2021
Tage bis Beginn: 257,0
Dosis: 1
Route/Site: OT / -

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

Antibody test Blood pressure measurement Dizziness Hypotension Vaccination site erythema Myalgia Vaccination site pain

Symptomtext

Blood pressure dropped very low; felt like fainting; pain and redness on the injection site; pain and redness on the injection site; This spontaneous case was reported by a patient and describes the occurrence of HYPOTENSION (Blood pressure dropped very low), DIZZINESS (felt like fainting), VACCINATION SITE PAIN (pain and redness on the injection site) and VACCINATION SITE ERYTHEMA (pain and redness on the injection site) in a 74-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 014F21A, 042L20A and 011J20A) for COVID-19 prophylaxis. No Medical History information was reported. On 17-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 19-Feb-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 21-Oct-2021, received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. In October 2021, the patient experienced HYPOTENSION (Blood pressure dropped very low), DIZZINESS (felt like fainting), VACCINATION SITE PAIN (pain and redness on the injection site) and VACCINATION SITE ERYTHEMA (pain and redness on the injection site). At the time of the report, HYPOTENSION (Blood pressure dropped very low), DIZZINESS (felt like fainting), VACCINATION SITE PAIN (pain and redness on the injection site) and VACCINATION SITE ERYTHEMA (pain and redness on the injection site) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): In October 2021, Blood pressure measurement: dropped very low. On an unknown date, Antibody test: >150. No relevant concomitant medications were reported. After the 2nd primary shot and after the First Moderna Booster and after Pfizer Booster, within 24 hours after the shot, her Blood pressure dropped very low and she felt like fainting. The patient had pain and redness on the injection site. No treatment information was provided. This case was linked to MOD-2021-023445, MOD-2021-662209 (Patient Link).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypotension
Hospital-Tage: -
Labordaten: Test Name: Antibody test; Result Unstructured Data: >150; Test Date: 202110; Test Name: Blood pressure; Result Unstructured Data: dropped very low
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2486062

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: RI
Alter: 64,0
Geschlecht: F
Eingang: 22.10.2022
Impfdatum: 07.01.2021
Beginn: 07.01.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / -

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

Dyspnoea Pruritus

Symptomtext

itching in her lower arms; Shortness of breath; This spontaneous case was reported by a patient and describes the occurrence of PRURITUS (itching in her lower arms) and DYSPNOEA (Shortness of breath) in a 64-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 011J20A and 609F21A) for COVID-19 vaccination. Concurrent medical conditions included Penicillin allergy, Sulfonamide allergy (sulfa antibiotics), Allergy to antibiotic (Z-pak), Asthma (since early 20s Recent change in status: stable with medications except for asthma attack after 2nd dose using Albuterol, Pulmicort.) and Blood pressure high (2 years ago Recent change in status: stable) since 2020. Concomitant products included ALBUTEROL [SALBUTAMOL] and BUDESONIDE (PULMICORT) for Asthma, DILTIAZEM, THIORIDAZINE, ASCORBIC ACID, CALCIUM, MINERALS NOS, RETINOL, TOCOPHERYL ACETATE, VITAMIN B NOS, VITAMINS NOS, ZINC (CENTRUM SILVER [ASCORBIC ACID;CALCIUM;MINERALS NOS;RETINOL;TOCOPHERYL ACETATE;VITAMIN B NOS;VITAMINS NOS;ZINC]), IBUPROFEN (ADVIL [IBUPROFEN]), IRON, MOMETASONE FUROATE (FLONASE [MOMETASONE FUROATE]) and CALCIUM CITRATE for an unknown indication. On 07-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 03-Dec-2021, received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 07-Jan-2021, the patient experienced PRURITUS (itching in her lower arms) and DYSPNOEA (Shortness of breath). On 07-Jan-2021, PRURITUS (itching in her lower arms) and DYSPNOEA (Shortness of breath) had resolved. mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) and mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) dosing remained unchanged. Patient had no history of COVID-19 infection and no history of Myocarditis or pericarditis. Patient did not receive any other vaccine within 1 month prior to Moderna COVID-19 vaccine. After 1st dose patient experienced itching in her lower arms and shortness of breath during 1 hour. After 1st booster she experienced again itching and shortness of breath during 10 or 15 minutes.. Patient called her pulmonologist to seek medical care for Adverse events. Cardiac related signs and symptoms: Patient experienced the symptom shortness of breath on 7Jan2021, 4Feb2021, and 3Dec2021 and related with 1st, 2nd and 1st booster dose and resolved. No timeline of symptoms, including Cardiac Lab values cause determined. No history of Myocarditis/pericarditis. This case was linked to MOD-2022-661757 (Patient Link).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Allergy to antibiotic (Z-pak); Asthma (since early 20s Recent change in status: stable with medications except for asthma attack after 2nd dose using Albuterol, Pulmicort.); Blood pressure high (2 years ago Recent change in status: stable); Penicillin allergy; Sulfonamide allergy (sulfa antibiotics)
Vorgeschichte: -
Andere Medikamente: DILTIAZEM; ALBUTEROL [SALBUTAMOL]; PULMICORT; THIORIDAZINE; CENTRUM SILVER [ASCORBIC ACID;CALCIUM;MINERALS NOS;RETINOL;TOCOPHERYL ACETATE;VITAMIN B NOS;VITAMINS; ADVIL [IBUPROFEN]; IRON; FLONASE [MOMETASONE FUROATE]; CALCIUM CITRATE
Allergien: -
Vorherige Impfungen: -

VAERS 2457818

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: -
Alter: 85,0
Geschlecht: F
Eingang: 24.09.2022
Impfdatum: 28.07.2020
Beginn: 01.10.2021
Tage bis Beginn: 430,0
Dosis: 2
Route/Site: OT / -

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

Blood pressure measurement Femur fracture Hypotension Incoherent Infusion Muscular weakness Parkinson's disease Post procedural complication Urinary tract infection X-ray

Symptomtext

Broke right femur; Worsens Parkinson's symptoms; Urinary tract infection; Lower extremities weakness of; Low blood pressure; Infusion; Postoperative complication; Incoherent; This spontaneous case was reported by a consumer and describes the occurrence of FEMUR FRACTURE (Broke right femur) and PARKINSON'S DISEASE (Worsens Parkinson's symptoms) in an 85-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 011J20A, 028L20A and 051F21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Co-suspect products included non-company products CARBIDOPA, LEVODOPA (DUOPA) gastroenteral suspension for an unknown indication and MORPHINE for an unknown indication. The patient's past medical history included Spasms, Back surgery and Surgery. Previously administered products included for Drug use for unknown indication: SULFAMETHOXAZOLE (Allergy with sulfa manifested by rash) and CODEINE PHOSPHATE (Allergy with codeine manifested by vomiting/phosphate powder allergy). Past adverse reactions to the above products included Drug allergy with CODEINE PHOSPHATE and SULFAMETHOXAZOLE. Concurrent medical conditions included Non-tobacco user and Abstains from alcohol. Concomitant products included DROXIDOPA (NORTHERA), NAPROXEN SODIUM (ALEVE), ARIPIPRAZOLE, METHOCARBAMOL, CANNABIS SATIVA (CBD COMPLEX), CALCIUM CARBONATE, COLECALCIFEROL (CALTRATE [CALCIUM CARBONATE;COLECALCIFEROL]), QUETIAPINE FUMARATE, BETAXOLOL HYDROCHLORIDE (BETOPTIC), TRAVOPROST (TRAVATAN), MIRTAZAPINE, CARBIDOPA, LEVODOPA (CARBIDOPA/LEVODOPA), LEVOTHYROXINE SODIUM, LORAZEPAM, PROBIOTIC 10 [BIFIDOBACTERIUM BIFIDUM;BIFIDOBACTERIUM LACTIS;LACTOBACILLUS ACIDOPHILUS;LACTOBACILLUS BREVIS;LACTOBACILLUS BULGARICUS;LACTOBACILLUS CASEI;LACTOBACILLUS PARACASEI;LACTOBACILLUS PLANTARUM;LACTOBACILLUS RHAMNOSUS;LACTOBACILLUS SALIVARIUS], CARBIDOPA, ASCORBIC ACID, COPPER GLUCONATE, FISH OIL, TOCOPHEROL, XANTOFYL, ZEAXANTHIN, ZINC OXIDE (OCUVITE ADULT 50+ [ASCORBIC ACID;COPPER GLUCONATE;FISH OIL;TOCOPHEROL;XANTOFYL;ZEAXANTHIN;ZINC OXIDE]) and CARBIDOPA, LEVODOPA (CARBIDOPA/LEVODOPA) for an unknown indication. On 28-Jul-2020, the patient started CARBIDOPA, LEVODOPA (DUOPA) (Intestinal use) at an unspecified dose. On 06-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 05-Mar-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 11-Sep-2021, received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On an unknown date, the patient started MORPHINE (unknown route) at an unspecified dose. On 08-Oct-2021, the patient experienced FEMUR FRACTURE (Broke right femur) (seriousness criteria hospitalization, disability and medically significant). In October 2021, the patient experienced INCOHERENT (Incoherent). On an unknown date, the patient experienced PARKINSON'S DISEASE (Worsens Parkinson's symptoms) (seriousness criterion medically significant), URINARY TRACT INFECTION (Urinary tract infection), MUSCULAR WEAKNESS (Lower extremities weakness of), HYPOTENSION (Low blood pressure), INFUSION (Infusion) and POST PROCEDURAL COMPLICATION (Postoperative complication). The patient was treated with PARACETAMOL (TYLENOL) at an unspecified dose and frequency. On 08-Oct-2021, FEMUR FRACTURE (Broke right femur) had resolved. In October 2021, INCOHERENT (Incoherent) had resolved. At the time of the report, PARKINSON'S DISEASE (Worsens Parkinson's symptoms), HYPOTENSION (Low blood pressure) and INFUSION (Infusion) had not resolved, URINARY TRACT INFECTION (Urinary tract infection) and MUSCULAR WEAKNESS (Lower extremities weakness of) was resolving and POST PROCEDURAL COMPLICATION (Postoperative complication) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 08-Oct-2021, X-ray: Broken right femur. On an unknown date, Blood pressure measurement: Low. On an unknown date, X-ray: Three weeks post surgery and stated the placement of rods and screws were still in place.. It was unknown if patient was enrolled in a COVID-19 Vaccine Trial. Memory impairment, Delusion, Confusional state, Gait disturbance, Mental status changes and Tremor subsumed under Parkinson's disease. Asthenia, Dehyration, Pain, Anxiety and Physical disability subsumed under Post procedural complication Loss of personal independence in daily activities, Bedridden, fall subsumed under fracture femur. This case was identified as part of a retrospective clean-up activity where certain emails received in the Moderna mailbox were missed to be booked-in. Route of administration for Duopa provided as Percutaneous J-tube. Company comment: This spontaneous case concerns an 85-years-old female patient, with medical history reported, who experienced the unexpected serious (hospitalization, disability and medically significant) event of femur fracture which occurred 28 days after the third dose mRNA-1273 vaccination. The patient also experienced unexpected serious (medically significant) event of Parkinson's disease in context to third dose of vaccination. It was reported that patient had fall with fractured right femur treated with unknown surgery and visited physical therapy three times a week and occupational therapy two times a week. She received unknown nasal pain medication given by the paramedic. Post-surgery for femur, hospital staff had trouble arousing patient, even with chest compressions. The events fracture femur was resolved, and event Parkinson's disease was not recovered. The benefit-risk relationship of mRNA-1273 Vaccine is not affected by this report. Event seriousness assessed as per medical judgement. This case was linked to MOD-2021-623359 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 28-Dec-2021: Significant follow-up appended(event, seriousness updated); Sender's Comments: This spontaneous case concerns an 85-years-old female patient, with medical history reported, who experienced the unexpected serious (hospitalization, disability and medically significant) event of femur fracture which occurred 28 days after the third dose mRNA-1273 vaccination. The patient also experienced unexpected serious (medically significant) event of Parkinson's disease in context to third dose of vaccination. It was reported that patient had fall with fractured right femur treated with unknown surgery and visited physical therapy three times a week and occupational therapy two times a week. She received unknown nasal pain medication given by the paramedic. Post-surgery for femur, hospital staff had trouble arousing patient, even with chest compressions. The events fracture femur was resolved, and event Parkinson's disease was not recovered. The benefit-risk relationship of mRNA-1273 Vaccine is not affected by this report. Event seriousness assessed as per medical judgement.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypotension
Hospital-Tage: -
Labordaten: Test Name: blood pressure; Result Unstructured Data: Low; Test Name: X ray of the right femur; Result Unstructured Data: Three weeks post surgery and stated the placement of rods and screws were still in place.; Test Date: 20211008; Test Name: X ray of the right femur; Result Unstructured Data: Broken right femur
Aktuelle Erkrankungen: Abstains from alcohol; Non-tobacco user
Vorgeschichte: Medical History/Concurrent Conditions: Back surgery; Spasms; Surgery
Andere Medikamente: NORTHERA; ALEVE; ARIPIPRAZOLE; METHOCARBAMOL; CBD COMPLEX; CALTRATE [CALCIUM CARBONATE;COLECALCIFEROL]; QUETIAPINE FUMARATE; BETOPTIC; TRAVATAN; MIRTAZAPINE; CARBIDOPA/LEVODOPA; LEVOTHYROXINE SODIUM; LORAZEPAM; PROBIOTIC 10 [BIFIDOBACTERIUM
Allergien: -
Vorherige Impfungen: -

VAERS 2457780

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: -
Alter: 85,0
Geschlecht: F
Eingang: 24.09.2022
Impfdatum: 28.07.2020
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: OT / -

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

Blood pressure measurement Dehydration Hypotension Inappropriate schedule of product administration Parkinson's disease Urinary tract infection

Symptomtext

WORSENS PARKINSON'S SYMPTOMS; First dose on 06-JAN-2021 and second dose on 05-MAR-2021; DEHYDRATION; URINARY TRACT INFECTION; LOW BLOOD PRESSURE; This spontaneous case was reported by a consumer and describes the occurrence of PARKINSON'S DISEASE (WORSENS PARKINSON'S SYMPTOMS) in an 85-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 028L20A, 011J20A and 051F21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Co-suspect products included non-company products CARBIDOPA, LEVODOPA (DUOPA) for Parkinson's disease and MORPHINE for an unknown indication. The patient was a non-tobacco user and has abstained from alcohol. The patient's past medical history included Spasms, Back surgery and Surgery. Previously administered products included for Product used for unknown indication: SULFAMETHOXAZOLE and CODEINE PHOSPHATE. Past adverse reactions to the above products included Drug allergy with SULFAMETHOXAZOLE; and Vomiting with CODEINE PHOSPHATE. Concurrent medical conditions included Parkinson's disease, Drug allergy and Drug allergy. Concomitant products included DROXIDOPA (NORTHERA), NAPROXEN SODIUM (ALEVE), ARIPIPRAZOLE, METHOCARBAMOL, CANNABIS SATIVA (CBD COMPLEX), CALCIUM CARBONATE, COLECALCIFEROL (CALTRATE + D [CALCIUM CARBONATE;COLECALCIFEROL]), QUETIAPINE FUMARATE, BETAXOLOL HYDROCHLORIDE (BETOPTIC), TRAVOPROST (TRAVATAN), MIRTAZAPINE, CARBIDOPA, LEVODOPA (CARBIDOPA/LEVODOPA), LEVOTHYROXINE SODIUM, LORAZEPAM, PROBIOTIC 10 [BIFIDOBACTERIUM BIFIDUM;BIFIDOBACTERIUM LACTIS;LACTOBACILLUS ACIDOPHILUS;LACTOBACILLUS BREVIS;LACTOBACILLUS BULGARICUS;LACTOBACILLUS CASEI;LACTOBACILLUS PARACASEI;LACTOBACILLUS PLANTARUM;LACTOBACILLUS RHAMNOSUS;LACTOBACILLUS SALIVARIUS], CARBIDOPA and ASCORBIC ACID, COPPER GLUCONATE, FISH OIL, TOCOPHEROL, XANTOFYL, ZEAXANTHIN, ZINC OXIDE (OCUVITE ADULT 50+ [ASCORBIC ACID;COPPER GLUCONATE;FISH OIL;TOCOPHEROL;XANTOFYL;ZEAXANTHIN;ZINC OXIDE]) for an unknown indication. On 28-Jul-2020, the patient CARBIDOPA, LEVODOPA (DUOPA) (unknown route) dosage was changed to 100 milliliter. On 18-Aug-2020, CARBIDOPA, LEVODOPA (DUOPA) (unknown route) dosage was changed to 100 milliliter. On 06-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 05-Mar-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 11-Sep-2021, received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On an unknown date, the patient started CARBIDOPA, LEVODOPA (DUOPA) (unknown route) 1 dosage form and MORPHINE (unknown route) at an unspecified dose. On an unknown date, the patient experienced PARKINSON'S DISEASE (WORSENS PARKINSON'S SYMPTOMS) (seriousness criteria disability and medically significant), INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (First dose on 06-JAN-2021 and second dose on 05-MAR-2021), DEHYDRATION (DEHYDRATION), URINARY TRACT INFECTION (URINARY TRACT INFECTION) and HYPOTENSION (LOW BLOOD PRESSURE). The patient was treated with PARACETAMOL (TYLENOL) at a dose of 1 dosage form. At the time of the report, PARKINSON'S DISEASE (WORSENS PARKINSON'S SYMPTOMS), INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (First dose on 06-JAN-2021 and second dose on 05-MAR-2021), URINARY TRACT INFECTION (URINARY TRACT INFECTION) and HYPOTENSION (LOW BLOOD PRESSURE) outcome was unknown and DEHYDRATION (DEHYDRATION) had not resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, Blood pressure measurement: Low. It was unknown if patient was enrolled in a COVID-19 Vaccine Trial. Concomitant drug included PROBIOTIC 10B. Duopa was administered through Percutaneous (J-tube) route. It was reported that, Pump Serial Number: 566056 and Gel Cassette Lot number: 1152316. Primary reporter did not have the lot number information, because the packaging was discarded for second regimen. It was reported that, 24 HOURS DUOPA INFUSION, PATIENTS TUBING WAS STARTING TO SEPERATE AT VALVE/Y CONNECTOR CAME LOOSE/INNER TUBE AND OUTER TUBE KIND OF SEPARATED/CONNECTION OF Y CAME UNSCREWED A LITTLE BIT AND UNCLAMPED OUTER TUBE, PATIENT COULD NOT FEED SELF OR PULL PANTS DOWN, URINARY TRACT INFECTION, LEG WEAKNESS, LOW BLOOD PRESSURE, INTESTINAL TUBE DISLOCATIONM and SHAKY. On unknown dates, the patient experienced DEBILITATED, PATIENT WAS BEDRIDDEN, MENTALLY AND PHYSICALLY UNCAPABLE, MENTAL STATUS DOWNHILL, CONFUSION, MEMORY ISSUES, ANXIETY, NEED ASSISTANCE WALKING (LEG WEAKNESS), SHAKY all are the symptoms of PARKINSON'S. This case was identified as part of a retrospective clean-up activity where certain emails received in the Moderna mailbox were missed to be booked-in. Company comment-This spontaneous case concerns a 85-year-old female patient, with relevant medical history of Parkinson's disease on DUOPA reported, who experienced the unexpected serious (medically significant/Disability) event of Parkinson's disease (reported as WORSENS PARKINSON'S SYMPTOMS) on an unknown date after receiving the 2nd dose of mRNA-1273 vaccine. Additionally , Inappropriate schedule of product administration was noted as patient received 1st and 2nd doses of mRNA-1273 vaccine approximately 2 months apart, and 3rd dose was given 6 months later, which is not in accordance with the recommended vaccine interval. Patient also had confusion, memory issues, anxiety, weakness in legs, needed assistance to walk. She was bedridden, physically and mentally uncapable for day today activities. No further info This case was linked to MOD-2021-623469 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 28-Dec-2021: Significant follow-up appended, seriousness updated. Patient's medical history, concomitant medications, Co-suspect indication and doses were updated. Worsens Parkinson's symptoms, dehydration, urinary tract infection and low blood pressure were added as events. Treatment drug was added. Reporter causality was updated. Company comment: This spontaneous case concerns a 85-year-old female patient, with relevant medical history of Parkinson's disease on DUOPA reported, who experienced the unexpected serious (medically significant/Disability) event of Parkinson's disease (reported as WORSENS PARKINSON'S SYMPTOMS) on an unknown date after receiving the 2nd dose of mRNA-1273 vaccine. Additionally , Inappropriate schedule of product administration was noted as patient received 1st and 2nd doses of mRNA-1273 vaccine approximately 2 months apart, and 3rd dose was given 6 months later, which is not in accordance with the recommended vaccine interval. Patient also had confusion, memory issues, anxiety, weakness in legs, needed assistance to walk. She was bedridden, physically and mentally uncapable for day today activities. No further information on detailed clinical course, investigations, treatment of the events was available in the report. Outcome of the event was not known at the time of report. Relevant medical history remains a confounder and Concomitant drug QUETIAPINE FUMARATE can be considered as contributory to the event. The benefit-risk relationship of mRNA-1273 is not affected by this report.; Sender's Comments: This spontaneous case concerns a 85-year-old female patient, with relevant medical history of Parkinson's disease on DUOPA reported, who experienced the unexpected serious (medically significant/Disability) event of Parkinson's disease (reported as WORSENS PARKINSON'S SYMPTOMS) on an unknown date after receiving the 2nd dose of mRNA-1273 vaccine. Additionally , Inappropriate schedule of product administration was noted as patient received 1st and 2nd doses of mRNA-1273 vaccine approximately 2 months apart, and 3rd dose was given 6 months later, which is not in accordance with the recommended vaccine interval. Patient also had confusion, memory issues, anxiety, weakness in legs, needed assistance to walk. She was bedridden, physically and mentally uncapable for day today activities. No further information on detailed clinical course, investigations, treatment of the events was available in the report. Outcome of the event was not known at the time of report. Relevant medical history remains a confounder and Concomitant drug QUETIAPINE FUMARATE can be considered as contributory to the event. The benefit-risk relationship of mRNA-1273 is not affected by this report.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dehydration
Hospital-Tage: -
Labordaten: Test Name: Blood pressure; Result Unstructured Data: Low
Aktuelle Erkrankungen: Drug allergy; Parkinson's disease
Vorgeschichte: Medical History/Concurrent Conditions: Back surgery; Spasms; Surgery; Comments: The patient was a non-tobacco user and has abstained from alcohol.
Andere Medikamente: NORTHERA; ALEVE; ARIPIPRAZOLE; METHOCARBAMOL; CBD COMPLEX; CALTRATE + D [CALCIUM CARBONATE;COLECALCIFEROL]; QUETIAPINE FUMARATE; BETOPTIC; TRAVATAN; MIRTAZAPINE; CARBIDOPA/LEVODOPA; LEVOTHYROXINE SODIUM; LORAZEPAM; PROBIOTIC 10 [BIFIDOBACTE
Allergien: -
Vorherige Impfungen: -

VAERS 2327200

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011j20a

moderat

Staat: MI
Alter: 76,0
Geschlecht: M
Eingang: 22.06.2022
Impfdatum: 12.02.2021
Beginn: 27.05.2022
Tage bis Beginn: 469,0
Dosis: 1
Route/Site: UN / UN

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

Abdominal cavity drainage Asthenia Biopsy colon normal Biopsy liver COVID-19 Chills Colostomy Computerised tomogram abnormal Constipation Culture Cytology Explorative laparotomy General physical health deterioration Iatrogenic injury Imaging procedure abnormal Intestinal dilatation Intestinal obstruction Large intestinal obstruction

Symptomtext

Provider summary "77-year-old male with a past medical history significant for prostate cancer status post radiation treatments in 2019 who was found after recent workup for weakness and chills, to have a sigmoid stricture. This progressed to a partial large bowel obstruction. Biopsies of the sigmoid colon were negative for neoplasm, but preoperative imaging did demonstrate significant retroperitoneal lymphadenopathy; PSA normal. The patient underwent an exploratory laparotomy and Hartmann procedure for progressive bowel distension on 6/2/22; at the time of the operation, 1 L of ascites was removed and was sent for cytology. Postoperatively, patient had ongoing sepsis and peritonitis Repeat imaging raised suspicion for retained foreign body. Underwent reopening of laparotomy and removal of a retained foreign body on 6/5/22. Due to worsening tachycardia and clinical deterioration yesterday, and concern for possible perforated viscous, patient was taken back to the OR for reopening of his laparotomy. No evidence of perforated viscous or intra-abdominal sepsis was identified. Ascites was sent for cytology and liver biopsies x2 were performed, due to a cirrhotic-appearing liver. On 6/8, the patient again showed evidence of clinical deterioration. Repeat COVID test was positive. Patient started on Remdesivir (therapy completed on 6/13) and dexamethasone (to continue through 6/18). Fluconazole added d/t peritoneal cultures (d/c'd 6/14 per ID's recommendations). The patient continued to improve clinically and diet was advanced appropriately. He will be discharged to a skilled nursing facility in stable condition. Patient discharged with prescription for beta blocker per Hospitalist recommendation given inpatient tachycardia."

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tachycardia
Hospital-Tage: 25,0
Labordaten: COVID PCR Negative 5/28/22 COVID PCR Positive 6/8/22
Aktuelle Erkrankungen: -
Vorgeschichte: Primary osteoarthritis of left hip 3/3/2022 Former smoker 11/19/2012 Gastroesophageal reflux disease 5/27/2022 Hypertension 5/27/2022 History of prostate cancer 5/28/2022 Abnormal CT scan Unknown Severe protein-calorie malnutrition 5/30/2022 Constipation 5/30/2022 Generalized weakness 5/30/2022 Proctitis 5/30/2022 Thrombocytopenia 6/13/2022
Andere Medikamente: allopurinol 100 mg Oral Daily cyanocobalamin (vitamin B-12) 3,000 mcg Oral Daily losartan potassium 50 mg Oral Daily metoprolol tartrate 12.5 mg Oral 2 times daily pantoprazole sodium 40 mg Oral Daily primidone 50 mg Oral EVERY MORNING
Allergien: Lisinopril
Vorherige Impfungen: -

VAERS 2254875

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: FL
Alter: 86,0
Geschlecht: F
Eingang: 27.04.2022
Impfdatum: 04.02.2021
Beginn: 25.04.2022
Tage bis Beginn: 445,0
Dosis: 1
Route/Site: - / -

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

Burning sensation COVID-19 Chest X-ray abnormal Chest pain Cough Fatigue Pneumonia SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Covid19 breakthrough. 1st vaccine received on 01/04/2021. 87 y/o female with PMHx Breast Cancer s/p bilat mastectomies, DM, HTN, Hypothyroid, Thrombocytopenia presents to ED with c/o Chest burning radiating to back and down her arms. Pt states she also has had chronic fatigue and cough since originally had Covid in January 2022. Pt afebrile, room air sats 97% and CXR consistent with Pneumonia. Pt treated with IV abx.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: SARS CoV 2 PCR Covid19-Detected on 04/25/2022
Aktuelle Erkrankungen: -
Vorgeschichte: Breast CA/Bilat Mastectomies, DM, HTN, Hypothyroid, TTP, UTI
Andere Medikamente: -
Allergien: Bactrim, Ciprofloxacin, Codeine, Morphine
Vorherige Impfungen: -

VAERS 2251491

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: -
Alter: 69,0
Geschlecht: F
Eingang: 26.04.2022
Impfdatum: 09.01.2021
Beginn: 01.01.2022
Tage bis Beginn: 357,0
Dosis: 1
Route/Site: OT / -

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

Diarrhoea Headache Insomnia Mobility decreased Tinnitus Vomiting

Symptomtext

in bed for 3 days; throwing up; diarrhea; horrible headache; trouble sleeping with the sound; tinnitus,some days worse than others,hissing sound; This spontaneous case was reported by a consumer and describes the occurrence of MOBILITY DECREASED (in bed for 3 days), VOMITING (throwing up), DIARRHOEA (diarrhea), HEADACHE (horrible headache) and TINNITUS (tinnitus,some days worse than others,hissing sound) in a 69-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 029K20A and 011J20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concurrent medical conditions included Asthma and Blood pressure high. Concomitant products included SALBUTAMOL SULFATE (INHALERIN) for Asthma, LOVASTATIN for Cholesterol. On 09-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 06-Feb-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. In January 2022, the patient experienced TINNITUS (tinnitus,some days worse than others,hissing sound). On an unknown date, the patient experienced MOBILITY DECREASED (in bed for 3 days), VOMITING (throwing up), DIARRHOEA (diarrhea), HEADACHE (horrible headache) and INSOMNIA (trouble sleeping with the sound). The patient was treated with PARACETAMOL (TYLENOL [PARACETAMOL]) at an unspecified dose and frequency and LORATADINE (CLARITINE) for Tinnitus, at an unspecified dose and frequency. At the time of the report, MOBILITY DECREASED (in bed for 3 days), VOMITING (throwing up), DIARRHOEA (diarrhea), HEADACHE (horrible headache), TINNITUS (tinnitus,some days worse than others,hissing sound) and INSOMNIA (trouble sleeping with the sound) outcome was unknown. Patient taking blood pressure pill as concomitant. Patient was on nose spray for tinnitus. Most recent FOLLOW-UP information incorporated above includes: On 21-Apr-2022: Non Significant Follow-up received

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Asthma; Blood pressure high.
Vorgeschichte: -
Andere Medikamente: INHALERIN; LOVASTATIN.
Allergien: -
Vorherige Impfungen: -

VAERS 2243494

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: -
Alter: 48,0
Geschlecht: F
Eingang: 20.04.2022
Impfdatum: 05.01.2021
Beginn: 12.09.2021
Tage bis Beginn: 250,0
Dosis: UNK
Route/Site: - / -

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

Blood glucose increased COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

9/12/21 PMH of Asthma, HTN, Hyperlipidemia and Type II DM who presented to ER with c/o SOB and uncontrolled sugars over 300

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 9/12/21 SARS-CoV-2 (COVID-19) by NAA, Micro Detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2225513

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20a

moderat

Staat: NY
Alter: 35,0
Geschlecht: F
Eingang: 10.04.2022
Impfdatum: 01.08.2021
Beginn: 01.09.2021
Tage bis Beginn: 31,0
Dosis: 1
Route/Site: IM / RA

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

Chest pain Dyspnoea Echocardiogram Heart rate increased Hypertension

Symptomtext

Chest pain starts midline and moves up toward left side, shortness of breath, high blood pressure. High heart rate. All the time

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Echo done 1/8/22
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Baby aspirin 81mg
Allergien: None
Vorherige Impfungen: Moderna booster shot, 7 hours after injection shortness of breath

VAERS 2200812

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011j20a

moderat

Staat: MA
Alter: 41,0
Geschlecht: F
Eingang: 27.03.2022
Impfdatum: 06.01.2021
Beginn: 06.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Arrhythmia Cardiac disorder Cardiac stress test abnormal Echocardiogram abnormal Electrocardiogram ambulatory abnormal Heart rate increased Supraventricular extrasystoles Supraventricular tachycardia Ventricular extrasystoles Ventricular tachycardia

Symptomtext

With First Vaccination , shortly after, I had increased heart rate, 120s/130s (old apple watch no ekg) tachycardia. I felt shakey, light headed, cold hands, clammy and felt like I was going to pass out. I called the team over. They monitored me extra, gave me juice and cookies, and the feelings subsided. One month later 2/1/21 I got my second dose and I again felt my heart rate increase to 120/130s at rest old apple watch/no ekg), but did not have other symptoms. That was Moderna Lot 028L2oA I have not had a booster because of this, and my new onset heart problems. I have since been followed by my PCP and a cardiloogy for onset of SVT/arrythmia. (healthy, no meds, no supplements, no changes to diet, weight, exercise. I do not drink alcohol regularly,, no smoking, no drugs. 1 cup of coffee a day.) Cardiology work up, stress test, ECHO, Zio patch indicating runs of SVT, VT , frequent PVCs, atrial ectopy. prior to vaccination I have never had any heart or health conditions. I have not been with cold or fever over the last 2 years, , and I have never been sick. I have never tested positive for Covid ( I need to get weekly test for my clinical site).

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Praegender Schweregrund: Arrhythmia
Hospital-Tage: -
Labordaten: 1/5/2022 out of the blue SVT HR 180 and settled to 120/130s for approx 3 hrs. Called PCP next morning 1/6/2022 virtual appointment with PCP 1/7/2022 EKG, Labs visit with PCP in office 1/11/2022 Zio patch placement at cardiology 1/19/2022 virtual appointment with cardiology dr. 1/24/22 mailed back zio patch 2/9/22 Echocardiogram and stress test, follow up with cardiology
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2162508

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: OH
Alter: 52,0
Geschlecht: F
Eingang: 07.03.2022
Impfdatum: 21.10.2021
Beginn: 30.01.2022
Tage bis Beginn: 101,0
Dosis: 1
Route/Site: IM / RA

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

COVID-19 Coronavirus test positive Cough Diarrhoea Dyspnoea Fatigue Headache Myalgia Nausea Parosmia Pyrexia Rhinorrhoea Vomiting Wheezing

Symptomtext

Patient tested positive on 01/26/2022. Admitted to the hospital on 01/30/2022 with symptoms: feverish, muscle aches, runny nose, cough, wheezing, shortness of breath, nausea or vomiting, headache, fatigue, diarrhea, olfactory disorder, difficulty breathing. No date of discharge was listed. Patient has multiple pre-existing health conditions.

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 2019 Novel Coronavirus RNA: Positive 01/26/2022
Aktuelle Erkrankungen: hypertension, severe obesity, asthma, immunocompromised, rheumatoid arthritis, allergies
Vorgeschichte: hypertension, severe obesity, asthma, immunocompromised, rheumatoid arthritis, allergies
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2130719

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: OK
Alter: 49,0
Geschlecht: M
Eingang: 22.02.2022
Impfdatum: 28.12.2020
Beginn: 28.12.2020
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / -

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

Dizziness Heart rate Tachycardia

Symptomtext

Tachycardia (fast heart rate); Lightheaded; This spontaneous case was reported by a nurse and describes the occurrence of TACHYCARDIA (Tachycardia (fast heart rate)) and DIZZINESS (Lightheaded) in a 49-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 011J20A) for COVID-19 vaccination. The patient's past medical history included No adverse event (No reported medical history). Concomitant products included METOPROLOL TARTRATE (LOPRESSOR) for an unknown indication. On 28-Dec-2020, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 28-Dec-2020, the patient experienced TACHYCARDIA (Tachycardia (fast heart rate)) and DIZZINESS (Lightheaded). On 28-Dec-2020, TACHYCARDIA (Tachycardia (fast heart rate)) and DIZZINESS (Lightheaded) had resolved. Unknown DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 28-Dec-2020, Heart rate: 140 140 heart beats per minute. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments.; Reporter's Comments: This case concerns a 49-year-old male patient, who experienced non-serious unexpected events of Tachycardia an Dizziness. The events occurred 3 to 5 minutes after first dose of mRNA-1273, lot # 011J20A. Treatment details were not provided. Based on the current available information and temporal association between the use of the product and onset of the events a causal relationship cannot be excluded.

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Praegender Schweregrund: Tachycardia
Hospital-Tage: -
Labordaten: Test Date: 20201228; Test Name: Pulse; Result Unstructured Data: 140 heart beats per minute
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: No adverse event (No reported medical history)
Andere Medikamente: LOPRESSOR
Allergien: -
Vorherige Impfungen: -

VAERS 2113154

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: FL
Alter: 74,0
Geschlecht: F
Eingang: 15.02.2022
Impfdatum: 10.02.2021
Beginn: 13.02.2022
Tage bis Beginn: 368,0
Dosis: UNK
Route/Site: - / -

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

COVID-19 Chest X-ray normal Chest discomfort Cough Dizziness Dyspnoea Headache Orthopnoea Palpitations SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Covid19 breakthrough. 1st Vaccine received on 01/08/2021. 75 y/o PMHx of HTN, DM, Hypothyroid, Diverticulitis, GERD presents to ED with c/o 2 day history of Chest pressure, orthopnea, palpitations, HA and dizziness. Pt states initially tested positive for Covid19 at MD office on 01/07/2022 and has also had Cough and SOB since. CXR-no infiltrates or effusions. Room air sat 100%, Afebrile.

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: SARS CoV 2 PCR Covid19 -Detected on 02/13/2022. Pt also has SARS CoV AG office- Positive on 01/07/2022.
Aktuelle Erkrankungen: -
Vorgeschichte: Hypothyroid, Diverticulitis, GERD, HTN, DM
Andere Medikamente: -
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 2095814

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: LA
Alter: 59,0
Geschlecht: F
Eingang: 08.02.2022
Impfdatum: 04.02.2021
Beginn: 04.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Blood thyroid stimulating hormone Cardiac stress test Chest discomfort Chest pain Computerised tomogram thorax Condition aggravated Dyspnoea exertional Echocardiogram Electrocardiogram Fatigue Full blood count Glycosylated haemoglobin Headache Lipids Malaise Metabolic function test Nasal congestion Nausea

Symptomtext

Increased pain in left arm, increased fatigue, headache, fever 102 F, nasal and chest congestion, malaise, nausea, vomiting, new onset palpitations, tachycardia, chest pain, chest tightness and increased shortness of breath with any activity and New onset renal insufficiency.

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Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: EKG, Chest CT, Echo, Cardiac Stress Test, CBC, CMP, HgbA1C, Lipid Panel, TSH, Etriodol level, Vitamin D and vitamin B13 levels, Sleep Apnea Test
Aktuelle Erkrankungen: Had COVID19 Pneumonia in 12/27/19-2/21/20 (approximately 8 weeks), followed by symptoms of Long COVID - fatigue, shortness of breath, gi upset, brain fog, GERD, eye infections 3/9/290, scalp rashes 4/17/20, 5/11/20, skin rashes 8/5/20, 9/9/20 with continued sob, fatigue, GI upset, brain fog.
Vorgeschichte: Asthma, Mixed HLD, L3-5, S1-S2 Herniated Disc, DDD, Chronic Back Pain, Allergic Rhinitis, Steroid induced Hyperglycemia, Vit D Deficiency, Smoker
Andere Medikamente: Allegra 180 mg PO QD Vitamin D 50k IU PO Q Week Ibuprofen 800 mg PO BID Metformin 500 mg PO BID Repaglinide 1 mg PO BID Estriodol 0.1 mg PO QD Amlodipine 5 mg PO QD Olmesartan Medoximil 40 mg PO QPM Protonix 40 mg PO QD Cyanocobalamin 1000
Allergien: Penicillin, Statins, Indocin If drug manufacturers are changed may have allergic reaction. Very sensitive to medications.
Vorherige Impfungen: Shingles

VAERS 2058848

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: TN
Alter: 37,0
Geschlecht: M
Eingang: 24.01.2022
Impfdatum: 21.01.2021
Beginn: 27.02.2021
Tage bis Beginn: 37,0
Dosis: 1
Route/Site: IM / LA

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

Blood magnesium normal Blood thyroid stimulating hormone normal Cardiac monitoring abnormal Chest pain Echocardiogram normal Laboratory test Metabolic function test normal Palpitations Thyroxine free normal Ventricular extrasystoles

Symptomtext

Around 1 month after receiving my second dose I began to experience frequent (10-12 per minute) heart palpitations and occasional chest pain. Went to see my primary care physician who ordered lab work and a cardiac monitor. The cardiac monitor showed frequent isolated PVCs. Cardiac markers were not drawn with the lab work so the results came back as normal. I was started on Toprol XL with no relief. After a follow up visit on 5/21 I requested to be referred to a cardiologist. The cardiologist recommended an echocardiogram. By the time I was able to schedule the echo my symptoms had resolved. The echo showed no abnormalities. My palpitations stopped on 6/11/21.

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Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 3/01 Labs - Magnesium, Free T4, TSH, and BMP all within normal limits.
Aktuelle Erkrankungen: none
Vorgeschichte: Asthma
Andere Medikamente: none
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2051167

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20a

moderat

Staat: FL
Alter: 90,0
Geschlecht: M
Eingang: 20.01.2022
Impfdatum: 27.10.2021
Beginn: 20.01.2022
Tage bis Beginn: 85,0
Dosis: 1
Route/Site: IM / -

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

Bradycardia Dyspnoea

Symptomtext

Patient is a 90-year-old male with PMHx significant for HTN, HLD, DM, OSA, s/p MVR who presented to the ED via EMS for dyspnea. Per chart review, the pt was also bradycardic with a HR of 29 bpm for which he received Atropine. The pt denies chest pain, nausea, vomiting, dizziness, or HA. Upon arrival to the ED, his HR was 30 with BP 134/58. He received an 500 cc NS bolus, Zofran, calcium gluconate, glucagon with improvement in HR to 49-50 with adequate BP. Case was discussed with Dr. who accepted the pt for evaluation and recommended against pacing as the pt is not symptomatic. He was transferred to another hospital for further evaluation. He arrives on a Dopamine gtt in no acute distress and with

Weitere VAERSDATA-Felder

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

VAERS 2043383

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: AK
Alter: 32,0
Geschlecht: F
Eingang: 18.01.2022
Impfdatum: 12.01.2021
Beginn: 12.01.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / RA

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

Abdominal pain Dizziness Dyspnoea Fatigue Feeling abnormal Female reproductive tract disorder Headache Heart rate increased Immediate post-injection reaction Lethargy Lung disorder Nausea Nervous system disorder Pain Pyrexia Vaginal haemorrhage Vomiting

Symptomtext

First injection (1/12/21) and second injection (2/9/21) both with similar side effects, however after the second, they were profoundly worse. Immediate dizziness, fever, body aches, piercing abdominal cramps, nausea, and emesis episodes. Immediate then chronic horrible "orbiting" headaches that felt like 1,000 knives piercing my brain- severe headaches, fatigue, lethargy, brain fog, vaginal bleeding, new dx female reproductive virus diagnosis 3 months after 2nd injection, shortness of breath, rapidly increasing heart rate with minimal exertion, impaired neurological and pulmonary function. I'm a marathon running and multi Marathon Qualifier; my training and competition capabilities have been profoundly impaired.

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Learned too late about D-Dimer testing and other potential treatments.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Vitamin D
Allergien: None
Vorherige Impfungen: -

VAERS 2042837

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: FL
Alter: 74,0
Geschlecht: M
Eingang: 18.01.2022
Impfdatum: 11.02.2021
Beginn: 13.01.2022
Tage bis Beginn: 336,0
Dosis: UNK
Route/Site: - / -

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

Asthenia COVID-19 Chest X-ray abnormal Dyspnoea Oropharyngeal pain Pneumonia Pyrexia SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Covid19 breakthrough. 1st vaccine received on 01/07/2021. 74 y/o PMH Multiple myeloma, immunocompromised host on Revlimid, BPH, HLD, HTN presents to ED 1/14/2022 after calling 911 for progressive weakness, SOB, Fever, sore throat and room air SATS of 80%. Patient had tested positive for Covid on 01/13/2022 at Local Care Center. CXR-Bibasilar PNA. Started on IV ABX, IV Steroids and Remdesivir.

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: SARS CoV AG Office- Positive 01/13/2022 (Local Care Center).
Aktuelle Erkrankungen: -
Vorgeschichte: Bone CA-Multiple myeloma (in current TX with Revlimid), Immunocompromised, BPH, HLD, HTN
Andere Medikamente: -
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 2039039

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: FL
Alter: 73,0
Geschlecht: F
Eingang: 17.01.2022
Impfdatum: 22.01.2021
Beginn: 04.01.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: OT / LA

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

Aphasia Condition aggravated Dysarthria Dyskinesia Dysphemia Feeling abnormal Gait inability Hypoaesthesia oral Hypokinesia Memory impairment Tremor

Symptomtext

Feel like there's a jolt & wake up to see that it's her lower extremities making the bed move/ For her hands & arms, she just hold them until they quit; She get this feeling in her head & can't remember what she was saying/ her clear thinking is what's really bothering her; She see what she was trying to say, but she can't speak it/ she try to tell people something & she can't get it out; Her mouth starts getting numb; She think it's messed up Her whole body/ she was scared; Her legs wouldn't walk/ needed help going to the bathroom; Her legs wouldn't move; Tremors in her hands, arms, & legs/ can't make them stop/ Right now her right arm & hand is shaking; Slurred speech; She stuttered; Her conditions are getting worse; This spontaneous case was reported by a consumer and describes the occurrence of GAIT INABILITY (Her legs wouldn't walk/ needed help going to the bathroom) and HYPOKINESIA (Her legs wouldn't move) in a 73-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 0271-121B, 016M20A and 011J20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 22-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 17-Feb-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 17-Dec-2021, received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 04-Jan-2021, the patient experienced CONDITION AGGRAVATED (Her conditions are getting worse). On 19-Dec-2021, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced GAIT INABILITY (Her legs wouldn't walk/ needed help going to the bathroom) (seriousness criterion disability), HYPOKINESIA (Her legs wouldn't move) (seriousness criterion disability), TREMOR (Tremors in her hands, arms, & legs/ can't make them stop/ Right now her right arm & hand is shaking), DYSARTHRIA (Slurred speech) and DYSPHEMIA (She stuttered). On 04-Jan-2022, the patient experienced DYSKINESIA (Feel like there's a jolt & wake up to see that it's her lower extremities making the bed move/ For her hands & arms, she just hold them until they quit). 04-Jan-2022, the patient experienced MEMORY IMPAIRMENT (She get this feeling in her head & can't remember what she was saying/ her clear thinking is what's really bothering her), APHASIA (She see what she was trying to say, but she can't speak it/ she try to tell people something & she can't get it out), HYPOAESTHESIA ORAL (Her mouth starts getting numb) and FEELING ABNORMAL (She think it's messed up Her whole body/ she was scared). At the time of the report, GAIT INABILITY (Her legs wouldn't walk/ needed help going to the bathroom), HYPOKINESIA (Her legs wouldn't move), TREMOR (Tremors in her hands, arms, & legs/ can't make them stop/ Right now her right arm & hand is shaking), DYSARTHRIA (Slurred speech), DYSPHEMIA (She stuttered), DYSKINESIA (Feel like there's a jolt & wake up to see that it's her lower extremities making the bed move/ For her hands & arms, she just hold them until they quit), MEMORY IMPAIRMENT (She get this feeling in her head & can't remember what she was saying/ her clear thinking is what's really bothering her), APHASIA (She see what she was trying to say, but she can't speak it/ she try to tell people something & she can't get it out), HYPOAESTHESIA ORAL (Her mouth starts getting numb), FEELING ABNORMAL (She think it's messed up Her whole body/ she was scared) and CONDITION AGGRAVATED (Her conditions are getting worse) had not resolved. No concomitant medications were provided. No treatment medications were reported. The patient is usually an active person. She take long hikes with her daughter, & she kayak. Company Comment: This case concerns a 73-year-old, female patient with no relevant medical history, who experienced the unexpected serious events of Gait Inability, Hypokinesia, Tremor, Dysarthria, Dysphemia, Dyskinesia, Memory Impairment, Aphasia, Hypoesthesia, Feeling Abnormal, and Condition Agrravated. The events of gait inability, hypokinesia, tremor, dysarthria, and dysphemia occurred approximately 2 days after the third dose of mRNA-1273 (Moderna covid-19 vaccine); while dyskinesia, memory impairment, aphasia, hypoesthesia, feeling abnormal, and condition aggravated occurred 18 days after the third dose. The rechallenge was not applicable as events occurred after third dose. The benefit-risk relationship of mRNA-1273 (Moderna covid-19 vaccine) is not affected by this report. This case was linked to MOD-2022-438710, MOD-2022-438711 (Patient Link).; Sender's Comments: This case concerns a 73-year-old, female patient with no relevant medical history, who experienced the unexpected serious events of Gait Inability, Hypokinesia, Tremor, Dysarthria, Dysphemia, Dyskinesia, Memory Impairment, Aphasia, Hypoesthesia, Feeling Abnormal, and Condition Agrravated. The events of gait inability, hypokinesia, tremor, dysarthria, and dysphemia occurred approximately 2 days after the third dose of mRNA-1273 (Moderna covid-19 vaccine); while dyskinesia, memory impairment, aphasia, hypoesthesia, feeling abnormal, and condition aggravated occurred 18 days after the third dose. The rechallenge was not applicable as events occurred after third dose. The benefit-risk relationship of mRNA-1273 (Moderna covid-19 vaccine) is not affected by this report.

Weitere VAERSDATA-Felder

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

VAERS 2034128

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: KY
Alter: 65,0
Geschlecht: F
Eingang: 14.01.2022
Impfdatum: 12.01.2021
Beginn: 29.10.2021
Tage bis Beginn: 290,0
Dosis: 1
Route/Site: OT / RA

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

Blood pressure measurement Body temperature Cardiac flutter Dyspnoea Exercise tolerance decreased Heart rate Palpitations Peripheral swelling Respiratory rate

Symptomtext

Palpitations; Decrease exercise tolerance; fluttering heart; leg started to swelled; shortness of breath/ Difficulty breathing / Dyspnoea; This spontaneous case was reported by a consumer and describes the occurrence of CARDIAC FLUTTER (fluttering heart) in a 65-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 939904, 031L20A. and 011J20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included Pulmonary embolism. Concurrent medical conditions included DVT. Concomitant products included APIXABAN (ELIQUIS) for DVT. On 12-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 09-Feb-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 26-Oct-2021, received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 29-Oct-2021, the patient experienced CARDIAC FLUTTER (fluttering heart) (seriousness criterion medically significant), PERIPHERAL SWELLING (leg started to swelled) and DYSPNOEA (shortness of breath/ Difficulty breathing / Dyspnoea). On an unknown date, the patient experienced PALPITATIONS (Palpitations) and EXERCISE TOLERANCE DECREASED (Decrease exercise tolerance). The patient was treated with DIPHENHYDRAMINE HYDROCHLORIDE (BENADRYL [DIPHENHYDRAMINE HYDROCHLORIDE]) ongoing since an unknown date at an unspecified dose and frequency. At the time of the report, CARDIAC FLUTTER (fluttering heart) and PERIPHERAL SWELLING (leg started to swelled) had not resolved, DYSPNOEA (shortness of breath/ Difficulty breathing / Dyspnoea) and PALPITATIONS (Palpitations) had resolved and EXERCISE TOLERANCE DECREASED (Decrease exercise tolerance) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, Blood pressure measurement: 138/75 138/75 mmHg. On an unknown date, Body temperature: 97 97 degree F. On an unknown date, Heart rate: 94 94 beats per minute. On an unknown date, Respiratory rate: 70 70 breaths per minute. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter considered DYSPNOEA (shortness of breath/ Difficulty breathing / Dyspnoea), PALPITATIONS (Palpitations) and EXERCISE TOLERANCE DECREASED (Decrease exercise tolerance) to be not related. No further causality assessments were provided for CARDIAC FLUTTER (fluttering heart) and PERIPHERAL SWELLING (leg started to swelled). Patient was taking Eliquis from years. Patient went to the ER were they checked for blood clots and did not find blood clot, also performed an ultrasound and since the patient is allergic to the contrast chemical was indicated Benadryl and steroids. Patient has no previous heart conditions nor has had covid-19. Patient had inquired if symptoms are common and whether it would prevent from getting. another Moderna vaccine in the future. Patient had difficulty in breathing and palpitations. Patient went to emergency room for Palpitations and Dyspnea on 18 Nov 2021 and had a doctor office visit on 23 Nov 2021. Causality for dyspnea, palpitations and decreased exercise tolerance was likely not related to the vaccine and anxiety was other possible cause of the events. Company comment: This case concerns a 65-year-old, female patient with medical history of pulmonary embolism and deep vein thrombosis, who experienced the unexpected, serious (Medically significant) and AESI of cardiac flutter, among other non-serious events. The event of cardiac flutter (described as fluttering heart) occurred approximately 3 days after receiving a dose, considered as the third dose of mRNA-1273. Follow up information by patient's physician stated that the patient suffered palpitations along with dyspnoea, that could be explained by patient's anxiety and decreased tolerance to exercise. The patient was concerned for a blot clot, however this was ruled out on images. Patient's physician does not considered that the reaction was not related to the vaccine. The rechallenge was not applicable as events occurred after third dose and no further dosing was reported. The medical history of pulmonary embolism and deep vein thrombosis remain as confounders. The benefit-risk relationship of mRNA-1273 is not affected by this report. This case was linked to MOD-2021-400069 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 04-Jan-2022: Follow up contains new events, secondary reporter, patient details, laboratory data, concomitant medication and date of vaccination was added and outcome of the event dyspnea was updated.; Sender's Comments: This case concerns a 65-year-old, female patient with medical history of pulmonary embolism and deep vein thrombosis, who experienced the unexpected, serious (Medically significant) and AESI of cardiac flutter, among other non-serious events. The event of cardiac flutter (described as fluttering heart) occurred approximately 3 days after receiving a dose, considered as the third dose of mRNA-1273. Follow up information by patient's physician stated that the patient suffered palpitations along with dyspnoea, that could be explained by patient's anxiety and decreased tolerance to exercise. The patient was concerned for a blot clot, however this was ruled out on images. Patient's physician does not considered that the reaction was not related to the vaccine. The rechallenge was not applicable as events occurred after third dose and no further dosing was reported. The medical history of pulmonary embolism and deep vein thrombosis remain as confounders. The benefit-risk relationship of mRNA-1273 is not affected by this report.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Test Name: Blood Pressure; Result Unstructured Data: 138/75 mmHg; Test Name: Body temperature; Result Unstructured Data: 97 degree F; Test Name: Heart rate; Result Unstructured Data: 94 beats per minute; Test Name: Respiratory Rate; Result Unstructured Data: 70 breaths per minute
Aktuelle Erkrankungen: DVT
Vorgeschichte: Medical History/Concurrent Conditions: Pulmonary embolism
Andere Medikamente: ELIQUIS
Allergien: -
Vorherige Impfungen: -

VAERS 2009873

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: NC
Alter: -
Geschlecht: F
Eingang: 05.01.2022
Impfdatum: 28.01.2021
Beginn: 13.12.2021
Tage bis Beginn: 319,0
Dosis: 1
Route/Site: - / -

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

COVID-19 Mobility decreased Muscle spasms Rash Rash erythematous SARS-CoV-2 test positive Skin warm

Symptomtext

I got the 1st COVID vaccine 1/28, 9 days later I had a red rash come up on my arm in the same area with the injection, reported it. So now I tested positive for COVID on 12/7- received antibodies injection on 12/8 and 7 days later I start having cramping in the arm and area with injection site, no redness, reported it also, yesterday I had a red area come up hot to touch in the same spot as the cramping now I can hardly even use my arm without pain. I actually have a picture documentation from 2/6 and 12/13

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Non smoker, non drinking and not pregnant
Vorgeschichte: Hypertension
Andere Medikamente: Losartan, Wellbutrin, Celexa, Melatonin
Allergien: PCN
Vorherige Impfungen: -

VAERS 1998906

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: NC
Alter: 47,0
Geschlecht: M
Eingang: 03.01.2022
Impfdatum: 31.12.2020
Beginn: 01.02.2021
Tage bis Beginn: 32,0
Dosis: 1
Route/Site: IM / RA

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

Cardiac pacemaker insertion Catheter placement Dizziness Dyspnoea Heart rate decreased Loss of personal independence in daily activities Stress echocardiogram

Symptomtext

I started to have trouble breathing and exercising, started feeling light headed within three months sometime in February and March, I was thinking it was related to distant heart issues. I had had a procedure and had problems after the vaccine. I started to become asymptomatic, light SOB, was not able to do what I could do, my heart rate was extremely low. They did a stress echo test, then they did catheterization and they did put me a pacemaker and this would now allow me to work how I did and thus I had to retire out. I do not know if the procedure I received caused these symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Stress echo test, catheterization. Pacemaker was also placed.
Aktuelle Erkrankungen: None reported
Vorgeschichte: Treated Afib; Prostate BPH (swollen prostate)
Andere Medikamente: Wellbutrin; Ambien; Flomax; Tylenol; Ibuprofen; Gencine; St. John's Wart
Allergien: Penicillin; B-venom
Vorherige Impfungen: -

VAERS 1996782

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: FL
Alter: 38,0
Geschlecht: F
Eingang: 31.12.2021
Impfdatum: 29.12.2020
Beginn: 01.02.2021
Tage bis Beginn: 34,0
Dosis: 1
Route/Site: OT / -

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

Fatigue Feeling cold Headache Inappropriate schedule of product administration Pyrexia Tremor

Symptomtext

first dose of Moderna COVID-19 Vaccine (29Dec2020, lot #011J20A) Second dose was injected IM on 03Feb2021; Cold Chills; Shakes; Low grade fever; Headache; Fatigue/ Tiredness; This spontaneous case was reported by an other health care professional and describes the occurrence of FEELING COLD (Cold Chills), TREMOR (Shakes), PYREXIA (Low grade fever), HEADACHE (Headache) and FATIGUE (Fatigue/ Tiredness) in a 38-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 028L20A and 011J20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 29-Dec-2020, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 03-Feb-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 03-Feb-2021, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (first dose of Moderna COVID-19 Vaccine (29Dec2020, lot #011J20A) Second dose was injected IM on 03Feb2021). In February 2021, the patient experienced FEELING COLD (Cold Chills), TREMOR (Shakes), PYREXIA (Low grade fever), HEADACHE (Headache) and FATIGUE (Fatigue/ Tiredness). On 03-Feb-2021, INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (first dose of Moderna COVID-19 Vaccine (29Dec2020, lot #011J20A) Second dose was injected IM on 03Feb2021) had resolved. In February 2021, FEELING COLD (Cold Chills), TREMOR (Shakes), PYREXIA (Low grade fever), HEADACHE (Headache) and FATIGUE (Fatigue/ Tiredness) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No Concomitant medication were reported. No treatment medication were reported. This case was linked to MOD-2021-430596.

Weitere VAERSDATA-Felder

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

VAERS 1992419

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: OH
Alter: 33,0
Geschlecht: M
Eingang: 30.12.2021
Impfdatum: 13.12.2021
Beginn: 15.12.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / LA

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

Abnormal behaviour Amnesia Blood creatine phosphokinase normal Blood thyroid stimulating hormone normal Chest X-ray normal Chest pain Chills Confusional state Dizziness Dyspnoea Electrocardiogram normal Fibrin D dimer normal Full blood count normal Hallucination Headache Lethargy Metabolic function test normal Palpitations

Symptomtext

Within 24 hours of the 3rd dose, (Booster), I developed fever, chills, shortness of breath and headache. Between 24-48 hours after, I became very lethargic and confused. I do not remember Tuesday 12/13/21 at all. I was hallucinating and not acting normal according to my wife. Starting on Wednesday 12/14/21, I began to have substernal chest pain, fluctuating in pain throughout the day with increased headaches and tachycardia. The chest pain has been increasing everyday and the tachycardia happens multiple times a day now unprovoked. With the tachycardia i get short of breath and dizzy. On Wednesday 12/23/21, the pain in my chest with the tachycardia was to the point that I went to Emergency Room. I have had a follow up with my PCP on 12/29/21 and now have an Echocardiogram scheduled for 1/6/22. I continue to have tachycardia throughout the day with palpitations that are only increasing in pain and duration. I never had these issues prior to my Covid Booster. Nothing in my medical history has changed in the past year.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 12/23/21 Emergency Room - 12 lead (SVT), D Dimer, CPK, PTT, Protime, HS Troponin I, BMP, CBC, TSH 3rd Generation, Assay Free Thyroxine. All within normal ranges. Chest X-Ray Normal. Echocardiogram scheduled for 1/6/22 at Hospital.
Aktuelle Erkrankungen: None. I have never had any cardiac issues in my life.
Vorgeschichte: ADHD
Andere Medikamente: Adderall 20mg, Prozac 20mg, Prozason 4mg
Allergien: Sulfa allergy, I have had bad reactions to the first 2 vaccines. No food or other products
Vorherige Impfungen: All Moderna, age 32, 12/30/20, 1/29/21, 12/13/21, IM Injection, Moderna

VAERS 1966716

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: LA
Alter: 73,0
Geschlecht: M
Eingang: 21.12.2021
Impfdatum: 18.01.2021
Beginn: 08.12.2021
Tage bis Beginn: 324,0
Dosis: 1
Route/Site: OT / LA

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

Feeling abnormal Neuropathic pruritus Paraesthesia Vaccination site pain

Symptomtext

had a neuropathic itch on sole of left foot. Not a regular itch.; Like pins; very annoying; Nothing at the injection site except sore; This spontaneous case was reported by a pharmacist and describes the occurrence of NEUROPATHIC PRURITUS (had a neuropathic itch on sole of left foot. Not a regular itch. ), PARAESTHESIA (Like pins), FEELING ABNORMAL (very annoying) and VACCINATION SITE PAIN (Nothing at the injection site except sore) in a 73-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 031H21A, 017B21A and 011J20A) for COVID-19 vaccination. No Medical History information was reported. On 18-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 31-Mar-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 08-Dec-2021, received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 08-Dec-2021, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced VACCINATION SITE PAIN (Nothing at the injection site except sore). On 13-Dec-2021, the patient experienced NEUROPATHIC PRURITUS (had a neuropathic itch on sole of left foot. Not a regular itch. ), PARAESTHESIA (Like pins) and FEELING ABNORMAL (very annoying). At the time of the report, NEUROPATHIC PRURITUS (had a neuropathic itch on sole of left foot. Not a regular itch. ), PARAESTHESIA (Like pins), FEELING ABNORMAL (very annoying) and VACCINATION SITE PAIN (Nothing at the injection site except sore) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. The patient denied to provide concomitant medications. The patient received the booster of the Moderna COVID-19 vaccine in the left upper arm. The patient had no rash. The reactions came and went. The patient did not receive any treatments but planning to take Allegra. This case was linked to MOD-2021-416481, MOD-2021-416488 (Patient Link).

Weitere VAERSDATA-Felder

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

VAERS 2545394

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: -
Alter: 48,0
Geschlecht: M
Eingang: 14.12.2021
Impfdatum: 23.12.2020
Beginn: 03.02.2021
Tage bis Beginn: 42,0
Dosis: 1
Route/Site: IM / LA

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

Anticoagulant therapy Dyspnoea Hypoxia

Symptomtext

hypoxia, severe dyspnea, dx with bilateral PE Narrative: Severe dyspnea, hypoxia with sats in 80. Hospitalized 2 days, heparin, DOAC to continue until Sept 2021

Weitere VAERSDATA-Felder

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

VAERS 1937996

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: KY
Alter: 54,0
Geschlecht: F
Eingang: 10.12.2021
Impfdatum: 12.01.2021
Beginn: 29.10.2021
Tage bis Beginn: 290,0
Dosis: 1
Route/Site: OT / RA

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

Cardiac flutter Dyspnoea Peripheral swelling

Symptomtext

fluttering heart; leg started to swelled; shortness of breath; This spontaneous case was reported by a consumer and describes the occurrence of CARDIAC FLUTTER (fluttering heart) in a 65-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 939904, 031L20A. and 011J20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included Pulmonary embolism. On 12-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 09-Feb-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 26-Oct-2021, received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 29-Oct-2021, the patient experienced CARDIAC FLUTTER (fluttering heart) (seriousness criterion medically significant), PERIPHERAL SWELLING (leg started to swelled) and DYSPNOEA (shortness of breath). The patient was treated with APIXABAN (ELIQUIS) at an unspecified dose and frequency and DIPHENHYDRAMINE HYDROCHLORIDE (BENADRYL [DIPHENHYDRAMINE HYDROCHLORIDE]) at an unspecified dose and frequency. At the time of the report, CARDIAC FLUTTER (fluttering heart), PERIPHERAL SWELLING (leg started to swelled) and DYSPNOEA (shortness of breath) had not resolved. Concomitant medication was not provided by the reporter. Patient went to the ER were they checked for blood clots and did not find blood clot, also performed an ultrasound and since the patient is allergic to the contrast chemical was indicated Benadryl and steroids. Patient has no previous heart conditions nor has had covid-19. Patient had inquired if symptoms are common and whether it would prevent from getting. another Moderna vaccine in the future. Company comment: This case concerns a 65-year-old, female patient with medical history of pulmonary embolism, who experienced the unexpected event cardiac flutter and non serious events of peripheral swelling and dyspnoea. The event of cardiac flutter (described as fluttering heart) occurred approximately 3 days after the third dose of mRNA-1273. Very limited information was provided regarding diagnostic findings. The rechallenge was not applicable as events occurred after third dose and no further dosing was reported or planned, based on information provided. The above mentioned medical history remains a confounder. The benefit-risk relationship of mRNA-1273 is not affected by this report. This case was linked to MOD-2021-400069 (Patient Link).; Sender's Comments: This case concerns a 65-year-old, female patient with medical history of pulmonary embolism, who experienced the unexpected event cardiac flutter and non serious events of peripheral swelling and dyspnoea. The event of cardiac flutter (described as fluttering heart) occurred approximately 3 days after the third dose of mRNA-1273. Very limited information was provided regarding diagnostic findings. The rechallenge was not applicable as events occurred after third dose and no further dosing was reported or planned, based on information provided. The above mentioned medical history remains a confounder. The benefit-risk relationship of mRNA-1273 is not affected by this report.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Pulmonary embolism
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1935297

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: KY
Alter: -
Geschlecht: U
Eingang: 09.12.2021
Impfdatum: 12.01.2021
Beginn: 30.10.2021
Tage bis Beginn: 291,0
Dosis: 2
Route/Site: OT / RA

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

Cardiac flutter Dyspnoea Peripheral swelling

Symptomtext

fluttering heart; shortness of breath; legs started to swell; This spontaneous case was reported by a consumer and describes the occurrence of CARDIAC FLUTTER (fluttering heart) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 939904, 011J20A and 031L20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included Pulmonary embolism. On 12-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 09-Feb-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 26-Oct-2021, received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 30-Oct-2021, the patient experienced CARDIAC FLUTTER (fluttering heart) (seriousness criterion medically significant), DYSPNOEA (shortness of breath) and PERIPHERAL SWELLING (legs started to swell). At the time of the report, CARDIAC FLUTTER (fluttering heart), DYSPNOEA (shortness of breath) and PERIPHERAL SWELLING (legs started to swell) had not resolved. No concomitant medication were reported. No treatment medication were reported. Company comment: This case concerns a patient, unknown gender and age, with medical history of pulmonary embolism, who experienced the serious, unexpected, event of cardiac flutter. The event occurred 4 days after booster dose of mRNA 1273 vaccine. The patient's leg swelled up and experienced difficulty of breathing and fluttering heart, patient went to the ER where an ultrasound was done, no blood clots were found. The rechallenge is not applicable as there is no additional dose expected. The patient's history of pulmonary embolism remains a confounder to the events. The benefit-risk relationship of mRNA 1273 vaccine is not affected by this report. This case was linked to MOD-2021-400023 (Patient Link).; Sender's Comments: This case concerns a patient, unknown gender and age, with medical history of pulmonary embolism, who experienced the serious, unexpected, AESI event of cardiac flutter. The event occurred 4 days after booster dose of mRNA 1273 vaccine. The patient's leg swelled up and experienced difficulty of breathing and fluttering heart, patient went to the ER where an ultrasound was done, no blood clots were found. The rechallenge is not applicable as there is no additional dose expected. The patient's history of pulmonary embolism remains a confounder to the events. The benefit-risk relationship of mRNA 1273 vaccine is not affected by this report.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Pulmonary embolism
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1909860

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: NY
Alter: 27,0
Geschlecht: F
Eingang: 30.11.2021
Impfdatum: 22.12.2020
Beginn: 19.01.2021
Tage bis Beginn: 28,0
Dosis: 1
Route/Site: IM / LA

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

Blindness Cardiac stress test Chills Disturbance in attention Dizziness Electrocardiogram ambulatory normal Electrocardiogram normal Fall Fatigue Memory impairment Orthostatic hypotension Tilt table test positive Ultrasound Doppler normal

Symptomtext

After 1st vaccine, I experienced fatigue and chills the morning afterwards. I also had a rash appear on my L deltoid a few days later that lasted about 4-5 days. After the 2nd vaccine (1/19) on 2/11 I stood up out of bed, lost vision and fell over. Throughout the past 8 months I have had multiple instances of my vision going black and falling over when standing up. I have dizziness, decreased concentration, decreased memory, and fatigue. My blood pressure has also been very low. I was worked up by cardiology and was diagnosed with Neurogenic orthostatic hypotension. I have been treated with increased water intake, increased salt intake, compression stockings and Midodrine 10mg x 3 per day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Orthostatic hypotension
Hospital-Tage: -
Labordaten: I have had an EKG, ECG, Holter, transcranial doppler and stress test- all negative for significant findings. I also had a tilt table test on July 7th with a positive result of type I mixed
Aktuelle Erkrankungen: N/A
Vorgeschichte: - Hashimoto's (antibodies, thyroid function still normal) - Chronic Fatigue
Andere Medikamente: - drospirenone/ethinyl estradiol/ levomefolate calcium tablets (birth control) - zyrtec 10 mg - sertraline 150 mg
Allergien: N/A
Vorherige Impfungen: -

VAERS 1904080

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: OR
Alter: 54,0
Geschlecht: M
Eingang: 27.11.2021
Impfdatum: 29.01.2021
Beginn: 12.03.2021
Tage bis Beginn: 42,0
Dosis: 2
Route/Site: IM / RA

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

Abdominal discomfort Abdominal pain Condition aggravated Diarrhoea Dyspepsia Gastric polyps Gastrooesophageal reflux disease Haematochezia Hypergastrinaemia Oropharyngeal pain Regurgitation

Symptomtext

Exacerbated gastroesophageal reflux disease and hypergastrinemia. Abdominal pain, cramping, discomfort, heartburn and acid regurgitation increased, as well as occurrence of new symptoms including sore throat, diarrhea and blood in the stool. Additionally, gastric polyps were diagnosed through endoscopic surgery. Patient was previously using sporadic histamine-2 blockers and occasional, low dose, short term proton-pump inhibitors to treat symptoms, which became ineffective. Patient was prescribed daily proton-pump inhibitors to manage symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Upper and lower endoscopic surgery.
Aktuelle Erkrankungen: None
Vorgeschichte: gastroesophageal reflux disease
Andere Medikamente: famotidine 20mg
Allergien: None
Vorherige Impfungen: -

VAERS 1889624

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: FL
Alter: 35,0
Geschlecht: M
Eingang: 22.11.2021
Impfdatum: 05.02.2021
Beginn: 15.05.2021
Tage bis Beginn: 99,0
Dosis: 1
Route/Site: IM / RA

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

Cardiac stress test normal Chest pain Echocardiogram Electrocardiogram ambulatory normal Electrocardiogram normal Exercise tolerance decreased Heart rate increased Magnetic resonance imaging normal Palpitations

Symptomtext

Chest pain with palpitations and higher than normal heart rate at random times throughout day - with no prior history or having experiencing these symptoms previously in my lifetime. Initially ~5-10 "episodes" per day. Nothing significant yielded from Cardiac tests, yet symptoms persisted. In early November, I noticed symptoms have improved and have resumed moderate cardio-fitness workouts.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: I went to Clinic for a full cardiac workup: EKG - Normal sinus rhythm, Echocardiogram - Good Exercise stress test - Normal although recovery time was longer than usual Cardiac Holter Monitor - 13 days with normal sinus rhythm Chest MRI - No signs of clots or pulmonary embolism Nothing significant yielded from Cardiac tests, yet symptoms persist
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Finasteride - 1mg (daily)
Allergien: None
Vorherige Impfungen: -

VAERS 1882633

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: NY
Alter: 49,0
Geschlecht: F
Eingang: 18.11.2021
Impfdatum: 23.12.2020
Beginn: 19.01.2021
Tage bis Beginn: 27,0
Dosis: 1
Route/Site: SYR / LA

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

Asthma Breast mass Breast swelling Condition aggravated Mammogram Ultrasound breast Ultrasound scan

Symptomtext

Lump and swelling in left breast for first vaccine ; had an emergency doctors office visit with a breast surgeon; had an ultrasound . Also had a follow up diagnostic mammogram and ultrasound . 2nd vaccine I suffered with asthmatic exacerbation and was hospitalized. I have had asthma my entire life and never experienced this before.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: 12/26/20 sonogram January 2021 diagnostic mammogram and ultrasound. March /April 2021 Asthmatic exacerbation was in ER with nebulizer treatment ; steroid IV injections . PFT ?s to follow and multiple follow up visits with a pulmonologist.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Vitamin C / Super B complex / Fish oil
Allergien: Penicillins/Vancomyocin
Vorherige Impfungen: -

VAERS 1879784

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: TX
Alter: -
Geschlecht: F
Eingang: 18.11.2021
Impfdatum: 21.01.2021
Beginn: 30.10.2021
Tage bis Beginn: 282,0
Dosis: 1
Route/Site: OT / RA

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

Tachycardia Vaccination complication

Symptomtext

AE to the Moderna Booster; experienced tachycardia; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION COMPLICATION (AE to the Moderna Booster) and TACHYCARDIA (experienced tachycardia) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 039D21A, 032L20A and 011J20A) for COVID-19 vaccination. No Medical History information was reported. On 21-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 20-Feb-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 28-Oct-2021, received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 30-Oct-2021, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced TACHYCARDIA (experienced tachycardia). On an unknown date, the patient experienced VACCINATION COMPLICATION (AE to the Moderna Booster). The patient was treated with ASPIRIN [ACETYLSALICYLIC ACID] for Adverse event, at an unspecified dose and frequency. On 30-Oct-2021, TACHYCARDIA (experienced tachycardia) had resolved. At the time of the report, VACCINATION COMPLICATION (AE to the Moderna Booster) outcome was unknown. No concomitant medications were provided. Patient had reported that the tachycardia came on at 2 PM on 30 Oct 2021 and lasted until 7 PM in the evening. She stated she went to a clinic for evaluation but should have went to the emergency room. Most recent FOLLOW-UP information incorporated above includes: On 10-Nov-2021: The recent follow-up contains significant information due to additional event and patient gender updated. Reporter were also updated.

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

VAERS 1876631

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: KS
Alter: 41,0
Geschlecht: F
Eingang: 17.11.2021
Impfdatum: 11.02.2021
Beginn: 17.09.2021
Tage bis Beginn: 218,0
Dosis: 1
Route/Site: IM / AR

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

COVID-19 Diarrhoea Dyspnoea Fatigue Pain Pyrexia Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

Congestion, fatigue, fever, body aches, diarrhea, shortness of breath

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Tested positive for COVID-19
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Multi-vitamins
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 1825340

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: FL
Alter: 64,0
Geschlecht: F
Eingang: 28.10.2021
Impfdatum: 29.12.2020
Beginn: 10.10.2021
Tage bis Beginn: 285,0
Dosis: 1
Route/Site: IM / UN

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

Blood creatinine increased Bundle branch block right COVID-19 Chest X-ray abnormal Dyspnoea Electrocardiogram abnormal Exposure to SARS-CoV-2 Lung infiltration Lung opacity Pleural effusion Prohormone brain natriuretic peptide increased SARS-CoV-2 test positive

Symptomtext

Case of a 65 years old female with past medical history of high blood pressure, HFrEF, COPD, CAD with CABG x 5 and hyperlipidemia presents to the ED due to complaints of shortness of breath, On EMS arrival patient was found in the 70s O2 room air, given breathing treatments during route to the ED, she is vaccinated against covid. She has been exposed to family members at home. Denies any hx of diarrheas, abdominal pain, headache, fever or other associated symptoms. Urine and bowel pattern within normal limits, patient is also aware that she has a mass in her lung and she has been unable to have a CT, since she has been denies twice by her insurance. Patient is independent ADLs and instrumental ADLs. Denies any toxic habits/ former smoker On admission: ProBNP is 29783. Her creatinine is noted to be 5.2. Previous creatinine from September of 2021 was 2.4. EKG shows sinus rhythm at 73 beats per minute with incomplete right bundle-branch block. XR Chest 1V 1. Focal masslike opacity in the left midlung. This may reflect a well-defined focus of consolidation or pneumonia however a mass is not ruled out. Further characterization with CT chest recommended. 2. Left basilar infiltrates and adjacent mild left-sided effusion. 3. Background of COPD and scattered fine reticular opacities suspected chronic. Tested + COVID 10/10/2021 1256

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

VAERS 1818083

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011j20a

moderat

Staat: MO
Alter: 47,0
Geschlecht: F
Eingang: 26.10.2021
Impfdatum: 28.01.2021
Beginn: 19.08.2021
Tage bis Beginn: 203,0
Dosis: UNK
Route/Site: SYR / RA

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

Alopecia COVID-19 Depression Disturbance in attention Dizziness Fatigue Fungal infection Headache Impaired work ability Mobility decreased Nasopharyngitis Nausea Pain Pain in extremity Sensation of foreign body Urticaria

Symptomtext

was positive for covid on 8/21/2021. on 8/23/2021 was given the infusion. on 8/27/2021 began z pack and steroids. was down for 4 weeks. went back to work finally. I have since missed work and continued to be sick with dizziness, faintness, nauseness, headaches, no concentration, depression, fatigue, body aches, cold like systems, something "stuck" in my throat, another round of antibodics, a yeast infections, loss of hair, extreme pain in the bottom of my feet, random break out of hives.

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Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: doctor visit, just keeps putting me on antibodics and steroids and steroid shots.
Aktuelle Erkrankungen: -
Vorgeschichte: lupus asthma ibs fibromyalgia
Andere Medikamente: plaquneil gabepentine topamax duloxetine norco bentyl
Allergien: n/a
Vorherige Impfungen: -

VAERS 1790654

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: CA
Alter: 50,0
Geschlecht: F
Eingang: 16.10.2021
Impfdatum: 04.01.2021
Beginn: 04.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / -

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

Abdominal pain upper Asthma Blood disorder Chest discomfort Dyspnoea Fatigue Headache Hyperventilation Off label use Pain in extremity SARS-CoV-2 test Salivary hypersecretion Secretion discharge Tachycardia Throat irritation Throat tightness

Symptomtext

Asthma; She had a telemedicine appointment with her doctor the following week who recommended that she not take an additional dose of the vaccine at at time; Heart beat which was very rapid; Mucous started running; A sore arm; Headaches; Felt tired; Feeling pressure on her chest; Throat was getting smaller/ like it was starting to close up; Throat was starting to burn; Felt is was hard to breathe; Hyperventilating; Felt her blood was bubbling; Stomach started hurting; She had saliva like she needed to spit; Had a headache; Sore arm; Felt tired; This spontaneous case was reported by a consumer and describes the occurrence of CHEST DISCOMFORT (Feeling pressure on her chest), THROAT TIGHTNESS (Throat was getting smaller/ like it was starting to close up), THROAT IRRITATION (Throat was starting to burn), DYSPNOEA (Felt is was hard to breathe), HYPERVENTILATION (Hyperventilating), BLOOD DISORDER (Felt her blood was bubbling), ABDOMINAL PAIN UPPER (Stomach started hurting), SALIVARY HYPERSECRETION (She had saliva like she needed to spit), ASTHMA (Asthma), TACHYCARDIA (Heart beat which was very rapid), SECRETION DISCHARGE (Mucous started running), PAIN IN EXTREMITY (A sore arm), HEADACHE (Headaches) and the first episode of FATIGUE (Felt tired) in a 50-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 011J20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concurrent medical conditions included Blood pressure high and High cholesterol. On 04-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 04-Jan-2021, the patient experienced CHEST DISCOMFORT (Feeling pressure on her chest) (seriousness criteria medically significant and life threatening), THROAT TIGHTNESS (Throat was getting smaller/ like it was starting to close up) (seriousness criteria medically significant and life threatening), THROAT IRRITATION (Throat was starting to burn) (seriousness criteria medically significant and life threatening), DYSPNOEA (Felt is was hard to breathe) (seriousness criteria medically significant and life threatening), HYPERVENTILATION (Hyperventilating) (seriousness criteria medically significant and life threatening), BLOOD DISORDER (Felt her blood was bubbling) (seriousness criteria medically significant and life threatening), ABDOMINAL PAIN UPPER (Stomach started hurting) (seriousness criteria medically significant and life threatening), SALIVARY HYPERSECRETION (She had saliva like she needed to spit) (seriousness criteria medically significant and life threatening), TACHYCARDIA (Heart beat which was very rapid) (seriousness criteria medically significant and life threatening), SECRETION DISCHARGE (Mucous started running) (seriousness criteria medically significant and life threatening), PAIN IN EXTREMITY (A sore arm) (seriousness criteria medically significant and life threatening), HEADACHE (Headaches) (seriousness criteria medically significant and life threatening) and the first episode of FATIGUE (Felt tired) (seriousness criteria medically significant and life threatening). In 2021, the patient experienced HEADACHE (Had a headache), PAIN IN EXTREMITY (Sore arm) and the second episode of FATIGUE (Felt tired). On an unknown date, the patient experienced ASTHMA (Asthma) (seriousness criteria medically significant and life threatening) and OFF LABEL USE (She had a telemedicine appointment with her doctor the following week who recommended that she not take an additional dose of the vaccine at at time). The patient was treated with DIPHENHYDRAMINE HYDROCHLORIDE (BENADRYL [DIPHENHYDRAMINE HYDROCHLORIDE]) at a dose of 1 dosage form. On 04-Jan-2021, CHEST DISCOMFORT (Feeling pressure on her chest), THROAT TIGHTNESS (Throat was getting smaller/ like it was starting to close up), THROAT IRRITATION (Throat was starting to burn), DYSPNOEA (Felt is was hard to breathe), HYPERVENTILATION (Hyperventilating), BLOOD DISORDER (Felt her blood was bubbling), ABDOMINAL PAIN UPPER (Stomach started hurting), SALIVARY HYPERSECRETION (She had saliva like she needed to spit), TACHYCARDIA (Heart beat which was very rapid) and SECRETION DISCHARGE (Mucous started running) had resolved. On 07-Jan-2021, PAIN IN EXTREMITY (A sore arm) and HEADACHE (Headaches) had resolved. At the time of the report, ASTHMA (Asthma), OFF LABEL USE (She had a telemedicine appointment with her doctor the following week who recommended that she not take an additional dose of the vaccine at at time), HEADACHE (Had a headache), PAIN IN EXTREMITY (Sore arm) and the last episode of FATIGUE (Felt tired) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): In March 2020, SARS-CoV-2 test: negative (Negative) Negative. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. No concomitant medications were provided. Within 15-20 minutes after receiving the vaccine the patient's throat was getting smaller and starting to burn, like it was starting to close up. The patient then started feeling pressure on her chest, felt it was hard to breathe and she was hyperventilating, felt her blood was bubbling, her stomach started hurting, mucous started running, she had saliva like she needed to spit, and she had headaches. This lasted for 2-3 hours. Events Sore arm, Fatigue and Headache are duplicated in the case because they were included in the Structured fields and also reported with unknown start date in the Narrative of the case. Conservatively, both events are included in the case. Company Comment: This case concerns a 50 year-old female patient with no relevant medical history reported, who experienced the unexpected serious events of Chest discomfort, Throat tightness, Throat irritation, Dyspnoea, Hyperventilation, Blood disorder, Abdominal pain upper, Salivary hypersecretion, Tachycardia, Secretion discharge, Pain in extremity, Asthma and events as Headache and Fatigue, which are considered unlisted because of the seriousness of the case (Medically significant and Life-Threatening). Most events started 15-20 minutes after the first dose of an inappropriate schedule of administration of Moderna Covid-19 vaccine and resolved in 2 to 3 hours after the administration of Benadryl. The event asthma started on an unknown date after the vaccine administration and the outcome is unknown. The rechallenge is unknown for all the events reported, since the patient never received a second dose. The patient was advised by her Health Care Provider not to take the second dose of the vaccine and based on that information, the Non serious event Off label use was added to the case. The benefit-risk relationship of Moderna Covid-19 Vaccine is not affected by this report.; Sender's Comments: This case concerns a 50 year-old female patient with no relevant medical history reported, who experienced the unexpected serious events of Chest discomfort, Throat tightness, Throat irritation, Dyspnoea, Hyperventilation, Blood disorder, Abdominal pain upper, Salivary hypersecretion, Tachycardia, Secretion discharge, Pain in extremity, Asthma and events as Headache and Fatigue, which are considered unlisted because of the seriousness of the case (Medically significant and Life-Threatening). Most events started 15-20 minutes after the first dose of an inappropriate schedule of administration of Moderna Covid-19 vaccine and resolved in 2 to 3 hours after the administration of Benadryl. The event asthma started on an unknown date after the vaccine administration and the outcome is unknown. The rechallenge is unknown for all the events reported, since the patient never received a second dose. The patient was advised by her Health Care Provider not to take the second dose of the vaccine and based on that information, the Non serious event Off label use was added to the case. The benefit-risk relationship of Moderna Covid-19 Vaccine is not affected by this report.

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Test Date: 202003; Test Name: COVID-19 test; Test Result: Negative ; Result Unstructured Data: Negative
Aktuelle Erkrankungen: Blood pressure high; High cholesterol
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1768268

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: FL
Alter: 63,0
Geschlecht: F
Eingang: 07.10.2021
Impfdatum: 06.01.2021
Beginn: 02.02.2021
Tage bis Beginn: 27,0
Dosis: 1
Route/Site: IM / RA

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

Cardiomyopathy Computerised tomogram thorax Dyspnoea exertional Echocardiogram Electrocardiogram Fatigue Heart rate irregular Laboratory test Petechiae Scan with contrast Thrombocytopenia Ultrasound liver

Symptomtext

9/8/21 Went to ER for petechiae on bilateral legs, feeling tired, low grade temp, SOB on exertion and irregular heartbeat. Admitted to hospital for thrombocytopenia and cardiomyopathy.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea exertional
Hospital-Tage: 3,0
Labordaten: 9/9/21 Ekg, CT Lung with contrast, Cardiac Echo, Labs, Liver ultrasound
Aktuelle Erkrankungen: Covid
Vorgeschichte: N/A
Andere Medikamente: Levothyroid, Pantoprazole, Atorvastatin, Estradiol
Allergien: Macrobid
Vorherige Impfungen: -

VAERS 1763990

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: NY
Alter: 63,0
Geschlecht: F
Eingang: 06.10.2021
Impfdatum: 05.01.2021
Beginn: 10.01.2021
Tage bis Beginn: 5,0
Dosis: 2
Route/Site: OT / -

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

Cardiac stress test Chest discomfort Computerised tomogram thorax Echocardiogram Extrasystoles Heart rate Palpitations Pulmonary function test SARS-CoV-2 antibody test

Symptomtext

Chest pressure; heart pounding/ pounding while sedentary/Irregular heart rate; SKIPPED BEATS/ skipping while sedentary; This spontaneous case was reported by a consumer and describes the occurrence of PALPITATIONS (heart pounding/ pounding while sedentary/Irregular heart rate), EXTRASYSTOLES (SKIPPED BEATS/ skipping while sedentary) and CHEST DISCOMFORT (Chest pressure) in a 63-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 011J20A and 028L20a) for COVID-19 vaccination. The patient's past medical history included Pericardial effusion on 29-Dec-2020, Heartbeats skipped (Last spring, patient noticed that during strenuous hikes, her heart, when pounding, would skip beats now and then. By fall, it was skipping beats every 2 to 5 beats.) in 2021, Urticaria and Hay fever. Previously administered products included for an unreported indication: SWINE FLU VACCINE in 1977. Past adverse reactions to the above products included Light headedness with SWINE FLU VACCINE. Concurrent medical conditions included Environmental allergy (Headaches, congestion), Allergy to chemicals (Nausea, vomiting, hives all over my body starting with where I had contact with the airline seats) since 17-Feb-2014, Drug allergy (Caused irregular heartbeat for a few hours about 12 hours after use/ Extreme heart arythmia) since 2007, Drug allergy (Allergy to Singulair, Disrupted sleep, increased stress/ psychological reaction), Food allergy (headaches, congestion.), Hypothyroidism since 2018, Asthma and Hypertension since 2006. Concomitant products included FEXOFENADINE from 2015 to an unknown date for Allergy, ZAFIRLUKAST from 2008 to an unknown date for Asthma, IBUPROFEN (ADVIL [IBUPROFEN]) for Headache, LISINOPRIL from 2015 to an unknown date for Hypertension, LEVOTHYROXINE from 2016 to an unknown date for Hypothyroidism. On 05-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 02-Feb-2021 at 12:15 PM, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 10-Jan-2021, the patient experienced PALPITATIONS (heart pounding/ pounding while sedentary/Irregular heart rate) and EXTRASYSTOLES (SKIPPED BEATS/ skipping while sedentary). On 15-Jan-2021, the patient experienced CHEST DISCOMFORT (Chest pressure). On 29-Jan-2021, PALPITATIONS (heart pounding/ pounding while sedentary/Irregular heart rate), EXTRASYSTOLES (SKIPPED BEATS/ skipping while sedentary) and CHEST DISCOMFORT (Chest pressure) had resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 18-Dec-2020, Cardiac stress test: normal (normal) Good. On 18-Dec-2020, Echocardiogram: abnormal (abnormal) pre-vaccine echo showed some pericardial effusion.. On 29-Dec-2020, Computerised tomogram thorax: normal (normal) Heart appeared normal. On 26-Jan-2021, Pulmonary function test: normal (normal) normal to above normal. On an unknown date, Heart rate: abnormal (abnormal) Heart rate irregular. On an unknown date, SARS-CoV-2 antibody test: negative (Negative) Sars-Cov-2 Antibody IGA- negative, positive (Positive) Sars-Cov-2 Antibody IGG- positive. and negative (Negative) Sars-Cov-2 Antibody IGM- negative. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. Patient stated that after the medications used for a month for pericarditis, pounding stopped, but not the pressure or skipping. Patient Wearing a heart monitor for a month showed nothing of note (heart skipping an average of 2%). increase in Levothyroxine (75 MCG to 88 MCG) finally ended the heart skipping and chest pressure. No treatment medications were reported. This case was linked to US-MODERNATX, INC.-MOD-2021-010524 (Linked Report). Most recent FOLLOW-UP information incorporated above includes: On 25-May-2021: Follow up received, contains no new information On 13-Aug-2021: Follow up includes: updated consumer weight in KG's. added food allergy& updated description box for some of relevant history. added medical history: Hay fever, added lab tests:Sars-Cov-2 Antibody IGM, IGA, IGG and their results, added 2nd dose details and concomitant medications: Advil & updated start date for other concomitants, event causes the patient to visit doctor's office.; Sender's Comments: US-MODERNATX, INC.-MOD-2021-010524: second dose case

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: Test Date: 20201218; Test Name: Stress test; Result Unstructured Data: Good; Test Date: 20201229; Test Name: chest CT; Result Unstructured Data: Heart appeared normal; Test Date: 20201218; Test Name: echocardiogram; Result Unstructured Data: pre-vaccine echo showed some pericardial effusion; Test Name: Heart rate; Result Unstructured Data: Heart rate irregular; Test Date: 20210126; Test Name: Pulmonary function test; Result Unstructured Data: normal to above normal; Test Name: Sars-Cov-2 Antibody IGA; Test Result: Negative; Result Unstructured Data: Sars-Cov-2 Antibody IGA- negative; Test Name: Sars-Cov-2 Antibody IGG; Test Result: Positive ; Result Unstructured Data: Sars-Cov-2 Antibody IGG- positive; Test Name: Sars-Cov-2 Antibody IGM; Test Result: Negative; Result Unstructured Data: Sars-Cov-2 Antibody IGM- negative.
Aktuelle Erkrankungen: Allergy to chemicals (Nausea, vomiting, hives all over my body starting with where I had contact with the airline seats); Asthma; Drug allergy (Caused irregular heartbeat for a few hours about 12 hours after use/ Extreme heart arrhythmia); Drug allergy (Allergy to Singulair, Disrupted sleep, increased stress/ psychological reaction); Environmental allergy (Headaches, congestion); Food allergy (headaches, congestion.); Hypertension; Hypothyroidism.
Vorgeschichte: Medical History/Concurrent Conditions: Hay fever; Heartbeats skipped (Last spring, patient noticed that during strenuous hikes, her heart, when pounding, would skip beats now and then. By fall, it was skipping beats every 2 to 5 beats.); Pericardial effusion; Urticaria.
Andere Medikamente: Zafirlukast; Lisinopril; Levothyroxine; Fexofenadine; Advil [Ibuprofen]
Allergien: -
Vorherige Impfungen: -

VAERS 1761510

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: CA
Alter: 45,0
Geschlecht: F
Eingang: 05.10.2021
Impfdatum: 23.12.2020
Beginn: 23.12.2020
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Arthralgia Condition aggravated Fatigue Impaired work ability Visual impairment

Symptomtext

Moderna Covid-19 vaccine EUA Joint pain, headaches, fatigue, vision worsening

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: I have seen the doctors multiple times from December 23-present. I missed 4 days of work after the first shot and 5 days after the second. I have never been the same since the shots.
Aktuelle Erkrankungen: Hypothyroidism, hearing impairment, arthritis, post hysterectomy from uterine cancer, insomnia, anxiety, depression, obesity.
Vorgeschichte: hearing impairment, anxiety, depression, insomnia, radical hysterectomy from uterine cancer, arthritis, obesity.
Andere Medikamente: Levothyroxine
Allergien: PCN,CIPRO
Vorherige Impfungen: -

VAERS 1745568

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011j20a

moderat

Staat: CO
Alter: 45,0
Geschlecht: F
Eingang: 29.09.2021
Impfdatum: 23.12.2020
Beginn: 23.01.2021
Tage bis Beginn: 31,0
Dosis: 1
Route/Site: IM / LA

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

Injected limb mobility decreased Injection site pain Injection site rash Injection site swelling Magnetic resonance imaging X-ray

Symptomtext

1st covid dose - unable to left the left arm for three days with pain , swelling , tenderness 2nd covid dose- red rash at left arm injection site litttle by little started with left arm pain, loss of the left arm movement

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Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: left arm x-rays let arm MRI
Aktuelle Erkrankungen: none
Vorgeschichte: hypothyroid diabetic type 2
Andere Medikamente: Levothyroxine metformin Glipizide
Allergien: nkda
Vorherige Impfungen: -

VAERS 1732385

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: NC
Alter: 54,0
Geschlecht: F
Eingang: 24.09.2021
Impfdatum: 07.01.2021
Beginn: 14.01.2021
Tage bis Beginn: 7,0
Dosis: UNK
Route/Site: IM / LA

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

Arthralgia Condition aggravated Psoriatic arthropathy

Symptomtext

worsened psoriatic arthritis joint pain which did improve over time but flared again after 2nd vaccine and 3rd booster injection. Has not completely resolved

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: NA
Aktuelle Erkrankungen: -
Vorgeschichte: chronic psoriatic arthritis and psoriasis, hypertension, hyperlipidemia
Andere Medikamente: Xanax 0.5 mg tablet ( Take 1 tablet(s) by oral route , 1 time per day , for 30 days ) losartan 50 mg-hydrochlorothiazide 12.5 mg tablet Humira rosuvastatin 10 mg tablet milk thistle; Fish oil; Co-enzyme Q10; Fiber; Vitamin D; Zinc
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1730256

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: NC
Alter: 82,0
Geschlecht: F
Eingang: 24.09.2021
Impfdatum: 15.01.2021
Beginn: 19.01.2021
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: OT / RA

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

Echocardiogram Enzyme level test Fatigue Heart rate Palpitations Product dose omission issue Tachycardia

Symptomtext

palpitation; has just been tired since then/lingering tiredness; tachycardia; did not take the second dose; This spontaneous case was reported by a consumer and describes the occurrence of TACHYCARDIA (tachycardia), PALPITATIONS (palpitation) and FATIGUE (has just been tired since then/lingering tiredness) in an 82-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 011J20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concurrent medical conditions included Tachycardia. On 15-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 19-Jan-2021, the patient experienced TACHYCARDIA (tachycardia) (seriousness criteria hospitalization prolonged and medically significant) and PRODUCT DOSE OMISSION ISSUE (did not take the second dose). On an unknown date, the patient experienced PALPITATIONS (palpitation) (seriousness criteria hospitalization prolonged and medically significant) and FATIGUE (has just been tired since then/lingering tiredness) (seriousness criterion hospitalization prolonged). The patient was hospitalized on sometime in February 2021 due to FATIGUE, PALPITATIONS and TACHYCARDIA. The patient was treated with METOPROLOL for Heart disorder, at an unspecified dose and frequency. At the time of the report, TACHYCARDIA (tachycardia), PALPITATIONS (palpitation), FATIGUE (has just been tired since then/lingering tiredness) and PRODUCT DOSE OMISSION ISSUE (did not take the second dose) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 19-Jan-2021, Echocardiogram: did not have a heart attack. On 19-Jan-2021, Enzyme level test: high (High) High. On 19-Jan-2021, Heart rate: high (High) 140 and 150. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. No concomitant medications were provided. The patient was hospitalized for day and a half where they catharized her and did an echocardiogram. This is a case of product dose omission for this 82-year-old, female patient with medical history of tachycardia who experienced the unexpected event of tachycardia, palpitation and the expected event of fatigue. The events started 4 days after the first dose of Spikevax. The rechallenge was not applicable, as the events happened after the first dose. The events were considered related to the product per the reporter's assessment. The medical history of tachycardia and advanced age remains as confounder. The event fatigue is consistent with the current understanding of the mechanism of action of the vaccine. The benefit-risk relationship of Spikevax in not affected by this report.; Sender's Comments: This is a case of product dose omission for this 82-year-old, female patient with medical history of tachycardia who experienced the unexpected event of tachycardia, palpitation and the expected event of fatigue. The events started 4 days after the first dose of Spikevax. The rechallenge was not applicable, as the events happened after the first dose. The events were considered related to the product per the reporter's assessment. The medical history of tachycardia and advanced age remains as confounder. The event fatigue is consistent with the current understanding of the mechanism of action of the vaccine. The benefit-risk relationship of Spikevax in not affected by this report.

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Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: Test Date: 20210119; Test Name: Echocardiogram; Result Unstructured Data: did not have a heart attack; Test Date: 20210119; Test Name: enzyme; Result Unstructured Data: High; Test Date: 20210119; Test Name: heart rate; Result Unstructured Data: 140 and 150
Aktuelle Erkrankungen: Tachycardia
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1715330

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: FL
Alter: 66,0
Geschlecht: F
Eingang: 20.09.2021
Impfdatum: 11.02.2021
Beginn: 17.09.2021
Tage bis Beginn: 218,0
Dosis: 1
Route/Site: IM / -

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

COVID-19 Decreased appetite Dyspnoea Oedema peripheral Productive cough SARS-CoV-2 test positive

Symptomtext

9/14/21: Patient arrived at the ER due to shortness of breath and cough. The patient tested positive for COVID-19 on 08/23/202. At that time she was managed with symptomatic therapy including albuterol inhaler. After testing COVID negative on 09/08/2021, she was getting symptomatically better. But since last 4 days she has worsening of cough and SOB. Shortness of breath is present even at rest, previously orthopnea/ PND absent. She complains of productive cough, associated with loss of appetite and pedal edema. Per patient, her nurse noted that her bp was 152/93 and oxygen saturation of 79%. She had televisit where she complained of home BP 170s-190s and oxygen sat was 79-85 % at room air. Patient received first dose Moderna vaccine on 1/08/2021 Lot # 011J20A and the second dose on 2/11/2021 Lot # 029K20A

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: HTN, hypothyroidism, base of tongue cancer, tonsillar cancer and fibromyalgia
Andere Medikamente: -
Allergien: Norvasc
Vorherige Impfungen: -

VAERS 1715152

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: NY
Alter: 39,0
Geschlecht: F
Eingang: 20.09.2021
Impfdatum: 07.01.2021
Beginn: 08.01.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Bursitis Mobility decreased Pain in extremity

Symptomtext

First vaccine I had extreme sore arm for day 2-4 day 5 I couldn?t move my arm at all and end up with bursitis for 3 weeks.

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Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: PTSD
Andere Medikamente: Vyvanse
Allergien: Bee?s, orange, guava
Vorherige Impfungen: -

VAERS 1679154

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: WI
Alter: 49,0
Geschlecht: F
Eingang: 07.09.2021
Impfdatum: 28.12.2020
Beginn: 03.09.2021
Tage bis Beginn: 249,0
Dosis: 1
Route/Site: IM / -

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

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

Symptomtext

Patient was admitted to the ER with shortness of breath. She tested positive for COVID-19 on 9/02/21.

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

VAERS 1662404

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011j20a

moderat

Staat: NY
Alter: 43,0
Geschlecht: F
Eingang: 01.09.2021
Impfdatum: 16.02.2021
Beginn: 20.02.2021
Tage bis Beginn: 4,0
Dosis: 2
Route/Site: IM / LA

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

Hyperacusis Migraine Photophobia

Symptomtext

Ever since having the injection I have been having 2-3 Migraines a month. I have never had Headaches such as these. Extremely sensitive to light, sound, and movement

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Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Coedine
Vorherige Impfungen: -

VAERS 1656310

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: HI
Alter: 49,0
Geschlecht: F
Eingang: 30.08.2021
Impfdatum: 23.12.2020
Beginn: 20.01.2021
Tage bis Beginn: 28,0
Dosis: 1
Route/Site: SYR / -

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

Condition aggravated Dizziness Laboratory test Vertigo positional

Symptomtext

Dizziness

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Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: basic labs done at emergency department on 2/20/2021
Aktuelle Erkrankungen: -
Vorgeschichte: Tinnitus, BPPV, T2DM, Dyslipidemia. She had exacerbation of her long standing BPPV after vaccination.
Andere Medikamente: Clonazepam, losartan, sertraline, semaglutide, rosuvastatin, tylenol
Allergien: Seafood, metformin
Vorherige Impfungen: -

VAERS 1916119

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: DE
Alter: 69,0
Geschlecht: F
Eingang: 28.08.2021
Impfdatum: 23.02.2021
Beginn: 25.02.2021
Tage bis Beginn: 2,0
Dosis: UNK
Route/Site: - / -

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

Barium swallow normal Cardiac monitoring abnormal Cardiac stress test normal Chest discomfort Chest pain Echocardiogram abnormal Gastrointestinal disorder Pain Palpitations Pericardial effusion Supraventricular tachycardia Ventricular extrasystoles

Symptomtext

Received #2 COVID vaccine 2/23/21. While taking bedtime meds pm 2/25/21, sudden onset very severe chest pain/pressure midsternum as if pill swallowed "sideways". No changes in BP, pulse or ECG trcing on fitness watch. Felt pain due to GI issue. Pain (less severe) con't through weekend, also noticed onset of palpitations. Saw primary dr 3/2/21. She ordered labs, barium swallow, ziopatch x 7 days, GI consult, did ECG in office. Only ziopatch showed results with runs of SVT, & PVC's. My primary Dr ordered a cardiac consult. Cardiologist ordered stress test (essentially normal), echocardiogram. Cardiologist said echocardiogram showed some pericardial effusion - didn't know why I woulld have that. I will have a repeat echocaRdiogram on 8/31/21. Have Not yet discussed possible vacciNe event with cardiologist. To see cardiologist 9/10/21.

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Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: barium swallow 3/4/21 - neg; ziopatch 3/9/21-3/16/21 - runs of SVT, PVC's; echocardiogram 6/8/21 - pericardial effusion; stress test 5/20/21 - NoRMal
Aktuelle Erkrankungen: No acute illnesses
Vorgeschichte: asthma, HTN, chRonic back pain, meNopausal syNdRome
Andere Medikamente: LosaRtiN, Hydrochlorathiazide, TRazadoNe, Estrodial, PRogesteRoNe, gabopeNtiN
Allergien: NoNe
Vorherige Impfungen: -

VAERS 1651380

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: CA
Alter: 40,0
Geschlecht: F
Eingang: 28.08.2021
Impfdatum: 01.02.2021
Beginn: 01.03.2021
Tage bis Beginn: 28,0
Dosis: 1
Route/Site: IM / LA

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

Blood creatine phosphokinase Computerised tomogram head Condition aggravated Disturbance in attention Full blood count Headache Loss of personal independence in daily activities Magnetic resonance imaging head Metabolic function test Migraine with aura

Symptomtext

Intractable H/A for 5 weeks. Severe, intense, no ability to concentrate, aura, light sensitivity, pounding, etc. Treatment with Imitrex (oral), Trazodone (then temporarily replaced with cyclobenzaprine, and subsequently tizanidine); OTC: Tylenol. Peaking throughout the first 3.5 weeks, then waning. Then, got 2nd dose of vax and H/A began to peak again 3 days later. Took injectable imitrex once, resolved to very low grade H/A within 45 min. Then was nearly completely gone by 3/8/21. 2/5/21 H/A began. Increased in intensity to the most intense, severe, mentally distracting/unable to focus or function normally H/A I ever experience. Intractable H/A. Cannot take Advil and Tylenol was barely helping at all. The intensity kept increasing over the course of a week, where I finally realized it's not going away and I need to seek care. 2/8/21 & 2/12/21 Telehealth visit with my PCP. DX: R51.9; RX: Trazodone (25mg/night), Sumatriptan 50 mg tablet (total of 9 tablets). 2/26/21: In person Urgent Care visit per PCP advice, as her schedule wasn't open. Dx: G43.011. RX: Sumatriptan 6 mg/0.5 mL injection pen kit (used 1 pen dose 3/4/21), Reglan (did not take raglan). 3/4/21: Spike in H/A that was reducing intensity the week prior. Began with an aura, began peaking, realized what this was, took the Sumatriptan injection, within 45 min stopped the peaking of the H/A. 3/8/21: E- Consult Peer to Peer: Neuro to PCP; By this time, the headache had waned to nearly gone, no meds needed. 4/7/21: Telehealth Neuro Consult - concluded this was vax rxn, as I have no prior hx of anything remotely similar.

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Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: 2/12/21: CT Head 2/26/21: MRI Brain 2/12/21: Labs: CMP; CBC; Creatine Kinase; Vit b12; Zinc
Aktuelle Erkrankungen: N/A
Vorgeschichte: Ulcerative colitis (in remission at the time) Endometriosis
Andere Medikamente: Vidolizumab /Entyvio 300 mg Digestive enzymes, probiotics, adaptogenic herbs, trans-resveratrol, cur cumin BCM-95, vitex/chasteberry, multi-vitamin, collagen peptides, acacia fiber, tretinoin (ointment, skin application), glutathione, beef
Allergien: Sulfa, Amoxicillin, Remicade/Infliximab, 5-ASA/Mesalamine.
Vorherige Impfungen: Shingrix 10/23/19, 12/30/21; after each dose: 3 days flu-like illness, body and muscle aches, bed ridden with 100-101d F fever x

VAERS 1641269

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: FL
Alter: 52,0
Geschlecht: M
Eingang: 27.08.2021
Impfdatum: 04.03.2021
Beginn: 06.08.2021
Tage bis Beginn: 155,0
Dosis: 2
Route/Site: IM / -

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

C-reactive protein increased COVID-19 Chest pain Fibrin D dimer increased Inflammatory marker increased Pneumonia Pyrexia SARS-CoV-2 test positive

Symptomtext

8/6/21: This is a 52 year old Dentist with no Past Medical History. He is Admitted to PCU for COVID19, Multifocal Community Pneumonia, Chest Pain, Positive D-Dimer, Elevated CPR Inflammatory, and Low-grade Fever. Patient has been sick with COVID for approximately 11 days. Has had low-grade fevers Note: Patient previously vaccinated with Moderna COVID-19 Vaccine: First Dose: 01/28/2021 Lot Number 028L20A and Second Dose: 03/04/2021 Lot Number 011J20A. 8/11/2021: patent discharged

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Praegender Schweregrund: Chest pain
Hospital-Tage: 5,0
Labordaten: SARS CoV 2 PCR COVID-19 Positive on 8/6/2021
Aktuelle Erkrankungen: -
Vorgeschichte: No chronic problems
Andere Medikamente: Lisinopril, Vitamin C, Vitamin B Complex
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 1634909

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: PR
Alter: 70,0
Geschlecht: F
Eingang: 26.08.2021
Impfdatum: 28.12.2020
Beginn: 28.12.2020
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: OT / LA

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

Anxiety Aphasia Depressed level of consciousness Disturbance in attention Dysgraphia Memory impairment Palpitations Urticaria Vaccination site erythema Vaccination site swelling

Symptomtext

Problems with concentration, couldn't concentrate; Trouble finding her words, could't speak properly, experience kind of aphasia symptoms; Mind fogginess, brain fog; Hives; Difficulty remembering names; Difficult to do writing tasks; Heart race; nervousness of getting the vaccine; Swallen in the injection site; Redness in the injection site; A spontaneous report was received from a 70-year-old, female consumer who received Moderna's COVID-19 vaccine and developed problems with concentration, could not speak properly, trouble finding her words, brain fog/ mind fogginess, hives, redness and swelling at the injection site, difficult to do writing tasks, difficulty remembering things, increment in heartbeat, heart racing, nervousness of getting the vaccine. The patient's past medical history, as provided by the reporter, included long lasting, bad side effects following the influenza vaccine. Concomitant medication reported included vitamins. On 28 Dec 2020, prior to the onset of the events, the patient received their first of two planned doses of mRNA-1273 (Lot number: 011J20A) intramuscularly in the left arm for prophylaxis of COVID-19 infection. On 28 Dec 2020, four hours after receiving the vaccine, the patient developed problems with concentration, trouble finding her words, mind fogginess, hives, redness and swelling at the injection site, difficult to do writing tasks, difficulty remembering things, increment heart beat. Treatment for the event included tylenol and ibuprofen. Action taken with the second dose of mRNA-1273 in response to the event was not reported. The outcome for the events, developed problems with concentration, trouble finding her words, mind fogginess, hives, redness and swelling at the injection site, increment heartbeat were considered as recovered on 30 Dec 2020. At the time of report outcome of the events difficult to do writing tasks, difficulty remembering things was unknown. The reporter's assessment of causality for the events was not applicable. Additional information received on 31 Dec 2020: Events updated. Follow up received on 23Mar2021, included no new information.; Reporter's Comments: Based on the current available information and temporal association between the use of the product and the start date of the events, a causal relationship cannot be excluded.

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Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Reaction to previous exposure to any vaccine (She does not receive the influenza vaccine anymore due to bad side effects that are long-lasting (months).)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1633793

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: CO
Alter: 62,0
Geschlecht: M
Eingang: 25.08.2021
Impfdatum: 24.02.2021
Beginn: 26.02.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: - / LA

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

Arthralgia Back pain Magnetic resonance imaging abnormal Muscular weakness Neck pain Nerve conduction studies Neuralgic amyotrophy Paraesthesia

Symptomtext

Stated with severe pain in left shoulder, back and neck a couple days after 2nd shot. One week after 2nd shot, parasthesia & weakness in left arm. Pain resolved in about a month. Parasthesia and weakness did not resolve for about 2 1/2 months.

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Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: MRI -- no nerve impigment Nerve conductiont tests -- diagnosed as brachial plexitits
Aktuelle Erkrankungen: none
Vorgeschichte: Sleep Apnea
Andere Medikamente: Vitamin D
Allergien: none
Vorherige Impfungen: -

VAERS 1626387

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: IN
Alter: 54,0
Geschlecht: M
Eingang: 24.08.2021
Impfdatum: 31.03.2021
Beginn: 31.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / LA

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

Blood pressure measurement Body temperature increased Headache Heart rate Hypertension Nausea Oxygen saturation Pain

Symptomtext

generalized pain to bilateral shoulders and legs; His B/P 160/110; nausea; headache; This spontaneous case was reported by a nurse and describes the occurrence of PAIN (generalized pain to bilateral shoulders and legs), HYPERTENSION (His B/P 160/110), NAUSEA (nausea) and HEADACHE (headache) in a 54-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 011J20A) for COVID-19 vaccination. No Medical History information was reported. On 31-Mar-2021 at 2:08 PM, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 31-Mar-2021 at 2:12 PM, the patient experienced PAIN (generalized pain to bilateral shoulders and legs), HYPERTENSION (His B/P 160/110), NAUSEA (nausea) and HEADACHE (headache). The patient was treated with DIPHENHYDRAMINE HYDROCHLORIDE (BENADRYL [DIPHENHYDRAMINE HYDROCHLORIDE]) (oral) on 31-Mar-2021 for Nausea, Headache, General body pain and Hypertension, at a dose of 1 dosage form. On 31-Mar-2021 at 3:00 PM, PAIN (generalized pain to bilateral shoulders and legs), NAUSEA (nausea) and HEADACHE (headache) outcome was unknown. At the time of the report, HYPERTENSION (His B/P 160/110) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 31-Mar-2021, Blood pressure measurement: 160/110 (High) 160/110 at 14:12 and 150/100 150/100 at 15:00. On 31-Mar-2021, Body temperature increased: 98.1 (normal) 98.1. On 31-Mar-2021, Heart rate: 75 (normal) 75. On 31-Mar-2021, Oxygen saturation: 96% (normal) 96%. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medications were reported. Most recent FOLLOW-UP information incorporated above includes: On 16-Jun-2021: Follow up received on 16-JUN-2021 contains significant information includes, Patient demographics, event outcome, vaccination Facility information.

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Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: Test Date: 20210331; Test Name: blood pressure; Result Unstructured Data: 160/110 at 14:12; Test Date: 20210331; Test Name: blood pressure; Result Unstructured Data: 150/100 at 15:00; Test Date: 20210331; Test Name: temperature; Result Unstructured Data: 98.1; Test Date: 20210331; Test Name: heart rate; Result Unstructured Data: 75; Test Date: 20210331; Test Name: oxygen saturation; Result Unstructured Data: 96%
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1626218

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: CA
Alter: 33,0
Geschlecht: F
Eingang: 24.08.2021
Impfdatum: 23.12.2020
Beginn: 09.02.2021
Tage bis Beginn: 48,0
Dosis: 2
Route/Site: - / -

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

COVID-19 Dyspnoea Fatigue Headache Pain SARS-CoV-2 test negative SARS-CoV-2 test positive

Symptomtext

tested positive for COVID; headaches; shortness of breath; bodyache; felt fatigued; A spontaneous report was received from a healthcare professional concerning a 33-years-old female patient who received Moderna's COVID-19 vaccine (mRNA-1273) and experienced events headaches, shortness of breath, body aches, felt fatigued, tested positive for covid. The patient's medical history was not provided. Concomitant medications reported were birth control medication. On 23 Dec 2020, prior to the onset of the events the patient received their first of two planned doses of mRNA-1273 (lot/batch: 011J20A) ivia unknown route for prophylaxis of COVID-19 infection. On 20 Jan 2021, prior to the onset of the events the patient received their second of two planned doses of mRNA-1273 (lot/batch: 042L20A) via unknown route for prophylaxis of COVID-19 infection. On 9 Feb 2021, the patient experienced the events- headache, shortness of breath, body aches and felt fatigued. On 11 Feb 2021, the patient tested positive for covid. She stated the symptoms subsided on their own On 11 Feb 2021, the lab data performed included- Rapid test (negative) and PCR test (positive). No treatment information was provided. Action taken with mRNA-1273 in response to the events was not reported. The outcome of events- headaches,shortness of breath, body aches, fatigue and Covid 19 positive- was Recovering/Resolving.

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Test Date: 20210211; Test Name: Covid Test-Rapid test; Test Result: Negative ; Test Date: 20210211; Test Name: Covid Test-PCR; Test Result: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: No adverse event
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1626035

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: NY
Alter: -
Geschlecht: M
Eingang: 24.08.2021
Impfdatum: 28.12.2020
Beginn: 29.12.2020
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: OT / RA

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

Ageusia Anosmia Chills Fatigue Migraine Oropharyngeal pain Vaccination site erythema Vaccination site pain

Symptomtext

Migraine headache; Red and blotchy on the injection site; Sore throat; Lost his sense of smell and taste; Lost his sense of smell and taste; Fatigue; Arm is sore; Chills; A spontaneous report was received from a consumer who was a male patient who received Moderna's COVID-19 Vaccine, and who experienced chills, arm was sore, fatigue, lost his sense of smell and taste, sore throat, red and blotchy on the injection site and migraine headache. The patient's medical history was not provided. Concomitant product use was not provided by the reporter. On 28-Dec-2020, approximately one day prior to the onset of the symptoms, the patient received his first of two planned doses of mRNA-1273 (LOT 011J20A) intramuscularly in the right arm for prophylaxis of COVID-19 infection. The next day, on 29-Dec-2020, he began to have chills and his arm was sore. Two days later, on 01-Jan-2021, he felt fatigued. On 04-Jan-2020, he reported losing his sense of smell and sense of taste. He reported a sore throat one day later on 05-Jan-2021 and stated that on 06-Jan-2021, his injection site was red and blotchy. Finally, on 07-Jan-2021, patient said that he experienced a migraine headache. He reported that for the migraine headache, he took six tablets of paracetamol which did not help. He stated that he then took three, 81 mg tablets of baby aspirin which did provide some relief. Action taken with mRNA-1273 in response to the events was not provided. The outcome of the events were not provided.; Sender's Comments: Based on the current available information and temporal association between the use of the product and the start date of the events, a causal relationship cannot be excluded. However, events loss of smell and taste is unlikely related to mRNA-1273. Further information is requested.

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Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: No adverse event (No medical history reported.)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1625442

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: OH
Alter: 44,0
Geschlecht: F
Eingang: 24.08.2021
Impfdatum: 29.12.2020
Beginn: 29.12.2020
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Chest discomfort Dyspnoea Eye pruritus Eye swelling

Symptomtext

Severe bilateral eye swelling and itching. Tightness in chest slight difficulty breathing SpO2 97%. Took Benadryl and Pepcid. Monitored myself symptoms decreased.

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Anemia
Andere Medikamente: Slow Fe, B12, Loratadine, potassium, magnesium, calcium, zinc, adderal
Allergien: Amoxicillin
Vorherige Impfungen: -

VAERS 1623342

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: NC
Alter: 52,0
Geschlecht: F
Eingang: 23.08.2021
Impfdatum: 01.02.2021
Beginn: 01.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Burning sensation Hypoaesthesia Pain in extremity Paraesthesia

Symptomtext

Within 20 minutes of receiving injection, experienced acute onset of diffuse paresthesia (pins and needles). Intensity and frequency lessened over time but did not completely resolve for approximately 6 months. Approximately 8 weeks after injection, began experiencing acute and transient burning in left foot toes (injection was on left side). Within 2 weeks, burning progressed into numbness and transient stabbing pain in left foot toes that radiated into leg, and transient numbness in left fingertips (primarily 5th digit) radiating at times into left hand and arm. Neurologist indicated possible idiopathic small nerve fiber neuropathy.

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Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Brain MRI; extensive blood panels; electromyography
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: OTC B12 supplements; Apri (birth control)
Allergien: -
Vorherige Impfungen: -

VAERS 1622462

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: NC
Alter: 64,0
Geschlecht: F
Eingang: 23.08.2021
Impfdatum: 30.12.2020
Beginn: 30.12.2020
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / RA

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

Headache Hypoaesthesia Pain in extremity Paraesthesia Product dose omission issue Vaccination site bruising

Symptomtext

Missed Dose; vaccination site bruising; pain in arm/arm aching down to elbow,from elbow to fingertips/severe pain in right arm below injection site; tingling feet/hands/pretty good tingling/tingling right arm/leg; numbness generalized/hip to below knew,dull and numbish;from below knee thru toes,same tingling as fingers/side of the face and jaw; dull and numbish/numbness right thigh and right side of face; Headache; This case was received via an unknown source (no reference has been entered for a health authority or license partner) on 05-Jun-2021 and was forwarded to Moderna on 07-Jun-2021. This spontaneous case was reported by a consumer and describes the occurrence of PRODUCT DOSE OMISSION ISSUE (Missed Dose), PAIN IN EXTREMITY (pain in arm/arm aching down to elbow,from elbow to fingertips/severe pain in right arm below injection site), PARAESTHESIA (tingling feet/hands/pretty good tingling/tingling right arm/leg), HYPOAESTHESIA (numbness generalized/hip to below knew,dull and numbish;from below knee thru toes,same tingling as fingers/side of the face and jaw; dull and numbish/numbness right thigh and right side of face) and VACCINATION SITE BRUISING (vaccination site bruising) in a 64-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 011J20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included Cold sores (Cold Sore Virus) and Guillain Barre syndrome in 1995. Concurrent medical conditions included Drug allergy (Allergic to Niacin), Plastic sensitivity, Food allergy (Allergic to Onions), Food allergy (Allergic to Mint), Diabetes, Hypertension (Blood Pressure) since 1995, Cholesterol since 1995 and Latex allergy. Concomitant products included FENOFIBRATE for Cholesterol, VALACICLOVIR HYDROCHLORIDE (VALTREX) for Cold sores, METFORMIN for Diabetes, QUINAPRIL HYDROCHLORIDE (ACCUPRIL), HYDROCHLOROTHIAZIDE and AMLODIPINE. On 30-Dec-2020 at 4:30 PM, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 30-Dec-2020 at 4:30 PM, the patient experienced HEADACHE (Headache). On 31-Dec-2020, the patient experienced HYPOAESTHESIA (numbness generalized/hip to below knew,dull and numbish;from below knee thru toes,same tingling as fingers/side of the face and jaw; dull and numbish/numbness right thigh and right side of face). On 31-Dec-2020 at 4:00 AM, the patient experienced PAIN IN EXTREMITY (pain in arm/arm aching down to elbow,from elbow to fingertips/severe pain in right arm below injection site) and PARAESTHESIA (tingling feet/hands/pretty good tingling/tingling right arm/leg). On an unknown date, the patient experienced PRODUCT DOSE OMISSION ISSUE (Missed Dose) and VACCINATION SITE BRUISING (vaccination site bruising). At the time of the report, PRODUCT DOSE OMISSION ISSUE (Missed Dose), PAIN IN EXTREMITY (pain in arm/arm aching down to elbow,from elbow to fingertips/severe pain in right arm below injection site), VACCINATION SITE BRUISING (vaccination site bruising) and HEADACHE (Headache) outcome was unknown and PARAESTHESIA (tingling feet/hands/pretty good tingling/tingling right arm/leg) and HYPOAESTHESIA (numbness generalized/hip to below knew,dull and numbish;from below knee thru toes,same tingling as fingers/side of the face and jaw; dull and numbish/numbness right thigh and right side of face) had not resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Accupril, Amlodipine and Hydrochlorthiazide are used for Blood Pressure This case was linked to MOD-2021-009337 (Patient Link).

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Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Cholesterol; Diabetes; Drug allergy (Allergic to Niacin); Food allergy (Allergic to Onions); Food allergy (Allergic to Mint); Hypertension (Blood Pressure); Latex allergy; Plastic sensitivity
Vorgeschichte: Medical History/Concurrent Conditions: Cold sores (Cold Sore Virus); Guillain Barre syndrome
Andere Medikamente: ACCUPRIL; HYDROCHLOROTHIAZIDE; FENOFIBRATE; AMLODIPINE; METFORMIN; VALTREX
Allergien: -
Vorherige Impfungen: -

VAERS 1616389

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: CO
Alter: 74,0
Geschlecht: M
Eingang: 22.08.2021
Impfdatum: 09.01.2021
Beginn: 06.02.2021
Tage bis Beginn: 28,0
Dosis: 1
Route/Site: OT / RA

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

Ageusia Anosmia Body temperature Cough Dyspnoea Fatigue Headache Myalgia Pyrexia Raynaud's phenomenon Rhinitis SARS-CoV-2 test Vaccination complication Vaccination site pain

Symptomtext

A slight loss of taste and smell but not completely gone; Rhinitis; Shortness of breath; A slight loss of taste and smell but not completely gone; Feeling off \ generally don't feel well; Cough; Headaches; General fatigue; Achy muscles \ muscle aches; Didn't really feel bad but had a temperature of 99.3 degrees; A really sore arm at injection site for 2 to 3 days/a sore arm at injection site; Feet turns red and then white; This spontaneous case was reported by a consumer and describes the occurrence of RAYNAUD'S PHENOMENON (Feet turns red and then white), ANOSMIA (A slight loss of taste and smell but not completely gone), RHINITIS (Rhinitis), DYSPNOEA (Shortness of breath) and AGEUSIA (A slight loss of taste and smell but not completely gone) in a 74-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 029L20A and 011J20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No medical history was provided by the reporter. Concomitant products included APIXABAN (ELIQUIS), SOTALOL, PARACETAMOL (TYLENOL), ALBUTEROL [SALBUTAMOL], EMPAGLIFLOZIN (JARDIANCE), FINASTERIDE (PROSCAR), FLUTICASONE PROPIONATE (FLONASE [FLUTICASONE PROPIONATE]), FLUTICASONE PROPIONATE, SALMETEROL XINAFOATE (ADVAIR), FUROSEMIDE SODIUM (LASIX [FUROSEMIDE SODIUM]), GABAPENTIN, MAGNESIUM OXIDE, METFORMIN, MONTELUKAST SODIUM (SINGULAIR), MORNIFLUMATE (FLOMAX [MORNIFLUMATE]), VITAMIN B6 and VITAMIN B12 [VITAMIN B12 NOS] for an unknown indication. On 09-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 06-Feb-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 06-Feb-2021, the patient experienced RAYNAUD'S PHENOMENON (Feet turns red and then white), RHINITIS (Rhinitis), DYSPNOEA (Shortness of breath), AGEUSIA (A slight loss of taste and smell but not completely gone), VACCINATION COMPLICATION (Feeling off \ generally don't feel well), COUGH (Cough), HEADACHE (Headaches), FATIGUE (General fatigue), MYALGIA (Achy muscles \ muscle aches), PYREXIA (Didn't really feel bad but had a temperature of 99.3 degrees) and VACCINATION SITE PAIN (A really sore arm at injection site for 2 to 3 days/a sore arm at injection site). On an unknown date, the patient experienced ANOSMIA (A slight loss of taste and smell but not completely gone). At the time of the report, RAYNAUD'S PHENOMENON (Feet turns red and then white), ANOSMIA (A slight loss of taste and smell but not completely gone), RHINITIS (Rhinitis), DYSPNOEA (Shortness of breath), AGEUSIA (A slight loss of taste and smell but not completely gone), VACCINATION COMPLICATION (Feeling off \ generally don't feel well), COUGH (Cough), HEADACHE (Headaches), FATIGUE (General fatigue) and MYALGIA (Achy muscles \ muscle aches) had not resolved and PYREXIA (Didn't really feel bad but had a temperature of 99.3 degrees) and VACCINATION SITE PAIN (A really sore arm at injection site for 2 to 3 days/a sore arm at injection site) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 19-Nov-2020, SARS-CoV-2 test: negative (Negative) Negative. On 29-Dec-2020, SARS-CoV-2 test: negative (Negative) negative. On 18-Jan-2021, SARS-CoV-2 test: negative (Negative) negative test for his CoV-2 antibodies Nucleocapsid Protein IgG Antibody Test. On 06-Feb-2021, Body temperature: 99.3 (Inconclusive) 99.3 degrees. On 22-Feb-2021, SARS-CoV-2 test: negative (Negative) negative. On 31-Mar-2021, SARS-CoV-2 test: negative (Negative) negative. No treatment information was reported.

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Test Date: 20210206; Test Name: Body temperature; Test Result: Inconclusive ; Result Unstructured Data: 99.3 degrees; Test Date: 20201229; Test Name: SARS-CoV-2 test; Test Result: Negative ; Result Unstructured Data: negative; Test Date: 20210118; Test Name: SARS-CoV-2 test; Test Result: Negative ; Result Unstructured Data: negative test for his CoV-2 antibodies Nucleocapsid Protein IgG Antibody Test,; Test Date: 20210222; Test Name: SARS-CoV-2 test; Test Result: Negative ; Result Unstructured Data: negative; Test Date: 20210331; Test Name: SARS-CoV-2 test; Test Result: Negative ; Result Unstructured Data: negative; Test Date: 20201119; Test Name: SARS-CoV-2 test; Test Result: Negative ; Result Unstructured Data: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: No medical history was provided by the reporter.
Andere Medikamente: ELIQUIS; SOTALOL; TYLENOL; ALBUTEROL [SALBUTAMOL]; JARDIANCE; PROSCAR; FLONASE [FLUTICASONE PROPIONATE]; ADVAIR; LASIX [FUROSEMIDE SODIUM]; GABAPENTIN; MAGNESIUM OXIDE; METFORMIN; SINGULAIR; FLOMAX [MORNIFLUMATE]; VITAMIN B6; VITAMIN B12 [V
Allergien: -
Vorherige Impfungen: -

VAERS 1611265

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: CA
Alter: 51,0
Geschlecht: F
Eingang: 22.08.2021
Impfdatum: 10.01.2021
Beginn: 26.03.2021
Tage bis Beginn: 75,0
Dosis: 1
Route/Site: OT / LA

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

Acoustic stimulation tests Deafness Hypotension Magnetic resonance imaging head Tinnitus

Symptomtext

hearing loss; Left ear tinnitus; Hypotensive episode; This spontaneous case was reported by a consumer and describes the occurrence of HYPOTENSION (Hypotensive episode), DEAFNESS (hearing loss) and TINNITUS (Left ear tinnitus) in a 51-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 016M20A and 011J20A) for COVID-19 vaccination. The patient's past medical history included Anaphylaxis, Hypersensitivity reaction and Urticaria. Concurrent medical conditions included Allergy to vaccine (Rabies vax(uticaria, anaphylaxis, received EPI)) since 1995 and Allergy to vaccine (Flu shot(lip swelling, cough, dysgeusia)) since 2011. Concomitant products included ETHINYLESTRADIOL, NORETHISTERONE ACETATE (NORETHINDRONE ACETATE AND ETHINYL ESTRADIOL) for Birth control. On 10-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 07-Feb-2021 at 1:00 PM, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 26-Mar-2021, the patient experienced HYPOTENSION (Hypotensive episode). On an unknown date, the patient experienced DEAFNESS (hearing loss) and TINNITUS (Left ear tinnitus). At the time of the report, HYPOTENSION (Hypotensive episode), DEAFNESS (hearing loss) and TINNITUS (Left ear tinnitus) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 03-Mar-2021, Acoustic stimulation tests: abnormal (abnormal) acute left sided sensorineural hearing loss. On 19-Apr-2021, Acoustic stimulation tests: abnormal (abnormal) acute left sided sensorineural hearing loss. On 03-May-2021, Magnetic resonance imaging head: negative (Negative) negative. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Treatment information include dexamethasone injection to left ear and started me on oral predisone and discontinued the diurectic. Most recent FOLLOW-UP information incorporated above includes: On 10-Jun-2021: Non-Significant follow up appended to AER

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Praegender Schweregrund: Hypotension
Hospital-Tage: -
Labordaten: Test Date: 20210303; Test Name: hearing test; Result Unstructured Data: acute left sided sensorineural hearing loss; Test Date: 20210419; Test Name: hearing test; Result Unstructured Data: acute left sided sensorineural hearing loss; Test Date: 20210503; Test Name: BRAIN MRI with w/wo contrast; Test Result: Negative ; Result Unstructured Data: negative
Aktuelle Erkrankungen: Allergy to vaccine (Rabies vax(uticaria, anaphylaxis, received EPI)); Allergy to vaccine (Flu shot(lip swelling, cough, dysgeusia))
Vorgeschichte: Medical History/Concurrent Conditions: Anaphylaxis; Hypersensitivity reaction; Urticaria
Andere Medikamente: NORETHINDRONE ACETATE AND ETHINYL ESTRADIOL
Allergien: -
Vorherige Impfungen: -

VAERS 1610214

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: NC
Alter: 51,0
Geschlecht: F
Eingang: 22.08.2021
Impfdatum: 31.03.2021
Beginn: 31.03.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: OT / LA

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

Allergy to vaccine Arthralgia Back pain Chills Dizziness Fatigue Joint stiffness Mobility decreased Movement disorder Muscle spasms Myalgia Nervousness Pain Pyrexia Restlessness

Symptomtext

This spontaneous case was reported by a consumer and describes the occurrence of MUSCLE SPASMS (muscle spasms waste down), MOVEMENT DISORDER (can hardly walk), NERVOUSNESS (shaky at times), MUSCLE SPASMS (back spasms) and BACK PAIN (Lower back pain) in a 51-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 011J20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. Concurrent medical conditions included Hypertension since 30-Jan-2015, Type 1 diabetes mellitus since 30-May-1999 and Drug allergy (opioid allergy). Concomitant products included INSULIN GLARGINE (LANTUS), INSULIN LISPRO (HUMALOG) and DULOXETINE HYDROCHLORIDE (CYMBALTA) for Diabetes, LISINOPRIL for Hypertension, TOPIRAMATE (TOPAMAX) for Migraine. On 31-Mar-2021 at 4:30 PM, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 31-Mar-2021, the patient experienced MUSCLE SPASMS (muscle spasms waste down), MOVEMENT DISORDER (can hardly walk), NERVOUSNESS (shaky at times), MUSCLE SPASMS (back spasms), BACK PAIN (Lower back pain), MYALGIA (Body aches), CHILLS (Chills) and ARTHRALGIA (joint pain). On 08-Apr-2021, the patient experienced ALLERGY TO VACCINE (Allergic reaction to vaccine). On 09-Apr-2021, the patient experienced MUSCLE SPASMS (spasms throughout body uncontrollably). On an unknown date, the patient experienced PAIN (Extreme pain joints, legs, hips). The patient was treated with Physical therapy for Movement disorder; Physical therapy for Back pain; Physical therapy for Pain; Physical therapy for Pain and Physical therapy for Arthralgia. On 01-Apr-2021, CHILLS (Chills) had resolved. At the time of the report, MUSCLE SPASMS (muscle spasms waste down), MOVEMENT DISORDER (can hardly walk), NERVOUSNESS (shaky at times), MUSCLE SPASMS (back spasms), ALLERGY TO VACCINE (Allergic reaction to vaccine), MUSCLE SPASMS (spasms throughout body uncontrollably) and MYALGIA (Body aches) outcome was unknown and BACK PAIN (Lower back pain), PAIN (Extreme pain joints, legs, hips) and ARTHRALGIA (joint pain) had not resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. This case was linked to MOD-2021-166743. Most recent FOLLOW-UP information incorporated above includes: On 25-May-2021: Significant Fu added. On 26-May-2021: Case merged with earlier duplicate case. Case marked for deletion.

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Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Drug allergy (opioid allergy); Hypertension; Type 1 diabetes mellitus
Vorgeschichte: Comments: No Medical History information was reported.
Andere Medikamente: LANTUS; HUMALOG; CYMBALTA; TOPAMAX; LISINOPRIL
Allergien: -
Vorherige Impfungen: -

VAERS 1609780

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: VA
Alter: 30,0
Geschlecht: M
Eingang: 22.08.2021
Impfdatum: 27.01.2021
Beginn: 09.02.2021
Tage bis Beginn: 13,0
Dosis: 1
Route/Site: OT / LA

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

Arthralgia Chest pain Chills Condition aggravated Dyspnoea Electrocardiogram Eyelid ptosis Eyelid sensory disorder Fatigue Hyperhidrosis Hypoaesthesia Influenza like illness Influenza virus test Magnetic resonance imaging Muscle spasms Muscle twitching Myalgia Pain

Symptomtext

Ringing in ears; Numbness under eyelid; Twitching; Significant change in quality of life; Eyelid on right feels drooping; Chest hurting; Hard time breathing; Tingling all over body; visit for spreading numbness; Worsening of symptoms; Extreme fatigue; Fatigue; Join pain in knee, wrist and feet; Body aches; Flu-like symptoms; Sweating; Heavy breathing; Cramping in lower left leg; Chills; Muscle pain in lower legs; This spontaneous case was reported by a consumer and describes the occurrence of INFLUENZA LIKE ILLNESS (Flu-like symptoms), HYPERHIDROSIS (Sweating), DYSPNOEA (Heavy breathing), MUSCLE SPASMS (Cramping in lower left leg) and PAIN (Body aches) in a 30-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 003A21A and 011J20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 27-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 09-Feb-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 09-Feb-2021, the patient experienced INFLUENZA LIKE ILLNESS (Flu-like symptoms), HYPERHIDROSIS (Sweating), DYSPNOEA (Heavy breathing), MUSCLE SPASMS (Cramping in lower left leg), CHILLS (Chills) and MYALGIA (Muscle pain in lower legs). On 20-Feb-2021, the patient experienced PAIN (Body aches), ARTHRALGIA (Join pain in knee, wrist and feet) and FATIGUE (Fatigue). On 27-Feb-2021, the patient experienced CONDITION AGGRAVATED (Worsening of symptoms) and FATIGUE (Extreme fatigue). On 05-Apr-2021, the patient experienced HYPOAESTHESIA (visit for spreading numbness). On 09-Apr-2021, the patient experienced PARAESTHESIA (Tingling all over body). On 12-Apr-2021, the patient experienced CHEST PAIN (Chest hurting). 12-Apr-2021, the patient experienced DYSPNOEA (Hard time breathing). On an unknown date, the patient experienced TINNITUS (Ringing in ears), EYELID SENSORY DISORDER (Numbness under eyelid), MUSCLE TWITCHING (Twitching), QUALITY OF LIFE DECREASED (Significant change in quality of life) and EYELID PTOSIS (Eyelid on right feels drooping). The patient was treated with MELOXICAM on 05-Apr-2021 for Joint pain, at an unspecified dose and frequency; IBUPROFEN (ADVIL [IBUPROFEN]) on 09-Mar-2021 for Adverse event, at an unspecified dose and frequency and IBUPROFEN (MOTRIN [IBUPROFEN]) on 01-Apr-2021 for Adverse event, at an unspecified dose and frequency. On 10-Feb-2021, INFLUENZA LIKE ILLNESS (Flu-like symptoms), HYPERHIDROSIS (Sweating), DYSPNOEA (Heavy breathing) and CHILLS (Chills) had resolved. At the time of the report, MUSCLE SPASMS (Cramping in lower left leg), PAIN (Body aches), CONDITION AGGRAVATED (Worsening of symptoms), HYPOAESTHESIA (visit for spreading numbness), PARAESTHESIA (Tingling all over body), CHEST PAIN (Chest hurting), DYSPNOEA (Hard time breathing), QUALITY OF LIFE DECREASED (Significant change in quality of life), ARTHRALGIA (Join pain in knee, wrist and feet), FATIGUE (Extreme fatigue) and MYALGIA (Muscle pain in lower legs) outcome was unknown and TINNITUS (Ringing in ears), EYELID SENSORY DISORDER (Numbness under eyelid), MUSCLE TWITCHING (Twitching), EYELID PTOSIS (Eyelid on right feels drooping) and FATIGUE (Fatigue) had not resolved. Not Provided DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 28-Feb-2021, Influenza virus test: negative (Negative) negative. On 28-Feb-2021, SARS-CoV-2 test: negative (Negative) negative. On 12-Apr-2021, Electrocardiogram: normal (normal) normal. On an unknown date, Magnetic resonance imaging: normal (normal) Everything was clear.. No concomitant medications were reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Test Date: 20210412; Test Name: EKG; Result Unstructured Data: normal; Test Date: 20210228; Test Name: Flu Test; Test Result: Negative; Result Unstructured Data: negative; Test Name: MRI; Result Unstructured Data: Everything was clear.; Test Date: 20210228; Test Name: COVID-19; Test Result: Negative; Result Unstructured Data: negative.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1607281

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: -
Alter: 47,0
Geschlecht: M
Eingang: 22.08.2021
Impfdatum: 24.12.2020
Beginn: 30.12.2020
Tage bis Beginn: 6,0
Dosis: 2
Route/Site: OT / LA

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

Alanine aminotransferase normal Albumin globulin ratio Anion gap Aspartate aminotransferase decreased Basophil count Blood albumin Blood alkaline phosphatase Blood bilirubin Blood calcium Blood chloride Blood creatinine Blood potassium Blood sodium Blood urea Blood urea nitrogen/creatinine ratio C-reactive protein Carbon dioxide Eosinophil count

Symptomtext

Left arm axillary swelling; Painful deep lymph node; This spontaneous case was reported by a health care professional and describes the occurrence of PERIPHERAL SWELLING (Left arm axillary swelling) and LYMPHADENOPATHY (Painful deep lymph node) in a 47-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 011J20A and 004M20A) for COVID-19 vaccination. The patient's past medical history included Swelling (Axillary swelling in the arm where he receive the injection) on 20-Jan-2021, Chills and Fever. Concurrent medical conditions included Drug allergy (allergic to tramadol) and Hypertension since 2014. Concomitant products included CHLORDIAZEPOXIDE HYDROCHLORIDE, CLIDINIUM BROMIDE (LIBRAX [CHLORDIAZEPOXIDE HYDROCHLORIDE;CLIDINIUM BROMIDE]) for Anxiety. On 24-Dec-2020, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 23-Jan-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 30-Dec-2020, the patient experienced PERIPHERAL SWELLING (Left arm axillary swelling) and LYMPHADENOPATHY (Painful deep lymph node). The patient was treated with COLECALCIFEROL (VITAMIN D [COLECALCIFEROL]) (oral) in May 2020 for Supplementation therapy, at a dose of 400 mg once a day and VITAMIN C [ASCORBIC ACID] (oral) in May 2020 for Supplementation therapy, at a dose of 500 mg once a day. On 20-Jan-2021, PERIPHERAL SWELLING (Left arm axillary swelling) had resolved with sequelae. At the time of the report, LYMPHADENOPATHY (Painful deep lymph node) outcome was unknown. Not Provided DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, Alanine aminotransferase normal (10.00-44.00): 17.40 17.40. On an unknown date, Albumin globulin ratio (0.70-2.30): 2.18 2.18. On an unknown date, Anion gap (5.00-25.00): 17.66 17.66. On an unknown date, Aspartate aminotransferase decreased (10.00-34.00): 16.30 16.30. On an unknown date, Basophil count (0.00-0.04 %): 0.03 % 0.03 and 0.3 % 0.3. On an unknown date, Blood albumin (3.50-5.00 g/dL): 5.10 g/dL 5.10. On an unknown date, Blood alkaline phosphatase (32.00-122.00 U/L): 60.00 U/L 60.00. On an unknown date, Blood bilirubin (0.20-1.00 mg/dl): 1.17 mg/dl 1.17. On an unknown date, Blood calcium (8.50-10.50 mg/dl): 10.16 mg/dl 10.16. On an unknown date, Blood chloride (98.00-110.00 10 thousand per litre): 100.70 10 thousand per litre 100.70. On an unknown date, Blood creatinine (0.50-1.20 mg/dl): 0.99 mg/dl 0.99. On an unknown date, Blood potassium (3.50-5.30 10 thousand per litre): 4.76 10 thousand per litre 4.76. On an unknown date, Blood sodium (136.00-147.00 10 thousand per litre): 138.00 10 thousand per litre 138.00. On an unknown date, Blood urea (8.00-25.00 mg/dl): 12.20 mg/dl 12.20. On an unknown date, Blood urea nitrogen/creatinine ratio (7.00-40.00): 12.32 12.32. On an unknown date, C-reactive protein: positive positive and positive. On an unknown date, Carbon dioxide (22.00-32.00 10 thousand per litre): 24.40 10 thousand per litre. On an unknown date, Eosinophil count (0.03-0.62 %): 0.03 % 0.03 and 0.3 % 0.3. On an unknown date, Globulin (2.10-4.60): 2.34 2.34. On an unknown date, Glomerular filtration rate: >60 >60 and >60. On an unknown date, Glucose tolerance impaired (100-125 mg/dl): >=126mg/dl mg/dl >=126mg/dl. On an unknown date, Haematocrit (39.4-49.3 %): 46.4 % 46.4. On an unknown date, Haemoglobin (13.4-16.9 g/dL): 16.3 g/dL 16.3. On an unknown date, Influenza: negative negative and negative negative. On an unknown date, Lymphocyte count (0.68-3.16 %): 1.06 % 1.06 and 10.3 % 10.3. On an unknown date, Mean cell haemoglobin (27.55-32.83 pg/ml): 29.80 pg/ml 29.80. On an unknown date, Mean cell haemoglobin concentration (32.72-35.76 g/dL): 35.13 g/dL 35.13. On an unknown date, Mean cell volume (81.26-95.11 fL): 84.83 fL 84.83. On an unknown date, Monocyte count (0.35-1.19 %): 0.83 % 0.83 and 8.1 % 8.1. On an unknown date, Neutrophil count (1.51-6.67 %): 8.31 % 8.31 and 81.0 % 81.0. On an unknown date, Platelet count (145-321): 171 171. On an unknown date, Pneumonia mycoplasmal: non-reactive non-reactive and non-reactive non-reactive. On an unknown date, Post laminectomy syndrome (70.00-99.00 mg/dl): 114.80 mg/dl 114.80. On an unknown date, Protein total (6.30-8.30 g/dL): 7.44 g/dL 7.44. On an unknown date, Red blood cell count (4.39-5.69): 5.47 5.47. On an unknown date, Red cell distribution width increased (11.6-14.7 %): 12.2 % 12.2. On an unknown date, White blood cell count (4.36-10.46): 10.26 10.26. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Most recent FOLLOW-UP information incorporated above includes: On 13-Apr-2021: No specific follow-up information recorded.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pneumonia mycoplasmal
Hospital-Tage: -
Labordaten: Test Name: alp; Test Result: Inconclusive ; Result Unstructured Data: 17.40; Test Name: a/g; Test Result: Inconclusive ; Result Unstructured Data: 2.18; Test Name: anion; Test Result: Inconclusive ; Result Unstructured Data: 17.66; Test Name: ast; Test Result: Inconclusive ; Result Unstructured Data: 16.30; Test Name: baso; Test Result: Inconclusive ; Result Unstructured Data: 0.03; Test Name: baso; Test Result: Inconclusive ; Result Unstructured Data: 0.3; Test Name: albumin; Test Result: Inconclusive ; Result Unstructured Data: 5.10; Test Name: alkaline; Test Result: Inconclusive ; Result Unstructured Data: 60.00; Test Name: bi; Test Result: Inconclusive ; Result Unstructured Data: 1.17; Test Name: calcium; Test Result: Inconclusive ; Result Unstructured Data: 10.16; Test Name: chloride; Test Result: Inconclusive ; Result Unstructured Data: 100.70; Test Name: creatinine; Test Result: Inconclusive ; Result Unstructured Data: 0.99; Test Name: potassium; Test Result: Inconclusive ; Result Unstructured Data: 4.76; Test Name: sodium; Test Result: Inconclusive ; Result Unstructured Data: 138.00; Test Name: blood urea nitrogen; Test Result: Inconclusive ; Result Unstructured Data: 12.20; Test Name: bun/creatinine; Test Result: Inconclusive ; Result Unstructured Data: 12.32; Test Name: co2; Test Result: Inconclusive ; Result Unstructured Data: 24.40; Test Name: c-reactive; Test Result: Positive ; Result Unstructured Data: positive; Test Name: c-reactive; Test Result: Positive ; Result Unstructured Data: positive; Test Name: eos; Test Result: Inconclusive ; Result Unstructured Data: 0.03; Test Name: eos; Test Result: Inconclusive ; Result Unstructured Data: 0.3; Test Name: globulin; Test Result: Inconclusive ; Result Unstructured Data: 2.34; Test Name: g; Test Result: Inconclusive ; Result Unstructured Data: >60; Test Name: gfr; Test Result: Inconclusive ; Result Unstructured Data: >60; Test Name: pre dia; Test Result: Inconclusive ; Result Unstructured Data: >=126mg/dl; Test Name: hemac; Test Result: Inconclusive ; Result Unstructured Data: 46.4; Test Name: hemo; Test Result: Inconclusive ; Result Unstructured Data: 16.3; Test Name: influenza; Test Result: Inconclusive ; Result Unstructured Data: negative; Test Name: influenza; Test Result: Inconclusive ; Result Unstructured Data: negative; Test Name: lymp; Test Result: Inconclusive ; Result Unstructured Data: 1.06; Test Name: lympho; Test Result: Inconclusive ; Result Unstructured Data: 10.3; Test Name: mch; Test Result: Inconclusive ; Result Unstructured Data: 29.80; Test Name: mchc; Test Result: Inconclusive ; Result Unstructured Data: 35.13; Test Name: mcv; Test Result: Inconclusive ; Result Unstructured Data: 84.83; Test Name: mono; Test Result: Inconclusive ; Result Unstructured Data: 0.83; Test Name: monocytes; Test Result: Inconclusive ; Result Unstructured Data: 8.1; Test Name: neutro; Test Result: Inconclusive ; Result Unstructured Data: 8.31; Test Name: neutrophils; Test Result: Inconclusive ; Result Unstructured Data: 81.0; Test Name: platelet; Test Result: Inconclusive ; Result Unstructured Data: 171; Test Name: mycoplasm; Test Result: Inconclusive ; Result Unstructured Data: non-reactive; Test Name: mycoplasm; Test Result: Inconclusive ; Result Unstructured Data: non-reactive; Test Name: fbs; Test Result: Inconclusive ; Result Unstructured Data: 114.80; Test Name: protein; Test Result: Inconclusive ; Result Unstructured Data: 7.44; Test Name: rbc; Test Result: Inconclusive ; Result Unstructured Data: 5.47; Test Name: rdw; Test Result: Inconclusive ; Result Unstructured Data: 12.2; Test Name: wbc; Test Result: Inconclusive ; Result Unstructured Data: 10.26
Aktuelle Erkrankungen: Drug allergy (allergic to tramadol); Hypertension
Vorgeschichte: Medical History/Concurrent Conditions: Chills; Fever; Swelling (Axillary swelling in the arm where he receive the injection)
Andere Medikamente: LIBRAX [CHLORDIAZEPOXIDE HYDROCHLORIDE;CLIDINIUM BROMIDE]
Allergien: -
Vorherige Impfungen: -

VAERS 1602902

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: CA
Alter: 53,0
Geschlecht: F
Eingang: 21.08.2021
Impfdatum: 01.02.2021
Beginn: 01.05.2021
Tage bis Beginn: 89,0
Dosis: 1
Route/Site: SYR / LA

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

Cough Headache Influenza A virus test Influenza B virus test Malaise Pain Pneumonia Pyrexia SARS-CoV-2 test negative Sneezing

Symptomtext

I got sick at the end of May. I had a fever for 5 days, headache, body aches. Covid like symptoms. 2 covid tests negative, and flu tests negative. I got sick again 4 days ago. Again high fever for 2 days this time coughing, sneezing, body aches, headache and now it has been determined I have pneumonia. 2 covid tests negative. I have never been this sick this often in my life to this extent.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pneumonia
Hospital-Tage: -
Labordaten: Covid tests negative Flu a and b negative
Aktuelle Erkrankungen: Rheumatoid Arthritis, and osteoarthritis
Vorgeschichte: Rheumatoid and Osteoarthritis
Andere Medikamente: Multivitamins, Percocet, aspirin. I was taking Humira but stopped a month before 1st vaccine for better effect of the Coronavirus vaccine
Allergien: Raw eggs, flu vaccine, sesame seed
Vorherige Impfungen: -

VAERS 1597951

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: NY
Alter: 35,0
Geschlecht: F
Eingang: 21.08.2021
Impfdatum: 13.01.2021
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: OT / LA

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

Antinuclear antibody Aphasia Atrial tachycardia Fatigue Feeling abnormal Heart rate Heart rate increased Insomnia Nervous system disorder Paraesthesia oral Tachycardia Vaccination site pain

Symptomtext

Anomia; Elevated heart rate/felt like it got to over 100; Tachycardia; Paroxysmal atrial tachycardia (PAT); Uncomfortable feeling on the nervous system, like it's overactivated; Adrenaline feeling/hormonal or neuorchemical feeling; Brain fog; Tingling in the mouth; Feel so tired, and is having a hard time sleeping; Feel so tired, and is having a hard time sleeping; Arm sore; This spontaneous case was reported by a health care professional (subsequently medically confirmed) and describes the occurrence of APHASIA (Anomia), HEART RATE INCREASED (Elevated heart rate/felt like it got to over 100), TACHYCARDIA (Tachycardia), ATRIAL TACHYCARDIA (Paroxysmal atrial tachycardia (PAT)) and NERVOUS SYSTEM DISORDER (Uncomfortable feeling on the nervous system, like it's overactivated) in a 35-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 011J20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 13-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On an unknown date, the patient experienced APHASIA (Anomia), HEART RATE INCREASED (Elevated heart rate/felt like it got to over 100), TACHYCARDIA (Tachycardia), ATRIAL TACHYCARDIA (Paroxysmal atrial tachycardia (PAT)), NERVOUS SYSTEM DISORDER (Uncomfortable feeling on the nervous system, like it's overactivated), FEELING ABNORMAL (Adrenaline feeling/hormonal or neuorchemical feeling), FEELING ABNORMAL (Brain fog), PARAESTHESIA ORAL (Tingling in the mouth), INSOMNIA (Feel so tired, and is having a hard time sleeping), FATIGUE (Feel so tired, and is having a hard time sleeping) and VACCINATION SITE PAIN (Arm sore). At the time of the report, APHASIA (Anomia), HEART RATE INCREASED (Elevated heart rate/felt like it got to over 100), TACHYCARDIA (Tachycardia), ATRIAL TACHYCARDIA (Paroxysmal atrial tachycardia (PAT)), NERVOUS SYSTEM DISORDER (Uncomfortable feeling on the nervous system, like it's overactivated), FEELING ABNORMAL (Adrenaline feeling/hormonal or neuorchemical feeling), FEELING ABNORMAL (Brain fog), PARAESTHESIA ORAL (Tingling in the mouth), INSOMNIA (Feel so tired, and is having a hard time sleeping), FATIGUE (Feel so tired, and is having a hard time sleeping) and VACCINATION SITE PAIN (Arm sore) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): In January 2021, Heart rate: 125 (High) heart rate was 125 bpm. On 27-Feb-2021, Antinuclear antibody: positive (High) Positive ANA so high, highest possible.. mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was withdrawn on an unknown date. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Treatment includes Cold showers, Compression stocking, Fluid intake.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Atrial tachycardia
Hospital-Tage: -
Labordaten: Test Date: 20210227; Test Name: ANA; Result Unstructured Data: Positive ANA so high, highest possible.; Test Date: 202101; Test Name: Heart rate; Result Unstructured Data: heart rate was 125 bpm
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1596555

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: -
Alter: 35,0
Geschlecht: F
Eingang: 21.08.2021
Impfdatum: 30.03.2021
Beginn: 03.03.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: OT / -

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

Paraesthesia oral Swollen tongue

Symptomtext

mild tongue swelling; tingling lips; This spontaneous case was reported by a nurse and describes the occurrence of SWOLLEN TONGUE (mild tongue swelling) and PARAESTHESIA ORAL (tingling lips) in a 35-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 011J20A) for COVID-19 vaccination. No Medical History information was reported. On 30-Mar-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 03-Mar-2021, the patient experienced SWOLLEN TONGUE (mild tongue swelling) and PARAESTHESIA ORAL (tingling lips). The patient was treated with DIPHENHYDRAMINE HYDROCHLORIDE (BENADRYL [DIPHENHYDRAMINE HYDROCHLORIDE]) (oral) for Adverse event, at a dose of 25 milligram once. At the time of the report, SWOLLEN TONGUE (mild tongue swelling) and PARAESTHESIA ORAL (tingling lips) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medications provided.

Weitere VAERSDATA-Felder

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

VAERS 1595032

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: -
Alter: 23,0
Geschlecht: M
Eingang: 21.08.2021
Impfdatum: 04.03.2021
Beginn: 04.03.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / -

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

Abdominal pain Arthralgia Body temperature Body temperature increased Chills Headache Injection site pain Lacrimation increased Nausea Salivary hypersecretion Tremor

Symptomtext

joint pain; increased saliva production; chills; temperature was 98.4; eyes were tearing; shaking; pain at the injection site; headache; nausea; abdominal pain; This spontaneous case was reported by a nurse and describes the occurrence of ABDOMINAL PAIN (abdominal pain), SALIVARY HYPERSECRETION (increased saliva production), LACRIMATION INCREASED (eyes were tearing), TREMOR (shaking) and ARTHRALGIA (joint pain) in a 23-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 011J20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 04-Mar-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 04-Mar-2021, the patient experienced ABDOMINAL PAIN (abdominal pain), LACRIMATION INCREASED (eyes were tearing), TREMOR (shaking), INJECTION SITE PAIN (pain at the injection site), HEADACHE (headache), NAUSEA (nausea) and BODY TEMPERATURE INCREASED (temperature was 98.4). On an unknown date, the patient experienced SALIVARY HYPERSECRETION (increased saliva production), ARTHRALGIA (joint pain) and CHILLS (chills). On 04-Mar-2021, ABDOMINAL PAIN (abdominal pain), SALIVARY HYPERSECRETION (increased saliva production), LACRIMATION INCREASED (eyes were tearing), TREMOR (shaking), ARTHRALGIA (joint pain), INJECTION SITE PAIN (pain at the injection site), HEADACHE (headache), NAUSEA (nausea), CHILLS (chills) and BODY TEMPERATURE INCREASED (temperature was 98.4) had resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 04-Mar-2021, Body temperature: 98.4 degree Celsius. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Concomitant medications were not reported. Treatment information in response to events was not provided.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: Test Date: 20210304; Test Name: Body temperature; Test Result: Inconclusive ; Result Unstructured Data: 98.4
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1594869

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: LA
Alter: 70,0
Geschlecht: F
Eingang: 21.08.2021
Impfdatum: 19.01.2021
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: OT / RA

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

Erythema Paraesthesia Swelling

Symptomtext

Tingling at the right side of her face; Swelling at the right side of her face; Redness in the right side of her face; A spontaneous report was received from a Healthcare Professional concerning a 70-years-old female patient who received Moderna's COVID-19 vaccine (mRNA-1273) and experienced events redness, swelling and tingling . The patient's medical history was not provided. The patient was allergic to a bird. Concomitant medications reported were Aspirin. On 19 Jan 2021, prior to the onset of the events the patient received their first of two planned doses of mRNA-1273 (lot/batch: 011J20A) via unknown route in the right arm for prophylaxis of COVID-19 infection. On unknown date the patient reported experienced redness, swelling and tingling in the right side of the face for 5 days No treatment information was provided. Action taken with mRNA-1273 in response to the events was not reported. On an unknown date the outcome redness, swelling, tingling was not reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: No adverse event (No medical history reported)
Andere Medikamente: ASPIRIN [ACETYLSALICYLIC ACID]
Allergien: -
Vorherige Impfungen: -

VAERS 1594757

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: -
Alter: -
Geschlecht: F
Eingang: 21.08.2021
Impfdatum: 22.01.2021
Beginn: 22.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / LA

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

Dyspnoea Fatigue Headache Incontinence Pain Pain in extremity Pyrexia

Symptomtext

Incontinence; Aches all over the body; Shortness of breath; Fever > 102?F; Headache; Pain in the arm of the injection; Tiredness; A Spondaneous report was received from a Healthcare professional concerning a 70 Years-old female patient who received Moderna's COVID-19 vaccine (mRNA-1273) and experienced Pain in the arm of the injection, Tiredness, Incontinence, Fever > 102?F, Aches all over the body, Headache, Shortness of breath, sore arm The patient's medical history was not given. No information about the concomitant medication was given. On 22-01-2021, prior to the onset of the events, the patient received their second of two planned doses of mRNA-1273 batch no: 011J20A intramuscularly in the left arm for prophylaxis of COVID-19 infection. On 22-01-2021, The patient experienced Pain in the arm of the injection, Tiredness. On 23-01-2021, the patient experienced incontinence, Fever > 102?F, Aches all over the body, headache, Shortness of Breath, Sore arm. The laboratory information is not given. The patient was given Tylenol as treatment medication. Action taken with mRNA-1273 in response to the events was not reported. The outcome of the events pain in the arm of the injection, Tiredness, Incontinence was resolved on 24-01-2021. The outcome of the events , Fever > 102?F, Aches all over the body, headache, Shortness of Breath, Sore arm are unknown.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: No adverse event
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1594553

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: -
Alter: -
Geschlecht: F
Eingang: 21.08.2021
Impfdatum: 14.01.2021
Beginn: 14.01.2019
Tage bis Beginn: -
Dosis: 1
Route/Site: OT / RA

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

Arthralgia Chills Fatigue Migraine Myalgia Nausea Pyrexia Urticaria Vaccination site movement impairment Vaccination site pain Vaccination site swelling Vaccination site urticaria

Symptomtext

itchy hives at the injection site; severe pain at the injection site; episodes of chills; felt feverish; her highest measured; nausea; muscle and joint pain; muscle and joint pain; fatigue; injection site swelling; limits the mobility of that [right] arm; migraine headache; 3" x 3" patch of itchy, painful hives on her right thigh; This spontaneous case was reported by an other health care professional and describes the occurrence of VACCINATION SITE MOVEMENT IMPAIRMENT (limits the mobility of that [right] arm), MIGRAINE (migraine headache), URTICARIA (3" x 3" patch of itchy, painful hives on her right thigh), VACCINATION SITE URTICARIA (itchy hives at the injection site) and VACCINATION SITE PAIN (severe pain at the injection site) in a 48-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 011J20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 14-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 14-Jan-2019, the patient experienced MIGRAINE (migraine headache) and URTICARIA (3" x 3" patch of itchy, painful hives on her right thigh). On 14-Jan-2021, the patient experienced VACCINATION SITE MOVEMENT IMPAIRMENT (limits the mobility of that [right] arm), VACCINATION SITE URTICARIA (itchy hives at the injection site), VACCINATION SITE PAIN (severe pain at the injection site), CHILLS (episodes of chills), PYREXIA (felt feverish; her highest measured), NAUSEA (nausea), MYALGIA (muscle and joint pain), ARTHRALGIA (muscle and joint pain), FATIGUE (fatigue) and VACCINATION SITE SWELLING (injection site swelling). At the time of the report, VACCINATION SITE MOVEMENT IMPAIRMENT (limits the mobility of that [right] arm), MIGRAINE (migraine headache), URTICARIA (3" x 3" patch of itchy, painful hives on her right thigh), VACCINATION SITE URTICARIA (itchy hives at the injection site), VACCINATION SITE PAIN (severe pain at the injection site), CHILLS (episodes of chills), PYREXIA (felt feverish; her highest measured), NAUSEA (nausea), MYALGIA (muscle and joint pain), ARTHRALGIA (muscle and joint pain), FATIGUE (fatigue) and VACCINATION SITE SWELLING (injection site swelling) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medications were reported. No treatment related information has been reported.; Sender's Comments: Based on the current available information and temporal association between the use of the product and the start date of the events, a causal relationship cannot be excluded.

Weitere VAERSDATA-Felder

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

VAERS 1591902

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: FL
Alter: 46,0
Geschlecht: F
Eingang: 20.08.2021
Impfdatum: 27.01.2021
Beginn: 04.08.2021
Tage bis Beginn: 189,0
Dosis: 1
Route/Site: IM / -

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

COVID-19 Diarrhoea Dyspnoea Myalgia Nausea Pyrexia SARS-CoV-2 test positive Vomiting

Symptomtext

8/8/21: Patient was sent to clinic by PCP to request orders for bamlanivimab infusion-Pt reports testing positive at a testing center on Wednesday and has been symptomatic for 7 days. Pt states she also brought husband to Clinic due to COVID like symptoms and husband was recommended to go to the ED due to hypoxia. Presents to ED with SOB. She states over the last 5 days she has had symptoms of generalized myalgias, fevers, nausea, vomiting and diarrhea. 8 8/8/21: Patient received rapid COVID test at clinic which resulted as negative. 8/8/21: Patient tested COVID positive upon admission 8/12/21: Pt discharged home

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 5,0
Labordaten: COVID-19 Pos as per pt on 8/4/2021 (outlying facility), Neg as per clinic 8/8/21 (rapid test) SARS CoV 2 PCR COVID-19 Positive: Confirmed with testing upon admission on 8/8/2021
Aktuelle Erkrankungen: Sage I papillary thyroid carcinoma s/p total thyroidectomy 12/2020
Vorgeschichte: HTN, CKD Stage 3, thyroid cancer s/p radiation/thyroidectomy, kidney stones, arthritis
Andere Medikamente: ascorbic acid, calcium gluconate, cholecalciferol, collagen, hctz, losartan, MVI, fish oil, oxycodone-acetaminophen prn for moderate pain, potassium citrate
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1586934

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011j20a

moderat

Staat: WI
Alter: 55,0
Geschlecht: F
Eingang: 19.08.2021
Impfdatum: 15.01.2021
Beginn: 15.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Arthralgia Blood test Cardiac flutter Diplopia Feeling abnormal Feeling hot Hot flush Magnetic resonance imaging neck Neck pain Palpitations Paraesthesia Spinal X-ray Tinnitus Tremor

Symptomtext

multi system involvement with substantial disruption in daily life, palpitations, shakiness, fluttering heart, tingling left and right arm, neck and shoulder pain (all muscles), fuzzy head, rigning ears, double vision, heat sensations in brain, face, arms, neck, shoulders, hot flashes, treatment has been PT, chiro, muscle relaxants, ibuprofen, tylenol, tylenolPM, trigger point injections, massage,

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: cervical x-ray, cervical MRI, lymes, thyroid, anti inflammatory, sugar, estrogen, blodd panel,
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: multi vitamin
Allergien: neosporin, some anesthesia components,
Vorherige Impfungen: -

VAERS 1582753

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011j20a

moderat

Staat: MA
Alter: 27,0
Geschlecht: F
Eingang: 18.08.2021
Impfdatum: 23.04.2021
Beginn: 24.04.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / LA

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

Cardiac monitoring abnormal Echocardiogram normal Heavy menstrual bleeding Palpitations Supraventricular extrasystoles Ventricular extrasystoles

Symptomtext

Beginning the same weekend of the second moderna vaccine (April 2021) I began to have infrequent heart palpitations and heavy menstrual cycle. Over about two months I reduced by caffiene and alcohol intake to see if the heart palpitations would subside. When they did not I contacted my PCP in June 2021. So far I have had an heart monitor which should PAC/PVC's and an echocardigram which came back normal. Heavy menstrual cycles also began the same weekend as the second vaccine. My period now lasts 6-8 days and is so heavy I can't use tampons anymore. My period used to be 4-5 days and relatively light since I am on hormonal birth control.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: Heart monitor June 26 - July 10th(ish). Heart Monitor showed PAC/PVC's but no other abnormalities. Echocardigam on July 27th was normal. My doctor also ordered a heart MRI with contrast which has not been scheduled yet.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Glycopyrrolate (2mg/day), Nexplanon
Allergien: Bactrim, Shellfish
Vorherige Impfungen: -

VAERS 1580144

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: OH
Alter: 52,0
Geschlecht: F
Eingang: 18.08.2021
Impfdatum: 09.01.2021
Beginn: 09.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / -

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

Heart rate increased Paraesthesia Paraesthesia oral Pruritus

Symptomtext

Tingling in the face and lips; Tingling face; itching face and arm(not at the injection site); a little fast heart beat; This spontaneous case was reported by a consumer and describes the occurrence of PARAESTHESIA ORAL (Tingling in the face and lips), PARAESTHESIA (Tingling face), PRURITUS (itching face and arm(not at the injection site)) and HEART RATE INCREASED (a little fast heart beat) in a 52-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 011J20A) for COVID-19 vaccination. Concomitant products included SECUKINUMAB (COSENTYX) for Psoriatic arthritis, METOPROLOL for Sinus tachycardia. On 09-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 09-Jan-2021, the patient experienced PARAESTHESIA ORAL (Tingling in the face and lips), PARAESTHESIA (Tingling face), PRURITUS (itching face and arm(not at the injection site)) and HEART RATE INCREASED (a little fast heart beat). At the time of the report, PARAESTHESIA ORAL (Tingling in the face and lips), PARAESTHESIA (Tingling face), PRURITUS (itching face and arm(not at the injection site)) and HEART RATE INCREASED (a little fast heart beat) had not resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Reporter did not allow further contact

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: No adverse event
Andere Medikamente: COSENTYX; METOPROLOL
Allergien: -
Vorherige Impfungen: -

VAERS 1580122

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: CT
Alter: -
Geschlecht: F
Eingang: 18.08.2021
Impfdatum: 22.12.2020
Beginn: 22.12.2020
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / LA

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

Dyspnoea Erythema Feeling hot Hypersensitivity Myalgia Oropharyngeal discomfort Oropharyngeal pain Pharyngeal paraesthesia Product dose omission issue Swollen tongue Throat irritation Tongue discomfort

Symptomtext

Tongue swelling; Throat tingle; Missed dose; Muscles hurt, muscles pain; Face became all red again; Hard time breathing, difficulty breathing; Back of throat still hurts; She had an allergic reaction; She was really hot, entire body and ears hot; Itchy throat; Funny feeling in her throat; Felt her tongue was bigger; This spontaneous case was reported by an other health care professional and describes the occurrence of HYPERSENSITIVITY (She had an allergic reaction), FEELING HOT (She was really hot, entire body and ears hot), THROAT IRRITATION (Itchy throat), OROPHARYNGEAL DISCOMFORT (Funny feeling in her throat) and TONGUE DISCOMFORT (Felt her tongue was bigger) in a 62-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 011J20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concomitant products included FAMOTIDINE and ONDANSETRON for an unknown indication. On 22-Dec-2020, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 22-Dec-2020, the patient experienced HYPERSENSITIVITY (She had an allergic reaction), FEELING HOT (She was really hot, entire body and ears hot), THROAT IRRITATION (Itchy throat), OROPHARYNGEAL DISCOMFORT (Funny feeling in her throat), TONGUE DISCOMFORT (Felt her tongue was bigger) and OROPHARYNGEAL PAIN (Back of throat still hurts). On 25-Dec-2020, the patient experienced ERYTHEMA (Face became all red again), DYSPNOEA (Hard time breathing, difficulty breathing) and MYALGIA (Muscles hurt, muscles pain). On an unknown date, the patient experienced SWOLLEN TONGUE (Tongue swelling), PHARYNGEAL PARAESTHESIA (Throat tingle) and PRODUCT DOSE OMISSION ISSUE (Missed dose). The patient was treated with DIPHENHYDRAMINE HYDROCHLORIDE (BENADRYL [DIPHENHYDRAMINE HYDROCHLORIDE]) for Adverse event, at an unspecified dose and frequency; PREDNISONE for Adverse event, at an unspecified dose and frequency and ALUMINIUM HYDROXIDE GEL, DRIED, MAGNESIUM CARBONATE (PEPCID [ALUMINIUM HYDROXIDE GEL, DRIED;MAGNESIUM CARBONATE]) for Adverse event, at an unspecified dose and frequency. On 22-Dec-2020, HYPERSENSITIVITY (She had an allergic reaction) and FEELING HOT (She was really hot, entire body and ears hot) had resolved. On 23-Dec-2020, THROAT IRRITATION (Itchy throat) and OROPHARYNGEAL DISCOMFORT (Funny feeling in her throat) had resolved. On 12-Jan-2021, TONGUE DISCOMFORT (Felt her tongue was bigger), ERYTHEMA (Face became all red again), DYSPNOEA (Hard time breathing, difficulty breathing) and MYALGIA (Muscles hurt, muscles pain) had resolved. At the time of the report, OROPHARYNGEAL PAIN (Back of throat still hurts) and PRODUCT DOSE OMISSION ISSUE (Missed dose) had resolved and SWOLLEN TONGUE (Tongue swelling) and PHARYNGEAL PARAESTHESIA (Throat tingle) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. It was reported that the patient was premeditated before taking the first dose. She also wanted to know if she could mix vaccine. Most recent FOLLOW-UP information incorporated above includes: On 07-Jun-2021: Follow up received contains No new information On 02-Aug-2021: NNI Case. On 02-Aug-2021: Significant follow up received. Concomitant medications and additional events of throat tingle, missed dose, tongue tingle were added.; Sender's Comments: Based on the current available information and temporal association between the use of the product and the start date of the event, a causal relationship cannot be excluded.

Weitere VAERSDATA-Felder

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

VAERS 1578942

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: KY
Alter: 56,0
Geschlecht: M
Eingang: 17.08.2021
Impfdatum: 13.01.2021
Beginn: 27.01.2021
Tage bis Beginn: 14,0
Dosis: 1
Route/Site: IM / LA

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

Bifascicular block Blood immunoglobulin M increased Blood thyroid stimulating hormone Cardiac stress test Chest X-ray Differential white blood cell count Electrocardiogram abnormal Electrocardiogram ambulatory Fatigue Full blood count Metabolic function test Palpitations Pulse waveform SARS-CoV-2 antibody test positive Sinus bradycardia Troponin T

Symptomtext

VACCINE GIVEN. 2 WEEKS LATER I WAS EXPERIENCING EXTREME FATIGUE. I AM A PHARMACIST AND PERFORMED AN ANTIBODY TEST AT WORK. IT WAS POSITVE FOR IgM antibodies to Covid19. NO IgG present. ANTIBODY TEST PERFORMED ON 01/12/2021 WAS NEGATIVE FOR IgM AND IgG AT THAT TIME. FATIGUE CONTINUED. HEART PALPITATIONS BEGAN SHORTLY THEREAFTER. I FINALLY WENT TO GET THESE PALPITATIONS EXAMINED AT MY DOCTOR'S OFFICE ON 06/16/2021. 12 LEAD ECG SHOWED SINUS BRADYCARDIA AND BIFASCICULAR BLOCK.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: 2,0
Labordaten: ANTIBODY TESTS: 12/21/2020; 01/12/2021, 01/27/2021 AND 08/14/2021 POCT EKG 06/16/2021; TSH REFLEX 06/16/2021; CMP 06/16/2021; CBC WITH DIFFERENTIAL 06/16/2021; HOSPITAL ADMISSION 06-18-2021 WITH BMP, TROPONIN-T REPORT; XR CHEST AP PORTABLE; ECG AND WAVEFORM 06/19/2021; HM HOLTER MONITOR 06/28/2021; ST STRESS TEST EXERCISE 07/08/2021; EKG 12-LEAD 08/12/2021. NO STRUCTURAL ABNORMALITIES; NO STENOSIS; 3 DIFFERENT EKG-12 LEADS HAVE SHOWN BIFASCICULAR BLOCK
Aktuelle Erkrankungen: NONE; FIRST VACCINE GIVEN 1/13/2021; SECOND VACCINE GIVEN 02/12/2021;ANTIBODY TEST POSTIVE FOR IgM 01/21/2021 and 08/14/2021.FATIGUE STARTED AROUND 01/21/2021 AND THAT IS WHY AN ANTIBODY TEST WAS COMPLETED. URGENT CARE VISIT FOR HEART ISSUES FIRST ON 06/16/2021
Vorgeschichte: NOW, HEART BLOCK.
Andere Medikamente: LOSARTAN 100MG QD, SERTRALINE 100MG QD, MULTIVITAMIN DAILY
Allergien: BUPROPION HCL
Vorherige Impfungen: -

VAERS 1577609

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: NY
Alter: 59,0
Geschlecht: M
Eingang: 17.08.2021
Impfdatum: 04.01.2021
Beginn: 07.01.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: OT / LA

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

Body temperature Cough Dyspnoea Fatigue Headache Malaise Pyrexia Rhinorrhoea SARS-CoV-2 test

Symptomtext

Shortness of breath; Runny nose; Cough off and on; Fever; Headaches; Fatigue; felt sick; This spontaneous case was reported by a consumer and describes the occurrence of MALAISE (felt sick), DYSPNOEA (Shortness of breath), RHINORRHOEA (Runny nose), COUGH (Cough off and on) and PYREXIA (Fever) in a 59-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 011J20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 04-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .5 ml. On 07-Jan-2021, the patient experienced MALAISE (felt sick). On 09-Jan-2021, the patient experienced DYSPNOEA (Shortness of breath), RHINORRHOEA (Runny nose), COUGH (Cough off and on), PYREXIA (Fever), HEADACHE (Headaches) and FATIGUE (Fatigue). The patient was treated with PARACETAMOL (TYLENOL) for Adverse event, at a dose of UNK dosage form. On 16-Jan-2021, RHINORRHOEA (Runny nose), COUGH (Cough off and on), HEADACHE (Headaches) and FATIGUE (Fatigue) had resolved. At the time of the report, MALAISE (felt sick), DYSPNOEA (Shortness of breath) and PYREXIA (Fever) had resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 09-Jan-2021, SARS-CoV-2 test: positive (Positive) positive.. In January 2021, Body temperature: 100-101 (High) between 100 to 101.. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Concomitant medicationswere not provided.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Test Date: 20210109; Test Name: Covid-19; Test Result: Positive ; Result Unstructured Data: positive.; Test Date: 202101; Test Name: Body temperature; Result Unstructured Data: between 100 to 101.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1573429

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20a

moderat

Staat: -
Alter: 54,0
Geschlecht: F
Eingang: 16.08.2021
Impfdatum: 13.01.2021
Beginn: 01.01.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: OT / -

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

COVID-19 Chills Cough Diarrhoea Dyspnoea Headache Mouth swelling Pyrexia SARS-CoV-2 test Tenderness

Symptomtext

positive for covid; chills; Fever; headache; loose stool; swelling in mouth; tenderness in her mouth; slight cough; shortness of breath; This spontaneous case was reported by a consumer (subsequently medically confirmed) and describes the occurrence of DIARRHOEA (loose stool), MOUTH SWELLING (swelling in mouth), TENDERNESS (tenderness in her mouth), COUGH (slight cough) and DYSPNOEA (shortness of breath) in a 54-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 011J20a) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical history was reported. Concomitant products included VITAMINS NOS for an unknown indication. On 13-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. In January 2021, the patient experienced DIARRHOEA (loose stool), MOUTH SWELLING (swelling in mouth), TENDERNESS (tenderness in her mouth), COUGH (slight cough), DYSPNOEA (shortness of breath), CHILLS (chills), PYREXIA (Fever) and HEADACHE (headache). On 23-Jan-2021, the patient experienced COVID-19 (positive for covid). At the time of the report, DIARRHOEA (loose stool), MOUTH SWELLING (swelling in mouth), TENDERNESS (tenderness in her mouth), COUGH (slight cough), DYSPNOEA (shortness of breath), COVID-19 (positive for covid), CHILLS (chills), PYREXIA (Fever) and HEADACHE (headache) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 23-Jan-2021, SARS-CoV-2 test: positive Positive. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Additional concomitant medications included blood pressure pills. The patient went to the emergency room on 23-Jan-2021 because of the side effects. While in the ER she was tested for COVID because of her symptoms and tested positive. The patient was experiencing a fever at that time which has gone down, had slight cough, her breathing was better but she was having shortness of breath. She was not admitted. On 25-Jan-2021, the patient was treated with an antibody infusion. She was told by her doctor she cannot get the second shot for 90 days because of the antibody treatment.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Test Date: 20210123; Test Name: Covid test; Result Unstructured Data: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: No Medical history was reported.
Andere Medikamente: VITAMINS NOS
Allergien: -
Vorherige Impfungen: -

VAERS 1573133

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: NC
Alter: 41,0
Geschlecht: F
Eingang: 16.08.2021
Impfdatum: 14.01.2021
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: OT / RA

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

Ageusia Bone pain Fatigue Feeling cold Headache Nausea Pain Pyrexia Rash Tremor Vision blurred Vomiting

Symptomtext

Sense of taste lost; Blurry vision; Fever; Shaking; I couldn't get warm enough; Nausea; I threw up; Hurt all over; My bones hurt; I was tired; Headache; rash; This spontaneous case was reported by a pharmacist and describes the occurrence of AGEUSIA (Sense of taste lost), VISION BLURRED (Blurry vision), PYREXIA (Fever), TREMOR (Shaking) and FEELING COLD (I couldn't get warm enough) in a 41-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 028L20A and 011J20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concurrent medical conditions included Seizures and Migraine. Concomitant products included RIZATRIPTAN BENZOATE (MAXALT) for Migraine, ESLICARBAZEPINE ACETATE (APTIOM) for Seizure, PANTOPRAZOLE SODIUM SESQUIHYDRATE (PANTOPRAZOLE 40), TIZANIDINE and FLUOXETINE HYDROCHLORIDE (PROZAC) for an unknown indication. On 14-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 11-Feb-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 AGEUSIA (Sense of taste lost), VISION BLURRED (Blurry vision), PYREXIA (Fever), TREMOR (Shaking), FEELING COLD (I couldn't get warm enough), NAUSEA (Nausea), VOMITING (I threw up), PAIN (Hurt all over), BONE PAIN (My bones hurt), FATIGUE (I was tired), HEADACHE (Headache) and RASH (rash). At the time of the report, AGEUSIA (Sense of taste lost), VISION BLURRED (Blurry vision), PYREXIA (Fever), TREMOR (Shaking), FEELING COLD (I couldn't get warm enough), NAUSEA (Nausea), VOMITING (I threw up), PAIN (Hurt all over) and BONE PAIN (My bones hurt) had resolved and FATIGUE (I was tired), HEADACHE (Headache) and RASH (rash) had not resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Most recent FOLLOW-UP information incorporated above includes: On 15-Feb-2021: No specific follow-up information recorded.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Migraine; Seizures
Vorgeschichte: -
Andere Medikamente: APTIOM; PANTOPRAZOLE 40; TIZANIDINE; PROZAC; MAXALT
Allergien: -
Vorherige Impfungen: -

VAERS 1573128

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: NC
Alter: 41,0
Geschlecht: F
Eingang: 16.08.2021
Impfdatum: 14.01.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: OT / RA

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

Ageusia Fatigue Headache Nausea Pain in extremity Pyrexia Resorption bone increased Tremor Vision blurred

Symptomtext

Pain in arm; sense of taste lost; blurry vision; Fever; shaking; nausea; my bones hurt; I was tired; headache; This spontaneous case was reported by a pharmacist and describes the occurrence of PAIN IN EXTREMITY (Pain in arm), AGEUSIA (sense of taste lost), VISION BLURRED (blurry vision), PYREXIA (Fever) and TREMOR (shaking) in a 41-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 011J20A and 028L20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concurrent medical conditions included Seizures and Migraine. Concomitant products included RIZATRIPTAN BENZOATE (MAXALT) for Migraine, ESLICARBAZEPINE ACETATE (APTIOM) for Seizures, PANTOPRAZOLE SODIUM SESQUIHYDRATE (PANTOPRAZOLE 40) and TIZANIDINE for an unknown indication, FLUOXETINE HYDROCHLORIDE (PROZAC). On 14-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 11-Feb-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 PAIN IN EXTREMITY (Pain in arm), AGEUSIA (sense of taste lost), VISION BLURRED (blurry vision), PYREXIA (Fever), TREMOR (shaking), NAUSEA (nausea), RESORPTION BONE INCREASED (my bones hurt), FATIGUE (I was tired) and HEADACHE (headache). At the time of the report, PAIN IN EXTREMITY (Pain in arm), AGEUSIA (sense of taste lost), VISION BLURRED (blurry vision), PYREXIA (Fever), TREMOR (shaking), NAUSEA (nausea), RESORPTION BONE INCREASED (my bones hurt), FATIGUE (I was tired) and HEADACHE (headache) had not resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Migraine; Seizures
Vorgeschichte: -
Andere Medikamente: APTIOM; PANTOPRAZOLE 40; TIZANIDINE; PROZAC; MAXALT
Allergien: -
Vorherige Impfungen: -

VAERS 1573036

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: -
Alter: 47,0
Geschlecht: F
Eingang: 16.08.2021
Impfdatum: 08.01.2021
Beginn: 13.01.2021
Tage bis Beginn: 5,0
Dosis: 1
Route/Site: OT / -

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

Chest discomfort Fatigue Headache Herpes zoster Hypertension Lymphadenopathy Oral mucosal blistering Pain Pain in extremity Swelling

Symptomtext

Arm pain; neck swollen; high blood pressure; chest still tight; body aches everywhere,; blisters in mouth; Fatigued; Headache; swollen lymph nodes in the neck; Shingles on roof of mouth and stomach; This spontaneous case was reported by a consumer and describes the occurrence of HERPES ZOSTER (Shingles on roof of mouth and stomach), PAIN IN EXTREMITY (Arm pain), SWELLING (neck swollen), HYPERTENSION (high blood pressure) and CHEST DISCOMFORT (chest still tight) in a 47-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 029L204 and 011J20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included Hashimoto's disease in 2001 and Anxiety in 2001. Concurrent medical conditions included Hypothyroidism in 2002 and Blood pressure high in 2001. Concomitant products included ESCITALOPRAM OXALATE (LEXAPRO) for Anxiety, METOPROLOL for Hypertension, LEVOTHYROXINE SODIUM (SYNTHROID) for Hypothyroidism. On 08-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 18-Feb-2021 at 1:15 PM, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 2 dosage form. On 13-Jan-2021, the patient experienced HERPES ZOSTER (Shingles on roof of mouth and stomach). On an unknown date, the patient experienced PAIN IN EXTREMITY (Arm pain), SWELLING (neck swollen), HYPERTENSION (high blood pressure), CHEST DISCOMFORT (chest still tight), PAIN (body aches everywhere,), ORAL MUCOSAL BLISTERING (blisters in mouth), FATIGUE (Fatigued), HEADACHE (Headache) and LYMPHADENOPATHY (swollen lymph nodes in the neck). At the time of the report, HERPES ZOSTER (Shingles on roof of mouth and stomach) had resolved, PAIN IN EXTREMITY (Arm pain), SWELLING (neck swollen), CHEST DISCOMFORT (chest still tight), PAIN (body aches everywhere,), ORAL MUCOSAL BLISTERING (blisters in mouth), FATIGUE (Fatigued), HEADACHE (Headache) and LYMPHADENOPATHY (swollen lymph nodes in the neck) outcome was unknown and HYPERTENSION (high blood pressure) had not resolved. Treatment included anti-viral medicine, famber, for shingles. she was given a second prescription because she got shingles on her stomach This case was linked to MOD-2021-097373 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 23-Apr-2021: Medical history, concomitant medications, therapy details and new events were added. Patient age was updated.

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Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Anxiety; Blood pressure high; Hashimoto's disease; Hypothyroidism
Andere Medikamente: SYNTHROID; METOPROLOL; LEXAPRO
Allergien: -
Vorherige Impfungen: -

VAERS 1572745

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: FL
Alter: 69,0
Geschlecht: F
Eingang: 16.08.2021
Impfdatum: 13.01.2021
Beginn: 13.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / LA

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

Diarrhoea Discomfort Headache Limb discomfort Nightmare Pain in extremity Palpitations Pyrexia

Symptomtext

Diarrhea comes and goes; Heavy nightmares; Palpitations; Body has felt a little off; Bad headaches; Arm felt heavy and painful; Arm felt heavy; Fever; This spontaneous case was reported by a consumer and describes the occurrence of DIARRHOEA (Diarrhea comes and goes), NIGHTMARE (Heavy nightmares), PALPITATIONS (Palpitations), DISCOMFORT (Body has felt a little off) and PAIN IN EXTREMITY (Arm felt heavy and painful) in a 69-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 011J20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concurrent medical conditions included Penicillin allergy, Drug allergy (darvacet and darvan.) and Blood pressure high. Concomitant products included LOSARTAN, VITAMIN D3 and CORTISONE for an unknown indication. On 13-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 13-Jan-2021, the patient experienced PAIN IN EXTREMITY (Arm felt heavy and painful), LIMB DISCOMFORT (Arm felt heavy) and PYREXIA (Fever). On 15-Jan-2021, the patient experienced DIARRHOEA (Diarrhea comes and goes), NIGHTMARE (Heavy nightmares), PALPITATIONS (Palpitations), DISCOMFORT (Body has felt a little off) and HEADACHE (Bad headaches). At the time of the report, DIARRHOEA (Diarrhea comes and goes), NIGHTMARE (Heavy nightmares), PALPITATIONS (Palpitations), DISCOMFORT (Body has felt a little off), PAIN IN EXTREMITY (Arm felt heavy and painful), LIMB DISCOMFORT (Arm felt heavy), PYREXIA (Fever) and HEADACHE (Bad headaches) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown.; Sender's Comments: Very limited information regarding this events has been provided at this time. Further information has been requested. Company assessed the events to be unlikely related to company product.

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Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure high; Drug allergy (darvacet and darvan.); Penicillin allergy
Andere Medikamente: LOSARTAN; VITAMIN D3; CORTISONE
Allergien: -
Vorherige Impfungen: -

VAERS 1572639

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: MA
Alter: 55,0
Geschlecht: F
Eingang: 16.08.2021
Impfdatum: 30.12.2020
Beginn: 09.01.2021
Tage bis Beginn: 10,0
Dosis: 1
Route/Site: OT / LA

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

Blood pressure measurement Breast discomfort Breast swelling Computerised tomogram Fibrin D dimer Ligament sprain Musculoskeletal chest pain X-ray

Symptomtext

Breast heaviness; chest pain; Breast swelling; Sprain; This spontaneous case was reported by a nurse and describes the occurrence of BREAST DISCOMFORT (Breast heaviness), MUSCULOSKELETAL CHEST PAIN (chest pain), BREAST SWELLING (Breast swelling) and LIGAMENT SPRAIN (Sprain) in a 55-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 011J20A) for COVID-19 vaccination. Concurrent medical conditions included Hypertension. On 30-Dec-2020, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .5 milliliter. On 09-Jan-2021, the patient experienced BREAST DISCOMFORT (Breast heaviness), MUSCULOSKELETAL CHEST PAIN (chest pain), BREAST SWELLING (Breast swelling) and LIGAMENT SPRAIN (Sprain). At the time of the report, BREAST DISCOMFORT (Breast heaviness), MUSCULOSKELETAL CHEST PAIN (chest pain), BREAST SWELLING (Breast swelling) and LIGAMENT SPRAIN (Sprain) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, Blood pressure measurement: Hypertension. On an unknown date, Computerised tomogram: negative (Negative) Unclear. On an unknown date, Fibrin D dimer: d-dimer Elevated, rule out DVT. On an unknown date, X-ray: x-ray Not clear. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Treatment included motrin and Lidoderm patch. No concomitant medication was provided.

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Praegender Schweregrund: Musculoskeletal chest pain
Hospital-Tage: -
Labordaten: Test Name: Blood pressure; Result Unstructured Data: Hypertension; Test Name: CT; Test Result: Negative ; Result Unstructured Data: Unclear; Test Name: Fibrin; Result Unstructured Data: Elevated, rule out DVT; Test Name: X-ray; Result Unstructured Data: Not clear
Aktuelle Erkrankungen: Hypertension
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1572329

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: OK
Alter: -
Geschlecht: F
Eingang: 16.08.2021
Impfdatum: 15.01.2021
Beginn: 15.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Fatigue Feeling cold Headache Tremor Vaccination site induration Vaccination site pain Vaccination site swelling

Symptomtext

sore arm; swelling at injection site; it was hard; horrible headache, from shoulder to base of neck to other shoulder; Felt really tired; feeling really cold; woke up shaking; A spontaneous report was received from a Consumer concerning a 70 Years-old female patient who received Moderna's COVID-19 vaccine (mRNA-1273) and experienced , sore arm, shaking and feeling really cold, headache from shoulder to base of neck to other shoulder, tired, swelling at injection site and it was hard. The patient's medical history included Blood pressure and high cholesterol. The concomitant medications taken by the patient, for unspecified indications, levothyroxine, metoprolol, Torvavastin, omeprazole and baby aspirin. On 15 Jan 2021, prior to the onset of the events, the patient received their first of two planned doses of mRNA-1273 (batch: 011J20A) intramuscularly in the upper left arm for prophylaxis of COVID-19 infection. On 15 Jan 2021, the patient experienced sore arm, horrible headache from shoulder to base of neck to the shoulder, shaking and feeling really cold, swelling at the injection site. Patient treated with Tylenol. Action taken with mRNA-1273 in response to the events was not reported. At the time of this report, the outcome of the event(s) (sore arm, headaches, swelling at injection site, shaking and feeling cold, injection site pain) was unknown.

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Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Blood pressure
Vorgeschichte: Medical History/Concurrent Conditions: Blood cholesterol; Drug hypersensitivity (Allergic to Zocor); Seasonal allergy
Andere Medikamente: LEVOTHYROXINE; METOPROLOL; Toravastin; OMEPRAZOLE; BABY ASPIRIN
Allergien: -
Vorherige Impfungen: -

VAERS 1571710

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: CA
Alter: -
Geschlecht: F
Eingang: 16.08.2021
Impfdatum: 07.01.2021
Beginn: 07.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / LA

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

Heart rate increased Injection site swelling Injection site warmth Mobility decreased Vaccination site pain

Symptomtext

Hard to lift arm; elevated heart rate; warm; little bit of swelling at the injection site; Super painful; This spontaneous case was reported by a consumer (subsequently medically confirmed) and describes the occurrence of MOBILITY DECREASED (Hard to lift arm), HEART RATE INCREASED (elevated heart rate), INJECTION SITE WARMTH (warm), INJECTION SITE SWELLING (little bit of swelling at the injection site) and VACCINATION SITE PAIN (Super painful) in a 25-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 011J20A) for COVID-19 vaccination. The patient's past medical history included No adverse effect. On 07-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 07-Jan-2021, the patient experienced MOBILITY DECREASED (Hard to lift arm), HEART RATE INCREASED (elevated heart rate), INJECTION SITE WARMTH (warm), INJECTION SITE SWELLING (little bit of swelling at the injection site) and VACCINATION SITE PAIN (Super painful). At the time of the report, MOBILITY DECREASED (Hard to lift arm), HEART RATE INCREASED (elevated heart rate), INJECTION SITE WARMTH (warm), INJECTION SITE SWELLING (little bit of swelling at the injection site) and VACCINATION SITE PAIN (Super painful) had not resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments.; Reporter's Comments: Based on the current available information and temporal association between the use of the product and the start date of the events, a causal relationship cannot be excluded.

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Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: No adverse effect
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1568406

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: NC
Alter: -
Geschlecht: U
Eingang: 15.08.2021
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: OT / -

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

Condition aggravated Contusion Vaccination site erythema Vaccination site pain Vaccination site swelling

Symptomtext

Bruise; Symptoms worsening; Redness at injection site; Swelling at injection site; Pain at injection site; A spontaneous report was received from a pharmacist concerning a patient who received Moderna's COVID-19 Vaccine, and experienced bruise/ contusion, symptoms worsening/ condition aggravated, redness at injection site/ vaccination site erythema, swelling at injection site/ vaccination site swelling, pain at injection site/ vaccination site pain. The patient's medical history was not provided. Concomitant product use was not provided by the reporter. On an unknown date, the patient received their first of two planned doses of mRNA-1273 (LOT# 011J20A) on an undisclosed date intramuscularly for prophylaxis of COVID-19 infection. A pharmacist called to report that 70 patients received their Moderna vaccine. He stated that the patients reported redness, swelling and pain at the injection site and bruising Additionally, pharmacist said that some of the patients have stated that their symptoms have worsened. Treatment information was not provided. Action taken with mRNA-1273 in response to the events were not provided. The outcome of the events, bruise, symptoms worsening, redness at injection site, swelling at injection site, pain at injection site were unknown.; Reporter's Comments: Based on the current available information and temporal association between the use of the product and the start date of the events, a causal relationship cannot be excluded.

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Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: No adverse event (No medical history reported.)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1568323

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: OK
Alter: 41,0
Geschlecht: F
Eingang: 15.08.2021
Impfdatum: 04.01.2021
Beginn: 04.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / LA

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

COVID-19 Condition aggravated Dysgeusia Dysphonia Flushing Headache Influenza like illness Nasopharyngitis Nausea Oropharyngeal discomfort Sluggishness Vaccination site pain

Symptomtext

Severe headache; Nausea; feels like when she catches a cold; Throat feels funny; Voice is scratchy; Cheeks flush/rosy; Feels sluggish; Iron/chemical taste in mouth; Feels like she does when she's catching a cold; Symptoms getting worse as the day goes on; Arm was really sore; A spontaneous report was received from a consumer concerning a 41 year old female patient, who received Moderna's COVID-19 vaccine (mRNA-1273) and experienced sore arm, severe headache, throat feels funny, voice was scratchy, cheeks flush/rosy, nausea, feels sluggish, an iron/chemical taste in the mouth and feels like she was catching a cold. The patient's medical history was not provided. No relevant concomitant medications were reported. On 04 Jan 2021, prior to the onset of the events, the patient received their first of two planned doses of mRNA-1273 (Batch No: 011J20A) in the left arm for prophylaxis of COVID-19 infection. On 04 Jan 2021, After receiving the vaccine, she stated that her arm was really sore. On 05 Jan 2021, the patient woke up with a severe headache. The patient experienced sore arm, severe headache, throat feels funny, voice was scratchy, cheeks flush/rosy, nausea, feels sluggish, an iron/chemical taste in the mouth and feels like she was catching a cold. The patient stated that the symptoms seem to be getting worse as the day goes on. The patient also stated she was in contact with several COVID positive individuals before being vaccinated but two separate COVID tests came back negative, however she was feeling sick the week prior to getting vaccinated. Treatment for the event included migraine medication. Action taken with mRNA-1273 in response to the events was not reported. The outcome of the events experienced sore arm, throat feels funny, severe headache, voice is scratchy, cheeks flush/rosy, nausea, feels sluggish, an iron/chemical taste in the mouth and feels like she's catching a cold was unknown.; Reporter's Comments: Based on the current available information and temporal association between the use of the product and the start date of these events, a causal relationship cannot be excluded.

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Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Test Name: covid-19; Test Result: Negative ; Test Name: covid-19; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: No adverse event (No reported medical history)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1568317

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: PA
Alter: -
Geschlecht: F
Eingang: 15.08.2021
Impfdatum: 05.01.2021
Beginn: 05.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / LA

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

Chest discomfort Chills Decreased appetite Dyspnoea Fatigue Headache Injection site pain Musculoskeletal discomfort Pyrexia Sinus disorder Sneezing

Symptomtext

shortness of breath; tightness across her chest; soreness around her check and back of neck; sinus issues; sneezing; no appetite; tiredness; left arm began to hurt; chills; headache; felt an elevated body temperature, temperature of 99.8 degrees Fahrenheit; A spontaneous report was received from a pharmacist who was also 67-year-old, female patient who received Moderna's COVID-19 vaccine (mRNA-1273) and experienced a headache, her left arm began to hurt, felt an elevated body temperature, measured temperature of 99.8 degrees Fahrenheit, chills, tiredness, no appetite, shortness of breath, tightness across the chest, soreness around her chest and back of neck, sinus issues and sneezing. The patient's medical history was not provided. No relevant concomitant medications were reported. On 05 Jan 2021, the patient received their first of two planned doses of mRNA-1273 (Lot: 011J20A) intramuscularly in the left deltoid for prophylaxis of COVID-19 infection. On 05 Jan 2021, 8 hours post injection, the patient developed headache, her left arm began to hurt, felt an elevated body temperature, measured temperature of 99.8 degrees Fahrenheit, chills and tiredness. On 06 Jan 2021, the patient stated that she slept all day. On 07 Jan 2021, she experienced shortness of breath, tightness across her chest, soreness around her chest and back of neck, sinus issues, sneezing, productive blowing of her nose. On 08 Jan 2021, the patient stated that when she woke up, she felt completely back to her normal self. Treatment included pseudoephedrine hydrochloride and ibuprofen. Action taken with mRNA-1273 in response to the event was not reported. The outcome of the events, headache, her left arm began to hurt, felt an elevated body temperature, measured temperature of 99.8 degrees Fahrenheit, chills, tiredness, no appetite, shortness of breath, tightness across the chest, soreness around her chest and back of neck, sinus issues and sneezing, were considered resolved on 08 Jan 2021.; Reporter's Comments: Based on the current available information and temporal association between the use of the product and the start date of the event, a causal relationship cannot be excluded.

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: No adverse event (No reported medical history)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1566916

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: IN
Alter: 24,0
Geschlecht: M
Eingang: 15.08.2021
Impfdatum: 14.03.2021
Beginn: 14.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / RA

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

Chills Heart rate Nausea Oxygen saturation Respiratory rate Skin warm Tachycardia Vomiting

Symptomtext

warm face; Nausea/vomiting; Nausea/vomiting; Chills; tachycardia; This spontaneous case was reported by a nurse and describes the occurrence of TACHYCARDIA (tachycardia), NAUSEA (Nausea/vomiting), SKIN WARM (warm face), VOMITING (Nausea/vomiting) and CHILLS (Chills) in a 24-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 011J20A) for COVID-19 vaccination. Concurrent medical conditions included Anxiety. On 14-Mar-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 14-Mar-2021, the patient experienced TACHYCARDIA (tachycardia), NAUSEA (Nausea/vomiting), VOMITING (Nausea/vomiting) and CHILLS (Chills). On an unknown date, the patient experienced SKIN WARM (warm face). At the time of the report, TACHYCARDIA (tachycardia), NAUSEA (Nausea/vomiting), SKIN WARM (warm face), VOMITING (Nausea/vomiting) and CHILLS (Chills) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 14-Mar-2021, Heart rate: 115-120 (High) 115-120. On 14-Mar-2021, Oxygen saturation: 98 percent (Inconclusive) 98%. On 14-Mar-2021, Respiratory rate: 16 (Inconclusive) 16. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Patient was monitored for 30 minutes by the onsite nurse. No concomitant medications were reported. No treatment details were reported. Most recent FOLLOW-UP information incorporated above includes: On 24-May-2021: This follow-up was received on 24-MAY-2021 which updated historical condition, lab data, dosage details and new events.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tachycardia
Hospital-Tage: -
Labordaten: Test Date: 20210314; Test Name: Heart rate; Result Unstructured Data: 115-120; Test Date: 20210314; Test Name: Oxygen saturation; Test Result: Inconclusive 98 %; Result Unstructured Data: 98%; Test Date: 20210314; Test Name: Respiratory rate; Test Result: Inconclusive ; Result Unstructured Data: 16
Aktuelle Erkrankungen: Anxiety
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1566586

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: CO
Alter: 28,0
Geschlecht: F
Eingang: 15.08.2021
Impfdatum: 19.01.2021
Beginn: 16.02.2021
Tage bis Beginn: 28,0
Dosis: 1
Route/Site: OT / RA

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

Chills Electrocardiogram Heart rate Pyrexia Tachycardia

Symptomtext

Lowgrade fever; Chills; Tachycardia; This spontaneous case was reported by a consumer and describes the occurrence of TACHYCARDIA (Tachycardia), PYREXIA (Lowgrade fever) and CHILLS (Chills) in a 28-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 031L20A and 011J20A) for COVID-19 vaccination. Concurrent medical conditions included Seasonal allergy. Concomitant products included LEVONORGESTREL (KYLEENA) for Birth control, VITAMIN C [ASCORBIC ACID] for Immune disorder (NOS), CLARITHROMYCIN (CLARITIN [CLARITHROMYCIN]) for Seasonal allergy, COLECALCIFEROL (VITAMIN D [COLECALCIFEROL]) for Vitamin D deficiency. On 19-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 16-Feb-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 16-Feb-2021 at 8:30 AM, the patient experienced TACHYCARDIA (Tachycardia). On an unknown date, the patient experienced PYREXIA (Lowgrade fever) and CHILLS (Chills). The patient was treated with PARACETAMOL (TYLENOL) at an unspecified dose and frequency and IBUPROFEN at an unspecified dose and frequency. On 18-Feb-2021, TACHYCARDIA (Tachycardia) had resolved. At the time of the report, PYREXIA (Lowgrade fever) and CHILLS (Chills) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, Electrocardiogram: normal (normal) normal. On an unknown date, Heart rate: 140 (High) heart rate remained high for about 15 hours.. Treatment included fluids. Action taken with mRNA-1273 in response to the events was not Applicable This case was linked to MOD-2021-044470 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 07-Jun-2021: Follow up received on 7-Jun-2021, reporter details, patient demographics, patient date of birth, concomitant medications, event (tachycardia) start date, stop date were added. Outcome for the event tachycardia was updated to recovered from unknown.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tachycardia
Hospital-Tage: -
Labordaten: Test Name: EKG; Result Unstructured Data: normal; Test Name: Heart rate; Result Unstructured Data: heart rate remained high for about 15 hours.
Aktuelle Erkrankungen: Seasonal allergy
Vorgeschichte: -
Andere Medikamente: CLARITIN [CLARITHROMYCIN]; VITAMIN D [COLECALCIFEROL]; VITAMIN C [ASCORBIC ACID]; KYLEENA
Allergien: -
Vorherige Impfungen: -

VAERS 1564044

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: IN
Alter: 43,0
Geschlecht: M
Eingang: 15.08.2021
Impfdatum: 07.03.2021
Beginn: 07.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / RA

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

Dyspnoea Hypersensitivity Throat irritation

Symptomtext

This spontaneous case was reported by a nurse and describes the occurrence of DYSPNOEA (Shortness of breath), THROAT IRRITATION (Scratchy throat) and HYPERSENSITIVITY (Hypersensitivity reaction) in a 43-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 011J20A) for COVID-19 vaccination. Concurrent medical conditions included Asthma, Obesity, Penicillin allergy, Shellfish allergy and Oil allergy (Grape seed oil allergy.). Concomitant products included PREDNISONE for Asthma. On 07-Mar-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 07-Mar-2021, the patient experienced DYSPNOEA (Shortness of breath), THROAT IRRITATION (Scratchy throat) and HYPERSENSITIVITY (Hypersensitivity reaction). At the time of the report, DYSPNOEA (Shortness of breath), THROAT IRRITATION (Scratchy throat) and HYPERSENSITIVITY (Hypersensitivity reaction) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Treatment activities for event was done with diphenhydramine (Benadryl) 25 mg oral and was monitored by an onsite nurse for 30 minutes. Patient felt better and was sent home. Most recent FOLLOW-UP information incorporated above includes: On 06-May-2021: hypersensitivity form- Add medical history, allergies.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Asthma; Obesity; Oil allergy (Grape seed oil allergy.); Penicillin allergy; Shellfish allergy
Vorgeschichte: -
Andere Medikamente: PREDNISONE
Allergien: -
Vorherige Impfungen: -

VAERS 1562639

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: NY
Alter: 55,0
Geschlecht: F
Eingang: 15.08.2021
Impfdatum: 09.01.2021
Beginn: 16.01.2021
Tage bis Beginn: 7,0
Dosis: 1
Route/Site: OT / -

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

Paraesthesia Rash macular Vaccination site erythema Vaccination site pain Vaccination site warmth

Symptomtext

Red Blotchy Patches Like a Round Ring around Injection Site; Hot to the touch Injection Site post first vaccine; Tingling Injection Site / Tingling Fingers; Redness below the injection site; Soreness; This spontaneous case was reported by a nurse and describes the occurrence of RASH MACULAR (Red Blotchy Patches Like a Round Ring around Injection Site), VACCINATION SITE WARMTH (Hot to the touch Injection Site post first vaccine), PARAESTHESIA (Tingling Injection Site / Tingling Fingers), VACCINATION SITE ERYTHEMA (Redness below the injection site) and VACCINATION SITE PAIN (Soreness) in a 55-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 011J20A) for COVID-19 vaccination. No Medical History information was reported. On 09-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 16-Jan-2021, the patient experienced RASH MACULAR (Red Blotchy Patches Like a Round Ring around Injection Site), VACCINATION SITE WARMTH (Hot to the touch Injection Site post first vaccine), PARAESTHESIA (Tingling Injection Site / Tingling Fingers), VACCINATION SITE ERYTHEMA (Redness below the injection site) and VACCINATION SITE PAIN (Soreness). On 30-Jan-2021, RASH MACULAR (Red Blotchy Patches Like a Round Ring around Injection Site), VACCINATION SITE WARMTH (Hot to the touch Injection Site post first vaccine), PARAESTHESIA (Tingling Injection Site / Tingling Fingers), VACCINATION SITE ERYTHEMA (Redness below the injection site) and VACCINATION SITE PAIN (Soreness) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Treatment information was not provided. Concomitant medication was not provided. This case was linked to MOD-2021-056348 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 30-Jun-2021: Follow up received on Jun 30 2021 contains no significant information

Weitere VAERSDATA-Felder

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

VAERS 1562324

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: PR
Alter: 32,0
Geschlecht: F
Eingang: 15.08.2021
Impfdatum: 29.12.2020
Beginn: 29.12.2020
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / LA

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

Blood pressure measurement Body temperature Dizziness Heart rate Hypersensitivity Hypertension Respiratory rate Tachycardia

Symptomtext

Tachycardia; Allergic reaction; Dizziness; High BP; This spontaneous case was reported by a health care professional and describes the occurrence of TACHYCARDIA (Tachycardia), HYPERSENSITIVITY (Allergic reaction), DIZZINESS (Dizziness) and HYPERTENSION (High BP) in a 32-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 011J20A) for COVID-19 vaccination. Concurrent medical conditions included Hypersensitivity reaction (Past allergies). On 29-Dec-2020, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 29-Dec-2020, the patient experienced TACHYCARDIA (Tachycardia), HYPERSENSITIVITY (Allergic reaction), DIZZINESS (Dizziness) and HYPERTENSION (High BP). On 29-Dec-2020, TACHYCARDIA (Tachycardia), DIZZINESS (Dizziness) and HYPERTENSION (High BP) had resolved. At the time of the report, HYPERSENSITIVITY (Allergic reaction) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 29-Dec-2020, Blood pressure measurement: 174/110 mmhg (High) High. On 29-Dec-2020, Body temperature: 36.6 (normal) Normal. On 29-Dec-2020, Heart rate: 137 (High) High pulse rate. On 29-Dec-2020, Respiratory rate: 20 bpm (normal) Normal. On 08-Jan-2021, Blood pressure measurement: 155/82 mmhg (High) High. On 08-Jan-2021, Body temperature: 37.6 (normal) Normal. On 08-Jan-2021, Heart rate: 123 (High) High. On 08-Jan-2021, Respiratory rate: 19 bpm (normal) Normal. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant product use was reported Treatment included: Blood pressure medications and oxygen It was also stated that Tachycardia was the residual effect of the events Most recent FOLLOW-UP information incorporated above includes: On 21-Jul-2021: Follow up received on 21-JUL-2021 contains: Updated reporter information; Updated patient details; Updated Lab data; Updated Event- Difficulty breathing; Updated Stop dates of events;

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Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: Test Date: 20201229; Test Name: Blood pressure; Result Unstructured Data: High; Test Date: 20210108; Test Name: Blood pressure; Result Unstructured Data: High; Test Date: 20201229; Test Name: Body Temperature; Result Unstructured Data: Normal; Test Date: 20210108; Test Name: Body Temperature; Result Unstructured Data: Normal; Test Date: 20201229; Test Name: Pulse rate; Result Unstructured Data: High pulse rate; Test Date: 20210108; Test Name: Pulse rate; Result Unstructured Data: High; Test Date: 20201229; Test Name: Respiratory rate; Result Unstructured Data: Normal; Test Date: 20210108; Test Name: Respiratory rate; Result Unstructured Data: Normal
Aktuelle Erkrankungen: Hypersensitivity reaction (Past allergies)
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1560593

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: NM
Alter: 73,0
Geschlecht: F
Eingang: 15.08.2021
Impfdatum: 06.01.2021
Beginn: 07.02.2021
Tage bis Beginn: 32,0
Dosis: 1
Route/Site: OT / LA

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

Chills Dizziness Dyspnoea Fatigue Headache Heart rate irregular Influenza like illness Nausea Pain Palpitations Pyrexia Somnolence

Symptomtext

An erratic pulse; Palpitations; Shortness of breath; Flu-like symptom; Felt sleepy; Aches; Dizziness; Chills; Had fatigue; A headache; Lots of nausea; Low grade fever; This spontaneous case was reported by a nurse and describes the occurrence of HEART RATE IRREGULAR (An erratic pulse), PALPITATIONS (Palpitations), DYSPNOEA (Shortness of breath), INFLUENZA LIKE ILLNESS (Flu-like symptom) and SOMNOLENCE (Felt sleepy) in a 73-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 011J20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included Ventricular arrhythmia. Concurrent medical conditions included Iodine allergy. On 06-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 06-Feb-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 2 dosage form. On 07-Feb-2021, the patient experienced HEART RATE IRREGULAR (An erratic pulse), PALPITATIONS (Palpitations), DYSPNOEA (Shortness of breath), INFLUENZA LIKE ILLNESS (Flu-like symptom), SOMNOLENCE (Felt sleepy), PAIN (Aches), DIZZINESS (Dizziness), CHILLS (Chills), FATIGUE (Had fatigue), HEADACHE (A headache), NAUSEA (Lots of nausea) and PYREXIA (Low grade fever). On 08-Feb-2021, HEART RATE IRREGULAR (An erratic pulse), PALPITATIONS (Palpitations), DYSPNOEA (Shortness of breath), INFLUENZA LIKE ILLNESS (Flu-like symptom), SOMNOLENCE (Felt sleepy), PAIN (Aches), DIZZINESS (Dizziness), CHILLS (Chills), FATIGUE (Had fatigue), HEADACHE (A headache), NAUSEA (Lots of nausea) and PYREXIA (Low grade fever) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Patient Take Benadryl on 07Feb2021 and Carvedilol and a low dose of Statins as a Treatment medication. This case was linked to MOD-2021-044875 (Patient Link).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Iodine allergy
Vorgeschichte: Medical History/Concurrent Conditions: Ventricular arrhythmia
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1560411

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: MI
Alter: 83,0
Geschlecht: F
Eingang: 15.08.2021
Impfdatum: 14.01.2021
Beginn: 16.01.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: OT / LA

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

Ageusia COVID-19 Corneal irritation Dry eye Fatigue Hypertension Incomplete course of vaccination Malaise Rash pruritic Thinking abnormal Urticaria

Symptomtext

Passed the 36 day window to get the second shot; High blood pressure 169/95 for last 2 weeks; Corneal irritation; Felt tired; Could not think clearly; Had no taste; Not feeling well; Tested positive for Covid-19; Dry eyes/ eyes have been so dry, has made reading uncomfortable; Itchiness of the jaw line/ Rash on the face, left/right cheek/ itchy/rash on both cheeks, lower left/right cheek, pimple like and itchy; Hives / Two welts; This spontaneous case was reported by a consumer and describes the occurrence of INCOMPLETE COURSE OF VACCINATION (Passed the 36 day window to get the second shot), COVID-19 (Tested positive for Covid-19), URTICARIA (Hives / Two welts), DRY EYE (Dry eyes/ eyes have been so dry, has made reading uncomfortable) and RASH PRURITIC (Itchiness of the jaw line/ Rash on the face, left/right cheek/ itchy/rash on both cheeks, lower left/right cheek, pimple like and itchy) in an 83-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 011J20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concomitant products included PROPRANOLOL, LEVOTHYROXINE, LOSARTAN, ALLOPURINOL, SERTRALINE and ALENDRONATE SODIUM for an unknown indication. On 14-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 16-Jan-2021, the patient experienced URTICARIA (Hives / Two welts) and RASH PRURITIC (Itchiness of the jaw line/ Rash on the face, left/right cheek/ itchy/rash on both cheeks, lower left/right cheek, pimple like and itchy). On 01-Mar-2021, the patient experienced DRY EYE (Dry eyes/ eyes have been so dry, has made reading uncomfortable). On 26-Mar-2021, the patient experienced COVID-19 (Tested positive for Covid-19), THINKING ABNORMAL (Could not think clearly), AGEUSIA (Had no taste), MALAISE (Not feeling well) and FATIGUE (Felt tired). On 08-Apr-2021, the patient experienced CORNEAL IRRITATION (Corneal irritation). On 15-Apr-2021, the patient experienced HYPERTENSION (High blood pressure 169/95 for last 2 weeks). On an unknown date, the patient experienced INCOMPLETE COURSE OF VACCINATION (Passed the 36 day window to get the second shot). At the time of the report, INCOMPLETE COURSE OF VACCINATION (Passed the 36 day window to get the second shot) had resolved, COVID-19 (Tested positive for Covid-19), THINKING ABNORMAL (Could not think clearly), AGEUSIA (Had no taste), MALAISE (Not feeling well), CORNEAL IRRITATION (Corneal irritation), HYPERTENSION (High blood pressure 169/95 for last 2 weeks) and FATIGUE (Felt tired) outcome was unknown, URTICARIA (Hives / Two welts) and DRY EYE (Dry eyes/ eyes have been so dry, has made reading uncomfortable) had not resolved and RASH PRURITIC (Itchiness of the jaw line/ Rash on the face, left/right cheek/ itchy/rash on both cheeks, lower left/right cheek, pimple like and itchy) was resolving. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Treatment for the event, included a gel, eyedrops, topical creams, and steroid eye ointment. Most recent FOLLOW-UP information incorporated above includes: On 08-Apr-2021: follow information received on 08-Apr-2021, events added On 29-Apr-2021: Follow up information received on 29-apr-2021, events were added; Sender's Comments: This report refers to a case of incomplete course of vaccination for mRNA-1273, lot # 011J20A with associated AEs rash pruritic, urticaria and dry eye. Based on the current available information and temporal association between the use of the product and the start date of the event, a causal relationship cannot be excluded.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: PROPRANOLOL; LEVOTHYROXINE; LOSARTAN; ALLOPURINOL; SERTRALINE; ALENDRONATE SODIUM
Allergien: -
Vorherige Impfungen: -

VAERS 1558402

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: OH
Alter: 60,0
Geschlecht: M
Eingang: 14.08.2021
Impfdatum: 01.12.2020
Beginn: 31.12.2020
Tage bis Beginn: 30,0
Dosis: 1
Route/Site: IM / RA

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

Condition aggravated Ear discomfort Tinnitus

Symptomtext

New onset bilateral Ear fullness and doubling of volume of high pitched dog whistle like preexisting baseline bilateral tinnitus ears associated with more difficult hearing in noisy environments, sleep. Interference, distraction with trying to rest or meditate. Tinnitus will increase if tired, too many computer demands, idiopathic, weather change and if over worked. Pressure in ears and fullness increases without reason. So far sleep helps Unchanged problem from start 8 months ago in end DEC 2020.

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Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Discussed with personal internist May 2020 but no testing done as I hoped would decrease or go away. Have tried OTC tinnitus masking noise device but not successful for me. I will likely get referral to ENT andalso audiologist but as physician I know must adapt to live w this intrusive condition affecting quality of life.
Aktuelle Erkrankungen: Atrial fibrillation treated rate control Hypertension treated controlled BMI 36 Insomnia treated with Lunesta and nortriptyline Chronic bilateral tinnitus since 2009 stable baseline Chronic cervical sprain and post concussion headaches stable
Vorgeschichte: See above.
Andere Medikamente: Propranolol, bupropion, lexapro, rosuvastatin, Eliquis,Lunesta, Vit D, Coenzyme Q10, acetaminophen, nortryptyline,
Allergien: Naproxen anaphylaxis Compazine akathasia Seasonal hay fever
Vorherige Impfungen: -

VAERS 1556447

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: NC
Alter: 73,0
Geschlecht: F
Eingang: 14.08.2021
Impfdatum: 26.01.2021
Beginn: 26.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / LA

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

Blood pressure measurement Body temperature Hypertension Myalgia Vaccination site erythema Vaccination site pain Vaccination site swelling Vaccination site warmth

Symptomtext

Muscle aches in my right hip and leg; Blood pressure was slightly elevated; Warm; Red patch at the site of the injection; Swollen; Sore at the injection site; This spontaneous case was reported by a consumer and describes the occurrence of HYPERTENSION (Blood pressure was slightly elevated), VACCINATION SITE WARMTH (Warm), MYALGIA (Muscle aches in my right hip and leg), VACCINATION SITE ERYTHEMA (Red patch at the site of the injection) and VACCINATION SITE SWELLING (Swollen) in a 73-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 024M20A and 011J20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concurrent medical conditions included Hypertension. Concomitant products included DILTIAZEM from 03-May-2012 to an unknown date, VALSARTAN (DIOVAN) from 22-Jan-2014 to an unknown date, HYDROCHLOROTHIAZIDE, TRIAMTERENE (TRIAMTERENE/HYDROCHLOROTHIAZIDE) from 27-Mar-2012 to an unknown date and POTASSIUM from 15-Oct-2014 to an unknown date for Hypertension, LACTOBACILLUS ACIDOPHILUS (FLORAJEN) from 26-Jun-2020 to an unknown date for Probiotic therapy, IVERMECTIN (SOOLANTRA) from 13-Feb-2019 to an unknown date for Rosacea. On 26-Jan-2021 at 4:27 PM, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 22-Feb-2021 at 3:52 PM, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 26-Jan-2021, the patient experienced VACCINATION SITE PAIN (Sore at the injection site). On 05-Feb-2021, the patient experienced VACCINATION SITE WARMTH (Warm), VACCINATION SITE ERYTHEMA (Red patch at the site of the injection) and VACCINATION SITE SWELLING (Swollen). On an unknown date, the patient experienced HYPERTENSION (Blood pressure was slightly elevated) and MYALGIA (Muscle aches in my right hip and leg). The patient was treated with Physical therapy (ave been to orthopedist and physical therapist and exercises recommended) for Myalgia. At the time of the report, HYPERTENSION (Blood pressure was slightly elevated) and VACCINATION SITE PAIN (Sore at the injection site) outcome was unknown and VACCINATION SITE WARMTH (Warm), MYALGIA (Muscle aches in my right hip and leg), VACCINATION SITE ERYTHEMA (Red patch at the site of the injection) and VACCINATION SITE SWELLING (Swollen) had resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, Blood pressure measurement: elevated (High) slightly elevated. On an unknown date, Body temperature: 100 degree (Inconclusive) low grade fever. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Treatment information not provided. Have been to orthopedist and physical therapist and exercises recommended. Most recent FOLLOW-UP information incorporated above includes: On 22-Apr-2021: The significant follow up received in which patient race information is added Medical History information is added. Second dose information is added. Concomitant medications were added. Events were added. Outcome of the events are updated.(Unknown to Recovered). On 12-Jul-2021: Follow-up information received does not contain any new information.

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Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: Test Name: Blood pressure; Result Unstructured Data: slightly elevated; Test Name: Body temperature; Test Result: Inconclusive ; Result Unstructured Data: low grade fever
Aktuelle Erkrankungen: Hypertension
Vorgeschichte: -
Andere Medikamente: DILTIAZEM; DIOVAN; TRIAMTERENE/HYDROCHLOROTHIAZIDE; POTASSIUM; SOOLANTRA; FLORAJEN
Allergien: -
Vorherige Impfungen: -

VAERS 1555126

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: CA
Alter: 61,0
Geschlecht: F
Eingang: 13.08.2021
Impfdatum: 15.01.2021
Beginn: 15.01.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: OT / LA

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

Blood test Burning sensation Electromyogram Erythema Headache Hypoaesthesia Injection site pain Paraesthesia Skin disorder

Symptomtext

every pore on her skin looks like it has been pin pricked; burning sensation/episodes of hot,burning; redness feet and hands; numbness and tingling in her limbs/ all extremeties(feet, legs, hands, arm); numbness and tingling in her limbs/pins and needles sensation/ tingling in all extremeties(feet, legs, hands, arm); headache; soreness on the injection site; This spontaneous case was reported by a nurse and describes the occurrence of HYPOAESTHESIA (numbness and tingling in her limbs/ all extremeties(feet, legs, hands, arm)), BURNING SENSATION (burning sensation/episodes of hot,burning), SKIN DISORDER (every pore on her skin looks like it has been pin pricked), PARAESTHESIA (numbness and tingling in her limbs/pins and needles sensation/ tingling in all extremeties(feet, legs, hands, arm)) and ERYTHEMA (redness feet and hands) in a 61-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 011J20A and 013M20a) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included Tinnitus (it was constant) on 12-May-2021, Lumbar radiculopathy since an unknown date and Peripheral neuropathy (worsening) since 16-Jan-2021. Concurrent medical conditions included Chronic back pain (Flares on and off), Erythromelalgia (worsening) since 21-Jan-2021, Drug allergy (Gabapentin) and Drug allergy (steroids (oral and injection)). Concomitant products included LORAZEPAM (ATIVAN) from 12-Jan-2015 to an unknown date for Anxiety, NORTRIPTYLINE from 05-Jan-2002 to an unknown date for Depression. On 15-Jan-2021 at 3:20 PM, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 13-Feb-2021 at 2:15 PM, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 2 dosage form. On 15-Jan-2021, the patient experienced HEADACHE (headache) and INJECTION SITE PAIN (soreness on the injection site). On 16-Jan-2021, the patient experienced HYPOAESTHESIA (numbness and tingling in her limbs/ all extremeties(feet, legs, hands, arm)) and PARAESTHESIA (numbness and tingling in her limbs/pins and needles sensation/ tingling in all extremeties(feet, legs, hands, arm)). On 21-Jan-2021, the patient experienced BURNING SENSATION (burning sensation/episodes of hot,burning) and ERYTHEMA (redness feet and hands). On 23-Jan-2021, the patient experienced SKIN DISORDER (every pore on her skin looks like it has been pin pricked). The patient was treated with PARACETAMOL (TYLENOL) for Adverse event, at a dose of UNK dosage form and NAPROXEN SODIUM (ALEVE) for Adverse event, at an unspecified dose and frequency. On 15-Jan-2021, HEADACHE (headache) and INJECTION SITE PAIN (soreness on the injection site) had resolved. At the time of the report, HYPOAESTHESIA (numbness and tingling in her limbs/ all extremeties(feet, legs, hands, arm)), BURNING SENSATION (burning sensation/episodes of hot,burning), PARAESTHESIA (numbness and tingling in her limbs/pins and needles sensation/ tingling in all extremeties(feet, legs, hands, arm)) and ERYTHEMA (redness feet and hands) had not resolved and SKIN DISORDER (every pore on her skin looks like it has been pin pricked) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): In 2021, Blood test: normal (normal) normal. In 2021, Electromyogram: normal (normal) large fiber neuro-normal. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. On an unknown date, patient have done COVOD-19 test twice.it was negative both times. The patient reported patient now have these symptoms on and off for over 5 months. They have been intermittent on all days. The patient has seen his medical provider via viedo appointment. She wanted to know if wants to know if there have been reports of Guillain Barre syndrome after the administration of the Moderna Covid-19 vaccine. Most recent FOLLOW-UP information incorporated above includes: On 29-Jun-2021: Significant follow up was received on the date 29-JUN-2021, reporter and patient details, lab data, medical history concomitant drugs, event terms, corrective treatment, events outcome were updated

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Test Date: 2021; Test Name: Blood work; Result Unstructured Data: normal; Test Date: 2021; Test Name: EMG; Result Unstructured Data: large fiber neuro-normal
Aktuelle Erkrankungen: Chronic back pain (Flares on and off); Drug allergy (steroids (oral and injection)); Drug allergy (Gabapentin); Erythromelalgia (worsening); Lumbar radiculopathy; Peripheral neuropathy (worsening)
Vorgeschichte: Medical History/Concurrent Conditions: Tinnitus (it was constant)
Andere Medikamente: NORTRIPTYLINE; ATIVAN
Allergien: -
Vorherige Impfungen: -

VAERS 1555088

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: RI
Alter: 50,0
Geschlecht: F
Eingang: 13.08.2021
Impfdatum: 28.12.2020
Beginn: 28.12.2020
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / LA

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

Headache Palpitations

Symptomtext

Palpitations; Headache; This spontaneous case was reported by a patient and describes the occurrence of PALPITATIONS (Palpitations) and HEADACHE (Headache) in a 50-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 011J20A) for COVID-19 vaccination. Concurrent medical conditions included Asthma, Hypertension and Sulfonamide allergy. Concomitant products included HYDROCHLOROTHIAZIDE and LISINOPRIL for Hypertension, SERTRALINE for an unknown indication. On 28-Dec-2020 at 6:15 AM, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 28-Dec-2020 at 6:45 AM, the patient experienced PALPITATIONS (Palpitations) and HEADACHE (Headache). At the time of the report, PALPITATIONS (Palpitations) and HEADACHE (Headache) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Based on the current available information and temporal association between the use of the product and the start date of the events within 30 minutes after vaccination, a causal relationship cannot be excluded. Further information has been requested; Reporter's Comments: Based on the current available information and temporal association between the use of the product and the start date of the events within 30 minutes after vaccination, a causal relationship cannot be excluded. Further information has been requested

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Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Asthma; Hypertension; Sulfonamide allergy
Vorgeschichte: -
Andere Medikamente: HYDROCHLOROTHIAZIDE; LISINOPRIL; SERTRALINE
Allergien: -
Vorherige Impfungen: -

VAERS 1553113

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: FL
Alter: 48,0
Geschlecht: F
Eingang: 13.08.2021
Impfdatum: 30.12.2020
Beginn: 26.01.2021
Tage bis Beginn: 27,0
Dosis: 2
Route/Site: OT / RA

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

Antineutrophil cytoplasmic antibody Chills Malaise Tremor

Symptomtext

Her myeloperoxidase level went from 234 - 756; very sick; shaking; chills; A spontaneous report was received from a healthcare professional concerning a 48-years-old female patient who received Moderna's COVID-19 vaccine (mRNA-1273) and experienced events very sick, shaking, chills, her myeloperoxidase level went from 234 - 756. The patient's medical history was not provided. No relevant concomitant medications were reported. On 30 Dec 2020, prior to the onset of the events the patient received first of two planned doses of mRNA-1273 (lot/batch: 011J20A) via unknown route in the right arm for prophylaxis of COVID-19 infection. On 26 Jan 2021, prior to the onset of the events the patient received their second of two planned doses of mRNA-1273 (lot/batch: 028L20A) via unknown route in the right arm for prophylaxis of COVID-19 infection. On 26 Jan 2021, the patient experienced the event(s) very sick, shaking, chills. On 16 Feb 2021, the patient experienced the event(s) her myeloperoxidase level went from 234 - 756. No treatment information was provided. Action taken with mRNA-1273 in response to the events was not reported. On 28 Jan 2021 the outcome of event(s), very sick, shaking, chills was resolved. On23 Feb 2021 the outcome of event(s), her myeloperoxidase level went from 234 - 756 was resolved.

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Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: No adverse event
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1552957

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: FL
Alter: 87,0
Geschlecht: F
Eingang: 13.08.2021
Impfdatum: 16.01.2021
Beginn: 16.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / LA

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

Chest discomfort Dyspnoea Hyperhidrosis Vaccination site erythema Vaccination site pain

Symptomtext

red mark at the injection site that's about 6 inches long; felt like somebody grabbed me in the chest; I started pouring sweat; I could hardly catch my breath; Arm was sore at the injection site; A spontaneous report was received from a Consumer concerning a 87 Years-old female patient who received Moderna's COVID-19 vaccine (mRNA-1273) and experienced events- chest discomfort, hyperhidrosis, dyspnea, vaccination site pain and vaccination site erythema. The patient's medical history was not provided. No relevant concomitant medications were reported. On 16/Jan/2021, prior to the onset of the events, the patient received their first of two planned doses of mRNA-1273 (lot/batch: 011J20A) intramuscularly in the left arm for prophylaxis of COVID-19 infection. On 16 Jan 2021, the patient experienced that her arm was sore at the injection site that night. She also reported that on Tuesday night (02Feb2021), she bent over to pick something up and had a cardiac episode. She describes it as if "somebody grabbed me in the chest and I started pouring sweat, and I could hardly catch my breath." She reported 2 such episodes that same evening (02Feb2021). She also reported that she currently has a red mark at the injection site that's about 6 inches long (4 Feb 2021) Laboratory details were not provided. No treatment information was provided. The patient did not go to the hospital, but did inform her doctor and set an appointment. Action taken with mRNA-1273 in response to the events was not reported. At the time of this report, the outcome of the events- chest discomfort, hyperhidrosis, dyspnoea, vaccination site pain and vaccination site erythema was considered unknown.; Reporter's Comments: This case concerns a 87 Years-old, female patient who experienced events of chest discomfort, hyperhidrosis, dyspnea, vaccination site pain and vaccination site erythema. Based on the current available information and temporal association between the use of the product and the start date of the event, a causal relationship cannot be excluded. Further information has been requested.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: No adverse event (No reported medical history.)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1552482

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: CA
Alter: 74,0
Geschlecht: F
Eingang: 13.08.2021
Impfdatum: 19.02.2021
Beginn: 19.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / LA

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

Back pain Decreased appetite Diarrhoea Dyspnoea Erythema Fatigue Hypersensitivity Induration Somnolence Swelling

Symptomtext

she's so tired; really bad low backache; diarrhea; I slept all day; didn't eat; She feels she has less appetite; Real bad allergy; she couldn't breathe very well; her arm was red; her arm was swollen; her arm was hard; A spontaneous report was received from a consumer concerning a 74-years-old female patient who received Moderna's COVID-19 vaccine (mRNA-1273) and experienced events real bad allergy, she couldn't breathe very well, her arm was red, her arm was swollen, her arm was hard, slept all day, didn't eat, she's so tired, really bad low backache, diarrhea, and she feels she has less appetite. The patient's medical history was not provided. Concomitant medications reported were losartan, atorvastatin, bupropion for drug use for unknown indication. On 19 Feb 2021, prior to the onset of the events the patient received first of two planned doses of mRNA-1273 (lot/batch: 011J20A) intramuscularly in the left arm for prophylaxis of COVID-19 infection. On 19 Feb 2021, the patient experienced the events real bad allergy, she couldn't breathe very well, her arm was red, her arm was swollen, and her arm was hard. On 20 Feb 2021, the patient experienced the events I slept all day, and didn't eat. On 21 Feb 2021, the patient experienced the events she's so tired, really bad low backache, diarrhea, and she feels she has less appetite. Treatment details included Tylenol. Action taken with mRNA-1273 in response to the events was not reported. On 21 Feb 2021, the outcome of events real bad allergy and she couldn't breathe very well was resolved. On 20 Feb 2021, the outcome of events, slept all day, didn't eat and diarrhea was resolved. The outcome of events her arm was red, her arm was swollen, her arm was hard, she's so tired, really bad low backache, and she feels she has less appetite was unknown.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: No adverse event
Andere Medikamente: LOSARTAN; ATORVASTATIN; WELLBUTRIN
Allergien: -
Vorherige Impfungen: -

VAERS 1552292

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: PA
Alter: 57,0
Geschlecht: F
Eingang: 13.08.2021
Impfdatum: 04.01.2021
Beginn: 03.02.2021
Tage bis Beginn: 30,0
Dosis: 1
Route/Site: OT / -

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

Anxiety Arthralgia Headache Pain in extremity Tremor

Symptomtext

Shaking; anxiety; arm pain that went worse after the second dose; joint pain; Headaches; This spontaneous case was reported by a consumer (subsequently medically confirmed) and describes the occurrence of TREMOR (Shaking), ANXIETY (anxiety), PAIN IN EXTREMITY (arm pain that went worse after the second dose), ARTHRALGIA (joint pain) and HEADACHE (Headaches) in a 57-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 029L20A and 011J20A) for COVID-19 vaccination. Concomitant products included DULOXETINE HYDROCHLORIDE (CYMBALTA) and INDOMETHACIN [INDOMETACIN] for an unknown indication. On 04-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 03-Feb-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 03-Feb-2021, the patient experienced TREMOR (Shaking), ANXIETY (anxiety), PAIN IN EXTREMITY (arm pain that went worse after the second dose), ARTHRALGIA (joint pain) and HEADACHE (Headaches). At the time of the report, TREMOR (Shaking) was resolving and ANXIETY (anxiety), PAIN IN EXTREMITY (arm pain that went worse after the second dose), ARTHRALGIA (joint pain) and HEADACHE (Headaches) outcome was unknown. Treatment information was not provided. On an unknown date, post-vaccination, the patient was seen by a neurologist for the shaking. Per the reporter, the neurologist stated they were unsure if the patient had a movement disorder but the tremors will slowly go away. This case was linked to MOD-2021-022325 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 07-Jun-2021: Follow up received on 07 Jun 2021. Updated reporter information, concomitant medications and events.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: CYMBALTA; INDOMETHACIN [INDOMETACIN]
Allergien: -
Vorherige Impfungen: -

VAERS 1551992

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: LA
Alter: 76,0
Geschlecht: F
Eingang: 13.08.2021
Impfdatum: 15.01.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: OT / RA

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

COVID-19 Dehydration Diarrhoea Nausea Vomiting

Symptomtext

COVID-19; DEHYDRATION; Diarrhea; Nausea; Vomiting; This spontaneous case was reported by a pharmacist and describes the occurrence of COVID-19 (COVID-19), DEHYDRATION (DEHYDRATION), DIARRHOEA (Diarrhea), NAUSEA (Nausea) and VOMITING (Vomiting) in a 76-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 011J20A and 024M20A) for COVID-19 vaccination. Concurrent medical conditions included Crohn's disease. On 15-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 11-Feb-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On an unknown date, the patient experienced COVID-19 (COVID-19), DEHYDRATION (DEHYDRATION), DIARRHOEA (Diarrhea), NAUSEA (Nausea) and VOMITING (Vomiting). At the time of the report, COVID-19 (COVID-19), DIARRHOEA (Diarrhea), NAUSEA (Nausea) and VOMITING (Vomiting) outcome was unknown and DEHYDRATION (DEHYDRATION) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Concomitant product use was not provided by the reporter. ?No treatment information was provided. ? Most recent FOLLOW-UP information incorporated above includes: On 26-Jul-2021: Follow up added. New events added.

Weitere VAERSDATA-Felder

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

VAERS 1551853

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: AZ
Alter: 48,0
Geschlecht: F
Eingang: 13.08.2021
Impfdatum: 08.01.2021
Beginn: 08.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / RA

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

Agitation Back pain Dyspnoea Fatigue

Symptomtext

Feeling tired; t's hard to breath; Get's agitated a lot; Back pain when she lays down; This spontaneous case was reported by a physician and describes the occurrence of FATIGUE (Feeling tired), DYSPNOEA (t's hard to breath), AGITATION (Get's agitated a lot) and BACK PAIN (Back pain when she lays down) in a 48-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 011J20A) for COVID-19 vaccination. no medical history is provided and concomitant drugs are provided. Concomitant products included PREGABALIN, LEVOTHYROXINE SODIUM (EUTHYROX), ASCORBIC ACID (VIT C), ZINC and FISH OIL for an unknown indication. On 08-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 08-Jan-2021, the patient experienced FATIGUE (Feeling tired), DYSPNOEA (t's hard to breath), AGITATION (Get's agitated a lot) and BACK PAIN (Back pain when she lays down). At the time of the report, FATIGUE (Feeling tired), DYSPNOEA (t's hard to breath), AGITATION (Get's agitated a lot) and BACK PAIN (Back pain when she lays down) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: no medical history is provided and concomitant drugs are provided.
Andere Medikamente: PREGABALIN; EUTHYROX; VIT C; ZINC; FISH OIL.
Allergien: -
Vorherige Impfungen: -

VAERS 1551771

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: LA
Alter: -
Geschlecht: F
Eingang: 13.08.2021
Impfdatum: 12.01.2021
Beginn: 12.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / LA

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

Blood pressure measurement Fatigue Feeling abnormal Hypersensitivity Hypertension Injection site pain Malaise Pruritus Rash Skin warm Vaccination site swelling

Symptomtext

Blood pressure was very very high; Felt terrible; Itching; Rash goin gall the way to elbow; Left arm was hot; Swollen; allergic reaction unspecified/adverse allergic reaction; Didn't feel good; Feel very tired; Left arm was sore; This spontaneous case was reported by a consumer (subsequently medically confirmed) and describes the occurrence of MALAISE (Didn't feel good), SKIN WARM (Left arm was hot), VACCINATION SITE SWELLING (Swollen), HYPERTENSION (Blood pressure was very very high) and FEELING ABNORMAL (Felt terrible) in a 70-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 011J20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concurrent medical conditions included Blood pressure high (Unspecified blood pressure) and Glaucoma. Concomitant products included HYDROCHLOROTHIAZIDE, VALSARTAN (VALSARTAN HCTZ) for Blood pressure abnormal, NAPHAZOLINE HYDROCHLORIDE (EYE DROPS [NAPHAZOLINE HYDROCHLORIDE]) for Glaucoma, SIMVASTATIN for an unknown indication. On 12-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 12-Jan-2021, the patient experienced INJECTION SITE PAIN (Left arm was sore). On 18-Jan-2021, the patient experienced MALAISE (Didn't feel good) and FATIGUE (Feel very tired). On 21-Jan-2021, the patient experienced SKIN WARM (Left arm was hot), VACCINATION SITE SWELLING (Swollen), RASH (Rash goin gall the way to elbow) and HYPERSENSITIVITY (allergic reaction unspecified/adverse allergic reaction). On 22-Jan-2021, the patient experienced HYPERTENSION (Blood pressure was very very high), FEELING ABNORMAL (Felt terrible) and PRURITUS (Itching). The patient was treated with PREDNISONE for Adverse event, at an unspecified dose and frequency; PEPSIN for Adverse event, at an unspecified dose and frequency and DIPHENHYDRAMINE HYDROCHLORIDE (BENADRYL [DIPHENHYDRAMINE HYDROCHLORIDE]) for Adverse event, at an unspecified dose and frequency. At the time of the report, MALAISE (Didn't feel good), SKIN WARM (Left arm was hot), VACCINATION SITE SWELLING (Swollen), HYPERTENSION (Blood pressure was very very high), FEELING ABNORMAL (Felt terrible), PRURITUS (Itching), INJECTION SITE PAIN (Left arm was sore) and FATIGUE (Feel very tired) had resolved, RASH (Rash goin gall the way to elbow) was resolving and HYPERSENSITIVITY (allergic reaction unspecified/adverse allergic reaction) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 22-Jan-2021, Blood pressure measurement: 166/100 166/100. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Most recent FOLLOW-UP information incorporated above includes: On 23-Mar-2021: NNI No specific follow-up information recorded.

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Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: Test Date: 20210122; Test Name: Blood pressure; Result Unstructured Data: 166/100; Comments: 166/100
Aktuelle Erkrankungen: Blood pressure high (Unspecified blood pressure)
Vorgeschichte: Medical History/Concurrent Conditions: Glaucoma
Andere Medikamente: VALSARTAN HCTZ; SIMVASTATIN; EYE DROPS [NAPHAZOLINE HYDROCHLORIDE]
Allergien: -
Vorherige Impfungen: -

VAERS 1551597

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: MD
Alter: -
Geschlecht: F
Eingang: 13.08.2021
Impfdatum: 16.01.2021
Beginn: 16.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / -

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

Condition aggravated Injection site discolouration Injection site erythema Injection site pain Injection site pruritus Injection site swelling Injection site warmth Pain in extremity

Symptomtext

Arm sore; injection site became red, hot and swollen; injection site became red, hot and swollen; injection site became red, hot and swollen; there was little bit itching on there; injection site exactly is a darker shade.; still tender; it started growing, the redness spread.; This spontaneous case was reported by a consumer and describes the occurrence of INJECTION SITE ERYTHEMA (injection site became red, hot and swollen), INJECTION SITE WARMTH (injection site became red, hot and swollen), INJECTION SITE SWELLING (injection site became red, hot and swollen), INJECTION SITE PRURITUS (there was little bit itching on there) and PAIN IN EXTREMITY (Arm sore) in a 46-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 011J20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No medical history was provided by the reporter. Concomitant products included VITAMINS NOS for an unknown indication. On 16-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 16-Jan-2021, the patient experienced CONDITION AGGRAVATED (it started growing, the redness spread.) and INJECTION SITE PAIN (still tender). On 26-Jan-2021, the patient experienced INJECTION SITE DISCOLOURATION (injection site exactly is a darker shade.). On an unknown date, the patient experienced INJECTION SITE ERYTHEMA (injection site became red, hot and swollen), INJECTION SITE WARMTH (injection site became red, hot and swollen), INJECTION SITE SWELLING (injection site became red, hot and swollen), INJECTION SITE PRURITUS (there was little bit itching on there) and PAIN IN EXTREMITY (Arm sore). The patient was treated with PARACETAMOL (TYLENOL) at an unspecified dose and frequency. At the time of the report, INJECTION SITE ERYTHEMA (injection site became red, hot and swollen), INJECTION SITE WARMTH (injection site became red, hot and swollen), INJECTION SITE SWELLING (injection site became red, hot and swollen), INJECTION SITE PRURITUS (there was little bit itching on there), PAIN IN EXTREMITY (Arm sore), CONDITION AGGRAVATED (it started growing, the redness spread.), INJECTION SITE DISCOLOURATION (injection site exactly is a darker shade.) and INJECTION SITE PAIN (still tender) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. This case was linked to MOD-2021-017910 (Linked Report).; Sender's Comments: MOD-2021-017910:Same reporter/ Different patient (Daughter)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: No medical history was provided by the reporter.
Andere Medikamente: VITAMINS NOS
Allergien: -
Vorherige Impfungen: -

VAERS 1551165

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: FL
Alter: 72,0
Geschlecht: F
Eingang: 13.08.2021
Impfdatum: 06.01.2021
Beginn: 08.01.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: OT / RA

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

Burning sensation Chest discomfort Confusional state Dizziness Dyspnoea Ear pain Facial pain Fatigue Flushing Headache Intentional product use issue Palpitations Quality of life decreased Vaccination site pain

Symptomtext

dizziness and lightheadedness especially from rising from a lying down position; flushing in the neck, face and ears when I attempted to walk for exercise; chest tightness; burning on the left side of my face on from the edge of the check to my ear.; piercing nerve ending pain in my right ear which comes and goes; The side of my face also becaume very sore to the touch.; symptoms affected quality of life; Intentional deviation from dosage regimen; Brain fog; Injection site Soreness; intermittent and recurring headaches; Palpitation / irregular heart rate; Shortness of breath; Fatigue; This spontaneous case was reported by a consumer and describes the occurrence of PALPITATIONS (Palpitation / irregular heart rate), DYSPNOEA (Shortness of breath), DIZZINESS (dizziness and lightheadedness especially from rising from a lying down position), FLUSHING (flushing in the neck, face and ears when I attempted to walk for exercise) and CHEST DISCOMFORT (chest tightness) in a 72-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 011J20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concurrent medical conditions included Trigeminal neuralgia. Concomitant products included AMITRIPTYLINE from 02-Jan-1994 to an unknown date for Trigeminal neuralgia. On 06-Jan-2021 at 9:15 AM, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 08-Jan-2021, the patient experienced PALPITATIONS (Palpitation / irregular heart rate), DYSPNOEA (Shortness of breath) and FATIGUE (Fatigue). On an unknown date, the patient experienced DIZZINESS (dizziness and lightheadedness especially from rising from a lying down position), FLUSHING (flushing in the neck, face and ears when I attempted to walk for exercise), CHEST DISCOMFORT (chest tightness), BURNING SENSATION (burning on the left side of my face on from the edge of the check to my ear.), EAR PAIN (piercing nerve ending pain in my right ear which comes and goes), FACIAL PAIN (The side of my face also becaume very sore to the touch.), QUALITY OF LIFE DECREASED (symptoms affected quality of life), INTENTIONAL PRODUCT USE ISSUE (Intentional deviation from dosage regimen), CONFUSIONAL STATE (Brain fog), VACCINATION SITE PAIN (Injection site Soreness) and HEADACHE (intermittent and recurring headaches ). At the time of the report, PALPITATIONS (Palpitation / irregular heart rate), DYSPNOEA (Shortness of breath), DIZZINESS (dizziness and lightheadedness especially from rising from a lying down position), FLUSHING (flushing in the neck, face and ears when I attempted to walk for exercise), CHEST DISCOMFORT (chest tightness), BURNING SENSATION (burning on the left side of my face on from the edge of the check to my ear.), EAR PAIN (piercing nerve ending pain in my right ear which comes and goes), FACIAL PAIN (The side of my face also becaume very sore to the touch.), QUALITY OF LIFE DECREASED (symptoms affected quality of life), CONFUSIONAL STATE (Brain fog), VACCINATION SITE PAIN (Injection site Soreness), FATIGUE (Fatigue) and HEADACHE (intermittent and recurring headaches ) had not resolved and INTENTIONAL PRODUCT USE ISSUE (Intentional deviation from dosage regimen) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Treatment information was not provided by the reporter. Most recent FOLLOW-UP information incorporated above includes: On 08-Jul-2021: Follow-up received and events added and event outcomes updated.

Weitere VAERSDATA-Felder

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

VAERS 1550448

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: PR
Alter: 61,0
Geschlecht: F
Eingang: 12.08.2021
Impfdatum: 08.01.2021
Beginn: 13.01.2021
Tage bis Beginn: 5,0
Dosis: 1
Route/Site: OT / LA

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

Arthralgia Lymphadenopathy Tachycardia

Symptomtext

Tachycardia; Lymphadenopathy; Arthralgia in the fingers; A spontaneous report was received from a consumer concerning a 61-Years-old female patient who received Moderna's COVID-19 vaccine (mRNA-1273) and experienced arthralgia in the fingers, lymphadenopathy and tachycardia. The patient's medical history was not provided. Concomitant medications reported included Synthroid (levothyroxine sodium) and Lipitor (atorvastatin calcium). On 08 Jan 2021, 6 days prior to the onset of the event Arthralgia in the fingers the patient received their first of two planned doses of mRNA-1273 (011J20A) in the left arm for prophylaxis of COVID-19 infection. On 13 Jan 2021, the patient experienced arthralgia in the fingers. On 15 Jan 2021, the patient experienced lymphadenopathy in the left arm. On 25 Jan 2021, the patient experienced tachycardia. No treatment information was provided. Action taken with mRNA-1273 in response to the event was not reported. On 25 Jan 2021, the outcome of the event tachycardia was resolved. The outcome of the events arthralgia in the fingers and lymphadenopathy was not reported.; Reporter's Comments: This case concerns a 61-year-old female who experienced a nonserious unexpected event of tachycardia and nonserious expected events of lymphadenopathy and arthralgia. Event onset was 6 days after the first dose of mRNA-1273. Treatment not reported. Tachycardia resolved, but other event outcomes unknown. Based on current available information and temporal association between the use of the product and the start date of the event, a causal relationship cannot be excluded.

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Praegender Schweregrund: Tachycardia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: No adverse event (No reported medical history.)
Andere Medikamente: SYNTHROID; LIPITOR
Allergien: -
Vorherige Impfungen: -

VAERS 1550133

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: -
Alter: -
Geschlecht: F
Eingang: 12.08.2021
Impfdatum: 29.12.2020
Beginn: 29.12.2020
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / LA

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

Blood pressure increased Chills Cold sweat Dizziness Headache Heart rate increased Hypertension Oxygen saturation Palpitations Tachycardia

Symptomtext

felt dizzy; Plapitation; tachycardia; Blood pressure went up; clammy; headache; cold and clammy; A spontaneous report was received from a physician concerning a 74 year old, female patient who received first dose of Moderna's COVID-19 vaccine and experienced headache, dizzy feeling, chill, palpitation, blood pressure went up, clummy and tachycardia. The patient's medical history was not provided. Concomitant product used was not provided by the reporter. On 29 DEC 2020, the patient received their first of two planned doses of mRNA-1273 (lot no: 011J20A) intramuscularly in the left arm for prophylaxis of COVID-19 infection. The patient experienced headache, dizzy feeling, started getting palpitation, her heart beats was 132 bpm. her blood pressure increased and oxygen levels were normal and the patient did not required oxygen. She started feeling cold and clammy and was in injection area of hospital for 2 hours with constant monitoring. She did not take any medication but drank lots of water. The patient was concerned of whether she should receive the second dose given the symptoms experienced after the first dose. Action taken with mRNA-1273 in response to the events were not reported. The outcome of the events headache, dizzy feeling, chill, palpitation, clammy, blood pressure went up and tachycardia were unknown.; Reporter's Comments: Based on the current available information and temporal association between the use of the product and the start date of these events, a causal relationship cannot be excluded.

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Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: Test Date: 20201229; Test Name: Blood pressure went up; Result Unstructured Data: Increased; Test Date: 20201229; Test Name: heart rate went up; Result Unstructured Data: Increased; Test Date: 20201229; Test Name: Oxygen level; Result Unstructured Data: normal
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: No adverse event (No reported medical history.)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1547517

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: LA
Alter: -
Geschlecht: F
Eingang: 12.08.2021
Impfdatum: 23.12.2020
Beginn: 24.12.2020
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: OT / LA

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

Injection site hypersensitivity Joint stiffness Migraine Pain

Symptomtext

Migraine; Joint stiffness; Skin feels hypersensitive especially at injection site; Body aches; A spontaneous report was received from a nurse concerning a 25-years-old, white, female patient who was participating in the mRNA-1273 Emergency Use Program and experienced multiple events of migraine, body aches, joint stiffness and skin feels hypersensitive at injection site. The patient's medical history as provided by the reporter, included COVID-19 and allergy to amoxicillin/ clavulanic acid. Concomitant medications reported included fish oil, colecalciferol, cetirizine hydrochloride and vitamins. On 23 Dec 2020, approximately sixteen hours prior to the onset of the symptoms, the patient received their first of two planned doses of mRNA-1273 (lot number: 011J20A) intramuscularly in the left arm for COVID-19 prophylaxis. On 24 Dec 2020, the patient experienced migraine, body aches, joint stiffness and injection site hypersensitivity. The treatment for the events included paracetamol, and the symptoms improved. Action taken with mRNA-1273 in response to the events was not reported. The outcome for the events, migraine, body aches, joint stiffness and skin feels hypersensitive at injection site, were unknown.; Reporter's Comments: This case concerns a 25-years-old, white, female patient who received their first of two planned doses of mRNA-1273 (Lot-# 011J20A; expiration date- unknown), reporting an unexpected event of migraine, joint stiffness, injection site hypersensitivity and an expected event of pain (body aches). The event occurred 15 hrs. 52 min after vaccine administration. Due to the temporal association between the onset of events and administration of vaccine, a causal relationship cannot be excluded.

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Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Drug allergy (Augmentin)
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19
Andere Medikamente: FISH OIL; VITAMIN D [COLECALCIFEROL]; ZYRTEC [CETIRIZINE HYDROCHLORIDE]; DAILY VITAMINS
Allergien: -
Vorherige Impfungen: -

VAERS 1544301

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: CA
Alter: 33,0
Geschlecht: F
Eingang: 11.08.2021
Impfdatum: 23.12.2020
Beginn: 01.01.2021
Tage bis Beginn: 9,0
Dosis: 1
Route/Site: OT / LA

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

COVID-19 Chills Dyspnoea Headache Influenza like illness Myalgia Pyrexia

Symptomtext

Covid-19; shortness of breath; headache; flu-like symptoms; body aches; fever of 101; chills; This spontaneous case was reported by a consumer and describes the occurrence of INFLUENZA LIKE ILLNESS (flu-like symptoms), DYSPNOEA (shortness of breath), COVID-19 (Covid-19), MYALGIA (body aches) and PYREXIA (fever of 101) in a 33-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 042L20A and 011J20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 23-Dec-2020, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 01-Jan-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 01-Jan-2021, the patient experienced INFLUENZA LIKE ILLNESS (flu-like symptoms), MYALGIA (body aches), PYREXIA (fever of 101) and CHILLS (chills). On 10-Feb-2021, the patient experienced DYSPNOEA (shortness of breath) and HEADACHE (headache). On 11-Feb-2021, the patient experienced COVID-19 (Covid-19). On 02-Jan-2021, INFLUENZA LIKE ILLNESS (flu-like symptoms), MYALGIA (body aches), PYREXIA (fever of 101) and CHILLS (chills) had resolved. At the time of the report, DYSPNOEA (shortness of breath), COVID-19 (Covid-19) and HEADACHE (headache) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No relevant concomitant medication reported. Patient took Tylenol and Ibuprofen for treatment.

Weitere VAERSDATA-Felder

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

VAERS 1544069

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: FL
Alter: -
Geschlecht: F
Eingang: 11.08.2021
Impfdatum: 29.12.2020
Beginn: 30.12.2020
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: OT / LA

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

Burning sensation COVID-19 Hypoaesthesia Paraesthesia

Symptomtext

Positive for Covid-19 after receiving vaccine; burning; tingling; numbness; This spontaneous case was reported by a nurse (subsequently medically confirmed) and describes the occurrence of COVID-19 (Positive for Covid-19 after receiving vaccine), BURNING SENSATION (burning), PARAESTHESIA (tingling) and HYPOAESTHESIA (numbness) in a 45-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 011J20A and 028L20A) for COVID-19 vaccination. Concurrent medical conditions included Respiratory disorder (Chronic respiratory conditions, asthma) and Obesity. On 29-Dec-2020, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On an unknown date, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 30-Dec-2020 at 12:00 PM, the patient experienced BURNING SENSATION (burning), PARAESTHESIA (tingling) and HYPOAESTHESIA (numbness). On an unknown date, the patient experienced COVID-19 (Positive for Covid-19 after receiving vaccine). At the time of the report, COVID-19 (Positive for Covid-19 after receiving vaccine) outcome was unknown and BURNING SENSATION (burning), PARAESTHESIA (tingling) and HYPOAESTHESIA (numbness) had not resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, COVID-19: (Positive) positive. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medications reported. Treatment information was unknown. Most recent FOLLOW-UP information incorporated above includes: On 20-Apr-2021: Follow up information included reporter details, patient demographics details , product details, event information and causality.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Test Name: covid-19; Test Result: Positive ; Result Unstructured Data: positive
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Obesity; Respiratory disorder (Chronic respiratory conditions, asthma)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1543585

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: MA
Alter: -
Geschlecht: F
Eingang: 11.08.2021
Impfdatum: 30.12.2020
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: OT / LA

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

Blood pressure measurement Breast enlargement Breast swelling Chest pain Computerised tomogram Electrocardiogram Fibrin D dimer Ligament sprain Lymphadenopathy X-ray

Symptomtext

lymph node enlargement; Left breat was heavier than right; If I press around the lining by the chest or sternum, it hurts; Sprain; Felt some swelling on the lining of the brest; This spontaneous case was reported by a nurse and describes the occurrence of LYMPHADENOPATHY (lymph node enlargement), CHEST PAIN (If I press around the lining by the chest or sternum, it hurts), LIGAMENT SPRAIN (Sprain) and BREAST SWELLING (Felt some swelling on the lining of the brest) in a 55-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 011J20A) for COVID-19 vaccination. Concurrent medical conditions included Hypertension. On 30-Dec-2020, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .5 ml. On an unknown date, the patient experienced LYMPHADENOPATHY (lymph node enlargement), CHEST PAIN (If I press around the lining by the chest or sternum, it hurts), LIGAMENT SPRAIN (Sprain) and BREAST SWELLING (Felt some swelling on the lining of the brest). At the time of the report, LYMPHADENOPATHY (lymph node enlargement), CHEST PAIN (If I press around the lining by the chest or sternum, it hurts), LIGAMENT SPRAIN (Sprain) and BREAST SWELLING (Felt some swelling on the lining of the brest) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, Blood pressure measurement: mmHg Inconclusive. On an unknown date, Computerised tomogram: negative Negative. On an unknown date, Electrocardiogram: Inconclusive. On an unknown date, Fibrin D dimer: high ng/mL (High) The D-Dimer was elevated which indicated a chance for DVT. On an unknown date, X-ray: (Inconclusive) The X-ray taken was unclear. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No treatment information was provided. No concomitant medication was provided.

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Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Test Name: EKG; Test Result: Inconclusive ; Test Name: D-Dimer; Result Unstructured Data: The D-Dimer was elevated which indicated a chance for DVT; Test Name: X-Ray; Test Result: Inconclusive ; Result Unstructured Data: The X-ray taken was unclear; Test Name: blood pressure; Test Result: Inconclusive ; Test Name: CT; Test Result: Negative
Aktuelle Erkrankungen: Hypertension
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1543547

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: NV
Alter: 45,0
Geschlecht: F
Eingang: 11.08.2021
Impfdatum: 28.12.2020
Beginn: 30.12.2020
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: OT / RA

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

Asthenia Dizziness Dysstasia Pruritus Skin burning sensation Tremor Urticaria Vision blurred

Symptomtext

Tremors; Can hardly stand up; Blurred vision; Itching everywhere; Burning of the skin; Light headedness, dizziness; Weakness; Hives; This spontaneous case was reported by a consumer (subsequently medically confirmed) and describes the occurrence of TREMOR (Tremors), DYSSTASIA (Can hardly stand up), VISION BLURRED (Blurred vision), PRURITUS (Itching everywhere) and SKIN BURNING SENSATION (Burning of the skin) in a 45-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 011J20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included No adverse event (No medical history was reported.) Concomitant products included PREDNISONE for an unknown indication. On 28-Dec-2020, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 30-Dec-2020, the patient experienced TREMOR (Tremors), DYSSTASIA (Can hardly stand up), VISION BLURRED (Blurred vision), PRURITUS (Itching everywhere), SKIN BURNING SENSATION (Burning of the skin), DIZZINESS (Light headedness, dizziness), ASTHENIA (Weakness) and URTICARIA (Hives). At the time of the report, TREMOR (Tremors), DYSSTASIA (Can hardly stand up), VISION BLURRED (Blurred vision), PRURITUS (Itching everywhere), SKIN BURNING SENSATION (Burning of the skin), DIZZINESS (Light headedness, dizziness), ASTHENIA (Weakness) and URTICARIA (Hives) had not resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Concomitant product use was not provided by the reporter. Company Comment: Based on the current available information and temporal association between the use of the product and the start date of the events, a causal relationship cannot be excluded.; Reporter's Comments: Based on the current available information and temporal association between the use of the product and the start date of the events, a causal relationship cannot be excluded.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: No adverse event (No medical history was reported.)
Andere Medikamente: PREDNISONE
Allergien: -
Vorherige Impfungen: -

VAERS 1543151

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: KS
Alter: 49,0
Geschlecht: F
Eingang: 11.08.2021
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: OT / LA

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

Dizziness Dyspnoea Feeling abnormal Maternal exposure during pregnancy Pain in extremity Swollen tongue Throat tightness

Symptomtext

Tongue started feelin weird and swollen, swelling of upper airways; Tongue started feelin weird and swollen; Dizzy; Little trouble breathing, difficulty breathing; Arm hurt something terrible; Sensation of throat closing; Maternal exposure during pregnancy; This spontaneous prospective pregnancy case was reported by an other health care professional (subsequently medically confirmed) and describes the occurrence of SWOLLEN TONGUE (Tongue started feelin weird and swollen, swelling of upper airways), FEELING ABNORMAL (Tongue started feelin weird and swollen), DIZZINESS (Dizzy), DYSPNOEA (Little trouble breathing, difficulty breathing) and PAIN IN EXTREMITY (Arm hurt something terrible) in a 49-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 011J20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included Anaphylaxis. Concurrent medical conditions included Asthma, Hay fever since 1971, Drug allergy (Claritin - anaphylaxis/hives) in 2002, Drug allergy (Penicillin - anaphylaxis/hives) in 1972, Drug allergy (Robutissin - Red blotches/itching) in 1984, Reactive airways disease (Has improved) since 1971, Fatty liver (Improved with healthier diet) since December 2020 and Diverticulosis (Improved with healthier diet) since December 2020. Concomitant products included DIPHENHYDRAMINE HYDROCHLORIDE (BENADRYL [DIPHENHYDRAMINE HYDROCHLORIDE]) for Allergy, BACILLUS COAGULANS (PROBIOTIC GUMMIES) for Diverticulitis, TOCOPHEROL (VITAMIN E [TOCOPHEROL]) for Fatty liver, ASCORBIC ACID (VITAMIN C PLUS [ASCORBIC ACID]) for Immunisation, CIMICIFUGA RACEMOSA RHIZOME, CIMICIFUGA RACEMOSA ROOT (BLACK COHOSH [CIMICIFUGA RACEMOSA RHIZOME;CIMICIFUGA RACEMOSA ROOT]) for Menopause. On an unknown date, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. Last menstrual period and estimated date of delivery were not provided. On an unknown date, the patient experienced SWOLLEN TONGUE (Tongue started feelin weird and swollen, swelling of upper airways), FEELING ABNORMAL (Tongue started feelin weird and swollen), DIZZINESS (Dizzy), DYSPNOEA (Little trouble breathing, difficulty breathing), PAIN IN EXTREMITY (Arm hurt something terrible), THROAT TIGHTNESS (Sensation of throat closing) and MATERNAL EXPOSURE DURING PREGNANCY (Maternal exposure during pregnancy). On 16-Jan-2021, PAIN IN EXTREMITY (Arm hurt something terrible) had resolved. At the time of the report, SWOLLEN TONGUE (Tongue started feelin weird and swollen, swelling of upper airways), FEELING ABNORMAL (Tongue started feelin weird and swollen), DIZZINESS (Dizzy), DYSPNOEA (Little trouble breathing, difficulty breathing) and THROAT TIGHTNESS (Sensation of throat closing) outcome was unknown and MATERNAL EXPOSURE DURING PREGNANCY (Maternal exposure during pregnancy) had resolved. Not Provided The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Treatment medication was not reported. Reporter did not allow further contact Most recent FOLLOW-UP information incorporated above includes: On 22-Mar-2021: Completed ADR form. Address /phone number correction, race, ethnicity, height, weight, past medical history, pregnancy status, previous allergic reactions, concomitant medications, event outcome received.; Sender's Comments: Based on the current available information and temporal association between the use of the product and the start date of the events, a causal relationship cannot be excluded.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Asthma; Diverticulosis (Improved with healthier diet); Fatty liver (Improved with healthier diet); Hay fever; Reactive airways disease (Has improved)
Vorgeschichte: Medical History/Concurrent Conditions: Anaphylaxis; Drug allergy (Robutissin - Red blotches/itching); Drug allergy (Penicillin - anaphylaxis/hives); Drug allergy (Claritin - anaphylaxis/hives)
Andere Medikamente: BENADRYL [DIPHENHYDRAMINE HYDROCHLORIDE]; VITAMIN E [TOCOPHEROL]; VITAMIN C PLUS [ASCORBIC ACID]; PROBIOTIC GUMMIES; BLACK COHOSH [CIMICIFUGA RACEMOSA RHIZOME;CIMICIFUGA RACEMOSA ROOT]
Allergien: -
Vorherige Impfungen: -

VAERS 1542897

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: NC
Alter: 64,0
Geschlecht: F
Eingang: 11.08.2021
Impfdatum: 30.12.2020
Beginn: 30.12.2020
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / RA

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

Headache Hypoaesthesia Limb discomfort Muscle atrophy Pain in extremity Paraesthesia Vaccination site bruising Vaccination site mass

Symptomtext

Muscle loss in legs; Injection site got bruised; Red lump in arm like a hard boiled; Inability to completely raise arms; Pain that went all the way from below injection site in right arm and to the elbow; fingertips were tingly, tingling right arm/leg; from hip to knee was dull and numb and also went to the toes and jawline, numbness right thigh and right side of face; Headache; This spontaneous case was reported by a consumer and describes the occurrence of PAIN IN EXTREMITY (Pain that went all the way from below injection site in right arm and to the elbow), PARAESTHESIA (fingertips were tingly, tingling right arm/leg), HYPOAESTHESIA (from hip to knee was dull and numb and also went to the toes and jawline, numbness right thigh and right side of face), VACCINATION SITE BRUISING (Injection site got bruised) and VACCINATION SITE MASS (Red lump in arm like a hard boiled) in a 64-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 011J20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concurrent medical conditions included Syndrome Guillain-Barre, Allergy to antibiotic (Niacin), Plastic sensitivity, Vegetable allergy (Onions), Vegetable allergy (Mint), Latex allergy, Cold sores (Cold sore virus), Blood pressure (Start date: 08/1995), Diabetes and Cholesterol (Start date: 08/1995). Concomitant products included QUINAPRIL HYDROCHLORIDE (ACCUPRIL) from August 1995 to an unknown date, AMLODIPINE from August 1995 to an unknown date and HYDROCHLOROTHIAZID for Blood pressure, FENOFIBRATE for Cholesterol, VALACICLOVIR HYDROCHLORIDE (VALTREX) for Cold sores, METFORMIN for Diabetes. On 30-Dec-2020 at 4:30 PM, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 30-Dec-2020 at 4:30 PM, the patient experienced HEADACHE (Headache). On 31-Dec-2020 at 4:00 AM, the patient experienced PAIN IN EXTREMITY (Pain that went all the way from below injection site in right arm and to the elbow), PARAESTHESIA (fingertips were tingly, tingling right arm/leg) and HYPOAESTHESIA (from hip to knee was dull and numb and also went to the toes and jawline, numbness right thigh and right side of face). On 31-Dec-2020 at 4:30 AM, the patient experienced LIMB DISCOMFORT (Inability to completely raise arms). On 02-Jan-2021, the patient experienced VACCINATION SITE BRUISING (Injection site got bruised) and VACCINATION SITE MASS (Red lump in arm like a hard boiled). On an unknown date, the patient experienced MUSCLE ATROPHY (Muscle loss in legs). On 03-Jan-2021, PARAESTHESIA (fingertips were tingly, tingling right arm/leg) and HYPOAESTHESIA (from hip to knee was dull and numb and also went to the toes and jawline, numbness right thigh and right side of face) had resolved with sequelae, VACCINATION SITE BRUISING (Injection site got bruised) and VACCINATION SITE MASS (Red lump in arm like a hard boiled) had resolved. At the time of the report, PAIN IN EXTREMITY (Pain that went all the way from below injection site in right arm and to the elbow), LIMB DISCOMFORT (Inability to completely raise arms) and HEADACHE (Headache) outcome was unknown and MUSCLE ATROPHY (Muscle loss in legs) had not resolved. mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was withdrawn on an unknown date. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter considered PAIN IN EXTREMITY (Pain that went all the way from below injection site in right arm and to the elbow), PARAESTHESIA (fingertips were tingly, tingling right arm/leg) and HYPOAESTHESIA (from hip to knee was dull and numb and also went to the toes and jawline, numbness right thigh and right side of face) to be related. No further causality assessments were provided for VACCINATION SITE BRUISING (Injection site got bruised), VACCINATION SITE MASS (Red lump in arm like a hard boiled), MUSCLE ATROPHY (Muscle loss in legs), LIMB DISCOMFORT (Inability to completely raise arms) and HEADACHE (Headache). No treatment information was provided. This case was linked to MOD-2021-211777 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 05-Jun-2021: Events added, reporter causality updated, reporter and patient information updated.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Allergy to antibiotic (Niacin); Blood pressure (Start date: 08/1995); Cholesterol (Start date: 08/1995); Cold sores (Cold sore virus); Diabetes; Latex allergy; Plastic sensitivity; Syndrome Guillain-Barre; Vegetable allergy (Onions); Vegetable allergy (Mint)
Vorgeschichte: -
Andere Medikamente: ACCUPRIL; AMLODIPINE; HYDROCHLOROTHIAZID; FENOFIBRATE; METFORMIN; VALTREX
Allergien: -
Vorherige Impfungen: -

VAERS 1542882

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: OH
Alter: 37,0
Geschlecht: F
Eingang: 11.08.2021
Impfdatum: 23.12.2020
Beginn: 27.12.2020
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: OT / -

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

Asthenia COVID-19 Chest discomfort Chest pain Cough Diarrhoea Dyspnoea Headache Hyposmia Musculoskeletal stiffness Upper-airway cough syndrome

Symptomtext

diarrhea; massive headache; weakness; shortness of breath; chest pain; chest pressure; cough; tested positive for Covid; hyposmia; postnasal drip; stiffness; This spontaneous case was reported by a nurse (subsequently medically confirmed) and describes the occurrence of COVID-19 (tested positive for Covid), UPPER-AIRWAY COUGH SYNDROME (postnasal drip), MUSCULOSKELETAL STIFFNESS (stiffness), HYPOSMIA (hyposmia) and DIARRHOEA (diarrhea) in a 37-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 011J20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 23-Dec-2020, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 27-Dec-2020, the patient experienced UPPER-AIRWAY COUGH SYNDROME (postnasal drip) and MUSCULOSKELETAL STIFFNESS (stiffness). On 30-Dec-2020, the patient experienced HYPOSMIA (hyposmia). On 31-Dec-2020, the patient experienced COVID-19 (tested positive for Covid), DIARRHOEA (diarrhea), HEADACHE (massive headache), ASTHENIA (weakness), DYSPNOEA (shortness of breath), CHEST PAIN (chest pain), CHEST DISCOMFORT (chest pressure) and COUGH (cough). At the time of the report, COVID-19 (tested positive for Covid), UPPER-AIRWAY COUGH SYNDROME (postnasal drip), MUSCULOSKELETAL STIFFNESS (stiffness), HYPOSMIA (hyposmia), DIARRHOEA (diarrhea), HEADACHE (massive headache), ASTHENIA (weakness), DYSPNOEA (shortness of breath), CHEST PAIN (chest pain) and COUGH (cough) outcome was unknown. Not Provided The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Treatment medications include Sudafed, Tylenol, zinc , vitamin c, Z-pak and inhaler. No concomitant medications were provided by reporter.

Weitere VAERSDATA-Felder

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

VAERS 1542769

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: CT
Alter: 68,0
Geschlecht: F
Eingang: 11.08.2021
Impfdatum: 22.12.2020
Beginn: 22.12.2020
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / -

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

Hypoaesthesia Paraesthesia Vaccination site erythema Vaccination site pain

Symptomtext

Pain on the injection site; A little redness on the injection site; Numbness in the face; Tingling in the face; This spontaneous case was reported by a nurse and describes the occurrence of VACCINATION SITE PAIN (Pain on the injection site), VACCINATION SITE ERYTHEMA (A little redness on the injection site), HYPOAESTHESIA (Numbness in the face) and PARAESTHESIA (Tingling in the face) in a 68-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 011J20A) for COVID-19 vaccination. No Medical History information was reported. On 22-Dec-2020, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 22-Dec-2020, the patient experienced HYPOAESTHESIA (Numbness in the face) and PARAESTHESIA (Tingling in the face). On 24-Dec-2020, the patient experienced VACCINATION SITE PAIN (Pain on the injection site) and VACCINATION SITE ERYTHEMA (A little redness on the injection site). On 22-Dec-2020, HYPOAESTHESIA (Numbness in the face) and PARAESTHESIA (Tingling in the face) had resolved. On 25-Dec-2020, VACCINATION SITE PAIN (Pain on the injection site) and VACCINATION SITE ERYTHEMA (A little redness on the injection site) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments.; Sender's Comments: Based on the current available information and temporal association between the use of the product and the start date of the event, a causal relationship cannot be excluded.

Weitere VAERSDATA-Felder

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

VAERS 1542693

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: TN
Alter: 68,0
Geschlecht: F
Eingang: 11.08.2021
Impfdatum: 26.12.2020
Beginn: 26.12.2020
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / RA

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

Limb discomfort Musculoskeletal chest pain

Symptomtext

terrible deep pain in my rib cage; arm was extremely sore for about 4 days; This spontaneous case was reported by a pharmacist (subsequently medically confirmed) and describes the occurrence of MUSCULOSKELETAL CHEST PAIN (terrible deep pain in my rib cage) and LIMB DISCOMFORT (arm was extremely sore for about 4 days) in a 68-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 011J20A) for COVID-19 vaccination. The patient's past medical history included No adverse event. On 26-Dec-2020, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 26-Dec-2020, the patient experienced MUSCULOSKELETAL CHEST PAIN (terrible deep pain in my rib cage) and LIMB DISCOMFORT (arm was extremely sore for about 4 days). At the time of the report, MUSCULOSKELETAL CHEST PAIN (terrible deep pain in my rib cage) and LIMB DISCOMFORT (arm was extremely sore for about 4 days) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Musculoskeletal chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: No adverse event
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1542609

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: NC
Alter: 46,0
Geschlecht: F
Eingang: 11.08.2021
Impfdatum: 30.12.2020
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: OT / LA

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

Dyspnoea Vaccination site erythema Vaccination site pain Vaccination site pruritus Vaccination site rash Vaccination site swelling Vaccination site warmth

Symptomtext

Shortness of breath; Arm is red; Arm is hot; Swollen arm; Vaccination site blotchiness; Vaccination site pain; Vaccination site pruritus; Puffy; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION SITE PAIN (Vaccination site pain), VACCINATION SITE PRURITUS (Vaccination site pruritus) and VACCINATION SITE SWELLING (Puffy) in a 46-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 011J20A) for COVID-19 vaccination. No Medical History information was reported. On 30-Dec-2020, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On an unknown date, the patient experienced VACCINATION SITE PAIN (Vaccination site pain), VACCINATION SITE PRURITUS (Vaccination site pruritus) and VACCINATION SITE SWELLING (Puffy). At the time of the report, VACCINATION SITE PAIN (Vaccination site pain), VACCINATION SITE PRURITUS (Vaccination site pruritus) and VACCINATION SITE SWELLING (Puffy) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Concomitant product use was not provided. No treatment medication was reported.; Sender's Comments: Based on the current available information and temporal association between the use of the product and the start date of the events, a causal relationship cannot be excluded.

Weitere VAERSDATA-Felder

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

VAERS 1542143

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: NY
Alter: -
Geschlecht: F
Eingang: 11.08.2021
Impfdatum: 11.01.2021
Beginn: 12.01.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: OT / LA

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

Dyspnoea

Symptomtext

Some difficulty breathing; A spontaneous report was received from a consumer who was also a 45-year-old, female patient, who received Moderna's COVID-19 vaccine (mRNA-1273) and experienced some difficulty breathing. The patient's medical history was not provided. No relevant concomitant medications were reported. On 11 Jan 2021, approximately one day prior to the onset of the events, the patient received their first of two planned doses of mRNA-1273 (Lot number: 11J20A) intramuscularly in the left arm for prophylaxis of COVID-19 infection. On 12 Jan 2021, in the evening, the patient had some difficulty breathing and used her inhaler once. She also reported using her inhaler twice on the same day. Treatment included an inhaler (not specified). Action taken with mRNA-1273 in response to the event was not reported. The event, some difficulty breathing, was not resolved.; Reporter's Comments: This case concerns a 45-year old female patient. The medical history is not provided. The patient experienced an unexpected non-serious event of Difficulty breathing approximately one day after receiving their first of two planned doses of mRNA-1273 (Lot number: 11J20A). Based on temporal association between the use of the product and the onset of the event, a causal relationship cannot be excluded and the event is considered possibly related to the vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: No adverse event (No medical history reported)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1540112

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: NY
Alter: -
Geschlecht: M
Eingang: 10.08.2021
Impfdatum: 09.01.2021
Beginn: 09.01.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / LA

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

Condition aggravated Cough Dyspnoea Pyrexia

Symptomtext

Coughing; difficulty breathing worsened; difficulty breathing; Fever; This spontaneous case was reported by a consumer and describes the occurrence of DYSPNOEA (difficulty breathing), CONDITION AGGRAVATED (difficulty breathing worsened), COUGH (Coughing) and PYREXIA (Fever) in a 31-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 011J20A) for COVID-19 vaccination. No Medical History information was reported. On 09-Jan-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 09-Jan-2021, the patient experienced DYSPNOEA (difficulty breathing) and PYREXIA (Fever). On 11-Jan-2021, the patient experienced CONDITION AGGRAVATED (difficulty breathing worsened). On an unknown date, the patient experienced COUGH (Coughing). At the time of the report, DYSPNOEA (difficulty breathing), CONDITION AGGRAVATED (difficulty breathing worsened) and COUGH (Coughing) had not resolved and PYREXIA (Fever) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. On 11-Jan-2021, coughing and difficulty breathing worsened. Concomitant medications were not provided. Treatment information was not reported.; Sender's Comments: Based on the current available information and temporal association between the use of the product and the start dates of the events, a causal relationship cannot be excluded.

Weitere VAERSDATA-Felder

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

VAERS 1540080

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: MI
Alter: -
Geschlecht: F
Eingang: 10.08.2021
Impfdatum: 08.01.2021
Beginn: 09.01.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: OT / RA

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

Chest pain Dyspnoea Fatigue Gastroenteritis viral

Symptomtext

it's like the worst stomach flu I've ever had; shortness of breath; physical chest pain; so tired; A spontaneous report was received from a non-healthcare professional concerning a 33 years old female patient who received Moderna's COVID-19 vaccine (mRNA-1273) and experienced it's like the worst stomach flu I've ever had, shortness of breath, physical chest pain, so tired. No medical history was reported. No concomitant medication was reported. On 08-Jan-2021, prior to the onset of the events like the worst stomach flu I've ever had, shortness of breath, physical chest pain, so tired, the patient received their first of two planned doses of mRNA-1273 (lot/batch: 011J20A) via an intramuscular route in right arm for prophylaxis of COVID-19 infection. On 13-Jan-2021, the patient experienced like the worst stomach flu I've ever had, shortness of breath, physical chest pain, so tired. Laboratory details was not provided. Treatment medication was not reported. Action taken with mRNA-1273 in response to the events like the worst stomach flu I've ever had, shortness of breath, physical chest pain, so tired was not provided. The outcome of the events like the worst stomach flu I've ever had, shortness of breath, physical chest pain, so tired was not provided. The reporter did not provide the assessment of the events like the worst stomach flu I've ever had, shortness of breath, physical chest pain, so tired to study drug.; Sender's Comments: Very limited information regarding this events has been provided at this time. Further information has been requested. Company assessed the events to be unlikely related to company product.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: No adverse event (No reported medical history)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1539900

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: ME
Alter: 43,0
Geschlecht: F
Eingang: 10.08.2021
Impfdatum: 23.12.2020
Beginn: 23.12.2020
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / LA

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

Dry mouth Erythema Feeling abnormal Feeling hot Hypotension Inappropriate affect Lethargy Limb discomfort Pruritus

Symptomtext

Lethargic; Legs began feeling heavy; Couldn't focus/felt like I wasn't sober/felt like she was on medication; Felt hot; Itching; Cotton mouth; Blood pressure became really low; red; Firm; Uncontrollable laughing; This spontaneous case was reported by a consumer (subsequently medically confirmed) and describes the occurrence of LETHARGY (Lethargic), LIMB DISCOMFORT (Legs began feeling heavy), FEELING ABNORMAL (Couldn't focus/felt like I wasn't sober/felt like she was on medication), FEELING HOT (Felt hot) and PRURITUS (Itching) in a 43-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 011J20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concurrent medical conditions included Drug allergy (Allergic to Sulfa.). On 23-Dec-2020, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 23-Dec-2020, the patient experienced LETHARGY (Lethargic), LIMB DISCOMFORT (Legs began feeling heavy), FEELING ABNORMAL (Couldn't focus/felt like I wasn't sober/felt like she was on medication), FEELING HOT (Felt hot), PRURITUS (Itching), DRY MOUTH (Cotton mouth), HYPOTENSION (Blood pressure became really low), ERYTHEMA (red), FEELING ABNORMAL (Firm) and INAPPROPRIATE AFFECT (Uncontrollable laughing). On 23-Dec-2020, LETHARGY (Lethargic), LIMB DISCOMFORT (Legs began feeling heavy), FEELING ABNORMAL (Couldn't focus/felt like I wasn't sober/felt like she was on medication), FEELING HOT (Felt hot), PRURITUS (Itching), DRY MOUTH (Cotton mouth), ERYTHEMA (red), FEELING ABNORMAL (Firm) and INAPPROPRIATE AFFECT (Uncontrollable laughing) had resolved. At the time of the report, HYPOTENSION (Blood pressure became really low) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. Concomitant product use was not provided by the reporter. Treatment information was not provided.; Sender's Comments: This case concerns a 43-year-old female with a nonserious unexpected events of hypotension, pruritus, erythema, dry mouth, lethargy, feeling hot, feeling abnormal, inappropriate affect, and limb discomfort. Event onset the same day as first dose mRNA-1273. Event outcomes unknown. Based on current available information and temporal association between the use of the product and the start date of the event, a causal relationship cannot be excluded.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypotension
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Drug allergy (Allergic to Sulfa.)
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1539878

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: HI
Alter: 52,0
Geschlecht: F
Eingang: 10.08.2021
Impfdatum: 22.12.2020
Beginn: 22.12.2020
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / RA

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

Formication Headache Inappropriate schedule of product administration Injection site swelling Paraesthesia Vaccination site induration Vaccination site pain

Symptomtext

inappropriate schedule of vaccine administered; Mild paresthesia on right thigh area like tingling sensation; tingling crawling sensation; Head ache; Pain and swelling site of injection; Localized pain; 1/2 inch diameter at site of injection; Hardness on area; This spontaneous case was reported by a nurse and describes the occurrence of PARAESTHESIA (Mild paresthesia on right thigh area like tingling sensation), FORMICATION (tingling crawling sensation), VACCINATION SITE INDURATION (Hardness on area), HEADACHE (Head ache) and INJECTION SITE SWELLING (Pain and swelling site of injection) in a 52-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 011J20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concurrent medical conditions included Hypertension in 2003, Allergy to animal dander (Allergic to cat dander) and Shellfish allergy (Allergic to raw shrimp). Concomitant products included LOSARTAN and HYDROCHLOROTHIAZIDE for Hypertension, MEDROXYPROGESTERONE, POTASSIUM CHLORIDE (K-TAB) and MULTIVITAMIN [VITAMINS NOS] for an unknown indication. On 22-Dec-2020, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 22-Dec-2020, the patient experienced VACCINATION SITE INDURATION (Hardness on area), INJECTION SITE SWELLING (Pain and swelling site of injection) and VACCINATION SITE PAIN (Localized pain; 1/2 inch diameter at site of injection). On 23-Dec-2020, the patient experienced PARAESTHESIA (Mild paresthesia on right thigh area like tingling sensation), FORMICATION (tingling crawling sensation) and HEADACHE (Head ache). On 05-Feb-2021, the patient experienced INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (inappropriate schedule of vaccine administered). On 25-Dec-2020, VACCINATION SITE INDURATION (Hardness on area), INJECTION SITE SWELLING (Pain and swelling site of injection) and VACCINATION SITE PAIN (Localized pain; 1/2 inch diameter at site of injection) had resolved. On 05-Feb-2021, INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (inappropriate schedule of vaccine administered) had resolved. At the time of the report, PARAESTHESIA (Mild paresthesia on right thigh area like tingling sensation) and FORMICATION (tingling crawling sensation) had not resolved and HEADACHE (Head ache) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. The patient did not seek treatment or advise from her physician. Most recent FOLLOW-UP information incorporated above includes: On 07-Jun-2021: Medical history updated, patient demographic details updated, concomitant medications updated, event outcome updated, new event inappropriate schedule of vaccine added based on 2nd dose information received; Sender's Comments: Based on the current available information and temporal association between the use of the product and the start date of the events, a causal relationship cannot be excluded.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Allergy to animal dander (Allergic to cat dander); Shellfish allergy (Allergic to raw shrimp)
Vorgeschichte: Medical History/Concurrent Conditions: Hypertension
Andere Medikamente: LOSARTAN; HYDROCHLOROTHIAZIDE; MEDROXYPROGESTERONE; K-TAB; MULTIVITAMIN [VITAMINS NOS]
Allergien: -
Vorherige Impfungen: -

VAERS 1539554

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: OH
Alter: 40,0
Geschlecht: F
Eingang: 10.08.2021
Impfdatum: 05.01.2021
Beginn: 05.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / LA

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

Aphthous ulcer Candida infection Facial pain Headache Influenza like illness Limb discomfort Malaise Myalgia Nausea Pain in extremity Paraesthesia oral Peripheral swelling Pruritus Vaccination site erythema

Symptomtext

nauseous; Random pains in right arm too (not injection site arm); injection site redness; body aches; arm was super itchy; thrush; mouth felt funny; Canker sores; pain in cheeks; pain in legs; swollen arm; arm was super sore; felt fluish; Feeling off; headache; This spontaneous case was reported by a health care professional (subsequently medically confirmed) and describes the occurrence of CANDIDA INFECTION (thrush), PARAESTHESIA ORAL (mouth felt funny), APHTHOUS ULCER (Canker sores), FACIAL PAIN (pain in cheeks) and PAIN IN EXTREMITY (pain in legs) in a 40-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 011J20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included No adverse effect. On 05-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 05-Jan-2021, the patient experienced LIMB DISCOMFORT (arm was super sore), INFLUENZA LIKE ILLNESS (felt fluish), MALAISE (Feeling off) and HEADACHE (headache). On 06-Jan-2021, the patient experienced CANDIDA INFECTION (thrush), PARAESTHESIA ORAL (mouth felt funny), APHTHOUS ULCER (Canker sores), FACIAL PAIN (pain in cheeks), PAIN IN EXTREMITY (pain in legs), PERIPHERAL SWELLING (swollen arm), PRURITUS (arm was super itchy), VACCINATION SITE ERYTHEMA (injection site redness) and MYALGIA (body aches). On 07-Jan-2021, the patient experienced PAIN IN EXTREMITY (Random pains in right arm too (not injection site arm)). On 08-Jan-2021, the patient experienced NAUSEA (nauseous). At the time of the report, CANDIDA INFECTION (thrush), PARAESTHESIA ORAL (mouth felt funny), APHTHOUS ULCER (Canker sores), FACIAL PAIN (pain in cheeks), PAIN IN EXTREMITY (pain in legs), PERIPHERAL SWELLING (swollen arm), LIMB DISCOMFORT (arm was super sore), INFLUENZA LIKE ILLNESS (felt fluish), MALAISE (Feeling off), PRURITUS (arm was super itchy), PAIN IN EXTREMITY (Random pains in right arm too (not injection site arm)), HEADACHE (headache), NAUSEA (nauseous), VACCINATION SITE ERYTHEMA (injection site redness) and MYALGIA (body aches) outcome was unknown. ER visit 07-Jan-2021 details not provided The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments.; Sender's Comments: Based on the current available information and temporal association between the use of the product and the start date of the events, a causal relationship cannot be excluded.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia oral
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: No adverse effect
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1539542

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: GA
Alter: -
Geschlecht: M
Eingang: 10.08.2021
Impfdatum: 06.01.2021
Beginn: 06.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / -

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

Chest discomfort Ear discomfort Fatigue Headache Heart rate Oropharyngeal discomfort Palpitations

Symptomtext

Tired; His ear towards the upper tip felt little warm; Heart palpitations; Odd feeling in chest; Throat discomfort; Headache; This spontaneous case was reported by an other health care professional (subsequently medically confirmed) and describes the occurrence of EAR DISCOMFORT (His ear towards the upper tip felt little warm), PALPITATIONS (Heart palpitations), CHEST DISCOMFORT (Odd feeling in chest), OROPHARYNGEAL DISCOMFORT (Throat discomfort) and HEADACHE (Headache) in a 33-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 011J20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included No adverse event (No adverse event). On 06-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 06-Jan-2021, the patient experienced EAR DISCOMFORT (His ear towards the upper tip felt little warm), PALPITATIONS (Heart palpitations), CHEST DISCOMFORT (Odd feeling in chest), OROPHARYNGEAL DISCOMFORT (Throat discomfort) and HEADACHE (Headache). On 07-Jan-2021, the patient experienced FATIGUE (Tired). On 08-Jan-2021, EAR DISCOMFORT (His ear towards the upper tip felt little warm), PALPITATIONS (Heart palpitations), CHEST DISCOMFORT (Odd feeling in chest), OROPHARYNGEAL DISCOMFORT (Throat discomfort), HEADACHE (Headache) and FATIGUE (Tired) had resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 06-Jan-2021, Heart rate: The beats per minute were starting at 122 jumped to 133 then 150 then 170 and then to 179. The heart rate decreased to 95 beats per minute. After 5 minutes the bpm was 170 for 1-2 minutes and then dropped to 90 bpm. Then went to 120-130 bpm at ER. Turned to 75bpm after sitting. After getting home HR increased to 122 bpm then lowered to 85-115. At home range went to 75-80 bpm.. On 07-Jan-2021, Heart rate: Resting Heart rate Normal.. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No relevant concomitant medications were reported. No treatment received at the ER. Patient was transferred to the ER. Company Comment: Based on the current available information and temporal association between the use of the product and the start date of the event, a causal relationship cannot be excluded. Further information has been requested.; Sender's Comments: Based on the current available information and temporal association between the use of the product and the start date of the event, a causal relationship cannot be excluded. Further information has been requested.

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Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: Test Date: 20210106; Test Name: Heart Rate; Result Unstructured Data: The beats per minute were starting at 122 jumped to 133 then 150 then 170 and then to 179. The heart rate decreased to 95 beats per minute. After 5 minutes the bpm was 170 for 1-2 minutes and then dropped to 90 bpm. Then went to 120-130 bpm at ER. Turned to 75bpm after sitting. After getting home HR increased to 122 bpm then lowered to 85-115. At home range went to 75-80 bpm.; Test Date: 20210107; Test Name: Heart Rate; Result Unstructured Data: Resting Heart rate Normal.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: No adverse event
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1537580

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: MA
Alter: -
Geschlecht: F
Eingang: 09.08.2021
Impfdatum: 23.12.2020
Beginn: 23.12.2020
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / LA

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

Chills Nasal congestion Nasal dryness Paraesthesia Paraesthesia oral Vaccination site erythema Vaccination site lymphadenopathy Vaccination site pain

Symptomtext

stuffy nose/congestion; chills; swollen lymp nodes on left arm injection site; nose always dry; arm pain; erythema around the vaccine site; tingly sensation on the lips; tingly sensation on the tip of nose; A spontaneous report was received from a 38 year old female consumer who received Moderna's COVID-19 vaccine (mRNA-1273) and experienced tingly sensation on tip of nose (paraesthesia) and lips (paraesthesia oral), weird stuffy nose (nasal congestion) and dryness (nasal dryness), arm pain (pain in extremity), swollen lymph nodes on left arm injections site (injection site lymphadenopathy), chills, and erythema around injection site (injection site erythema). The patient's medical history was not provided. No relevant concomitant medications were reported. On 23 Dec 2020, prior to the onset of the events, the patient received their first of two planned doses of mRNA-1273 (Lot 011J20A) intramuscularly in the left arm for prophylaxis of COVID-19 infection. On 23 Dec 2020 after the vaccine was administered, the patient reports that she had immediate reaction, tingly sensation on the tip of nose and lips. After, the patient experienced weird stuff nose, not congested but dry, arm pain, swollen lymph nodes on left arm injection site and chills. On 30 Dec 2020, the patient experienced erythema around the vaccine site. No treatment information was provided. Action taken with mRNA-1273 in response to the events was not reported. The outcome of the events of weird stuffy nose and dryness, arm pain, swollen lymph nodes on left arm injections site, chills and erythema around injection site, were unknown. The events of tingly sensation on tip of nose and lips was resolved on 23 Dec 2020.; Reporter's Comments: Based on the current available information and temporal association between the use of the product and the start date of the event, a causal relationship cannot be excluded.

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Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: No adverse event (No reported medical history.)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1536972

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: PA
Alter: 43,0
Geschlecht: F
Eingang: 09.08.2021
Impfdatum: 28.12.2020
Beginn: 28.12.2020
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: OT / LA

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

Amenorrhoea Limb discomfort Menstruation irregular Paraesthesia Vaccination site pain

Symptomtext

missing period since first dose; Irregular menstrual period, got very little discharge on 22Feb2021; Tingling in left foot immediately after the injection/tingling more in right foot; Feels like ball is rolling around in the sole of foot; arm pain where she got the injection; This spontaneous case was reported by a dentist (subsequently medically confirmed) and describes the occurrence of AMENORRHOEA (missing period since first dose), MENSTRUATION IRREGULAR (Irregular menstrual period, got very little discharge on 22Feb2021), PARAESTHESIA (Tingling in left foot immediately after the injection/tingling more in right foot), LIMB DISCOMFORT (Feels like ball is rolling around in the sole of foot) and VACCINATION SITE PAIN (arm pain where she got the injection) in a 43-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 011J20A and 028L20A) for COVID-19 vaccination. Concurrent medical conditions included Thyroid disorder (Patient is on thyroid medication). Concomitant products included LEVOTHYROXINE for Thyroid disorder. On 28-Dec-2020, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 28-Jan-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 28-Dec-2020, the patient experienced AMENORRHOEA (missing period since first dose), MENSTRUATION IRREGULAR (Irregular menstrual period, got very little discharge on 22Feb2021), PARAESTHESIA (Tingling in left foot immediately after the injection/tingling more in right foot), LIMB DISCOMFORT (Feels like ball is rolling around in the sole of foot) and VACCINATION SITE PAIN (arm pain where she got the injection). The patient was treated with IBUPROFEN (MOTRIN [IBUPROFEN]) at an unspecified dose and frequency. In December 2020, VACCINATION SITE PAIN (arm pain where she got the injection) had resolved. At the time of the report, AMENORRHOEA (missing period since first dose), MENSTRUATION IRREGULAR (Irregular menstrual period, got very little discharge on 22Feb2021) and PARAESTHESIA (Tingling in left foot immediately after the injection/tingling more in right foot) had not resolved and LIMB DISCOMFORT (Feels like ball is rolling around in the sole of foot) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Treatment included ibuprofen. Consumer stated she had her period in Dec-2020, did not have it in Jan-2021, had very little discharge on 22-Feb-2021, did not have it in Mar-2021, and had not had it in Apr-2021. She visited a gynecologist, and blood tests performed to check her hormone levels had normal results. Consumer visited a physician for the tingling sensation. Blood tests from this visit also had normal results. The patient also stated that she was emotionally distressed, it affects her a lot and it also changed her body. Most recent FOLLOW-UP information incorporated above includes: On 12-Apr-2021: The patient information, 1st and 2nd dose of vaccine information along with batch number, concomitant drug, additional events amenorrhea and menstruation irregular were updated. On 26-Apr-2021: No new information was provided.; Sender's Comments: Based on the current available information and temporal association beteen the use of the product and the start date of the events a causal relationship cannot be excluded.

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Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Thyroid disorder (Patient is on thyroid medication)
Vorgeschichte: -
Andere Medikamente: LEVOTHYROXINE
Allergien: -
Vorherige Impfungen: -

VAERS 1536794

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: NY
Alter: 36,0
Geschlecht: M
Eingang: 09.08.2021
Impfdatum: 23.12.2020
Beginn: 23.12.2020
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / LA

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

Chills Dizziness Dyspnoea Fatigue Headache Injection site pain Pain

Symptomtext

body ache; dizziness; having hard time breathing; body chills; very fatigue; headache; injection site pain; A spontaneous report was received from a non-HCP concerning a 36-year old, male patient who experienced body ache, dizziness, having hard time breathing, body chills, very fatigue, headache, and injection site pain. The patient's medical history was not provided by the reporter. Concomitant product use was not provided by the reporter. On 23 DEC 2020, the patient received one of two planned doses of mRNA-1273 (LOT/BATCH# 011J20A) intramuscularly in the Left Deltoid for prophylaxis of COVID-19 infection. On 23 DEC 2020, the patient experienced body chill, headache, very fatigue, body ache, dizziness, injection site pain, and having a hard time breathing. Treatment for the events included 400mg ibuprofen Action taken with mRNA-1273 in response to the events was not reported. The events very fatigue, injection site pain, and having a hard time breathing were considered not recovered/not resolved. The events body ache, dizziness, and body chill were considered recovered/resolved on 24 DEC 2020. The event headache was considered recovered/resolved on 25 DEC 2020 The reporter did not provide an assessment for the events body ache, dizziness, having hard time breathing, body chills, very fatigue, headache, and injection site pain.; Reporter's Comments: This case concerns a 36-year-old, male patient. The patient's medical history was not provided. The patient experienced the non serious, unexpected event of body ache, dyspnea, dizziness and, expected event of chills, fatigue, headache and injection site pain. The event occurred the day the patient received one of the two doses of mRNA-1273 (LOT/BATCH# 011J20A). Based on the current available information and temporal association between the use of the product and the start date of the events, a causal relationship cannot be excluded.

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: No adverse event (No reported medical history)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1536781

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: MA
Alter: 25,0
Geschlecht: F
Eingang: 09.08.2021
Impfdatum: 30.12.2020
Beginn: 30.12.2020
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / LA

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

Hypoaesthesia Paraesthesia Paraesthesia oral

Symptomtext

Tingling in feet and toes; Numbness in feet / Numbness in toes; Left side of mouth tingling; This spontaneous report was received from a consumer of age 25 years old, female who was participating in the mRNA-1273COVID-19 Vaccine, Emergency Use Authorization Program and experienced multiple events of tingling in feet and toes, numbness in feet / numbness in toes and left side of mouth tingling. The patient's medical history was not reported. No concomitant medications were reported. On 30 Dec 2020, approximately 3 minutes earlier to the onset of the events, the patient received her first of two planned doses of mRNA-1273 (Lot number 011J20A) intramuscularly in the deltoid muscle of the left arm for prophylaxis of COVID-19 infection. On 30 Dec 2020, two to three minutes after the injection, the patient experienced tingling and numbness in left foot and toes. She started to walk around bit but the feeling persisted. A few minutes later the same tingling and numbness in right foot and toes developed. After ten minutes, the patient experienced tingling in her left lip. The patient was then treated with Benadryl and taken to the emergency medical technician (EMT) to be monitored. After 35 minutes and having the patient's vitals checked twice the patient was cleared to go. The patient informed that after she left the site she did not experienced any tingling or numbness. The Action taken with mRNA-1273 Vaccine in response to the events was not reported. The outcome for the events, tingling and numbness in left foot and toes, tingling and numbness in right foot and toes and tingling in my left lip were considered recovered/ resolved on the same date. The reporter did not provide an assessment for the events.; Reporter's Comments: This case concerns a 25-year-old, female patient, who experienced non-serious unexpected events of Paraesthesia and Hypoaesthesia extremities and Paraesthesia oral left side . The events of Paraesthesia and Hypoaesthesia extremities and Paraesthesia oral left side , occurred 1 day (same day) after first dose of mRNA-1273, COVID-19 Vaccine lot # 011J20A. Treatment included Benadryl. Based on the current available information and temporal association between the use of the product and onset of the events a causal relationship cannot be excluded.

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Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: No adverse event (No reported medical history)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1536748

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: PA
Alter: -
Geschlecht: M
Eingang: 09.08.2021
Impfdatum: 23.12.2020
Beginn: 23.12.2020
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / -

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

Chills Fatigue Myalgia Nausea Pain Tremor

Symptomtext

Fatigue; Chills; Shaking; Body aches; Muscle pain; Nausea; Initial MOD-2020-001401 A report was received from a physician concerning a male patient of unknown age and race participating in the mRNA-1273 Emergency Use Program and experienced fatigue, tiredness, muscle pain, body aches, chills, shaking, feeling cold, nausea, achy, and the verbatim term of "felt run down". The patient's medical history was not provided. No relevant concomitant medications were reported. On 23 December 2020 at 4pm prior to the onset of the events, the patient received their first of two planned doses of mRNA-1273 (BATCH# 011J20A) by injection for prophylaxis of COVID-19 infection. Patient experienced fatigue, tiredness, muscle pain, body aches, chills, shaking, feeling cold, nausea, achy, and the verbatim term of "felt run down", on the same day as the injection start date. It is unknown if patient has recovered from the events. No treatment was administered to treat the events. Action taken with mRNA-1273 in response to the events was not reported. The outcome of the events fatigue, tiredness, muscle pain, body aches, chills, shaking, feeling cold, nausea, achy, and the verbatim term of "felt run down" was not reported. The causality assessment of the reported events fatigue, tiredness, muscle pain, body aches, chills, shaking, feeling cold, nausea, achy, and the verbatim term of "felt run down", is unknown to the study drug.; Reporter's Comments: This case concerns a male patient of unknown age. The patient's medical history was not provided. The patient experienced the expected event of fatigue, myalgia, chills, nausea and unexpected event of Pain, tremors, feeling cold and feeling abnormal. The event occurred the day the first dose of mRNA-1273 (BATCH# 011J20A) was administered. Based on the current available information and temporal association between the use of the product and the start date of the event, a causal relationship cannot be excluded.

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Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: No adverse event (No reported medical history)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1535823

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: WI
Alter: 40,0
Geschlecht: F
Eingang: 09.08.2021
Impfdatum: 28.12.2020
Beginn: 28.12.2020
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / LA

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

Blood pressure increased Blood pressure measurement Dizziness Headache Heart rate Hyperhidrosis Tachycardia

Symptomtext

Heart rate increased from 98 to 114; Dizziness; Hyperhidrosis; Blood pressure increased; Headache; This spontaneous case was reported by an other health care professional and describes the occurrence of TACHYCARDIA (Heart rate increased from 98 to 114), DIZZINESS (Dizziness), HYPERHIDROSIS (Hyperhidrosis), BLOOD PRESSURE INCREASED (Blood pressure increased) and HEADACHE (Headache) in a 40-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 011J20A) for COVID-19 vaccination. Concurrent medical conditions included Drug hypersensitivity (allergy to sulfa) and Drug allergy (allergy to codeine). Concomitant products included SPIRONOLACTONE, NALTREXONE+BUPROPIN, PHENTERMINE, ROPINIROLE HYDROCHLORIDE (REQUIP), OMEPRAZOLE (PROTONIX [OMEPRAZOLE]), VITAMINS NOS (MULTIVITAMINUM) and IBUPROFEN for an unknown indication, SERTRALINE and trazadone. On 28-Dec-2020, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 28-Dec-2020, the patient experienced TACHYCARDIA (Heart rate increased from 98 to 114), DIZZINESS (Dizziness), HYPERHIDROSIS (Hyperhidrosis), BLOOD PRESSURE INCREASED (Blood pressure increased) and HEADACHE (Headache). At the time of the report, TACHYCARDIA (Heart rate increased from 98 to 114), DIZZINESS (Dizziness), HYPERHIDROSIS (Hyperhidrosis), BLOOD PRESSURE INCREASED (Blood pressure increased) and HEADACHE (Headache) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 28-Dec-2020, Blood pressure measurement: 142/88 (High) elevated BP ranging from 138/72- 142/88. On 28-Dec-2020, Heart rate: 114 (High) elevated HR from 98-114 After sitting HR went down to 88. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments.; Sender's Comments: Based on the current available information and temporal association between the use of the product and the start dates of the events, a causal relationship cannot be excluded.

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Praegender Schweregrund: Tachycardia
Hospital-Tage: -
Labordaten: Test Date: 20201228; Test Name: blood pressure; Result Unstructured Data: elevated BP ranging from 138/72- 142/88; Comments: After sitting Blood pressure went down to 129/81; Test Date: 20201228; Test Name: heart rate; Result Unstructured Data: elevated HR from 98-114 After sitting HR went down to 88
Aktuelle Erkrankungen: Drug hypersensitivity (allergy to sulfa)
Vorgeschichte: Medical History/Concurrent Conditions: Drug allergy (allergy to codeine)
Andere Medikamente: SPIRONOLACTONE; SERTRALINE; NALTREXONE+BUPROPIN; PHENTERMINE; REQUIP; PROTONIX [OMEPRAZOLE]; MULTIVITAMINUM; IBUPROFEN; trazadone
Allergien: -
Vorherige Impfungen: -

VAERS 1529126

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011 J20A

moderat

Staat: FL
Alter: 56,0
Geschlecht: F
Eingang: 05.08.2021
Impfdatum: 30.12.2020
Beginn: 01.04.2021
Tage bis Beginn: 92,0
Dosis: 1
Route/Site: IM / LA

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

Cardiac stress test Dyspnoea

Symptomtext

shortness of breath

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Attended Cardiologist, ordered stress test, recommended to follow up with Pulmonology/schedule Diagnostic cardiac Cath
Aktuelle Erkrankungen: None
Vorgeschichte: Hypothyroid
Andere Medikamente: Levothyroxine, Liothyronine, Estrogen, Progesterone, Trazodone, Gabapentin, Ezetimibe
Allergien: None
Vorherige Impfungen: -

VAERS 1528980

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: MA
Alter: 35,0
Geschlecht: F
Eingang: 05.08.2021
Impfdatum: 07.01.2021
Beginn: 12.01.2021
Tage bis Beginn: 5,0
Dosis: 1
Route/Site: IM / LA

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

Axillary pain Chills Decreased appetite Dyspnoea Eye pain Fatigue Grip strength decreased Headache Heart rate abnormal Hyperhidrosis Hypophagia Injection site pain Injection site swelling Lymphadenopathy Myalgia Nausea Oxygen saturation decreased Pain

Symptomtext

Adverse events after my 1st dose (day 0= 01/07/21): Day 1- local tenderness; Day 2- local tenderness + fatigue Day 3-4= felt ok, N/A; Day 5 evening- started to have mild/moderate body aches- took 1 xTylenol in the evening. I was able to complete my daily activities; Day 6- moderate body/muscle ache, headache and pain in my left armpit (lymphadenopathy)- took Tylenol every 6-8hrs. I was able to complete my daily activities, with moderate fatigue; Day 6/7 over night= Same symptoms as a day 6 plus Moderate/ serve bone -pain woke me up from my sleep. Took Tylenol; I was able to complete daily activities but with moderate/severe fatigue; Day 7/8= Overnight Less pain, localized mainly in upper back. Persistent headaches and lymphadenopathy on my left armpit. Took Advil over night and during the day at q6-8 hrs. Worked from home that day with moderate/severe fatigue. Day 9= No more headache, pain localized upper back, between my arm plates. But new today chest tightness (difficulty breathing) with dry cough. At this time I called the occupational health at the hospital (my workplace) and scheduled a COVID test. COVID PCR Test results were NEGATIVE. The dry cough persisted for a period of time. Adverse events after my 2nd dose (Day 0= 02/04/21): I got my 2nd COVID 19 (Moderna) vaccine at 5.30pm. No immediate reactions post administration. I went back to work and completed the duties until 10pm (a very busy day in the department). Day 0/1: Around 11.30/midnight pm when I went to bed and I started to have chills and tremor like I have never had in my life (the bed was shaking). I could not talk and barely hold my phone in my hand. The next morning I was suppose to give a talk, but when I saw my symptoms I decided to notify the organizers. I barely managed to email them. Please see my reports on the v-safe for more details. Briefly: presented also with fever, very severe pain at the injection site+swelling. Painful lymphadenopathy on my hight armpit. Headache, muscle and body aches, severe fatigue, nausea (I have never been that sick in my life). Loss of appetite- I couldn't eat anything for >48hrs; I forced myself to keep hydrated. Along all these symptoms I also presented a profuse sweat (for 2 days night and day- at times I changed cloths every 30min-1hr), high HR, and heavy breathing, severe fatigue. I had an oximeter at home and the O2 saturation was below 90% at RT. One of the most alarming symptom that I had was the severe/unbearable headache/eye pain (felt like brain swelling), almost called 911.

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Called my Telemedicine and spoke with Dr. on 2/6/21, who recommended to increase the medicine doses (Tylenol and Advil) and if no effect to go to ER. Had a follow- up call with my PCP on 4/8/21.
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 1528616

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: KY
Alter: 54,0
Geschlecht: F
Eingang: 05.08.2021
Impfdatum: 12.01.2021
Beginn: 01.03.2021
Tage bis Beginn: 48,0
Dosis: 1
Route/Site: SYR / LA

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

Acoustic stimulation tests Magnetic resonance imaging head Migraine Tinnitus

Symptomtext

tinnitus migraine headaches (cervicogenic migraine headaches)

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Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: Hearing test MRI
Aktuelle Erkrankungen: -
Vorgeschichte: various auto-immune symptoms
Andere Medikamente: none
Allergien: penicillin, ampicillin by-products, sulfur
Vorherige Impfungen: -

VAERS 1519853

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: SD
Alter: 44,0
Geschlecht: F
Eingang: 02.08.2021
Impfdatum: 28.12.2020
Beginn: 28.12.2020
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Asthenia Back pain Burning sensation Chest X-ray Computerised tomogram thorax Dyspnoea Ear discomfort Ear pain Facial pain Fatigue Fibrin D dimer increased Full blood count Gait disturbance Headache Hypersensitivity Hypoaesthesia Immediate post-injection reaction Metabolic function test

Symptomtext

I had severe muscle cramping and pain within a couple hours of receiving my first Covid Vaccine, so bad I could barely walk up the stairs to my house. The pain decreased over the course of the following 2 weeks, but still had residual cramping/pain in my lower back. I received my 2nd dose on Jan. 28, 2021, and immediately started having debilitating headaches, pretty much everyday, had fatigue regularly after 2nd dose also. Then I noticed my allergies, generally not severe, got markedly more severe this year. About a month and a half ago, I started getting a facial parathesia on occasion. This includes a burning, painful, numb ears/face. The attacks of parathesia have increased in pain and numbness every time I get an onset, the last one happened 2 weeks ago. Also a couple weeks ago I started having a lot of issues breathing, so was seen by a doctor to get better inhalers/medicines. Last week I started having severe issues with breathing and over production of mucus. I also have an elevated D-Dimer, had to have a chest CT to make sure I did not have an pulmonary embolism. I still continue to have breathing issues and nobody can figure out exactly what is wrong with me. All reactions seem to be inflammatory in nature and all my issues started after the Moderna Covid Vaccine. I never had these issues prior and had no long term medical illnesses or underlying conditions.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: I have had CBC's multiple times (7/14/21 and 7/28/21), metabolic panels, Chest Xrays (7/28/21), Chest CT (7/29/2021), D-Dimer (elevated) 7/29/21, Covid Test (negative 7/28/2021),
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Vitamin D
Allergien: Fenagren anti nausea med.
Vorherige Impfungen: -

VAERS 1512587

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: AR
Alter: 55,0
Geschlecht: F
Eingang: 29.07.2021
Impfdatum: 19.01.2021
Beginn: 29.07.2021
Tage bis Beginn: 191,0
Dosis: 2
Route/Site: IM / RA

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

Anger Crying Fatigue Feeling abnormal Limb discomfort Mood altered Paraesthesia

Symptomtext

I feel very tired and fatigue all the time. On edge all the time. I feel empty on the inside, my head feels like I am in a fog all the time. Am very emotional all the time. I consider myself a very strong person. But every since the vaccine, am very mody, crying and angry all the time. I have no patience for people anymore. I was never like that at first. I was a out going type and now I always want to be a lone. Both of my arms feel very heavy and tingling all the time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: No
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: No
Allergien: No
Vorherige Impfungen: -

VAERS 1505328

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: -
Alter: 55,0
Geschlecht: F
Eingang: 27.07.2021
Impfdatum: 18.01.2021
Beginn: 18.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / -

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

Chills Dizziness Injection site pain Pyrexia Tremor

Symptomtext

Severe chills, whole body shook constantly, fever, light headed, faint feeling, sore arm at injection site.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None.
Vorgeschichte: None.
Andere Medikamente: None.
Allergien: None.
Vorherige Impfungen: -

VAERS 1498540

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: CT
Alter: 70,0
Geschlecht: F
Eingang: 23.07.2021
Impfdatum: 23.01.2021
Beginn: 12.02.2021
Tage bis Beginn: 20,0
Dosis: 1
Route/Site: IM / LA

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

Arthralgia Blood pressure increased Condition aggravated Joint swelling Musculoskeletal stiffness Tendonitis X-ray limb abnormal

Symptomtext

Approximately 2 weeks after 2nd dose: 1. increased arthritic pain, new ankle swelling pain - needed to use an air cast and ultimately diagnosed as Posterior tibial tendonitis on 6/3/2021 2. muscles so stiff in AM that it was hard to straighten legs -On 3-12-2021 Discussed with Dr. Infectious Dis specialist - treated with new anti-inflammatory herbs and herbs that stabilize mast cells - ? Quercetin 400 mg BID, ginger root 500 mg bid ? cucumin as Meriva 500-SF (Soy Free) 1 BID Dr. added low dose naltrexone now at 3 mg/d. 3. loss of control of blood pressure - 130/80 to 180/90 - increased lisinopril from 10 mg/d to 20 mg/day

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: BP checks at home under advice of PCP February 2021 X-rays of ankle 6/3/2021
Aktuelle Erkrankungen: None
Vorgeschichte: fibromyalgia 18 documented and treated episodes of lyme disease with persisting symptoms - fatigue, brain fog- with persistent high elevations of multiple Iglobulins on the Western Blot tests diabetes type 2 treated with diet, mild hypertension hypothyroidism restless leg syndrome ,idiopathic hypersomnia (sleep studies with MSLT) osteoarthritis in hands
Andere Medikamente: Armour Thyroid 120 mg 8 am fastng Armodafinil 250 mg mg q am for idiopathic hypersomnia Duloxetine 60 mg for fibromyalgia pain and loss of balance estradiol 0.05 mg patch applied approximately every wk medroxyprogesterone 5 mg da
Allergien: penicillin, cephalosporins crab, soy, peanuts, beans, peas
Vorherige Impfungen: -

VAERS 1490564

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: RI
Alter: 39,0
Geschlecht: M
Eingang: 21.07.2021
Impfdatum: 17.02.2021
Beginn: 18.03.2021
Tage bis Beginn: 29,0
Dosis: 1
Route/Site: SYR / LA

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

Chest discomfort Dyspnoea Fatigue Nasal congestion Respiratory tract congestion Respiratory tract infection

Symptomtext

Seemingly high susceptibility to respiratory infection. Historically, I have not had back to back respiratory conditions. Twice since the injections I have experienced a prolonged respiratory infection with symptoms lasting well over one month. Uncommon fatigue and heavy chest. Significant head congestion without runny nose or perceivable "drainage". I am currently sick with a respiratory infection that has gone on for appx. 6 weeks with heavy symptoms recently (i.e. bed ridden, extreme difficulty breathing, heavy congestion, etc.)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1487411

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: CA
Alter: 63,0
Geschlecht: F
Eingang: 20.07.2021
Impfdatum: 31.12.2020
Beginn: 31.12.2020
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / RA

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

Injected limb mobility decreased Periarthritis X-ray normal

Symptomtext

Arm could not move (frozen shoulder) due to the placement of the vaccine. Went to Primary Care, been sent to PT, did not work, going to see ortho, and get cortisone shot, but did not give full relief, still issues with mobility, can not put behind the chest. Can raise overhead more now.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: X-ray, was normal
Aktuelle Erkrankungen: -
Vorgeschichte: High blood pressure
Andere Medikamente: Losartin
Allergien: -
Vorherige Impfungen: -

VAERS 1481749

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: NC
Alter: 43,0
Geschlecht: M
Eingang: 18.07.2021
Impfdatum: 05.01.2021
Beginn: 25.02.2021
Tage bis Beginn: 51,0
Dosis: 1
Route/Site: OT / LA

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

Chest discomfort Dyspnoea Palpitations Rash Ventricular tachycardia

Symptomtext

Nonsustained ventricular tachycardia; Chest discomfort; Rash; S.O.B; Palpitations; This spontaneous case was reported by a consumer and describes the occurrence of VENTRICULAR TACHYCARDIA (Nonsustained ventricular tachycardia), DYSPNOEA (S.O.B), PALPITATIONS (Palpitations), CHEST DISCOMFORT (Chest discomfort) and RASH (Rash) in a 43-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 030C20A and 011J20A) for COVID-19 vaccination. Concurrent medical conditions included COPD (Frequent exacerbation), Hypertension, Diabetes, Shellfish allergy and Allergy to antibiotic (Cipro allergy). Concomitant products included METOPROLOL for Arrhythmia, SALBUTAMOL SULFATE (ALBUTEROL [SALBUTAMOL SULFATE]) for COPD, ATORVASTATIN for Hyperchloremia, HYDROCHLOROTHIAZIDE, LISINOPRIL (LISINOPRIL HCTZ) and AMLODIPINE for Hypertension. On 05-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 04-Feb-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 25-Feb-2021, the patient experienced DYSPNOEA (S.O.B) (seriousness criterion hospitalization), PALPITATIONS (Palpitations) (seriousness criterion hospitalization) and RASH (Rash) (seriousness criterion hospitalization). On 27-Mar-2021 at 12:06 PM, the patient experienced CHEST DISCOMFORT (Chest discomfort) (seriousness criterion hospitalization). On 26-May-2021, the patient experienced VENTRICULAR TACHYCARDIA (Nonsustained ventricular tachycardia) (seriousness criteria hospitalization and medically significant). The patient was hospitalized on 25-Feb-2021 due to DYSPNOEA and PALPITATIONS, then on 27-Mar-2021 due to CHEST DISCOMFORT, then on 25-May-2021 due to RASH, and then on 26-May-2021 due to VENTRICULAR TACHYCARDIA. At the time of the report, VENTRICULAR TACHYCARDIA (Nonsustained ventricular tachycardia), DYSPNOEA (S.O.B), PALPITATIONS (Palpitations), CHEST DISCOMFORT (Chest discomfort) and RASH (Rash) had not resolved. Patient reported that he visited cardiologist, primary care, emergency room multiple more times. He experienced unknown rash from beginning and continues. One of the emergency room visit on 27-May-2021 and went for palpitation, shortness breath and non sustained ventricular tachycardia was present. He admitted to hospital. He experienced rash on arm, then face, torso and now mid section and thighs have rah. Experiencing palpitation/ arrhythmias daily as well shortness of breath. Treatment information was not provided. Based on the current available information and temporal association between the use of mRNA-1273 and the onset of the events, a causal relationship cannot be excluded. However, the cardiac related disorders are confounded by the patient's underlying cardiac conditions) hypertension, arrhythmia, hypercholesterolemia) and diabetes; Sender's Comments: Based on the current available information and temporal association between the use of mRNA-1273 and the onset of the events, a causal relationship cannot be excluded. However, the cardiac related disorders are confounded by the patient's underlying cardiac conditions) hypertension, arrhythmia, hypercholesterolemia) and diabetes

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Allergy to antibiotic (Cipro allergy); COPD (Frequent exacerbation); Diabetes; Hypertension; Shellfish allergy
Vorgeschichte: -
Andere Medikamente: LISINOPRIL HCTZ; AMLODIPINE; ATORVASTATIN; METOPROLOL; ALBUTEROL [SALBUTAMOL SULFATE]
Allergien: -
Vorherige Impfungen: -

VAERS 1450210

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: NV
Alter: 57,0
Geschlecht: F
Eingang: 06.07.2021
Impfdatum: 29.12.2020
Beginn: 01.03.2021
Tage bis Beginn: 62,0
Dosis: 1
Route/Site: IM / LA

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

Blood test Chest X-ray Dyspnoea Echocardiogram Palpitations Thyroid function test Ultrasound scan Weight decreased

Symptomtext

I experienced racing heart, weight loss and shortness of breath.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Cardiogram-06/05/2021 Blood test-06/05/2021 Thyroid-06/05/2021 Ultrasound-06/05/2021 Chest X-ray-06/05/2021
Aktuelle Erkrankungen: No other ilnesses
Vorgeschichte: No chronic or long standing health conditions
Andere Medikamente: I take adderall
Allergien: I am allergic to sulfa cream
Vorherige Impfungen: -

VAERS 1441100

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: OR
Alter: 60,0
Geschlecht: F
Eingang: 01.07.2021
Impfdatum: 11.01.2021
Beginn: 28.01.2021
Tage bis Beginn: 17,0
Dosis: 1
Route/Site: SYR / LA

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

Cardiac stress test Chest pain Dyspnoea Electrocardiogram

Symptomtext

Woke up in morning to get ready for work. Went into the bathroom to urinate, had crushing chest pain, got back to bed. Subsided after after a couple minutes. Very scary, took my breath away. I cried and called into work to say I wouldn't be in. Called MD clinic when they opened and got seen. As an RN, I knew the serious nature of heat pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: EKG, Stress Test
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Estrogen Patch, Vit. C, Vit. D
Allergien: E-Mycin, Pseudoephedrine, Omeprazole
Vorherige Impfungen: -

VAERS 1440964

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: CT
Alter: 48,0
Geschlecht: F
Eingang: 01.07.2021
Impfdatum: 30.12.2020
Beginn: 30.12.2020
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Cardiac function test Chest discomfort Chest pain Dysgeusia Electrocardiogram Salivary hypersecretion Urticaria

Symptomtext

Within a few minutes, my mouth began to produce excessive amounts of saliva w/a metallic test, followed by hives and severe tightening of the chest. went home sick from work and ended going to the emergency department w/increased severe chest pains.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: EKG w/cardiac labs drawn. observation for several hours. 1-1-2021
Aktuelle Erkrankungen: none
Vorgeschichte: asthma and PVC's
Andere Medikamente: pro-air as needed.
Allergien: sulfa drugs
Vorherige Impfungen: -

VAERS 1434257

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: FL
Alter: 62,0
Geschlecht: M
Eingang: 29.06.2021
Impfdatum: 03.02.2021
Beginn: 01.04.2021
Tage bis Beginn: 57,0
Dosis: 1
Route/Site: IM / LA

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

Angiogram Atrial fibrillation Cardiac monitoring abnormal Cardiomyopathy Dyspnoea Ejection fraction decreased Electrocardiogram abnormal Palpitations Stress echocardiogram abnormal

Symptomtext

March/April 2021 began having palpitations and shortness of breath. EKG at PCP office confirmed new onset atrial fibrillation. Stress ECHO and Holter monitor confirmed a reduced ejection fraction and mild cardiomyopathy. Cardiac angiography confirmed suboptimal ejection fraction

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: See above
Aktuelle Erkrankungen: Hypertension Hypothyroidism
Vorgeschichte: same as above
Andere Medikamente: Losartan Cardura Synthroid
Allergien: none
Vorherige Impfungen: -

VAERS 1421094

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: MT
Alter: 74,0
Geschlecht: F
Eingang: 23.06.2021
Impfdatum: 13.01.2021
Beginn: 24.01.2021
Tage bis Beginn: 11,0
Dosis: UNK
Route/Site: IM / RA

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

Chest X-ray Cough Decreased appetite Diarrhoea Dyspnoea Full blood count Lethargy Metabolic function test Pain Pyrexia SARS-CoV-2 test positive Urine analysis

Symptomtext

Received Moderna 1/13/2021, began having poor appetite, loose stools on 1/24/2021. On 1/31/2021 patient had dry cough, fever, shortness of breath, body aches, lethargy and was admitted to the hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 6,0
Labordaten: 1/31/2021 - CBC, CMP, UA, Sars Co-V 2 positive, CXR
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Osteoarthritis Rheumatoid Arthritis Immunosuppression Gastritis Breast Cancer Spinal Stenosis Osteoporosis
Andere Medikamente: Ativan Cymbalta Prolia Rinvoq Topamax Diclofenac Gabapentin Tizanidine Flexeril Humira Nexium Premarin Synthroid Folic Acid Losartan
Allergien: Codeine Leflunomide Sulfadiazine
Vorherige Impfungen: -

VAERS 1415221

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: KY
Alter: 73,0
Geschlecht: F
Eingang: 21.06.2021
Impfdatum: 05.01.2021
Beginn: 21.06.2021
Tage bis Beginn: 167,0
Dosis: 1
Route/Site: IM / LA

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

COVID-19 Chest X-ray abnormal Dyspnoea Pneumonia SARS-CoV-2 test positive

Symptomtext

DIAGNOSED AND HOSPITALIZED WITH COVID-19 AND PNEUMONIA ON 6/21/21 AFTER BEING VACCINATED WITH MODERNA VACCINE IN JAN/FEB. SHE HAS HAD INCREASING SHORTNESS OF BREATH FOR SEVERAL DAYS AND SAW HER PCP TODAY. SHE IS ON STEROID MEDS AND NEB TREATMENTS FREQUENTLY.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 6/21/21-COVID-19 TEST AND CHEST X-RAY
Aktuelle Erkrankungen: HEART FAILURE AND LUNG PROBLEMS
Vorgeschichte: HEART FAILURE AND LUNG PROBLEMS
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1408221

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: WI
Alter: 55,0
Geschlecht: F
Eingang: 17.06.2021
Impfdatum: 15.01.2021
Beginn: 15.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Laboratory test Magnetic resonance imaging Paraesthesia X-ray

Symptomtext

On 01/15/2021 10:00 PM I had tingling like pins and needles down left and right arm and it is still continuing today. I had an office visit with my Doctor and I've had an x-ray of neck, MRI, blood tests. They do not know what's going on.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Lab tests, MRI, Neck X-ray
Aktuelle Erkrankungen: None.
Vorgeschichte: None.
Andere Medikamente: None.
Allergien: Components of anesthesia, adhesive sensitivity, Neosporin
Vorherige Impfungen: -

VAERS 1399044

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: AL
Alter: 34,0
Geschlecht: F
Eingang: 15.06.2021
Impfdatum: 28.12.2020
Beginn: 07.04.2021
Tage bis Beginn: 100,0
Dosis: 1
Route/Site: IM / LA

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

Angiogram Atrial fibrillation Atrial tachycardia Catheterisation cardiac Chest X-ray Dyspnoea Fatigue Fibrin D dimer Fibrin D dimer increased

Symptomtext

Episode of atrial fibrillation/atrial tachycardia- responded to propranolol-had blood work which showed elevated d-dimer-had a neg cta-had an echocardiogram which showed elevated right sided heart pressures-follow-up right heart cath showed elevated pulmonary artery pressures with exercise- 2 points away from being dx with exercise induced pulmonary htn-6 min walk test oxygen dropped to 93 and heart rate was elevated-awaiting PFTs Since early april have been have significant SOB with mild acitivity along with episodes of tachycardia and bradycardia-also days with significant fatigue

Weitere VAERSDATA-Felder

Praegender Schweregrund: Atrial tachycardia
Hospital-Tage: -
Labordaten: chest xray-april 14-normal D-Dimer 379-April 14 2021- went to ER that evening and had a neg CTA Echo-elevated right sided heart pressures-4/19/21 Right heart cath may 20 2021-PA systolic 36 Diastolic 18
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Prenatal Vitamins
Allergien: none
Vorherige Impfungen: -

VAERS 1397020

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: OR
Alter: 30,0
Geschlecht: F
Eingang: 14.06.2021
Impfdatum: 03.01.2021
Beginn: 07.01.2021
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Electrocardiogram Electrocardiogram ambulatory Laboratory test Nausea Palpitations Tachycardia

Symptomtext

Palpitations, dizziness, and nausea with associated intermittent tachycardia. Worse with exertion.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: EKG, labs and (1/7), Holter monitor (1/13)
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: topiramate
Allergien: Peanuts, erythromycin, PCN
Vorherige Impfungen: -

VAERS 1385188

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011j20a

moderat

Staat: MA
Alter: 54,0
Geschlecht: F
Eingang: 09.06.2021
Impfdatum: 26.01.2021
Beginn: 27.01.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Blood pressure increased Blood test Chest discomfort Dizziness Dyspnoea Echocardiogram normal Headache Heart rate abnormal Palpitations

Symptomtext

01/27/2021 I felt dizzy, I had a headache, around the afternoon around 4, I felt short of breath, tightness in chest, maybe around 6pm I started feeling my heart racing and I could feel abnormal heart rate, my pulse 180, my watch does an EKG and I did one and it said irregular heart rate possible Afib, seek medical care, went to ER. Saw cardiologist for an echo and it was okay. By the 28th of Jan I was fully recovered

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Pulse shot to 180 at ER. Bloodwork EKG, a lot of premature beats. Elevated BP, cannot recall number but lowered upon discharge
Aktuelle Erkrankungen: None
Vorgeschichte: Common Variable Immune deficiency disorder
Andere Medikamente: Multivitamin Loratadine Effexor Wellbutrin Adderall XR
Allergien: Bactrim
Vorherige Impfungen: -

VAERS 1372288

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: NY
Alter: 51,0
Geschlecht: F
Eingang: 03.06.2021
Impfdatum: 06.01.2021
Beginn: 06.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Biopsy Blood test normal Flushing Heavy menstrual bleeding Impaired work ability Insomnia Palpitations Polyp Rash Skin burning sensation Ultrasound scan normal Uterine dilation and curettage

Symptomtext

Right off that bat, I noticed heart palpitations and also flushing on the chest. I was getting a rash on chest. The EMT there told me to go home and take Benadryl. I took two of them. It didn't help with the symptoms. I called the doctor - he told me to take three Benadryl every six hours. I didn't really sleep that night - I was tired due to Benadryl. I put ice on my chest in the middle of the night because it was on fire. I remembered that I tried to go to work the next day but I couldn't. I went to the doctor. He told me to take 2 Benadryl one hour before the next shot. It took awhile for the symptoms to go away - I took Benadryl during the next week. I still had the rash on my chest. I went to the OB/GYN after that for my annual exam and after that I was bleeding and I thought it had been from my pap smear. I was bleeding very heavily - altogether it was three months of heavy bleeding. Medication to stop bleeding: Filled on Provera - 10 mg - on 2/8/2021 - they told me to take it for 10 days. Tranexamic acid -650 mg 2 tablets 3 times a day for up to 5 days.. They did bloodwork. I did a Sonogram. I had to leave during my work duties a couple of time (I'm a surgical assistant in surgeries) because I was bleeding and my co-workers told me I didn't look good. Had second dose of vaccine (lot number 004M20A) on 2/5/2021 - the bleeding got heavier (and in fact, immediately after I had the shot, I had to go to the bathroom I started bleeding so heavily - heavier than I had ever bled before) after the 2nd vaccine and the rash that I had after the first vaccine was still there but would come and go with Benadryl. I did testing on April 20th - for pre-surgery. I had a DNC on April 27th and after the DNC I felt so much better. The rash is gone; I'm not as tired. And I feel better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: 2,0
Labordaten: bloodwork - was done Sonogram - Gynecology office - they didn't see anything at that point. He said to wait. At that time, I was on medication to stop the bleeding: See above for dates of the first doses of the two meds to stop the bleeding. On 2/24/2021 - did another dose of Provera and I refilled another prescription of Tranexamic acid on 2/22/2021 Biopsy - Gynecology office - 2/24/2021 - they had me go to an Oncologist after this because they found something there and they didn't know if it was cancerous. Oncologist - he took over the case because after the biopsy, the gynecologist wasn't sure what was going on. They did a DNC deeper biopsy to find out. At the end - he said it was a polyp. There was no cancer. I had a DNC -After the surgery, I feel so much better - rash is gone; not as tired and I feel better.
Aktuelle Erkrankungen: no
Vorgeschichte: no
Andere Medikamente: I'm on Synthroid for thyroid
Allergien: sulfur
Vorherige Impfungen: -

VAERS 1346453

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: NC
Alter: 40,0
Geschlecht: M
Eingang: 25.05.2021
Impfdatum: 08.01.2021
Beginn: 08.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / RA

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

Acute kidney injury Blood test Chest X-ray Dyspnoea Echocardiogram Fatigue Heart injury Liver injury Pain

Symptomtext

Acute Liver and Kidney Injuries, severe fatigue, difficulty breathing, heart damage, body aches, etc.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Bloodwork - Numerous times, Echocardiogram - May 7th, 2021, Lung and heart x-ray - prior to May 7th, 2021, numerous doctor visits.
Aktuelle Erkrankungen: None
Vorgeschichte: -
Andere Medikamente: Andro-gel, Synthroid, multi-vitamin
Allergien: None
Vorherige Impfungen: -

VAERS 1324049

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: NJ
Alter: 49,0
Geschlecht: F
Eingang: 17.05.2021
Impfdatum: 19.01.2021
Beginn: 08.02.2021
Tage bis Beginn: 20,0
Dosis: 1
Route/Site: IM / -

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

Chest pain Computerised tomogram abnormal Dyspnoea Electrocardiogram Myocardial necrosis marker normal SARS-CoV-2 test negative

Symptomtext

I developed shortness of breath with exertion several weeks after the Moderna vaccine around February 8th. The shortness of breath became worse around the first week of April and I went to Non-urgent clinic on 4/4/21. Was given albuterol and recommended f/u with pulmonary specialist I also have had left-sided chest pain started around 4/20-4/21. I went to non-urgent clinic on 4/30/21 and chest pain felt to be costochondritis. Was recommended f/u with cardiology on routine basis.. I have not diagnosis yet. I am being followed by cardiologist and pulmonologist. I am reporting these symptoms because they started about 3 weeks-1 months after my first Moderna vaccine. I do not know if the Moderna vaccine caused these symptoms I am just stating it may be a possiblity.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 4/4/21-CT of chest-was told mild scarring EKG Rapid COVID negative 4/30/21-EKG negative , cardiac enzymes negative, Rapid COVID negative
Aktuelle Erkrankungen: -
Vorgeschichte: Arthritis Recurrent Depression Hyperlipidemia
Andere Medikamente: 1)Lithium Carbonate 600 mg twice a day 2)Prozac 20 mg daily 3)Topiramate 50 mg twice a day 4)Multivitamin one daily 5)Magnesium Oxide 250 mg daily 6)Vitamin D3 1000 IU twice daily 7)Cetirizine 10 mg daily 8)Fluticasone 1-2 sprays each nost
Allergien: CT iodine contrast
Vorherige Impfungen: -

VAERS 1317279

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: GA
Alter: 92,0
Geschlecht: M
Eingang: 14.05.2021
Impfdatum: 23.02.2021
Beginn: 17.04.2021
Tage bis Beginn: 53,0
Dosis: 1
Route/Site: IM / UN

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

Cough Dyspnoea

Symptomtext

Hospitalization due to shortness of breath and excessive coughing

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: No
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1317279

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: GA
Alter: 92,0
Geschlecht: M
Eingang: 14.05.2021
Impfdatum: 23.02.2021
Beginn: 17.04.2021
Tage bis Beginn: 53,0
Dosis: 2
Route/Site: IM / UN

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

Cough Dyspnoea

Symptomtext

Hospitalization due to shortness of breath and excessive coughing

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: No
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1315852

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: CO
Alter: 49,0
Geschlecht: M
Eingang: 13.05.2021
Impfdatum: 29.04.2021
Beginn: 29.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / RA

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

Blood test Hypertension

Symptomtext

Uncontrolled high blood pressure after second vaccination shot. Have no history of high blood pressure prior.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: Medical tests / blood work came back negative
Aktuelle Erkrankungen: No
Vorgeschichte: ADHD / high cholesterol
Andere Medikamente: Simvastatin Focalin Wellbutrin Prozac
Allergien: Bee stings
Vorherige Impfungen: -

VAERS 1299508

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: NY
Alter: 68,0
Geschlecht: M
Eingang: 08.05.2021
Impfdatum: 23.12.2020
Beginn: 15.01.2021
Tage bis Beginn: 23,0
Dosis: 1
Route/Site: IM / LA

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

Condition aggravated Dysaesthesia Malaise Pain Pain of skin Sensitive skin

Symptomtext

Marked local pain for 3 days. Approximately 3 weeks later regional painful skin to upper left chest , left scapula and then left upper outer arm and upper left back, all very sensitive to touch. This was CRPS reaction to shot, or shingles without rash. I had previously been vaccinated with Zostavax and both Shingrix shots. Now over three months later, my left upper back remains with dysphasia. There developed some intensely pruritic and painful papules to my left upper back. Never vesicles. I got a little relief from topical lidocaine and oral Gabapentin. My neurologist and I came to same opinion that ?something triggered by COVID shot?. Second COVID shot no big deal at all....just malaise hangover in first 12-48 hours.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: MI, CAD, DM
Andere Medikamente: Trulicity, ASA, Plavix, Farxiga, Metformin, Carvedilol, Lexapro, lisinopril, potassium citrate
Allergien: None
Vorherige Impfungen: -

VAERS 1270004

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: KS
Alter: 43,0
Geschlecht: F
Eingang: 29.04.2021
Impfdatum: 08.01.2021
Beginn: 08.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / LA

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

Anxiety Blood pressure increased Blood pressure measurement Feeling hot Heart rate Heart rate increased Nausea Panic reaction Paraesthesia Peripheral swelling Respiratory rate Swelling face Vaccination complication

Symptomtext

Felt bad but went to work; Panic feeling; Extreme nausea; Anxiety; Facial swelling; Warm tingling at the injection site; Left arm swelling; Hot all over the body; Pulse was up; Blood pressure up; This spontaneous case was reported by a nurse (subsequently medically confirmed) and describes the occurrence of SWELLING FACE (Facial swelling) in a 43-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 011J20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included Fever. Concurrent medical conditions included Asthma and Pollen allergy. On 08-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 08-Jan-2021, the patient experienced SWELLING FACE (Facial swelling) (seriousness criterion medically significant), PARAESTHESIA (Warm tingling at the injection site), PERIPHERAL SWELLING (Left arm swelling), FEELING HOT (Hot all over the body), HEART RATE INCREASED (Pulse was up), BLOOD PRESSURE INCREASED (Blood pressure up), ANXIETY (Anxiety) and NAUSEA (Extreme nausea). On an unknown date, the patient experienced VACCINATION COMPLICATION (Felt bad but went to work) and PANIC REACTION (Panic feeling). At the time of the report, SWELLING FACE (Facial swelling), PARAESTHESIA (Warm tingling at the injection site), PERIPHERAL SWELLING (Left arm swelling), FEELING HOT (Hot all over the body), HEART RATE INCREASED (Pulse was up), VACCINATION COMPLICATION (Felt bad but went to work), ANXIETY (Anxiety), PANIC REACTION (Panic feeling) and NAUSEA (Extreme nausea) outcome was unknown and BLOOD PRESSURE INCREASED (Blood pressure up) had not resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 08-Jan-2021, Blood pressure measurement: 140/98 (Inconclusive) 140/98 mmHg and 182/108 (Inconclusive) 182/108 mmHg. On 08-Jan-2021, Heart rate: 118 (Inconclusive) 118 beats per minute and 132 (Inconclusive) 132 beats per minute. On 08-Jan-2021, Respiratory rate: 24 (Inconclusive) 24 breaths per minute. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Based on the current available information and temporal association between the use of the product and the start date of the events, a causal relationship cannot be excluded. This case was linked to MODERNATX, INC.-MOD-2021-005905 (E2B Linked Report). Most recent FOLLOW-UP information incorporated above includes: On 14-Apr-2021: follow up received on 14-Apr-2021 included historical condition (asthma and fever), Allergically condition pollen allergy, lab data (blood pressure, heart rate and respiratory rate), concomitant medications (Symbicort Inhaler), treatment medication (Benadryl and Xanax), event (Panic Feeling).; Sender's Comments: Based on the current available information and temporal association between the use of the product and the start date of the events, a causal relationship cannot be excluded. MODERNATX, INC.-MOD-2021-005905:

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Test Date: 20210108; Test Name: blood pressure; Test Result: Inconclusive ; Result Unstructured Data: 140/98 mmHg; Test Date: 20210108; Test Name: blood pressure; Test Result: Inconclusive ; Result Unstructured Data: 182/108 mmHg; Test Date: 20210108; Test Name: heart rate; Test Result: Inconclusive ; Result Unstructured Data: 118 beats per minute; Test Date: 20210108; Test Name: heart rate; Test Result: Inconclusive ; Result Unstructured Data: 132 beats per minute; Test Date: 20210108; Test Name: Respiratory rate; Test Result: Inconclusive ; Result Unstructured Data: 24 breaths per minute
Aktuelle Erkrankungen: Asthma; Pollen allergy
Vorgeschichte: Medical History/Concurrent Conditions: Fever
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1235464

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: CA
Alter: 50,0
Geschlecht: F
Eingang: 20.04.2021
Impfdatum: 02.01.2021
Beginn: 18.01.2021
Tage bis Beginn: 16,0
Dosis: 1
Route/Site: SYR / LA

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

COVID-19 Chest discomfort Chest pain Diarrhoea Headache Infusion Pain Pharyngeal swelling Pyrexia SARS-CoV-2 test positive

Symptomtext

I was exposed to Covid 5 days after vaccine. I tested positive 10 days after vaccine. 12 days after has headache , aches, diarrhea. Got the Regeneron monoclonal antibody infusion s 1/18 and had throat swelling about 1 hour into the infusion and got benedryl. Improved so went home then about 5 hours after the infusion. I had chest pain and chest tightness so went to the ER with concern if re action to this infusion. Took benedryl and xopenex and that help. I went home ER after PE and MI ruled out Had fever a few days later so got augmentin. The headache and aches from Covid slowly resolved. No further chest pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: CT of chest. D dimer. Ekg.
Aktuelle Erkrankungen: Covid,
Vorgeschichte: Mast cell disorder , gerd, svt, allergies , asthma , low igg
Andere Medikamente: Verapamil , Zyrtec , singular, Pepcid, nexium, Regeneron
Allergien: Sulfa, codeine, cefzil, Omnicef, toradol, levaquin
Vorherige Impfungen: Influenza- not sure brand. Throat itching

VAERS 1230511

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: CA
Alter: 56,0
Geschlecht: F
Eingang: 19.04.2021
Impfdatum: 28.12.2020
Beginn: 29.12.2020
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / RA

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

Anxiety Arthralgia Chills Dyspnoea Insomnia Pyrexia

Symptomtext

C/o worsening insomnia/anxiety after 2nd dose COVID-19 vaccine administered 03/26/21. Per HCW, anxiety presents at night when trying to sleep and is unsure if anxiety is causing insomnia or vice-versa. Per HCW, she slept well this weekend after taking herbal supplement "Ashwagandha" on night of 04/17/21 and 04/18/21. Unsure if insomnia/anxiety is resolved. Reported fever, chills, joint pain, difficulty breathing and insomnia/anxiety approx. 24-48 hours post 1st dose of COVID Vaccine on 12/28/2021. Per HCW, she missed 4 days of work after initial dose. Initial symptoms resolved using rest and Tylenol. Per HCW, her PCP felt s/s were consistent with Flu. Per HCW, PCP approved her to take 2nd COVID vaccine dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: No
Aktuelle Erkrankungen: Insomnia induced by COVID vaccine. Flu like S/S post vaccine
Vorgeschichte: Hypertension maintained by Maxzide.
Andere Medikamente: Maxzide 37.5 mg PO Every day.
Allergien: Flu Shot Allergy. Had MD Note to proceed with COVID Vaccine
Vorherige Impfungen: Approx. 5 years experienced lip swelling and difficulty breathing with Flu Vaccine.

VAERS 1229067

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: GA
Alter: 53,0
Geschlecht: F
Eingang: 19.04.2021
Impfdatum: 04.01.2021
Beginn: 17.01.2021
Tage bis Beginn: 13,0
Dosis: 1
Route/Site: IM / -

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

Chest pain Dyspnoea Palpitations

Symptomtext

Palpitations, particularly when supine, as well as chest pain and shortness of breath which lasted approximately 2 weeks. She was seen in the hospital ER without cause found and labs were normal. Palpitations self-resolved within 6-8 weeks after initiation.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Full records from hospital not available at time of report
Aktuelle Erkrankungen: None
Vorgeschichte: Type 2 Diabetes Mellitus, HTN, neuropathy
Andere Medikamente: Gabapentin, Metformin, Farxiga, Lantus, Novolog
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1226427

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: MO
Alter: 49,0
Geschlecht: M
Eingang: 18.04.2021
Impfdatum: 23.12.2020
Beginn: 20.03.2021
Tage bis Beginn: 87,0
Dosis: 2
Route/Site: IM / RA

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

Blindness Blood creatinine increased COVID-19 Computerised tomogram head abnormal Dehydration Laboratory test Mydriasis Optic neuritis Petechiae Pyrexia SARS-CoV-2 test positive

Symptomtext

Petechiae to arms, chest, abdomen, and back. Fever of 104 on 1/11/21. Elevated creatnine. Admitted to Emergency room for dehydration and diagnosed with covid 19. On 3/20/21 lost vision to left eye. Saw the doctor and diagnosed with optic neuritis. On 4/11/21 lost vision to right eye. Went to emergency room, at the local medical center emergency room and the doctor also diagnosed with optic neuritis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dehydration
Hospital-Tage: 1,0
Labordaten: CT brain, eyes dilated and labs drawn.
Aktuelle Erkrankungen: none
Vorgeschichte: high blood pressure
Andere Medikamente: amlododipine
Allergien: none
Vorherige Impfungen: -

VAERS 1213027

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: NC
Alter: 29,0
Geschlecht: F
Eingang: 15.04.2021
Impfdatum: 22.01.2021
Beginn: 22.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Fatigue Headache Hyperacusis Migraine Nausea Photophobia

Symptomtext

Severe migraine, complicated with nausea and sensitivity to light and sound, not alleviated by general migraine medications, lasted approximately 6 hours. Significant fatigue and headache following day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: none
Vorgeschichte: hx migraines, gerd, asthma, depression, anxiety, endometriosis
Andere Medikamente: zonisomide, aygestin, wellbutrin, geodon, melatonin, nexium, imitrex, phenergan
Allergien: latex
Vorherige Impfungen: -

VAERS 1207902

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: NY
Alter: 76,0
Geschlecht: M
Eingang: 14.04.2021
Impfdatum: 29.12.2020
Beginn: 03.01.2021
Tage bis Beginn: 5,0
Dosis: 1
Route/Site: IM / LA

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

Antibody test negative Injection site pain Mobility decreased SARS-CoV-2 antibody test

Symptomtext

Persistent pain in left upper arm over three months after first injection. Worse at night. For the first month, some loss of function in left arm/shoulder but that has resolved now. Dull pain persists.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: My doctor ordered an antibody test but IgG was negative. However, test used by lab does not measure the Spike Protein, only the nucleocapsid protein so not surprising.
Aktuelle Erkrankungen: None
Vorgeschichte: Controlled hypertension, Gout, osteoarthritis
Andere Medikamente: Aspirin, Chlorthalidone, Lisinopril, Allopurinol, Vit. D, Multivitamin, Atorvastin, Primidone
Allergien: None
Vorherige Impfungen: -

VAERS 1206878

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: MA
Alter: 57,0
Geschlecht: F
Eingang: 14.04.2021
Impfdatum: 16.01.2021
Beginn: 16.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / -

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

Paraesthesia oral Swollen tongue

Symptomtext

Tingling tongue; Tongue swelling; This spontaneous case was reported by a non-health professional and describes the occurrence of PARAESTHESIA ORAL (Tingling tongue) and SWOLLEN TONGUE (Tongue swelling) in a 57-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 011J20A) for COVID-19 vaccination. The patient's past medical history included No adverse event (No adverse event history). On 16-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 16-Jan-2021, the patient experienced PARAESTHESIA ORAL (Tingling tongue) (seriousness criterion medically significant) and SWOLLEN TONGUE (Tongue swelling) (seriousness criterion medically significant). At the time of the report, PARAESTHESIA ORAL (Tingling tongue) and SWOLLEN TONGUE (Tongue swelling) was resolving. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown Route) was unknown. Treatment provided was Benadryl 50mg. This case concerns a 57-year-old female with a serious unexpected event of paraesthesia oral and swollen tongue. Event onset about 20 minutes after first dose mRNA-1273. Treated with Benadryl. Events resolving. Based on current available information and temporal association between the use of the product and the start date of the event, a causal relationship cannot be excluded. Reporter did not allow further contact; Sender's Comments: This case concerns a 57-year-old female with a serious unexpected event of paraesthesia oral and swollen tongue. Event onset about 20 minutes after first dose mRNA-1273. Treated with Benadryl. Events resolving. Based on current available information and temporal association between the use of the product and the start date of the event, a causal relationship cannot be excluded.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia oral
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: No adverse event (No adverse event history)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1202652

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: NC
Alter: 84,0
Geschlecht: F
Eingang: 13.04.2021
Impfdatum: 05.02.2021
Beginn: 07.04.2021
Tage bis Beginn: 61,0
Dosis: 1
Route/Site: IM / LA

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

COVID-19 Pneumonia aspiration SARS-CoV-2 test positive

Symptomtext

PERSON RECEIVED MODERNA COVID VACCINE DOSE 1 & DOSE 2 AT COUNTY HEALTH DEPARTMENT. TESTED POSITIVE FOR COVID 4/7/21 AND WAS ADMITTED TO HOSPITAL FOR ASPIRATION PNEUMONIA 4/11/21.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pneumonia aspiration
Hospital-Tage: 2,0
Labordaten: N/A
Aktuelle Erkrankungen: UNSURE
Vorgeschichte: UNSURE
Andere Medikamente: UNSURE
Allergien: UNSURE
Vorherige Impfungen: -

VAERS 1197239

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: IN
Alter: 58,0
Geschlecht: F
Eingang: 12.04.2021
Impfdatum: 09.04.2021
Beginn: 10.04.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Blood test Chills Disorientation Dyspnoea Fatigue Injection site erythema Injection site pruritus Injection site swelling Pain Pharyngeal swelling Scan Swelling face X-ray

Symptomtext

I was notified by on 4/12/21 @ 9:00 AM. Neither nor I was contacted by the employee. I called and left her a message to contact me. @ 11:51 she contacted me from work and stated on 4/9/21, Friday ~1800 just got very tired so she laid down. She stated she had chills and had body aches. She awoke at 2 AM ?grasping for air? and took her nebulizer. She stated the episode was different from normal shortness of breath with COPD, but the treatment helped. She stated her face was swollen, and her left deltoid at the injection site was red & swollen. She stated shortly an hour or so after the injection the site became ?itchy? but she thought was from the band-aid which she removed. On 4/10/21 morning she called in leave time because she thought was due to her COPD. 4/10/21 ~ 7 pm or 8 pm she called an ambulance and was transported to health center due to shortness and felt like ?throat was swollen. She stated she slept and stated felt ?disoriented.? She stated the hospital gave her IV steroids (one dose only she thinks). She stated the night and discharged on 4/11/21 morning with no new prescriptions. The attending physician. She was told to follow up with her provider, in 5-7 days. Vaccinated on 4/9/21 @ 14:30, Left deltoid: Redness at injection site improving on 4/12/21 per employee.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 1,0
Labordaten: Per Patient the hospital did an x-ray, blood work, and ?some sort of scan to rule out blood clot in my lungs, which was ruled out.? Unable to verify or did not see results.
Aktuelle Erkrankungen: Stated having memory loss and started work up for it, no acute illness.
Vorgeschichte: Known COPD
Andere Medikamente: Unknown
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 975647

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: NY
Alter: 35,0
Geschlecht: F
Eingang: 08.04.2021
Impfdatum: 13.01.2021
Beginn: 13.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Cardiovascular evaluation Dyspnoea Electrocardiogram Electrocardiogram ambulatory Fatigue Computerised tomogram Echocardiogram Feeling jittery Flushing Feeling abnormal Heart rate increased Laboratory test Malaise Nervousness Tachycardia Palpitations Paraesthesia Sleep disorder

Symptomtext

After the vaccine, I walked up stair to leave. I felt flush, and my heart began to race. That evening, I noticed I was out of breath, more than usual. Then the next day, I was in tachycardia while resting. Climbing the stairs at home, my heart rate was above 140 BPM. I was trying to not move around alot to keep my heart rate down. It was an uncomfortable feeling. I called my doctor and had a video visit on 01/18/2021 and the on 01/21/2021 my heart rate was up over 100 BPM while just sitting. It felt like something was off with the biochemistry of my body. I saw Cardiology on 01/22/2021 and on 01/23/2021 they sent me to see a POTTS specialists. When I took a shower on 01/25/2021 my heart rate went up and my nervous system was activated. I started taking cold showers afterwards. It seems to help. On 01/29/2021 I started getting tingling in my feet that moved to my hands. It flairs up when I am stressed. On 02/27/2021 I had bloodwork that shows my ANA as POS with the numbers greater than 2,560. I know that 6 months prior, I had NEG ANA results. I also experienced fatigue, trouble sleeping and brain fog.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: I had a cardiac work up with an EKG, Holter Monitor and labs drawn.
Aktuelle Erkrankungen: No other illnesses at the time of vaccination and up to one month prior.
Vorgeschichte: No chronic or long-standing health conditions.
Andere Medikamente: I was not taking any prescriptions, over-the-counter medications, dietary supplements or herbal remedies.
Allergien: I am allergic to bactrim.
Vorherige Impfungen: -

VAERS 975647

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: NY
Alter: 35,0
Geschlecht: F
Eingang: 08.04.2021
Impfdatum: 13.01.2021
Beginn: 13.01.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Cardiovascular evaluation Dyspnoea Electrocardiogram Electrocardiogram ambulatory Fatigue Computerised tomogram Echocardiogram Feeling jittery Flushing Feeling abnormal Heart rate increased Laboratory test Malaise Nervousness Tachycardia Palpitations Paraesthesia Sleep disorder

Symptomtext

After the vaccine, I walked up stair to leave. I felt flush, and my heart began to race. That evening, I noticed I was out of breath, more than usual. Then the next day, I was in tachycardia while resting. Climbing the stairs at home, my heart rate was above 140 BPM. I was trying to not move around alot to keep my heart rate down. It was an uncomfortable feeling. I called my doctor and had a video visit on 01/18/2021 and the on 01/21/2021 my heart rate was up over 100 BPM while just sitting. It felt like something was off with the biochemistry of my body. I saw Cardiology on 01/22/2021 and on 01/23/2021 they sent me to see a POTTS specialists. When I took a shower on 01/25/2021 my heart rate went up and my nervous system was activated. I started taking cold showers afterwards. It seems to help. On 01/29/2021 I started getting tingling in my feet that moved to my hands. It flairs up when I am stressed. On 02/27/2021 I had bloodwork that shows my ANA as POS with the numbers greater than 2,560. I know that 6 months prior, I had NEG ANA results. I also experienced fatigue, trouble sleeping and brain fog.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: I had a cardiac work up with an EKG, Holter Monitor and labs drawn.
Aktuelle Erkrankungen: No other illnesses at the time of vaccination and up to one month prior.
Vorgeschichte: No chronic or long-standing health conditions.
Andere Medikamente: I was not taking any prescriptions, over-the-counter medications, dietary supplements or herbal remedies.
Allergien: I am allergic to bactrim.
Vorherige Impfungen: -

VAERS 1171572

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011j20A

moderat

Staat: AZ
Alter: 46,0
Geschlecht: F
Eingang: 06.04.2021
Impfdatum: 07.01.2021
Beginn: 07.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Axillary pain Dizziness Headache Injection site pain Injection site swelling Mobility decreased Nausea Pain Pyrexia

Symptomtext

With first shot. Extreme pain on arm of immunized arm. Swelling and decreased mobility. same day of injection 01/07/21 around 6pm. Next day Friday January 08 2021 missed work due to mild body aches, head ache, severe pain on arm, decreased mobility. Under arm pain and swelling on arm of vaccine given. Temp of 99.5-99.9 Had symptoms for 2 full days. 2nd shot. Same day of immunization of 02/04/21 right arm mildly ached. Later on that day around 7-8 pm still had mild pain on arm . Moderate body aches, headache, nausea. The next day 02/05/21 Extreme body aches, horrible headache concentrated on eyes. 100.1 -100.5 temp for 2 days. Symptoms of dizziness and extreme body aches lasted for 4 days and then slowly left.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: Depression Anxiety Hypothyroidism
Andere Medikamente: Prozac, Levothyroxine, Collagen,
Allergien: none
Vorherige Impfungen: -

VAERS 1171329

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: IN
Alter: 56,0
Geschlecht: F
Eingang: 06.04.2021
Impfdatum: 30.03.2021
Beginn: 30.03.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Chest discomfort Hypertension Pain Pyrexia Urticaria

Symptomtext

Patient was vaccinated on 03/30/2021 @ 1340. At 1159 the same day, patient started with hives all over her body, tightening in her chest, HTN (186/119), fever and body aches. Patient went to the Emergency Room and was treated for an allergic reaction and released. She called our onsite RN on 31MAR21 to report.

Weitere VAERSDATA-Felder

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

VAERS 2555620

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011j20A

moderat

Staat: -
Alter: 53,0
Geschlecht: F
Eingang: 31.03.2021
Impfdatum: 31.03.2021
Beginn: 02.01.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: IM / LA

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

Arthralgia Migraine Myalgia Oropharyngeal pain Pyrexia

Symptomtext

Myalgia, Arthralgia, Fever, migraine, sore thorat Narrative:

Weitere VAERSDATA-Felder

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

VAERS 1147198

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: -
Alter: 58,0
Geschlecht: F
Eingang: 30.03.2021
Impfdatum: 26.12.2020
Beginn: 14.01.2021
Tage bis Beginn: 19,0
Dosis: 1
Route/Site: IM / RA

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

COVID-19 pneumonia Lung opacity Parotid gland enlargement Parotitis SARS-CoV-2 test positive Tachycardia

Symptomtext

58 yo female, BMI 41, PMHx of diabetes and HTN, admitted for COVID-19 pneumonia, tachycardia, L parotid tenderness and swelling and possible volume depletion on 1/14/2021. CT of chest from 1/14/21 reveals scattered groundglass opacities (B). COVID treated with supportive care, parotiditis treated with vancomycin. Patient discharged to home on 1/19/2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1146734

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: AK
Alter: 29,0
Geschlecht: F
Eingang: 30.03.2021
Impfdatum: 26.01.2021
Beginn: 26.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dysgeusia Oral discomfort Paraesthesia oral Swollen tongue

Symptomtext

About 30 minutes after receiving her first dose of Moderna Vaccine, she started to feel burning in her mouth, swollen tongue, and taste of metal. In the weeks to follow, it progressed to burning/tingling lips.

Weitere VAERSDATA-Felder

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

VAERS 1138103

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: CA
Alter: 31,0
Geschlecht: M
Eingang: 26.03.2021
Impfdatum: 15.01.2021
Beginn: 17.01.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / LA

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

Influenza like illness Migraine Pyrexia

Symptomtext

On the third day after vaccination, I started to get a Migraine. It was localized Migraine on the left side of my face which was the same side as I was vaccinated on. I have never had a Migraine before. The migraine lasted for three days I got the second dose and had felt like I had the flu with a fever for 14 hours but no Migraine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Vitamin c Athletic Grains Probiotic Zinc Fish oil Klonopin as needed rarely
Allergien: Penicillin drugs-hives as child
Vorherige Impfungen: -

VAERS 1132308

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: NH
Alter: 51,0
Geschlecht: M
Eingang: 25.03.2021
Impfdatum: 24.03.2021
Beginn: 24.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Flushing Hypoaesthesia Paraesthesia

Symptomtext

flushing, left arm tingling and numbness resolving within 30 minutes

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None known
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: none known
Vorherige Impfungen: -

VAERS 1130999

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: OH
Alter: 49,0
Geschlecht: F
Eingang: 24.03.2021
Impfdatum: 23.12.2020
Beginn: 30.12.2020
Tage bis Beginn: 7,0
Dosis: 1
Route/Site: IM / LA

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

Alopecia Arthralgia Condition aggravated Swelling Swelling face

Symptomtext

I noticed that I started swelling - my hands and my feet especially; my Provider noticed it - she noticed my face was really swollen (I work at the office of my provider). It happened a week after the vaccine - she put me on Lasix to help with the swelling and my joints had pain. It flared up my joint pain from Fibromyalgia. Two weeks after that I started losing a lot of hair - it was more handfuls then I had ever lost before. It lasted up through when I got the second shot. The Lasix brought the swelling down in my face but it didn't bring it down in my legs. Fibromyalgia symptoms and swelling and still a little hair loss (although hair loss was slowing down)was happening at time of second vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: no
Aktuelle Erkrankungen: none
Vorgeschichte: Fibromyalgia; High ANA - weakened immune system; Reynaud's disease; Lump on my thyroid
Andere Medikamente: I didn't take my allergy shots; Benefiber; CoQ10; Apple Cider Vinegar Pills; Propranolol; Pravastatin
Allergien: Sucrose; Sulpha; Celebrex
Vorherige Impfungen: -

VAERS 1127685

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: CA
Alter: 50,0
Geschlecht: M
Eingang: 23.03.2021
Impfdatum: 14.01.2021
Beginn: 14.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Aphasia Bone pain Carpal tunnel syndrome Dizziness Dysgeusia Electrocardiogram normal Feeling abnormal Hypopnoea Impaired work ability Influenza like illness Mental impairment Mouth breathing Nasal congestion Nerve injury Pain Paraesthesia oral SARS-CoV-2 test negative

Symptomtext

After I got the shot, on the way home, I started feeling tingling on tongue and lips; had a metallic taste. I felt like I had allergies - I was a little congested - but the next morning, 04:00 am - I was still congested - and was still breathing short and shallow. I get to work and I'm open mouth breathing - not breathing correctly. It felt like my lungs were swollen on the inside and throat was swollen on inside. Couldn't palpate and feel it but just couldn't access the lower lungs breathing-wise. Started getting dizzy and couldn't think - from 05:00 am to 09:00 am - and I decided I couldn't work anymore. I went to headquarters and I couldn't talk from lack of breathing - would have to stop just to think or just to breathe. I drove by the clinic where I was got my vaccine and decided to go in - I was so dizzy and I realized I shouldn't be driving. They told me to get up and move and I told them I couldn't breathe and I'm not one to say that but they called an ambulance that took me ER. (I was a LPN at one time so I wasn't anxious.) And they told me it was anxiety - and they kept telling me to breathe. But it wasn't an anxiety attack at all. My heartrate was normal. I was shallow breathing. They gave me a paper bag to breathe into. That's it .I was there for a couple of hours. They had told me to rest. I shouldn't have gotten out of bed that morning - my body just didn't want to move. I felt a little better after a couple of hours and people helped me from there to get home. After that, I felt better - about 4 pm or 5 pm. Second vaccine - felt flu like symptoms for three days after. I still feel a little weird - my bones hurt and I'm achy. Just not feeling right. Note: When I was in the emergency room - my hands were purple. Circulation was weird.They told me my oxygen levels were fine and that I just needed to breathe. It caused carpal tunnel in my wrist - I had nerve damage on that about three weeks - I have about 80 percent nerve damage from previous and so when something irritates it - it takes a while to recover from it but I have. I consulted with a doctor about the reaction to first vaccine before getting the second vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia oral
Hospital-Tage: -
Labordaten: EKGs - everything was just fine - at ER
Aktuelle Erkrankungen: three weeks prior - had a cold and was negative for COVID
Vorgeschichte: no
Andere Medikamente: no
Allergien: no except- seasonal type allergies - pollen
Vorherige Impfungen: -

VAERS 1109712

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: CA
Alter: 52,0
Geschlecht: F
Eingang: 17.03.2021
Impfdatum: 14.01.2021
Beginn: 03.02.2021
Tage bis Beginn: 20,0
Dosis: 1
Route/Site: IM / -

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

Acoustic stimulation tests Dyspnoea Hyperacusis Hypoacusis Vertigo

Symptomtext

Muffled /decreased hearing in both ears, voices seemed too loud and harsh. Very bad shorteness of breath, vertigo

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 02/12/2021 Medical facility over the phone consultation. Placed on Amoxicillin 1000mg twice a day for 7 days. 02/14/2021 Medical facility. Placed on Prednisone 40mg once daily for 5 days, Meclizine 50 mg a day, Claritin 10mg a day 02/22/2021 Medical facility over the phone consultation for referral to ENT 03/04/2021 Hearing test done at Medical facility 03/12/2021 ENT appointment in person at Medical facility
Aktuelle Erkrankungen: 12/14/2021 dry cough
Vorgeschichte: None
Andere Medikamente: None
Allergien: Pseudoephedrine
Vorherige Impfungen: -

VAERS 1104079

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011j20a

moderat

Staat: PA
Alter: 23,0
Geschlecht: F
Eingang: 16.03.2021
Impfdatum: 02.02.2021
Beginn: 12.03.2021
Tage bis Beginn: 38,0
Dosis: 2
Route/Site: IM / LA

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

Abdominal pain Arthralgia COVID-19 Chest pain Dysphagia Dyspnoea Fatigue Headache Impaired work ability Nausea Pain Pain in jaw Pyrexia SARS-CoV-2 test negative Vomiting White blood cell count increased

Symptomtext

Abdominal pain, nausea, vomiting, low grade fever, headache, body-aches, fatigue, joint pain, jaw pain, sharp chest pain when breathing and swallowing, etc. Was seen in hospital ED on 3/14/2021. Covid-19 tested negative on 3/14/2021. Missed work two days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: WBC was elevated
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: BC pills and multivitamins
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 1101598

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: AK
Alter: 50,0
Geschlecht: F
Eingang: 15.03.2021
Impfdatum: 20.01.2021
Beginn: 01.02.2021
Tage bis Beginn: 12,0
Dosis: 2
Route/Site: IM / -

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

Condition aggravated Pemphigoid

Symptomtext

Caused a Flare-up of Bullous Pemphigoid (flushed burning skin, with bullous blisters)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Chronic pain, low thyroid,
Andere Medikamente: Buproprion 300 mg XL Levothyroxine 75 mcg Naltrexon 25 mg topirimate 75 mg
Allergien: morphine, phenergan iv, reglan, oxycillin, avelox, amitryptyline,
Vorherige Impfungen: -

VAERS 1098582

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: MO
Alter: 61,0
Geschlecht: M
Eingang: 14.03.2021
Impfdatum: 25.01.2021
Beginn: 08.02.2021
Tage bis Beginn: 14,0
Dosis: 1
Route/Site: IM / RA

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

Arthralgia Asthenia Dyspnoea Fatigue Headache Pyrexia Rash

Symptomtext

After first shot in series, I developed slight headache, minor weakness, minor shoulder pain. After second shot in series, 8 hours post-injection, I developed headache, moderate to severe joint pain throughout, fever around 100, extreme fatigue and weakness, slight difficulty breathing. Went to bed for 19 hours and began to feel better with recovery in two days. 14 days post-injection, I developed a systemic rash throughout my body. Consulted with my PC physician. Was prescribed Medrol Dose Pack. This had very minor effect on rash. Returned to physician for consult upon completion of steroid series. I then received a steroid shot intramuscular in right hip and one week oral steroid protocol. This achieved a more positive result, almost clearing up the rash. I had a consult with a dermatologist on 03/02/2021 who confirmed the opinion that the rash was probably a side effect of the Moderna vaccine. The rash has returned fully as of 3/14/2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Heart Disease
Andere Medikamente: Fish Oil Multi Vitamin
Allergien: NKA
Vorherige Impfungen: -

VAERS 1088203

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: OH
Alter: 32,0
Geschlecht: F
Eingang: 10.03.2021
Impfdatum: 30.12.2020
Beginn: 04.01.2021
Tage bis Beginn: 5,0
Dosis: 1
Route/Site: IM / RA

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

Asthma Chest discomfort Chest pain Chills Dyspnoea Headache Nausea Pain Pain in extremity Vaccination complication Wheezing

Symptomtext

Symptoms from vaccine did not start until Day 5. I woke up at 0900 with a sore arm, nausea, headache, generalized aches, chills. By that evening (unsure of time), started with my usual asthma flare-up symptoms. These include, soreness of breath, chest tightness and pain, wheezing. I started treatment at home with q4h DuoNeb breathing treatments and a decreasing prednisone prescription. This treatment did not work so I followed up with my pulmonologist and his PA-C for a follow-up. They made the decision that this flare up was caused "by my immune response to the covid vaccine."

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Decreasing prednisone prescription for 7 days started Tuesday, January 5th, 2021. Second prescription of decreasing prednisone for 7 days started Friday, January 15th, 2021.
Aktuelle Erkrankungen: none
Vorgeschichte: Persistent severe asthma
Andere Medikamente: Breo 200/25 1 inhalation daily at HS. Singulair 10mg PO daily at HS. Lexapro 20mg PO daily at HS. Magnesium glycinate 240mg PO daily at HS. NuvaRing - vaginal insertion, keep in for 3 weeks at a time. Vitamin D3 125mcg PO daily. Vitamin B1
Allergien: Adverse Reactions to Advair (causing involuntary muscle spasms) and Benzodiazepines (causes seizures).
Vorherige Impfungen: -

VAERS 1087594

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: IN
Alter: 43,0
Geschlecht: M
Eingang: 10.03.2021
Impfdatum: 07.03.2021
Beginn: 07.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Dyspnoea Throat irritation

Symptomtext

Patient received a COVID-19 vaccine on 07MAR21 @ 1900. At 2111, he complained of a scratchy throat and shortness of breath. He has a history of asthma and uses Prednisone and nebulizers at home. He was given Benadryl 25 mg po at 2111 by our onsite nurse and was monitored an additional 30 minutes.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Obesity Asthma
Andere Medikamente: -
Allergien: Penicillin Shellfish Grape Seed Oil
Vorherige Impfungen: -

VAERS 1084720

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: KS
Alter: 42,0
Geschlecht: F
Eingang: 09.03.2021
Impfdatum: 31.12.2020
Beginn: 04.01.2021
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: SYR / RA

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

Fatigue Feeling abnormal Headache Nausea SARS-CoV-2 test negative Tremor

Symptomtext

12/31/2020 vaccination 1/4 I had to leave work. I started to get a bad HA, shaky, 'brain fog'. No fever. Kept feeling extreme nauseous. I went and called dr., said it sounded vaccine related. She did a rapid test; negative. I was extremely fatigued. She did prescribe Zofran.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: COVID; neg
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: Allergy medicine, Effexor 75mg
Allergien: sulfa
Vorherige Impfungen: -

VAERS 1076152

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: NY
Alter: 40,0
Geschlecht: F
Eingang: 05.03.2021
Impfdatum: 06.01.2021
Beginn: 08.01.2021
Tage bis Beginn: 2,0
Dosis: UNK
Route/Site: - / LA

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

Condition aggravated Feeling abnormal Fibromyalgia Malaise Myalgia

Symptomtext

Fibromyalgia flare after 12 years of remission. Extreme myalgia, brain fog , malaise x 4 weeks post 1st dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Fibromyalgia in remission
Andere Medikamente: N/A
Allergien: Fish, Codeine, Eggplant
Vorherige Impfungen: -

VAERS 1075815

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: IN
Alter: 23,0
Geschlecht: M
Eingang: 05.03.2021
Impfdatum: 04.03.2021
Beginn: 04.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Abdominal pain Arthralgia Chills Headache Injection site pain Lacrimation increased Nausea Salivary hypersecretion Tremor

Symptomtext

Patient received a COVID-19 vaccine on 04MAR21 @ 1400. At 1645, he returned to the vaccine room shaking and his eyes were tearing up. He complained of pain at the injection site, headache, nausea, abdominal pain, chills and joint pain. His temperature was 98.4 @ 1712. He also complained of increased saliva production. He laid down on a cot and an emergency rescue blanket was applied. He was reassured and monitored by our onsite RN. He was stable and left at 1755.

Weitere VAERSDATA-Felder

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

VAERS 1074995

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: IN
Alter: 35,0
Geschlecht: F
Eingang: 05.03.2021
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: IM / LA

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

Paraesthesia oral Swollen tongue

Symptomtext

The above patient received COVID-19 vaccine at 1400 on 03MAR21. She came to the EH&S office at 1430 complaining of tingling lips and mild tongue swelling. She was given Benadryl 25 mg po at 1437 by RN. The patient emailed later that same day at 2139 and stated that she was completely fine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia oral
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: Peanuts Seasonal Shrimp Store Fruit
Vorherige Impfungen: -

VAERS 1073162

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: SD
Alter: 78,0
Geschlecht: F
Eingang: 04.03.2021
Impfdatum: 22.12.2020
Beginn: 01.01.2021
Tage bis Beginn: 10,0
Dosis: 1
Route/Site: IM / RA

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

Blood potassium decreased Blood sodium decreased COVID-19 Convalescent plasma transfusion Cough Diarrhoea Diarrhoea haemorrhagic Escherichia test positive Gastroenteritis Escherichia coli Hypotension Nausea Platelet count decreased Pyrexia SARS-CoV-2 test positive Vomiting

Symptomtext

Pt had received dose 1 of COVID vaccine on 12/22/20. On 01/01/21 pt presented to the emergency department for intractable nausea, vomiting, cough, and non bloody diarrhea. Pt had tested positive for COVID 19 on 12/30/2020. Pt was spiking high fevers and was hypotensive. Pt was admitted to the hospital from 1/01-1/06 and treated with dexamethasone, remdesivir, and convalescent plasma.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypotension
Hospital-Tage: 5,0
Labordaten: COVID 19 PCR positive 12/30, Platelets 97, Sodium 124, Potassium 2.9, GI viral panel positive for enteropathogenic E coli
Aktuelle Erkrankungen: None noted
Vorgeschichte: Multiple myeloma, hypertension, hypothyroidism
Andere Medikamente: Hhydrochlorothiazide, Synthroid, Potassium Chloride
Allergien: Loevofloxacin, Sulfamethoxazole
Vorherige Impfungen: -

VAERS 1072768

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: AZ
Alter: 35,0
Geschlecht: F
Eingang: 04.03.2021
Impfdatum: 23.12.2020
Beginn: 23.12.2020
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Fatigue Migraine Nausea Pain in extremity

Symptomtext

After my first vaccine, I experienced left arm soreness and fatigue. Two days later I experienced severe migraine headaches, nausea and dizziness. I take Humira medication for my Crohn's disease.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Chronic disease for Crohn's disease
Andere Medikamente: Multi-vitamins, probiotics, Acetometaphin
Allergien: Sulfa based medication, penicillin, adhesives, tramadol medication
Vorherige Impfungen: Tdap injection and booster injection

VAERS 928635

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: IA
Alter: 62,0
Geschlecht: F
Eingang: 04.03.2021
Impfdatum: 07.01.2021
Beginn: 07.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Erythema Fatigue Malaise Rash Skin warm Flushing Nausea Oral pruritus Tongue pruritus Tremor Swelling

Symptomtext

Within 5 minutes I had a rash through my body (hot tot he touch) and as quickly as that came it went away. I sat for a little bit and the same thing happen again. My BP started going up and my face started getting red and I just did not feel well, they got concerned with that it progressed to the insides of my cheeks and we were concerned about throat swelling, so they sent me to the ER where I got Benadryl by IV and they also gave me Epi and some other meds and I don't remember what they were. I was there for about 4 hours. About 2AM it started coming back again, inside my cheeks started feeling like it was swelling again and I took Benadryl (I was home). I took another dose in the morning and in the afternoon. In fact I kept taking Benadryl pretty regularly for the next 3-4 days. I decided to go to my PCP and he prescribed something else that made me really drowsy, so I went back to the Benadryl and it took another couple of days to feel that the cheeks stopped with the feeling of swelling. (PCP at the hospital. At this time I still feel tired, energy levels are just not what used to be before vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: Heart monitor and I think EKG and BP, Oxygen stuff.
Aktuelle Erkrankungen: no
Vorgeschichte: allergic rhinitis hypertension hypothyroidism
Andere Medikamente: labetalol, lisinopril, salmon oil, magnesium oxide, multivitamin, loratadine, calcium, amlodipine, turmeric, CoQ10
Allergien: cashew, lisinopril, sulfa drugs and environmental allergies
Vorherige Impfungen: -

VAERS 928635

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: IA
Alter: 62,0
Geschlecht: F
Eingang: 04.03.2021
Impfdatum: 07.01.2021
Beginn: 07.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Erythema Fatigue Malaise Rash Skin warm Flushing Nausea Oral pruritus Tongue pruritus Tremor Swelling

Symptomtext

Within 5 minutes I had a rash through my body (hot tot he touch) and as quickly as that came it went away. I sat for a little bit and the same thing happen again. My BP started going up and my face started getting red and I just did not feel well, they got concerned with that it progressed to the insides of my cheeks and we were concerned about throat swelling, so they sent me to the ER where I got Benadryl by IV and they also gave me Epi and some other meds and I don't remember what they were. I was there for about 4 hours. About 2AM it started coming back again, inside my cheeks started feeling like it was swelling again and I took Benadryl (I was home). I took another dose in the morning and in the afternoon. In fact I kept taking Benadryl pretty regularly for the next 3-4 days. I decided to go to my PCP and he prescribed something else that made me really drowsy, so I went back to the Benadryl and it took another couple of days to feel that the cheeks stopped with the feeling of swelling. (PCP at the hospital. At this time I still feel tired, energy levels are just not what used to be before vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: Heart monitor and I think EKG and BP, Oxygen stuff.
Aktuelle Erkrankungen: no
Vorgeschichte: allergic rhinitis hypertension hypothyroidism
Andere Medikamente: labetalol, lisinopril, salmon oil, magnesium oxide, multivitamin, loratadine, calcium, amlodipine, turmeric, CoQ10
Allergien: cashew, lisinopril, sulfa drugs and environmental allergies
Vorherige Impfungen: -

VAERS 1066828

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: AZ
Alter: 55,0
Geschlecht: F
Eingang: 02.03.2021
Impfdatum: 23.12.2020
Beginn: 10.01.2021
Tage bis Beginn: 18,0
Dosis: 1
Route/Site: IM / LA

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

Blood catecholamines normal Blood thyroid stimulating hormone Fatigue Free haemoglobin Full blood count Haemoglobin normal Hypertension Lipids Lymphadenopathy Metabolic function test Pain Pain in extremity Vitamin D

Symptomtext

normal vaccine reactions (sore arm, swollen lymph nodes, tiredness, body aches) developed sudden hypertension 1/10/2021 (urgent hypertensive crisis), PCP put me on metroprolol succinate ER 50mg q24

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: 2/12/2021 Catecholamines fractionated plasma and Metanephrines, Fractionated, Free Plasma--all normal 1/11/2021 CBC, TSH, CMP, Vitamin D, Hgb A1C, lipid panel--all normal
Aktuelle Erkrankungen: none
Vorgeschichte: HSV2
Andere Medikamente: norethindrone 2.5mg q24 estradiol 0.5mg q24 valcyclovir 1 tablet daily as needed
Allergien: nka
Vorherige Impfungen: -

VAERS 1065462

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: FL
Alter: 63,0
Geschlecht: F
Eingang: 02.03.2021
Impfdatum: 18.02.2021
Beginn: 18.02.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Arthralgia Back pain Condition aggravated Fibromyalgia Gait disturbance Myalgia

Symptomtext

Widespread Muscle pain, more so than with just fibromyalgia. lower back and hip pain making it hard to walk. Still hurting pretty bad after over a week. Either caused a fibromyalgia flare up or really affected my muscles. Never had the hip pain like this.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Fibromyalgia
Andere Medikamente: Synthroid, Cytomel, Vit C, Vit D, Zinc, Celebrex, Magnesium
Allergien: None
Vorherige Impfungen: -

VAERS 1058395

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: GA
Alter: 68,0
Geschlecht: F
Eingang: 26.02.2021
Impfdatum: 13.01.2021
Beginn: 14.01.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Headache Migraine Myalgia Nausea

Symptomtext

Nausea. Overall muscle aches. Migraines that responded to the 2 different drugs lists, but manifested repeatedly such that the nausea and very severe head pain woke me. My response was to take a different drug in each 24 hour period. Using sumatriptan first and then 24 hours later after the pain ceased and then reestablished itself, using Migrainol, and so on. The drugs worked, but the projectile vomiting and head pain consistently came and went. Injection #1 was a bit shorter and slightly less intense, but the last time I experienced projectile vomiting due to migraines was in 1999.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: No other illnesses.
Vorgeschichte: Restless Leg Syndrome. Precautionary Gabapentin after left side temporal lobectomy
Andere Medikamente: Gabapentin Migrainol Sumatriptan Biotin Compound Testosterone 10/ DHEA 10/Preg 50 Capsules Compound Estrao.75/Prog160 Capsules Levothyroxine Gabapentin Centrum Silver 88 mg Aspirin Chelated Magnesium Brown Seaweed Extract
Allergien: Grass Pollens. Diary products, except Yogurt. Mylantin a drug removed from the market in the 1960's.
Vorherige Impfungen: -

VAERS 1054667

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: OH
Alter: 38,0
Geschlecht: F
Eingang: 25.02.2021
Impfdatum: 12.01.2021
Beginn: 09.02.2021
Tage bis Beginn: 28,0
Dosis: 1
Route/Site: IM / RA

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

Decreased appetite Feeling cold Hallucination Injected limb mobility decreased Insomnia Paraesthesia Pyrexia

Symptomtext

PT STATES 'ON 2-9-21 SHE STARTED SEEING AND TALKING TO DEAD PEOPLE, SHE WAS UNABLE TO EAT OR SLEEP FOR A WEEK'. SHE ALSO HAD FEVER, CHILLS AND A SORE ARM AFTER THE SHOT. SHE WEN TO THE ER ON 2-22-21 AND WAS RELEASED WITHOUT TREATMENT. SHE ALSO SAW HER PCP ON 2-22-21 AND WAS GIVEN ZOLOFT WHICH HAS HELPED SOME. SHE STATES SHE 'TOOK HERSELF OFF ALL HER MEDS SO HER SYSTEM WOULD BE CLEAN FOR THE SHOT.' 2-24-21 9AM TC - STATES 'LEGS TINGLE TODAY'. ADVISED HER TO CALL HER PCP ABOUT GETTING BACK ON HER MEDS TO HELP HER FEEL BETTER, STATES SHE 'WILL CALL PCP TODAY'.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: CONCUSION 2019
Andere Medikamente: -
Allergien: PCN
Vorherige Impfungen: -

VAERS 1053265

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011j20a

moderat

Staat: CA
Alter: 45,0
Geschlecht: F
Eingang: 24.02.2021
Impfdatum: 18.01.2021
Beginn: 23.01.2021
Tage bis Beginn: 5,0
Dosis: 1
Route/Site: SYR / RA

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

Mobility decreased Pain in extremity Spinal pain Tendon pain

Symptomtext

Pain along lower spine, bilateral Achilles? tendon and bilateral heels. Decrease mobility.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Hypothyroidism
Andere Medikamente: Levothyroxine
Allergien: Carrots, sulfa, propylene glycol
Vorherige Impfungen: -

VAERS 1050206

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: MD
Alter: 30,0
Geschlecht: F
Eingang: 23.02.2021
Impfdatum: 08.01.2021
Beginn: 11.01.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: IM / LA

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

Fatigue Impaired work ability Injected limb mobility decreased Injection site pain Oropharyngeal pain Pain Throat irritation Urticaria

Symptomtext

I had hives despite having taken my daily dose of Claritin that seemed to get worse as the day continued. I reached out to my Healthcare clinic and they were unsure if there was a simple treatment and almost required me to go the emergency room for this. I conducted a telehealth consultation with a doc who was not my primary care physician and was unfamiliar with my preexisting exercise urticaria condition that occasionally results in light hives but never anaphylaxis for me without Claritin. I declined going to the emergency room since this did not seem that serious and instead took another Claritin to try to get the somewhat worsening hives with no apparent cause to stop without an unnecessarily escalated situation. My throat was slightly itchy but I never became anaphylactic likely due to taking an additional Claritin and not doing anything requiring physical effort for the day beyond telecons from home because I left the office to telework mid morning after I started getting continually slightly worse hives. By evening I was ok and the next day just had a slightly sore throat but was able to work and just started the day with 2 Claritin without any further instance of hives appearing. The day after that I returned to my standard 1 Claritin dose with no ill effects. From this event, it seems clear that a 72 hour downing period from dose 1 is insufficient and should be upped to 96 hours. Prior to this more severe event, I had, on days 2 and 3, a sore left arm at injection site that prevented me from even reasonably lifting my arm to a height sufficient to grab my cell phone off it's charger while lying in bed without serious discomfort. That level of arm discomfort prevented me from working out or would have prevented me from anything other than light office work involving my vaccine arm. My level of tiredness for the couple days following this dose also required that I take an hour long nap days 1 and 2, and no nap at all is usually the norm for me.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Exercise induced urticaria (controlled by one daily Claritin)
Andere Medikamente: Claritin, Ibuprofen, Mirena
Allergien: None
Vorherige Impfungen: -

VAERS 1049714

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: NH
Alter: 20,0
Geschlecht: M
Eingang: 23.02.2021
Impfdatum: 29.01.2021
Beginn: 01.02.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: IM / LA

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

Asthenia Grip strength decreased Hemiparesis Muscular weakness Tremor

Symptomtext

About 3d after shot, patient was at gym and noticed L arm had decreased strength and decreased grip strength. No improvement since. Now has noticed some intermittent L hand tremors and L leg weakness. This was all disclosed when patient returned for shot #2. Shot #2 not given. Patient advised to discuss with PCP first.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Unknown
Andere Medikamente: Unknown
Allergien: Unknown
Vorherige Impfungen: -

VAERS 1049126

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: NY
Alter: 66,0
Geschlecht: M
Eingang: 23.02.2021
Impfdatum: 08.01.2021
Beginn: 12.01.2021
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: IM / LA

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

COVID-19 pneumonia Malaise Nucleic acid test Oxygen saturation Oxygen saturation decreased Pyrexia Systemic inflammatory response syndrome

Symptomtext

Tested 1/14/2021 positive, fever & malaise 1/19-21/21, admitted with severe CoVID pneumonia 1/22/2021 ? 1/25/2021, required supplemental O2 1/22-24.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: -
Labordaten: NAA positive 1/14/2021 and confirmed 1/22/2021, met SIRS criteria with multiple biomarkers positive on 1/22/2021. Pulse ox dropped below 89% on 1/22/2021 six hours after admission.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1047566

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: LA
Alter: 78,0
Geschlecht: F
Eingang: 22.02.2021
Impfdatum: 14.01.2021
Beginn: 14.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Heart rate irregular Palpitations

Symptomtext

Approximately 10 minutes after receiving the Moderna vaccine patient started complaining of heart racing. After assessing the patient her heart rate was 117 and irregular, her bp was 172/100. We advised the patient to go to the emergency room for evaluation, she refused transport by ambulance but agreed for her friend to bring her.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: Unknown
Aktuelle Erkrankungen: unknown
Vorgeschichte: Anxiety
Andere Medikamente: Unknown
Allergien: no known drug allergies
Vorherige Impfungen: -

VAERS 1046940

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: CA
Alter: 52,0
Geschlecht: F
Eingang: 22.02.2021
Impfdatum: 29.01.2021
Beginn: 29.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Oral pruritus Paraesthesia Paraesthesia oral Pruritus genital

Symptomtext

Within 15 minutes of receiving the vaccine, the patient described feeling prickly sensation and pruritus around mouth and labial region. She also noted within 20 minutes of receiving the vaccine that her tongue felt larger than normal. 50 mg Diphenydramine (BENADRYL) was administered within 5 minutes of symptom report, patient noted she was feeling less, itchy, her tongue still felt larger than normal. Patient was able to swallow the two caplets without any difficulty and a visual exam of her mouth, tongue and pharynx at time of symptom report and before leaving the clinic was normal with no enlargement noticed. ER precautions reviewed and the patient was encouraged to call clinic immediately for any concerns, worsening or non-improvement Patient was advised to take Diphenhydramine (BENADRYL) 50 mg in about 5-6 hours. The patient was called at home around 8 PM , she still felt some residual symptoms and agreed to take Diphenhydramine 50 mg (second dose). She is also advised to take Allegra (Fexofenadrine) 180 mg daily for 14 days. Patient referred to an allergist for advice on whether or not to receive Moderna #2 due four weeks follwoing initial dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: PCN, Baclofen
Vorherige Impfungen: -

VAERS 1046579

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: NY
Alter: 58,0
Geschlecht: F
Eingang: 22.02.2021
Impfdatum: 27.01.2021
Beginn: 06.02.2021
Tage bis Beginn: 10,0
Dosis: 2
Route/Site: IM / LA

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

Blood thyroid stimulating hormone normal Burning sensation Pain in extremity Paraesthesia

Symptomtext

burning, tingling, pain started in upper extremities during the daytime ! started about 9 days after second dose of Moderna Vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: TSH results WNL, started on Neurontin 2/17/2021 EMG test pending for 2/26/2021
Aktuelle Erkrankungen: no illnesses
Vorgeschichte: HTN, Type II Diabetes well contolled,
Andere Medikamente: Magnesium, Metformin, Hydrochlorothiazide, Avapro, Estrogen, Zinc, Green Tea Extract with EGCG + Vitamin C pill form, Synthroid, Zenwise Digestive Enzymes and Prevagen
Allergien: Sulfur drugs
Vorherige Impfungen: -

VAERS 1043677

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: CA
Alter: 61,0
Geschlecht: F
Eingang: 20.02.2021
Impfdatum: 30.01.2021
Beginn: 01.02.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: IM / RA

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

Blood test Dyspnoea Electrocardiogram Fatigue Palpitations Pruritus Tremor X-ray therapy to lung

Symptomtext

woke with unusual itching all over scalp in middle of the night. two hours later, awoke again shaking uncontrollably. no fever. shortness of breath. heart pounding 180 beats/min this continued for 45 minutes. shortness of breath continued 10 days. feeling fatigued since then. unsure if I should take second dose of vaccine in a week.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: ekg, lung xray, blood tests
Aktuelle Erkrankungen: mild shingles episodes since initial infection on 12/16/2019
Vorgeschichte: shingles nerve pain
Andere Medikamente: vitamin B,, C, E algea fish oil vegetarian, multi vitamin
Allergien: none
Vorherige Impfungen: flu shot twice, mild heart palpitations and shortness of breath for three days.

VAERS 2488042

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: -
Alter: 79,0
Geschlecht: M
Eingang: 19.02.2021
Impfdatum: 12.01.2021
Beginn: 12.01.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Asthenia Bradycardia Dizziness Hypotension

Symptomtext

Narrative: Patient is a 78 year old man who received COVID19 vaccine from the clinic on 1/12/21. A half an hour after her received the vaccine, he lowered himself to the ground due to feeling very dizzy and light headed. Per RN note the pt hit his head, however, per ER MD/NP note he denied hitting his head. The patient was hypotensive and bradycardic and brought to the ER where he was treated with a bolus of normal saline. Per post-discharge note, the pt denied any more syncopal episodes however did still feel week.

Weitere VAERSDATA-Felder

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

VAERS 1041350

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: SC
Alter: 86,0
Geschlecht: F
Eingang: 19.02.2021
Impfdatum: 21.01.2021
Beginn: 22.01.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Arthralgia Hypoaesthesia Injection site erythema Injection site induration Injection site pain Injection site swelling Pain Pain in extremity Paraesthesia

Symptomtext

Pt reports day after vaccine 01/22/2021 she had approx. a quarter size, red, harden, elevated area to LUA . She states it was extremely painful and days following injection pain worsened to radiate down her arm which started to cause numbness and tingling. She presented today for 2nd covid injection which was not recommended by her PCP due to current ongoing problem since her last vaccine. She was wearing splint to left wrist upon arrival per pt report due to pain and some numbness that she has been having. Pt states per PCP looked at area and she was referred to neurologist for nerve conduction study due to ongoing serve pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Pt referred by her outside PCP to a neurologist for nerve conduction study per pt report which is scheduled for March 02,2021.
Aktuelle Erkrankungen: None
Vorgeschichte: cardiac
Andere Medikamente: gabapentin, fursomide
Allergien: PCN
Vorherige Impfungen: -

VAERS 1040864

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: NC
Alter: 61,0
Geschlecht: M
Eingang: 19.02.2021
Impfdatum: 20.01.2021
Beginn: 21.01.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / RA

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

Condition aggravated Dizziness Vertigo Vitreous floaters

Symptomtext

Received at approximately 2:30pm. At just after midnight following vaccine, woke up and had what appeared to be Vertigo/dizziness. This has not completely gone away since onset on 1/21/2021. I began having "floaters" in my vision beginning about 8am following vaccine. This has not gone away. I did have a bout of vertigo in January 2020, that had not reoccurred since that time. I have not had "floaters" prior to the 2nd dose of the vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: None. I do have an eye exam scheduled for 2/22/2021.
Aktuelle Erkrankungen: -
Vorgeschichte: HTN, High cholesterol, Type II Diabetes, kidney stones, seasonal allergies, arthritis/osteoarthritis
Andere Medikamente: Pravastatin, Glipizide, Metformin, Ibuprofen, Vitamin C, Aspirin (81mg), Fexofenadine, Lisinopril-HCTZ, Fluticasone, Azelastine HCI, Tamsulosin
Allergien: Erythromycin, Dyazide
Vorherige Impfungen: chills, fever, shakes after 2nd shingles vaccine on 9/15/20

VAERS 1040436

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: RI
Alter: 47,0
Geschlecht: F
Eingang: 18.02.2021
Impfdatum: 26.01.2021
Beginn: 26.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Chills Electrocardiogram Electrocardiogram ambulatory Headache Heart rate increased Hypoaesthesia Palpitations Tachycardia

Symptomtext

I had headache within hours of both vaccines.There were chills but no fever with vaccine one. Vaccine one caused left sided numbness from neck to toes. I had tachycardia within hours but it subsided within a week. Vaccine 2 has caused tachycardia and palpitations within hours. Heart rate was in the 150's lying down and higher when standing. The palpitations and tachycardia were not going away so I contacted my cardiologist as I only get like that when my thyroid medication is too high or blood pressure too low. I had to wear a holter monitor. Follow up showed thyroid panel normal and blood pressure was not low. EKG showed NSR. It's over 3 weeks later and I still have periods of palpitations even without the tachycardia. My heart rate is still elevated but improving. Now 110-120 standing. I think something in the vaccine causes the immune system to ramp up so much that the thyroid produces too much and it causes the levels to be too high and causes the heart issues. I have several female friends and coworkers with autoimmune disorders and they have all had palpitations and tachycardia with vaccine 2.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: Holter monitor 2/4-2/5. EKG and office visit 2/11.
Aktuelle Erkrankungen: -
Vorgeschichte: Hashimoto's, IBS, GERD, Asthma, migraines, orthostatic hypotension, orthostatic tachycardia when bp is low
Andere Medikamente: Lansoprazole 30mg daily, Levothyroxine 88mcg daily
Allergien: Pork, raspberries, caffeine intollerant, azthiromycin, erithomycine antibiotics, sulpha antibiotics, penicillin, amoxicillin, doxycycline, tetracycline, tetanus toxoid, nuts
Vorherige Impfungen: PPD test tuberculin toxin

VAERS 1039353

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: WI
Alter: 32,0
Geschlecht: F
Eingang: 18.02.2021
Impfdatum: 10.02.2021
Beginn: 12.02.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: - / -

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

Migraine Pyrexia

Symptomtext

FEVER MIGRAINE

Weitere VAERSDATA-Felder

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

VAERS 1039260

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: FL
Alter: 68,0
Geschlecht: M
Eingang: 18.02.2021
Impfdatum: 09.01.2021
Beginn: 10.01.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Ataxia Chills Dehydration Headache Pyrexia

Symptomtext

Later that night I developed significant ataxia, fever and a significant headache. It felt as if I was paralytic. I treated it with ibueprophen and tylenol. I was given a liter of fluid because I felt dehydrated which did make me feel better and the symptoms lasted about 6hrs but the headache and chills lasted about 24 hr and symptoms subsided after that.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dehydration
Hospital-Tage: -
Labordaten: no
Aktuelle Erkrankungen: no
Vorgeschichte: Hypertension, Pre-Diabetes
Andere Medikamente: HCTZ, Protonics, Losartan, Metformin, Multivitamin, Aglemibride, Plavix, Atorvostatin, baby aspirin
Allergien: Pril family meds, bee stings
Vorherige Impfungen: -

VAERS 1039059

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: -
Alter: 64,0
Geschlecht: F
Eingang: 18.02.2021
Impfdatum: 07.01.2021
Beginn: 07.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Heart rate increased Palpitations

Symptomtext

Rapid Heart rate , Heart palpitations within 15 minutes of receiving vaccine. Pulse 122. when checked by EMT. Waited half hour longer went home. About 4 hours later went to . ER B/p 204/104 Pulse 108 at check in.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: hypertension
Andere Medikamente: Lisinopril, Hydrochlorothiazide, Potassium chloride ER, aspirin, Multivitamin/multimineral, Refresh tears eye drops
Allergien: Latex, seasonal allergies
Vorherige Impfungen: -

VAERS 2673733

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: -
Alter: 68,0
Geschlecht: M
Eingang: 17.02.2021
Impfdatum: 22.12.2021
Beginn: 23.12.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Condition aggravated Confusional state Fall

Symptomtext

fall, low grade temp 99.8 Narrative: 67 yo patient with lewey body dementia, with h/o of falls had 2 falls within 3 days of covid 19 vaccination on 12/22/2021, with falls on 12/23 and and 12/24. Vet with noted confusion that was noted to be exacerbated by recent vaccination. No additional notation of orthostastic Bp or other noted symptoms to confound fall besides mechanical.

Weitere VAERSDATA-Felder

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

VAERS 1034252

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: NY
Alter: 51,0
Geschlecht: F
Eingang: 16.02.2021
Impfdatum: 05.01.2021
Beginn: 16.02.2021
Tage bis Beginn: 42,0
Dosis: 1
Route/Site: IM / RA

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

Angiogram Blood test Catheterisation cardiac Chest pain Stent placement

Symptomtext

After 1st dose 1/6/21 at 6:10am I had severe chest pain, Went to ER . Had a cardiac cath that day and a stent placed in my LAD

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 2,0
Labordaten: Cardiac Cath, CTA, Blood
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension controlled, Elevated Cholesterol ,
Andere Medikamente: Otzela, Losartan, Metroprol, Fluoxetine, Asprin, Zyrtec, valacyclovir
Allergien: None
Vorherige Impfungen: -

VAERS 973021

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: -
Alter: 57,0
Geschlecht: M
Eingang: 16.02.2021
Impfdatum: 30.12.2020
Beginn: 25.01.2021
Tage bis Beginn: 26,0
Dosis: 1
Route/Site: IM / RA

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

Abdominal pain Chest pain Chills Dyspnoea Headache Influenza like illness SARS-CoV-2 test negative Influenza virus test negative Pyrexia

Symptomtext

Patient is seen with flu-like illness for one day. Low likelihood COVID-19 given no hotspot travel, no known contacts, and currently symptomatic with viral syndrome and negative COVID antigen. Will rx meds for symptoms, dc to f/u as outpatient, have return to ER for new or worse symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: UNK
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1032621

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: CA
Alter: 28,0
Geschlecht: F
Eingang: 15.02.2021
Impfdatum: 21.01.2021
Beginn: 21.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Arthralgia Chest discomfort Chest pain Neck pain Pain in extremity

Symptomtext

After the vaccination, within a few hours, I felt soreness on my left arm. The soreness increased throughout the day and eventually expanded to my left hip and left neck. I think about a week or 2 later, I started to also feel a slight pain in my right chest (to the right of sternum) when I occasionally took deep breaths. For the past two weeks, in addition to the pain, I feel an overall tightness/heaviness across my chest. Sometimes, I push or gently pound on my chest to try to massage the area. That said, I do not have any difficulty breathing and am overall quite an active person (exercise at least 3x/wk).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: N/A. Just yesterday, I have reported these symptoms to my doctor. Doctor has not yet responded and as such, I have not yet scheduled any medical visits.
Aktuelle Erkrankungen: N/A
Vorgeschichte: Genetic disorder (Mutation in Keratin-14 gene; skin condition).
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 1031678

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: LA
Alter: 40,0
Geschlecht: F
Eingang: 15.02.2021
Impfdatum: 05.01.2021
Beginn: 05.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Chest discomfort Chills Fatigue Feeling abnormal Gastrooesophageal reflux disease Goitre Hypoaesthesia Impaired work ability Injection site erythema Injection site swelling Malaise Pain in extremity Paraesthesia SARS-CoV-2 test negative Thyroid disorder Tremor Ventricular extrasystoles

Symptomtext

I had pretty bad arm pain; some redness and some swelling that lasted about three days. January 6 - I noticed frequent PVC's with my heart all day long. January 7 - I didn't notice anything different. January 8 - things got intense: my right arm when I got to work; it was tingling and I was real shaky. I was administering vaccines that day and I had issues with my hand shaking really bad. I ate chocolate to see if that would help and it didn't go away. A few hours later - I left work at 2:30 - my left arm went numb and started tingling, too. I had a lot of discomfort in my chest and heart area. I didn't feel right. I tried to take a nap - but it felt like impending doom; I had extreme chills but I had no fever - like I was going to have a heart attack. I called my husband. I took an Ativan (I had some that was five years old). I went to sleep. I woke u next morning and felt extremely ill and felt very fatigued. January 9th, I went to Urgent care - to get a COVID test and it was negative. The issues with my heart was a reason for me not to get the 2nd dose of the vaccine. My Dr (at the Urgent Care) palpated my thyroid and said it was enlarged and I never have had an issue with my thyroid. Follow up on the 25th with my primary care doctor for my thyroid because they couldn't do blood work at Urgent Care. Since I've had the vaccine, I have been having bad reflux and I've had to take medicine for it and I've had pain in my hands (with the joints) - like arthritis. When I'm holding my phone, for example, my hands hurt.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: COVID test - January 9th -negative result
Aktuelle Erkrankungen: no
Vorgeschichte: Heart arrhythmia - that has been kind of dormant for past 5 years
Andere Medikamente: Aldactone
Allergien: no
Vorherige Impfungen: -

VAERS 1031550

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: AL
Alter: 69,0
Geschlecht: F
Eingang: 15.02.2021
Impfdatum: 05.01.2021
Beginn: 12.01.2021
Tage bis Beginn: 7,0
Dosis: 1
Route/Site: IM / LA

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

Injection site pain Injection site swelling Loss of personal independence in daily activities Mobility decreased

Symptomtext

About a week after my first vaccine, I noticed a pain in my left shoulder near the injection site that felt similar to a shoulder injury I had 3 years ago when I tore my shoulder ligament resulting in a hairline fracture in my humerus. I thought it was just swollen from the shot in my muscle and would go away in a week or so. 5 weeks later, I am experiencing pain in my shoulder that feels exactly like my injury 3 years ago. Can't lift my arm, can't pull up my pants or put my seatbelt on, have difficulty putting my arm in a sleeve when dressing, have significantly reduced mobility in that arm and it has not gotten any better. Seems worse. Haven't seen a doctor yet. Still hoping it will get better and not sure which doctor to see. Trying to find out if this was caused by the vaccine injection before deciding if I should see my internist or shoulder doc.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: None yet
Aktuelle Erkrankungen: -
Vorgeschichte: Diabetes, Heart Disease, Spinal Arthritis, Osteo-arthritis
Andere Medikamente: Insulin, Atorvastatin, Losartan, Baby aspirin, Zyrtec, Vitamin D3, Vitamin B12
Allergien: Sulfa, Minocin
Vorherige Impfungen: -

VAERS 1026846

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: GA
Alter: 85,0
Geschlecht: F
Eingang: 12.02.2021
Impfdatum: 11.01.2021
Beginn: 13.01.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / LA

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

Catheterisation cardiac Malaise Pneumonia Stent placement Urinary tract infection

Symptomtext

Patients husband called office on February 3rd wanted to let us know his wife was in the hospital and my not be out to get her 2nd Moderna COVID-19 vaccine on Monday February 8th. I talked with the husband briefly about why his wife was hospitalized. He reported she got sick 2 days after getting her first COVID-19 vaccine. He states she had pneumonia, had a urinary tract infection and had to have a heart catherization with stent placement. We moved her second vaccine appointment to February 17th. The spouse came in on February 8th for his 2nd dose. He told me the doctors did not believe his wife's hospitalization was related to the first COVID vaccine and he said the doctor's told him that she needed her 2nd dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pneumonia
Hospital-Tage: 7,0
Labordaten: Patient was hospitalized on January 13, 2021 and discharged January 20, 2021
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1026148

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: GA
Alter: 66,0
Geschlecht: F
Eingang: 12.02.2021
Impfdatum: 27.01.2021
Beginn: 27.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Flushing Paraesthesia Taste disorder

Symptomtext

Patient reported flushed feeling, bad taste in mouth and tingling on the outside of right cheek. Administered Benadryl 25mg 0.5cc IM RD muscle at 2:46pm. Patient did not have a rash, redness, nor swelling. Patient was not in any distress. Patient left facility alert, awake at 3:20pm. Symptoms had subsided and patient had no further complaints.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Vital signs 2:50pm BP 124/71, HR 65 Vital signs 3:20pm BP 136/75 HR 60
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: Penicillin-skin rash
Vorherige Impfungen: -

VAERS 1025545

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: OH
Alter: 49,0
Geschlecht: F
Eingang: 12.02.2021
Impfdatum: 29.12.2020
Beginn: 29.12.2020
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Ageusia Anosmia COVID-19 Hypoaesthesia Mobility decreased Pain in extremity SARS-CoV-2 test positive

Symptomtext

About 30 minutes after receiving the Moderna vaccine my whole face went numb. It felt like a had been given a dose of novocaine. It lasted about 24 hours then went away. I also had severe pain in my left arm and was unable to lift my arm for about 24 hours. Two days later I developed sinus symptoms and 6 days later I lost my sense of taste and smell and tested positive for COVID

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Vitamin E, vitamin D, Probiotics, Claritin, Biotin, Vitamin B 6
Allergien: none
Vorherige Impfungen: -

VAERS 1025093

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: VA
Alter: 39,0
Geschlecht: F
Eingang: 12.02.2021
Impfdatum: 06.02.2021
Beginn: 06.02.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Mobility decreased Nausea Pain Pain in extremity Pyrexia Skin swelling Skin warm Urticaria

Symptomtext

I got the vaccine in the morning and late that evening I started getting hives again on my abdomen, fever of 102.0, body aches, extreme right arm pain (to the point where I could not raise it), localized swelling and heat. The next day body aches and nausea.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: triamcinolone acetonide 0.1% azelaic acid 15% gel ketoconazole 2% cream multivitamin
Allergien: Ciprofloxacin chlorhexidine gluconate adhesive tape lactose
Vorherige Impfungen: First Moderna Vaccine, already filed a previous report

VAERS 1012755

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: PR
Alter: 72,0
Geschlecht: M
Eingang: 12.02.2021
Impfdatum: 15.01.2021
Beginn: 15.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Chills Dehydration Diarrhoea Full blood count Pyrexia Rash Thrombocytopenia Viral test SARS-CoV-2 test Vomiting

Symptomtext

Patient states having a skin rash that started in the trunk, back, spreading to extremities in 24 hours. Patient refer vomiting, diarrhea, fever (38C), Chills. Patient says he was dehydrated. Patient states he was hospitalized from January 19 to January 21, 2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dehydration
Hospital-Tage: 3,0
Labordaten: Dengue fever test, COVID, CBC
Aktuelle Erkrankungen: N/A
Vorgeschichte: DIABETES, HYPERTENSION, ARTRITIS, FIBROMIALGIA, IRRITABLE BOWEL SYNDROME, LOWER RESP SYNDROME,PTSD
Andere Medikamente: ALPRAZOLAM 0.5 GABAPENTIN 100mg SULIDAC 150mg LISINOPRIL 40MG ACETAMINOPHEN 325mg BUPROPION HCL 150 mg AMLODIPINE BESYLATE 10mg SIMVASTATIN 80mg HYDROCHLOROTHIAZIDE 50mg SINGULAIR 10mg CETIRIZINE 10mg GLIMEPIRIDE 2mg PANTOPRAZOLE OLSALAZINE
Allergien: DYE,METFORMIN, PENICILLIN, HYDROCHLORIDE(SUN)
Vorherige Impfungen: -

VAERS 1006357

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011j20a

moderat

Staat: PR
Alter: 42,0
Geschlecht: F
Eingang: 12.02.2021
Impfdatum: 04.02.2021
Beginn: 04.02.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / RA

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

Abdominal pain upper Headache Pain Tracheal inflammation Paraesthesia

Symptomtext

Symptoms started 10 minutes after the Moderna vaccine dose. The patient started feeling a tingling sensation on her throat. She was given an intramuscular diphenhydramine (Benadryl) 50mg dose.

Weitere VAERSDATA-Felder

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

VAERS 959170

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: OR
Alter: 48,0
Geschlecht: F
Eingang: 12.02.2021
Impfdatum: 05.01.2021
Beginn: 06.01.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Erythema Mobility decreased Musculoskeletal stiffness Pain in extremity Peripheral swelling Tenderness Skin warm

Symptomtext

1/5 Vaccination; 1/6 24 hours later, i woke up and unable to use arm. Stiff, red and hot to the touch, extremely painful; 1/7 redness spread. Put on antibiotic with doctor that Friday. Went back the following Monday *unable to work until 1/14 due to arm pain, swelling; **COVID + July 2020; lingering symptoms

Weitere VAERSDATA-Felder

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

VAERS 959170

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: OR
Alter: 48,0
Geschlecht: F
Eingang: 12.02.2021
Impfdatum: 05.01.2021
Beginn: 06.01.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Erythema Mobility decreased Musculoskeletal stiffness Pain in extremity Peripheral swelling Tenderness Skin warm

Symptomtext

1/5 Vaccination; 1/6 24 hours later, i woke up and unable to use arm. Stiff, red and hot to the touch, extremely painful; 1/7 redness spread. Put on antibiotic with doctor that Friday. Went back the following Monday *unable to work until 1/14 due to arm pain, swelling; **COVID + July 2020; lingering symptoms

Weitere VAERSDATA-Felder

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

VAERS 1024295

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: TX
Alter: 39,0
Geschlecht: F
Eingang: 11.02.2021
Impfdatum: 04.01.2021
Beginn: 07.01.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: IM / LA

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

Bundle branch block right Chest pain Injection site pain Injection site rash Vomiting

Symptomtext

I exp sore arm and rash around the injection site. Then 3 days later had chest pains and vomiting went to the hospital.I was diagnosed with partial right bundle branch block. I'm still exp chest pains intermediately.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Anxiety, Migraine medications
Allergien: No
Vorherige Impfungen: -

VAERS 1022292

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: LA
Alter: 73,0
Geschlecht: M
Eingang: 11.02.2021
Impfdatum: 09.02.2021
Beginn: 10.02.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Blood bilirubin increased Blood glucose increased Chest X-ray abnormal Chills Dyspnoea Electrocardiogram ST segment abnormal Glycosylated haemoglobin Lung infiltration Pancytopenia Platelet count decreased Pneumonia White blood cell count decreased

Symptomtext

Reported to ER at MC 2/10 with shortness of breath and chills and patient attributed his symptoms to the second vaccination. Lab work in ER revealed WBC of 3.8 and platelet count of 122(baseline usually around 100), Total Bili 3.1. EKG NSR with prolonged ST interval. Chest xray mild left basilar infiltrate - admitted to acute care as observation with diagnosis of pancytopenia. Started on Rocephin for Pneumonia, IV fluids for hydration, accuchecks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: WBC 3.8 2/10, 3.5 2/11 Platelet- 122 2/10, 110 2/11, Glucose 160's, HgbA1C - 6.2, Total Bili 3.1
Aktuelle Erkrankungen: -
Vorgeschichte: Diabetes
Andere Medikamente: Gabapentin, Glimepiride, Metformin, Quinapril, Sertraline
Allergien: NKA
Vorherige Impfungen: -

VAERS 957235

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: NY
Alter: 53,0
Geschlecht: F
Eingang: 11.02.2021
Impfdatum: 12.01.2021
Beginn: 12.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Angioedema Hypoaesthesia oral Pruritus Urticaria Lip swelling Paraesthesia oral Swollen tongue Wheezing

Symptomtext

Patient sitting on exam table, speaking in full sentences and breathing comfortably but having diffuse itching. Stated feels like internal itching. Within 3 to 5 minutes lower lip felt numb " like when get dental procedure'. Tongue also a little numb. Given Benadryl 50 mg IM in the right deltoid. At 12:10 pm Itching persisted then given Prednisone 40 mg PO at 12:30pmUrticaria and angioedema starting within 3 minutes of the vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia oral
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Osteoarthritis, hypertension, dysthymic disorder, prediabetes
Andere Medikamente: albuterol, diclofenac, cetirizine, estradiol, famotidine,
Allergien: Lisinopril
Vorherige Impfungen: -

VAERS 2671918

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011j20a

moderat

Staat: -
Alter: 50,0
Geschlecht: F
Eingang: 10.02.2021
Impfdatum: 05.02.2021
Beginn: 05.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Chills Decreased appetite Dizziness Fatigue Headache Immediate post-injection reaction Myalgia Nausea Paraesthesia Paraesthesia oral Vomiting

Symptomtext

Dizziness, Headache, Myalgia, NauseaVomiting, loss of appetite, tingling of lips and extremities immediately after injection, chills,fatigue, 3 days later. Narrative: Other Relevant History:

Weitere VAERSDATA-Felder

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

VAERS 1020599

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: SD
Alter: 83,0
Geschlecht: F
Eingang: 10.02.2021
Impfdatum: 25.01.2021
Beginn: 27.01.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / LA

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

Metabolic function test Pain in extremity Pyrexia Tachycardia Tachypnoea

Symptomtext

arm pain, fever, tachycardia, tachypnea

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tachycardia
Hospital-Tage: -
Labordaten: Complete metabolic panel
Aktuelle Erkrankungen: unknown
Vorgeschichte: diabetes hypertension
Andere Medikamente: unknown
Allergien: none
Vorherige Impfungen: -

VAERS 1020478

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: OH
Alter: 55,0
Geschlecht: F
Eingang: 10.02.2021
Impfdatum: 01.12.2020
Beginn: 31.12.2020
Tage bis Beginn: 30,0
Dosis: UNK
Route/Site: IM / RA

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

Condition aggravated Pain in extremity Tendonitis

Symptomtext

12/31/20 RT ARM PAIN, SAW PCP SAID IT WAS BICEP TENDONITIS AGGRAVATED BY COVID 19 VACCINATION, MULTIPLE APPTS WITH PCP FOR CONTINUED RT ARM PAIN, ANTI-INFLAMMATORY PRESCRIBED, AS OF TODAY, 2/10/21, IT IS SOMEWHAT BETTER (4/10 PAIN SCALE), TOLERABLE BUT STILL FRUSTRATING

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: PCP APPTS 1/4/21, 1/11/21, 1/15/21, 1/20/21, AND 1/22/21
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: estradiol, vit c, vit d, zinc, vit b
Allergien: na
Vorherige Impfungen: -

VAERS 1019913

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: TN
Alter: 67,0
Geschlecht: F
Eingang: 10.02.2021
Impfdatum: 03.02.2021
Beginn: 07.02.2021
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: IM / RA

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

Atrial fibrillation Cerebral infarction Chest discomfort Computerised tomogram head abnormal Dizziness postural Dyspnoea Heart rate increased Visual field defect

Symptomtext

Chest discomfort with high heart rate and shortness of breath, dizzy upon standing. In ER HR was 156 with atrial fibrillation with RVR. BP 146/89. 2/7/21 1546 - Patient complaining of left side peripheral field deficit, CT showed subacute right occipital lobe infarct

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Hypertensive disorder, Curvature of spine, Raynaud's disease, Degeneration of intervertebral disc, Arthritis, GERD
Andere Medikamente: Lostartan 25mg PO Daily Lovastatin 20mg PO Bedtime Lortab 5-325mg PO BIDPRN Celecoxib 200mg PO Daily
Allergien: NKA
Vorherige Impfungen: Moderna COVID19 Vaccine 1/4/21 @ 1031, headache, fatigue, sore arm

VAERS 1002381

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: KS
Alter: 23,0
Geschlecht: F
Eingang: 10.02.2021
Impfdatum: 05.01.2021
Beginn: 05.01.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: SYR / LA

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

Blister Cold sweat Fatigue Injection site pain Migraine Decreased appetite Malaise Nausea Pain

Symptomtext

Reports felt Nauseated and decreased appetite gen. malaise until 01/16/21. Then developed blisters on hands-feet-joints. Felt better after blisters appeared. Dr. (her HCP) advised take #2 dose if desires

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: NO
Vorgeschichte: NO
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1017326

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: TX
Alter: 46,0
Geschlecht: F
Eingang: 09.02.2021
Impfdatum: 31.12.2020
Beginn: 31.12.2020
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Erythema Palpitations

Symptomtext

I felt like racing in chest and had little red spots around chest area(appearance ringworms 40-50 in count).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: No
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Cholesterol, Metformin
Allergien: Morphine
Vorherige Impfungen: -

VAERS 1017163

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: OH
Alter: 40,0
Geschlecht: F
Eingang: 09.02.2021
Impfdatum: 05.01.2020
Beginn: 06.01.2020
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Injection site erythema Injection site pain Injection site warmth Migraine Nausea Urticaria Vomiting

Symptomtext

On 1/6 at 3:30am woke up with severe migraine that made me nauseous and vomiting. Lasted until about 6pm. Spoke with my doctor who told me to take advil. Then on morning of 1/13 work up with a welt the size of a baseball at the injection site that was red, painful, and hot to touch. Was sent to urgent care by my PCP. Welt continued to grow. They didn't know if it was an infection at the injection site or an delayed allergic reaction. They put me on antibiotics and benadryl cream. Finally stopped growing and started to clear up by the 17th.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: none
Andere Medikamente: Synthroid
Allergien: Phenergan, Ambian.
Vorherige Impfungen: -

VAERS 1016646

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: NY
Alter: 68,0
Geschlecht: F
Eingang: 09.02.2021
Impfdatum: 19.01.2021
Beginn: 19.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Chills Migraine Pain Pyrexia

Symptomtext

Chills Fever migraine headache, acheyness

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Hyper thyroid
Andere Medikamente: Levothyroxine Vitamin D Emergen-c
Allergien: No allergies
Vorherige Impfungen: -

VAERS 1016016

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: OH
Alter: 51,0
Geschlecht: F
Eingang: 09.02.2021
Impfdatum: 31.12.2020
Beginn: 01.01.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Back pain Chest X-ray normal Chest discomfort Cough Dyspnoea Headache Heart rate increased Impaired work ability Increased upper airway secretion Malaise Paraesthesia Rash SARS-CoV-2 test negative Tremor Urticaria

Symptomtext

About 5 minutes after the vaccine, I felt like the vaccine going through my body, mu fingers kept tingling, heart rate started to race. They game me some orange juice and monitored me for about 15 minutes. I went back to work and I felt shaky for about 3-4 hours. I then had a terrible headaches and back ache. That same night I got some hives and chest tightness with increased in throat production and the headache continued that night. The next day I still felt tired and achy, felt like a mild flu. I had chest tightness with difficulty breathing. I continued to feel sick Saturday and Sunday and Monday I had a Covid test done, which was negative. On Monday I had rashes on my arms and legs and continued to have the hives and on Tuesday I started to feel a bit better with a dry cough. On Tuesday 01-12-220 I had a chest x-ray which was negative. On Wednesday, I woke up and felt much worse and that's when I called the NP and she prescribed three inhalers for my breathing issues. On 01-27-2020, since I was still feeling not better I called off work. As now, I am slowly getting better, but I still continued with the hives.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Covid test, negative
Aktuelle Erkrankungen: 11-26-20; I got tested for Covid, was negative
Vorgeschichte: HBP
Andere Medikamente: Lisinopril 10mg, Ibuprofen 400mg
Allergien: Amoxycillin, Percocet, Morphine
Vorherige Impfungen: -

VAERS 1014411

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: AK
Alter: 64,0
Geschlecht: F
Eingang: 08.02.2021
Impfdatum: 05.01.2021
Beginn: 05.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Blood test normal Contusion Dark circles under eyes Electrocardiogram normal Headache Hypertension Liver function test normal Nightmare Palpitations Platelet function test normal Renal function test normal Sleep disorder Thirst

Symptomtext

I had extremely high blood pressure; my heart was throbbing. I was told to go to ER at work but I didn't and went home and rested. That went on for days. I called my doctor and she put me on Metrozal to help with heart rate and BP and that brought that back down again. I'm taking this every day now in addition to my other blood pressure medicine. It has helped. I had headaches; I had terrible dreams and couldn't sleep. My eyes turned all dark - like when you need to drink water (underneath eyes). Had a terrible thirst. I drink water constantly. I had bruising on various parts of my body - legs; arms etc. It's calmed down with all these symptoms within a couple of weeks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: Dr: She did a series of tests on my - kidneys; liver; blood; blood; platelets; EKG and everything came back normal. 1/23/2021
Aktuelle Erkrankungen: broken foot;
Vorgeschichte: high blood pressure
Andere Medikamente: Hydrochlorothiazide 12 mg; locartin 100 mg; Vit D
Allergien: cats; dogs
Vorherige Impfungen: flu shots - usually get the flu symptoms after them including this years.

VAERS 1012887

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: NC
Alter: 38,0
Geschlecht: F
Eingang: 08.02.2021
Impfdatum: 04.01.2021
Beginn: 04.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / RA

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

Burning sensation Dizziness Hyperhidrosis Paraesthesia Vertigo

Symptomtext

1/4/2021 vaccination. About 5 pm, tingling and burning all over extremities. Sweating. Super dizzy at 8pm. Vertigo. Went to bed. Woke up . PCP wouldn't see me. Went to Urgent Care. Afibrille. Vitals were stable. Rest, fluids. F/up with neurologist.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: n/a
Vorgeschichte: IBS, migraines
Andere Medikamente: topiranate, serpraline, vyvanse
Allergien: latex, sulfa, morphine, erythromycin, reglan
Vorherige Impfungen: -

VAERS 1011402

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: MA
Alter: 40,0
Geschlecht: F
Eingang: 08.02.2021
Impfdatum: 05.01.2021
Beginn: 16.01.2021
Tage bis Beginn: 11,0
Dosis: 1
Route/Site: IM / RA

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

Angiotensin converting enzyme Blood folate Burning sensation Chills Fatigue Full blood count normal Hypoaesthesia Injection site erythema Injection site mass Injection site pruritus Injection site rash Injection site swelling Laboratory test normal Loss of personal independence in daily activities Magnetic resonance imaging abnormal Neurological examination normal Pain Pain in extremity

Symptomtext

Previously healthy 40 y/o female with sulfa allergy and received dose #1 of Moderna COVID-19 vaccine on 1/5/21. Experienced fatigue, chills, bodyaches on 1/6/21 and resolved by 1/7/21. Rash below injection site appeared on 1/9/21 that was red, itchy, and inflamed with a palpable lump. Rash slowly dissipated by 1/15/21. On 1/16/21, experienced generalized pruritis and tingling in hands, feet, and legs. Over the course of the next 3 days, experienced tingling, numbness, burning, and pain in upper and lower extremities that interfered with sleep and daily function and was not resolved with self mediation with acetaminophen and diphenhydramine. On 1/19/21, primary care provider was contacted. PCP consulted allergist/immunologist who did not think symptoms were related to an allergic reaction to the vaccine. Referred to neurologist for further workup and prescribed gapabentin for symptom control. Neuropathy slowly resolved over the following week by around 1/25/21-1/27/21.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: All workup was normal/negatve: neuro exam, Chem 7, CBC with diff, vitamin B12, folic acid, antinuclear antibody, angiotensin converting enzyme, lyme disease screen, covid 19 nasal swab, MRI of the spine and brain.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Sulfa drugs
Vorherige Impfungen: -

VAERS 1010209

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: CA
Alter: 41,0
Geschlecht: F
Eingang: 08.02.2021
Impfdatum: 14.01.2021
Beginn: 14.01.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: SYR / RA

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

Chills Decreased appetite Fatigue Headache Nervousness Pain Palpitations Pyrexia

Symptomtext

Racing heart, nervousness, severe fatigue, chills, body aches, fever of 101.6, headache, loss of appetite,

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Slightly elevated inflammation
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1010040

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: ME
Alter: 57,0
Geschlecht: F
Eingang: 07.02.2021
Impfdatum: 29.12.2020
Beginn: 29.12.2020
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / -

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

Dermatochalasis Hypoaesthesia oral Paraesthesia oral Swelling of eyelid

Symptomtext

Lower lip left side (vaccine in left shoulder) became tingling, numb, pins and needles feeling 45 mins to 1 hour after shot, and eyelids were puffy and slightly sagging. Lip felt that way for 3-4 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia oral
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: AREDS-2 eye vitamins
Allergien: Aspirin, PEG
Vorherige Impfungen: -

VAERS 1008972

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: NY
Alter: 48,0
Geschlecht: F
Eingang: 07.02.2021
Impfdatum: 29.12.2020
Beginn: 29.12.2020
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Arthralgia Loss of personal independence in daily activities Mobility decreased Pain in extremity

Symptomtext

When my first dose was administered on this day I felt a pain go down my arm. I continue to have pain in my elbow/forearm area. I cannot lift or reach for objects as i was able to prior to the shot. My day to day duties continue to be affected.

Weitere VAERSDATA-Felder

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

VAERS 1007587

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: AL
Alter: 54,0
Geschlecht: F
Eingang: 06.02.2021
Impfdatum: 23.12.2020
Beginn: 18.01.2021
Tage bis Beginn: 26,0
Dosis: 1
Route/Site: SYR / RA

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

Erythema Impaired work ability Injection Injection site erythema Injection site induration Injection site pruritus Injection site swelling Injection site warmth Joint range of motion decreased Laboratory test Magnetic resonance imaging Mobility decreased Musculoskeletal stiffness Neck pain Pain in extremity Pain of skin Peripheral swelling Spinal X-ray

Symptomtext

Arm turned red at injection site and hot. There was really no pain and went away within a couple of day but turned red again exactly a week later from injection date. This time it was hard, hot, red, itchy, and bigger. Dr treated it with clindamycin and dose pack of steroids. It got better after a few days. Next, I got a UTI and called my primary care physician. She ordered CIPRO and phenazopyridine. That got better but before CIPRO was finished, I got a crick in my neck that turned into excruciating pain in my neck and was unable to turn head from side to side. At the same time, my left foot became painful, red and swelled. I have been treated for arthritis in that foot 6 years ago with an injection. I have not had any problems with it since the injection. Dr. treated my neck problem with Robaxin and a steroid dose pack. This seemed to help my foot too temporarily. Neck pain improved but not gone. It was excruciating pain up the back of my scalp at times. I can turn my head some now but it's not back normal. Can't turn it all the way. Dr. did another injection in my foot but did not work this time. I got worse and I can no longer put any weight on that foot. I have not been able to work since January 20. Have had to apply for leave of absence and short-term disability

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: X-ray of foot and neck. MRI of foot. Lab work
Aktuelle Erkrankungen: None
Vorgeschichte: Hypothyroidism, arthritis
Andere Medikamente: Levothyroxine, multivitamin, vitamin D, meloxicam, atorvastatin, ambien
Allergien: Penicillin, sulfa
Vorherige Impfungen: -

VAERS 1015834

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: OR
Alter: 85,0
Geschlecht: F
Eingang: 05.02.2021
Impfdatum: 08.01.2021
Beginn: 08.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dyspnoea Pharyngeal swelling

Symptomtext

Patient observed for 15 m, left clinic was at a restaurant for a bit (~ 1 hr after) & developed throat swelling and shortness of breath & returned to clinic & was observed, vitals & EKG were stable & patient was discharged

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: Afib, HTN, glaucoma
Vorgeschichte: "
Andere Medikamente: alendronate weekly, atorvastatin, Lisinopril, Sertraline, digoxin
Allergien: Fuorescein, propranolol, codeine- unknown if "true" allergy
Vorherige Impfungen: -

VAERS 1006991

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: MA
Alter: 22,0
Geschlecht: F
Eingang: 05.02.2021
Impfdatum: 05.02.2021
Beginn: 05.02.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Dyspnoea Eye irritation Throat irritation Throat tightness Wheezing

Symptomtext

About 2m after second COVID shot patient began feeling burning eyes and slight difficulty breathing. Paramedic onsite immediately listened to lungs and heard diffuse wheezing bilaterally. Within 1m minute patient felt throat tickling and then tightening and breathing was more difficult. Paramedic gave patient EpiPen with resolution of symptoms in less than 1-2 minutes. Ambulance called and arrived very quickly. Patient was transported to hospital. As way to hospital patient felt breathing getting worse again and was given solumedrol and benadryl IV and a second EpiPen. Don't yet know what happened beyond this.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Immediately after event, BP = 150/100, P=110, O2 = 92%.
Aktuelle Erkrankungen: None
Vorgeschichte: None known
Andere Medikamente: unknown
Allergien: Strawberries
Vorherige Impfungen: -

VAERS 1005621

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: VA
Alter: 60,0
Geschlecht: F
Eingang: 05.02.2021
Impfdatum: 02.02.2021
Beginn: 02.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Paraesthesia

Symptomtext

C/O tingling of left hand and ring finger approximately 30 minutes after receiving Moderna Vaccine #1.

Weitere VAERSDATA-Felder

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

VAERS 1005454

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: MO
Alter: 32,0
Geschlecht: F
Eingang: 05.02.2021
Impfdatum: 28.01.2021
Beginn: 28.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Chest discomfort Dysphagia Ear pruritus Paraesthesia oral Throat irritation

Symptomtext

An hour after vaccination- tingling lips, itchy ears, frequent urge to swallow, scratchy throat, chest tightening. Immediately began Benadryl. These symptoms persisted, so I continued Benadryl every 4 hours for 2 days. On Saturday 01/30/2021, when symptoms continued. She advised switching from Benadryl to a once daily dose of Claritin and Pepcid AC. Switched to Claritin and Pepcid, symptoms persisted but started to diminish in severity. Planned appointment with Primary Care Physician is scheduled for 02/19/2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia oral
Hospital-Tage: -
Labordaten: None at this time.
Aktuelle Erkrankungen: None.
Vorgeschichte: None.
Andere Medikamente: Norethindrone 0,35mg
Allergien: Minor allergic reaction hives to Keflex in high school.
Vorherige Impfungen: -

VAERS 1005218

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: OR
Alter: 32,0
Geschlecht: F
Eingang: 05.02.2021
Impfdatum: 04.01.2021
Beginn: 04.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Abdominal pain Dizziness Hyperhidrosis Pallor Tremor Vision blurred

Symptomtext

It started with abdominal pain (like hunger pain). I sat down for dinner and took one bit and abdominal pain got worse. I felt like I was going to pass out. I started sweating and my vision was blurry, I had the shakes. The sensation like your low sugar. I was pale and my skin was sweaty . After about 45minutes it cleared up.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: NAC (supplement) -600mg/daily Active B- complex Magnesium -300mg/daily Cetirizine- 10mg/ daily Birth control (implant) Tylenol (occasionally) Inbroken (occasionally)
Allergien: Sulfa
Vorherige Impfungen: Flu shot- I get sick every time I get a shot.

VAERS 1005139

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: -
Alter: 38,0
Geschlecht: M
Eingang: 05.02.2021
Impfdatum: 03.02.2021
Beginn: 03.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Arthralgia Fatigue Injection site pain Migraine Myalgia

Symptomtext

Pain at injection site, Migraine which started a few hours after injection, fatigue, and muscle/ joint pain for following 30 plus hours. Fatigue for 38 hours.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Degenerative Disc Disorder, Reactive Airway Disease, Diverticulitis
Andere Medikamente: None
Allergien: None known
Vorherige Impfungen: -

VAERS 1004198

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: OR
Alter: 62,0
Geschlecht: F
Eingang: 05.02.2021
Impfdatum: 22.12.2020
Beginn: 22.12.2020
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / LA

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

Abdominal pain Chills Computerised tomogram abdomen abnormal Diarrhoea Diarrhoea haemorrhagic Haemorrhoids Muscle spasms Nausea Pain Tremor

Symptomtext

hemorrhoid pain; bloody diarrhea; severe diarrhea; Nausea; abdominal pain; shaking chills; Severe leg cramps; A spontaneous report was received from a 62 year old, female patient who received Moderna's COVID-19 vaccine (mRNA-1273) and experienced severe leg cramps, severe diarrhea, nausea, abdominal pain, shaking chills, hemorrhoid pain and the serious event of bloody diarrhea. The patient's medical history included diverticulitis. No relevant concomitant medications were reported. On 22 Dec 2020, about 4pm, the patient received their first of two planned doses of mRNA-1273 (Lot #011J20A) intramuscularly in the left arm for prophylaxis of COVID-19 infection. On 22 Dec 2020, around 7pm, the patient experienced severe leg cramps. On 23 Dec 2020, she experienced severe diarrhea, nausea, abdominal pain, shaking chills and bloody diarrhea. Treatment for nausea was ondansetron. On 24 Dec 2020, the patient experienced terrible hemorrhoid pain and abdominal pain. On 25 Dec 2020, the patient went to the emergency room where she received a computed tomography scan. The computed tomography scan of the lower abdomen showed that earlier diagnosis of diverticulitis 27 Nov 2020 "inflammation" had gotten better. Action taken with mRNA-1273 in response to the events were not reported. The outcome for events, severe leg cramps, severe diarrhea, nausea, abdominal pain, shaking chills, bloody diarrhea and hemorrhoid pain, were unknown.; Reporter's Comments: This case concerns a 62-year-old female patient with medical history of diverticulitis, who received their first of two planned doses of mRNA-1273 (Lot 011J20A), and who experienced the serious unlisted event of bloody diarrhea, the non-serious listed events of nausea and chills, and the non-serious unlisted events of severe leg cramps, severe diarrhea, abdominal pain, and hemorrhoid pain. Based on the current available information and temporal association between the use of the product and the onset of events after vaccination, a causal relationship cannot be excluded and the events are considered possibly related to the vaccine. The patient's history of diverticulitis is noted.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: Test Date: 20201225; Test Name: CT of lower abdomen; Result Unstructured Data: Earlier diagnosis of diverticulitis on 27/NOV/2020 inflation had gotten better
Aktuelle Erkrankungen: Diverticulitis
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 928663

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: AR
Alter: 20,0
Geschlecht: F
Eingang: 05.02.2021
Impfdatum: 04.02.2021
Beginn: 04.02.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Chills Dyspnoea Fatigue Headache Nausea Pain Pyrexia Pain in extremity Vomiting

Symptomtext

fever, body aches, chills, nausea, vomitting, headache

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Birth control and probiotics
Allergien: penicillen
Vorherige Impfungen: Moderna

VAERS 928663

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: AR
Alter: 20,0
Geschlecht: F
Eingang: 05.02.2021
Impfdatum: 04.02.2021
Beginn: 04.02.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / RA

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

Chills Dyspnoea Fatigue Headache Nausea Pain Pyrexia Pain in extremity Vomiting

Symptomtext

fever, body aches, chills, nausea, vomitting, headache

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Birth control and probiotics
Allergien: penicillen
Vorherige Impfungen: Moderna

VAERS 1003662

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: MA
Alter: 55,0
Geschlecht: M
Eingang: 04.02.2021
Impfdatum: 25.01.2021
Beginn: 28.01.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: IM / LA

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

Dyspnoea Electrocardiogram Palpitations Sinus tachycardia Tachycardia Vital signs measurement

Symptomtext

palpitations, tachycardia, mild dyspnea which lasted several minutes; recurred several hours later then resolved

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Vital signs - HR 117; BP 130/75; O2 sat 94% 1/29/21 EKG - sinus tachycardia
Aktuelle Erkrankungen: Healthy
Vorgeschichte: None
Andere Medikamente: None
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1001995

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: IN
Alter: 71,0
Geschlecht: M
Eingang: 04.02.2021
Impfdatum: 06.01.2021
Beginn: 15.01.2021
Tage bis Beginn: 9,0
Dosis: UNK
Route/Site: SYR / LA

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

Arthralgia Mobility decreased Myalgia Tendonitis

Symptomtext

Severe tendonitis and muscle pain in both shoulders and both hips. Sustained up to 2nd shot and morning after 2nd shot could hardly move. I get some relief with NSAID's.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: High Blood Pressure Bladder Cancer (in remission)
Andere Medikamente: Aspirin (81 mg) Fish Oil (1000 mg) Complete Senior Vitamin Tamsulosin (.4 mg) Nifedipine (30 mg) Spironolacton-E-hctz (25-25)
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 998539

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: OK
Alter: 25,0
Geschlecht: F
Eingang: 03.02.2021
Impfdatum: 03.02.2021
Beginn: 03.02.2021
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 cold Headache Migraine Pyrexia Tremor Vomiting

Symptomtext

2/2/2021 vaccination . About 6pm cold chills, fever, vomiting, HA. Still experiencing fever and migraine. Really 'shaky'. Did not experience this with the first vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: pneumonia; 01/2021
Vorgeschichte: endometreosis
Andere Medikamente: n/a
Allergien: microbid
Vorherige Impfungen: -

VAERS 997954

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: AZ
Alter: 36,0
Geschlecht: F
Eingang: 03.02.2021
Impfdatum: 28.12.2020
Beginn: 30.12.2020
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / LA

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

Arthralgia Chills Decreased appetite Fatigue Headache Hyperhidrosis Hypersomnia Impaired work ability Mobility decreased Myalgia Pyrexia SARS-CoV-2 test negative White blood cell count decreased

Symptomtext

Two days after I got the vaccine - muscle and joint aches - lasted a week and increased in severity as days went on; also had a headaches. In the weekend I was getting fatigued and really bad chills and sweats on the second. The 3rd of January, I could barely walk to the bathroom because I was so fatigued. Low fever on the 4th - 99.4. Couldn't have a full visit to dr on the 4th.Tested for COVID on 4th; Negative result. Couldn't go back to work until the 7th. I was completely exhausted, no appetite; muscles aches; had a bit of a headache, too, but the fatigue was so overwhelming that I just slept for those three days 5th, 6th, 7th. I went back to work on the 7th - it was rough but over the weekend I started doing better and the following week was better for me.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: Blood work - January 6th - my white count was very low and I'm getting it repeated today to check it. January 6th - they did a SED rate (normal) and maybe a metabolic panel (normal)
Aktuelle Erkrankungen: no
Vorgeschichte: Ulcerative colitis - but nothing active
Andere Medikamente: no
Allergien: no
Vorherige Impfungen: -

VAERS 997952

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: NH
Alter: 47,0
Geschlecht: F
Eingang: 03.02.2021
Impfdatum: 22.12.2020
Beginn: 26.12.2020
Tage bis Beginn: 4,0
Dosis: UNK
Route/Site: IM / LA

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

COVID-19 Cough Dyspnoea Injection site pain Oropharyngeal pain Pain Pyrexia SARS-CoV-2 test positive

Symptomtext

From 22nd to the 25th sore arm at injection of Dec. 26 -27 Cough, sore through, fever, shortness of breath and body aches then Dec. 27 COVID PCR for covid and 28 DEC the PCR positive

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: COVID PCR
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Viibryd 30mg, Multi- Vitamin
Allergien: Sulfur Antibiotics
Vorherige Impfungen: -

VAERS 996208

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: GA
Alter: 56,0
Geschlecht: M
Eingang: 02.02.2021
Impfdatum: 30.12.2020
Beginn: 31.12.2020
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Chills Headache Myalgia Tremor

Symptomtext

Received 1st dose of Moderna COVID-19 vaccine on 12/30/2021 at 0830 am. Called on 01/04/2021 to report extreme chills/shaking, headache and muscle aches that started 12/31/20. Reports symptoms resolved in 24 hours.

Weitere VAERSDATA-Felder

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

VAERS 995373

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: NY
Alter: 31,0
Geschlecht: F
Eingang: 02.02.2021
Impfdatum: 30.12.2020
Beginn: 06.01.2021
Tage bis Beginn: 7,0
Dosis: 1
Route/Site: IM / LA

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

Erythema Hypoaesthesia Mobility decreased Muscular weakness Pain Pain in extremity Peripheral swelling Pruritus Urticaria

Symptomtext

Pain and soreness was felt the fist 2 days after vaccine however on the 6th day pain 20/10, numbness, all the way to thumb was felt on L arm, swelling, redness, itching, hives and pain only on L arm and temp of 99.4. Pain in L thumb still hurts even more than a month later sometimes is even hard to pop out pill or open or hold stuff with that hand and thumb. Benadryl ibuprofen tylenol was taken for 1st and second dose. Did not help much!!

Weitere VAERSDATA-Felder

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

VAERS 994825

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: TN
Alter: 36,0
Geschlecht: F
Eingang: 02.02.2021
Impfdatum: 23.12.2020
Beginn: 24.12.2020
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Arthralgia Dyspnoea Fatigue Headache Illness Influenza virus test negative Injection site erythema Injection site pain Injection site pruritus Injection site swelling Migraine Pyrexia Respiratory symptom SARS-CoV-2 test negative Wheezing

Symptomtext

(Starting at about 12 hours post vaccine) Developed severe headache (turned into Migraine) that lasted about 4 days, Fever (100.8) x 24 hours (medicated with Tylenol Q 4 hours), joint pain and fatigue. Developed moderate amount of swelling at the injection site day 2 and a large red area (about the size of an orange) that lasted over a week. The red area burned and itched. January 1, became very ill with Upper Respiratory symtoms. Shortness of breath, wheezing, fatigue, fever. Saw PCP who tested for Covid 19 (negative) and flu (negative). Returned to PCP on January 3 with worsening symptoms of shortness of breath. Another Covid 19 test run (negative) and presc. for Steriods given. Took 1 week to recover.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Covid 19/Flu tests Jan.1 Negative (unsure if symptoms related to vaccine or other virus) Covid 19 test Jan. 3 Negative
Aktuelle Erkrankungen: None
Vorgeschichte: Migraine (Hemiplegic/classic), Hypothyroid, PCOS, Endometriosis, Asthma, Anxiety/Depression(Well Controlled),
Andere Medikamente: Metformin Daily(PCOS), Levothyroxine Daily, Zyrtec Daily,
Allergien: Hydrocode
Vorherige Impfungen: Unknown if considered "Adverse" 10-17-2016 Pneumovax- Starting at 24 hr post vaccine- 103 temp,

VAERS 993091

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: FL
Alter: 46,0
Geschlecht: F
Eingang: 01.02.2021
Impfdatum: 29.12.2020
Beginn: 29.12.2020
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Arthralgia Burning sensation Chest pain Dyspnoea Electroencephalogram Hypoaesthesia Pain in extremity Paraesthesia Rash

Symptomtext

After 30 minutes facial numbness, left hand pain and elbow pain. Intermittent facial numbness since. Tonight (2/1/21) a burning feeling of face, like a sunburn with slight rash and left cheek, chin and forehead tingling and slight numbness. One episode at one week after shot (1/4/21) of facial numbness with shortness of breath two episodes in same day and sternum or chest soreness for a short period of time. Went to be seen and evaluated at Hospital. Released since all vitals were ok. Continuing facial numbness (especially on left) off and on since first vaccine dose with no history of ever having this in my life. No treatments given and no imaging tests were performed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 1/4/21 EEG and ER staff evaluation/ blood pressure
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Amoxicillin, Sulfa Drugs, morphine, phenergen, MSG, citric acid
Vorherige Impfungen: -

VAERS 991389

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: OH
Alter: 80,0
Geschlecht: F
Eingang: 01.02.2021
Impfdatum: 28.01.2021
Beginn: 30.01.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / RA

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

Chest discomfort Dyspnoea Fatigue Headache Musculoskeletal stiffness Pain Pain in extremity Sinus disorder

Symptomtext

hours after vaccination arm soreness, stiffness in hands, two days after vaccination fatigue, breathing difficulty-feeling of tightness around rib cage, heart felt tight, headache, body aches, sinus trouble

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Osteoporosis, High Cholesterol
Andere Medikamente: None
Allergien: Cephalexin
Vorherige Impfungen: -

VAERS 991173

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011j20a

moderat

Staat: NC
Alter: 30,0
Geschlecht: F
Eingang: 01.02.2021
Impfdatum: 26.01.2021
Beginn: 27.01.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / RA

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

Heart rate increased Muscle spasms Tachycardia

Symptomtext

I have been experiencing tachycardia since 0700 am 1/27/21 heart rate reaching 130 just standing and walking from one door to the next it was 153 , Also I have been experiencing muscle spasms all over as if 1/28/21 and as if today 2/1/21 I?m still experiencing the same two reactions .

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tachycardia
Hospital-Tage: -
Labordaten: I work at hospital, my vs were taking by a nurse on unit.
Aktuelle Erkrankungen: No
Vorgeschichte: Asthmatic
Andere Medikamente: No
Allergien: Vancomycin, penicillin ,some Nuts and fruits
Vorherige Impfungen: -

VAERS 991132

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: OH
Alter: 45,0
Geschlecht: F
Eingang: 01.02.2021
Impfdatum: 11.01.2021
Beginn: 13.01.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / LA

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

Arthralgia Fatigue Herpes zoster Injection site pain Paraesthesia Rash

Symptomtext

Vaccine Monday 1/11/2021 1530. Wednesday 1/13/2021 woke up with mild site pain, fatigue, arthralgia. 1/14/2021 Pain in shoulder blade area. 1/16/2021-1/17/2021 developed painful, unilateral truncal rash and tingling pain. Sought help with PCP; Dx. with SHINGLES; started on Valtrex, etc.. Positive COVID history 12/9/2021. States when had her blood tested to donate in January the week before her vaccine she tested negative.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: unknown, states none
Aktuelle Erkrankungen: none
Vorgeschichte: none, healthy
Andere Medikamente: allegra, Vit. D3, zinc tablets, magnesium, Vit B6
Allergien: Cats, dust, seasonal
Vorherige Impfungen: -

VAERS 989672

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: NY
Alter: 57,0
Geschlecht: F
Eingang: 31.01.2021
Impfdatum: 21.12.2020
Beginn: 23.12.2020
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: SYR / LA

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

Body temperature increased Headache Hypoaesthesia Paraesthesia Paraesthesia oral Tenderness

Symptomtext

2 days after the vaccine I started experiencing numbness and tingling on the left side of my face statring at my lips and moving up to under my eye. This would last up to 1 & 1/2 hrs. I let my Infection Control Nurses know as soon as it happened. It has continued with the left sides of my face sor to touch near my cheekbone & jawbone, teeth both upper and lower contantly aching with the numbness & tingling still prominet. My gums feel swollen and teeth feel loose. They are not. Just the constant tingling that is the real issue. I had my second dose on 01/18/2021 with lot # of 001L20A. Woke up @ 2 am the next morning with a massive headache and ran a 101.3 temp for 2 & 1/2 days. Numbness and tingling continues.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: ulcertive Colitis
Andere Medikamente: None
Allergien: Kelflex, Remicade, Levothorxine
Vorherige Impfungen: -

VAERS 989638

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: FL
Alter: 80,0
Geschlecht: F
Eingang: 31.01.2021
Impfdatum: 13.01.2021
Beginn: 21.01.2021
Tage bis Beginn: 8,0
Dosis: 1
Route/Site: SYR / LA

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

Feeling abnormal Injection site rash Malaise Paraesthesia

Symptomtext

8 days after the first dose, my Mom developed a rash at the site of the injection. It lasted for about 6 days and it was the size of the palm of a hand. She saw her primary care Doctor on 1/25/21 for a regular physical. He saw the rash (which had subsided) and advised her to take one Benadryl 30 minutes before she has the second dose of the Moderna vaccine on 2/10/21. On 1/30/21 she had an episode where her face was tingling and she was not feeling well and a somewhat out of it. Today, 1/31/21, she is feeling better but still has tingling in her face.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: -
Vorgeschichte: Heart valve issues, diverticulitis
Andere Medikamente: Crestor (20 mg), Bayer (81 mg), Losartan (50 mg), Amlodipine (2.5 mg), Toprol XL (25 mg), Vitamin D3 (1000IU)
Allergien: Allergie to generic versions of Crestor, Allergic to Ciprofloxacin, Allergic to Lipitor, Alergic to Bactrin (sulfa drug catergory), Allergic to hydrocodone (7.5 mg)
Vorherige Impfungen: -

VAERS 989635

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: NC
Alter: 65,0
Geschlecht: F
Eingang: 31.01.2021
Impfdatum: 20.01.2021
Beginn: 20.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Tachycardia

Symptomtext

Approximately 2 hours later, tachycardia 120-130 bpm for 3 hours. Also, when checked BP 80-90/ 40-50 running concurrently with the tachycardia.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tachycardia
Hospital-Tage: -
Labordaten: None. I would not go to ED. I pushed fluids and ate pretzels. I did tell one of my supervising physicians later that evening.
Aktuelle Erkrankungen: None I am a health professional. Nurse Practitioner
Vorgeschichte: Obesity Chronic Kidney Disease Osteoarthritis HTN
Andere Medikamente: Atenolol, alupurinol, Lasix, hydrochlorothiazide, mag oxide, potassium chloride, B12, vitamin D3, prozac
Allergien: PCN, topomax, alcohol sugars
Vorherige Impfungen: -

VAERS 989333

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: CA
Alter: 69,0
Geschlecht: M
Eingang: 31.01.2021
Impfdatum: 31.12.2020
Beginn: 13.01.2021
Tage bis Beginn: 13,0
Dosis: 1
Route/Site: SYR / LA

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

Anxiety Blood test normal Cardiac stress test normal Echocardiogram normal Electrocardiogram normal Hypertension Insomnia Palpitations

Symptomtext

Out of know where on 1-13-21 awoke at 3:00 AM with severe anxiety which has continued to date, 1-31-21 but not as severe. Unable to sleep, no matter what medication given. At beginning had high blood pressure which is unusual for me and heart palpitations. Had two trips to the ER , 1-13-21 9:00 PM, released and 1-15-21 10:00 PM and admitted, kept for one day. Heart palpitations decreased within the first week and blood pressure came down to normal. Unable to sleep, after being given Hydroxyzine Hydrochloride-25mg and later Alprazolam-.5 mg. Tried taking herbs before taking Alprazolam due to the addiction factor. Took Kava , Deep Sleep and CBD. Took Alprazolam after herbs didn't seem to help but it made me feel bad and didn't help with the sleep so went to over the counter sleep aid.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: 1,0
Labordaten: EKG - NEG., STRESS TEST-NEG, ECHO CARDIOGRAM-NEG. Multiple blood tests-all good.
Aktuelle Erkrankungen: -
Vorgeschichte: High Cholesterol
Andere Medikamente: Rosuvastatin-20mg, Fish oil-1000mg, Aspirin-low dose, Cinnamon-1000mg.
Allergien: Lipitor
Vorherige Impfungen: -

VAERS 989106

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: KS
Alter: 32,0
Geschlecht: F
Eingang: 31.01.2021
Impfdatum: 30.12.2020
Beginn: 15.01.2021
Tage bis Beginn: 16,0
Dosis: 1
Route/Site: SYR / LA

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

Condition aggravated Herpes zoster Rash

Symptomtext

Developed shingles within 2.5 week of injection (haven't had shingles since I was 5), rash on chest (3 weeks after shot) Moderna COVID?19 Vaccine EUA

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: n/a
Vorgeschichte: 5 years old - shingles
Andere Medikamente: n/a
Allergien: latex, kiwi
Vorherige Impfungen: -

VAERS 974840

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: OR
Alter: 40,0
Geschlecht: F
Eingang: 30.01.2021
Impfdatum: 02.01.2021
Beginn: 02.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Dizziness Dysphagia Erythema Hypertension Oropharyngeal discomfort Dyspnoea Mouth swelling Swelling face Pruritus Throat clearing Urticaria Wheezing Swollen tongue Throat irritation

Symptomtext

The patient received the 1st dose of Moderna vaccine. She waited 20 minutes for observation without any symptoms. She left and began to drive home in her car when she felt her tongue begin to swell. She returned to the vaccine clinic observation area and was transferred to the ED. Her overall symptoms included tongue swelling, throat irriation, oral and facial swelling, lightheadedness, shortness of breath, wheezing, hypertension (170/118; HR=83), urticaria over chest wall. The patient had self-administered oral prednisone prior to ED transfer. Was further treated with diphenhydramine, famotidine, and dexamethasone. Discharged to home after 3 hours. Follow-up notes report symptoms resolved by 2 days post-discharge.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: asthma, hypertension
Andere Medikamente: albuterol MDI, tylenol with codeine, duloxetine, loratadine
Allergien: peanuts (anaphylaxis), oranges, dust, molds, soybean, fish
Vorherige Impfungen: -

VAERS 974840

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: OR
Alter: 40,0
Geschlecht: F
Eingang: 30.01.2021
Impfdatum: 02.01.2021
Beginn: 02.01.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / RA

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

Dizziness Dysphagia Erythema Hypertension Oropharyngeal discomfort Dyspnoea Mouth swelling Swelling face Pruritus Throat clearing Urticaria Wheezing Swollen tongue Throat irritation

Symptomtext

The patient received the 1st dose of Moderna vaccine. She waited 20 minutes for observation without any symptoms. She left and began to drive home in her car when she felt her tongue begin to swell. She returned to the vaccine clinic observation area and was transferred to the ED. Her overall symptoms included tongue swelling, throat irriation, oral and facial swelling, lightheadedness, shortness of breath, wheezing, hypertension (170/118; HR=83), urticaria over chest wall. The patient had self-administered oral prednisone prior to ED transfer. Was further treated with diphenhydramine, famotidine, and dexamethasone. Discharged to home after 3 hours. Follow-up notes report symptoms resolved by 2 days post-discharge.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: asthma, hypertension
Andere Medikamente: albuterol MDI, tylenol with codeine, duloxetine, loratadine
Allergien: peanuts (anaphylaxis), oranges, dust, molds, soybean, fish
Vorherige Impfungen: -

VAERS 966491

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: WI
Alter: 55,0
Geschlecht: F
Eingang: 30.01.2021
Impfdatum: 01.01.2021
Beginn: 21.01.2021
Tage bis Beginn: 20,0
Dosis: 1
Route/Site: IM / RA

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

Alanine aminotransferase increased Anion gap Aphasia Basophil count Blood alkaline phosphatase normal Cardiac function test Coordination abnormal Dyspnoea Electrocardiogram Blood bilirubin normal Blood chloride normal Blood creatinine normal Blood potassium decreased Blood sodium normal Carbon dioxide decreased Chest discomfort Eosinophil count normal Formication

Symptomtext

Hives, seizure like spasms, triggered migraine, lost ability to speak, unable to hold pen and unable to write my name, sweats but had cold skin, racing heart rate, difficulty breathing, unable to track what was happening around me, burning and itching skin

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: EKG, blood tests for kidney and liver functioning and testing for heart complications
Aktuelle Erkrankungen: No illness but did have a fall on ice 4 days prior to vaccine
Vorgeschichte: Diabetic, Migraines, Fibromyalgia, contact Dermatitis
Andere Medikamente: Metformin, Farxiga, Lamictal, Gaubapentine, Loradidine, Effector, Attenanol
Allergien: Oxytocin, Hydrocodine, Morphine, Ultram, Vicodine, Percoset, Demoral, Latex
Vorherige Impfungen: -

VAERS 2662356

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: -
Alter: 31,0
Geschlecht: F
Eingang: 29.01.2021
Impfdatum: 25.01.2020
Beginn: 25.01.2021
Tage bis Beginn: 366,0
Dosis: 2
Route/Site: IM / LA

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

Headache Migraine Myalgia Neck pain Pain in extremity

Symptomtext

Headache, Myalgia, SORE ARM AND NECK Narrative: 1/25: pt experienced sore arm and neck. On 1/26 she experienced muscle aches and migraine. On 1/28 she had a headache.

Weitere VAERSDATA-Felder

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

VAERS 988604

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: OH
Alter: 32,0
Geschlecht: F
Eingang: 29.01.2021
Impfdatum: 12.01.2021
Beginn: 12.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Balance disorder Cold sweat Condition aggravated Dizziness Electrocardiogram normal Fatigue Feeling cold Feeling drunk Full blood count normal Hyperhidrosis Metabolic function test normal Pregnancy test urine negative Pruritus Tinnitus Urine analysis normal Vertigo

Symptomtext

Employee states she had her vaccine 1545 and after sitting in chair 'a little more than 20-25 minutes,' she began to feel faint, dizzy, sweaty, cold and clammy hands but felt sweaty. Developed ringing in her ears and vertigo; like she is drunk and spinning, off balance. Taken to ER, BP up at 152/80's and HR in the 90's. Testing completed; all normal per employee. Went home and felt extreme fatigue, and as of 1/18/2021 her arm is still achy, running down her arm to her fingertips and down her backside on the left side in the upper part of the back. Has no PCP, discussed f/u with an Urgent Care or other Health Care Provider if lost any sensation or developed further symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: In ER reports BMP, CBC, urine pregnancy test and UA, EKG, all normal results.
Aktuelle Erkrankungen: none
Vorgeschichte: Asthma, Fibrocystic Breast. Hx. of fainting with ringing in her ears with her periods when younger.
Andere Medikamente: Birth Control Pills, Vitamen C
Allergien: seafood; rash, hives, shortness of breath.
Vorherige Impfungen: -

VAERS 987576

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: VA
Alter: 52,0
Geschlecht: F
Eingang: 29.01.2021
Impfdatum: 21.01.2021
Beginn: 28.01.2021
Tage bis Beginn: 7,0
Dosis: 1
Route/Site: SYR / RA

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

Axillary pain Dyspnoea Injection site erythema Injection site induration Injection site pain Injection site pruritus Injection site swelling Injection site warmth Lymphadenopathy

Symptomtext

Itching, Swelling, hardness, tenderness and redness on injection site (right arm) Feels warm to touch. Discomfort and slight swelling under right arm pit. Symptoms started 7 days after vaccination. Also felt a little out of breath on day 8.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: Asthma Diverticulitis Migraines Degenerative disc disease Arthritis Pre diabetes
Vorgeschichte: Asthma Diverticulitis Migraines Degenerative disc disease Arthritis
Andere Medikamente: Omeprazole Albuterol inhaler
Allergien: None known
Vorherige Impfungen: Flu shot. 11/2020, redness and itchiness on shot site.

VAERS 987556

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: OK
Alter: 33,0
Geschlecht: F
Eingang: 29.01.2021
Impfdatum: 28.01.2021
Beginn: 28.01.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Chills Diarrhoea Dizziness Fatigue Headache Injection site discomfort Musculoskeletal stiffness Myalgia Pyrexia Tachycardia

Symptomtext

Local discomfort at injection site, diarrhea, chills, dizziness, fever, headache, myalgia, muscle stiffness, tachycardia, fatigue

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tachycardia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: No
Vorgeschichte: Juvenile dermatomyositis, endometriosis, hypothyroidism, dyslipidemia, obesity
Andere Medikamente: Orilissa 150mg, levothyroxine 0.25mcg, vitamin d3 1000 units, hydroxychloroquine 200mg, rosuvastatin 10mg all once daily
Allergien: Cetirizine, mushrooms, penicillin, sulfamethoxazole/trimethoprim, clindamycin
Vorherige Impfungen: -

VAERS 986218

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: PA
Alter: 45,0
Geschlecht: F
Eingang: 29.01.2021
Impfdatum: 11.01.2021
Beginn: 12.01.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / UN

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

Chills Dyspnoea Palpitations

Symptomtext

1 day after recipient received the vaccine she developed heart palpitations, chills, and shortness of breath that resolved within 12 hours.

Weitere VAERSDATA-Felder

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

VAERS 986172

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 011J20A

moderat

Staat: NC
Alter: 47,0
Geschlecht: F
Eingang: 29.01.2021
Impfdatum: 08.01.2021
Beginn: 11.01.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: IM / RA

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

Asthenia Back pain Body temperature increased Chest discomfort Chest pain Cough Dyspnoea Fatigue Feeling cold Impaired work ability Injection site pain Injection site pruritus Injection site rash Injection site warmth Joint stiffness Muscle spasms Musculoskeletal stiffness Neck pain

Symptomtext

" COVID-19 Vaccine EUA" Day 3 following injection 1-11-21--Difficult breating, chest pressure all day and night. Extreme fatique and weakness. Day 4 following---continued difficulty breathing and chest pressure continuous. Moderate fatique and weakness. Day 5 following--- breathing difficulty improved significantly. Right arm muscle spasms and severe pain radiating to neck and chest and back (right side only), and stiffening of right hand and fingers. Tingling in are and pale color along with it feeling very cold. Small rash also at injection site. Moderate fatique and weakness. Day 6 following---breathing back to normal. Arm stiffening better. Still severe pain in right arm, neck, chest and back muscles. Less fatique and weakness. Day 7 following---Pain in right side of body continued. Chest tightness and cough started. 100 Temperature at 7pm. Fatique and weakness worsened. Day 8 following--- Pain in right side of body continued w a little less severity. Chest tightness and cough w 99.8 temperature. Day 9 -10following--- Pain in right side continues now with injection site (R arm) red, itcy and warm at site. Days 11-18----symptoms at there least. Overall felt well. Day 19 following--- sore throat, heavy chest tightness and cough w slight breathing difficulty. Day 20 following ---Severe body aches, cough, lowgrade fever of 99, Extreme fatigue. Sore throat. Difficulty breathing, moderately. Unable to work. Day 21 (today 1-29-21)---chest tightness, cough, lowgrade fever 99.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma; IBD; Degenerative spine disease
Andere Medikamente: Citalopram 40mg; Claritin 10mg; Trulance 3mg; Singular 10mg; Tizanidine 4mg Whole Food Multi Vitamins; Vitamin D 5000iu liquid drop; Vit B6
Allergien: Alinia (antibiotic); Latex
Vorherige Impfungen: -