VAERS Reports #038K20A

VAERS 2670071

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

kritisch

Staat: FL
Alter: 74,0
Geschlecht: U
Eingang: 11.08.2023
Impfdatum: 26.02.2021
Beginn: 04.08.2023
Tage bis Beginn: 889,0
Dosis: 1
Route/Site: - / -

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

Acute respiratory failure COVID-19 pneumonia Sepsis

Symptomtext

Sepsis with Acute hypoxic respiratory failure -2/2 COVID-19 PNA. Currently on-on NC. Titrate to keep sats 92-96% Remdesivir- yes

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Osteoarthritis, HLD, nicotine dependence in the past, class 1 obesity,
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2593087

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

kritisch

Staat: MI
Alter: 88,0
Geschlecht: F
Eingang: 08.03.2023
Impfdatum: 30.03.2021
Beginn: 02.03.2023
Tage bis Beginn: 702,0
Dosis: 1
Route/Site: IM / LA

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

Acute respiratory failure COVID-19 Encephalopathy Pneumonia Pneumonia aspiration Respiratory viral panel SARS-CoV-2 RNA SARS-CoV-2 test positive

Symptomtext

acute hypoxic respiratory failure, COVID-19 infection, Possible aspiration pneumonia versus community-acquired pneumonia, acute encephalopathy

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 5,0
Labordaten: Respiratory Panel PCR - detected presence of SARS-CoV-2 RNA on 3/2/2023
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2584867

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

kritisch

Staat: FL
Alter: 91,0
Geschlecht: M
Eingang: 21.02.2023
Impfdatum: 13.04.2022
Beginn: 04.02.2023
Tage bis Beginn: 297,0
Dosis: 1
Route/Site: IM / -

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

COVID-19 Death Pneumonia SARS-CoV-2 test positive Urinary tract infection

Symptomtext

Hospitalization: 2/4/2023 - 2/8/2023 (4 days) Presentation to the ED: BILATERAL PNEUMONIA & UTI. COVID + date: 2/4/23. Treatment: steroids Discharge to: HOSPICE - EXPIRED 2/9/23. 038K20A 1/29/2021 023M20A 2/26/2021 047C21A 11/4/2021 027L21A 4/13/2022

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Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: PAF, HTN, CVA, UTI, BPH, ANXIETY
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2584853

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

kritisch

Staat: FL
Alter: 87,0
Geschlecht: M
Eingang: 21.02.2023
Impfdatum: 06.11.2021
Beginn: 16.01.2023
Tage bis Beginn: 436,0
Dosis: 1
Route/Site: IM / -

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

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

Symptomtext

Hospitalization: 1/16/2023 - 1/25/2023 (9 days) Presentation to the ED: hypoxia COVID + date: 1/16/2023 Treatment: remdesivir & Decadron Discharge to: home with hospice. patient expired 1/30/2023. 038K20A 2/2/2021 031M20A 3/2/2021 051F21A 11/6/2021

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Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: COPD/hypertension/colon cancer
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2548834

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

kritisch

Staat: MI
Alter: 66,0
Geschlecht: M
Eingang: 03.01.2023
Impfdatum: 02.02.2021
Beginn: 19.12.2022
Tage bis Beginn: 685,0
Dosis: 1
Route/Site: - / -

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

COVID-19 Influenza virus test negative SARS-CoV-2 test positive Septic shock

Symptomtext

Pt admitted on 12/19 for septic shock with possible sources being UTI or pneumonia. Pt was COVID and influenza negative on admission. Pt was tested for COVID on 12/31 at discharge due to requiring SNF placement and was found to be COVID positive.

Weitere VAERSDATA-Felder

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

VAERS 2405639

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

kritisch

Staat: MI
Alter: 67,0
Geschlecht: F
Eingang: 09.08.2022
Impfdatum: 07.01.2022
Beginn: 05.08.2022
Tage bis Beginn: 210,0
Dosis: 1
Route/Site: IM / UN

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

Acute respiratory failure Anticoagulant therapy COVID-19 Chronic obstructive pulmonary disease Condition aggravated Coronary artery disease Cough Discomfort Dyspnoea Electrocardiogram Headache Laboratory test Malaise Obstructive sleep apnoea syndrome Orthostatic hypotension Presyncope Pyrexia Rhonchi

Symptomtext

Chief Complaint: Syncopal episode. Cough and shortness of breath. Additional Medical History: This 67-year-old obese female with a history of coronary artery disease, COPD, diabetes mellitus, hypertension, hyperlipidemia, migraine, irritable bowel syndrome, seizure and sleep apnea was brought to the ED by an ambulance after she suffered a syncopal episode in a camper just prior to arrival. The patient states that she has not been feeling well today. She has been having a nonproductive cough and shortness of breath for the last 3 days. She denies any fever, chills, nausea, vomiting, chest pain or diaphoresis. The patient is uncomfortable at the time of this examination. She has a headache. Associated Symptoms: cough, headache, shortness of breath

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 3,0
Labordaten: The oxygen saturation of the patient was 85% while breathing room air. She needed supplemental oxygen to keep the saturation above 90%. The patient was given Solu-Medrol 125 mg intravenously upon arrival. She received multiple inhaler treatments using Combivent. The patient tested positive for the COVID-19 infection. I reviewed all the lab results, EKG and radiological findings. The patient was observed in the ED. The physical examination revealed a persistent expiratory wheezing. It was decided to admit her for further care. I discussed the case with Dr. the hospitalist on-call. Problem 1: Acute exacerbation of chronic obstructive pulmonary disease Plan 1: Possibly due to COVID-19 infection however other infectious process cannot be ruled out. Patient has bilateral rhonchi in the lower lobes. Plan: -Start patient on IV antibiotics azithromycin and ceftriaxone. -Obtain respiratory pathogen panel -Start Solu-Medrol 80 mg 3 times daily. -DuoNeb for bronchodilation. -Incentive spirometer -Continue with nasal cannula oxygen, titrate as needed. Problem 2: COVID-19 Plan 2: Patient reported was vaccinated for COVID-19. She has fever now. -We will obtain C-reactive protein. -Patient will be on steroid and azithromycin as above. -Continue with nasal cannula oxygen, titrate as needed. -We will monitor overnight, and if her oxygen requirement worsen by the morning, will consider remdesivir. -Tylenol for fever. -Encourage oral hydration. Problem 3: Acute hypoxemic respiratory failure Plan 3: Secondary to COPD exacerbation COVID-19 infection and management will be the same as above. Problem 4: Coronary artery disease without angina pectoris Plan 4: History of coronary artery disease but was not following up with cardiology lately. She has scheduled echocardiogram as outpatient and has an appointment with a new cardiologist. Patient presented with syncope. -We will trend another troponin -We will obtain cardiogram if the patient stay in the hospital Monday. -Resume home medication Plavix. -Continuous cardiac monitoring. Problem 5: Syncope and collapse Plan 5: Likely vasovagal versus orthostatic hypotension. Patient syncopized from a standing position. Patient reported multiple syncope episode over the last few months. Patient was sick for 3 days, and had fever in the camp. Plan: -Continuous telemetry monitoring overnight monitor for arrhythmias. -Trend another troponin. -Will give gentle IV fluid hydration overnight -Encourage oral hydration. -Continuous cardiac monitoring. Problem 6: Type 2 diabetes mellitus Plan 6: On multiple medication at home. Confirm or resume home medication including Victoza We anticipate her blood glucose level to be elevated especially with steroid use. Problem 7: OSA on CPAP Plan 7: Resume CPAP with home setting. Plan 8: CODE STATUS: Full code DVT prophylaxis: Lovenox GI prophylaxis: Pantoprazole
Aktuelle Erkrankungen: unknown
Vorgeschichte: obesity CAD COPD DM HTN IBS Seizure sleep apnea
Andere Medikamente: Current Home Medications 1. albuterol 2.5 mg/3 mL (0.083%) inhalation solution : 3 milliliter(s) inhaled 4 times a day 2. clopidogrel 75 mg oral tablet : 1 tab(s) orally once a day 3. glipiZIDE : milligram(s) orally once a day 4. lisinopril
Allergien: none known
Vorherige Impfungen: -

VAERS 2390940

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

kritisch

Staat: MI
Alter: 74,0
Geschlecht: F
Eingang: 26.07.2022
Impfdatum: 02.12.2021
Beginn: 25.07.2022
Tage bis Beginn: 235,0
Dosis: 1
Route/Site: SYR / UN

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

Acute respiratory failure COVID-19 Cough Dyspnoea Kyphoscoliosis Lymphoedema Obesity Rheumatoid arthritis SARS-CoV-2 test positive

Symptomtext

Patient is a 75-year-old female with past medical history significant for hypertension and CHF who is presenting today for evaluation for cough and shortness of breath. Patient was tested positive for COVID 19 2 days before presentation. Patient came into the emergency department for further evaluation based on direction by her PCP. Patient says that she has a nonproductive cough, occasional shortness of breath. No significant medical history. Patient denies any fevers, chills, nausea, vomiting, diarrhea.

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 1,0
Labordaten: 5:52 PM: Patient was evaluated emergency department initially for COVID-19. Test positive COVID-19 rapid. Given 4 mg dexamethasone. Patient placed on 3 L nasal cannula. Patient improved SPO2. Patient is otherwise stable in emergency department. Patient PCP was contacted doctor admitted to his service. Problem 1: Acute hypoxemic respiratory failure due to COVID-19 Plan 1: Started oxygen supplementation Started on IV steroid, IV remdesivir and IV Zithromax. Placed on nebulizer treatment as needed Problem 2: Rheumatoid arthritis Plan 2: On methotrexate Problem 3: Kyphoscoliosis Problem 4: Moderate obesity Plan 4: With BMI of 33 Problem 5: Lymphedema of extremity Plan 5: Continue on pressure stocking
Aktuelle Erkrankungen: unknown
Vorgeschichte: HTN CHF GERD
Andere Medikamente: Current Home Medications 1. aspirin 81 mg oral tablet : 1 tab(s) orally once a day 2. bumetanide : 1.5 milligram(s) orally once a day 3. bumetanide 1 mg oral tablet : 1 tab(s) orally once a day 4. folic acid 1 mg oral tablet : 1 tab(s) oral
Allergien: codeine
Vorherige Impfungen: -

VAERS 2258995

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038k20a

kritisch

Staat: MI
Alter: 81,0
Geschlecht: F
Eingang: 29.04.2022
Impfdatum: 30.03.2021
Beginn: 05.12.2021
Tage bis Beginn: 250,0
Dosis: 2
Route/Site: IM / -

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

Asthenia Atelectasis COVID-19 Chest X-ray abnormal Cough Death Decreased appetite Diet refusal Hypoxia Lung disorder Mental status changes Pain Pleural effusion Respiratory tract congestion Urinary incontinence Weight decreased

Symptomtext

Pt presented to the ER 12/5/2021 complaining of altered mentation, decreased appetite, weight loss of 20 lb over 1 month. Patient also having urinary incontinence. Patient had been refusing to eat. Patient's husband present at bedside. Husband and patient's son who both live with the patient are both positive for COVID-19. He stated that patient has been getting worse over the last month complaining of generalized pain all the time. He was unable to care for the patient so he called ER. Patient also had a cough that been going on "for a while", at least 4 months. Patient had been having increasing weakness. On 12/11 Overnight patient developed hypoxia and needed 5 liters supplemental oxygen. CXR showed right perihilar and basilar atelactasis and increasing left lower love airspace disease with small left pleural effusion. She received decadron, Patient was having congestion, which is slowly getting better, which I hope will continue to get better as she recovers from COVID-19. She is on Mucinex DM and Claritin. Her oxygenation issues is resolved and now she is off supplemental oxygen and saturating in 90s on RA. Due to complication from other chronic illnesses, pt passed away on 12/24/21

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Praegender Schweregrund: Death
Hospital-Tage: 11,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: 2-10-2020 Atrial fibrillation 12/30/2019 Bilateral dry eyes 8/12/19 Presence of Watchman left atrial appendage closure device 3/2001 Stroke Date Unknown Anxiety and depression Date Unknown Arthritis Date Unknown Asthma Date Unknown Balance disorder Date Unknown Blood transfusion Date Unknown DOE (dyspnea on exertion) Date Unknown Dysphagia Date Unknown GERD (gastroesophageal reflux disease) Date Unknown HTN (hypertension) Date Unknown Irritable bowel disease Date Unknown Migraine Date Unknown Panic attacks Date Unknown PONV (postoperative nausea and vomiting) Date Unknown Poor short term memory Date Unknown Prophylactic antibiotic Date Unknown Pseudophakia Date Unknown Squamous blepharitis left eye, upper and lower eyelids Date Unknown Squamous blepharitis of both upper and lower eyelid of right eye Date Unknown Vitreous degeneration and detachment of right eye Surgical History 31 items 02/10/2020 Echo transesoph 08/12/2019 Echo transesoph 02/21/2019 Watchman 10/30/2018 Echo transesoph 03/13/2018 Hchg myelogram lumbar 10/26/2017 Ablation 6/1/2016 Laminectomy lumbar spine w/ fusion 4/15/15 Hchg egd with dilation 9/22/2014 Ablation 9/12/14 Echo transesoph 9/12/14 Cardioversion 08-05-11 Ablation 5/3/2011 Esophagogastroduodenoscopy with biopsy 4/15/2011 Esophagogastroduodenoscopy (orderset) 05/04/09 Procedure 03/2008 Hx pacemaker placement 2005 Hx heart catheterization age 11 yr Appendectomy last one 1/2008 Cardioversion Date Unknown Cholecystectomy laparoscopic Date Unknown Hx cataract removal (Bilateral) 1999 and 2000 Hx craniotomy ~1960's Hx hemorrhoidectomy 2004, 2006 Hx knee replacment (Bilateral) ~1970's & 1980's Hx lumbar fusion Date Unknown Hx lumbar laminectomy ~1980's Hx tmj arthotomy as child Hx tonsil and adenoidectomy ~1970's Hx vein stripping Date Unknown Hysterectomy abdominal total w/ bilateral salpingo oophorectomy Date Unknown Pr total knee arthroplasty (Bilateral)
Andere Medikamente: albuterol (PROAIR HFA) 108 (90 BASE) MCG/ACT HFA inhaler aspirin EC (ECOTRIN) 325 MG tablet butalbital-acetaminophen-caffeine (ESGIC) 50-325-40 MG tablet dextromethorphan-guaifenesin (MUCINEX DM) 30-600 MG SR tablets diltiazem (DILACOR-
Allergien: Latex, Demerol, lubricating jelly, morphine, sulfa, Penicillin.
Vorherige Impfungen: -

VAERS 2179721

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

kritisch

Staat: MI
Alter: 91,0
Geschlecht: M
Eingang: 15.03.2022
Impfdatum: 12.02.2021
Beginn: 13.02.2022
Tage bis Beginn: 366,0
Dosis: 2
Route/Site: UN / UN

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

Acute kidney injury Acute myocardial infarction Ammonia increased Anticoagulant therapy Blood creatinine increased Brain natriuretic peptide increased COVID-19 Cardiac failure acute Chronic kidney disease Decubitus ulcer Deep vein thrombosis Fibrin D dimer increased Hypermagnesaemia Hypertransaminasaemia Influenza A virus test negative Influenza B virus test Lactic acidosis Leukocytosis

Symptomtext

Attending Physician: DO;* Date of Admission: 2/13/2022 CC: HPI: This is a 92y.o. male with medical history of A. fib , HTN, CAD, CHF, multiple myeloma s/p chemotherapy, baseline bedbound, from ECF, presents to the ED for mental status change. Check patient in the ER, he is unresponsive. Called to talk to his son, baseline orientated, bedbound, in the ER start heparin drip, received IV bolus 1 L in the ED, admit inpatient for further evaluation and management, infection disease consult# Metabolic encephalopathy/mental status change/unresponsiveness/elevated ammonia level # Sepsis/ COVID-19 infection without hypoxia # Non-STEMI/elevated troponin /hx of A fib # Transaminitis # Acute heart failure , elevated BNP level, unknown EF # Lactic acidosis, improving, # Urinary retention/UTI/leukocytosis # AKI on CKD IV, elevated Cr. Level # RLE DVT /elevated D dimer # stage III pressure ulcer coccyx , no s/s infection # hypermagnesemia

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Praegender Schweregrund: Acute myocardial infarction
Hospital-Tage: 9,0
Labordaten: NOCOVER> 1 HEALTH SYSTEM LABORATORY Chart Review Copy HAR: 22325542501 DOB: (92 yrs) PT CLASS: Inpatient CSN: 243640753 DEPT: PATIENT STATUS: Discharged GENDER: male BED: ORD DR: AUTH DR: Results Covid-19, Flu, RSV by NAA (Order) Contains abnormal data Covid-19, Flu, RSV by NAA Order: Status: Final result Visible to patient: No (inaccessible in myChart) Next appt: None Specimen Information: Nasopharyngeal; Swab 0 Result Notes Component Ref Range & Units Influenza A Not Detected Not Detected Influenza B Not Detected Not Detected RSV Not Detected Not Detected SARS-CoV-2 (COVID-19) by NAA, Micro Not Detected Detected Abnormal Narrative Methodology: Nucleic Acid Amplification(NAA)/Polymerase Chain Reaction(PCR) The SARS-CoV-2 (COVID-19) test is for in vitro diagnostic use under the FDA Emergency Use Authorization (EUA) for laboratories certified under CLIA to perform high complexity testing. This test has not been FDA cleared or approved. Specimen Collected: 02/12/22 10:59 AM Last Resulted: 02/12/22 12:13 PM
Aktuelle Erkrankungen: ? A-fib ? CHF (congestive heart failure)
Vorgeschichte: -
Andere Medikamente: acetaminophen (TYLENOL) 325 MG PO Tab take 650 mg by mouth every 6 hours as needed. Unknown Unknown time atorvastatin (LIPITOR) 20 MG PO Tab take 20 mg by mouth once every night at bedtime. Unknown Unknown time bisacodyl (DULCOLAX) 5 MG PO
Allergien: not listed
Vorherige Impfungen: -

VAERS 2075677

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

kritisch

Staat: MI
Alter: 72,0
Geschlecht: F
Eingang: 31.01.2022
Impfdatum: 01.04.2021
Beginn: 04.01.2022
Tage bis Beginn: 278,0
Dosis: 1
Route/Site: IM / AR

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

Acute kidney injury Adult failure to thrive Anaemia Angiogram pulmonary abnormal Anticoagulant therapy Anticoagulation drug level above therapeutic Antinuclear antibody positive Asthenia Atrial fibrillation Blood test normal Condition aggravated DNA antibody positive Death Deep vein thrombosis Dyspnoea COVID-19 CSF culture negative Chest wall mass

Symptomtext

Patient is now DECEASED; Hospitalized (12.11.21 - 1.20.22); COVID-19 positive (1.4.22); Fully vaccinated (no booster) Admission Date: 12/11/2021 Date of Death: 1/20/22 Time of Death: 3:04 PM Preliminary Cause of Death: Acute encephalopathy DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Tachypnea Failure to thrive in adult AKI (acute kidney injury) Atrial fibrillation with rapid ventricular response Atrial fibrillation with RVR Altered mental state Sepsis HOSPITAL COURSE: Patient is a 73 year old woman who was recently admitted to hospital and had extensive work up for fever presented with altered mental status. She was on bactrim for concern for toxoplasma infection. She was found to have a.fib with RVR as well. She was started on IV cardizem. Echo was normal. Cardiology was consulted for assistance with rate control. She was transitioned to lopressor and digoxin with improvement and weaned off cardizem gtt. Neurology consult was obtained. She had MRI, LP and EEG. All of them did not reveal any organic etiology for her presentation. As her mental status did not improve, corpak was placed and she was started on tube feeds. ID consulted for toxoplasma infection. Unclear if patient with active infection Bactrim initially continued and stopped due to LFTs trending up given low suspicion for active infection and completing extended antibiotic course from admission at hospital recently. Karius test was ordered and was negative. Overnight on 12/24, pt was found to be tachycardic, tachypneic hypotensive and hypoxic. A RAP was called, pt was given 3 L IVF and 3 doses of albumin with slow improvement of blood pressures. She was quickly weaned back to RA. Her hgb was found to have dropped to 7.0 and 1 unit PRBC ordered. She had CT thorax which did show right upper lobe PE and CT abd/pelvis showing proctitis. US showed bilateral LE dvt. Her Eliquis was changed to Lovenox. GI was consulted with acutre drops in hgb and felt no acute GI bleed. Pt then had worsening fevers, tachycardia and tachypnea on 12/26. She had repeat CT Angio thorax which showed worsening clot burden. A LMWH level was checked and found to be supratherapeutic. Hematology was consulted and she was switched to heparin drip. Neurology was reconsulted with ongoing AMS and fevers. She was moved to ICU as CC2 for closer monitoring. Patient remained stable over the night in the ICU and transferred back to the general floor. Heparin gtt continued as patient had a decrease in hgb, may transition back to eliquis if hgb stabilizes. Lasix resumed, but minimal output even with addition of metolazone and eventually transitioned to lasix drip that was weaned off. She continued to require intermittent diuresis. With persistent encephalopathy, neurology and ID was reconsulted. Repeat LP was done 1/5/22 with a negative CSF. A repeat 2 hour EEG 1/12 continue to show moderate encephalopathy. Per ID 1/12 no further infectious work up recommended unless increased fever curve and new leukocytosis. Rheumatology was then contacted who recommended checking ANA and Anti Ds DNA. ANA and anti smith antibody found to be positive. She was started on plaquenil 400 mg daily for possible lupus cognitive impairment. She continued to have persistent tachycardia and tachypnea. She was originally seen by cardiology. She was started on metoprolol, dilitiazem, and digoxin with some improvement in HR however still at times elevated. She had persistent tachypnea as high as 60. Her O2 remained stable. Did not note any improvement with suctioning. The patient was positive for COVID 1/4/22. Remain on RA and imaging with mild disease burden. She also continued to receive intermittent diuresis. She was then started on morphine for work of breathing. The patient was noted to be anemic and required multiple blood transfusions. Could consider GI evaluation once hemodynamically stable. She was also noted to have persistently worsening sacral wound. Wound was consulted who recommended dressing changes, offloading. Concern for pressure ulcer vs kennedy ulcer. Noted that may need to consider plastics for debridement in OR however pt too hemodynamically unstable to pursue. With prolonged hospitalization, palliative, hospice and ethics were consulted. Family was agreeable to change code status to DNR/DNI. Hospice continued to follow. Family wanted to wait to see after initiating plaquenil if any improvement in mentation in 7-10 days. Mentation failed to improve. On 1/19, she was transitioned to comfort care and was admitted under inpatient hospice status. She was started on morphine and versed infusions. Multiple family members were present at bedside. The patient passed away at 3:04 pm on 1/20/22. Hospice present and will follow up with family for funeral home selection.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 40,0
Labordaten: -
Aktuelle Erkrankungen: Admitted to hospital from 11.12.21 through 12.7.21 - Fever, unspecified fever cause (Primary Dx); Weakness generalized; Mass in chest; Pyrexia of unknown origin; Tremor; Neuropathy
Vorgeschichte: Patient is a 73 y.o. female with past medical history of diabetes mellitus, hypertension, low back pain, blastomycoses infection, and MALT lymphoma of orbit (recently with multiple falls and weight loss) Acute encephalopathy Toxoplasmosis Atrial fibrillation with RVR Type 2 diabetes mellitus with hyperglycemia, without long-term current use of insulin Pressure injury of right buttock, unstageable Hemoptysis Acute pulmonary embolism without acute cor pulmonale Deep venous thrombosis Elevated temperature Abnormal LFTs Goals of care, counseling/discussion Multiple comorbid conditions
Andere Medikamente: aspirin (ASPIRIN) 81 MG enteric coated tablet B Complex Vitamins (BL VITAMIN B COMPLEX PO) Calcium 600 MG TABS Coenzyme Q10 (COQ10 PO) cyanocobalamin (VITAMIN B-12) 1000 MCG tablet ferrous sulfate 325 (65 Fe) MG tablet insulin aspart (NOVOL
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2050891

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

kritisch

Staat: MI
Alter: 77,0
Geschlecht: M
Eingang: 20.01.2022
Impfdatum: 12.02.2021
Beginn: 07.01.2022
Tage bis Beginn: 329,0
Dosis: 2
Route/Site: IM / LA

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

Acute respiratory failure Alanine aminotransferase normal Angiogram pulmonary abnormal Anion gap Anticoagulant therapy Arrhythmia Arterial catheterisation Aspartate aminotransferase normal Asthenia Atrial fibrillation Back pain Basophil count decreased Basophil percentage decreased Blood albumin decreased Blood alkaline phosphatase normal Blood bicarbonate increased Blood bilirubin normal Blood calcium normal

Symptomtext

Hospitalized (1.7.22 - 1.13.22 / RE-ADMITTED 1.17.22 for GI Bleed duodenal ulcer, acute blood loss anemia); COVID-19 positive (1.1.22 - home test/ 1.7.22 hospital); Fully vaccinated - moderna x2 d/c summary from 1.13.22: Discharge Summary MD (Physician) ? ? General Medicine BRIEF OVERVIEW: Discharge Provider: MD Primary Care Provider: DO Admission Date: 1/7/2022 Discharge Date: Jan 13, 2022 Active Hospital Problems Diagnosis Date Noted POA ? Type 2 diabetes mellitus with hyperglycemia 01/08/2022 Yes ? Acute respiratory failure with hypoxia and hypercapnia 01/08/2022 Unknown ? Acute hypoxemic respiratory failure due to COVID-19 01/03/2022 Unknown ? Pseudoarthrosis of lumbar spine 05/18/2018 Yes ? Cardiomyopathy 08/16/2017 Yes ? Atrial fibrillation 08/16/2017 Yes ? Allergic rhinitis Yes ? Hypercholesterolemia 07/13/2010 Yes ? Hypertension Yes ? GERD (gastroesophageal reflux disease) Yes Resolved Hospital Problems No resolved problems to display. Pre-Existing Active Problems Diagnosis Date Noted POA ? Hardware complicating wound infection, subsequent encounter 06/08/2018 Unknown ? Edema, unspecified type 08/30/2017 Unknown ? ED (erectile dysfunction) 09/25/2012 Unknown ? Eczema Unknown ? DJD (degenerative joint disease) 03/01/2010 Unknown Discharge Disposition: home health care svc DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Hypoxia [R09.02] Acute hypoxemic respiratory failure due to COVID-19 [U07.1, J96.01] Pneumonia due to COVID-19 virus [U07.1, J12.82] Acute respiratory failure with hypoxia and hypercapnia [J96.01, J96.02] COVID-19 [U07.1] HOSPITAL COURSE: per HPI: Patient is a 78 y.o. male with past medical history significant for atrial fibrillation recently started on Eliquis, history of cardiomyopathy with recovered EF, chronic lower extremity edema, hypertension, hyperlipidemia, non-insulin-dependent type 2 diabetes, hypothyroidism and chronic low back pain with chronic opioid use who presents to the emergency department approximately 1 week after being diagnosed with COVID-19 (01/01/2022) with worsening shortness of breath. Patient began showing symptomatic with generalized fatigue, body aches, sore throat, dyspnea and productive cough. He received monoclonal antibody treatment on 01/04 but continued to have increased shortness of breath so presented to ED today. He has been vaccinated with Moderna x2 in 02/2021 but not the booster vaccine. He is fully oriented but ill-appearing and very fatigued so I question if some of his recall is accurate. He endorses a mildly productive cough originally streaked with bright red sputum but since has become dark brown/dark red and is improving. He has maintained a decent appetite and continued to take all of his medications including Lasix. Has chronic lower extremity edema appears stable to him. Was originally diagnosed with AFib multiple years ago but not on anticoagulation until 2 weeks ago when his PCP recommended restarting Eliquis. No noted fevers, chest pain, abdominal pain, nausea, vomiting, diarrhea or difficulty urinating. Non smoking, minimal ETOH use. On arrival to the emergency room, patient was hypoxic to 75% on room air and tachypneic to respirations 34 and he ultimately required 6 L nasal cannula to maintain O2 sats greater than 92%. He was quite hypertensive with blood pressure 180s to 200s mmHg systolic which improved after IV hydralazine. Labs show potassium 3.2, hyperglycemia, NT proBNP 1400, troponins indeterminate downtrending, procalcitonin 0.06 and no leukocytosis. COVID-19 PCR positive. CT angiogram thorax was negative for PE but demonstrated scattered diffuse mixed ground-glass opacities and consolidations consistent with COVID-19 pneumonia along with a small left pleural effusion. Left lower extremity duplex ultrasound was negative for DVT. Independent review of EKG shows atrial fibrillation at a rate of 89 ppm in without acute ischemic changes from prior. He was given IV hydralazine 10 mg, home metoprolol 50 mg, Decadron 10 mg and admitted to hospital medicine for acute hypoxic respiratory failure secondary to COVID-19 pneumonia. in-house: patient admitted for severe sepsis 2/2 COVID-19 pneumonia with acute hypoxemic respiratory failure as well as acute CHF. moving patient out of the ED was difficult due to his oxygenation requirements possibly necessitating being sent to the ICU, he was on BiPAP and requiring more than 50% FiO2. he was started on decadron, lasix, but not remdesivir due to concerns for fluid overload; he was also started on lantus due to concern for hyperglycemia from his steroids. echocardiogram was unremarkable, no DVT on RLE venous doppler U/S. patient's pCO2 and pH were elevated as well as stable after several hours on BiPAP, he also remained lethargic. ICU was called and he was moved to the unit a few hours after admission on 1/8. patient was placed on BiPAP there and monitored as ICU was planning on intubating him. however he turned around and was stable for transfer later on 1/8. transfer did not take place right away due to bed availability. on 1/10 patient was AAOx4 and said his SOB and cough had improved, he had no other complaints at the time. Hypoxia improved and patient was continued on Decadron, remdesivir during hospitalization. Patient was subsequently evaluated by pulmonary rehab prior to discharge recommended 3 L at rest and with activity. Patient was discharged to complete 10 days of oral Decadron. Patient required insulin during the hospitalization. Evaluated by Endocrinology who did not think that patient to be discharged on insulin which was discontinued. Patient was evaluated by PT and OT recommended home with home health. Patient was discharged in medically stable condition. Discharge instructions were discussed with patient. CONSULTS / RECOMMENDATION: Consult Orders (From admission, onward) IP CONSULT TO DIABETES & ENDOCRINOLOGY Provider: Diabetes And Endocrinology INPATIENT PROCEDURES: BP 152/100 | Pulse 97 | Temp 36.4 ?C (Axillary) | Resp 21 | Ht 1.803 m | Wt 83.7 kg | SpO2 95% | BMI 25.74 kg/m? FIO2 (%): (S) 40 % 1/8/22 H&P: Admission History and Physical CHIEF COMPLAINT dyspnea Assessment/Plan ASSESSMENT Principal Problem: Acute hypoxemic respiratory failure due to COVID-19 Active Problems: Hypertension GERD (gastroesophageal reflux disease) Hypercholesterolemia Allergic rhinitis Atrial fibrillation Cardiomyopathy Pseudoarthrosis of lumbar spine Type 2 diabetes mellitus with hyperglycemia PLAN FULL MEDICATION RECONCILIATION PENDING review of medications w/ wife later this AM by pharmacy tech. Many inconsistencies between pharmacy dispense history and patient reported medications. Patient memory questionable due to fatigue from current illness. Ordered eliquis 5 mg BID for afib (started two weeks ago by patient, possibly a sample, no pharmacy Rx visible), lasix, metoprolol and synthroid. Pending verification of eliquis, cozaar, metformin and PPI. Addendum 0330: VBG shows significant hypercarbia and respiratory acidosis w/ venous pCO2 93 and pH 7.23. C/w ongoing lethargy. Likely multifactorial from poor respiratory compensation for COVID, suspected pulm edema from significant hypertension (flash edema?) and possible oversedation chronic narcotics. No COPD hx. Lethargic but he seems be alert enough to remove a mask. Will trial BIPAP as able due to underlying COVID. IV lasix 40 mg x 1 with concurrent IV potassium 40 mEq. Goal systolic BP 140-160 mmHg. Addendum 0630: CO2 improving on BIPAP w/ O2 sats > 95% on 100% BIPAP. Placed on this level of FIO2 per respiratory because he keeps ripping of BIPAP mask and desaturating -- not due to any desaturations on lower level FIO2. Requested safety attendant and for respiratory to reduce FIO2 to maintain sat > 92%. After which time, he should be appropriate for a GMB bed. Approx 600 mL UOP within 1.5 hours of IV lasix. A1c 8.0 and remains hyperglycemic. Started lantus 20 units daily basal bolus insulin (first dose 9 AM) Lethargy Acute hypoxic respiratory failure 2/2 COVID 19 pneumonia Small left pleural effusion Bilateral mucous plugging CTA thorax 1/8: negative for PE, scattered diffuse mixed ground-glass opacities and consolidations consistent with COVID-19 pneumonia, small left pleural effusion, diffuse peribronchial thickening, scattered mucus plugging bilaterally -Currently requiring 6 L NC with significant tachypnea and conversational dyspnea -Symptom onset 1/1 (7 days PTA), vaccinated w/ moderna x 2 (2/2021) -Doubt bacterial superinfection w/ low procal (0.06) -Outpatient monoclonal antibody infusion on 1/4/21 -Decadron started 1/7 - present -Agreeable to remdesivir but have not started due to concern of volume overload. Re-evaluate after lasix -Concerned for pulmonary edema w/ significant lower extremity edema and accelerated hypertension -Start lasix IV 40 mg BID when potassium replete (home: lasix 40 mg daily) -Update limited echo w/ significant lower extremity edema -Check VBG due to lethargy -CPT and scheduled mucinex for mucous plugging -Daily weights/strict I& O -Trend CMP, CBC, D dimer and CRP -Proning and incentive spirometry discussed and encouraged -Continuous oximetry and telemetry Asymmetric chronic lower extremity edema, R > L -Unclear if worse from baseline due to poor patient history -Doppler USV left lower extremity negative for DVT, pending RLE U/S -Updating limited echo -Checking urine protein:creatine ratio -Continue lasix per above Acute on chronic CHF exacerbation? History of cardiomyopathy w/ recovered EF, in setting of post-operative spinal surgery -EF 40% 8/2017 in setting of post-op complications following -- > 53% 9/2017 -EKG w/o ischemic changes, trops indeterminate and downtrending, NT pro BNP 1500 (no baseline) -Updating limited echo due to ongoing edema -Lasix per above, daily weights, strict I/O Accelerated hypertension Hyperlipidemia -Very hypertensive on presentation in setting of respiratory distress -Improved after IV hydralazine -Endorses antihypertensive compliance but exact home regimen unclear, pharmacy tech to clarify later this AM -Continue metoprolol, lasix and statin. Hold on Cozaar in setting of acute illness -IV hydralazine 10 mg IV q 4 hours prn for systolic BP >160 mmHg -Hold on IV BB pending echo evaluation of systolic function -Goal systolic BP 140-169 mmHg Atrial fibrillation -Rates adequately controlled thus far -Recently started eliquis 2 weeks PTA -Continue metoprolol and eliquis Non-insulin-dependent type 2 diabetes mellitus -Diet controlled. Maybe on metformin? -A1 c 6.9 on 03/2021, will recheck -Moderate dose corrective insulin started in anticipation of steroid induced hyperglycemia Asymptomatic bilateral nephrolithiasis -incidental finding on CT a/p Hypothyroidism -Continue Synthroid -TSH 2.3 on 12/2021 GERD -Continue PPI Chronic low back pain -continue Norco 5 mg-325 mg every 8 hours hours p.r.n. pending improvement in mentation -MAPS confirmed DVT ppx: Eliquis Diet: Diabetic liberal Code status: Full Code per discussion with patient on admission Updated wife via phone about clinical status and plan of care at 0630. She is home recovering from COVID and would like an update later today. Son added as potential visitor but she is unsure if phone number is correct. Above assessment and plan discussed with Dr. whose insight is reflected above. Subjective HISTORY OF PRESENT ILLNESS Patient is a 78 y.o. male with past medical history significant for atrial fibrillation recently started on Eliquis, history of cardiomyopathy with recovered EF, chronic lower extremity edema, hypertension, hyperlipidemia, non-insulin-dependent type 2 diabetes, hypothyroidism and chronic low back pain with chronic opioid use who presents to the emergency department approximately 1 week after being diagnosed with COVID-19 (01/01/2022) with worsening shortness of breath. Patient began showing symptomatic with generalized fatigue, body aches, sore throat, dyspnea and productive cough. He received monoclonal antibody treatment on 01/04 but continued to have increased shortness of breath so presented to ED today. He has been vaccinated with Moderna x2 in 02/2021 but not the booster vaccine. He is fully oriented but ill-appearing and very fatigued so I question if some of his recall is accurate. He endorses a mildly productive cough originally streaked with bright red sputum but since has become dark brown/dark red and is improving. He has maintained a decent appetite and continued to take all of his medications including Lasix. Has chronic lower extremity edema appears stable to him. Was originally diagnosed with AFib multiple years ago but not on anticoagulation until 2 weeks ago when his PCP recommended restarting Eliquis. No noted fevers, chest pain, abdominal pain, nausea, vomiting, diarrhea or difficulty urinating. Non smoking, minimal ETOH use. On arrival to the emergency room, patient was hypoxic to 75% on room air and tachypneic to respirations 34 and he ultimately required 6 L nasal cannula to maintain O2 sats greater than 92%. He was quite hypertensive with blood pressure 180s to 200s mmHg systolic which improved after IV hydralazine. Labs show potassium 3.2, hyperglycemia, NT proBNP 1400, troponins indeterminate downtrending, procalcitonin 0.06 and no leukocytosis. COVID-19 PCR positive. CT angiogram thorax was negative for PE but demonstrated scattered diffuse mixed ground-glass opacities and consolidations consistent with COVID-19 pneumonia along with a small left pleural effusion. Left lower extremity duplex ultrasound was negative for DVT. Independent review of EKG shows atrial fibrillation at a rate of 89 ppm in without acute ischemic changes from prior. He was given IV hydralazine 10 mg, home metoprolol 50 mg, Decadron 10 mg and admitted to hospital medicine for acute hypoxic respiratory failure secondary to COVID-19 pneumonia. Patient Active Problem List Diagnosis ? Hypertension ? GERD (gastroesophageal reflux disease) ? DJD (degenerative joint disease) ? Hypercholesterolemia ? Eczema ? Allergic rhinitis ? ED (erectile dysfunction) ? Atrial fibrillation ? Cardiomyopathy ? Edema, unspecified type ? Pseudoarthrosis of lumbar spine ? Hardware complicating wound infection, subsequent encounter ? Acute hypoxemic respiratory failure due to COVID-19 ? Type 2 diabetes mellitus with hyperglycemia REVIEW OF SYSTEMS Review of Systems Constitutional: Positive for appetite change and fatigue. Negative for chills and fever. HENT: Positive for sore throat. Respiratory: Positive for cough and shortness of breath. Cardiovascular: Positive for leg swelling. Negative for chest pain. Gastrointestinal: Negative for abdominal pain, diarrhea, nausea and vomiting. Genitourinary: Negative for difficulty urinating. Musculoskeletal: Positive for back pain (chronic). Skin: Negative for rash. Neurological: Positive for weakness. Negative for headaches. Hematological: Bruises/bleeds easily. Objective OBJECTIVE BP 177/98 | Pulse 91 | Temp 97.7 ?F (36.5 ?C) (Oral) | Resp 24 | Ht 1.803 m (5' 11") | Wt 95.7 kg (210 lb 15.7 oz) | SpO2 96% | BMI 29.43 kg/m? Physical Exam Vitals and nursing note reviewed. Constitutional: Appearance: He is ill-appearing. Comments: Sleepy but rouses to voice, tachypenic and conversationally dyspneic HENT: Mouth/Throat: Mouth: Mucous membranes are dry. Pharynx: Oropharynx is clear. Eyes: Extraocular Movements: Extraocular movements intact. Cardiovascular: Rate and Rhythm: Tachycardia present. Rhythm irregular. Pulses: Normal pulses. Heart sounds: Normal heart sounds. No murmur heard. Pulmonary: Effort: No respiratory distress. Breath sounds: Wheezing and rales (throughout all lung fields) present. Comments: Conversationally dyspneic and tachypenic, increased work of breathing with abdominal accessory muscle use but does not appear in respiratory distress Abdominal: General: Bowel sounds are normal. There is no distension. Palpations: Abdomen is soft. Tenderness: There is no abdominal tenderness. Musculoskeletal: General: No tenderness. Right lower leg: Edema (3+ pitting edema to thigh) present. Left lower leg: Edema (2+ pitting edema of calf) present. Skin: General: Skin is dry. Comments: Cool extremities but dorsalis pedis pulses strong Neurological: Mental Status: He is alert and oriented to person, place, and time. Comments: Very tired and falls asleep during questions but fully oriented and rouses easily to voice 1/18/22 MICU H&P: MICU ATTENDING ATTESTATION I personally saw and examined the patient and discussed with the resident. I assessed/reviewed this patient's hemodynamics, cardiopulmonary status, renal function, fluid balance, medications, labs, imaging, analog sedation, mental status (delirium), mobility, nutrition, glycemic control, line-tube-drain necessity, skin status, prophylaxis, disposition, patient/family concerns and daily goals. I developed a detailed management plan on the basis of these assessments. Brief exam: He was obtunded on initial exam when rapid response was called, covered in hematochezia with small amount of epistaxis. After resuscitation he was alert and conversant. Cool, pale. Brief History and Medical Decision-Making: This is a 78 yo male with recent COVID pneumonia, discharged on 1/13 s/p MAB and steroid treatment. Presented with GIB. Found to have duodenal ulcer on EGD 1/17 s/[p cautery and Epi injection. ICU responded to code blue on floor when he had a syncopal event and was acutely hypotensive after passing large amount of hematochezia. ---Hemorrhagic shock secondary to Duodenal ulcer s/p Endoscopic intervention Resuscitated with PRBCs, 1 unit on 1/17 and an additional 2 units overnight Discussed with GI, but recommended IR intervention, now s/p embolization of the GDAm and duodenal perforator. Monitor H&H q6 hr Continue protonix gtt. NPO Off vasopressors Lactic acidosis secondary to shock Restrictive lung disease: chronically elevated serum bicarbonate consistent with hypoventilation, avoid hyperoxygenation. Wean for SpO2 goal of 92-96% --atrial fibrillation Holding metoprolol and Eliquis Diabetes Mellitus SSI and lantus Principal Problem: Acute blood loss anemia Active Problems: Atrial fibrillation Type 2 diabetes mellitus with hyperglycemia Melena Hemorrhagic shock COVID-19 virus detected This patient is critically ill and is requiring active support and intensive surveillance to prevent life threatening clinical deterioration. I spent a total of 80 minutes in the evaluation and management of this patient excluding all procedures. MD Pulmonary and Critical Care Medicine Medical Group Expand All Collapse All Hide copied text Hover for details CHIEF COMPLAINT: Acute blood loss anemia Assessment/Plan ASSESSMENT / PLAN: Patient is a 78 y.o. male with a past medical history of afib on eliquis, recent hospitalization for covid-19 pna 1/7-1/13 discharge on 3L nasal cannula, currently admitted for GI bleeding. Transferred to ICU for continued bleeding and hemodynamic compromise requiring norepinephrine Hemorrhagic Shock Acute Blood Loss Anemia Upper GI Bleed 2/2 Duodenal Ulcers EGD on 1/17 remarkable for duodenal ulcers treated with epinephrine and cautery, esophageal exudates suspicious for candida Deteriorated on general medical floors with continued melena, hematemesis, and hypotension Last Hgb 6.8, last lactic acid 8.5 Plan - GI consulted, discussed with on-call physician Dr. who recommend IR embolization - IR consulted for urgent embolization - Continue IV PPi - Ordered 2 units pRBC (will be 3 total since admission), consider adding platelets to next transfusion round, if necessary. Transfuse hgb <7.0 - CBC q6 hours, lactic acid q6 hours - Vasopressors prn for hemodynamic support - Hold Eliquis, last dose 1/16 Covid-19 PNA Fully vaccinated, not boosted. Tested positive 1/7, hospitalized 1/7-1/13 S/p monoclonal abs, dexamethasone and Remdesivir, discharged on 3L Plan - Currently on non-rebreather - Last ABG consistent with respiratory acidosis, repeat prn Atrial Fibrillation Plan - Holding Eliquis and Metoprolol given bleeding and hypotension Diabetes Mellitus Last A1c 8.0% 1/7 Plan - Basal bolus insulin with 8 units Lantus at night and moderate dose corrective Humalog - Holding home hypoglycemics Hypertension Plan - Hold home meds given hypotension Hypothyroid Plan - Home synthroid Lines: L art line (1/17), L IJ CVC (1/17) Drains: n/a Airway: non-rebreather Diet: NPO VTE Prophylaxis: Contraindicated with GI bleed Code Status: Full - Unknown GI Prophylaxis: IV PPi Plan was discussed with attending Dr., please see their attestation for further recommendations DO Internal Medicine HISTORY OF PRESENT ILLNESS: Patient is a 78 y.o. male with a history of afib on eliquis, DM, hypothyroid, HTN, recent hospitalization from 1/7-1/13 for covid-19 pneumonia discharged on 3L nasal cannula and dexamethasone. Since that time patient has been progressively more fatigued and weak, also noting episodes of melena. Patient was admitted to the general medical floors on 1/17 and underwent EGD which found duodenal ulcers s/p epinephrine and cautery to stop the bleeding. He required 1 unit pRBC at that time. The evening of 1/17 a "code blue" was called due to change in mental status, hypotension, and hematemesis with concern for lack of pulses. ICU team arrived and found pulses remained strong, no ACLS performed. Patient was transferred to the ICU for requiring norepinephrine to maintain adequate mean arterial pressures. Family was updated via telephone Patient Active Problem List Diagnosis ? Hypertension ? GERD (gastroesophageal reflux disease) ? DJD (degenerative joint disease) ? Hypercholesterolemia ? Eczema ? Allergic rhinitis ? ED (erectile dysfunction) ? Atrial fibrillation ? Cardiomyopathy ? Edema, unspecified type ? Pseudoarthrosis of lumbar spine ? Hardware complicating wound infection, subsequent encounter ? Acute hypoxemic respiratory failure due to COVID-19 ? Type 2 diabetes mellitus with hyperglycemia ? Acute respiratory failure with hypoxia and hypercapnia ? Acute blood loss anemia ? Melena OBJECTIVE: BP (!) 149/37 | Pulse 118 | Temp 36.6 ?C | Resp 24 | Ht 1.803 m | Wt 86 kg | SpO2 100% | BMI 26.46 kg/m? Physical Exam Vitals reviewed. Constitutional: Appearance: He is toxic-appearing. HENT: Head: Normocephalic and atraumatic. Cardiovascular: Rate and Rhythm: Tachycardia present. Rhythm irregular. Pulses: Normal pulses. Heart sounds: Normal heart sounds. No murmur heard. No gallop. Pulmonary: Effort: Respiratory distress present. Breath sounds: No wheezing or rales. Comments: Accessory muscle use On non-rebreather mask Abdominal: General: Abdomen is flat. Bowel sounds are normal. There is no distension. Palpations: Abdomen is soft. There is no mass. Tenderness: There is no abdominal tenderness. There is no guarding or rebound. Musculoskeletal: Right lower leg: No edema. Left lower leg: No edema. Skin: Comments: Lower extremities are cold Neurological: Mental Status: He is alert. Motor: No weakness

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 9,0
Labordaten: D-Dimer (Normal) Collected: 01/13/22 0707 Order Status: Completed Specimen: Blood, Venous Updated: 01/13/22 0842 D-Dimer Quant 440 0 - 500 ng/mL FEU Comprehensive Metabolic Panel (CMP) (Abnormal) Collected: 01/13/22 0707 Order Status: Completed Specimen: Blood, Venous Updated: 01/13/22 0819 Sodium Level 144 134 - 146 mmol/L Potassium Level 3.9 3.4 - 5.0 mmol/L Chloride 101 98 - 112 mmol/L HCO3 36 High 21 - 29 mmol/L Anion Gap 7 Low 9 - 18 mmol/L Glucose Level 91 70 - 99 mg/dL Blood Urea Nitrogen 24 High 8 - 20 mg/dL Creatinine 0.64 0.60 - 1.30 mg/dL MDRD eGFR >60 >=60 mL/min/1.73 m2 CG eCrCl 101 mL/min/1.73 m2 Calcium Level Total 9.1 8.6 - 10.4 mg/dL Protein Total 6.2 6.0 - 8.0 g/dL Albumin Level 2.6 Low 3.5 - 5.0 g/dL Bilirubin Total 0.7 0.2 - 1.0 mg/dL Alkaline Phosphatase 85 40 - 129 IU/L Alanine Aminotransferase 18 10 - 40 IU/L Aspartate Aminotransferase 18 10 - 40 IU/L C Reactive Protein (CRP), Blood Level (Abnormal) Collected: 01/13/22 0707 Order Status: Completed Specimen: Blood, Venous Updated: 01/13/22 0819 C-Reactive Protein 7.2 High <=5.0 mg/L Complete Blood Count w/Differential (Abnormal) Collected: 01/13/22 0707 Order Status: Completed Specimen: Blood, Venous Updated: 01/13/22 0803 White Blood Cell 13.62 High 4.00 - 10.80 x10*3/uL Red Blood Cell 5.11 4.60 - 6.00 x10*6/uL Hemoglobin 13.9 Low 14.0 - 18.0 g/dL Hematocrit 44.6 42.0 - 52.0 % Mean Cell Volume 87.3 80.0 - 100.0 fL Mean Cell Hemoglobin 27.2 27.0 - 33.0 pg Mean Cell Hemoglobin Concentration 31.2 Low 32.0 - 37.0 g/dL Red Cell Diameter Width 13.3 11.0 - 16.0 % NRBC Absolute Count 0.00 0.00 - 0.01 x10*3/uL NRBC Automated 0.0 0.0 - 0.1 %WBC Platelet 422 High 140 - 400 x10*3/uL Mean Platelet Volume 10.0 7.4 - 11 fL Neutrophil Automated 82.6 High 35.0 - 80.0 % Immature Granulocyte Automated 0.4 0.0 - 0.6 % Lymphocyte Automated 7.3 Low 20.0 - 50.0 % Monocytes Automated 9.3 2.0 - 12.0 % Eosinophil Automated 0.3 0.0 - 6.0 % Basophil Automated 0.1 0.0 - 2.0 % Neutrophil Absolute Count 11.24 High 1.80 - 7.80 x10*3/uL Immature Granulocyte Absolute Count 0.06 High 0.00 - 0.05 x10*3/uL Lymphocyte Absolute Count 1.00 1.00 - 4.00 x10*3/uL Monocyte Absolute Count 1.26 High 0.00 - 0.90 x10*3/uL Eosinophil Absolute Count 0.04 0.00 - 0.50 x10*3/uL Basophil Absolute Count 0.02 0.00 - 0.20 x10*3/uL
Aktuelle Erkrankungen: -
Vorgeschichte: Past Medical History: Diagnosis Date ? Allergic rhinitis ? Arthritis ? Atrial fibrillation ? Cardiomyopathy ? Cough ? Diabetes mellitus, type II ? Eczema ? Edema, unspecified type 8/30/2017 ? Fracture Left ankle, snowmobile accident, 1979 ? GERD (gastroesophageal reflux disease) ? Hypercholesterolemia ? Hyperlipidemia ? Hypertension ? Hypothyroidism ? Low testosterone ? Nephrolithiasis ? Osteopenia ? Pneumonia due to organism ? Pseudoarthrosis of lumbar spine
Andere Medikamente: Ascorbic Acid 500 mg Oral Daily Atorvastatin Calcium 40 MG TAKE 1 BY MOUTH DAILY. Need to be seen by PCP for additional refills Cholecalciferol 2,000 Units Oral Daily Furosemide 20 mg Oral PRN HYDROcodone-Acetaminophen 10-325 MG No dose, ro
Allergien: ramipril - cough tomatoe - upset stomach
Vorherige Impfungen: -

VAERS 2043208

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

kritisch

Staat: MI
Alter: 65,0
Geschlecht: M
Eingang: 18.01.2022
Impfdatum: 23.01.2021
Beginn: 12.01.2022
Tage bis Beginn: 354,0
Dosis: 2
Route/Site: - / -

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

Acute respiratory failure Anaemia COVID-19 Cardiac failure acute SARS-CoV-2 test positive

Symptomtext

Pt was admitted for symptomatic anemia and acute decompensated heart failure with acute respiratory failure with hypoxia. Pt was tested for COVID on day 2 of admission and positive.

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

VAERS 1933071

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

kritisch

Staat: IL
Alter: 89,0
Geschlecht: M
Eingang: 08.12.2021
Impfdatum: 25.03.2021
Beginn: 26.11.2021
Tage bis Beginn: 246,0
Dosis: 1
Route/Site: IM / -

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

Asthenia Cardiac arrest Cough Death Dyspnoea Endotracheal intubation Therapy cessation

Symptomtext

Cough, SOB, weakness, pt suffered cardiac arrest, was intubated, pt was given remdesivir, care was withdrawn and pt passed away on 12/2/2021

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Praegender Schweregrund: Cardiac arrest
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Diabetes AFIB Multiple CVA's Cancer Chronic kidney disease
Andere Medikamente: -
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1919872

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

kritisch

Staat: MI
Alter: 76,0
Geschlecht: M
Eingang: 03.12.2021
Impfdatum: 12.02.2021
Beginn: 28.11.2021
Tage bis Beginn: 289,0
Dosis: 2
Route/Site: UN / UN

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

Acute kidney injury Acute respiratory failure Alanine aminotransferase normal Anion gap normal Aortic disorder Arteriosclerosis Arteriosclerosis coronary artery Aspartate aminotransferase increased Asthenia Atrial fibrillation Basophil percentage decreased Blood albumin decreased Blood alkaline phosphatase normal Blood bicarbonate normal Blood bilirubin normal Blood calcium decreased Blood chloride decreased Blood creatinine increased

Symptomtext

Patient currently inpatient at (5) days. Pt is a 77 y.o. male with past medical history significant for paroxysmal AFib on Coumadin, CVA, hypertension, type 2 diabetes who presents to the emergency department with generalized weakness and dyspnea on exertion. Patient tested positive for COVID-19 on a home test yesterday. He developed symptoms 2 days ago. He is fully vaccinated with his last vaccine in February 2021 and has not received a booster. Patient developed progressive generalized weakness, dyspnea on exertion, dry cough, wheezing, and malaise over the last 48 hours. They called his PCP today who sent him into the emergency department. He reports poor appetite. No nausea, vomiting, diarrhea. His wife is currently admitted. In the emergency department patient was hypoxic and placed on 6 L nasal cannula. Was weaned to 4 L. Chest x-ray shows COVID pneumonia. He was given Decadron. COVID-19 pneumonia Acute hypoxic respiratory failure Vaccinated, last vaccination February 2021 Positive home test 11/27, symptom onset 11/26 Chest x-ray shows COVID pneumonia Currently on 4 L nasal cannula Decadron PO Remdesivir IV Albuterol q6hr for wheezing mucinex BID Acapella, IS Prone as able Daily CBC, CMP, CRP, Ddimer AKI on CKD stage 3 BUN 28, creatinine 1.48 with baseline creatinine 1.2 Hold ACE-I Normal saline 100 mL/hr for 1 L then Hep-Lock Trend BMP in a.m. Recent left eye cataract surgery Left cataract surgery 1 and half weeks ago Family is unsure if he needs prednisolone and trimethoprim polymyxin B eyedrops still, will check bottles when they go home and call us with dosing instructions Paroxysmal atrial fibrillation Continue atenolol On Coumadin with subtherapeutic INR 1.2 Pharmacy consult to manage Coumadin Daily INR Will place on Lovenox 40 mg subQ daily while INR is subtherapeutic for DVT prophylaxis Generalized weakness PT/OT History of CVA Mild residual cognitive deficits Continue statin, Coumadin per above Essential hypertension Hold ACE-inhibitor Continue amlodipine, atenolol Diabetes mellitus type 2, insulin dependent Hold metformin, not on sliding scale insulin at home Decrease home Lantus from 60 units to 45 units and continue moderate dose sliding scale corrective Mood disorder Paxil Diet: General VTE ppx: lovenox subQ daily while INR is subtherapeutic Code status: Full code per patient and son at bedside. Patient's sons share medical power of attorney for patient. Disposition: admitted as inpatient for COVID pneumonia. Anticipated LOS > 2 midnights.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 5,0
Labordaten: Prothrombin Time (PT with INR) Status: Abnormal Result Value Ref Range Status Prothrombin Time 13.5 (H) 9.5 - 12.0 second(s) Final INR 1.2 0.9 - 1.2 Ratio Final DR CHEST 2 VIEWS FRONTAL AND LATERAL Status: None Narrative EXAMINATION: Frontal and Lateral View Chest EXAM DATE: 11/28/2021 2:31 PM TECHNIQUE: Frontal and lateral views INDICATION: dyspnea covid. COMPARISON: 3/8/2017 ENCOUNTER: Not applicable _________________________ Impression Mild patchy hazy opacities bilaterally, in conjunction with history, likely due to Covid pneumonia. No confluent consolidation, pleural effusion or pneumothorax. Cardiomegaly. Tortuous aorta with atherosclerotic calcifications. COVID-19 PCR Detected (A) Electrocardiogram, Complete Status: None (Preliminary result) Narrative Ventricular Rate 74 BPM Atrial Rate 93 BPM QRS Duration 96 ms Q-T Interval 370 ms QTC Calculation(Bazett) 410 ms Calculated R Axis 44 degrees Calculated T Axis 124 degrees Diagnosis Atrial fibrillation ST & T wave abnormality, consider inferior ischemia Abnormal ECG When compared with ECG of 01-NOV-2021 12:24, No significant change was found Result Value Ref Range Status White Blood Cell 7.45 4.00 - 10.80 x10*3/uL Final Red Blood Cell 3.97 (L) 4.60 - 6.00 x10*6/uL Final Hemoglobin 12.5 (L) 14.0 - 18.0 g/dL Final Hematocrit 37.4 (L) 42.0 - 52.0 % Final Mean Cell Volume 94.2 80.0 - 100.0 fL Final Mean Cell Hemoglobin 31.5 27.0 - 33.0 pg Final Mean Cell Hemoglobin Concentration 33.4 32.0 - 37.0 g/dL Final Red Cell Diameter Width 14.4 11.0 - 16.0 % Final NRBC Absolute Count 0.00 0.00 - 0.01 x10*3/uL Final NRBC Automated 0.0 0.0 - 0.1 %WBC Final Platelet 220 140 - 400 x10*3/uL Final Mean Platelet Volume 10.0 7.4 - 11 fL Final Neutrophil Automated 83.3 (H) 35.0 - 80.0 % Final Immature Granulocyte Automated 0.1 0.0 - 0.6 % Final Lymphocyte Automated 6.7 (L) 20.0 - 50.0 % Final Monocytes Automated 9.8 2.0 - 12.0 % Final Eosinophil Automated 0.0 0.0 - 6.0 % Final Basophil Automated 0.1 0.0 - 2.0 % Final Neutrophil Absolute Count 6.20 1.80 - 7.80 x10*3/uL Final Immature Granulocyte Absolute Count 0.01 0.00 - 0.05 x10*3/uL Final Lymphocyte Absolute Count 0.50 (L) 1.00 - 4.00 x10*3/uL Final Monocyte Absolute Count 0.73 0.00 - 0.90 x10*3/uL Final Eosinophil Absolute Count 0.00 0.00 - 0.50 x10*3/uL Final Basophil Absolute Count 0.01 0.00 - 0.20 x10*3/uL Final Comprehensive Metabolic Panel (CMP) Status: Abnormal Result Value Ref Range Status Sodium Level 133 (L) 134 - 146 mmol/L Final Potassium Level 3.0 (L) 3.4 - 5.0 mmol/L Final Chloride 95 (L) 98 - 112 mmol/L Final HCO3 22 21 - 29 mmol/L Final Anion Gap 16 9 - 18 mmol/L Final Glucose Level 99 70 - 99 mg/dL Final Blood Urea Nitrogen 28 (H) 8 - 20 mg/dL Final Creatinine 1.48 (H) 0.60 - 1.30 mg/dL Final MDRD eGFR 46 (L) >=60 mL/min/1.73 m2 Final CG eCrCl 39 mL/min/1.73 m2 Final Calcium Level Total 8.9 8.6 - 10.4 mg/dL Final Protein Total 6.7 6.0 - 8.0 g/dL Final Albumin Level 3.4 (L) 3.5 - 5.0 g/dL Final Bilirubin Total 0.5 0.2 - 1.0 mg/dL Final Alkaline Phosphatase 53 40 - 129 IU/L Final Alanine Aminotransferase 28 10 - 40 IU/L Final Aspartate Aminotransferase 183 (H) 10 - 40 IU/L Final C Reactive Protein (CRP), Blood Level Status: Abnormal Result Value Ref Range Status C-Reactive Protein 164.9 (H) <=5.0 mg/L Final
Aktuelle Erkrankungen: -
Vorgeschichte: Diabetes mellitus, type II, insulin dependent (HCC) HTN (hypertension) High cholesterol History of CVA with residual deficit GERD (gastroesophageal reflux disease) Adjustment disorder with depressed mood Obesity, Class I, BMI 30-34.9 Persistent atrial fibrillation (HCC) Degenerative scoliosis in adult patient Microalbuminuria
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet Alcohol Swabs (ALCOHOL PREP) 70 % PADS amlodipine-benazepril (LOTREL) 10-40 MG per capsule atenolol (TENORMIN) 100 MG tablet atorvastatin (LIPITOR) 80 MG tablet Centrum Silver (CENTRUM SILVER) tablet Do
Allergien: Codeine- stomach pain
Vorherige Impfungen: -

VAERS 1885226

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

kritisch

Staat: MI
Alter: 88,0
Geschlecht: M
Eingang: 19.11.2021
Impfdatum: 04.03.2021
Beginn: 11.11.2021
Tage bis Beginn: 252,0
Dosis: 1
Route/Site: IM / AR

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

Asthenia Atrial fibrillation Brain death Breath sounds normal COVID-19 Computerised tomogram head normal Computerised tomogram spine Condition aggravated Confusional state Electrocardiogram abnormal Fall Fatigue Head injury Laboratory test Lethargy Pacemaker generated rhythm Painful respiration SARS-CoV-2 test positive

Symptomtext

Hospitalized 11/11/2021-still currently admitted; COVID-19 positive 11/11/2021; fully vaccinated Fatigue Subjective HISTORY OF PRESENT ILLNESS: Patient is an 89-year-old man with severe dementia, hypertension, hyperlipidemia, seizures, AFib, depression and anxiety. Patient was brought from facility the ER due to increased fatigue, lethargy and being covered positive 11/09/2021. Patient is too lethargic/demented to give any assistance for HPI. His wife is also being admitted here and tells me that patient has been lethargic 8-10 hours a day for months now. I spoke with patient's son and he stated that his dad has been getting more lethargic for a few weeks now. Recently saw PCP who did increase his Keppra thinking he was having partial seizures/postictal state causing lethargy. Patient has not been started on this yet. Son states though that can significantly worse and about Sunday. Patient had a fall that at that time and then was seen on 11/0 9 he was tested positive for COVID-19 straight back home. We discussed code status and son states patient is to be a full code, later on it determined brain dead hand and sister would determine when to ?pull the plug?. 11/13/2021 note: Discussed at length with patient's son and daughter. We went over that hospice goals would be to not do any additional testing, medications or x-rays. They are in agreement with this. They reiterated that comfort care was their desire. 2. COVID. Treatment has been stopped due to desire for hospice care. 11/18/2021 note: Discussed possible hospice at home vs facility. Initially told me they would be ok learning more about home hospice but have since told care mgmt that they would only be able to do facility and unable to care for him at home. Per CM, earliest would be 11/21 when out of iso.

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Praegender Schweregrund: Brain death
Hospital-Tage: 8,0
Labordaten: -
Aktuelle Erkrankungen: ER visit 11/09/2021 note: Discharge MEDICAL DECISION MAKING: The patient presents emergency department by EMS after a fall 2 days ago. This was witnessed by his wife. Patient's wife refused care at that time. Patient was sent to the emergency department today as he has been appearing more weak. He has dementia listed in his clinical history was unclear what his baseline orientation is. Patient initially was activated trauma code due to fall with head injury reported confusion. Primary survey completed. Airway pain. Breath sounds equal and clear. Heart regular rate rhythm with 2+ peripheral pulses. GCS 14 due to confusion. Patient was fully exposed and no identifiable traumatic injury seen. Given mechanism injury he was maintained in his cervical collar. CT imaging head and cervical spine also ordered along with lab work, EKG, and urinalysis. EKG showed atrial fibrillation is rate controlled at 69 with occasional ventricular paced rhythm. No acute ischemic change seen or change when compared to prior EKG. Pacemaker was also interrogated due to the son's concern regarding potential bradycardia causing his fall. There is no evidence of bradycardia with lowest heart rate being greater than 60. The patient's son and daughter arrived the emergency department and confirmed he is at his baseline mentation. CT imaging reviewed showed no traumatic injury. Lab work and urinalysis were reassuring. Was able to clear cervical collar in no pain in the neck with palpation or range of motion. Patient has been ambulatory since the fall given the reassuring clinical picture she is appropriate for discharge. Family members were requesting to take him home from the emergency department which I feel is appropriate this time. I recommended close follow-up with her PCP and return for worsening symptoms which were discussed. They were in agreement with this plan all questions were answered
Vorgeschichte: Acute Bilateral Cerebellar Ischemic Infarcts R > L s/p No tPA no EVT Ataxia Essential hypertension Other hyperlipidemia Nonintractable epilepsy without status epilepticus (HCC) Dementia without behavioral disturbance (HCC) Urinary retention Coronary artery disease involving native coronary artery of native heart without angina pectoris Lightheadedness Atrial flutter (HCC) Acute cystitis without hematuria Acute metabolic encephalopathy Acute renal insufficiency Allergic rhinitis Arthritis of multiple sites Blepharitis Cataract extraction status Chronic diarrhea Corneal opacity Dermatochalasis Elevated PSA Nonexudative age-related macular degeneration Exudative age-related macular degeneration (HCC) Glaucoma suspect Hay fever Impaction of colon (HCC) Memory changes Myogenic ptosis Non-rheumatic mitral regurgitation Obstipation Obstructive sleep apnea syndrome Other specified postprocedural states Polyp of colon Pseudophakia PVD (peripheral vascular disease) (HCC) Squamous cell carcinoma, face Seizure disorder (HCC) SSS (sick sinus syndrome) (HCC) Mixed hyperlipidemia History of recent stroke
Andere Medikamente: LORazepam (ATIVAN) 2 MG/ML concentrated solution
Allergien: Environmental pollen extract
Vorherige Impfungen: -

VAERS 1880395

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

kritisch

Staat: MI
Alter: 75,0
Geschlecht: M
Eingang: 18.11.2021
Impfdatum: 09.03.2021
Beginn: 17.11.2021
Tage bis Beginn: 253,0
Dosis: 1
Route/Site: UN / UN

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

Acute kidney injury Acute respiratory failure COVID-19 pneumonia Leukocytosis Pneumonia

Symptomtext

Acute hypoxemic respiratory failure; COVID-19 viral pneumonia; Superimposed community acquired pneumonia; Acute kidney injury; Leukocytosis

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

VAERS 1876785

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

kritisch

Staat: KY
Alter: 76,0
Geschlecht: M
Eingang: 17.11.2021
Impfdatum: 20.02.2021
Beginn: 01.11.2021
Tage bis Beginn: 254,0
Dosis: 1
Route/Site: IM / RA

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

Blood creatinine increased Blood urea increased Cardio-respiratory arrest Cardiomegaly Chest X-ray abnormal Cough Death Endotracheal intubation Fatigue Glomerular filtration rate decreased Haemodialysis Haemoglobin decreased Hypervolaemia Lung opacity Resuscitation SARS-CoV-2 test negative White blood cell count increased

Symptomtext

HOSPITAL COURSE: The patient was a 77 yr/o-year-old male with a history of CKD, COPD and OSA who presented to hospital 10/20/21 with cough, fatigue, and overall decline. Labs showed WBC 11.3; Hg 7.1; BUN/Cr 71/5.03, eGFR 11; COVID negative. Chest xray showed cardiomegaly and multifocal airspace disease bilaterally. He was treated for volume overload and was initiated on hemodialysis. His hospital course was further complicated by acute cardiopulmonary arrest requiring ACLS with ROSC after 6 minutes. He was intubated as part of post-arrest care. He was extubated 10/28/21 but failed to improve. His family ultimately opted for comfort-focused care. He was transferred to the Inpatient Care Center for continued care. Upon admission to the Hospital the pt had a PPS of 10% and prognosis judged to be limited to hours to days. Parenteral medications including fentanyl were ordered for comfort. The interdisciplinary team provided ongoing pt and family support. The pt continued to decline and died on 11/1/21 @ 12:33.

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Praegender Schweregrund: Cardio-respiratory arrest
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: CKD; hypokalemia; hypothyroidism; UTI; erythropoietin deficiency anemia;
Vorgeschichte: Cardiovascular and Mediastinum Hypertension Acute on chronic diastolic CHF (congestive heart failure) Coronary artery disease Carotid artery stenosis Benign essential HTN Arrhythmia Acute on chronic diastolic congestive heart failure Vagal autonomic bradycardia Diastolic congestive heart failure Stricture of artery Cardiopulmonary arrest with successful resuscitation Respiratory Chronic obstructive pulmonary disease Sleep apnea OSA on CPAP HCAP (healthcare-associated pneumonia) Acute hypoxemic respiratory failure Sepsis due to pneumonia Acute on chronic respiratory failure with hypoxia Pneumonia of right lower lobe due to infectious organism Digestive GERD (gastroesophageal reflux disease) GI bleed Chronic diarrhea Esophagitis due to ASA of 2020 Adenoma of ascending colon of 2019 Endocrine Diabetes Hypothyroid Diabetes mellitus Type 2 diabetes mellitus, uncontrolled Hyperprolactinemia Type II or unspecified type diabetes mellitus without mention of complication, uncontrolled Hypothyroidism Hypothyroidism (acquired) Diabetic polyneuropathy associated with type 2 diabetes mellitus Type 2 diabetes mellitus with stage 4 chronic kidney disease Type 2 diabetes, HbA1c goal < 7% Nervous and Auditory Acute metabolic encephalopathy Musculoskeletal and Integument Alopecia Genitourinary BPH (benign prostatic hyperplasia) End-stage renal disease Renal cell carcinoma of right kidney of 2017 Acute on chronic renal failure ATN (acute tubular necrosis) Contrast dye induced nephropathy Acute kidney failure, unspecified Erythropoietin deficiency anemia Stage 5 chronic kidney disease Malignant neoplasm of kidney Chronic kidney disease, stage IV (severe) Other Hyperlipemia Hypercholesterolemia Carotid bruit Family history of colonic polyps Hx of colonic polyps Diarrhea Hypomagnesemia Acute blood loss anemia Lactic acidosis Perinephric hematoma Severe anemia Hypovolemic shock Leukemoid reaction Hematoma, right perihepatic and right perinephric hematoma Syncope and collapse Stroke-like symptoms Anemia requiring transfusions Cancer related pain Iron deficiency anemia due to chronic blood loss Acute on chronic blood loss anemia Anemia in chronic kidney disease Edema Hypocalcemia Proteinuria Vitamin D deficiency Enlarged prostate
Andere Medikamente: Non
Allergien: Hydromorphone
Vorherige Impfungen: -

VAERS 1873017

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

kritisch

Staat: MI
Alter: 80,0
Geschlecht: F
Eingang: 16.11.2021
Impfdatum: 26.10.2021
Beginn: 06.11.2021
Tage bis Beginn: 11,0
Dosis: 1
Route/Site: IM / AR

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

Acute respiratory failure Azotaemia COVID-19 COVID-19 pneumonia Chest X-ray abnormal Chest pain Condition aggravated Confusional state Dialysis Dyspnoea Haemodialysis Hyperhidrosis Hypertension Hypoxia Lung disorder Lung infiltration Malaise Positive airway pressure therapy

Symptomtext

Hospitalized 11/6/2021; COVID-19 positive 11/6/2021; fully vaccinated BRIEF OVERVIEW: Admission Date: 11/6/2021 Discharge Date: 11/10/2021 DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Hypoxia. Patient is a 80-year-old female admitted with acute respiratory failure with hypoxia secondary to COVID19. She has a past medical history for end-stage renal disease on dialysis Monday Wednesday Friday, coronary artery disease, chronic obstructive pulmonary disease, hypertension. She presented to emergency room on 11/06 with dyspnea and chest pain. She was found to be hypoxic requiring 3.5 L of nasal cannula for support. Her COVID PCR was positive. Chest x-ray showed changes consistent with COVID pneumonia. She had missed several dialysis sessions because she was feeling unwell likely from COVID. Of note patient did receive COVID-19 vaccination, most recently a booster shot. She was admitted to Medicine Service further assessment and management. Nephrology were consulted for dialysis. Patient was started on Decadron. She was monitored on continuous pulse oximetry. She was dialyzed per her regular schedule. Following dialysis patient experience some improvement in her symptoms. She was discharged with home health per her and family wishes (PT/OT recommended SAR) on home O2 of 3L NC and will temporarily need to get dialysis on Mon, Wed, Fri at 7:45am until out of COVID19 isoliation.

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 5,0
Labordaten: Readmission Note on 11/15/2021: HISTORY OF PRESENT ILLNESS: Patient is a 80 y.o. female with past medical history of ESRD on HD Monday, Wednesday, Friday, CAD, COPD on 3L oxygen, HTN, and recent hospitalization for COVID-19 pneumonia (11/6-11/10). Patient presents from the ED with acute hypoxic respiratory failure and uremia requiring emergent hemodialysis. Patient had missed her dialysis session on Friday (11/12). Per discussion with daughter she did not receive the proper address or contact information for dialysis where patient is suppose to have dialysis temporarily until out of COVID19 isolation. Over the weekend, patient had progressively worsening SOB, diaphoretic, and confused thus, she was brought to the ED for further evaluation and treatment. Upon arrival to the outlying emergency department, patient was afebrile, tachycardia, hypertensive with blood pressure to 233/89 and hypoxic at 84% on 6 L nasal cannula. CXR showing diffuse hazy/patchy infiltrate throughout both lungs could represent pulmonary edema and/or diffuse bilateral pneumonia. Focal airspace disease in RLL. She was placed on BiPAP for increase work of breathing and respiratory acidosis. She was transferred to hospital in stable condition for emergent hemodialysis. Patient will be admitted to Health clinic for further treatment and evaluation.
Aktuelle Erkrankungen: -
Vorgeschichte: Lupus erythematosus Hyperlipidemia Anxiety state HTN (hypertension) Peripheral arterial occlusive disease Renal artery stenosis Stress incontinence Tremor CAD s/p stent ESRD (end stage renal disease) Right flank pain Chronic right shoulder pain Closed fracture of right proximal humerus Chronic diastolic heart failure Dizziness Secondary hyperparathyroidism of renal origin Vasculitis Dermatitis Shoulder arthritis GERD (gastroesophageal reflux disease) Anemia in chronic kidney disease CAD (coronary artery disease) Heart failure, unspecified Polycystic kidney, adult type AVF (arteriovenous fistula) Acute on chronic respiratory failure Respiratory failure COPD (chronic obstructive pulmonary disease) Suspected elder abuse, initial encounter Community acquired bacterial pneumonia Acute respiratory failure with hypoxia Respiratory failure with hypoxia
Andere Medikamente: albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler Aloe Vera GEL amLODIPine (NORVASC) 5 MG tablet aspirin 81 MG chewable tablet calcitriol (ROCALTROL) 0.25 MCG capsule carvedilol (COREG) 6.25 MG tablet cho
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1833633

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

kritisch

Staat: -
Alter: 87,0
Geschlecht: M
Eingang: 01.11.2021
Impfdatum: 01.04.2021
Beginn: 21.05.2021
Tage bis Beginn: 50,0
Dosis: UNK
Route/Site: - / -

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

Acute respiratory failure Arthralgia COVID-19 Death Fall Mental status changes Respiratory failure SARS-CoV-2 test positive Surgery

Symptomtext

Pt. presents to facility 05/21/2021 with R hip pain after mechanical fall; underwent surgery and on 06/03/2021 transfered to alternative facility; on 06/22 returns to original facility from secondary with altered mental status. On 06/23/21 pt. passed away due to Acute hypoxic, hypercarbic respiratory failure.

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: -
Labordaten: 12/21/2020 SARS-CoV-2 (COVID-19) detected by PCR; 05/21/2021 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1825023

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

kritisch

Staat: MI
Alter: 80,0
Geschlecht: F
Eingang: 28.10.2021
Impfdatum: 12.02.2021
Beginn: 21.10.2021
Tage bis Beginn: 251,0
Dosis: 2
Route/Site: IM / LA

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

Acute respiratory failure COVID-19 Condition aggravated Cough Decreased appetite Diarrhoea Dyspnoea Exposure to SARS-CoV-2 Faeces discoloured Frequent bowel movements Hypoxia Impaired self-care Laboratory test normal Magnetic resonance imaging head Musculoskeletal pain Proctalgia SARS-CoV-2 test positive Scan with contrast

Symptomtext

Hospitalized (10.21.21 - still admitted / current); COVID-19 positive (10.21.21); fully vaccinated Date of Admission: 10/21/2021 Chief complaint Diarrhea due to COVID-19 History of Present Illness Patient is a 81 y.o. female who presents today with diarrhea. Patient has a history of chronic respiratory failure with hypoxia on 2 L nasal cannula baseline, chronic obstructive pulmonary disease, history of DVT/PE on Eliquis, hypothyroid, squamous cell lung cancer, type 2 diabetes, obesity. She is mostly wheelchair bound. She lives at home alone and has visiting nurses who come twice a day. Per patient, she began having diarrhea about 4 days ago, which is very frequent and yellow in color. She states that her rectal and buttock area is very painful and brought this point. She has noted some mild shortness of breath and more coughing and states that every time she coughs she passes stool. She denies any fevers/chills, abdominal pain, nausea/vomiting. She has had decreased appetite over the past few days. Her daughter, who is a caregiver tested positive for COVID recently. The patient is vaccinated. In the emergency department, the patient was found to be hemodynamically stable. She was on 2 L nasal cannula with saturations of 96%. Labs were stable. COVID testing was positive. Initially, it was felt that the patient could go home, however, upon further discussion with the patient's family was felt that this was an unsafe discharge plan as the patient is home alone most of the day and cannot get to the bathroom herself. Her daughter also tells me that the home health agency told them that nobody would be coming in tonight either. Due to her very frequent diarrhea and inability to care for self, as well as not having a caregiver who is available to take care of her, it was felt that patient should be admitted for further observation. Family feels that patient may benefit from a rehab facility. Progress note from 10.27.21: Covid-19 positive / infection Acute on chronic Hypoxic respiratory failure Vaccination complete Sx onset 10/17/21 (daughter with Covid) Covid + 10/21/21 Baseline 2L NC for COPD increased to 4 then 6 so started tx Decadron 6 d x10 d Remdesivir x5 d

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 8,0
Labordaten: -
Aktuelle Erkrankungen: 9.21.21: MRI Brain with and without contrast
Vorgeschichte: Chronic shoulder pain Wheelchair bound nightime CPAP and daytime O2 noncompliance Hypersomnia Pneumonia due to infectious organism, unspecified laterality, unspecified part of lung Gastroesophageal reflux disease without esophagitis Morbid obesity with BMI of 40.0-44.9, adult History of ESBL E. coli infection OAB (overactive bladder) COPD with acute exacerbation Acute on chronic hypoxemic respiratory failure Laryngeal stridor OSA (obstructive sleep apnea)
Andere Medikamente: ALBUTEROL 108 (90 Base) MCG/ACT inhaler apixaban (ELIQUIS) 5 MG tablet baclofen (LIORESAL) 10 MG tablet Cholecalciferol (VITAMIN D) 1000 units TABS erythromycin (ROMYCIN) ophthalmic ointment fluticasone-umeclidin-vilant (TRELEGY ELLIPTA) 10
Allergien: LisinoprilAngioedema CodeineUnknown Nickel Penicillins Sulfa Drugs
Vorherige Impfungen: -

VAERS 1818541

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

kritisch

Staat: MI
Alter: 82,0
Geschlecht: M
Eingang: 26.10.2021
Impfdatum: 25.03.2021
Beginn: 16.10.2021
Tage bis Beginn: 205,0
Dosis: 1
Route/Site: IM / AR

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

Acute respiratory failure COVID-19 COVID-19 pneumonia Chest X-ray abnormal Decreased appetite Dyspnoea Hypoxia Lung opacity Polyuria SARS-CoV-2 test positive

Symptomtext

Hospitalized (10.16.21 - current, still admitted); COVID-19 positive (10.16.21); fully vaccinated CHIEF COMPLAINT: Hypoxia; HPI: HISTORY OF PRESENT ILLNESS: Patient is a 82 y.o. male who presents today with worsening shortness of breath since couple of day. He uses 2 liters of oxygen at baseline. For last couple of days his oxygen saturation is staying in 70's. He denies chest pain. He feels much better after oxygen. His appetite has been poor as well. No abdominal pain. No leg swelling. No dizziness or shortness of breath. He denies dizziness. ASSESSMENT / PLAN: Acute on chronic hypoxic respiratory failure: Covid 19 pneumonia: - Fully vaccinated - decadron - CT angio ordered - remdesevir ordered - not a candidate for MAB due to hypoxia - does not appear fluid overloaded on exam Progress Note - Assessment and Plan from 10.26.21: Acute on chronic (2L baseline) hypoxemic respiratory failure, secondary to COVID-19 PNA - Fully vaccinated Moderna Feb and March 2021 - s/p Remdesivir 10/16-10/21 - Decadron (6 mg daily PO x 10 days, 10/17-10/26) - Pulmonary toiletting - Wean O2 as able, goal >92 - Off of HFNC today, on 6L - Consider pulm consult if unable to further wean. - CXR 10/25 improved bilateral heterogenous pulm opacities, no acute cardiopulm abnormality - Lasix decreased to 20mg IV daily; will hold further diuresis now.

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 11,0
Labordaten: -
Aktuelle Erkrankungen: 10.12.21: Primary Care office visit - Back Pain (Compression fracture of body of thoracic vertebra (Primary Dx); Closed compression fracture of body of first lumbar vertebra; Immunization due; Urinary frequency) 10.16.21: ED - hypoxia, SOB, COVID-19 (transferred / hospital admission)
Vorgeschichte: Dyslipidemia Acute kidney injury AKI (acute kidney injury) Grade II Diastolic dysfunction CAD s/p CABG x2 Emphysema Heart failure with reduced ejection fraction echo with EF 48% Hypertension
Andere Medikamente: albuterol HFA (PROAIR HFA) 108 (90 Base) MCG/ACT inhaler aspirin 81 MG tablet atorvastatin (LIPITOR) 40 MG tablet budesonide/formoterol (SYMBICORT) 80-4.5 MCG/ACT inhaler dilTIAZem (CARDIZEM CD) 240 MG 24 hr capsule fluticasone (FLONASE) 50
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1818174

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

kritisch

Staat: MI
Alter: 71,0
Geschlecht: F
Eingang: 26.10.2021
Impfdatum: 19.02.2021
Beginn: 15.10.2021
Tage bis Beginn: 238,0
Dosis: 2
Route/Site: IM / AR

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

Acute respiratory failure Blood glucose normal COVID-19 COVID-19 pneumonia Chest X-ray abnormal Condition aggravated Cough Dyspnoea Fatigue Fluid retention Hyperglycaemia Hypoxia Lung infiltration Nasal congestion Oropharyngeal pain Polyuria Pyrexia SARS-CoV-2 test positive

Symptomtext

Hospitalized (10.15-10.22); COVID-19 positive (10.15); fully vaccinated Discharge Provider: MD Primary Care Provider: PA-C Admission Date: 10/15/2021 Discharge Date: Oct 22, 2021 DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Acute respiratory failure with hypoxia Pneumonia due to COVID-19 virus HOSPITAL COURSE: Is a 72-year-old COVID-vaccinated female who presented with fever cough and shortness of breath 2 physician, with findings in the office of a pulse oximetry of 86% on room air. In the emergency room her COVID PCR test was positive and her chest x-ray showed bilateral interstitial pulmonary infiltrates consistent with COVID pneumonia. On supplemental oxygen her pulse oximetry was 93%. Patient was treated with 5 days of remdesivir, as well as Decadron until the day of discharge. She required 3-5 L of oxygen through most of her hospital stay. Two days prior to her discharge it was noted that she had gained 3 kg of fluid weight, and she was started on IV Lasix diuresis. With that she had a diuresis of about 6 L of fluid and by the day of discharge she had successfully weaned to room air. Through her hospital stay she required significant basal bolus insulin dosing for hyperglycemia due to the corticosteroids, but on the day of discharge her blood sugar was down into the 80s and she was not discharged on corticosteroids and therefore is expected to be able to manage her diabetes with her home regimen of oral hypoglycemics. Her only new discharge medication was Lasix 20 mg daily as needed for edema or shortness of breath. She was requested to follow-up with Dr. in 1 week. The patient had timed out from isolation in the hospital and was not required to quarantine at discharge.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 8,0
Labordaten: -
Aktuelle Erkrankungen: 10.15.21: Seen at PCP office - cough, hypoxia (sats < 91%); sore throat; nasal congestion; fatigue
Vorgeschichte: Endometrial cancer Type 2 diabetes mellitus with hyperglycemia, without long-term current use of insulin Hypertension Gout Fatty liver Heart murmur DM type 2 (diabetes mellitus, type 2) Hypertension CAD (coronary artery disease) Fatty liver
Andere Medikamente: blood glucose test strips lancet misc OneTouch Ultra 2 Blood Glucose Monitor allopurinol (ZYLOPRIM) 100 MG tablet aspirin 81 MG tablet atorvastatin (LIPITOR) 40 MG tablet furosemide (LASIX) 20 MG tablet glipiZIDE (GLUCOTROL) 5 MG tablet lis
Allergien: Bactrim [Sulfamethoxazole W-trimethoprim]Hives Celebrex [Celecoxib] Lisinopril Cough Losartan Cough
Vorherige Impfungen: -

VAERS 1795377

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

kritisch

Staat: MI
Alter: 67,0
Geschlecht: M
Eingang: 18.10.2021
Impfdatum: 17.02.2021
Beginn: 09.10.2021
Tage bis Beginn: 234,0
Dosis: 2
Route/Site: IM / AR

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

Acute respiratory failure Atrial fibrillation COVID-19 Cardioversion Chest X-ray abnormal Condition aggravated Cough Diarrhoea Dyspnoea Heart rate increased Hypotension Hypoxia Lung opacity Oedema Palpitations Pyrexia Respiratory rate increased SARS-CoV-2 test positive

Symptomtext

Hospitalized 10/10/2021; COVID-19 positive 10/9/2021; fully vaccinated Discharge Summary General Medicine BRIEF OVERVIEW: Admission Date: 10/10/2021 Discharge Date: Oct 15, 2021 Discharge Disposition: home or self care Active Issues Requiring Follow-up: DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Acute on chronic respiratory failure with hypoxia HOSPITAL COURSE: Patient is a 67M with h/o CAD with ischemic cardiomyopathy s/p ICD, CHF, PAF on chronic Coumadin, HTN, HLD, COPD on 2L home O2, OSA and obesity who presented to ED for SOB that started 10/3 with associated palpitations. He has had increased edema, but no orthopnea. He reports dry , non-productive cough for a couple days without associated fevers, chills, sweats or rigors. He reports episode of diarrhea In the ER, he was febrile with temp 38.1, normotensive, tachycardic with HR up to 136, and tachypneic with RR up to 31. He was hypoxic to 88% on baseline 2L and is now on 3L. COVID 19 positive ( he is vaccinated against COVID) CXR showed patchy opacity of the posterior LLL. He was treated for AFib with RVR using IV Cardizem pushes, but became hypotensive and was subsequently cardioverted. He also received CAP coverage with Rocephin/Zithromax

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Chronic systolic heart failure ? Old myocardial infarction ? Neck pain ? Muscle weakness (generalized) ? Decreased range of motion of neck ? Low back pain, unspecified back pain laterality, unspecified chronicity, unspecified whether sciatica present ? Chronic obstructive pulmonary disease, unspecified COPD type ? Cough ? SOB (shortness of breath) on exertion ? Diffusion capacity of lung (dl), decreased ? Hyperinflation of lungs ? Tobacco abuse, in remission ? Cardiomyopathy ? Obesity, unspecified obesity severity, unspecified obesity type ? Physical deconditioning ? Abnormality of lung on chest x-ray ? OSA on CPAP ? Sustained VT (ventricular tachycardia) ? ICD (implantable cardiac defibrillator) in place ? Dyslipidemia ? Cardiomyopathy, ischemic ? AF (paroxysmal atrial fibrillation) ? Pulmonary emphysema ? Left Cephalic Vein Thrombosis ? DM type 2 (diabetes mellitus, type 2) ? Hematuria ? CAD (coronary artery disease) ? Hypothyroidism ? Stage 3b chronic kidney disease ? Anemia
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet albuterol (PROVENTIL, VENTOLIN, PROAIR) 108 (90 BASE) MCG/ACT inhaler allopurinol (ZYLOPRIM) 300 MG tablet aspirin 81 MG EC tablet atorvastatin (LIPITOR) 40 MG tablet budesonide/formoterol (SYMBICORT) 1
Allergien: wine
Vorherige Impfungen: -

VAERS 1794786

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

kritisch

Staat: MI
Alter: 82,0
Geschlecht: F
Eingang: 18.10.2021
Impfdatum: 13.02.2021
Beginn: 11.10.2021
Tage bis Beginn: 240,0
Dosis: 2
Route/Site: IM / AR

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

Acute respiratory failure Agitation Angiogram pulmonary abnormal Blood culture negative COVID-19 COVID-19 pneumonia Computerised tomogram thorax abnormal Cough Decreased appetite Dehydration Diarrhoea Disorientation Dyspnoea Electrocardiogram T wave peaked Fatigue Hypophagia Hypothermia Hypoxia

Symptomtext

Hospitalized 10/11/2021; COVID-19 positive 10/11/2021; fully vaccinated Assessment/Plan DIAGNOSIS at time of disposition: 1. COVID-19 2. Acute respiratory failure with hypoxia ED Disposition ED Disposition Hospitalized MEDICAL DECISION MAKING Patient presents to the emergency department with concern for nausea and loss of appetite which is been progressive over the last several weeks, especially worse in the last 3 days. It at triage patient was noted to be saturating 86% on room air. She was placed on 2 L nasal cannula and improved to 93%. Of note patient is not on home oxygen. Her physical exam is remarkable for a fatigued appearing elderly woman, with crackles across the lung fields bilaterally. Differential diagnosis includes but is not limited to viral versus bacterial pneumonia, pancreatitis, biliary pathology. IV access was established she was given 1 L of IV fluids for hydration given reports of poor oral intake, as well as Zofran for nausea. EKG is obtained which does not demonstrate peaked T-waves, evidence of ischemia, or right axis deviation. No significant changes when compared to EKG from 08/04/2021. Patient has a workup which is significant for positive COVID-19 PCR. Patient is a CT thorax which shows findings consistent with a viral pneumonia, no evidence of underlying bacterial process. Given patient's hypoxia on room air as well as her tachypnea, she will be admitted to the hospitalist service for continued management. Patient did not have clinical deterioration while in the emergency department. 10/13/2021 note: ASSESSMENT / PLAN: Patient is an 83 year old female with CAD status post stenting in 2005, type 2 diabetes mellitus, hypertension, hypertriglyceridemia, and CKD who presented with approximately one month of fatigue and malaise as well as progressive shortness of breath, loss of appetite, and diarrhea. She was found to be COVID-19 positive, despite being fully vaccinated. #COVID-19 pneumonia CT thorax showed peripheral areas of ground glass opacities, consistent with COVID-19 pneumonia. Procalcitonin 0.37, have low suspicion for superimposed bacterial pneumonia, especially given no focal consolidation on imaging. Exact date of symptom onset difficult to ascertain; therefore, is outside the window for remdesivir. National shortage of tocilizumab currently. Plan: - Continue dexamethasone 6mg daily x10 days total or until discharge. - Tessalon perles for cough. - Supplemental oxygen therapy as needed 10/15/2021 note: ASSESSMENT / PLAN: Patient is an 83 year old female with CAD status post stent placement in 2005, type 2 diabetes mellitus, hypertension, hypertriglyceridemia, and CKD who presented with 3-4 weeks of fatigue and malaise as well as progressive shortness of breath, loss of appetite, and diarrhea. She was found to be COVID-19 positive. Her oxygen requirements have been relatively stable; however, she has been intermittently disoriented and agitated, requiring PRN Zyprexa. #COVID-19 pneumonia Patient's oxygen requirements have been stable to improving. She was on 70% FiO2/50 L/min on high flow nasal cannula at the time of my exam. Plan: - Continue dexamethasone 6mg daily x10 days total or until discharge. - Supplemental oxygen therapy as needed. - Tessalon perles for cough. #Hypoxia Most likely secondary to COVID-19 pneumonia, which appeared worse on CTA 10/13 compared to imaging on 10/11. Low suspicion for PE, given no evidence of PE on CTA. Management as above. 10/17/2021 note: Assessment/Plan Patient is an 83 year old female with CAD status post stent placement in 2005, type 2 diabetes mellitus, hypertension, hypertriglyceridemia, and CKD who presented with 3-4 weeks of fatigue and malaise as well as progressive shortness of breath, loss of appetite, and diarrhea. She was found to be COVID-19 positive, admitted for acute hypoxic respiratory failure likely secondary to COVID pneumonia. # Acute hypoxic respiratory failure #COVID-19 pneumonia # Borderline hypothermia, concern for bacterial pneumonia Patient has required up to 100% FiO2 over the last 24 hours to maintain her oxygen saturations. CTA performed yesterday, 10/16, for episode of hypoxia out of concern for PE, which was negative for PE but demonstrated worsening pneumonia and left lower lobe airspace disease. Was started on empiric therapy for possible hospital acquired pneumonia yesterday, 10/16. Blood cultures collected 10/16 show NGTD. MRSA nares pending. If negative, can likely discontinue vancomycin. Due to her variable mental state and concern for drying her secretions rendering them more difficult to expectorate, patient would likely not be a good candidate for BiPAP should her respiratory needs continue to escalate. Discussed the option of comfort care with husband, who is patient's DPOA. He was in favor of this but asked me to speak with his daughter, as well.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 7,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Additional heart attack (inferior wall) AKI (acute kidney injury) Arthritis Chronic back pain Coronary atherosclerosis of native coronary artery Diabetes mellitus GERD (gastroesophageal reflux disease) Hypercholesteremia Hyperlipidemia LDL goal < 70 Hyperparathyroidism, primary Hypertension Hyperthyroidism Hypertriglyceridemia Hypothyroidism Iron deficiency anemia Lactose intolerance Menopause Multinodular non-toxic goiter Myocardial infarction Non-toxic multinodular goiter Obesity Severe sepsis Type II or unspecified type diabetes mellitus without mention of complication, not stated as uncontrolled UTI (urinary tract infection) Venous insufficiency
Andere Medikamente: amLODIPine (NORVASC) 10 MG tablet aspirin EC 81 MG enteric coated tablet clopidogrel (PLAVIX) 75 MG tablet ezetimibe (ZETIA) 10 MG tablet furosemide (LASIX) 40 MG tablet losartan (COZAAR) 100 MG tablet metformin-XR (GLUCOPHAGE-XR) 500 MG 24
Allergien: Aliskiren-hydrochlorothiazideOther Candesartan Cilexetil-hctzOther Dust Erythromycin [Akne-mycin] Hydralazine Latex Lipitor [Hmg-coa-r Inhibitors] Lisinopril Macrolides Milk Mold Olmesartan Medoxomil-hctz Penicillins Soy Allergy Sulfa Drugs Tetanus Immune Globulin Valsartan
Vorherige Impfungen: -

VAERS 1778983

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

kritisch

Staat: MI
Alter: 85,0
Geschlecht: M
Eingang: 12.10.2021
Impfdatum: 11.02.2021
Beginn: 11.10.2021
Tage bis Beginn: 242,0
Dosis: 2
Route/Site: UN / UN

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

Acute respiratory failure Asthenia COVID-19 Confusional state Gait inability

Symptomtext

Hospitalization - acute respiratory failure with hypoxia; COVID-19; Unable to ambulate; generalized weakness; confusion

Weitere VAERSDATA-Felder

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

VAERS 1765475

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

kritisch

Staat: MI
Alter: 67,0
Geschlecht: F
Eingang: 06.10.2021
Impfdatum: 13.03.2021
Beginn: 29.09.2021
Tage bis Beginn: 200,0
Dosis: 1
Route/Site: IM / AR

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

Abdominal pain Biopsy liver COVID-19 Colonoscopy Computerised tomogram abdomen abnormal Condition aggravated Death Dyspnoea General physical health deterioration Hypoxia Intestinal perforation Laparotomy Leukocytosis Mass Metastatic squamous cell carcinoma Neuroendocrine tumour Oesophagogastroduodenoscopy SARS-CoV-2 test positive

Symptomtext

Deceased (10.4.21); Hospitalized (9.14.21); COVID-19 positive (9.29.21); fully vaccinated Admission Date: 9/14/2021 Date of Death: 10/4/21 Time of Death: 6:56 AM Preliminary Cause of Death: Hypoxia DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Perforated abdominal viscus Bowel perforation a 68 y.o. female with past medical history significant for Crohn's disease on immunosuppressive therapy, history of stroke, and PAD who presented to the emergency department with severe abdominal pain. CT concerning for bowel perforation and Colorectal took patient for urgent laparotomy and was treated with broad spectrum antibiotics and antifungals. CT also with concern for liver metastasis and biopsy done in the OR showing metastatic neuroendocrine tumor. Workup further showed a cardiac mass which was biopsied via RHC showing metastatic SCC indicating patient having two primary metastatic diseases. Patient continued to decline and developed dyspnea; unfortunately she tested positive for COVID19. Patient ultimately wished to be made comfort care and so hospice was consulted and comfort care orders initiated. Medicine service took over care to facilitate this on 10/2. Patient expired on 10/4/2021 at 6:56am.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 21,0
Labordaten: -
Aktuelle Erkrankungen: 8.26.21: EGD/Colonoscopy 9.9.21: Office visit - follow-up Crohn's disease 9.10.21: Infusion - vedolizumab (ENTYVIO) 300 mg in sodium chloride... 300 mg 9.14.21: ED - abdominal pain; perforated viscus; sepsis; leukocytosis; new cancer - transferred to another hospital - admitted
Vorgeschichte: PVD (peripheral vascular disease) Other osteoporosis without current pathological fracture Diverticulosis of sigmoid colon Vitamin D deficiency Colitis Right upper quadrant abdominal pain Crohn's disease of small intestine with complication Closed pilon fracture of left tibia Essential hypertension, benign Crohn's disease and perforation s/p right colon resection and end ileostomy with long hartmann's pouch, liver biopsy 9/14/21 Bowel perforation Mass of heart Leukocytosis Allergy to trimethoprim/sulfamethoxazole COVID-19
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet Adhesive Tape (KENDALL PAPER 2"X10YD) TAPE albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler amitriptyline (ELAVIL) 100 MG tablet aspirin 81 MG EC tablet azaTHIOprine
Allergien: BaclofenOther, Difficulty concentrating Septra [Sulfamethoxazole W-trimethoprim]Hives AtorvastatinOther Boniva [Bisphosphonates]Other CodeineOther Fosamax [Alendronic Acid]Other Hydrocodone-acetaminophenConfusion Ileostomy Restricted Foods Sulfamethoxazole Trimethoprim
Vorherige Impfungen: -

VAERS 1722888

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

kritisch

Staat: CA
Alter: 72,0
Geschlecht: M
Eingang: 22.09.2021
Impfdatum: 08.02.2021
Beginn: 18.02.2021
Tage bis Beginn: 10,0
Dosis: 2
Route/Site: IM / LA

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

Cardiac failure congestive Cardiomyopathy Catheterisation cardiac normal Death Echocardiogram abnormal Oedema

Symptomtext

Patient presented with Edema and developed CHF and Cardiomyopathy progressing to death on 08/15/2021

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: Heart cath found no CAD. echocardiogram shows cardiomyopathy
Aktuelle Erkrankungen: OSA DJD
Vorgeschichte: OSA on CPAp, knee arthritis
Andere Medikamente: Levitra
Allergien: none
Vorherige Impfungen: -

VAERS 1718822

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

kritisch

Staat: MI
Alter: 68,0
Geschlecht: M
Eingang: 21.09.2021
Impfdatum: 13.03.2021
Beginn: 13.09.2021
Tage bis Beginn: 184,0
Dosis: 1
Route/Site: IM / AR

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

Acute respiratory failure Angiogram pulmonary abnormal Blood uric acid normal COVID-19 COVID-19 pneumonia Chest X-ray abnormal Chronic obstructive pulmonary disease Condition aggravated Diarrhoea Dyspnoea Feeling abnormal Fibrin D dimer increased Hypoxia Lung infiltration Lung opacity Oxygen saturation decreased Pneumonia Productive cough

Symptomtext

Hospitalized (9.13.21 - present); Symptoms started week prior; COVID-19 positive (9.13.21); Fully Vaccinated Pt is a 69 y.o. male who presents to hospital with difficulty breathing. The patient is known to have history of multiple comorbidities including chronic obstructive pulmonary disease, obstructive sleep apnea on CPAP, hypertension, pneumonia in the past, tobacco use, hypertension, and diabetes mellitus type 2. On September 9, 2021, the patient was presented to his primary care physician office because of increasing productive cough with poly phlegm, and increase of difficulty breathing. At that time he did not have any fever. Also the patient had some diarrhea at that time. He was given a course of Zithromax. However since then, the patient did not improve. Instead he has been feeling feverish with productive cough, and more difficulty breathing. He came back to the emergency department for evaluation. The patient COVID-19 PCR rapid test came back positive. The chest x-ray showed mild bibasilar hazy and streaky opacities right greater than left compatible with pneumonia. The patient was hypoxic in the emergency department with oxygen saturation 84% on room air. He has been requiring high-flow nasal cannula initially with FiO2 90% and later it went down to 35%. The patient is being admitted to the hospital for further evaluation treatment. Assessment and Plan Medical Decision Making This is a 69 years old gentleman who was presented to the emergency department because of 5 days complaining of productive cough with yellow phlegm, difficulty breathing, and diarrhea. On presentation he was hypoxic with oxygen saturation 85% on room air. The patient is requiring oxygen supplement via high-flow nasal cannula. The chest x-rays showed bibasilar infiltrations compatible with pneumonia. The PCR rapid test for COVID came back positive. 1. Acute hypoxic respiratory failure. Present on admission. Associated with COVID-19 pneumonia and chronic obstructive pulmonary disease exacerbation. The patient is requiring right now high-flow nasal cannula with FiO2 35%. We will keep monitoring. The patient is full code. 2. COVID-19 pneumonia. Present on admission. The patient is on dexamethasone and remdesivir. Will re-evaluate in the morning. We will do daily COVID-19 lab care set. 3. Chronic obstructive pulmonary disease exacerbation. Present on admission. The patient has already failed outpatient Zithromax orally. We will continue breathing treatment. Notes from 9.20.21: ASSESSMENT / PLAN: Acute on chronic hypoxic respiratory failure Severe COVID-19 pneumonia s/p vaccination COPD exacerbation - Continue HFNC and titrate to maintain saturations of 90-94% - Continue Decadron; s/p Remdesivir - Maintain euvolemia and diurese prn -Antitussives prn, encourage IS use and prone - Continue duonebs q 6h prn - Mucinex - Dulera and spiriva and Singulair **DDimer was increasing; no PE noted, small acute thrombus in the cephalic vein that does not require full dose anticoagulation. CTA does show PA dilation; likely c/w PAH.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 9,0
Labordaten: -
Aktuelle Erkrankungen: 9.8.21: Office Visit - COPD exacerbation IMPRESSION AND PLAN 1. Chronic obstructive pulmonary disease exacerbation. We will treat with Zithromax. The patient's oxygen level is 92%. He does not appear acutely distressed, so at this point, we will not use any oral steroids. He will let us know if symptoms do not gradually improve with the above treatment. Call if he has further difficulties. The patient does see Pulmonary and has been changing his inhalers also. He will contact them with any concerns regarding his inhalers. Continue albuterol on a p.r.n. basis for acute symptoms. 2. Chronic diarrhea. Lab orders placed. He has been referred back to Gastroenterology and awaiting line up for colonoscopy. 3. History of gout. Uric acid level is satisfactory. He has not had any recent flare-ups of gout. We will continue current dose of allopurinol. He has had labs in July for monitoring of this medication. Continue current dose. 9.10.21 - called office feeling worse 9.13.21: ED, admitted to hospital, COVID-19 positive
Vorgeschichte: Non-Hospital Scrotal mass Rosacea Blepharitis of both eyes with rosacea Senile nuclear cataract, bilateral Class 2 obesity Bleeding from the nose COPD exacerbation (HCC) Abscess of back Wound check, abscess Early dry stage nonexudative age-related macular degeneration of both eyes Squamous blepharitis of upper and lower eyelids of both eyes Morbid (severe) obesity due to excess calories (HCC) Essential hypertension Acute gout involving toe of left foot, unspecified cause Nocturnal hypoxemia due to obstructive chronic bronchitis (HCC)
Andere Medikamente: Outpatient Medications albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler allopurinol (ZYLOPRIM) 100 MG tablet Budeson-Glycopyrrol-Formoterol (BREZTRI AEROSPHERE) 160-9-4.8 MCG/ACT AERO fluticasone-salmete
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1625050

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

kritisch

Staat: CO
Alter: 87,0
Geschlecht: M
Eingang: 23.08.2021
Impfdatum: 21.01.2021
Beginn: 24.01.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: SYR / -

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

Cerebrovascular accident Dysstasia Gait inability Hemiparesis Incontinence Loss of personal independence in daily activities Movement disorder Thrombosis Wheelchair user

Symptomtext

This individual suffered a severe stroke three days after receiving the Covid19 vaccine in January 2021. He was admitted to the hospital and suffered a second stroke 3 days later. While in the hospital, a blood clot was also discovered in his leg. The previous month (December 2020), this individual's carotid arteries were checked by a doctor, and he was given a "clean bill of health." Prior to the strokes, this individual was living (with his wife) independently in their house, driving, and exercising regularly. The stroke left him with severe left-side weakness, unable to stand, walk, or use his left hand. He is now wheelchair-bound, incontinent, and requires around-the-clock care.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 17,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1392054

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

kritisch

Staat: KY
Alter: 73,0
Geschlecht: M
Eingang: 11.06.2021
Impfdatum: 06.02.2021
Beginn: 16.02.2021
Tage bis Beginn: 10,0
Dosis: 1
Route/Site: IM / UN

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

B-cell lymphoma Computerised tomogram Death Fatigue Full blood count Lymphoma Magnetic resonance imaging Pain

Symptomtext

He died after being diagnosed with Lymphoma. Double hit , B cell. He was fatigued a couple weeks after vaccine, fatigue worsened, then developed severe pain. Diagnosis to death was 11 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 14,0
Labordaten: CBC, mri, CT, hematologists, oncologist etc etc
Aktuelle Erkrankungen: Knee replacement surgery
Vorgeschichte: A-fib
Andere Medikamente: Tikosyn Warfarin
Allergien: None known
Vorherige Impfungen: -

VAERS 1367850

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

kritisch

Staat: -
Alter: 77,0
Geschlecht: F
Eingang: 02.06.2021
Impfdatum: 25.02.2021
Beginn: 14.05.2021
Tage bis Beginn: 78,0
Dosis: UNK
Route/Site: - / -

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

Blood osmolarity decreased Cerebrovascular accident Facial paresis Hyponatraemia Immune system disorder

Symptomtext

I63.9 - Cerebrovascular accident (CVA), unspecified mechanism (CMS/HCC) E87.1 - Hypo-osmolality and hyponatremia R29.810 - Facial weakness

Weitere VAERSDATA-Felder

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

VAERS 1351548

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

kritisch

Staat: IL
Alter: 46,0
Geschlecht: F
Eingang: 26.05.2021
Impfdatum: 01.02.2021
Beginn: 24.03.2021
Tage bis Beginn: 51,0
Dosis: 2
Route/Site: IM / AR

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

Cerebrovascular accident Computerised tomogram abnormal Laboratory test abnormal Magnetic resonance imaging abnormal Thunderclap headache Visual field defect Visual impairment X-ray

Symptomtext

On March 24th, I awoke from sleeping to a thunderclap headache, 6/10 pain. I tried to treat the pain with Tylenol and benadryl, but it wouldn't go away. I also developed visual aura of zig zag lines on my peripheral vision. I presented to the ER on March 26th, and they did an MRI. MRI showed multiple bilateral strokes. My hospitalist stated I should report it to VAERS.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 4,0
Labordaten: 3/26/21 - 3/29/21: MRI, CT, multiple lab services, x-ray, speech therapy, PT, OT
Aktuelle Erkrankungen: None
Vorgeschichte: Depression
Andere Medikamente: Prozac 20mg daily
Allergien: Levaquin, PCN
Vorherige Impfungen: -

VAERS 1273804

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

kritisch

Staat: MI
Alter: 68,0
Geschlecht: U
Eingang: 30.04.2021
Impfdatum: 31.03.2021
Beginn: 10.04.2021
Tage bis Beginn: 10,0
Dosis: 2
Route/Site: - / -

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

COVID-19 Death Gastrointestinal haemorrhage Respiratory failure

Symptomtext

GI Hemorrhage Covid + Respiratory Failure

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None known
Vorgeschichte: HTN S/P Heart Transplant Hyperparathyroidism Reflux End stage renal disease
Andere Medikamente: Cardizem Norco Neurontin banophen Plavix
Allergien: Aspirin Atrorvastatin Crestor Haldol Haloperidol Lipitor Lisinopril Oxycodone Aldactone Hydralazine
Vorherige Impfungen: -

VAERS 1261534

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

kritisch

Staat: AR
Alter: 76,0
Geschlecht: M
Eingang: 27.04.2021
Impfdatum: 11.02.2021
Beginn: 18.02.2021
Tage bis Beginn: 7,0
Dosis: 2
Route/Site: OT / LA

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

Cerebrovascular accident Computerised tomogram Gait disturbance Magnetic resonance imaging Movement disorder

Symptomtext

stroke; trouble walking; Difficulty getting out of bed; This spontaneous case was reported by a consumer (subsequently medically confirmed) and describes the occurrence of CEREBROVASCULAR ACCIDENT (stroke) in a 76-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 038K20A and 038K20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 11-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 11-Mar-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 18-Feb-2021, the patient experienced CEREBROVASCULAR ACCIDENT (stroke) (seriousness criteria hospitalization and medically significant). On 19-Feb-2021, the patient experienced MOVEMENT DISORDER (Difficulty getting out of bed). On an unknown date, the patient experienced GAIT DISTURBANCE (trouble walking). The patient was hospitalized for 3 days due to CEREBROVASCULAR ACCIDENT. The patient was treated with Rehabilitation therapy for Cerebrovascular accident; Rehabilitation therapy for Movement disorder and Rehabilitation therapy for Gait disturbance. At the time of the report, CEREBROVASCULAR ACCIDENT (stroke), MOVEMENT DISORDER (Difficulty getting out of bed) and GAIT DISTURBANCE (trouble walking) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): In 2021, Computerised tomogram: unknown unknown. In 2021, Magnetic resonance imaging: abnormal Abnormal. mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosing remained unchanged. The patient got worse so was sent for MRI was done and showed something. The patient stated the stroke has affected his right side and has trouble walking. He was in the hospital for 3 days. He then went back for rehab hospital and there for about a week. He is now home and doing out patient rehab. No concomitant medications were reported. Company comment: Limited information regarding the events has been provided at this time and a causal relationship cannot be excluded; Sender's Comments: Limited information regarding the events has been provided at this time and a causal relationship cannot be excluded

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 3,0
Labordaten: Test Date: 2021; Test Name: CT Scan; Result Unstructured Data: unknown; Test Date: 2021; Test Name: MRI; Result Unstructured Data: Abnormal
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1167768

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

kritisch

Staat: IL
Alter: 72,0
Geschlecht: F
Eingang: 05.04.2021
Impfdatum: 03.03.2021
Beginn: 07.03.2021
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: IM / RA

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

Cerebrovascular accident Condition aggravated

Symptomtext

On 3/7/2021, the patient experienced a cerebrovascular accident, was hospitalized for acute care then rehabilitation until 4/1/2021. Patient has a previous history of CVA.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 8,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: allergic rhinitis, anxiety, cerebrovascular accident, chronic back pain, degeneration of intervertebral disc, depressive disorder, essential hypertension, exposure to SARS-CoV-2, gastroesophageal reflux disease, gastroesophageal reflux disease with hiatal hernia, hiatal hernia, hyperlipidemia, obesity, osteopenia, posttraumatic stress disorder, prolapsed lumbar intervertebral disc, sleep apnea
Andere Medikamente: acetaminophen, atorvastatin, Calcium 500 + D, ClearLax, cyanocobalamin (vitamin B-12), Effexor XR, Eliquis, enalapril maleate, hydroxyzine pamoate, levothyroxine, metoprolol succinate, omeprazole, verapamil, Vitamin D3, Xanax
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1155464

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

kritisch

Staat: IL
Alter: 86,0
Geschlecht: F
Eingang: 01.04.2021
Impfdatum: 05.02.2021
Beginn: 08.02.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: IM / RA

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

Death

Symptomtext

Patient passed away 2/23/21

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Fluid overload, shortness of breath (hospitalized 1/27)
Vorgeschichte: hypertension, hyperlipidemia, heart failure, afib, hyperparathyroidism, osteopenia, osteoarthritis, osteodystrophy, anemia, renal dysfunction, CKD end stage, fluid overload
Andere Medikamente: Norco, Metoprolol XL, Famotidine, midodrine, Calcitonin, Pravastatin, Raloxifene
Allergien: no known allergies
Vorherige Impfungen: -

VAERS 1111645

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

kritisch

Staat: IL
Alter: 94,0
Geschlecht: F
Eingang: 18.03.2021
Impfdatum: 10.02.2021
Beginn: 18.03.2021
Tage bis Beginn: 36,0
Dosis: 2
Route/Site: IM / -

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

Areflexia Death Dysphagia Oxygen saturation decreased Productive cough

Symptomtext

Patient was a resident on a LTC wing. Received Covid-19 vaccine on 1/13/21 & 2/10/21. Pt stated she felt phlegm in her throat 3/14/21. On 3/15/21 patient started having trouble swallowing, and started needing supplemental oxygen for low oxygen saturation and needing suctioned for c/o being unable to swallow.. ST eval showed no gag reflex and inability to swallow effectively or safely. Pt needed 5L/O2 and unable to hold saturations above 90%. Patient became ?comfort care?, and passed away 3/18/21.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Hx: CAD, HTN, GERD, anxiety
Vorgeschichte: Hx: CAD, HTN, GERD, anxiety
Andere Medikamente: -
Allergien: NKA
Vorherige Impfungen: -

VAERS 1075349

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

kritisch

Staat: IL
Alter: 103,0
Geschlecht: F
Eingang: 05.03.2021
Impfdatum: 25.01.2021
Beginn: 25.02.2021
Tage bis Beginn: 31,0
Dosis: 2
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: Fosamax chlorthalidone losartan clonidine toprol
Allergien: -
Vorherige Impfungen: -

VAERS 1075090

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

kritisch

Staat: IL
Alter: 96,0
Geschlecht: M
Eingang: 05.03.2021
Impfdatum: 25.01.2021
Beginn: 23.02.2021
Tage bis Beginn: 29,0
Dosis: 2
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: Aricept Lexapro lisinopril Toprol vit D Norvasc Seroquel Flomax
Allergien: -
Vorherige Impfungen: -

VAERS 1075057

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

kritisch

Staat: IL
Alter: 91,0
Geschlecht: M
Eingang: 05.03.2021
Impfdatum: 25.01.2021
Beginn: 12.02.2021
Tage bis Beginn: 18,0
Dosis: 2
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: amlodipine Asa 81 ,glipizide Lexapro losartan Prilosec seroquel
Allergien: NKA
Vorherige Impfungen: -

VAERS 1073361

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

kritisch

Staat: IL
Alter: 106,0
Geschlecht: F
Eingang: 04.03.2021
Impfdatum: 25.01.2021
Beginn: 19.02.2021
Tage bis Beginn: 25,0
Dosis: 2
Route/Site: IM / RA

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

Death

Symptomtext

passed away

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: allopurinol, iron, cytomel, duoneb, prilosec, levothyroxine
Allergien: PCN, ASA, Amantadine, IVP dye
Vorherige Impfungen: -

VAERS 1067942

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038k20a

kritisch

Staat: MD
Alter: -
Geschlecht: M
Eingang: 03.03.2021
Impfdatum: 04.02.2021
Beginn: 05.02.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: OT / LA

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

Cerebrovascular accident

Symptomtext

Stroke; A spontaneous report was received from a Consumer and Other HCP concerning a 84Years-old male patient who received Moderna's COVID-19 vaccine (mRNA-1273) and experienced event like Stroke. The patient's medical history provided no adverse event. Relevant concomitant medications were reported like atorvastatin calcium, ezetimibe, niacin, metoprolol, acetylsalicylic acid, levothyroxine sodium, and iron supplement. On 4th Feb 2021, prior to the onset of the events, the patient received their first of two planned doses of mRNA-1273 (lot/batch: 038k20a) intramuscularly in the left arm for prophylaxis of COVID-19 infection. On date 5th Feb 2021, The patient experienced the event like Stroke, which required hospitalization. It was noted the patient's speech was getting better, but the left side of his body was still paralyzed. There was no treatment information provided There were no laboratory details provided. Action taken with mRNA-1273 in response to the events was not reported. The outcome of the event is unknown.; Reporter's Comments: Although a temporal association exit, provided information is not adequate to assess the causal association between the event and mRNA-1273. Critical details such as the medical history and diagnostic report is lacking. Causality is also confounded by the patient's advanced age and suspected cardiac related condition (patient is on antihypertensive noted in conmed)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: No adverse event (No medical history reported)
Andere Medikamente: STATIN EZ; NIACIN; METOPROLOL; ASPIRIN (E.C.); SYNTHROID; IRON SUPPLEMENT
Allergien: -
Vorherige Impfungen: -

VAERS 1066770

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

kritisch

Staat: IL
Alter: 97,0
Geschlecht: M
Eingang: 02.03.2021
Impfdatum: 25.01.2021
Beginn: 09.02.2021
Tage bis Beginn: 15,0
Dosis: 2
Route/Site: IM / RA

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

Death

Symptomtext

died

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: lasix, seroquel, kcl, coreg, eliquis, vasotec,omeprazole, tylenol, rocephin
Allergien: NKA
Vorherige Impfungen: -

VAERS 1058447

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

kritisch

Staat: PA
Alter: 47,0
Geschlecht: M
Eingang: 26.02.2021
Impfdatum: 23.02.2021
Beginn: 24.02.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Accidental overdose Death Drug abuse Drug screen positive Toxicity to various agents Urine analysis abnormal

Symptomtext

Moderna COVID- 19 Vaccine EUA Patient was found deceased in the community near his home address on 2/24/21. The Medical Examiner's cause of death is currently listed as "Drug Intoxication - Accidental Overdose." Per the MEO, post mortem urine toxicology was positive for cocaine and fentanyl. His death is believed to be related to a cocaine product that was adulterated with fentanyl and is not believed to be related in any way to the Moderna COVID-19 vaccine. This was explicitly stated by the Medical Examiner's Office.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: Urine toxicology on 2/24/21: positive for cocaine and fentanyl
Aktuelle Erkrankungen: None known
Vorgeschichte: Opioid use disorder, cocaine use disorder, hypertension, asthma, hepatitis C (treated), tobacco use, bipolar
Andere Medikamente: Albuterol, abilify, mirtazapine, buprenorphine/naloxone,
Allergien: Lamotrigine
Vorherige Impfungen: -

VAERS 1036437

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038k20A

kritisch

Staat: OH
Alter: 86,0
Geschlecht: M
Eingang: 17.02.2021
Impfdatum: 26.01.2021
Beginn: 17.02.2021
Tage bis Beginn: 22,0
Dosis: 1
Route/Site: IM / RA

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

Death

Symptomtext

Patient is deceased. Family called the pharmacy on 2-17-21 to let us know he would not be coming for his second appointment. When the pharmacist tried to call the family back for more info, the phone number on file doesn't work.

Weitere VAERSDATA-Felder

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

VAERS 1025398

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

kritisch

Staat: IL
Alter: 77,0
Geschlecht: F
Eingang: 12.02.2021
Impfdatum: 05.02.2021
Beginn: 07.02.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / LA

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

Death Unresponsive to stimuli

Symptomtext

Patient received vaccine on 2/5. We were told on 2/9 that the patient visited another emergency department on 2/6 but no information was given as to what prompted that visit. She was sent home. Daughter found her on 2/6 or 2/ 7 unresponsive and she died.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: COPD, type II diabetes, HTN
Andere Medikamente: -
Allergien: Latex, Abilify, Gadolinium contrast media
Vorherige Impfungen: -

VAERS 1009866

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038k20a

kritisch

Staat: FL
Alter: 85,0
Geschlecht: F
Eingang: 07.02.2021
Impfdatum: 29.01.2021
Beginn: 30.01.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Death Haemorrhagic stroke

Symptomtext

pt was given vaccine on the afternoon of 01-29-2021. Pt was administered the moderna covid-19 shot into the deltoid muscle of this pt. Pt was observed and left pharmacy. on 2-6, pts daughter calls pharmacy, and says the night of 1-29, after recieveing the vaccine, her mother had a hemmorhagic stroke and passed away

Weitere VAERSDATA-Felder

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

VAERS 1012073

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

kritisch

Staat: IL
Alter: -
Geschlecht: F
Eingang: 05.02.2021
Impfdatum: -
Beginn: 23.01.2020
Tage bis Beginn: -
Dosis: UNK
Route/Site: IM / -

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

Acute myocardial infarction

Symptomtext

Patient received BAM therapy on 12/10/2020 and received Moderna vaccine on 1/23/2021. Acute STEMI after BAM therapy

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute myocardial infarction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Acute combined heart failure, DM with Stage 3 chronic kidney disease, Venous Stasis dermatitis, Osteopenia, FMS, PVD,GERD, Acute STEMI after BAM therapy.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1005455

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038k20a

kritisch

Staat: IL
Alter: 78,0
Geschlecht: M
Eingang: 05.02.2021
Impfdatum: 29.01.2021
Beginn: 30.01.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / RA

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

Death Respiratory arrest Retching Withdrawal of life support

Symptomtext

We don't know what happened. 25 hours after the shot, he started gagging and stopped breathing. He was pronounced at OSF at 8:07pm after we took him off life support.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Gallbladder not working, one kidney functioning at 25%
Vorgeschichte: Rheumatoid arthritis
Andere Medikamente: -
Allergien: n/a
Vorherige Impfungen: -

VAERS 1005217

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038k20a

kritisch

Staat: IN
Alter: 99,0
Geschlecht: F
Eingang: 05.02.2021
Impfdatum: 27.01.2021
Beginn: 28.01.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / UN

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

Death General physical health deterioration

Symptomtext

Nursing home called 911 for decline in condition. Patient transported to ER where she was admitted to inpatient care and expired 1/30 at 16:13

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: asthma, CHF, Hypokalemia, hypothyroidism
Andere Medikamente: albuteron, gabapentin, levothyroxine, loperamide, pantoprazole, potassium, pravastatin, triamterine, ventolin
Allergien: Morphine, penicillin, quinidine
Vorherige Impfungen: -

VAERS 995346

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

kritisch

Staat: IL
Alter: 61,0
Geschlecht: M
Eingang: 02.02.2021
Impfdatum: 05.01.2021
Beginn: 27.01.2021
Tage bis Beginn: 22,0
Dosis: 2
Route/Site: IM / LA

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

Blood test Chest discomfort Computerised tomogram thorax Deep vein thrombosis Echocardiogram Electrocardiogram Insomnia Myocardial necrosis marker Painful respiration Pulmonary embolism Scan with contrast Sleep disorder Ultrasound scan Ventilation/perfusion scan

Symptomtext

Tightness in chest several times about 1 week and 2 weeks after 1st round. Difficulty sleeping on left side 20 and 21 days following 1st round. Severe pain with inhaling AM of 22 day. Diagnosed at ER Hospital, with DVT left calf and PE both lungs. On Heparin IV for 4 days inpatient. Now on Eloquis 10mg BID for a week, 5mg BID thereafter.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 4,0
Labordaten: QV, CT chest, CT with die marker, EKG, ultrasound both legs, cardiac echo, cardiac enzymes, numerous other blood work, etc.
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: CT die marker
Vorherige Impfungen: -

VAERS 2280933

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

schwer

Staat: SC
Alter: 68,0
Geschlecht: F
Eingang: 17.05.2022
Impfdatum: 08.02.2021
Beginn: 08.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Fatigue Mobility decreased Movement disorder Paralysis Rash Rash erythematous Rash vesicular

Symptomtext

1- extremely tired couldn't get out of the bed for several hours (5-6hours) 2- entire body paralyzed for 1-2 hours couldn't move any extremity in bed had to have help to turn over #3 BOOSTER had red blistery rash from top of fingers to elbows and across upper chest that lasted for 5-6weeks very painful

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paralysis
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: No
Vorgeschichte: borderline diabetes
Andere Medikamente: Metformin, Vitamin E, Vitamin D, Baclofen, Singular, Cymbalta, Cinnamon, Turmeric
Allergien: Fentanyl
Vorherige Impfungen: -

VAERS 2222596

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

schwer

Staat: FL
Alter: 76,0
Geschlecht: F
Eingang: 08.04.2022
Impfdatum: 02.02.2021
Beginn: 05.04.2022
Tage bis Beginn: 427,0
Dosis: 1
Route/Site: OT / LA

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

Asthenia Dizziness Fatigue Headache Presyncope Vomiting

Symptomtext

Fourth shot made patient weak; Fourth shot felt light headed almost passed out; Fourth shot felt light headed almost passed out; Fourth shot gave patient a headache; Fourth shot made patient vomit; Today patient feels better but tired; This spontaneous case was reported by a consumer and describes the occurrence of ASTHENIA (Fourth shot made patient weak), PRESYNCOPE (Fourth shot felt light headed almost passed out), DIZZINESS (Fourth shot felt light headed almost passed out), FATIGUE (Today patient feels better but tired) and HEADACHE (Fourth shot gave patient a headache) in a 76-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 002M21A, 052E21A, 031M20A and 038K20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient does not have any allergies, did not test positive for COVID-19 and did not receive any other vaccine within 1 month prior to Moderna. The patient had 3 heart stents and lung emphysema prior to vaccination and did not register any change to illness status post vaccination. Concurrent medical conditions included Emphysema pulmonary (Lung Emphysema prior to vaccination.). Concomitant products included ATORVASTATIN for Cholesterol, THEOPHYLLINE for Lung disorder NOS, METOPROLOL, DILTIAZEM, TIOTROPIUM BROMIDE MONOHYDRATE (SPIRIVA) and FLUTICASONE PROPIONATE, SALMETEROL XINAFOATE (ADVAIR) for an unknown indication. On 02-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 02-Mar-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 17-Aug-2021, received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 03-Apr-2022, received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 05-Apr-2022, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced FATIGUE (Today patient feels better but tired). On an unknown date, the patient experienced ASTHENIA (Fourth shot made patient weak), PRESYNCOPE (Fourth shot felt light headed almost passed out), DIZZINESS (Fourth shot felt light headed almost passed out), HEADACHE (Fourth shot gave patient a headache) and VOMITING (Fourth shot made patient vomit). At the time of the report, ASTHENIA (Fourth shot made patient weak), DIZZINESS (Fourth shot felt light headed almost passed out), HEADACHE (Fourth shot gave patient a headache) and VOMITING (Fourth shot made patient vomit) was resolving, PRESYNCOPE (Fourth shot felt light headed almost passed out) outcome was unknown and FATIGUE (Today patient feels better but tired) had not resolved. The patient confirmed that the patient did not seek medical care post vaccination. The patient did not experience a similar event in the past. On 05-Apr-2022 it was reported that the patient felt better but tired after receiving the 2nd booster shot on the 03-Apr-2022. No treatment was taken by the patient. This case was linked to MOD-2022-533315, MOD-2022-533310, MOD-2022-533304 (Patient Link).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Emphysema pulmonary (Lung Emphysema prior to vaccination.)
Vorgeschichte: Comments: The patient does not have any allergies, did not test positive for COVID-19 and did not receive any other vaccine within 1 month prior to Moderna. The patient had 3 heart stents and lung emphysema prior to vaccination and did not register any change to illness status post vaccination.
Andere Medikamente: METOPROLOL; DILTIAZEM; ATORVASTATIN; THEOPHYLLINE; SPIRIVA; ADVAIR
Allergien: -
Vorherige Impfungen: -

VAERS 2068830

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

schwer

Staat: FL
Alter: 87,0
Geschlecht: M
Eingang: 27.01.2022
Impfdatum: 25.02.2021
Beginn: 18.01.2022
Tage bis Beginn: 327,0
Dosis: 1
Route/Site: IM / -

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

Blood pH normal Brain natriuretic peptide increased COVID-19 Chest X-ray abnormal Dyspnoea Heart rate increased Hypoxia International normalised ratio increased PCO2 decreased PO2 decreased Pneumonia Respiratory distress SARS-CoV-2 test positive Tachycardia Troponin White blood cell count increased

Symptomtext

88-year-old male, past with a history of chronic atrial fibrillation on warfarin , presented with a 2-day history of worsening shortness of breath. The patient's stepdaughter noted his heart rate to be elevated, sats were in the mid 80s. He has received his COVID vaccination. in the emergency room in moderate respiratory distress, hypoxemic, tachycardic. Chest x-ray revealed probable bilateral pneumonia. COVID was positive. The patient was admitted for further monitoring and evaluation. in ED WBC 15 , INR 11 , BNP 16181, TROP 34 , ABG PH 7.4, PCO2 29 , PO2 69 given Cardizem ivp in ED , hr WAS IN 100 , started on metoprolol 25 mg bid currently 100 % on RA. Pt vaccinated with Moderna 1/28/21 & 2/25/21. patient discharged from hospital 1/25/22

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Praegender Schweregrund: Respiratory distress
Hospital-Tage: 5,0
Labordaten: COVID-19 PCR + 1/20/22
Aktuelle Erkrankungen: -
Vorgeschichte: a-fib on warfarin
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2021238

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

schwer

Staat: IL
Alter: 43,0
Geschlecht: F
Eingang: 10.01.2022
Impfdatum: 04.02.2021
Beginn: 01.03.2021
Tage bis Beginn: 25,0
Dosis: 2
Route/Site: IM / AR

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

Cheilitis Electric shock sensation Facial pain Headache Herpes zoster

Symptomtext

The following day I took off of work for the typical symptoms and I recovered within 48 hours. Around the middle of March, the right side of my face hurt and felt like there was electricity shooting through it, and I noticed a sore developing above my lip. As my symptoms worsened with a terrible headache, I used my telehealth service and uploaded a picture of my face and they diagnosed me with Shingles and gave me antiviral medications and it cleared within a week. About 6 months later in August 2021, I had a recurrence in the same spot but it was mild, and I haven't had another incident since.

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Praegender Schweregrund: Electric shock sensation
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Blood Pressure Hydrochlorothiazide, Bupropion.
Allergien: Bactrim, Vicodin, Penicillin
Vorherige Impfungen: -

VAERS 1783135

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

schwer

Staat: IL
Alter: 74,0
Geschlecht: M
Eingang: 13.10.2021
Impfdatum: 29.01.2021
Beginn: 23.02.2021
Tage bis Beginn: 25,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Feeling abnormal Heart rate increased Laboratory test Presyncope

Symptomtext

After a fews days of taking the vaccine he started feeling bad. His heart rate was going up he had the feeling of being light headed and about to pass out. He was taken to the ER and admitted on 2/23/21

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Praegender Schweregrund: Presyncope
Hospital-Tage: 4,0
Labordaten: yes
Aktuelle Erkrankungen: no
Vorgeschichte: high blood pressure
Andere Medikamente: lorsartan, hydrothyroize
Allergien: no
Vorherige Impfungen: -

VAERS 1772353

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

schwer

Staat: NY
Alter: 71,0
Geschlecht: M
Eingang: 08.10.2021
Impfdatum: 24.01.2021
Beginn: 21.02.2021
Tage bis Beginn: 28,0
Dosis: 2
Route/Site: SYR / LA

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

Blood test Computerised tomogram Dyspnoea Fatigue Feeling jittery Magnetic resonance imaging Pulmonary thrombosis Thrombosis Ultrasound scan

Symptomtext

On 7/28/21 was diagnosed with large blood clots, 1 in each lung and 1 in leg. Shortness of breath, fatigue,and jittery were symptoms leading to hospital visit. Was in hospital for a week.

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Praegender Schweregrund: Pulmonary thrombosis
Hospital-Tage: 7,0
Labordaten: Multiple MRI's, CT's, Ultrasounds and blood draws between 7/28/21 and 8/3/21.
Aktuelle Erkrankungen: none
Vorgeschichte: Afib Cerebral amyloid angiopathy Dementia High Blood Pressure
Andere Medikamente: Lisinopril/Hctz Atorvastatin Metoprolol Succinate ER Famciclovir Fluoxetine Hcl Rivastigmine Centrum Silver Multivitamin
Allergien: none
Vorherige Impfungen: -

VAERS 1713464

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

schwer

Staat: IL
Alter: 72,0
Geschlecht: F
Eingang: 18.09.2021
Impfdatum: 08.03.2021
Beginn: 28.04.2021
Tage bis Beginn: 51,0
Dosis: 2
Route/Site: IM / LA

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

Anticoagulant therapy Computerised tomogram abnormal Dyspnoea exertional Pain in extremity Thrombosis Varicose vein

Symptomtext

Blood clots. After long car trip on April 18th; returning on April 22nd, noticed shortness of breathe when walking. Made appointment with cardiologist with complete cardiology work up. Everything OK. Then saw doctor, my regular doctor, because shortness of breathe continued. She ordered CT scan which showed multiple blood clots. Doctor immediately prescribed Eliquis for six months. Of note, I also have varicose veins with leg swelling after 8 to 10+ hours riding in car, but I have never had blood clots. Shortness of breathe seems to have been resolved.

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Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: 6/08/21 CT scan
Aktuelle Erkrankungen: None
Vorgeschichte: GERD
Andere Medikamente: Levothyroxin, Omeprazole, Qunol ultra CoQ10, NatureMade Multi For Her 50+, NatureMade Magnesium citrate 250 mg, NatureMade Calcium 600 mg
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1548470

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

schwer

Staat: SC
Alter: -
Geschlecht: F
Eingang: 12.08.2021
Impfdatum: 10.02.2021
Beginn: 01.02.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: OT / LA

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

Chills Decreased appetite Hyperhidrosis Loss of consciousness Nausea Pain in extremity Pyrexia Vomiting

Symptomtext

Passed out for about one minute; Vomiting; Chills; Sweat; Decreased appetite; Mild fever/Higher fever; Sore arm; Nauseated; A spontaneous report, was received from a health care professional (patient's husband), concerning a 33-year-old female patient, unknown race and ethnicity, who was administered Moderna's COVID-19 vaccine, and experienced passed out for about one minute (loss of consciousness), sore arm (pain in extremity), sweat (hyperhidrosis), decreased appetite, mild fever/higher fever (pyrexia), chills, vomiting, and nauseated (nausea). The patient's medical history was not provided. No relevant concomitant medications were reported. No information on allergies were provided. The reported stated that the patient was physically and mentally healthy before vaccination. On 10 Feb 2021, prior to the onset of events, the patient received their second planned dose of mRNA-1273 (lot number: 038K20), intramuscularly into left upper arm for the prophylaxis of COVID-19 infection. On 10 Feb 2021, after the second dose of vaccine, the patient experienced sore arm, and mild fever/higher fever. On 11 Feb 2021, the patient developed chills, sweat, and decreased appetite. The patient has passed out for about a minute and started vomiting on 12 Feb 2021. The patient did not seek any medical emergency. The patient was nauseated on an unknown date in Feb 2021. The patient received treatment medication with ibuprofen twice within 12 hours of adverse events apart. The patient was currently not taking any other medications. The outcome for the events, passed out for about one-minute, sore arm, sweat, decreased appetite, mild fever/higher fever, chills, vomiting, and nauseate, were reported 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 event, a causal relationship cannot be excluded.

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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 1322955

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

schwer

Staat: NJ
Alter: 66,0
Geschlecht: M
Eingang: 17.05.2021
Impfdatum: 09.02.2021
Beginn: 24.02.2021
Tage bis Beginn: 15,0
Dosis: 2
Route/Site: IM / LA

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

Abdominal pain Anticoagulant therapy Computerised tomogram Decreased appetite Deep vein thrombosis Embolism Essential hypertension Ligament rupture Muscle strain Musculoskeletal stiffness Nausea Pain in extremity Ultrasound Doppler abnormal Vomiting

Symptomtext

2 weeks later developed DVT (leg pain, also found to have ACL tear of unknown duration), loss of appetite, and bilateral stiffness in hands. Hospitalized for DVT on blood thinners since Diagnosis: Acute embolism and thrombosis of unspecified deep veins of right lower extremity ; Unspecified abdominal pain ; Nausea with vomiting, unspecified ; Strain of muscle, fascia and tendon of the posterior muscle group at thigh level, left thigh, initial encounter ; Essential (primary) hypertension

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Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: 5,0
Labordaten: CT & doppler US to detect DVT
Aktuelle Erkrankungen: Bipolar PTSD tremour High cholesterol (off medication)
Vorgeschichte: Marijuana use
Andere Medikamente: Geodon, Hydroxyzine
Allergien: Pennicillin & Fluoride
Vorherige Impfungen: -

VAERS 1317645

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

schwer

Staat: MI
Alter: 82,0
Geschlecht: F
Eingang: 14.05.2021
Impfdatum: 12.02.2021
Beginn: 12.03.2021
Tage bis Beginn: 28,0
Dosis: 1
Route/Site: SYR / RA

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

CSF protein increased Guillain-Barre syndrome Hypoaesthesia Magnetic resonance imaging neck Magnetic resonance imaging thoracic Muscular weakness Radicular pain

Symptomtext

Guillain Barre syndrome. Presented with rapid onset L >R leg weakness, numbness and radicular pain. Symptoms came on overnight. 3 days later developing hand symptoms.

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Praegender Schweregrund: Guillain-Barre syndrome
Hospital-Tage: -
Labordaten: CSF protein elevated at 53 (5/14/21). MRI cervical and thoracic spine negative for spinal cord abnormality (5/12/21)
Aktuelle Erkrankungen: None active
Vorgeschichte: PAST MEDICAL HISTORY: 1. GERD. 2. Hypertension. 3. Hyperlipidemia. 4. Arthritis. 5. Hypothyroidism. 6. Allergic rhinitis. 7. History of DVT with likely PE. 8. Anxiety. 9. Asthma.
Andere Medikamente: allegra, Eliquis, Benicar, paxil, omeprazole, albuterol, Symbicort, levothyroxine, singulair, clonidine
Allergien: Iodine, Keflex, latex, naproxen, penicillin
Vorherige Impfungen: -

VAERS 1301443

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038k20A

schwer

Staat: IL
Alter: 42,0
Geschlecht: F
Eingang: 09.05.2021
Impfdatum: 29.01.2021
Beginn: 29.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Anaphylactic reaction

Symptomtext

Anaphylactic reaction

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Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma and allergies
Andere Medikamente: Claritin,pro air as needed.
Allergien: Penicillin, sulfa, keflex
Vorherige Impfungen: -

VAERS 1272190

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

schwer

Staat: MD
Alter: 64,0
Geschlecht: F
Eingang: 29.04.2021
Impfdatum: 27.01.2021
Beginn: 28.03.2021
Tage bis Beginn: 60,0
Dosis: 1
Route/Site: IM / RA

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

Pneumonia Pulmonary thrombosis

Symptomtext

BLOOD CLOT IN THE LUNGS AND PNEUMONIA (AS REPORTED PER PATIENT)

Weitere VAERSDATA-Felder

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

VAERS 1246335

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

schwer

Staat: IN
Alter: 71,0
Geschlecht: F
Eingang: 23.04.2021
Impfdatum: 28.01.2021
Beginn: 16.03.2021
Tage bis Beginn: 47,0
Dosis: 1
Route/Site: SYR / LA

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

Chest X-ray Echocardiogram Electroencephalogram Magnetic resonance imaging head Seizure Ultrasound Doppler

Symptomtext

Seizure

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Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: Brain MRI; Chest X-ray; EEG; Heart Ultrasound; Carotid artery ultrasound; 24-hr. heart monitor
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Lovastatin 20 mg; Lisinopril-HCTZ 10-12.5 mg.; Tylenol 500 mg.; Fish Oil 1000 mg.; Turmeric; Calcium 1200 mg.; Glucosamine Chondroitin; Vitamin C. 1000 mg; Centrum Silver Women 50+; Probiotic
Allergien: -
Vorherige Impfungen: -

VAERS 1235684

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

schwer

Staat: IL
Alter: 71,0
Geschlecht: F
Eingang: 21.04.2021
Impfdatum: 05.02.2021
Beginn: 08.03.2021
Tage bis Beginn: 31,0
Dosis: 1
Route/Site: OT / -

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

Chills Hearing disability Ischaemic stroke Meningitis viral Vision blurred

Symptomtext

If not 100 % sure but she may had an ischemic stroke,This is not normal; viral meningitis; chills; vision problems,vision problem was bad; hearing problems; This spontaneous case was reported by a consumer and describes the occurrence of ISCHAEMIC STROKE (If not 100 % sure but she may had an ischemic stroke,This is not normal) and MENINGITIS VIRAL (viral meningitis) in a 71-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. QQ2A21 and 038K20A) 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 05-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 07-Mar-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 08-Mar-2021, the patient experienced VISION BLURRED (vision problems,vision problem was bad) and HEARING DISABILITY (hearing problems). On an unknown date, the patient experienced ISCHAEMIC STROKE (If not 100 % sure but she may had an ischemic stroke,This is not normal) (seriousness criterion medically significant), MENINGITIS VIRAL (viral meningitis) (seriousness criterion medically significant) and CHILLS (chills). At the time of the report, ISCHAEMIC STROKE (If not 100 % sure but she may had an ischemic stroke,This is not normal), MENINGITIS VIRAL (viral meningitis), VISION BLURRED (vision problems,vision problem was bad), HEARING DISABILITY (hearing problems) and CHILLS (chills) outcome was unknown. Action taken with mRNA-1273 in response to the events was not Applicable. Treatment medication includes: Blood thinner Rosuvastatin, 81mg aspirin. Additional information:After second dose had chills but she hear from people who had fever, chills and etc. Woke up on Monday March 8 with vision problems, hearing problems. She waited 8 days until she went to the doctor because everybody says had a reaction but this was getting worse. Went to eye doctor because of vision problem was bad, on March 18 4 weeks after first symptoms appears, optometrist send to her internist and after consultation, on March 23 had 2 MRI head and brain. March 26 had contrast MRI brain, send her for a carotid study in her neck. Went to the internist again, April 2 send to spinal test. April 5 echocardiogram, yesterday went to first appointment with her vision therapeutics. This morning went to the neurologist send her for 2 more brain MRI. If not 100 % sure but she may had an ischemic stroke, doctor will confirm it with the studies. Neurologist confirm she has viral meningitis and the symptoms are similar with ischemic stroke, but that is not confirmed yet. 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 is 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 is requested.

Weitere VAERSDATA-Felder

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

VAERS 1231024

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

schwer

Staat: TN
Alter: 36,0
Geschlecht: F
Eingang: 19.04.2021
Impfdatum: 02.02.2021
Beginn: 03.02.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Blood pressure decreased Chills Cold sweat Cyanosis Hyperhidrosis Hypotension Loss of consciousness Vision blurred

Symptomtext

Suddenly became hypotensive, diaphoretic and clammy, vision got swimmy. I was able to sit down and then lie down before passing out. Then I got the chills and fingers were a bit cyanotic. Blood pressure was checked--it was low 60s/40s. Pulse ox was checked--that was fine, 99 or 100. Temp was checked--that was also normal. Laid down for a few hours and drank lots of fluids, (water and juice). Blood pressure slowly came back up as the day progressed, but not back to normal. It took two weeks for my blood pressure to fully stabilize back to my normal range. I checked my blood pressure daily for probably three weeks and drank juice/gatorade daily to help.

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Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: None
Vorgeschichte: migraine, Gilbert's, hypothyroidism
Andere Medikamente: Bystolic, levothyroxine, multivitamin, Zyrtec
Allergien: N/A
Vorherige Impfungen: -

VAERS 1137224

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

schwer

Staat: -
Alter: 83,0
Geschlecht: F
Eingang: 26.03.2021
Impfdatum: 26.02.2021
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: OT / LA

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

Peripheral swelling Thrombosis

Symptomtext

Develop a blood clot on their left knee; Left leg kept swelling up; A spontaneous report was received from a physician concerning a 83-year-old, female patient, who received Moderna's COVID-19 Vaccine (mRNA-1273) and experienced a blood clot on her left knee and left leg kept swelling up. The patient's medical history included cholesterol unspecified. Products known to have been used by the patient, within two weeks prior to the event, included vitamin D and medications for cholesterol. On 26 Feb 2021, prior to the onset of the symptoms, the patient received her first of two planned doses of mRNA-1273 (Batch number: 038K20A) intramuscularly in the left arm for prophylaxis of COVID-19 infection. On an unspecified date after the vaccination patient developed blood clot on left leg, leg also kept swelling. Relevant treatment for the event included blood thinners and aspirin. Action taken with mRNA-1273 in response to the events was not provided. The outcome of the events, blood clot on their left knee and left leg kept swelling up, 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 events, a causal relationship cannot be excluded.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: High cholesterol
Vorgeschichte: -
Andere Medikamente: VITAMIN D [VITAMIN D NOS]
Allergien: -
Vorherige Impfungen: -

VAERS 1110290

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

schwer

Staat: IL
Alter: 63,0
Geschlecht: M
Eingang: 18.03.2021
Impfdatum: 12.03.2021
Beginn: 17.03.2021
Tage bis Beginn: 5,0
Dosis: 1
Route/Site: IM / -

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

Alanine aminotransferase normal Aspartate aminotransferase normal Blood albumin normal Blood alkaline phosphatase normal Blood bilirubin Blood calcium decreased Blood chloride decreased Blood creatinine normal Blood glucose increased Blood lactic acid Blood potassium normal Blood sodium normal Blood urea normal Blood urine absent Brain natriuretic peptide normal Carbon dioxide normal Cardiomegaly Chest X-ray normal

Symptomtext

3/17/21 63 y.o. male who presents with sudden onset of chest pain and palpitations, which occurred while patient was exerting himself. Pain is substernal, radiated to the left arm, associated with lightheadedness. Denies diaphoresis or nausea. Per EMS there were short runs of nonsustained ventricular tachycardia 3/18: - remains inpatient admission as of 3/18/21 @ 0900 63 y.o. male with a past medical history of nonsustained ventricular tachycardia. He states he was lifting a couch yesterday and his heart started beating fast. He did not really have any chest pain, but felt a little bit lightheaded. He called an ambulance and they brought into the ER. In the emergency room his EKG did show some frequent PVCs. However, he did not really require any intervention. He was given 3 nitro, but it really did not make any difference in the way he was feeling. The patient denies multiple times that he actually had chest pain. He states he just felt like his heart was beating funny. The patient's most recent stress test was a nuclear stress test in May of 2019. Overnight, the patient has felt very well. He denies any significant chest pain. He denies any further heart palpitations. On the monitor he would occasionally going to bigeminy, which is not abnormal for him. EKG this morning was unremarkable. After speaking with the patient's wife, she told me that he has had a several month history of very limited exertion. She states every time he exerts he becomes extremely dyspneic and has heart palpitations and sometimes almost passes out. She states last night he was extremely diaphoretic and very nearly passed out.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: 2,0
Labordaten: XR CHEST PORTABLE Final Result EXAM DESCRIPTION: XR CHEST PORTABLE INDICATIONS: Chest pain COMPARISON: 2014 TECHNIQUE: Single AP portable FINDINGS: Cardiac silhouette is mildly enlarged. Lungs are clear. IMPRESSION: No acute findings ECG: EKG from the emergency room showed sinus rhythm with frequent PVCs and no ischemic change. EKG from this morning showed normal sinus rhythm with no ischemic change Lab Review CBC Recent Labs Lab 03/17/21 1934 03/10/21 1116 WBC 7.9 7.3 HGB 14.8 15.5 HCT 42.2 46.5 PLT 227 238 MCV 87.7 87.7 RBC 4.81 5.30 CHEMISTRY Recent Labs Lab 03/17/21 1938 03/10/21 1116 GLU 158* 162* BUN 19* 17 CREATININE 1.0 1.1 NA 139 138 K 4.0 4.2 CL 85* 102 CO2 25 24 CALCIUM 8.1* 9.0 LABALBU 3.4 4.0 ALT 26 28 AST 27 20 ALKPHOS 80 62 LABBILI 0.3 0.5 LACTATE 2.2* -- GI No results for input(s): AMYLASE, LIPASE in the last 70080 hours. COAGS No results for input(s): PROTIME, PTT, INR in the last 70080 hours. CARDIAC Recent Labs Lab 03/18/21 0705 03/17/21 2317 03/17/21 1938 TROPONINI 0.00 < > 0.01 BNP -- -- 52 < > = values in this interval not displayed. URINE Recent Labs Lab 03/17/21 2002 LEUKOCYTESUR NEGATIVE NITRITE NEGATIVE BLOODU NEGATIVE WBCU 0 to 5 SPECGRAV 1.010 KETONESU NEGATIVE PROTEINUA NEGATIVE PHUR 6.0
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Medications Administrations Status Frequency Start Date End Date metFORMIN (GLUCOPHAGE) tablet 1,000 mg Order Report Active 2 TIMES DAILY WITH MEALS 03/18/21 09/14/21 fish oil omega-3 fatty acids capsule 2,000 mg Order Report Active DAILY
Allergien: nka
Vorherige Impfungen: -

VAERS 1106505

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

schwer

Staat: MI
Alter: 74,0
Geschlecht: F
Eingang: 16.03.2021
Impfdatum: 25.02.2021
Beginn: 27.02.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / RA

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

Arteriogram carotid normal Electrocardiogram Eye infarction Magnetic resonance imaging Scan with contrast Thrombosis Visual field defect Visual impairment

Symptomtext

Ocular stroke. A black curtain dropped down over right eye. Went to ER on the 28th, and was admitted. Had a blood clot in the right eye. Carotid artery right side did not have stenosis, they do not know why she had a stroke. Doctor can't say that it was caused by the vaccine. She now has a permanent blind spot in right eye.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: 2,0
Labordaten: Did contrast dye on carotid artery, ECG, MRI
Aktuelle Erkrankungen: no
Vorgeschichte: no
Andere Medikamente: Rosuvastatin 5mg, Levothyroxine 1mg, Baby Aspirin, CoQ10, D3, Tumeric
Allergien: Sulfur Drugs, egg based products
Vorherige Impfungen: Flu vaccine

VAERS 1082334

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

schwer

Staat: IL
Alter: 60,0
Geschlecht: F
Eingang: 08.03.2021
Impfdatum: 05.03.2021
Beginn: 05.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Anaphylactic reaction Anxiety Arachnoiditis Asthenia Bursitis Condition aggravated Conjunctivitis Dyspnoea Fatigue Headache Injection site oedema Mobility decreased Muscle contractions involuntary Myalgia Pain in extremity Paraesthesia oral Thirst

Symptomtext

No rxn to dose 1. Dose 2: @10 min had tingling of lips; at 12 min had tingling of tongue [and anxiety from the tingling]; @ 15 min had some SOB and knew this was not just anxiety. Had zero intention of being taken to ER as I could easily tx myself. Took inhalers, extra cetirizine. Did not take epi, though have several pens. @4 hour started feeling weak, severe arm pain. At 6 hours, unbearable arm pain, extreme weakness [did not take BP or pulse ox--though I can and wish I had]. Exceeding thirst, could not get water down fast enough. Reactivation of arachnoiditis symptoms. Started unusual muscle fasciculations in arms, leg, and face [face not normal for me]-took valium and baclofen. Next 36 hours unable Additional information for Item 18: next 48 hours, unable to get out of bed other than to get water. Severe HA upon waking [@16 H post injection]. Severe myalgias, but in areas of known arachnoiditis that have been quiescent for quite some time. Forgot to mention, as I find this strange: prior to going to sleep I had left eye conjunctivitis. Left eye only that still is slightly persistent and doesn't require any care [for me at least] I am currently 72 hours post. Still with HA and some fatigue, though worked today [I WAH for a population health company]. L arm is not as painful as the excruciating pain @ hour 4-16, and no need for additional acetaminophen. I have an exceedingly high pain tolerance due to the arachnoiditis, but this was the first time I took a narcotic in 5 years. 2 .5 mg oxycodone x1, then 600 mg ibuprofen x1, then 1 gm acetaminophen 2 over next 24 hours and nothing since, but it is still quite painful today. Different today than yesterday is the development of what feels like left shoulder bursitis. We'll have to see how this goes over time. There is extensive edema at the site, but not clear erythema [I'm dark skinned]. Still just can't seem to get enough water. Had my first meal last night [made chicken soup]. It's still pretty early on. I'm not even at the 72 hour mark yet, so hopefully things will settle down over the next weeks. I checked the box as life threatening because that was likely early anaphylaxis -- though at first I seriously thought at first I was just anxious because of the lip tingling. This is in defense of the fact I did not self administer epi when I became SOB. I likely should have, but know myself well and did fine without it and with asthma and allergy care. I didn't need extra albuterol after the first 24 hours [though writing this makes me feel SOB just from reliving it]. This second dose is a doozy. Hope this was helpful. I provided you guys with my cell but if you want to follow up, I use my phone for work so if you text first I cant tell you availability.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: seasonal allergies
Vorgeschichte: arachnoiditis, controlled asthma, seasonal allergies, high cholesterol
Andere Medikamente: cetirizine, monteleukast, gabapentin, duloxetine, baclofen, pr
Allergien: bee/wasps
Vorherige Impfungen: -

VAERS 1079995

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

schwer

Staat: IL
Alter: 36,0
Geschlecht: M
Eingang: 07.03.2021
Impfdatum: 15.01.2021
Beginn: 15.01.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / -

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

Abdominal discomfort Cold sweat Diabetic ketoacidosis Glycosylated haemoglobin increased Intensive care Malaise

Symptomtext

Ith the first vaccination I had upset stomach and clamy forehead about an hour after vaccination. Then within a 3 week time period I kept getting sicker then, the day after my second dose (which caused me no reaction, which I thought was weird as everyone reported that one having more side effects) I had become so sick that I went to the ER and found I had diabetic ketoacidosis. It runs in my family to have type 2 but later in life. What was also strange is that Inhad a physical not long before the vaccine through my PCP Dr. and my A1C labs came back elevated but within normal limits....

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 5,0
Labordaten: Due to my ICU stay at Hospital there are too many labs to note, but you are welcome to request them from the hospital if it will help others.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Blood pressure medication Amlodipine
Allergien: Allergic to cats and some pollens
Vorherige Impfungen: -

VAERS 1072809

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

schwer

Staat: IL
Alter: 85,0
Geschlecht: F
Eingang: 04.03.2021
Impfdatum: 09.02.2021
Beginn: 12.02.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: SYR / LA

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

Bell's palsy Blood test Magnetic resonance imaging

Symptomtext

Bell's Palsy occurred on right side of face , beginning 3 days after injection. Treated with steroids by primary care physician. Followed up with neurologist who ordered bloodwork and MRI (awaiting results). 3 weeks later, palsy still has not resolved. It was advised to wait at least 6 weeks and until the palsy is resolved before getting the second Moderna shot.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: Bloodwork 2/26/21 -- awaiting results MRI 3/3/21 -- awaiting results
Aktuelle Erkrankungen: -
Vorgeschichte: high blood pressure
Andere Medikamente: high blood pressure medications, thyroid medication
Allergien: -
Vorherige Impfungen: -

VAERS 1064312

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

schwer

Staat: MI
Alter: 77,0
Geschlecht: M
Eingang: 01.03.2021
Impfdatum: 26.02.2021
Beginn: 27.02.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Asthenia Blood chloride decreased Blood creatine normal Blood glucose normal Blood sodium decreased Chills Cold sweat Dizziness Drooling Eye movement disorder Facial paralysis Gait disturbance Haemoglobin decreased Loss of consciousness Malaise Nausea Syncope Unresponsive to stimuli

Symptomtext

Reported via Nurse Triage / PCP: Fainted earlier, eyes rolled back, mouth was drooping. Nausea, weakness, and chills. BP was 107/75, HR in the 70s. Currently alert and resting. States that patient had his 2nd covid vaccine yesterday AM and then develop chills and clammy skin last night. Symptoms worsened today and patient became weak and fainted. Was unconscious for about 5 minutes and while unconscious, mouth was open and drooling and became incontinent and eyes rolled back in head. Is awake and alert now, but still weak and only able to take 1 or 2 steps. No chest pain or breathing difficulty and no fever. Feeling very nauseous. Caller requesting prescription for zofran. Yesterday AM 2nd vaccine. Last night chills. This AM feeling weak. Today at 11am he felt weak with ambulation. He fainted. Was unconscious for 5 min. Had drooping of the face. He was unresponsive during this time. Had incontinence of urine. Then became awake but very weak still. Only able to walk a few steps. He is communicating. No chest pain. No current fever. No shortness of breath. BP 107/75 with HR 70. He has been very nauseated. He is drinking only small sips of water. Does not seem like a usually COVID-19 vaccine reaction. Given the LOC with urinary incontinence and sustained weakness, I advised ER evaluation to rule out neurological issues. Pt's daughter in agreement. They will go to ER. From Emergency Department: Patient presenting with chief complaint of syncopal episode which was witnessed by his wife. He reported the got dizzy and lightheaded and then passed out while seated. The reported duration of his loss of consciousness was somewhat inconsistent, unclear how long he passed out for, there was however no postictal state. He was not noted have any shaking or seizure activity, he did have an episode of urinary incontinence. He has not been feeling well ever since receiving his 2nd COVID-19 vaccine. By the time of my exam patient states that he is completely asymptomatic, he states he is feeling much better after receiving IV fluids. His lab work is remarkable for a slightly low sodium, compared to his previous levels which were many months ago. Unclear of the acuity of this, although upon further discussion with the patient he has been drinking large amounts of water since his vaccine trying to stay hydrated. I advised him to substitute to some electrolyte balanced fluids and to have his sodium rechecked by his PCP to ensure that this is transient. With negative testing and resolution of his symptoms he is stable for discharge home. Close return precautions were given.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: -
Labordaten: Na = 126; Cl = 94; Glucose = 156; SCR = 0.9; Hgb = 13.5
Aktuelle Erkrankungen: NA
Vorgeschichte: hyperglycemia, BPH, LUTS, hyperlipidemia, elevated PSA, BPH with urinary tract symptoms / obstruction, seborrheic keratosis, senile nuclear sclerosis, bilateral, posterior vitreous detachment bilateral, impaired fasting glucose, seasonal allergies,
Andere Medikamente: finasteride, hydrocortisone cream, saw palmetto capsules, naproxen, fish oil, ondansetron, tamsulosin
Allergien: keflex, doxycycline, penicillin, sulfa drugs
Vorherige Impfungen: -

VAERS 1063860

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

schwer

Staat: MI
Alter: 51,0
Geschlecht: F
Eingang: 01.03.2021
Impfdatum: 24.02.2021
Beginn: 24.02.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Anaphylactic reaction Blood alkaline phosphatase increased Blood alkaline phosphatase normal Blood glucose increased Chest X-ray normal Dyspnoea Neutrophil percentage increased Platelet count increased Red blood cell count decreased Respiratory distress Stridor Urticaria Wheezing White blood cell count increased

Symptomtext

Pt presented to the ED in acute anaphylaxis 20 minutes after receiving vaccine dose, in respiratory distress with stridor, wheezing, and difficulty breathing, as well as hives across her chest and arms. Pt had Epipen with her and ED staff assisted her in administering it. Pt received solu-medrol, pepcid, benadryl, and albuterol in the ED. Pt significantly improved within 1 hour and was admitted to the hospital to be monitored overnight.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: 1,0
Labordaten: CBC 2/25 significant for WBC 24.32, Platelet 451, neutrophil 90.2,%. Chest xray 2/25 normal. CBC 2/26 significant for WBC 19.46, RBC 4.10, Platelet 420, neutrophil 88.6%. CMP 2/26 significant for glucose 127, alkaline phosphatase 108
Aktuelle Erkrankungen: -
Vorgeschichte: breast mass, colon polyps, gastritis, GERD, hyperlipidemia, hypogammaglobulinemia, IBS, immune deficiency disorder, osteoarthritis, recurrent sinus infections
Andere Medikamente: lipitor, prenatal 27-1mg tabs, xarelto, albuterol, flexeril, diflucan, ambien, valtrex, xanax, singulair, tylenol, calcium citrate-vitamin D, vitamin D, cymbalta, allegra, hizentra, magnesium oxide, prilosec, zofran, vitamin B12
Allergien: bactrim, blood root, ceftin, tree nuts, kiwi fruit, sulfa drugs, trimethoprim, COVID-19 vaccine (added 2/24/2021)
Vorherige Impfungen: -

VAERS 1058337

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

schwer

Staat: IL
Alter: 26,0
Geschlecht: F
Eingang: 26.02.2021
Impfdatum: 26.01.2021
Beginn: 27.01.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Chills Fatigue Fluid intake reduced Myalgia Nausea Pyrexia Syncope Vomiting

Symptomtext

About 7:00 am - fatigue and chills, muscle aches. Starting around noon, my fever was getting higher and higher - to 103. At 2:00 pm, I tried to sit up in my bed - I proceeded to throw up and faint. I contacted doctor to see if I should take anything. I took an ibuprofen and drank fluid - but didn't drink as much as normal because of nausea. I was nauseated all day. It stayed about 102 until about 8:00 pm. At about 10:00 pm that night, I started feeling a bit better. The next day fever was 99.7 and with more ibuprofen it normalized to 98.6. If I didn't take ibuprofen for awhile it went back up to 99. something so I had to keep taking ibuprofen for the rest of that third day. Fourth day - mild fatigue and muscle aches. Everything was normal other than that. Fatigue and muscle aches were gone about Friday morning.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: no
Aktuelle Erkrankungen: Ear infection
Vorgeschichte: cluster headaches; asthma
Andere Medikamente: no except - I have Immuno therapy allergy shots - I do them once a month : January 21st, 2021
Allergien: Compazine
Vorherige Impfungen: -

VAERS 1058035

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

schwer

Staat: IL
Alter: 45,0
Geschlecht: F
Eingang: 26.02.2021
Impfdatum: 12.02.2021
Beginn: 13.02.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: - / LA

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

Arthralgia Cold sweat Dizziness Loss of consciousness Pain Pyrexia Spinal pain

Symptomtext

Saturday morning after waking up I felt extreme dizziness, fever, cold sweats, aches throughout shoulders, spine, and hips, and after getting up passed out twice.

Weitere VAERSDATA-Felder

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

VAERS 1055160

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038k20a

schwer

Staat: AR
Alter: 79,0
Geschlecht: F
Eingang: 25.02.2021
Impfdatum: 25.02.2021
Beginn: 25.02.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Cold sweat Feeling abnormal Heart rate decreased Syncope

Symptomtext

Pt felt "off" some minutes after receiving vaccine. reported to staff and fainted upon standing. eased her to floor and elevated legs. regained consciousness immediately. called 911. heart rate low blood pressure normal. clammy before faint quickly regained color. EMS took over and transported pt to hospital

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: unknown
Vorgeschichte: no
Andere Medikamente: unknown
Allergien: no
Vorherige Impfungen: -

VAERS 1053976

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

schwer

Staat: IL
Alter: 21,0
Geschlecht: F
Eingang: 25.02.2021
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: ja

Hypoacusis Loss of consciousness Pain in extremity Unresponsive to stimuli

Symptomtext

Moderna COVID-19 Vaccine EUA Approximately 3 minutes after her vaccine pt became unconscious and unresponsive for a short time. Pt was quickly awoken by RN. Pt states that she has a history of syncope following venipuncture that she forgot to disclose. Approximately 15 post episode pt stated that her vision had been restored but her hearing still felt "off". Pt was given 12 oz water, crackers and juice. Pt called roommate to pick her up to bring her home. Approximately 25 minutes later, pt reports some left arm pain but was feeling better. At 1345 pt was discharged by her own choice and left with her roommate. Pt still felt "off" but reported that this was likely just due to anxiety. Pt and roommate given instructions to go to nearest ER if symptoms returned.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: -
Vorgeschichte: Hx of migraines Hx of syncope (especially with needles)
Andere Medikamente: Kyleena IUD
Allergien: Penicillin - unknown
Vorherige Impfungen: -

VAERS 1045538

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

schwer

Staat: FL
Alter: -
Geschlecht: F
Eingang: 22.02.2021
Impfdatum: 29.01.2021
Beginn: 04.02.2021
Tage bis Beginn: 6,0
Dosis: 1
Route/Site: OT / LA

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

Facial paralysis Musculoskeletal stiffness Oral discomfort

Symptomtext

bell's pausy; strange feeling in my lip; stiff neck; A spontaneous report was received from a consumer concerning a 73-year old, female patient who received Moderna's COVID-19 vaccine (mRNA-1273) and developed Bell's Palsy (facial paralysis), stiff neck (musculoskeletal stiffness), and a strange feeling in her lip (oral discomfort). The patient's medical history was not provided. Products known to have been used by the patient, within two weeks prior to the event, included vitamins, atorvastatin calcium and calcium On 29 Jan 2021, the patient received their first of two planned doses of mRNA-1273 (Batch number: 038K20A) intramuscularly in the left arm for prophylaxis of COVID-19 infection. On 04 Feb 2021, the patient developed a very stiff neck and had a restless sleep. On 06 Feb 2021, the patient reported awaking with a strange feeling in her lip. She was advised by her primary care physician. On 07 Feb 2021, the symptoms had worsened, and her facial muscle had twisted. Treatment for the event included prednisone and valacyclovir. Action taken with mRNA-1273 in response to the events was not provided/unknown. The events, Bell's Palsy, stiff neck and strange feeling in lip, was considered not recovered/not resolved.; Reporter's Comments: Although a temporal relationship exists, there is not enough information to assess the causal relationship of the reported events with the administration of mRNA-1273 (Batch number: 038K20A). Critical details such as patient's medical history and relevant diagnostic test are lacking. Additional information have been requested.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: No adverse event (No reported medical history)
Andere Medikamente: VITAMINS NOS; LIPITOR; CALCIUM
Allergien: -
Vorherige Impfungen: -

VAERS 1045521

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

schwer

Staat: IL
Alter: -
Geschlecht: F
Eingang: 22.02.2021
Impfdatum: 04.02.2021
Beginn: 04.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / -

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

Diarrhoea Nausea Pyrexia Syncope

Symptomtext

Fainted; Diarrhea; Nausea; Warm body temperature; A spontaneous report was received from a consumer, regarding herself, a 82-year-old, female consumer who received Moderna's COVID-19 vaccine (mRNA-1273) and experienced fainted, diarrhea, nausea and warm body temperature. The patient's medical history reported included ulcerative colitis. Concomitant product use was not provided. On 04 Feb 2021, prior to the onset of the events, the patient received their first of two planned doses of mRNA-1273 (lot Number: 038K20A) intramuscularly for prophylaxis of COVID-19 infection. On 04 Feb 2021, in the evening, after receiving the vaccine, the patient was fainted and started to experience diarrhea, nausea and warm body temperature. The event fainted was considered to be medically significant. Treatment for the events not provided. Action taken with the second dose of mRNA-1273 in response to the events were not reported. The outcome for the events, fainted, diarrhea, nausea and warm body temperature were resolved on 05 Feb 2021.; 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: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Ulcerative colitis
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1036369

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

schwer

Staat: FL
Alter: 67,0
Geschlecht: F
Eingang: 17.02.2021
Impfdatum: 01.02.2021
Beginn: 14.02.2021
Tage bis Beginn: 13,0
Dosis: 1
Route/Site: IM / LA

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

Bell's palsy Blood test

Symptomtext

Experienced Bell's Palsy on right side of face. Noticeable when smiling.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: Seen by Dr. on Monday, Feb. 15 at 2:30pm. Blood tests taken Tuesday, Feb. 16th at Quest Diagnostic
Aktuelle Erkrankungen: None
Vorgeschichte: high bp, pre-diabetic, high cholesterol - this was determined after examination by primary doctor. Not under medication at the time of reaction.
Andere Medikamente: Advance Formula ,Adults multivitamins with 25mcg Vitamin D3 and multimineral supplement by Publix (compare to Centrum), one tablet per day; Essential Zinc 50mg by Sundown, one tablet per day.
Allergien: None
Vorherige Impfungen: -

VAERS 980074

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038k20A

schwer

Staat: IL
Alter: 36,0
Geschlecht: F
Eingang: 16.02.2021
Impfdatum: 27.01.2021
Beginn: 27.01.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Anxiety Blood test Computerised tomogram Condition aggravated Dizziness Blood glucose normal Bruxism Dyspnoea Muscle contractions involuntary Partial seizures Dysarthria Dyskinesia Electrocardiogram normal Electroencephalogram Laboratory test normal Magnetic resonance imaging Mobility decreased Movement disorder

Symptomtext

On Jan. 27, 2021 was scheduled to have my 2nd dose of the Moderna Covid-19 Vaccine at 4:40pm at Health Clinic. The vaccine was injected on my right arm at around 4:50pm. I was then told to wait in the waiting room for 15 mins. When I walked in to the waiting room the nurse announced that there were donuts and hot chocolate for everyone. I pulled a chair from on the tables to set my coat and purse down then I went to serve myself hot chocolate and a donut. I had then went to sit down and while I was talking to my co-worker I began to feel my blood rushing to my head and felt dizzy, my eyes began to close involuntary, and then I began to start twitching and lost control of my body. My eyes and mouth shut completely but I could hear everything that was going on. Everyone at the office began to panic and someone injected me with an epipen. I was then taken by an ambulance to the nearest hospital. At the hospital I had about 5 seizure episodes, had slurred speech and was unable to move much. All they kept telling me was that I was fine. I was then discharged after running a few tests and was told that I had an anxiety attack. When I arrived home I had 3 more seizures and my husband took me to the hospital. I was then hospitalized for 4 days. There at the hospital I continued to have the same symptoms and after doing more tests everyday the doctors said that all the tests resulted normal and that they were unable to figure out what was the actual cause of all this. I was told to follow up with my PCP and with a Neurologists.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Partial seizures
Hospital-Tage: 4,0
Labordaten: Cat Scan and Blood Work on 01/27/21 at Hospital. EKG and Blood work on 01/27/21 at Hospital. EEG and Blood Work on 01/28/21 Hospital. 24 Hour EEG, MRI and blood work on 01/29/21 Hospital. Blood work on 01/30/21 Hospital.
Aktuelle Erkrankungen: Seizures and compulsions
Vorgeschichte: Asthma, hypothyroidism, and seasonal allergies
Andere Medikamente: EpiPen
Allergien: Avelox
Vorherige Impfungen: -

VAERS 980074

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

schwer

Staat: IL
Alter: 36,0
Geschlecht: F
Eingang: 16.02.2021
Impfdatum: 27.01.2021
Beginn: 27.01.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Anxiety Blood test Computerised tomogram Condition aggravated Dizziness Blood glucose normal Bruxism Dyspnoea Muscle contractions involuntary Partial seizures Dysarthria Dyskinesia Electrocardiogram normal Electroencephalogram Laboratory test normal Magnetic resonance imaging Mobility decreased Movement disorder

Symptomtext

On Jan. 27, 2021 was scheduled to have my 2nd dose of the Moderna Covid-19 Vaccine at 4:40pm at Health Clinic. The vaccine was injected on my right arm at around 4:50pm. I was then told to wait in the waiting room for 15 mins. When I walked in to the waiting room the nurse announced that there were donuts and hot chocolate for everyone. I pulled a chair from on the tables to set my coat and purse down then I went to serve myself hot chocolate and a donut. I had then went to sit down and while I was talking to my co-worker I began to feel my blood rushing to my head and felt dizzy, my eyes began to close involuntary, and then I began to start twitching and lost control of my body. My eyes and mouth shut completely but I could hear everything that was going on. Everyone at the office began to panic and someone injected me with an epipen. I was then taken by an ambulance to the nearest hospital. At the hospital I had about 5 seizure episodes, had slurred speech and was unable to move much. All they kept telling me was that I was fine. I was then discharged after running a few tests and was told that I had an anxiety attack. When I arrived home I had 3 more seizures and my husband took me to the hospital. I was then hospitalized for 4 days. There at the hospital I continued to have the same symptoms and after doing more tests everyday the doctors said that all the tests resulted normal and that they were unable to figure out what was the actual cause of all this. I was told to follow up with my PCP and with a Neurologists.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Partial seizures
Hospital-Tage: 4,0
Labordaten: Cat Scan and Blood Work on 01/27/21 at Hospital. EKG and Blood work on 01/27/21 at Hospital. EEG and Blood Work on 01/28/21 Hospital. 24 Hour EEG, MRI and blood work on 01/29/21 Hospital. Blood work on 01/30/21 Hospital.
Aktuelle Erkrankungen: Seizures and compulsions
Vorgeschichte: Asthma, hypothyroidism, and seasonal allergies
Andere Medikamente: EpiPen
Allergien: Avelox
Vorherige Impfungen: -

VAERS 1028652

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

schwer

Staat: MI
Alter: 27,0
Geschlecht: F
Eingang: 13.02.2021
Impfdatum: 12.02.2021
Beginn: 13.02.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / RA

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

Syncope Vision blurred

Symptomtext

The following morning around 7:30am, these symptoms occurred after both doses (1st dose was 1/15 at 4:30pm at same location): pounding in ears, blurred vision, and feeling like I would pass out. This happened any time I tried to sit up, for the first two hours of the day. Went away after that, but still occasionally would get pounding in ears for the next 24 hours.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: IBS
Andere Medikamente: Amitriptyline 50mg, probiotic
Allergien: Raw celery
Vorherige Impfungen: -

VAERS 1026497

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

schwer

Staat: IL
Alter: 65,0
Geschlecht: F
Eingang: 12.02.2021
Impfdatum: 02.02.2021
Beginn: 03.02.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / RA

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

Presyncope

Symptomtext

Vasovagal reaction

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: IBS
Andere Medikamente: Tamoxifen, Centrum Multi Vitamin, OsCal calcium, Zyrtec
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 1022391

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

schwer

Staat: IL
Alter: 42,0
Geschlecht: F
Eingang: 11.02.2021
Impfdatum: 10.02.2021
Beginn: 11.02.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / RA

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

Chills Dizziness Face injury Hyperhidrosis Loss of consciousness Pain in extremity

Symptomtext

MODERNA COVID-19 vaccine EUA Received first shot yesterday (2/10/21 @ 2:42pm) had chills off and on overnight and sore arm. Got up at 6:30 am today (2/11/21), used the bathroom, felt very dizzy and lightheaded, started sweating profusely, tried to make it back to bed, took 4 steps and passed out, hitting my face on dresser. This has only happened one other time, 16 years ago when I was pregnant, flying on vacation and hadn?t eaten, blood sugar dropped and I passed out momentarily. No history of fainting, not diabetic, no health issues whatsoever. Healthy weight, fit and in shape.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: No health issues
Andere Medikamente: None
Allergien: No allergies. Sensitivity to darvoset and pergoset, makes me sick
Vorherige Impfungen: -

VAERS 1016123

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

schwer

Staat: IN
Alter: 38,0
Geschlecht: F
Eingang: 09.02.2021
Impfdatum: 07.02.2021
Beginn: 08.02.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / LA

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

Arthralgia Chills Decreased appetite Epistaxis Fatigue Headache Injection site urticaria Pain Pyrexia Thrombosis

Symptomtext

Day after (2/8/21): Severe chills, tiredness, body aches, headache, loss of appetite, fever (101.4), bloody nose w/blood clots (left nostril only). 2 days after (2/9/21): Intermittent headache, aches in joints, bloody nose w/blood clots (left nostril only), hive around injection site.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Not applicable
Vorgeschichte: Breast Cancer Survivor
Andere Medikamente: Anastrozole
Allergien: Not applicable
Vorherige Impfungen: -

VAERS 1009827

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038k20a

schwer

Staat: MI
Alter: 28,0
Geschlecht: M
Eingang: 07.02.2021
Impfdatum: 04.02.2021
Beginn: 06.02.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: IM / LA

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

Catheterisation cardiac Chest pain Echocardiogram Electrocardiogram abnormal Laboratory test Magnetic resonance imaging Pericarditis Troponin increased X-ray

Symptomtext

Chest pain- pericarditis. Elevated troponin. Heart cath. PCU hospital admit. No previous heart hx. Ekg abnormal. Echo, mri.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: 2,0
Labordaten: Heart cath, labs. Echo, mri X-ray ekg
Aktuelle Erkrankungen: Nasal congestion/ cough three to four weeks prior
Vorgeschichte: Adhd; mood swings; sleep apnea
Andere Medikamente: Concerta , abilify, clonidine
Allergien: None
Vorherige Impfungen: -

VAERS 1005208

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038k20a

schwer

Staat: IL
Alter: 25,0
Geschlecht: F
Eingang: 05.02.2021
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: ja Erholt: ja

Adverse event Blood test normal Chest X-ray normal Dizziness Electrocardiogram Loss of consciousness Malaise Nausea Pregnancy test negative Vital signs measurement Vomiting

Symptomtext

10:50 am: received vaccination, no adverse events immediately afterwards, went back to work. 9pm: felt ill, took temp., temp was 98.6. Then felt nauseous, went to the bathroom to vomit. Felt faint, sat with head between legs for 1 minute, then passed out on the floor. Woke up 30 seconds later and vomited. Still felt lightheaded 10 minutes after adverse event. Called EMS and went to Emergency Room.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: In Emergency room: All bloodwork was normal, negative pregnancy test, vitals signs within normal limits, normal chest x-ray. EKG was abnormal, with flipped T waves. Repeat EKG was also abnormal, persistent flipped T waves. ER doctor recommends I see a cardiologist.
Aktuelle Erkrankungen: none in the past month (but had COVID-19 in November 2020)
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1005088

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

schwer

Staat: IL
Alter: 49,0
Geschlecht: F
Eingang: 05.02.2021
Impfdatum: 27.01.2021
Beginn: 28.01.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / RA

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

Bell's palsy Chills Headache Lymphadenopathy Nausea Pain Pyrexia Swelling face

Symptomtext

Day 1:Swelling on left side of face, swollen lymph nodes, chills, fever, body ache, headache; Day 2:extreme headache, nausea; Day 3:headache; Day 4:headache; Day 5: Doctor diagnosed with acute Bell's Palsy.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: Doctor appointment on February 1st. Diagnosed with acute Bell's Palsy.
Aktuelle Erkrankungen: NONE
Vorgeschichte: NONE
Andere Medikamente: NONE
Allergien: NONE
Vorherige Impfungen: -

VAERS 1004913

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

schwer

Staat: VT
Alter: 21,0
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: ja Erholt: nein

Dizziness Seizure Tachycardia Tremor

Symptomtext

After receiving vaccine, Employee complained of tachycardia (P=100), some dizziness. Employee drank water and juice. Employee appeared like she might vomit and started shaking, employee was lifted from her chair to the floor. Employee was turned to her right side and was having a seizure. CODE Team was called and Employee was taken to Emergency room via stretcher.

Weitere VAERSDATA-Felder

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

VAERS 1002484

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

schwer

Staat: MI
Alter: 77,0
Geschlecht: F
Eingang: 04.02.2021
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: ja

Postictal paralysis Seizure

Symptomtext

Pt has a hx of seizure disorder. Vaccine given at 0942. Seizure started at approximately 0944 and lasted until 0948. Patient was unable to converse- was attempting. It lasted approximately 4-5 minutes. Her partner was with us and assured us she was okay and did not need medical tx. She states vaccines can "sometimes shock system" but it had been a long time since she had a seizure. Second seizure occurred at 10:10 and occurred for approximately 3 minutes. Patient states she took her medication: Lamictal 150mg BID for her seizures. Partner states that seizures can be normal for her and declined need for ambulance.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Postictal paralysis
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: No known
Vorgeschichte: Hx of Seizure Disorder
Andere Medikamente: Lamictal 150 mg BID
Allergien: No known
Vorherige Impfungen: -

VAERS 998224

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

schwer

Staat: IL
Alter: 28,0
Geschlecht: F
Eingang: 03.02.2021
Impfdatum: 25.01.2021
Beginn: 25.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Abdominal pain upper Anaphylactic reaction Asthma Chest discomfort Chills Cough Diarrhoea Dizziness Dyspnoea Feeling abnormal Headache Malaise Nausea Pyrexia Throat tightness Toothache Vomiting

Symptomtext

Anaphylaxis. Epi Pen given and ambulance called. Given anaphylaxis cocktail in ER. 2:30pm: Vaccine administered 3:30pm: Headache & teeth ache which continued 7:00pm asthmatic cough which continued throughout 11:00pm fever and chills 9:00am felt generally very ill--stomach pain (more anaphylactic type pain) 10:00am nausea, severe stomach pain, diarreaha, vomiting, lungs very tight, continued coughing 11:00am excruciating stomach pain (stomach on fire) Throat felt "thick", feeling faint, brain fog, dizzy (These are my typical anaphylactic reactions) Epi pen administered & ambulance called Anaphylaxis symptoms returned in ER. The pain was the worst since my bowel obstructions several years ago.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: mast cell activation syndrome oral allergy syndrome Hashimoto's thyroiditis hydradenitis supperativa psoriasis/ eczema depression/anxiety
Andere Medikamente: synthroid vitamin D claritin iron supplement montelukast clindamiacin topical lexapro prazosin lamictal
Allergien: Food: banana, kiwi, avocado, strawberry, sesame, hazelnut, macadamia nuts, Drugs: biaxin
Vorherige Impfungen: -

VAERS 996026

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

schwer

Staat: MI
Alter: 80,0
Geschlecht: F
Eingang: 02.02.2021
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: ja Erholt: nein

Chest discomfort Dyspnoea Syncope

Symptomtext

pt c/o chest tightness, hx of chest in last week, took 1 nitro glycerine , appeared to faint with heavy breaths. 1505 bp 130/80, p76,o2sat 97% became diaphoretic nauseated , threw up ,became more alert 911 called O2 applied 1520 bp118/74 p61 o2sat 96% Ambulance arrived transport to ED

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: hx of cardiac disease with 4 stents and recent Emeregency Room visit for chestpain
Vorgeschichte: Cardiac
Andere Medikamente: unknown
Allergien: LEVAQUIN
Vorherige Impfungen: -

VAERS 994848

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

schwer

Staat: IL
Alter: 60,0
Geschlecht: M
Eingang: 02.02.2021
Impfdatum: 01.02.2021
Beginn: 02.02.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / RA

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

Fatigue Pain in extremity Syncope

Symptomtext

sore arm, fatique, fainting

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: hypoglycemia
Andere Medikamente: dutasteride, finasteride
Allergien: none
Vorherige Impfungen: -

VAERS 994507

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

schwer

Staat: IL
Alter: 41,0
Geschlecht: F
Eingang: 02.02.2021
Impfdatum: 01.02.2021
Beginn: 02.02.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Asthenia Chills Headache Loss of consciousness Mydriasis Nausea Pain Vomiting

Symptomtext

Severe headache during the day after vaccine given. Then around midnight , woke up with extreme chills, body aches, weakness, nausea.. Got up to go to bathroom to throw up, at this time my husband was with me and when I got to bathroom, I passed out. He was holding me, stated my eyes were open and pupils very dilated. He had to wake me out if it (maybe just under 1 min) When I woke up, I vomited a little. Then until about 4 am I continued to have extreme chills, body aches and threw up a few more times. Still currently (9:30 am) feeling very weak and have a bad headache .

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Ibuprofen 600mg taken before vaccine.
Allergien: None
Vorherige Impfungen: -

VAERS 991187

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

schwer

Staat: IL
Alter: 63,0
Geschlecht: F
Eingang: 01.02.2021
Impfdatum: 28.01.2021
Beginn: 28.01.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Anaphylactic reaction Dyspnoea Peripheral swelling Swelling Urticaria

Symptomtext

Developed hives within 2 hrs/took Benadryl that night; swelling that traveled up the arm and neck in the morning with shortness of breath/used rescue inhaler at 0400 and then again at 0800; and then anaphylaxis by 0900. Treated in ED with EpiPen then IV Solumedrol, Benadryl and Famotidine. Recovered and started on prednisone taper pack starting at 6 tabs for 3 days etc. Suggested to make follow up Dr appt for one week following incident/set for Feb 8

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: B/P=250/210 when first arriving at ED, B/P was 156/78 when leaving ED with HR at 125
Aktuelle Erkrankungen: Severe reaction to this years flu shot end of October: Fever 103.4 for 4 days which started 3 days after receiving the vaccine-2 Neg COVID tests during that time period
Vorgeschichte: asthma, allergies, OA, elevated cholesterol, GERD
Andere Medikamente: Zyrtek, Omeprazole, Zetia, Aleve, Singular
Allergien: Cantaloupe, Lilium Candidum (Lilies), Macadamia Nut, Ragweed, Codeine, Poison Ivy, and intolerance to Statins
Vorherige Impfungen: Extreme immune response this past OCT after this year's flu vaccine. Elevated fever of 103.4 for 4 days

VAERS 987386

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

schwer

Staat: -
Alter: 70,0
Geschlecht: F
Eingang: 29.01.2021
Impfdatum: 29.01.2021
Beginn: 29.01.2021
Tage bis Beginn: 0,0
Dosis: 6
Route/Site: IM / RA

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

Flushing Hyperhidrosis Muscular weakness Presyncope Tremor

Symptomtext

pt was vaccinated with no reported issues. pt waited required 15 minutes in pharmacy area with no reported issues. when pt sat up from chair and began walking to care they experienced the following: tremors, flushing, sweating, near fainting like symptoms, muscle weakness. symptoms lasted approximately 5-10 minutes and were resolved completely after given cold water and after sitting for an extra 15 minutes.

Weitere VAERSDATA-Felder

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

VAERS 986911

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

schwer

Staat: IL
Alter: 57,0
Geschlecht: F
Eingang: 29.01.2021
Impfdatum: 25.01.2021
Beginn: 25.01.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

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

Chills Dizziness Headache Hyperhidrosis Loss of consciousness Nausea Pyrexia

Symptomtext

"Moderna COVID-19 Vaccine EUA". I started with dizziness around 2pm. 9pm started extreme chills, teeth chattering. 1am nausea, sweating profusely, headache. 4:30 am worse headache, light headed, passed out on kitchen floor. Woke up around 1pm on Tuesday and temp was 37.8. Took Ibuprofen for h/a and fever once my stomach felt better. Headache remained until Weds am. I felt great today (Friday).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Preservision 2x/dly, Fish Oil 1200mg dly, Vitamin C 500mg dly, Magnesium 250mg dly. No prescription meds.
Allergien: N/A
Vorherige Impfungen: -

VAERS 985164

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

schwer

Staat: IL
Alter: 49,0
Geschlecht: F
Eingang: 29.01.2021
Impfdatum: 27.01.2021
Beginn: 27.01.2021
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 Chest pain Dizziness Nausea Pharyngeal swelling Vomiting

Symptomtext

Presented to ED @ 0815 (approx 45 mins after 2nd Moderna vaccine) c.o. dizziness, N/V, chest pain. Patient reports throat swelling although no obvious facial/throat swelling on exam, no wheezing. Treated as anaphylaxis. Temp 36.2, BP 186/103, HR 70, RR 24, O2 sat 99. Benadryl 50mg IV, Epinephrine 0.5mg IM, Pepcid 20mg IV, Zofran 4mg IV, Solu-Medrol 125mg IV, Tylenol 1000mg po, 1L NS IV bolus. H/o covid infection ~ 3 months ago, now recovered from COVID PNA as well.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: no known allergies
Vorherige Impfungen: -

VAERS 979465

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

schwer

Staat: NY
Alter: 73,0
Geschlecht: F
Eingang: 27.01.2021
Impfdatum: 25.01.2021
Beginn: 25.01.2021
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 lactic acid increased Chills Dizziness Fall Head injury Injection site pain Nausea Pyrexia Syncope

Symptomtext

Injection site pain, Nausea, light headed same day (1/25//2021) after injection. That evening, Nausea, fever and chills. Took Tylenol. Next day (1/26/2021) Nausea, fever and chills continued. On 1/27/2021 in the morning became faint and weak and fell or fainted. Due to fall hit her head. Daughter living in same house treated her with Ice Pack and brought her to Hospital ER for evaluation. Hospital identified fever and began antibiotic treatment and fluids.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: 1,0
Labordaten: Lactic Acid high. Injection site soar. Plan: Antibiotics, Fluids and observe for 24 hours. Plan to release next day.
Aktuelle Erkrankungen: None
Vorgeschichte: Post Bypass, HTN, Diabetes
Andere Medikamente: Metoprolol, Metformin, Lisinopril, Aspirin 81mg, Lovastatin, Vitamin D 2000IU
Allergien: None
Vorherige Impfungen: -

VAERS 977309

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

schwer

Staat: IL
Alter: 48,0
Geschlecht: F
Eingang: 27.01.2021
Impfdatum: 27.01.2021
Beginn: 27.01.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Electrocardiogram Metabolic function test Syncope

Symptomtext

Pt fainted after 5 minutes in receiving the vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: EKG, bloodwork, ER MD exam.
Aktuelle Erkrankungen: -
Vorgeschichte: thyroid removed due to cancer, appendectomy, rotator cuff repair.
Andere Medikamente: Synthroid/Vit C/Vit D3, magnesium
Allergien: dilaudid - rash
Vorherige Impfungen: -

VAERS 2676539

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: FL
Alter: 80,0
Geschlecht: F
Eingang: 25.08.2023
Impfdatum: 27.02.2021
Beginn: 24.08.2023
Tage bis Beginn: 908,0
Dosis: 1
Route/Site: - / -

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

COVID-19 Pneumonia

Symptomtext

Pneumonia due to infectious organism, unspecified laterality, unspecified part of lung (POA: Yes) COVID-19 infection with not requiring oxygen. Continues azithromycin IV/ceftriaxone IV

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pneumonia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Coronary artery disease Congestive heart failure Atrial flutter Diabetes mellitus Hypertension
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2673533

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: FL
Alter: 71,0
Geschlecht: F
Eingang: 18.08.2023
Impfdatum: 29.11.2021
Beginn: 01.07.2023
Tage bis Beginn: 579,0
Dosis: 1
Route/Site: IM / -

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

Cough Dyspnoea Pyrexia

Symptomtext

038K20A 2/3/2021 031M20A 3/3/2021 058H21A 11/29/2021 past medical history significant for hypertension and hyperlipidemia presented to emergency room complain of fever cough associated shortness of breath 3on oxygen support via nasal cannula started on Decadron IV patient offered remdesivir but she declined the offer she also treated with ceftriaxone IV as well as azithromycin IV

Weitere VAERSDATA-Felder

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

VAERS 2616040

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: MI
Alter: 68,0
Geschlecht: M
Eingang: 17.04.2023
Impfdatum: 08.12.2021
Beginn: 13.04.2023
Tage bis Beginn: 491,0
Dosis: 1
Route/Site: - / -

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

Aspiration pleural cavity Bacterial test COVID-19 Chest pain Computerised tomogram thorax abnormal Dyspnoea Exposure to SARS-CoV-2 Gram stain Hypoxia Malaise Oxygen saturation decreased Pleural effusion Pulmonary mass SARS-CoV-2 test positive

Symptomtext

Brief Summary of Hospital Stay: (Include Significant Findings and Invasive Procedures) Patient is a 69 year old male with significant smoking history, who recently had CT which showed RIGHT lung nodule concerning for cancer. Repeat scan showed the nodule was decreased in size significantly, however did show large LEFT pleural effusion, causing patient chest pain and dyspnea. Patient admitted for further workup and management COVID positive by PCR, also reports that he was positive at home in late March, son had moderate symptoms and tested positive; patient tested after this result. He had minimal symptoms at onset. Was noted to be slightly hypoxic on room air, to 89%. Was placed on 2L oxygen, and was weaned off. During home O2 eval patient did desat to 89% on day of discharge, but had no symptoms of dyspnea or chest pain. Discharged home without O2 (88% cutoff used). Thoracentesis performed, positive Light's criteria. No malignant cells seen, potentially parapneumonic effusion based on COVID infection. However with recent imaging, unable to rule out malignant effusion. Given loculated nature of effusion prescribed antibiotics for three weeks. Gram stain with bacteria but culture did not result with anything. Recommend repeat imaging with PCP, for effusion as well as for lung nodule. Chronic issues including hypertension, hyperlipidemia, GERD treated with home medications. Stable on discharge Issues Requiring Follow Up: (Who, what, when, and how communicated?) Right lung nodule on CT imaging Loculated effusion may require follow up imaging as well to ensure resolution

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 3,0
Labordaten: COVID positive PCR 4/13/2023
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2616040

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: MI
Alter: 68,0
Geschlecht: M
Eingang: 17.04.2023
Impfdatum: 08.12.2021
Beginn: 13.04.2023
Tage bis Beginn: 491,0
Dosis: 2
Route/Site: - / -

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

Aspiration pleural cavity Bacterial test COVID-19 Chest pain Computerised tomogram thorax abnormal Dyspnoea Exposure to SARS-CoV-2 Gram stain Hypoxia Malaise Oxygen saturation decreased Pleural effusion Pulmonary mass SARS-CoV-2 test positive

Symptomtext

Brief Summary of Hospital Stay: (Include Significant Findings and Invasive Procedures) Patient is a 69 year old male with significant smoking history, who recently had CT which showed RIGHT lung nodule concerning for cancer. Repeat scan showed the nodule was decreased in size significantly, however did show large LEFT pleural effusion, causing patient chest pain and dyspnea. Patient admitted for further workup and management COVID positive by PCR, also reports that he was positive at home in late March, son had moderate symptoms and tested positive; patient tested after this result. He had minimal symptoms at onset. Was noted to be slightly hypoxic on room air, to 89%. Was placed on 2L oxygen, and was weaned off. During home O2 eval patient did desat to 89% on day of discharge, but had no symptoms of dyspnea or chest pain. Discharged home without O2 (88% cutoff used). Thoracentesis performed, positive Light's criteria. No malignant cells seen, potentially parapneumonic effusion based on COVID infection. However with recent imaging, unable to rule out malignant effusion. Given loculated nature of effusion prescribed antibiotics for three weeks. Gram stain with bacteria but culture did not result with anything. Recommend repeat imaging with PCP, for effusion as well as for lung nodule. Chronic issues including hypertension, hyperlipidemia, GERD treated with home medications. Stable on discharge Issues Requiring Follow Up: (Who, what, when, and how communicated?) Right lung nodule on CT imaging Loculated effusion may require follow up imaging as well to ensure resolution

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 3,0
Labordaten: COVID positive PCR 4/13/2023
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2592410

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: MI
Alter: 80,0
Geschlecht: M
Eingang: 07.03.2023
Impfdatum: 03.11.2022
Beginn: 05.03.2023
Tage bis Beginn: 122,0
Dosis: 1
Route/Site: - / -

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

COVID-19 Dyspnoea Fatigue Heart rate increased Pneumonia SARS-CoV-2 test positive

Symptomtext

Pt transferred from a local Hospital due to fatigue and increased heart rate and shortness of breath. Pt tested positive for COVID and was found to have pneumonia and was transferred. He has a PMH of CAD s/p multiple cardiovascular stents, CHF, and liver cirrhosis.

Weitere VAERSDATA-Felder

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

VAERS 2586894

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: MI
Alter: 77,0
Geschlecht: M
Eingang: 24.02.2023
Impfdatum: 02.06.2022
Beginn: 26.12.2022
Tage bis Beginn: 207,0
Dosis: 1
Route/Site: - / -

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

Acute kidney injury Blood pressure increased COVID-19 Drug level Dyspnoea Glomerular filtration rate decreased Metabolic function test Nausea Peripheral vascular disorder Pyrexia SARS-CoV-2 test positive Vomiting

Symptomtext

"Patient with 4 COVID vaccines who admitted with COVID detected PCR. Provider d/c note: ""Hospital Course: No notes on file These were his acute medical issues addressed: 1. Intractable N/V. -- may have been a viral gastroenteritis vs COVID infection. -- resolved with supportive care. -- tolerating a full diet at discharge. 2. COVID-19 patient; Vaccinated x 2 (Moderna); NOT boosted. -- No fever, cough, SOB or hypoxia. 3. CKD-3 baseline GFR in the 20's. -- sl decreased GFR into the teens after presenting symptoms. -- needs repeat BMP next week. -- did resume ARB at discharge. 4. AKI due to #1 -- ARB held this hospitalization, but continued at discharge as BP was rising. 5. Kidney transplant patient (Cadaveric- 2004). 6. Chronically immunosuppressed from #5 (Prednisone/ Cellcept/ Tacrolimus). -- Tacrolimus levels WNL. 7. HTN -- ARB resumed at discharge. 8. PVD DC home in stable condition. To return to ED is +fever/ SOB/ difficulty breathing, or any untoward symptom."

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 2,0
Labordaten: COVID detected PCR 12/27/2022
Aktuelle Erkrankungen: -
Vorgeschichte: Kidney transplant status, cadaveric Common iliac aneurysm (HCC) Benign localized prostatic hyperplasia with lower urinary tract symptoms (LUTS) Hypertension CKD/AV Access Urge incontinence Aneurysm of infrarenal abdominal aorta CKD (chronic kidney disease) stage 4, GFR 15-29 ml/min (HCC) Arthritis Dyslipidemia Cerebral infarction (HCC) Other chest pain General weakness Immunocompromised (HCC) Anemia Rising PSA level Secondary hyperparathyroidism (HCC) GERD (gastroesophageal reflux disease) History of GI bleed Hypertensive nephrosclerosis Immunosuppressive management encounter following kidney transplant Nephrotic syndrome Peptic ulcer disease Vitamin D deficiency Lung nodule Adenomatous polyp of transverse colon Cognitive impairment Polyneuropathy associated with underlying disease (HCC)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2581663

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: FL
Alter: 76,0
Geschlecht: M
Eingang: 14.02.2023
Impfdatum: 16.12.2022
Beginn: 20.01.2023
Tage bis Beginn: 35,0
Dosis: 1
Route/Site: IM / -

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

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

Symptomtext

Hospitalization: 1/5/2023 - 1/20/2023 (15 days) Presentation to the ED: upper chest pain COVID + date: 1/20/2023. Treatment: none, patient was discovered positive on a transfer screen to ltcf placement. Discharge to: SNF 038K20A 2/5/2021 025A21A 3/5/2021 017F21A 10/27/2021 001M21A 4/14/2022 Moderna Bivalent AS7168B 12/16/2022

Weitere VAERSDATA-Felder

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

VAERS 2566712

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: MI
Alter: 91,0
Geschlecht: M
Eingang: 24.01.2023
Impfdatum: 18.11.2021
Beginn: 24.12.2022
Tage bis Beginn: 401,0
Dosis: 1
Route/Site: - / -

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

COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

12/24/22 presents to ED for "SOB". PMHx of "thrombocytopenia, hyperlipidemia, and hypertension"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 12/24/22 SARS-CoV-2 (COVID-19) detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2555823

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: MI
Alter: 88,0
Geschlecht: F
Eingang: 10.01.2023
Impfdatum: 05.02.2021
Beginn: 26.11.2022
Tage bis Beginn: 659,0
Dosis: 1
Route/Site: - / -

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

Chest pain Cough

Symptomtext

11/26/22 presents to ED for "cough, chest pain". PMHx of "MCI, urinary incontinence, HTN and CKD 3b"

Weitere VAERSDATA-Felder

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

VAERS 2537836

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: FL
Alter: 76,0
Geschlecht: F
Eingang: 20.12.2022
Impfdatum: 04.11.2021
Beginn: 21.11.2022
Tage bis Beginn: 382,0
Dosis: 1
Route/Site: IM / -

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

COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

Hospitalization: 11/21/2022 - 11/29/2022 Presentation to the ED: COVID POSITIVE 1 WEEK BEFORE ARRIVING TO ED, INCREASING SHORTNESS OF BREATH. COVID + date: 11/21/2022 Treatment: 5 days of remdesivir. Discharge to: Inpatient Rehab Facility. MODERNA LOT#038K20A 1/30/2021 MODERNA LOT#031M20A 2/26/2021 MODERNA LOT#050E21A 11/4/2021

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: hypertension, hyperlipidemia, depression, anxiety, insomnia, osteoarthritis and rheumatoid arthritis
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2529913

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: MI
Alter: 77,0
Geschlecht: M
Eingang: 13.12.2022
Impfdatum: 03.03.2021
Beginn: 20.11.2022
Tage bis Beginn: 627,0
Dosis: 1
Route/Site: - / -

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

COVID-19 Mental status changes Pneumonia SARS-CoV-2 test positive

Symptomtext

Patient with history of 3 COVID vaccines who admitted with altered mental status and pneumonia. COVID test initially "not detected" upon admission on 11/20/22. Retesting on 11/29/22 resulted detected. Issues resolved and patient d/c back to facility.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pneumonia
Hospital-Tage: 17,0
Labordaten: COVID Detected PCR on 11/29/2022
Aktuelle Erkrankungen: -
Vorgeschichte: Cardiovascular Essential hypertension PAF (paroxysmal atrial fibrillation) Chronic systolic (congestive) heart failure Hyperlipidemia Digestive Dysphagia Psychological Anxiety and depression Vascular dementia Respiratory History of adenicarcinoma of rigtht lung Allergic rhinitis Other BPH (benign prostatic hyperplasia) History of stroke Anxiety state Constipation ED (erectile dysfunction) Insomnia Prediabetes Spinal stenosis of lumbar region without neurogenic claudication Mediastinal adenopathy Hip pain, left Alcohol use Sepsis due to Enterobacter species QT prolongation COVID-19 virus infection
Andere Medikamente: -
Allergien: Codeine PhosphateHallucination Effexor [Venlafaxine]Diarrhea GabapentinUnknown Lipitor [Atorvastatin] NortriptylineOther (See Comments) Simvastatin Wellbutrin [Bupropion Hcl]
Vorherige Impfungen: -

VAERS 2525361

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038k20a

moderat

Staat: MI
Alter: 69,0
Geschlecht: F
Eingang: 07.12.2022
Impfdatum: 20.02.2021
Beginn: 06.12.2022
Tage bis Beginn: 654,0
Dosis: 2
Route/Site: IM / -

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

Blood test normal Brain natriuretic peptide increased COVID-19 Cardiac failure congestive Catheterisation cardiac abnormal Condition aggravated Dyspnoea Dyspnoea exertional Dyspnoea paroxysmal nocturnal Ejection fraction decreased Electrocardiogram normal Laboratory test Orthopnoea Patent ductus arteriosus SARS-CoV-2 test positive Troponin Weight increased

Symptomtext

Patient is nontoxic-appearing 70-year-old female with a history of coronary artery disease and CHF with a LifeVest on and recent heart catheterization at the end of November with patent vessels and a EF of 20 to 25% presents the emergency department ambulatory for shortness of breath. Patient states that is gotten worse over the last 24 hours. She denies any productive cough. She has no leg swelling however states that she normally does not get leg swelling whenever she puts on water weight. Yesterday she weighed 170 pounds this morning she was 178. Denies any chest pain. No fevers. Associated Symptoms: orthopnea, paraoxysmal nocturnal dyspnea, shortness of breath

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 2,0
Labordaten: o ED Clinical Course Patient was seen immediately on arrival to the emergency department and plan of care was discussed with the patient. Patient will have an IV established blood work will be obtained will lock the IV due to her history of fluid overload. EKG reviewed as above nonischemic. We will plan for chest x-ray. She is saturating 96% on room air however has marked dyspnea on exertion and conversation. This does improve at rest. Laboratory studies are reviewed. Patient's troponin is 0.06. BNP is markedly elevated in the 4000's. Last BNP was 1200. COVID test is positive. Remainder of blood work is unremarkable. Patient had a recent heart catheterization within the last 2 weeks. This showed patent vessels. I did I discussed the case with Dr. who graciously accepts this admission for CHF exacerbation. Admitting diagnosis CHF exacerbation COVID-19
Aktuelle Erkrankungen: unknown
Vorgeschichte: CHF, DM, HTN, CAD
Andere Medikamente: unknown
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2497647

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: MI
Alter: 86,0
Geschlecht: F
Eingang: 03.11.2022
Impfdatum: 29.03.2021
Beginn: 02.11.2022
Tage bis Beginn: 583,0
Dosis: 1
Route/Site: SYR / UN

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

Brain natriuretic peptide increased COVID-19 Chest X-ray normal Cough Dyspnoea Dyspnoea exertional Fatigue Hypoxia Oxygen saturation decreased Respiratory symptom SARS-CoV-2 test positive Troponin normal Wheezing White blood cell count decreased

Symptomtext

Patient is an 89-year-old female with an extensive past medical history that includes but is not limited to hypertension, high cholesterol, type 2 diabetes and GERD who presents to the emergency department with complaint of shortness of breath and a positive test for COVID yesterday. Patient is not the best historian is difficult to get information out of her she basically says she has been having trouble breathing off and on over the entire summer but she was getting worse a few days ago family had her take a COVID test at home and it came back positive. Reports shortness of breath nonproductive cough wheezing and exertional dyspnea. Nursing staff reports to me that the patient ambulating from her car to the hospital bed her oxygen saturation fell to 85%. They placed her on supplemental O2 before my exam. Patient denies any history of asthma or COPD but per nursing staff she has a nebulizer at home. Associated Symptoms: cough, fatigue, shortness of breath, URI symptoms, wheezing

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 2,0
Labordaten: Patient's BNP is elevated, however chest x-ray does not appear to be consistent with congestive heart failure her troponin is normal. Her white blood cell count is only 4.6 which is consistent with COVID which she tested positive for. She has been hypoxemic here she is dropped her sats down to 85% so she required supplemental oxygen since she is requiring supplemental oxygen I gave her Decadron 6 mg IV and a aerosol treatment.
Aktuelle Erkrankungen: unknown
Vorgeschichte: DM COPD Obesity HTN Depression GERD
Andere Medikamente: Current Home Medications 1. ALPRAZolam 0.25 mg oral tablet : 1 tab(s) orally 2 times a day 2. aspirin 81 mg oral tablet : 1 tab(s) orally once a day 3. Centrum Silver oral tablet : 1 tab(s) orally once a day 4. cetirizine 10 mg oral tablet
Allergien: Allergy: - codeine; (Drug) Other See Desc - morphine; (Drug) Itching - sulfa drugs; (Drug Category) Hives - sulfamethoxazole; (Drug) Itching
Vorherige Impfungen: -

VAERS 2493906

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: MI
Alter: 84,0
Geschlecht: M
Eingang: 31.10.2022
Impfdatum: 12.11.2021
Beginn: 24.10.2022
Tage bis Beginn: 346,0
Dosis: 1
Route/Site: SYR / UN

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

Asthenia Atrial fibrillation Atrial flutter COVID-19 Cough Dyspnoea Dyspnoea exertional Fatigue Fibrin D dimer increased Hypoxia Laboratory test Mobility decreased Oxygen saturation decreased Respiratory symptom SARS-CoV-2 test positive Tachycardia

Symptomtext

Chief Complaint: COVID-positive/generalized weakness/shortness of breath Additional Medical History: Patient is an 85-year-old male with a history of coronary artery disease with prior MI, congestive heart failure, atrial fibrillation, hypertension, COPD (normally requires 4 L of oxygen 24 hours a day), prior stroke, seizures and anxiety. Patient tested positive for COVID 9 days ago. He tested positive after other family members tested positive and he developed some upper respiratory type symptoms. I saw this patient 6 days ago in the emergency room for some generalized fatigue and worsening cough with shortness of breath. He had a full work-up at that time and was on Paxlovid. He felt better and was ultimately discharged home on steroids. Patient states he did really well for couple of days however over the last 3 to 4 days has continued to become weaker and weaker and feel more short of breath with a worsening cough. Patient states he is having a very difficult time getting around his house and normally would be able to do so without any difficulty. He lives at home with his wife. He has also required increased oxygen at 6 L up from his normal 4 L. Patient states every time he attempts to get up or walk around his oxygen saturations fall into the high 80s. He denies any associated chest pain. Denies fever or chills. His main complaint at this time is weakness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 2,0
Labordaten: Patient is an 85-year-old male with a history of advanced COPD on 4 L nasal cannula at home the patient also have history of coronary artery disease with prior MI, congestive heart failure, atrial fibrillation, hypertension, prior stroke, seizures and anxiety. Patient tested positive for COVID 9 days ago. He tested positive after other family members tested positive and he developed some upper respiratory symptoms. The patient was seen in this emergency room but he was not admitted. He finished a full course of Paxlovid this Friday. The patient also received short course of steroids. Patient states he did really well for couple of days however over the last 3 to 4 days has continued to become weaker and weaker and feel more short of breath with a worsening cough. Patient states he is having a very difficult time getting around his house and normally would be able to do so without any difficulty. He lives at home with his wife. He has also required increased oxygen at 6 L up from his normal 4 L. Patient states every time he attempts to get up or walk around his oxygen saturations fall into the high 80s. He denies any associated chest pain. Denies fever or chills. Problem 1: COVID-19 viremia Plan 1: The patient received full course of Plaxovid, steroids and he is on home oxygen. The patient is admitted with Combivent, oxygen and steroids I will add Zithromax as anti-inflammatory. The patient does have tachycardia and hypoxia his D-dimer is elevated we will rule out pulmonary embolus. Problem 2: Generalized weakness Plan 2: Most likely secondary to COVID. Add vitamin C and zinc sulfate. Physical therapy will be helpful in the next 24 to 48 hours. Problem 3: Atrial fibrillation and flutter Plan 3: His heart rate seems regular on physical exam the patient is not anticoagulated. In any case his heart rate is borderline tachycardic. Problem 4: Chronic obstructive pulmonary disease Plan 4: Heavy smoker in the past 2-3 packs/day according to his wife quit 15 years ago. Treatment as above Problem 5: DVT prophylaxis Plan 5: The patient will be on both mechanical and pharmaceutical agent.
Aktuelle Erkrankungen: -
Vorgeschichte: Afib/flutter COPD Obesity CAD HTN arthritis Depression/anxiety
Andere Medikamente: Current Home Medications 1. aspirin 81 mg oral tablet : 1 tab(s) orally once a day 2. Bystolic 10 mg oral tablet : 1 tab(s) orally once a day 3. desvenlafaxine (as base) 100 mg oral tablet, extended release : orally once a day 4. Flonase 50
Allergien: None known
Vorherige Impfungen: -

VAERS 2481623

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038k20a

moderat

Staat: FL
Alter: 74,0
Geschlecht: F
Eingang: 18.10.2022
Impfdatum: 09.04.2022
Beginn: 23.09.2022
Tage bis Beginn: 167,0
Dosis: 1
Route/Site: IM / LA

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

COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

Hospitalization: 9/23/2022 - 10/6/2022 (13 days) Presentation to the ED: SHORTNESS OF BREATH. COVID-19 + date: 9/23/22. Treatment: STEROIDS. Discharge to: SNF.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: hypertension, hyperlipidemia, diabetes mellitus type 2 with diabetic neuropathy, morbid obesity
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2473484

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: MI
Alter: 79,0
Geschlecht: M
Eingang: 10.10.2022
Impfdatum: 08.02.2021
Beginn: 05.10.2022
Tage bis Beginn: 604,0
Dosis: 1
Route/Site: - / -

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

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

Symptomtext

Pt arrived due to shortness of breath. He has a PMH of a previous stroke with aphasia. His wife is at home with COVID. He also has a cough. He was admitted due to dyspnea and COVID positivity.

Weitere VAERSDATA-Felder

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

VAERS 2419429

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: FL
Alter: -
Geschlecht: M
Eingang: 24.08.2022
Impfdatum: 19.04.2021
Beginn: 16.08.2022
Tage bis Beginn: 484,0
Dosis: 2
Route/Site: SYR / LA

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

Asthenia Cardiovascular disorder Chest pain Dizziness Dyspnoea

Symptomtext

Hospitalization: admitted 8/14/2022; discharged 8/20/2022. Presentation to the ED: chief complaint "weakness, dizziness, chest pain, and shortness of breath". Treatment: patient was treated for cardiovascular issues and placed on oxygen therapy. No documentation of COVID prophalyxis, or steroids. Discharge to home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 6,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Afib, SIRS, anemia, type 2 diabetes, raynaud's disease, thyroid cancer, hyperlipidemia, neuropathy.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2405965

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: IL
Alter: 65,0
Geschlecht: F
Eingang: 09.08.2022
Impfdatum: 23.03.2021
Beginn: 01.06.2021
Tage bis Beginn: 70,0
Dosis: 2
Route/Site: IM / RA

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

Purpura Rash Tachycardia

Symptomtext

Bilateral purpuric rash of lower legs; mild tachycardia.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tachycardia
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: none
Vorgeschichte: hypertension, hyperlipidemia, rheumatoid arthritis, osteoporosis,
Andere Medikamente: Maxide, amlodipine, rosuvastatin, prednisone, sulfasalazine, vitamin D, vitamin C, folic acid, quercetin, zinc, probiotics
Allergien: Covid vaccine
Vorherige Impfungen: -

VAERS 2403018

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: MI
Alter: 85,0
Geschlecht: M
Eingang: 05.08.2022
Impfdatum: 08.03.2021
Beginn: 19.07.2022
Tage bis Beginn: 498,0
Dosis: 1
Route/Site: - / -

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

COVID-19 Cough Dyspnoea Hypoxia Productive cough SARS-CoV-2 test positive Sputum discoloured

Symptomtext

Patient with COVID vaccines who admitted to hospital with a COVID detected test. Provider d/c note: "86 YO male with h/o ESRD on HD (MWF), DMI, HTN who is presenting to the ED for evaluation of hypoxia noted at his residence earlier today. He had an O2 sat in the 40s per chart review and EMS was called. He had a non productive cough and shortness of breath a couple of days ago and had a home COVID test taken which was found to be positive. He was initially seen in medical and transferred to hospital due to having ESRD and being on 2L NC (initially on 4LNC). He states he has some shortness of breath and cough with clear to yellow colored sputum at times. He has not missed dialysis. Denied fevers, chills, nausea, vomiting. Patient, though required supplemental oxygenation, was quickly weaned off and tolerating RA. He initially received decadron which was then stopped and home cortef was continued. Patient worked with therapy once symptom resolution occurred while receiving scheduled HD. Hospitalization was prolonged due to Covid recovery timeline required by rehabilitation. "

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 11,0
Labordaten: COVID detected PCR on 07/18/22.
Aktuelle Erkrankungen: -
Vorgeschichte: Secondary hyperparathyroidism of renal origin (Chronic) 12/5/2014 Hyperlipemia (Chronic) Diabetes mellitus (Chronic) Hypertension (Chronic) Hydronephrosis of left kidney 12/5/2014 Anemia, chronic renal failure (Chronic) 12/11/2014 ESRD (end stage renal disease) (Chronic) 12/11/2014 Pituitary adenom
Andere Medikamente: Rocalcitrol Trusopt Biofreeze Midodrine Protonix Timolol Metamucil Albuterol-ipratroprium Elavil Aspirin Lipitor Alphagan Parlodel Sensipar Mircera Florinef Flonase Cortef Venofer Synthroid Renvela Travatan
Allergien: Hydrochlorothiazide Triamterene-hydrochlorothiaziad
Vorherige Impfungen: -

VAERS 2388249

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: MI
Alter: 83,0
Geschlecht: M
Eingang: 25.07.2022
Impfdatum: 01.02.2022
Beginn: 01.07.2022
Tage bis Beginn: 150,0
Dosis: 1
Route/Site: - / -

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

Asthenia Atrial fibrillation CHA2DS2-VASc-score COVID-19 COVID-19 pneumonia Condition aggravated Dementia General physical health deterioration Haematuria Mental impairment Montreal cognitive assessment abnormal Pneumonia Pyrexia SARS-CoV-2 test positive

Symptomtext

Provider D/C note: "83-year-old male with a past medical history significant for persistent atrial fibrillation not on anticoagulation, dilated cardiomyopathy with history of have breath that was recovered, aortic stenosis, hypothyroid, hypertension, BPH and dementia who presented with weakness and fever. Patient was treated for a right lower lobe pneumonia but ultimately was found to have COVID prior to discharge. Patient defervesced and was in isolation for 10 days. Patient had no acute events and was doing well. Patient has had a recent decline per the hospital visits and a recent decline in mental status as well. Moca 2/30 was repeated this hospitalization as well the last patient has severe dementia. Patient was discharged for rehab unlikely placement. Hospital Course: COVID PNA, resolved - patient was treated with antibiotics prior to COVID(+), completed course with possible right lower lobe pneumonia - COVID positive 07/07/2022, discontinued precautions 07/17/2022 Persistent Atrial fibrillation, CHADS-VASC=5 - not on anticoagulation due to intermittent hematuria - rate controlled with metoprolol Dilated Cardiomyopathy w/ Hx of HFrEF, recovered - continue home bb, mra, ace-i - stopped home lasix as patient is euvolemic, monitor weights, can restarted patient needs. Severe Aortic Stenosis - follows with cardiology they were monitoring progression Hypothyroid - continue home levothyroxine HTN, controlled - continue ace-i BPH - continue home tamsulosin Severe Dementia with Depression, High risk delirium - seroquel nightly - sertraline, bupropion - MOCA 2/30 - Severe dementia Issues Requiring Follow Up: PCP - post hospital follow-up and to help with placement with PACE"

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 21,0
Labordaten: COVID detected PCR 07/07/22.
Aktuelle Erkrankungen: -
Vorgeschichte: Hypothyroidism Anxiety and depression Benign localized prostatic hyperplasia without lower urinary tract symptoms (LUTS) Cancer of prostate with intermediate recurrence risk (stage T2b-c or Gleason 7 or PSA 10-20) (*) HTN (hypertension) Hyperlipidemia, unspecified Hypertensive heart disease without heart failure Mitral valve disorder Nonrheumatic aortic valve stenosis Gait disorder Obesity Paroxysmal atrial fibrillation (HCC) DCM (dilated cardiomyopathy) (*) Dementia (*)
Andere Medikamente: Wellbutrin Drisdol Xalatan Synthroid Prinivil Toprol XL Miralax Seroquel Senna S Zoloft Aldactone Flomax
Allergien: Vicodin
Vorherige Impfungen: -

VAERS 2364545

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: IL
Alter: 68,0
Geschlecht: M
Eingang: 11.07.2022
Impfdatum: 09.03.2021
Beginn: 06.01.2022
Tage bis Beginn: 303,0
Dosis: 2
Route/Site: IM / -

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

Asthenia Blood creatinine increased Blood potassium decreased COVID-19 Cough Decreased appetite Dehydration Diarrhoea Dysarthria Dyspnoea Electrolyte substitution therapy Feeling cold Gait disturbance Headache Hypotension Hypoxia Inappropriate schedule of product administration Pneumonia

Symptomtext

Moderna Dose 1 2/8/21 (038K20A) Moderna Dose 2 3/9/21 (038K20A) COVID Positive 1/9/22 1/9/22: Patient is a 69-year-old male with past medical history significant for type 2 diabetes mellitus, hypertension, OSA on CPAP, CAD s/p bypass grafting, hyperlipidemia, Hx CVA with right-sided weakness, depression, hx diarrhea, obesity has come to the emergency room with complaints of cough, diarrhea and increased weakness for 3 days. Patient has dysarthric speech and at times difficult to understand. Some of the information has been gathered from the emergency room providers report and a phone call to patient's wife. Patient told me that the reason for him coming to the hospital was because of the diarrhea. He also admits to cough and shortness of breath. He is unable to contribute much to the history. Patient's wife reports that patient was at baseline assisted with a gait belt and 1 person assist to ambulate. He started having generalized weakness since Friday he also complained about headache and feeling of cold. Patient had to be put in a wheelchair for getting him to the bathroom from Friday. Patient did not have any appetite. He had nasal drainage on Friday. He started having cough yesterday and this morning he had multiple episodes of loose stools that she had to change the diapers multiple times. His wife also reports that she herself and her grandson sick and having fevers, cough and stuffy nose and sore throat that they are worried about COVID-19. Patient apparently is a vaccinated for COVID-19 with Moderna vaccine x2. He did not receive a booster dose. Patient denied any chest pain or palpitation. He denied any abdominal pain or headache at my exam. He denied any nausea or vomiting. In the emergency room patient was noted to have mild dehydration with a creatinine elevated to 1.4. Mild potassium deficiency at 3.3. Patient did not have any leukocytosis. His COVID test is pending. Patient was hypotensive in the 70s to 90s systolic while in the ER. His O2 saturations were low 90s on room air and was placed on 2 L O2 nasal cannula. He is being admitted for further management. 1/19/22: 69-year-old male with past medical history significant for type 2 diabetes mellitus, hypertension, OSA on CPAP, CAD s/p bypass grafting, hyperlipidemia, Hx CVA with right-sided weakness, depression, hx diarrhea, obesity has come to the emergency room with complaints of cough, diarrhea and increased weakness for 3 days. He tested positive for COVID-19. He is noted to have hypotension and also developed hypoxemia in the emergency room. Patient had to be started on oxygen. He was on IV pressors and IV fluids overnight in the emergency room on 1/9/22. Patient was noted to have right lung pneumonia thought to be from COVID-19 infection. Patient was started on remdesivir and IV Decadron. He was also started on azithromycin and Rocephin. He needed the multiple electrolyte replacements. He needed up to 15 L high flow oxygen on 1/9/22. His kidney function recovered with IV fluids. The patient was needing between 3-4 L of oxygen on the medical floor. Patient was vaccinated for COVID-19. Patient had positive blood cultures but the final report came back as Coag-negative staph with 2 different species. Patient was started on vancomycin which was discontinued after the repeat cultures were negative. He improved over the next few days and was the restarted back on his blood pressure meds. He was weaned from oxygen. He is s/p remdesivir. He he has complete IV Decadron as of today. Patient was accepted at a skilled nursing facility is and is planned for discharge today.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dehydration
Hospital-Tage: 11,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: DM type 2 HTN OSA CAD s/p bypass grafting HLD h/o CVA with right-sided weakness depressoin diarrhea obesity
Andere Medikamente: amantadine 100 mg PO QD aspirin 81 mg Po QD atorvastatin 80 mg PO QD calcium carbonate 500 mg PO TID PRN carvedilol 25 mg PO BIDWM clopidogrel 75 mg PO QD dextromethorphan-quinidine 20-10 mg PO Q12h doxazosin 2 mg PO QD finasteride 5 mg PO
Allergien: NKA
Vorherige Impfungen: -

VAERS 2357665

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: MI
Alter: 65,0
Geschlecht: F
Eingang: 05.07.2022
Impfdatum: 01.02.2021
Beginn: 26.06.2022
Tage bis Beginn: 510,0
Dosis: 2
Route/Site: - / -

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

Arthralgia COVID-19 Fall Musculoskeletal chest pain SARS-CoV-2 test positive

Symptomtext

6/26 67y.o. female with history of breast cancer, fibroids status post hysterectomy, presented with complaints of rib pain, left hip pain after a fall.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Musculoskeletal chest pain
Hospital-Tage: -
Labordaten: 6/26 SARS-CoV-2 by NAA, Detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2326916

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: MI
Alter: 86,0
Geschlecht: F
Eingang: 22.06.2022
Impfdatum: 02.12.2021
Beginn: 21.06.2022
Tage bis Beginn: 201,0
Dosis: 2
Route/Site: IM / UN

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

Blood creatinine increased Blood urea increased Brain natriuretic peptide increased COVID-19 Cardiac failure chronic Cardiac failure congestive Cardiomegaly Chest X-ray abnormal Dyspnoea Haemoglobin decreased Malaise SARS-CoV-2 test positive Troponin

Symptomtext

86-year-old female with a history of coronary artery disease, defibrillator/pacemaker placement, hypertension and chronic renal insufficiency was brought to the ED by an ambulance for the concern of a shortness of breath. The patient is accompanied by her neighbor. The neighbor states that the patient lives 2 blocks away from her house. The patient walked to her neighbor's house in the morning without any problem. It appears that they traveled to visit a mutual friend. The neighbor states that the patient was not "feeling well" when they left. The neighbor observed that the patient was not able to get into the car in a rest area while returning back to the home. She felt short of breath and her neighbor called for the ambulance service. The patient denied any shortness of breath when the paramedics arrived at the scene. The patient denies any specific complaint at the time of this examination. She uses 2 L of supplemental oxygen at the home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 1,0
Labordaten: The hemoglobin was low at 9.9. The creatinine was elevated at 2.0. The BUN was 63. The BNP was elevated at 1780. There was no previous lab result available for a comparison. The chest x-ray revealed a cardiomegaly. The troponin level was 0.07. The patient tested positive for the COVID-19 infection. The patient most probably had a chronic congestive heart failure. The possibility of an acute exacerbation could not be ruled out. The troponin was elevated at 0.07. Therefore, it was decided to admit the patient for observation. I discussed the case with Dr., the hospitalist on-call. The patient received Lasix 40 mg intravenously.
Aktuelle Erkrankungen: -
Vorgeschichte: CHF CAD/pacemaker HTN Renal insufficiency
Andere Medikamente: Current Home Medications 1. allopurinol 100 mg oral tablet : 1 orally once a day 2. bisoprolol 5 mg oral tablet : 1 orally once a day (at bedtime) 3. Bumex 0.5 mg oral tablet : 1 orally 2 times a day 4. calcitriol 0.25 mcg oral capsule :
Allergien: none known
Vorherige Impfungen: -

VAERS 2282939

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038k20a

moderat

Staat: IL
Alter: 61,0
Geschlecht: F
Eingang: 18.05.2022
Impfdatum: 02.11.2021
Beginn: 17.05.2022
Tage bis Beginn: 196,0
Dosis: 1
Route/Site: SYR / -

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

Dyspnoea Wheezing

Symptomtext

Patient presents to ER with SOB and wheezing.

Weitere VAERSDATA-Felder

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

VAERS 2273558

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038k20a

moderat

Staat: FL
Alter: 63,0
Geschlecht: F
Eingang: 12.05.2022
Impfdatum: 28.02.2021
Beginn: 09.05.2022
Tage bis Beginn: 435,0
Dosis: UNK
Route/Site: - / -

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

Bronchitis Dyspnoea Sepsis Wheezing

Symptomtext

Pt came to hospital with shortness of breath and wheezing. sepsis r/t bronchitits 3L of oxygen, antibiotics given and steroids.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: HTN, COPD, hyperlipidemia, ashthma
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2270894

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: -
Alter: 76,0
Geschlecht: M
Eingang: 11.05.2022
Impfdatum: 10.02.2021
Beginn: 08.02.2022
Tage bis Beginn: 363,0
Dosis: UNK
Route/Site: - / -

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

COVID-19 Hypoglycaemia Hypotension SARS-CoV-2 test positive

Symptomtext

02/08/22 presents to ED for "Hypoglycemia and hypotension". PMHx of "CAD with CABG x2 in 2009, ischemic cardiomyopathy with ICD, Paroxysmal Afib, OSA with BIPAP on oxygen atnight, COPD on 4L of home oxygen, sick sinus syndrome with pacemaker in place in 2017, CHF, Factor V Leiden, TIA, DM2, HTN, HLD and GERD with hiatal hernia, pancreatic cyst"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypotension
Hospital-Tage: -
Labordaten: 02/09/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2270812

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: -
Alter: 87,0
Geschlecht: F
Eingang: 11.05.2022
Impfdatum: 04.02.2021
Beginn: 28.02.2022
Tage bis Beginn: 389,0
Dosis: UNK
Route/Site: - / -

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

COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

02/28/22 presents to ED for "shortness of breath". PMHx of "CKD, IDDM, third degree heart block w Pacemaker"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 02/28/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2269025

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: -
Alter: 85,0
Geschlecht: F
Eingang: 10.05.2022
Impfdatum: 06.02.2021
Beginn: 05.05.2022
Tage bis Beginn: 453,0
Dosis: 1
Route/Site: IM / UN

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

COVID-19 pneumonia Dyspnoea

Symptomtext

Hospitalization for shortness of breath from COVID-19 Pneumonia on dates 5/5/2022- 5/10/2022. Treated with dexamethasone, aformoterol nebulizer BID, budesonide 0.5mg inhaled BID, Symbicort Inhaler 2 puffs BID, baricitinib 2mg PO daily, vitamin C 1,000 mg PO daily, vitamin D 25 mcg PO daily, zinc 50 mg PO daily.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: codeine, fluvastatin, sulfonamide antibiotics
Vorherige Impfungen: -

VAERS 1999681

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: MI
Alter: 81,0
Geschlecht: M
Eingang: 02.05.2022
Impfdatum: 14.01.2021
Beginn: 07.12.2021
Tage bis Beginn: 327,0
Dosis: 2
Route/Site: - / -

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

COVID-19 Dyspnoea Dyspnoea exertional SARS-CoV-2 test positive Wheezing

Symptomtext

12/07/21 presents to ED for "DOE" "labored breathing w/ wheezing". PMHx of "non-ischemic cardiomyopathy, CAD s/p CABG, asthma, TIA (2014)"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 12/07/21 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1999681

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: MI
Alter: 81,0
Geschlecht: M
Eingang: 02.05.2022
Impfdatum: 14.01.2021
Beginn: 07.12.2021
Tage bis Beginn: 327,0
Dosis: UNK
Route/Site: - / -

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

COVID-19 Dyspnoea Dyspnoea exertional SARS-CoV-2 test positive Wheezing

Symptomtext

12/07/21 presents to ED for "DOE" "labored breathing w/ wheezing". PMHx of "non-ischemic cardiomyopathy, CAD s/p CABG, asthma, TIA (2014)"

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 12/07/21 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2256704

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: MI
Alter: 92,0
Geschlecht: M
Eingang: 28.04.2022
Impfdatum: 22.12.2021
Beginn: 27.04.2022
Tage bis Beginn: 126,0
Dosis: 1
Route/Site: IM / UN

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

Asthenia C-reactive protein increased COVID-19 Comminuted fracture Computerised tomogram abnormal Computerised tomogram head normal Confusional state Cough Dehydration Dyspnoea Dyspnoea exertional Fall Gait disturbance Humerus fracture Hypophagia Impacted fracture Mental status changes Myalgia

Symptomtext

his is a 92-year-old male with a past medical history significant for coronary artery disease, DVT, GERD, subdural hemorrhage and craniotomy and cholecystectomy, who presents to the emergency department with complaints of progressive symptoms of cough, shortness of breath and altered mentation for approximately 1-1/2 days. This occurs in the setting of a recent fall. Patient was seen in the emergency department on 4/22/2022 for fall when he tripped while using his walker. The patient suffered a comminuted impacted fracture of the neck of the right humerus. Patient's radiographic studies in the emergency department on that day were x-rays of the shoulder as well as CT scans of the shoulder. He did not have any other scans of the head neck as he had denied any head injury no loss of consciousness. Patient has presently a nonproductive cough shortness of breath and increased dyspnea on exertion and per the son is more confused

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Praegender Schweregrund: Dehydration
Hospital-Tage: 1,0
Labordaten: Problem 1: COVID-19 Plan 1: Patient presents with symptoms of confusion, generalized weakness, muscle ache, poor oral intake. No shortness of breath, cough, or fever reported. Patient was vaccinated for COVID-19. Plan: -Patient has significantly elevated C-reactive protein and ESR -We will start Solu-Medrol 40 mg twice daily. -Since the patient is not requiring oxygen so far, and there is no significant cough or fever, will hold remdesivir for now. -Gentle IV fluid hydration. -Tylenol for fever. -Patient is anticoagulated with Eliquis. Problem 2: Confusion Plan 2: Secondary to COVID-19 infection, and poor hydration. CT head is negative for acute intracranial pathology. -His mental status is improving. -Gentle IV fluid hydration as above. Problem 3: Generalized weakness Plan 3: Secondary to viral infection. Hydration and pain control as above. -We will obtain OT/PT evaluation. Patient lives with his son. He might need short-term rehab. He had a recent fall with a fracture of the right humeral neck that is requiring sling for now. Problem 4: Closed fracture of right humerus Plan 4: Secondary to a fall. His son describes a mechanical fall happened at the backyard. Patient was seen by orthopedics, had CT scan that showed impacted fracture. Recommendation was to use a supporting sling and immobilization. -Optimize pain control. -OT/PT evaluation Problem 5: History of DVT (deep vein thrombosis) Plan 5: Patient is on Eliquis. We will continue during this hospitalization Problem 6: History of hypothyroidism Plan 6: Interestingly the patient is on levothyroxine and liothyronine not sure why. We will resume home medication Problem 7: Coronary artery disease without angina pectoris Plan 7: Patient has a history of coronary artery disease and 1 stent. He is on Plavix which will continue. There is no chest pain. Problem 8: OSA on CPAP Plan 8: Continue nocturnal CPAP same home settings
Aktuelle Erkrankungen: unknown
Vorgeschichte: hypothyroidism CAD/angina GERD CRF sleep apnea HTN diabetes
Andere Medikamente: Current Home Medications 1. Coenzyme Q10 200 mg oral capsule : 1 tab(s) orally once a day 2. dorzolamide-timolol 2%-0.5% preservative-free ophthalmic solution : 1 drop(s) to each affected eye 2 times a day 3. Eliquis 2.5 mg oral tablet : 1
Allergien: contrast dye
Vorherige Impfungen: -

VAERS 2247803

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: SC
Alter: 53,0
Geschlecht: F
Eingang: 22.04.2022
Impfdatum: 17.04.2021
Beginn: 01.05.2021
Tage bis Beginn: 14,0
Dosis: 2
Route/Site: SYR / RA

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

Asthma Blood test normal Chest X-ray abnormal Computerised tomogram thorax abnormal Dyspnoea Electrocardiogram abnormal Nasal operation Nasal polyps Pneumonitis

Symptomtext

In May 2021 I had more difficulty breathing than normal. I had surgery the year before on polyps in my nose. Then my breathing got so bad I had to use a nebulizer and my doctor prescribed medication for that. I started using my albuterol more. My doctor switched me to a different inhaler, and it did nothing more. I was referred to a pulmonologist. The pulmonologist switched my inhaler and it worked for a while. Then I started having more trouble again. The pulmonologist recommended I go on a biologic medicine which has not been approved by insurance yet. I was diagnosed with eosinophilic asthma.

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: CT, abnormal, inflammation in lungs. Chest x-rays, abnormal. EKG, normal, blood work, abnormal.
Aktuelle Erkrankungen: None
Vorgeschichte: Psoriatic Arthritis; Fibromyalgia; Eosinophilic; Severe Rhino sinusitis with polyps; Semperis
Andere Medikamente: Gabapentin; Symbicort Inhaler; Allegra; Zyrtec; Flonase nasal spray; turmeric; Loestrin; daily fiber pill; daily multivitamin; albuterol
Allergien: Penicillin; azithromycin; erythromycin; Cipro; Betadine
Vorherige Impfungen: -

VAERS 2237369

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: MI
Alter: 69,0
Geschlecht: M
Eingang: 16.04.2022
Impfdatum: 05.02.2021
Beginn: 05.03.2021
Tage bis Beginn: 28,0
Dosis: 1
Route/Site: OT / -

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

Fatigue Heart rate Pyrexia Tachycardia

Symptomtext

Pulse raised between 90 and 100; Fever; Fatigue; This spontaneous case was reported by a consumer and describes the occurrence of TACHYCARDIA (Pulse raised between 90 and 100), PYREXIA (Fever) and FATIGUE (Fatigue) in a 70-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 030A21A and 038K20A) for COVID-19 vaccination. The patient had no allergies, never had COVID-19 positive test or diagnosis. And patient was on diuretic therapy. The patient's past medical history included Heart disease, unspecified (Since 30 years ago and no recent change in status such as improvement or worsening) and Open heart surgery. Previously administered products included for Product used for unknown indication: INFLUENZA VACCINE. Past adverse reactions to the above products included No adverse event with INFLUENZA VACCINE. Concurrent medical conditions included Type II diabetes mellitus (Since 4 years ago and no recent change in status such as improvement or worsening) and Blood pressure high (Since 30 years ago and no recent change in status such as improvement or worsening). Concomitant products included METFORMIN and DAPAGLIFLOZIN PROPANEDIOL MONOHYDRATE (FARXIGA) for Diabetes, HYDROCHLOROTHIAZIDE for Diuretic therapy. On 05-Feb-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) (unknown route) dosage was changed to 1 dosage form. On 05-Mar-2021, the patient experienced TACHYCARDIA (Pulse raised between 90 and 100), PYREXIA (Fever) and FATIGUE (Fatigue). On 07-Mar-2021, TACHYCARDIA (Pulse raised between 90 and 100), PYREXIA (Fever) and FATIGUE (Fatigue) had resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 05-Mar-2021, Heart rate: 90 to 100 Pulse raised between 90 and 100 for 3 days. Other concomitant medication includes: Beta Blockers for an unknown indication. Patient stated that AE did not caused patient to seek medical care and the patient did not experienced similar events in the past. No treatment was given to the patient. This case was linked to MOD-2022-535597, MOD-2022-535624, MOD-2022-535625 (Patient Link).

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Praegender Schweregrund: Tachycardia
Hospital-Tage: -
Labordaten: Test Date: 20210305; Test Name: Pulse rate; Result Unstructured Data: Pulse raised between 90 and 100 for 3 days
Aktuelle Erkrankungen: Blood pressure high (Since 30 years ago and no recent change in status such as improvement or worsening); Type II diabetes mellitus (Since 4 years ago and no recent change in status such as improvement or worsening)
Vorgeschichte: Medical History/Concurrent Conditions: Heart disease, unspecified (Since 30 years ago and no recent change in status such as improvement or worsening); Open heart surgery; Comments: The patient had no allergies, never had COVID-19 positive test or diagnosis. And patient was on diuretic therapy.
Andere Medikamente: METFORMIN; FARXIGA; HYDROCHLOROTHIAZIDE
Allergien: -
Vorherige Impfungen: -

VAERS 2193779

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: MI
Alter: 53,0
Geschlecht: F
Eingang: 23.03.2022
Impfdatum: 12.03.2021
Beginn: 10.04.2021
Tage bis Beginn: 29,0
Dosis: 1
Route/Site: OT / LA

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

Eye disorder Limb mass Mobility decreased Suspected product quality issue Vaccination site inflammation

Symptomtext

At the moment, she cant lift her arm up; Surgery Doctor said that "It was a 3, 5, 6 mass and never saw something like that before"; Her eyes are getting bad now; The second shot messed up my arm/"Something was wrong with the shot",/My Doctor said that i can't get any more shots"; An hour later of receiving the second shot, my arm swallowed up like the size of a grapefruit/Arm inflammation lasted for a month; This spontaneous case was reported by a consumer and describes the occurrence of MOBILITY DECREASED (At the moment, she cant lift her arm up) and LIMB MASS (Surgery Doctor said that "It was a 3, 5, 6 mass and never saw something like that before") in a 53-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 032M20A and 038K20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included Arm operation in November 2021. Previously administered products included for COVID-19 vaccination: Moderna COVID-19 vaccine on 12-Mar-2021. Past adverse reactions to the above products included No adverse event with Moderna COVID-19 vaccine. Concurrent medical conditions included Drug allergy (Patient was allergic to Aminophylline). On 12-Mar-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 10-Apr-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 10-Apr-2021, the patient experienced VACCINATION SITE INFLAMMATION (An hour later of receiving the second shot, my arm swallowed up like the size of a grapefruit/Arm inflammation lasted for a month). On an unknown date, the patient experienced MOBILITY DECREASED (At the moment, she cant lift her arm up) (seriousness criterion disability), LIMB MASS (Surgery Doctor said that "It was a 3, 5, 6 mass and never saw something like that before") (seriousness criterion medically significant), EYE DISORDER (Her eyes are getting bad now) and SUSPECTED PRODUCT QUALITY ISSUE (The second shot messed up my arm/"Something was wrong with the shot",/My Doctor said that i can't get any more shots"). At the time of the report, MOBILITY DECREASED (At the moment, she cant lift her arm up), LIMB MASS (Surgery Doctor said that "It was a 3, 5, 6 mass and never saw something like that before"), EYE DISORDER (Her eyes are getting bad now), VACCINATION SITE INFLAMMATION (An hour later of receiving the second shot, my arm swallowed up like the size of a grapefruit/Arm inflammation lasted for a month) and SUSPECTED PRODUCT QUALITY ISSUE (The second shot messed up my arm/"Something was wrong with the shot",/My Doctor said that i can't get any more shots") outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Patient never tested positive for COVID-19 and did not receive any other vaccine within one month prior to Moderna vaccine. At the time of the vaccination, she did not have any acute or chronic illnesses and she was not taking any concomitant medication. Company Comment: This spontaneous case concerns a 53-year-old, female patient, with no relevant medical history, who experienced an unexpected, disabling, and ongoing serious event of Mobility decreased and an unexpected, medically significant serious event of Limb mass that occurred on an unspecified date after receiving dose 2 of mRNA-1273 vaccine. An hour after receiving her second dose of mRNA-1273, the patient reportedly experienced her arm swelled up to a size of a grapefruit and the inflammation lasted for a month. The patient added that she underwent an unspecified arm surgery due to a "3, 5, 6 mass" 7 months post-vaccination with dose 2 of mRNA-1273. The patient also reported that her eyes are getting bad now. The patient suspected product quality issue (The second shot messed up my arm/"Something was wrong with the shot",/My Doctor said that i can't get any more shots") with her second dose of mRNA-1273 vaccine. The benefit-risk relationship of mRNA-1273 is not affected by this report. Most recent FOLLOW-UP information incorporated above includes: On 16-Mar-2022: Live non-significant follow-up received. No new information was added.; Sender's Comments: This spontaneous case concerns a 53-year-old, female patient, with no relevant medical history, who experienced an unexpected, disabling, and ongoing serious event of Mobility decreased and an unexpected, medically significant serious event of Limb mass that occurred on an unspecified date after receiving dose 2 of mRNA-1273 vaccine. An hour after receiving her second dose of mRNA-1273, the patient reportedly experienced her arm swelled up to a size of a grapefruit and the inflammation lasted for a month. The patient added that she underwent an unspecified arm surgery due to a "3, 5, 6 mass" 7 months post-vaccination with dose 2 of mRNA-1273. The patient also reported that her eyes are getting bad now. The patient suspected product quality issue (The second shot messed up my arm/"Something was wrong with the shot",/My Doctor said that i can't get any more shots") with her second dose of mRNA-1273 vaccine. The benefit-risk relationship of mRNA-1273 is not affected by this report.

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Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Drug allergy (Patient was allergic to Aminophylline)
Vorgeschichte: Medical History/Concurrent Conditions: Arm operation
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2168084

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: NJ
Alter: 68,0
Geschlecht: F
Eingang: 09.03.2022
Impfdatum: 25.02.2021
Beginn: 19.03.2021
Tage bis Beginn: 22,0
Dosis: 2
Route/Site: SYR / LA

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

Chest X-ray normal Chest discomfort Cough Dyspnoea Electrocardiogram Fatigue SARS-CoV-2 test negative

Symptomtext

3/19/2021 for 3 days hard coughing, slight tightness of chest and tired. Drank plenty of fluids and rested. Saw doctor 3/29/21. Some coughing continued on and off after this. August 23 went to Urgent Care with trouble breathing and coughing. Put me on Predisone for 1 week, took Covid tests rapid and other - both negative. Saw general doctor 8/30 and was going to put me on Advair, but did not get approval until 9/3. Had milk protein, allergy to milk products on record, I did not take. Went to Emergency room 9/4 coughing hard and some trouble breathing. They took EKG, chest x-ray, tested for Covid rapid and other- both negative, gave me 2 nebulizar treatments and some predisone there. They sent me home on 2 weeks of predisone and to use rescue inhaler four times a day. Saw general doctor 9/17 and they put me on Flovent inhaler and to use rescue inhaler as needed. I was still using my rescue inhaler about once a day. I asked to see a plumonologist. Saw him 11/1/21. He put me on Symbicort. I saw him 12/28 and he said I could try going off if it. If after two days, I did not have trouble, but if after 2 weeks, I did, he could change it to only one type of med. I tried it and was able to go until the two weeks. I started it back up. I had my Covid booster shot 1/11/2022. I finally was able to reach my doctor to change my medicine. But I tried going off the Symbicort again and started coughing within a day. I am stilll taking the Symbicort as of now. The doctor gave me a Flovent disc inhaler with milk protein so I need to check with him on this. I had allergies before all this, but only running nose with a sinus infection once in a while. I used to have pneumonia once in a while, but not since about 1996.

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Chest x-ray showed nothing
Aktuelle Erkrankungen: -
Vorgeschichte: cad, asthma, high blood pressure, beginning of cataracts and masculardegeneration,
Andere Medikamente: 81 mg aspirin, calcium, ferrous sulfate, Alaway eye drops, magnesium, metoprolol, One-A-Day Women's 50 plus vitamins, omega 3, PreserVision AREDS-2, Flonase nasal spray, albuterol sulfate rescue inhaler
Allergien: Penicillins, atorvastatin, Sulfa (Sulfonamide antibiotics), ibandronate sodium, moxifloxacin, sulfamethoxazole, trimethoprim, cephalexin, when young allergic to milk and milk products and egg whites, allergists says I am allergic to mold, milddew and dust.
Vorherige Impfungen: -

VAERS 2124392

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: IL
Alter: 49,0
Geschlecht: F
Eingang: 18.02.2022
Impfdatum: 17.02.2021
Beginn: 01.02.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / LA

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

Blood test Colitis ulcerative Condition aggravated Stool analysis Vaccine positive rechallenge

Symptomtext

I've been in remission for ulcerative colitis for years. After taking the 1st dose, I had a flare up of the ulcerative colitis. And after the 2nd dose, I had another bad flare up that needed treatment. This has never happened to me in years. I've been taking Prednisone as treatment. I am still dealing with these flare ups.

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Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Blood test; Stool test.
Aktuelle Erkrankungen: None
Vorgeschichte: Ulcerative colitis
Andere Medikamente: Lialda Prednisone
Allergien: Latex Sulfa
Vorherige Impfungen: 1st dose of Moderna.

VAERS 2082472

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: MI
Alter: 71,0
Geschlecht: M
Eingang: 02.02.2022
Impfdatum: 03.02.2021
Beginn: 30.12.2021
Tage bis Beginn: 330,0
Dosis: UNK
Route/Site: IM / -

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

Dyspnoea

Symptomtext

Worsening DIB resulting in admission

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: 15,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Anemia, deficiency Aortic valve disorder Benign essential hypertension Dry skin End stage renal disease on dialysis Gastroesophageal reflux disease without esophagitis Keratosis Left leg weakness Lumbosacral plexopathy Peripheral arterial disease Pure hypercholesterolemia SBE (subacute bacterial endocarditis) prophylaxis candidate Stage IV adenocarcinoma of bladder Type 1 diabetes mellitus with nephropathy
Andere Medikamente: -
Allergien: Levaquin, Aspirin, Nafcillin
Vorherige Impfungen: -

VAERS 2075573

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: IL
Alter: 22,0
Geschlecht: F
Eingang: 31.01.2022
Impfdatum: 30.01.2021
Beginn: 20.12.2021
Tage bis Beginn: 324,0
Dosis: 2
Route/Site: IM / LA

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

Abdominal pain upper Ageusia Anosmia COVID-19 Malaise Migraine Nausea Pain Pyrexia SARS-CoV-2 test negative SARS-CoV-2 test positive Ultrasound abdomen

Symptomtext

On Monday December 20.2021 work through the day was fine then fever 104, body aches, migraines, stomach cramping. I called my dad cause I felt super sick. Then next day I got tested December 21, 2021 positive for Covid-19 experienced really bad nausea. I started having issues with no taste, smell on December 24,2021. I applied Vick's vapor rub that night to help with the smell. Upon me waking up on December 25, 2021 my smell had came back. On December 26, 2021 I went to retest Covid (negative) and still having nausea. I had a Ultrasound of abdomen on January 3,2022 and a follow up with Radiologist for Ultrasound of pelvis and uterus .

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Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: 2 Covid-19 (positive) (negative), Ultrasound (abdomen).
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Adderall, Liletta
Allergien: No
Vorherige Impfungen: -

VAERS 2051533

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: IL
Alter: 46,0
Geschlecht: F
Eingang: 20.01.2022
Impfdatum: 28.01.2021
Beginn: 06.01.2022
Tage bis Beginn: 343,0
Dosis: 1
Route/Site: IM / LA

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

Angiogram pulmonary abnormal COVID-19 COVID-19 pneumonia Lung disorder Lung opacity SARS-CoV-2 test positive

Symptomtext

Received Moderna vaccine on 01/28/21 and 2/26/21. COVID positive 1/6/22. Presented to ER on 1/11/22 and admitted. admitted on 1/11/22 for COVID-19 pneumonia. Respiratory therapy was supplemental oxygen as needed was offered. Remdesivir and dexamethasone therapy but COVID-19 treatment protocol also initiated. Patient improved with resolution of symptoms. BP control optimization was employed. The patient was ultimately discharged home in stable condition and will follow-up with her PCP within 1 week. Discharged on 1/18/22

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Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 7,0
Labordaten: 1/6/22 COVID19: positive 1/11/22 CTA chest: Multifocal bilateral airspace disease and somewhat nodular opacities most consistent with multifocal COVID-19 pneumonia.
Aktuelle Erkrankungen: -
Vorgeschichte: Anemia ? Arthritis ? DUB (dysfunctional uterine bleeding) ? Hyperlipidemia ? Hypertension ? Morbid obesity ? Osteoarthritis ? Ovarian cyst
Andere Medikamente: amLODIPine 10 MG Tabs Commonly known as: NORVASC 10 mg, Oral, DAILY celecoxib 200 MG Caps Commonly known as: CeleBREX TAKE 1 CAPSULE BY MOUTH EVERY DAY potassium chloride CR 10 MEQ Tab-cont-rel Commonly known as: KLORCON TAKE 1 TABLET
Allergien: none
Vorherige Impfungen: -

VAERS 2032226

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: MI
Alter: 78,0
Geschlecht: M
Eingang: 13.01.2022
Impfdatum: 19.02.2021
Beginn: 05.01.2022
Tage bis Beginn: 320,0
Dosis: 2
Route/Site: IM / -

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

Alanine aminotransferase increased Amnesia Anion gap Anuria Aspartate aminotransferase increased Asthenia Bladder catheter replacement Bladder catheterisation Bladder outlet obstruction Blood albumin decreased Blood alkaline phosphatase increased Blood bicarbonate normal Blood bilirubin normal Blood calcium normal Blood chloride normal Blood creatinine normal Blood glucose normal Blood lactic acid

Symptomtext

Hospitalized (1.5.22 - 1.11.22); COVID-19 positive (12.29.21); Fully vaccinated - moderna x2 d/c summary: Discharge Summary MD (Resident) ? ? General Medicine Cosigned by: MD at 1/11/2022 4:00 PM Attestation signed by, MD at 1/11/2022 4:00 PM I discussed the history/exam with the Resident on 1/11/2022. I agree with the findings and the Plan of Care as documented in the resident's note. I saw and evaluated the patient. I spent 35 minutes performing this hospital discharge. BRIEF OVERVIEW: Discharge Provider: MD Primary Care Provider: MD Admission Date: 1/5/2022 Discharge Date: Jan 11, 2022 Hospital problems: Generalized weakness Multiple falls at home Urinary retention with Foley in place Possible traumatic Foley Benign prostatic hyperplasia COVID-19 infection Transaminitis Essential hypertension Coronary artery disease Hyperlipidemia Seizure disorder Dementia At risk for falls Anxiety and depression Gastroesophageal reflux disease Peripheral nerve disease Restless leg syndrome Medication List CHANGE how you take these medications tamsulosin 0.4 MG capsule Commonly known as: FLOMAX take 2 capsules by mouth once daily What changed: o how much to take o when to take this DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Generalized weakness [R53.1] COVID-19 [U07.1] HOSPITAL COURSE: 77 year old male with PMHx coronary disease, chronic renal insufficiency, dementia, indwelling Foley catheter admitted for generalized weakness, falls, and urinary retention. Patient presented to the emergency department with ongoing generalized weakness leading to difficulty ambulating with his walker and multiple falls at home. ED course: Troponins normal at 9, 10. CBC without leukocytosis, anemia, or thrombocytopenia. Urinalysis showing >300 protein, moderate leukocytes, >75 RBCs, 8 WBCs. No hyaline casts or squamous epithelial cells to indicate contamination. Urine grossly bloody. EKG with normal sinus rhythm, ventricular rate of 95, QTc 459 ms. Left axis deviation. Nonspecific ST and T-wave abnormality seen. 500 mL fluid bolus given. Accepted for admission under observation to the general medicine service. In the hospital he was seen by Physical therapy and Occupational therapy. They recommended subacute rehab. He received 2 days of Rocephin 1 g daily for suspicion for urinary tract infection but urine culture grew resident flora. Benadryl as a sleep aid was discontinued. His Dilantin levels were drawn and shown to be low. He will need follow-up with Neurology. Orthostatic vital signs normal. He continued to be stable throughout the admission with continuing signs of generalized weakness. He was transferred to subacute rehab for further care. CONSULTS / RECOMMENDATION: Consult Orders (From admission, onward) None INPATIENT PROCEDURES: BP 116/62 | Pulse 91 | Temp 36.5 ?C (Oral) | Resp 18 | Ht 1.727 m | Wt 90.4 kg | SpO2 96% | BMI 30.30 kg/m? Physical Exam Constitutional: General: He is not in acute distress. Appearance: He is obese. He is not diaphoretic. HENT: Head: Normocephalic. Right Ear: External ear normal. Left Ear: External ear normal. Nose: Nose normal. Mouth/Throat: Mouth: Mucous membranes are moist. Eyes: General: Right eye: No discharge. Left eye: No discharge. Cardiovascular: Rate and Rhythm: Normal rate and regular rhythm. Pulmonary: Effort: No respiratory distress. Breath sounds: Normal breath sounds. Abdominal: General: Abdomen is flat. There is no distension. Palpations: Abdomen is soft. Tenderness: There is no abdominal tenderness. Musculoskeletal: Right lower leg: No edema. Left lower leg: No edema. Comments: Trembling with movement Skin: General: Skin is warm and dry. Capillary Refill: Capillary refill takes less than 2 seconds. Neurological: Mental Status: He is alert and oriented to person, place, and time. Psychiatric: Mood and Affect: Mood normal. H&P: Attestation signed by, DO at 1/5/2022 10:24 PM I have personally interviewed and examined the patient on 1/5/2022. Management was discussed with Dr. I agree with the documented findings and plan of care in his/her note. Brief exam: alert, elderly man in no acute distress. Oriented to person, place, time and general situation though some details seem difficult for him to recall. Foley in place with reddish urine. Non-tender abdomen. No focal neurologic deficits. Non labored respirations and heart sounds have RRR. Brief history and medical decision making: 77-year-old man with recent diagnosis of COVID-19 and multiple falls at home over the past several weeks. Wife noticed him trip on his Foley catheter and subsequent blood in the Foley. Seen initially at outside hospital and discharged after Foley replacement and initiation of Keflex for possible urinary tract infection. Today he is admitted for generalized weakness suspected to be from COVID-19 infection; diagnosed at outside hospital on 12/29/2021. Symptom onset 12/28. Vaccinated but without booster and received monoclonal antibodies 3-4 days ago. Denies shortness of breath and is on room air. Will obtain PT & OT evaluation and recommendations. Patient also noted to have hematuria, likely traumatic in nature based on history but may have associated urinary tract infection. Urine culture pending. Will plan for Rocephin daily and follow urine culture. History of E coli and Proteus infections. Patient and wife expressed do not resuscitate/DNI wishes. Expand All Collapse All Hide copied text Hover for details Inpatient Hospitalist History & Physical CHIEF COMPLAINT: Generalized weakness Falls at home Subjective HISTORY OF PRESENT ILLNESS: Patient is a 77 year old male with past medical history significant for coronary artery disease with STEMI s/p DES to RCA in 2018, hypertension, hyperlipidemia, GERD, anxiety, depression, seizure disorder, BPH, indwelling Foley catheter, restless leg syndrome, peripheral nerve disease, and current COVID-19 infection presents emergency department with chief complaint of generalized weakness and multiple falls at home. Past majority of the history is obtained by chart review and previous records. Also obtained by wifeover the phone. Patient has been to an outside hospital emergency department 2 times in the past 2 days, 1/3/22 and 1/4/22. Each time, he was sent home. Most recently, he was sent home with Keflex to treat a urinary tract infection and recommendations for home health care services. However, his wife never picked up the Keflex. Per chart review, the patient's wife states he has been experiencing increasingly worsening generalized weakness leading to difficulty holding his body up, ambulating with his walker, and multiple falls at home. He is not hit his head or lost consciousness per his wife but does have some bruising on his buttock and extremities. He has an indwelling catheter that was placed several months ago for chronic out obstruction. He follows with a Urologist. The patient's wife called his Urology office yesterday stating that she had not seen any urine in his catheter bag since 3:00 a.m. the night before. She was also noticing blood in his bag. She does report that she noticed he tripped on his foley the other night, which might have caused some of the bleeding, but she isn't sure. Reportedly, his catheter was replaced yesterday at Facility with return of urine. She does not feel she can adequately take care of him at home and is hoping he will go to a rehab facility to get stronger prior to returning home. She says that each time he falls, she has to call EMS and it takes 3 people to get him up and into a chair or bed. ED course: Labs ordered including complete blood count, CMP, troponin, urinalysis. Troponins normal at 9, 10. CBC without leukocytosis, anemia, or thrombocytopenia. Electrolytes including sodium (136), potassium (4.2), chloride (101), bicarbonate (21) all within normal range. Glucose mildly elevated to 127. Renal function normal with GFR >60, BUN 11, and Cr 0.74. Alkaline phosphatase mildly elevated to 132, AST elevated to 77, ALT elevated to 42, bilirubin normal at 0.5. Urinalysis showing >300 protein, moderate leukocytes, >75 RBCs, 8 WBCs. No hyaline casts or squamous epithelial cells to indicate contamination. Urine grossly bloody. EKG with normal sinus rhythm, ventricular rate of 95, QTc 459 ms. Left axis deviation. Nonspecific ST and T-wave abnormality seen. 500 mL fluid bolus given. Accepted for admission under observation to the general medicine service. Review of Systems Constitutional: Positive for chills and malaise/fatigue. Negative for fever. HENT: Negative for congestion and sore throat. Eyes: Negative for pain and redness. Respiratory: Negative for cough, shortness of breath and wheezing. Cardiovascular: Negative for chest pain, palpitations and leg swelling. Gastrointestinal: Negative for abdominal pain, blood in stool, nausea and vomiting. Genitourinary: Positive for hematuria. Negative for dysuria and flank pain. Musculoskeletal: Positive for falls and myalgias. Skin: Negative for rash. Neurological: Positive for weakness. Negative for dizziness. Psychiatric/Behavioral: Positive for memory loss (short term, chronic Objective OBJECTIVE: BP 120/59 | Pulse 94 | Temp 36.9 ?C (Oral) | Resp 15 | Ht 1.727 m | Wt 90.4 kg | SpO2 94% | BMI 30.30 kg/m? Physical Exam Vitals reviewed. Constitutional: General: He is not in acute distress. Appearance: He is obese. He is ill-appearing. Comments: Lying on his right side in the hospital bed, visibly shaking. States he is cold. Stops shaking after 2nd blanket placed over him. He appears very tired. HENT: Head: Normocephalic and atraumatic. Right Ear: External ear normal. Left Ear: External ear normal. Nose: Nose normal. Mouth/Throat: Pharynx: Oropharynx is clear. Eyes: Extraocular Movements: Extraocular movements intact. Conjunctiva/sclera: Conjunctivae normal. Pupils: Pupils are equal, round, and reactive to light. Cardiovascular: Rate and Rhythm: Normal rate and regular rhythm. Heart sounds: No murmur heard. Pulmonary: Effort: Pulmonary effort is normal. No respiratory distress. Breath sounds: No wheezing or rales. Abdominal: General: Bowel sounds are normal. There is no distension. Palpations: Abdomen is soft. Tenderness: There is no abdominal tenderness. There is no right CVA tenderness or left CVA tenderness. Genitourinary: Comments: Foley catheter in place Musculoskeletal: Cervical back: Neck supple. Right lower leg: No edema. Left lower leg: No edema. Skin: General: Skin is warm and dry. Findings: No rash. Neurological: General: No focal deficit present. Mental Status: He is alert and oriented to person, place, and time. Comments: Able to tell me his full name, date of birth, where he is located, and why he is in the hospital. He is having trouble speaking at times due to fatigue. Psychiatric: Mood and Affect: Mood normal. Behavior: Behavior normal.

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Praegender Schweregrund: Tremor
Hospital-Tage: 6,0
Labordaten: Lab Results Component Value Date WBC 7.49 01/05/2022 RBC 4.81 01/05/2022 HGB 14.2 01/05/2022 HCT 41.7 (L) 01/05/2022 MCV 86.7 01/05/2022 PLATELET 190 01/05/2022 NEUTABSOLU 6.17 01/05/2022 Lab Results Component Value Date GLUCOSE 127 (H) 01/05/2022 SODIUM 136 01/05/2022 POTASSIUM 4.2 01/05/2022 CHLORIDE 101 01/05/2022 TOTALCO2 25 09/20/2017 HCO3 21 01/05/2022 ANIONGAP 14 01/05/2022 BUN 11 01/05/2022 CREATININE 0.74 01/05/2022 EGFR >60 01/05/2022 EGFRML >60 09/20/2017 Troponin: 9, 10 AST: 77, ALT 42, bilirubin 0.5 Lactate at OSH on 1/4/22: 1.4 Urinalysis showing over 300 protein, moderate leukocytes, >75 RBCs, 8 WBCs. No hyaline casts or squamous epithelial cells to indicate contamination. Urine grossly bloody. Urine culture 1/5/22: pending Blood culture x2 1/5/22: pending Electrocardiogram 01/05/2022: Normal sinus rhythm with ventricular rate of 95. QTc 459 ms. Left axis deviation. Nonspecific ST and T-wave abnormality seen. Chest x-ray 01/04/2022 at Facility: Normal heart size, no pulmonary vascular congestion, mild airspace infiltration bilaterally, no segmental consolidation or pleural effusion. Impression was probable bilateral interstitial pneumonitis. Comprehensive Metabolic Panel (CMP) (Abnormal) Collected: 01/11/22 0513 Order Status: Completed Specimen: Blood, Venous Updated: 01/11/22 0615 Sodium Level 140 134 - 146 mmol/L Potassium Level 4.0 3.4 - 5.0 mmol/L Chloride 106 98 - 112 mmol/L HCO3 22 21 - 29 mmol/L Anion Gap 12 9 - 18 mmol/L Glucose Level 92 70 - 99 mg/dL Blood Urea Nitrogen 10 8 - 20 mg/dL Creatinine 0.79 0.60 - 1.30 mg/dL MDRD eGFR >60 >=60 mL/min/1.73 m2 CG eCrCl 75 mL/min/1.73 m2 Calcium Level Total 8.5 Low 8.6 - 10.4 mg/dL Protein Total 6.8 6.0 - 8.0 g/dL Albumin Level 2.3 Low 3.5 - 5.0 g/dL Bilirubin Total 0.5 0.2 - 1.0 mg/dL Alkaline Phosphatase 177 High 40 - 129 IU/L Alanine Aminotransferase 44 High 10 - 40 IU/L Aspartate Aminotransferase 46 High 10 - 40 IU/L Complete Blood Count without Differential (Abnormal) Collected: 01/11/22 0512 Order Status: Completed Specimen: Blood, Venous Updated: 01/11/22 0555 White Blood Cell 7.62 4.00 - 10.80 x10*3/uL Red Blood Cell 4.36 Low 4.60 - 6.00 x10*6/uL Hemoglobin 12.7 Low 14.0 - 18.0 g/dL Hematocrit 38.0 Low 42.0 - 52.0 % Mean Cell Volume 87.2 80.0 - 100.0 fL Mean Cell Hemoglobin 29.1 27.0 - 33.0 pg NRBC Absolute Count 0.00 0.00 - 0.01 x10*3/uL NRBC Automated 0.0 0.0 - 0.1 %WBC Mean Cell Hemoglobin Concentration 33.4 32.0 - 37.0 g/dL Red Cell Diameter Width 12.2 11.0 - 16.0 % Platelet 442 High 140 - 400 x10*3/uL Mean Platelet Volume 10.5 7.4 - 11 fL
Aktuelle Erkrankungen: 1/3/22 - visit to Ed for weakness/falls/COVID 19 infection 1/4/22 - visit to ED for urinary retention
Vorgeschichte: Past medical history: Benign prostatic hyperplasia Essential hypertension Peripheral nerve disease Seizure disorder Restless leg syndrome Dementia Hypercholesterolemia Diverticulosis Generalized anxiety disorder GERD Hiatal hernia Obesity At risk for falls Depression B12 deficiency Chronic pain of both knees Chondrocalcinosis Coronary artery disease History of STEMI (inferior wall, s/p DES to RCA 11/8/18) Former smoker Restrictive lung disease CKD Cataracts
Andere Medikamente: Aspirin 81 MG Oral, 1 tablet daily Atorvastatin Calcium 80 MG take 1 tablet by mouth NIGHTLY Carvedilol 6.25 MG take 1 tablet by mouth twice a day Clotrimazole-Betamethasone 1-0.05 % Apply to skin BiD as needed Cyanocobalamin 1,000 mcg Oral
Allergien: penicillins - hives
Vorherige Impfungen: -

VAERS 1993228

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: IL
Alter: 56,0
Geschlecht: F
Eingang: 30.12.2021
Impfdatum: 27.01.2021
Beginn: 11.03.2021
Tage bis Beginn: 43,0
Dosis: 2
Route/Site: SYR / AR

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

Alanine aminotransferase normal Angiogram cerebral normal Anion gap normal Antibody test negative Aspartate aminotransferase normal Basophil count normal Blood albumin normal Blood alkaline phosphatase normal Blood bilirubin normal Blood calcium normal Blood chloride normal Blood cholesterol increased Blood creatinine normal Blood glucose normal Blood potassium normal Blood sodium normal Blood triglycerides normal Blood urea normal

Symptomtext

Painless left eye optic nueritis on 3/11/21 noticed, went to optometrist, referred to Opthamologist saw at 11 am 3/12/21, visual fields, eye exam, verified swelling in left optic nerve. sent to ED for stroke workup. MRI Brain, CTA Head, stroke protocol and various lab tests. No findings to indicate stroke, assigned to Nuerologist admit for further acute retinal artery ischemia workup. IV Steroids (methylprednisolone) for 2 days, discharged and recieved 1 day OP IV steroids, followed by 14 days oral predisone, followup with Dr. (and primary Dr.); no known diagnosis by hospital nuerologist or Dr., Refered to a Nuero/Opthamologist Dr. in state on 4/30/2021. Full optical workup, visual fields, photographs and lab script for MOG antibody test. MOG antibody test 5/7/21 Negative. Swelling of Optic Nerve is gone, additional Visual Field loss in left eye. Only have bottom outside quadrant of vision after this episode, .

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Praegender Schweregrund: Condition aggravated
Hospital-Tage: 2,0
Labordaten: MRI Brain, CTA Head 3/12/21; , MOG Antibody 5/7/21 all tests negative, Visual fields 3/11/21 Lab tests run 3/12-3/15/21 - Hemoglobin, Hematocrit, RBC, MCV, MCH, MCHC, RDW, WBC, Continued lab tests: absolute neutrohils, absolute basophils, absolute eosinophils, absolute monocytes, absolute lymphocytes, Nuetrophils, Eosinophils, Basophils, Monocytes, Lymphocytes, Platelets, Sodium, potassium, chloride,CO2, Anion gap, BUN, Creatinine, Creatinine, Istat, eFGR-AA, eGFR-non AA, Glucose, Calcium, Alk phos, AST, ALT, Bilirubin (total), Total protein, Albumin, Hemoglobin A1C, Procalcitorin (all witihin normal ranges) Cholesterol, HDL, Triglycerides CRP - Chol 214 all others in range and ratios good.
Aktuelle Erkrankungen: No illnesses
Vorgeschichte: atypical bilateral optic nueritis (last episode 2002), no known cause
Andere Medikamente: Multi vitamin daily
Allergien: Penicillin & Tetracyclin
Vorherige Impfungen: -

VAERS 1958837

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: MI
Alter: 67,0
Geschlecht: F
Eingang: 17.12.2021
Impfdatum: 04.02.2021
Beginn: 18.02.2021
Tage bis Beginn: 14,0
Dosis: 2
Route/Site: IM / LA

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

Arthralgia Back pain Condition aggravated Cyanosis Full blood count Laboratory test abnormal Magnetic resonance imaging Monoclonal gammopathy Neuralgia Pain in extremity Paraesthesia Peripheral coldness Urine analysis X-ray normal

Symptomtext

2 weeks after the vaccine I developed cold, tingly, painful feet. My feet were blue. My back going into my hip area was very painful so I saw my PCP who injected a steroid injection in my back to try to help with the nerve pain in my feet, but didn't work. I saw a neurosurgeon who performed a MRI on my back because the pain was so intense but didn't see anything that would explain the painful feet. Labs were done and a pre-cancerous condition M-Gust was found. I was referred to a cancer doctor and is currently being monitored watching to ensure cancer doesn't appear. I was prescribed gabapentin for the nerve pain which has helped with the severity of the pain but the pain is still there to date and the back pain is still present to date as well with Tylenol to help with that. I saw a rheumatologist who did rule out arthritis as well. A total x-ray of my entire body was also performed to check for lesion but none were found.

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Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: MRI; CBC; extensive blood work and labs; total body x-ray; urinalysis
Aktuelle Erkrankungen: No
Vorgeschichte: Back pain
Andere Medikamente: Multivitamin, Ambien, Flonase, Lisinopril
Allergien: No
Vorherige Impfungen: -

VAERS 1927806

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: IL
Alter: 78,0
Geschlecht: F
Eingang: 07.12.2021
Impfdatum: 03.02.2021
Beginn: 17.03.2021
Tage bis Beginn: 42,0
Dosis: 1
Route/Site: OT / -

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

Arthralgia Neck pain Pain Pain in extremity Paraesthesia Vaccination site pain

Symptomtext

left hand tingling, fingers tingling, maybe they hit a nerve, been going on for several months; experience pain in her upper arm above the injection site; pain then traveled to shoulder, pain in back of shoulder; pain in the upper arm where they gave shot/pain in the injection site/pain comes and goes, injection spot pain is always there/pain keeps me up at night/arm feels heavy/like lead.; my therapist told me I'm not the only one who has had the pain from the vaccine/hurts and hurts and hurts.; pain she has been experiencing in her shoulder and neck has gotten worse; This spontaneous case was reported by a patient and describes the occurrence of PAIN (my therapist told me I'm not the only one who has had the pain from the vaccine/hurts and hurts and hurts.), NECK PAIN (pain she has been experiencing in her shoulder and neck has gotten worse), PARAESTHESIA (left hand tingling, fingers tingling, maybe they hit a nerve, been going on for several months), PAIN IN EXTREMITY (experience pain in her upper arm above the injection site) and ARTHRALGIA (pain then traveled to shoulder, pain in back of shoulder) in a 78-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concurrent medical conditions included Blood pressure abnormal and Blood cholesterol abnormal. Concomitant products included OLMESARTAN MEDOXOMIL (BENICAR) for Blood pressure, ATORVASTATIN for Cholesterol, VITAMINS NOS for an unknown indication. On 03-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 03-Mar-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 17-Mar-2021, the patient experienced PAIN (my therapist told me I'm not the only one who has had the pain from the vaccine/hurts and hurts and hurts.), NECK PAIN (pain she has been experiencing in her shoulder and neck has gotten worse), ARTHRALGIA (pain then traveled to shoulder, pain in back of shoulder) and VACCINATION SITE PAIN (pain in the upper arm where they gave shot/pain in the injection site/pain comes and goes, injection spot pain is always there/pain keeps me up at night/arm feels heavy/like lead.). 17-Mar-2021, the patient experienced PAIN IN EXTREMITY (experience pain in her upper arm above the injection site). On an unknown date, the patient experienced PARAESTHESIA (left hand tingling, fingers tingling, maybe they hit a nerve, been going on for several months). The patient was treated with GABAPENTIN at an unspecified dose and frequency; PARACETAMOL (TYLENOL [PARACETAMOL]) at an unspecified dose and frequency; NAPROXEN SODIUM (ALEVE) at an unspecified dose and frequency and Physical therapy for Vaccination site pain. At the time of the report, PAIN (my therapist told me I'm not the only one who has had the pain from the vaccine/hurts and hurts and hurts.), NECK PAIN (pain she has been experiencing in her shoulder and neck has gotten worse), PARAESTHESIA (left hand tingling, fingers tingling, maybe they hit a nerve, been going on for several months), PAIN IN EXTREMITY (experience pain in her upper arm above the injection site), ARTHRALGIA (pain then traveled to shoulder, pain in back of shoulder) and VACCINATION SITE PAIN (pain in the upper arm where they gave shot/pain in the injection site/pain comes and goes, injection spot pain is always there/pain keeps me up at night/arm feels heavy/like lead.) had not resolved. The patient reported 2 weeks after receiving the 2nd dose of the Moderna vaccine, she started experiencing pain in the upper arm at the injection site. As time went on, she didn't do anything about the pain, and it got worse. She then started to experience pain in her upper arm above the injection site, and the pain traveled to her shoulder, back of the shoulder, and neck. This all happened over a matter of several months. She said that on a scale of 1-10, her pain would be a 10. She had been undergoing physical therapy to help with the pain. She also stated that nobody seems to know what has been going on with her. Her shoulder and neck had gotten worse and was scaring her. All the pain was in her right arm, where she received the injection. After the pain started, she started experiencing tingling in her left hand and fingers as well. The tingling was ongoing for several months as well. She stated that may be the vaccination provider hit a nerve while giving the injection, but she was not sure. She said that the physical therapy seems to help with the pain in the shoulder and neck, as well as the tingling in her left hand and fingers. She did not experience it all the time, the pain came and went. However, the injection site pain was there no matter how much therapy she got and no matter what she was doing. Also stated that she was watching tv and the pain was just there. It kept getting worse. The pain also kept her up at night. She had a hard time reaching into the cupboard and doing her hair. She said that her arm felt heavy, like lead. Most recent FOLLOW-UP information incorporated above includes: On 02-Dec-2021: Significant follow up. Updated Product (Dose information), Events(added events neck pain, shoulder pain, Paresthesia upper limb) and Narrative.

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Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Blood cholesterol abnormal; Blood pressure abnormal
Vorgeschichte: -
Andere Medikamente: BENICAR; ATORVASTATIN; VITAMINS NOS
Allergien: -
Vorherige Impfungen: -

VAERS 1919876

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: MI
Alter: 75,0
Geschlecht: F
Eingang: 03.12.2021
Impfdatum: 12.02.2021
Beginn: 26.11.2021
Tage bis Beginn: 287,0
Dosis: 2
Route/Site: UN / UN

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

Acute left ventricular failure Asthenia Atrial fibrillation COVID-19 Chest X-ray normal Chronic left ventricular failure Condition aggravated Dyspnoea Echocardiogram normal Ejection fraction normal Faeces discoloured Haemoglobin normal Hepatocellular injury Impaired self-care Liver function test decreased Melaena Oedema Pulmonary hypertension

Symptomtext

Patient discharged from (8) day inpatient admission and returned to ED same day for generalized weakness and inability to cae for herself. Requesting home care. The patient is a 76 y.o. female with a history of chronic diastolic CHF, a.fib on eliquis, HTN, HLD, and GERD admitted on 11/26/2021 with progressive SOB and edema secondary to acute on chronic diastolic heart failure in the setting of diuretic non adnerence. Pt reported dark stool prior to admission as well. +COVID test on admission. A fib with RVR present at time of admission. Pt initiated on supplemental O2 and IV diuresis. Significant COVID pneumonia not suspected given CXR findings, respiratory failure felt to be secondary to CHF instead. Decadron was started, remdesivir held as no significant pneumonia on x-ray and transaminitis. RUQ U/S showed mild increased liver echogenicity, suggesting underlying hepatocellular disease. LFTs down-trended. Recent echo 8/2021 with EF 61%, mild pulmonary HTN. She diuresed well and was weaned to room air. Transitioned back to oral torsemide. She reported melena on admission so home eliquis held initally. Hemoglobin remained stable without signs of bleeding and eliquis was resumed without evidence of bleeding. PT/OT evaluated and recommended discharge home with assist and HHC. Patient had stopped taking torsemide at home and she felt it was causing her to feel "unwell". Discharge plans coordinated with cardiology, advised discharge on lasix 40 mg daily with KCl 20meq. She was advised to monitor her weights closely and have follow up labs checked within 5-7 days. Cardiology arranged virtual appointment on 12/6. She was felt stable for discharge on 12/2. She will complete remaining 3 days of torsemide for 10 day course. She was discharged home in stable condition with family.

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Praegender Schweregrund: Condition aggravated
Hospital-Tage: 8,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Respiratory OSA (obstructive sleep apnea) Dyspnea on exertion Multiple lung nodules Mixed restrictive and obstructive lung disease (HCC) Obstructive lung disease (HCC) Non-allergic rhinitis Acute hypoxemic respiratory failure (HCC) Circulatory Essential hypertension Venous insufficiency Premature atrial contraction Persistent atrial fibrillation (HCC) Acute on chronic diastolic heart failure (HCC) Atrial fibrillation with RVR (HCC) Hypercoagulable state due to atrial fibrillation (HCC) Digestive Class 1 obesity due to excess calories with body mass index (BMI) of 33.0 to 33.9 in adult GERD (gastroesophageal reflux disease) Hepatomegaly Irritable bowel syndrome with diarrhea Infectious/Inflammatory Arthritis of right shoulder region Diverticulitis COVID-19 virus infection Hematologic MDS (myelodysplastic syndrome) (HCC) Nervous Glaucoma Genitourinary Duplicated renal collecting system Urinary incontinence in female Endocrine/Metabolic Non-toxic multinodular goiter Prediabetes Other PLMD (periodic limb movement disorder) Generalized anxiety disorder Personal history of colonic polyps Hoarseness of voice Visual field defect Bilateral lower extremity edema Insomnia, unspecified Pelvic mass Abnormal CT of the chest Vertigo Hx of macrocytic anemia Balance problem
Andere Medikamente: acetaminophen (TYLENOL) 325 MG tablet apixaban (ELIQUIS) 5 MG tablet atorvastatin (LIPITOR) 20 MG tablet benzonatate (TESSALON) 100 MG capsule Cholecalciferol (VITAMIN D PO) Cyanocobalamin (VITAMIN B-12 PO) dexamethasone (DECADRON) 6 MG tab
Allergien: Betadine [Povidone Iodine]Rash
Vorherige Impfungen: -

VAERS 1916406

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038k20A

moderat

Staat: PA
Alter: 53,0
Geschlecht: F
Eingang: 02.12.2021
Impfdatum: 13.02.2021
Beginn: 20.02.2021
Tage bis Beginn: 7,0
Dosis: 2
Route/Site: SYR / RA

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

Feeling abnormal Hypoaesthesia Paraesthesia Tinnitus Vaccine positive rechallenge Visual impairment

Symptomtext

a1c went up i had no idea until i saw something on social media and i was like that's what happened to me and now that i got my 3rd i see it for myself my eye site is a mess and i was doing fine until the vaccine numbness and tingling in fingers and toes my bottom of right foot went numb ringing in my ears brain fogs and this is every time i get my shot i have had all three

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Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: none! i didn't know what to do i mentioned to my doctor and he said he had not heard of these side effects
Aktuelle Erkrankungen: -
Vorgeschichte: high blood pressure diabetes high cholesterol
Andere Medikamente: janumet losartan omeprazole rostovasatin gapapatin trulicity
Allergien: -
Vorherige Impfungen: -

VAERS 1909326

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: MI
Alter: 68,0
Geschlecht: M
Eingang: 30.11.2021
Impfdatum: 03.03.2021
Beginn: 29.11.2021
Tage bis Beginn: 271,0
Dosis: 1
Route/Site: IM / -

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

Acute kidney injury Anosmia Asthenia Blood glucose increased COVID-19 COVID-19 pneumonia Chest X-ray abnormal Chills Cough Decreased appetite Diarrhoea Dizziness Dyspnoea Fatigue Feeling abnormal Hypophagia Malaise Pollakiuria

Symptomtext

Chief Complaint: 69 y m c/o feeling punky for a week and his sugars are elevated, respiratory complaints cough, dyspnea (SOB) and URI symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 1,0
Labordaten: o History of Present Illness This is a 69-year-old male significant past medical history of CAD status post CABG, hypertension, hyperlipidemia, peripheral arterial disease status post carotid endarterectomy, daily alcohol use and tobacco abuse that presented to the hospital with chief complaint of cough and generally feeling unwell for about 6 days. Patient states that he started to feel unwell with cough, congestion and loss of smell. The patient took an outpatient Covid test at home and was negative. So he thought he just had the flu. He had a very poor appetite and was not eating and drinking very well at all. He was not checking his glucose and was not taking his insulin. The patient states his breathing has been okay but he was intermittently dyspneic. Patient did have his Covid vaccinations earlier in the year and his wife just recently got the booster. The patient has had chills but no fevers. He has been weak, fatigued and having malaise. The patient has had some intermittent diarrhea but no abdominal pain. He has not had any nausea or vomiting. Patient denies any chest pain. He did have some mild intermittent lightheadedness and dizziness. The patient states he does drink a few beers a day. Patient denies any history of chronic kidney disease. He notes that he did have pretty significant urinary frequency over the past few days. In the emergency room department, the patient was found to have acute renal failure. His chest x-ray showed Covid pneumonia. And his COVID-19 swab was positive. Patient was not hypoxemic on room air.
Aktuelle Erkrankungen: unknown
Vorgeschichte: Peripheral artery disease CAD HTN Diabetes
Andere Medikamente: Current Home Medications 1. amLODIPine 10 mg oral tablet : 1 tab(s) orally once a day 2. Aspir 81 oral delayed release tablet : 1 tab(s) orally once a day 3. atorvastatin 40 mg oral tablet : 1 tab(s) orally once a day 4. Cardura 1 mg oral t
Allergien: niacin (anaphylaxis)
Vorherige Impfungen: -

VAERS 1889865

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: IL
Alter: 44,0
Geschlecht: F
Eingang: 22.11.2021
Impfdatum: 23.02.2021
Beginn: 24.02.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / RA

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

Arthralgia Blood test normal Computerised tomogram abnormal Headache Hepatic failure Hepatic steatosis Impaired work ability Musculoskeletal chest pain Pyrexia Sleep disorder Ultrasound scan normal

Symptomtext

I got the vaccine and missed 3 days of work. The night of my vaccine 2/23/21, I started running a low grade fever and had achy joints and a headache. The night of the 24th my fever got up to 103.5 and stayed that way for a few hours, I woke up that night with pain in the rib cage. I took a hot bath to help relax my muscles, that did not help so I drove to the ER. They did ultrasounds and couldn't find anything. They sent me home with a possible UTI. By the time I left the ER on the 24th, with an antibiotic, the pain continued. I think on the 25th I saw my doctor. The pain has never went away, just would get better but then progressively worse. I sought treatment again in September with my doctor and had a cat scan in October. I was diagnosed with a fatty liver with deterioration. The pain is slowly getting better, I had to change my diet.

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Praegender Schweregrund: Musculoskeletal chest pain
Hospital-Tage: -
Labordaten: CT- fatty liver; bloodwork- no finding; ultrasound- no finding.
Aktuelle Erkrankungen: No
Vorgeschichte: Asthma
Andere Medikamente: Singulair; Xyzal; Omeprazole; Advair inhaler
Allergien: No
Vorherige Impfungen: -

VAERS 1869553

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: NJ
Alter: 60,0
Geschlecht: F
Eingang: 15.11.2021
Impfdatum: 04.02.2021
Beginn: 01.02.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: IM / LA

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

Atrophy Back pain Headache Hypoaesthesia Insomnia Muscle contractions involuntary Muscular weakness Neck pain Pain in extremity Tinnitus Tremor

Symptomtext

Headaches, Insomnia, Fasciculations(muscle twitches) Body Tremors, Atrophy, Limb Weakness, Ear Ringing, Neck & Back pain , Numb Toes , Aching fingers

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Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: Numerous Blood Works, Brain MRI, EEG, EMG, Neck Ultrasound, Back MRI Thoracic, cervical, Lumbar. Physical Exams from Neurologists and Primary
Aktuelle Erkrankungen: -
Vorgeschichte: Pre Diabetes High Cholesterol High Blood Pressure History of Breast Cancer
Andere Medikamente: Metformin Valsartan HCT Atrovastatin Letrozole Potassium CL
Allergien: None Known
Vorherige Impfungen: -

VAERS 1857023

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: FL
Alter: 49,0
Geschlecht: F
Eingang: 10.11.2021
Impfdatum: 03.02.2021
Beginn: 03.03.2021
Tage bis Beginn: 28,0
Dosis: 1
Route/Site: OT / LA

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

Anxiety Arthritis Biliary colic Body temperature Chest discomfort Computerised tomogram Dyspnoea Electrocardiogram Endoscopy Feeling abnormal Gastritis Headache Multisystem inflammatory syndrome in adults Myalgia Neck pain Nephrolithiasis Noninfective gingivitis Oesophagitis

Symptomtext

Flank pain that wrapped around my back & the front of my stomach; chest tightness; sinus tachycardia; shortness of breath; response; Pericardial effusion; They found 100 tiny kidney stones; Gallbladder pain; I had kidney pain.; Gums were inflamed; My whole body was inflamed; inflammation in my stomach; inflammation in my esophagus.; I'm having more anxiety & panic attacks since this happened. pain on the right neck; I'm having more anxiety & panic attacks since this happened. Arthritis; pain on the right arm; pain on the right side of my head; I felt a little strange; I had a low grade fever of 99.9 or 100F; Muscle aches/ Body ache; This spontaneous case was reported by a consumer and describes the occurrence of MULTISYSTEM INFLAMMATORY SYNDROME IN ADULTS (MISA response), PERICARDIAL EFFUSION (Pericardial effusion), CHEST DISCOMFORT (chest tightness), SINUS TACHYCARDIA (sinus tachycardia), DYSPNOEA (shortness of breath) and FLANK PAIN (Flank pain that wrapped around my back & the front of my stomach) in a 49-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 011A21A and 038K20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 03-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 03-Mar-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 03-Mar-2021, the patient experienced PYREXIA (I had a low grade fever of 99.9 or 100F) and MYALGIA (Muscle aches/ Body ache). On 18-Mar-2021, the patient experienced FLANK PAIN (Flank pain that wrapped around my back & the front of my stomach) (seriousness criterion hospitalization) and FEELING ABNORMAL (I felt a little strange). On an unknown date, the patient experienced MULTISYSTEM INFLAMMATORY SYNDROME IN ADULTS (MISA response) (seriousness criterion medically significant), PERICARDIAL EFFUSION (Pericardial effusion) (seriousness criterion medically significant), CHEST DISCOMFORT (chest tightness) (seriousness criterion hospitalization), SINUS TACHYCARDIA (sinus tachycardia) (seriousness criterion hospitalization), DYSPNOEA (shortness of breath) (seriousness criterion hospitalization), NEPHROLITHIASIS (They found 100 tiny kidney stones), BILIARY COLIC (Gallbladder pain), RENAL PAIN (I had kidney pain.), NONINFECTIVE GINGIVITIS (Gums were inflamed), INFLAMMATION (My whole body was inflamed), GASTRITIS (inflammation in my stomach), OESOPHAGITIS (inflammation in my esophagus.), PANIC ATTACK (I'm having more anxiety & panic attacks since this happened.), NECK PAIN (pain on the right neck), ANXIETY (I'm having more anxiety & panic attacks since this happened.), ARTHRITIS (Arthritis), PAIN IN EXTREMITY (pain on the right arm) and HEADACHE (pain on the right side of my head). The patient was hospitalized from 18-Mar-2021 to 21-Mar-2021 due to FLANK PAIN, then for 2 days due to CHEST DISCOMFORT, DYSPNOEA and SINUS TACHYCARDIA. The patient was treated with PARACETAMOL (TYLENOL [PARACETAMOL]) ongoing from 03-Mar-2021 for Fever, Muscle ache and Ache, at an unspecified dose and frequency and FAMOTIDINE (PEPCID AC) ongoing since an unknown date for Inflammation stomach, at an unspecified dose and frequency. At the time of the report, MULTISYSTEM INFLAMMATORY SYNDROME IN ADULTS (MISA response), PERICARDIAL EFFUSION (Pericardial effusion), CHEST DISCOMFORT (chest tightness), SINUS TACHYCARDIA (sinus tachycardia), DYSPNOEA (shortness of breath), FLANK PAIN (Flank pain that wrapped around my back & the front of my stomach), NEPHROLITHIASIS (They found 100 tiny kidney stones), BILIARY COLIC (Gallbladder pain), RENAL PAIN (I had kidney pain.), NONINFECTIVE GINGIVITIS (Gums were inflamed), INFLAMMATION (My whole body was inflamed), FEELING ABNORMAL (I felt a little strange), GASTRITIS (inflammation in my stomach), OESOPHAGITIS (inflammation in my esophagus.), PANIC ATTACK (I'm having more anxiety & panic attacks since this happened.), NECK PAIN (pain on the right neck), ANXIETY (I'm having more anxiety & panic attacks since this happened.), ARTHRITIS (Arthritis), PAIN IN EXTREMITY (pain on the right arm), HEADACHE (pain on the right side of my head), PYREXIA (I had a low grade fever of 99.9 or 100F) and MYALGIA (Muscle aches/ Body ache) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available):On 03-Mar-2021, Body temperature: 99.9f or 100f (High) low grade fever of 99.9F or 100F.On 18-Mar-2021, Computerised tomogram: abnormal (abnormal) pericardial effusion.On 18-Mar-2021, Electrocardiogram: abnormal (abnormal) pericardial effusion.On 18-Mar-2021, Ultrasound scan: abnormal (abnormal) pericardial effusion. In August 2021, Endoscopy: abnormal (abnormal) inflammation in my esophagus & my stomach.. In August 2021, SARS-CoV-2 antibody test: positive (Positive) H 7.69. In October 2021, X-ray: abnormal (abnormal) arthritis.On an unknown date, Rhesus antigen negative: negative (Negative) Negative. Concomitant medications were not reported. The patient reported that, she would keep taking deep breaths, on 18-mar-2021 she had Colitis. Company Comment: This case concerns a 49 year-old female patient with no reported medical history, who experienced the unexpected serious events of Multisystem inflammatory syndrome in adults (AESI), Pericardial effusion, Sinus tachycardia, Dyspnoea, and Flank pain, and the unexpected non-serious AESI of Arthritis. The events occurred an unknown number of days after the second dose of mRNA-1273 vaccine, except for the event of Flank pain which occurred 15 days after the second dose. Details of the clinical events and chronology of symptoms were not clearly reported for this case. The benefit-risk relationship of mRNA-1273 vaccine is not affected by this report. This case was linked to MOD-2021-370456 (Patient Link). Sender's Comments: This case concerns a 49 year-old female patient with no reported medical history, who experienced the unexpected serious events of Multisystem inflammatory syndrome in adults (AESI), Pericardial effusion, Sinus tachycardia, Dyspnoea, and Flank pain, and the unexpected non-serious AESI of Arthritis. The events occurred an unknown number of days after the second dose of mRNA-1273 vaccine, except for the event of Flank pain which occurred 15 days after the second dose. Details of the clinical events and chronology of symptoms were not clearly reported for this case. The benefit-risk relationship of mRNA-1273 vaccine is not affected by this report.

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: 4,0
Labordaten: Test Date: 20210303; Test Name: Body temperature; Result Unstructured Data: low grade fever of 99.9F or 100F.; Test Date: 20210318; Test Name: CT Scan; Result Unstructured Data: pericardial effusion; Test Date: 20210318; Test Name: electrocardiogram; Result Unstructured Data: pericardial effusion; Test Date: 202108; Test Name: Endoscopy; Result Unstructured Data: inflammation in my esophagus & my stomach.; Test Name: Rh; Test Result: Negative ; Result Unstructured Data: Negative; Test Date: 202108; Test Name: Quantum CoV test; Test Result: Positive ; Result Unstructured Data: H 7.69; Test Date: 20210318; Test Name: Ultrasound; Result Unstructured Data: pericardial effusion; Test Date: 202110; Test Name: X-Ray; Result Unstructured Data: arthritis.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1833915

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038k20a

moderat

Staat: MI
Alter: 94,0
Geschlecht: M
Eingang: 01.11.2021
Impfdatum: 05.03.2021
Beginn: 29.10.2021
Tage bis Beginn: 238,0
Dosis: 1
Route/Site: - / -

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

Cough Dyspnoea SARS-CoV-2 test

Symptomtext

SOB Cough

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: 3,0
Labordaten: rapid covid
Aktuelle Erkrankungen: unknown
Vorgeschichte: CAD
Andere Medikamente: Aspirin Enteric Coated 81 mg oral delayed release tablet, 81 mg= 1 tab(s), PO (oral), qDay, Unable to obtain: reviewed external, updated meds, unable to verify use and compliance of medications with the patient atorvastatin 10 mg oral ta
Allergien: KNA
Vorherige Impfungen: -

VAERS 1814931

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: MI
Alter: 79,0
Geschlecht: F
Eingang: 25.10.2021
Impfdatum: 04.02.2021
Beginn: 17.10.2021
Tage bis Beginn: 255,0
Dosis: 1
Route/Site: - / -

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

COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

SOB

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: 6,0
Labordaten: Positive on admission 10.17.21
Aktuelle Erkrankungen: -
Vorgeschichte: HTN, IBS, acquired hypothroidism, osteoporosis, BCC,
Andere Medikamente: Tessalon, vit. D, boniva, atrovent, levoxyl, prilosec, oscal
Allergien: -
Vorherige Impfungen: -

VAERS 1778836

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: MI
Alter: 60,0
Geschlecht: F
Eingang: 12.10.2021
Impfdatum: 14.02.2021
Beginn: 11.04.2021
Tage bis Beginn: 56,0
Dosis: 2
Route/Site: IM / RA

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

Asthenia Blood pressure increased Cardiac stress test Chest X-ray Computerised tomogram thorax Condition aggravated Dyspnoea Echocardiogram Electrocardiogram Fall Fatigue Foot fracture Laboratory test Limb injury Muscular weakness Nausea Pulmonary function test normal Systemic lupus erythematosus

Symptomtext

leg weakness. On Arpil 11,2021 I fell, hit the rght side of my body against a tree and landed on the ground. Had a hard time breathing when I fell. I went to ER on 4/12 . no fracture on ribs, left tiny avulsion fracture on foot. Seen primary care provider on 4/20 was sent to ER due to increase shortness of breath. Was put in hospital observation 24 hours and had a stress stress test, echo and labs . have been to ER twice for same issue. I have had 2 complete pulmonary function tests- negative., CT High Resolution, CT PE protocol, numerous labs, chest xray. I have seen Pulmonologist, Rheumatologist and my primary care provider , I have leg weakness, fatigue, lack of energy, shortness of breath walking more than 50 feet, increase blood pressure, my Lupus has flared up, lack of vocal cord usage, muscle weakness and nausea.. Since seeing my primary care provider I have been put on other medications, Coreg, Losartan, Zofran, Clonidine.

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Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: EKG's in ER , Complete pulmonary function tests- 5/26/21 and 8/3/21 CTA Chest ER 4/20/21 CT HIgh resolution ER 8/3/21 Labs - Munson Medical Center Stress test 4/21/21 USV Renal Ultrasound 8/25/21 Chest x-ray 4/21/21 Echocardiogram 4/21/21
Aktuelle Erkrankungen: none
Vorgeschichte: Cancer, Non Hodgkins Lymphoma of Parotid Glands, Diabetes Type 2, Lupus, Sjogrens syndrome, Rheumatoid arthritis, Hypothyroidism, Dry eyes/dry mouth
Andere Medikamente: Ozempic, Levothyroxine
Allergien: Scopolamine patch, Compazine, Tramadol, Levaquin, Bumex, Metformin, Pravastatin, Januvia, Norco
Vorherige Impfungen: -

VAERS 1766989

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: PA
Alter: 83,0
Geschlecht: F
Eingang: 07.10.2021
Impfdatum: 13.02.2021
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: OT / -

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

Abdominal discomfort Arthralgia Chills Diarrhoea Gait disturbance Hyperhidrosis Mobility decreased Myalgia Pain

Symptomtext

Upset stomach; Cannot lift her arms/cannot bend fingers; Difficulty walking; Severe sweating; Diarrhea; Greatest pain on right side; Excruciating pain in shoulder/excruciating pain in hands, through knees/pain in all joints, fingers; All joints in pain; Chills; This spontaneous case was reported by a physician and describes the occurrence of ABDOMINAL DISCOMFORT (Upset stomach), MOBILITY DECREASED (Cannot lift her arms/cannot bend fingers), GAIT DISTURBANCE (Difficulty walking), HYPERHIDROSIS (Severe sweating) and DIARRHOEA (Diarrhea) in an 83-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 0173NA, 040A21A and 038K20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included Colectomy. Concurrent medical conditions included Immunocompromised. On 13-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 14-Mar-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 14-Sep-2021, received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On an unknown date, the patient experienced ABDOMINAL DISCOMFORT (Upset stomach), MOBILITY DECREASED (Cannot lift her arms/cannot bend fingers), GAIT DISTURBANCE (Difficulty walking), HYPERHIDROSIS (Severe sweating), DIARRHOEA (Diarrhea), PAIN (Greatest pain on right side), MYALGIA (Excruciating pain in shoulder/excruciating pain in hands, through knees/pain in all joints, fingers), ARTHRALGIA (All joints in pain) and CHILLS (Chills). The patient was treated with IBUPROFEN at an unspecified dose and frequency; PARACETAMOL (TYLENOL) at an unspecified dose and frequency and MAGNESIUM SALICYLATE at an unspecified dose and frequency. At the time of the report, ABDOMINAL DISCOMFORT (Upset stomach), MOBILITY DECREASED (Cannot lift her arms/cannot bend fingers), GAIT DISTURBANCE (Difficulty walking), HYPERHIDROSIS (Severe sweating), DIARRHOEA (Diarrhea), PAIN (Greatest pain on right side), MYALGIA (Excruciating pain in shoulder/excruciating pain in hands, through knees/pain in all joints, fingers), ARTHRALGIA (All joints in pain) and CHILLS (Chills) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Patient is on no concomitant medications, but she takes a lot of vitamins.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Immunocompromised
Vorgeschichte: Medical History/Concurrent Conditions: Colectomy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1765312

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038k20a

moderat

Staat: NJ
Alter: 46,0
Geschlecht: F
Eingang: 06.10.2021
Impfdatum: 11.03.2021
Beginn: 29.09.2021
Tage bis Beginn: 202,0
Dosis: 1
Route/Site: SYR / RA

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

Arthralgia Condition aggravated Fatigue Genital herpes Herpes simplex test positive Pain Rheumatoid arthritis

Symptomtext

First ever genital herpes outbreak during Rheumatoid Arthritis flare. Blister on genitals, fatigue and all over body pain in joints RA/muscles. Never had any symptoms of Herpes before. Medical practitioner mentioned that the vaccine could possibly awaken dormant viruses. I am immuno suppressed.

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Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: September 30, 2021 at Labcorp. Positive for Herpes simplex virus type-2. Typing was confirmed by monoclonal antibody microscopic immunofluorescence.
Aktuelle Erkrankungen: -
Vorgeschichte: Rheumatoid Arthritis Obesity
Andere Medikamente: Enbrel 50mg/ml sureclick Methotrexate 20mg 1x/wk Sertraline 50mg/day Wellbutrin HCL XL 300mg/day Rosuvastatin 10mg/day Folic acid 1mg/day Fluticasone nasal Women?s Multi vitamin 1/day Vitamin C 500mg/day Fish oil 1000mg 1x/day D3 25mcg-1
Allergien: None
Vorherige Impfungen: -

VAERS 1757490

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: IL
Alter: 53,0
Geschlecht: F
Eingang: 03.10.2021
Impfdatum: 27.02.2021
Beginn: 20.09.2021
Tage bis Beginn: 205,0
Dosis: 1
Route/Site: SYR / -

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

Migraine Muscle twitching

Symptomtext

Sept 20 my facial muscles started to twitch and I had consistent migraines with lasting over 8 hours. Icing or taking medication only reduced the severity of migraine but it did not go away.

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Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: I have been getting vitamin infusions with B complex vitamin C and glutathione
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: Shellfish,nuts,avacado,,aloe
Vorherige Impfungen: -

VAERS 1751967

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: FL
Alter: 64,0
Geschlecht: F
Eingang: 01.10.2021
Impfdatum: 31.01.2021
Beginn: 01.02.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: OT / LA

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

Atrial fibrillation Echocardiogram Heart rate Heart rate irregular Hepatic function abnormal Platelet count Platelet count decreased Troponin Vaccination site cellulitis Vaccination site erythema Vaccination site pain Vaccination site swelling Vaccination site warmth Ventricular tachycardia Vitamin D decreased

Symptomtext

Ventricular Tachycardia (VTach); Atrial Fibrillation (AFib); Hot to touch; she has had abnormal level of her liver function; Painful at the Injection site; Irregular heart beat; Vitamin D decreased; Platelet count decreased; Arm was swollen; Redness; thought it was cellulitis; This spontaneous case was reported by a patient and describes the occurrence of VENTRICULAR TACHYCARDIA (Ventricular Tachycardia (VTach)) and ATRIAL FIBRILLATION (Atrial Fibrillation (AFib)) in a 65-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included Overweight. Concomitant products included DIPHTHERIA VACCINE from 09-Mar-2021 to an unknown date for an unknown indication. On 31-Jan-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. In February 2021, the patient experienced VACCINATION SITE CELLULITIS (thought it was cellulitis), VACCINATION SITE SWELLING (Arm was swollen) and VACCINATION SITE ERYTHEMA (Redness). On 07-Mar-2021, the patient experienced VENTRICULAR TACHYCARDIA (Ventricular Tachycardia (VTach)) (seriousness criteria hospitalization and medically significant), ATRIAL FIBRILLATION (Atrial Fibrillation (AFib)) (seriousness criteria hospitalization and medically significant), PLATELET COUNT DECREASED (Platelet count decreased) and VITAMIN D DECREASED (Vitamin D decreased). On 17-May-2021, the patient experienced HEART RATE IRREGULAR (Irregular heart beat). On an unknown date, the patient experienced VACCINATION SITE WARMTH (Hot to touch), HEPATIC FUNCTION ABNORMAL (she has had abnormal level of her liver function) and VACCINATION SITE PAIN (Painful at the Injection site). The patient was treated with CEFALEXIN MONOHYDRATE (KEFLEX [CEFALEXIN MONOHYDRATE]) ongoing since an unknown date for Vaccination site cellulitis, at a dose of 1 dosage form; MUPIROCIN ongoing since an unknown date for Vaccination site cellulitis, at a dose of 1 dosage form; ACRIVASTINE (BENADRYL ALLERGY RELIEF) ongoing since an unknown date for Adverse event, at a dose of 1 dosage form; APIXABAN (ELIQUIS) ongoing since an unknown date for Atrial fibrillation, at a dose of 1 dosage form, blood thinner; VITAMIN D NOS ongoing since an unknown date for Vitamin deficiency, at a dose of 1 dosage form and METOPROLOL ongoing since an unknown date for Adverse event, at a dose of 25 mg as required. On 07-Mar-2021, VENTRICULAR TACHYCARDIA (Ventricular Tachycardia (VTach)) and ATRIAL FIBRILLATION (Atrial Fibrillation (AFib)) had resolved. At the time of the report, HEART RATE IRREGULAR (Irregular heart beat), VACCINATION SITE CELLULITIS (thought it was cellulitis) and VITAMIN D DECREASED (Vitamin D decreased) had resolved and VACCINATION SITE WARMTH (Hot to touch), PLATELET COUNT DECREASED (Platelet count decreased), HEPATIC FUNCTION ABNORMAL (she has had abnormal level of her liver function), VACCINATION SITE PAIN (Painful at the Injection site), VACCINATION SITE SWELLING (Arm was swollen) and VACCINATION SITE ERYTHEMA (Redness) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 29-Apr-2021, Echocardiogram: normal (normal) Test was performed on 16th March. On 29-Apr-2021, Heart rate: 130 or 140 (abnormal) Irregular pulse of 130 or 140. On 29-Apr-2021, Platelet count: 105,000 (abnormal) abnormal platelet level 105,000 on 7th March 2021 and low (abnormal) platelets count of 137,000 [normal level: 150,000-450,000] on 6-JUN-2021. On 29-Apr-2021, Troponin: 0.0033 (normal) 0.0033 [Normal: lower than 0.045]. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Patient went on to consult with her HCP thought of vaccination site was Cellulitis and it had Infiltrated the tissue at injection site. Patient stated that she has had abnormal level of her liver function. The doctor performed a CAT scan and blood work and was diagnosed with Arrhythmia with Atrial Fibrillation and Ventricular Tachycardia. On 09 Mar 2021, Patient was told to get the Pneumonia Vaccine along with DPT [diphtheria] vaccine. Patient received both of the vaccine in each arm. Patient had no idea which vaccine was given on the left arm. But again her left arm was swollen, redness, and painful. She stated that in the past never had blood work done. But since the incident, her blood work had been abnormal. Particularly her platelets had been dropping. So patient said her blood work was done on March 7, March 9, April 29th (platelets level were 105,000 then normal), May 3, May 12, and May 17th. She had followed up with Hematologist who informed her that this go eventually go away and it can come back to normal level. She also confirmed that they did not take any medicine or over the counter medicine prior to receiving COVID-19 vaccine and said that her HCP are looking into to see if she can potentially get the 3rd dose or not of the Moderna COVID-19 vaccine. Patient stated that she had risk factor of Over weight. This case concerns a 65-year-old female patient with no details on previous relevant medical history, who experienced the unexpected serious events of Atrial fibrillation and Ventricular tachycardia and the non-serious AESI of Platelet count decreased with other associated non serious events after (mRNA- 1273 vaccine / Moderna COVID-19 Vaccine). The onset of the events occurred approximately 1 month and 8 days after the second dose. The rechallenge is not applicable, since the events occurred after the second dose. The benefit-risk relationship of vaccine is not affected by this report. This case was linked to MOD-2021-330876 (Patient Link).; Sender's Comments: This case concerns a 65-year-old female patient with no details on previous relevant medical history, who experienced the unexpected serious events of Atrial fibrillation and Ventricular tachycardia and the non-serious AESI of Platelet count decreased with other associated non serious events after (mRNA- 1273 vaccine / Moderna COVID-19 Vaccine). The onset of the events occurred approximately 1 month and 8 days after the second dose. The rechallenge is not applicable, since the events occurred after the second dose. The benefit-risk relationship of vaccine is not affected by this report.

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Praegender Schweregrund: Ventricular tachycardia
Hospital-Tage: -
Labordaten: Test Date: 20210429; Test Name: ECHO; Result Unstructured Data: Test was performed on 16th March; Test Date: 20210429; Test Name: Pulse Rate; Result Unstructured Data: Irregular pulse of 130 or 140; Test Date: 20210429; Test Name: Platelet level; Result Unstructured Data: abnormal platelet level 105,000 on 7th March 2021; Test Date: 20210429; Test Name: platelets count; Result Unstructured Data: platelets count of 137,000 [normal level: 150,000-450,000] on 6-JUN-2021; Test Date: 20210429; Test Name: Troponin; Result Unstructured Data: 0.0033 [Normal: lower than 0.045]
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Overweight
Andere Medikamente: DIPHTHERIA VACCINE
Allergien: -
Vorherige Impfungen: -

VAERS 1731138

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: MI
Alter: 84,0
Geschlecht: M
Eingang: 24.09.2021
Impfdatum: 12.03.2021
Beginn: 20.09.2021
Tage bis Beginn: 192,0
Dosis: 1
Route/Site: IM / UN

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

COVID-19 Condition aggravated Confusional state Cough Dyspnoea Malaise Pneumonia Respiratory tract congestion SARS-CoV-2 test positive Tremor

Symptomtext

85-year-old male presents emergency department by private automobile in mild distress. He is tremulous. Patient has a history of COPD and tremors. He is currently being treated for lung cancer with metastasis to the brain as well. He is on antibiotics for a diagnosis of pneumonia on Monday. He started feeling sick on Monday with cough and congestion. He was seen by his doctor and placed on antibiotics. Today his tremors got worse and he was increasingly short of breath. He has home oxygen but only wears it occasionally. They checked his O2 saturation at home and it was 78%. He does not complain of any chest pain. He is mildly confused. No nausea or vomiting.

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Praegender Schweregrund: Condition aggravated
Hospital-Tage: 2,0
Labordaten: SARS CoV-2 RNA (NAAT)= Detected
Aktuelle Erkrankungen: unknown
Vorgeschichte: COPD, lung cancer w brain metastasis
Andere Medikamente: Current Home Medications 1. Aspir 81 oral delayed release tablet : 1 tab(s) orally once a day 2. levoFLOXacin 500 mg oral tablet : 1 tab(s) orally every 24 hours 3. metoprolol tartrate 25 mg oral tablet : 1 tab(s) orally once a day 4. potas
Allergien: penicillin
Vorherige Impfungen: -

VAERS 1716115

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: MI
Alter: 91,0
Geschlecht: F
Eingang: 20.09.2021
Impfdatum: 13.02.2021
Beginn: 12.09.2021
Tage bis Beginn: 211,0
Dosis: 2
Route/Site: UN / UN

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

Acute kidney injury Asthenia Blood sodium decreased COVID-19 Chest X-ray normal Condition aggravated Hypomagnesaemia Hyponatraemia Monoclonal antibody unconjugated therapy SARS-CoV-2 test positive

Symptomtext

Patient is a 92-year-old female who presented with weakness. The patient has a history of HTN, CKD 3, GERD. In the ER the patient was found to be COVID positive, she is fully vaccinated. She did not have any hypoxia. Her labs showed hyponatremia with sodium of 126, AKI and hypomagnesemia. The patient had a CXR which was negative. She was admitted for further management. The patient was agreeable to monoclonal antibody therapy and this was completed on 9/12. She was given some IVF and her renal function normalized. On the morning of discharge she was feeling much better. Her sodium level had improved. She worked with OT who recommended home with home health PT/OT and nursing. The patient's daughter agreed to stay with her initially and make sure things were continuing to go well at home. Care management helped arrange home health care for the patient. The patient was advised to follow up with her PCP after discharge and discharged home in stable condition with her daughter.

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Praegender Schweregrund: Condition aggravated
Hospital-Tage: 1,0
Labordaten: DR CHEST SINGLE VIEW [244473878] Resulted: 09/12/21 1152 Order Status: Completed Updated: 09/12/21 1154 Narrative: EXAMINATION: Single View Chest EXAM DATE: 9/12/2021 11:35 AM TECHNIQUE: Portable upright AP view. INDICATION: URI symptoms COMPARISON: 3/29/2013 ENCOUNTER: Not applicable _________________________ FINDINGS: There is cut off of the right lateral angle. Chin dominant positioning limits detail at the thoracic inlet. The heart is normal in size. There is no pulmonary vascular congestion. No effusion, pneumothorax or acute pulmonary process is seen. _________________________ Impression: Negative for acute cardiopulmonary process. Procedure Component Value Ref Range Date/Time COVID-19 PCR, Rapid [244473868] (Abnormal) Collected: 09/12/21 1113 Order Status: Completed Specimen: Swabbed Collection from Nasopharynx Updated: 09/12/21 1128 COVID-19 PCR Detected Abnormal Not Detected Comment: COVID-19 (SARS-CoV-2) test is positive. Clinical correlation with patient history and other diagnostic information is necessary to determine infection status. This test has received Emergency Use Authorization (EUA) by the FDA, but performance has not been evaluated for asymptomatic patients. Testing was performed using a nucleic acid amplification method. The specimen source may have been changed from the original order per patient situation or symptoms. Covid 19 Result Comment See Comment Comment: COVID-19 results reported as "detected" means COVID-19 positive. Positive patients should self-isolate for 10 days or 24 hours after fever resolves and other symptoms are improving, whichever is longer: - Stay home except to get medical care and wear a facemask if you must leave - Separate yourself from other people in your home, known as home isolation - Cover your coughs and sneezes - Wash your hands often - Avoid sharing household items - Clean high-touch surfaces everyday - If you have a medical emergency and need to call 911, notify dispatch personnel that you may have COVID-19 and put on a facemask before emergency medical services arrive. If the result is "inconclusive" or "invalid" and you have not been contacted by a medical professional from us about your result or if you have questions about COVID-19, your symptoms, or need a return to work/school note, please contact your primary care provider (PCP).
Aktuelle Erkrankungen: Chronic renal insufficiency, stage 3 (moderate)
Vorgeschichte: Respiratory DOE (dyspnea on exertion) Circulatory Hypertension, benign Digestive GERD (gastroesophageal reflux disease) Vitamin D deficiency Infectious/Inflammatory COVID-19 virus infection Nervous Chest pain, unspecified type Genitourinary Chronic renal insufficiency, stage 3 (moderate) Endocrine/Metabolic Hyperlipemia Hyponatremia Hypomagnesemia Other Osteopenia Generalized weakness
Andere Medikamente: ALPRAZolam (XANAX) 0.5 MG tablet amLODIPine (NORVASC) 5 MG tablet aspirin (ASPIRIN LOW DOSE) 81 MG tablet atenolol (TENORMIN) 50 MG tablet escitalopram (LEXAPRO) 5 MG tablet furosemide (LASIX) 20 MG tablet hydrALAZINE (APRESOLINE) 25 MG tab
Allergien: No Active Allergies
Vorherige Impfungen: -

VAERS 1714252

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: FL
Alter: 67,0
Geschlecht: F
Eingang: 19.09.2021
Impfdatum: 01.02.2021
Beginn: 01.02.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

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

Computerised tomogram head Dizziness Dyskinesia Fall Head injury Malaise Mobility decreased Pain Pyrexia Walking aid user

Symptomtext

Approximately one hour after receiving the Moderna vaccine, I returned home. As I was walking into the house, I became dizzy and lightheaded. I braced myself against the wall so I wouldn't fall. My husband then walked me slowly to the nearest chair. After about 20 seconds, the dizzy spell stopped. However, while I was braced against the wall, I lost control of my right arm. It fell away from the wall and started flopping around uncontrollably. I had never had this happen before, but have had repeated dizzy spells since then with the same uncontrolled movements of my right arm. In fact, after receiving the Moderna booster shot on 9-1-21, I had a similar experience the next day. I was using a walker for stability as I was not feeling well, with body aches and a low fever. As I was walking with the walker, I had a dizzy spell come on, and lost control of my right arm which let go of the walker handle. As a result, I fell and hit my head on the floor. I did not lose consciousness.

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Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: CT of head 5-21-2021
Aktuelle Erkrankungen: Bronchiectasis Mycobacterium avium complex - lung infection Osteoporosis Depression
Vorgeschichte: Mycobacterium avium complex - lung infection See Item 11 above
Andere Medikamente: Omeprazole 20 mg daily Azithromycin 500 mg daily Eliquis 5 mg twice daily Dexamethasone 2 mg 5 days/week; 1 mg 2 days/week Floranex 1 tablet twice daily Levothyroxine .025 mg daily Metoprolol Succinate ER 25 mg - 1/2 tablet daily Mirtaz
Allergien: Soy
Vorherige Impfungen: -

VAERS 1705009

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: NJ
Alter: 46,0
Geschlecht: F
Eingang: 16.09.2021
Impfdatum: 11.02.2021
Beginn: 18.02.2021
Tage bis Beginn: 7,0
Dosis: 1
Route/Site: IM / RA

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

Condition aggravated Rash Rash pruritic Rheumatoid arthritis Swelling

Symptomtext

RASH: On 2/20 (after dose 1) I had a small itchy bump and pale rash about 4? below the injection site. It lasted 2 days and faded. (Also, the site of my tdap vaccine on the opposite arm a month earlier was now red and itchy). The same injection site rash returned 4? below the site on 3/12 after dose 2. It was tender and itchy. It lasted a few days and faded, but returned about 2 weeks later and faded over a week. RA FLARES: Rheumatoid Arthritis symptoms flared mildly after first dose of the vaccine, but got progressively worse beginning 1 day after the 2nd dose. Systemic flares of swelling, pain, and inflammation in multiple joints, including: both elbows, both knees, multiple fingers, both wrists, right side jaw, and left toes. Symptoms increased in severity as time progressed, causing difficulty with daily activities and intense pain up to level 8-10. After using a medrol dose pack to try and reduce flares, pain returned when the pack was complete. 5mg/ day of Prednisone was added but removed after 1 week due to not feeling well. At that point it was determined that my current treatment was no longer working and the Enbrel was dropped from my regimen and replaced with Xeljanz XR. 10mg daily Prednisone was added back in to bridge the 6-8 week timeframe of waiting for the new treatment to kick in. As of the current date, the prednisone is being tapered off as flare symptoms have all but disappeared with the effectiveness of the Xeljanz. **NOTE: my Rheumatoid Arthritis was not completely controlled at time of the vaccine and there had already been discussion between my doctor and me regarding possible treatment change. To receive each dose of the vaccine I had to stop taking both the methotrexate and Enbrel each week of the shot. We believe that the combined lack of meds with the disease activity made my immune system go hyperactive when it woke up to create Covid antibodies, which also caused my immune system to attack me.

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Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: 2/10/2021 (labs 1 day prior to shot 1) Sed Rate: 63 CRP: 9 6/18/2021 (first labs after both shots and before new meds) Sed Rate: 87 CRP: 39 5/25/2021 VECTRA SCORE: 51 (Prior vectra score was 47on 10/29/2020)
Aktuelle Erkrankungen: None
Vorgeschichte: Rheumatoid Arthritis Obesity
Andere Medikamente: Enbrel 50mg/ml sureclick Methotrexate 20mg 1x/wk Sertraline 50mg/day Wellbutrin HCL XL 300mg/day Rosuvastatin 10mg/day Folic acid 1mg/day Fluticasone nasal Women?s Multi vitamin 1/day Vitamin C 500mg/day Fish oil 1000mg 1x/day D3 25mcg-1
Allergien: None
Vorherige Impfungen: -

VAERS 1700269

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: MI
Alter: 82,0
Geschlecht: F
Eingang: 15.09.2021
Impfdatum: 12.02.2021
Beginn: 08.09.2021
Tage bis Beginn: 208,0
Dosis: 2
Route/Site: IM / RA

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

Asthenia Bedridden COVID-19 Condition aggravated Culture urine positive Diarrhoea Dysphagia Multiple sclerosis Muscular weakness Pyuria SARS-CoV-2 test positive Wheelchair user

Symptomtext

Hospitalization; COVID-19 positive (9.8.21); fully immunized Admission Date: 9/8/2021 Discharge Date: 9/11/2021 Discharge Disposition: home health care svc Active Issues Requiring Follow-up: PCP , will need help on procuring interferon beta DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Generalized weakness [R53.1] HOSPITAL COURSE: Patient is a 82 y.o. female with PMH of multiple sclerosis, neurogenic bladder s/p chronic Foley, hyperlipidemia, hypertension, DVT, and CVA with chronic left-sided weakness who presented to the ED 9/8 for generalized weakness. The patient is wheelchair/bed bound as a result of MS and previous CVA. Over the past 3 weeks she noted increasing generalized weakness particularly of her bilateral upper extremities. This had been much worse within the last week. She was concerned that this was related to MS because she stopped taking her q48hr Interferon beta in July because it was too expensive. Her acute on chronic weakness was felt to be due to progression of MS off of Interferon beta and COVID. PT rec discharge home with assist which CM ensured was in place prior to discharge. SLP evaluated and recommended dysphagia diet. No hypoxemia, imaging findings, or significant respiratory symptoms to suggest COVID pneumonia during admission. She had diarrhea on presentation that self resolved. She had asymptomatic pyuria and was given Ceftriaxone in the ED, urine cultures showed mixed flora antibiotics were not continued during admission.

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Praegender Schweregrund: Condition aggravated
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: NA
Vorgeschichte: Multiple sclerosis Urinary tract infection associated with indwelling urethral catheter Irritable bowel Recurrent UTI H/O Clostridium difficile infection Septic shock Bladder dysfunction Essential hypertension Acute respiratory failure with hypoxia Lower GI bleed Previous (DVT) of femoral vein of right lower extremity Steroid-induced hyperglycemia Acute blood loss anemia AKI (acute kidney injury) Proctitis Multiple sclerosis Weakness generalized Hypokalemia Chronic indwelling Foley catheter Gastroenteritis Bowel dysfunction Wheelchair bound Foot drop, right Spasticity Cellulitis of right lower extremity Generalized weakness
Andere Medikamente: (TYLENOL) 500 MG (NORVASC) 10 MG (LIORESAL) 10 MG (REFRESH OPTIVE ADVANCED) 0.5-1-0.5 % SOLN (ZYRTEC) 10 MG (ANUSOL-HC) 25 MG (BETASERON) 0.25 mg/mL (ACIDOPHILUS) (LOPRESSOR) 25 MG (DITROPAN) 5 MG (PRAVACHOL) 40 MG (RISPERDAL) 0.25 MG
Allergien: Latex
Vorherige Impfungen: -

VAERS 1695840

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038k20a

moderat

Staat: IN
Alter: 60,0
Geschlecht: F
Eingang: 14.09.2021
Impfdatum: 31.01.2021
Beginn: 01.05.2021
Tage bis Beginn: 90,0
Dosis: 2
Route/Site: SYR / RA

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

Anxiety Arthralgia Asthenia Blood test Bradyphrenia Condition aggravated Depression Feeling abnormal Memory impairment Myalgia Pain Thyroid hormones test

Symptomtext

Starting approximately 90 days after getting vaccine and progressing with no let-up, I am in pain most of the time now - joints and muscles. Any normal muscle ache I had before vaccine is now amplified 60% every single day. I have 40% less energy and have waves of depression and anxiety - all that have escalated and highly exceed any emotions prior to vaccine. Memory and thinking are much more foggy and slower than before. I am not in the same health as I was a year ago. I regret ever getting vaccine -

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Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Hormones are level - thyroid included. Nothing on my bloodwork shows any reason for this pain. bloodwork taken 2nd or 3rd qtr of 2021
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Wellbutrin Adderall Losartin (been taking for a long period of time before vac date)
Allergien: none
Vorherige Impfungen: -

VAERS 1682472

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: -
Alter: 73,0
Geschlecht: M
Eingang: 08.09.2021
Impfdatum: 02.03.2021
Beginn: 02.09.2021
Tage bis Beginn: 184,0
Dosis: 1
Route/Site: IM / UN

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

Asthenia COVID-19 Cough Dyspnoea Fatigue SARS-CoV-2 test positive

Symptomtext

This is a very pleasant 73-year-old male with hypertension, hyperlipidemia, peripheral neuropathy, patient presented to the emergency department due to progressively worsening cough and shortness of breath, he has known positive COVID-19 infection in the outpatient setting, he reports that he is vaccinated with Moderna vaccine 1st dose in April 2021 and the 2nd dose in May 2021, P started to have symptoms about 7-10 days ago, he also received a dose of Regenerone in the outpatient setting about 4 days ago per his report, he denies any known sick contacts, lives with his wife at home, his symptoms have been progressively worsening including shortness of breath, nonproductive cough, overall generalized weakness and fatigue. He denies any chest pain, nausea, vomiting, sweating, dizziness or focal weaknesses. In the emergency department, his resting pulse ox is 90-91%, requiring minimal supplemental O2 via nasal cannula. Nothing seems to improve or worsen his symptoms. He is currently afebrile and hemodynamically stable Tested positive on 9/2/2021

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: hypertension, hyperlipidemia, peripheral neuropathy
Andere Medikamente: -
Allergien: doxycyvcline monohydrate, augmentin
Vorherige Impfungen: -

VAERS 1678179

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: IN
Alter: 72,0
Geschlecht: F
Eingang: 07.09.2021
Impfdatum: 23.01.2021
Beginn: 06.02.2021
Tage bis Beginn: 14,0
Dosis: 1
Route/Site: SYR / RA

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

Electrocardiogram Fatigue Laboratory test Pain in extremity Palpitations Paraesthesia Tachycardia Weight decreased

Symptomtext

Sore arm, tingling all over. Fatigue, palpitations, tachycardia, weight loss

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Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: EKG, labs
Aktuelle Erkrankungen: Arthritis
Vorgeschichte: Arthritis
Andere Medikamente: Lisinopril
Allergien: NKA
Vorherige Impfungen: -

VAERS 1658468

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: FL
Alter: 67,0
Geschlecht: F
Eingang: 31.08.2021
Impfdatum: 01.02.2021
Beginn: 20.07.2021
Tage bis Beginn: 169,0
Dosis: UNK
Route/Site: IM / -

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

Asthenia COVID-19 Chest X-ray Chest pain Chills Dyspnoea Fatigue Nausea Pain Pyrexia SARS-CoV-2 test positive

Symptomtext

Pt came to ER c/o weakness and fatigue, lack of strength, chest pain, nausea, SOB, fever, chills, and achy. Onset 1 week prior was recently diagnosed with Covid.

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Praegender Schweregrund: Chest pain
Hospital-Tage: 7,0
Labordaten: 7/20/20: CXR, 7/6/20: Covid test positive.
Aktuelle Erkrankungen: -
Vorgeschichte: COPD, HTN, PEG tube, cancer of tongue, cancer of throat, PVD,
Andere Medikamente: -
Allergien: Levaquin
Vorherige Impfungen: -

VAERS 1637623

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038k20a

moderat

Staat: IL
Alter: 36,0
Geschlecht: F
Eingang: 26.08.2021
Impfdatum: 03.02.2021
Beginn: 01.03.2021
Tage bis Beginn: 26,0
Dosis: 2
Route/Site: IM / RA

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

Migraine

Symptomtext

Migraines multiple times a week

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Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Interstitial Cystitis, adenomyosis, anxiety, IBS
Andere Medikamente: Fish oil, multivitamin, Lexapro, Xanax (as needed)
Allergien: Triptans, monistat
Vorherige Impfungen: -

VAERS 1631841

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: IL
Alter: 78,0
Geschlecht: F
Eingang: 25.08.2021
Impfdatum: 27.02.2021
Beginn: 27.03.2021
Tage bis Beginn: 28,0
Dosis: 1
Route/Site: OT / RA

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

Dyspnoea Vaccination site erythema

Symptomtext

Difficulty breathing; multiple red, hot, itchy lumps at the injection site; This spontaneous case was reported by a consumer and describes the occurrence of DYSPNOEA (Difficulty breathing) and VACCINATION SITE ERYTHEMA (multiple red, hot, itchy lumps at the injection site) in a 78-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 011A21A and 038K20A) for COVID-19 vaccination. Concurrent medical conditions included COPD. Concomitant products included WARFARIN, ATORVASTATIN, METOPROLOL and PARACETAMOL (TYLENOL) for an unknown indication. On 27-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 27-Mar-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 27-Mar-2021, the patient experienced DYSPNOEA (Difficulty breathing) and VACCINATION SITE ERYTHEMA (multiple red, hot, itchy lumps at the injection site). At the time of the report, DYSPNOEA (Difficulty breathing) and VACCINATION SITE ERYTHEMA (multiple red, hot, itchy lumps at the injection site) was resolving. Concomitant medications taken were Heart medication No treatment medications were reported Action taken with mRNA-1273 in response to the events were Not Applicable

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COPD
Andere Medikamente: WARFARIN; ATORVASTATIN; METOPROLOL; TYLENOL
Allergien: -
Vorherige Impfungen: -

VAERS 1624153

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: IL
Alter: 36,0
Geschlecht: F
Eingang: 23.08.2021
Impfdatum: 08.02.2021
Beginn: 09.02.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / AR

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

Anxiety Back pain Condition aggravated Headache Muscle tightness Musculoskeletal discomfort Neck pain Spinal X-ray abnormal Spinal X-ray normal

Symptomtext

I have thoracic back pain that started after a physical therapist pushed on my back doing a spinal mobilization on 2/8/21. I had my COVID vaccine in the morning and my physical therapy appointment in the afternoon. The pain started after my PT appointment. After a myofascial release massage on 5/26/21, I have had neck pain and a headache. Both of these conditions have been described as musculoskeletal problems. Overall the back pain has improved. My neck pain and headache have not improved. I have had a lot of muscle tightness and anxiety. I also hadn't worked out a lot so I think my muscles weren't as strong as they should be.

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Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: thoracic spine x-ray on 3/23/21- normal cervical spine x-ray on 6/27/21- minimal narrowing C6-C7
Aktuelle Erkrankungen: anxiety
Vorgeschichte: anxiety
Andere Medikamente: Prenatal vitamin
Allergien: None
Vorherige Impfungen: -

VAERS 1623565

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: PA
Alter: 40,0
Geschlecht: M
Eingang: 23.08.2021
Impfdatum: 24.01.2021
Beginn: 25.03.2021
Tage bis Beginn: 60,0
Dosis: 2
Route/Site: IM / LA

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

Anticoagulant therapy Arthralgia Chills Condition aggravated Fatigue Feeling abnormal International normalised ratio increased Pain in extremity Prothrombin time prolonged Therapy change

Symptomtext

After receiving my first shot on 1/24/21 I had a sore are and felt tired. After receiving my second Moderna shot on 2/21/21 I had severe chills and felt awful for the next 48 hours. I had a very sore shoulder as well. I have been on Warfarin for almost 20 years due to having Factor V Leiden with a history of DVT in my left leg and a PE in my lungs. I have been on a stable regimen of Warfarin for almost two decades and after the second Moderna shot my protimes have been running very high. I have had numerous conversations with multiple providers and my medicine has been adjusted and my daily dose has been lowered four times now and my INR is still running high. As of this morning I checked my INR on my home monitor and it was a 4.1, which is well outside of the normal range even though the dose of my Warfarin has been lowered multiple times. I am very concerned about what is going on and I've seen my hematologist and primary care doctor. I've been working with the Clinic and they have been working with me to try to get my INR in a stable range but it has yet to get in one. It has been six months of unstable INR results and now I am reaching out to you for help and guidance. Please let me know how you can assist.

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Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Numerous results of out of range INR's over the last six months after the second dose of the Moderna vaccine.
Aktuelle Erkrankungen: N/A
Vorgeschichte: Factor V Leiden deficiency with a history of DVT in left leg and PE in lungs (2002 & 2003).
Andere Medikamente: Warfarin (blood thinners)
Allergien: Augmentin, Hydrocortisone cream
Vorherige Impfungen: -

VAERS 1622430

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: FL
Alter: -
Geschlecht: M
Eingang: 23.08.2021
Impfdatum: 28.01.2021
Beginn: 26.02.2021
Tage bis Beginn: 29,0
Dosis: 1
Route/Site: OT / LA

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

Influenza like illness Mobility decreased Myalgia Paraesthesia

Symptomtext

experiencing tingling in legs and problem getting up with muscles; problem getting up with muscles; Sore arm; flu like symptoms; This spontaneous case was reported by a consumer and describes the occurrence of INFLUENZA LIKE ILLNESS (flu like symptoms), PARAESTHESIA (experiencing tingling in legs and problem getting up with muscles), MOBILITY DECREASED (problem getting up with muscles) and MYALGIA (Sore arm) in a male patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 013M20A and 038K20A) for COVID-19 vaccination. Concomitant products included OMEPRAZOLE for an unknown indication. On 28-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 25-Feb-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 26-Feb-2021, the patient experienced INFLUENZA LIKE ILLNESS (flu like symptoms) and MYALGIA (Sore arm). On 02-Apr-2021, the patient experienced PARAESTHESIA (experiencing tingling in legs and problem getting up with muscles) and MOBILITY DECREASED (problem getting up with muscles). On 27-Feb-2021, INFLUENZA LIKE ILLNESS (flu like symptoms) and MYALGIA (Sore arm) had resolved. At the time of the report, PARAESTHESIA (experiencing tingling in legs and problem getting up with muscles) and MOBILITY DECREASED (problem getting up with muscles) had not resolved. No treatment details were reported.

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

VAERS 1622411

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: MI
Alter: 68,0
Geschlecht: M
Eingang: 23.08.2021
Impfdatum: 06.02.2021
Beginn: 06.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / -

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

Arthralgia Condition aggravated Pain

Symptomtext

soreness in my shoulder/right hand started experiencing a lot of pain in the joints; shoulder and hand throbbing and it keeps me up; The soreness didn't go away and has gotten worse over time; This spontaneous case was reported by a consumer and describes the occurrence of ARTHRALGIA (soreness in my shoulder/right hand started experiencing a lot of pain in the joints), PAIN (shoulder and hand throbbing and it keeps me up) and CONDITION AGGRAVATED (The soreness didn't go away and has gotten worse over time) in a 68-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 040A21A and 038K20A) for COVID-19 vaccination. No medical history was provided by the reporter. Concomitant products included ATORVASTATIN for Cholesterol, CLOPIDOGREL for Stent placement, LISINOPRIL and METOPROLOL for an unknown indication. On 06-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 06-Mar-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 06-Feb-2021, the patient experienced ARTHRALGIA (soreness in my shoulder/right hand started experiencing a lot of pain in the joints), PAIN (shoulder and hand throbbing and it keeps me up) and CONDITION AGGRAVATED (The soreness didn't go away and has gotten worse over time). The patient was treated with ACETYLSALICYLIC ACID, CAFFEINE, PARACETAMOL (EXCEDRIN [ACETYLSALICYLIC ACID;CAFFEINE;PARACETAMOL]) at an unspecified dose and frequency. At the time of the report, ARTHRALGIA (soreness in my shoulder/right hand started experiencing a lot of pain in the joints), PAIN (shoulder and hand throbbing and it keeps me up) and CONDITION AGGRAVATED (The soreness didn't go away and has gotten worse over time) had not resolved. Treatment information also include Arthritis HOT Ointment. The soreness didn't go away and has gotten worse over time. Their right hand also started experiencing a lot of pain in the joints. The patient waited and thought it would subside but hasn't yet. The soreness really bothers them more at night compared to any other time when they have a lot of movement. When they lay on their left side at night and their right side is elevated, their shoulder and hand begin throbbing and keeps them up. This case was linked to MOD-2021-211615 (Patient Link).

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Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: No medical history was provided by the reporter.
Andere Medikamente: LISINOPRIL; METOPROLOL; ATORVASTATIN; CLOPIDOGREL
Allergien: -
Vorherige Impfungen: -

VAERS 1608630

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: IL
Alter: 76,0
Geschlecht: F
Eingang: 22.08.2021
Impfdatum: 05.02.2021
Beginn: 01.03.2021
Tage bis Beginn: 24,0
Dosis: 1
Route/Site: OT / LA

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

Dizziness Dyspnoea Fatigue Gait disturbance Headache Pain in extremity Tinnitus Tremor

Symptomtext

dizzy; shakiness that has stayed now in her left hand; legs started hurting; has to use a walker in order to walk; after walking she then will have to sit down and is so tired that she then gasps for breath to have get the breath; after walking she then will have to sit down and is so tired that she then gasps for breath to have; started getting headaches; feeling lightheaded; hears pounding and scraping sounds as if someone is hammering or building in her right ear; has shakiness, describing that she is shaky; This spontaneous case was reported by a consumer and describes the occurrence of PAIN IN EXTREMITY (legs started hurting), GAIT DISTURBANCE (has to use a walker in order to walk), DYSPNOEA (after walking she then will have to sit down and is so tired that she then gasps for breath to have get the breath), DIZZINESS (feeling lightheaded) and DIZZINESS (dizzy) in a 76-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included Pneumonia and Heart transplant. Concomitant products included CARVEDILOL, OMEPRAZOLE, ATORVASTATIN, ALLOPURINOL, PRIMIDONE and DULOXETINE for an unknown indication. On 05-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 06-Mar-2021, the patient experienced PAIN IN EXTREMITY (legs started hurting), GAIT DISTURBANCE (has to use a walker in order to walk), DYSPNOEA (after walking she then will have to sit down and is so tired that she then gasps for breath to have get the breath), FATIGUE (after walking she then will have to sit down and is so tired that she then gasps for breath to have) and HEADACHE (started getting headaches). In March 2021, the patient experienced DIZZINESS (feeling lightheaded), TREMOR (has shakiness, describing that she is shaky) and TINNITUS (hears pounding and scraping sounds as if someone is hammering or building in her right ear). On an unknown date, the patient experienced DIZZINESS (dizzy) and TREMOR (shakiness that has stayed now in her left hand). The patient was treated with PARACETAMOL (TYLENOL) at a dose of 1 dosage form. At the time of the report, PAIN IN EXTREMITY (legs started hurting), GAIT DISTURBANCE (has to use a walker in order to walk), DYSPNOEA (after walking she then will have to sit down and is so tired that she then gasps for breath to have get the breath), DIZZINESS (feeling lightheaded), DIZZINESS (dizzy), TREMOR (has shakiness, describing that she is shaky), TREMOR (shakiness that has stayed now in her left hand), TINNITUS (hears pounding and scraping sounds as if someone is hammering or building in her right ear), FATIGUE (after walking she then will have to sit down and is so tired that she then gasps for breath to have) and HEADACHE (started getting headaches) outcome was unknown. Not Provided This case was linked to US-MODERNATX, INC.-MOD-2021-079309 (Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2021-079309:

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Heart transplant; Pneumonia
Andere Medikamente: CARVEDILOL; OMEPRAZOLE; ATORVASTATIN; ALLOPURINOL; PRIMIDONE; DULOXETINE
Allergien: -
Vorherige Impfungen: -

VAERS 1597746

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: IL
Alter: 74,0
Geschlecht: F
Eingang: 21.08.2021
Impfdatum: 15.02.2021
Beginn: 10.03.2021
Tage bis Beginn: 23,0
Dosis: 1
Route/Site: OT / -

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

Abdominal pain upper Asthenia Blood glucose increased Blood pressure measurement Body temperature Burning sensation Chills Diarrhoea Dizziness postural Dyspnoea Dysstasia Feeding disorder Heart rate Hyperhidrosis Hypersensitivity Illness Mobility decreased Pyrexia

Symptomtext

This spontaneous case was reported by a consumer (subsequently medically confirmed) and describes the occurrence of ILLNESS (?i had very bad side effects , i was sick for 3 weeks?.), BURNING SENSATION (had high ( around 100F ) and low temperature ( 95F) her forehead sometimes was burning), DIZZINESS POSTURAL (felt dizzy: couldn't stand up to the chair, i asked my husband his walker, that i do not need to use), SWELLING (she was swelling, then freezing again) and HYPERHIDROSIS (hair, neck, head was sweated) in a 74-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concurrent medical conditions included Allergy (Allergic to bees), Hypertension, Diabetes, Cholesterol and Allergy to insect sting (Bess.). On 15-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 10-Mar-2021, the patient experienced DYSSTASIA (felling better when she tried to grab something from the floor and called her husband to pulled her). On an unknown date, the patient experienced ILLNESS (?i had very bad side effects , i was sick for 3 weeks?.), BURNING SENSATION (had high ( around 100F ) and low temperature ( 95F) her forehead sometimes was burning), DIZZINESS POSTURAL (felt dizzy: couldn't stand up to the chair, i asked my husband his walker, that i do not need to use), SWELLING (she was swelling, then freezing again), HYPERHIDROSIS (hair, neck, head was sweated), ASTHENIA (felt very weak: not able to stand up), DIARRHOEA (diarrhea), MOBILITY DECREASED (Could hardly function), ABDOMINAL PAIN UPPER (stomach cramps/ abdominal pain), FEEDING DISORDER (could hardly get the food, tried to eat something to get her pills), WEIGHT DECREASED (Lost 13 pounds in 3 weeks.), HYPERSENSITIVITY (started feeling her throat was closing, like the time she had the allergic reaction with the bees, she), DYSPNOEA (shortness of breath), CHILLS (shivering) and PYREXIA (had high ( around 100F ) and low temperature ( 95F) her forehead sometimes was burning). The patient was treated with PARACETAMOL (TYLENOL) at a dose of 1 dosage form. At the time of the report, ILLNESS (?i had very bad side effects , i was sick for 3 weeks?.), BURNING SENSATION (had high ( around 100F ) and low temperature ( 95F) her forehead sometimes was burning), DIZZINESS POSTURAL (felt dizzy: couldn't stand up to the chair, i asked my husband his walker, that i do not need to use), SWELLING (she was swelling, then freezing again), HYPERHIDROSIS (hair, neck, head was sweated), ASTHENIA (felt very weak: not able to stand up), DIARRHOEA (diarrhea), MOBILITY DECREASED (Could hardly function), ABDOMINAL PAIN UPPER (stomach cramps/ abdominal pain), FEEDING DISORDER (could hardly get the food, tried to eat something to get her pills), WEIGHT DECREASED (Lost 13 pounds in 3 weeks.), HYPERSENSITIVITY (started feeling her throat was closing, like the time she had the allergic reaction with the bees, she), DYSPNOEA (shortness of breath), DYSSTASIA (felling better when she tried to grab something from the floor and called her husband to pulled her), CHILLS (shivering) and PYREXIA (had high ( around 100F ) and low temperature ( 95F) her forehead sometimes was burning) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, Blood glucose increased (130-140 mg/dl): 195 mg/dl (High) High. On an unknown date, Blood pressure measurement: 212 mmHg (High) High. On an unknown date, Body temperature: 100 (High) 100F and 95 (Low) 95F. On an unknown date, Heart rate: high heart beats per minute (High) High. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. Concomitant medications include blood pressure medicine, Cholesterol medicine, diabetic pills. Most recent FOLLOW-UP information incorporated above includes: On 26-Jul-2021: Reporter's mail address updated.

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Test Name: Blood sugar; Test Result: 195 mg/dl; Result Unstructured Data: High; Test Name: Blood pressure; Result Unstructured Data: 212mmHg; Test Name: Body temperature; Result Unstructured Data: 100F; Test Name: Body temperature; Result Unstructured Data: 95F; Test Name: Heart rate; Result Unstructured Data: High
Aktuelle Erkrankungen: Allergy (Allergic to bees); Cholesterol; Diabetes; Hypertension
Vorgeschichte: Medical History/Concurrent Conditions: Allergy to insect sting (Bess.)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1581490

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: FL
Alter: 67,0
Geschlecht: F
Eingang: 18.08.2021
Impfdatum: 02.02.2021
Beginn: 02.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / -

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

Discomfort Dizziness Dysphagia Dysphonia Flushing Nausea Palpitations Vaccination site pain Vaccination site reaction

Symptomtext

flushing; Reaction; Soreness; Nausea; "Rush" Throughout body; Dizziness; Heart Racing; Hard to Swallow; hoarseness which continued for 24 hours; This spontaneous case was reported by a consumer and describes the occurrence of DISCOMFORT ("Rush" Throughout body), DIZZINESS (Dizziness), PALPITATIONS (Heart Racing), DYSPHAGIA (Hard to Swallow) and FLUSHING (flushing) in a 67-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included No adverse event. Concurrent medical conditions included Osteoporosis. Concomitant products included ALENDRONATE SODIUM (FOSAMAX) for an unknown indication. On 02-Feb-2021 at 2:30 PM, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 02-Feb-2021, the patient experienced DISCOMFORT ("Rush" Throughout body), DIZZINESS (Dizziness), PALPITATIONS (Heart Racing), DYSPHAGIA (Hard to Swallow), VACCINATION SITE PAIN (Soreness) and NAUSEA (Nausea). On 02-Feb-2021 at 2:32 PM, the patient experienced VACCINATION SITE REACTION (Reaction). On an unknown date, the patient experienced FLUSHING (flushing) and DYSPHONIA (hoarseness which continued for 24 hours). At the time of the report, DISCOMFORT ("Rush" Throughout body), DIZZINESS (Dizziness), PALPITATIONS (Heart Racing), DYSPHAGIA (Hard to Swallow), FLUSHING (flushing), DYSPHONIA (hoarseness which continued for 24 hours), VACCINATION SITE REACTION (Reaction) and NAUSEA (Nausea) had resolved and VACCINATION SITE PAIN (Soreness) 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. Treatment information was not provided. Most recent FOLLOW-UP information incorporated above includes: On 20-Jul-2021: Significant follow-up information received.

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Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Osteoporosis
Vorgeschichte: Medical History/Concurrent Conditions: No adverse event
Andere Medikamente: FOSAMAX
Allergien: -
Vorherige Impfungen: -

VAERS 1580791

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: FL
Alter: 36,0
Geschlecht: F
Eingang: 18.08.2021
Impfdatum: 29.01.2021
Beginn: 01.02.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: OT / LA

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

Chills Diarrhoea Dyspnoea Myalgia

Symptomtext

diarrhea; chills; body aches; shortness of breath, when she woke up in the morning; This case was received via an unknown source (no reference has been entered for a health authority or license partner) on 02-Feb-2021 and was forwarded to Moderna on 03-Feb-2021. This spontaneous case was reported by a consumer and describes the occurrence of DYSPNOEA (shortness of breath, when she woke up in the morning), DIARRHOEA (diarrhea), CHILLS (chills) and MYALGIA (body aches) in a 36-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. The patient's past medical history included No adverse event. On 29-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 DYSPNOEA (shortness of breath, when she woke up in the morning). On 02-Feb-2021, the patient experienced DIARRHOEA (diarrhea), CHILLS (chills) and MYALGIA (body aches). On 01-Feb-2021, DYSPNOEA (shortness of breath, when she woke up in the morning) outcome was unknown. At the time of the report, DIARRHOEA (diarrhea), CHILLS (chills) and MYALGIA (body aches) 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 includes Tylenol for diarrhea. Concomitant medication for depression and anxiety.

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: No adverse event
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1573122

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: FL
Alter: -
Geschlecht: M
Eingang: 16.08.2021
Impfdatum: 29.01.2021
Beginn: 01.02.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: OT / -

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

Arthralgia Muscular weakness Neck pain Pain in extremity Paraesthesia Peripheral swelling Pruritus

Symptomtext

This spontaneous case was reported by a consumer and describes the occurrence of PAIN IN EXTREMITY (left arm started to ache and went right across to the other arm), NECK PAIN (neck hurt and he could not turn it), PERIPHERAL SWELLING (Both arms swelled up and were itchy and tingly), ARTHRALGIA (excruciating pain through his shoulders and arms and could not even make a fist, pain spread to his knees. They felt weak, shoulder pain) and PRURITUS (Itchy) in a 76-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included Knee replacement. Concomitant products included VALSARTAN, LOVASTATIN, ACETYLSALICYLIC ACID (BABY ASPIRIN) and VITAMIN 15. On 29-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 PAIN IN EXTREMITY (left arm started to ache and went right across to the other arm), NECK PAIN (neck hurt and he could not turn it), PERIPHERAL SWELLING (Both arms swelled up and were itchy and tingly), ARTHRALGIA (excruciating pain through his shoulders and arms and could not even make a fist, pain spread to his knees. They felt weak, shoulder pain), PRURITUS (Itchy) and PARAESTHESIA (tingly). On 09-Feb-2021, the patient experienced MUSCULAR WEAKNESS (barley able to lift up his arms, lost all strength in his hands). On 07-Feb-2021, PAIN IN EXTREMITY (left arm started to ache and went right across to the other arm), NECK PAIN (neck hurt and he could not turn it), PERIPHERAL SWELLING (Both arms swelled up and were itchy and tingly), ARTHRALGIA (excruciating pain through his shoulders and arms and could not even make a fist, pain spread to his knees. They felt weak, shoulder pain), PRURITUS (Itchy) and PARAESTHESIA (tingly) had resolved. At the time of the report, MUSCULAR WEAKNESS (barley able to lift up his arms, lost all strength in his hands) 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 included prednisone, Benadryl, immodine. This case was linked to US-MODERNATX, INC.-MOD-2021-015074 (E2B Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2021-015074:

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Knee replacement
Andere Medikamente: VALSARTAN; LOVASTATIN; BABY ASPIRIN; VITAMIN 15
Allergien: -
Vorherige Impfungen: -

VAERS 1571475

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: PA
Alter: -
Geschlecht: F
Eingang: 16.08.2021
Impfdatum: 16.02.2021
Beginn: 16.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / LA

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

Dyspnoea Nausea Pain in extremity

Symptomtext

pain in arm; feel like i cant breath; little a nauseous a couple hours after the vaccine; This spontaneous case was reported by a consumer and describes the occurrence of PAIN IN EXTREMITY, DYSPNOEA, and NAUSEA in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. #038K20A) for COVID-19 vaccination. No Medical History information was reported. On 16-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 16-Feb-2021, the patient experienced PAIN IN EXTREMITY, DYSPNOEA, and NAUSEA. At the time of the report, PAIN IN EXTREMITY, DYSPNOEA, and NAUSEA outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown.

Weitere VAERSDATA-Felder

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

VAERS 1567735

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: FL
Alter: 58,0
Geschlecht: F
Eingang: 15.08.2021
Impfdatum: 12.03.2021
Beginn: 13.03.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: OT / LA

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

Lymphadenopathy Mobility decreased Swelling Vaccination site erythema Vaccination site mass Vaccination site pain

Symptomtext

Cannot raise her arm up due to pain; Lump the size of a golf ball at the injection site; swelling seemed to be moving down her left side; Lymph nodes started swelling under her left arm, swelling seemed to be moving her left side; Red at the injection site; Sore arm; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION SITE MASS (Lump the size of a golf ball at the injection site), SWELLING (swelling seemed to be moving down her left side), MOBILITY DECREASED (Cannot raise her arm up due to pain), VACCINATION SITE PAIN (Sore arm) and LYMPHADENOPATHY (Lymph nodes started swelling under her left arm, swelling seemed to be moving her left side) in a 58-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 12-Mar-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 13-Mar-2021, the patient experienced VACCINATION SITE PAIN (Sore arm). On 14-Mar-2021, the patient experienced VACCINATION SITE MASS (Lump the size of a golf ball at the injection site), SWELLING (swelling seemed to be moving down her left side), LYMPHADENOPATHY (Lymph nodes started swelling under her left arm, swelling seemed to be moving her left side) and VACCINATION SITE ERYTHEMA (Red at the injection site). On 17-Mar-2021, the patient experienced MOBILITY DECREASED (Cannot raise her arm up due to pain). The patient was treated with IBUPROFEN on 12-Mar-2021 at a dose of UNK dosage form. At the time of the report, VACCINATION SITE MASS (Lump the size of a golf ball at the injection site) and VACCINATION SITE PAIN (Sore arm) was resolving and SWELLING (swelling seemed to be moving down her left side), MOBILITY DECREASED (Cannot raise her arm up due to pain), LYMPHADENOPATHY (Lymph nodes started swelling under her left arm, swelling seemed to be moving her left side) and VACCINATION SITE ERYTHEMA (Red at the injection site) had not resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. Concomitant medications were not provided by the reporter.

Weitere VAERSDATA-Felder

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

VAERS 1567393

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: IL
Alter: 82,0
Geschlecht: M
Eingang: 15.08.2021
Impfdatum: 15.02.2021
Beginn: 18.02.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: OT / -

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

Chills Diarrhoea Tremor Vomiting

Symptomtext

Shaking like a leaf; Chills; Vomited; Diarrhea, it was so bad,; This spontaneous case was reported by a patient and describes the occurrence of DIARRHOEA (Diarrhea, it was so bad,), TREMOR (Shaking like a leaf), VOMITING (Vomited) and CHILLS (Chills) in an 82-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. The patient's past medical history included Pneumonia (had pneumonia several years ago), Memory impairment (medication for memory), Torticollis (torticollis medicine.) and Blood disorder (blood thinner medicine). Concurrent medical conditions included Hypertension (Blood pressure medicine,). On 15-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 18-Feb-2021, the patient experienced DIARRHOEA (Diarrhea, it was so bad,). On 20-Feb-2021, the patient experienced VOMITING (Vomited). On an unknown date, the patient experienced TREMOR (Shaking like a leaf) and CHILLS (Chills). At the time of the report, DIARRHOEA (Diarrhea, it was so bad,), TREMOR (Shaking like a leaf), VOMITING (Vomited) and CHILLS (Chills) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Concomitant medicines included medcines for blood pressure, blood thinner, memory and torticollis. No treatment information reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Hypertension (Blood pressure medicine,)
Vorgeschichte: Medical History/Concurrent Conditions: Blood disorder (blood thinner medicine); Memory impairment (medication for memory); Pneumonia (had pneumonia several years ago); Torticollis (torticollis medicine.)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1562640

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: NJ
Alter: 50,0
Geschlecht: F
Eingang: 15.08.2021
Impfdatum: 06.02.2021
Beginn: 06.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / LA

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

Dysgeusia Nausea Pain in extremity Paraesthesia oral

Symptomtext

soreness on the left arm; metallic taste in mouth; slight tingling on top of her tongue; Nausea; This spontaneous case was reported by a consumer and describes the occurrence of PAIN IN EXTREMITY (soreness on the left arm), DYSGEUSIA (metallic taste in mouth), PARAESTHESIA ORAL (slight tingling on top of her tongue) and NAUSEA (Nausea) in a 50-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. No Medical History information was reported. On 06-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 06-Feb-2021, the patient experienced PAIN IN EXTREMITY (soreness on the left arm), DYSGEUSIA (metallic taste in mouth), PARAESTHESIA ORAL (slight tingling on top of her tongue) and NAUSEA (Nausea). At the time of the report, PAIN IN EXTREMITY (soreness on the left arm), DYSGEUSIA (metallic taste in mouth), PARAESTHESIA ORAL (slight tingling on top of her tongue) and NAUSEA (Nausea) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. No concomitant medication was reported. No treatment medication was reported.

Weitere VAERSDATA-Felder

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

VAERS 1562531

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: IL
Alter: 39,0
Geschlecht: F
Eingang: 15.08.2021
Impfdatum: 01.02.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: OT / LA

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

Cough Dyspnoea Fatigue

Symptomtext

Coughing; coughing up mucus; fatigue; shortness of breath; This spontaneous case was reported by a consumer and describes the occurrence of COUGH (Coughing), COUGH (coughing up mucus), FATIGUE (fatigue) and DYSPNOEA (shortness of breath) in a 39-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 038K20A and 006M20A) for COVID-19 vaccination. The patient's past medical history included No adverse event. On 01-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 01-Mar-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On an unknown date, the patient experienced COUGH (Coughing), COUGH (coughing up mucus), FATIGUE (fatigue) and DYSPNOEA (shortness of breath). At the time of the report, COUGH (Coughing), COUGH (coughing up mucus), FATIGUE (fatigue) and DYSPNOEA (shortness of breath) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. Concomitant information were not provided by the reporter. Treatment information were not provided by the reporter.

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 1562471

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: FL
Alter: 86,0
Geschlecht: F
Eingang: 15.08.2021
Impfdatum: 04.02.2021
Beginn: 02.03.2021
Tage bis Beginn: 26,0
Dosis: 1
Route/Site: OT / LA

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

Dental paraesthesia Toothache

Symptomtext

Woke up with a tooth bothering; Sensitivity on the front sensitivity to the front tooth the cheeck feeling like cold; This spontaneous case was reported by a consumer and describes the occurrence of DENTAL PARAESTHESIA (Sensitivity on the front sensitivity to the front tooth the cheeck feeling like cold) and TOOTHACHE (Woke up with a tooth bothering) in an 86-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. No Medical History information was reported. On 04-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 02-Mar-2021, the patient experienced DENTAL PARAESTHESIA (Sensitivity on the front sensitivity to the front tooth the cheeck feeling like cold). On 03-Mar-2021, the patient experienced TOOTHACHE (Woke up with a tooth bothering). At the time of the report, DENTAL PARAESTHESIA (Sensitivity on the front sensitivity to the front tooth the cheeck feeling like cold) and TOOTHACHE (Woke up with a tooth bothering) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. No relevant concomitant medications were reported. No treatment information was provided. Most recent FOLLOW-UP information incorporated above includes: On 20-Jul-2021: Follow up received included No New Information

Weitere VAERSDATA-Felder

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

VAERS 1561807

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: NY
Alter: 61,0
Geschlecht: F
Eingang: 15.08.2021
Impfdatum: 25.01.2021
Beginn: 25.01.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / -

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

COVID-19 Decreased appetite Diarrhoea Heart rate Palpitations Pyrexia Vaccination site rash

Symptomtext

Covid symptoms; Diarrhea; Red rash; Fever of 101.6; Fast heart beat/Pulse of 100-110; Not having an appetite; This spontaneous case was reported by a consumer and describes the occurrence of DECREASED APPETITE (Not having an appetite), PALPITATIONS (Fast heart beat/Pulse of 100-110), COVID-19 (Covid symptoms), DIARRHOEA (Diarrhea) and VACCINATION SITE RASH (Red rash) in a 61-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included COVID-19 in March 2021. On 25-Jan-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 25-Jan-2021, the patient experienced PALPITATIONS (Fast heart beat/Pulse of 100-110) and PYREXIA (Fever of 101.6). On 27-Jan-2021, the patient experienced VACCINATION SITE RASH (Red rash). On 28-Jan-2021, the patient experienced COVID-19 (Covid symptoms) and DIARRHOEA (Diarrhea). On an unknown date, the patient experienced DECREASED APPETITE (Not having an appetite). On 28-Jan-2021, VACCINATION SITE RASH (Red rash) outcome was unknown. On 01-Feb-2021, COVID-19 (Covid symptoms) outcome was unknown. At the time of the report, DECREASED APPETITE (Not having an appetite) had resolved, PALPITATIONS (Fast heart beat/Pulse of 100-110) had not resolved and DIARRHOEA (Diarrhea) and PYREXIA (Fever of 101.6) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 25-Jan-2021, Heart rate: 100-110 (abnormal) 100-110. On 25-Jan-2021, Pyrexia: 101.6 (High) High. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. No relevant concomitant medications reported. No treatment information was provided.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: Test Date: 20210125; Test Name: heart beat; Result Unstructured Data: 100-110; Test Date: 20210125; Test Name: fever; Result Unstructured Data: High
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1559781

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: FL
Alter: 79,0
Geschlecht: F
Eingang: 15.08.2021
Impfdatum: 29.01.2021
Beginn: 03.02.2021
Tage bis Beginn: 5,0
Dosis: 1
Route/Site: OT / LA

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

Burning sensation Erythema Fatigue Formication Hyperhidrosis Lip swelling Night sweats Palpitations Pruritus Rash Sunburn Swelling face Urine analysis Urticaria

Symptomtext

Urticaria/hives; Burning sensation; Face swelling; crawling skin; she experienced a face sunburn; bottom lip swelling; sweats; Rash/rash went from her neck to up side of face and back; Itchy; got almost like a sunburn, It's on my face, like my cheeks and nose; extremely tired and slept; Night sweats; Palpitations; This spontaneous case was reported by a consumer and describes the occurrence of ERYTHEMA (got almost like a sunburn, It's on my face, like my cheeks and nose), NIGHT SWEATS (Night sweats), PALPITATIONS (Palpitations), URTICARIA (Urticaria/hives) and BURNING SENSATION (Burning sensation) in a 79-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 031M20A and 038K20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included Cesarean section and Gallbladder removal. Concurrent medical conditions included Sulfonamide allergy (Allergy to Sulphur drugs.) and Blood pressure high (Controlled with medication.). Concomitant products included IRBESARTAN for Blood pressure high, VITAMIN B12 NOS and CENTRUM SILVER FORTE for an unknown indication. On 29-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 26-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 NIGHT SWEATS (Night sweats) and PALPITATIONS (Palpitations). On 27-Feb-2021, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced ERYTHEMA (got almost like a sunburn, It's on my face, like my cheeks and nose) and FATIGUE (extremely tired and slept). On an unknown date, the patient experienced URTICARIA (Urticaria/hives), BURNING SENSATION (Burning sensation), SWELLING FACE (Face swelling), FORMICATION (crawling skin), SUNBURN (she experienced a face sunburn), LIP SWELLING (bottom lip swelling), HYPERHIDROSIS (sweats), RASH (Rash/rash went from her neck to up side of face and back) and PRURITUS (Itchy). The patient was treated with PREDNISONE ACETATE (PREDNISONE [PREDNISONE ACETATE]) ongoing from 17-Feb-2021 for Adverse event, at a dose of 4 mg; DIPHENHYDRAMINE HYDROCHLORIDE (BENADRYL [DIPHENHYDRAMINE HYDROCHLORIDE]) ongoing from 02-Feb-2021 for Adverse event, at a dose of 2 dosage form; ASPIRIN [ACETYLSALICYLIC ACID] ongoing from 26-Feb-2021 for Adverse event, at a dose of 1 dosage form; PARACETAMOL (TYLENOL) ongoing from 26-Feb-2021 for Adverse event, at a dose of 1 dosage form and PREDNISONE for Urticaria, at an unspecified dose and frequency. At the time of the report, ERYTHEMA (got almost like a sunburn, It's on my face, like my cheeks and nose), NIGHT SWEATS (Night sweats), PALPITATIONS (Palpitations), URTICARIA (Urticaria/hives), BURNING SENSATION (Burning sensation), SWELLING FACE (Face swelling), FORMICATION (crawling skin), SUNBURN (she experienced a face sunburn), LIP SWELLING (bottom lip swelling), HYPERHIDROSIS (sweats), RASH (Rash/rash went from her neck to up side of face and back), FATIGUE (extremely tired and slept) and PRURITUS (Itchy) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 17-Feb-2021, Urine analysis: abnormal (abnormal) high white blood cell count. The patient reported a return of her hives within 2 to 3 days after completing a 6 day Prednisone taper. This case was linked to MOD-2021-029577 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 19-Jul-2021: Significant follow up

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Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: Test Date: 20210217; Test Name: urinalysis; Result Unstructured Data: high white blood cell count
Aktuelle Erkrankungen: Blood pressure high (Controlled with medication.); Sulfonamide allergy (Allergy to Sulphur drugs.)
Vorgeschichte: Medical History/Concurrent Conditions: Cesarean section; Gallbladder removal
Andere Medikamente: IRBESARTAN; VITAMIN B12 NOS; CENTRUM SILVER FORTE
Allergien: -
Vorherige Impfungen: -

VAERS 1559776

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: FL
Alter: 79,0
Geschlecht: F
Eingang: 15.08.2021
Impfdatum: 29.01.2021
Beginn: 05.02.2021
Tage bis Beginn: 7,0
Dosis: 1
Route/Site: OT / LA

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

Night sweats Palpitations Pruritus Rash Rash pruritic Urticaria White blood cell count

Symptomtext

irregular heart beat; itchy rash; itch; rash across my chest. Rash all over my trunk and up and down my leg/rash went from her neck to up side of face and back; I had large welts/hives/hives on trunk of my body and back of legs; night sweats/Heavy, heavy night sweat; This spontaneous case was reported by a pharmacist and describes the occurrence of URTICARIA (I had large welts/hives/hives on trunk of my body and back of legs), NIGHT SWEATS (night sweats/Heavy, heavy night sweat), PALPITATIONS (irregular heart beat), RASH PRURITIC (itchy rash) and RASH (rash across my chest. Rash all over my trunk and up and down my leg/rash went from her neck to up side of face and back) in a 79-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included Cesarean section and Gallbladder removal. Concurrent medical conditions included Blood pressure (Controlled with medication) since 1996 and Drug hypersensitivity (Allergic to Sulphur drugs). Concomitant products included IRBESARTAN for Blood pressure, VITAMIN B12 NOS and 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]) for an unknown indication. On 29-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 05-Feb-2021, the patient experienced URTICARIA (I had large welts/hives/hives on trunk of my body and back of legs). 05-Feb-2021, the patient experienced NIGHT SWEATS (night sweats/Heavy, heavy night sweat) and RASH (rash across my chest. Rash all over my trunk and up and down my leg/rash went from her neck to up side of face and back). On an unknown date, the patient experienced PALPITATIONS (irregular heart beat), RASH PRURITIC (itchy rash) and PRURITUS (itch). The patient was treated with METHYLPREDNISOLONE ongoing since an unknown date at a dose of 400 milligram; DIPHENHYDRAMINE HYDROCHLORIDE (BENADRYL [DIPHENHYDRAMINE HYDROCHLORIDE]) ongoing since an unknown date at a dose of 1 dosage form and PREDNISONE ongoing since an unknown date for Hives, at a dose of 4 MG. At the time of the report, URTICARIA (I had large welts/hives/hives on trunk of my body and back of legs), NIGHT SWEATS (night sweats/Heavy, heavy night sweat), PALPITATIONS (irregular heart beat), RASH PRURITIC (itchy rash) and PRURITUS (itch) outcome was unknown and RASH (rash across my chest. Rash all over my trunk and up and down my leg/rash went from her neck to up side of face and back) had resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): In 2021, White blood cell count: elevated wbc (High) elevated WBC. 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. This case was linked to MOD-2021-029584 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 19-Jul-2021: Significant follow up :- AE update

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: Test Date: 2021; Test Name: WBC; Result Unstructured Data: elevated WBC
Aktuelle Erkrankungen: Blood pressure (Controlled with medication); Drug hypersensitivity (Allergic to Sulphur drugs)
Vorgeschichte: Medical History/Concurrent Conditions: Cesarean section; Gallbladder removal
Andere Medikamente: IRBESARTAN; VITAMIN B12 NOS; CENTRUM SILVER [ASCORBIC ACID; CALCIUM; MINERALS NOS; RETINOL; TOCOPHERYL ACETATE; VITAMIN B NOS; VITAMINS
Allergien: -
Vorherige Impfungen: -

VAERS 1556586

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: NJ
Alter: -
Geschlecht: F
Eingang: 14.08.2021
Impfdatum: 04.02.2021
Beginn: 04.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / -

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

Chest discomfort Dyspnoea Fatigue Headache Heart rate Nausea Oxygen saturation Oxygen saturation abnormal Pyrexia Tachycardia

Symptomtext

tachycardia up to 130; tightness in chest , discomfort in chest; low pulse ox of 94; out of breath; fever of 101.2; nausea; headache; fatigue; This spontaneous case was reported by a consumer and describes the occurrence of TACHYCARDIA (tachycardia up to 130), CHEST DISCOMFORT (tightness in chest , discomfort in chest), OXYGEN SATURATION ABNORMAL (low pulse ox of 94), DYSPNOEA (out of breath) and PYREXIA (fever of 101.2) in a 44-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concurrent medical conditions included Asthmatic. Concomitant products included INHALER for Asthma. On 04-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 04-Feb-2021, the patient experienced TACHYCARDIA (tachycardia up to 130), CHEST DISCOMFORT (tightness in chest , discomfort in chest), OXYGEN SATURATION ABNORMAL (low pulse ox of 94), DYSPNOEA (out of breath), PYREXIA (fever of 101.2), NAUSEA (nausea), HEADACHE (headache) and FATIGUE (fatigue). At the time of the report, TACHYCARDIA (tachycardia up to 130) and OXYGEN SATURATION ABNORMAL (low pulse ox of 94) had resolved and CHEST DISCOMFORT (tightness in chest , discomfort in chest), DYSPNOEA (out of breath), PYREXIA (fever of 101.2), NAUSEA (nausea), HEADACHE (headache) and FATIGUE (fatigue) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 04-Feb-2021, Heart rate: 130 (High) tachycardia up to 130. On 04-Feb-2021, Oxygen saturation: 94 Low. On 04-Feb-2021, Pyrexia: 101.2 High. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No treatment information was provided., patient reported feeling like using inhaler because she is asthmatic, but it is unknown if she used it.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Test Date: 20210204; Test Name: heart rate; Result Unstructured Data: tachycardia up to 130; Test Date: 20210204; Test Name: pulse ox; Test Date: 20210204; Test Name: fever
Aktuelle Erkrankungen: Asthmatic
Vorgeschichte: -
Andere Medikamente: INHALER
Allergien: -
Vorherige Impfungen: -

VAERS 1556090

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: FL
Alter: 67,0
Geschlecht: F
Eingang: 14.08.2021
Impfdatum: 28.01.2021
Beginn: 05.01.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: OT / LA

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

Chest discomfort Dyspepsia Dyspnoea Fatigue Pruritus Rash Swelling Vaccination site erythema Vaccination site induration Vaccination site swelling

Symptomtext

heartburn; heaviness in chest.; Swelling; difficulty breathing; itchy; rash spread; very tired; Vaccination site induration; Vaccination site swelling; Vaccination site erythema; This spontaneous case was reported by a consumer and describes the occurrence of DYSPNOEA (difficulty breathing), PRURITUS (itchy), RASH (rash spread), DYSPEPSIA (heartburn) and CHEST DISCOMFORT (heaviness in chest.) in a 67-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) 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) since an unknown date. On 28-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 VACCINATION SITE ERYTHEMA (Vaccination site erythema). On 05-Feb-2021, the patient experienced VACCINATION SITE INDURATION (Vaccination site induration) and VACCINATION SITE SWELLING (Vaccination site swelling). On 06-Feb-2021, the patient experienced PRURITUS (itchy), RASH (rash spread) and FATIGUE (very tired). On 07-Feb-2021, the patient experienced DYSPNOEA (difficulty breathing), DYSPEPSIA (heartburn), CHEST DISCOMFORT (heaviness in chest.) and SWELLING (Swelling). At the time of the report, DYSPNOEA (difficulty breathing), PRURITUS (itchy), RASH (rash spread), DYSPEPSIA (heartburn), CHEST DISCOMFORT (heaviness in chest.), SWELLING (Swelling), FATIGUE (very tired), VACCINATION SITE INDURATION (Vaccination site induration), VACCINATION SITE SWELLING (Vaccination site swelling) and VACCINATION SITE ERYTHEMA (Vaccination site erythema) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. No treatment information was reported.

Weitere VAERSDATA-Felder

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

VAERS 1555124

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: FL
Alter: 71,0
Geschlecht: F
Eingang: 13.08.2021
Impfdatum: 03.02.2021
Beginn: 03.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / -

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

Chills Feeling cold Myalgia Tremor

Symptomtext

chills; body ache; felt so cold; Shaking; A spontaneous report was received from a Healthcare Professional Dear concerning a 72? Years-old female patient who received Moderna's COVID-19 vaccine (mRNA-1273) and experienced events, very strong chills, shaking, body ache, and felt so cold. The patient's medical history was not provided. Concomitant medications reported were Humaira Once a week (last injection Monday 01 Feb 2021), Atorvastatin: 20 mg Once daily in the morning, Lisinopril HCTZ 20-12.5 mg Once daily, Amlodipine: 5 mg Once daily, Baby aspirin for drug use for unknown indication. On unknown date, prior to the onset of the events, the patient received their first of two planned doses of mRNA-1273 (lot batch: 038K20A) intramuscularly for prophylaxis of COVID-19 infection. On 3 Feb 2021, the patient experienced the events, very strong chills. shaking, body ache, and felt so cold. Treatment details included Tylenol Extra Strength Rapid Release gel 500 mg: 2 tablet in the morning at 9 am. Action taken with mRNA-1273 in response to the events, very strong chills, shaking, body ache, felt so cold was not reported. On 4 Feb 2021 the outcome of events, very strong chills was resolved and shaking was resolved. On an unknown date the outcome of events include body ache and felt so cold 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 event, 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
Andere Medikamente: ATORVASTATIN; LISINOPRIL + HIDROCLOROTIAZIDA; AMLODIPINE; BABY ASPIRIN; Humaira
Allergien: -
Vorherige Impfungen: -

VAERS 1552242

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20a

moderat

Staat: IL
Alter: 73,0
Geschlecht: F
Eingang: 13.08.2021
Impfdatum: 02.02.2021
Beginn: 12.02.2021
Tage bis Beginn: 10,0
Dosis: 1
Route/Site: OT / LA

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

Erythema Fatigue Feeling hot Influenza like illness Injection site swelling Lymphadenopathy Palpitations Piloerection

Symptomtext

flu-like symptoms; Extreme fatigue; heart palpitations of and on; Smooth bright red area on arm; Swelling at injection site; Swollen lymph nodes under arm; Arm felt hot; Bumpy 6x3 inch red circle on arm; This spontaneous case was reported by a consumer and describes the occurrence of FEELING HOT (Arm felt hot), PILOERECTION (Bumpy 6x3 inch red circle on arm), PALPITATIONS (heart palpitations of and on), INFLUENZA LIKE ILLNESS (flu-like symptoms) and ERYTHEMA (Smooth bright red area on arm) in a 73-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20a) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No medical history was reported by the reporter. Concurrent medical conditions included Insect bite allergy (Insect bites: Swollen and red for days/even weeks). Concomitant products included LEVOTHYROXINE SODIUM (SYNTHROID) for an unknown indication. On 02-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 12-Feb-2021, the patient experienced FEELING HOT (Arm felt hot) and PILOERECTION (Bumpy 6x3 inch red circle on arm). On 13-Feb-2021, the patient experienced PALPITATIONS (heart palpitations of and on), ERYTHEMA (Smooth bright red area on arm), INJECTION SITE SWELLING (Swelling at injection site) and LYMPHADENOPATHY (Swollen lymph nodes under arm). On an unknown date, the patient experienced INFLUENZA LIKE ILLNESS (flu-like symptoms) and FATIGUE (Extreme fatigue). At the time of the report, FEELING HOT (Arm felt hot), PILOERECTION (Bumpy 6x3 inch red circle on arm), PALPITATIONS (heart palpitations of and on), INFLUENZA LIKE ILLNESS (flu-like symptoms), ERYTHEMA (Smooth bright red area on arm), INJECTION SITE SWELLING (Swelling at injection site), LYMPHADENOPATHY (Swollen lymph nodes under arm) and FATIGUE (Extreme fatigue) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Treatment information was not provided. Most recent FOLLOW-UP information incorporated above includes: On 15-Jul-2021: Follow-up received on 15-Jul-2021 contains significant information. Other relevant history added, dose information updated, Patient demographics updated, Events updated

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Insect bite allergy (Insect bites: Swollen and red for days/even weeks)
Vorgeschichte: Comments: No medical history was reported by the reporter.
Andere Medikamente: SYNTHROID
Allergien: -
Vorherige Impfungen: -

VAERS 1543548

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: FL
Alter: 86,0
Geschlecht: F
Eingang: 11.08.2021
Impfdatum: 29.01.2021
Beginn: 01.02.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: OT / LA

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

Arthralgia Blood test Gait inability Mobility decreased Motor dysfunction Musculoskeletal stiffness Myalgia Pain Pain in extremity Red blood cell sedimentation rate Skin irritation

Symptomtext

My hands were so sore; Two sores on buttocks; Pain in legs and shoulders; had pain in legs and shoulders; Unable to bend or lift; I had stiffness all over my body/stiff neck; polymyalgia/muscular problems all through my body; it was painful; I couldn't even get off the toilet; I was unable to walk after the 1st dose; This spontaneous case was reported by a consumer and describes the occurrence of MUSCULOSKELETAL STIFFNESS (I had stiffness all over my body/stiff neck), MOTOR DYSFUNCTION (Unable to bend or lift), PAIN (it was painful), MOBILITY DECREASED (I couldn't even get off the toilet) and GAIT INABILITY (I was unable to walk after the 1st dose) in an 86-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 038K20A and 013M20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concurrent medical conditions included Osteoporosis. On 29-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 01-Feb-2021, the patient experienced PAIN (it was painful), MOBILITY DECREASED (I couldn't even get off the toilet), GAIT INABILITY (I was unable to walk after the 1st dose) and MYALGIA (polymyalgia/muscular problems all through my body). On 03-Feb-2021, the patient experienced MUSCULOSKELETAL STIFFNESS (I had stiffness all over my body/stiff neck). On 07-Feb-2021, the patient experienced MOTOR DYSFUNCTION (Unable to bend or lift), PAIN IN EXTREMITY (had pain in legs and shoulders) and ARTHRALGIA (Pain in legs and shoulders). On 08-Mar-2021, the patient experienced SKIN IRRITATION (Two sores on buttocks). On 18-Mar-2021, the patient experienced PAIN IN EXTREMITY (My hands were so sore). The patient was treated with ATORVASTATIN CALCIUM (STATIN [ATORVASTATIN CALCIUM]) on 07-Feb-2021 at an unspecified dose and frequency; PREDNISONE on 08-Feb-2021 for Muscular pain, Stiffness, Pain of extremities, Shoulder pain and Mobility decreased, at a dose of 20 mg; PREDNISONE (oral) on 19-Mar-2021 for Muscular pain, Stiffness, Pain of extremities, Shoulder pain and Mobility decreased, at a dose of 10 mg; PREDNISONE on 26-Mar-2021 for Muscular pain, Stiffness, Pain of extremities, Shoulder pain and Mobility decreased, at a dose of 5 mg; PREDNISONE on 10-May-2021 for Muscular pain, Stiffness, Pain of extremities, Shoulder pain and Mobility decreased, at a dose of 8 mg; PREDNISONE 18-Mar-2021 for Hand pain, at an unspecified dose and frequency; PREDNISONE 23-Feb-2021 for Hand pain, at an unspecified dose and frequency and MUPIROCIN from 08-Mar-2021 to 18-Mar-2021 for Skin irritation, at a dose of UNK UNK, bid. At the time of the report, MUSCULOSKELETAL STIFFNESS (I had stiffness all over my body/stiff neck), MOTOR DYSFUNCTION (Unable to bend or lift), PAIN (it was painful), MOBILITY DECREASED (I couldn't even get off the toilet), GAIT INABILITY (I was unable to walk after the 1st dose), PAIN IN EXTREMITY (had pain in legs and shoulders), PAIN IN EXTREMITY (My hands were so sore), ARTHRALGIA (Pain in legs and shoulders) and MYALGIA (polymyalgia/muscular problems all through my body) outcome was unknown and SKIN IRRITATION (Two sores on buttocks) had not resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 10-Feb-2021, Blood test: within normal limits (normal) Patient reported that all of her blood work was fine. No details were provided.. On 10-Feb-2021, Red blood cell sedimentation rate: within normal limits (normal) Patient reported that her sed rate was fine. No details were provided.. On 02-Mar-2021, Red blood cell sedimentation rate: 80 (High) No reference range was reported.. 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. No concomitant products reported This case was linked to INC.-MOD-2021-161587 (E2B Linked Report). Most recent FOLLOW-UP information incorporated above includes: On 21-May-2021: Follow up received: added treatments, added events and subsumed some, AI has the details On 21-May-2021: Added Patient History, Product in Event tab, On 01-Jul-2021: Non-Significant follow up appended to adverse event report; possible NNI; Sender's Comments: INC.-MOD-2021-161587:Same reporter

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: Test Date: 20210210; Test Name: Blood work; Result Unstructured Data: Patient reported that all of her blood work was fine. No details were provided.; Test Date: 20210210; Test Name: High sed rate of 80; Result Unstructured Data: Patient reported that her sed rate was fine. No details were provided.; Test Date: 20210302; Test Name: High sed rate of 80; Result Unstructured Data: No reference range was reported.
Aktuelle Erkrankungen: Osteoporosis
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1543274

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20a

moderat

Staat: NC
Alter: -
Geschlecht: M
Eingang: 11.08.2021
Impfdatum: 22.01.2021
Beginn: 21.01.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

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

Chest pain Dizziness Dysarthria Dyspnoea

Symptomtext

Difficulty breathing; Slurred speech; Odd chest pain; Dizzy; This spontaneous case was reported by a consumer and describes the occurrence of DYSARTHRIA (Slurred speech), CHEST PAIN (Odd chest pain), DIZZINESS (Dizzy) and DYSPNOEA (Difficulty breathing) in a male patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20a) for COVID-19 vaccination. The patient's past medical history included Cardiac disorder. On 22-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 21-Jan-2021, the patient experienced DYSARTHRIA (Slurred speech), CHEST PAIN (Odd chest pain) and DIZZINESS (Dizzy). On an unknown date, the patient experienced DYSPNOEA (Difficulty breathing). At the time of the report, DYSARTHRIA (Slurred speech), CHEST PAIN (Odd chest pain), DIZZINESS (Dizzy) and DYSPNOEA (Difficulty breathing) was resolving. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown Route) was unknown. Concomitant medications were not provided. Treatment medications were not provided Most recent FOLLOW-UP information incorporated above includes: On 21-Jan-2021: No specific follow-up information recorded.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Cardiac disorder
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1512358

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: MI
Alter: 35,0
Geschlecht: F
Eingang: 29.07.2021
Impfdatum: 05.02.2021
Beginn: 05.02.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Chest discomfort Dyspnoea Heart rate increased Injection site erythema Injection site pain Injection site swelling

Symptomtext

Shortness of breath, tightness in chest, rapid heartbeat, throat closing in, Right arm of injection site extremely swollen and red.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Estradiol 0.1mg derma patch
Allergien: None
Vorherige Impfungen: -

VAERS 1446591

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: MI
Alter: 66,0
Geschlecht: M
Eingang: 04.07.2021
Impfdatum: 16.02.2021
Beginn: 01.03.2021
Tage bis Beginn: 13,0
Dosis: 2
Route/Site: IM / LA

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

Asthenia C-reactive protein increased Gait disturbance Joint stiffness Laboratory test Mobility decreased Muscular weakness Red blood cell sedimentation rate increased Systemic inflammatory response syndrome

Symptomtext

Pt was healthy prior. Approx 4-6 weeks after the 2nd vaccine injection the pt was noted to have joint stiffness in the R shoulder which then progressed to knuckles, wrists, and legs with weakness at his artificial knees. Stiffness was initially worse in the am and was without relief with NSAIDS. Pt had trouble with ambulation and getting up and down from chairs/sitting. He became significantly debilitated and f/u with MD ensued. Steroid dose pack helped but after several days post completion the s/s returned. C-RP & ESR were elevated but all other RA and autoimmune markers were neg on his labs. Repeat f/u with MD a Ketorolac Injection was given that didn't touch the s/s. As the s/s continued the pt was then put on Celebrex 200mg bid and instructed to f/u with Rheumatology. The pt gets relief with the Celebrex bid but if the dose is decreased to 200mg x 1 q day > the pt has immediate return of s/s. Repeat C-RP and ESR were again elevated on the second set of labs also. We are in the process of follow up with Rheumatology who after first visit said he didn't know what was wrong with him. We are pending additional labs and xrays this week. The pt has always been very active and healthy with no medical problems other then slight hypertension. His body has gone into a systemic inflammatory response acutely for no reason.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: see above note
Aktuelle Erkrankungen: none
Vorgeschichte: slight hypertension
Andere Medikamente: losartan 50 mg
Allergien: none
Vorherige Impfungen: -

VAERS 1410457

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: WI
Alter: 73,0
Geschlecht: M
Eingang: 18.06.2021
Impfdatum: 30.01.2021
Beginn: 01.06.2021
Tage bis Beginn: 122,0
Dosis: 1
Route/Site: IM / -

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

Chest discomfort Chest pain Cough Dyspnoea Nasal congestion Rhinorrhoea

Symptomtext

Vaccinated with Moderna on 1/30/21 and 2/27/21. Symptom onset 6/1/21 with cough, runny nose, shortness of breath, nasal congestion and pain/pressure in the chest. Patient does have a history of lung and sinus infections. Sample sent for genomic sequencing.

Weitere VAERSDATA-Felder

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

VAERS 1394063

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: IL
Alter: 67,0
Geschlecht: M
Eingang: 12.06.2021
Impfdatum: 30.01.2021
Beginn: 01.03.2021
Tage bis Beginn: 30,0
Dosis: 1
Route/Site: OT / -

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

Asthenia Atrioventricular block complete Dyspnoea Fatigue Gait disturbance Heart rate

Symptomtext

Complete heart block; He feel out of breath; Feeling tired; Weakness in legs; Could not walk 20 steps/Can not climb staircase; This spontaneous case was reported by a consumer and describes the occurrence of ATRIOVENTRICULAR BLOCK COMPLETE (Complete heart block) in a 67-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 012M21A and 038K20A) for COVID-19 immunisation. The occurrence of additional non-serious events is detailed below. The patient's past medical history included Bone marrow disorder and Pacemaker insertion (cardiac) since 03-Mar-2021. Concomitant products included MYCOPHENOLATE MOFETIL (MYCOPHENOLATE) for Bone marrow disorder. On 30-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 28-Feb-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 01-Mar-2021, the patient experienced ASTHENIA (Weakness in legs) and FATIGUE (Feeling tired). 01-Mar-2021, the patient experienced GAIT DISTURBANCE (Could not walk 20 steps/Can not climb staircase). On 02-Mar-2021, the patient experienced ATRIOVENTRICULAR BLOCK COMPLETE (Complete heart block) (seriousness criteria hospitalization, medically significant and intervention required) and DYSPNOEA (He feel out of breath). The patient was hospitalized on 02-Mar-2021 due to ATRIOVENTRICULAR BLOCK COMPLETE. At the time of the report, ATRIOVENTRICULAR BLOCK COMPLETE (Complete heart block), ASTHENIA (Weakness in legs), GAIT DISTURBANCE (Could not walk 20 steps/Can not climb staircase), DYSPNOEA (He feel out of breath) and FATIGUE (Feeling tired) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 02-Mar-2021, Heart rate: 23-27 (abnormal) heart rate was irregular and went down to 23-27 beats per minute'.. patient of Bone marrow disease and taking Mycophenolate for last 4 years. Treatment medication information was not provided. 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. 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 events, a causal relationship cannot be excluded. Further information has been requested.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Test Date: 20210302; Test Name: heart rate; Result Unstructured Data: heart rate was irregular and went down to 23-27 beats per minute'.
Aktuelle Erkrankungen: Pacemaker insertion (cardiac)
Vorgeschichte: Medical History/Concurrent Conditions: Bone marrow disorder
Andere Medikamente: MYCOPHENOLATE
Allergien: -
Vorherige Impfungen: -

VAERS 1380720

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: GA
Alter: 71,0
Geschlecht: F
Eingang: 08.06.2021
Impfdatum: 08.02.2021
Beginn: 01.03.2021
Tage bis Beginn: 21,0
Dosis: 1
Route/Site: OT / RA

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

Blood magnesium Blood phosphorus Chills Dehydration Diarrhoea Endoscopy Fall Nausea Neuropathy peripheral Oral candidiasis Pyrexia Renal impairment Sigmoidoscopy normal Unresponsive to stimuli Urinary tract infection Vomiting Walking aid user Weight decreased

Symptomtext

unresponsive to stimuli; urinary tract infections; candida in her throat; dehydrated; neuropathy in both legs and has fallen 3 times; She had lost 25 lbs but she had gained back 3 lbs; nausea; vomiting; fever; chills; diarrhea; started using a cane and progressed to a walker; fallen 3 times; This spontaneous case was reported by a patient (subsequently medically confirmed) and describes the occurrence of UNRESPONSIVE TO STIMULI (unresponsive to stimuli) in a 71-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 002A21A and 038K20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included Essential tremor and Kidney transplant. Concomitant products included CEVIMELINE for Dry mouth, VITAMIN B3, VACCINIUM MACROCARPON FRUIT (CRANBERRY [VACCINIUM MACROCARPON FRUIT]), CYANOCOBALAMIN (VITAMIN B12 [CYANOCOBALAMIN]), TACROLIMUS, MYCOPHENOLIC ACID, PREDNISONE, PRIMIDONE, RABEPRAZOLE, ROSUVASTATIN CALCIUM and FLUOXETINE HYDROCHLORIDE (PROZAC) for Kidney disorder, LORAZEPAM (ATIVAN) for Nerve pain, ACETAMINOPHEN for Pain, FLUTICASONE PROPIONATE (PROAIR [FLUTICASONE PROPIONATE]) for an unknown indication. On 08-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 08-Mar-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 09-Mar-2021, the patient experienced WEIGHT DECREASED (She had lost 25 lbs but she had gained back 3 lbs), DIARRHOEA (diarrhea), NAUSEA (nausea), VOMITING (vomiting), PYREXIA (fever) and CHILLS (chills). On 13-Mar-2021, the patient experienced NEUROPATHY PERIPHERAL (neuropathy in both legs and has fallen 3 times) and DEHYDRATION (dehydrated). In March 2021, the patient experienced WALKING AID USER (started using a cane and progressed to a walker) and FALL (fallen 3 times). On 12-Apr-2021, the patient experienced ORAL CANDIDIASIS (candida in her throat). On 20-May-2021, the patient experienced URINARY TRACT INFECTION (urinary tract infections). On an unknown date, the patient experienced UNRESPONSIVE TO STIMULI (unresponsive to stimuli) (seriousness criteria hospitalization and medically significant). The patient was hospitalized from 12-May-2021 to 16-May-2021 due to UNRESPONSIVE TO STIMULI. The patient was treated with PARACETAMOL (TYLENOL) on 13-Mar-2021 for Fever, at an unspecified dose and frequency; ONDANSETRON (ZOFRAN [ONDANSETRON]) for Candida of mouth, at an unspecified dose and frequency; PROMETHAZINE HYDROCHLORIDE (PHENERGAN [PROMETHAZINE HYDROCHLORIDE]) on 19-Apr-2021 for Candida infection, at an unspecified dose and frequency; DOXYCYCLINE for Urinary tract infection, at an unspecified dose and frequency; FLUCONAZOLE (DIFLUCAN) at an unspecified dose and frequency and PHOSPHORUS at an unspecified dose and frequency. On 09-Apr-2021, PYREXIA (fever) had resolved. On 14-Apr-2021, ORAL CANDIDIASIS (candida in her throat) had resolved. At the time of the report, UNRESPONSIVE TO STIMULI (unresponsive to stimuli), NEUROPATHY PERIPHERAL (neuropathy in both legs and has fallen 3 times), WEIGHT DECREASED (She had lost 25 lbs but she had gained back 3 lbs), WALKING AID USER (started using a cane and progressed to a walker), FALL (fallen 3 times) and URINARY TRACT INFECTION (urinary tract infections) outcome was unknown and DIARRHOEA (diarrhea), DEHYDRATION (dehydrated), NAUSEA (nausea), VOMITING (vomiting) and CHILLS (chills) had not resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 14-May-2021, Blood magnesium: low (Low) low. On 14-May-2021, Blood phosphorus: low (Low) low. On 14-May-2021, Endoscopy: candida in throat (abnormal) candida in throat. On 14-May-2021, Renal impairment: normal (normal) normal. On 14-May-2021, Sigmoidoscopy normal: normal (normal) normal. By 19 Apr 2021, the transplant team office was called as she was not responding. They ran bloodwork and found the Diflucan had caused issues with the tacrolimus which she takes for the kidney transplant. They went to the hospital on 10 May 2021 and 11 May 2021 but could not wait. She was finally admitted on 12 May 2021. On 14 May 2021 another endoscopy showed that the candida was better. Bloodwork indicated her phosphorus was critically low and magnesium was low. She was given fluids and phosphorus. Her kidney function test was normal. She was released on 16 May 2021. 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 subject's use of steroids can be a confounding factor to oral candidiasis. Furthermore the interaction between Diflucan and Tacrolimus can also be a confounding factor. This case was linked to MOD-2021-169089 (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 subject's use of steroids can be a confounding factor to oral candidiasis. Furthermore the interaction between Diflucan and Tacrolimus can also be a confounding factor.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dehydration
Hospital-Tage: 5,0
Labordaten: Test Date: 20210514; Test Name: magnesium; Result Unstructured Data: low; Test Date: 20210514; Test Name: phosphorus; Result Unstructured Data: low; Test Date: 20210514; Test Name: endoscopy; Result Unstructured Data: candida in throat; Test Date: 20210514; Test Name: Kidney Function; Result Unstructured Data: normal; Test Date: 20210514; Test Name: sigmoidoscopy; Result Unstructured Data: normal
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Essential tremor; Kidney transplant
Andere Medikamente: VITAMIN B3; CRANBERRY [VACCINIUM MACROCARPON FRUIT]; VITAMIN B12 [CYANOCOBALAMIN]; TACROLIMUS; MYCOPHENOLIC ACID; PREDNISONE; CEVIMELINE; PRIMIDONE; RABEPRAZOLE; ROSUVASTATIN CALCIUM; PROZAC; ATIVAN; ACETAMINOPHEN; PROAIR [FLUTICASONE PROPI
Allergien: -
Vorherige Impfungen: -

VAERS 1361000

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: MI
Alter: 66,0
Geschlecht: F
Eingang: 29.05.2021
Impfdatum: 03.03.2021
Beginn: 19.03.2021
Tage bis Beginn: 16,0
Dosis: 2
Route/Site: SYR / RA

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

Abdominal pain Asthenia Chest pain Exercise tolerance decreased Fatigue Feeling abnormal Musculoskeletal chest pain Pain of skin Rash Tenderness

Symptomtext

On the morning of 3/21/2021 I awoke to skin pain on my LEFT side (Bilateral mastectomy lymph glands only on right) from midsternal through the left scapula. Any touch was painful, sheets clothing etc. It felt like Shingles but no rash was there. day 3-7 terrible spleen pain with pressure under my left ribs radiating to my back to the base of my scapula. On day 8 the shingles rash appeared on my RIGHT side and I was put on Valtrex. Because of the sternal and rib pain I thought perhaps I was constipated so I took several laxatives to no avail. The rib pain was crushing even to the touch. It finally slowly dissipated staring day 9

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Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Doctor visit I believe on 3-27-21. I was fatigued for weeks. I normally lap swim 4 days a week for 1 hour but simply did not have the energy. When I returned to swimming I could only tolerate 20 minutes due to my heart rate over 200 and muscle fatigue
Aktuelle Erkrankungen: none
Vorgeschichte: Diabetes, sleep Apnea
Andere Medikamente: levothyroid, Metformin,Repaglimine, Ozempic,
Allergien: Iodine
Vorherige Impfungen: -

VAERS 1282645

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: IL
Alter: 35,0
Geschlecht: F
Eingang: 03.05.2021
Impfdatum: 12.02.2021
Beginn: 28.03.2021
Tage bis Beginn: 44,0
Dosis: 2
Route/Site: IM / LA

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

Arthralgia Bacterial infection Blood test abnormal Bursal fluid accumulation Central venous catheterisation Magnetic resonance imaging abnormal Mobility decreased Pain in extremity Periarthritis Product administered at inappropriate site Shoulder operation X-ray normal

Symptomtext

She got her vaccine, and she remembers very clearly that she had mentioned to her husband that whoever was administering the vaccine had given it high up on the arm and did not cover it with a band-aide. For the next couple of days had the usual sore arm. Eventually about 1 to 1/2 weeks after she was taking some anti-inflammatory medication for 3-4 weeks. Once that wore off 2 days later she had severe pain in her left shoulder, and it was out of the ordinary, no trauma to that shoulder, nothing to have caused that pain. She went to take a shower and got dressed and noticed that she had a sore arm within 5-10 minutes had full blown sharp pain. She went to the closest ER and asked her about the vaccine and did not look into that, and took an x-ray and gave her pain medication. She took that and it did not help her much and then saw her physician. When they saw how much pain that she was in and could not move her arm at all and were suspicious for an inflammatory process. She had an MRI that showed a good to moderate amount of fluid in her left arm bursa and that this should be looked into. Her blood work came back as showing that she had some sort of infection going on. She was told to go to an ER immediately so that they could tap the fluid and see what was going on. She went to another ER and then they started investigated and she had a lot of infected shoulder bursa that was isolated to that area and said that it had to be inoculated. Eventually she had to have surgery to get the shoulder bursa cleaned out and found that it was a common bacteria on the skin, and administered by inoculation. She mentioned to her orthopedic that she had the vaccine and no band-aide and that he agreed it was due to that. She was on anti-inflammatories that masked the pain so that's why it took so long to find it. She now has a frozen shoulder, and has a PICC line inserted so she can get antibiotics 3 times a day for a full month and is finishing that course today. The surgery was 4/6/21 and started that a day or two before the surgery.

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Praegender Schweregrund: Mobility decreased
Hospital-Tage: 8,0
Labordaten: See above with hospitalization.
Aktuelle Erkrankungen: None.
Vorgeschichte: None.
Andere Medikamente: None.
Allergien: Rocephin (SOB and itchy eyes).
Vorherige Impfungen: -

VAERS 1268317

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: IL
Alter: 73,0
Geschlecht: M
Eingang: 28.04.2021
Impfdatum: 18.02.2021
Beginn: 01.04.2021
Tage bis Beginn: 42,0
Dosis: UNK
Route/Site: IM / -

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

COVID-19 Computerised tomogram thorax abnormal Convalescent plasma transfusion Cough Immunosuppression Malaise Pneumonia Pyrexia SARS-CoV-2 test positive

Symptomtext

Patient became ill with fever and cough on 4/1/21. Patient had completed COVID vaccination series on 2/18/21. Patient was found to be COVID positive. Patient presented to ED on 4/6/21 and found to have LLL pneumonia on CT chest. Patient had been treated with bamlanivimab as an outpatient prior to presentation on 3/16/21. Patient was treated with oxygen, antibiotics, steroids, convalescent plasma. Per ID consult, patient unlikely to mount a adequate response to COVID-19 infection due to immunosuppresion. Patient improved and was discharged to home.

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Praegender Schweregrund: Pneumonia
Hospital-Tage: 15,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: CLL, neutropenia, CHF, hypogammaglobulinemia, CAD, drug induced neutropenia
Andere Medikamente: obinutuzumab, venetoclax
Allergien: -
Vorherige Impfungen: -

VAERS 1233633

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: MI
Alter: 82,0
Geschlecht: F
Eingang: 20.04.2021
Impfdatum: 04.02.2021
Beginn: 15.04.2021
Tage bis Beginn: 70,0
Dosis: 1
Route/Site: IM / LA

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

COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

During Hospitalization, patient tested positive for COVID-19 post vaccination. Patient experienced shortness of breath requiring supplemental oxygen

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: NAA PCR COVID test: Positive for COVID-19 on 4/15/21
Aktuelle Erkrankungen: -
Vorgeschichte: CKD, DM, HTN, Cardiomyopathy
Andere Medikamente: Lasix, coreg, altace, entresto, zyloprim, xanax
Allergien: Latex and penicillins
Vorherige Impfungen: -

VAERS 1227133

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: PA
Alter: 79,0
Geschlecht: M
Eingang: 18.04.2021
Impfdatum: 13.01.2021
Beginn: 03.04.2021
Tage bis Beginn: 80,0
Dosis: 1
Route/Site: OT / RA

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

Anxiety Blood pressure measurement Blood test Chest pain Computerised tomogram Fall Heart rate Limb discomfort Tremor Weight Weight decreased

Symptomtext

chest pain; Shaking legs/ Tremors in hands; legs buckled; anxiety; Weight loss; fell to ground; This spontaneous case was reported by a consumer (subsequently medically confirmed) and describes the occurrence of CHEST PAIN (chest pain), TREMOR (Shaking legs/ Tremors in hands) and LIMB DISCOMFORT (legs buckled) in a 79-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 012L20A and 038K20A) 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 13-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 03-Apr-2021, the patient experienced CHEST PAIN (chest pain) (seriousness criterion hospitalization). On 06-Apr-2021, the patient experienced FALL (fell to ground) and WEIGHT DECREASED (Weight loss). On an unknown date, the patient experienced TREMOR (Shaking legs/ Tremors in hands) (seriousness criterion disability), LIMB DISCOMFORT (legs buckled) (seriousness criterion disability) and ANXIETY (anxiety). On 04-Apr-2021, CHEST PAIN (chest pain) had resolved. At the time of the report, TREMOR (Shaking legs/ Tremors in hands), LIMB DISCOMFORT (legs buckled), FALL (fell to ground), ANXIETY (anxiety) and WEIGHT DECREASED (Weight loss) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): In March 2021, Blood test: normal (normal) Normal. In March 2021, Computerised tomogram: normal (normal) Normal. In March 2021, Weight: 148 (Inconclusive) Inconclusive. On 06-Apr-2021, Weight: 125 (Inconclusive) Inconclusive. On an unknown date, Blood pressure measurement: elevated (High) BP Elevated. On an unknown date, Heart rate: elevated (High) Elevated. The patient underwent CAT scan of the stomach, complete gastro work-up and complete blood work up. All tests were result normal. On 3 Apr 2021 he experienced severe chest pain and was transported to the hospital they concluded it was not heart related but he was hospitalized overnight. His BP and heart rate were also elevated. Concomitant product use was not provided.Treatment information was unknown. Very limited information regarding these events has been provided at this time. Further information has been requested.; Sender's Comments: Very limited information regarding these events has been provided at this time. Further information has been requested.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Test Date: 202104; Test Name: BP; Result Unstructured Data: BP Elevated; Test Date: 202103; Test Name: Complete blood work; Result Unstructured Data: Normal; Test Date: 202103; Test Name: CT scan abdomen; Result Unstructured Data: Normal; Test Date: 202104; Test Name: heart rate; Result Unstructured Data: Elevated; Test Date: 202103; Test Name: Body weight; Test Result: Inconclusive ; Result Unstructured Data: Inconclusive; Test Date: 20210406; Test Name: Body weight; Test Result: Inconclusive ; Result Unstructured Data: Inconclusive
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: No adverse event (No reported medical history)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1188837

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038k20a

moderat

Staat: FL
Alter: 50,0
Geschlecht: F
Eingang: 10.04.2021
Impfdatum: 29.01.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

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

Hypoaesthesia Impaired work ability Peripheral swelling Renal failure Renal pain Tremor Weight decreased

Symptomtext

3b kidney failure; hands were swollen; numb (hands); not eating because she gets kidney pains; lost 10 pounds; essential tremor got much worse; cannot work a 5 day week; This spontaneous case was reported by a health care professional and describes the occurrence of RENAL FAILURE (3b kidney failure) in a 50-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 038k20a and 031m20a) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included Arthritis. Concomitant products included HYDROXYZINE, TOLTERODINE, URO MP, MELOXICAM and CYCLOBENZAPRINE HYDROCHLORIDE (CYCLOBENZAPRIN) for an unknown indication. On 29-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 26-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 RENAL FAILURE (3b kidney failure) (seriousness criterion medically significant), PERIPHERAL SWELLING (hands were swollen), HYPOAESTHESIA (numb (hands)), RENAL PAIN (not eating because she gets kidney pains), WEIGHT DECREASED (lost 10 pounds), TREMOR (essential tremor got much worse) and IMPAIRED WORK ABILITY (cannot work a 5 day week). At the time of the report, RENAL FAILURE (3b kidney failure), PERIPHERAL SWELLING (hands were swollen), HYPOAESTHESIA (numb (hands)), RENAL PAIN (not eating because she gets kidney pains), WEIGHT DECREASED (lost 10 pounds), TREMOR (essential tremor got much worse) and IMPAIRED WORK ABILITY (cannot work a 5 day week) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Treatment for the event included hydrochlorothiazide and propranolol. Reporter states has current medical condition autoimmune issues, Interstitial cystitis, essential tremor, spastic pelvic floor, arthritis. Reporter did not allow further contact; 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. The patient's current medical condition of autoimmune issues, interstitial cystitis, essential tremor, spastic pelvic floor, arthritis and product usage of NSAIDS remains confounders.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Arthritis
Andere Medikamente: HYDROXYZINE; TOLTERODINE; URO MP; MELOXICAM; CYCLOBENZAPRIN
Allergien: -
Vorherige Impfungen: -

VAERS 1138317

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: PA
Alter: 28,0
Geschlecht: F
Eingang: 26.03.2021
Impfdatum: 23.03.2021
Beginn: 23.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Immediate post-injection reaction Injection site pain Mobility decreased Muscular weakness Pain Paraesthesia

Symptomtext

Pain immediately upon completion of injection, with slight tingling in hand. Within 2 minutes of injection, pain was experienced at site of injection in the arm. Within 30 minutes of injection, arm had very limited range of motion resulting in inability to lift arm away from myself and severe pain. Discussed symptoms with pharmacist at clinic and was told if symptoms do not improve within 4 days, contact doctor and to take ibuprofen for symptoms in the meantime. Contacted PCP 2 hours post injection due to how severe pain was and was told pain was normal and should clear up. 24 hours post injection- symptoms still remained - very limited range of motion of arm and severe pain at site of injection and surrounding area in arm and into shoulder and neck. 48 hours post injection- pain less severe and increased range of motion in arm. 72 hours post injection- slight increase from 48 hours in terms of range of motion and slight decrease of pain. Currently still monitoring symptoms and taking ibuprofen.

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Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Obesity, asthma, minor seasonal allergies
Andere Medikamente: Multivitamin and probiotic taken daily
Allergien: N/A
Vorherige Impfungen: -

VAERS 1134181

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: IN
Alter: 57,0
Geschlecht: F
Eingang: 25.03.2021
Impfdatum: 03.02.2021
Beginn: 16.03.2021
Tage bis Beginn: 41,0
Dosis: 2
Route/Site: IM / RA

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

Chest pain Computerised tomogram Cough Dyspnoea Electrocardiogram Feeling cold Nasal congestion Pyrexia SARS-CoV-2 test negative

Symptomtext

I had my second covid vaccination on 2/3/21. On the morning of 3/16 I woke up short of breath, chilling, chest pain, chest congestion and cough, and a fever of 101F which rose to 102.5F. I was monitoring my pulse ox which would range from 90 to 91% but at times dropped to 84%. I had to mentally take deep breaths to get my pulse ox to 90%. These symptoms lasted 12 hours. Next day, short of breath at times and tired. Called the health department on 3/18 and was told to get a rapid test which was negative. The NP thought I might have pneumonia or a pulmonary embolus. I was sent to the ED and a CTa scan was done and everything was normal including 12 lead ekg, pulse ox and vital signs. The physician thought it was GERD. I'm a nurse and have GERD, this was not GERD. The PA that took care of me agreed the symptoms were, 'weird' and I should report this incident.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Chemo gram 12 Lead EKG Urinalysis Ct A scan to rule out a pulmonary embolus vital signs and pulse ox were within normal limits. All labs and diagnostic tests were normal.
Aktuelle Erkrankungen: None
Vorgeschichte: GERD IBS
Andere Medikamente: Prevacid OTC once a day Multiple vitamin once a day Calcium supplement once a day Fluoxietine HCL 20 mg once a day Estradial 1 mg once a day Prevalite powder 4 gm once a day
Allergien: None
Vorherige Impfungen: -

VAERS 1124754

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038k20a

moderat

Staat: PA
Alter: 39,0
Geschlecht: F
Eingang: 22.03.2021
Impfdatum: 09.02.2021
Beginn: 10.02.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / RA

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

Abdominal pain Computerised tomogram pelvis Fatigue Full blood count abnormal Gastrointestinal disorder Hypoacusis Palpitations Pyrexia Ultrasound pelvis abnormal

Symptomtext

Heart palpitations, hearing a loud pulse in R ear, extreme fatigue, GI disturbance (bloating, pain), severe pain RLQ resulting in ER visit on 2/10/21, fever x 1 day. Sound in ear & fatigue persist, will f/u w/ cardiology 3/26

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Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: Er visit w/ complete blood count & imaging for pain (ct pelvis, us pelvis) on 2/10/21. Blood results abnormal, imaging revealed ovarian cysts. Was offered pain meds and sent home same day
Aktuelle Erkrankungen: Ovarian cyst; diagnosed with endometriosis within 1 month after
Vorgeschichte: None known prior
Andere Medikamente: Omega 3 Multi vit Vit d Melatonin
Allergien: Nickel, penicillin, latex
Vorherige Impfungen: -

VAERS 1121846

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: FL
Alter: -
Geschlecht: F
Eingang: 22.03.2021
Impfdatum: 02.02.2021
Beginn: 04.02.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: OT / -

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

Arrhythmia Fatigue Hypertension Vaccination site pain

Symptomtext

Abnormal Implant afib link recorder reading; Pain at injection site; Fatigue; High blood pressure; A spontaneous report was received from a 77 year old female patient who received Moderna's COVID-19 vaccine (mRNA-1273) and who experienced high blood pressure, abnormal afib implant recorder reading, pain at injection site, and fatigue. The patient's medical history included atrial fibrillation and . The concomitant medications included Eliquist (apixaban). On 02-Feb-2021, the patient received their first of two planned doses of mRNA-1273 (Lot number: 038K20A) intramuscularly for prophylaxis of COVID-19 infection. On 04-Feb-2021 the patient experienced high blood pressure. On 05-Feb-2021, the patient experienced pain at injection site, fatigue and abnormal afib implant recorder readings. On 09-Feb-2021, the patient consulted a physician for abnormal afib implant recorder readings. Treatment information was unknown. Action taken with mRNA-1273 was unknown. The outcome of the events, high blood pressure, abnormal afib implant recorder reading, pain at injection site, and fatigue., was unknown.; Reporter's Comments: Very limited information regarding these events has been provided at this time. Further information has been requested.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arrhythmia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Atrial fibrillation; Device implant NOS
Andere Medikamente: ELIQUIS
Allergien: -
Vorherige Impfungen: -

VAERS 1110052

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: PA
Alter: 39,0
Geschlecht: M
Eingang: 18.03.2021
Impfdatum: 22.02.2021
Beginn: 22.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Dysphagia Ear pain Feeling abnormal Headache Pain in extremity Palpitations

Symptomtext

Already listed previously

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: I felt a little ?off? about 15 minutes after the first shot but didn?t think anything of it until I got to the car and sat down. I had heart palpitations after about 25-30 minutes, felt mentally foggy, and when I went to get a drink of water, I had trouble swallowing. This was strange, the ?trouble? was not actually with water making its way down my throat, the trouble was more to do with using my mouth/jaw movements in order to complete a swallow. I felt this way the rest of the evening and had to take Benadryl to go to sleep. I?ve also had sharp random headaches up to 3 days after the vaccine. I would say my symptoms got lighter as time went by but till this day, I have tenderness in my left temple /ear and am not sure if it?s related to vaccine or seasonal allergies. I have had post nasal drip for a few weeks now due to the weather changes(cold to warm to cold). I took Tylenol last night and that helped with my headache. I also have a lot stress (work, 2 toddlers, school) so I have only been sleeping 5-6 hours a night and it?s often broken up sleep.
Vorgeschichte: Lower back pain Allergies
Andere Medikamente: None
Allergien: Seasonal allergies(grass, hay, trees, pollen), allergies to mold spores, allergies to cats and dogs, allergic to cipro(medication to treat stomach bug).
Vorherige Impfungen: -

VAERS 1102863

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: IL
Alter: 66,0
Geschlecht: F
Eingang: 15.03.2021
Impfdatum: 02.02.2021
Beginn: 21.02.2021
Tage bis Beginn: 19,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Fatigue Headache Hypotension

Symptomtext

On 2/21/21 she noticed a headache, dizziness, fatigue and low blood pressure. She noticed the s/s because she had this same delayed reaction after the Shingrix vaccine in 2018.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypotension
Hospital-Tage: -
Labordaten: She did visit her PCP Dr. and she wanted advice on getting dose #2. He told her it was a personal decesion. She saw him on Marah 4, 2021. Was treated with medication for headache. At this time she has decided to not get dose #2.
Aktuelle Erkrankungen: None
Vorgeschichte: None that she is aware of.
Andere Medikamente: Multivitamin one daily
Allergien: NKA
Vorherige Impfungen: Shingrix 5/16/2018 and 7/16/2018

VAERS 1094209

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: MI
Alter: 45,0
Geschlecht: F
Eingang: 12.03.2021
Impfdatum: 02.02.2021
Beginn: 02.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Chest X-ray Chest discomfort Chest pain Hyperventilation Increased appetite Pleurisy Respiratory rate increased

Symptomtext

While patient was shopping after receiving her vaccine she started feeling "pressure"/"tightening" in the left chest/shoulder area and then in the front and back of upper torso. She stated it continued to increase and became painful. Her respirations increased and she felt like she was panting. She states it didn't feel like her previous anaphylaxis where her throat "felt like a rubber chicken" and she was unable to speak and had swelling in her throat.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: She went to the ER where they did a chest x-ray and bloodwork. She states she was diagnosed with pleurisy. SHe was there during shift change and one physician told her it was unrelated to the vaccine and the other told her it most likely was.
Aktuelle Erkrankungen: none
Vorgeschichte: mitral valve prolapse
Andere Medikamente: Calan 20mg
Allergien: PCN-unknown Zomig- anaphylaxis multiple food allergies
Vorherige Impfungen: -

VAERS 1092208

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: IL
Alter: 70,0
Geschlecht: F
Eingang: 11.03.2021
Impfdatum: 05.02.2021
Beginn: 12.02.2021
Tage bis Beginn: 7,0
Dosis: 1
Route/Site: IM / RA

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

Condition aggravated Hypoaesthesia Pain in extremity Paraesthesia Peripheral swelling Pruritus Rash

Symptomtext

2/12: developed leg swelling, pain, numbness and tingling. 2/19 developed rash on face and both arms with itching. 2/26 ED visit diagnosed with worsening of peripheral neuropathy. 3/3 - office visit complaining of worsening peripheral edema

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Asthma, kidney disease, CAD, Diabetes, Fibromyalgia, ganglioneuroma, HTN
Andere Medikamente: -
Allergien: iodine, contrast media, barium sulfate, codeine, Sulfa, Shellfish. Cardura
Vorherige Impfungen: -

VAERS 1091802

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: IL
Alter: 46,0
Geschlecht: F
Eingang: 11.03.2021
Impfdatum: 11.02.2021
Beginn: 19.02.2021
Tage bis Beginn: 8,0
Dosis: 2
Route/Site: IM / RA

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

Dizziness Flushing Nausea Palpitations

Symptomtext

The team member reported her heart was racing, she became dizzy, nauseated, flushed, and felt like she was going to pass out.

Weitere VAERSDATA-Felder

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

VAERS 1089091

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: -
Alter: 64,0
Geschlecht: M
Eingang: 10.03.2021
Impfdatum: 12.02.2021
Beginn: 22.02.2021
Tage bis Beginn: 10,0
Dosis: 1
Route/Site: IM / RA

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

COVID-19 Chest pain Dialysis Dyspnoea Hypoxia SARS-CoV-2 test positive Troponin increased

Symptomtext

Patient received 1st COVID vaccine on 2.12.21. Reported to local ER with chest pain and increased ShOB on 2.22.21. Found to be positive for COVID, elevated troponin. Transferred to medical center. Patient was mildly hypoxic on the floor but never required more than 2L nasal prongs. Patient is currently on dialysis. Patient received dexamethasone therapy only while on the floor. Discharged home on 3.4.2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 10,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1086040

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: IL
Alter: -
Geschlecht: M
Eingang: 09.03.2021
Impfdatum: 27.01.2021
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: OT / -

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

Dyspnoea Fluid retention

Symptomtext

Breathing problems; Retaining a lot of fluids; A spontaneous report received from a Consumer, concerning 75-year-old male patient who received Moderna COVID-19 vaccine ((mRNA-1273) and experienced breathing problems and retaining a lot of fluids. The patient's medical history included breathing problem and retaining fluid. No relevant concomitant medications were reported. On 27-JAN-2021, the patient received his first of two planned doses of mRNA-1273 (Lot number: 038K20A) through an unknown route in an unknown arm for prophylaxis of COVID-19 infection. On an unspecified date, the patient had experienced breathing problems and was retaining a lot of fluids. The patient was hospitalized on 24-JAN-2021. The patient was placed on a ventilator (defibrillator). The patient was discharged from the hospital on 28-JAN-2021. The patient stated that this had happened to him prior to getting the first dose of the vaccine. Action taken with mRNA-1273 in response to the event was not reported. Outcome of the events of having breathing problems and retaining a lot of fluids was unknown.; Reporter's Comments: Very limited information regarding this events has been provided at this time. Further information has been requested.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: Breathing difficult; Fluid retention
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1082773

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: KY
Alter: 73,0
Geschlecht: F
Eingang: 08.03.2021
Impfdatum: 17.02.2021
Beginn: 02.03.2021
Tage bis Beginn: 13,0
Dosis: 1
Route/Site: SYR / LA

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

Condition aggravated

Symptomtext

In about a week and a half after receiving the vaccine, my neuropathy went from just in my feet to going up my leg almost to my knee.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: I have mild neuropathy in both of my feet.
Vorgeschichte: -
Andere Medikamente: none
Allergien: sulfur, codeine, latex
Vorherige Impfungen: -

VAERS 1076117

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038k20A

moderat

Staat: IL
Alter: 35,0
Geschlecht: F
Eingang: 05.03.2021
Impfdatum: 12.02.2021
Beginn: 13.02.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / RA

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

Chest X-ray Chills Dizziness Echocardiogram Headache Laboratory test Magnetic resonance imaging head Magnetic resonance imaging spinal Malaise Palpitations Pyrexia Tachycardia

Symptomtext

intermittent episodes of subjective fever chills tachycardia nearly passing out headaches. Symptoms started approximately 9 days ago after having a second maternal vaccine. She states she is intermittently been feeling ill in terms of diffuse myalgias headaches today she had a racing heart rate and near syncope. Denies any chest pain shortness of breath abdominal pain nausea vomiting diarrhea.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: Work-up was initiated in the ER including MRI of the brain MRI of the spine Echo Chest x-ray Lab work Body Guardian
Aktuelle Erkrankungen: None
Vorgeschichte: Scarlet fever Edit Overview Change Dx Resolve Overview scarlet tina Palpitations Create Overview Change Dx Resolve IBS (irritable bowel syndrome) Create Overview Change Dx Resolve Chicken pox (From Hx) Cardiomyopathy (HCC)
Andere Medikamente: Escitalopram Oxalate (Tab) LEXAPRO 10 MG Take 10 mg by mouth daily. Gabapentin (Cap) NEURONTIN 100 MG Take 1 capsule (100 mg total) by mouth 2 (two) times daily as needed. Norgestimate-Eth Estradiol (Tab) ORTHO-CYCLEN 0.25-35 MG-MCG Take
Allergien: NKA
Vorherige Impfungen: -

VAERS 1074885

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038k20a

moderat

Staat: IL
Alter: 70,0
Geschlecht: F
Eingang: 05.03.2021
Impfdatum: 02.01.2021
Beginn: 05.02.2021
Tage bis Beginn: 34,0
Dosis: 1
Route/Site: IM / RA

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

Blood glucose Burning sensation Haemoglobin Neuropathy peripheral Pain in extremity Paraesthesia Pruritus Rash Skin burning sensation

Symptomtext

I did not experience an immediate reaction to the shot as they had me wait 30 mins to assure that I was not allergic to the shot as I do have allergies. Not sure if the medical complications that I experience a week later after having the shot is related to the shot or not and my primary doctor or my endocrinology dr. is not sure either and had concerns as to weather I should take the second shot or not. I went to the emergency dr. because the (burning, itching, pain, pins/needles) were so bad in my upper and lower extremities. They prescribe me pain med and another med that has help a lot. I visited my endocrinology dr. for my dietetics. After running all kinds of test she stated that my A1C levels were a 6.point. She could not attributed my severe neuropathy to diabetics or to the virus shot. She set me for an appointment to see a neurologist. I also developed a week later severe bumps on my face, neck and both arms. I went to urgent care and they gave me a shot of some sort and sent me home with steroids and take Benadryl. My skin cleared up in a few days. I had never had that happen to me.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: AC1, not sure of all the types of test taken in the emergency. Glucose test
Aktuelle Erkrankungen: Dietetics, Asthma, high blood pressure, Stint in heart and pace maker
Vorgeschichte: The same as above
Andere Medikamente: Zyrtec, Tylenol
Allergien: sea food, Idoline, sulfur, codeine
Vorherige Impfungen: -

VAERS 1073961

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: MI
Alter: 79,0
Geschlecht: F
Eingang: 04.03.2021
Impfdatum: 11.02.2021
Beginn: 12.02.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: - / LA

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

Blood electrolytes normal Disorientation Dizziness Electrocardiogram normal Inflammation Thyroid function test normal Tremor Urine analysis normal

Symptomtext

Dizziness and trembling following shot. Slight sinus inflammation. Steroids prescribed. Dizziness and head disorientation continued after prescription over. Took blood. Everything including thyroid and electrolytes were normal. Dizziness and unsteadiness left after 19 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: Blood tests for thryroid and electrolytes performed on 2/26/2021 EKG normal: 2/26/2021 Urine test: 2/26/2021 All normal
Aktuelle Erkrankungen: No symptoms
Vorgeschichte: None
Andere Medikamente: Levothyroxine Tabs
Allergien: Penicillin, mold, trees, grasses
Vorherige Impfungen: -

VAERS 1060195

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: PA
Alter: 33,0
Geschlecht: F
Eingang: 27.02.2021
Impfdatum: 22.02.2021
Beginn: 22.02.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Axillary pain Chest discomfort Headache Heart rate increased Hypertension Hypoaesthesia Neck pain Pharyngeal swelling

Symptomtext

2.5 hours after receiving 2nd vaccine I developed left lower facial numbness. And additional 30-45 minutes after that I began having throat swelling/tightness and chest tightness. I went to the ER and was found to have and elevated heart rate and blood pressure. I had taken Benadryl prior to going to the ER and was given IV prednisone and Pepcid there. After a 2 hour observation my symptoms had subsided and I was released. The next morning I began having chest tightness again. My PCP called in a script for prednisone and advised me to also take Benadryl and Motrin as needed. I am still have intermittent facial/neck numbness, anterior and posterior neck pain; as well as intermittent headaches and axillary pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Amoxicillin, latex, peanuts, milk
Vorherige Impfungen: -

VAERS 1053841

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: -
Alter: 48,0
Geschlecht: F
Eingang: 25.02.2021
Impfdatum: 21.02.2021
Beginn: 21.02.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Electrocardiogram Heart rate increased Laboratory test Malaise Paraesthesia

Symptomtext

Following vaccine administration, patient complained of feeling increased heart rate to observation nurse. Vital signs checked and initially her heart rate was 115 but decreased to 75 with next set of vitals. Patients BP was 140/78, pulse ox 98. No SOB, no signs of anaphylaxis. Patient has h/o of anxiety and felt this was related. Patient was monitored for 30 min and felt some intermittent tingling in her hands. Patient was transported to the ED for further evaluation as she was still not feeling well after she was offered a snack and a drink. Patient monitored in ED, workup included EKG and labwork. Symptoms resolved and patient discharged to home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: anxiety, depression, IBS
Andere Medikamente: -
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 1049676

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: IL
Alter: 63,0
Geschlecht: F
Eingang: 23.02.2021
Impfdatum: 17.02.2021
Beginn: 17.02.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: UN / LA

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

Paraesthesia

Symptomtext

Starting at 6 pm in 17 the. Feelings of electrical shocks in various places in my body every 15 to 20 minutes stopping at 5 pm the 18 the. A sensation like getting a shock from an exposed outlet but not on skin, it was inside my body. Enough of a shock to be startling. One time it would be in right upper arm then upper leg, lower leg, sides, etc...

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Hypo thyroid, graves
Andere Medikamente: Levothyroxine, previous, pepto bismol, melatonin
Allergien: Eggs
Vorherige Impfungen: -

VAERS 1047641

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038k20A

moderat

Staat: MI
Alter: 52,0
Geschlecht: F
Eingang: 22.02.2021
Impfdatum: 12.02.2021
Beginn: 12.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Asthenia Confusional state Dizziness Feeling hot Headache Injection site rash Injection site urticaria Nausea Palpitations

Symptomtext

Moderna covid-19 vaccine eua. About 15 min after injection I felt hot (very unusual for me), then dizzy, racing heart, weak then very nauseous. I told the nurse. He asked me to lay down. I did not get worse. After 20 min or so I sat up and did not feel worse. Just stable nausea and dizzy. I asked if I could leave. After verifying I had people at home I was allowed to go. I felt exhausted and nauseous for the rest of the day. I was confused the next morning about what day it was and had some hives at injection site. I felt normal after figuring out what day it was. I walked 8 miles and aside from the hives at the injection site was normal. One week later I had headache, exhaustion and had an uncomfortable rash at the site. The rash is still on my arm. Should I get the second dose?

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Hashimoto thyroid
Andere Medikamente: None
Allergien: Many, bee and other wasp stings, latex, crustaceans, erythromycin, ceclore, sulfur
Vorherige Impfungen: DPT, high fever, age 40

VAERS 1044868

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: MI
Alter: 45,0
Geschlecht: M
Eingang: 21.02.2021
Impfdatum: 17.02.2021
Beginn: 18.02.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / LA

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

Asthenia Chills Erythema Fatigue Feeling cold Malaise Mobility decreased Pain Peripheral swelling Tremor Vomiting

Symptomtext

Began with severe fatigue and transitioned into severe shaking, body chills, aches that stayed for a prolonged period. In the course of trying to bring warmth to the body, I showered and ended up having severe vomiting. The body aches, fatigue, and overall sickness stayed with me for over 48 hours. Two days post vaccination, my left arm was swollen with severe redness. I am still struggling with fatigue and body aches (4 days later) but have regained mobility and strength.

Weitere VAERSDATA-Felder

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

VAERS 1043710

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: IL
Alter: 21,0
Geschlecht: F
Eingang: 20.02.2021
Impfdatum: 20.02.2021
Beginn: 20.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Chest discomfort Chest pain Dizziness Dyspnoea

Symptomtext

Immediately following the vaccine administration pt started to c/o dizziness, chest pain and pressure, SOB. VSS at 122/58, 103, 22, 98%.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Called EMT to take her to ED at 1409. Left vaccine clinic at 1420.
Aktuelle Erkrankungen: None
Vorgeschichte: Anxiety
Andere Medikamente: Buspar, Lexapro, Xyzal
Allergien: Sulfa and PCN
Vorherige Impfungen: -

VAERS 1043558

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: IL
Alter: 79,0
Geschlecht: F
Eingang: 20.02.2021
Impfdatum: 18.02.2021
Beginn: 19.02.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: - / -

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

Abdominal pain upper Arthralgia Chills Constipation Diarrhoea Neck pain Pain in extremity Paraesthesia

Symptomtext

On the 19th by about 4 pm pain in both arms not just the pain in a left arm muscle which was expected Pins and needles and pain in both hands Neck and shoulder pain Later that night chills Stomach ache and constipation followed by loose bowel later These were milder versions of my reaction when I had Covid-19 in November except the pins and needles in hands. That came on after I got over Covid. These pains went away after a couple of courses of Tylenol extra strength. Except the chills and stomach ache recurred and my stomach is still a little achy

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None Had Covid-19 in early November 2021
Vorgeschichte: High blood pressure Slightly high cholesterol Gout
Andere Medikamente: Losartan 100 m Allopurinal 100 mg Ezetimebe 10 mg GNC Probiotic Biotin forte with zinc 3mg Ocuvite adult
Allergien: Erythromiacin Levaquin
Vorherige Impfungen: -

VAERS 1042952

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: IL
Alter: 44,0
Geschlecht: F
Eingang: 20.02.2021
Impfdatum: 08.02.2021
Beginn: 09.02.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Chest pain Chills Dyspnoea Headache Lymphadenopathy Nausea Oropharyngeal pain Pain Respiratory viral panel SARS-CoV-2 test negative

Symptomtext

Headache,body Ache,Nausea,SOB,Chest pain,Chills,Sore Throat,Swollen lymph nodes

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Covid test,Respiratory Viral test
Aktuelle Erkrankungen: none
Vorgeschichte: Asthma(controlled for 3 yrs)
Andere Medikamente: Vitamin C and D3
Allergien: Trees and Dust mites
Vorherige Impfungen: -

VAERS 1041166

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: -
Alter: 52,0
Geschlecht: F
Eingang: 19.02.2021
Impfdatum: 10.02.2021
Beginn: 10.02.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Dizziness postural Feeling abnormal Hyperhidrosis Hyperventilation Tachycardia

Symptomtext

During the 15 min observation period state 'not feeling right.' When evaluated, patient was tachycardic, diaphoretic, hyperventilating, continued this way for several minutes. Tried to stand but felt dizzy. Medical emergency was called and patient was sent to the emergency room for further observation.

Weitere VAERSDATA-Felder

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

VAERS 1039412

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: MT
Alter: 53,0
Geschlecht: F
Eingang: 18.02.2021
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

Hypoaesthesia Paraesthesia

Symptomtext

Patient stated that approximately 11:30 am she noted left facial cheek feeling numb and tingling. Then became tingling all over face that lasted for approximately on hour. Patient returned to Clinic to report symptoms at approximately 1445. Patient stated that symptoms had resolved prior to arrival. Patient was seen for symptoms by FNP.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: No laboratory tests were done at time of visit.
Aktuelle Erkrankungen: None reported
Vorgeschichte: None reported
Andere Medikamente: None reported
Allergien: Hydrocodone, Tylenol #3, Oxycodone, Lisinopril, Ketotifen, Morphine
Vorherige Impfungen: -

VAERS 1036110

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: IL
Alter: 63,0
Geschlecht: F
Eingang: 17.02.2021
Impfdatum: 03.02.2021
Beginn: 03.02.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Arthralgia Fatigue Injected limb mobility decreased Injection site erythema Injection site pain Injection site swelling Injection site warmth Malaise Pain

Symptomtext

Mild body aches and fatigue started at 10:00 pm, approximately 11 hours after injection. Next morning body aches and fatigue increased, generalized ill-feeling, also with joint achiness. Surface swelling, redness and warmth with approx 4 inch circumference at site of injection. Painful to move arm that had injection; raising arm above shoulder level (over head) extremely painful, almost impossible. All symptoms fading after 48 hours. All symptoms resolved within 72 hours except warmth and tenderness at injection site. Injection site back to normal without symptoms 7 days after injection.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: hypothyroid, osteopenia, atherosclerosis
Andere Medikamente: Hydrochlorthiazide 1.25 mg Levothyroxine 112mcg Centrum Silver for Women multivitamin magnesium 200mg vitamin D 1000IU aspirin 81 mg Theracurmin (curcumin) 60mg Align probiotic
Allergien: none
Vorherige Impfungen: -

VAERS 1032894

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: NC
Alter: 64,0
Geschlecht: F
Eingang: 16.02.2021
Impfdatum: 10.02.2021
Beginn: 10.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / RA

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

Anxiety Diarrhoea Dizziness Paraesthesia oral Pharyngeal paraesthesia Pharyngeal swelling Swollen tongue

Symptomtext

Throat and tongue tingling and sensation of swelling, diarrhea and took benadryl. At 8 hrs post vaccine got dizziness, throat swelling, anxiety, and had to use epipen. Went to hospital by ambulance and was further treated with prednisone and benadryl and Zofran.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia oral
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Multiple sclerosis, hypertension, GERD, gastric polyps, thyroid nodules, multiple allergies, histamine intolerance, high cholesterol, arrhythmia, mild asthma, mild depression, constipation
Andere Medikamente: Bystolic, Pantoprazole, Zetia, zyrtec, vitamin D, vitamin B12, calcium, Baclofen, Diltiazem ER, cymbalta, magnesium, flonase
Allergien: Penicillin, sulfa, lidocaine, latex, aspirin, NSAIDs, nitrofurantoin, tetracycline, doxycycline, Clindamycin , Crestor, Lipitor, Lyrica, levaquin, shellfish, tree nuts, mango, eggplant, coconut, bananas, avocado.
Vorherige Impfungen: -

VAERS 1032733

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: FL
Alter: 77,0
Geschlecht: F
Eingang: 16.02.2021
Impfdatum: 03.02.2021
Beginn: 04.02.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Fatigue Hypersensitivity Paraesthesia Sneezing

Symptomtext

summary of her symptoms: 1 hr post vaccination - feeling tired and sneezing excessively for a couple of days. 3rd day post vaccination-skin tingling sensation all over that resolved with oatmeal bath. 5th day post vaccination-was seen by pcp who told she was fine. received a call from pa from office to inform her she had an allergic rxn and was not to receive the second vaccine. today-she is asymptomatic.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: saw her PA yesterday, and the PA said those were just allergic reactions
Aktuelle Erkrankungen: -
Vorgeschichte: Breast cancer 3 years ago, cholesterol. glaucoma, heart disease, bone density
Andere Medikamente: Niacin 500 mg tablet Aspirin 81 mg tablet Multivitamin Calcium with Vitamin D Lumigan eye drops
Allergien: -
Vorherige Impfungen: -

VAERS 1030937

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: IL
Alter: 61,0
Geschlecht: F
Eingang: 15.02.2021
Impfdatum: 10.02.2021
Beginn: 11.02.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / RA

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

Disturbance in attention Fatigue Headache Impaired work ability Injection site erythema Injection site pain Injection site reaction Injection site swelling Injection site warmth Musculoskeletal stiffness Nausea Pain Tachycardia

Symptomtext

2/10/21 - 915AM - tachycardia for 10 minutes - 30 minutes after receiving vaccine. 2/11/21 - 8AM - injection site stiffness, swelling, redness, hot to touch body aches with severe headache and nausea inability to focus at work (RN duties) 2/11/21 - 12PM - Sent home from work - tylenol for pain/headache, slept for 18 hours. 2/12/21 - 8AM - Returned to work - body aches resolved - headache controlled with tylenol, Feeling of fatigue Continued injection site tenderness, swelling and redness 2/13/21 - Symptoms resolved

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tachycardia
Hospital-Tage: -
Labordaten: No testing completed
Aktuelle Erkrankungen: None
Vorgeschichte: Hypothyroidism Hyperlipidemia Asthma Obesity Anxiety
Andere Medikamente: Levothyroxine 112mcg, sertraline HCl 50mg, atorvastatin 40mg, Vyvanse 40mg, symbicort 80/4.5, ibuprofen 200mg
Allergien: Tetanus - vaccines penicillin
Vorherige Impfungen: Flu Vaccine - Rec'd 2011

VAERS 1029117

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: PA
Alter: 64,0
Geschlecht: F
Eingang: 14.02.2021
Impfdatum: 07.01.2021
Beginn: 24.01.2021
Tage bis Beginn: 17,0
Dosis: 2
Route/Site: IM / LA

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

Migraine Pain Pyrexia

Symptomtext

after first vaccine: increased ocular migraines - no treatment. after second vaccine: 101.5 fever - took 2 ibuprofen; slept 15 hours; moderately sore are 5 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: intermittent hyperactive airways
Andere Medikamente: fluticasone nasal spray; gingko biloba; B12; calcium with vitamin D
Allergien: none
Vorherige Impfungen: -

VAERS 1027297

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: IL
Alter: 39,0
Geschlecht: F
Eingang: 12.02.2021
Impfdatum: 25.01.2021
Beginn: 27.01.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: SC / RA

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

Arthralgia Asthenia Burning sensation Injection site joint pain Injection site pain Paraesthesia

Symptomtext

I have had joint pain in my right arm since the 2nd vaccine. I received both doses in that arm. The pain varies from my shoulder to my elbow and at times my wrist. Sometimes it radiates from my shoulder down to my fingers. I also at times feel tingling in my fingers. There's no rhythm or pattern to where the pain is. I describe the pain as burning and weakness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: I have not been seen about it yet.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1026472

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: FL
Alter: 69,0
Geschlecht: F
Eingang: 12.02.2021
Impfdatum: 05.02.2021
Beginn: 06.02.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Abdominal discomfort Chills Dizziness Fatigue Heart rate irregular Influenza like illness Injection site erythema Injection site pain Injection site warmth Insomnia Lethargy Palpitations Pyrexia

Symptomtext

Woke up at 1:00 AM with heart pounding and beating very fast, dizzy, chills followed by high fever. This lasted 2+ hours. Then my heart beat so faintly, that I was afraid to go back to sleep for fear I would not wake up. Felt a little sick to my stomach. Next day, I felt like I had the flu all day, lethargic, tired but couldn't sleep. The injection site of the shot was very sore, big red circle about the size of a peach, hot to the touch and this lasted until day 5. Concerned about 2nd dose, because if the reaction was worse than this, I don't think my heart can take it.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: Made an appointment with my primary care physician to discuss this and his recommendation for 2nd dose.
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Candesartan
Allergien: Sulfur, DMAPA, Cobalt (ll) Chloride Hexahydrate
Vorherige Impfungen: -

VAERS 1026382

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: CA
Alter: 26,0
Geschlecht: F
Eingang: 12.02.2021
Impfdatum: 09.02.2021
Beginn: 09.02.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Dyspnoea Injection site erythema Injection site rash Injection site swelling

Symptomtext

PATIENT COMPLAINED OF REDNESS AND SWELLING TO LEFT ARM THAT IS MOVING UP ARM TO SHOULDER, BROKE OUT IN RASH WITH SLIGHT SHORTNESS OF BREATH.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: NONE
Vorgeschichte: OBESITY
Andere Medikamente: PATIENT TOOK NYQUIL
Allergien: IBUPROFEN AND BENADRYL
Vorherige Impfungen: -

VAERS 1025269

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: MI
Alter: 36,0
Geschlecht: F
Eingang: 12.02.2021
Impfdatum: 11.02.2021
Beginn: 11.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Chills Hypoaesthesia Pain in extremity Paraesthesia Paraesthesia oral

Symptomtext

I had a sore arm a couple hours later. Approximately 2- 2 1/2 hours after the injection the right side of my face started tingling, not completely numb but mild numbness. The feeling is similar to Novacane wearing off from dental work. Around 8 p.m. while laying down, my lips tingled for awhile. As on 10 a.m. on 2/12/2021 I still have mild tingling in my right side of face and upper lip area on the right side. I have had mild chills.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: None as of now
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Lo-Estrin birth control, Motrin 600 mg. Multi-vitamin, vitamin D and Zinc.
Allergien: Sulfa drugs. Mild reaction to the Pertussis vaccine
Vorherige Impfungen: Pertussis, under 10 years old and mild reaction

VAERS 1023881

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: IL
Alter: 78,0
Geschlecht: F
Eingang: 11.02.2021
Impfdatum: 10.02.2021
Beginn: 11.02.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / LA

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

Dry mouth Dyspnoea Painful respiration Throat tightness Wheezing

Symptomtext

about 3:30 the next morning i woke up with dry mouth and went to the bath room and tried to drink water and my throat had closed up and i couldn't breathe I was not able to drink water and and kept gasping for air. finally after a few minutes i was able to catch my breath and i started to wheeze and then my chest hurt when i would breath. And then i woke up today and i was fine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: sycosis of liver, A fib
Andere Medikamente: potassium Citrate 5 mg, baby aspirin 80 mg, calcium 600 mg, vitamin D3, Iron 65 mg, centrum multivitamin, coQTen, Align pro biotics, Eliquis 5 mg twice a day, carvedilol 12 mg twice a day, Olmesartan 40 mg ,
Allergien: codeine, upper Brazil nut
Vorherige Impfungen: -

VAERS 1023022

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: FL
Alter: 74,0
Geschlecht: F
Eingang: 11.02.2021
Impfdatum: 03.02.2021
Beginn: 05.02.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / LA

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

Arthralgia Erythema Injected limb mobility decreased

Symptomtext

Intense erythema, arthralgia, myalgia left shoulder and left deltoid. Shoulder injured in a jogging injury/ fall twenty years ago (subachromial impingement), but have had no problem with since, became "frozen" and extraordinarily painful (on pain scale its a 9). It is post-vaccine day 10 now and it appears to be showing no signs of abating. Only relief is 400mg ibuprofen on a prn basis. Cannot lift left arm or extend left arm (abduction). Believe the vaccine may have caused a vigorous immune response (great!), however it may be an "cytokine storm" which has caused an acute arthritis event. Concerned about immunization #2.

Weitere VAERSDATA-Felder

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

VAERS 1022765

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: PA
Alter: 51,0
Geschlecht: F
Eingang: 11.02.2021
Impfdatum: 03.02.2021
Beginn: 03.02.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Chills Injected limb mobility decreased Injection site pain Pain Peripheral swelling Pyrexia Rash erythematous

Symptomtext

pt stated that after her vax that her left arm developed swelling, red rash, pain around the injection site extending from her shoulder to her elbow. Pt had a slight fever with chills and body aches which kept her in bed the entire day after the injection. Pt has contacted her PCP and waiting to hear back from them for medical advice since she states she still has pain, swelling, redness and can hardly move her left arm.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: no
Aktuelle Erkrankungen: no
Vorgeschichte: thyroid and concussions
Andere Medikamente: declined
Allergien: corn, soy, egg
Vorherige Impfungen: -

VAERS 1019275

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: IL
Alter: 25,0
Geschlecht: F
Eingang: 10.02.2021
Impfdatum: 27.01.2021
Beginn: 03.02.2021
Tage bis Beginn: 7,0
Dosis: 2
Route/Site: IM / LA

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

Chest pain Fatigue Heart rate increased

Symptomtext

The patient complained of chest pain, increased heart rate (130), BA, fatigue. Advised to seek treatment/ED for chest pain

Weitere VAERSDATA-Felder

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

VAERS 1020141

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: IL
Alter: 55,0
Geschlecht: F
Eingang: 09.02.2021
Impfdatum: 02.02.2021
Beginn: 02.02.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Chest discomfort Hypoaesthesia oral Joint swelling Lip swelling Lymph node pain Paraesthesia oral Throat tightness

Symptomtext

Developed throat tightness and chest tightness later in day of vaccine admin. ~ albuterol neb relieved symptoms. The following day in the mid-morning, she had a reoccurrence of throat and chest tightness and also subsequently developed swollen, tingling and numb lips. She took Allegra 180 mg, prednisone 30 mg ~ symptoms did improve with these. For the next several days, she had intermittent lip tingling and swelling. 3 days s/p vaccine, she developed throat and chest tightness again - no improvement with albuterol but did get improvement with Benadryl. She also developed intermittent tenderness of cervical and occipital LNs and swelling and tenderness in some of her joints (bilateral knees and wrists)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia oral
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: No
Vorgeschichte: mild intermittent asthma, G.E.R.D, depression, elevated triglycerides , s/p breast cancer without node involvement, recurrent acne, allergic rhinitis
Andere Medikamente: wellbutrin, lexepro, lamictal, serquel, montelukast, arimidex, arnruity protonix, fenofibrate, calcium, vitamin D, MVI, tumeric, vitamin C with rose hips, spironlacton, aleve, meloxicam, ibuprofen, fluticasone nasal
Allergien: No known drug allergies
Vorherige Impfungen: -

VAERS 1017451

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: IL
Alter: 49,0
Geschlecht: F
Eingang: 09.02.2021
Impfdatum: 02.02.2021
Beginn: 02.02.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Asthma Chest X-ray normal Dizziness Dyspnoea Electrocardiogram normal Heart rate increased Palpitations Throat tightness

Symptomtext

Approx 15 minutes after vaccination patient complained of a sensation that her throat is closing and difficulty breathing. She was given benadryl and utilized her home albuterol inhaler. She asked to be taken to the ED. In the ED patient received albuterol nebulizer (@1327), epinephrine 0.3 mg (@1345), famotidine 20 mg (@1327) and methylprednisolone 125 mg (@1327). She was discharged with a prednisone prescription. Symptoms seemed to improve with albuterol and steroids. Epinephrine did not seem to improve symptoms. Patient was discharged with a diagnosis of asthma exacerbation. Patient reported to ED again on 2/9 with feelings of lightheadedness and palpitations. All diagnostic evaluations were negative. Increased heart rate contributed to prednisone use for previous mentioned asthma exacerbation.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: EKG 2/9 Chest Xray 2/9
Aktuelle Erkrankungen: n/a
Vorgeschichte: asthma
Andere Medikamente: zolpidem, albuterol, diclofenac, mirtazapine, alprazolam, chlorpromazine, latuda, duloxetine, propranolol
Allergien: aminophylline, doxycycline, duoneb, lamictal, sulfa drugs, theophylline, azithromycin
Vorherige Impfungen: -

VAERS 1016148

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: IL
Alter: 19,0
Geschlecht: F
Eingang: 09.02.2021
Impfdatum: 27.01.2021
Beginn: 30.01.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: IM / LA

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

Blood creatine phosphokinase MB increased C-reactive protein increased Chest pain Chills Computerised tomogram thorax normal Dyspnoea Electrocardiogram ST segment elevation Electrocardiogram abnormal Fall Fibrin D dimer Injection site erythema Injection site oedema Injection site warmth Myalgia Pain Painful respiration Red blood cell sedimentation rate increased SARS-CoV-2 test negative

Symptomtext

Patient is a 19yo female presenting to the ED with chest pain. Patient received her second Moderna vaccine two days. Since then she has been having symptoms of chills and myalgias. This morning she had severe chest pain in the middle of her chest. It made it difficult to breathe. Patient had no side effects from 1st dose of vaccine and denies any symptoms prior to receiving 2nd dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: VSS PE: No abnormalities on cardiac exam. No pulsus paradoxus. No improvement of chest pain with leaning forward although poor effort by patient due to pain from a fall two days ago. Mild erythema, edema and warmth surround injection site. EKG: possible pericarditis with minimal ST elevations in leads II, III, AVF, V2 and V6. Labs: Elevated Trop 2.25-- >2.66; CKMB 9.7; Ddimer 1433; ESR 35; CRP 11.40. CT Chest: No PE or pericardial effusion. Of note per the CT tech the IV blew during the exam and was not sure if enough contrast had passed for a valid read. No comments of any issue from radiologist. Patient chest pain still present but not as severe as this morning and continued worsening with deep inspiration. COVID antigen negative COVID PCR negative Recommend patient have an ECHO to r/o pericarditis vs pericardial effusion or any other cardiac abnormality before discharging home with appropriate treatment. Blessing called for transfer 11am. Accepted to Med/Surg. Patient had been started on Heparin prior to CT. This was discontinued after CT results. Patient was administered Toradol 30mg IV and Colchicine 1.2mg.
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Unknown
Andere Medikamente: Unknown
Allergien: Unknown
Vorherige Impfungen: -

VAERS 1011702

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: CO
Alter: 55,0
Geschlecht: M
Eingang: 08.02.2021
Impfdatum: 02.02.2021
Beginn: 03.02.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Dehydration Injection site pain Pyrexia

Symptomtext

shortness of breath, low oxygen level from COVID-19 1st week of November 2020. After vaccination on 2/2/21, developed high temp (104.1F), severe dehydration, and pain at injection site

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dehydration
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: pneumonia Jan 22, 2020
Vorgeschichte: Type II diabetes, hypercholesterolemia
Andere Medikamente: losartan, glipizide
Allergien: sulfa drugs
Vorherige Impfungen: -

VAERS 1011125

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: IL
Alter: 31,0
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: nein

Pain in extremity Paraesthesia

Symptomtext

Prickly feeling in left arm by brachial artery and also in right lower leg, outer calf muscle. Very sore left arm.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Supraventricular tachycardia
Andere Medikamente: None
Allergien: Sudafed and others heart stimulants
Vorherige Impfungen: -

VAERS 1010006

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: IL
Alter: 39,0
Geschlecht: F
Eingang: 07.02.2021
Impfdatum: 07.02.2021
Beginn: 07.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Hypoaesthesia Paraesthesia

Symptomtext

After about 15 minutes my face felt tingly. Like a slight numbness to my face. I felt it in my forehead, chin, nose, and cheeks. When I got home I took a Benadryl. After about 3 hours my face felt normal again.

Weitere VAERSDATA-Felder

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

VAERS 1009034

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: IL
Alter: 36,0
Geschlecht: M
Eingang: 07.02.2021
Impfdatum: 03.02.2021
Beginn: 03.02.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Body temperature increased Chills Headache Hyperhidrosis Tremor

Symptomtext

103 fever, chills, shakes, sweats, headache. 100.2 temperature started at 5pm. By 7pm, fever rose to 103. Temperature did not drop below 100 degrees until 9am on 2-4-2021. Sweats ended by noon on 2-4-2021. All symptoms resolved by 9pm on 2-4-2021. Only medication taken was Tylenol starting at 9pm on 2-3-2021. 2 pills every 6 hours. 3 doses of Tylenol total.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Eczema
Andere Medikamente: Dupixent
Allergien: Formaldehyde, Quaternium 15
Vorherige Impfungen: -

VAERS 1007119

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: FL
Alter: 61,0
Geschlecht: M
Eingang: 05.02.2021
Impfdatum: 04.02.2021
Beginn: 05.02.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Chills Dizziness Lethargy Pain in extremity Paraesthesia Pyrexia

Symptomtext

102 degree fever, shivering, lethargy, sore arm, skin tingling, very dizzy

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: diabetes controlled with insulin and medication
Andere Medikamente: None
Allergien: NKA
Vorherige Impfungen: -

VAERS 1006803

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038k20a

moderat

Staat: FL
Alter: 65,0
Geschlecht: F
Eingang: 05.02.2021
Impfdatum: 27.01.2021
Beginn: 27.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / -

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

Fatigue Feeling abnormal Headache Injection site erythema Injection site rash Mobility decreased Pain in extremity Paraesthesia oral Peripheral swelling Skin warm

Symptomtext

On 1-27-21 in the afternoon her mouth felt "tingly" and at around 5p.m. patient felt pain in arm. and the arm swelled. it also hurt for her to mover her arm. She also felt fatigued and she rested the rest of the evening. The next day she also felt fatigued. Her arm felt warm to the touch. She also had a headache and felt "spacey." She took a Benadryl to see if it would make her feel better. Today (Feb 5, 2021) she noticed redness at 2 p.m. around the site of injection and it looked a little "rashy." Patient applied Vaseline intensive care to rash. She says it still feels warm to the touch.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Benadryl, esgic, crestor, Tylenol, Pepcid, prilosec
Allergien: seafood
Vorherige Impfungen: -

VAERS 1005375

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: IL
Alter: 66,0
Geschlecht: F
Eingang: 05.02.2021
Impfdatum: 04.02.2021
Beginn: 04.02.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: SYR / RA

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

Paraesthesia oral Rash macular Tongue disorder

Symptomtext

Tongue tingling, thickening, red blotches, Took Benadryl to relieve symptoms,

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia oral
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: UTI
Vorgeschichte: Degenerative Disk Disease in spine, neck and lower back; arthritis in joints; Pacemaker; hypertension;
Andere Medikamente: Aspirin-81 mg; Biotin-800 mcg; Vitamin D-2000 mg; Lisinopril-20 mg; Montelukast-10 mg; Omeprazole-20 mg; Escitalopram-10 mg; Probiotic; Furosemide-20 mg; Bystolic-5 mg; Ezetimibe-10 mg; Cefdinir-300 mg;
Allergien: Avelox-rash; Flexerill-rash; Iodine-rash; Lebquin-rash; Penicillins-rash; Sulfa-rash; Vicodin-rash; Betadine-rash
Vorherige Impfungen: Slight reaction to Flu Shot, September 14, 2020 and Pneumonia Shot-Prevnar 13. Took Benadryl for relief. I don?t remember if I

VAERS 1005335

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: IN
Alter: 45,0
Geschlecht: M
Eingang: 05.02.2021
Impfdatum: 03.02.2021
Beginn: 04.02.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / RA

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

Dizziness Fatigue Headache Hypoaesthesia Pain Paraesthesia Pyrexia

Symptomtext

Extreme Fatigue Dizziness Fever, body aches Tingling, and numbness to the injected arm (right) Severe headache

Weitere VAERSDATA-Felder

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

VAERS 1001050

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: IN
Alter: 28,0
Geschlecht: F
Eingang: 04.02.2021
Impfdatum: 02.02.2021
Beginn: 02.02.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Arthralgia Cold sweat Decreased appetite Dyspnoea Fatigue Headache Hot flush Night sweats Pain Palpitations Pyrexia

Symptomtext

fatigue (extreme, could barely keep eyes open), headache, painful deep breaths, heart racing, fever over night with night sweats, body aches/ joint pain, hot/cold flashes, loss of appetite- all happened with in 2/2 to 2/3. Symptoms began to resolve on 2/4

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: Asthma
Andere Medikamente: birth control medication
Allergien: Morphine
Vorherige Impfungen: -

VAERS 1000423

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: FL
Alter: 41,0
Geschlecht: F
Eingang: 04.02.2021
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

Balance disorder Chills Disturbance in attention Dyspnoea Epistaxis Fatigue Headache Mental impairment Muscle fatigue Musculoskeletal stiffness Myalgia Nausea Pain Pyrexia

Symptomtext

Within 12 hours of receiving vaccine I began to feel fatigue in my muscles and a mild headache. The next morning I experienced brain fog, inability to formulate thoughts correctly, difficulty thinking, lack of concentration, muscle soreness, aches all over body, tired easily, shortness of breath, fever, chills, and nausea. 36 hours after receiving vaccine, I still feel uneasy on my feet, light headedness, muscle soreness, stiff neck, nose bleeds, headache, nausea and extreme fatigue.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: no
Aktuelle Erkrankungen: NO
Vorgeschichte: NO
Andere Medikamente: NONE
Allergien: MACROBID
Vorherige Impfungen: -

VAERS 999333

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: IL
Alter: 45,0
Geschlecht: F
Eingang: 03.02.2021
Impfdatum: 01.02.2021
Beginn: 01.02.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Arthralgia Chills Headache Impaired work ability Myalgia Pain Pyrexia Tachycardia Tremor

Symptomtext

Approximately 14 hours after receiving second dose of vaccine had severe body aches and chills, uncontrolled shaking for 6hrs, tachycardia, fever 103, joint and muscle pain, severe headache, fever did not respond well to tylenol taken, lowest got was 101.9. Continued to remain symptomatic until present day 02/03/2021 with body aches, severe headache and 102 fever. Had to call in sick to work 02/03/2021. Called Covid hotline and they advised me to complete this form and to notify them if not better by 02/04/2021 or go to urgent care if fevers remain still tomorrow.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tachycardia
Hospital-Tage: -
Labordaten: None as of 02/03/2021
Aktuelle Erkrankungen: I have Menieres Disease, chronic inner ear autoimmune disorder as well as Sjogrens an autoimmune disorder. Have been having facial rashes and flushing over past few months with ear issues. No new meds ordered or no new treatments started.
Vorgeschichte: Meneires Disease Deaf left ear IBS Sjogrens disease chronic anemia
Andere Medikamente: meloxicam, neurontin
Allergien: latex allergy, allergy to some fruits, milk sensitivity, chocolate sensitivity and nickel sensitivity
Vorherige Impfungen: -

VAERS 997961

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: FL
Alter: 67,0
Geschlecht: F
Eingang: 03.02.2021
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: ja

Dizziness Dysphagia Feeling abnormal Nausea Palpitations

Symptomtext

feeling foggy, woozy, a little dizzy and nauseated, racing hearthard to swallow

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: generic Fosamax once a week
Allergien: none
Vorherige Impfungen: -

VAERS 997933

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038k20a

moderat

Staat: IN
Alter: 53,0
Geschlecht: F
Eingang: 03.02.2021
Impfdatum: 01.02.2021
Beginn: 01.02.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / RA

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

Dizziness Feeling abnormal Impaired work ability Injection site erythema Injection site inflammation Injection site swelling Migraine

Symptomtext

Felt increased wooziness/dizziness/feeling off for several hours. Progressed to a migraine (not a person to ever have had migraines)x 24 hrs. Resulted in not going to work the next day. Also a large, raised, redden/inflamed injection site remains on the right deltoid.

Weitere VAERSDATA-Felder

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

VAERS 995982

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: IL
Alter: 26,0
Geschlecht: F
Eingang: 02.02.2021
Impfdatum: 02.02.2021
Beginn: 02.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Blood glucose Chills Dysgeusia Dyspnoea Electrocardiogram Headache Nausea Paraesthesia

Symptomtext

Shortness of breath, chills. tingling, metallic taste, nausea, headache

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: EKG 2/2/21, glucose test, blood pressure
Aktuelle Erkrankungen: None
Vorgeschichte: SVT, asthma
Andere Medikamente: Metoprolol, lo lost in, albuterol, dulera
Allergien: Ferrous sulfate
Vorherige Impfungen: -

VAERS 994578

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: NC
Alter: 74,0
Geschlecht: F
Eingang: 02.02.2021
Impfdatum: 27.01.2021
Beginn: 27.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Chest discomfort Chills Hot flush Hypoaesthesia Paraesthesia

Symptomtext

The first one was some fullness in chest, and I left the clinic and I had some flushing in my face, nothing you wouldn't expect, had some light chills. Around four hours later I had some tingling in my feet and then began to progress up the leg, I began to realize I didn't have feeling in my feet so I began to walk around for about four to five hours, and began to get some relief and and laid down around 2 o clock in the morning, and when she woke up she had numbness in the bottom of her feet. It took about 36 hours for the numbness to go away.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: No.
Aktuelle Erkrankungen: -
Vorgeschichte: chronic sinus issues CAD coronary artery disease high blood pressure s'jrogens morphea lichens schloresis
Andere Medikamente: clobestosol propenate .05 as needed Restasis .05 twice daily nitroglycerin as needed .4 mg isosorbide mononitrate 90 mg. amlodipine besylate 5 mg daily pilocaprin 5 mg twice daily montiltus 10 mg daily linzess 145 mg as needed ezetimibe
Allergien: clindamycine clonzepam crestor lipator polysporin methrotexate acrolytes fragrances trees molds grasses
Vorherige Impfungen: 2019 adverse reaction to Flu vaccine

VAERS 991180

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: IN
Alter: 71,0
Geschlecht: M
Eingang: 01.02.2021
Impfdatum: 30.01.2021
Beginn: 31.01.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Condition aggravated Neuropathy peripheral

Symptomtext

Increase in severity of peripheral neuropathy.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: Preexisting peripheral neuropathy.
Andere Medikamente: Plavix 75 mg. (morning) 1/day Aspirin 81 mg. (morning) 1/day Flomax 4 mg. (morning) 1/day Centrum Silver (morning) 1/day Prilosec 20 mg. (morning) 1/day Toprol XL 12.5 mg. (morning) 1/day Colace 100 mg.
Allergien: None
Vorherige Impfungen: -

VAERS 989261

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: FL
Alter: 71,0
Geschlecht: F
Eingang: 31.01.2021
Impfdatum: 28.01.2021
Beginn: 29.01.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: IM / LA

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

Influenza like illness Injected limb mobility decreased

Symptomtext

Flu like symptoms beginning about 8 hours after injection & lasting about 36 hours. Also unable to lift arm used for injection which lasted about 16 hours.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: GERD, intermittent palpitations, controlled high cholesterol
Andere Medikamente: Atorvastatin, nadolol, Omeprazole, calcium+D, magnesium, Metamucil
Allergien: Sulfa, macrodantin
Vorherige Impfungen: -

VAERS 988056

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: FL
Alter: 72,0
Geschlecht: M
Eingang: 30.01.2021
Impfdatum: 29.01.2021
Beginn: 30.01.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Asthenia Body temperature increased Decreased appetite Headache Heart rate increased Hypertension Injection site pain Pain

Symptomtext

Headache, Temperature 100.6, Body Ache in all joints, severe pain in left arm at injection site, overall weakness, no appetite, high heart beat, blood pressure high,

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Type 2 Diabetic
Andere Medikamente: Xaralto, Metformin,Atovarsatin, Losartin,carvedilol,nifedipine,jardiance,novolog
Allergien: NO
Vorherige Impfungen: -

VAERS 987682

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: FL
Alter: 67,0
Geschlecht: M
Eingang: 30.01.2021
Impfdatum: 29.01.2021
Beginn: 30.01.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / RA

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

Paraesthesia Rash macular

Symptomtext

Red blotchiness on both legs from the ankle to mid-calf. No pain but tingling sensation when touched.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: None to date
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Rosuvastatin , 1 per day Alfuzosin , 1 per day Turmeric , 2 per day Centrum Silver, 1 per day
Allergien: None
Vorherige Impfungen: -

VAERS 985254

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038k20a

moderat

Staat: FL
Alter: 65,0
Geschlecht: F
Eingang: 29.01.2021
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: ja Erholt: nein

Paraesthesia oral Tongue discomfort

Symptomtext

Patient reported a tingling tongue and burning on the tip of her tongue

Weitere VAERSDATA-Felder

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

VAERS 984827

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: IL
Alter: 40,0
Geschlecht: F
Eingang: 29.01.2021
Impfdatum: 27.01.2021
Beginn: 28.01.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / RA

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

Abdominal pain lower Blood glucose normal Condition aggravated Crying Diarrhoea Dizziness Dysstasia Feeling hot Feeling of body temperature change Full blood count Hyperhidrosis Laboratory test Metabolic function test Nausea Pain in extremity Pallor Retching Reynold's syndrome

Symptomtext

210 am woke up hot. Walked downstairs had ringing in my ear and saw stars, held the wall almost passed out. Began profusely sweating drenching my clothes. Nausea began. Went back upstairs sat on my bathroom floor due to nausea/ dry heave. All of a sudden SEVERE abdominal pain began 10/10. Cried for my husband. Dripping sweat gave me a cold rag and foam large diarrhea began. Still 10/10 pain in abdomen. Felt like my lower abdomen was getting ripped out. About 45 minutes or so later still 10/10 wanted to go to ER. I could not stand. If I stood my legs and body felt like I wanted to curl in a ball on the floor. He called an ambulance. I was pale as a ghost, no fever, normal vital signs. Went into full reynauds flare from body stress. Ambulance was unable to get oxygen sat and glucose at the time due to flare. Arrived at the ER labs drawn. WBC 10.9 and Glucose 194. I am not or never have been diabetic. Vaccine related. Like a lightswitch all symptoms stopped except sweating hot and cold spells, sore arm and drowsiness. Discharged at 6am

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Bolus 0.9 NS 1 liter CBC BMP
Aktuelle Erkrankungen: None
Vorgeschichte: Reynauds
Andere Medikamente: Vitamin C Vitamin D
Allergien: Prevacid
Vorherige Impfungen: -

VAERS 983474

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: IL
Alter: 36,0
Geschlecht: M
Eingang: 28.01.2021
Impfdatum: 27.01.2021
Beginn: 28.01.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Chills Cough Fatigue Hyperhidrosis Palpitations Pyrexia Wheezing

Symptomtext

chills, fever, 101 temp, weezing, sweating, fatigue, cough, heart racing over 100 bpm

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: n/a
Allergien: n/a
Vorherige Impfungen: -

VAERS 983253

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: IL
Alter: 49,0
Geschlecht: F
Eingang: 28.01.2021
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: ja Erholt: nein

Dyspnoea Emotional distress Flushing Hypoaesthesia Hypoaesthesia oral Pharyngeal hypoaesthesia

Symptomtext

Patient began feeling like tongue was numb after approximately 12 minutes. She was taken to the emergency room immediately and felt short of breath, flushed, numbness in limbs, and felt like throat and tongue were numb. Appeared in distress and began on 4 L of oxygen per nasal cannula (SPO2 remained at 100%). Epinephrine 0.3 mg was given IM at 1501, Benadryl 50 mg was given IM at 1502 and Alprazolam 0.5 mg PO at 1520. Patient's BP was 152/91 at 1501 but decreased back down to 133/63 at 1508. Heart rate remained in the 80's and respiratory rate decreased from 24 at 1501 to 20 at 1521

Weitere VAERSDATA-Felder

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

VAERS 975781

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038k20a

moderat

Staat: PA
Alter: 55,0
Geschlecht: F
Eingang: 26.01.2021
Impfdatum: 26.01.2021
Beginn: 26.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Chills Dizziness Dyspnoea Hypoaesthesia

Symptomtext

patient complained of feeling light-headed, dizzy, short of breath, chills and numbness in her chest.

Weitere VAERSDATA-Felder

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

VAERS 971678

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: IL
Alter: 66,0
Geschlecht: F
Eingang: 25.01.2021
Impfdatum: 22.01.2021
Beginn: 24.01.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / LA

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

Blood creatine phosphokinase normal Blood glucose normal Erythema Full blood count Haematocrit normal Mean cell haemoglobin concentration decreased Metabolic function test Monocyte count normal Paraesthesia Pruritus Rash Red blood cell sedimentation rate normal

Symptomtext

Pt began having itching and tingling sensation and rash and redness to b/l hands on Sunday 01/24/2021. She present to the ER at hospital on Monday 01/25/2021. Pt had blood testing and was prescribed on discharge benadryl and prednisone.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: CBC, CMP, ESR, and CK. All tests were WNL except the following: Hematocrit elevated 46.1, Monocyte absolute count elevated 0.5, Mean cell hemoglobin concentration low -31.9 and Glucose elevated at 116
Aktuelle Erkrankungen: COPD, OA, Allergic Rhinitis, Insomnia
Vorgeschichte: see Item 11
Andere Medikamente: Albuterol HHN, MVI Alive, Benadryl, Zyrtec, Flonase, Ipratropium HHN, Singulair, Symbicort
Allergien: Bee stings, wasps stings, sulfa, mosquitoes, Lasix, PCN
Vorherige Impfungen: -

VAERS 966478

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

moderat

Staat: IL
Alter: 82,0
Geschlecht: F
Eingang: 22.01.2021
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: ja Erholt: ja

Dyspnoea Oropharyngeal discomfort Throat tightness

Symptomtext

About 10 minutes after receiving the vaccine, pt began complaining of a tickle in her throat and mild SOB. After 13 minutes she began complaining of her throat feeling tight.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Pt was taken immediately to the Hospital ER. No Medical test or laboratory testing was done. Pt was given a Saline lock and IV Solumedrol and Benadryl.
Aktuelle Erkrankungen: CAD, Diverticulosis, gerd, oa, dm type 2, seasonal allergies Hyperlipidemia, anxiety
Vorgeschichte: See Item 11
Andere Medikamente: ASA 81mg daily, Buspar, coreg, cozaar, eye itch relief, flonase, ibuprophen, jardiance, MVI, prilosec, pravachol, tylenol, xanax, zyrtec,
Allergien: crestor, hydrocodone, lipitor, PCN, vicodin, zetia, welchol
Vorherige Impfungen: -

VAERS 2673534

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: FL
Alter: 68,0
Geschlecht: F
Eingang: 18.08.2023
Impfdatum: 07.12.2021
Beginn: 01.07.2023
Tage bis Beginn: 571,0
Dosis: 1
Route/Site: IM / -

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

COVID-19 Nausea SARS-CoV-2 test positive Vomiting

Symptomtext

7/1/2023 - 7/3/2023 (2 days) presented to the emergency room complaining of nausea and vomiting for the last 2 days after being tested positive for COVID-19 treated with supportive care 038K20A 2/3/2021 031M20A 3/3/2021 045J21A 12/7/2021

Weitere VAERSDATA-Felder

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

VAERS 2616462

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: -
Alter: 69,0
Geschlecht: F
Eingang: 18.04.2023
Impfdatum: 01.02.2021
Beginn: 02.02.2021
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: OT / -

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

Arthralgia Chills Erythema Fatigue Headache Myalgia Nausea Pruritus Pyrexia Swelling Vaccination site pain Vaccination site swelling

Symptomtext

Swelling; Redness; itching; Pain at the injection site; moderate headache; mild nausea; Mild Joint pain; Low grade Fever; Chills; Mild muscle body aches; Fatigue; Pain at the injection site; Swelling at the injection site; Headache; Joint pain; Nausea; This spontaneous case was reported by a patient and describes the occurrence of SWELLING (Swelling), ERYTHEMA (Redness), PRURITUS (itching), the second episode of VACCINATION SITE PAIN (Pain at the injection site) and HEADACHE (moderate headache) in a 69-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 031M20A and 038K20A) for COVID-19 prophylaxis. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 01-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 01-Mar-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 14-Aug-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 received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 02-Feb-2021, the patient experienced the first episode of VACCINATION SITE PAIN (Pain at the injection site), VACCINATION SITE SWELLING (Swelling at the injection site), HEADACHE (Headache), ARTHRALGIA (Joint pain) and NAUSEA (Nausea). On 02-Mar-2021, the patient experienced SWELLING (Swelling), ERYTHEMA (Redness), PRURITUS (itching), the second episode of VACCINATION SITE PAIN (Pain at the injection site), HEADACHE (moderate headache), NAUSEA (mild nausea), ARTHRALGIA (Mild Joint pain), PYREXIA (Low grade Fever), CHILLS (Chills), MYALGIA (Mild muscle body aches) and FATIGUE (Fatigue). At the time of the report, SWELLING (Swelling), the last episode of VACCINATION SITE PAIN (Pain at the injection site), HEADACHE (moderate headache), NAUSEA (mild nausea) and ARTHRALGIA (Mild Joint pain) outcome was unknown and ERYTHEMA (Redness), PRURITUS (itching), VACCINATION SITE SWELLING (Swelling at the injection site), HEADACHE (Headache), ARTHRALGIA (Joint pain), NAUSEA (Nausea), PYREXIA (Low grade Fever), CHILLS (Chills), MYALGIA (Mild muscle body aches) and FATIGUE (Fatigue) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medications were reported. Patient reported no adverse events after 1st and 2nd Moderna monovalent booster dose. No treatment information was provided.

Weitere VAERSDATA-Felder

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

VAERS 2603313

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: MI
Alter: 89,0
Geschlecht: F
Eingang: 24.03.2023
Impfdatum: 07.12.2021
Beginn: 20.03.2023
Tage bis Beginn: 468,0
Dosis: 1
Route/Site: UN / UN

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

COVID-19 Discomfort Fall Gait disturbance Glomerular filtration rate decreased Head injury Hip fracture Pain SARS-CoV-2 test positive X-ray of pelvis and hip abnormal

Symptomtext

Discharge Summary "Hospital Course: No notes on file Pt is a 90 YO female that presented to the ED with c/o ground level fall. Patient reports after dinner tonight she got in the closet to get some popcorn stumbled back and fell. She landed on her left side and pumped her head. She states she will not call it a hit of her head. She denies dizziness prior to fall. She reports being alert through the whole event. She denies any headache. States pain in much controlled since being here. She denies loosing consciousness. In the ED, VSS. Labs reviewed and notes EGFR 54. XR notes left hip fracture (HPI per NP) Patient is a 90yr old female with a history of HTN, CAD s/p stents, HLD, CKD, Carotid stenosis s/p bilateral stents who presented following a GLF. She apparently stumbled on her way to the closet to get some popcorn, falling on left side sustaining left hip fracture. Today she is seen laying in bed, uncomfortable due to pain. "

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: 3,0
Labordaten: Positive COVID PCR on 3/20/23
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2507154

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: IL
Alter: 48,0
Geschlecht: F
Eingang: 14.11.2022
Impfdatum: 25.02.2021
Beginn: 05.03.2022
Tage bis Beginn: 373,0
Dosis: 2
Route/Site: IM / LA

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

Facial pain Headache Trigeminal neuralgia

Symptomtext

Diagnosis of Trigeminal Nueralgia- Pain in my face and head on the left side.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial pain
Hospital-Tage: -
Labordaten: MRI
Aktuelle Erkrankungen: None
Vorgeschichte: -
Andere Medikamente: -
Allergien: The cold- I get hives when the temperature drops too fast and is rainy or wet.
Vorherige Impfungen: -

VAERS 2495065

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: IL
Alter: 74,0
Geschlecht: F
Eingang: 01.11.2022
Impfdatum: 27.04.2022
Beginn: 11.08.2022
Tage bis Beginn: 106,0
Dosis: 2
Route/Site: IM / LA

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

Arthralgia COVID-19 Chills Headache Myalgia Nasal congestion Oropharyngeal pain SARS-CoV-2 test positive

Symptomtext

Started on Aug. 11 at 3:00a.m. Woke up with plugged up head and terrible headache. Took a home Covid test and tested positive for Covid. Called pulmonologist that morning and he wanted me on Paxlovid. I called my doctor and she called in a prescription for Paxlovid. Started it on the 12th of August. I did a home rest every other day and they were positive until Aug. 16 when it was negative. I tested negative every other day for 8 days. My symptoms were an extremely congested head and a headache. I also had chills but no fever. Sore muscles and joints and a sore throat. I never did get a cough. Was able to work in yard and do the usual things I have to do. Rested as much as possible.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: Just did home tests and took Paxlovid.
Aktuelle Erkrankungen: None
Vorgeschichte: COPD
Andere Medikamente: Calcium, Vit.D, daily multivitamin, probiotic, Anoro Ellipta inhaler
Allergien: Hydrocodone
Vorherige Impfungen: -

VAERS 2429750

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: FL
Alter: 90,0
Geschlecht: M
Eingang: 06.09.2022
Impfdatum: 04.03.2021
Beginn: 19.08.2022
Tage bis Beginn: 533,0
Dosis: 1
Route/Site: IM / LA

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

Asthenia COVID-19 Cellulitis Confusional state Diarrhoea SARS-CoV-2 test positive

Symptomtext

Hospitalization: admitted 8/19/22, discharged 8/21/22. Presentation to the ED: Presented with generalized weakness, increased confusion, diarrhea. COVID-19 + date: 8/19/22. Treatment: Receiving doxycycline for right lower extremity cellulitis. Did not receive remdesivir therapy or steroid therapy. Discharge to: Home or Self Care.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Hyperlipidemia, hypertension, neuropathy, stented coronary artery, anemia.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2427660

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: MI
Alter: 78,0
Geschlecht: M
Eingang: 02.09.2022
Impfdatum: 22.12.2021
Beginn: 16.08.2022
Tage bis Beginn: 237,0
Dosis: 1
Route/Site: - / -

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

Angiogram normal Blood pressure systolic decreased COVID-19 Computerised tomogram head normal Computerised tomogram spine Dizziness Fall Headache Osteoarthritis SARS-CoV-2 test positive Stenosis Vomiting

Symptomtext

Patient up to date with COVID vaccinations who admitted to hospital with potential complications from COVID. Provider d/c note: "Patient with past medical history of Meniere's disease presented to the emergency department with complaint of ground level fall secondary to dizziness and emesis. Patient stated that he was standing in the restroom when he got dizzy. He states that he grabbed his grab bar to support himself and managed to pull it off the wall while falling. Patient denies hitting his head. Patient was incidentally found to have COVID-19. CT cervical spine without contrast shows lower cervical DJD without fracture or acute malalignment, CT head without contrast shows no acute intracranial abnormality. Upon admission patient's symptom of dizziness and headache had resolved, and he was eager to go home. Patient was kept overnight for presyncopal workup. CTA head and neck added and showed no large vessel occlusions. There were multiple mild to moderate intracranial stenoses with no definite flow limitation and minimal carotid plaque present. Orthostatic blood pressures were positive with a 33 mm mercury drop in systolic blood pressure from sitting to standing. Decreased patient's Hyzaar by half and discussed changing positions slowly to prevent future syncopal episodes. Patient discharged with PCP follow-up on 08/25/22. Ten-day prescription of meclizine provided for patient's Meniere's. "

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: 3,0
Labordaten: COVID detected PCR on 08/16/22
Aktuelle Erkrankungen: -
Vorgeschichte: CKD Stage 3 DM 2 HTN Rheumatoid arthritis A-fib
Andere Medikamente: -
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2400501

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: MI
Alter: 69,0
Geschlecht: M
Eingang: 03.08.2022
Impfdatum: 01.05.2022
Beginn: 27.07.2022
Tage bis Beginn: 87,0
Dosis: 1
Route/Site: SYR / AR

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

COVID-19 Fatigue Influenza Laboratory test Liver function test normal Nasopharyngitis Pain Renal function test normal Respiratory tract congestion Rhinorrhoea Vaccine breakthrough infection

Symptomtext

N OTE: On the date above, I recived the first in the series of vaccinations. I received the second on 01/MAR/2021, and Boosters on 17NOV 21 and on 01MAY22. The adverse event is a breakthrough case of COVID-19. Day Zero on 27JUL 22. On 30JUL22, I started a course of treatment with PAXLOVID. the first day or two of infection caused symptoms consistent with a bad cold or flu, aches, extreme fatigue, runny nose, and chest congestion. Those have been improving with each passing day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Labs, CHEM 6 prior to Rx of PAXLOVID - Renal and hepatic functions all OK.
Aktuelle Erkrankungen: -
Vorgeschichte: Asthma, CAD, BPH, RBBB, GERD
Andere Medikamente: fluticasone- Umeclidinium vilanterol ?Trelegy? inhaler ? asthma control - daily montelukast ?Singular? 10 mg ? asthma control ?daily rampril ?Altace? ? 2.5mg - ACE inhibitor BP control ? daily metoprolol ?Toprol-XL? 25mg ? Beta Blocker BP
Allergien: NKA
Vorherige Impfungen: -

VAERS 2399136

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: MI
Alter: 54,0
Geschlecht: M
Eingang: 02.08.2022
Impfdatum: 28.01.2021
Beginn: 01.08.2022
Tage bis Beginn: 550,0
Dosis: 2
Route/Site: - / -

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

Gangrene Osteomyelitis Pyrexia Respiratory tract congestion SARS-CoV-2 test

Symptomtext

Pt was admitted to the hospital on 7/27 for gangrene of the toe of the right foot (with osteomyelitis). He was tested for COVID on 8/1 after having a fever and congestion the day prior.

Weitere VAERSDATA-Felder

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

VAERS 2386910

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: FL
Alter: 76,0
Geschlecht: F
Eingang: 23.07.2022
Impfdatum: 29.01.2021
Beginn: 22.05.2022
Tage bis Beginn: 478,0
Dosis: 3
Route/Site: OT / LA

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

Asthenia Dysstasia Fall Immunisation reaction Malaise Muscular weakness

Symptomtext

still did not feel good; legs were weak/arms were weak/still with some weakness on her legs; a terrible reaction after getting the 2nd booster dose of the Moderna; whole body was weak/was very weak/still weak but can walk around with walker; She fell 3x that day; could barely stand up; This spontaneous case was reported by a patient and describes the occurrence of MALAISE (still did not feel good), MUSCULAR WEAKNESS (legs were weak/arms were weak/still with some weakness on her legs), IMMUNISATION REACTION (a terrible reaction after getting the 2nd booster dose of the Moderna), ASTHENIA (whole body was weak/was very weak/still weak but can walk around with walker) and FALL (She fell 3x that day) in a 76-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 038K20A, 031M20A and 034F21A) for COVID-19 prophylaxis. The occurrence of additional non-serious events is detailed below. Previously administered products included for Product used for unknown indication: flu vaccine in 2021. Past adverse reactions to the above products included No adverse event with flu vaccine. Concurrent medical conditions included Allergic reaction to drug, Drug allergy (reactions to a lot of meds), Hypertension (both present prior to getting the vaccine) and Anxiety (both present prior to getting the vaccine). Concomitant products included METOPROLOL and ALPRAZOLAM (XANAX) for an unknown indication. On 29-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 26-Feb-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 09-Nov-2021, received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 21-May-2022, received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 22-May-2022, the patient experienced MUSCULAR WEAKNESS (legs were weak/arms were weak/still with some weakness on her legs), IMMUNISATION REACTION (a terrible reaction after getting the 2nd booster dose of the Moderna), ASTHENIA (whole body was weak/was very weak/still weak but can walk around with walker), FALL (She fell 3x that day) and DYSSTASIA (could barely stand up). On 24-May-2022, the patient experienced MALAISE (still did not feel good). The patient was treated with OXYGEN at an unspecified dose and frequency. At the time of the report, MALAISE (still did not feel good) had not resolved and MUSCULAR WEAKNESS (legs were weak/arms were weak/still with some weakness on her legs), IMMUNISATION REACTION (a terrible reaction after getting the 2nd booster dose of the Moderna), ASTHENIA (whole body was weak/was very weak/still weak but can walk around with walker), FALL (She fell 3x that day) and DYSSTASIA (could barely stand up) was resolving. Patient did not diagnose with or tested positive for Covid-19. Patient calls in to report a terrible reaction after getting the 2nd booster dose of the Moderna Covid-19 vaccine. She states that in the morning after she got the 2nd booster dose (22-May-2022), her whole body, legs and arms were weak and she could barely stand up. She fell thrice that day because she was very weak. On her 3rd fall, she called the paramedics and she was brought to the emergency room (ER) early in the morning of 23-May-2022. She was put on oxygen and was given IV fluids with antibiotics and antihistamines. She stayed in the ER for about 5 hours and was sent home. She was still weak, can walk around but with a walker. The paramedics and the doctors who attended to her in the ER thought that her condition was from the booster.On 24-May-2022, she went to an urgent care because she still did not feel good. On 06-Jun-2022, she consulted her primary care physician and was told that she worked through her reaction to the vaccine. The AE cause patient to seek medical care (ER) the patient did not experience a similar event in the past. The patient symptoms improved. Lot number for the second booster dose was 042(?)21A

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Allergic reaction to drug; Anxiety (both present prior to getting the vaccine); Drug allergy (reactions to a lot of meds); Hypertension (both present prior to getting the vaccine)
Vorgeschichte: -
Andere Medikamente: METOPROLOL; XANAX
Allergien: -
Vorherige Impfungen: -

VAERS 2306281

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: CO
Alter: 80,0
Geschlecht: F
Eingang: 02.06.2022
Impfdatum: 05.02.2021
Beginn: 20.05.2022
Tage bis Beginn: 469,0
Dosis: 1
Route/Site: OT / LA

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

Blister Rash pruritic

Symptomtext

Developed a few blisters on legs; developed an itchy rash on right side of back--from waist to shoulder blade running diagonally toward spine; This spontaneous case was reported by a consumer and describes the occurrence of BLISTER (Developed a few blisters on legs) and RASH PRURITIC (developed an itchy rash on right side of back--from waist to shoulder blade running diagonally toward spine) in an 80-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 001M21A, 003F21A, 010M20A and 038K20A) for COVID-19 vaccination. Co-suspect product included non-company product NIRMATRELVIR, RITONAVIR (PAXLOVID) for COVID-19 treatment. Patient did not have any drug allergy. Concomitant products included SIMVASTATIN from January 2019 to 19-May-2022 for an unknown indication. On 05-Feb-2021 at 11:00 AM, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 05-Mar-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 08-Nov-2021, received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 08-Apr-2022 at 12:00 PM, received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 19-May-2022, the patient started NIRMATRELVIR, RITONAVIR (PAXLOVID) (unknown route) at an unspecified dose. On 20-May-2022, the patient experienced BLISTER (Developed a few blisters on legs) and RASH PRURITIC (developed an itchy rash on right side of back--from waist to shoulder blade running diagonally toward spine). At the time of the report, BLISTER (Developed a few blisters on legs) and RASH PRURITIC (developed an itchy rash on right side of back--from waist to shoulder blade running diagonally toward spine) was resolving. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. It was reported that patient was in generally good health. Patient was not taking any other medications/products within 2 weeks of starting COVID-19 treatment. Reportedly, Events appeared on the first or second day of taking Paxlovid. They remains, though is not itchy, 12 days after starting Paxlovid and seven days after finishing it. Treatment details was not reported by the reporter. Pfizer have permission to contact them and also have permission to contact the patient's healthcare provider about this report . The device date was reported as 30-May-2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash pruritic
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: Patient did not have any drug allergy.
Andere Medikamente: SIMVASTATIN; PAXLOVID
Allergien: -
Vorherige Impfungen: -

VAERS 2286510

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: FL
Alter: 82,0
Geschlecht: F
Eingang: 20.05.2022
Impfdatum: 30.01.2021
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: OT / RA

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

Fatigue Vaccination site pain

Symptomtext

tiredness; sore arm when she touched the injection site; This spontaneous case was reported by a patient and describes the occurrence of FATIGUE (tiredness) and VACCINATION SITE PAIN (sore arm when she touched the injection site) in an 82-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. No Medical History information was reported. On 30-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On an unknown date, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced FATIGUE (tiredness) and VACCINATION SITE PAIN (sore arm when she touched the injection site). At the time of the report, FATIGUE (tiredness) and VACCINATION SITE PAIN (sore arm when she touched the injection site) outcome was unknown. No concomitant medication was reported. No treatment medication was reported.

Weitere VAERSDATA-Felder

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

VAERS 2286508

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: FL
Alter: 82,0
Geschlecht: F
Eingang: 20.05.2022
Impfdatum: 30.01.2021
Beginn: 30.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / RA

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

Fatigue Vaccination site pain

Symptomtext

sore right injection site arm; she was tired; This spontaneous case was reported by a patient and describes the occurrence of VACCINATION SITE PAIN (sore right injection site arm) and FATIGUE (she was tired) in an 82-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. No Medical History information was reported. On 30-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 30-Jan-2021, the patient experienced VACCINATION SITE PAIN (sore right injection site arm) and FATIGUE (she was tired). At the time of the report, VACCINATION SITE PAIN (sore right injection site arm) and FATIGUE (she was tired) outcome was unknown. mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) dosing remained unchanged. No concomitant medications was reported. No treatment drug details was reported. This case was linked to MOD-2022-569659, MOD-2022-569293 (Patient Link).

Weitere VAERSDATA-Felder

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

VAERS 2247830

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: MI
Alter: 74,0
Geschlecht: M
Eingang: 22.04.2022
Impfdatum: 08.02.2021
Beginn: 19.04.2022
Tage bis Beginn: 435,0
Dosis: 1
Route/Site: - / -

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

Arthralgia COVID-19 Renal transplant SARS-CoV-2 test positive Transplant rejection

Symptomtext

Pt had a renal transplant in January 2022. Pt has had ongoing issues with rejection and other medication adjustments. Pt arrived to ER due to arthralgias, but denies any other COVID symptoms. Pt was COVID-19 positive.

Weitere VAERSDATA-Felder

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

VAERS 2237371

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: MI
Alter: 69,0
Geschlecht: M
Eingang: 16.04.2022
Impfdatum: 05.02.2021
Beginn: 31.03.2022
Tage bis Beginn: 419,0
Dosis: 1
Route/Site: OT / -

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

Fatigue Heart rate Heart rate increased Pyrexia

Symptomtext

pulse raised to 100; fever; fatigue; This spontaneous case was reported by a consumer and describes the occurrence of HEART RATE INCREASED (pulse raised to 100), PYREXIA (fever) and FATIGUE (fatigue) in a 70-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 026L21B, 026D21A, 030A21A and 038K20A) for COVID-19 vaccination. Patient never had COVID-19 positive diagnosis or test and no allergy including medications, food and other products. It was reported patient was concerned because he had an open heart surgery. Previously administered products included for Product used for unknown indication: Flu shot (Flu shot 1 month ago). Past adverse reactions to the above products included No adverse event with Flu shot. Concurrent medical conditions included Type 2 diabetes mellitus (Since 4 years ago and no recent change in status such as improvement or worsening), Blood pressure high (Since 30 years ago and no recent change in status such as improvement or worsening) and Heart disease, unspecified (Since 30 years ago and no recent change in status such as improvement or worsening). Concomitant products included METFORMIN and DAPAGLIFLOZIN PROPANEDIOL MONOHYDRATE (FARXIGA) for Diabetes, HYDROCHLOROTHIAZIDE for Diuretic therapy. On 05-Feb-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) (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 31-Mar-2022, received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 31-Mar-2022, the patient experienced HEART RATE INCREASED (pulse raised to 100), PYREXIA (fever) and FATIGUE (fatigue). On 05-Apr-2022, PYREXIA (fever) and FATIGUE (fatigue) had resolved. At the time of the report, HEART RATE INCREASED (pulse raised to 100) had not resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 31-Mar-2022, Heart rate: 100 (High) Pulse raised to 100 for 4 days. Normal pulse of the patient was between 60 and 65. Other relevant concomitant medication included Beta blockers. Patient took 1st booster shot on 26Oct2021, and 2nd booster dose on 31Mar2022. After 2nd booster dose, pulse raised also to 100 for 4 days, and currently then coming down and improving, but still not in the normal range and patient did not experience a similar event in the past and the adverse event did not cause him to seek medical care including office visit, Urgent care, ER and hospitalized. No treatment given for his symptoms. This case was linked to MOD-2022-535597, MOD-2022-535621, MOD-2022-535624 (Patient Link).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Test Date: 20220331; Test Name: Pulse rate; Result Unstructured Data: Pulse raised to 100 for 4 days
Aktuelle Erkrankungen: Blood pressure high (Since 30 years ago and no recent change in status such as improvement or worsening); Heart disease, unspecified (Since 30 years ago and no recent change in status such as improvement or worsening); Type 2 diabetes mellitus (Since 4 years ago and no recent change in status such as improvement or worsening)
Vorgeschichte: Comments: Patient never had COVID-19 positive diagnosis or test and no allergy including medications, food and other products. It was reported patient was concerned because he had an open heart surgery.
Andere Medikamente: METFORMIN; FARXIGA; HYDROCHLOROTHIAZIDE
Allergien: -
Vorherige Impfungen: -

VAERS 2237368

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: MI
Alter: 70,0
Geschlecht: M
Eingang: 16.04.2022
Impfdatum: 05.02.2021
Beginn: 05.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / -

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

Fatigue Heart rate Pyrexia

Symptomtext

fever; fatigue; This spontaneous case was reported by a consumer and describes the occurrence of PYREXIA (fever) and FATIGUE (fatigue) in a 70-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. Patient never had COVID-19 positive diagnosis or test and no allergy including medications, food and other products. The patient's past medical history included Heart disease, unspecified (Started since 30 years ago and no recent change in status such as improvement or worsening.) and Open heart surgery. Previously administered products included for Product used for unknown indication: Flu shot (Flu shot were given one month ago.). Past adverse reactions to the above products included No adverse event with Flu shot. Concurrent medical conditions included Type 2 diabetes mellitus (Started since 4 years ago and no recent change in status such as improvement or worsening.) and Blood pressure high (Started since 30 years ago and no recent change in status such as improvement or worsening.). Concomitant products included METFORMIN and DAPAGLIFLOZIN PROPANEDIOL MONOHYDRATE (FARXIGA) for Diabetes, HYDROCHLOROTHIAZIDE for Diuretic effect. On 05-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 05-Feb-2021, the patient experienced PYREXIA (fever) and FATIGUE (fatigue). On 07-Feb-2021, PYREXIA (fever) and FATIGUE (fatigue) had resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 05-Feb-2021, Heart rate: 90 and 100 (High) After 1 dose pulse raised between 90 and 100 for 3 days.. mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosing remained unchanged. It was reported that patient did not experienced a similar event in the past and this adverse event didnt cause patient to seek medical care including office visit, Urgent care, ER and hospitalized. Other concomitant medicine: Beta Blockers for an unknown indication. No treatment information were provided by the reporter. This case was linked to MOD-2022-535621, MOD-2022-535624, MOD-2022-535625 (Patient Link).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Test Date: 20210205; Test Name: Pulse rate; Result Unstructured Data: After 1 dose pulse raised between 90 and 100 for 3 days.
Aktuelle Erkrankungen: Blood pressure high (Started since 30 years ago and no recent change in status such as improvement or worsening.); Type 2 diabetes mellitus (Started since 4 years ago and no recent change in status such as improvement or worsening.)
Vorgeschichte: Medical History/Concurrent Conditions: Heart disease, unspecified (Started since 30 years ago and no recent change in status such as improvement or worsening.); Open heart surgery; Comments: Patient never had COVID-19 positive diagnosis or test and no allergy including medications, food and other products.
Andere Medikamente: METFORMIN; FARXIGA; HYDROCHLOROTHIAZIDE
Allergien: -
Vorherige Impfungen: -

VAERS 2222592

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: FL
Alter: 76,0
Geschlecht: F
Eingang: 08.04.2022
Impfdatum: 02.02.2021
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: OT / LA

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

Fatigue SARS-CoV-2 test Feeling abnormal Nausea

Symptomtext

Third shot make me nausea; This spontaneous case was reported by a consumer and describes the occurrence of NAUSEA (Third shot make me nausea) in a 76-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 052E21A, 038K20A and 031M20A) for COVID-19 vaccination. The patient did not have any allergies, did not tested positive for COVID-19 and did not received any other vaccine within 1 month prior to Moderna's. The patient's past medical history included Stent placement (3 Heart Stents). Concurrent medical conditions included Emphysema (Lung Emphysema, prior vaccination), Cholesterosis and Lung disorder NOS. Concomitant products included ATORVASTATIN for Cholesterosis, THEOPHYLLINE for Lung disorder NOS, METOPROLOL, DILTIAZEM, TIOTROPIUM BROMIDE MONOHYDRATE (SPIRIVA) and FLUTICASONE PROPIONATE, SALMETEROL XINAFOATE (ADVAIR) for an unknown indication. On 02-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 02-Mar-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 17-Aug-2021, received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On an unknown date, the patient experienced NAUSEA (Third shot make me nausea). At the time of the report, NAUSEA (Third shot make me nausea) outcome was unknown. Patient stated that she did not register any change on her illness status post vaccination, did not seek for medical care post vaccination and did not experienced a similar event in the past. No treatment was taken by the patient. This case was linked to MOD-2022-533310, MOD-2022-533316, MOD-2022-533304 (Patient Link).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Cholesterosis; Emphysema (Lung Emphysema, prior vaccination); Lung disorder NOS
Vorgeschichte: Medical History/Concurrent Conditions: Stent placement (3 Heart Stents); Comments: The patient did not have any allergies, did not tested positive for COVID-19 and did not received any other vaccine within 1 month prior to Moderna's.
Andere Medikamente: METOPROLOL; DILTIAZEM; ATORVASTATIN; THEOPHYLLINE; SPIRIVA; ADVAIR
Allergien: -
Vorherige Impfungen: -

VAERS 2222592

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: FL
Alter: 76,0
Geschlecht: F
Eingang: 08.04.2022
Impfdatum: 02.02.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: OT / LA

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

Fatigue SARS-CoV-2 test Feeling abnormal Nausea

Symptomtext

Third shot make me nausea; This spontaneous case was reported by a consumer and describes the occurrence of NAUSEA (Third shot make me nausea) in a 76-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 052E21A, 038K20A and 031M20A) for COVID-19 vaccination. The patient did not have any allergies, did not tested positive for COVID-19 and did not received any other vaccine within 1 month prior to Moderna's. The patient's past medical history included Stent placement (3 Heart Stents). Concurrent medical conditions included Emphysema (Lung Emphysema, prior vaccination), Cholesterosis and Lung disorder NOS. Concomitant products included ATORVASTATIN for Cholesterosis, THEOPHYLLINE for Lung disorder NOS, METOPROLOL, DILTIAZEM, TIOTROPIUM BROMIDE MONOHYDRATE (SPIRIVA) and FLUTICASONE PROPIONATE, SALMETEROL XINAFOATE (ADVAIR) for an unknown indication. On 02-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 02-Mar-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 17-Aug-2021, received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On an unknown date, the patient experienced NAUSEA (Third shot make me nausea). At the time of the report, NAUSEA (Third shot make me nausea) outcome was unknown. Patient stated that she did not register any change on her illness status post vaccination, did not seek for medical care post vaccination and did not experienced a similar event in the past. No treatment was taken by the patient. This case was linked to MOD-2022-533310, MOD-2022-533316, MOD-2022-533304 (Patient Link).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Cholesterosis; Emphysema (Lung Emphysema, prior vaccination); Lung disorder NOS
Vorgeschichte: Medical History/Concurrent Conditions: Stent placement (3 Heart Stents); Comments: The patient did not have any allergies, did not tested positive for COVID-19 and did not received any other vaccine within 1 month prior to Moderna's.
Andere Medikamente: METOPROLOL; DILTIAZEM; ATORVASTATIN; THEOPHYLLINE; SPIRIVA; ADVAIR
Allergien: -
Vorherige Impfungen: -

VAERS 2219787

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: -
Alter: 89,0
Geschlecht: F
Eingang: 07.04.2022
Impfdatum: 29.01.2021
Beginn: 04.04.2022
Tage bis Beginn: 430,0
Dosis: 1
Route/Site: OT / LA

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

Chills Headache Nausea Pain in extremity

Symptomtext

Nauseated; Experienced chills; 24 hours later sore left arm; Headache; This spontaneous case was reported by a consumer and describes the occurrence of NAUSEA (Nauseated), CHILLS (Experienced chills), PAIN IN EXTREMITY (24 hours later sore left arm) and HEADACHE (Headache) in an 89-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 012F21A and 038K20A) for COVID-19 vaccination. Previously administered products included for Product used for unknown indication: Flu Vaccine in 2021. Past adverse reactions to the above products included No adverse event with Flu Vaccine. Concurrent medical conditions included Seafood allergy and Seafood allergy. Concomitant products included VITAMIN D NOS for an unknown indication. On 29-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .5 milliliter. On 26-Feb-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to .5 milliliter. On 05-Nov-2021, received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to .25 milliliter. On 03-Apr-2022, received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to .25 milliliter. On 04-Apr-2022, the patient experienced NAUSEA (Nauseated), CHILLS (Experienced chills), PAIN IN EXTREMITY (24 hours later sore left arm) and HEADACHE (Headache). On 05-Apr-2022, CHILLS (Experienced chills), PAIN IN EXTREMITY (24 hours later sore left arm) and HEADACHE (Headache) had resolved. At the time of the report, NAUSEA (Nauseated) had resolved. No Treatment information was provided. Other medications: Preservision Vitamins, Low dose blood pressure medication- For use as a Prevention This case was linked to MOD-2022-533478 (Patient Link). Reporter did not allow further contact

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Seafood allergy
Vorgeschichte: -
Andere Medikamente: VITAMIN D NOS
Allergien: -
Vorherige Impfungen: -

VAERS 2219783

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: -
Alter: 88,0
Geschlecht: F
Eingang: 07.04.2022
Impfdatum: 29.01.2021
Beginn: 29.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / LA

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

Vaccination site pain

Symptomtext

slightly sore left arm (1st dose); This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION SITE PAIN (slightly sore left arm (1st dose)) in an 88-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. Patient had never tested positive for COVID. Previously administered products included for Product used for unknown indication: seasonal flu vaccine (Sometime in 2021) in 2021. Past adverse reactions to the above products included No adverse event with seasonal flu vaccine. Concurrent medical conditions included Seafood allergy (Shrimp) and Seafood allergy (Lobster). Concomitant products included ASCORBIC ACID, BETACAROTENE, CUPRIC OXIDE, TOCOPHERYL ACETATE, ZINC OXIDE (PRESERVISION) and VITAMIN D [VITAMIN D NOS] for an unknown indication. On 29-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .5 milliliter. On 29-Jan-2021, the patient experienced VACCINATION SITE PAIN (slightly sore left arm (1st dose)). At the time of the report, VACCINATION SITE PAIN (slightly sore left arm (1st dose)) had resolved. mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosing remained unchanged. Concomitant medications included unknown low blood pressure medication used as preventative. No treatment information was provided. This case was linked to MOD-2022-533478, MOD-2022-533479 (Patient Link). Reporter did not allow further contact

Weitere VAERSDATA-Felder

Praegender Schweregrund: Vaccination site pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Seafood allergy (Shrimp); Seafood allergy (Lobster)
Vorgeschichte: Comments: Patient had never tested positive for COVID.
Andere Medikamente: PRESERVISION; VITAMIN D [VITAMIN D NOS]
Allergien: -
Vorherige Impfungen: -

VAERS 2215565

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: FL
Alter: 77,0
Geschlecht: F
Eingang: 05.04.2022
Impfdatum: 29.01.2021
Beginn: 01.03.2022
Tage bis Beginn: 396,0
Dosis: 1
Route/Site: OT / -

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

Cold sweat Decreased appetite Fatigue Loss of personal independence in daily activities Nausea Pain in extremity Vertigo

Symptomtext

This spontaneous case was reported by a consumer and describes the occurrence of VERTIGO (on very short period of time I've had feeling of vertigo/it wasn't long when turning head felt vertigo/ this morning seems to be worst never had vertigo before at 5:30 turn in bed, room was spinning), COLD SWEAT (cold sweat), DECREASED APPETITE (just had lack of appetite), LOSS OF PERSONAL INDEPENDENCE IN DAILY ACTIVITIES (patient needed help from husband to walk to the bathroom) and PAIN IN EXTREMITY (sore arm) in a 77-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 066K21A, 049E21A, 031M20A and 038K20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included Surgery (underwent Surgery for breast cancer) in February 2006. Concurrent medical conditions included Breast cancer since 2005 and Emphysema. Concomitant products included LANSOPRAZOLE, THEOPHYLLINE, PRAVASTATIN and FLUTICASONE FUROATE, UMECLIDINIUM BROMIDE, VILANTEROL TRIFENATATE (TRELEGY) for an unknown indication. On 29-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 26-Feb-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 21-Aug-2021, received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 26-Mar-2022, received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. In March 2022, the patient experienced COLD SWEAT (cold sweat), DECREASED APPETITE (just had lack of appetite), LOSS OF PERSONAL INDEPENDENCE IN DAILY ACTIVITIES (patient needed help from husband to walk to the bathroom) and NAUSEA (some nausea). March 2022, the patient experienced PAIN IN EXTREMITY (sore arm) and FATIGUE (fatigue). On 27-Mar-2022, the patient experienced VERTIGO (on very short period of time I've had feeling of vertigo/it wasn't long when turning head felt vertigo/ this morning seems to be worst never had vertigo before at 5:30 turn in bed, room was spinning). At the time of the report, VERTIGO (on very short period of time I've had feeling of vertigo/it wasn't long when turning head felt vertigo/ this morning seems to be worst never had vertigo before at 5:30 turn in bed, room was spinning) had not resolved and COLD SWEAT (cold sweat), DECREASED APPETITE (just had lack of appetite), LOSS OF PERSONAL INDEPENDENCE IN DAILY ACTIVITIES (patient needed help from husband to walk to the bathroom), PAIN IN EXTREMITY (sore arm), FATIGUE (fatigue) and NAUSEA (some nausea) outcome was unknown. It was reported that the patient did not have any allergies to medication, food and other products. The patient had never been diagnosed with/ tested positive for COVID-19. Patient stayed in bed till about 2 o?clock and didn't have any other symptom at 3 o clock I was able to get out of bed and have a normal day. Patient needed help from husband to walk to the bathroom after that went back to bed and experience the same vertigo feeling, patient mention that this vertigo experiences are for a short period of time but seems to be worsened. Patient had nothing, no side effect, no previous health condition, or medications, never had been an issue, never had reaction before. No treatment medication was reported by the reporter. This case was linked to MOD-2022-528604, MOD-2022-528616, MOD-2022-528619 (Patient Link).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Breast cancer; Emphysema
Vorgeschichte: Medical History/Concurrent Conditions: Surgery (underwent Surgery for breast cancer)
Andere Medikamente: Lansoprazole; Theophylline; Pravastatin; Trelegy
Allergien: -
Vorherige Impfungen: -

VAERS 2213527

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: FL
Alter: 76,0
Geschlecht: F
Eingang: 04.04.2022
Impfdatum: 29.01.2021
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: OT / -

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

Fatigue Pain in extremity

Symptomtext

sore arm; fatigue; This spontaneous case was reported by a consumer and describes the occurrence of PAIN IN EXTREMITY (sore arm) and FATIGUE (fatigue) in a 77-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 031M20A and 038K20A) for COVID-19 vaccination. Concurrent medical conditions included Breast cancer (diagnosed in late 2005 and underwent unspecified surgery in Feb-2006) since 2005 and Emphysema. Concomitant products included LANSOPRAZOLE, THEOPHYLLINE, PRAVASTATIN and FLUTICASONE FUROATE, UMECLIDINIUM BROMIDE, VILANTEROL TRIFENATATE (TRELEGY) for an unknown indication. On 29-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 26-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 (sore arm) and FATIGUE (fatigue). At the time of the report, PAIN IN EXTREMITY (sore arm) and FATIGUE (fatigue) was resolving. Patient's height was 5.3 (160.02 cm). It was reported that the patient had no allergies and COVID-19 in the past. The patient experienced sore arm and fatigue after vaccination, however felt better in 24. Treatment information was not provided. This case was linked to MOD-2022-528604, MOD-2022-528619, MOD-2022-528626 (Patient Link).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Breast cancer (diagnosed in late 2005 and underwent unspecified surgery in Feb-2006); Emphysema
Vorgeschichte: -
Andere Medikamente: LANSOPRAZOLE; THEOPHYLLINE; PRAVASTATIN; TRELEGY
Allergien: -
Vorherige Impfungen: -

VAERS 2213526

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: FL
Alter: 76,0
Geschlecht: F
Eingang: 04.04.2022
Impfdatum: 29.01.2021
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: OT / -

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

Fatigue Pain in extremity

Symptomtext

This spontaneous case was reported by a consumer and describes the occurrence of PAIN IN EXTREMITY (sore arm) and FATIGUE (fatigue) in a 77-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. The patient's past medical history included Surgery in 2006. Concurrent medical conditions included Breast cancer (Breast cancer diagnosed in late 2005) since 2005 and Emphysema. Concomitant products included LANSOPRAZOLE, THEOPHYLLINE, PRAVASTATIN and FLUTICASONE FUROATE, UMECLIDINIUM BROMIDE, VILANTEROL TRIFENATATE (TRELEGY) for an unknown indication. On 29-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced PAIN IN EXTREMITY (sore arm) and FATIGUE (fatigue). At the time of the report, PAIN IN EXTREMITY (sore arm) and FATIGUE (fatigue) outcome was unknown. mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) dosing remained unchanged. Patient height mentioned as 5.3. No treatment information was provided by the reporter. This case was linked to MOD-2022-528616, MOD-2022-528619, MOD-2022-528626 (Patient Link).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Breast cancer (Breast cancer diagnosed in late 2005); Emphysema
Vorgeschichte: Medical History/Concurrent Conditions: Surgery
Andere Medikamente: LANSOPRAZOLE; THEOPHYLLINE; PRAVASTATIN; TRELEGY
Allergien: -
Vorherige Impfungen: -

VAERS 2213459

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: FL
Alter: 77,0
Geschlecht: F
Eingang: 04.04.2022
Impfdatum: 29.01.2021
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: OT / -

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

Fatigue Pain in extremity

Symptomtext

sore arm; fatigue; This spontaneous case was reported by a consumer and describes the occurrence of PAIN IN EXTREMITY (sore arm) and FATIGUE (fatigue) in a 77-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 049E21A, 031M20A and 038K20A) for COVID-19 vaccination. The patient's past medical history included Surgery in February 2006. Concurrent medical conditions included Breast cancer (Breast cancer diagnosed in late 2005) and Emphysema. Concomitant products included LANSOPRAZOLE, THEOPHYLLINE, PRAVASTATIN and FLUTICASONE FUROATE, UMECLIDINIUM BROMIDE, VILANTEROL TRIFENATATE (TRELEGY) for an unknown indication. On 29-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 26-Feb-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 21-Aug-2021, received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On an unknown date, the patient experienced PAIN IN EXTREMITY (sore arm) and FATIGUE (fatigue). At the time of the report, PAIN IN EXTREMITY (sore arm) and FATIGUE (fatigue) had resolved. Patient information: Height 5.3. No treatment medications were reported. This case was linked to MOD-2022-528604, MOD-2022-528616, MOD-2022-528626 (Patient Link).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Breast cancer (Breast cancer diagnosed in late 2005); Emphysema
Vorgeschichte: Medical History/Concurrent Conditions: Surgery
Andere Medikamente: LANSOPRAZOLE; THEOPHYLLINE; PRAVASTATIN; TRELEGY
Allergien: -
Vorherige Impfungen: -

VAERS 2145645

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: DE
Alter: 72,0
Geschlecht: M
Eingang: 26.02.2022
Impfdatum: 27.01.2021
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: OT / -

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

Pain in extremity

Symptomtext

sore arm after first dose; This spontaneous case was reported by a patient family member or friend and describes the occurrence of PAIN IN EXTREMITY (sore arm after first dose) in a 72-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. Concomitant products included ACETYLSALICYLIC ACID (BABY ASPIRIN) for an unknown indication. On 27-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 PAIN IN EXTREMITY (sore arm after first dose). At the time of the report, PAIN IN EXTREMITY (sore arm after first dose) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. No treatment medications were reported. This case was linked to MOD-2021-281266, MOD-2021-128083 (Patient Link).

Weitere VAERSDATA-Felder

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

VAERS 2145110

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: FL
Alter: 61,0
Geschlecht: M
Eingang: 26.02.2022
Impfdatum: 05.03.2021
Beginn: 03.04.2021
Tage bis Beginn: 29,0
Dosis: 1
Route/Site: OT / LA

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

Headache Vertigo

Symptomtext

vertigo; headache; This spontaneous case was reported by a consumer and describes the occurrence of VERTIGO (vertigo) and HEADACHE (headache) in a 61-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 038K20A and 038K20A) for COVID-19 vaccination. No Medical History information was reported. On 05-Mar-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 02-Apr-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 03-Apr-2021, the patient experienced HEADACHE (headache). On an unknown date, the patient experienced VERTIGO (vertigo). The patient was treated with PARACETAMOL (TYLENOL) for Adverse event, at a dose of 1 dosage form and IBUPROFEN (ADVIL [IBUPROFEN]) for Adverse event, at a dose of 1 dosage form. At the time of the report, VERTIGO (vertigo) and HEADACHE (headache) outcome was unknown. Concomitantly the patient was on unspecified medications for blood pressure.

Weitere VAERSDATA-Felder

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

VAERS 2137603

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: -
Alter: 68,0
Geschlecht: M
Eingang: 24.02.2022
Impfdatum: 04.02.2021
Beginn: 21.12.2021
Tage bis Beginn: 320,0
Dosis: UNK
Route/Site: - / -

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

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

Symptomtext

12/21/21 presents to EC ED for "cough and fevers". PMHx of "HLD, OSA, Lung CA s/p resection (2018), and COPD."

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: 12/22/21 SARS-CoV-2 (COVID-19) detected.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2105271

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: PA
Alter: 76,0
Geschlecht: F
Eingang: 11.02.2022
Impfdatum: 01.01.2021
Beginn: 16.06.2021
Tage bis Beginn: 166,0
Dosis: UNK
Route/Site: IM / LA

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

Dermatologic examination Pruritus Urticaria

Symptomtext

Hives after 5 minutes in the sun. Extreme itching, anti itch cream, stay out of the sun or cover up. Sun block doesn't prevent, seems to be getting worse. I have seen allergists and dermatologist .

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: none
Vorgeschichte: hypertension, hypothyroidism, GERD, vertigo
Andere Medikamente: levothyroxine, losartan potassium, atenolol, omeprazole DR, b-12, b complex, Icaps, aspirin
Allergien: amoxicillin
Vorherige Impfungen: -

VAERS 2087684

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: KY
Alter: 29,0
Geschlecht: F
Eingang: 04.02.2022
Impfdatum: 16.08.2021
Beginn: 31.12.2021
Tage bis Beginn: 137,0
Dosis: 2
Route/Site: IM / LA

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

Back pain Blood creatinine increased Blood potassium decreased COVID-19 Chills Cough Exposure to SARS-CoV-2 Fatigue Feeling abnormal Pain SARS-CoV-2 test positive Taste disorder

Symptomtext

Patient is a 30 yof who presented with 1 day of cough and positive COVID-19 test. She states that there was an outbreak at a location she visited and thinks this is where she was exposed. She states she wore her mask the entire time she was at the location. She was feeling in her usual state of health until yesterday when she developed a cough. She was tested for COVID-19 yesterday and the result was positive today. She notes that "stuff tasted bad yesterday" but thought it was due to her usual sinus issues/sinus infection. She also says that she felt "foggy" and very fatigued this morning when she woke up. She denies fevers, saying she never runs a fever even with Strep, but does endorse cold chills. She also complains of feeling "sore" diffusely, especially in her back. She denies shortness of breath, N/V, diarrhea. Patient was on room air and with stable vital signs. She was admitted for observation overnight at request of transplant nephrology and her home mycophenolate and lasix were held. Patient remained stable and on room air. She did have a slight increase in creatinine, possibly due to dehydration vs acute illness. She was counseled to hold her lasix for two days. Her potassium was replete and she received IV fluid. She will be discharged with a pulse oximeter for home monitoring and will follow-up in clinic. Discharge Disposition/Condition Disposition: Home Condition: Stable (s/sx potential problems absent or manageable)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Back pain
Hospital-Tage: 3,0
Labordaten: COVID PCR positive on 12/31/21
Aktuelle Erkrankungen: N/A
Vorgeschichte: She has a past medical history of Chronic kidney disease, unspecified, Chronic kidney disease, unspecified, Conversions - Other, Conversions - Other, Conversions - Other, Encounter for surveillance of contraceptive pills, Excessive and frequent menstruation with irregular cycle, Other specified disorders of nose and nasal sinuses, Other specified disorders of nose and nasal sinuses, Personal history of other diseases of the female genital tract, Personal history of other diseases of the respiratory system, Personal history of other diseases of the respiratory system, Personal history of peptic ulcer disease, Polyp of cervix uteri, Scoliosis, unspecified, and Scoliosis, unspecified.
Andere Medikamente: amitriptylene belatacept biotin bisacodyl calcium carbonate-vitamin D cholecalciferol coenzyme Q10 furosemide
Allergien: Nifedipine Er Rash, Swelling High Allergy 10/21/2019 redness, swelling and rash in bilateral lower extremities from knees to feet redness, swelling and rash in bilateral lower extremities from knees to feet redness, swelling and rash in bilateral lower extremities from knees to feet Sodium Bicarbonate Sodium Bicarbonate Swelling, Other High Allergy 4/14/2020 headache, dizziness and abdominal pain headache, dizziness and abdominal pain Sirolimus Sirolimus Hives, Unknown Medium Allergy 9/19/2011 Deletion Reason: Amoxicillin Amoxicillin Unknown Low Allergy 1/22/2015 Cefaclor Cefaclor Unknown Low Allergy 1/22/2015 Linaclotide Linaclotide Other Low Allergy 12/30/2019 DIARRHEA, BLOATING, MIGRANES Mycophenolate Mycophenolate Rash, Unknown Low Allergy 11/7/2007 Promethazine Promethazine Other, Unknown Low Allergy 7/24/2017 lost ability to speak, caused vision complications Vancomycin Vancomycin Unknown Low Allergy 11/7/2007 Red man syndrome Adverse Reactions/Drug Intolerances Guaifenesin Er Guaifenesin Er Dizziness Low Intolerance 12/11/2019 Rituximab Rituximab Other Low Intolerance 4/30/2021
Vorherige Impfungen: -

VAERS 2037553

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: MI
Alter: 67,0
Geschlecht: F
Eingang: 15.01.2022
Impfdatum: 22.02.2021
Beginn: 22.03.2021
Tage bis Beginn: 28,0
Dosis: 1
Route/Site: OT / LA

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

Electrocardiogram Feeling abnormal Myalgia Vaccination site pain

Symptomtext

felt icky with mild aches for 24; mild aches for 24 hours; Sore left injection site arm; This spontaneous case was reported by a consumer and describes the occurrence of FEELING ABNORMAL (felt icky with mild aches for 24), MYALGIA (mild aches for 24 hours) and VACCINATION SITE PAIN (Sore left injection site arm) in a 67-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 030A21A and 038K20A) for COVID-19 vaccination. The patient's past medical history included Atrial fibrillation and Palpitations (Fluttering heart with the sensation of skipping.). On 22-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 22-Mar-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 22-Mar-2021, the patient experienced FEELING ABNORMAL (felt icky with mild aches for 24), MYALGIA (mild aches for 24 hours) and VACCINATION SITE PAIN (Sore left injection site arm). On 23-Mar-2021, FEELING ABNORMAL (felt icky with mild aches for 24) and MYALGIA (mild aches for 24 hours) had resolved. At the time of the report, VACCINATION SITE PAIN (Sore left injection site arm) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 04-Dec-2021, Electrocardiogram: normal (normal) normal. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant drugs were reported. No treatment information was reported. The patient received the vaccine in her left arm shoulder deltoid muscle. She felt icky with mild aches for 24 hours. Sore left injection site arm. This case was linked to MOD-2022-447985, MOD-2022-447895 (Patient Link).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myalgia
Hospital-Tage: -
Labordaten: Test Date: 20211204; Test Name: Electrocardiogram; Result Unstructured Data: normal
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Atrial fibrillation; Palpitations (Fluttering heart with the sensation of skipping.)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2034816

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: MI
Alter: 67,0
Geschlecht: F
Eingang: 14.01.2022
Impfdatum: 22.02.2021
Beginn: 22.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / LA

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

Feeling abnormal Pain Vaccination site pain

Symptomtext

mild icky feeling; felt achy; injection site left arm was sore; This spontaneous case was reported by a consumer and describes the occurrence of FEELING ABNORMAL (mild icky feeling), PAIN (felt achy) and VACCINATION SITE PAIN (injection site left arm was sore) in a 67-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. The patient's past medical history included Atrial fibrillation and Palpitations. On 22-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 22-Feb-2021, the patient experienced FEELING ABNORMAL (mild icky feeling), PAIN (felt achy) and VACCINATION SITE PAIN (injection site left arm was sore). On 23-Feb-2021, FEELING ABNORMAL (mild icky feeling) and PAIN (felt achy) had resolved. At the time of the report, VACCINATION SITE PAIN (injection site left arm was sore) outcome was unknown. mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) dosing remained unchanged. Treatment medication was not reported. Relevant concomitant medications were not provided by the reporter. This case was linked to MOD-2022-447964, MOD-2022-447985 (Patient Link).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Atrial fibrillation; Palpitations
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2017856

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: -
Alter: 75,0
Geschlecht: M
Eingang: 08.01.2022
Impfdatum: 05.02.2021
Beginn: 04.01.2022
Tage bis Beginn: 333,0
Dosis: 2
Route/Site: OT / -

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

Dizziness Hyperhidrosis

Symptomtext

covered in sweat; dizzy; This spontaneous case was reported by a consumer and describes the occurrence of HYPERHIDROSIS (covered in sweat) and DIZZINESS (dizzy) in a 75-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 041J21A, 038K20A and 030A21A) for COVID-19 vaccination. Concurrent medical conditions included Blood cholesterol abnormal and Blood pressure high. On 05-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 05-Mar-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 03-Jan-2022, received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 04-Jan-2022, the patient experienced HYPERHIDROSIS (covered in sweat) and DIZZINESS (dizzy). At the time of the report, HYPERHIDROSIS (covered in sweat) and DIZZINESS (dizzy) outcome was unknown. The patient's took medicines for cholesterol and high blood pressure. Patient did not take any medication for the symptoms. It was reported that the patient woke up 20 minutes ago covered in sweat and was dizzy.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Blood cholesterol abnormal; Blood pressure high
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2006018

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: IL
Alter: 93,0
Geschlecht: M
Eingang: 05.01.2022
Impfdatum: 27.03.2021
Beginn: 30.12.2021
Tage bis Beginn: 278,0
Dosis: 1
Route/Site: IM / UN

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

Asthenia Atrial fibrillation COVID-19 Chest X-ray normal Chills Electrocardiogram abnormal Pyrexia SARS-CoV-2 test positive Troponin increased Urinary tract infection

Symptomtext

12/30 Patient to ER with fever, weakness recently with UTI and did not complete antibiotics EKG with afib heart in the 70s Tmax 101.5 Elevated troponin Reported chills and fever (1 day prior admission, 12/29) so covid test was obtained patient not requiring supplemental oxygen

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Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: 12/30/2021 troponin 622 12/31/2021 COVID19 PCR positive 12/30/2021 CXR no focal infiltrate, effusion or pneumothorax is seen
Aktuelle Erkrankungen: -
Vorgeschichte: Carotid artery stenosis Chronic diastolic heart failure Chronic kidney disease, stage 3 Coronary artery disease Elevated troponin ESBL Escherichia coli Hypertension Personal history of bladder cancer Personal history of prostate cancer Postprocedural anterior bulbous urethral stricture, male S/P CABG (coronary artery bypass graft) Subclavian artery stenosis Ureteral calculi Ureteral stricture, right Urethral stricture in male
Andere Medikamente: acetaminophen 325 mg oral tablet, 650 mg= 2 TAB, PO, Q4H (Every 4 hours), PRN aspirin, 81 mg, PO, Daily bumetanide 1 mg oral tablet, 1 mg= 1 TAB, PO, Daily Coreg 12.5 mg oral tablet, 12.5 mg= 1 TAB, PO, BID (2 times a day) dilTIAZem 240
Allergien: shrimp iodine compounds
Vorherige Impfungen: -

VAERS 1992102

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: IN
Alter: 65,0
Geschlecht: F
Eingang: 30.12.2021
Impfdatum: 04.03.2021
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: IM / UN

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

Allergy test Rash pruritic

Symptomtext

Itching Rash which lasted all summer--moving from one part of body to another. Treated by a dermatologist--all summer--used topical steroid, benadryl, and po visteril--did allergy testing--attempted to stay away from food that was on list--unsuccessful and started on Dupixent, which has helped.

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Praegender Schweregrund: Rash pruritic
Hospital-Tage: -
Labordaten: Allergy testing in August
Aktuelle Erkrankungen: none
Vorgeschichte: -
Andere Medikamente: Synthroid, Ramipril, Janumet, Farxiga, Vytorin, Lasix, KCL, Ropinirol, Neurotin, Vitamin D weekly, Plaquinil, Toprol XL, Omega 3 Acid Etyhyl Esters, Baby ASA, B 12, Glucosamie/chondrotin, Magnesium, Probiotic, Fergon, Multivitamin, topical
Allergien: Latex, Formaldehyde (and derivatives), /bacitracin
Vorherige Impfungen: -

VAERS 1951643

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: IN
Alter: 48,0
Geschlecht: F
Eingang: 15.12.2021
Impfdatum: 02.02.2021
Beginn: 02.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / RA

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

Adverse event Chills Fatigue Pain Pain in extremity

Symptomtext

I had fatigue, soreness in the arm, body aches and chills. These adverse health events lasted for about 3days.

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Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma Depression Anxiety Panic Disorder Migraine Hypertension Hypothyroidism TMJ GERD
Andere Medikamente: Sertraline 50mg; Trazodone 50mg; Wellbutrin 100mg; Buspirone 40mg/daily; Levothyroxine 125 mcg; Lisinopril 5mg; Atenolol 25mg; Pepcid 40mg; Xyzal 5mg; Vitamin D 3 5000units; Sinovent 220mch; l-methyl folate; Ventolin 90mcg
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1942607

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038k20a

mild

Staat: IL
Alter: 58,0
Geschlecht: F
Eingang: 12.12.2021
Impfdatum: 05.02.2021
Beginn: 05.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Abdominal pain upper Chills Computerised tomogram abnormal Diverticulitis Pyrexia

Symptomtext

Diverticulitis, chills, fever. Symptoms (chills, fever, and stomach pain) became pronounced around 3:00 p.m. but most likely began around 7:00 a.m., with the patient not recognizing the symptom as diverticulitis. Because the symptoms began before the actual immunization, the event is not related to the immunization, but since all adverse reactions were requested to be reported, the patient did so.

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Praegender Schweregrund: Abdominal pain upper
Hospital-Tage: -
Labordaten: Emergency room admission and CT scan which showed diverticulitis.
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma, high blood pressure, high cholesterol, stroke syndrome
Andere Medikamente: Losartan/HCTZ, , Plavix, Zyrtec, Lipitor, Singulair
Allergien: Shellfish, salmon, bass
Vorherige Impfungen: -

VAERS 1923575

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: MI
Alter: 70,0
Geschlecht: F
Eingang: 04.12.2021
Impfdatum: 04.02.2021
Beginn: 01.02.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: SYR / LA

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

Computerised tomogram Constipation Faecal volume increased Pain

Symptomtext

Constipation; large amount of stool volume within colon. Pain on left side that started week and 1/2 prior to 11/27.

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Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: CT Scan 11/27/21
Aktuelle Erkrankungen: -
Vorgeschichte: Superventicular Tachycardia
Andere Medikamente: Losartan Diltizem Metropol Potassium CoQ10 Vitamin D3 Low Dose Asprin
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1910025

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: IL
Alter: 54,0
Geschlecht: M
Eingang: 30.11.2021
Impfdatum: 01.02.2021
Beginn: 08.02.2021
Tage bis Beginn: 7,0
Dosis: 2
Route/Site: IM / RA

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

Computerised tomogram normal Culture urine negative Cystoscopy Hydronephrosis Mycobacterium tuberculosis complex test Pain Scan with contrast abnormal Ultrasound kidney abnormal Ureteral stent insertion Ureteric obstruction Ureteroscopy Urine analysis normal Urogram abnormal X-ray abnormal

Symptomtext

Starting 8 Feb severe acute pain which was suspected of kidney stones but CT Stone protocol was clear. Pain continued for three months during which several imaging protocols were done and showed mild hydronephrosis and mid-level constriction in the ureter on the left side. On 16 mar 2021, a "Cystoscopy /Ureteroscopy & Indwell Stent Insertion with string" procedure was performed to relieve the obstruction. The stent was removed on 22 Mar 2021. Starting about AUgust the pain subsided and subsequent imaging showed a relief in hydronephrosis and ureteral obstruction. Further imaging tests scheduled for February 2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: 1,0
Labordaten: UA and Urine culture (110 Feb 2021) - rvealed no infection. CT Stone protocol (11 Feb 2021) - revealed no stones. CT Urogram w/o & w contract (17 Feb 2021) - revealed hydronephrosis and ureteral obstruction on Left side. Ultrasound kidney (8 Mar 2021) - showed some possible fibrosis as potential obstruction of ureter. X-ray retrograde in OR (16 Mar 2021) confirmed the imaging findings. Tests for tuberculosis (Quantiferon Gold on 20 Jul 2021) and Urine culture for tuberculosis (4 Aug 2021) were both negative.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Pepcid
Allergien: None
Vorherige Impfungen: -

VAERS 1909915

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: MI
Alter: 73,0
Geschlecht: F
Eingang: 30.11.2021
Impfdatum: 03.03.2021
Beginn: 04.11.2021
Tage bis Beginn: 246,0
Dosis: 1
Route/Site: - / -

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

Asthenia COVID-19 Fatigue Hypophagia SARS-CoV-2 test positive

Symptomtext

Patient fully vaccinated for COVID who admitted to hospital with COVID positive test. Provider discharge note: "74-year-old female who presented to the emergency department with decreased oral intake and generalized weakness. Patient was recently hospitalized a week prior to admission and she developed sudden onset fatigue and weakness without focal symptoms. Patient recently had COVID diagnosis however she is out of isolation window. She was hydrated with IV fluids. She did not have any respiratory signs or symptoms. Physical therapy was ordered and after evaluation she was cleared for home discharge."

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: 2,0
Labordaten: COVID detected test on 11/04/21.
Aktuelle Erkrankungen: -
Vorgeschichte: UPJ obstruction - right Renal cyst CAD (coronary artery disease) History of bilateral knee arthroplasty Hypertension Obesity Thyroid nodule Rheumatoid arthritis (*) Hyperparathyroidism (*) Depression GERD (gastroesophageal reflux disease) Low HDL (under 40) Osteopenia DNS (deviated nasal septum) Hypertrophy of both inferior nasal turbinates Crohn's disease of small intestine without complication (*) Major depressive disorder with single episode, in full remission (*) Generalized weakness Polyneuropathy, idiopathic progressive Cerebral embolism without cerebral infarction Vascular dementia without behavioral disturbance (*) Stage 3 chronic kidney disease (*) Small vessel disease (*) Adenocarcinoma of right lung (*)
Andere Medikamente: Norvasc, Aspirin, Calcium with D3, Clonidine, Valium, Benadryl, colace, folic acid, prevacid, methotrexate, multivitamin, K-dur, probiotic, zoloft, micardis,
Allergien: Iodine, betadine, lisinopril, levaquin, sulfa antibiotics
Vorherige Impfungen: -

VAERS 1879384

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: FL
Alter: 72,0
Geschlecht: M
Eingang: 18.11.2021
Impfdatum: 03.02.2021
Beginn: 08.11.2021
Tage bis Beginn: 278,0
Dosis: 1
Route/Site: OT / -

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

Feeling abnormal Myalgia Restlessness

Symptomtext

a little restless; brain fogginess/looped out in my head; sore arms; This spontaneous case was reported by a consumer and describes the occurrence of RESTLESSNESS (a little restless), FEELING ABNORMAL (brain fogginess/looped out in my head) and MYALGIA (sore arms) in a 72-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 939905, 025A21A and 038K20A) for COVID-19 vaccination. No Medical History information was reported. On 03-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 03-Mar-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 08-Nov-2021, received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 08-Nov-2021, the patient experienced RESTLESSNESS (a little restless) and MYALGIA (sore arms). 08-Nov-2021, the patient experienced FEELING ABNORMAL (brain fogginess/looped out in my head). The patient was treated with TRAZODONE for Adverse event, at an unspecified dose and frequency. At the time of the report, RESTLESSNESS (a little restless) and FEELING ABNORMAL (brain fogginess/looped out in my head) had not resolved and MYALGIA (sore arms) was resolving. Concomitant drugs were not reported. Treatment included swim spa. The patient thought that might have received a incorrect dosage. This case was linked to MOD-2021-381283 (Patient Link).

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

VAERS 1873767

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: IL
Alter: 40,0
Geschlecht: F
Eingang: 16.11.2021
Impfdatum: 04.02.2021
Beginn: 01.02.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: SYR / UN

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

Urticaria

Symptomtext

In February, I dealt with Hives. I thought it was because of the insulation due to a remodeling I was doing. It was on and off. It lasted about 2 to 3 weeks. I don't remember very well, due to not really paying much attention to them. It was all over my body in different spots.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Urticaria
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: -
Vorgeschichte: Auto Immune Deficiency Misconnected tissue disease, Lupus Rheumatoid Arthritis Sjogren Hashimoto Thyroiditis
Andere Medikamente: Levothyroxine 100mg once a day Vitamin D3 2000 IU once a day
Allergien: Seasonal Allergies Pollen
Vorherige Impfungen: -

VAERS 1867114

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: PA
Alter: 66,0
Geschlecht: F
Eingang: 13.11.2021
Impfdatum: 28.01.2021
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: OT / -

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

Chills Headache Myalgia

Symptomtext

chills; body ache; headache; This spontaneous case was reported by a consumer and describes the occurrence of CHILLS (chills), MYALGIA (body ache) and HEADACHE (headache) in a 66-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 007M20A and 038K20A) for COVID-19 vaccination. No Medical History information was reported. On 28-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 25-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 CHILLS (chills), MYALGIA (body ache) and HEADACHE (headache). At the time of the report, CHILLS (chills), MYALGIA (body ache) and HEADACHE (headache) outcome was unknown. No concomitant medications were reported. No treatment medications were reported. This case was linked to MOD-2021-369478.

Weitere VAERSDATA-Felder

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

VAERS 1856704

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: NY
Alter: 78,0
Geschlecht: F
Eingang: 10.11.2021
Impfdatum: 28.01.2021
Beginn: 25.10.2021
Tage bis Beginn: 270,0
Dosis: 1
Route/Site: OT / LA

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

Arthralgia Axillary pain Bone pain Feeling cold Pain in extremity Vaccination site erythema Vaccination site movement impairment Vaccination site pruritus Vaccination site rash

Symptomtext

Left shoulder hurts when moving after booster shot; Felt very cold; Left collar bone aches; Under left arm pit feels uncomfortable; Red rash on the injection site; Red rash on the injection site; Itching on the injection site; Left arm started aching/Left arm aches worst than the second shot; Shoulder problem got worst after booster shot/The left shoulder hurts when moving; This spontaneous case was reported by a consumer and describes the occurrence of PAIN IN EXTREMITY (Left arm started aching/Left arm aches worst than the second shot), BONE PAIN (Left collar bone aches), VACCINATION SITE MOVEMENT IMPAIRMENT (Left shoulder hurts when moving after booster shot), FEELING COLD (Felt very cold) and ARTHRALGIA (Shoulder problem got worst after booster shot/The left shoulder hurts when moving) in a 78-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 017F21A, 031M20A and 038K20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concurrent medical conditions included Shoulder discomfort. On 28-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 25-Feb-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 25-Oct-2021, received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 25-Oct-2021, the patient experienced PAIN IN EXTREMITY (Left arm started aching/Left arm aches worst than the second shot) and ARTHRALGIA (Shoulder problem got worst after booster shot/The left shoulder hurts when moving). On 26-Oct-2021, the patient experienced BONE PAIN (Left collar bone aches), FEELING COLD (Felt very cold), AXILLARY PAIN (Under left arm pit feels uncomfortable), VACCINATION SITE ERYTHEMA (Red rash on the injection site), VACCINATION SITE RASH (Red rash on the injection site) and VACCINATION SITE PRURITUS (Itching on the injection site). On 02-Nov-2021, the patient experienced VACCINATION SITE MOVEMENT IMPAIRMENT (Left shoulder hurts when moving after booster shot). At the time of the report, PAIN IN EXTREMITY (Left arm started aching/Left arm aches worst than the second shot), BONE PAIN (Left collar bone aches), FEELING COLD (Felt very cold), AXILLARY PAIN (Under left arm pit feels uncomfortable), VACCINATION SITE ERYTHEMA (Red rash on the injection site), VACCINATION SITE RASH (Red rash on the injection site) and VACCINATION SITE PRURITUS (Itching on the injection site) outcome was unknown and VACCINATION SITE MOVEMENT IMPAIRMENT (Left shoulder hurts when moving after booster shot) and ARTHRALGIA (Shoulder problem got worst after booster shot/The left shoulder hurts when moving) had not resolved. Concomitant information was not provided. Treatment information was not provided. This case was linked to MOD-2021-372494 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 02-Nov-2021: Follow-up information received on 04-NOV-2021 contains no new information.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Shoulder discomfort
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1856700

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: NY
Alter: 78,0
Geschlecht: F
Eingang: 10.11.2021
Impfdatum: 28.01.2021
Beginn: 25.02.2021
Tage bis Beginn: 28,0
Dosis: 1
Route/Site: OT / -

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

Feeling cold Pain in extremity

Symptomtext

Mild feeling cold after second shot; Left arm ached a little after second shot; This spontaneous case was reported by a consumer and describes the occurrence of FEELING COLD (Mild feeling cold after second shot) and PAIN IN EXTREMITY (Left arm ached a little after second shot) in a 78-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 031M20A and 038K20A) for COVID-19 vaccination. Concurrent medical conditions included Shoulder discomfort (Left Shoulder problem prior vaccination.). On 28-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 25-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 FEELING COLD (Mild feeling cold after second shot) and PAIN IN EXTREMITY (Left arm ached a little after second shot). At the time of the report, FEELING COLD (Mild feeling cold after second shot) and PAIN IN EXTREMITY (Left arm ached a little after second shot) outcome was unknown. No concomitant medications were reported. No treatment medications were reported. This case was linked to MOD-2021-372539 (Patient Link).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Shoulder discomfort (Left Shoulder problem prior vaccination.)
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1853509

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: FL
Alter: 49,0
Geschlecht: F
Eingang: 09.11.2021
Impfdatum: 03.02.2021
Beginn: 03.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / LA

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

Fatigue

Symptomtext

I got the 1st dose of the Moderna Covid-19 vaccine. I was tired.; This spontaneous case was reported by a consumer and describes the occurrence of FATIGUE (I got the 1st dose of the Moderna Covid-19 vaccine. I was tired.) in a 49-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. No Medical History information was reported. On 03-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 03-Feb-2021, the patient experienced FATIGUE (I got the 1st dose of the Moderna Covid-19 vaccine. I was tired.). At the time of the report, FATIGUE (I got the 1st dose of the Moderna Covid-19 vaccine. I was tired.) outcome was unknown. mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) dosing remained unchanged. Concomitant medications details was not reported by the reporter. This case was linked to MOD-2021-370421 (Patient Link).

Weitere VAERSDATA-Felder

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

VAERS 1850594

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: MI
Alter: 68,0
Geschlecht: F
Eingang: 08.11.2021
Impfdatum: 04.03.2021
Beginn: 07.11.2021
Tage bis Beginn: 248,0
Dosis: 1
Route/Site: IM / -

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

Acute kidney injury Asthenia COVID-19 Chest X-ray abnormal Cough Diarrhoea Fatigue Hyponatraemia Lung infiltration Malaise Nausea SARS-CoV-2 test positive Vomiting

Symptomtext

This is a 69-year-old female with significant past medical history of end-stage renal disease on dialysis that received her renal transplant, hypertension, type 2 diabetes and CKD that presented to the hospital with chief complaint of progressively worsening nausea and vomiting over the past several days. Patient states that she has been sick for about 10 days with nausea vomiting and diarrhea. She has been unable to keep food or drink down. She states that she missed multiple days of medications due to her nausea and vomiting. The patient notes diarrhea as well. The patient denied any significant abdominal pain fevers or chills. Patient did note a slight cough but was not short of breath. The patient was vaccinated for Covid with a bone neurovaccine earlier in the year. The patient denies any chest pain, palpitations, lightheadedness or dizziness. Patient denies any dysuria, hematuria urinary frequency. Patient started to feel weak and fatigued as well.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: 1,0
Labordaten: In the emergency room department, the patient was found to be in acute renal failure with hyponatremia. Incidentally she was noted to be COVID-19 positive. Chest x-ray showed some bibasilar infiltrates but she was not hypoxemic or dyspneic. She was hemodynamically stable and afebrile. She was given a liter of fluid in the ER.
Aktuelle Erkrankungen: unknown
Vorgeschichte: renal transplant recipient Hyptertension Diabetes hyperlipidemia
Andere Medikamente: atorvastatin 10 mg oral tablet : 1 tab(s) orally once a day (at bedtime) 3. calcitriol 0.25 mcg oral capsule : 1 cap(s) orally every other day 4. Effexor XR 75 mg oral capsule, extended release : 1 cap(s) orally once a day 5. insulin aspart
Allergien: N/A
Vorherige Impfungen: -

VAERS 1845299

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: NJ
Alter: 51,0
Geschlecht: F
Eingang: 05.11.2021
Impfdatum: 25.02.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: OT / -

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

Chills Fatigue Headache Pain

Symptomtext

achy; tired; chills; pounding head ache; This spontaneous case was reported by a consumer and describes the occurrence of PAIN (achy), FATIGUE (tired), CHILLS (chills) and HEADACHE (pounding head ache) in a 51-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. No Medical History information was reported. On 25-Feb-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced PAIN (achy), FATIGUE (tired), CHILLS (chills) and HEADACHE (pounding head ache). The patient was treated with CAFFEINE, PARACETAMOL (EXCEDRIN [CAFFEINE;PARACETAMOL]) for Headache, at an unspecified dose and frequency. At the time of the report, PAIN (achy) and FATIGUE (tired) outcome was unknown and CHILLS (chills) and HEADACHE (pounding head ache) had resolved. No concomitant medications were reported This case was linked to MOD-2021-366207 (Patient Link).

Weitere VAERSDATA-Felder

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

VAERS 1836125

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: NJ
Alter: 80,0
Geschlecht: F
Eingang: 02.11.2021
Impfdatum: 02.03.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: OT / -

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

Decreased appetite Dysstasia Feeling abnormal Inflammation Rash macular Vaccination complication Vaccination site pain

Symptomtext

quite reaction to booster shot; appetite decreased; felt like I was gonna die clarified as "felt like whole system was taken over in some negative way "; barely able to get out of recliner; felt like my whole body was inflamed; pink icy looking blotches on left arm; left arm started to become sore, left arm hurt; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION COMPLICATION (quite reaction to booster shot), DECREASED APPETITE (appetite decreased), FEELING ABNORMAL (felt like I was gonna die clarified as "felt like whole system was taken over in some negative way "), DYSSTASIA (barely able to get out of recliner) and INFLAMMATION (felt like my whole body was inflamed) in an 80-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 037C21A, 038K20A and 022M20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Co-suspect product included non-company product HYDROXYCHLOROQUINE for Dermatomyositis. The patient's past medical history included Dermatomyositis. Concurrent medical conditions included Autoimmune disorder. Concomitant products included LOSARTAN POTASSIUM (COZAAR), IPRATROPIUM BROMIDE, SALBUTAMOL SULFATE (ALBUTEROL SULFATE AND IPRATROPIUM BROMIDE) and BECLOMETASONE DIPROPIONATE (QVAR) for an unknown indication. On 02-Mar-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 03-May-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 20-Oct-2021, received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On an unknown date, the patient started HYDROXYCHLOROQUINE (unknown route) at an unspecified dose. On an unknown date, the patient experienced VACCINATION COMPLICATION (quite reaction to booster shot), DECREASED APPETITE (appetite decreased), FEELING ABNORMAL (felt like I was gonna die clarified as "felt like whole system was taken over in some negative way "), DYSSTASIA (barely able to get out of recliner), INFLAMMATION (felt like my whole body was inflamed), RASH MACULAR (pink icy looking blotches on left arm) and VACCINATION SITE PAIN (left arm started to become sore, left arm hurt). The patient was treated with LORAZEPAM ongoing since an unknown date at a dose of 0.5 mg and PARACETAMOL (TYLENOL) for Dermatomyositis, at an unspecified dose and frequency. At the time of the report, VACCINATION COMPLICATION (quite reaction to booster shot), DECREASED APPETITE (appetite decreased), FEELING ABNORMAL (felt like I was gonna die clarified as "felt like whole system was taken over in some negative way "), DYSSTASIA (barely able to get out of recliner), INFLAMMATION (felt like my whole body was inflamed), RASH MACULAR (pink icy looking blotches on left arm) and VACCINATION SITE PAIN (left arm started to become sore, left arm hurt) outcome was unknown. No concomitant medications was reported. No treatment drug details was reported. Concomitant medication includes aseltine floacazone for unknown indication. Most recent FOLLOW-UP information incorporated above includes: On 25-Oct-2021: Significant F/U Received contains patient details, relevant medical history, vaccine batch number/date for all doses, suspect products.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash macular
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Autoimmune disorder.
Vorgeschichte: Medical History/Concurrent Conditions: Dermatomyositis.
Andere Medikamente: COZAAR; ALBUTEROL SULFATE AND IPRATROPIUM BROMIDE; QVAR.
Allergien: -
Vorherige Impfungen: -

VAERS 1799503

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: OH
Alter: 88,0
Geschlecht: F
Eingang: 20.10.2021
Impfdatum: 24.01.2021
Beginn: 18.10.2021
Tage bis Beginn: 267,0
Dosis: 1
Route/Site: IM / LA

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

COVID-19 Malaise SARS-CoV-2 test positive

Symptomtext

patient admitted to hospital due to covid symptoms

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: 10/19/21-tested positive for covid
Aktuelle Erkrankungen: unknown
Vorgeschichte: CHF, malnutrition, atrial fib,
Andere Medikamente: unknown
Allergien: sulfa
Vorherige Impfungen: -

VAERS 1782394

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: MI
Alter: 65,0
Geschlecht: F
Eingang: 13.10.2021
Impfdatum: 11.02.2021
Beginn: 02.10.2021
Tage bis Beginn: 233,0
Dosis: 2
Route/Site: IM / -

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

COVID-19 Chest discomfort Cough Exposure to SARS-CoV-2 Pain SARS-CoV-2 test positive

Symptomtext

Patient presented to emergency department on 10/2/2021 with cough, chest discomfort, and body aches. She had a COVID-19 exposure a week prior. Shew as found to be COVID-19 positive and was admitted for further management. She was treated with remdesivir, decadron, and supplemental oxygen. She was discharged home on 10/6/2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: 4,0
Labordaten: COVID-19 positive on 10/2/2021.
Aktuelle Erkrankungen: None known
Vorgeschichte: DDD (degenerative disc disease), lumbar Vitamin D deficiency Essential hypertension Obstructive sleep apnea on CPAP History of endometrial cancer
Andere Medikamente: ascorbic acid (VITAMIN C) 250 MG tablet benazepril-hctz (LOTENSIN HCT) 10-12.5 MG tablet Cholecalciferol (VITAMIN D3) 2000 UNIT TABS magnesium oxide (MAG OX) 250 MG tablet multivitamin/beta carotene (TAB-A-VITE/BETA CAROTENE) tab TABS table
Allergien: Lisinopril (muscle cramps), losartan (muscle cramps), simvastatin (cramps)
Vorherige Impfungen: -

VAERS 1775950

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: MI
Alter: 73,0
Geschlecht: M
Eingang: 11.10.2021
Impfdatum: 12.02.2021
Beginn: 12.03.2021
Tage bis Beginn: 28,0
Dosis: 1
Route/Site: OT / -

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

Headache Thermal burn

Symptomtext

Left shoulder burned; Headache; This spontaneous case was reported by a consumer and describes the occurrence of THERMAL BURN (Left shoulder burned) and HEADACHE (Headache) in a 73-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 023M20A and 038K20A) for COVID-19 vaccination. No Medical History information was reported. On 12-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 12-Mar-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 12-Mar-2021, the patient experienced THERMAL BURN (Left shoulder burned) and HEADACHE (Headache). At the time of the report, THERMAL BURN (Left shoulder burned) and HEADACHE (Headache) outcome was unknown. No treatment information was provided. No concomitant medication was provided This case was linked to MOD-2021-338314, MOD-2021-338407 (Patient Link).

Weitere VAERSDATA-Felder

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

VAERS 1771104

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: -
Alter: 61,0
Geschlecht: F
Eingang: 08.10.2021
Impfdatum: 12.02.2021
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: OT / -

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

Headache

Symptomtext

headache; This spontaneous case was reported by a consumer and describes the occurrence of HEADACHE (headache) in a 61-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. No Medical History information was reported. On 12-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced HEADACHE (headache). At the time of the report, HEADACHE (headache) outcome was unknown. mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) dosing remained unchanged. Concomitant medication of the patient was not reported. No treatment information was provided by the reporter. This case was linked to MOD-2021-338542, MOD-2021-338560 (Patient Link).

Weitere VAERSDATA-Felder

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

VAERS 1771098

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: MI
Alter: 73,0
Geschlecht: M
Eingang: 08.10.2021
Impfdatum: 12.02.2021
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: OT / -

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

Headache Thermal burn

Symptomtext

left shoulder burned; headache; This spontaneous case was reported by a consumer and describes the occurrence of THERMAL BURN (left shoulder burned) and HEADACHE (headache) in a 73-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. No Medical History information was reported. On 12-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. In 2021, the patient experienced THERMAL BURN (left shoulder burned) and HEADACHE (headache). At the time of the report, THERMAL BURN (left shoulder burned) and HEADACHE (headache) outcome was unknown. mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) dosing remained unchanged. No concomitant and treatment information provided. After first dose patient had a headache and left shoulder burned. This case was linked to MOD-2021-338406, MOD-2021-338407 (Patient Link).

Weitere VAERSDATA-Felder

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

VAERS 1770524

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: -
Alter: 62,0
Geschlecht: F
Eingang: 08.10.2021
Impfdatum: 12.02.2021
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: OT / -

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

Dizziness Pain in extremity

Symptomtext

severe pain from her waist down to her thigh; felt dizzy; This spontaneous case was reported by a consumer and describes the occurrence of PAIN IN EXTREMITY (severe pain from her waist down to her thigh) and DIZZINESS (felt dizzy) in a 62-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 088D21A, 023M20A and 038K20A) for COVID-19 vaccination. No Medical History information was reported. On 12-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 12-Mar-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 23-Aug-2021, received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On an unknown date, the patient experienced PAIN IN EXTREMITY (severe pain from her waist down to her thigh) and DIZZINESS (felt dizzy). At the time of the report, PAIN IN EXTREMITY (severe pain from her waist down to her thigh) and DIZZINESS (felt dizzy) outcome was unknown. Concomitant product use was not provided by the reporter. Treatment information was not provided. It was reported that patient was not aware if she was eligible for booster dose or not. This case was linked to MOD-2021-338524 (Patient Link).

Weitere VAERSDATA-Felder

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

VAERS 1767286

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: PA
Alter: 84,0
Geschlecht: M
Eingang: 07.10.2021
Impfdatum: 13.02.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: OT / -

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

Abdominal discomfort Abdominal pain upper Muscle discomfort

Symptomtext

Slight muscular discomfort; Stomach discomfort / Abdomen discomfort; Stomach pain/ Abdomen pain; This spontaneous case was reported by a physician and describes the occurrence of MUSCLE DISCOMFORT (Slight muscular discomfort), ABDOMINAL DISCOMFORT (Stomach discomfort / Abdomen discomfort) and ABDOMINAL PAIN UPPER (Stomach pain/ Abdomen pain) in an 85-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 0173NA, 038K20A and 040A21A) for COVID-19 vaccination. Concurrent medical conditions included Immunocompromised (Went through a series of cancer treatments). On 13-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 14-Mar-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 14-Sep-2021, received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On an unknown date, the patient experienced MUSCLE DISCOMFORT (Slight muscular discomfort), ABDOMINAL DISCOMFORT (Stomach discomfort / Abdomen discomfort) and ABDOMINAL PAIN UPPER (Stomach pain/ Abdomen pain). At the time of the report, MUSCLE DISCOMFORT (Slight muscular discomfort), ABDOMINAL DISCOMFORT (Stomach discomfort / Abdomen discomfort) and ABDOMINAL PAIN UPPER (Stomach pain/ Abdomen pain) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. The patient is on a number of different medications (name was unspecified). No treatment information was provided. The patient received third dose of vaccine and reports slight muscular discomfort, not severe with stomach and abdomen discomfort and pain. The patient had went through series of cancer treatments and considered as immunocompromised.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain upper
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Immunocompromised (Went through a series of cancer treatments.)
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1767061

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: IL
Alter: 71,0
Geschlecht: F
Eingang: 07.10.2021
Impfdatum: 28.01.2021
Beginn: 23.09.2021
Tage bis Beginn: 238,0
Dosis: 1
Route/Site: OT / LA

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

Bursitis COVID-19 Drug ineffective Fatigue Illness Injection site pain Pain in extremity

Symptomtext

Arm pain forever; Bursitis; Sick; injection site pain; Some fatigue; COVID positive / just getting over COVID; Lack of drug effect; This spontaneous case was reported by a consumer and describes the occurrence of PAIN IN EXTREMITY (Arm pain forever), BURSITIS (Bursitis), ILLNESS (Sick), COVID-19 (COVID positive / just getting over COVID) and DRUG INEFFECTIVE (Lack of drug effect) in a 71-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 013M20A and 038K20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included Shoulder replacement. Previously administered products included for an unreported indication: FLU. Concomitant products included ROSUVASTATIN CALCIUM (CRESTOR) and ALENDRONATE SODIUM (FOSAMAX) for an unknown indication. On 28-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 26-Feb-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 23-Sep-2021, the patient experienced COVID-19 (COVID positive / just getting over COVID) and DRUG INEFFECTIVE (Lack of drug effect). On an unknown date, the patient experienced PAIN IN EXTREMITY (Arm pain forever), BURSITIS (Bursitis), ILLNESS (Sick), INJECTION SITE PAIN (injection site pain) and FATIGUE (Some fatigue). At the time of the report, PAIN IN EXTREMITY (Arm pain forever), BURSITIS (Bursitis), ILLNESS (Sick), COVID-19 (COVID positive / just getting over COVID), DRUG INEFFECTIVE (Lack of drug effect), INJECTION SITE PAIN (injection site pain) and FATIGUE (Some fatigue) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 23-Sep-2021, SARS-CoV-2 test: positive (Positive) COVID positive. No Treatment were reported. Patient mentioned flu shot caused bursitis and tendonitis. Most recent FOLLOW-UP information incorporated above includes: On 29-Sep-2021: follow up received on 29-SEP-2021 includes Event was added On 04-Oct-2021: follow up received contains medical history , events for flu shot; Sender's Comments: This case concerns a 71-year-old, female with reported history of Flu vaccination and shoulder replacement, who experienced the unexpected AESI event of Drug ineffective because of COVID 19 infection more than 15 days after the second dose of the vaccine within a correct interval with the first dose. The event occurred approximately 7 months and 26 days after the first dose and 6 month and 27 days after the most recent dose (second dose) of mRNA-1273 Moderna vaccine (Spikevax). The rechallenge was unknown since the patient is planning on getting the booster. Several other non serious or AESI events were reported, such as pain in extremity, tendinitis and bursitis that could be confounded by the history of shoulder replacement and the co suspect of flu vaccine. The benefit-risk relationship of mRNA-1273 Moderna vaccine in not affected by this report

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Test Date: 20210923; Test Name: COVID-19; Test Result: Positive ; Result Unstructured Data: COVID positive
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Shoulder replacement
Andere Medikamente: CRESTOR; FOSAMAX
Allergien: -
Vorherige Impfungen: -

VAERS 1764228

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: FL
Alter: 88,0
Geschlecht: M
Eingang: 06.10.2021
Impfdatum: 02.02.2021
Beginn: 20.09.2021
Tage bis Beginn: 230,0
Dosis: 1
Route/Site: OT / -

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

Cough Nasopharyngitis Pain in extremity Rhinorrhoea

Symptomtext

Full blown cold; Sniffles; Dry cough; Arm soreness; This spontaneous case was reported by a patient and describes the occurrence of COUGH (Dry cough), PAIN IN EXTREMITY (Arm soreness), RHINORRHOEA (Sniffles) and NASOPHARYNGITIS (Full blown cold) in an 88-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 047C21A, 031M20A and 038K20A) for COVID-19 vaccination. The patient's past medical history included Mouth cancer, Tongue neoplasm NOS, Knee replacement (Total right knee replacement surgery) and Radiation therapy. Concurrent medical conditions included Type 2 diabetes mellitus and Loss of taste. On 02-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 02-Mar-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 20-Sep-2021, received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 20-Sep-2021, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced PAIN IN EXTREMITY (Arm soreness). On 23-Sep-2021, the patient experienced COUGH (Dry cough). On 24-Sep-2021, the patient experienced RHINORRHOEA (Sniffles). On 27-Sep-2021, the patient experienced NASOPHARYNGITIS (Full blown cold). In September 2021, PAIN IN EXTREMITY (Arm soreness) and RHINORRHOEA (Sniffles) had resolved. On 24-Sep-2021, COUGH (Dry cough) had resolved. At the time of the report, NASOPHARYNGITIS (Full blown cold) had not resolved. No Concomitant medications were reported. No Treatment medications were reported. This case was linked to MOD-2021-042571 (Patient Link).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Loss of taste; Type 2 diabetes mellitus
Vorgeschichte: Medical History/Concurrent Conditions: Knee replacement (Total right knee replacement surgery); Mouth cancer; Radiation therapy; Tongue neoplasm NOS
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1759420

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: MI
Alter: 66,0
Geschlecht: M
Eingang: 04.10.2021
Impfdatum: 06.02.2021
Beginn: 20.09.2021
Tage bis Beginn: 226,0
Dosis: 1
Route/Site: - / -

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

COVID-19 Chemotherapy Decreased appetite Fatigue SARS-CoV-2 test positive

Symptomtext

Pt had a history of right lower lobe small cell lung cancer and emphysema. He reports a feeling of fatigue and loss of appetite. He is still receiving chemotherapy. He was found to be COVID positive.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: 10,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1737786

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: IL
Alter: 67,0
Geschlecht: F
Eingang: 27.09.2021
Impfdatum: 01.02.2021
Beginn: 01.07.2021
Tage bis Beginn: 150,0
Dosis: 1
Route/Site: IM / RA

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

Blood test Pain in extremity Sensory disturbance

Symptomtext

Weird feeling in feet/lower legs. Pain/aching, feels as if wearing socks. Have appt with neurologist in October

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: Blood tests. Slightly elevated B12
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Celexa, gabapentin, Vit B12
Allergien: Naproxen, nickel
Vorherige Impfungen: -

VAERS 1736886

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: OK
Alter: 67,0
Geschlecht: F
Eingang: 27.09.2021
Impfdatum: 26.02.2021
Beginn: 22.09.2021
Tage bis Beginn: 208,0
Dosis: 2
Route/Site: IM / LA

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

Ageusia Anosmia COVID-19 Chills Fatigue Myalgia SARS-CoV-2 test positive

Symptomtext

CHILLS, LOSS OF TASTE/SMELL, MUSCLE PAIN, FATIGUE

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: 09/22/21: POSITIVE POC SARS COVID RAPID ANTIGEN
Aktuelle Erkrankungen: LOW BACK PAIN, SACRAL BACK PAIN, NEURALGIA
Vorgeschichte: EDEMA, PALPITATIONS, ANXIETY DISORDER, PAIN OF BREAST, HYPERLIPIDEMIA, INSOMNIA, HYPOCHONDRIASIS, HTN, OBSTRUCTIVE SLEEP APNEA, GERD
Andere Medikamente: GABAPENTIN, HYDROXYZINE, KEOTIFEN, LISOCAINE MOUTH WASH, WARLICK SOLN, AMLODIPINE, BISACODYL, MIRALAX, OFLOXACIN, NYSTATIN POWDER, OMEPRAZOLE, DICLOFENAC GEL, PROPRANOLOL, MULTIVITAMIN, ACETAMINOPHEN, ASPIRIN, IBUPROFEN, CALCIUM CITRATE
Allergien: NKA
Vorherige Impfungen: -

VAERS 1721803

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: PA
Alter: 58,0
Geschlecht: F
Eingang: 22.09.2021
Impfdatum: 02.02.2021
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: OT / -

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

Discomfort Fatigue Headache Illness Malaise Myalgia Pyrexia

Symptomtext

sick for 2 days; felt yucky; didn't feel well; sore arm; fever/ highest was 101.2 F; really tired; headachy; This spontaneous case was reported by a consumer and describes the occurrence of ILLNESS (sick for 2 days), DISCOMFORT (felt yucky), MALAISE (didn't feel well), MYALGIA (sore arm) and PYREXIA (fever/ highest was 101.2 F) in a 58-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 031M20A and 038K20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No medical history was reported by reporter. Concurrent medical conditions included Cancer. Concomitant products included IMATINIB MESILATE (GLEEVEC) for Chemotherapy. On 02-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 02-Mar-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On an unknown date, the patient experienced ILLNESS (sick for 2 days), DISCOMFORT (felt yucky), MALAISE (didn't feel well), MYALGIA (sore arm), PYREXIA (fever/ highest was 101.2 F), FATIGUE (really tired) and HEADACHE (headachy). The patient was treated with PARACETAMOL (TYLENOL) for Adverse event, at a dose of 1 dosage form. At the time of the report, ILLNESS (sick for 2 days), DISCOMFORT (felt yucky), MALAISE (didn't feel well), MYALGIA (sore arm), PYREXIA (fever/ highest was 101.2 F), FATIGUE (really tired) and HEADACHE (headachy) outcome was unknown.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Cancer
Vorgeschichte: Comments: No medical history was reported by reporter.
Andere Medikamente: GLEEVEC
Allergien: -
Vorherige Impfungen: -

VAERS 1696384

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038k20a

mild

Staat: -
Alter: 53,0
Geschlecht: F
Eingang: 14.09.2021
Impfdatum: 25.02.2021
Beginn: 11.03.2021
Tage bis Beginn: 14,0
Dosis: 1
Route/Site: - / LA

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

Pruritus Rash Scratch

Symptomtext

itching and scratching on stomach, both underarms has raw rash, groin, ear, face nothing working

Weitere VAERSDATA-Felder

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

VAERS 1696293

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: FL
Alter: 82,0
Geschlecht: M
Eingang: 14.09.2021
Impfdatum: 30.01.2021
Beginn: 23.02.2021
Tage bis Beginn: 24,0
Dosis: UNK
Route/Site: IM / -

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

Asthenia Chest X-ray Fatigue Jaundice SARS-CoV-2 test

Symptomtext

Pt came to ER for jaundice on 2/23. Seen in ED again on 2/27 for weakness and fatigue.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: 5,0
Labordaten: Covid test on 2/23/21 and cxr.
Aktuelle Erkrankungen: -
Vorgeschichte: Cdiff, gout, HTN, skin cancer.
Andere Medikamente: -
Allergien: Bactrim, benzoin topical tincture, cephalexin, ciprofloxacin, clindamycin, doxycycline, fluorouracil, polysporin, solaraze, tape, telfa, vicryl stiches.
Vorherige Impfungen: -

VAERS 1689017

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: PA
Alter: 51,0
Geschlecht: M
Eingang: 10.09.2021
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: unbekannt Erholt: nein

Acoustic stimulation tests abnormal Deafness Ear pain Tinnitus

Symptomtext

Later that night I developed a ringing in my left ear and it was painful. I reached out to my PCP who scheduled an ENT specialist appt. An ear examination and Audiology test was done and as a result of the test it has been discovered that I have since lost some hearing in what is called my high frequency range only in the left ear. ENT complete the routine exam and looked with a camera up my nostrils. I never associated it with the vaccine until the ENT was asking various questions and that's when I realized that the ringing started the same day I got the 1st injection and just had carried over still to date 6 months later. The ENT advised to wait awhile so I have an appointment set for late Nov to see if it will heal itself by then and if not other treatments will be accessed then. The soreness went away after about 1 month and the volume of the ringing varies throughout the day, but its still there.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Ear pain
Hospital-Tage: -
Labordaten: Hearing Exam; Audiology Test-hearing loss
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Lisinopril; vit D3
Allergien: Iodine in shellfish
Vorherige Impfungen: -

VAERS 1683584

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: SC
Alter: 65,0
Geschlecht: F
Eingang: 08.09.2021
Impfdatum: 10.02.2021
Beginn: 20.08.2021
Tage bis Beginn: 191,0
Dosis: 1
Route/Site: OT / -

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

Allergy to vaccine Decreased appetite Diarrhoea Fatigue Myalgia Nasopharyngitis Pain Pyrexia Sinus disorder

Symptomtext

diarrhea; feels very sinusy but nose is not running; it feels like when you have an allergy; cold like symptoms mainly in nose and eyes; pain; loss of appetite; fatigue; body aches/arm was sore; runned a fever of a 100; This spontaneous case was reported by a consumer and describes the occurrence of PAIN (pain), DECREASED APPETITE (loss of appetite), NASOPHARYNGITIS (cold like symptoms mainly in nose and eyes), DIARRHOEA (diarrhea) and SINUS DISORDER (feels very sinusy but nose is not running) in a 66-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 038K20A, 27A21A and 038K20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No medical history was reported. Concomitant products included CLONAZEPAM for an unknown indication. On 10-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 10-Mar-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 20-Aug-2021, received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 20-Aug-2021, the patient experienced PAIN (pain), DECREASED APPETITE (loss of appetite), FATIGUE (fatigue), MYALGIA (body aches/arm was sore) and PYREXIA (runned a fever of a 100). On 21-Aug-2021, the patient experienced NASOPHARYNGITIS (cold like symptoms mainly in nose and eyes), SINUS DISORDER (feels very sinusy but nose is not running) and ALLERGY TO VACCINE (it feels like when you have an allergy). On 23-Aug-2021, the patient experienced DIARRHOEA (diarrhea). On 21-Aug-2021, DECREASED APPETITE (loss of appetite) and PYREXIA (runned a fever of a 100) had resolved. On 22-Aug-2021, PAIN (pain) and MYALGIA (body aches/arm was sore) had resolved. On 24-Aug-2021, DIARRHOEA (diarrhea) had resolved. At the time of the report, NASOPHARYNGITIS (cold like symptoms mainly in nose and eyes), SINUS DISORDER (feels very sinusy but nose is not running), ALLERGY TO VACCINE (it feels like when you have an allergy) and FATIGUE (fatigue) outcome was unknown. Patient is immunocompromised since she had her spleen removed No treatment information was received This case was linked to MOD-2021-295308 (Patient Link).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: No medical history was reported
Andere Medikamente: CLONAZEPAM
Allergien: -
Vorherige Impfungen: -

VAERS 1662463

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038k20a

mild

Staat: MI
Alter: 69,0
Geschlecht: F
Eingang: 01.09.2021
Impfdatum: 08.03.2021
Beginn: 06.04.2021
Tage bis Beginn: 29,0
Dosis: 2
Route/Site: IM / LA

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

Chills Decreased appetite Headache Lethargy

Symptomtext

Every 27-29 days since my last shot on March 8, I get a combination of headache, lethargy, no appetite and chills.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Stem cell transplant survivor 2-19-2014 Stage 3 kidney disease Neuropathy Ocular migraines Macular degeneration Suppressed immune system Cataracts Follicular lymphoma-cured by stem cell transplant
Andere Medikamente: Nebupent, albuteral, cod liver oil, valcyclovier, multi vitamin, magnesium, lutein, zeaxanthin, vit d
Allergien: Dapsone Tegaderm patches Ursodiol Tramadol
Vorherige Impfungen: -

VAERS 1645346

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: IL
Alter: 61,0
Geschlecht: M
Eingang: 28.08.2021
Impfdatum: 27.01.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: OT / -

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

Blindness Diplopia Eye disorder Pain Photophobia

Symptomtext

Legally blind in both eyes; In pain; Had double & triple vision; Extreme light sensitivity; Multiple diseases on multiple layers of his eyes; This spontaneous case was reported by a consumer and describes the occurrence of BLINDNESS (Legally blind in both eyes), PAIN (In pain), DIPLOPIA (Had double & triple vision), PHOTOPHOBIA (Extreme light sensitivity) and EYE DISORDER (Multiple diseases on multiple layers of his eyes) in a 61-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 007M20A, 038K20A and 052E21A) for COVID-19 vaccination. The patient's past medical history included Eye discomfort (Patient has history of eye problems dating back 30years) in 1991, Blepharoconjunctivitis, unspecified and Uveitis. Concurrent medical conditions included Immunocompromised. Concomitant products included PREDNISONE for an unknown indication. 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. On 16-Aug-2021, received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On an unknown date, the patient experienced BLINDNESS (Legally blind in both eyes) (seriousness criteria hospitalization and medically significant), PAIN (In pain) (seriousness criterion hospitalization), DIPLOPIA (Had double & triple vision) (seriousness criterion hospitalization), PHOTOPHOBIA (Extreme light sensitivity) (seriousness criterion hospitalization) and EYE DISORDER (Multiple diseases on multiple layers of his eyes) (seriousness criterion hospitalization). At the time of the report, BLINDNESS (Legally blind in both eyes), PAIN (In pain), DIPLOPIA (Had double & triple vision), PHOTOPHOBIA (Extreme light sensitivity) and EYE DISORDER (Multiple diseases on multiple layers of his eyes) was resolving. Patient went to Clinic, Hospital, and a another major eye clinic for treatment after the 2nd shot & they never connected it with the vaccine. They found multiple diseases on multiple layers of his eyes. No treatment information was provided. It was reported that within 24hrs of receiving the 3rd dose patient was bedridden 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. This case was linked to MOD-2021-292150 (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.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Immunocompromised
Vorgeschichte: Medical History/Concurrent Conditions: Blepharoconjunctivitis, unspecified; Eye discomfort (Patient has history of eye problems dating back 30years); Uveitis
Andere Medikamente: PREDNISONE
Allergien: -
Vorherige Impfungen: -

VAERS 1644603

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: IL
Alter: 78,0
Geschlecht: M
Eingang: 28.08.2021
Impfdatum: 04.02.2021
Beginn: 05.03.2021
Tage bis Beginn: 29,0
Dosis: 1
Route/Site: OT / -

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

Body temperature Fatigue Feeling abnormal Oropharyngeal pain Pain in extremity Poor quality sleep Rhinorrhoea

Symptomtext

today I feel kind of tired; last night I felt kind of bad; I didn't sleep well; developed a runny nose; sore throat; arm was a little sore; This spontaneous case was reported by a consumer and describes the occurrence of PAIN IN EXTREMITY (arm was a little sore), RHINORRHOEA (developed a runny nose), OROPHARYNGEAL PAIN (sore throat), FEELING ABNORMAL (last night I felt kind of bad) and POOR QUALITY SLEEP (I didn't sleep well) in a 78-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 012A21A and 038K20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concomitant products included AMLODIPINE, LOVASTATIN, ESOMEPRAZOLE MAGNESIUM TRIHYDRATE (NEXIUM [ESOMEPRAZOLE MAGNESIUM TRIHYDRATE]) and LISINOPRIL for an unknown indication. On 04-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 04-Mar-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 05-Mar-2021, the patient experienced PAIN IN EXTREMITY (arm was a little sore). On 08-Aug-2021, the patient experienced RHINORRHOEA (developed a runny nose) and OROPHARYNGEAL PAIN (sore throat). On 09-Aug-2021, the patient experienced FEELING ABNORMAL (last night I felt kind of bad) and POOR QUALITY SLEEP (I didn't sleep well). On 10-Aug-2021, the patient experienced FATIGUE (today I feel kind of tired). On 05-Mar-2021, PAIN IN EXTREMITY (arm was a little sore) had resolved. At the time of the report, RHINORRHOEA (developed a runny nose), OROPHARYNGEAL PAIN (sore throat), FEELING ABNORMAL (last night I felt kind of bad), POOR QUALITY SLEEP (I didn't sleep well) and FATIGUE (today I feel kind of tired) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): In August 2021, Body temperature: 98.6 (High) usually around 97.7 degrees Fahrenheit and it increased to 98.6 degrees Fahrenheit. No treatment medications was provided by reporter. On 09-AUG-2021 patient felt a little uncomfortable. This case was linked to MOD-2021-282798 (Patient Link).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Test Date: 202108; Test Name: Body temperature; Result Unstructured Data: usually around 97.7 degrees Fahrenheit and it increased to 98.6 degrees Fahrenheit
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: AMLODIPINE; LOVASTATIN; NEXIUM [ESOMEPRAZOLE MAGNESIUM TRIHYDRATE]; LISINOPRIL
Allergien: -
Vorherige Impfungen: -

VAERS 1644601

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: IL
Alter: 78,0
Geschlecht: M
Eingang: 28.08.2021
Impfdatum: 04.02.2021
Beginn: 04.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / -

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

Vaccination site pain

Symptomtext

arm was little sore; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION SITE PAIN (arm was little sore) in a 78-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 012A21A and 038K20A) for COVID-19 vaccination. Concomitant products included AMLODIPINE, LOVASTATIN, ESOMEPRAZOLE MAGNESIUM (NEXIUM [ESOMEPRAZOLE MAGNESIUM]) and LISINOPRIL for an unknown indication. On 04-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 04-Mar-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 04-Feb-2021, the patient experienced VACCINATION SITE PAIN (arm was little sore). On 05-Feb-2021, VACCINATION SITE PAIN (arm was little sore) had resolved. No treatment medications were provided This case was linked to MOD-2021-282847 (Patient Link).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Vaccination site pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: AMLODIPINE; LOVASTATIN; NEXIUM [ESOMEPRAZOLE MAGNESIUM]; LISINOPRIL
Allergien: -
Vorherige Impfungen: -

VAERS 1636398

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: FL
Alter: 79,0
Geschlecht: M
Eingang: 26.08.2021
Impfdatum: 02.02.2021
Beginn: 25.07.2021
Tage bis Beginn: 173,0
Dosis: UNK
Route/Site: IM / -

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

Malaise Myalgia Productive cough Pyrexia SARS-CoV-2 test

Symptomtext

Fever 102, productive cough, malaise, myalgia x 1 week.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: Covid test
Aktuelle Erkrankungen: -
Vorgeschichte: Acid reflux, angina, anxiety, HTN, vagotomy.
Andere Medikamente: -
Allergien: NKA
Vorherige Impfungen: -

VAERS 1636349

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: OH
Alter: 89,0
Geschlecht: M
Eingang: 26.08.2021
Impfdatum: 24.02.2021
Beginn: 25.08.2021
Tage bis Beginn: 182,0
Dosis: 1
Route/Site: IM / LA

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

COVID-19 Cough Dizziness Nausea Respiratory tract congestion SARS-CoV-2 test positive Vaccine breakthrough infection Vomiting

Symptomtext

Breakthrough COVID admission in fully vaccinated patient. Presented with dizziness, nausea, vomiting, 2 week history of cough and congestion. SpO2 96% on room air

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: 8/25 SARS-CoV-2 detected
Aktuelle Erkrankungen: -
Vorgeschichte: arthritis, BPH, DVT, diabetes
Andere Medikamente: unknown
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1634947

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: NJ
Alter: 22,0
Geschlecht: F
Eingang: 26.08.2021
Impfdatum: 25.01.2021
Beginn: 25.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / LA

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

Myalgia Vaccination site erythema Vaccination site mass

Symptomtext

small lump, like a ball at the injection site; It is red; muscle soreness in the arm of the injection; This spontaneous case was reported by a pharmacist and describes the occurrence of MYALGIA (muscle soreness in the arm of the injection), VACCINATION SITE MASS (small lump, like a ball at the injection site) and VACCINATION SITE ERYTHEMA (It is red) in a 22-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. No Medical History information was reported. On 25-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 25-Jan-2021, the patient experienced MYALGIA (muscle soreness in the arm of the injection). On 02-Feb-2021, the patient experienced VACCINATION SITE MASS (small lump, like a ball at the injection site) and VACCINATION SITE ERYTHEMA (It is red). At the time of the report, MYALGIA (muscle soreness in the arm of the injection) had resolved and VACCINATION SITE MASS (small lump, like a ball at the injection site) and VACCINATION SITE ERYTHEMA (It is red) outcome was unknown. Not Provided The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. No treatment information was provided. No relevant concomitant medications were reported.

Weitere VAERSDATA-Felder

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

VAERS 1631477

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: MI
Alter: 72,0
Geschlecht: F
Eingang: 25.08.2021
Impfdatum: 03.02.2021
Beginn: 10.02.2021
Tage bis Beginn: 7,0
Dosis: 1
Route/Site: OT / -

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

Erythema Pruritus Rash

Symptomtext

itchiness; rash; redness; This spontaneous case was reported by a consumer and describes the occurrence of PRURITUS (itchiness), RASH (rash) and ERYTHEMA (redness) in a 72-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. No medical history was provided by the reporter. . Concomitant products included ACETYLSALICYLIC ACID (BABY ASPIRIN), METOPROLOL and CALCIUM CARBONATE, COLECALCIFEROL (VITAMIN D 2000) for an unknown indication. On 03-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 10-Feb-2021, the patient experienced PRURITUS (itchiness), RASH (rash) and ERYTHEMA (redness). On 11-Feb-2021, PRURITUS (itchiness) and ERYTHEMA (redness) had resolved. At the time of the report, RASH (rash) 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.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: No medical history was provided by the reporter.
Andere Medikamente: BABY ASPIRIN; METOPROLOL; VITAMIN D 2000
Allergien: -
Vorherige Impfungen: -

VAERS 1631464

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: -
Alter: -
Geschlecht: U
Eingang: 25.08.2021
Impfdatum: 02.03.2021
Beginn: 03.03.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: OT / -

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

Chills Fatigue Pain in extremity Pyrexia

Symptomtext

Fever of 100.6F; chills; fatigue; sore arm; This spontaneous case was reported by a consumer and describes the occurrence of PYREXIA (Fever of 100.6F), CHILLS, FATIGUE (fatigue) and PAIN IN EXTREMITY (sore arm) in a 79-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. No medical history was provided by the reporter. On 02-Mar-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 03-Mar-2021, the patient experienced PYREXIA (Fever of 100.6F), CHILLS, FATIGUE (fatigue) and PAIN IN EXTREMITY (sore arm). At the time of the report, PYREXIA (Fever of 100.6F), CHILLS, FATIGUE (fatigue) and PAIN IN EXTREMITY (sore arm) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. No concomitant medications reported. No treatment reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: No medical history was provided by the reporter
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1631329

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: -
Alter: 76,0
Geschlecht: F
Eingang: 25.08.2021
Impfdatum: 03.02.2021
Beginn: 04.02.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: OT / -

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

Arthralgia Bedridden Chills Fatigue Myalgia

Symptomtext

In bed all day; Fatigue; Chills; Muscle pain; Joint pain; This spontaneous case was reported by a physician and describes the occurrence of BEDRIDDEN (In bed all day), FATIGUE (Fatigue), CHILLS (Chills), MYALGIA (Muscle pain) and ARTHRALGIA (Joint pain) in a 76-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. The patient's past medical history included No adverse event. Concomitant products included INSULIN for an unknown indication. On 03-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 04-Feb-2021, the patient experienced BEDRIDDEN (In bed all day), FATIGUE (Fatigue), CHILLS (Chills), MYALGIA (Muscle pain) and ARTHRALGIA (Joint pain). On 05-Feb-2021, BEDRIDDEN (In bed all day), FATIGUE (Fatigue), CHILLS (Chills), MYALGIA (Muscle pain) and ARTHRALGIA (Joint pain) 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 included Tylenol; 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: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: No adverse event
Andere Medikamente: INSULIN
Allergien: -
Vorherige Impfungen: -

VAERS 1626502

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: NJ
Alter: -
Geschlecht: F
Eingang: 24.08.2021
Impfdatum: 09.02.2021
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: OT / -

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

Arthralgia Asthenia Discomfort Fatigue Gait disturbance Myalgia Pain in extremity Pyrexia

Symptomtext

very weak; bones and body started to ache a lot; slight fever; she couldn't even walk, now she can't walk; pain in her left leg, it burns like fire; shoulder hurts, her neck; extremely exhausted; sensation; This spontaneous case was reported by a consumer and describes the occurrence of ASTHENIA (very weak), MYALGIA (bones and body started to ache a lot), PYREXIA (slight fever), GAIT DISTURBANCE (she couldn't even walk, now she can't walk) and PAIN IN EXTREMITY (pain in her left leg, it burns like fire) in a 66-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for an unknown indication. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 09-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1. On an unknown date, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) at an unspecified dose. On an unknown date, the patient experienced ASTHENIA (very weak), MYALGIA (bones and body started to ache a lot), PYREXIA (slight fever), GAIT DISTURBANCE (she couldn't even walk, now she can't walk), PAIN IN EXTREMITY (pain in her left leg, it burns like fire), ARTHRALGIA (shoulder hurts, her neck), FATIGUE (extremely exhausted) and DISCOMFORT (sensation). Not Provided The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) and mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown Route) was unknown. Reporter did not allow further contact

Weitere VAERSDATA-Felder

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

VAERS 1622398

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: MI
Alter: 68,0
Geschlecht: M
Eingang: 23.08.2021
Impfdatum: 06.02.2021
Beginn: 06.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / -

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

Arthralgia

Symptomtext

Soreness in my shoulder; This spontaneous case was reported by a patient and describes the occurrence of ARTHRALGIA (Soreness in my shoulder) in a 68-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. The patient's past medical history included Stent placement. Concurrent medical conditions included Hypercholesterolemia. Concomitant products included ATORVASTATIN for Hypercholesterolemia, CLOPIDOGREL for Stent placement, LISINOPRIL and METOPROLOL for an unknown indication. On 06-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 06-Feb-2021, the patient experienced ARTHRALGIA (Soreness in my shoulder). The patient was treated with CAFFEINE, PARACETAMOL (EXCEDRIN [CAFFEINE;PARACETAMOL]) at an unspecified dose and frequency and MENTHOL, METHYL SALICYLATE (ARTHRITIS HOT) at an unspecified dose and frequency. At the time of the report, ARTHRALGIA (Soreness in my shoulder) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. This case was linked to MOD-2021-211636 (Patient Link).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Hypercholesterolemia
Vorgeschichte: Medical History/Concurrent Conditions: Stent placement
Andere Medikamente: LISINOPRIL; METOPROLOL; ATORVASTATIN; CLOPIDOGREL
Allergien: -
Vorherige Impfungen: -

VAERS 1621635

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: FL
Alter: 80,0
Geschlecht: M
Eingang: 23.08.2021
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: UNK
Route/Site: OT / -

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

Balance disorder Dizziness Fall Injury

Symptomtext

Extremely, extremely dizzy; Lost his balance; Had a serious fall; Fell and hurt himself; This spontaneous case was reported by a consumer and describes the occurrence of DIZZINESS (Extremely, extremely dizzy), BALANCE DISORDER (Lost his balance), FALL (Had a serious fall) and INJURY (Fell and hurt himself) in an 80-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced DIZZINESS (Extremely, extremely dizzy), BALANCE DISORDER (Lost his balance), FALL (Had a serious fall) and INJURY (Fell and hurt himself). At the time of the report, DIZZINESS (Extremely, extremely dizzy), BALANCE DISORDER (Lost his balance), FALL (Had a serious fall) and INJURY (Fell and hurt himself) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. No concomitant medications were provided. Treatment medications were unknown. Most recent FOLLOW-UP information incorporated above includes: On 03-Jun-2021: Follow-up information received on 03-JUN-2021 contains significant information: Added new event "Hurt".

Weitere VAERSDATA-Felder

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

VAERS 1621361

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038k20a

mild

Staat: IL
Alter: 78,0
Geschlecht: M
Eingang: 23.08.2021
Impfdatum: 22.01.2021
Beginn: 26.02.2021
Tage bis Beginn: 35,0
Dosis: 2
Route/Site: - / LA

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

Chills Decreased activity Dry skin Movement disorder Oedema peripheral Pityriasis rubra pilaris Rash Rash erythematous Rash pruritic Skin exfoliation

Symptomtext

Dry skin after 2nd dose; Pityriasis rubra pilaris (PRP) after 2nd dose; Legs and feet swelled up after 2nd dose; Can't even get into his tractor after 2nd dose; Not as active after 2nd dose/he was very active, but not so much now; Skin just flakes off after 2nd dose; Shivering after 2nd dose; itched and scratched until he couldn't take it; Red rash all over his entire body after 2nd dose; Red rash all over his entire body after 2nd dose \it is getting worse and is getting on his ears and eyelids now; This spontaneous case was reported by a patient (subsequently medically confirmed) and describes the occurrence of RASH PRURITIC (itched and scratched until he couldn't take it), DRY SKIN (Dry skin after 2nd dose), PITYRIASIS RUBRA PILARIS (Pityriasis rubra pilaris (PRP) after 2nd dose), OEDEMA PERIPHERAL (Legs and feet swelled up after 2nd dose) and MOVEMENT DISORDER (Can't even get into his tractor after 2nd dose) in a 78-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 038k20a and 013m20a) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included Bypass surgery. On 22-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 25-Feb-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 26-Feb-2021, the patient experienced RASH PRURITIC (itched and scratched until he couldn't take it), RASH ERYTHEMATOUS (Red rash all over his entire body after 2nd dose) and RASH (Red rash all over his entire body after 2nd dose \it is getting worse and is getting on his ears and eyelids now). On an unknown date, the patient experienced DRY SKIN (Dry skin after 2nd dose), PITYRIASIS RUBRA PILARIS (Pityriasis rubra pilaris (PRP) after 2nd dose), OEDEMA PERIPHERAL (Legs and feet swelled up after 2nd dose), MOVEMENT DISORDER (Can't even get into his tractor after 2nd dose), DECREASED ACTIVITY (Not as active after 2nd dose/he was very active, but not so much now), SKIN EXFOLIATION (Skin just flakes off after 2nd dose) and CHILLS (Shivering after 2nd dose). The patient was treated with TRIAMCINOLONE ACETONIDE (KENALOG [TRIAMCINOLONE ACETONIDE]) for Adverse event, at an unspecified dose and frequency and ADALIMUMAB (HUMIRA) for Adverse event, at an unspecified dose and frequency. At the time of the report, RASH PRURITIC (itched and scratched until he couldn't take it), DRY SKIN (Dry skin after 2nd dose), PITYRIASIS RUBRA PILARIS (Pityriasis rubra pilaris (PRP) after 2nd dose), OEDEMA PERIPHERAL (Legs and feet swelled up after 2nd dose), MOVEMENT DISORDER (Can't even get into his tractor after 2nd dose), DECREASED ACTIVITY (Not as active after 2nd dose/he was very active, but not so much now), SKIN EXFOLIATION (Skin just flakes off after 2nd dose), RASH ERYTHEMATOUS (Red rash all over his entire body after 2nd dose), RASH (Red rash all over his entire body after 2nd dose \it is getting worse and is getting on his ears and eyelids now) and CHILLS (Shivering after 2nd dose) outcome was unknown. No concomitant medications were reported. The patient went to the emergency room on 04Mar2021. The patient was given a steroid shot called Kenalog and ointment. The patient reported it didn't help and he went to the dermatologist that week. He says he got another steroid shot and more prescriptions, which didn't help. He went to another dermatologist and then went to a specialist who diagnosed it as pityriasis rubra pilaris (PRP) and that it was a reaction to the vaccine. The patient reported his wife was sweating and he was shivering. Caller's wife was also on the phone and reported that the PRP could go into remission, but would never go away. She also reported the doctor said that he should not get any more COVID-19 vaccines. She reported he had no allergies.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Bypass surgery
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1620902

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: FL
Alter: 68,0
Geschlecht: U
Eingang: 23.08.2021
Impfdatum: 27.01.2021
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: OT / LA

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

Chills Injection site erythema Nausea

Symptomtext

chills; nausea; Local Erythema; This spontaneous case was reported by a consumer and describes the occurrence of CHILLS (chills), NAUSEA (nausea) and INJECTION SITE ERYTHEMA (Local Erythema) in a 68-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 031M20A and 038K20A) for COVID-19 vaccination. The patient's past medical history included Vomiting, Stomach cramps and Wheezing. Concurrent medical conditions included Crohns disease aggravated since July 2012, Allergy to molds, Drug allergy (Allergic to Demerol induced vomiting and pass out), Allergic reaction to antibiotics (Allergic to Augmentin) and Asthma. Concomitant products included MESALAZINE (LIALDA) for Crohn's, ESTRADIOL (VAGIFEM) from 2018 to an unknown date for Dryness of eyes, LANSOPRAZOLE (PREVACID) from 2000 to an unknown date for Reflux esophagitis, L-THYROXINE [LEVOTHYROXINE] for Thyroid disorder. On 27-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 27-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 CHILLS (chills), NAUSEA (nausea) and INJECTION SITE ERYTHEMA (Local Erythema). The patient was treated with DIPHENHYDRAMINE HYDROCHLORIDE (BENADRYL [DIPHENHYDRAMINE HYDROCHLORIDE]) from 27-Feb-2021 to 03-Mar-2021 at an unspecified dose and frequency and BISMUTH SUBSALICYLATE, CALCIUM CARBONATE (PEPTO BISMOL [BISMUTH SUBSALICYLATE;CALCIUM CARBONATE]) 28-Feb-2001 at an unspecified dose and frequency. On 04-Mar-2021, CHILLS (chills), NAUSEA (nausea) and INJECTION SITE ERYTHEMA (Local Erythema) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) was not applicable. This case was linked to MOD-2021-028875 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 30-Jun-2021: Non-Significant Follow-up; 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: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Allergic reaction to antibiotics (Allergic to Augmentin); Allergy to molds; Asthma; Crohns disease aggravated; Drug allergy (Allergic to Demerol induced vomiting and pass out)
Vorgeschichte: Medical History/Concurrent Conditions: Stomach cramps; Vomiting; Wheezing
Andere Medikamente: LIALDA; PREVACID; L-THYROXINE [LEVOTHYROXINE]; VAGIFEM
Allergien: -
Vorherige Impfungen: -

VAERS 1619086

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A.

mild

Staat: GA
Alter: 71,0
Geschlecht: F
Eingang: 22.08.2021
Impfdatum: 08.02.2021
Beginn: 09.02.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: OT / RA

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

Endoscopy Fatigue Mass Renal function test Sigmoidoscopy Vaccination site pain

Symptomtext

vaccination site pain; lump arm; Fatigue; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION SITE PAIN (vaccination site pain), MASS (lump arm) and FATIGUE (Fatigue) in a 71-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 038K20A. and 002A21A) for COVID-19 vaccination. The patient's past medical history included Kidney transplant and Urinary tract infection from 20-May-2021 to 21-May-2021. Concomitant products included RABEPRAZOLE for Acid reflux (oesophageal), CEVIMELINE for Dry mouth, VITAMIN B3, CRANBERRY [VACCINIUM MACROCARPON], CYANOCOBALAMIN (VITAMIN B12 [CYANOCOBALAMIN]), TACROLIMUS, MYCOPHENOLIC ACID, PREDNISONE, PRIMIDONE, ROSUVASTATIN CALCIUM, FLUOXETINE HYDROCHLORIDE (PROZAC), LORAZEPAM (ATIVAN), HYDROCODONE, FLUTICASONE PROPIONATE, SALMETEROL XINAFOATE (ADVAIR) and SALBUTAMOL SULFATE (PROAIR [SALBUTAMOL SULFATE]) for an unknown indication. On 08-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 08-Mar-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 09-Feb-2021, the patient experienced VACCINATION SITE PAIN (vaccination site pain), MASS (lump arm) and FATIGUE (Fatigue). The patient was treated with PARACETAMOL (TYLENOL) at an unspecified dose and frequency; FLUCONAZOLE (DIFLUCAN) at an unspecified dose and frequency; ONDANSETRON (ZOFRAN [ONDANSETRON]) at an unspecified dose and frequency; PROMETHAZINE (PHENERGAN [PROMETHAZINE]) at an unspecified dose and frequency; PHOSPHORUS at an unspecified dose and frequency and DOXYCYCLINE at an unspecified dose and frequency. On 16-Feb-2021, VACCINATION SITE PAIN (vaccination site pain) and MASS (lump arm) had resolved. At the time of the report, FATIGUE (Fatigue) had not resolved. Not Provided DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 12-Apr-2021, Endoscopy: candida candida in her throat. On an unknown date, Renal function test: normal normal (normal) normal. On an unknown date, Sigmoidoscopy: normal normal (normal) normal. Treatment information also included fluids. This case was linked to MOD-2021-169159 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 25-May-2021: follow up received on 25-may-2021 contains Non significant follow up

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Test Date: 20210412; Test Name: endoscopy; Result Unstructured Data: candida in her throat; Comments: candida in her throat; Test Name: kidney function test; Result Unstructured Data: normal; Test Name: flex sigmoidoscopy; Result Unstructured Data: normal
Aktuelle Erkrankungen: Urinary tract infection
Vorgeschichte: Medical History/Concurrent Conditions: Kidney transplant
Andere Medikamente: VITAMIN B3; CRANBERRY [VACCINIUM MACROCARPON]; VITAMIN B12 [CYANOCOBALAMIN]; TACROLIMUS; MYCOPHENOLIC ACID; PREDNISONE; CEVIMELINE; PRIMIDONE; RABEPRAZOLE; ROSUVASTATIN CALCIUM; PROZAC; ATIVAN; HYDROCODONE; ADVAIR; PROAIR [SALBUTAMOL SULFAT
Allergien: -
Vorherige Impfungen: -

VAERS 1616985

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: NY
Alter: 42,0
Geschlecht: F
Eingang: 22.08.2021
Impfdatum: 25.01.2021
Beginn: 07.03.2021
Tage bis Beginn: 41,0
Dosis: 2
Route/Site: OT / -

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

Mechanical urticaria

Symptomtext

Dermatographia all over body; This spontaneous case was reported by a consumer and describes the occurrence of MECHANICAL URTICARIA (Dermatographia all over body) in a 42-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 038K20A and 014M20A) for COVID-19 vaccination. No Medical History information was reported. On 25-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 01-Mar-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 07-Mar-2021, the patient experienced MECHANICAL URTICARIA (Dermatographia all over body). At the time of the report, MECHANICAL URTICARIA (Dermatographia all over body) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Treatment information was not provided. No concomitant medication was provided.

Weitere VAERSDATA-Felder

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

VAERS 1616716

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: FL
Alter: 91,0
Geschlecht: F
Eingang: 22.08.2021
Impfdatum: 29.01.2021
Beginn: 03.03.2021
Tage bis Beginn: 33,0
Dosis: 1
Route/Site: OT / -

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

Adverse drug reaction Erythema Pain Pruritus Skin discolouration Skin mass Swelling

Symptomtext

upper arm is still slightly pink in color with some small bumps; upper arm is still slightly pink in color with some small bumps; Patient had a bad reaction after the 2nd dose; Patient had a pain after the 2nd dose; Swelling; Redness; Itch; This spontaneous case was reported by a consumer and describes the occurrence of ADVERSE DRUG REACTION (Patient had a bad reaction after the 2nd dose), PAIN (Patient had a pain after the 2nd dose), SKIN DISCOLOURATION (upper arm is still slightly pink in color with some small bumps), SKIN MASS (upper arm is still slightly pink in color with some small bumps) and SWELLING (Swelling) in a 91-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 031M20A and 038K20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No medical history was provided by reporter. Concomitant products included ATENOLOL for Blood pressure management, PRAVASTATIN for Cholesterol, TRAVOPROST (TRAVATANZ) for Glaucoma, LEVOTHYROXINE for Thyroid disorder. On 29-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 26-Feb-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 2 dosage form. On 03-Mar-2021, the patient experienced SWELLING (Swelling). 03-Mar-2021, the patient experienced ERYTHEMA (Redness) and PRURITUS (Itch). On 26-Mar-2021, the patient experienced ADVERSE DRUG REACTION (Patient had a bad reaction after the 2nd dose). 26-Mar-2021, the patient experienced PAIN (Patient had a pain after the 2nd dose). On an unknown date, the patient experienced SKIN DISCOLOURATION (upper arm is still slightly pink in color with some small bumps) and SKIN MASS (upper arm is still slightly pink in color with some small bumps). On 09-Apr-2021, SWELLING (Swelling), ERYTHEMA (Redness) and PRURITUS (Itch) had resolved with sequelae. At the time of the report, ADVERSE DRUG REACTION (Patient had a bad reaction after the 2nd dose) and PAIN (Patient had a pain after the 2nd dose) had resolved and SKIN DISCOLOURATION (upper arm is still slightly pink in color with some small bumps) and SKIN MASS (upper arm is still slightly pink in color with some small bumps) had not resolved. No treatment medications were provided. Most recent FOLLOW-UP information incorporated above includes: On 19-Jul-2021: Patient DOB added, Updated suspect drug start date and Added batch/lot number , Added Concomitant medications and Added New events - Considered significant On 19-Jul-2021: significant follow up contains no new information.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: No medical history was provided by reporter
Andere Medikamente: TRAVATANZ; LEVOTHYROXINE; ATENOLOL; PRAVASTATIN
Allergien: -
Vorherige Impfungen: -

VAERS 1613766

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: PA
Alter: -
Geschlecht: F
Eingang: 22.08.2021
Impfdatum: 25.03.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

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

Asthenia Fatigue Influenza like illness

Symptomtext

This spontaneous case reported by a consumer, describes the occurrence of influenza-like illness (flu-like symptoms), asthenia (in bed for one whole day) and fatigue (extreme tiredness for about 3-4 days) in a female patient, of an unknown age, who received mRNA-1273 (Moderna COVID-19 vaccine, batch# 038K20A) for COVID-19 immunization. No medical history reported. On Mar 25, 2021, patient received the second dose of mRNA-1273 (Moderna COVID-19 vaccine), unknown route; 1 dosage form. On an unknown date, patient experienced influenza-like illness (flu-like symptoms), asthenia (in bed for one whole day) and fatigue (extreme tiredness for about 3-4 days). At the time of the report, influenza-like illness (flu-like symptoms), asthenia (in bed for one whole day) and fatigue (extreme tiredness for about 3-4 days) outcome: unknown/not provided The reporter did not provide any causality assessments. Treatment: Tylenol- didn't help. Concomitant product details not provided. This case linked to MOD-2021-039893 (patient link).

Weitere VAERSDATA-Felder

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

VAERS 1612905

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20a

mild

Staat: MI
Alter: 66,0
Geschlecht: F
Eingang: 22.08.2021
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

Pain in extremity

Symptomtext

sore arm; This spontaneous case was reported by a consumer and describes the occurrence of PAIN IN EXTREMITY (sore arm) in a 66-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20a) 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 09-Jan-2021, the patient experienced PAIN IN EXTREMITY (sore arm). At the time of the report, PAIN IN EXTREMITY (sore arm) outcome was unknown. mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosing remained unchanged. Concomitant medications included blood pressure and thyroid medications. No treatment information was provided.

Weitere VAERSDATA-Felder

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

VAERS 1609320

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: NJ
Alter: 66,0
Geschlecht: F
Eingang: 22.08.2021
Impfdatum: 09.02.2021
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: OT / LA

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

Arthralgia Burning sensation Malaise Neck pain Pain

Symptomtext

His leg burns and feels like a burn.; affected her to make her neck and the ball she had in her neck and clavicle; whole body hurts; she feels worse every day,; hip hurts; This spontaneous case was reported by a consumer and describes the occurrence of BURNING SENSATION (His leg burns and feels like a burn.), NECK PAIN (affected her to make her neck and the ball she had in her neck and clavicle), PAIN (whole body hurts), MALAISE (she feels worse every day,) and ARTHRALGIA (hip hurts) in a 66-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 030A21A and 038K20A) for COVID-19 vaccination. The patient's past medical history included Fall. On 09-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 09-Mar-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 BURNING SENSATION (His leg burns and feels like a burn.), NECK PAIN (affected her to make her neck and the ball she had in her neck and clavicle), PAIN (whole body hurts), MALAISE (she feels worse every day,) and ARTHRALGIA (hip hurts). At the time of the report, BURNING SENSATION (His leg burns and feels like a burn.), NECK PAIN (affected her to make her neck and the ball she had in her neck and clavicle), PAIN (whole body hurts), MALAISE (she feels worse every day,) and ARTHRALGIA (hip hurts) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medications were provided. Treatment medication included the vitamins and stopped taking anti-inflammatory drugs.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Fall
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1608606

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: IL
Alter: 76,0
Geschlecht: F
Eingang: 22.08.2021
Impfdatum: 05.02.2021
Beginn: 06.02.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: OT / -

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

Abdominal discomfort Pain Pain in extremity

Symptomtext

felt a little achy; felt a little off, described as having a little stomach upset; left arm hurt up in the muscle; This spontaneous case was reported by a consumer and describes the occurrence of PAIN (felt a little achy), ABDOMINAL DISCOMFORT (felt a little off, described as having a little stomach upset) and PAIN IN EXTREMITY (left arm hurt up in the muscle) in a 76-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 002A21A and 038K20A) for COVID-19 vaccination. The patient's past medical history included Pneumonia and Transplant (heart valve transplant). Concomitant products included CARVEDILOL, OMEPRAZOLE, ATORVASTATIN, ALLOPURINOL, PRIMIDONE and DULOXETINE for an unknown indication. On 05-Feb-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 06-Feb-2021, the patient experienced PAIN (felt a little achy), ABDOMINAL DISCOMFORT (felt a little off, described as having a little stomach upset) and PAIN IN EXTREMITY (left arm hurt up in the muscle). The patient was treated with PARACETAMOL (TYLENOL) at an unspecified dose and frequency. On 06-Feb-2021, PAIN (felt a little achy), ABDOMINAL DISCOMFORT (felt a little off, described as having a little stomach upset) and PAIN IN EXTREMITY (left arm hurt up in the muscle) had resolved. Not Provided For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. This case was linked to US-MODERNATX, INC.-MOD-2021-079337 (E2B Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2021-079337:

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Pneumonia; Transplant (heart valve transplant)
Andere Medikamente: CARVEDILOL; OMEPRAZOLE; ATORVASTATIN; ALLOPURINOL; PRIMIDONE; DULOXETINE
Allergien: -
Vorherige Impfungen: -

VAERS 1606841

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: FL
Alter: 79,0
Geschlecht: F
Eingang: 22.08.2021
Impfdatum: 29.01.2021
Beginn: 04.02.2021
Tage bis Beginn: 6,0
Dosis: 2
Route/Site: OT / -

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

Full blood count Heart rate irregular Night sweats Pruritus Rash Urine analysis Urticaria

Symptomtext

night sweats; irregular heartbeat; itchy; large welts/hives/hives on trunk of my body,and back of legs; Rash across my chest and rash all over my trunk and up and down my leg; This spontaneous case was reported by a consumer and describes the occurrence of NIGHT SWEATS (night sweats), HEART RATE IRREGULAR (irregular heartbeat), PRURITUS (itchy), URTICARIA (large welts/hives/hives on trunk of my body,and back of legs) and RASH (Rash across my chest and rash all over my trunk and up and down my leg) in a 79-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 038K20A and 031M20A) for COVID-19 vaccination. Concurrent medical conditions included Hypertension (BP) since 1996 and Drug allergy (Allergy to Sulphur). Concomitant products included IRBESARTAN from an unknown date to 23-Jun-2021 for Blood pressure high, 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]), VITAMIN B12 NOS and HYDROXYZINE HCL for an unknown indication. On 29-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) (unknown route) 1 dosage form. On 04-Feb-2021, the patient experienced NIGHT SWEATS (night sweats), HEART RATE IRREGULAR (irregular heartbeat), PRURITUS (itchy), URTICARIA (large welts/hives/hives on trunk of my body,and back of legs) and RASH (Rash across my chest and rash all over my trunk and up and down my leg). The patient was treated with METHYLPREDNISOLONE ongoing from 17-Feb-2021 for Allergy, at a dose of 4 milligram; CETIRIZINE HYDROCHLORIDE (ZYRTEC [CETIRIZINE HYDROCHLORIDE]) ongoing from 17-Feb-2021 at a dose of 10 milligram twice a day; OMALIZUMAB (XOLAIR) for Chronic idiopathic urticaria, at a dose of 300 milligram, 3 doses; DIPHENHYDRAMINE HYDROCHLORIDE (BENADRYL [DIPHENHYDRAMINE HYDROCHLORIDE]) on 15-Jun-2021 for Hives, at a dose of 1 dosage form once and DEXAMETHASONE ACETATE (DECADRON [DEXAMETHASONE ACETATE]) on 15-Jun-2021 for Hives, at a dose of 1 dosage form once. At the time of the report, NIGHT SWEATS (night sweats), HEART RATE IRREGULAR (irregular heartbeat), PRURITUS (itchy), URTICARIA (large welts/hives/hives on trunk of my body,and back of legs) and RASH (Rash across my chest and rash all over my trunk and up and down my leg) had not resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 31-Jan-2021, Full blood count: normal normal. On 31-Jan-2021, Urine analysis: high wbc count abnormal. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) and mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown Route) was unknown. Most recent FOLLOW-UP information incorporated above includes: On 19-Jul-2021: Follow-up information received on 20-Jul-2021. Events, patient information, treatment, and batch number updated.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: Test Date: 20210131; Test Name: CBC; Test Date: 20210131; Test Name: Urine analysis
Aktuelle Erkrankungen: Drug allergy (Allergy to Sulphur); Hypertension (BP)
Vorgeschichte: -
Andere Medikamente: CENTRUM SILVER [ASCORBIC ACID;CALCIUM;MINERALS NOS;RETINOL;TOCOPHERYL ACETATE;VITAMIN B NOS;VITAMINS; VITAMIN B12 NOS; HYDROXYZINE HCL; IRBESARTAN
Allergien: -
Vorherige Impfungen: -

VAERS 1606388

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: FL
Alter: 65,0
Geschlecht: M
Eingang: 22.08.2021
Impfdatum: 30.01.2021
Beginn: 27.02.2021
Tage bis Beginn: 28,0
Dosis: 2
Route/Site: OT / LA

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

Chills Dysstasia Feeling abnormal Hyperhidrosis Hypoaesthesia Night sweats Pain Peripheral swelling Pyrexia Tenderness

Symptomtext

Sweating; Soaking in bed; can't stand; feeling fuzzy; intermittent numbness in face; Pain; pain, tenderness, and swelling in arm; pain, tenderness, and swelling in arm; shivering/chills; High fever; This spontaneous case was reported by a consumer and describes the occurrence of HYPERHIDROSIS (Sweating), NIGHT SWEATS (Soaking in bed), DYSSTASIA (can't stand), FEELING ABNORMAL (feeling fuzzy) and HYPOAESTHESIA (intermittent numbness in face) in a 65-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 038K20A and 023M20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concomitant products included ALPRAZOLAM (XANAX) for an unknown indication. On 30-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 27-Feb-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 27-Feb-2021, the patient experienced HYPERHIDROSIS (Sweating), NIGHT SWEATS (Soaking in bed), DYSSTASIA (can't stand), FEELING ABNORMAL (feeling fuzzy), HYPOAESTHESIA (intermittent numbness in face), PAIN (Pain), TENDERNESS (pain, tenderness, and swelling in arm), PERIPHERAL SWELLING (pain, tenderness, and swelling in arm), CHILLS (shivering/chills) and PYREXIA (High fever). The patient was treated with IBUPROFEN (ADVIL [IBUPROFEN]) for Fever, at a dose of 1 dosage form and ACETAMINOPHEN for Fever, at a dose of 1 dosage form. At the time of the report, HYPERHIDROSIS (Sweating), NIGHT SWEATS (Soaking in bed), DYSSTASIA (can't stand), FEELING ABNORMAL (feeling fuzzy), HYPOAESTHESIA (intermittent numbness in face), PAIN (Pain), TENDERNESS (pain, tenderness, and swelling in arm), PERIPHERAL SWELLING (pain, tenderness, and swelling in arm), CHILLS (shivering/chills) and PYREXIA (High fever) outcome was unknown. Relevant concomitant medications included BP medications, thyroid medications,diabetic medications. Action taken with mRNA-1273 in response to the event was not applicable

Weitere VAERSDATA-Felder

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

VAERS 1605692

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: MI
Alter: 66,0
Geschlecht: F
Eingang: 22.08.2021
Impfdatum: 05.03.2021
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: OT / -

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

Arthralgia Neck pain Vaccination site pain

Symptomtext

Severe neck pain; Severe shoulder pain; Pain under the ampit at the injection site; This spontaneous case was reported by a consumer (subsequently medically confirmed) and describes the occurrence of NECK PAIN (Severe neck pain), ARTHRALGIA (Severe shoulder pain) and VACCINATION SITE PAIN (Pain under the ampit at the injection site) in a 66-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 015M20A and 038K20A) for COVID-19 vaccination. The patient's past medical history included No adverse event (No reported medical history). On 05-Mar-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 02-Apr-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 NECK PAIN (Severe neck pain), ARTHRALGIA (Severe shoulder pain) and VACCINATION SITE PAIN (Pain under the ampit at the injection site). The patient was treated with PARACETAMOL at an unspecified dose and frequency. At the time of the report, NECK PAIN (Severe neck pain), ARTHRALGIA (Severe shoulder pain) and VACCINATION SITE PAIN (Pain under the ampit at the injection site) outcome was unknown. No relevant concomitant medications were reported. Action taken with mRNA-1273 in response to the events was not applicable.

Weitere VAERSDATA-Felder

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

VAERS 1605451

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038k20a

mild

Staat: AZ
Alter: 73,0
Geschlecht: F
Eingang: 22.08.2021
Impfdatum: 05.02.2021
Beginn: 12.02.2021
Tage bis Beginn: 7,0
Dosis: 1
Route/Site: OT / -

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

Pruritus Vaccination site reaction

Symptomtext

"COVID arm"; itchiness; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION SITE REACTION ("COVID arm") and PRURITUS (itchiness) in a 74-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038k20a) for COVID-19 vaccination. Concurrent medical conditions included Cholesterol and Blood pressure. On 05-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 12-Feb-2021, the patient experienced VACCINATION SITE REACTION ("COVID arm") and PRURITUS (itchiness). On 19-Feb-2021, VACCINATION SITE REACTION ("COVID arm") and PRURITUS (itchiness) had resolved. Not Provided The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Patient was scarred to take the second dose and therefore she decided not to take it. Concomitant products included were blood pressure meds ,cholesterol meds. Treatment included antihistamines and "put ice on it".; 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: Pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Blood pressure; Cholesterol.
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1602146

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: -
Alter: -
Geschlecht: M
Eingang: 21.08.2021
Impfdatum: 01.03.2021
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: OT / -

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

Burning sensation Chills Feeling abnormal Feeling hot Pain

Symptomtext

was burning up; certain parts of his body were hot like stomach and back; still feels achy; run down; had chills; This case was received via an unknown source (no reference has been entered for a health authority or license partner) on 30-Mar-2021 and was forwarded to Moderna on 30-Mar-2021. This spontaneous case was reported by a consumer and describes the occurrence of BURNING SENSATION (was burning up), FEELING HOT (certain parts of his body were hot like stomach and back), PAIN (still feels achy), FEELING ABNORMAL (run down) and CHILLS (had chills) in a male patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 038K20A and 038K20A) for COVID-19 vaccination. The patient's past medical history included No adverse event. On 01-Mar-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 29-Mar-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On an unknown date, the patient experienced BURNING SENSATION (was burning up), FEELING HOT (certain parts of his body were hot like stomach and back), PAIN (still feels achy), FEELING ABNORMAL (run down) and CHILLS (had chills). At the time of the report, BURNING SENSATION (was burning up), FEELING HOT (certain parts of his body were hot like stomach and back), PAIN (still feels achy), FEELING ABNORMAL (run down) and CHILLS (had chills) outcome was unknown. No concomitant medication provided. Patient received Tylenol treatment for the symptoms. Patient has registered for Vsafe. Reporter did not allow further contact

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: No adverse event
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1600990

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: -
Alter: -
Geschlecht: F
Eingang: 21.08.2021
Impfdatum: 01.03.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: OT / -

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

Arthralgia Back pain Feeling abnormal

Symptomtext

her hips and back hurt a little bit; felt run down; her hips and back hurt a little bit; This spontaneous case was reported by a consumer and describes the occurrence of BACK PAIN (her hips and back hurt a little bit), FEELING ABNORMAL (felt run down) and ARTHRALGIA (her hips and back hurt a little bit) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 038K20A and 038K20A) for COVID-19 vaccination. No Medical History information was reported. On 01-Mar-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 29-Mar-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On an unknown date, the patient experienced BACK PAIN (her hips and back hurt a little bit), FEELING ABNORMAL (felt run down) and ARTHRALGIA (her hips and back hurt a little bit). At the time of the report, BACK PAIN (her hips and back hurt a little bit), FEELING ABNORMAL (felt run down) and ARTHRALGIA (her hips and back hurt a little bit) outcome was unknown. No Concomitant medications were provided No Treatment information provided This case was linked to MOD21-065465, MOD-2021-065604 (E2B Linked Report). Reporter did not allow further contact; Sender's Comments: MOD21-065465:cross link MOD-2021-065604:Crosslinked

Weitere VAERSDATA-Felder

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

VAERS 1600572

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: MI
Alter: 74,0
Geschlecht: F
Eingang: 21.08.2021
Impfdatum: 09.02.2021
Beginn: 10.03.2021
Tage bis Beginn: 29,0
Dosis: 1
Route/Site: OT / RA

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

Pain in extremity Rash Vaccination site erythema

Symptomtext

Arm was sore; Rash on neck, chest, and both arms; arms were red; This spontaneous case was reported by a consumer and describes the occurrence of PAIN IN EXTREMITY (Arm was sore), RASH (Rash on neck, chest, and both arms) and VACCINATION SITE ERYTHEMA (arms were red) in a 74-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 030A21A and 038K20A) for COVID-19 vaccination. No Medical History information was reported. On 09-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 10-Mar-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 10-Mar-2021, the patient experienced PAIN IN EXTREMITY (Arm was sore), RASH (Rash on neck, chest, and both arms) and VACCINATION SITE ERYTHEMA (arms were red). The patient was treated with PARACETAMOL (TYLENOL) for Pain in arm, at a dose of 1 dosage form. On 11-Mar-2021, RASH (Rash on neck, chest, and both arms) and VACCINATION SITE ERYTHEMA (arms were red) had resolved. On 12-Mar-2021, PAIN IN EXTREMITY (Arm was sore) had resolved. Not Provided Concomitant medication information was not reported. Treatment- Ibuprofen Action taken with mRNA-1273 (Moderna COVID-19 Vaccine) is considered as not applicable. Most recent FOLLOW-UP information incorporated above includes: On 05-May-2021: Follow up was attached on 05 May 2021 and contains No NewInformation. On 22-Jun-2021: Follow up received on 22-JUN-2021:contains No new information

Weitere VAERSDATA-Felder

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

VAERS 1599336

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: NY
Alter: -
Geschlecht: F
Eingang: 21.08.2021
Impfdatum: 21.01.2021
Beginn: 31.01.2021
Tage bis Beginn: 10,0
Dosis: 2
Route/Site: OT / LA

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

Arthralgia Pain in extremity

Symptomtext

experienced pain in left arm; shoulder pain; This spontaneous case was reported by a consumer and describes the occurrence of PAIN IN EXTREMITY (experienced pain in left arm) and ARTHRALGIA ( shoulder pain) in a 78-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 038K20A and 004m20A) for COVID-19 vaccination. The patient's past medical history included No adverse event. Concomitant products included MELOXICAM (MOBIC), AMOXICILLIN TRIHYDRATE, CLARITHROMYCIN, ESOMEPRAZOLE MAGNESIUM (NEXIUM 1-2-3), ESTRADIOL (ESTROGEN), VITAMIN D NOS, ASCORBIC ACID, ROSA CANINA FRUIT (VITAMIN C & ROSEHIP), FISH OIL and CENTRUM SILVER +50 for an unknown indication. On 21-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .5 milliliter. On 18-Feb-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to .5 milliliter. On 31-Jan-2021, the patient experienced ARTHRALGIA ( shoulder pain). On 28-Feb-2021, the patient experienced PAIN IN EXTREMITY (experienced pain in left arm). The patient was treated with PARACETAMOL (TYLENOL) at an unspecified dose and frequency. At the time of the report, PAIN IN EXTREMITY (experienced pain in left arm) and ARTHRALGIA ( shoulder pain) outcome was unknown.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: MOBIC; NEXIUM 1-2-3; ESTROGEN; VITAMIN D NOS; VITAMIN C & ROSEHIP; FISH OIL; CENTRUM SILVER +50
Allergien: -
Vorherige Impfungen: -

VAERS 1597440

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: FL
Alter: 72,0
Geschlecht: F
Eingang: 21.08.2021
Impfdatum: 30.01.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: OT / -

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

Body temperature increased Chills Delusion Feeling of body temperature change Hyperhidrosis Influenza like illness Pyrexia Rash Unevaluable event

Symptomtext

Flue like symptoms but only stronger; system completely blocked; Sweats; Took it's clothes off because it was cold and hot; Delusional because of the fever; Rash on the arm; Chills, Shivering; Fever of 40?C; This spontaneous case was reported by a consumer and describes the occurrence of INFLUENZA LIKE ILLNESS (Flue like symptoms but only stronger), UNEVALUABLE EVENT (system completely blocked), HYPERHIDROSIS (Sweats), FEELING OF BODY TEMPERATURE CHANGE (Took it's clothes off because it was cold and hot) and DELUSION (Delusional because of the fever) in a 72-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 038K20A and 039K20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included COVID-19 in July 2020. Concurrent medical conditions included Hypertension. On 30-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 06-Mar-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 INFLUENZA LIKE ILLNESS (Flue like symptoms but only stronger), UNEVALUABLE EVENT (system completely blocked), HYPERHIDROSIS (Sweats), FEELING OF BODY TEMPERATURE CHANGE (Took it's clothes off because it was cold and hot), DELUSION (Delusional because of the fever), RASH (Rash on the arm), CHILLS (Chills, Shivering) and PYREXIA (Fever of 40?C). At the time of the report, INFLUENZA LIKE ILLNESS (Flue like symptoms but only stronger), UNEVALUABLE EVENT (system completely blocked), HYPERHIDROSIS (Sweats), FEELING OF BODY TEMPERATURE CHANGE (Took it's clothes off because it was cold and hot), DELUSION (Delusional because of the fever), RASH (Rash on the arm), CHILLS (Chills, Shivering) and PYREXIA (Fever of 40?C) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, Body temperature increased: 40 degree Celsius (Inconclusive) 40?C. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Patient was doing ok at the time of report. Products known to have been used by the patient, within two weeks prior to the event, included unspecified blood pressure pills. No treatment information was provided. This case was linked to MOD-2021-049333 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 05-May-2021: Clinical course information.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Test Name: Temperature; Result Unstructured Data: 40?C
Aktuelle Erkrankungen: Hypertension
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1596924

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: FL
Alter: 65,0
Geschlecht: M
Eingang: 21.08.2021
Impfdatum: 08.02.2021
Beginn: 08.03.2021
Tage bis Beginn: 28,0
Dosis: 2
Route/Site: OT / -

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

Myalgia Pain in extremity Pyrexia

Symptomtext

Sore arm; Fever; Muscle ache; This spontaneous case was reported by a consumer and describes the occurrence of PAIN IN EXTREMITY (Sore arm), PYREXIA (Fever) and MYALGIA (Muscle ache) in a 65-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 038K20A and 031M20A) for COVID-19 vaccination. No medical history was provided by the reporter. On 08-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 08-Mar-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 08-Mar-2021, the patient experienced PAIN IN EXTREMITY (Sore arm), PYREXIA (Fever) and MYALGIA (Muscle ache). At the time of the report, PAIN IN EXTREMITY (Sore arm), PYREXIA (Fever) and MYALGIA (Muscle ache) had not resolved. No treatment information was provided. No relevant concomitant medications were reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myalgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: No medical history was provided by the reporter.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1596719

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: PA
Alter: 79,0
Geschlecht: F
Eingang: 21.08.2021
Impfdatum: 05.02.2021
Beginn: 06.03.2021
Tage bis Beginn: 29,0
Dosis: 2
Route/Site: OT / -

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

Body temperature Headache Myalgia Pain in extremity Pyrexia

Symptomtext

sore arm; Fever; headache; muscle aches; This spontaneous case was reported by a consumer and describes the occurrence of PAIN IN EXTREMITY (sore arm), PYREXIA (Fever), HEADACHE (headache) and MYALGIA (muscle aches) in a 79-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 038K20A and 048A121A) for COVID-19 vaccination. No Medical History information was reported. On 05-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 05-Mar-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 06-Mar-2021, the patient experienced PAIN IN EXTREMITY (sore arm), PYREXIA (Fever), HEADACHE (headache) and MYALGIA (muscle aches). On 07-Mar-2021, PYREXIA (Fever) had resolved. At the time of the report, PAIN IN EXTREMITY (sore arm), HEADACHE (headache) and MYALGIA (muscle aches) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 06-Mar-2021, Body temperature: 101.2 (High) 101.2. No corrective treatment was reported

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: Test Date: 20210306; Test Name: body temperature; Result Unstructured Data: 101.2
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1596079

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: IL
Alter: 72,0
Geschlecht: F
Eingang: 21.08.2021
Impfdatum: 03.02.2021
Beginn: 12.02.2021
Tage bis Beginn: 9,0
Dosis: 1
Route/Site: OT / LA

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

Erythema Pruritus Urticaria

Symptomtext

itches , hives , and redness at the left arm; itches , hives , and redness at the left arm; itches , hives , and redness at the left arm; A spontaneous report was received from a consumer concerning a 72-years-old female patient who received Moderna's COVID-19 vaccine (mRNA-1273) and experienced events itches at the injection arm/pruritis, hives at the injection arm/Urticaria, redness at the injection arm/Erythema. The patient's medical history was not provided. No relevant concomitant medications were reported. On 3 Feb 2021, prior to the onset of the events the patient received their first of two planned doses of mRNA-1273 (lot/batch: unknown) intramuscularly in the left arm for prophylaxis of COVID-19 infection. On 12 Feb 2021, the patient experienced the event(s) itches, hives and redness at the left arm/pruritis . On 12 Feb 2021, the patient experienced the event(s) itches, hives and redness at the left arm/Urticaria . On 12 Feb 2021, the patient experienced the event(s) itches, hives and redness at the left arm/Erythema. . No treatment information was provided. Action taken with mRNA-1273 in response to the events was not reported. The outcome of event(s), itches at the injection arm was unknown.The outcome of event(s), hives at the injection arm was unknown.The outcome of event(s), redness at the injection arm was unknown..

Weitere VAERSDATA-Felder

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

VAERS 1596059

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: FL
Alter: 79,0
Geschlecht: F
Eingang: 21.08.2021
Impfdatum: 02.02.2021
Beginn: 13.02.2021
Tage bis Beginn: 11,0
Dosis: 1
Route/Site: OT / LA

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

Injection site discomfort Injection site induration Injection site swelling Insomnia

Symptomtext

woke up in middle of night; injection site hurt; injection site hard; injection site swelling; A spontaneous report was received from a Consumer concerning a 79-years-old female patient who received Moderna's COVID-19 vaccine (mRNA-1273) and experienced events woke up in the middle of the night, hurting injection site, hard injection site, swollen injection site. The patient's medical history was not provided. No relevant concomitant medications were reported. On 2 Feb 2021, prior to the onset of the events the patient received their first of two planned doses of mRNA-1273 (lot/batch: 038K20A) intramuscularly in the left arm for prophylaxis of COVID-19 infection. On 13 Feb 2021, the patient experienced the events woke up in the middle of the night. hurting injection site, hard injection site, swollen injection site. No treatment information was provided. Action taken with mRNA-1273 in response to the events were not applicable On an unknown date the outcome of events, woke up in the middle of the night, On an unknown date the outcome of events, hurting injection site, On an unknown date the outcome of events, hard injection site, On an unknown date the outcome of events, swollen injection site was not reported.

Weitere VAERSDATA-Felder

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

VAERS 1595725

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: MI
Alter: 86,0
Geschlecht: F
Eingang: 21.08.2021
Impfdatum: 12.02.2021
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: OT / LA

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

Injection site erythema Injection site mass Injection site pruritus

Symptomtext

arm red; arm hard lump; arm itchy; A spontaneous report was received from a consumer concerning a 86-years-old female patient who received Moderna's COVID-19 vaccine (mRNA-1273) and experienced events arm red(Injection site erythema), arm hard lump(Injection site mass), arm itchy(Injection site pruritus). The patient's medical history was not provided. No relevant concomitant medications were reported. On 12 Feb 2021, prior to the onset of the events the patient received their first of two planned doses of mRNA-1273 (lot/batch: 038K20A) intramuscularly in the left arm for prophylaxis of COVID-19 infection. Patient experienced arm red, arm hard lump, arm itchy. No treatment information was provided. Action taken with mRNA-1273 in response to the events was not reported. The outcome of event(s), arm red, arm hard lump,arm itchy was unknown.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: No adverse event
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1595706

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: MI
Alter: 75,0
Geschlecht: F
Eingang: 21.08.2021
Impfdatum: 05.02.2021
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: IM / RA

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

Injection site joint swelling Injection site pain

Symptomtext

This spontaneous case reported by a consumer, describes the occurrence of injection site pain (arm sore after the injection) and injection site joint swelling (bright pink circle around the injection site about 1 inch in diameter) in a 75-year-old female patient who received mRNA-1273 (Moderna COVID-19 vaccine, batch# 038K20A) for COVID-19 immunization. No medical history reported. On Feb 5, 2021, patient received the first dose of mRNA-1273 (Moderna COVID-19 vaccine), intramuscular; 1 dosage form. On an unknown date, patient experienced injection site pain (arm sore after the injection) and injection site joint swelling (bright pink circle around the injection site about 1 inch in diameter). At the time of the report, injection site pain (arm sore after the injection) and injection site joint swelling (bright pink circle around the injection site about 1 inch in diameter) outcome: unknown. The action taken with mRNA-1273 (Moderna COVID-19 vaccine), intramuscular: unknown. Products known to have been used by the patient within two weeks prior to the event, not reported. Treatment information not provided.

Weitere VAERSDATA-Felder

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

VAERS 1595141

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: PA
Alter: 68,0
Geschlecht: M
Eingang: 21.08.2021
Impfdatum: 28.01.2021
Beginn: 29.01.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: OT / -

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

Arthralgia Pruritus Vaccination site erythema

Symptomtext

Redness below injection site; 2 inches wide and 3 inches long; Itchy shoulder; Shoulder soreness; A spontaneous report was received from a consumer concerning a 68-years-old male patient who received Moderna's COVID-19 vaccine (mRNA-1273) and experienced shoulder soreness/ arthralgia, itchy shoulder/ pruritus, redness belowinjection site/ vaccination site erythema. The patient's medical history was not provided. Concomitant product use was not provided by the reporter. On 28 Jan 2021, prior to the onset of the events ,the patient received first of two planned doses of mRNA-1273 (Batch number: 038K20A) intramuscularly for prophylaxis of COVID-19 infection. On 29 Jan 2021, approximately 1 day after vaccination, the patient experienced shoulder soreness that lasted for few days and subsided. On 03 Feb 2021, the patient experienced itchy shoulder and 2 days later, on 5 Feb 2021, the patient discovered that area was itchy and red. The affected area was below the injection site and it was 2 inches wide and 3 inches long. The patient reported that the itchiness was subsided and redness was still there. Treatment for the events included Hydrocortisone, OTC Benadryl. Action taken with mRNA-1273 in response to the events was not reported. The outcome of events, shoulder soreness, itchy shoulder, were considered to be resolving at the time of report. the outcome of the event, redness below injection site, was considered not resolved at the time of report.

Weitere VAERSDATA-Felder

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

VAERS 1594872

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038k20a

mild

Staat: MI
Alter: 74,0
Geschlecht: M
Eingang: 21.08.2021
Impfdatum: 02.02.2021
Beginn: 04.02.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: OT / -

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

Diarrhoea

Symptomtext

Diarrhea; This spontaneous case was reported by a consumer and describes the occurrence of DIARRHOEA (Diarrhea) in a 74-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038k20a) for COVID-19 vaccination. No Medical History information was reported. On 02-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 04-Feb-2021, the patient experienced DIARRHOEA (Diarrhea). On 05-Feb-2021, DIARRHOEA (Diarrhea) had resolved. Not Provided The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. No treatment information was provided. No relevant concomitant medications reported.

Weitere VAERSDATA-Felder

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

VAERS 1581618

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: FL
Alter: -
Geschlecht: F
Eingang: 18.08.2021
Impfdatum: 02.02.2021
Beginn: 05.02.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: OT / -

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

Erythema Rash

Symptomtext

large red area on the arm; area was bumpy like a rash; A spontaneous report was received from a Consumer concerning a 83-years-old female patient who received Moderna's COVID-19 vaccine (mRNA-1273) and experienced events large red area on the arm(erythema), area was bumpy like a rash(rash). The patient's medical history was not provided. No relevant concomitant medications were reported. On 2 Feb 2021,approximately 4 days prior to the onset of the events the patient received their first of two planned doses of mRNA-1273 (lot/batch: 038K20A) intramuscularly in arm for prophylaxis of COVID-19 infection. On 5 Feb 2021, the patient experienced the event(s) large red area on the arm and area was bumpy like a rash. No treatment information was provided. Action taken with mRNA-1273 in response to the events was not reported. The outcome of event(s) large red area on the arm and area was bumpy like a rash was considered resolved on 15 Feb 2021. .

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: No adverse event
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1581428

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: IN
Alter: 83,0
Geschlecht: M
Eingang: 18.08.2021
Impfdatum: 02.02.2021
Beginn: 02.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / -

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

Erythema Pain Swelling Vaccination site mass

Symptomtext

Hard Lump,Lump increased in size; Pain; Redness,Redness became larger; Swelling; This spontaneous case was reported by a consumer and describes the occurrence of ERYTHEMA (Redness,Redness became larger), VACCINATION SITE MASS (Hard Lump,Lump increased in size), SWELLING (Swelling) and PAIN (Pain) in an 83-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. The patient's past medical history included No adverse event. On 02-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 02-Feb-2021, the patient experienced ERYTHEMA (Redness,Redness became larger) and SWELLING (Swelling). On 03-Feb-2021, the patient experienced VACCINATION SITE MASS (Hard Lump,Lump increased in size) and PAIN (Pain). At the time of the report, ERYTHEMA (Redness,Redness became larger), VACCINATION SITE MASS (Hard Lump,Lump increased in size), SWELLING (Swelling) and PAIN (Pain) outcome was unknown. Not Provided The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: No adverse event
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1581064

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038k20A

mild

Staat: IL
Alter: 59,0
Geschlecht: F
Eingang: 18.08.2021
Impfdatum: 24.01.2021
Beginn: 25.01.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: OT / LA

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

Back pain Chills Fatigue Injection site erythema Malaise Pain in extremity Pyrexia

Symptomtext

severe spine pain; felt really tired; could not get out of bed; exhausted; arm a little red; chills; arm sore; fever; slept the entire next day; This spontaneous case was reported by a health care professional (subsequently medically confirmed) and describes the occurrence of BACK PAIN (severe spine pain), MALAISE (felt really tired), FATIGUE (could not get out of bed; exhausted), INJECTION SITE ERYTHEMA (arm a little red) and CHILLS (chills) in a 59-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 026L20A and 038k20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No medical history reported. Concomitant products included ASCORBIC ACID, FOLIC ACID, IRON, RETINOL, ZINC (SUPLEMENTO DE MICRONUTRIENTES), VITAMINS NOS, LEVOTHYROXINE and ALBUTEROL SULFATE for an unknown indication. On 24-Jan-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On an unknown date, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 25-Jan-2021, the patient experienced BACK PAIN (severe spine pain), MALAISE (felt really tired), FATIGUE (could not get out of bed; exhausted), INJECTION SITE ERYTHEMA (arm a little red), CHILLS (chills), PAIN IN EXTREMITY (arm sore), PYREXIA (fever) and FATIGUE (slept the entire next day). The patient was treated with PARACETAMOL (TYLENOL) for Fever, at a dose of 500 milligram. At the time of the report, BACK PAIN (severe spine pain), MALAISE (felt really tired), FATIGUE (could not get out of bed; exhausted), INJECTION SITE ERYTHEMA (arm a little red), CHILLS (chills), PAIN IN EXTREMITY (arm sore), PYREXIA (fever) and FATIGUE (slept the entire next day) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No treatment information provided.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Back pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: No medical history reported.
Andere Medikamente: SUPLEMENTO DE MICRONUTRIENTES; VITAMINS NOS; LEVOTHYROXINE; ALBUTEROL SULFATE
Allergien: -
Vorherige Impfungen: -

VAERS 1581034

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: NC
Alter: 73,0
Geschlecht: F
Eingang: 18.08.2021
Impfdatum: 23.01.2021
Beginn: 24.01.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: OT / -

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

Abdominal pain Insomnia

Symptomtext

Abdominal cramps; night time awaking, can't sleep; This spontaneous case was reported by a consumer and describes the occurrence of ABDOMINAL PAIN (Abdominal cramps) and INSOMNIA (night time awaking, can't sleep) in a 73-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. No Medical History information was reported. On 23-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 24-Jan-2021, the patient experienced ABDOMINAL PAIN (Abdominal cramps) and INSOMNIA (night time awaking, can't sleep). At the time of the report, ABDOMINAL PAIN (Abdominal cramps) and INSOMNIA (night time awaking, can't sleep) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown.

Weitere VAERSDATA-Felder

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

VAERS 1580972

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: NY
Alter: 82,0
Geschlecht: F
Eingang: 18.08.2021
Impfdatum: 23.01.2021
Beginn: 25.01.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: OT / LA

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

Rash Rash pruritic

Symptomtext

Rash is a little bit itchy; Rash all over the body; This spontaneous case was reported by a consumer and describes the occurrence of RASH PRURITIC (Rash is a little bit itchy) and RASH (Rash all over the body) in an 82-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. Concurrent medical conditions included Sensitive skin (Medical history reported as Sensitive skin/Fair skin.). On 23-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 25-Jan-2021, the patient experienced RASH PRURITIC (Rash is a little bit itchy) and RASH (Rash all over the body). At the time of the report, RASH PRURITIC (Rash is a little bit itchy) and RASH (Rash all over the body) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Most recent FOLLOW-UP information incorporated above includes: On 26-Jan-2021: ADR form contains NNI

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Sensitive skin (Medical history reported as Sensitive skin/Fair skin.)
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1580953

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: FL
Alter: 68,0
Geschlecht: F
Eingang: 18.08.2021
Impfdatum: 03.02.2021
Beginn: 15.02.2021
Tage bis Beginn: 12,0
Dosis: 1
Route/Site: OT / -

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

Discomfort Headache Lethargy Tinnitus

Symptomtext

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 events headache, ringing in ears/tinnitus, dull discomfort upon movement/discomfort, lethargy. The patient's medical history was not provided. No relevant concomitant medications were reported. On 3 Feb 2021, prior to the onset of the events the patient received first of two planned doses of mRNA-1273 (lot/batch: 038K20A) intramuscularly for prophylaxis of COVID-19 infection. On an unknown date, the patient experienced the event(s) headache, ringing in ears, dull discomfort upon movement, lethargy. No treatment information was provided. Action taken with mRNA-1273 in response to the events was not reported. The outcome of event(s), headache, ringing in ears, dull discomfort upon movement, lethargy was unknown.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: No adverse event
Andere Medikamente: OMEGA 3 FISH OILS
Allergien: -
Vorherige Impfungen: -

VAERS 1580845

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: FL
Alter: 69,0
Geschlecht: U
Eingang: 18.08.2021
Impfdatum: 31.01.2021
Beginn: 01.02.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: OT / LA

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

Acne Vaccination site pain

Symptomtext

This spontaneous case was reported by a consumer and describes the occurrence of ACNE (Pimple outside of lip) and VACCINATION SITE PAIN (Pain at injection site) in a 69-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. No Medical History information was reported. On 31-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 ACNE (Pimple outside of lip) and VACCINATION SITE PAIN (Pain at injection site). At the time of the report, ACNE (Pimple outside of lip) and VACCINATION SITE PAIN (Pain at injection site) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Concomitant medications were not provided.

Weitere VAERSDATA-Felder

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

VAERS 1580677

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: MI
Alter: 69,0
Geschlecht: F
Eingang: 18.08.2021
Impfdatum: 02.02.2021
Beginn: 02.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / -

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

Chills Fatigue Nausea Pain in extremity

Symptomtext

legs started to hurt; she is tired (kind of flu tired); chills; she is feeling like vomit; This spontaneous case was reported by a non-health professional (subsequently medically confirmed) and describes the occurrence of PAIN IN EXTREMITY (legs started to hurt), FATIGUE (she is tired (kind of flu tired)), CHILLS (chills) and NAUSEA (she is feeling like vomit) in a 69-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. The patient's past medical history included Heart transplant. On 02-Feb-2021 at 12:40 PM, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 02-Feb-2021, the patient experienced PAIN IN EXTREMITY (legs started to hurt), FATIGUE (she is tired (kind of flu tired)), CHILLS (chills) and NAUSEA (she is feeling like vomit). The patient was treated with PARACETAMOL (TYLENOL) on 02-Feb-2021 for Adverse reaction, at an unspecified dose and frequency. At the time of the report, PAIN IN EXTREMITY (legs started to hurt), FATIGUE (she is tired (kind of flu tired)), CHILLS (chills) and NAUSEA (she is feeling like vomit) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Patient's concomitant medication included unspecified rejection medicine taking for heart transplant.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Heart transplant
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1580564

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: OH
Alter: 79,0
Geschlecht: M
Eingang: 18.08.2021
Impfdatum: 23.01.2021
Beginn: 23.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / -

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

Arthralgia Chills Fatigue Malaise Myalgia Pyrexia SARS-CoV-2 test

Symptomtext

Malaise; Body ache; Arthralgia; Fever; Fatigue; Chills; This spontaneous case was reported by a consumer and describes the occurrence of MALAISE (Malaise), MYALGIA (Body ache), ARTHRALGIA (Arthralgia), FATIGUE (Fatigue) and CHILLS (Chills) in a 79-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 038K20A and 038K20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included No adverse event. On 23-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 23-Jan-2021, received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 23-Jan-2021, the patient experienced FATIGUE (Fatigue) and CHILLS (Chills). On 25-Jan-2021, the patient experienced MALAISE (Malaise), MYALGIA (Body ache), ARTHRALGIA (Arthralgia) and PYREXIA (Fever). On 26-Jan-2021, PYREXIA (Fever) had resolved. At the time of the report, MALAISE (Malaise), MYALGIA (Body ache), ARTHRALGIA (Arthralgia), FATIGUE (Fatigue) and CHILLS (Chills) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): In 2021, SARS-CoV-2 test: Negative. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. No relevant concomitant medications were reported. Treatment details included Tylenol. Reporter did not allow further contact; 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: Arthralgia
Hospital-Tage: -
Labordaten: Test Date: 2021; Test Name: SARS CoV-2 test; Result Unstructured Data: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: No adverse event
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1580332

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: IL
Alter: 42,0
Geschlecht: M
Eingang: 18.08.2021
Impfdatum: 26.01.2021
Beginn: 26.01.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: OT / RA

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

Myalgia Pyrexia Vaccination site pain

Symptomtext

fever; body aches; sore arm; A spontaneous report was received from a consumer concerning a 42-years-old male patient who received Moderna's COVID-19 vaccine (mRNA-1273) and experienced events flu like symptoms (fever, sore arm, and body ache). The patient's medical history was not provided. No relevant concomitant medications were reported. On 26 Jan 2021, prior to the onset of the events the patient received their last of two planned doses of mRNA-1273 (lot batch: 038K20A) intramuscularly in the right arm for prophylaxis of COVID-19 infection. On 26 Jan 2021, the patient experienced the events flu like symptoms (fever sore arm, and body ache) and was treated with ibuprofen. Action taken with mRNA-1273 in response to the events was not reported. The outcome of events 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: Myalgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: No adverse event (No reported medical history.)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1580286

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: PA
Alter: 74,0
Geschlecht: F
Eingang: 18.08.2021
Impfdatum: 26.01.2021
Beginn: 02.02.2021
Tage bis Beginn: 7,0
Dosis: 1
Route/Site: OT / -

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

Vaccination site rash Vaccination site swelling Vaccination site warmth

Symptomtext

Warm; Swollen arm; rash on her arm/the size of the rash was about the size of a tennis ball; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION SITE WARMTH (Warm), VACCINATION SITE SWELLING (Swollen arm) and VACCINATION SITE RASH (rash on her arm/the size of the rash was about the size of a tennis ball) in a 74-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. No medical history was provided by the reporter. On 26-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 02-Feb-2021, the patient experienced VACCINATION SITE WARMTH (Warm), VACCINATION SITE SWELLING (Swollen arm) and VACCINATION SITE RASH (rash on her arm/the size of the rash was about the size of a tennis ball). The patient was treated with ASPIRIN [ACETYLSALICYLIC ACID] (oral) at an unspecified dose and frequency. At the time of the report, VACCINATION SITE WARMTH (Warm), VACCINATION SITE SWELLING (Swollen arm) and VACCINATION SITE RASH (rash on her arm/the size of the rash was about the size of a tennis ball) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. Concomitant medication was not provided. Treatment includes ice on and off. Most recent FOLLOW-UP information incorporated above includes: On 11-Jun-2021: follow up received from 11-JUN-2021 :Patient said she is doing fine and declined for further follow-up

Weitere VAERSDATA-Felder

Praegender Schweregrund: Vaccination site rash
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: No medical history was provided by the reporter
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1580127

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: IL
Alter: 42,0
Geschlecht: M
Eingang: 18.08.2021
Impfdatum: 26.01.2021
Beginn: 26.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / RA

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

Myalgia Pain in extremity Pyrexia

Symptomtext

Sore arm; Body ache; Fever; This spontaneous case was reported by a consumer and describes the occurrence of PAIN IN EXTREMITY (Sore arm), MYALGIA (Body ache) and PYREXIA (Fever) in a 42-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. No medical history was provided by the reporter. On 26-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 26-Jan-2021, the patient experienced PAIN IN EXTREMITY (Sore arm), MYALGIA (Body ache) and PYREXIA (Fever). The patient was treated with IBUPROFEN ongoing since an unknown date at an unspecified dose and frequency. At the time of the report, PAIN IN EXTREMITY (Sore arm), MYALGIA (Body ache) and PYREXIA (Fever) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Reporter did not allow further contact

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myalgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: No medical history was provided by the reporter.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1573857

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: OK
Alter: 51,0
Geschlecht: M
Eingang: 16.08.2021
Impfdatum: 30.03.2021
Beginn: 12.08.2021
Tage bis Beginn: 135,0
Dosis: 1
Route/Site: IM / LA

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

Headache Pyrexia SARS-CoV-2 test positive

Symptomtext

FEVER, HEADACE

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: 08/12/21: POSITIVE SARS-COV-2 RNA
Aktuelle Erkrankungen: NA
Vorgeschichte: CHRONIC HYPOXEMIC RESPIRATORY FAILURE, TYPE 2 DIABETES, DIABETIC FOOT ULCER, MULTIPLE JOINT PAIN, MYOPIA, ASTIGMATISM, PRESBYOPIA, ALCOHOL ABUSE, ONYCHOMYCOSIS OF TOENAILS
Andere Medikamente: LEVEMIR, NOVOLOG, IBUPROFEN, METFORMIN, ERGOCALCIFEROL, ALBUTEROL, DICOLFENAC, CETIRIZINE, FLUTICASONE/SALMETEROL, ALOGLIPTIN, MONTELUKAST, GABAPENTIN, ASPIRIN, SILDENAFIL, LISINOPRIL, ATORVASTATIN, METOPROLOL, NITROGLYCERIN
Allergien: NKA
Vorherige Impfungen: -

VAERS 1573189

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: MI
Alter: 86,0
Geschlecht: F
Eingang: 16.08.2021
Impfdatum: 05.02.2021
Beginn: 14.02.2021
Tage bis Beginn: 9,0
Dosis: 1
Route/Site: OT / LA

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

Vaccination site rash

Symptomtext

Rash, two and a half inches around the vaccination area.; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION SITE RASH (Rash, two and a half inches around the vaccination area.) in an 86-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. Concomitant products included PANTOPRAZOLE, METOPROLOL and APIXABAN (ELIQUIS) for an unknown indication. On 05-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 14-Feb-2021, the patient experienced VACCINATION SITE RASH (Rash, two and a half inches around the vaccination area.). At the time of the report, VACCINATION SITE RASH (Rash, two and a half inches around the vaccination area.) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. Treatment Patient did not treat the rash. Most recent FOLLOW-UP information incorporated above includes: On 27-Apr-2021: No specific follow-up information recorded.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Vaccination site rash
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: PANTOPRAZOLE; METOPROLOL; ELIQUIS
Allergien: -
Vorherige Impfungen: -

VAERS 1573042

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K 20A

mild

Staat: FL
Alter: 75,0
Geschlecht: F
Eingang: 16.08.2021
Impfdatum: 29.01.2021
Beginn: 06.02.2021
Tage bis Beginn: 8,0
Dosis: 1
Route/Site: OT / LA

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

Axillary pain Injection site pain Injection site pruritus Pyrexia Rash macular

Symptomtext

Burning; Itching; Really red and really big blotchy reaction at the site of injection; Glands in her armpit are sore; Low grade fever; This spontaneous case was reported by a consumer and describes the occurrence of INJECTION SITE PAIN (Burning), INJECTION SITE PRURITUS (Itching), RASH MACULAR (Really red and really big blotchy reaction at the site of injection), AXILLARY PAIN (Glands in her armpit are sore) and PYREXIA (Low grade fever) in a 75-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K 20A) for COVID-19 vaccination. No Medical History information was reported. On 29-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 06-Feb-2021, the patient experienced INJECTION SITE PAIN (Burning), INJECTION SITE PRURITUS (Itching), RASH MACULAR (Really red and really big blotchy reaction at the site of injection), AXILLARY PAIN (Glands in her armpit are sore) and PYREXIA (Low grade fever). At the time of the report, INJECTION SITE PAIN (Burning), INJECTION SITE PRURITUS (Itching), RASH MACULAR (Really red and really big blotchy reaction at the site of injection), AXILLARY PAIN (Glands in her armpit are sore) and PYREXIA (Low grade fever) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Treatment include ice and hydrocortisone cream. No concomitant medications were reported.

Weitere VAERSDATA-Felder

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

VAERS 1572851

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: FL
Alter: 66,0
Geschlecht: F
Eingang: 16.08.2021
Impfdatum: 29.01.2021
Beginn: 30.01.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: OT / LA

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

Fatigue Headache Vaccination site pain

Symptomtext

Injection site arm got sore; Very fatigued; Headache; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION SITE PAIN (Injection site arm got sore), FATIGUE (Very fatigued) and HEADACHE (Headache) in a 66-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. No Medical History information was reported. On 29-Jan-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 30-Jan-2021, the patient experienced FATIGUE (Very fatigued) and HEADACHE (Headache). On an unknown date, the patient experienced VACCINATION SITE PAIN (Injection site arm got sore). At the time of the report, VACCINATION SITE PAIN (Injection site arm got sore), FATIGUE (Very fatigued) and HEADACHE (Headache) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Concomitant medication list was not provided. Treatment information was not provided.

Weitere VAERSDATA-Felder

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

VAERS 1568095

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: IL
Alter: 75,0
Geschlecht: F
Eingang: 15.08.2021
Impfdatum: 09.02.2021
Beginn: 20.02.2021
Tage bis Beginn: 11,0
Dosis: 1
Route/Site: OT / LA

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

Rash papular Rash pruritic

Symptomtext

raised bump 1/4-half dollar in size on forehead and scalp/ rash was on scalp and forehead; Rash itched bad; This spontaneous case was reported by a consumer (subsequently medically confirmed) and describes the occurrence of RASH PAPULAR (raised bump 1/4-half dollar in size on forehead and scalp/ rash was on scalp and forehead) and RASH PRURITIC (Rash itched bad) in a 75-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. No Medical History information was reported. On 09-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 20-Feb-2021, the patient experienced RASH PAPULAR (raised bump 1/4-half dollar in size on forehead and scalp/ rash was on scalp and forehead) and RASH PRURITIC (Rash itched bad). The patient was treated with LORATADINE (CLARITIN [LORATADINE]) for Rash, at an unspecified dose and frequency. At the time of the report, RASH PAPULAR (raised bump 1/4-half dollar in size on forehead and scalp/ rash was on scalp and forehead) and RASH PRURITIC (Rash itched bad) had not resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Treatment details included a topical corticosteroid, and to use a cold rag for rash. No concomitant medications were reported. Patient visited dermatologist. She received her second shot on 09-Mar-2021 (batch lot 006M20A) in right arm.

Weitere VAERSDATA-Felder

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

VAERS 1567713

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: PA
Alter: 60,0
Geschlecht: F
Eingang: 15.08.2021
Impfdatum: 28.01.2021
Beginn: 25.02.2021
Tage bis Beginn: 28,0
Dosis: 1
Route/Site: OT / LA

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

Abdominal discomfort Abdominal pain upper Dysgeusia Dyspepsia Endoscopy Fatigue Gastrooesophageal reflux disease Headache Myalgia Pain in extremity Pyrexia

Symptomtext

thinking its acid reflux; Burning in stomach; Hurting in stomach/some pain in stomach; Metallic taste in her mouth; She had some fever; Headache; Tiredness; Body aches; About 12 hours after receiving 2nd dose, her arm started to get sore; Stomach discomfort/feels discomfort and heaviness on top of the stomach; This spontaneous case was reported by a consumer (subsequently medically confirmed) and describes the occurrence of PAIN IN EXTREMITY (About 12 hours after receiving 2nd dose, her arm started to get sore), ABDOMINAL DISCOMFORT (Stomach discomfort/feels discomfort and heaviness on top of the stomach), GASTROOESOPHAGEAL REFLUX DISEASE (thinking its acid reflux), DYSPEPSIA (Burning in stomach) and ABDOMINAL PAIN UPPER (Hurting in stomach/some pain in stomach) in a 60-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 007M20A and 038K20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No medical information was provided by the reporter. Concomitant products included MONTELUKAST SODIUM (SINGULAIR), LEVOTHYROXINE, MULTIVITAMIN [VITAMINS NOS] and FISH OIL for an unknown indication. On 28-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 25-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 PAIN IN EXTREMITY (About 12 hours after receiving 2nd dose, her arm started to get sore), ABDOMINAL DISCOMFORT (Stomach discomfort/feels discomfort and heaviness on top of the stomach) and HEADACHE (Headache). 25-Feb-2021, the patient experienced DYSGEUSIA (Metallic taste in her mouth), PYREXIA (She had some fever), FATIGUE (Tiredness) and MYALGIA (Body aches). On 26-Feb-2021, the patient experienced DYSPEPSIA (Burning in stomach). 26-Feb-2021, the patient experienced ABDOMINAL PAIN UPPER (Hurting in stomach/some pain in stomach). On an unknown date, the patient experienced GASTROOESOPHAGEAL REFLUX DISEASE (thinking its acid reflux). The patient was treated with FAMOTIDINE (PEPCID AC) at an unspecified dose and frequency; OMEPRAZOLE (PRILOSEC [OMEPRAZOLE]) at an unspecified dose and frequency and ESOMEPRAZOLE MAGNESIUM TRIHYDRATE (NEXIUM [ESOMEPRAZOLE MAGNESIUM TRIHYDRATE]) at an unspecified dose and frequency. On 26-Feb-2021, PAIN IN EXTREMITY (About 12 hours after receiving 2nd dose, her arm started to get sore), HEADACHE (Headache), FATIGUE (Tiredness) and MYALGIA (Body aches) had resolved. At the time of the report, ABDOMINAL DISCOMFORT (Stomach discomfort/feels discomfort and heaviness on top of the stomach), GASTROOESOPHAGEAL REFLUX DISEASE (thinking its acid reflux), DYSPEPSIA (Burning in stomach), DYSGEUSIA (Metallic taste in her mouth) and PYREXIA (She had some fever) outcome was unknown and ABDOMINAL PAIN UPPER (Hurting in stomach/some pain in stomach) had resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, Endoscopy: unknown (Inconclusive) Unknown. It was reported that about 12 hours after receiving 2nd dose, patient arm started to get sore. She had some fever, headache and stomach discomfort, tiredness and body aches. After 24 hours later(26Feb2021), she only had stomach discomfort with burning and hurting in stomach. She feels discomfort and heaviness on top of the stomach. patient reported metallic taste in her mouth that started on 25-Feb-2021. She wants to know about commonly reported side effects It was reported that the patient experienced a lot of stomach problems, burning. She took a lot of medications. She went through tests, saw doctors. She said her symptoms didn't end a day or two after the vaccine and it is still a problem. She said it might have changed. She is on medication now. Ten days before second dose the symptoms went away. After the second dose, on the first day she had fever and wasn't feeling well. On the second day, problem came back, and it was worse. She had burning and some pain in stomach. She started taking antacids, tried several different medicines. A month into it, started taking Nexium over the counter. It helped a little bit. She went to GI doctor, did endoscopy, checked gall bladder. They put her on diet to see if it's gall bladder. Pain went away with diet. Now they're thinking its acid reflux. Treatment provided Tums, Milk of magnesia . Action taken with mRNA-1273 in response to the event was not applicable. This case was linked to US-MODERNATX, INC.-MOD-2021-024653 (E2B Linked Report). Most recent FOLLOW-UP information incorporated above includes: On 10-May-2021: Follow up received on 10-May-2021 and included significant information such as New events were added, Treatment information about the patient was added, New lab test was added and details about doctor consultation was added.; Sender's Comments: US-MODERNATX, INC.-MOD-2021-024653:1st dose

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain upper
Hospital-Tage: -
Labordaten: Test Name: endoscopy; Test Result: Inconclusive ; Result Unstructured Data: Unknown
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: No medical information was provided by the reporter.
Andere Medikamente: SINGULAIR; LEVOTHYROXINE; MULTIVITAMIN [VITAMINS NOS]; FISH OIL
Allergien: -
Vorherige Impfungen: -

VAERS 1567028

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: SC
Alter: 70,0
Geschlecht: F
Eingang: 15.08.2021
Impfdatum: 10.02.2021
Beginn: 10.03.2011
Tage bis Beginn: -
Dosis: 1
Route/Site: OT / LA

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

Back pain Echocardiogram Erythema Feeling abnormal Myalgia Pain Pain in extremity Peripheral swelling Pruritus Vaccination site discolouration

Symptomtext

Pink at injection site; Pain in back; Not feeling good; Whole body hurting; Pain in muscles; Right arm hurting, swollen; Right arm red, itchy; Right arm hurting, swollen; Right arm red, itchy; This spontaneous case was reported by a consumer (subsequently medically confirmed) and describes the occurrence of BACK PAIN (Pain in back), FEELING ABNORMAL (Not feeling good), VACCINATION SITE DISCOLOURATION (Pink at injection site), ERYTHEMA (Right arm red, itchy) and PAIN IN EXTREMITY (Right arm hurting, swollen) in a 70-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 011A2A and 038K20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 10-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 10-Mar-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 10-Mar-2011, the patient experienced ERYTHEMA (Right arm red, itchy) and PERIPHERAL SWELLING (Right arm hurting, swollen). On 10-Mar-2021, the patient experienced PAIN IN EXTREMITY (Right arm hurting, swollen) and PRURITUS (Right arm red, itchy). On 11-Mar-2021, the patient experienced BACK PAIN (Pain in back), FEELING ABNORMAL (Not feeling good), PAIN (Whole body hurting) and MYALGIA (Pain in muscles). On 16-Mar-2021, the patient experienced VACCINATION SITE DISCOLOURATION (Pink at injection site). The patient was treated with IBUPROFEN at an unspecified dose and frequency. At the time of the report, BACK PAIN (Pain in back), FEELING ABNORMAL (Not feeling good), VACCINATION SITE DISCOLOURATION (Pink at injection site), ERYTHEMA (Right arm red, itchy), PAIN IN EXTREMITY (Right arm hurting, swollen), PERIPHERAL SWELLING (Right arm hurting, swollen), PRURITUS (Right arm red, itchy), PAIN (Whole body hurting) and MYALGIA (Pain in muscles) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, Echocardiogram: other (normal) other. No Concomitant medications was reported

Weitere VAERSDATA-Felder

Praegender Schweregrund: Back pain
Hospital-Tage: -
Labordaten: Test Name: Echocardiogram; Result Unstructured Data: other
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1566812

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: NY
Alter: 75,0
Geschlecht: F
Eingang: 15.08.2021
Impfdatum: 22.01.2021
Beginn: 22.01.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: OT / LA

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

Night sweats Vaccination site pain

Symptomtext

Night sweat; Injection site pain; This spontaneous case was reported by a consumer and describes the occurrence of NIGHT SWEATS (Night sweat) and VACCINATION SITE PAIN (Injection site pain) in a 75-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 038K20A and 010M20A) for COVID-19 vaccination. The patient's past medical history included No adverse reaction. On 22-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 19-Feb-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 22-Jan-2021, the patient experienced VACCINATION SITE PAIN (Injection site pain). On 25-Jan-2021, the patient experienced NIGHT SWEATS (Night sweat). On 25-Jan-2021, NIGHT SWEATS (Night sweat) and VACCINATION SITE PAIN (Injection site pain) had resolved. No concomitant medications were provided. Treatment information provided mentioned Tylenol, Zyrtec, and hydrocortisone 2.5%. Action taken with mRNA-1273 in response to the event was not applicable as patient received both doses of the vaccine. This case was linked to MOD-2021-058663 (Patient Link).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Vaccination site pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: No adverse reaction
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1566598

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: FL
Alter: 76,0
Geschlecht: F
Eingang: 15.08.2021
Impfdatum: 05.03.2021
Beginn: 08.03.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: OT / LA

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

Pruritus Swelling

Symptomtext

Bumps and lumps are spread all over the body; Patient started with bumps and lumps that started itching; When she goes out in Sun, they get aggravated; This spontaneous case was reported by a consumer and describes the occurrence of PRURITUS (Patient started with bumps and lumps that started itching), PRURITUS (When she goes out in Sun, they get aggravated) and SWELLING (Bumps and lumps are spread all over the body) in a 76-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. Concurrent medical conditions included Drug allergy (Sulfa allergy). Concomitant products included CALCIUM and VITAMIN C [ASCORBIC ACID] for an unknown indication. On 05-Mar-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .5 ml. On 08-Mar-2021, the patient experienced PRURITUS (Patient started with bumps and lumps that started itching) and PRURITUS (When she goes out in Sun, they get aggravated). On 15-Mar-2021, the patient experienced SWELLING (Bumps and lumps are spread all over the body). The patient was treated with DIPHENHYDRAMINE HYDROCHLORIDE (BENADRYL [DIPHENHYDRAMINE HYDROCHLORIDE]) at an unspecified dose and frequency and CETIRIZINE HYDROCHLORIDE (ZYRTEC [CETIRIZINE HYDROCHLORIDE]) at an unspecified dose and frequency. At the time of the report, PRURITUS (Patient started with bumps and lumps that started itching), PRURITUS (When she goes out in Sun, they get aggravated) and SWELLING (Bumps and lumps are spread all over the body) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Concomitant medication also included acidophillus. Treatment medication also included steroid cream.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Drug allergy (Sulfa allergy)
Vorgeschichte: -
Andere Medikamente: CALCIUM; VITAMIN C [ASCORBIC ACID]
Allergien: -
Vorherige Impfungen: -

VAERS 1565605

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: MI
Alter: 74,0
Geschlecht: F
Eingang: 15.08.2021
Impfdatum: 09.02.2021
Beginn: 09.02.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: OT / RA

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

Headache Influenza like illness Pain Pyrexia

Symptomtext

Feelin achy; Slight temp of 99 degrees; Felt like had the flu for couple of days; Headache; This case was received via an unknown source (no reference has been entered for a health authority or license partner) on 12-Mar-2021 and was forwarded to Moderna on 12-Mar-2021. This spontaneous case was reported by a consumer (subsequently medically confirmed) and describes the occurrence of PAIN (Feelin achy), PYREXIA (Slight temp of 99 degrees), INFLUENZA LIKE ILLNESS (Felt like had the flu for couple of days) and HEADACHE (Headache) in a 74-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 038K20A and 030A21A) for COVID-19 vaccination. The patient's past medical history included Sarcoidosis since 01-Jan-2014. Concurrent medical conditions included Drug allergy (Codeine). Concomitant products included LOSARTAN POTASSIUM (COZAAR) from 01-Jan-2010 to an unknown date for Blood pressure, ATORVASTATIN CALCIUM (LIPITOR) from 01-Jan-2010 to an unknown date for High cholesterol. On 09-Feb-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 10-Mar-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 2 dosage form. On 09-Feb-2021, the patient experienced HEADACHE (Headache). On 10-Feb-2021, the patient experienced PAIN (Feelin achy), PYREXIA (Slight temp of 99 degrees) and INFLUENZA LIKE ILLNESS (Felt like had the flu for couple of days). On 10-Feb-2021, PAIN (Feelin achy), PYREXIA (Slight temp of 99 degrees) and INFLUENZA LIKE ILLNESS (Felt like had the flu for couple of days) outcome was unknown. On 16-Feb-2021, HEADACHE (Headache) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Treatment medication include Tylenol and ibuprofen. Most recent FOLLOW-UP information incorporated above includes: On 05-May-2021: Past medical history was updated. Concomitant medications were updated.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Drug allergy (Codeine); Sarcoidosis
Vorgeschichte: -
Andere Medikamente: LIPITOR; COZAAR
Allergien: -
Vorherige Impfungen: -

VAERS 1565255

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: MI
Alter: 71,0
Geschlecht: F
Eingang: 15.08.2021
Impfdatum: 09.02.2021
Beginn: 10.03.2021
Tage bis Beginn: 29,0
Dosis: 1
Route/Site: OT / LA

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

Dry throat Dysphagia Oropharyngeal pain Throat tightness

Symptomtext

Hard time going down, almost felt like it was restricted; during the night very dry throat; very sore throat; Almost felt it was closing up; This spontaneous case was reported by a consumer and describes the occurrence of DRY THROAT (during the night very dry throat), OROPHARYNGEAL PAIN (very sore throat), THROAT TIGHTNESS (Almost felt it was closing up) and DYSPHAGIA (Hard time going down, almost felt like it was restricted) in a 71-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 030A21A and 038K20A) for COVID-19 vaccination. Concurrent medical conditions included CPAP. On 09-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 10-Mar-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 10-Mar-2021, the patient experienced DRY THROAT (during the night very dry throat), OROPHARYNGEAL PAIN (very sore throat) and THROAT TIGHTNESS (Almost felt it was closing up). On 11-Mar-2021, the patient experienced DYSPHAGIA (Hard time going down, almost felt like it was restricted). The patient was treated with PARACETAMOL (TYLENOL) for Sore throat, at a dose of 2 dosage form. At the time of the report, DRY THROAT (during the night very dry throat), OROPHARYNGEAL PAIN (very sore throat), THROAT TIGHTNESS (Almost felt it was closing up) and DYSPHAGIA (Hard time going down, almost felt like it was restricted) outcome was unknown. Concomitant medications details were not reported by the reporter.

Weitere VAERSDATA-Felder

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

VAERS 1565003

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: MI
Alter: -
Geschlecht: F
Eingang: 15.08.2021
Impfdatum: 01.03.2021
Beginn: 01.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / LA

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

Pain in extremity Rash Vaccination complication Vaccination site induration Vaccination site swelling

Symptomtext

rash on upper left arm; hardness(injection site); swelling (injection site); sore arm; Patient believes injection was administered too quickly; felt so much pressure; This spontaneous case was reported by a consumer and describes the occurrence of PAIN IN EXTREMITY (sore arm), VACCINATION COMPLICATION (Patient believes injection was administered too quickly; felt so much pressure), RASH (rash on upper left arm), VACCINATION SITE INDURATION (hardness(injection site)) and VACCINATION SITE SWELLING (swelling (injection site)) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. No Medical History information was reported. On 01-Mar-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 01-Mar-2021, the patient experienced VACCINATION COMPLICATION (Patient believes injection was administered too quickly; felt so much pressure). On 02-Mar-2021, the patient experienced PAIN IN EXTREMITY (sore arm). On 10-Mar-2021, the patient experienced RASH (rash on upper left arm), VACCINATION SITE INDURATION (hardness(injection site)) and VACCINATION SITE SWELLING (swelling (injection site)). On 01-Mar-2021, VACCINATION COMPLICATION (Patient believes injection was administered too quickly; felt so much pressure) had resolved. At the time of the report, PAIN IN EXTREMITY (sore arm), RASH (rash on upper left arm), VACCINATION SITE INDURATION (hardness(injection site)) and VACCINATION SITE SWELLING (swelling (injection site)) had not resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. No concomitant medications were provided by the reporter. No treatment information was reported. Most recent FOLLOW-UP information incorporated above includes: On 11-Mar-2021: Reporter details provided, vaccine details provided, event outcome (ongoing) provided

Weitere VAERSDATA-Felder

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

VAERS 1563930

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: FL
Alter: 68,0
Geschlecht: F
Eingang: 15.08.2021
Impfdatum: 03.02.2021
Beginn: 03.03.2021
Tage bis Beginn: 28,0
Dosis: 1
Route/Site: OT / -

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

Pain in extremity Vaccination site bruising Vaccination site discolouration

Symptomtext

Injection site turned green; Injection site turned black/Injection site turned blue purple; sore all day; This spontaneous case was reported by a consumer and describes the occurrence of PAIN IN EXTREMITY (sore all day), VACCINATION SITE BRUISING (Injection site turned black/Injection site turned blue purple) and VACCINATION SITE DISCOLOURATION (Injection site turned green) in a 68-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 025A21A and 038K20A) for COVID-19 vaccination. Concomitant products included LOVASTATIN, LEVOTHYROXINE and ALENDRONATE SODIUM (FOSAMAX) for an unknown indication. On 03-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 03-Mar-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 03-Mar-2021, the patient experienced PAIN IN EXTREMITY (sore all day). On 04-Mar-2021, the patient experienced VACCINATION SITE BRUISING (Injection site turned black/Injection site turned blue purple). On 08-Mar-2021, the patient experienced VACCINATION SITE DISCOLOURATION (Injection site turned green). At the time of the report, PAIN IN EXTREMITY (sore all day), VACCINATION SITE BRUISING (Injection site turned black/Injection site turned blue purple) and VACCINATION SITE DISCOLOURATION (Injection site turned green) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Reporter did not allow further contact

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: LOVASTATIN; LEVOTHYROXINE; FOSAMAX
Allergien: -
Vorherige Impfungen: -

VAERS 1563748

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: PA
Alter: 78,0
Geschlecht: M
Eingang: 15.08.2021
Impfdatum: 03.02.2021
Beginn: 03.03.2021
Tage bis Beginn: 28,0
Dosis: 2
Route/Site: OT / LA

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

Agitation Dermatitis psoriasiform Fatigue Feeling abnormal Rash macular Vaccination site pruritus Vaccination site rash Vaccination site urticaria

Symptomtext

Psoriasis Reaction; hives; rash/ Rash that is bright red and bump from elbow to wrist, and lower back; itch; red blotches; tired; felt foggy; agitated; This spontaneous case was reported by a health care professional and describes the occurrence of FEELING ABNORMAL (felt foggy), AGITATION (agitated), DERMATITIS PSORIASIFORM (Psoriasis Reaction), RASH MACULAR (red blotches) and FATIGUE (tired) in a 78-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 038K20A and 025A21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included BPH. Concurrent medical conditions included Hypertension. Concomitant products included AMLODIPINE for Blood pressure, TADALAFIL, BETAMETHASONE from 05-Mar-2021 to an unknown date, METHYLPREDNISOLONE SODIUM SUCCINATE (SOLUMEDROL) from 16-Apr-2021 to 22-Apr-2021 and TRIAMCINOLONE from 27-Apr-2021 to an unknown date for an unknown indication, CETIRIZINE HYDROCHLORIDE (ZYRTEC ALLERGY) from 03-Mar-2021 to an unknown date and BETAMETHASONE. On 03-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 03-Mar-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 03-Mar-2021, the patient experienced FEELING ABNORMAL (felt foggy), AGITATION (agitated), RASH MACULAR (red blotches) and FATIGUE (tired). On an unknown date, the patient experienced DERMATITIS PSORIASIFORM (Psoriasis Reaction), VACCINATION SITE URTICARIA (hives), VACCINATION SITE RASH (rash/ Rash that is bright red and bump from elbow to wrist, and lower back) and VACCINATION SITE PRURITUS (itch). On 03-Mar-2021, FEELING ABNORMAL (felt foggy), AGITATION (agitated), RASH MACULAR (red blotches) and FATIGUE (tired) had resolved. At the time of the report, DERMATITIS PSORIASIFORM (Psoriasis Reaction), VACCINATION SITE URTICARIA (hives), VACCINATION SITE RASH (rash/ Rash that is bright red and bump from elbow to wrist, and lower back) and VACCINATION SITE PRURITUS (itch) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Treatment drug not reported. This case was linked to MOD-2021-033582 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 03-May-2021: Lower level term updated from Injection site itching to Vaccination site pruritus, Injection site hives to Vaccination site urticaria.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Hypertension
Vorgeschichte: Medical History/Concurrent Conditions: BPH
Andere Medikamente: AMLODIPINE; TADALAFIL; ZYRTEC ALLERGY; BETAMETHASONE; BETAMETHASONE; SOLUMEDROL; TRIAMCINOLONE
Allergien: -
Vorherige Impfungen: -

VAERS 1563731

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: FL
Alter: 93,0
Geschlecht: F
Eingang: 15.08.2021
Impfdatum: 29.01.2021
Beginn: 08.03.2021
Tage bis Beginn: 38,0
Dosis: 1
Route/Site: OT / -

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

Neck pain

Symptomtext

neck pain; This spontaneous case was reported by a consumer and describes the occurrence of NECK PAIN (neck pain) in a 93-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 031M20A and 038K20A) for COVID-19 vaccination. The patient's past medical history included Angina pectoris since an unknown date. Concomitant products included GLYCERYL TRINITRATE (NITROGLYCERIN TRANSDERMAL SYSTEM) for an unknown indication. On 29-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 26-Feb-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 08-Mar-2021, the patient experienced NECK PAIN (neck pain). At the time of the report, NECK PAIN (neck pain) outcome was unknown. Not Provided Treatment information was unknown Most recent FOLLOW-UP information incorporated above includes: On 03-May-2021: Follow-up received on 03-MAY-2021, contains no new information.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Neck pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Angina pectoris
Vorgeschichte: -
Andere Medikamente: NITROGLYCERIN TRANSDERMAL SYSTEM
Allergien: -
Vorherige Impfungen: -

VAERS 1563718

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: SC
Alter: 88,0
Geschlecht: F
Eingang: 15.08.2021
Impfdatum: 02.03.2021
Beginn: 02.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / LA

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

Swelling Vaccination site pain

Symptomtext

Neck swollen on left side; Sore left arm; This spontaneous case was reported by a consumer and describes the occurrence of SWELLING (Neck swollen on left side) and VACCINATION SITE PAIN (Sore left arm) in an 88-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. No Medical History information was reported. On 02-Mar-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 02-Mar-2021, the patient experienced SWELLING (Neck swollen on left side) and VACCINATION SITE PAIN (Sore left arm). The patient was treated with PARACETAMOL (TYLENOL) at an unspecified dose and frequency. At the time of the report, SWELLING (Neck swollen on left side) and VACCINATION SITE PAIN (Sore left arm) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Concomitant product use was not provided by the reporter.

Weitere VAERSDATA-Felder

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

VAERS 1563334

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: NJ
Alter: 75,0
Geschlecht: F
Eingang: 15.08.2021
Impfdatum: 04.02.2021
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: OT / LA

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

Herpes zoster Oral pain

Symptomtext

Broke up in shingles on the left side of their face; A lot of pain, mostly in their mouth; This spontaneous case was reported by a consumer and describes the occurrence of HERPES ZOSTER (Broke up in shingles on the left side of their face) and ORAL PAIN (A lot of pain, mostly in their mouth) in a 75-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. Concomitant products included BIFIDOBACTERIUM INFANTIS (ALIGN) for Supplementation therapy, ROSUVASTATIN CALCIUM (CRESTOR) and FAMOTIDINE (PEPCID [FAMOTIDINE]) for an unknown indication. On 04-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced HERPES ZOSTER (Broke up in shingles on the left side of their face) and ORAL PAIN (A lot of pain, mostly in their mouth). The patient was treated with IBUPROFEN (ADVIL [IBUPROFEN]) at an unspecified dose and frequency; VALACICLOVIR HYDROCHLORIDE (VALTREX) at a dose of 1 gram three times a day; LIDOCAINE at an unspecified dose and frequency; MUPIROCIN at an unspecified dose and frequency and METHYLPREDNISOLONE at an unspecified dose and frequency. At the time of the report, HERPES ZOSTER (Broke up in shingles on the left side of their face) and ORAL PAIN (A lot of pain, mostly in their mouth) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. This case was linked to MOD-2021-036002, MOD-2021-036002 (Patient Link).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oral pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: CRESTOR; PEPCID [FAMOTIDINE]; ALIGN
Allergien: -
Vorherige Impfungen: -

VAERS 1563023

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: MI
Alter: 85,0
Geschlecht: U
Eingang: 15.08.2021
Impfdatum: 04.02.2021
Beginn: 04.03.2021
Tage bis Beginn: 28,0
Dosis: 1
Route/Site: OT / -

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

Arthralgia Chills Decreased appetite Fatigue Pyrexia

Symptomtext

Loss appetite; Bone joints ache; Fever; Chills; Fatigue; This spontaneous case was reported by a consumer and describes the occurrence of DECREASED APPETITE (Loss appetite), ARTHRALGIA (Bone joints ache), PYREXIA (Fever), CHILLS (Chills) and FATIGUE (Fatigue) in an 85-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 030A21A and 038K20A) for COVID-19 vaccination. No Medical History information was reported. On 04-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 04-Mar-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 04-Mar-2021, the patient experienced DECREASED APPETITE (Loss appetite), ARTHRALGIA (Bone joints ache), PYREXIA (Fever), CHILLS (Chills) and FATIGUE (Fatigue). On 04-Mar-2021, CHILLS (Chills) had resolved. At the time of the report, DECREASED APPETITE (Loss appetite), ARTHRALGIA (Bone joints ache), PYREXIA (Fever) and FATIGUE (Fatigue) outcome was unknown. No concomitant medication was reported. Treatment medication was not provided by the reporter. Action taken with mRNA-1273 in response to the event was not applicable.

Weitere VAERSDATA-Felder

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

VAERS 1562588

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: FL
Alter: 71,0
Geschlecht: M
Eingang: 15.08.2021
Impfdatum: 04.02.2021
Beginn: 05.02.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: OT / -

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

Dizziness Nausea

Symptomtext

Nausea; Dizziness; light headedness; This spontaneous case was reported by a consumer and describes the occurrence of DIZZINESS (Dizziness), DIZZINESS (light headedness) and NAUSEA (Nausea) in a 71-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. The patient's past medical history included No adverse event (No medical history reported). On 04-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) at an unspecified dose. On 05-Feb-2021, the patient experienced DIZZINESS (Dizziness) and DIZZINESS (light headedness). On an unknown date, the patient experienced NAUSEA (Nausea). At the time of the report, DIZZINESS (Dizziness), DIZZINESS (light headedness) and NAUSEA (Nausea) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. No treatment information was reported. Most recent FOLLOW-UP information incorporated above includes: On 24-Mar-2021: No specific follow-up information recorded.

Weitere VAERSDATA-Felder

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

VAERS 1562163

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: FL
Alter: -
Geschlecht: F
Eingang: 15.08.2021
Impfdatum: 01.02.2021
Beginn: 08.02.2021
Tage bis Beginn: 7,0
Dosis: 1
Route/Site: OT / -

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

Diarrhoea Pyrexia

Symptomtext

fever; diarrhea; This spontaneous case was reported by a consumer and describes the occurrence of PYREXIA (fever) and DIARRHOEA (diarrhea) in a 78-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. No Medical History information was reported. On 01-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 08-Feb-2021, the patient experienced PYREXIA (fever) and DIARRHOEA (diarrhea). At the time of the report, PYREXIA (fever) and DIARRHOEA (diarrhea) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Concomitant medications were not reported. Treatment RX not given Drinking Pedialyte.

Weitere VAERSDATA-Felder

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

VAERS 1562122

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: SC
Alter: -
Geschlecht: F
Eingang: 15.08.2021
Impfdatum: 17.02.2021
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: OT / -

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

Injection site erythema Injection site pruritus Injection site swelling

Symptomtext

Swollen (Injection); Redness (Injection SIte); Itchiness (Injection Site); A spontaneous report was received from a consumer concerning a 66-years-old female patient who received Moderna's COVID-19 vaccine (mRNA-1273) and experienced events swollen (injection), redness (injection site), itchiness (injection site). The patient's medical history was not provided. No relevant concomitant medications were reported. On 17 Feb 2021, prior to the onset of the events the patient received first of two planned doses of mRNA-1273 (lot/batch: 038K20A) intramuscularly for prophylaxis of COVID-19 infection. On an unknown date, the patient experienced the event(s) Swollen (Injection), Redness (Injection SIte), Itchiness (Injection Site). No treatment information was provided. Action taken with mRNA-1273 in response to the events was not reported. The outcome of event(s), swollen (injection), redness (injection site), itchiness (injection site) was unknown.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: No adverse event
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1562062

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: FL
Alter: 77,0
Geschlecht: F
Eingang: 15.08.2021
Impfdatum: 01.02.2021
Beginn: 02.02.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: OT / -

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

Abdominal pain upper Diarrhoea Fatigue Headache Nausea Weight decreased

Symptomtext

stomach cramps; stomach pain; Diarrhea after every meal and snack; lost weight; eight pounds; very fatigued; nausea without throw up; headaches; This spontaneous case was reported by a consumer and describes the occurrence of ABDOMINAL PAIN UPPER (stomach pain), DIARRHOEA (Diarrhea after every meal and snack), ABDOMINAL PAIN UPPER (stomach cramps), WEIGHT DECREASED (lost weight; eight pounds) and FATIGUE (very fatigued) in a 77-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included No adverse reaction. Concomitant products included PANTOPRAZOLE for Acid reflux (oesophageal), LEVOTHYROXINE, METFORMIN and VITAMINS NOS for an unknown indication. On 01-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 02-Feb-2021, the patient experienced DIARRHOEA (Diarrhea after every meal and snack), WEIGHT DECREASED (lost weight; eight pounds), FATIGUE (very fatigued), NAUSEA (nausea without throw up) and HEADACHE (headaches). On an unknown date, the patient experienced ABDOMINAL PAIN UPPER (stomach pain) and ABDOMINAL PAIN UPPER (stomach cramps). At the time of the report, ABDOMINAL PAIN UPPER (stomach pain), DIARRHOEA (Diarrhea after every meal and snack), ABDOMINAL PAIN UPPER (stomach cramps), WEIGHT DECREASED (lost weight; eight pounds), FATIGUE (very fatigued), NAUSEA (nausea without throw up) and HEADACHE (headaches) 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 details include ibuprofen and vitamins.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain upper
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: No adverse reaction
Andere Medikamente: LEVOTHYROXINE; METFORMIN; VITAMINS NOS; PANTOPRAZOLE
Allergien: -
Vorherige Impfungen: -

VAERS 1562036

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: PA
Alter: 78,0
Geschlecht: M
Eingang: 15.08.2021
Impfdatum: 03.02.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: OT / LA

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

Erythema Rash Rash pruritic Urticaria Vaccination site rash

Symptomtext

redness; hives; rash on back and clavicle; (rash) very itchy; Rash at the injection site in the left arm; This spontaneous case was reported by an other health care professional (subsequently medically confirmed) and describes the occurrence of ERYTHEMA (redness), URTICARIA (hives), RASH (rash on back and clavicle), RASH PRURITIC ((rash) very itchy) and VACCINATION SITE RASH (Rash at the injection site in the left arm) in a 78-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 038K20A and 025A21A) for COVID-19 vaccination. Concurrent medical conditions included Hypertension and Benign prostatic hyperplasia. Concomitant products included AMLODIPINE for Blood pressure management, TADALAFIL for Enlarged prostate. On 03-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 03-Mar-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 ERYTHEMA (redness), URTICARIA (hives), RASH (rash on back and clavicle), RASH PRURITIC ((rash) very itchy) and VACCINATION SITE RASH (Rash at the injection site in the left arm). At the time of the report, ERYTHEMA (redness) and VACCINATION SITE RASH (Rash at the injection site in the left arm) outcome was unknown and URTICARIA (hives), RASH (rash on back and clavicle) and RASH PRURITIC ((rash) very itchy) had not resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Treatment medication includes Benadryl, Steroid Ointment and Body Wash. This case was linked to MOD-2021-037010 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 03-May-2021: Follow up information was received: Added Patient Demographics, Reporter Information, Medical History Information, Concomitant and Treatment Medications, Events associated with vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Benign prostatic hyperplasia; Hypertension
Vorgeschichte: -
Andere Medikamente: AMLODIPINE; TADALAFIL
Allergien: -
Vorherige Impfungen: -

VAERS 1561899

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038k20A

mild

Staat: FL
Alter: 78,0
Geschlecht: M
Eingang: 15.08.2021
Impfdatum: 09.02.2021
Beginn: 10.02.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: OT / LA

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

Arthralgia Fatigue Headache Myalgia Nausea

Symptomtext

Fatigue; Headache; Muscle Pain; Joint Pain; Nausea; This spontaneous case was reported by a consumer and describes the occurrence of FATIGUE (Fatigue), HEADACHE (Headache), MYALGIA (Muscle Pain), ARTHRALGIA (Joint Pain) and NAUSEA (Nausea) in a 78-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038k20A) for COVID-19 vaccination. Concurrent medical conditions included Diabetes (Patient is under medication). Concomitant products included INSULIN for Diabetes, GABAPENTIN for an unknown indication. On 09-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 10-Feb-2021, the patient experienced FATIGUE (Fatigue), HEADACHE (Headache), MYALGIA (Muscle Pain), ARTHRALGIA (Joint Pain) and NAUSEA (Nausea). At the time of the report, FATIGUE (Fatigue), HEADACHE (Headache), MYALGIA (Muscle Pain), ARTHRALGIA (Joint Pain) and NAUSEA (Nausea) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. The patient was not taking any medications to treat those side effects.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Diabetes (Patient is under medication)
Vorgeschichte: -
Andere Medikamente: INSULIN; GABAPENTIN
Allergien: -
Vorherige Impfungen: -

VAERS 1561843

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: MI
Alter: 70,0
Geschlecht: F
Eingang: 15.08.2021
Impfdatum: 02.02.2021
Beginn: 02.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Pain Vaccination site pain Vaccination site rash Vaccination site swelling

Symptomtext

little ache; little swollen; a rash and a round circle all around the injection site; her arm hurt for the first day or two; 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 events little ache/pain, little swollen/vaccination site swelling, her arm hurt for the first day or two,/vaccination site pain, a rash and a round circle all around the injection site/vaccination site rash. The patient's medical history was not provided. No relevant concomitant medications were reported. On 2 Feb 2021, prior to the onset of the events the patient received first of two planned doses of mRNA-1273 (lot/batch: 038K20A) via unknown route in the left arm for prophylaxis of COVID-19 infection. On 9 Feb 2021, the patient experienced the event(s) little ache, little swollen. On 2 Feb 2021, the patient experienced the event(s) her arm hurt for the first day or two, a rash and a round circle all around the injection site. Treatment details included None. Action taken with mRNA-1273 in response to the events was not reported. On 3 Feb 2021 the outcome of event(s), her arm hurt for the first day or two was resolved. The outcome of event(s), little ache, little swollen, a rash and a round circle all around the injection site was unknown.

Weitere VAERSDATA-Felder

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

VAERS 1561559

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: FL
Alter: 65,0
Geschlecht: F
Eingang: 15.08.2021
Impfdatum: 12.01.2021
Beginn: 12.01.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: OT / -

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

Pain

Symptomtext

Soreness; This spontaneous case was reported by a consumer and describes the occurrence of PAIN (Soreness) in a 65-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. No Medical History information was reported. On 12-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 12-Feb-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 12-Jan-2021, the patient experienced PAIN (Soreness). On 13-Jan-2021, PAIN (Soreness) had resolved. Not Provided mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) and mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) dosing remained unchanged. Treatment medications of the patient were provided. No concomitant medications were provided. Patient stated that on 8FEB2021 she was riding her bike when she was hit by a car she experienced whip lash and bruising from the accident

Weitere VAERSDATA-Felder

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

VAERS 1561354

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038k20a

mild

Staat: MI
Alter: 73,0
Geschlecht: F
Eingang: 15.08.2021
Impfdatum: 22.02.2021
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: OT / -

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

Feeling abnormal Injection site pruritus Vaccination site swelling

Symptomtext

Feeling strange; Itching at injection; Swollen at injection site; This spontaneous case was reported by a consumer and describes the occurrence of FEELING ABNORMAL (Feeling strange), INJECTION SITE PRURITUS (Itching at injection) and VACCINATION SITE SWELLING (Swollen at injection site) in a 73-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038k20a) for COVID-19 vaccination. Concurrent medical conditions included Blood pressure abnormal. Concomitant products included METFORMIN for an unknown indication. On 22-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On an unknown date, the patient experienced FEELING ABNORMAL (Feeling strange), INJECTION SITE PRURITUS (Itching at injection) and VACCINATION SITE SWELLING (Swollen at injection site). At the time of the report, FEELING ABNORMAL (Feeling strange), INJECTION SITE PRURITUS (Itching at injection) and VACCINATION SITE SWELLING (Swollen at injection site) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Patient's concomitant medications also included unspecified supplements and medicine for blood pressure. Treatment medications was not provided by the reporter

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure abnormal
Andere Medikamente: METFORMIN
Allergien: -
Vorherige Impfungen: -

VAERS 1560926

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: FL
Alter: 75,0
Geschlecht: F
Eingang: 15.08.2021
Impfdatum: 29.01.2021
Beginn: 29.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / LA

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

Bone pain Chills Fatigue Malaise Nausea Pyrexia Vaccination complication Vaccination site discolouration

Symptomtext

Had a severe reaction; Bones felt like electricity was going through them; Sick; Injection site was initially black and blue; Chills; Nauseas; A fever of 101; Tired; Didn't feel great for a day; This spontaneous case was reported by a consumer and describes the occurrence of MALAISE (Didn't feel great for a day), VACCINATION COMPLICATION (Had a severe reaction), BONE PAIN (Bones felt like electricity was going through them), VACCINATION COMPLICATION (Sick) and VACCINATION SITE DISCOLOURATION (Injection site was initially black and blue) in a 75-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 013M20A and 038K20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 29-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 26-Feb-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 29-Jan-2021, the patient experienced MALAISE (Didn't feel great for a day). On 26-Feb-2021, the patient experienced VACCINATION COMPLICATION (Had a severe reaction), BONE PAIN (Bones felt like electricity was going through them), VACCINATION COMPLICATION (Sick), VACCINATION SITE DISCOLOURATION (Injection site was initially black and blue), CHILLS (Chills), NAUSEA (Nauseas), PYREXIA (A fever of 101) and FATIGUE (Tired). At the time of the report, MALAISE (Didn't feel great for a day), VACCINATION COMPLICATION (Had a severe reaction), BONE PAIN (Bones felt like electricity was going through them), VACCINATION COMPLICATION (Sick), VACCINATION SITE DISCOLOURATION (Injection site was initially black and blue), CHILLS (Chills), NAUSEA (Nauseas), PYREXIA (A fever of 101) and FATIGUE (Tired) outcome was unknown. Not Provided No concomitant medication was reported. Treatment medication was not provided by the reporter. Action taken with mRNA-1273 in response to the event was not applicable.

Weitere VAERSDATA-Felder

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

VAERS 1560865

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: NY
Alter: 78,0
Geschlecht: F
Eingang: 15.08.2021
Impfdatum: 21.01.2021
Beginn: 31.01.2021
Tage bis Beginn: 10,0
Dosis: 2
Route/Site: OT / LA

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

Arthralgia

Symptomtext

both of her shoulders had knives in them(pain); This spontaneous case was reported by a consumer and describes the occurrence of ARTHRALGIA (both of her shoulders had knives in them(pain)) in a 78-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 038K20A and 004M20a) for COVID-19 vaccination. Concurrent medical conditions included Arthritis. Concomitant products included MELOXICAM (MOBIC), ESOMEPRAZOLE SODIUM (NEXIUM [ESOMEPRAZOLE SODIUM]), ESTRADIOL (ESTROGEN), COLECALCIFEROL (VITAMIN D 3), ASCORBIC ACID (VITAMIN C ACID), FISH OIL and CENTRUM SILVER [ASCORBIC ACID;BETACAROTENE;BIOTIN;CALCIUM;CHROMIUM;COLECALCIFEROL;COPPER;FOLIC ACID;IODINE;IRON;LYCOPENE;MAGNESIUM;MANGANESE;NICOTINAMIDE;PANTOTHENIC ACID;PHOSPHORUS;PHYTOMENADIONE;POTASSIUM;PYRIDOXINE HYDROCHLORIDE;RETINOL;RIBOFLAVIN for an unknown indication. On 21-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .5 milliliter. On 18-Feb-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 31-Jan-2021, the patient experienced ARTHRALGIA (both of her shoulders had knives in them(pain)). The patient was treated with PARACETAMOL (TYLENOL) at an unspecified dose and frequency. At the time of the report, ARTHRALGIA (both of her shoulders had knives in them(pain)) outcome was unknown. Treatment Medicines include Tylenol and Mobic that patient takes for Arthritis. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was not applicable.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Arthritis
Andere Medikamente: MOBIC; NEXIUM [ESOMEPRAZOLE SODIUM]; ESTROGEN; VITAMIN D 3; VITAMIN C ACID; FISH OIL; CENTRUM SILVER [ASCORBIC ACID;BETACAROTENE;BIOTIN;CALCIUM;CHROMIUM;COLECALCIFEROL;COPPER;FOLIC ACID;
Allergien: -
Vorherige Impfungen: -

VAERS 1560764

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: IL
Alter: 76,0
Geschlecht: F
Eingang: 15.08.2021
Impfdatum: 06.02.2021
Beginn: 07.02.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: OT / LA

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

Influenza like illness Myalgia Pain

Symptomtext

Feeling like getting the flu again; Body aches and pain; Body aches and pains; This spontaneous case was reported by a consumer and describes the occurrence of INFLUENZA LIKE ILLNESS (Feeling like getting the flu again), PAIN (Body aches and pain) and MYALGIA (Body aches and pains) in a 76-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 immunisation. The patient's past medical history included Breast cancer. Concurrent medical conditions included Cholesterol. On 06-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 07-Feb-2021, the patient experienced INFLUENZA LIKE ILLNESS (Feeling like getting the flu again), PAIN (Body aches and pain) and MYALGIA (Body aches and pains). At the time of the report, INFLUENZA LIKE ILLNESS (Feeling like getting the flu again), PAIN (Body aches and pain) and MYALGIA (Body aches and pains) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. No concomitant medication was provided. No treatment details were provided.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myalgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Cholesterol
Vorgeschichte: Medical History/Concurrent Conditions: Breast cancer
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1560730

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: PA
Alter: 70,0
Geschlecht: M
Eingang: 15.08.2021
Impfdatum: 17.02.2021
Beginn: 17.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / RA

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

Dizziness Rash pruritic

Symptomtext

Bad Itchy rash on both Arms & Legs; Dizzy; A spontaneous report was received from a consumer concerning a 70-years-old male patient who received Moderna's COVID-19 vaccine (mRNA-1273) and experienced events dizzy, bad itchy rash on both arms & legs. The patient's medical history was not provided. He stopped Lipitor prior to vaccination and has not restarted it. Concomitant medications reported were esomeprazole magnesium. On 17 Feb 2021, prior to the onset of the events the patient received their first of two planned doses of mRNA-1273 (lot/batch: 038K20A) intramuscularly in the right arm for prophylaxis of COVID-19 infection. On 17 Feb 2021, the patient felt a little dizzy for one day. On 19 Feb 2021, he developed an itchy rash on both arms and legs. On 20 Feb 2021, he went to the Hospital. The Emergency Room (ER) doctor administered one diphenhydramine injection to him, and discharged him the same day to continue diphenhydramine per oral at home. The rash lasted for five days. On 24 Feb 2021, the patient had very little symptoms. He took another diphenhydramine pill and it went away. Treatment details included diphenhydramine Injection, diphenhydramine capsules. Action taken with mRNA-1273 in response to the events was unknown. Outcome for the event of dizzy and bad itchy rash on both arms and legs was considered resolved.; 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: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: No adverse event (No medical history reported)
Andere Medikamente: ESOMEPRAZOLE MAGNESIUM
Allergien: -
Vorherige Impfungen: -

VAERS 1560728

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: PA
Alter: 66,0
Geschlecht: F
Eingang: 15.08.2021
Impfdatum: 03.02.2021
Beginn: 09.02.2021
Tage bis Beginn: 6,0
Dosis: UNK
Route/Site: OT / -

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

Headache Pain in extremity Pyrexia Rash

Symptomtext

Sore arm; Initially experiencing a headache; Rash on her chest, stomach, and back; Fever / temp was approximately 99.2F; A spontaneous report was received from a consumer concerning herself, a 66-year-old patient, who received Moderna's COVID-19 vaccine (mRNA-1273) and experienced headache, sore arm / pain in extremity, rash on her chest, stomach and back / rash, fever, temp was approximately 99.2F / pyrexia. The patient's medical history was not provided. Concomitant product use was not provided. On 03 Feb 2021, prior to the onset of the events, the patient received their planned doses of mRNA-1273 (Batch number: 038K20A) intramuscularly for prophylaxis of COVID-19 infection. On an unknown date the patient initially experienced headache and sore arm. On 09 Feb 2021, the patient experienced rash on her chest, stomach, and back. Patient also reported that her temp was approximately 99.2F and still has the rash. Treatment information included diphenhydramine. Action taken with mRNA-1273 in response to the events was not reported. The event rash was not resolved at the time of report. The outcome of the event, headache, sore arm, temp was approximately 99.2F was unknown.

Weitere VAERSDATA-Felder

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

VAERS 1560702

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: FL
Alter: 75,0
Geschlecht: F
Eingang: 15.08.2021
Impfdatum: 01.02.2021
Beginn: 02.02.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: OT / -

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

Diarrhoea Fatigue Pain in extremity Stomach mass

Symptomtext

pain in back of legs and arms; fatigue; diarrhea; knot in my stomach; This spontaneous case was reported by a consumer and describes the occurrence of STOMACH MASS (knot in my stomach), DIARRHOEA (diarrhea), FATIGUE (fatigue) and PAIN IN EXTREMITY (pain in back of legs and arms) in a 75-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. No Medical History information was reported. On 01-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 02-Feb-2021, the patient experienced STOMACH MASS (knot in my stomach). On 03-Feb-2021, the patient experienced DIARRHOEA (diarrhea) and FATIGUE (fatigue). On 04-Feb-2021, the patient experienced PAIN IN EXTREMITY (pain in back of legs and arms). On 06-Feb-2021, PAIN IN EXTREMITY (pain in back of legs and arms) had resolved. At the time of the report, STOMACH MASS (knot in my stomach), DIARRHOEA (diarrhea) and FATIGUE (fatigue) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. No relevant concomitant medications were reported. No treatment information was provided.

Weitere VAERSDATA-Felder

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

VAERS 1560624

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: FL
Alter: -
Geschlecht: F
Eingang: 15.08.2021
Impfdatum: 03.02.2021
Beginn: 11.02.2021
Tage bis Beginn: 8,0
Dosis: 1
Route/Site: OT / -

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

Vaccination site induration Vaccination site pruritus Vaccination site rash Vaccination site swelling Vaccination site warmth

Symptomtext

Injection site feels warm; Injection site feels hard; Injection site itching; Rash on the injection site; Injection site swollen; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION SITE WARMTH (Injection site feels warm), VACCINATION SITE INDURATION (Injection site feels hard), VACCINATION SITE PRURITUS (Injection site itching), VACCINATION SITE RASH (Rash on the injection site) and VACCINATION SITE SWELLING (Injection site swollen) in a 92-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. No Medical History information was reported. On 03-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 11-Feb-2021, the patient experienced VACCINATION SITE WARMTH (Injection site feels warm), VACCINATION SITE INDURATION (Injection site feels hard), VACCINATION SITE PRURITUS (Injection site itching), VACCINATION SITE RASH (Rash on the injection site) and VACCINATION SITE SWELLING (Injection site swollen). At the time of the report, VACCINATION SITE WARMTH (Injection site feels warm), VACCINATION SITE INDURATION (Injection site feels hard), VACCINATION SITE PRURITUS (Injection site itching), VACCINATION SITE RASH (Rash on the injection site) and VACCINATION SITE SWELLING (Injection site swollen) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. No relevant concomitant medications were reported. No treatment information was provided.

Weitere VAERSDATA-Felder

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

VAERS 1560580

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: IL
Alter: 75,0
Geschlecht: F
Eingang: 15.08.2021
Impfdatum: 27.01.2021
Beginn: 10.02.2021
Tage bis Beginn: 14,0
Dosis: 1
Route/Site: OT / RA

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

Cough Rash Rhinorrhoea Sneezing Throat irritation Vaccination site erythema Vaccination site induration Vaccination site pain Vaccination site pruritus Vaccination site swelling

Symptomtext

Runny Nose; Sneezing; Scratchy Throat; Cough; Hardness - Near Injection Site; Rash - Inside of Right Forearm; Itchy Sensation - Near Injection Site; Redness - Near Injection Site; Soreness - Near Injection Site; Swelling - Near Injection Site; This spontaneous case was reported by a consumer (subsequently medically confirmed) and describes the occurrence of RHINORRHOEA (Runny Nose), SNEEZING (Sneezing), THROAT IRRITATION (Scratchy Throat), COUGH (Cough) and VACCINATION SITE INDURATION (Hardness - Near Injection Site) in a 75-year-old female patient who received mRNA-1273 (batch no. 038K20A) 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 (Intramuscular) 1 dosage form. On 10-Feb-2021, the patient experienced RHINORRHOEA (Runny Nose), SNEEZING (Sneezing), THROAT IRRITATION (Scratchy Throat), COUGH (Cough), VACCINATION SITE INDURATION (Hardness - Near Injection Site), RASH (Rash - Inside of Right Forearm), VACCINATION SITE PRURITUS (Itchy Sensation - Near Injection Site), VACCINATION SITE ERYTHEMA (Redness - Near Injection Site), VACCINATION SITE PAIN (Soreness - Near Injection Site) and VACCINATION SITE SWELLING (Swelling - Near Injection Site). The patient was treated with CETIRIZINE HYDROCHLORIDE (BENADRYL ALLERGY [CETIRIZINE HYDROCHLORIDE]) at an unspecified dose and frequency and HYDROCORTISONE (CORTIZONE-10 [HYDROCORTISONE]) at an unspecified dose and frequency. At the time of the report, RHINORRHOEA (Runny Nose), SNEEZING (Sneezing), THROAT IRRITATION (Scratchy Throat), COUGH (Cough), VACCINATION SITE INDURATION (Hardness - Near Injection Site), RASH (Rash - Inside of Right Forearm), VACCINATION SITE PRURITUS (Itchy Sensation - Near Injection Site), VACCINATION SITE ERYTHEMA (Redness - Near Injection Site), VACCINATION SITE PAIN (Soreness - Near Injection Site) and VACCINATION SITE SWELLING (Swelling - Near Injection Site) had not resolved. Not Provided The action taken with mRNA-1273 (Intramuscular) was unknown. For mRNA-1273 (Intramuscular), the reporter did not provide any causality assessments.

Weitere VAERSDATA-Felder

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

VAERS 1560321

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: MI
Alter: 78,0
Geschlecht: F
Eingang: 15.08.2021
Impfdatum: 05.02.2021
Beginn: 07.02.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: OT / LA

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

Burning sensation Pruritus Rash Swelling

Symptomtext

has raised bumps on her chest; terrible rash; burning; itching; This spontaneous case was reported by a consumer and describes the occurrence of BURNING SENSATION (burning), PRURITUS (itching), SWELLING (has raised bumps on her chest) and RASH (terrible rash) in a 78-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. No Medical History information was reported. On 05-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 07-Feb-2021, the patient experienced BURNING SENSATION (burning), PRURITUS (itching) and RASH (terrible rash). On 03-Mar-2021, the patient experienced SWELLING (has raised bumps on her chest). At the time of the report, BURNING SENSATION (burning), PRURITUS (itching) and RASH (terrible rash) was resolving and SWELLING (has raised bumps on her chest) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. Concomitant product use was not reported Treatment information was not provided

Weitere VAERSDATA-Felder

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

VAERS 1560269

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: MI
Alter: 74,0
Geschlecht: F
Eingang: 15.08.2021
Impfdatum: 18.02.2021
Beginn: 25.02.2021
Tage bis Beginn: 7,0
Dosis: 1
Route/Site: OT / -

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

Dry mouth Oral discomfort Swollen tongue Urticaria

Symptomtext

Tongue swelling; Dry mouth; Burning; Body broke out in hives; This spontaneous case was reported by a consumer and describes the occurrence of SWOLLEN TONGUE (Tongue swelling), DRY MOUTH (Dry mouth), ORAL DISCOMFORT (Burning) and URTICARIA (Body broke out in hives) in a 74-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. No Medical History information was reported. On 18-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 25-Feb-2021, the patient experienced SWOLLEN TONGUE (Tongue swelling), DRY MOUTH (Dry mouth), ORAL DISCOMFORT (Burning) and URTICARIA (Body broke out in hives). The patient was treated with DIPHENHYDRAMINE HYDROCHLORIDE (BENADRYL [DIPHENHYDRAMINE HYDROCHLORIDE]) at an unspecified dose and frequency. At the time of the report, SWOLLEN TONGUE (Tongue swelling), DRY MOUTH (Dry mouth), ORAL DISCOMFORT (Burning) and URTICARIA (Body broke out in hives) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported.

Weitere VAERSDATA-Felder

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

VAERS 1560123

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: IL
Alter: 74,0
Geschlecht: F
Eingang: 15.08.2021
Impfdatum: 11.02.2021
Beginn: 15.02.2021
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: OT / RA

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

Abdominal discomfort Dizziness Nausea Vertigo

Symptomtext

Nausea; Woozy/Kind of dizzy-like; Upset stomach; Vertigo; This spontaneous case was reported by a consumer and describes the occurrence of NAUSEA (nausea), DIZZINESS (woozy), ABDOMINAL DISCOMFORT (Upset stomach), DIZZINESS (kind of dizzy-like) and VERTIGO (vertigo) in a 74-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. The patient's past medical history included Vertigo. On 11-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 15-Feb-2021, the patient experienced NAUSEA (nausea), DIZZINESS (woozy), ABDOMINAL DISCOMFORT (Upset stomach), DIZZINESS (kind of dizzy-like) and VERTIGO (vertigo). On 16-Feb-2021, NAUSEA (nausea), DIZZINESS (woozy), ABDOMINAL DISCOMFORT (Upset stomach), DIZZINESS (kind of dizzy-like) and VERTIGO (vertigo) 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. No concomitant medication details were provided. No treatment medication details were provided.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Vertigo
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1559978

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: FL
Alter: 71,0
Geschlecht: F
Eingang: 15.08.2021
Impfdatum: 02.02.2021
Beginn: 02.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / LA

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

Chills Fatigue Headache Illness Myalgia Parosmia Symptom recurrence

Symptomtext

fatigue; headache; body aches; chills; violently sick; like covid again; smells exhaust fumes; This spontaneous case was reported by a consumer and describes the occurrence of ILLNESS (violently sick), SYMPTOM RECURRENCE (like covid again), PAROSMIA (smells exhaust fumes), FATIGUE (fatigue) and HEADACHE (headache) in a 71-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included COVID-19. Concomitant products included GABAPENTIN and CLOZAPINE for an unknown indication. On 02-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 02-Feb-2021, the patient experienced PAROSMIA (smells exhaust fumes). On 03-Feb-2021, the patient experienced ILLNESS (violently sick), SYMPTOM RECURRENCE (like covid again), FATIGUE (fatigue), HEADACHE (headache), MYALGIA (body aches) and CHILLS (chills). The patient was treated with PARACETAMOL (TYLENOL) at an unspecified dose and frequency. On 07-Feb-2021, ILLNESS (violently sick), SYMPTOM RECURRENCE (like covid again), HEADACHE (headache), MYALGIA (body aches) and CHILLS (chills) had resolved. At the time of the report, PAROSMIA (smells exhaust fumes) outcome was unknown and FATIGUE (fatigue) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19
Andere Medikamente: GABAPENTIN; CLOZAPINE
Allergien: -
Vorherige Impfungen: -

VAERS 1559763

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: MI
Alter: -
Geschlecht: F
Eingang: 15.08.2021
Impfdatum: 01.02.2021
Beginn: 02.02.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: OT / RA

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

Vaccination site erythema Vaccination site pruritus Vaccination site rash

Symptomtext

Significantly redder and as big as can of coke; Really itchy; Slight pale rash; Skin would feel itchy at injection site; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION SITE PRURITUS (Skin would feel itchy at injection site), VACCINATION SITE PRURITUS (Really itchy), VACCINATION SITE RASH (Slight pale rash) and VACCINATION SITE ERYTHEMA (Significantly redder and as big as can of coke) in a 75-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. Concurrent medical conditions included Sensitive skin (The patient stated that she get rashes and itchiness very easily.). Concomitant products included LEVOCETIRIZINE DIHYDROCHLORIDE (XYZAL), LOSARTAN, ESTROGENS CONJUGATED (PREMARIN) and PREDNISONE ( same dose since 5-6 years) for an unknown indication. On 01-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 02-Feb-2021, the patient experienced VACCINATION SITE PRURITUS (Skin would feel itchy at injection site) and VACCINATION SITE RASH (Slight pale rash). On 08-Feb-2021, the patient experienced VACCINATION SITE PRURITUS (Really itchy). On 10-Feb-2021, the patient experienced VACCINATION SITE ERYTHEMA (Significantly redder and as big as can of coke). At the time of the report, VACCINATION SITE PRURITUS (Skin would feel itchy at injection site), VACCINATION SITE PRURITUS (Really itchy), VACCINATION SITE RASH (Slight pale rash) and VACCINATION SITE ERYTHEMA (Significantly redder and as big as can of coke) had not resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. Treatment details included body lotion. Patient reports "I'm putting lotion on it and its still the same"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Vaccination site pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Sensitive skin (The patient stated that she get rashes and itchiness very easily.)
Vorgeschichte: -
Andere Medikamente: XYZAL; LOSARTAN; PREMARIN; PREDNISONE
Allergien: -
Vorherige Impfungen: -

VAERS 1559751

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: NJ
Alter: 39,0
Geschlecht: F
Eingang: 15.08.2021
Impfdatum: 08.02.2021
Beginn: 08.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / -

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

Myalgia Pyrexia Vaccination site erythema Vaccination site swelling Vaccination site warmth

Symptomtext

On 08-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 08-Feb-2021, the patient experienced PYREXIA (Fever) and MYALGIA (Body aches). On 09-Feb-2021, the patient experienced VACCINATION SITE WARMTH (Injection site is super hot) and VACCINATION SITE SWELLING (Injection site is swollen). On 10-Feb-2021, the patient experienced VACCINATION SITE ERYTHEMA (Injection site is red). The patient was treated with PARACETAMOL (TYLENOL) at an unspecified dose and frequency. At the time of the report, VACCINATION SITE WARMTH (Injection site is super hot), VACCINATION SITE ERYTHEMA (Injection site is red) and VACCINATION SITE SWELLING (Injection site is swollen) outcome was unknown and PYREXIA (Fever) and MYALGIA (Body aches) was resolving. 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.

Weitere VAERSDATA-Felder

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

VAERS 1559654

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: PA
Alter: 68,0
Geschlecht: M
Eingang: 15.08.2021
Impfdatum: 28.01.2021
Beginn: 29.01.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: OT / -

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

Arthralgia Pruritus Vaccination site erythema

Symptomtext

Redness below injection site; Itchy shoulder; Shoulder soreness; This spontaneous case was reported by a consumer (subsequently medically confirmed) and describes the occurrence of PRURITUS (Itchy shoulder), VACCINATION SITE ERYTHEMA (Redness below injection site) and ARTHRALGIA (Shoulder soreness) in a 68-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. The patient's past medical history included No adverse event (No reported medical history). On 28-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 29-Jan-2021, the patient experienced ARTHRALGIA (Shoulder soreness). On 03-Feb-2021, the patient experienced PRURITUS (Itchy shoulder). On 05-Feb-2021, the patient experienced VACCINATION SITE ERYTHEMA (Redness below injection site). The patient was treated with HYDROCORTISONE for Itchy, at an unspecified dose and frequency and LORATADINE, PSEUDOEPHEDRINE HYDROCHLORIDE (BENADRYL 24 D) for Itchy, at an unspecified dose and frequency. At the time of the report, PRURITUS (Itchy shoulder) had resolved and VACCINATION SITE ERYTHEMA (Redness below injection site) and ARTHRALGIA (Shoulder soreness) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Treatment medications for itchy shoulder included hydrocortisone and OTC Benadryl.

Weitere VAERSDATA-Felder

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

VAERS 1559404

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: FL
Alter: 72,0
Geschlecht: F
Eingang: 15.08.2021
Impfdatum: 02.02.2021
Beginn: 02.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / LA

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

Rash Rash macular Symptom masked Vaccination site pain Vaccination site pruritus Vaccination site rash

Symptomtext

Symptoms woke her up in the middle of the night; Bad Rash on the Injection Site; Pain on the Injection Site; Itchy Injection Site; Big Blotch on the Injection Site; Rash on her face; This spontaneous case was reported by a consumer and describes the occurrence of SYMPTOM MASKED (Symptoms woke her up in the middle of the night), RASH MACULAR (Big Blotch on the Injection Site), RASH (Rash on her face), VACCINATION SITE RASH (Bad Rash on the Injection Site) and VACCINATION SITE PAIN (Pain on the Injection Site) in a 72-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 02-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 02-Feb-2021, the patient experienced RASH MACULAR (Big Blotch on the Injection Site), RASH (Rash on her face), VACCINATION SITE PAIN (Pain on the Injection Site) and VACCINATION SITE PRURITUS (Itchy Injection Site). On 09-Feb-2021, the patient experienced SYMPTOM MASKED (Symptoms woke her up in the middle of the night) and VACCINATION SITE RASH (Bad Rash on the Injection Site). The patient was treated with PARACETAMOL (TYLENOL) at an unspecified dose and frequency. At the time of the report, SYMPTOM MASKED (Symptoms woke her up in the middle of the night), RASH MACULAR (Big Blotch on the Injection Site), RASH (Rash on her face), VACCINATION SITE RASH (Bad Rash on the Injection Site), VACCINATION SITE PAIN (Pain on the Injection Site) and VACCINATION SITE PRURITUS (Itchy Injection Site) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Concomitant medications were not provided.

Weitere VAERSDATA-Felder

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

VAERS 1559378

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: FL
Alter: 68,0
Geschlecht: F
Eingang: 15.08.2021
Impfdatum: 30.01.2021
Beginn: 30.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / -

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

Erythema Hypersensitivity Injection site erythema Injection site warmth Vaccination site pain

Symptomtext

( whole arm) hot to the touch; whole arm was red; red spot near injection site; hypersensitivity reaction; arm soreness; This spontaneous case was reported by a consumer and describes the occurrence of INJECTION SITE WARMTH (( whole arm) hot to the touch), ERYTHEMA (whole arm was red), PAIN IN EXTREMITY (arm soreness), INJECTION SITE ERYTHEMA (red spot near injection site) and HYPERSENSITIVITY (hypersensitivity reaction) in a 68-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. Concurrent medical conditions included Asthma, Drug allergy (Demerol- vomit and pass out), Drug allergy (Augmentin- stomach cramps), Environmental allergy (mold- wheezing), Environmental allergy (mildew- wheezing) and Crohn's disease since July 2012. Concomitant products included MESALAZINE (LIALDA) for Crohn's, ESTRADIOL (VAGIFEM) for Dryness vaginal, LANSOPRAZOLE (PREVACID) for Reflux esophagitis, LEVOTHYROXINE, METHOCARBAMOL, CENTRUM SILVER +50, CALCIUM, ASCORBIC ACID, ECHINACEA PURPUREA (ECHINACEA + VITAMINA C VITATECH) and BIOTIN for an unknown indication. On 30-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 30-Jan-2021, the patient experienced PAIN IN EXTREMITY (arm soreness). On 06-Feb-2021, the patient experienced HYPERSENSITIVITY (hypersensitivity reaction). On 10-Feb-2021, the patient experienced INJECTION SITE ERYTHEMA (red spot near injection site). On an unknown date, the patient experienced INJECTION SITE WARMTH (( whole arm) hot to the touch) and ERYTHEMA (whole arm was red). The patient was treated with DIPHENHYDRAMINE HYDROCHLORIDE (BENADRYL [DIPHENHYDRAMINE HYDROCHLORIDE]) from 06-Feb-2021 to 03-Mar-2021 at an unspecified dose and frequency and BISMUTH SUBSALICYLATE (PEPTOBISMOL) 28-Feb-2021 at an unspecified dose and frequency. On 01-Feb-2021, PAIN IN EXTREMITY (arm soreness) had resolved. On 11-Feb-2021, HYPERSENSITIVITY (hypersensitivity reaction) had resolved. At the time of the report, INJECTION SITE WARMTH (( whole arm) hot to the touch), ERYTHEMA (whole arm was red) and INJECTION SITE ERYTHEMA (red spot near injection site) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Concomitant medication included evening primrose oil, used for unknown indication. This case was linked to MOD-2021-192267 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 01-Jun-2021: Follow-up was received on 01-JUN-2021 Contains significant information. added patient demographics, current condition and allergy details in medical history tab, updated dose and indication for concomitant medication, New treatment medication and new event were added. On 30-Jun-2021: Follow-up was received on 30-JUN-2021 contains No new information.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Asthma; Crohn's disease; Drug allergy (Demerol- vomit and pass out); Drug allergy (Augmentin- stomach cramps); Environmental allergy (mold- wheezing); Environmental allergy (mildew- wheezing)
Vorgeschichte: -
Andere Medikamente: LIALDA; PREVACID; VAGIFEM; LEVOTHYROXINE; METHOCARBAMOL; CENTRUM SILVER +50; CALCIUM; ECHINACEA + VITAMINA C VITATECH; BIOTIN
Allergien: -
Vorherige Impfungen: -

VAERS 1559119

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: FL
Alter: 65,0
Geschlecht: F
Eingang: 15.08.2021
Impfdatum: 29.01.2021
Beginn: 27.02.2021
Tage bis Beginn: 29,0
Dosis: 1
Route/Site: OT / LA

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

Balance disorder Fatigue Muscular weakness

Symptomtext

Weakness on both legs (she was taking small steps when she walked; Almost losing her balance; Feels tired; This spontaneous case was reported by a consumer and describes the occurrence of MUSCULAR WEAKNESS (Weakness on both legs (she was taking small steps when she walked), BALANCE DISORDER (Almost losing her balance) and FATIGUE (Feels tired) in a 65-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 031M20A and 038K20A) for COVID-19 vaccination. No Medical History information was reported. On 29-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 26-Feb-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 27-Feb-2021, the patient experienced MUSCULAR WEAKNESS (Weakness on both legs (she was taking small steps when she walked), BALANCE DISORDER (Almost losing her balance) and FATIGUE (Feels tired). On 27-Feb-2021, MUSCULAR WEAKNESS (Weakness on both legs (she was taking small steps when she walked) and BALANCE DISORDER (Almost losing her balance) had resolved. At the time of the report, FATIGUE (Feels tired) outcome was unknown. No relevant concomitant medications were reported. No treatment information was reported. Action taken with mRNA-1273 in response to the events was not applicable.; 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: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1559029

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: OH
Alter: 82,0
Geschlecht: M
Eingang: 15.08.2021
Impfdatum: 25.01.2021
Beginn: 25.02.2021
Tage bis Beginn: 31,0
Dosis: 1
Route/Site: OT / -

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

Chills Feeling abnormal Memory impairment Pain in extremity Sensory loss

Symptomtext

Sore Arm; Felt like in a daze; Memory lapse; Seems like he lost it; Got the chills; This spontaneous case was reported by a consumer and describes the occurrence of PAIN IN EXTREMITY (Sore Arm), FEELING ABNORMAL (Felt like in a daze), MEMORY IMPAIRMENT (Memory lapse), SENSORY LOSS (Seems like he lost it) and CHILLS (Got the chills) in an 82-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 002A21A and 038K20A) for COVID-19 vaccination. No Medical History information was reported. On 25-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 24-Feb-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 25-Feb-2021, the patient experienced PAIN IN EXTREMITY (Sore Arm), FEELING ABNORMAL (Felt like in a daze), MEMORY IMPAIRMENT (Memory lapse), SENSORY LOSS (Seems like he lost it) and CHILLS (Got the chills). At the time of the report, PAIN IN EXTREMITY (Sore Arm), FEELING ABNORMAL (Felt like in a daze), MEMORY IMPAIRMENT (Memory lapse), SENSORY LOSS (Seems like he lost it) and CHILLS (Got the chills) had resolved. No treatment information was provided.

Weitere VAERSDATA-Felder

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

VAERS 1558993

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: MI
Alter: 73,0
Geschlecht: F
Eingang: 15.08.2021
Impfdatum: 05.02.2021
Beginn: 05.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / -

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

Emergency care Pruritus Urticaria

Symptomtext

was taken to ER and given some treatment; Itchy; Hives, ended up spread in many parts of her body,; This spontaneous case was reported by a consumer and describes the occurrence of EMERGENCY CARE (was taken to ER and given some treatment), PRURITUS (Itchy) and URTICARIA (Hives, ended up spread in many parts of her body,) in a 73-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. Concurrent medical conditions included Cholesterol, Thyroid disorder NOS and Thrombocythemia. On 05-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 05-Feb-2021, the patient experienced EMERGENCY CARE (was taken to ER and given some treatment), PRURITUS (Itchy) and URTICARIA (Hives, ended up spread in many parts of her body,). The patient was treated with DIPHENHYDRAMINE HYDROCHLORIDE (BENADRYL [DIPHENHYDRAMINE HYDROCHLORIDE]) at a dose of 1 UNK and PREDNISONE at an unspecified dose and frequency. At the time of the report, EMERGENCY CARE (was taken to ER and given some treatment), PRURITUS (Itchy) and URTICARIA (Hives, ended up spread in many parts of her body,) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. Patient was given steroid injection,Benadryl injection and prednisone pills as a treatment medication. Concomitant Medication included unspecified cholesterol medication , thyroid medication, quimo drug pill for type. It was reported that that the patient had many problems after she had the shot and it was unknown if it was related to the shot. Her problems lasted for 3 months. Most recent FOLLOW-UP information incorporated above includes: On 21-Jun-2021: F/U received on 21-JUN-2021,Clinical course information and event outcome updated.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Cholesterol; Thrombocythemia; Thyroid disorder NOS
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1558943

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: FL
Alter: 68,0
Geschlecht: F
Eingang: 15.08.2021
Impfdatum: 30.01.2021
Beginn: 30.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / -

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

Fatigue Feeling abnormal Pruritus Vaccination site erythema Vaccination site pain

Symptomtext

Didn't feel real great; Tired; Redness and itching; Itching; Didn't feel real great; soreness at injection site; Redness and itching; This spontaneous case was reported by a consumer and describes the occurrence of the first episode of VACCINATION SITE ERYTHEMA (Redness and itching), VACCINATION SITE PAIN (soreness at injection site), PRURITUS (Itching), the second episode of VACCINATION SITE ERYTHEMA (Redness and itching) and the first episode of FEELING ABNORMAL (Didn't feel real great) in a 68-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included No adverse event. On 30-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 30-Jan-2021, the patient experienced the first episode of VACCINATION SITE ERYTHEMA (Redness and itching), VACCINATION SITE PAIN (soreness at injection site) and the first episode of FEELING ABNORMAL (Didn't feel real great). On 08-Feb-2021, the patient experienced PRURITUS (Itching). On 09-Feb-2021, the patient experienced the second episode of VACCINATION SITE ERYTHEMA (Redness and itching). On 10-Feb-2021, the patient experienced FATIGUE (Tired) and the second episode of FEELING ABNORMAL (Didn't feel real great). The patient was treated with PARACETAMOL (TYLENOL) at an unspecified dose and frequency. 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.

Weitere VAERSDATA-Felder

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

VAERS 1558925

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: FL
Alter: 68,0
Geschlecht: F
Eingang: 15.08.2021
Impfdatum: 30.01.2021
Beginn: 30.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / -

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

Erythema Fatigue Pruritus Vaccination complication Vaccination site erythema Vaccination site pain Vaccination site pruritus

Symptomtext

Tired / Not myself; Redness; Itching; Itching at injection site; Redness at injection site; Sore at the injection site; Didn't feel real great; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION COMPLICATION (Didn't feel real great), ERYTHEMA (Redness), PRURITUS (Itching), VACCINATION SITE PRURITUS (Itching at injection site) and VACCINATION SITE ERYTHEMA (Redness at injection site) in a 68-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 30-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 30-Jan-2021, the patient experienced VACCINATION COMPLICATION (Didn't feel real great), VACCINATION SITE PRURITUS (Itching at injection site), VACCINATION SITE ERYTHEMA (Redness at injection site) and VACCINATION SITE PAIN (Sore at the injection site). On 08-Feb-2021, the patient experienced PRURITUS (Itching). On 09-Feb-2021, the patient experienced ERYTHEMA (Redness). On 10-Feb-2021, the patient experienced FATIGUE (Tired / Not myself). The patient was treated with PARACETAMOL (TYLENOL) for Adverse event following immunisation, at an unspecified dose and frequency. On 01-Feb-2021, VACCINATION COMPLICATION (Didn't feel real great), VACCINATION SITE PRURITUS (Itching at injection site), VACCINATION SITE ERYTHEMA (Redness at injection site) and VACCINATION SITE PAIN (Sore at the injection site) had resolved. At the time of the report, ERYTHEMA (Redness), PRURITUS (Itching) and FATIGUE (Tired / Not myself) had not resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. No relevant concomitant medications were reported.

Weitere VAERSDATA-Felder

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

VAERS 1558799

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: KY
Alter: 65,0
Geschlecht: F
Eingang: 15.08.2021
Impfdatum: 03.01.2021
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

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

Fatigue Oropharyngeal pain

Symptomtext

sore throat that lasted for 24-36 hour; Slept all day due to Fatigue; A spontaneous report was received from a consumer concerning a 65-years-old female patient who received Moderna's COVID-19 vaccine (mRNA-1273) and experienced events sore throat that lasted for 24-36 hour, just slept all day due to fatigue. The patient's medical history was not provided. Concomitant medications reported were eliquis, Ambien, Atorvastatin for drug use for unknown indication. On 3 Feb 2021, prior to the onset of the events the patient received their second of two planned doses of mRNA-1273 (lot/batch: 038K20A) intramuscularly for prophylaxis of COVID-19 infection. On an unknown date, the patient experienced the event(s) sore throat that lasted for 24-36 hour, just slept all day due to fatigue. Treatment details included as no treatment taken. Action taken with mRNA-1273 in response to the events was not reported. The outcome of event(s), sore throat that lasted for 24-36 hour, just slept all day due to fatigue was unknown.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: No adverse event
Andere Medikamente: ELIQUIS; AMBIEN; ATORVASTATIN
Allergien: -
Vorherige Impfungen: -

VAERS 1557803

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: SC
Alter: 81,0
Geschlecht: M
Eingang: 14.08.2021
Impfdatum: 08.02.2021
Beginn: 08.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / -

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

Chills

Symptomtext

A little bit of chills; This spontaneous case was reported by a consumer and describes the occurrence of CHILLS (A little bit of chills) in an 81-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. No Medical History information was reported. On 08-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 08-Feb-2021, the patient experienced CHILLS (A little bit of chills). At the time of the report, CHILLS (A little bit of chills) outcome was unknown. Not Provided The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. No concomitant and treatment medication information 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 event, a causal relationship cannot be excluded.

Weitere VAERSDATA-Felder

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

VAERS 1557800

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038k20a

mild

Staat: -
Alter: 72,0
Geschlecht: F
Eingang: 14.08.2021
Impfdatum: 21.01.2021
Beginn: 21.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / LA

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

Acne Pruritus Rash

Symptomtext

on her right leg little red pimples that were itchy; a rash on her left leg that was itchy and spread more; rash on her left leg that was itchy and spread more; This spontaneous case was reported by a consumer and describes the occurrence of ACNE (on her right leg little red pimples that were itchy), RASH (a rash on her left leg that was itchy and spread more) and PRURITUS (rash on her left leg that was itchy and spread more) in a 72-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 013m20a and 038k20a) for COVID-19 vaccination. Concurrent medical conditions included Hypertension. On 21-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 18-Feb-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 21-Jan-2021, the patient experienced PRURITUS (rash on her left leg that was itchy and spread more). On 23-Feb-2021, the patient experienced ACNE (on her right leg little red pimples that were itchy) and RASH (a rash on her left leg that was itchy and spread more). At the time of the report, ACNE (on her right leg little red pimples that were itchy), RASH (a rash on her left leg that was itchy and spread more) and PRURITUS (rash on her left leg that was itchy and spread more) outcome was unknown. concomitants- High blood pressure pills treatment- "Cream" didn't remember which Action taken with mRNA-1273 (Moderna COVID-19 Vaccine) is considered as not applicable.

Weitere VAERSDATA-Felder

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

VAERS 1557792

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038k20a

mild

Staat: -
Alter: -
Geschlecht: F
Eingang: 14.08.2021
Impfdatum: 21.01.2021
Beginn: 21.01.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: OT / LA

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

Rash pruritic

Symptomtext

A rash on her left leg that was itchy and spread more; This spontaneous case was reported by a consumer and describes the occurrence of RASH PRURITIC (A rash on her left leg that was itchy and spread more) in a 72-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 038k20a and 013m20a) 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) (unknown route) 1 dosage form. On 18-Feb-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 21-Jan-2021, the patient experienced RASH PRURITIC (A rash on her left leg that was itchy and spread more). At the time of the report, RASH PRURITIC (A rash on her left leg that was itchy and spread more) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. Concomitant medication was not reported. Treatment included unspecified cream. This case was linked to MOD-2021-027643.

Weitere VAERSDATA-Felder

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

VAERS 1557716

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038k20a

mild

Staat: MI
Alter: 85,0
Geschlecht: F
Eingang: 14.08.2021
Impfdatum: 07.02.2021
Beginn: 08.02.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: OT / LA

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

Pain in extremity Vaccination site erythema Vaccination site warmth

Symptomtext

Injection site is very warm; Injection sire is more red; Arm more sore; This spontaneous case was reported by a consumer and describes the occurrence of PAIN IN EXTREMITY (Arm more sore), VACCINATION SITE WARMTH (Injection site is very warm) and VACCINATION SITE ERYTHEMA (Injection sire is more red) in an 85-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038k20a) for COVID-19 vaccination. No medical history was provided by the reporter. On 07-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 08-Feb-2021, the patient experienced PAIN IN EXTREMITY (Arm more sore). On 09-Feb-2021, the patient experienced VACCINATION SITE WARMTH (Injection site is very warm) and VACCINATION SITE ERYTHEMA (Injection sire is more red). The patient was treated with PARACETAMOL (TYLENOL) at an unspecified dose and frequency. At the time of the report, PAIN IN EXTREMITY (Arm more sore), VACCINATION SITE WARMTH (Injection site is very warm) and VACCINATION SITE ERYTHEMA (Injection sire is more red) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Reporter did not allow further contact

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: No medical history was provided by the reporter.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1557514

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: FL
Alter: 74,0
Geschlecht: F
Eingang: 14.08.2021
Impfdatum: 31.01.2021
Beginn: 01.02.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: OT / LA

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

Diarrhoea

Symptomtext

diarrhea; This spontaneous case was reported by a consumer and describes the occurrence of DIARRHOEA (diarrhea) in a 74-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. Concomitant products included VITAMIN D NOS, ASCORBIC ACID (VITAMIN C ACID), CALCIUM and LISINOPRIL for an unknown indication. On 31-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 DIARRHOEA (diarrhea). At the time of the report, DIARRHOEA (diarrhea) outcome was unknown. Not Provided The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. The patient did not take any treatment medication. This case was linked to MOD-2021-022461 (Patient Link).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: VITAMIN D NOS; VITAMIN C ACID; CALCIUM; LISINOPRIL
Allergien: -
Vorherige Impfungen: -

VAERS 1557400

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: MI
Alter: 81,0
Geschlecht: F
Eingang: 14.08.2021
Impfdatum: 08.02.2021
Beginn: 15.02.2021
Tage bis Beginn: 7,0
Dosis: 1
Route/Site: OT / -

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

Skin swelling Vaccination site erythema Vaccination site pruritus Vaccination site swelling

Symptomtext

puffiness; pinkish arm 3inches by 2 inches wide; itchy; Swollen; This spontaneous case was reported by a consumer and describes the occurrence of SKIN SWELLING (puffiness), VACCINATION SITE ERYTHEMA (pinkish arm 3inches by 2 inches wide), VACCINATION SITE PRURITUS (itchy) and VACCINATION SITE SWELLING (Swollen) in an 81-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. The patient's past medical history included No adverse event. On 08-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 15-Feb-2021, the patient experienced SKIN SWELLING (puffiness), VACCINATION SITE ERYTHEMA (pinkish arm 3inches by 2 inches wide), VACCINATION SITE PRURITUS (itchy) and VACCINATION SITE SWELLING (Swollen). At the time of the report, SKIN SWELLING (puffiness), VACCINATION SITE ERYTHEMA (pinkish arm 3inches by 2 inches wide), VACCINATION SITE PRURITUS (itchy) and VACCINATION SITE SWELLING (Swollen) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. Reporter did not allow further contact

Weitere VAERSDATA-Felder

Praegender Schweregrund: Vaccination site pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: No adverse event
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1557397

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: NC
Alter: 80,0
Geschlecht: F
Eingang: 14.08.2021
Impfdatum: 28.01.2021
Beginn: 26.02.2021
Tage bis Beginn: 29,0
Dosis: 2
Route/Site: OT / -

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

Headache

Symptomtext

tremendous headache; This spontaneous case was reported by a consumer and describes the occurrence of HEADACHE (tremendous headache) in an 80-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 038K20A and 014M20A) for COVID-19 vaccination. Concomitant products included ACETYLSALICYLIC ACID, DIPYRIDAMOLE (AGGRENOX) for Clot blood, LUBIPROSTONE (AMITIZA), ACETYLSALICYLIC ACID (BABY ASPIRIN) and PRAVASTATIN for an unknown indication. On 28-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 25-Feb-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 26-Feb-2021, the patient experienced HEADACHE (tremendous headache). The patient was treated with ACETAMINOPHEN at a dose of morning. At the time of the report, HEADACHE (tremendous headache) outcome was unknown.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: AGGRENOX; AMITIZA; BABY ASPIRIN; PRAVASTATIN
Allergien: -
Vorherige Impfungen: -

VAERS 1557323

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: MI
Alter: 69,0
Geschlecht: F
Eingang: 14.08.2021
Impfdatum: 10.02.2021
Beginn: 10.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / LA

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

Fatigue Hypoaesthesia Periorbital swelling Visual impairment

Symptomtext

my eyes have been puffy; my vision was kind of weird.; I've also felt fatigued; numbing that went from jawline /earlobe up to face, across cheek.; This spontaneous case was reported by a consumer and describes the occurrence of HYPOAESTHESIA (numbing that went from jawline /earlobe up to face, across cheek.), PERIORBITAL SWELLING (my eyes have been puffy), VISUAL IMPAIRMENT (my vision was kind of weird.) and FATIGUE (I've also felt fatigued) in a 69-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. Concomitant products included ROSUVASTATIN CALCIUM (CRESTOR), EZETIMIBE (ZETIA) and METOPROLOL for an unknown indication. On 10-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 10-Feb-2021, the patient experienced HYPOAESTHESIA (numbing that went from jawline /earlobe up to face, across cheek.). On an unknown date, the patient experienced PERIORBITAL SWELLING (my eyes have been puffy), VISUAL IMPAIRMENT (my vision was kind of weird.) and FATIGUE (I've also felt fatigued). On 10-Feb-2021, HYPOAESTHESIA (numbing that went from jawline /earlobe up to face, across cheek.) had resolved. At the time of the report, PERIORBITAL SWELLING (my eyes have been puffy) and VISUAL IMPAIRMENT (my vision was kind of weird.) outcome was unknown and FATIGUE (I've also felt fatigued) was resolving. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. No treatment details were reported. Most recent FOLLOW-UP information incorporated above includes: On 29-Apr-2021: Follow-up received on 29-April-2021 contains non-significant information. Contact information was updated.

Weitere VAERSDATA-Felder

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

VAERS 1557215

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: IL
Alter: 71,0
Geschlecht: M
Eingang: 14.08.2021
Impfdatum: 02.02.2021
Beginn: 02.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / LA

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

Joint stiffness Peripheral swelling Rash

Symptomtext

mild rash; stiff joints; lump on his arm; This spontaneous case was reported by a consumer and describes the occurrence of JOINT STIFFNESS (stiff joints), PERIPHERAL SWELLING (lump on his arm) and RASH (mild rash) in a 71-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. Co-suspect product included non-company product ACETYLSALICYLIC ACID (ASPIRIN (E.C.)) for Thrombosis. The patient's past medical history included COVID-19. Concurrent medical conditions included Allergy to antibiotic, Ragweed allergy, Drug allergy (Novocaine), Diabetes since 2006, Venous ulcer NOS since 2018 and Hypertension since 1998. Concomitant products included INSULIN for Blood glucose abnormal, ATENOLOL for Blood pressure management, MULTIVITAMINS [VITAMINS NOS], COLECALCIFEROL (VIT D [COLECALCIFEROL]), HYDROCHLOROTHIAZIDE, SPIRONOLACTONE (SPIRONOLACTONE AND HYDROCHLOROTHIAZIDE), ACETYLSALICYLIC ACID (BABY ASPIRIN) and CYANOCOBALAMIN (VIT B12) for an unknown indication. On 02-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On an unknown date, the patient started ACETYLSALICYLIC ACID (ASPIRIN (E.C.)) (unknown route) 83 mg. On 02-Feb-2021, the patient experienced JOINT STIFFNESS (stiff joints) and PERIPHERAL SWELLING (lump on his arm). On 07-Feb-2021, the patient experienced RASH (mild rash). The patient was treated with BETAMETHASONE at an unspecified dose and frequency. At the time of the report, JOINT STIFFNESS (stiff joints), PERIPHERAL SWELLING (lump on his arm) and RASH (mild rash) had resolved. mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosing remained unchanged. Patient received second dose on 02-MAR-2021. Most recent FOLLOW-UP information incorporated above includes: On 29-Apr-2021: Added relevant history, updated concomitant medications, updated second dose details.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Allergy to antibiotic; Diabetes; Drug allergy (Novocaine); Hypertension; Ragweed allergy; Venous ulcer NOS
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19
Andere Medikamente: MULTIVITAMINS [VITAMINS NOS]; VIT D [COLECALCIFEROL]; SPIRONOLACTONE AND HYDROCHLOROTHIAZIDE; ATENOLOL; BABY ASPIRIN; VIT B12; INSULIN
Allergien: -
Vorherige Impfungen: -

VAERS 1557203

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: SC
Alter: 79,0
Geschlecht: F
Eingang: 14.08.2021
Impfdatum: 08.02.2021
Beginn: 08.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / -

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

Arthralgia

Symptomtext

Pain in her shoulder; This spontaneous case was reported by a consumer and describes the occurrence of ARTHRALGIA (Pain in her shoulder) in a 79-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. No Medical History information was reported. On 08-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 08-Feb-2021, the patient experienced ARTHRALGIA (Pain in her shoulder). At the time of the report, ARTHRALGIA (Pain in her shoulder) outcome was unknown. Not Provided The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. No relevant Concomitant medications were reported. No Treatment information for the event was provided. This case was received via an unknown source (no reference has been entered for a health authority or license partner) on 09-Feb-2021 and was forwarded to Moderna on 09-Feb-2021. This spontaneous case was reported by a consumer and describes the occurrence of ARTHRALGIA (Pain in her shoulder) in a 79-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. No Medical History information was reported. On 08-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 08-Feb-2021, the patient experienced ARTHRALGIA (Pain in her shoulder). At the time of the report, ARTHRALGIA (Pain in her shoulder) outcome was unknown. Not Provided The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. No relevant Concomitant medications were reported. No Treatment information for the event was provided.

Weitere VAERSDATA-Felder

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

VAERS 1557082

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: PA
Alter: 64,0
Geschlecht: F
Eingang: 14.08.2021
Impfdatum: 17.02.2021
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: OT / RA

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

Chills Headache Lymph node pain Malaise Nausea

Symptomtext

felt very sick; lymph nodes in right arm pit very sore; chills; terrible nausea; bad headache; This spontaneous case was reported by a consumer and describes the occurrence of MALAISE (felt very sick), LYMPH NODE PAIN (lymph nodes in right arm pit very sore), CHILLS (chills), NAUSEA (terrible nausea) and HEADACHE (bad headache) in a 64-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. No Medical History information was reported. On 17-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On an unknown date, the patient experienced MALAISE (felt very sick), LYMPH NODE PAIN (lymph nodes in right arm pit very sore), CHILLS (chills), NAUSEA (terrible nausea) and HEADACHE (bad headache). At the time of the report, MALAISE (felt very sick), LYMPH NODE PAIN (lymph nodes in right arm pit very sore), CHILLS (chills), NAUSEA (terrible nausea) and HEADACHE (bad headache) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. No concomitant medications were provided No treatment information provided

Weitere VAERSDATA-Felder

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

VAERS 1556774

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: IL
Alter: 53,0
Geschlecht: F
Eingang: 14.08.2021
Impfdatum: 30.01.2021
Beginn: 30.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / LA

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

Pain in extremity Vaccination site pain

Symptomtext

Pain in right heel; Sore Left Arm; This spontaneous case was reported by a consumer and describes the occurrence of PAIN IN EXTREMITY (Pain in right heel) and VACCINATION SITE PAIN (Sore Left Arm) in a 53-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. Concurrent medical conditions included Bursitis. On 30-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 30-Jan-2021, the patient experienced PAIN IN EXTREMITY (Pain in right heel) and VACCINATION SITE PAIN (Sore Left Arm). On 03-Feb-2021, VACCINATION SITE PAIN (Sore Left Arm) had resolved. On 18-Feb-2021, PAIN IN EXTREMITY (Pain in right heel) 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 assessment. About three weeks after the first vaccine, on 18-FEB-2021, patient had a cortisone shot in the heel of her right foot. No concomitant medications were reported. Treatment information was not provided.

Weitere VAERSDATA-Felder

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

VAERS 1556761

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: FL
Alter: 70,0
Geschlecht: F
Eingang: 14.08.2021
Impfdatum: 26.01.2021
Beginn: 01.02.2021
Tage bis Beginn: 6,0
Dosis: 1
Route/Site: OT / LA

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

Injection site rash

Symptomtext

rash near injection site; This spontaneous case was reported by a consumer and describes the occurrence of INJECTION SITE RASH (rash near injection site) in a 70-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. Concurrent medical conditions included Seasonal allergy. Concomitant products included DENOSUMAB (PROLIA), LISINOPRIL, BETAHISTINE HYDROCHLORIDE (VERTEX [BETAHISTINE HYDROCHLORIDE]), FAMOTIDINE (PEPCID AC) and ESTRIOL for an unknown indication. On 26-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 INJECTION SITE RASH (rash near injection site). At the time of the report, INJECTION SITE RASH (rash near injection site) outcome was unknown. 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 which shows a temporal association between the use of mRNA-1273 and the onset of the events, a causal relationship cannot be excluded. Rash is consistent with the product known safety profile.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site rash
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Seasonal allergy
Andere Medikamente: PROLIA; LISINOPRIL; VERTEX [BETAHISTINE HYDROCHLORIDE]; PEPCID AC; ESTRIOL
Allergien: -
Vorherige Impfungen: -

VAERS 1556692

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038k20a

mild

Staat: MI
Alter: 74,0
Geschlecht: M
Eingang: 14.08.2021
Impfdatum: 06.02.2021
Beginn: 06.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / LA

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

Erythema Pain Pain in extremity

Symptomtext

He experienced redness and soreness on his arm following vaccination; redness and soreness on his arm following vaccination; redness and soreness on his arm following vaccination; This spontaneous case was reported by a consumer and describes the occurrence of PAIN (redness and soreness on his arm following vaccination), ERYTHEMA (redness and soreness on his arm following vaccination) and PAIN IN EXTREMITY (He experienced redness and soreness on his arm following vaccination) in a 74-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038k20a) for COVID-19 vaccination. No Medical History information was reported. On 06-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 06-Feb-2021, the patient experienced PAIN (redness and soreness on his arm following vaccination) and ERYTHEMA (redness and soreness on his arm following vaccination). On 18-Feb-2021, the patient experienced PAIN IN EXTREMITY (He experienced redness and soreness on his arm following vaccination). At the time of the report, PAIN (redness and soreness on his arm following vaccination), ERYTHEMA (redness and soreness on his arm following vaccination) and PAIN IN EXTREMITY (He experienced redness and soreness on his arm following vaccination) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. No concomitant medications were reported. No treatment medications were provided by the reporter. Most recent FOLLOW-UP information incorporated above includes: On 14-Jul-2021: TCR attached NNI case.

Weitere VAERSDATA-Felder

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

VAERS 1556590

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: OH
Alter: 82,0
Geschlecht: U
Eingang: 14.08.2021
Impfdatum: 23.01.2021
Beginn: 23.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / -

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

Cough Muscle spasms Pain Pharyngeal swelling Vomiting

Symptomtext

Terrible pain; Throat swollen; cough; muscle spasm neck moving to front; muscle spasium leg, back, arm left side,neck moving to front; vomit; This spontaneous case was reported by a consumer and describes the occurrence of MUSCLE SPASMS (muscle spasium leg, back, arm left side,neck moving to front), PHARYNGEAL SWELLING (Throat swollen), MUSCLE SPASMS (muscle spasm neck moving to front), COUGH (cough) and PAIN (Terrible pain) in an 82-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included Central vision loss and Sleep apnoea (c pap). Concurrent medical conditions included Drug allergy (to opioids). On 23-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 23-Jan-2021, the patient experienced VOMITING (vomit). On 25-Jan-2021, the patient experienced MUSCLE SPASMS (muscle spasium leg, back, arm left side,neck moving to front). On 26-Jan-2021, the patient experienced MUSCLE SPASMS (muscle spasm neck moving to front). On 29-Jan-2021, the patient experienced PHARYNGEAL SWELLING (Throat swollen) and COUGH (cough). On an unknown date, the patient experienced PAIN (Terrible pain). On 24-Jan-2021, VOMITING (vomit) outcome was unknown. On 27-Jan-2021, MUSCLE SPASMS (muscle spasium leg, back, arm left side,neck moving to front) outcome was unknown. On 29-Jan-2021, MUSCLE SPASMS (muscle spasm neck moving to front) outcome was unknown. At the time of the report, PHARYNGEAL SWELLING (Throat swollen), COUGH (cough) and PAIN (Terrible pain) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. No concomitant medications were reported. It was reported R/T: (Oxy 98 percent) Treatment :Applied heating pad Most recent FOLLOW-UP information incorporated above includes: On 22-Apr-2021: New event was added

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Drug allergy (to opioids)
Vorgeschichte: Medical History/Concurrent Conditions: Central vision loss; Sleep apnoea (c pap)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1556512

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: FL
Alter: 66,0
Geschlecht: F
Eingang: 14.08.2021
Impfdatum: 29.01.2021
Beginn: 29.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / LA

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

Burning sensation Ear pain Neck pain Oropharyngeal pain Pain in extremity Vaccination site pain Vaccination site pruritus

Symptomtext

Left ear hurt; Neck hurt; Left arm hurt; Left fingers hurt; Sore throat; Burning sensation from her shoulder to her finger tips; Itchiness; Soreness of arm; This spontaneous case was reported by a consumer and describes the occurrence of OROPHARYNGEAL PAIN (Sore throat), BURNING SENSATION (Burning sensation from her shoulder to her finger tips), EAR PAIN (Left ear hurt), NECK PAIN (Neck hurt) and PAIN IN EXTREMITY (Left arm hurt; Left fingers hurt) in a 66-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concurrent medical conditions included Arthritis. On 29-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 29-Jan-2021, the patient experienced VACCINATION SITE PRURITUS (Itchiness) and VACCINATION SITE PAIN (Soreness of arm). On 07-Feb-2021, the patient experienced BURNING SENSATION (Burning sensation from her shoulder to her finger tips). On 08-Feb-2021, the patient experienced OROPHARYNGEAL PAIN (Sore throat), EAR PAIN (Left ear hurt), NECK PAIN (Neck hurt) and PAIN IN EXTREMITY (Left arm hurt; Left fingers hurt). At the time of the report, OROPHARYNGEAL PAIN (Sore throat), BURNING SENSATION (Burning sensation from her shoulder to her finger tips), EAR PAIN (Left ear hurt), NECK PAIN (Neck hurt), PAIN IN EXTREMITY (Left arm hurt; Left fingers hurt), VACCINATION SITE PRURITUS (Itchiness) and VACCINATION SITE PAIN (Soreness of arm) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Treatment details included Tylenol. No relevant concomitant medications were reported.

Weitere VAERSDATA-Felder

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

VAERS 1556290

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: NC
Alter: 69,0
Geschlecht: F
Eingang: 14.08.2021
Impfdatum: 23.01.2021
Beginn: 24.01.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: OT / LA

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

Erythema Fatigue Headache Pain in extremity Peripheral swelling Pyrexia Vaccination site warmth

Symptomtext

Arm is still very inflammed; arm was red; arm was hot, still warm; arm was sore; Headache; Low grade fever; Fatigue; This spontaneous case was reported by a consumer and describes the occurrence of PERIPHERAL SWELLING (Arm is still very inflammed), ERYTHEMA (arm was red), VACCINATION SITE WARMTH (arm was hot, still warm), PAIN IN EXTREMITY (arm was sore) and HEADACHE (Headache) in a 69-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included COVID-19 (The illness lasted for 2 weeks and she did not have any major symptoms from it) in November 2020 and Appendectomy (Emergency appendectomy) on 20-Jun-2021. Concomitant products included ESCITALOPRAM OXALATE (LEXAPRO) for an unknown indication. On 23-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 24-Jan-2021, the patient experienced PERIPHERAL SWELLING (Arm is still very inflammed), ERYTHEMA (arm was red), VACCINATION SITE WARMTH (arm was hot, still warm), PAIN IN EXTREMITY (arm was sore), HEADACHE (Headache), PYREXIA (Low grade fever) and FATIGUE (Fatigue). The patient was treated with NAPROXEN SODIUM (ALEVE) at an unspecified dose and frequency. At the time of the report, PERIPHERAL SWELLING (Arm is still very inflammed), ERYTHEMA (arm was red) and VACCINATION SITE WARMTH (arm was hot, still warm) had not resolved and PAIN IN EXTREMITY (arm was sore), HEADACHE (Headache), PYREXIA (Low grade fever) and FATIGUE (Fatigue) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Other concomitant medications included blood pressure medications and hormone replacement therapy. Treatment information provided included application of ice on arm. Most recent FOLLOW-UP information incorporated above includes: On 06-Jul-2021: Follow-up received and added surgical procedure (emergency appendectomy) and updated reporter's contact information.; Sender's Comments: Based on the current available information which shows a strong temporal association between the use of the product and the start date of the reported event, a causal relationship with the event cannot be excluded. Headache, low grade fever and fatigue are consistent with the known safety profile of the mRNA-1273.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Appendectomy (Emergency appendectomy); COVID-19 (The illness lasted for 2 weeks and she did not have any major symptoms from it)
Andere Medikamente: LEXAPRO
Allergien: -
Vorherige Impfungen: -

VAERS 1556288

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: IL
Alter: 62,0
Geschlecht: F
Eingang: 14.08.2021
Impfdatum: 11.02.2021
Beginn: 17.02.2021
Tage bis Beginn: 6,0
Dosis: UNK
Route/Site: OT / RA

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

Feeling hot Inflammation Pain in extremity Vaccination site discolouration Vaccination site pruritus Vaccination site urticaria Vaccination site warmth

Symptomtext

Arm was hot to touch and itchy; Purple hue around the injection site; hot and warm from the elbow to her shoulder; Had inflammation; Arm was hot to touch and itchy; Sore arm; Welt that was hard and hot at the injection site; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION SITE WARMTH (Arm was hot to touch and itchy), VACCINATION SITE DISCOLOURATION (Purple hue around the injection site), FEELING HOT (hot and warm from the elbow to her shoulder), INFLAMMATION (Had inflammation) and VACCINATION SITE PRURITUS (Arm was hot to touch and itchy) in a 62-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concurrent medical conditions included Hypertension. Concomitant products included ATORVASTATIN and ESCITALOPRAM OXALATE (LEXAPRO) for an unknown indication. On 11-Feb-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 17-Feb-2021, the patient experienced VACCINATION SITE WARMTH (Arm was hot to touch and itchy), VACCINATION SITE DISCOLOURATION (Purple hue around the injection site), FEELING HOT (hot and warm from the elbow to her shoulder), INFLAMMATION (Had inflammation), VACCINATION SITE PRURITUS (Arm was hot to touch and itchy), PAIN IN EXTREMITY (Sore arm) and VACCINATION SITE URTICARIA (Welt that was hard and hot at the injection site). At the time of the report, VACCINATION SITE WARMTH (Arm was hot to touch and itchy), VACCINATION SITE DISCOLOURATION (Purple hue around the injection site), FEELING HOT (hot and warm from the elbow to her shoulder), INFLAMMATION (Had inflammation), VACCINATION SITE PRURITUS (Arm was hot to touch and itchy), PAIN IN EXTREMITY (Sore arm) and VACCINATION SITE URTICARIA (Welt that was hard and hot at the injection site) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Treatment medications include Benadryl and advil.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Hypertension
Vorgeschichte: -
Andere Medikamente: ATORVASTATIN; LEXAPRO
Allergien: -
Vorherige Impfungen: -

VAERS 1556213

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: FL
Alter: 76,0
Geschlecht: F
Eingang: 14.08.2021
Impfdatum: 27.01.2021
Beginn: 06.02.2021
Tage bis Beginn: 10,0
Dosis: 1
Route/Site: OT / -

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

Vaccination site pruritus Vaccination site rash

Symptomtext

Small rash at the site; the site of injection is incredibly itchy; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION SITE PRURITUS (the site of injection is incredibly itchy) and VACCINATION SITE RASH (Small rash at the site) in a 76-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. 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 06-Feb-2021, the patient experienced VACCINATION SITE PRURITUS (the site of injection is incredibly itchy). On 07-Feb-2021, the patient experienced VACCINATION SITE RASH (Small rash at the site). At the time of the report, VACCINATION SITE PRURITUS (the site of injection is incredibly itchy) and VACCINATION SITE RASH (Small rash at the site) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown.

Weitere VAERSDATA-Felder

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

VAERS 1556187

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: MD
Alter: 66,0
Geschlecht: F
Eingang: 14.08.2021
Impfdatum: 29.01.2021
Beginn: 29.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / LA

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

Induration Pain Pruritus Vaccination site erythema Vaccination site pain

Symptomtext

Traveling down to the elbow; Itchy; Felt hard; Injection site red; Injection site was sore; felt like it was burning; This spontaneous case was reported by a consumer and describes the occurrence of PAIN (Traveling down to the elbow), PRURITUS (Itchy), INDURATION (Felt hard), VACCINATION SITE ERYTHEMA (Injection site red) and VACCINATION SITE PAIN (Injection site was sore) in a 66-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concurrent medical conditions included Blood pressure, High cholesterol, Allergy (Adhesive tapes and band aids) and Penicillin allergy. Concomitant products included LISINOPRIL, ATORVASTATIN, EZETIMIBE (ZETIA), TOLTERODINE L-TARTRATE (DETROL LA), VITAMIN A [RETINOL] and COLECALCIFEROL (VITAMIN D [COLECALCIFEROL]) for an unknown indication. On 29-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 29-Jan-2021, the patient experienced PAIN (Traveling down to the elbow), PRURITUS (Itchy), INDURATION (Felt hard), VACCINATION SITE ERYTHEMA (Injection site red), VACCINATION SITE PAIN (Injection site was sore) and VACCINATION SITE PAIN (felt like it was burning). The patient was treated with CETIRIZINE HYDROCHLORIDE (ZYRTEC [CETIRIZINE HYDROCHLORIDE]) ongoing since an unknown date at an unspecified dose and frequency. At the time of the report, PAIN (Traveling down to the elbow), PRURITUS (Itchy), INDURATION (Felt hard), VACCINATION SITE ERYTHEMA (Injection site red), VACCINATION SITE PAIN (Injection site was sore) and VACCINATION SITE PAIN (felt like it was burning) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Allergy (Adhesive tapes and band aids)
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure; High cholesterol; Penicillin allergy
Andere Medikamente: LISINOPRIL; ATORVASTATIN; ZETIA; DETROL LA; VITAMIN A [RETINOL]; VITAMIN D [COLECALCIFEROL]
Allergien: -
Vorherige Impfungen: -

VAERS 1555945

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: PA
Alter: -
Geschlecht: F
Eingang: 14.08.2021
Impfdatum: 28.01.2021
Beginn: 28.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / LA

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

Abdominal pain upper Dyspepsia Flatulence Pain in extremity

Symptomtext

stomach problems, pain; stomach burning; gas; arm hurt; This spontaneous case was reported by a consumer and describes the occurrence of ABDOMINAL PAIN UPPER (stomach problems, pain), DYSPEPSIA (stomach burning), FLATULENCE (gas) and PAIN IN EXTREMITY (arm hurt) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. Concurrent medical conditions included Thyroid disorder and Allergy. On 28-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 28-Jan-2021, the patient experienced PAIN IN EXTREMITY (arm hurt). On an unknown date, the patient experienced ABDOMINAL PAIN UPPER (stomach problems, pain), DYSPEPSIA (stomach burning) and FLATULENCE (gas). On 30-Jan-2021, PAIN IN EXTREMITY (arm hurt) had resolved. At the time of the report, ABDOMINAL PAIN UPPER (stomach problems, pain), DYSPEPSIA (stomach burning) and FLATULENCE (gas) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Concomitant medications reported were Allergies medication, Thyroids pills for drug use for unknown indication. Treatment medications includes Tums, antacids and Nexium. Patient Went to see GI doctor did endoscopy she was on special diet and checked gall bladder. This case was linked to US-MODERNATX, INC.-MOD-2021-048047 (E2B Linked Report). Most recent FOLLOW-UP information incorporated above includes: On 10-May-2021: Follow up contains treatment details updated and new events were updated.; Sender's Comments: US-MODERNATX, INC.-MOD-2021-048047:Second dose

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain upper
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Allergy; Thyroid disorder
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1555918

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: IL
Alter: 76,0
Geschlecht: F
Eingang: 14.08.2021
Impfdatum: 02.02.2021
Beginn: 02.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / LA

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

Arthralgia Myalgia Neck pain Pruritus Vaccination site swelling

Symptomtext

soreness; swelling; pain in neck; joint pain; muscle pain; itching; This spontaneous case was reported by a consumer and describes the occurrence of MYALGIA (soreness), VACCINATION SITE SWELLING (swelling), NECK PAIN (pain in neck), ARTHRALGIA (joint pain) and MYALGIA (muscle pain) in a 76-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical history information was reported. On 02-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 02-Feb-2021, the patient experienced MYALGIA (soreness), VACCINATION SITE SWELLING (swelling), NECK PAIN (pain in neck), ARTHRALGIA (joint pain), MYALGIA (muscle pain) and PRURITUS (itching). The patient was treated with NAPROXEN SODIUM (ALEVE) at an unspecified dose and frequency. At the time of the report, MYALGIA (soreness), VACCINATION SITE SWELLING (swelling), NECK PAIN (pain in neck), ARTHRALGIA (joint pain), MYALGIA (muscle pain) and PRURITUS (itching) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. No relevant concomitant medications were reported. This case was received via an unknown source (no reference has been entered for a health authority or license partner) on 24-Feb-2021 and was forwarded to Moderna on 24-Feb-2021. This spontaneous case was reported by a consumer and describes the occurrence of MYALGIA (soreness), VACCINATION SITE SWELLING (swelling), NECK PAIN (pain in neck), ARTHRALGIA (joint pain) and MYALGIA (muscle pain) in a 76-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical history information was reported. On 02-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 02-Feb-2021, the patient experienced MYALGIA (soreness), VACCINATION SITE SWELLING (swelling), NECK PAIN (pain in neck), ARTHRALGIA (joint pain), MYALGIA (muscle pain) and PRURITUS (itching). The patient was treated with NAPROXEN SODIUM (ALEVE) at an unspecified dose and frequency. At the time of the report, MYALGIA (soreness), VACCINATION SITE SWELLING (swelling), NECK PAIN (pain in neck), ARTHRALGIA (joint pain), MYALGIA (muscle pain) and PRURITUS (itching) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. No relevant concomitant medications were reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: No Medical history information was reported.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1555343

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: IL
Alter: 77,0
Geschlecht: M
Eingang: 13.08.2021
Impfdatum: 09.02.2021
Beginn: 22.02.2021
Tage bis Beginn: 13,0
Dosis: 1
Route/Site: OT / LA

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

Vaccination site pruritus Vaccination site rash

Symptomtext

was itchy; rash at injection sight; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION SITE RASH (rash at injection sight) and VACCINATION SITE PRURITUS (was itchy) in a 77-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. No Medical History information was reported. On 09-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 22-Feb-2021, the patient experienced VACCINATION SITE RASH (rash at injection sight) and VACCINATION SITE PRURITUS (was itchy). The patient was treated with HYDROCORTISONE for Vaccination site pruritus, at an unspecified dose and frequency. At the time of the report, VACCINATION SITE RASH (rash at injection sight) and VACCINATION SITE PRURITUS (was itchy) outcome was unknown. Not Provided The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. No concomitant medications reported . At the time of report, rash was bigger. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments.

Weitere VAERSDATA-Felder

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

VAERS 1555301

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: IN
Alter: 75,0
Geschlecht: M
Eingang: 13.08.2021
Impfdatum: 26.01.2021
Beginn: 23.02.2021
Tage bis Beginn: 28,0
Dosis: 2
Route/Site: OT / LA

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

Asthenia Body temperature Chills Cold sweat Headache Pain Pyrexia

Symptomtext

fever 100.2 F; felt clammy; felt weak; Chills; headache; body hurt everywhere; This spontaneous case was reported by a consumer and describes the occurrence of COLD SWEAT (felt clammy), ASTHENIA (felt weak), CHILLS (Chills), HEADACHE (headache) and PAIN (body hurt everywhere) in a 75-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 038K20A and 015M20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concurrent medical conditions included COPD, Cholesterol, Blood pressure and Arthritis. On 26-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 23-Feb-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 23-Feb-2021, the patient experienced COLD SWEAT (felt clammy), ASTHENIA (felt weak), CHILLS (Chills), HEADACHE (headache) and PAIN (body hurt everywhere). On 24-Feb-2021, the patient experienced PYREXIA (fever 100.2 F). At the time of the report, COLD SWEAT (felt clammy), ASTHENIA (felt weak), CHILLS (Chills), HEADACHE (headache), PAIN (body hurt everywhere) and PYREXIA (fever 100.2 F) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 24-Feb-2021, Body temperature: 100.2 100.2. Concomitant medications reported were acid reflux medication, muscle pain med, arthritis med, blood thinner, cholesterol medication, blood pressure medication, inhaler for COPD. Treatment details included Tylenol (paracetamol). This case was linked to MOD-2021-024144 (Patient Link).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Test Date: 20210224; Test Name: BODY TEMPERATURE; Result Unstructured Data: 100.2
Aktuelle Erkrankungen: Arthritis; Blood pressure; Cholesterol
Vorgeschichte: Medical History/Concurrent Conditions: COPD
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1555291

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: IN
Alter: 71,0
Geschlecht: F
Eingang: 13.08.2021
Impfdatum: 26.01.2021
Beginn: 23.02.2021
Tage bis Beginn: 28,0
Dosis: 2
Route/Site: OT / LA

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

Chills Headache Muscular weakness Nausea Pain

Symptomtext

nausea; headache; pain all over; chills; legs and arms weak; This spontaneous case was reported by a consumer and describes the occurrence of MUSCULAR WEAKNESS (legs and arms weak), NAUSEA (nausea), HEADACHE (headache), PAIN (pain all over) and CHILLS (chills) in a 71-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 038K20A and 015M20A) for COVID-19 vaccination. Concurrent medical conditions included Hypertension, Cholesterol, Sarcoidosis, Diabetes, Autoimmune disorder NOS and Asthma. On 26-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 23-Feb-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 23-Feb-2021, the patient experienced MUSCULAR WEAKNESS (legs and arms weak), HEADACHE (headache), PAIN (pain all over) and CHILLS (chills). On an unknown date, the patient experienced NAUSEA (nausea). The patient was treated with PARACETAMOL (TYLENOL) for Headache and Pain, at an unspecified dose and frequency. At the time of the report, MUSCULAR WEAKNESS (legs and arms weak), NAUSEA (nausea), HEADACHE (headache), PAIN (pain all over) and CHILLS (chills) outcome was unknown. Concomitant medications reported were blood pressure medication, high cholesterol medication, sarcoid medication, diabetes medication, autoimmune disease medication, inhaler for asthma.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Asthma; Autoimmune disorder NOS; Cholesterol; Diabetes; Hypertension; Sarcoidosis
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1555255

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: FL
Alter: 82,0
Geschlecht: F
Eingang: 13.08.2021
Impfdatum: 03.02.2021
Beginn: 03.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / LA

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

Injection site discomfort Limb discomfort Pain Rash Rash erythematous Rash pruritic

Symptomtext

achy; uncomfortable; red rash on lower side of arm/red dots; itchy rash; oozing rash; arm very uncomfortable; This spontaneous case was reported by a consumer and describes the occurrence of PAIN (achy), INJECTION SITE DISCOMFORT (uncomfortable), RASH ERYTHEMATOUS (red rash on lower side of arm/red dots), RASH PRURITIC (itchy rash) and RASH (oozing rash) in an 82-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included Cancer. Concomitant products included BACITRACIN and HYDROCORTISONE (CORTIZONE 10). On 03-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 03-Feb-2021, the patient experienced PAIN (achy), INJECTION SITE DISCOMFORT (uncomfortable), RASH ERYTHEMATOUS (red rash on lower side of arm/red dots), RASH PRURITIC (itchy rash), RASH (oozing rash) and LIMB DISCOMFORT (arm very uncomfortable). On 05-Feb-2021, PAIN (achy) and INJECTION SITE DISCOMFORT (uncomfortable) had resolved. On 23-Feb-2021, RASH PRURITIC (itchy rash), RASH (oozing rash) and LIMB DISCOMFORT (arm very uncomfortable) had resolved. At the time of the report, RASH ERYTHEMATOUS (red rash on lower side of arm/red dots) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. No treatment details were provided.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site discomfort
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Cancer
Andere Medikamente: BACITRACIN; CORTIZONE 10
Allergien: -
Vorherige Impfungen: -

VAERS 1555223

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: FL
Alter: -
Geschlecht: F
Eingang: 13.08.2021
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: ja

Dizziness Fatigue Vision blurred

Symptomtext

Blurred vision; Dizziness; Very tired; This spontaneous case was reported by a consumer and describes the occurrence of VISION BLURRED (Blurred vision), DIZZINESS (Dizziness) and FATIGUE (Very tired) in a 67-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. No Medical History information was reported. 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 VISION BLURRED (Blurred vision), DIZZINESS (Dizziness) and FATIGUE (Very tired). At the time of the report, VISION BLURRED (Blurred vision), DIZZINESS (Dizziness) and FATIGUE (Very tired) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Concomitant medications were not provided. Treatment information was not reported.

Weitere VAERSDATA-Felder

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

VAERS 1555175

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: -
Alter: -
Geschlecht: F
Eingang: 13.08.2021
Impfdatum: 03.02.2021
Beginn: 03.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / -

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

Dizziness Fatigue Nausea

Symptomtext

Dizziness; tired; slightly nauseous; This spontaneous case was reported by a consumer and describes the occurrence of DIZZINESS (Dizziness), FATIGUE (tired) and NAUSEA (slightly nauseous) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. No Medical History information was reported. On 03-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 03-Feb-2021, the patient experienced DIZZINESS (Dizziness), FATIGUE (tired) and NAUSEA (slightly nauseous). At the time of the report, DIZZINESS (Dizziness), FATIGUE (tired) and NAUSEA (slightly nauseous) outcome was unknown. Not Provided The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. Concomitant medication details were not reported by the reporter. Treatment details was not reported by the reporter.

Weitere VAERSDATA-Felder

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

VAERS 1553239

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: IL
Alter: -
Geschlecht: F
Eingang: 13.08.2021
Impfdatum: 10.02.2021
Beginn: 17.02.2021
Tage bis Beginn: 7,0
Dosis: 1
Route/Site: OT / -

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

Colitis Crohn's disease Pain in extremity Vaccination site bruising Vaccination site pain

Symptomtext

bruising at injection site; sharp pain at the injection site, pain that wake me up from my sleep; Crohn's has acted up; colitis has acted up; Sore Arm; A spontaneous report was received from a consumer who was also an 83-year old, female patient who received Moderna's COVID-19 vaccine (mRNA-1273) and experienced Crohn's and colitis flare-up, sharp pain and bruising at the vaccine site, and sore arm. The patient's medical history was Crohn's disease and colitis. No relevant concomitant medications were reported. On 10 Feb 2021, prior to the onset of the events, the patient received their first of two planned doses of mRNA-1273 (lot/batch: 038K20A) for prophylaxis of COVID-19 infection. On 17 Feb 2021, the patient's Crohn's and colitis has acted up. She also experienced sharp pain at the injection site that wakes her up at night. On 23 Feb 2021, the patient's arm is still bruised at the injection site. Treatment details included Tylenol with codeine. Action taken with mRNA-1273 in response to the events was not reported. At the time of this report, the outcome of the events Crohn's and colitis flare-up, sharp pain and bruising at the vaccine site, and sore arm) was unknown. Patient's follow-up consent is not clear.; Reporter's Comments: Based on the current available information and temporal association between the use of the product and the start date of the vaccine site pain and bruising, a causal relationship cannot be excluded. Patient referred easily bruising which can be a cofounder. Very limited information regarding the Crohn's and colitis aggravation has been provided at this time. Further information has been requested.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Colitis; Crohn's disease
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1552967

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: PA
Alter: 80,0
Geschlecht: F
Eingang: 13.08.2021
Impfdatum: 12.02.2021
Beginn: 12.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / LA

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

Altered visual depth perception Blood pressure increased Erythema Feeling hot Hypersensitivity Insomnia Myalgia Rash Urticaria Visual impairment

Symptomtext

red marks all over face and hands; felt hot; couldn't sleep; allergy reactions; lost depth perception; psychedelic pattern in vision; insignificant arm pain; Blood pressure increased; Rash on forehead; hives; This spontaneous case was reported by a consumer and describes the occurrence of ERYTHEMA (red marks all over face and hands), FEELING HOT (felt hot), INSOMNIA (couldn't sleep), HYPERSENSITIVITY (allergy reactions) and ALTERED VISUAL DEPTH PERCEPTION (lost depth perception) in an 80-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concomitant products included METHENAMINE HIPPURATE (HIPREX [METHENAMINE HIPPURATE]) for Bladder infection, NORTRIPTYLINE for Facial pain, ATORVASTATIN, MULTIVITAMIN [VITAMINS NOS] and DENOSUMAB (PROLIA) for an unknown indication. On 12-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 12-Feb-2021, the patient experienced BLOOD PRESSURE INCREASED (Blood pressure increased), RASH (Rash on forehead) and URTICARIA (hives). On an unknown date, the patient experienced ERYTHEMA (red marks all over face and hands), FEELING HOT (felt hot), INSOMNIA (couldn't sleep), HYPERSENSITIVITY (allergy reactions), ALTERED VISUAL DEPTH PERCEPTION (lost depth perception), VISUAL IMPAIRMENT (psychedelic pattern in vision) and MYALGIA (insignificant arm pain). On 15-Feb-2021, URTICARIA (hives) had resolved. At the time of the report, ERYTHEMA (red marks all over face and hands), FEELING HOT (felt hot), INSOMNIA (couldn't sleep), HYPERSENSITIVITY (allergy reactions), ALTERED VISUAL DEPTH PERCEPTION (lost depth perception), VISUAL IMPAIRMENT (psychedelic pattern in vision), BLOOD PRESSURE INCREASED (Blood pressure increased), RASH (Rash on forehead) and MYALGIA (insignificant arm pain) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, Blood pressure increased: 180/135 (High) 180/135 mmHg. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. Treatment medication used was Benadryl Most recent FOLLOW-UP information incorporated above includes: On 28-Apr-2021: No specific follow-up information recorded. On 28-Apr-2021: NNI, additional info 2 On 28-Apr-2021: Additional info 3 On 29-Apr-2021: No specific follow-up information recorded.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myalgia
Hospital-Tage: -
Labordaten: Test Date: 20210212; Test Name: blood pressure increased; Result Unstructured Data: 180/135 mmHg
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: No medical history was reported.
Andere Medikamente: ATORVASTATIN; NORTRIPTYLINE; HIPREX [METHENAMINE HIPPURATE]; MULTIVITAMIN [VITAMINS NOS]; PROLIA
Allergien: -
Vorherige Impfungen: -

VAERS 1552747

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: IL
Alter: 51,0
Geschlecht: F
Eingang: 13.08.2021
Impfdatum: 29.01.2021
Beginn: 30.01.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: OT / RA

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

Dry skin Eye swelling Rash Skin tightness

Symptomtext

Skin on her face and neck felt tight; Skin on her face and neck felt dry; Swollen eyes; Had a Rash; This spontaneous case was reported by a consumer and describes the occurrence of SKIN TIGHTNESS (Skin on her face and neck felt tight), DRY SKIN (Skin on her face and neck felt dry), EYE SWELLING (Swollen eyes) and RASH (Had a Rash) in a 51-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. Concurrent medical conditions included Seasonal allergy and Allergy (The patient has outdoor allergy and takes allergy shots). On 29-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 30-Jan-2021, the patient experienced SKIN TIGHTNESS (Skin on her face and neck felt tight), DRY SKIN (Skin on her face and neck felt dry), EYE SWELLING (Swollen eyes) and RASH (Had a Rash). The patient was treated with DIPHENHYDRAMINE HYDROCHLORIDE (BENADRYL [DIPHENHYDRAMINE HYDROCHLORIDE]) for Adverse event, at a dose of UNK dosage form. At the time of the report, SKIN TIGHTNESS (Skin on her face and neck felt tight), DRY SKIN (Skin on her face and neck felt dry), EYE SWELLING (Swollen eyes) and RASH (Had a Rash) outcome was unknown. Not Provided The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Concomitant information was not provided. She took some Benadryl but it has not helped her symptoms much. She finds her symptoms more annoying than anything else.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Allergy (The patient has outdoor allergy and takes allergy shots); Seasonal allergy
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1552661

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: IL
Alter: 72,0
Geschlecht: F
Eingang: 13.08.2021
Impfdatum: 26.01.2021
Beginn: 03.02.2021
Tage bis Beginn: 8,0
Dosis: 1
Route/Site: OT / -

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

Myalgia Vaccination site erythema Vaccination site pruritus Vaccination site swelling

Symptomtext

Itchy Arm (Injection Site); Red Arm (Injection Site); Swollen Arm (Injection Site); Body Aches; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION SITE PRURITUS (Itchy Arm (Injection Site)), VACCINATION SITE ERYTHEMA (Red Arm (Injection Site)), VACCINATION SITE SWELLING (Swollen Arm (Injection Site)) and MYALGIA (Body Aches) in a 72-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. No Medical History information was reported. On 26-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 03-Feb-2021, the patient experienced VACCINATION SITE PRURITUS (Itchy Arm (Injection Site)), VACCINATION SITE ERYTHEMA (Red Arm (Injection Site)), VACCINATION SITE SWELLING (Swollen Arm (Injection Site)) and MYALGIA (Body Aches). At the time of the report, VACCINATION SITE PRURITUS (Itchy Arm (Injection Site)), VACCINATION SITE ERYTHEMA (Red Arm (Injection Site)), VACCINATION SITE SWELLING (Swollen Arm (Injection Site)) and MYALGIA (Body Aches) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. No concomitant medications were reported. No corrective treatment was provided.

Weitere VAERSDATA-Felder

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

VAERS 1552646

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: PA
Alter: 75,0
Geschlecht: F
Eingang: 13.08.2021
Impfdatum: 22.01.2021
Beginn: 03.02.2021
Tage bis Beginn: 12,0
Dosis: 1
Route/Site: OT / LA

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

Feeling hot Vaccination site erythema Vaccination site pain Vaccination site swelling

Symptomtext

This spontaneous case was reported by a consumer and describes the occurrence of FEELING HOT (Arm felt hot in the shoulder area), VACCINATION SITE ERYTHEMA (Red blotch about the size of patients' hand where patient received vaccine), VACCINATION SITE PAIN (Minor pain) and VACCINATION SITE SWELLING (Little bit swollen) in a 75-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. 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 03-Feb-2021, the patient experienced FEELING HOT (Arm felt hot in the shoulder area), VACCINATION SITE ERYTHEMA (Red blotch about the size of patients' hand where patient received vaccine), VACCINATION SITE PAIN (Minor pain) and VACCINATION SITE SWELLING (Little bit swollen). At the time of the report, FEELING HOT (Arm felt hot in the shoulder area), VACCINATION SITE ERYTHEMA (Red blotch about the size of patients' hand where patient received vaccine), VACCINATION SITE PAIN (Minor pain) and VACCINATION SITE SWELLING (Little bit swollen) had not resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. No relevant concomitant medications were reported. No treatment information was provided.

Weitere VAERSDATA-Felder

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

VAERS 1552635

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: IL
Alter: 72,0
Geschlecht: F
Eingang: 13.08.2021
Impfdatum: 26.01.2021
Beginn: 03.02.2021
Tage bis Beginn: 8,0
Dosis: 2
Route/Site: OT / -

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

Myalgia Vaccination site erythema Vaccination site pruritus Vaccination site swelling

Symptomtext

Injection site was itchy; Injection site was red; Injection site was swollen; Body ache; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION SITE PRURITUS (Injection site was itchy), VACCINATION SITE ERYTHEMA (Injection site was red), VACCINATION SITE SWELLING (Injection site was swollen) and MYALGIA (Body ache) in a 72-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. No Medical History information was reported. On 26-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) (unknown route) dosage was changed to 2 dosage form. On 03-Feb-2021, the patient experienced VACCINATION SITE PRURITUS (Injection site was itchy), VACCINATION SITE ERYTHEMA (Injection site was red), VACCINATION SITE SWELLING (Injection site was swollen) and MYALGIA (Body ache). At the time of the report, VACCINATION SITE PRURITUS (Injection site was itchy), VACCINATION SITE ERYTHEMA (Injection site was red), VACCINATION SITE SWELLING (Injection site was swollen) and MYALGIA (Body ache) outcome was unknown. Concomitant product use was not provided by the reporter. No treatment information was provided. The action taken with the drug was Not applicable.

Weitere VAERSDATA-Felder

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

VAERS 1552610

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: IL
Alter: 80,0
Geschlecht: M
Eingang: 13.08.2021
Impfdatum: 28.01.2021
Beginn: 28.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / RA

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

Fatigue Tenderness

Symptomtext

tiredness; tender arm; This spontaneous case was reported by a consumer and describes the occurrence of TENDERNESS (tender arm) and FATIGUE (tiredness) in an 80-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. Concurrent medical conditions included Cancer. On 28-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 28-Jan-2021, the patient experienced TENDERNESS (tender arm). On an unknown date, the patient experienced FATIGUE (tiredness). On 28-Jan-2021, TENDERNESS (tender arm) had resolved. At the time of the report, FATIGUE (tiredness) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. No relevant concomitant medications were reported. No treatment information was provided. This case was linked to US-MODERNATX, INC.-MOD-2021-016013 (E2B Linked Report). Most recent FOLLOW-UP information incorporated above includes: On 28-Jun-2021: Event added , relevant history added.; Sender's Comments: US-MODERNATX, INC.-MOD-2021-016013:Crosslinked (MOD21-020670)

Weitere VAERSDATA-Felder

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

VAERS 1552450

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: IL
Alter: -
Geschlecht: M
Eingang: 13.08.2021
Impfdatum: 25.01.2021
Beginn: 23.02.2021
Tage bis Beginn: 29,0
Dosis: 1
Route/Site: OT / -

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

Decreased appetite Dizziness Pain Pyrexia

Symptomtext

Body aches; No appetite; Feeling unsteady/dizzy; Fever (100.8? after taking Tylenol); This spontaneous case was reported by a consumer and describes the occurrence of PAIN (Body aches), DECREASED APPETITE (No appetite), DIZZINESS (Feeling unsteady/dizzy) and PYREXIA (Fever (100.8? after taking Tylenol)) in a male patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 038K20A and 038K20A) for COVID-19 vaccination. Concurrent medical conditions included Blood pressure abnormal and Cholesterol high. Concomitant products included OMEPRAZOLE MAGNESIUM (PRILOSEC [OMEPRAZOLE MAGNESIUM]). On 25-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 22-Feb-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 23-Feb-2021, the patient experienced PAIN (Body aches), DECREASED APPETITE (No appetite), DIZZINESS (Feeling unsteady/dizzy) and PYREXIA (Fever (100.8? after taking Tylenol)). The patient was treated with PARACETAMOL (TYLENOL) at a dose of unknown. At the time of the report, PAIN (Body aches), DECREASED APPETITE (No appetite), DIZZINESS (Feeling unsteady/dizzy) and PYREXIA (Fever (100.8? after taking Tylenol)) had not resolved. patient uses unspecified blood pressure and cholesterol medications as concomitants.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Blood pressure abnormal; Cholesterol high
Vorgeschichte: -
Andere Medikamente: PRILOSEC [OMEPRAZOLE MAGNESIUM]
Allergien: -
Vorherige Impfungen: -

VAERS 1552119

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038k20A

mild

Staat: MI
Alter: 74,0
Geschlecht: F
Eingang: 13.08.2021
Impfdatum: 03.02.2021
Beginn: 03.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / RA

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

Rash erythematous Rash pruritic Vaccination site pain

Symptomtext

Pinky rash upper breast; Itchy rash upper breast; Tenderness in right arm of injection; This spontaneous case was reported by a consumer and describes the occurrence of RASH ERYTHEMATOUS (Pinky rash upper breast), RASH PRURITIC (Itchy rash upper breast) and VACCINATION SITE PAIN (Tenderness in right arm of injection) in a 74-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038k20A) for COVID-19 vaccination. Concurrent medical conditions included Breast cancer, Hypertension, Diabetes and Alcohol allergy (Allergy: alcohol when drinking). On 03-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 03-Feb-2021, the patient experienced RASH ERYTHEMATOUS (Pinky rash upper breast), RASH PRURITIC (Itchy rash upper breast) and VACCINATION SITE PAIN (Tenderness in right arm of injection). At the time of the report, RASH ERYTHEMATOUS (Pinky rash upper breast), RASH PRURITIC (Itchy rash upper breast) and VACCINATION SITE PAIN (Tenderness in right arm of injection) outcome was unknown. Not Provided The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. patient uses unspecified medication for breast cancer survivor, blood pressure, diabetes as concomitant medications.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash erythematous
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Alcohol allergy (Allergy: alcohol when drinking); Breast cancer; Diabetes; Hypertension
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1551863

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: MI
Alter: 70,0
Geschlecht: F
Eingang: 13.08.2021
Impfdatum: 03.02.2021
Beginn: 03.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / LA

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

Abdominal pain upper Feeling abnormal Flushing Headache Myalgia Sleep deficit

Symptomtext

Face started to flush; Sick to her stomach; Did not sleep or feel well; Did not sleep or feel well; Aches and pains throughout her body; Bad headache; This spontaneous case was reported by a consumer and describes the occurrence of FLUSHING (Face started to flush), ABDOMINAL PAIN UPPER (Sick to her stomach), SLEEP DEFICIT (Did not sleep or feel well), FEELING ABNORMAL (Did not sleep or feel well) and MYALGIA (Aches and pains throughout her body) in a 70-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 03-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 03-Feb-2021, the patient experienced FLUSHING (Face started to flush), ABDOMINAL PAIN UPPER (Sick to her stomach), SLEEP DEFICIT (Did not sleep or feel well), FEELING ABNORMAL (Did not sleep or feel well), MYALGIA (Aches and pains throughout her body) and HEADACHE (Bad headache). The patient was treated with PARACETAMOL (TYLENOL) for Adverse event, at a dose of UNK dosage form. On 03-Feb-2021, FLUSHING (Face started to flush) had resolved. On 05-Feb-2021, ABDOMINAL PAIN UPPER (Sick to her stomach), SLEEP DEFICIT (Did not sleep or feel well), FEELING ABNORMAL (Did not sleep or feel well), MYALGIA (Aches and pains throughout her body) and HEADACHE (Bad headache) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown.

Weitere VAERSDATA-Felder

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

VAERS 1551709

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: FL
Alter: 57,0
Geschlecht: F
Eingang: 13.08.2021
Impfdatum: 01.02.2021
Beginn: 04.02.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: OT / LA

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

Feeling hot Neck pain Pruritus Rash Vaccination site pain

Symptomtext

Minor itchiness by the upper body; Pain going down from the side on my neck; Warm by the rash; Rash on the chest; Soreness at injection; This spontaneous case was reported by a consumer and describes the occurrence of PRURITUS (Minor itchiness by the upper body), NECK PAIN (Pain going down from the side on my neck), FEELING HOT (Warm by the rash), RASH (Rash on the chest) and VACCINATION SITE PAIN (Soreness at injection) in a 57-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. no specified medical history was reported. Concomitant products included LISINOPRIL and VITAMINS NOS for an unknown indication. On 01-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 04-Feb-2021, the patient experienced PRURITUS (Minor itchiness by the upper body), NECK PAIN (Pain going down from the side on my neck), FEELING HOT (Warm by the rash), RASH (Rash on the chest) and VACCINATION SITE PAIN (Soreness at injection). The patient was treated with LORATADINE, PSEUDOEPHEDRINE HYDROCHLORIDE (BENADRYL 24 D) at an unspecified dose and frequency. At the time of the report, PRURITUS (Minor itchiness by the upper body), NECK PAIN (Pain going down from the side on my neck), FEELING HOT (Warm by the rash), RASH (Rash on the chest) and VACCINATION SITE PAIN (Soreness at injection) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Neck pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: no specified medical history was reported
Andere Medikamente: LISINOPRIL; VITAMINS NOS
Allergien: -
Vorherige Impfungen: -

VAERS 1551552

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: -
Alter: 69,0
Geschlecht: F
Eingang: 13.08.2021
Impfdatum: 09.02.2021
Beginn: 10.02.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: OT / LA

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

Fatigue Pain in extremity Pyrexia

Symptomtext

This spontaneous case was reported by a consumer and describes the occurrence of PAIN IN EXTREMITY (sore arm next day), FATIGUE (very tired the next day) and PYREXIA (low grade fever 99.4) in a 69-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. The patient's past medical history included No adverse event. On 09-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 10-Feb-2021, the patient experienced PAIN IN EXTREMITY (sore arm next day) and FATIGUE (very tired the next day). On an unknown date, the patient experienced PYREXIA (low grade fever 99.4). The patient was treated with IBUPROFEN (ADVIL [IBUPROFEN]) at an unspecified dose and frequency. At the time of the report, PAIN IN EXTREMITY (sore arm next day), FATIGUE (very tired the next day) and PYREXIA (low grade fever 99.4) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: No adverse event
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1551533

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: FL
Alter: 67,0
Geschlecht: F
Eingang: 13.08.2021
Impfdatum: 09.02.2021
Beginn: 09.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / RA

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

Herpes zoster Pain in extremity Rash Swelling

Symptomtext

shingles; rash over their neck and upper back on the opposite side; with a little rash; was swollen on the bicep area; arm was sore immediately; A spontaneous report was received from a caregiver concerning a 67-years-old male patient who received Moderna's COVID-19 vaccine (mRNA-1273) and experienced events arm was sore immediately/pain in extremity, and was swollen on the bicep area/swelling, with a little rash/rash, rash over their neck and upper back on the opposite side/rash, shingles /herpes zoster. The patient's medical history was not provided. Concomitant medications reported were 0.5 mg lorazepam, 10mg amitriptyline, 5mg Lisinopril for drug use for unknown indication. On 9 Feb 2021, prior to the onset of the events the patient received first of two planned doses of mRNA-1273 (lot/batch: 038K20A) via unknown route in the right arm for prophylaxis of COVID-19 infection. On 9 Feb 2021, the patient experienced the event(s) arm was sore immediately, and was swollen on the bicep area, with a little rash. On 12 Feb 2021, the patient experienced the event(s) rash over their neck and upper back on the opposite side. Treatment details included Topical treatment for the initial rash., Valacyclovir for the shingles. Action taken with mRNA-1273 in response to the events was not reported. The outcome of event(s), arm was sore immediately, and was swollen on the bicep area, with a little rash, rash over their neck and upper back on the opposite side,shingles was unknown.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: No adverse event
Andere Medikamente: LORAZEPAM; AMITRIPTYLINE; LISINOPRIL
Allergien: -
Vorherige Impfungen: -

VAERS 1551530

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: IL
Alter: 45,0
Geschlecht: F
Eingang: 13.08.2021
Impfdatum: 10.02.2021
Beginn: 10.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / -

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

Injection site mass Injection site pain Injection site pruritus Injection site swelling Muscle tightness

Symptomtext

Huge Knot; swelling; itchiness; Tightness; Tenderness; A spontaneous report was received from a consumer concerning a 45-years-old patient who received Moderna's COVID-19 vaccine (mRNA-1273) and experienced events tenderness/injection site pain, huge knot/injection site mass, swelling/injection site swelling, itchiness/injection site pruritus, tightness/muscle tightness. The patient's medical history was not provided. Concomitant medications reported were medroxy progestrone, Bladder Pills., Menopause Medications for drug use for unknown indication. On 10 Feb 2021, prior to the onset of the events the patient received first of two planned doses of mRNA-1273 (lot/batch: 038K20A) intramuscularly for prophylaxis of COVID-19 infection. On 10 Feb 2021, the patient experienced the event(s) tenderness. On 19 Feb 2021, the patient experienced the event(s) huge knot, swelling, itchiness, tightness. Treatment details included Ibuprofen and diphenhydramine. Action taken with mRNA-1273 in response to the events was not reported. The outcome of event(s), tenderness, huge knot, swelling, itchiness, tightness was unknown.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site mass
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: No adverse event
Andere Medikamente: PROVERA
Allergien: -
Vorherige Impfungen: -

VAERS 1551429

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: NY
Alter: -
Geschlecht: F
Eingang: 13.08.2021
Impfdatum: 25.01.2021
Beginn: 26.01.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: OT / -

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

Decreased appetite Pyrexia Rash macular

Symptomtext

Arm of the injection has red spots/blotchy red, not just one dot; 100.2? F; Over 100? F; 99.1? F; No appetite; This spontaneous case was reported by a consumer and describes the occurrence of DECREASED APPETITE (No appetite), RASH MACULAR (Arm of the injection has red spots/blotchy red, not just one dot) and PYREXIA (100.2? F; Over 100? F; 99.1? F) in a 61-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for an unknown indication. The patient's past medical history included Autoimmune thyroid disorder (may be related to COVID), Premature atrial contraction and COVID-19 in March 2020. Concurrent medical conditions included Drug allergy (some antibiotics). Concomitant products included LEVOTHYROXINE SODIUM (LEVOTHYROXINE [LEVOTHYROXINE SODIUM]) for an unknown indication. On 25-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 26-Jan-2021, the patient experienced DECREASED APPETITE (No appetite) and PYREXIA (100.2? F; Over 100? F; 99.1? F). On 29-Jan-2021, the patient experienced RASH MACULAR (Arm of the injection has red spots/blotchy red, not just one dot). The patient was treated with PARACETAMOL (TYLENOL) for Fever, at an unspecified dose and frequency. On 28-Jan-2021, DECREASED APPETITE (No appetite) and PYREXIA (100.2? F; Over 100? F; 99.1? F) had resolved. At the time of the report, RASH MACULAR (Arm of the injection has red spots/blotchy red, not just one dot) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Autoimmune thyroid disorder (may be related to COVID); COVID-19; Drug allergy (some antibiotics); Premature atrial contraction
Andere Medikamente: LEVOTHYROXINE [LEVOTHYROXINE SODIUM]
Allergien: -
Vorherige Impfungen: -

VAERS 1550789

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: IL
Alter: -
Geschlecht: F
Eingang: 13.08.2021
Impfdatum: 10.02.2021
Beginn: 20.02.2021
Tage bis Beginn: 10,0
Dosis: 1
Route/Site: OT / RA

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

Pruritus

Symptomtext

Red itchy patch noted on her right arm (injection site); This spontaneous case was reported by a consumer and describes the occurrence of PRURITUS (Red itchy patch noted on her right arm (injection site)) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. The patient's past medical history included No adverse event. On 10-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 20-Feb-2021, the patient experienced PRURITUS (Red itchy patch noted on her right arm (injection site)). At the time of the report, PRURITUS (Red itchy patch noted on her right arm (injection site)) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. No relevant concomitant medications were reported. No treatment information was provided.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: No adverse event
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1550566

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: MI
Alter: 74,0
Geschlecht: F
Eingang: 12.08.2021
Impfdatum: 03.02.2021
Beginn: 16.02.2021
Tage bis Beginn: 13,0
Dosis: 1
Route/Site: OT / LA

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

Biopsy breast Catheterisation cardiac Myalgia Rash papular Skin lesion Vaccination site erythema Vaccination site pruritus Vaccination site rash Vaccination site warmth

Symptomtext

Chilblain-like lesions; Muscle aches; Warm reddened skin/self diagnosed warm red rash on upper left arm/warm reddened skin with slight bumpy rash appeared; Bumpy rash/ slight bumpy rash appeared; itchy at the injection site/Itching; rash at the injection site/self diagnosed warm red rash on upper left arm/warm reddened skin with slight bumpy rash appeared; Itchy red rash at injection site/self diagnosed warm red rash on upper left arm; This spontaneous case was reported by a patient and describes the occurrence of VACCINATION SITE WARMTH (Warm reddened skin/self diagnosed warm red rash on upper left arm/warm reddened skin with slight bumpy rash appeared), RASH PAPULAR (Bumpy rash/ slight bumpy rash appeared), SKIN LESION (Chilblain-like lesions), VACCINATION SITE PRURITUS (itchy at the injection site/Itching) and VACCINATION SITE RASH (rash at the injection site/self diagnosed warm red rash on upper left arm/warm reddened skin with slight bumpy rash appeared) in a 74-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included Bunionectomy (Also in 1970) in 1987, Hysterectomy in 1999, Cholecystectomy in 2004, Parathyroidectomy in 2004, Bladder suspension in 2007, Fracture repair in 2010, Fusion cervical spine in 2012, Cardiac pacemaker insertion on 28-Feb-2019, Cardioversion (Also on 21-JUN-2018, 01-MAR-2019, 18-JUL-2019, and 03-SEP-2019.) on 22-May-2018, Cardiac ablation (Also on 03-AUG-2018, and 29-AUG-2019.) on 24-Apr-2018 and Lumpectomy on 23-Dec-2020. Concurrent medical conditions included Cardiovascular disease, unspecified (Ongoing since 2017 - persistent atrial fibrillation /flutter - AV Node ablation and pacemaker.), Sulfonamide allergy (Early 1970s -1980s, red rash (reaction to Declostatin,swollen thumb with warm red rash)), Drug allergy (Declostatin, Early 1970s -1980s, red rash (reaction to Declostatin,swollen thumb with warm red rash)), Drug allergy (Allergy to Erythromycin.), Drug allergy (Allergy to Hydrochlorothiazide.), Drug allergy (Allergy to Niacin), Drug allergy (approximately in 2013, legs ached Allergy to Vytorin.) since 2013, Drug allergy (Extreme dizziness and irregular heartbeat) since 2019, Drug allergy (In 1970s.), Vitamin D low, Type 2 diabetes mellitus, Hypothyroidism, Heart disorder, Cardiac arrhythmia, Blood cholesterol abnormal, Bowel discomfort, Atrial fibrillation since 2017, Atrial flutter since 2017 and Type 2 diabetes mellitus. Concomitant products included RIVAROXABAN (XARELTO) for Anticoagulant therapy, CURCUMA LONGA, PIPER NIGRUM (TURMERIC & BLACK PEPPAR) and CURCUMIN for Antiinflammatory therapy, PRAVASTATIN for Blood cholesterol abnormal, PLANTAGO OVATA (METAMUCIL FIBRE THERAPY) for Bowel discomfort, METOPROLOL SUCCINATE for Cardiac arrhythmia, SITAGLIPTIN PHOSPHATE (JANUVIA) and METFORMIN HCL from 16-Mar-2020 to an unknown date for Diabetes, AZILSARTAN MEDOXOMIL, CHLORTALIDONE (EDARBYCLOR) from 16-Mar-2020 to an unknown date for Heart disorder, LEVOTHYROXINE SODIUM (LEVOTHYROXIN) for Hypothyroidism, LORATADINE for Runny nose, CHOLECALCIFEROL for Vitamin D, UBIDECARENONE (COQ10 [UBIDECARENONE]) and AMOXICILLIN for an unknown indication. On 03-Feb-2021 at 1:00 PM, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 16-Feb-2021, the patient experienced VACCINATION SITE WARMTH (Warm reddened skin/self diagnosed warm red rash on upper left arm/warm reddened skin with slight bumpy rash appeared) and VACCINATION SITE PRURITUS (itchy at the injection site/Itching). 16-Feb-2021, the patient experienced RASH PAPULAR (Bumpy rash/ slight bumpy rash appeared) and VACCINATION SITE ERYTHEMA (Itchy red rash at injection site/self diagnosed warm red rash on upper left arm). 16-Feb-2021, the patient experienced VACCINATION SITE RASH (rash at the injection site/self diagnosed warm red rash on upper left arm/warm reddened skin with slight bumpy rash appeared). On an unknown date, the patient experienced SKIN LESION (Chilblain-like lesions) and MYALGIA (Muscle aches). On 28-Feb-2021, VACCINATION SITE WARMTH (Warm reddened skin/self diagnosed warm red rash on upper left arm/warm reddened skin with slight bumpy rash appeared), RASH PAPULAR (Bumpy rash/ slight bumpy rash appeared), VACCINATION SITE PRURITUS (itchy at the injection site/Itching), VACCINATION SITE RASH (rash at the injection site/self diagnosed warm red rash on upper left arm/warm reddened skin with slight bumpy rash appeared) and VACCINATION SITE ERYTHEMA (Itchy red rash at injection site/self diagnosed warm red rash on upper left arm) had resolved. At the time of the report, SKIN LESION (Chilblain-like lesions) and MYALGIA (Muscle aches) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): In 2010, Catheterisation cardiac: unknown (Inconclusive) unknown. On 11-Sep-2020, Biopsy breast: unknown (Inconclusive) unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter considered VACCINATION SITE WARMTH (Warm reddened skin/self diagnosed warm red rash on upper left arm/warm reddened skin with slight bumpy rash appeared), RASH PAPULAR (Bumpy rash/ slight bumpy rash appeared), VACCINATION SITE PRURITUS (itchy at the injection site/Itching), VACCINATION SITE RASH (rash at the injection site/self diagnosed warm red rash on upper left arm/warm reddened skin with slight bumpy rash appeared) and VACCINATION SITE ERYTHEMA (Itchy red rash at injection site/self diagnosed warm red rash on upper left arm) to be possibly related. No further causality assessments were provided for SKIN LESION (Chilblain-like lesions) and MYALGIA (Muscle aches). On 20-FEB-2021, patient stated she still had rash but it was not itching. The rash was localized. The event did not cause patient to seek any medical care. The patient did not had any other symptoms. She had not taken any medicine or applied any creams. She was just letting it run its course. She was schedule for second dose on 03-MAR-2021. The patient had atrio-ventricular node ablation on 26 -SEP-2019. No treatment details were not reported. This case was linked to MOD-2021-255792 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 26-Apr-2021: Events Muscle aches, raised rash, feeling of warmth, vaccination site erythema added.patient ethnic group is updated. patient medical history is added.adverse event start date added. email id added. Rash at injection site, duration of days added. Chilblain-like lesions added. On 13-Jul-2021: Follow up received information about concomitant medications added, patient history updated, event dates, outcome updated, causality updated.

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Praegender Schweregrund: Myalgia
Hospital-Tage: -
Labordaten: Test Date: 20200911; Test Name: Breast Biopsy (Needle Core); Test Result: Inconclusive ; Result Unstructured Data: unknown; Test Date: 2010; Test Name: Heart Catherization; Test Result: Inconclusive ; Result Unstructured Data: unknown
Aktuelle Erkrankungen: Atrial fibrillation; Atrial flutter; Blood cholesterol abnormal; Bowel discomfort; Cardiac arrhythmia; Cardiovascular disease, unspecified (Ongoing since 2017 - persistent atrial fibrillation /flutter - AV Node ablation and pacemaker.); Drug allergy (In 1970s.); Drug allergy (Extreme dizziness and irregular heartbeat); Drug allergy (Declostatin, Early 1970s -1980s, red rash (reaction to Declostatin,swollen thumb with warm red rash)); Drug allergy (approximately in 2013, legs ached Allergy to Vytorin.); Drug allergy (Allergy to Niacin); Drug allergy (Allergy to Hydrochlorothiazide.); Drug allergy (Allergy to Erythromycin.); Heart disorder; Hypothyroidism; Sulfonamide allergy (Early 1970s -1980s, red rash (reaction to Declostatin,swollen thumb with warm red rash)); Type 2 diabetes mellitus; Vitamin D low
Vorgeschichte: Medical History/Concurrent Conditions: Bladder suspension; Bunionectomy (Also in 1970); Cardiac ablation (Also on 03-AUG-2018, and 29-AUG-2019.); Cardiac pacemaker insertion; Cardioversion (Also on 21-JUN-2018, 01-MAR-2019, 18-JUL-2019, and 03-SEP-2019.); Cholecystectomy; Fracture repair; Fusion cervical spine; Hysterectomy; Lumpectomy; Parathyroidectomy
Andere Medikamente: COQ10 [UBIDECARENONE]; CHOLECALCIFEROL; JANUVIA; LEVOTHYROXIN; EDARBYCLOR; METFORMIN HCL; METOPROLOL SUCCINATE; PRAVASTATIN; TURMERIC & BLACK PEPPAR; CURCUMIN; XARELTO; AMOXICILLIN; LORATADINE; METAMUCIL FIBRE THERAPY
Allergien: -
Vorherige Impfungen: -

VAERS 1550392

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: NJ
Alter: 64,0
Geschlecht: F
Eingang: 12.08.2021
Impfdatum: 10.02.2021
Beginn: 11.02.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: OT / LA

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

Fatigue Myalgia Oral pain Pain in extremity Palatal swelling Pruritus Rash

Symptomtext

Roof of the mouth sore; roof of my mouth is swollen; sore arm; Fatigue; Muscle ache; itching; rash spreading all over my torso and neck; rash on her thighs; This spontaneous case was reported by a consumer and describes the occurrence of PRURITUS (itching), ORAL PAIN (Roof of the mouth sore), PALATAL SWELLING (roof of my mouth is swollen), PAIN IN EXTREMITY (sore arm) and RASH (rash on her thighs) in a 64-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No medical history was reported by the reporter. Concomitant products included ESCITALOPRAM OXALATE (LEXAPRO) and DILTIAZEM (CARDIZEM [DILTIAZEM]) for an unknown indication. On 10-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 11-Feb-2021, the patient experienced RASH (rash on her thighs). On 16-Feb-2021, the patient experienced PRURITUS (itching) and RASH (rash spreading all over my torso and neck). On an unknown date, the patient experienced ORAL PAIN (Roof of the mouth sore), PALATAL SWELLING (roof of my mouth is swollen), PAIN IN EXTREMITY (sore arm), FATIGUE (Fatigue) and MYALGIA (Muscle ache). At the time of the report, PRURITUS (itching), PALATAL SWELLING (roof of my mouth is swollen), PAIN IN EXTREMITY (sore arm), RASH (rash on her thighs), RASH (rash spreading all over my torso and neck), FATIGUE (Fatigue) and MYALGIA (Muscle ache) outcome was unknown and ORAL PAIN (Roof of the mouth sore) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Treatment details was not reported by the reporter.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: No medical history was reported by the reporter.
Andere Medikamente: LEXAPRO; CARDIZEM [DILTIAZEM]
Allergien: -
Vorherige Impfungen: -

VAERS 1550375

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: IN
Alter: 72,0
Geschlecht: F
Eingang: 12.08.2021
Impfdatum: 01.02.2021
Beginn: 16.02.2021
Tage bis Beginn: 15,0
Dosis: 1
Route/Site: OT / LA

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

Headache

Symptomtext

persistent headache; This spontaneous case was reported by a health care professional and describes the occurrence of HEADACHE (persistent headache) in a 72-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. No medical history was reported by the reporter. Concomitant products included ROSUVASTATIN CALCIUM (CRESTOR), LEVOTHYROXINE SODIUM (SYNTHROID) and VITAMINS NOS for an unknown indication. On 01-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 16-Feb-2021, the patient experienced HEADACHE (persistent headache). The patient was treated with PARACETAMOL (TYLENOL) ongoing since an unknown date for Headache, at an unspecified dose and frequency. At the time of the report, HEADACHE (persistent 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.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: No medical history was reported by the reporter.
Andere Medikamente: CRESTOR; SYNTHROID; VITAMINS NOS
Allergien: -
Vorherige Impfungen: -

VAERS 1549942

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: MI
Alter: 71,0
Geschlecht: F
Eingang: 12.08.2021
Impfdatum: 06.02.2021
Beginn: 06.03.2021
Tage bis Beginn: 28,0
Dosis: 1
Route/Site: - / LA

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

Injection site erythema Injection site warmth Peripheral swelling

Symptomtext

On same day after the second dose injection site became red area of the redness has been; Arm is swollen; Arm patient received second dose in feels hot to the touch; This spontaneous case was reported by a consumer and describes the occurrence of INJECTION SITE ERYTHEMA (On same day after the second dose injection site became red area of the redness has been), PERIPHERAL SWELLING (Arm is swollen) and INJECTION SITE WARMTH (Arm patient received second dose in feels hot to the touch) in a 71-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 038K20A and 038K20A) for COVID-19 vaccination. The patient's past medical history included No Adverse Event (No medical history provided.) since an unknown date. Concomitant products included DIPHENHYDRAMINE, PARACETAMOL, PHENYLPROPANOLAMINE HYDROCHLORIDE (BENADRYL [DIPHENHYDRAMINE;PARACETAMOL;PHENYLPROPANOLAMINE HYDROCHLORIDE]) for an unknown indication. On 06-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) at an unspecified dose. On 06-Mar-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 06-Mar-2021, the patient experienced INJECTION SITE ERYTHEMA (On same day after the second dose injection site became red area of the redness has been), PERIPHERAL SWELLING (Arm is swollen) and INJECTION SITE WARMTH (Arm patient received second dose in feels hot to the touch). At the time of the report, INJECTION SITE ERYTHEMA (On same day after the second dose injection site became red area of the redness has been), PERIPHERAL SWELLING (Arm is swollen) and INJECTION SITE WARMTH (Arm patient received second dose in feels hot to the touch) outcome was unknown. Not Provided

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: No Adverse Event, Continue: true, Comment: No medical history provided.
Andere Medikamente: BENADRYL [DIPHENHYDRAMINE;PARACETAMOL;PHENYLPROPANOLAMINE HYDROCHLORIDE]
Allergien: -
Vorherige Impfungen: -

VAERS 1548740

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: IL
Alter: 69,0
Geschlecht: F
Eingang: 12.08.2021
Impfdatum: 27.01.2021
Beginn: 28.01.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: OT / -

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

Chills Oral herpes Pruritus

Symptomtext

She felt like he was developing cold sores in her body; She is very itchy; Chills; This spontaneous case was reported by a consumer and describes the occurrence of ORAL HERPES (She felt like he was developing cold sores in her body), PRURITUS (She is very itchy) and CHILLS (Chills) in a 69-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 038K20A and 026L20A) for COVID-19 vaccination. No Medical History information was reported. On 27-Jan-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On an unknown date, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 28-Jan-2021, the patient experienced CHILLS (Chills). On 31-Jan-2021, the patient experienced ORAL HERPES (She felt like he was developing cold sores in her body) and PRURITUS (She is very itchy). On 28-Jan-2021, CHILLS (Chills) had resolved. At the time of the report, ORAL HERPES (She felt like he was developing cold sores in her body) and PRURITUS (She is very itchy) outcome was unknown. Concomitant and Treatment medications were not provided. 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: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1548726

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: IL
Alter: 83,0
Geschlecht: F
Eingang: 12.08.2021
Impfdatum: 30.01.2021
Beginn: 31.01.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: OT / LA

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

Headache Hypersomnia

Symptomtext

Headache; Slept a lot; This spontaneous case was reported by a physician (subsequently medically confirmed) and describes the occurrence of HEADACHE (Headache) and HYPERSOMNIA (Slept a lot) in an 83-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. No Medical History information was reported. On 30-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 31-Jan-2021, the patient experienced HEADACHE (Headache) and HYPERSOMNIA (Slept a lot). On 31-Jan-2021, HYPERSOMNIA (Slept a lot) had resolved. On 01-Feb-2021, HEADACHE (Headache) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No relevant concomitant medications were reported Treatment details included Tylenol and pain killer.

Weitere VAERSDATA-Felder

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

VAERS 1548698

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: FL
Alter: 66,0
Geschlecht: M
Eingang: 12.08.2021
Impfdatum: 31.01.2021
Beginn: 31.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / LA

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

Body temperature Chills Decreased appetite Fatigue Headache Nausea Pyrexia

Symptomtext

has no appetite; fever up to 100.1F; headache; chills; nausea; was tired; This spontaneous case was reported by a consumer and describes the occurrence of DECREASED APPETITE (has no appetite), PYREXIA (fever up to 100.1F), HEADACHE (headache), CHILLS (chills) and NAUSEA (nausea) in a 66-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included Blood pressure since an unknown date. Concomitant products included VITAMINS NOS for an unknown indication. On 31-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 31-Jan-2021, the patient experienced DECREASED APPETITE (has no appetite), PYREXIA (fever up to 100.1F), HEADACHE (headache), CHILLS (chills), NAUSEA (nausea) and FATIGUE (was tired). The patient was treated with PARACETAMOL (TYLENOL) on 01-Feb-2021 at an unspecified dose and frequency. At the time of the report, DECREASED APPETITE (has no appetite), PYREXIA (fever up to 100.1F), HEADACHE (headache), CHILLS (chills), NAUSEA (nausea) and FATIGUE (was tired) was resolving. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 31-Jan-2021, Body temperature: 100.1 (Inconclusive) fever up to 100.1F. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Statins and blood pressure medication are the other concomitant medications reported by reporter.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Test Date: 20210131; Test Name: Body temperature; Test Result: Inconclusive ; Result Unstructured Data: fever up to 100.1F
Aktuelle Erkrankungen: Blood pressure
Vorgeschichte: -
Andere Medikamente: VITAMINS NOS
Allergien: -
Vorherige Impfungen: -

VAERS 1548553

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: PA
Alter: 79,0
Geschlecht: M
Eingang: 12.08.2021
Impfdatum: 24.01.2021
Beginn: 31.01.2021
Tage bis Beginn: 7,0
Dosis: 1
Route/Site: OT / -

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

Chills Pain Pyrexia

Symptomtext

A spontaneous report was received from a consumer concerning a 79-year-old, male patient who received Moderna's COVID-19 vaccine (mRNA-1273) and experienced chills, body aches/ pain and slight fever/ pyrexia. The patient's medical history was not provided. No relevant concomitant medications were reported. On 24 Jan 2021, prior to the onset of the events, the patient received their first of two planned doses of mRNA-1273 (Batch Number: 038K20A) intramuscularly for prophylaxis of COVID-19 infection. On 31 Jan 2021, the patient experienced chills, body aches and slight fever. No treatment information was provided. Action taken with mRNA-1273 in response to the events was not reported. On 1 Feb 2021, the outcome of event, slight fever was resolved. The outcome of the events, chills and body aches 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 event, a causal relationship cannot be excluded.

Weitere VAERSDATA-Felder

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

VAERS 1548113

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: FL
Alter: 80,0
Geschlecht: M
Eingang: 12.08.2021
Impfdatum: 27.01.2021
Beginn: 27.01.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / RA

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

Pain in extremity

Symptomtext

sore arm; This case was received via an unknown source (no reference has been entered for a health authority or license partner) on 18-Feb-2021 and was forwarded to Moderna on 18-Feb-2021. This spontaneous case was reported by a consumer and describes the occurrence of PAIN IN EXTREMITY (sore arm) in an 81-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. The patient's past medical history included Sleep apnea, Hypertension, Hyperthyroidism and Pacemaker insertion (cardiac). Concurrent medical conditions included Seasonal allergy and Drug allergy (certain prostate medication (unsure)). Concomitant products included RIVAROXABAN (XARELTO), LOSARTAN, AMLODIPINE and METOPROLOL for an unknown indication. On 27-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 27-Jan-2021, the patient experienced PAIN IN EXTREMITY (sore arm). At the time of the report, PAIN IN EXTREMITY (sore arm) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Treatment information was not provided. This case was linked to MODERNATX, INC. Most recent FOLLOW-UP information incorporated above includes: On 03-May-2021: Follow up included no new information as the follow up document contains information about wife.; Sender's Comments: MODERNATX, INC.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Drug allergy (certain prostate medication (unsure)); Seasonal allergy
Vorgeschichte: Medical History/Concurrent Conditions: Hypertension; Hyperthyroidism; Pacemaker insertion (cardiac); Sleep apnea
Andere Medikamente: XARELTO; LOSARTAN; AMLODIPINE; METOPROLOL
Allergien: -
Vorherige Impfungen: -

VAERS 1548110

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: FL
Alter: 68,0
Geschlecht: F
Eingang: 12.08.2021
Impfdatum: 27.01.2021
Beginn: 27.01.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: OT / LA

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

Bone marrow oedema Chills Diarrhoea Fatigue Feeling cold Headache Hot flush Illness Limb discomfort Pain in extremity Pyrexia Rash Synovial cyst Vomiting

Symptomtext

soreness in arm; reoccurring hot flashes up to 5 per day; could hardly walk; very cold; real sick; all her limbs felt very heavy; bad rash; vomiting; chills; fever; headaches; Looked like the bone popped up on top of the foot, by the last 2 toes/looked like it broke but it wasn't; Bone in right foot had a lump; Diarrhea; Bad headache; Complete exhaustion; Very tired; Felt like she had "50-pound leg weights; This case was received via an unknown source (no reference has been entered for a health authority or license partner) on 18-Feb-2021 and was forwarded to Moderna on 18-Feb-2021. This spontaneous case was reported by a consumer and describes the occurrence of SYNOVIAL CYST (Looked like the bone popped up on top of the foot, by the last 2 toes/looked like it broke but it wasn't), BONE MARROW OEDEMA (Bone in right foot had a lump), LIMB DISCOMFORT (Felt like she had "50-pound leg weights), DIARRHOEA (Diarrhea) and PAIN IN EXTREMITY (soreness in arm) in a 68-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 038K20A and 031M20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included Migraine, Hepatitis C, Post-traumatic stress disorder, ADD, Hypersensitivity, Atrial fibrillation, Pacemaker insertion (cardiac) in 2019 and Cardiac ablation. Concurrent medical conditions included Latex allergy, Sulfonamide allergy (allergy to sulfa drug) and Seasonal allergy. Concomitant products included DOFETILIDE, RIVAROXABAN (XARELTO), LEVOTHYROXINE SODIUM (SYNTHROID) and VITAMIN D3 for an unknown indication. On 27-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 25-Feb-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 27-Jan-2021, the patient experienced LIMB DISCOMFORT (Felt like she had "50-pound leg weights) and FATIGUE (Very tired). On 28-Jan-2021, the patient experienced SYNOVIAL CYST (Looked like the bone popped up on top of the foot, by the last 2 toes/looked like it broke but it wasn't), BONE MARROW OEDEMA (Bone in right foot had a lump), DIARRHOEA (Diarrhea), FATIGUE (Complete exhaustion) and HEADACHE (Bad headache). On an unknown date, the patient experienced PAIN IN EXTREMITY (soreness in arm), HOT FLUSH (reoccurring hot flashes up to 5 per day), PAIN IN EXTREMITY (could hardly walk), FEELING COLD (very cold), ILLNESS (real sick), LIMB DISCOMFORT (all her limbs felt very heavy), RASH (bad rash), VOMITING (vomiting), CHILLS (chills), PYREXIA (fever) and HEADACHE (headaches). At the time of the report, SYNOVIAL CYST (Looked like the bone popped up on top of the foot, by the last 2 toes/looked like it broke but it wasn't), BONE MARROW OEDEMA (Bone in right foot had a lump), LIMB DISCOMFORT (Felt like she had "50-pound leg weights), DIARRHOEA (Diarrhea), PAIN IN EXTREMITY (soreness in arm), HOT FLUSH (reoccurring hot flashes up to 5 per day), PAIN IN EXTREMITY (could hardly walk), FEELING COLD (very cold), ILLNESS (real sick), LIMB DISCOMFORT (all her limbs felt very heavy), RASH (bad rash), FATIGUE (Complete exhaustion), FATIGUE (Very tired), HEADACHE (Bad headache), VOMITING (vomiting), CHILLS (chills), PYREXIA (fever) and HEADACHE (headaches) outcome was unknown. No treatment information was provided. This case was linked to US-MODERNATX, INC.-MOD-2021-016250 (E2B Linked Report). Most recent FOLLOW-UP information incorporated above includes: On 03-May-2021: Follow up received on 3 may 2021,Added event, Added concomitant medication, Added dosage form; Sender's Comments: US-MODERNATX, INC.-MOD-2021-016250:

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Latex allergy; Seasonal allergy; Sulfonamide allergy (allergy to sulfa drug)
Vorgeschichte: Medical History/Concurrent Conditions: ADD; Atrial fibrillation; Cardiac ablation; Hepatitis C; Hypersensitivity; Migraine; Pacemaker insertion (cardiac); Post-traumatic stress disorder
Andere Medikamente: DOFETILIDE; XARELTO; SYNTHROID; VITAMIN D3
Allergien: -
Vorherige Impfungen: -

VAERS 1548062

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: FL
Alter: 66,0
Geschlecht: F
Eingang: 12.08.2021
Impfdatum: 17.02.2021
Beginn: 17.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / -

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

Fatigue Headache Myalgia Pyrexia

Symptomtext

fever(101.6); Fatigue; Headache; body aches; This spontaneous case was reported by a consumer and describes the occurrence of PYREXIA (fever(101.6)), FATIGUE (Fatigue), HEADACHE (Headache) and MYALGIA (body aches) in a 66-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. No medical history was provided by reporter. On 17-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 17-Feb-2021, the patient experienced PYREXIA (fever(101.6)), FATIGUE (Fatigue), HEADACHE (Headache) and MYALGIA (body aches). At the time of the report, PYREXIA (fever(101.6)), FATIGUE (Fatigue), HEADACHE (Headache) and MYALGIA (body aches) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. No relevant concomitant medications were reported No treatment information was provided.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: No medical history was provided by reporter
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1548025

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: IL
Alter: 71,0
Geschlecht: F
Eingang: 12.08.2021
Impfdatum: 28.01.2021
Beginn: 28.01.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: OT / RA

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

Pain in extremity

Symptomtext

This spontaneous case was reported by a consumer and describes the occurrence of PAIN IN EXTREMITY (Tender arm) in a 71-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. Concomitant products included CHOLESTEROL and THYROID THERAPY. On 28-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 01-Mar-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 28-Jan-2021, the patient experienced PAIN IN EXTREMITY (Tender arm). On 28-Jan-2021, PAIN IN EXTREMITY (Tender arm) had resolved. This case was linked to US-MODERNATX, INC.-MOD-2021-022449 (E2B Linked Report). This case was linked to MOD-2021-163880, MOD-2021-163880. Reporter did not allow further contact. Most recent FOLLOW-UP information incorporated above includes: On 24-May-2021: TCR; Sender's Comments: US-MODERNATX, INC.-MOD-2021-022449:Crosslinked (MOD21-020670)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: CHOLESTEROL; THYROID THERAPY
Allergien: -
Vorherige Impfungen: -

VAERS 1547927

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: OH
Alter: 72,0
Geschlecht: F
Eingang: 12.08.2021
Impfdatum: 03.02.2021
Beginn: 08.02.2021
Tage bis Beginn: 5,0
Dosis: 2
Route/Site: OT / LA

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

Abdominal pain Bacterial test Colitis Colonoscopy Culture stool Diarrhoea Erythema Headache Parasite stool test Pruritus Pyrexia Rash Vaccination site rash Vaccination site urticaria

Symptomtext

This spontaneous case was reported by a nurse and describes the occurrence of DIARRHEA (Diarrhea), PRURITUS (Generalized itching, some icthy areas on lower extremities), ERYTHEMA (generalized redness), ABDOMINAL PAIN (Abnormal cramping) and COLITIS (Colitis) in a 72-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 038K20A and 029A21) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concurrent medical conditions included Blood pressure high. Concomitant products included HYDROCHLOROTHIAZIDE, LISINOPRIL (LISINOPRIL HCTZ) for Hypertension, GABAPENTIN for Nerve pain, DICLOFENAC, OMEPRAZOLE and MIRABEGRON (MYRBETRIQ) for an unknown indication. On 03-Feb-2021 at 3:00 PM, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 03-Mar-2021 at 4:00 PM, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 08-Feb-2021, the patient experienced DIARRHOEA (Diarrhea). On 09-Feb-2021, the patient experienced PRURITUS (Generalized itching, some icthy areas on lower extremities), ERYTHEMA (generalized redness), ABDOMINAL PAIN (Abnormal cramping), VACCINATION SITE URTICARIA (generalized hives, concentrated around injection site.) and VACCINATION SITE RASH (Generalized rash on arms, concentrated around injection site). On 11-Feb-2021, the patient experienced RASH (Bi-lateral rash both arms). On 15-Feb-2021, the patient experienced PYREXIA (Fever) and HEADACHE (Headache). On an unknown date, the patient experienced COLITIS (Colitis). The patient was treated with PARACETAMOL (TYLENOL) for Adverse event, at an unspecified dose and frequency and CETIRIZINE HYDROCHLORIDE (ZYRTEC [CETIRIZINE HYDROCHLORIDE]) for Adverse event, at an unspecified dose and frequency. On 13-Feb-2021, RASH (Bi-lateral rash both arms) had resolved. On 15-Feb-2021, PYREXIA (Fever) and HEADACHE (Headache) had resolved. On 23-Feb-2021, PRURITUS (Generalized itching, some icthy areas on lower extremities), ERYTHEMA (generalized redness), ABDOMINAL PAIN (Abnormal cramping), VACCINATION SITE URTICARIA (generalized hives, concentrated around injection site.) and VACCINATION SITE RASH (Generalized rash on arms, concentrated around injection site) had resolved. At the time of the report, DIARRHOEA (Diarrhea) was resolving and COLITIS (Colitis) had resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 30-Dec-2020, Colonoscopy: normal (normal) Normal. On 15-May-2021, Colonoscopy: irrited area (abnormal) Showed an irritated area. On an unknown date, Bacterial test: negative (Negative) Negative. On an unknown date, Colonoscopy: irritated area like colitis (abnormal) Showed an irritated area like colitis. On an unknown date, Culture stool: negative (Negative) Negative. On an unknown date, Parasite stool test: negative (Negative) Negative. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) and mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) 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 20-Jun-2021: Updated patient demographics, lab data. Added Vaccine facility information. Added 2nd dose details.Updated Concomitant medication omeprazole and gabapentin dose,route of administration and indication. Added new concomitant medications Lisinopril, simvastatin and myrbetriq. Added new events -rash, urticaria, itching, erythema, abdominal pain with diarrhea. Updated outcome of the event diarrhea from unknown to recovering. On 20-Jun-2021: The follow-up was received on 20-Jun-21 contains no significant information.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain
Hospital-Tage: -
Labordaten: Test Name: C. diff stool test; Test Result: Negative ; Result Unstructured Data: Negative; Test Name: Colonoscopy; Result Unstructured Data: Showed an irritated area like colitis; Test Date: 20201230; Test Name: Colonoscopy; Result Unstructured Data: Normal; Test Date: 20210515; Test Name: Colonoscopy; Result Unstructured Data: Showed an irritated area; Test Name: Culture stool test; Test Result: Negative ; Result Unstructured Data: Negative; Test Name: Parasite stool test; Test Result: Negative ; Result Unstructured Data: Negative
Aktuelle Erkrankungen: Blood pressure high
Vorgeschichte: -
Andere Medikamente: DICLOFENAC; OMEPRAZOLE; GABAPENTIN; LISINOPRIL HCTZ; MYRBETRIQ
Allergien: -
Vorherige Impfungen: -

VAERS 1547795

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: MI
Alter: 74,0
Geschlecht: M
Eingang: 12.08.2021
Impfdatum: 12.02.2021
Beginn: 15.02.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: OT / LA

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

Dizziness

Symptomtext

dizziness; This spontaneous case was reported by a consumer and describes the occurrence of DIZZINESS (dizziness) in a 74-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. No medical history was provided by the reporter. Concomitant products included ATORVASTATIN, TAMSULOSIN, OMEPRAZOLE and LISINOPRIL for an unknown indication. On 12-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 15-Feb-2021, the patient experienced DIZZINESS (dizziness). The patient was treated with PARACETAMOL (TYLENOL) at an unspecified dose and frequency. At the time of the report, DIZZINESS (dizziness) had not resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: No medical history was provided by the reporter.
Andere Medikamente: ATORVASTATIN; TAMSULOSIN; OMEPRAZOLE; LISINOPRIL
Allergien: -
Vorherige Impfungen: -

VAERS 1547686

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: FL
Alter: 75,0
Geschlecht: F
Eingang: 12.08.2021
Impfdatum: 29.01.2021
Beginn: 30.01.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: OT / -

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

Erythema Pruritus

Symptomtext

Pruritus; Erythema; This spontaneous case was reported by a consumer and describes the occurrence of PRURITUS (Pruritus) and ERYTHEMA (Erythema) in a 75-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. The patient's past medical history included No adverse event. On 29-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 30-Jan-2021, the patient experienced PRURITUS (Pruritus) and ERYTHEMA (Erythema). At the time of the report, PRURITUS (Pruritus) and ERYTHEMA (Erythema) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: No adverse event
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1547618

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: MD
Alter: -
Geschlecht: F
Eingang: 12.08.2021
Impfdatum: 30.01.2021
Beginn: 07.02.2021
Tage bis Beginn: 8,0
Dosis: 1
Route/Site: OT / LA

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

Erythema Induration Pruritus Swelling

Symptomtext

Experiencing itching, swelling, hard, large red spot; Experiencing itching, swelling, hard, large red spot; Experiencing itching, swelling, hard, large red spot; Experiencing itching, swelling, hard, large red spot; This spontaneous case was reported by a consumer and describes the occurrence of PRURITUS (Experiencing itching, swelling, hard, large red spot), INDURATION (Experiencing itching, swelling, hard, large red spot), ERYTHEMA (Experiencing itching, swelling, hard, large red spot) and SWELLING (Experiencing itching, swelling, hard, large red spot) in a 71-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. Concomitant products included LEVOTHYROXINE, ROSUVASTATIN and ESTRADIOL for an unknown indication. On 30-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 07-Feb-2021, the patient experienced PRURITUS (Experiencing itching, swelling, hard, large red spot), INDURATION (Experiencing itching, swelling, hard, large red spot), ERYTHEMA (Experiencing itching, swelling, hard, large red spot) and SWELLING (Experiencing itching, swelling, hard, large red spot). The patient was treated with PARACETAMOL (TYLENOL) at an unspecified dose and frequency and CORTISONE ACETATE at a dose of UNK dosage form. At the time of the report, PRURITUS (Experiencing itching, swelling, hard, large red spot), INDURATION (Experiencing itching, swelling, hard, large red spot), ERYTHEMA (Experiencing itching, swelling, hard, large red spot) and SWELLING (Experiencing itching, swelling, hard, large red spot) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: LEVOTHYROXINE; ROSUVASTATIN; ESTRADIOL
Allergien: -
Vorherige Impfungen: -

VAERS 1544604

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: IL
Alter: -
Geschlecht: F
Eingang: 11.08.2021
Impfdatum: 28.01.2021
Beginn: 29.01.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: OT / LA

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

Abdominal discomfort Arthralgia Chills Diarrhoea Fatigue Injection site erythema Injection site swelling Myalgia

Symptomtext

muscle aches; Joint aches; Chills; feels fatigue; Diarrhea; Stomach upset; 4" x 4" injection site swelling; 4" x 4" injection site redness; This spontaneous case was reported by a consumer and describes the occurrence of INJECTION SITE SWELLING (4" x 4" injection site swelling), INJECTION SITE ERYTHEMA (4" x 4" injection site redness), MYALGIA (muscle aches), ARTHRALGIA (Joint aches) and CHILLS (Chills) in a 63-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included No adverse event. On 28-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 29-Jan-2021, the patient experienced INJECTION SITE SWELLING (4" x 4" injection site swelling) and INJECTION SITE ERYTHEMA (4" x 4" injection site redness). On 31-Jan-2021, the patient experienced MYALGIA (muscle aches), ARTHRALGIA (Joint aches), CHILLS (Chills), FATIGUE (feels fatigue), DIARRHOEA (Diarrhea) and ABDOMINAL DISCOMFORT (Stomach upset). At the time of the report, INJECTION SITE SWELLING (4" x 4" injection site swelling), INJECTION SITE ERYTHEMA (4" x 4" injection site redness), MYALGIA (muscle aches), ARTHRALGIA (Joint aches), CHILLS (Chills), FATIGUE (feels fatigue), DIARRHOEA (Diarrhea) and ABDOMINAL DISCOMFORT (Stomach upset) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Reporter did not allow further contact; 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: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: No adverse event
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1544584

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: FL
Alter: 70,0
Geschlecht: M
Eingang: 11.08.2021
Impfdatum: 01.02.2021
Beginn: 02.02.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: OT / -

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

Arthralgia Chills Feeling abnormal Headache Pain in extremity Pyrexia Visual acuity reduced

Symptomtext

decreased visual acuity; felt knocked off feet; significant left arm pain; low grade fever of 100.5; chills; headache; joint pain; This spontaneous case was reported by a physician and describes the occurrence of VISUAL ACUITY REDUCED (decreased visual acuity), FEELING ABNORMAL (felt knocked off feet), PAIN IN EXTREMITY (significant left arm pain), PYREXIA (low grade fever of 100.5) and CHILLS (chills) in a 70-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) 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 ROSUVASTATIN CALCIUM (CRESTOR), FLUOXETINE HYDROCHLORIDE (PROZAC), QUETIAPINE FUMARATE (SEROQUEL), ACETYLSALICYLIC ACID (BABY ASPIRIN), LOSARTAN, CETIRIZINE, MELOXICAM, PANTOPRAZOLE SODIUM SESQUIHYDRATE (TOPRAZOLE), ALPRAZOLAM, GABAPENTIN and FLUOXETINE for an unknown indication. On 01-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 02-Feb-2021, the patient experienced VISUAL ACUITY REDUCED (decreased visual acuity), FEELING ABNORMAL (felt knocked off feet), PAIN IN EXTREMITY (significant left arm pain), PYREXIA (low grade fever of 100.5), CHILLS (chills), HEADACHE (headache) and ARTHRALGIA (joint pain). On 04-Feb-2021, VISUAL ACUITY REDUCED (decreased visual acuity), PAIN IN EXTREMITY (significant left arm pain), PYREXIA (low grade fever of 100.5), CHILLS (chills), HEADACHE (headache) and ARTHRALGIA (joint pain) had resolved and FEELING ABNORMAL (felt knocked off feet) was resolving. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 02-Feb-2021, Pyrexia: 100.5 (abnormal) low grade fever of 100.5. 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. 04-feb-2021 Reporter states still a bit of discomfort, but feels better and back to work.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: Test Date: 20210202; Test Name: fever; Result Unstructured Data: low grade fever of 100.5
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: No medical history was provided by the reporter.
Andere Medikamente: CRESTOR; PROZAC; SEROQUEL; BABY ASPIRIN; LOSARTAN; CETIRIZINE; MELOXICAM; TOPRAZOLE; ALPRAZOLAM; GABAPENTIN; FLUOXETINE
Allergien: -
Vorherige Impfungen: -

VAERS 1544552

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 038K20A

mild

Staat: NY
Alter: 69,0
Geschlecht: F
Eingang: 11.08.2021
Impfdatum: 25.01.2021
Beginn: 02.02.2021
Tage bis Beginn: 8,0
Dosis: 1
Route/Site: OT / LA

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

Injection site erythema Injection site pruritus Injection site rash Injection site swelling Injection site warmth Urticaria

Symptomtext

hives; erupted in whelps at injection site; itchy at injection site; red at injection site; swollen at injection site; slightly hot at injection site; This case was received via an unknown source (no reference has been entered for a health authority or license partner) on 03-Feb-2021 and was forwarded to Moderna on 03-Feb-2021. This spontaneous case was reported by a consumer and describes the occurrence of INJECTION SITE RASH (erupted in whelps at injection site), INJECTION SITE PRURITUS (itchy at injection site), INJECTION SITE ERYTHEMA (red at injection site), INJECTION SITE SWELLING (swollen at injection site) and INJECTION SITE WARMTH (slightly hot at injection site) in a 69-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038K20A) 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 25-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 02-Feb-2021, the patient experienced INJECTION SITE RASH (erupted in whelps at injection site), INJECTION SITE PRURITUS (itchy at injection site), INJECTION SITE ERYTHEMA (red at injection site), INJECTION SITE SWELLING (swollen at injection site) and INJECTION SITE WARMTH (slightly hot at injection site). On an unknown date, the patient experienced URTICARIA (hives). On 03-Feb-2021, INJECTION SITE RASH (erupted in whelps at injection site), INJECTION SITE PRURITUS (itchy at injection site), INJECTION SITE ERYTHEMA (red at injection site), INJECTION SITE SWELLING (swollen at injection site) and INJECTION SITE WARMTH (slightly hot at injection site) had resolved. At the time of the report, URTICARIA (hives) was resolving. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. No treatment information was provided. No concomitant medication was provided. Reporter did not allow further contact

Weitere VAERSDATA-Felder

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