- Staat
- -
- Alter
- 85,0
- Geschlecht
- F
- Eingang
- 09.08.2023
- Impfdatum
- 14.01.2022
- Beginn
- 02.09.2022
- Tage bis Beginn
- 231,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute myocardial infarction
Pulmonary embolism
Symptom recurrence
Symptomtext
ACUTE NON ST ELEVATION MI ACUTE PULMONARY EMBOLISM 10/15/2022 -- RECURRENCE OF HOSPITALIZATION WITH SAME SYMPTOMS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute myocardial infarction
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 09.08.2023
- Impfdatum
- 14.01.2022
- Beginn
- 02.01.2023
- Tage bis Beginn
- 353,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute myocardial infarction
Symptomtext
ACUTE NON ST ELEVATION MI
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute myocardial infarction
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 82,0
- Geschlecht
- F
- Eingang
- 17.04.2023
- Impfdatum
- 24.12.2021
- Beginn
- 11.03.2023
- Tage bis Beginn
- 442,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
Arthralgia
Bronchiolitis
Bronchitis
COVID-19
Chest X-ray abnormal
Decubitus ulcer
Essential hypertension
Fall
Femur fracture
Hypotension
Hypoxia
Injury
Intramedullary rod insertion
SARS-CoV-2 test positive
X-ray of pelvis and hip abnormal
Symptomtext
Patient is a 83 y.o. female patient of MD with history of essential pretension, CAD, hyperlipidemia presented to Hospital with right hip pain secondary to ground-level fall found to have right femur fracture. Had R hip intramedullary nailing on 3/12/23 with no complications. Acute intertrochanteric fracture proximal right femur due to mechanical fall Fracture of right femur due to trauma alone S/p R hip TFN 3/12/23 S/p mechanical fall, x-ray right hip fracture Ortho consulted, taken to OR 3/12/23, tolerated procedure well. Recommend WBAT right lower extremity Lovenox for DVT prophylaxis PT/OT recommend up to 5 days of ST for 10 to 30 days SW following for DC needs. Pre-CERT approved. Plan for DC to SNF today as patient stable. Pt advised to f/u with her PCP Acute hypoxic respiratory failure Covid-19 virus infection Date of covid positive test: 3/12/2023 Vaccination status: vaccinated Imaging: Chest x-ray bronchitis, bronchiolitis Completed IV Remdesivir Continue Decadron Placed initially on 2 L of oxygen via NC, then weaned down to room air Hypoxic on 3/16 so placed on 3 L of oxygen Repeat CXR unchanged from previous Continue to wean down oxygen at the SNF Hypotension due to medications Primary HTN SBP 84 on 3/15, required 500 cc bolus, 110 after bolus Home BP meds held Will continue to hold coreg and lisinopril on discharge. Can be resumed out-pt as deemed appropriate by physician at SNF/PCP Stage 1 pressure injury of left heel present on admission Wound care consulted. Appreciate input.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 6,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 07.01.2023
- Impfdatum
- 16.09.2022
- Beginn
- 15.10.2022
- Tage bis Beginn
- 29,0
- Dosis
- 4
- Route/Site
- SYR / -
Tod: ja
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Death
Gastric cancer stage IV
Symptomtext
My dad's PSA levels skyrocketed from 2021 to 2022 resulting in a diagnosis of curable Prostate Cancer. As of the date of this diagnosis he had received 4 covid vaccinations. He received the 5th covid vaccination shortly after beginning radiation for curable Prostate Cancer. Prior to the 5th dose on 9/2022, my dad had no other cancers. The scans and bloodwork showed no metastases. On 10/2022 my dad was diagnosed with Stage 4 gastric cancer. Unrelated to the existing prostate cancer. The Gastric Cancer was a second primary - which is very rare. Additionally, his gastric cancer was PDL1 positive and metastasized at an unusually aggressive speed. He went to heaven on 12/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- 31,0
- Labordaten
- -
- Aktuelle Erkrankungen
- Stage 1 Prostate Cancer
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 90,0
- Geschlecht
- M
- Eingang
- 23.12.2022
- Impfdatum
- 04.01.2022
- Beginn
- 13.11.2022
- Tage bis Beginn
- 313,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
COVID-19
COVID-19 pneumonia
Chest X-ray abnormal
Cough
Echocardiogram normal
Ejection fraction normal
Hypoxia
Influenza virus test negative
Lacunar stroke
Lung infiltration
Motor dysfunction
Pleural effusion
Productive cough
SARS-CoV-2 test positive
Staphylococcus test positive
Symptomtext
Hospital Course: Patient is a 91 y.o. male patient with a history of hypertension, atrial fibrillation (on Eliquis), HFpEF (echo 8/29/2022 showed EF 56%), and recent lacunar stroke without residual motor deficits who presented to the ED complaining of persistent cough. Chest x-ray in the ED showed slight fluid and mild infiltrate concerning for pneumonia in the right lung base. He was found to be COVID-positive. He was started on Vanco/cefepime for concern of HAP, on further evaluation presentation appeared more consistent with viral etiology and antibiotics were discontinued. Was started on remdesivir and steroids. He has been afebrile and was weaned from 1LNC to room air. Found stable for discharge on 11/17. AMPAC 15/17. Per discussion with family, preferred to go home with previously established PRIVATE for disposition. OP follow-up with PCP, stroke clinic, and urology. Discharge Diagnoses: Acute hypoxemic respiratory failure COVID-pneumonia Cough Patient presented with productive cough since he left the hospital on 11/3/2022 Chest x-ray 11/13 showed slight fluid and mild infiltrate in the right lung base COVID positive 11/13/22, flu negative.MRSA nare swab positive Patient was hypoxic on admission, requiring 2 L nasal cannula. He was not showing any signs of acute respiratory distress. Corrected with supplemental oxygen and has been weaned to room air. -Remdesivir infusions and decadron given while inpatient, transitioned to oral prednisone taper at discharge
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 4,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 08.12.2022
- Impfdatum
- 21.04.2022
- Beginn
- 30.11.2022
- Tage bis Beginn
- 223,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Blood creatinine increased
Blood lactic acid
Brain natriuretic peptide normal
COVID-19
Cerebrovascular accident
Chest X-ray abnormal
Chills
Cough
Dyspnoea
Electrocardiogram normal
Haemoglobin decreased
Hypoxia
Lung disorder
Oropharyngeal pain
Pain
Procalcitonin
Productive cough
Symptomtext
"Patient with 4 COVID vaccines who admitted with COVID complications and a detected COVID PCR. Provider d/c note: ""78 YO-year-old male with PMHX of Afib on eliquis, COPD, HFrEF 35%, HX of CVA(9/2022) not on DAPT, HTN, BPH who presented via EMS to due to complaints of increased weakness, shortness of breath, and cough. Patient reports he started experiencing a fever with chills on Monday which have progressively worsened since then to include body aches, cough productive for clear to light yellow sputum, and sore throat. Patient is a poor historian as much of his speaking was hard to understand at the time which according to patient's niece is his baseline. Patient is vaccinated and denied any hospitalization for COVID any history. Patient did admit to having a sick contact with the past week which was reportedly his son who he resides with. At baseline patient is fully independent. Patient did have recent admission (9/22) for CVA of left temporal frontal lobes as well as left parietal lobe no longer on dapt. Patient otherwise denied any dizziness, lightheadedness, chest pain, palpitations, abdominal pain or any diarrhea/constipation ED vitals: Febrile 101.1 F, Tachypneic RR 22, 148/100, 86% room air ED labs: Cr: 1.3 HGB 11.7 BNP 13.1K Trope 47-- >56 lactate:1.7-- >0.7 procal:0.12 CXR: B/L airspace disease R>L has developed since 9/13/2022 RVP: covid + EKG: Normal Sinus Rhythm ED Course: Given DuoNebs En-route to emergency department, Lasix 40, Solumedrol, Ofirmev, Zofran. Upon admission, Patient completed 4 days of Remdesivir and decadron. He is to continue Dexamethasone 6mg daily through 12/10. His respiratory status greatly improved and cognition at baseline after discussion with patient's son. A walk test performed indicative of hypoxia upon ambulation to 84% with improvement of 1L Nasal cannula.. Patient is set up with Oxygen prior to discharge. He is to continue his home medications and follow with PCP. """
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebrovascular accident
- Hospital-Tage
- 4,0
- Labordaten
- COVID Detected PCR on 11/30/2022
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Hospital Cardiomyopathy (*) HTN (hypertension) Asymptomatic PVCs HFrEF (heart failure with reduced ejection fraction) (*) Cerebrovascular accident (CVA) Atrial fibrillation Major depressive disorder COVID-19 Acute on chronic respiratory failure Non-Hospital Elevated prostate specific antigen (PSA) Prostate nodule Bradycardia Ventricular tachycardia (paroxysmal) Hematuria, gross NSVT (nonsustained ventricular tachycardia)
- Andere Medikamente
- -
- Allergien
- EnalaprilatUnknown Labetalol HclUnknown PenicillinsUnknown ValsartanUnknown
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 20.09.2022
- Impfdatum
- 11.01.2022
- Beginn
- 08.09.2022
- Tage bis Beginn
- 240,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Agitation
Alcohol test negative
Back pain
COVID-19
Chest X-ray normal
Coma scale
Computerised tomogram head normal
Drug screen negative
Electroencephalogram abnormal
Endotracheal intubation
Hypercapnia
Intensive care
Intentional medical device removal by patient
Laboratory test normal
Mental status changes
Metabolic encephalopathy
Neurological examination normal
Procedural shock
Symptomtext
Discharge Provider: DO Primary Care Provider at Discharge: DO Admission Date: 9/8/2022 Discharge Date: 9/10/2022 PRESENTING PROBLEM: Acute metabolic encephalopathy HOSPITAL COURSE: 54 yo with HTN, DMTII, seizures, CKD, CVA, COPD on oxygen, chronic pain brought to ED 9/7 for AMS. She was found to be hypercapnic with low GCS for which she was intubated. COVID positive without infiltrates on CXR. Drug screen neg for drugs of abuse and alcohol level was negative. She had post intubation shock for which she required norepi. 9/8 pm, she self extubated. She did require precedex overnight for agitation which was only transient and with appropriate behavior. Recently prescribed baclofen, Lyrica, and Flagyl for back/vaginal pain. Negative head CT - history of CVA November of 2021 - managed with aspirin and statin therapy. Seen by Neurology exam without focal deficits, defer further neuroimaging. EEG with encephalopathy. Stop baclofen and lyrica. Patient transferred out of the intensive care unit to the general medical floor. She is breathing at her baseline oxygen level and requesting to go home as soon as possible. Mobilizing without difficulty in the room. Labs unremarkable this morning. Sputum did return with MRSA and due to severe episode will elect to treat for 5 days. Allergy to sulfa therefore prescribed doxycycline. At time of discharge, patient is hemodynamically stable and insistent on leaving asap.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Coma scale
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- Discharge Provider: MD Primary Care Provider: DO Admission Date: 1/4/2022 Discharge Date: 1/7/22 HOSPITAL DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Hypokalemia [E87.6] Acute exacerbation of chronic obstructive pulmonary disease (COPD) [J44.1] COPD with acute exacerbation [J44.1] Acute on chronic respiratory failure with hypoxia [J96.21]
- Vorgeschichte
- Chronic obstructive pulmonary disease with acute exacerbation Hypoxemia Obesity OSA (obstructive sleep apnea) History of tobacco abuse GERD (gastroesophageal reflux disease) Non-intractable vomiting with nausea Idiopathic hypotension Chronic bronchitis Hand abscess COPD (chronic obstructive pulmonary disease) Seizure Acute on chronic respiratory failure with hypoxia and hypercapnia Pain History of back pain COVID-19 virus infection CAP (community acquired pneumonia) due to MRSA (methicillin resistant Staphylococcus aureus)
- Andere Medikamente
- acetaminophen (TYLENOL) 500 MG tablet albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler amitriptyline (ELAVIL) 100 MG tablet aspirin EC 81 MG EC tablet atorvastatin (LIPITOR) 20 MG tablet budesonide/formo
- Allergien
- ErythromycinHives, Nausea and Vomiting MetforminHives, Nausea and Vomiting PenicillinsHives Sulfa DrugsHives MetoclopramideAnxiety
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 31.08.2022
- Impfdatum
- 03.02.2022
- Beginn
- 04.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Autopsy
Cardiac disorder
Condition aggravated
Death
Histology
Immunisation reaction
Toxicologic test
Symptomtext
Death due to cardiac disease exacerbated by the vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- Autopsy, histology, toxicology
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Hypertension
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 07.06.2022
- Impfdatum
- 19.01.2022
- Beginn
- 02.02.2022
- Tage bis Beginn
- 14,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Breast enlargement
Breast pain
Gynaecomastia
Mammogram normal
Pruritus
Symptomtext
Both my Breasts started growing 2 or 3 weeks after i had recieved my shot. I'm a skinny guy and my doctor was a little surprized it was happening. i was sent for a Mammo Gram ( somewhat Painful ) on March 2, 2022 resuluts came back as: A-Fatty, Benign for cancer, and little Gynecomastia. They said there just growing and i can go home. Now its June and my breasts are still growing, sometimes painful and at times they itch.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Gynaecomastia
- Hospital-Tage
- -
- Labordaten
- Mammo Gram proformed on March 2, 2022
- Aktuelle Erkrankungen
- ED/ Prostate, lower back/hip pains, Allergies
- Vorgeschichte
- HPV, High Blood Pre, Acid reflex
- Andere Medikamente
- Alfuzosin, ProstatePQ, Amlodipine, Meloxicam, Probiotic, Ginkgo Biloba, Famotidine, Azelastin-Fluticasone Propionate 137/50 Nasal Spray, Nasal Saline wash, Allegra, Zoloft, Mens 50+ Multi Vit, Vitamin D3, Metamucil.
- Allergien
- Gluten, Dairy, Parabens, some shell fish, Viagra
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 39,0
- Geschlecht
- M
- Eingang
- 23.01.2022
- Impfdatum
- 28.12.2021
- Beginn
- 19.01.2022
- Tage bis Beginn
- 22,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Acute myocardial infarction
Angioplasty
Blood creatine phosphokinase MB increased
Blood test
Coronary arterial stent insertion
Electrocardiogram ST segment elevation
Troponin increased
Symptomtext
Inferior ST elevation myocardial infarction, angioplasty and stenting of posterior descending coronary artery. In recovery.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute myocardial infarction
- Hospital-Tage
- -
- Labordaten
- ECG 19Jan2022 - ST elevation in inferior leads, acute MI. Blood test 19Jan2022 - Troponin 13.68, CKMB 80.8
- Aktuelle Erkrankungen
- Kidney stones
- Vorgeschichte
- Kidney stones
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- Chills, rash, fatigue after first (28Dec2020) and after the second dose (6Jan2021) of Moderna COVID19 vaccine.
- Staat
- IN
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 20.01.2022
- Impfdatum
- 12.01.2022
- Beginn
- 15.01.2022
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cerebral thrombosis
Cerebrovascular accident
Computerised tomogram
Electrocardiogram
Laboratory test
Magnetic resonance imaging
Symptomtext
stroke, blod clot in brain
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebrovascular accident
- Hospital-Tage
- 3,0
- Labordaten
- ct scam, mri, ekg, lab
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- hemachromatosis, copd, anxiety
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 20.01.2023
- Impfdatum
- 23.12.2021
- Beginn
- 25.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Anaphylactic reaction
Dyspnoea
Swelling
Urticaria
Symptomtext
On 01/20/2023 at 11:40am a 37 year old female, requested a Moderna Covid Bivalent Booster. She reported to RN that she got hives 2 days after receiving her previous Moderna Covid Booster lot#070H21A on 12/21/2021. Her hives went away the next day and she did not seek medical attention. No medical conditions. She did not report any reaction with the previous 2 primary series doses of Moderna Covid Vaccines. At 11:47 texted Dr. for a medical consult. "Good morning. We have a 37 yo female requesting Moderna Bivalent booster. She reports getting hives appearing 2 days following her last booster on 12/23/2021. She states she had no SOB, anaphylaxis or swelling. The hives went away the next day. She reports having hives previously in her teens possibly from seafood or cold weather. She is currently taking Benadryl. Please advise." At 11:48 am Dr. replied via text "No problem, she can receive booster. At 11:53 am, Client received a Moderna Covid Bivalent Booster lot#046H22A in the left deltoid by RN. Client was educated to seek medical attention if a severe allergic reaction were to occur. Client left with a steady gait after a 30 minute observation period.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Anaphylactic reaction
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- seafood or cold air
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 09.12.2022
- Impfdatum
- 24.03.2021
- Beginn
- 03.04.2021
- Tage bis Beginn
- 10,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: ja
Erholt: nein
Blood creatine phosphokinase MB
Blood pressure measurement
Brain natriuretic peptide
Chest discomfort
Chest pain
Cardiac disorder
Electrocardiogram
Foreign travel
Hypertension
Dizziness
Joint swelling
Myoglobin blood
Loss of personal independence in daily activities
Myocarditis
Pain in extremity
Peripheral swelling
Symptomtext
new onset chest pain, chest pain coming and going, chest pain comes back over time, never fully recovered; Pressure; Very high blood pressure; Dizziness; Daily left leg pain; Ankle swollen; pain on the left side of the torax onset 10 days after vaccination; This spontaneous case was reported by a patient and describes the occurrence of CHEST PAIN (new onset chest pain, chest pain coming and going, chest pain comes back over time, never fully recovered), CHEST DISCOMFORT (Pressure), HYPERTENSION (Very high blood pressure), DIZZINESS (Dizziness), PAIN IN EXTREMITY (Daily left leg pain) and JOINT SWELLING (Ankle swollen) in a 53-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 016B21A) for COVID-19 prophylaxis. The occurrence of additional non-serious events is detailed below. Active and healthy patient until she received Moderna's vaccine. Concurrent medical conditions included Penicillin allergy. On 24-Mar-2021 at 2:50 AM, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 03-Apr-2021, the patient experienced CHEST PAIN (pain on the left side of the torax onset 10 days after vaccination). On 14-Apr-2021 at 12:26 PM, the patient experienced CHEST PAIN (new onset chest pain, chest pain coming and going, chest pain comes back over time, never fully recovered) (seriousness criterion disability), CHEST DISCOMFORT (Pressure) (seriousness criterion disability), HYPERTENSION (Very high blood pressure) (seriousness criterion disability), DIZZINESS (Dizziness) (seriousness criterion disability), PAIN IN EXTREMITY (Daily left leg pain) (seriousness criterion disability) and JOINT SWELLING (Ankle swollen) (seriousness criterion disability). The patient was treated with IBUPROFEN at an unspecified dose and frequency. At the time of the report, CHEST PAIN (new onset chest pain, chest pain coming and going, chest pain comes back over time, never fully recovered), CHEST DISCOMFORT (Pressure), HYPERTENSION (Very high blood pressure), DIZZINESS (Dizziness), PAIN IN EXTREMITY (Daily left leg pain) and JOINT SWELLING (Ankle swollen) had not resolved and CHEST PAIN (pain on the left side of the torax onset 10 days after vaccination) had resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 14-Apr-2021, Blood creatine phosphokinase MB (0.0-4.3): less than 1.0 mg/mL. On 14-Apr-2021, Blood pressure measurement: High upper above 180. On 14-Apr-2021, Brain natriuretic peptide (0.0-100): 64.4 pg/ml. On 14-Apr-2021, Electrocardiogram: normal electrocardiogram with sinus rhythm and normal cardiac axis. On 14-Apr-2021, Myoglobin blood (0.0-107): 50.6 ng/mL. On an unknown date, Blood pressure measurement: High elevated upper blood pressure above 140., between 110/115 ? 55/60 and between 135/185 ? 75/110. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. Concomitant medications were not reported. On 14-Apr-2021 doctor did ECG check on heart with normal electrocardiogram with sinus rhythm and normal cardiac axis. On 14-Apr-2021, lab test TNI was performed and the result was less than 0.05ng/mL the normal range was provided as 0.00-0.40. On 14-Apr-2021, lab test DDIM was performed and the result was 101 ng/ml. Normal range was 0.0-400. Patient experiendced chest pain, pressure, very high blood pressure, and dizziness direclty after take off from airport, she took high dose of constant ibuprofen, no medical assistance on board, flight crew escorted her to in airport Emergency Clinic. Doctors measured very high blood pressure (upper above 180) and did ECG check on heart. Disallowed to fly further to final destination. She was prescribed pain treatment course and rest. She never fully recovered. Chest pain, left leg pain comes back over time, she cannot be active and perform sports or being active. Stay on high altitude ended in daily left leg pain, ankle swollen, elevtated upper blood pressure above 140. She Cannot go on scheduled flight. Company Comment: This is a spontaneous case regarding a 53-year-old female patient, with no relevant medical history, who experienced serious (disability) events of chest pain, chest discomfort, hypertension, dizziness, pain in extremity and swollen ankle after receiving first dose of mRNA-1273 vaccine. According to the report, patient experienced pain on the left side of the thorax 10 days after vaccination that subsided spontaneously. 21 days after vaccination, during a long haul flight, patient experienced new onset of chest pain accompanied by chest pressure, high blood pressure and dizziness. Patient took high dose of constant ibuprofen and was escorted to in airport Emergency Clinic where doctors measured blood pressure (upper above 180), performed ECG (normal result) and lab tests including CKMB, MYO, TnI, BNP and DDIM (all were between normal ranges). Patient was prescribed pain treatment course and rest, but she stated that she never fully recovered. Chest pain and left leg pain came back over time, she cannot perform sports or active life anymore and cannot fly. A stay on high altitude ended in daily left leg pain, ankle swollen, and elevated blood pressure above 140. She stated that her blood pressure was between 110/115 ? 55/60 and is now between 135/185 ? 75/110. No further details regarding clinical course, diagnostic tests or treatment performed were disclosed. The benefit-risk relationship of mRNA-1273 vaccine is not affected by this report.; Sender's Comments: This is a spontaneous case regarding a 53-year-old female patient, with no relevant medical history, who experienced serious (disability) events of chest pain, chest discomfort, hypertension, dizziness, pain in extremity and swollen ankle after receiving first dose of mRNA-1273 vaccine. According to the report, patient experienced pain on the left side of the thorax 10 days after vaccination that subsided spontaneously. 21 days after vaccination, during a long haul flight, patient experienced new onset of chest pain accompanied by chest pressure, high blood pressure and dizziness. Patient took high dose of constant ibuprofen and was escorted to in airport Emergency Clinic where doctors measured blood pressure (upper above 180), performed ECG (normal result) and lab tests including CKMB, MYO, TnI, BNP and DDIM (all were between normal ranges). Patient was prescribed pain treatment course and rest, but she stated that she never fully recovered. Chest pain and left leg pain came back over time, she cannot perform sports or active life anymore and cannot fly. A stay on high altitude ended in daily left leg pain, ankle swollen, and elevated blood pressure above 140. She stated that her blood pressure was between 110/115 ? 55/60 and is now between 135/185 ? 75/110. No further details regarding clinical course, diagnostic tests or treatment performed were disclosed. The benefit-risk relationship of mRNA-1273 vaccine is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myocarditis
- Hospital-Tage
- -
- Labordaten
- Test Date: 20210414; Test Name: CKMB; Result Unstructured Data: less than 1.0 mg/mL; Test Name: high blood pressure; Result Unstructured Data: High elevated upper blood pressure above 140.; Test Name: high blood pressure; Result Unstructured Data: between 110/115 ? 55/60; Test Name: high blood pressure; Result Unstructured Data: between 135/185 ? 75/110; Test Date: 20210414; Test Name: high blood pressure; Result Unstructured Data: High upper above 180; Test Date: 20210414; Test Name: BNP; Result Unstructured Data: 64.4 pg/ml; Test Date: 20210414; Test Name: ECG check; Result Unstructured Data: normal electrocardiogram with sinus rhythm and normal cardiac axis; Test Date: 20210414; Test Name: MYO; Result Unstructured Data: 50.6 ng/mL
- Aktuelle Erkrankungen
- Penicillin allergy
- Vorgeschichte
- Comments: Active and healthy patient until she received Moderna's vaccine.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 24.10.2022
- Impfdatum
- 30.12.2021
- Beginn
- 09.10.2022
- Tage bis Beginn
- 283,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Colitis
Computerised tomogram abdomen abnormal
Diarrhoea
Dyspnoea
Hypotension
Intensive care
Renal mass
SARS-CoV-2 test positive
Symptomtext
Patient with 3 COVID vaccines who admitted to hospital with COVID detected PCR. Provider d/c note: "79-year-old female with past medical history significant for chronic obstructive pulmonary disease, DVT and AFib. She presented to the emergency department on 10/10/2022 with a chief complaint of shortness of breath and diarrhea. On arrival she was found to have some colitis as well as positive for COVID-19 infection. She was originally admitted to the ICU due to borderline hypotension on arrival. CT imaging showed evidence of colitis as well as a renal mass. She was started on antibiotics as well as steroids. Her symptoms were slow to improve but continued to improve over the course of her stay. On day of discharge patient was tolerating her home oxygen and occasionally room air. She will be discharged home on the completion of her antibiotics and steroids. She will be sent home with home care and was told to follow-up with her PCP as well as she was sent a referral to Urology for the finding of this renal mass. On day of discharge she was in improved and stable condition, was ready to go home and was given strict return precautions to which she verbalized understanding"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Intensive care
- Hospital-Tage
- 5,0
- Labordaten
- COVID Detected on 10/10/2022
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Cardiovascular Essential hypertension Paroxysmal atrial fibrillation (*) Hx CVA incidental finding on CT Pulmonary embolism (*) NSTEMI (non-ST elevated myocardial infarction) (*) Digestive Chronic gastritis Gastritis, erosive PUD (peptic ulcer disease) Gastroenteritis due to 2019 novel coronavirus Endocrine Hyperthyroidism Psychological Depression Respiratory Chronic obstructive pulmonary disease (*) On home oxygen therapy Supplemental oxygen dependent Acute on chronic respiratory failure (*) Urinary Acute kidney injury (*) Right renal lesion concerning for renal cell carcinoma Other Chronic back pain Esophageal diverticulum History of heart attack Osteoarthritis Osteoporosis Frequent falls Hypomagnesemia Polycythemia Generalized abdominal pain Chronic bilateral low back pain with bilateral sciatica Severe protein-calorie malnutrition (*) Generalized muscle weakness Protein-calorie malnutrition (*) Chronic, continuous use of opioids
- Andere Medikamente
- -
- Allergien
- Mold, Shrimp, Augmentin, Bowel Prep, Clopidogrel, Coumadin, Fosamax, Tomato
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 20.05.2022
- Impfdatum
- 08.01.2022
- Beginn
- 08.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Abdominal pain
Arthralgia
Back pain
Blood test normal
Chest pain
Blood potassium
COVID-19
Costochondritis
Computerised tomogram normal
Dysgeusia
Dyspnoea
Flank pain
Gait disturbance
Dizziness
Dysstasia
Electrocardiogram
Extrasystoles
Feeding disorder
Symptomtext
Positive COVID-19 PCR test; Still has from time to time: Muscle knot and cramps on the back of the left leg.; Still has from time to time: Muscle knot and cramps on the back of the left leg.; Still has from time to time: dizziness; Still has from time to time headache; Diagnosed with Costochondritis (Inflammation in the chest wall); Pneumonia; Had a seizure and went to the emergency room at a Hospital; Potassium keeps dropping; Pain on the right side of hip & knee cap; Could not eat; Shortness Of Breath; Foggy brain; Could not stand up; Black outs; Racing Heart/Palpitation/Heart Palpitation continues from time to time 3 months after first vaccine; Diagnosed with Premature Heart Beat; Immediately after vaccination, she had a metallic taste in the mouth; Immediately after vaccination, itchiness started on her forehead and spread down the entire body.; At night she had pain on her back; This spontaneous case was reported by a patient and describes the occurrence of PNEUMONIA (Pneumonia), SEIZURE (Had a seizure and went to the emergency room at a Hospital), LOSS OF CONSCIOUSNESS (Black outs), HYPOKALAEMIA (Potassium keeps dropping) and COVID-19 (Positive COVID-19 PCR test) in a 37-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 070H21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 08-Jan-2022, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 08-Jan-2022, the patient experienced DYSGEUSIA (Immediately after vaccination, she had a metallic taste in the mouth), PRURITUS (Immediately after vaccination, itchiness started on her forehead and spread down the entire body.) and BACK PAIN (At night she had pain on her back). On 09-Jan-2022, the patient experienced LOSS OF CONSCIOUSNESS (Black outs) (seriousness criterion medically significant), PALPITATIONS (Racing Heart/Palpitation/Heart Palpitation continues from time to time 3 months after first vaccine), EXTRASYSTOLES (Diagnosed with Premature Heart Beat), DYSPNOEA (Shortness Of Breath), FEELING ABNORMAL (Foggy brain), DYSSTASIA (Could not stand up), FEEDING DISORDER (Could not eat) and ARTHRALGIA (Pain on the right side of hip & knee cap). On 14-Jan-2022, the patient experienced SEIZURE (Had a seizure and went to the emergency room at a Hospital) (seriousness criterion medically significant) and HYPOKALAEMIA (Potassium keeps dropping) (seriousness criterion medically significant). On 15-Jan-2022, the patient experienced PNEUMONIA (Pneumonia) (seriousness criterion medically significant). On 03-Feb-2022, the patient experienced COVID-19 (Positive COVID-19 PCR test) (seriousness criterion hospitalization) and COSTOCHONDRITIS (Diagnosed with Costochondritis (Inflammation in the chest wall)). On 18-Apr-2022, the patient experienced MUSCLE MASS (Still has from time to time: Muscle knot and cramps on the back of the left leg.), MUSCLE SPASMS (Still has from time to time: Muscle knot and cramps on the back of the left leg.), DIZZINESS (Still has from time to time: dizziness) and HEADACHE (Still has from time to time headache). The patient was hospitalized on 03-Feb-2022 due to COVID-19. The patient was treated with POTASSIUM for Supplementation therapy, at an unspecified dose and frequency; DEXAMETHASONE (DECADRON [DEXAMETHASONE]) for Heartbeats premature and Costochondritis, at a dose of at different times and PREDNISONE for Heartbeats premature and Costochondritis, at a dose of at different times. At the time of the report, PNEUMONIA (Pneumonia), SEIZURE (Had a seizure and went to the emergency room at a Hospital), LOSS OF CONSCIOUSNESS (Black outs), HYPOKALAEMIA (Potassium keeps dropping), COVID-19 (Positive COVID-19 PCR test), EXTRASYSTOLES (Diagnosed with Premature Heart Beat), DYSGEUSIA (Immediately after vaccination, she had a metallic taste in the mouth), PRURITUS (Immediately after vaccination, itchiness started on her forehead and spread down the entire body.), BACK PAIN (At night she had pain on her back), DYSPNOEA (Shortness Of Breath), FEELING ABNORMAL (Foggy brain), DYSSTASIA (Could not stand up), COSTOCHONDRITIS (Diagnosed with Costochondritis (Inflammation in the chest wall)), FEEDING DISORDER (Could not eat) and ARTHRALGIA (Pain on the right side of hip & knee cap) outcome was unknown and PALPITATIONS (Racing Heart/Palpitation/Heart Palpitation continues from time to time 3 months after first vaccine), MUSCLE MASS (Still has from time to time: Muscle knot and cramps on the back of the left leg.), MUSCLE SPASMS (Still has from time to time: Muscle knot and cramps on the back of the left leg.), DIZZINESS (Still has from time to time: dizziness) and HEADACHE (Still has from time to time headache) had not resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 14-Jan-2022, Blood potassium: low (Low) Keeps dropping. On 14-Jan-2022, Electrocardiogram: normal (normal) Normal. On 03-Feb-2022, SARS-CoV-2 test: positive (Positive) Positive. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. Patient was not on any medications prior to or during vaccination. In the morning of 09-Jan-2022, patient started having racing heart, premature heartbeat, palpitation, pain on the right side of hip and kneecap, and shortness of breath. The patient started wearing a heart monitor at home. On 03-Feb-2022, she ended up in the hospital. She states that she does not have a medical history of seizures and no medical history of heart disease. She was not breastfeeding during or after vaccination. She states that a month ago, she started getting better. On 18-May-2022, she was able to sit up and move around. She tried Betablockers, but she could not tolerate it and discontinued it. COMPANY COMMENT: This is an spontaneous case concerning an 37-years-old female patient with no medical history who experienced the unexpected events of COVID-19 (AESI, seriousness criterion Hospitalization), SEIZURE, PNEUMONIA, LOSS OF CONSCIOUSNESS, HYPOKALAEMIA (seriousness criterion IME), PRURITUS, BACK PAIN, DYSGEUSIA, PALPITATIONS, EXTRASYSTOLES, DYSPNOEA, FEELING ABNORMAL, DYSSTASIA, FEEDING DISORDER, COSTOCHONDRITIS, MUSCLE MASS, MUSCLE SPASMS. PALPITATIONS and other expected events beginning the same day after receiving the 1st dose of mRNA-1273 vaccine. The benefit-risk relationship of mRNA-1273 vaccine is not affected by this report.; Sender's Comments: COMPANY COMMENT: This is an spontaneous case concerning an 37-years-old female patient with no medical history who experienced the unexpected events of COVID-19 (AESI, seriousness criterion Hospitalization), SEIZURE, PNEUMONIA, LOSS OF CONSCIOUSNESS, HYPOKALAEMIA (seriousness criterion IME), PRURITUS, BACK PAIN, DYSGEUSIA, PALPITATIONS, EXTRASYSTOLES, DYSPNOEA, FEELING ABNORMAL, DYSSTASIA, FEEDING DISORDER, COSTOCHONDRITIS, MUSCLE MASS, MUSCLE SPASMS. PALPITATIONS and other expected events beginning the same day after receiving the 1st dose of mRNA-1273 vaccine. The benefit-risk relationship of mRNA-1273 vaccine is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220114; Test Name: Potassium; Result Unstructured Data: Keeps dropping; Test Date: 20220114; Test Name: EKG; Result Unstructured Data: Normal; Test Date: 20220203; Test Name: COVID-19 PCR test; Test Result: Positive ; Result Unstructured Data: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 20.05.2022
- Impfdatum
- 08.01.2022
- Beginn
- 08.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Abdominal pain
Arthralgia
Back pain
Blood test normal
Chest pain
Blood potassium
COVID-19
Costochondritis
Computerised tomogram normal
Dysgeusia
Dyspnoea
Flank pain
Gait disturbance
Dizziness
Dysstasia
Electrocardiogram
Extrasystoles
Feeding disorder
Symptomtext
Positive COVID-19 PCR test; Still has from time to time: Muscle knot and cramps on the back of the left leg.; Still has from time to time: Muscle knot and cramps on the back of the left leg.; Still has from time to time: dizziness; Still has from time to time headache; Diagnosed with Costochondritis (Inflammation in the chest wall); Pneumonia; Had a seizure and went to the emergency room at a Hospital; Potassium keeps dropping; Pain on the right side of hip & knee cap; Could not eat; Shortness Of Breath; Foggy brain; Could not stand up; Black outs; Racing Heart/Palpitation/Heart Palpitation continues from time to time 3 months after first vaccine; Diagnosed with Premature Heart Beat; Immediately after vaccination, she had a metallic taste in the mouth; Immediately after vaccination, itchiness started on her forehead and spread down the entire body.; At night she had pain on her back; This spontaneous case was reported by a patient and describes the occurrence of PNEUMONIA (Pneumonia), SEIZURE (Had a seizure and went to the emergency room at a Hospital), LOSS OF CONSCIOUSNESS (Black outs), HYPOKALAEMIA (Potassium keeps dropping) and COVID-19 (Positive COVID-19 PCR test) in a 37-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 070H21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 08-Jan-2022, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 08-Jan-2022, the patient experienced DYSGEUSIA (Immediately after vaccination, she had a metallic taste in the mouth), PRURITUS (Immediately after vaccination, itchiness started on her forehead and spread down the entire body.) and BACK PAIN (At night she had pain on her back). On 09-Jan-2022, the patient experienced LOSS OF CONSCIOUSNESS (Black outs) (seriousness criterion medically significant), PALPITATIONS (Racing Heart/Palpitation/Heart Palpitation continues from time to time 3 months after first vaccine), EXTRASYSTOLES (Diagnosed with Premature Heart Beat), DYSPNOEA (Shortness Of Breath), FEELING ABNORMAL (Foggy brain), DYSSTASIA (Could not stand up), FEEDING DISORDER (Could not eat) and ARTHRALGIA (Pain on the right side of hip & knee cap). On 14-Jan-2022, the patient experienced SEIZURE (Had a seizure and went to the emergency room at a Hospital) (seriousness criterion medically significant) and HYPOKALAEMIA (Potassium keeps dropping) (seriousness criterion medically significant). On 15-Jan-2022, the patient experienced PNEUMONIA (Pneumonia) (seriousness criterion medically significant). On 03-Feb-2022, the patient experienced COVID-19 (Positive COVID-19 PCR test) (seriousness criterion hospitalization) and COSTOCHONDRITIS (Diagnosed with Costochondritis (Inflammation in the chest wall)). On 18-Apr-2022, the patient experienced MUSCLE MASS (Still has from time to time: Muscle knot and cramps on the back of the left leg.), MUSCLE SPASMS (Still has from time to time: Muscle knot and cramps on the back of the left leg.), DIZZINESS (Still has from time to time: dizziness) and HEADACHE (Still has from time to time headache). The patient was hospitalized on 03-Feb-2022 due to COVID-19. The patient was treated with POTASSIUM for Supplementation therapy, at an unspecified dose and frequency; DEXAMETHASONE (DECADRON [DEXAMETHASONE]) for Heartbeats premature and Costochondritis, at a dose of at different times and PREDNISONE for Heartbeats premature and Costochondritis, at a dose of at different times. At the time of the report, PNEUMONIA (Pneumonia), SEIZURE (Had a seizure and went to the emergency room at a Hospital), LOSS OF CONSCIOUSNESS (Black outs), HYPOKALAEMIA (Potassium keeps dropping), COVID-19 (Positive COVID-19 PCR test), EXTRASYSTOLES (Diagnosed with Premature Heart Beat), DYSGEUSIA (Immediately after vaccination, she had a metallic taste in the mouth), PRURITUS (Immediately after vaccination, itchiness started on her forehead and spread down the entire body.), BACK PAIN (At night she had pain on her back), DYSPNOEA (Shortness Of Breath), FEELING ABNORMAL (Foggy brain), DYSSTASIA (Could not stand up), COSTOCHONDRITIS (Diagnosed with Costochondritis (Inflammation in the chest wall)), FEEDING DISORDER (Could not eat) and ARTHRALGIA (Pain on the right side of hip & knee cap) outcome was unknown and PALPITATIONS (Racing Heart/Palpitation/Heart Palpitation continues from time to time 3 months after first vaccine), MUSCLE MASS (Still has from time to time: Muscle knot and cramps on the back of the left leg.), MUSCLE SPASMS (Still has from time to time: Muscle knot and cramps on the back of the left leg.), DIZZINESS (Still has from time to time: dizziness) and HEADACHE (Still has from time to time headache) had not resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 14-Jan-2022, Blood potassium: low (Low) Keeps dropping. On 14-Jan-2022, Electrocardiogram: normal (normal) Normal. On 03-Feb-2022, SARS-CoV-2 test: positive (Positive) Positive. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. Patient was not on any medications prior to or during vaccination. In the morning of 09-Jan-2022, patient started having racing heart, premature heartbeat, palpitation, pain on the right side of hip and kneecap, and shortness of breath. The patient started wearing a heart monitor at home. On 03-Feb-2022, she ended up in the hospital. She states that she does not have a medical history of seizures and no medical history of heart disease. She was not breastfeeding during or after vaccination. She states that a month ago, she started getting better. On 18-May-2022, she was able to sit up and move around. She tried Betablockers, but she could not tolerate it and discontinued it. COMPANY COMMENT: This is an spontaneous case concerning an 37-years-old female patient with no medical history who experienced the unexpected events of COVID-19 (AESI, seriousness criterion Hospitalization), SEIZURE, PNEUMONIA, LOSS OF CONSCIOUSNESS, HYPOKALAEMIA (seriousness criterion IME), PRURITUS, BACK PAIN, DYSGEUSIA, PALPITATIONS, EXTRASYSTOLES, DYSPNOEA, FEELING ABNORMAL, DYSSTASIA, FEEDING DISORDER, COSTOCHONDRITIS, MUSCLE MASS, MUSCLE SPASMS. PALPITATIONS and other expected events beginning the same day after receiving the 1st dose of mRNA-1273 vaccine. The benefit-risk relationship of mRNA-1273 vaccine is not affected by this report.; Sender's Comments: COMPANY COMMENT: This is an spontaneous case concerning an 37-years-old female patient with no medical history who experienced the unexpected events of COVID-19 (AESI, seriousness criterion Hospitalization), SEIZURE, PNEUMONIA, LOSS OF CONSCIOUSNESS, HYPOKALAEMIA (seriousness criterion IME), PRURITUS, BACK PAIN, DYSGEUSIA, PALPITATIONS, EXTRASYSTOLES, DYSPNOEA, FEELING ABNORMAL, DYSSTASIA, FEEDING DISORDER, COSTOCHONDRITIS, MUSCLE MASS, MUSCLE SPASMS. PALPITATIONS and other expected events beginning the same day after receiving the 1st dose of mRNA-1273 vaccine. The benefit-risk relationship of mRNA-1273 vaccine is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220114; Test Name: Potassium; Result Unstructured Data: Keeps dropping; Test Date: 20220114; Test Name: EKG; Result Unstructured Data: Normal; Test Date: 20220203; Test Name: COVID-19 PCR test; Test Result: Positive ; Result Unstructured Data: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 07.05.2022
- Impfdatum
- 18.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cardiac stress test
Chest pain
Dyspnoea
Palpitations
Syncope
Symptomtext
Heart Palpitations, fainting ,shortness of breathe ,pain in chest.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- Nuclear Stress test
- Aktuelle Erkrankungen
- Heart Murmur
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 04.04.2022
- Impfdatum
- 01.04.2022
- Beginn
- 02.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pericarditis
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pericarditis
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 14.03.2022
- Impfdatum
- 09.03.2022
- Beginn
- 09.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Amnesia
Decreased appetite
Erythema
Gait disturbance
Hallucination, auditory
Loss of consciousness
Loss of personal independence in daily activities
Oropharyngeal pain
Pyrexia
Rash
Rash erythematous
Skin wrinkling
Vomiting
Symptomtext
Loss consciousness that evening of injection. Found next morning at 9am still unconscious. Loss of memory for 2 days. Fever for 2 days. Vomiting for 2 days, No appetite 5 days. Rash -red dots started on legs, now on arms, trunk. Toes are red / prune looking. Throat sore. Auditory hallucinations on Friday 11th. Unable to function for 2 days. Unable to perform ADL's. Needed someone to do everything for her. Was seen by home nurse. Is now able to get to the restroom by herself after 5 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Diabetes, HTN, Chronic kidney failure, COPD, Cancer, Lymphedema, CHF
- Andere Medikamente
- Insulin, Pain meds, Blood pressure, magnesium, potassium, steroids, Singulair, Effexor, D3, zinc, vitamin C, probiotic
- Allergien
- Levemir, rocephin, vancomycin, levofloxin, tetanus, versed-valium-Demerol in combo form (can take separately) IVP dye, Keflex
- Vorherige Impfungen
- -
- Staat
- NH
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 28.02.2022
- Impfdatum
- 07.01.2022
- Beginn
- 10.01.2022
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
Asthenia
Brain stem infarction
Dysstasia
Facial paralysis
Symptomtext
She was transferred to the hospital on 1/10/2022 with weakness, facial drop, inability to stand. Dx of Pontine Stroke. Returned to the facility 1/11/22 at baseline from Medical Center at baseline.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Facial paralysis
- Hospital-Tage
- 1,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- CHRONIC OBSTRUCTIVE PULMONARY DISEASE, UNSPECIFIED TYPE 2 DIABETES MELLITUS WITHOUT COMPLICATIONS MAJOR DEPRESSIVE DISORDER, RECURRENT, MILD ESSENTIAL (PRIMARY) HYPERTENSION PERSONAL HISTORY OF COVID-19 10/27/2021
- Andere Medikamente
- -
- Allergien
- Bumetanide, Metformin, Shell Fish
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 28.02.2022
- Impfdatum
- 02.01.2022
- Beginn
- 04.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blindness unilateral
Fear
Impaired work ability
Ophthalmological examination abnormal
Retinal artery occlusion
Blindness
Thrombosis
Retinal haemorrhage
Retinal oedema
Visual impairment
Symptomtext
Patient called the pharmacy on 2/28/2022 to report adverse event that she experienced a few days after receiving 2nd covid shot. Patient began to experience vision loss leading to a visit to Eye Associates. Patient states she formed blood clot in back of her eye.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Thrombosis
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none mentioned to provider
- Vorgeschichte
- none mentioned to provider
- Andere Medikamente
- None was mentioned by the patient
- Allergien
- no allergies known
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 28.02.2022
- Impfdatum
- 02.01.2022
- Beginn
- 04.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blindness unilateral
Fear
Impaired work ability
Ophthalmological examination abnormal
Retinal artery occlusion
Blindness
Thrombosis
Retinal haemorrhage
Retinal oedema
Visual impairment
Symptomtext
Patient called the pharmacy on 2/28/2022 to report adverse event that she experienced a few days after receiving 2nd covid shot. Patient began to experience vision loss leading to a visit to Eye Associates. Patient states she formed blood clot in back of her eye.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Thrombosis
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none mentioned to provider
- Vorgeschichte
- none mentioned to provider
- Andere Medikamente
- None was mentioned by the patient
- Allergien
- no allergies known
- Vorherige Impfungen
- -
- Staat
- ME
- Alter
- 22,0
- Geschlecht
- M
- Eingang
- 19.02.2022
- Impfdatum
- 08.02.2022
- Beginn
- 17.02.2022
- Tage bis Beginn
- 9,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood culture negative
CSF culture negative
CSF glucose normal
CSF lymphocyte count increased
CSF protein normal
Condition aggravated
Echocardiogram normal
Electroencephalogram abnormal
Endotracheal intubation
Headache
Laboratory test
Lumbar puncture abnormal
Magnetic resonance imaging head abnormal
Seizure
Toxicologic test abnormal
Urine analysis normal
Symptomtext
Presented 2/17 with ongoing seizures for >60 minutes. Received ativan and midazolam in the ER. Loaded with Keppra. Continued to seize. Intubated. Started on propofol but still having seizures. Loaded with fosphenytoin and started on midazolam infusion. Remains intubated and sedated. Sedation is being weaned and seizures are now controlled on Keppra 1500mg BID, fosphenytoin 100mg TID, and lamotrigine. Patient had been compliant with lamotrigine and not missed any doses. He had been complaining of severe headache after his COVID booster prior to presentation. His last seizure was 2 years prior to presentation.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- 3,0
- Labordaten
- MRI brain 2/17 showed known mesial temporal sclerosis, no new lesions, no inflammation, no stroke, no enhancement. Lumbar puncture 2/18 with normal protein and glucose, mild lymphocytic pleocytosis, negative culture. Other studies pending. Continuous EEG with seizures controlled on referenced medications. Urinalysis negative. Urine toxicology THC positive. Echo normal. Blood cultures negative.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- mesial temporal sclerosis with epilepsy
- Andere Medikamente
- lamotrigine
- Allergien
- no known allergies
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 12.02.2022
- Impfdatum
- 11.02.2022
- Beginn
- 11.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Fatigue
Feeling abnormal
Headache
Heart rate increased
Pain
Syncope
Symptomtext
Extremely faint, headache, body ache, shivering, fatigue, accelerated heartbeat, loopy
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- history of alpha gal
- Andere Medikamente
- Zoloft, birth control, trazodone
- Allergien
- -
- Vorherige Impfungen
- gardasil vaccine caused alpha gal approx 2013
- Staat
- FL
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 09.02.2022
- Impfdatum
- 21.12.2021
- Beginn
- 26.01.2022
- Tage bis Beginn
- 36,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute left ventricular failure
Anticoagulant therapy
Atrial fibrillation
Atrial pressure increased
Blood thyroid stimulating hormone normal
Borrelia test negative
Cardiac failure congestive
Cardiac stress test abnormal
Catheterisation cardiac abnormal
Chest X-ray abnormal
Chest discomfort
Chest pain
Computerised tomogram thorax normal
Confusional state
Dyspnoea
Echocardiogram abnormal
Ejection fraction decreased
Electrocardiogram abnormal
Symptomtext
She came to the ER with complaints of chest pain and palpitations that developed while she was having a stress test. EKG showed AFib with RVR and she was sent to the ER 1/26/22. She had this pain intermittently on and off for the last several days with associated orthopnea and shortness of breath. Orthopnea and shortness of breath worse during the night. Chest pain described as heaviness. Without any attenuating or accentuating factors. In the ER-patient received it could told medications for the AFib and was put on heparin drip. Also noted to have elevated troponin. For the concern of pulmonary embolism-CT PA was ordered-pending. COVID-19 vaccination status-received vaccination including booster.Admitted to hospital for acute systolic heart failure of unclear etiology, atrial fibrillation, elevated troponin, elevated proBNP, pleural effusion. Cardiology consulted 1/26/22: 75/F with new onset afib/CMY presents with increased shortness of breath, Continue on heparin drip, Plan for cath in accordance with early invasive approach, May need cardioversion as some component possibly tachycardia induced,Continue on diuresis. Echocardiogram showed EF 20-25%, moderate MR, moderately dilated left atrium and right atrium, mild-to-moderate TR, mild pulmonary hypertension, large pleural effusion. Cath was done 1/27/22: Impression: No significant coronary artery disease, Severely elevated left sided pressures. Acute systolic heart failure - unclear etiology, ProBNP > 11000. ? Vaccine related - received Moderna booster vaccination 1 week ?prior to hospitalization, negative respiratory panel, negative COVID-19 and influenza, negative RSV, pending lyme serology. Intermittently confused. D/C Summary Note: Hospital Course This is a pleasant 75-year-old female with a past medical history of hypertension, hyperlipidemia, dementia, osteoarthritis, nicotine use, daily alcohol use, chronic GERD, fully vaccinated against COVID-19 including a 3rd booster (Moderna), who presented the emergency department with complaints of chest pain and palpitations during her outpatient stress test. Apparently, 8 days after administration of her most recent booster, patient began developing shortness of breath and symptoms of congestive heart failure. In the ER, EKG positive for atrial fibrillation with rapid ventricular response with heart rate of 107. Troponin trended 691, 516, 563, 486. BNP 10000. Echocardiogram showed an ejection fraction of 20% with an RVSP of 38 with a large left pleural effusion. Chest x-ray positive for evidence of congestive heart failure. CT of the pulmonary arteries negative for PE. Bilateral lower extremity ultrasound negative for DVT. Patient met sirs criteria with heart rate of 110, respiratory rate 26. Hemoglobin 16.5. D-dimer 1.94. TSH 3.89 with a free T4 of 1.31. Respiratory viral panel negative. Lyme serology negative. Regarding her chest pain, present on admission. At this point, likely secondary to vaccine induced (Moderna) myocarditis versus viral myocarditis. Patient did have elevated troponins on admission. These were noted to down trend. Patient was taken for cardiac catheterization on 01/27/2022 which was negative for significant obstructive coronary artery disease and did note severely elevated left-sided pressures. Continue with aspirin and statin. Cardiology evaluation done. Follow-up with cardiology in the clinic. Follow-up with PCP as well. Patient discharged home with LifeVest on 2/3/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myocarditis
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Hypertension, HLD, dementia, osteoarthritis, nicotine dependence, alcohol use, GERD
- Andere Medikamente
- -
- Allergien
- Sulfa drugs
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 20.01.2022
- Impfdatum
- 10.01.2022
- Beginn
- 10.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Chest pain
Dizziness
Seizure
Symptomtext
A few hours after receiving vaccine, patient reported she had a seizure. She went to the emergency room. Her family members gave her aspirin 325mg and it helped. She experienced chest pain and dizziness. No history of seizures.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- N/A.
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 12.01.2022
- Impfdatum
- 11.01.2022
- Beginn
- 11.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Disease prodromal stage
Seizure
Symptomtext
Approximately twenty minutes after administering the vaccine the patient experienced symptoms consistent with her prodrome. The prodromal and ictal phases each lasted less than 5 minutes.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- Unknown
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Complete history unknown. Patient was recently diagnosed with epilepsy and is currently being treated with prescripiton medications.
- Andere Medikamente
- Unknown
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 31.12.2021
- Impfdatum
- 30.12.2021
- Beginn
- 31.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Feeling cold
Headache
Hyperhidrosis
Loss of consciousness
Pyrexia
Symptomtext
Fever and chills at 2am that continued until morning, sweating, dizzy, headache, PASSED OUT for a minute
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Thyroid disease
- Andere Medikamente
- Levothyroxine
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 30.12.2021
- Impfdatum
- 29.12.2021
- Beginn
- 29.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Eye movement disorder
Loss of consciousness
Syncope
Unresponsive to stimuli
Symptomtext
Systemic: Dizziness / Lightheadness-Medium, Systemic: Fainting / Unresponsive-Medium, Additional Details: Pt given flu shot and Moderna booster in L arm. She moved chairs so I could provide same thing to her dad: as I was providing his flu shot she said she felt lightheaded; When i finished his shot dad noticed she looked wobbly and her eyes were rolling around. I held her shoulders and asked if her dad could help me lay her down and keep her legs elevated. She lost consciousness briefly but opened her eyes pretty quickly when her mom asked her if she was ok (she replied YES);ems came & assessedher
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 39,0
- Geschlecht
- M
- Eingang
- 29.12.2021
- Impfdatum
- 20.12.2021
- Beginn
- 21.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood thrombin
Chest pain
Electrocardiogram
Fatigue
Loss of consciousness
Mobility decreased
Palpitations
Paraesthesia
Peripheral coldness
Sensation of blood flow
Sleep disorder
Syncope
Symptomtext
Woke up in the middle of the night with stabbing chest pains and a racing heart (no clock didn't know exact time, but put down 2 am on this form as it required a time and that is my best estimate.) I tried to get up and I could feel all the blood drain out of my head and upper reaches of my body and the best I could do was sort of crumple up and collapse downward in stages successfully managing to prevent any major drops that might result in a head injury, and then I passed out. I came too later (not sure exactly how long, again no clock in the room.) I managed to get back in bed, but it was hard and most of my body was painfully asleep and as I fumbled around I could feel lots of cold apparently mostly-stagnant blood run from various extremities back into the warmer more actively circulating part of my body. Exhaustion sent me back to sleep quickly. In the morning I went to the emergency room to check my heart and minus a brief six second sampling EKG and a quick thrombin test they refused to do anything that might actually properly look for things like pericarditis, myocarditis, or other adverse heart inflammation events. As such we will never be able to get the tests to actually know what we need to know.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- May have had COVID at time of vaccine but was not diagnosed with it until testing afterwards.
- Vorgeschichte
- -
- Andere Medikamente
- A few vitamins and supplements: multi + C, D, B, Calcium, Zinc, Flax seed oil
- Allergien
- Clindamycin
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 25.12.2021
- Impfdatum
- 24.12.2021
- Beginn
- 24.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Anaphylactic reaction
Blood pressure decreased
Dizziness
Oxygen saturation decreased
Syncope
Unresponsive to stimuli
Vomiting
Symptomtext
Systemic: Allergic: Anaphylaxis-Mild, Systemic: Dizziness / Lightheadness-Medium, Systemic: Fainting / Unresponsive-Medium, Systemic: drop in BP and O2sat and vomiting-Medium
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Anaphylactic reaction
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 24.12.2021
- Impfdatum
- 21.12.2021
- Beginn
- 21.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Hypertension
Injection site erythema
Injection site pruritus
Pruritus
Syncope
Tachycardia
Unresponsive to stimuli
Symptomtext
Site: Itching at Injection Site-Mild, Site: Redness at Injection Site-Mild, Systemic: Allergic: Itch (specify: facial area, extremeties)-Mild, Systemic: Fainting / Unresponsive-Medium, Systemic: Hypertension-Mild, Systemic: Tachycardia-Mild
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 23.12.2021
- Impfdatum
- 22.12.2021
- Beginn
- 22.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blindness
Dizziness
Fatigue
Lethargy
Pallor
Syncope
Symptomtext
Systemic: Dizziness / Lightheadness-Medium, Systemic: Exhaustion / Lethargy-Medium, Systemic: Fainting / Unresponsive-Severe, Additional Details: Patient lost color in her face and said that she could not see anymore...She was able to communicate and squeeze my hand for a bit before she stopped talking to me. Her friend and I laid her on the ground to prevent fainting and in doing so she ended up passing out. She was non responsive, but breathing. 911 was called. Pulse ox was placed on her finger and breathing checked. She came to in about 30 seconds and we kept her on the floor flat until EMS came. EMS arrived quickly and took over
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 22.12.2021
- Impfdatum
- 20.12.2021
- Beginn
- 21.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Fall
Head injury
Nausea
Pain
Syncope
Vomiting
Symptomtext
Extreme Chills and severe body aches developed while sleeping. Nauseous and fainted and hit head on way to puke. Now on concussion monitoring.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- Birth control, doxycycline, spironolactone
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 22.12.2021
- Impfdatum
- 21.12.2021
- Beginn
- 21.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Confusional state
Dizziness
Eye irritation
Flushing
Hyperhidrosis
Immediate post-injection reaction
Nausea
Syncope
Symptomtext
Chills-Mild, Confusion-Medium, Dizziness / Lightheadedness-Medium, Systemic: Flushed / Sweating-Medium, Systemic: Nausea-Mild, Additional Details: The patient received the booster of Moderna vaccine in the right deltoid, patient stated his right eye bothered him immediately then he fainted for about 20 sec , provider was instantly called patient woke back up and began to sweat and stated he was feeling nauseous. after watching the patient 15 mins he still did not recover to baseline so paramedics were called and patient was checked out but refused to go to the Emergency room and signed an AMA and left the clinic with his mother.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 25,0
- Geschlecht
- M
- Eingang
- 21.12.2021
- Impfdatum
- 20.12.2021
- Beginn
- 20.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Injection site pain
Paraesthesia
Seizure
Symptomtext
Site: Pain at Injection Site-Mild, Systemic: Seizure-Mild, Additional Details: Patient had seizure twice - within 5 minutes- reported some tingling in the arm of vaccine but after 5 minutes was feeling better
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 41,0
- Geschlecht
- M
- Eingang
- 20.12.2021
- Impfdatum
- 18.12.2021
- Beginn
- 20.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arrhythmia
Chest pain
Dizziness
Headache
Heart rate decreased
Heart rate irregular
Pain
Pyrexia
Syncope
Symptomtext
Main Symptom: Arrhythmia (Irregular Heartbeat), led to chest pain, dizziness, fainting, and drop in heart pulse. The day before AE symptoms: low grade fever, headache, body-ache.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- None, not yet.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- No
- Allergien
- No
- Vorherige Impfungen
- Similar but milder symptoms when I received the second dose of Moderna Covid-19 vaccine.
- Staat
- CA
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 15.12.2021
- Impfdatum
- 14.12.2021
- Beginn
- 14.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Flushing
Hyperhidrosis
Seizure
Syncope
Unresponsive to stimuli
Symptomtext
Systemic: Fainting / Unresponsive-Medium, Systemic: Flushed / Sweating-Medium, Systemic: Seizure-Medium, Additional Details: PATIENT SEIZED AFTER COVID VACCINE. RECOVERED AND WAS SEATED THEN SEIZED AGAIN. ABULANCE WAS CALLED AND TOOK PATIENT TO ER
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 18.04.2023
- Impfdatum
- 28.12.2021
- Beginn
- 01.01.2023
- Tage bis Beginn
- 369,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood test
Cardiac function test
Cardiac stress test
Chest discomfort
Electrocardiogram
Electrocardiogram ambulatory
Extrasystoles
Heart rate increased
Palpitations
Scan myocardial perfusion
Symptomtext
Chest pressure with palpitations and rapid heart beats. Skips beats when laying down or standing up suddenly.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- EKG, holter, nuclear heart test., stress test. A full blood work up to include all heart tests. I have had this done at 3 different cardiologist. Last one was March 2023.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Shellfish, iodine
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 06.03.2023
- Impfdatum
- 04.03.2022
- Beginn
- 25.01.2023
- Tage bis Beginn
- 327,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Dyspnoea
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
I had a lot of congestion with a lot of coughing. I had a lot of head and chest congestion which made it hard to breath.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- at home rapid COVID-19 test- 1/25/2023 POSITIVE
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Polimeri fibrosis
- Andere Medikamente
- Ofed; Amlodipine Besylate Vitamin D; Men's multivitamin; Glucosamine
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 02.03.2023
- Impfdatum
- 19.01.2022
- Beginn
- 27.02.2023
- Tage bis Beginn
- 404,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood alkaline phosphatase increased
Blood lactic acid increased
COVID-19
Chronic obstructive pulmonary disease
Condition aggravated
Dyspnoea
Influenza
Obesity
SARS-CoV-2 test positive
Spinal osteoarthritis
Symptomtext
Discharge summary "Patient is a 60-year-old female with a past medical history of oxygen-dependent chronic obstructive pulmonary disease (3-4 L), anxiety, bipolar, chronic pain who presents with shortness of breath. Found to have chronic obstructive pulmonary disease exacerbation secondary to acute COVID infection. Patient was treated with DuoNebs, Decadron, remdesivir. On the day of discharge patient was back on her 3-4 L home oxygen and felt back to her baseline. She was okay with getting a final dose of remdesivir and then discontinuing the course. She will complete a total of 10 days of Decadron at home. No antibiotics were given as I felt the cause of her chronic obstructive pulmonary disease exacerbation was likely the COVID infection. She was given Levaquin in the hospital in case there is a superimposed bacterial component, but did not tolerate it well and due to allergies there are limited other options."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- 2,0
- Labordaten
- COVID PCR positive on 2/27/23
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- COVID-19 2/28/2023 Anxiety and depression Unknown Insomnia (Chronic) Unknown COPD with acute exacerbation Unknown Osteoarthritis (Chronic) Unknown Borderline diabetes Unknown Dyslipidemia (Chronic) Unknown Hypertension (Chronic) Unknown COPD exacerbation (*) 1/1/2020 Acute respiratory insufficiency 1/1/2020 Second hand smoke exposure (Chronic) 1/1/2020 Acute on chronic respiratory failure with hypoxia 1/1/2020 Calculus of kidney 3/3/2020 Umbilical hernia 3/11/2020 Elevated d-dimer 10/20/2021 Tobacco abuse (Chronic) 10/20/2021 Diverticulitis 11/6/2021 Unspecified mood (affective) disorder 11/30/2021 Bipolar disorder (Chronic) 12/20/2021 Stress incontinence of urine (Chronic) 12/20/2021 Goiter 1/13/2022 Influenza A 3/13/2022 Cervical spondylosis 5/13/2022 Class 3 severe obesity with body mass index (BMI) of 40.0 to 44.9 in adult 9/12/2022 Elevated lactic acid level 9/12/2022 Alkaline phosphatase elevation 9/12/2022
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 92,0
- Geschlecht
- F
- Eingang
- 26.01.2023
- Impfdatum
- 20.12.2021
- Beginn
- 19.11.2022
- Tage bis Beginn
- 334,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Atrial fibrillation
COVID-19
Chest pain
Cough
Fatigue
Hypoxia
Myocardial ischaemia
Oxygen saturation decreased
SARS-CoV-2 test positive
Troponin increased
Symptomtext
Patient brought to the ED by EMS on 11/19 for chest pain, fatigue, and dry cough. COVID-19 PCR test done in the ED resulted positive. In the ED, her O2 sats intermittently dropped to 88%, therefore she was given a dose of decadron and placed on O2 NC. In the ED, patient's troponin was found to be elevated, and cardiology was consulted who recommended admission. Ultimately patient admitted 11/19/22 - 11/22/22. Discharge diagnosis included acute hypoxia felt due to COVID-19 infection. Elevated troponin suspected to have been demand ischemia due to Afib RVR and possibly due to COVID-19 infection.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 14.01.2023
- Impfdatum
- 22.12.2021
- Beginn
- 01.02.2022
- Tage bis Beginn
- 41,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Exercise tolerance decreased
Injection site pain
Insomnia
Mobility decreased
Myalgia
Pain
Symptomtext
Pain upon administration Pain beginning 2 weeks after shot and ongoing pain since. Now radiating around to muscle and causing pain when I try to exercise, reach, sleep, lift, etc.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- RA
- Andere Medikamente
- Humira pen Atorvastatin Pregabalin Calcium/Magnesium Niacin Probiotic Vitamin B1 Vitamin C Vitamin D3 CoQ10 Omega 3-6-9
- Allergien
- Avelox Crestor Leflunomide
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 48,0
- Geschlecht
- M
- Eingang
- 19.12.2022
- Impfdatum
- 14.12.2021
- Beginn
- 30.11.2022
- Tage bis Beginn
- 351,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dyspnoea
Feeling abnormal
Gait inability
SARS-CoV-2 test negative
Symptomtext
On Tuesday 11/29 I wasn't feeling good, next day I had shortness of breath, I did a COVID-test at home and came negative. I could not walk to the house; I had another test, and it was negative again. On Thursday I went to work and sent me home, I went to urgent care and had another test came negative, they sent me to ER and ordered a stress test for 12/29 and will see the Cardiologist on January 12th, 2023.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- 29NOV2022 - COVID-19 - Negative; 30NOV2022 - COVID-19 Test - Negative; 01DEC2022 - COVID-19 - Negative
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Asthma; Knee Pain
- Andere Medikamente
- Incruse; Advair; Antolin.
- Allergien
- Wellbutrin ; Benadryl
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 23.11.2022
- Impfdatum
- 07.01.2022
- Beginn
- 21.11.2022
- Tage bis Beginn
- 318,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Alanine aminotransferase increased
Angiogram
Anion gap
Anticoagulant therapy
Arrhythmia
Anxiety
Aspartate aminotransferase increased
Basophil count decreased
Basophil percentage
Blood albumin normal
Blood alkaline phosphatase normal
Basophil count normal
Basophil percentage increased
Blood bilirubin normal
Blood calcium decreased
Blood chloride normal
Blood creatinine normal
Blood glucose normal
Symptomtext
Document Type: History and Physical Document Subject: History & Physical Note Performed By: on November 22, 2022 06:49 Verified By: on November 22, 2022 06:49 Encounter Info: Hospital, Observation, 11/21/22 - * Final Report * Chief Complaint Palpitations History of Present Illness/Subjective This is a 66-year-old man with an extensive past medical history noted fully below, significant for liver transplant earlier this year secondary to HCC/hep C cirrhosis, and recent hospital admission at Hospital for introduction of Epclusa which is known to cause bradycardia, earlier this month the patient began having episodes of SVT and was seen by cardiology during this admission, they wanted him to continue to take flecainide twice daily however the patient states to me that he he doesn't see the reason for having to take a medication when he is not having arrhythmia and chooses to take it only when he is having the arrhythmia however today he did not do this and just came to the emergency room instead. In the ED he was found to have COVID 19, however he is not requiring any supplemental O2. He arrived in SVT with rates in the 170s converted to sinus rhythm with 1 dose of adenosine. Since that he says he has not felt any palpitations and feels much better. We will place him in observation overnight and possibly have cardiology evaluate in the a.m. Review of Systems A complete, 13-system review was performed and was negative except for as noted in the HPI. Physical Exam/Objective Vital Signs (most recent and range for last 24 hours) Temp (CEL) 37.0 (36.1-38) Temp (FAHR) 98.6 (97.0-100.4), BP 138/85 (115-138)/(63-94), HR 58 (55-174), RR 18 (17-22), O2Sat 95 (95-95) Neurologic (most recent and range for last 24 hours) GCS 15(15-15) Patient Weight Current Daily Weight: 72.7 kg 11/21/22 Previous Daily Weight: 72.7 kg 11/21/22 BMI: 26.7 11/21/22 Overweight (BMI 25-29.9) Patient Height Current Height: 165.1 cm 11/21/22 Constitutional: No acute distress, well-nourished Eyes: PERRL, EOMI, normal conjunctiva, no scleral icterus ENMT: Moist oral mucosa Neck: Supple, non-tender, intact range of motion Respiratory: Lungs CTAB, no respiratory distress, no wheezes or rales Cardiovascular: Regular rate and rhythm Gastrointestinal: Soft, non-tender, non-distended, large well-healed surgical incision consistent with liver transplant Musculoskeletal: No joint swelling, no deformity, intact ROM Integumentary: Intact, warm, dry no rashes Neurologic: Alert & Oriented x 3, no cognitive impairment, no focal deficits Psychiatric: Cooperative, appropriate mood and affect Assessment/Plan Place in observation in MedSurg 1. SVT (supraventricular tachycardia) Maintain telemetry, repeat troponin in a.m. initial trop is negative Monitor and replete electrolytes as needed Consider cardiology evaluation Resume home meds as appropriate 2. COVID-19 Given patient is not requiring supplemental O2 will provide supportive care, no role for steroids or remdesivir at this time 3. Liver transplant status 4. Immunocompromised patient Noted continue home medications and monitor LFTs 5. Chronic hepatitis C Noted. Continue home medications monitor for bradycardia secondary to Epclusa 6. Primary hypertension Noted. Continue home medications 7. DVT prophylaxis Noted. SCDs and Lovenox Orders: enoxaparin, 40 mg, Subcutaneous, Injection, Q24H, Routine, 11/21/22 21:00:00 2000 mg Sodium, 20 gm Saturated Fat Diet Assign To Auto Diff Call Blood Glucose Call Diastolic Blood Pressure Call Heart Rate Call Mental Status Changes Call O2 Saturation Call Respiratory Distress Call Respiratory Rate Call Systolic Blood Pressure Call Temperature Call Urine Output CBC w/Differential Comp Metabolic Panel Fall Precautions Initiate IV Care Protocols As Appropriate Initiate Mobility Protocol Initiate Skin and Wound Care Protocol Intake + Output Strict Level of Care Magnesium SerPl QN Medical Service OT Evaluation and Treatment Phosphorus SerPl QN PT Evaluation and Treatment Resp Evaluation or Assessment Resuscitation Status Sequential Compression Device Single Oxygen Saturation Telemetry Class III 24hr Recommendation Troponin-I High Sensitivity Vital Signs Weight Weight Code Status Resuscitation Status - Ordered -- 11/21/22 20:58:00 , Full Code Chronic Problem List Anemia Anxiety Chronic hepatitis C Coronary artery disease HCC (hepatocellular carcinoma) Immunosuppression due to drug therapy Impingement syndrome of right shoulder Liver transplanted Primary hypertension Supraventricular tachycardia Procedure/Surgical History ?Complete resection of colon ?gall bladder ?liver cancer ?Liver Transplant ?Sebaceous cyst removal Surgical History Internal 07/24/2022 Liver Transplant 02/25/2022 Angiogram 06/03/2021 Angiogram 05/06/2021 Angiogram 03/30/2021 Colonscpy Diagnostic/Screen 03/26/2021 EGD Diagnostic 03/20/2021 EGD Diagnostic Medications Home Medications (8) Active Epclusa 400 mg-100 mg oral tablet 1 Tablet, Orally, Daily flecainide 50 mg oral tablet 50 mg = 1 Tablet, Orally, Q12H hydroCODONE-acetaminophen 10 mg-325 mg oral tablet 1 Tablet, PRN, Orally, Q6H magnesium oxide 400 mg oral tablet 800 mg = 2 Tablet, Orally, BID methocarbamol 750 mg oral tablet 1,500 mg = 2 Tablet, PRN, Orally, TID multivitamin Therapeutic oral tablet 1 Tablet, Orally, Daily mycophenolic acid 360 mg oral delayed release tablet 360 mg = 1 Tablet, Orally, BID tacrolimus 1 mg oral capsule 2 mg = 2 Capsule, Orally, BID, Z 94.4 Active Scheduled Inpatient Medications enoxaparin, Injection, 40 mg, Subcutaneous, Q24H, Start: 11/21/22 21:00:00 One-Time Medications Given 11/21/22 00:00:00 TO 11/22/22 06:48:50 adenosine, Injection, 6 mg, IV Push, ONCE, (1 DOSE 11/21/22 15:38:00) metoPROLOL (metoPROLOL succinate), Tab, Extended Rel, 25 mg, Orally, ONCE, (1 DOSE 11/21/22 16:09:00) Sodium Chloride 0.9% (Sodium Chloride 0.9% - ED Bolus), Infusion, 1,000 mL, IVPB, ONCE, (1 DOSE 11/21/22 15:50:00) PRN Medications (0600 - 0559) from 11/21 - 11/22 None Reported Allergies Bee Stings (SOB) No Known Medication Allergies Social History Alcohol Denies Electronic Cigarette/Vaping E-Cigarette Use Never. Substance Abuse Denies Tobacco Tobacco Use: Former smoker, quit more than 30 days ago. Family History Dementia: Mother. Diabetes mellitus: Father. Heart attack: Father. Lab Results All Labs Last 24 hours (No Micro or Pathology) Hematology: WBC: 3.5 k/cumm Low (11/22/22 04:00:00) RBC: 4.36 million/cumm (11/22/22 04:00:00) Hgb: 12.6 GM/dL Low (11/22/22 04:00:00) Hct: 38.1 % Low (11/22/22 04:00:00) MCV: 87 fL (11/22/22 04:00:00) MCH: 28.8 pg (11/22/22 04:00:00) MCHC: 33 GM/dL (11/22/22 04:00:00) RDW: 14.2 % (11/22/22 04:00:00) Platelet: 88 k/cumm Low (11/22/22 04:00:00) MPV: 10.6 fL (11/22/22 04:00:00) Neutrophils %: 64 % (11/22/22 04:00:00) Lymphocytes %: 15 % (11/22/22 04:00:00) Monocytes %: 18 % (11/22/22 04:00:00) Eosinophils %: 2 % (11/22/22 04:00:00) Basophils %: 1 % (11/22/22 04:00:00) Absolute Neutrophil: 2.2 k/cumm (11/22/22 04:00:00) Absolute Lymphocyte: 0.5 k/cumm Low (11/22/22 04:00:00) Absolute Monocyte: 0.6 k/cumm (11/22/22 04:00:00) Absolute Eosinophil: 0.1 k/cumm (11/22/22 04:00:00) Absolute Basophil: 0 k/cumm (11/22/22 04:00:00) Chemistry: Sodium SerPl QN: 135 mmol/L (11/22/22 04:00:00) Potassium SerPl QN: 4.5 mmol/L (11/22/22 04:00:00) Chloride SerPl QN: 103 mmol/L (11/22/22 04:00:00) Carbon Dioxide SerPl QN: 25 mmol/L (11/22/22 04:00:00) Anion Gap: 7 mmol/L (11/22/22 04:00:00) BUN SerPl QN: 20 mg/dL (11/22/22 04:00:00) Creatinine SerPl QN: 1.09 mg/dL (11/22/22 04:00:00) Estimated GFR (CKD-EPI, no race): 75 mL/min/1.73m2 (11/22/22 04:00:00) Estimated CRCL (CG): 62 mL/min (11/22/22 04:00:00) Glucose SerPl QN: 76 mg/dL (11/22/22 04:00:00) Calcium Total SerPl QN: 8.8 mg/dL (11/22/22 04:00:00) Phosphorus SerPl QN: 5 mg/dL High (11/22/22 04:00:00) Alkaline Phos SerPl QN: 105 Units/L (11/22/22 04:00:00) ALT SerPl QN: 70 Units/L High (11/22/22 04:00:00) AST SerPl QN: 71 Units/L High (11/22/22 04:00:00) Bilirubin Total SerPl QN: 0.5 mg/dL (11/22/22 04:00:00) Total Protein SerPl QN: 5.8 GM/dL Low (11/22/22 04:00:00) Albumin SerPl QN: 3.6 GM/dL (11/22/22 04:00:00) Magnesium SerPl QN: 1.9 mg/dL (11/22/22 04:00:00) Troponin-I High Sensitivity: 18 ng/L (11/21/22 16:00:00) BNP Pl QN: 70 pg/mL (11/21/22 16:00:00) Coagulation: PT: 12.1 seconds (11/21/22 16:00:00) INR: 1.06 (11/21/22 16:00:00) All Other Labs: COVID 19 Specimen Source: Nasopharyngeal (11/21/22 15:44:00) Coronavirus SARS-CoV2 Rapid: Detected Abnormal (11/21/22 15:44:00) Micro - Last 7 days Rapid Influenza Method: PCR - Liat (11/21/22 15:44:00) Rapid Influenza A PCR: Not Detected (11/21/22 15:44:00) Rapid Influenza B PCR: Not Detected (11/21/22 15:44:00) Diagnostics Radiology Results - Last 24 hours Across Visits 11/21/2022 16:23 - XR Chest PA or AP IMPRESSION:1. No acute findings in the chest.Thank you for consulting our team of subspecialty radiologists. Healthcare providers wishing to discussthis case further can contact the Cardiothoracic Reading Room. For after-hours or emergency department cases, pleasecall. Signature Line Electronically Signed on 11/22/22 06:49 ________________________________________________________
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arrhythmia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 23.11.2022
- Impfdatum
- 07.01.2022
- Beginn
- 21.11.2022
- Tage bis Beginn
- 318,0
- Dosis
- 3
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Alanine aminotransferase increased
Angiogram
Anion gap
Anticoagulant therapy
Arrhythmia
Anxiety
Aspartate aminotransferase increased
Basophil count decreased
Basophil percentage
Blood albumin normal
Blood alkaline phosphatase normal
Basophil count normal
Basophil percentage increased
Blood bilirubin normal
Blood calcium decreased
Blood chloride normal
Blood creatinine normal
Blood glucose normal
Symptomtext
Document Type: History and Physical Document Subject: History & Physical Note Performed By: on November 22, 2022 06:49 Verified By: on November 22, 2022 06:49 Encounter Info: Hospital, Observation, 11/21/22 - * Final Report * Chief Complaint Palpitations History of Present Illness/Subjective This is a 66-year-old man with an extensive past medical history noted fully below, significant for liver transplant earlier this year secondary to HCC/hep C cirrhosis, and recent hospital admission at Hospital for introduction of Epclusa which is known to cause bradycardia, earlier this month the patient began having episodes of SVT and was seen by cardiology during this admission, they wanted him to continue to take flecainide twice daily however the patient states to me that he he doesn't see the reason for having to take a medication when he is not having arrhythmia and chooses to take it only when he is having the arrhythmia however today he did not do this and just came to the emergency room instead. In the ED he was found to have COVID 19, however he is not requiring any supplemental O2. He arrived in SVT with rates in the 170s converted to sinus rhythm with 1 dose of adenosine. Since that he says he has not felt any palpitations and feels much better. We will place him in observation overnight and possibly have cardiology evaluate in the a.m. Review of Systems A complete, 13-system review was performed and was negative except for as noted in the HPI. Physical Exam/Objective Vital Signs (most recent and range for last 24 hours) Temp (CEL) 37.0 (36.1-38) Temp (FAHR) 98.6 (97.0-100.4), BP 138/85 (115-138)/(63-94), HR 58 (55-174), RR 18 (17-22), O2Sat 95 (95-95) Neurologic (most recent and range for last 24 hours) GCS 15(15-15) Patient Weight Current Daily Weight: 72.7 kg 11/21/22 Previous Daily Weight: 72.7 kg 11/21/22 BMI: 26.7 11/21/22 Overweight (BMI 25-29.9) Patient Height Current Height: 165.1 cm 11/21/22 Constitutional: No acute distress, well-nourished Eyes: PERRL, EOMI, normal conjunctiva, no scleral icterus ENMT: Moist oral mucosa Neck: Supple, non-tender, intact range of motion Respiratory: Lungs CTAB, no respiratory distress, no wheezes or rales Cardiovascular: Regular rate and rhythm Gastrointestinal: Soft, non-tender, non-distended, large well-healed surgical incision consistent with liver transplant Musculoskeletal: No joint swelling, no deformity, intact ROM Integumentary: Intact, warm, dry no rashes Neurologic: Alert & Oriented x 3, no cognitive impairment, no focal deficits Psychiatric: Cooperative, appropriate mood and affect Assessment/Plan Place in observation in MedSurg 1. SVT (supraventricular tachycardia) Maintain telemetry, repeat troponin in a.m. initial trop is negative Monitor and replete electrolytes as needed Consider cardiology evaluation Resume home meds as appropriate 2. COVID-19 Given patient is not requiring supplemental O2 will provide supportive care, no role for steroids or remdesivir at this time 3. Liver transplant status 4. Immunocompromised patient Noted continue home medications and monitor LFTs 5. Chronic hepatitis C Noted. Continue home medications monitor for bradycardia secondary to Epclusa 6. Primary hypertension Noted. Continue home medications 7. DVT prophylaxis Noted. SCDs and Lovenox Orders: enoxaparin, 40 mg, Subcutaneous, Injection, Q24H, Routine, 11/21/22 21:00:00 2000 mg Sodium, 20 gm Saturated Fat Diet Assign To Auto Diff Call Blood Glucose Call Diastolic Blood Pressure Call Heart Rate Call Mental Status Changes Call O2 Saturation Call Respiratory Distress Call Respiratory Rate Call Systolic Blood Pressure Call Temperature Call Urine Output CBC w/Differential Comp Metabolic Panel Fall Precautions Initiate IV Care Protocols As Appropriate Initiate Mobility Protocol Initiate Skin and Wound Care Protocol Intake + Output Strict Level of Care Magnesium SerPl QN Medical Service OT Evaluation and Treatment Phosphorus SerPl QN PT Evaluation and Treatment Resp Evaluation or Assessment Resuscitation Status Sequential Compression Device Single Oxygen Saturation Telemetry Class III 24hr Recommendation Troponin-I High Sensitivity Vital Signs Weight Weight Code Status Resuscitation Status - Ordered -- 11/21/22 20:58:00 , Full Code Chronic Problem List Anemia Anxiety Chronic hepatitis C Coronary artery disease HCC (hepatocellular carcinoma) Immunosuppression due to drug therapy Impingement syndrome of right shoulder Liver transplanted Primary hypertension Supraventricular tachycardia Procedure/Surgical History ?Complete resection of colon ?gall bladder ?liver cancer ?Liver Transplant ?Sebaceous cyst removal Surgical History Internal 07/24/2022 Liver Transplant 02/25/2022 Angiogram 06/03/2021 Angiogram 05/06/2021 Angiogram 03/30/2021 Colonscpy Diagnostic/Screen 03/26/2021 EGD Diagnostic 03/20/2021 EGD Diagnostic Medications Home Medications (8) Active Epclusa 400 mg-100 mg oral tablet 1 Tablet, Orally, Daily flecainide 50 mg oral tablet 50 mg = 1 Tablet, Orally, Q12H hydroCODONE-acetaminophen 10 mg-325 mg oral tablet 1 Tablet, PRN, Orally, Q6H magnesium oxide 400 mg oral tablet 800 mg = 2 Tablet, Orally, BID methocarbamol 750 mg oral tablet 1,500 mg = 2 Tablet, PRN, Orally, TID multivitamin Therapeutic oral tablet 1 Tablet, Orally, Daily mycophenolic acid 360 mg oral delayed release tablet 360 mg = 1 Tablet, Orally, BID tacrolimus 1 mg oral capsule 2 mg = 2 Capsule, Orally, BID, Z 94.4 Active Scheduled Inpatient Medications enoxaparin, Injection, 40 mg, Subcutaneous, Q24H, Start: 11/21/22 21:00:00 One-Time Medications Given 11/21/22 00:00:00 TO 11/22/22 06:48:50 adenosine, Injection, 6 mg, IV Push, ONCE, (1 DOSE 11/21/22 15:38:00) metoPROLOL (metoPROLOL succinate), Tab, Extended Rel, 25 mg, Orally, ONCE, (1 DOSE 11/21/22 16:09:00) Sodium Chloride 0.9% (Sodium Chloride 0.9% - ED Bolus), Infusion, 1,000 mL, IVPB, ONCE, (1 DOSE 11/21/22 15:50:00) PRN Medications (0600 - 0559) from 11/21 - 11/22 None Reported Allergies Bee Stings (SOB) No Known Medication Allergies Social History Alcohol Denies Electronic Cigarette/Vaping E-Cigarette Use Never. Substance Abuse Denies Tobacco Tobacco Use: Former smoker, quit more than 30 days ago. Family History Dementia: Mother. Diabetes mellitus: Father. Heart attack: Father. Lab Results All Labs Last 24 hours (No Micro or Pathology) Hematology: WBC: 3.5 k/cumm Low (11/22/22 04:00:00) RBC: 4.36 million/cumm (11/22/22 04:00:00) Hgb: 12.6 GM/dL Low (11/22/22 04:00:00) Hct: 38.1 % Low (11/22/22 04:00:00) MCV: 87 fL (11/22/22 04:00:00) MCH: 28.8 pg (11/22/22 04:00:00) MCHC: 33 GM/dL (11/22/22 04:00:00) RDW: 14.2 % (11/22/22 04:00:00) Platelet: 88 k/cumm Low (11/22/22 04:00:00) MPV: 10.6 fL (11/22/22 04:00:00) Neutrophils %: 64 % (11/22/22 04:00:00) Lymphocytes %: 15 % (11/22/22 04:00:00) Monocytes %: 18 % (11/22/22 04:00:00) Eosinophils %: 2 % (11/22/22 04:00:00) Basophils %: 1 % (11/22/22 04:00:00) Absolute Neutrophil: 2.2 k/cumm (11/22/22 04:00:00) Absolute Lymphocyte: 0.5 k/cumm Low (11/22/22 04:00:00) Absolute Monocyte: 0.6 k/cumm (11/22/22 04:00:00) Absolute Eosinophil: 0.1 k/cumm (11/22/22 04:00:00) Absolute Basophil: 0 k/cumm (11/22/22 04:00:00) Chemistry: Sodium SerPl QN: 135 mmol/L (11/22/22 04:00:00) Potassium SerPl QN: 4.5 mmol/L (11/22/22 04:00:00) Chloride SerPl QN: 103 mmol/L (11/22/22 04:00:00) Carbon Dioxide SerPl QN: 25 mmol/L (11/22/22 04:00:00) Anion Gap: 7 mmol/L (11/22/22 04:00:00) BUN SerPl QN: 20 mg/dL (11/22/22 04:00:00) Creatinine SerPl QN: 1.09 mg/dL (11/22/22 04:00:00) Estimated GFR (CKD-EPI, no race): 75 mL/min/1.73m2 (11/22/22 04:00:00) Estimated CRCL (CG): 62 mL/min (11/22/22 04:00:00) Glucose SerPl QN: 76 mg/dL (11/22/22 04:00:00) Calcium Total SerPl QN: 8.8 mg/dL (11/22/22 04:00:00) Phosphorus SerPl QN: 5 mg/dL High (11/22/22 04:00:00) Alkaline Phos SerPl QN: 105 Units/L (11/22/22 04:00:00) ALT SerPl QN: 70 Units/L High (11/22/22 04:00:00) AST SerPl QN: 71 Units/L High (11/22/22 04:00:00) Bilirubin Total SerPl QN: 0.5 mg/dL (11/22/22 04:00:00) Total Protein SerPl QN: 5.8 GM/dL Low (11/22/22 04:00:00) Albumin SerPl QN: 3.6 GM/dL (11/22/22 04:00:00) Magnesium SerPl QN: 1.9 mg/dL (11/22/22 04:00:00) Troponin-I High Sensitivity: 18 ng/L (11/21/22 16:00:00) BNP Pl QN: 70 pg/mL (11/21/22 16:00:00) Coagulation: PT: 12.1 seconds (11/21/22 16:00:00) INR: 1.06 (11/21/22 16:00:00) All Other Labs: COVID 19 Specimen Source: Nasopharyngeal (11/21/22 15:44:00) Coronavirus SARS-CoV2 Rapid: Detected Abnormal (11/21/22 15:44:00) Micro - Last 7 days Rapid Influenza Method: PCR - Liat (11/21/22 15:44:00) Rapid Influenza A PCR: Not Detected (11/21/22 15:44:00) Rapid Influenza B PCR: Not Detected (11/21/22 15:44:00) Diagnostics Radiology Results - Last 24 hours Across Visits 11/21/2022 16:23 - XR Chest PA or AP IMPRESSION:1. No acute findings in the chest.Thank you for consulting our team of subspecialty radiologists. Healthcare providers wishing to discussthis case further can contact the Cardiothoracic Reading Room. For after-hours or emergency department cases, pleasecall. Signature Line Electronically Signed on 11/22/22 06:49 ________________________________________________________
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arrhythmia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 07.11.2022
- Impfdatum
- 17.12.2021
- Beginn
- 06.11.2022
- Tage bis Beginn
- 324,0
- Dosis
- 2
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Dyspnoea
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough COVID infection. Symptom of shortness of breath. Unsure of onset of symptoms. Reported positive test from nursing home around 10/31/2022, but unsure of exact timeline. Positive test collected 11/06/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Positive SARS-CoV-2 -COVID-19 collected 11/06/2022
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Essential hypertension, history of thyroid cancer, chronic obstructive pulmonary disease, peripheral artery disease, chronic kidney disease
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 04.11.2022
- Impfdatum
- 27.01.2022
- Beginn
- 26.10.2022
- Tage bis Beginn
- 272,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Asthma
COVID-19
Chest X-ray normal
Chest pain
Chills
Condition aggravated
Dyspnoea
Hyperhidrosis
Pain
Pleuritic pain
Pyrexia
SARS-CoV-2 test positive
Wheezing
Symptomtext
COVID+ 10/26/22. Vaccination status - Moderna x3 BRIEF OVERVIEW: Admission Date: 10/26/2022 Discharge Date: 10/29/2022 Active Hospital Problems Diagnosis Date Noted POA ? Dyspnea 10/27/2022 Unknown ? Acute asthma exacerbation 12/28/2020 Yes ? COVID-19 DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Dyspnea Acute exacerbation of mild persistent extrinsic asthma COVID-19 Acute asthma exacerbation HOSPITAL COURSE: The patient is a 44 y.o. male with PMH of asthma who presented to the ED due to shortness of breath for 2 days. He complains of accompanying fever, chills, sweats. Also recalls body aches. Also recalls wheezing and pleuritic chest pain left-sided. Self-medicated with NyQuil, DayQuil, vitamins, airborne. He also continued to use a his to inhalers. Despite this, remained short of breath. Presented to the emergency department, found to be wheezing. Chest x-ray negative. COVID-19 positive. Breathing treatments and steroids given. He was admitted for further medical management. He received IV remdesivir for COVID 19 and prednisone for asthma exacerbation. He received supportive care. He should follow up with his PCP as an outpatient. He was discharged home in stable condition on 10/29/2022. BP 135/94 | Pulse 95 | Temp 36.6 ?C (Oral) | Resp 18 | Ht 1.829 m | Wt 129.3 kg | SpO2 95% | BMI 38.65 kg/m? Physical Exam Constitutional: General: He is not in acute distress. Appearance: He is obese. HENT: Head: Normocephalic. Eyes: General: No scleral icterus. Conjunctiva/sclera: Conjunctivae normal. Cardiovascular: Rate and Rhythm: Normal rate and regular rhythm. Pulmonary: Effort: Pulmonary effort is normal. No respiratory distress. Breath sounds: No wheezing. Abdominal: General: Bowel sounds are normal. There is no distension. Palpations: Abdomen is soft. Tenderness: There is no abdominal tenderness. There is no guarding or rebound. Musculoskeletal: Right lower leg: No edema. Left lower leg: No edema. Skin: General: Skin is warm and dry. Neurological: Mental Status: He is alert.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Asthma ? Bronchitis ? Lumbar disc herniation 08/12/2015 ? Obesity ? OSA on CPAP
- Andere Medikamente
- Multivitamins-Ca-Iron-Minerals Tab Take by mouth albuterol (PROVENTIL) 2.5 mg /3 mL (0.083 %) nebulizer solution ipratropium-albuterol (DUO-NEB) 0.5 mg-3 mg(2.5 mg base)/3 mL nebulizer solution Inhale 3 mL through mouth 4 times dail
- Allergien
- Sulfa Drugs
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 77,0
- Geschlecht
- M
- Eingang
- 28.10.2022
- Impfdatum
- 14.04.2021
- Beginn
- 12.10.2022
- Tage bis Beginn
- 546,0
- Dosis
- 3
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
COVID-19
Dyspnoea
Mechanical ventilation
Rales
SARS-CoV-2 test positive
Wean from ventilator
Wheezing
Symptomtext
Pt to ED 10/12 for shortness of breath. PT COVID+ 10/12, maintained on Zosyn and vancomycin. 10/13 pt has been weaned off the ventilator, on supplemental oxygen. 10/14 Vital signs stable, pt A&Ox4. 10/15 Pt states shortness of breath has improved, crackles still present in bilateral lower lobes with slight expiratory wheeze in upper lobes. 10/18 pt respiratory status has been improving. 10/20 pt discharged.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- 9,0
- Labordaten
- see above
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Acute respiratory failure with hypoxia Acute respiratory failure Acute respiratory failure with hypoxemia Chronic hepatitis C without hepatic coma DM (diabetes mellitus), type 2, uncontrolled Diabetes Cardiomyopathy Chronic systolic congestive heart failure SOB (shortness of breath) Dyspnea on exertion Respiratory distress History of respiratory distress Mixed hyperlipidemia Essential hypertension Presence of heart assist device Tobacco use Nonrheumatic mitral valve regurgitation Chronic midline low back pain without sciatica Rhabdomyolysis RBBB Bradycardia Coronary artery disease involving native coronary artery of native heart without angina pectoris Syncope Stroke determined by clinical assessment Ischemic cardiomyopathy CHF (congestive heart failure) PAF (paroxysmal atrial fibrillation) S/P angioplasty with stent
- Andere Medikamente
- acetaminophen (TYLENOL) 325 MG PO Tab albuterol (PROVENTIL, VENTOLIN, PROAIR) HFA 108 (90 Base) MCG/ACT INHAL Aero Soln apixaban (Eliquis) 5 MG PO Tab aspirin 81 MG PO Chew Tab atorvastatin (LIPITOR) 40 MG PO Tab carvedilol (COREG) 12.5 MG
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 14.09.2022
- Impfdatum
- 16.12.2021
- Beginn
- 01.01.2022
- Tage bis Beginn
- 16,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anxiety
Dyspnoea
Tremor
Weight decreased
Symptomtext
Lost 25 pounds, tremors, shortness of breath, and anxiety
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Neurologist, gastroenterologist, pulmonologist and PCP
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Allopurinol, Amlodipine, Atenolol, Chlorthalidone, Ezetimide, Chromium Picolinate, CoQ10
- Allergien
- -
- Vorherige Impfungen
- Covid 19 vaccination, Moderna
- Staat
- -
- Alter
- 81,0
- Geschlecht
- M
- Eingang
- 01.09.2022
- Impfdatum
- 18.12.2021
- Beginn
- 29.08.2022
- Tage bis Beginn
- 254,0
- Dosis
- 3
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Cough
Dyspnoea
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 18.07.2022
- Impfdatum
- 23.12.2021
- Beginn
- 09.07.2022
- Tage bis Beginn
- 198,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
COVID-19 pneumonia
Hypertension
Nausea
Renal function test normal
SARS-CoV-2 test positive
Vomiting
Symptomtext
Discharge Provider: (name) Primary Care Provider: MD Admission Date: 7/9/2022 Discharge Date: Jul 12, 2022 PRESENTING PROBLEM: COVID-19 HOSPITAL COURSE: Patient is a 79 y/o woman with PMH significant for diastolic congestive heart failure, hypertension, CKD stage 4, coronary artery disease with PCI presented to emergency department with nausea and vomiting. On presentation to emergency department her blood pressure was very high 211/96 other vital signs were unremarkable. She was tested positive for COVID-19 pneumonia Patient is admitted to hospitalist service for COVID-19 infection. Is on admission patient was started on fluids. As patient was able to tolerate diet without any symptoms IV fluids were discontinued. She did not require steroids or remdesivir given clinical stability. As BP was high we increase Hydralazine to 50 mg TID ( was on 50 mh BID). BP is improved. Renal functions are stable. In stable condition patient is discharged home.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19 pneumonia
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- CAD (coronary artery disease) Hyperlipidemia, unspecified GERD (gastroesophageal reflux disease) Essential hypertension, benign Diastolic dysfunction Aortic stenosis GAD (generalized anxiety disorder) Gout Nonexudative senile macular degeneration of retina Sleep apnea Insomnia Senile nuclear cataract, bilateral Osteopenia CKD (chronic kidney disease) stage 4, GFR 15-29 ml/min (HCC) Myopia of both eyes Chronic bilateral low back pain with right-sided sciatica Chronic neck pain Dry eyes, bilateral Chronic diastolic congestive heart failure (HCC) Uses walker Moderate depressive disorder (HCC) chronic, currently active, not psychotic COVID-19
- Andere Medikamente
- allopurinol (ZYLOPRIM) 100 MG tablet amLODIPine (NORVASC) 5 MG tablet apoaequorin (PREVAGEN) 10 MG CAPS capsule calcitonin, salmon, (MIACALCIN) 200 UNIT/ACT nasal spray calcitriol (ROCALTROL) 0.25 MCG capsule cycloSPORINE (RESTASIS) 0.
- Allergien
- Bactrim [Sulfa Drugs]Other Contrast Dye [Ivp Dye, Iodine Containing]Other NsaidsOther
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 27.06.2022
- Impfdatum
- 19.12.2021
- Beginn
- 07.06.2022
- Tage bis Beginn
- 170,0
- Dosis
- 1
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Dyspnoea
Fatigue
Malaise
Pyrexia
SARS-CoV-2 test positive
Symptomtext
Fever, Malaise, Fatigue, Shortness of breath. Symptoms started on 06/07/2022, Received positive test on 06/08/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Mild Asthma
- Andere Medikamente
- Bupropion, Silodosin
- Allergien
- Sulfa
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 13.06.2022
- Impfdatum
- 26.12.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Arthritis
Chondrocalcinosis
Condition aggravated
Influenza like illness
Joint swelling
Laboratory test abnormal
Magnetic resonance imaging abnormal
Ultrasound scan abnormal
X-ray abnormal
Symptomtext
Severe onset 12/30/2021 severe pain and swelling in the left knee, have been previously diagnosed with CPPD but have not had any issues with CPPD flare in 6 years. Saw orthopedic and received cortizone shot and predispose pills which helped temporarily. But as soon as the pills wore off the pain came back. Also tried Euflexxa injections. Shots didn't help and pain expanded to right shoulder then left shoulder. Orthopedic doctor felt something else is going & referred to Rhuematologist. I saw Rheumatologist doctor in February 2021 he ran extensive tests & xrays and diagnosed with inflamatory Arthritis. Started treatments with prednisone and methotraxate. Now taking 25mg of Methotraxate Injection and Prednisone 5mg- and still in daily pain. To add to reaction from booster-I felt flu like symptoms about 24 hours after shot.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- Labs 2/16/22, 4/6/22, 5/11/22 Radiology-1/19/22 MRI, 1/27/22 Sonogram, 2/19/22 xrays
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High Blood Pressure, Glaucoma, Asthma, CPPD, Gastritis, Acid Reflux
- Andere Medikamente
- Quinapril, Carvedilol, Ecotrin, Omeprazole, Fenofibrate, Finastride, Combigan, Lumigan, Albuterol, Advair, Montelukast, Claritin
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 19,0
- Geschlecht
- M
- Eingang
- 07.06.2022
- Impfdatum
- 20.12.2021
- Beginn
- 14.01.2022
- Tage bis Beginn
- 25,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Anti-thyroid antibody increased
Autoimmune thyroiditis
Condition aggravated
Constipation
Depression
Fatigue
Gastrointestinal pain
Goitre
Heart rate decreased
Irritable bowel syndrome
Lethargy
Neck mass
Neck pain
Oropharyngeal pain
Peripheral coldness
Pharyngeal swelling
Suicide attempt
Ultrasound thyroid abnormal
Symptomtext
About three and a half weeks after my Moderna booster shot, my throat swelled up and I began to perceive a permanent lump and pain in my neck. Not debilitating, but very unpleasant. After a couple of months (around mid-March), I developed debilitating constipation and IBS and started feeling a slowed heart rate and chronic coldness in my extremities, so I decided to get it checked out medically. It turns out I have autoimmune thyroiditis, diagnosed as Hashimoto's. It has since gotten worse, and now I am fatigued, lethargic, and depressed (attempted suicide on April 23, 2022) on top of everything else. Throat is very painful, digestive system is very painful. I don't know if the damage will permanent (I read some case reports suggesting it might go away in a couple months), but it has not improved at all.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- April 22, 2022: Thyroglobulin and TPO antibody panels. Results: massively elevated above normal ranges. April 22, 2022: Thyroid ultrasound. Results: abnormally enlarged thyroid and with more blood vessels then normal.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None at the time. After developing thyroiditis, developed chronic chest pain, constipation, and IBS.
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 04.06.2022
- Impfdatum
- 24.02.2021
- Beginn
- 01.03.2021
- Tage bis Beginn
- 5,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Autoimmune disorder
C-reactive protein increased
Dyspnoea exertional
Immunoglobulins increased
Lymphoedema
Oedema
Pain
Symptomtext
Activation/exacerbation of autoimmune process resulting in exertional dyspnea, generalized subcutaneous edema/lymphedema and pain. Sxs were minimal after the first dose, barely noticeable, but were progressively more prominent with the subsequent 2 doses.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea exertional
- Hospital-Tage
- -
- Labordaten
- Elevated hsCRP and immunoglobulin levels in February 2022
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypothyroidism
- Andere Medikamente
- L-Thyroxine, Vitamin D, Viamin B12
- Allergien
- Penicillin (Anaphyaxis)
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 10.05.2022
- Impfdatum
- 27.01.2022
- Beginn
- 29.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Migraine
Symptomtext
Migraines began approx 48 hours after receiving Moderna booster vaccine. Since receiving this booster I have been having migraines 1-2 times weekly. Prior to receiving booster I would get a migraine once every couple years.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Positive for Covid 19 on 1/6/2022
- Vorgeschichte
- Now
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 12.04.2022
- Impfdatum
- 08.04.2022
- Beginn
- 09.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Condition aggravated
Dyspnoea
Hyperhidrosis
Pyrexia
Urticaria
Symptomtext
Patient felt sweaty and feverish, but did not take temperature. She broke out in hives. She has been having hives off and on since receiving the first covid immunizations. She also had shortness of breath for about 24 hours
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Lupus
- Andere Medikamente
- Levothyroxine 112 mcg daily Potassium Chloride 10 mEq 2 tablets three times a day Propranolol 10mg 2 tablets twice a day Omeprazole 40mg daily
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 07.04.2022
- Impfdatum
- 27.12.2021
- Beginn
- 28.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Asthenia
Breast pain
Chest pain
Symptomtext
The Moderna booster (lot# 070H21A) rcvd on 12/27/21 gave left arm, elbow, shoulder pain & weakness. Still today there is mostly elbow pain & weakness. Some left breast/chest pain initially.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- No treatment sought
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- BC pill/Resveratrol/Magnesium
- Allergien
- None known
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 31.03.2022
- Impfdatum
- 08.03.2021
- Beginn
- 05.04.2021
- Tage bis Beginn
- 28,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest discomfort
Chest pain
Dyspnoea
Tachycardia
Throat tightness
Symptomtext
Chest pain, chest tightness, tachycardia, shortness of breath, throat tightness.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Microgestin
- Allergien
- Sulfa, Vicodin
- Vorherige Impfungen
- Pain, sickness, tiredness, malaise; Flu shot; 47 years old; 2020
- Staat
- AZ
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 22.03.2022
- Impfdatum
- 25.02.2021
- Beginn
- 13.01.2022
- Tage bis Beginn
- 322,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Asymptomatic COVID-19
Atrial fibrillation
Blood glucose
Chest X-ray
Coagulation test
Dyspnoea exertional
Full blood count
Metabolic function test
SARS-CoV-2 test positive
Tachycardia
Troponin
Symptomtext
Patient is a 55yo female with a history of atrial fibrillation, heart failure with preserved ER (Echo at FMC 11/2020 EF 50-55%), DM, HTN who presented to the ED with DOE for about 1 week. Found to be in Afib with RVR and admitted to for further management. Also found to be COVID positive. Course detailed by problem below. Covid (+) Did not require oxygen and was asymptomatic. Incidental finding on admission. Given rapid resolution of dyspnea, anticipate this was secondary to tachyarrhythmia with possible component of heart failure contributing. Advised 10 day isolation (test positive 1/13/22).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea exertional
- Hospital-Tage
- 3,0
- Labordaten
- POCT glucose CBC, CMP, Troponin Chest xray Coag Covid
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Heart Failure A.Fib HTN DM
- Andere Medikamente
- Rivaroxaban Metoprolol Metformin Furosemide
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 51,0
- Geschlecht
- M
- Eingang
- 10.03.2022
- Impfdatum
- 01.03.2022
- Beginn
- 01.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Condition aggravated
Fatigue
Feeling abnormal
Headache
Injection site pain
Lymph node pain
Lymphadenopathy
Nausea
Pain
Pain in extremity
Pyrexia
Tinnitus
Symptomtext
Evening of shot, arm sore, slight nausea and headache. Woke up next morning arm hurt so bad could not lift above head, slight nausea, fatigue, headache and joint pain, slight fever. Multiple doses of alternating Tylenol and Motrin needed to combat. Also previous tinnitus heightened after booster shot. Woke up second day with sore/swollen lymph nodes left armpit. Fatigue/headache/joint pain subsided day three. Day four arm pain pretty much gone, still sore to touch at injection site. Day seven lymph nodes almost back to normal. Initial Covid doses were Pfizer administered on 3/26/21 and 4/23/21 by Hospital. No adverse reactions whatsoever to those, arm barely sore at injection site. After this Moderna booster, it is the worst I?ve felt in two years since I think I had Covid in March 2020 (limited testing then).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High cholesterol (managed)
- Andere Medikamente
- Atorvistatin, multivitamin, glucosamine/chondroitin
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 02.03.2022
- Impfdatum
- 21.12.2021
- Beginn
- 21.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypoaesthesia
Limb mass
Mobility decreased
Muscular weakness
Neuralgia
Pain in extremity
Symptomtext
Received booster shot on 12-21-21. Noticed pain in left arm immediately but figured it was normal since experienced that with first 2 shots as well. A couple of days after, noticed a lump on my arm which went away after about 1 month. Pain in arm did not disappear. Also experienced muscle weakness, nerve pain and loss of motion. Took ibuprofen OTC daily for 2 months. Since I am in between insurances, I didn't want to go see a MD. Friend referred me to acupunture. Started that middle of Feb weekly. Helped get rid of nerve pain but now pain is more of a numbing pain. Very painful at night and constant. Finally went to urgent care on 3-2-2022 where they referred me to sports medicine MD.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hep B carrier
- Andere Medikamente
- Estradiol Vaginal Cream
- Allergien
- Lidocaine
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 48,0
- Geschlecht
- M
- Eingang
- 28.02.2022
- Impfdatum
- 04.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Hypoaesthesia
Injection site pain
Pain
Paraesthesia
Symptomtext
Patient reports persistent pain at the site of injection and later, development of generalized right shoulder pain, worse with raising his right arm. Also notes numbness and tingling of the 5th, 4th and 3rd digit in the weeks following the vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- None identified
- Vorgeschichte
- None identified
- Andere Medikamente
- No known medications
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 26.02.2022
- Impfdatum
- 21.01.2022
- Beginn
- 21.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Adverse reaction
Arthralgia
Balance disorder
Dizziness
Headache
Injected limb mobility decreased
Pain in extremity
Pyrexia
Vomiting
Symptomtext
I received my booster shot on 1/20. I immediately started having an adverse reaction. Within hours I couldn't move my arm what so ever and I could feel debilitating pain radiating up the left side of my neck and down my finger tips. I couldn't move my neck to the left of my left wrist at all. I then began having nerve pain in my feet, severe headaches and dizziness, high fevers, excruciating joint pain, and vomiting. For approximately one week after I felt off balance and dizzy.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injected limb mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- 1/25/2021
- Staat
- OH
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 15.02.2022
- Impfdatum
- 21.12.2021
- Beginn
- 07.01.2022
- Tage bis Beginn
- 17,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Angiogram pulmonary normal
Blood electrolytes normal
Blood magnesium normal
Blood potassium decreased
Blood thyroid stimulating hormone normal
C-reactive protein normal
COVID-19
Cardiac murmur
Chest X-ray normal
Dehydration
Dizziness
Dyspnoea
Echocardiogram normal
Ejection fraction normal
Electrocardiogram ST segment abnormal
Exposure during pregnancy
Haematocrit normal
Haemoglobin normal
Symptomtext
1/7/22 Pt is a 31 year old female who tested positive for SARS-CoV-2 on 12/24. She returned to work on 1/7 after finishing isolation. She presented to the ED with lightheadedness, SOB and tachycardia. She works in a hospital and was reommended to present to the ED. Per D/C from the same day Murmur and recent Covid-19 dx who presented to Observation 1/7/2022 with chief complaint of heart palpitations and shortness of breath. Labs and imaging on admit: K 3.3, Mg 1.8, Trop x2 and NT-pro BNP negatibe, WBC 11.17. EKG sinus tachycardia non-specific ST abnormalities. CXR non-acute. BLEVD and CTPA negative. 1. Palpitations with Dyspnea: patient recently with Covid-19 as discussed, returned to work today and reportedly became lightheaded, short of breath and palpitations with HR 160's on fitbit after climbing a flight of stairs. No current chest pain but patient is concerned about myocarditis. Trop x2 and NT-pro BNP negative. EKG sinus tachycardia non-specific ST abnormalities. CXR non-acute. BLEVD and CTPA negative. Suspect in setting of dehydration and recent Covid, s/p 2L IVF bolus with improved rate 90's on tele in ED. OSV neg, repeat EKG with sinus tachycardia and TTE on 1/7/21 with EF: 69%, and essentially normal study CRP/TSH wnl. Tele.EP Evaluated and recommended no further inpt work up and no need for meds currently especially in light of pregnancy. If persistent, can consider outpt holter monitoring. Monitor. 2. Covid-19 Infection: Vaccinated and just got booster. Recent Dx 12/29/21. Patient endorsed congestion and stable on RA. CXR non-acute. BLEVD and CTPA negative. Currently on RA and out of isolation. 3. Hypokalemia: 3.3 on admit, Mg wnl. Monitor and replete PRN. Improved 1/8/22. Will give small dose to get K>4, mag level wnl. 4. Leukocytosis: 11 on admit. No infectious symptoms. Suspect reactive. Trended. 5. Pregnancy: +test on 1/6/21 at home.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dehydration
- Hospital-Tage
- -
- Labordaten
- 1/7 K+ 3.3, all other electrolytes including Mg were normal, Normal TSH WBC 11.7, Hgb 13.1, Hct 40, Plt 262 normal echocardiogram negative LE venous dopplers nl CXR and CTA pulm arteries
- Aktuelle Erkrankungen
- early pregnancy LMP 11/30/21
- Vorgeschichte
- -
- Andere Medikamente
- prenatal vitamin
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 11.02.2022
- Impfdatum
- 11.02.2022
- Beginn
- 11.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Flushing
Hot flush
Hypertension
Paraesthesia
Pruritus
Tachycardia
Symptomtext
Tingling in feet, Tachycardia, hypertension, itching, hot flashes, flushing
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypertension
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- hypothyroid
- Andere Medikamente
- synthroid
- Allergien
- IV contrast
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 11.02.2022
- Impfdatum
- 02.01.2022
- Beginn
- 03.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest pain
Tachycardia
Symptomtext
Severe chest pain for 5 hours on January 3rd starting at 1 am. Tachycardia for a day and a half.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Concerta
- Allergien
- PCN
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 09.02.2022
- Impfdatum
- 27.12.2021
- Beginn
- 27.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest pain
Dermatitis
Inflammation
Influenza like illness
Lymphadenopathy
Pruritus
Rash
Rash erythematous
Rash papular
Rash pruritic
Skin warm
Swelling
Swelling face
Symptomtext
Flu-like symptoms started approximately 6 hours after injection and lasted for approximately 24 hours afterward. Localized lymph node swelling began once flu-like symptoms subsided and lasted approximately one week. On 01/05/2022, base of scalp developed an itchy rash, swelling and bumps and occurred sporadically. Hot, itchy, inflamed skin then developed on forearms and back of hand, include deep itch in each palm. Face swelling about the ears, eyes, and lips. Torso, buttocks, and groin developed widespread inflammation, rash, raised red and white linear bumps. All come and go to varying extremes throughout the day, and are especially pronounced after a shower. Periodic chest pans are felt, top and central sternum. All symptoms continue to this day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Flu-like symptoms started approximately 6 hours after injection and lasted for approximately 24 hours afterward. Localized lymph node swelling began once flu-like symptoms subsided and lasted approximately one week. On 01/05/2022, base of scalp developed an itchy rash, swelling and bumps and occurred sporadically. Hot, itchy, inflamed skin then developed on forearms and back of hand, include deep itch in each palm. Face swelling about the ears, eyes, and lips. Torso, buttocks, and groin developed widespread inflammation, rash, raised red and white linear bumps. All come and go to varying extremes throughout the day, and are especially pronounced after a shower. Periodic chest pans are felt, top and central sternum. All symptoms continue to this day.
- Andere Medikamente
- None. However, a flu-shot was received during same visit.
- Allergien
- NKA
- Vorherige Impfungen
- General flu-like symptoms after each primary COVID vaccination (Moderna, 02/11/2021 & 03/10/2021). 510and 52 YO at respective d
- Staat
- MD
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 03.02.2022
- Impfdatum
- 28.01.2022
- Beginn
- 28.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Supraventricular tachycardia
Symptomtext
SVT occurred after shot
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Supraventricular tachycardia
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Mitral valve prolapse
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 38,0
- Geschlecht
- M
- Eingang
- 28.01.2022
- Impfdatum
- 24.01.2022
- Beginn
- 26.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Back pain
Chills
Condition aggravated
Headache
Pain
Pain in extremity
Swelling
Symptomtext
Patient was given his booster vaccination 1/24/2022. He had a headache and chills on 1/24/2022 & 1/25/2022 which subsided. On 1/26, he began to have pain in his right shoulder and lower back. The pain in his lower back went away at approximately 5pm that evening, but the shoulder pain continued. He took 7 Advil that day with little relief. On Thursday, 1/27/2022, he woke up with increased pain. The site of injection did not hurt and there was no redness or swelling noted. The pain is located in his rotator cuff area. No recent injury to his arm. Pain is 2/10 with no movement and up to 9/10 with movement. The pain radiates to his elbow. There is no numbness or tingling the the hand/fingers and he is able to move hand/fingers as normal. He took 2 extra strength Tylenol on Thursday 1/27 with some relief. 1/28/2022, pain has not resolved and he notes some swelling to pectoral region of right chest. He will be contacting his physician this morning. He had a similar experience of pain to arm following both previous COVID-19 vaccinations, but this has been more severe than the previous ones.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- Possible COVID-19 early January, but was cleared by physician to get vaccination on 1/24/2021
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 48,0
- Geschlecht
- M
- Eingang
- 27.01.2022
- Impfdatum
- 19.01.2022
- Beginn
- 22.01.2022
- Tage bis Beginn
- 3,0
- Dosis
- N/A
- Route/Site
- SC / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Amnesia
Arthralgia
Asthenia
Balance disorder
Cough
Disturbance in attention
Dyspnoea
Gait disturbance
Headache
Hemiparesis
Hypoaesthesia
Interchange of vaccine products
Muscular weakness
Pain
Symptomtext
On day one I had a fever 100, 100.3 lasted for 36 hours, treated with Tylenol and cold therapy. On the 3rd day of vaccination, I had whole body sever pain, joint pain, and weakness. Headaches, shortness of breath treated with inhaler and breathing exercise. Still have body and joint pain not tolerable, cough and shortness of breath. Starting January 25th, I had slight numbness and weakness on my lower extremity mainly on the Right side radiating to my back and hands. Couple of incidents tripping and loosing my balance due to the weakness and dragging my right leg lasting for a second or so. I still have the weakness and pain, intermittent lightning headache and continuous pain on my joints. Loss of focus and short memory while having the sudden headache.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- I am referred by employee Health to follow up with my PCP, waiting for appointment or telehealth. Taking OTC pain medications and inhalers meanwhile.
- Aktuelle Erkrankungen
- Heart Palpitations, headaches since COVID infection a year ago and J&J vaccination in August of 2021.
- Vorgeschichte
- None except Migraine headaches.
- Andere Medikamente
- None
- Allergien
- Penicillin, Ammonia, Compazine, Flue Shot and TDAP shots.
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 48,0
- Geschlecht
- M
- Eingang
- 25.01.2022
- Impfdatum
- 14.01.2022
- Beginn
- 21.01.2022
- Tage bis Beginn
- 7,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cardiac disorder
Chest discomfort
Electrocardiogram
Fatigue
Palpitations
Symptomtext
Approximately one week after vaccine (21 January 2022), experienced unusual fatigue and irregularities with chest/possible heart issues. I was experiencing intermittent chest discomfort before this (beginning on/or about 3 Jan 2022), so unsure if the issues experienced beginning 21 January are a continuation of existing conditions or possibly related to booster vaccine (Moderna). Cardiac-type events increased over the weekend and into this week that could be classified similar to heart palpitations (stops/skipping beats).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- Visited primary care on Monday, 24 January 2022 for check up. EKG and baseline vitals (heart/lung via stethoscope) indicated no adverse conditions with heart functionality. Referred to cardiologist for stress test (10 Feb 2022) and possible other testing.
- Aktuelle Erkrankungen
- Intermittent chest discomfort that started ~3 Jan 2022.
- Vorgeschichte
- Elevated blood pressure
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 20.01.2022
- Impfdatum
- 20.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Dysstasia
Paraesthesia
Sitting disability
Symptomtext
patient called about 2 hours after vaccination complaining about muscle tingle on both arms, dizziness and difficulty sitting and standing. advised patient to call md/report to the emergency department.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- Impfdatum
- 14.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Dysphagia
Hyperhidrosis
Myalgia
Pallor
Paraesthesia oral
Symptomtext
Patient given Moderna booster, had received Pfizer 1st and 2nd doase anaphylaxis history warranted 30 min observation period 2;20p, c/o tingling in lips, able to swallow comfortable\u 2;27p c/o difficulty swallowing, pale , diaphoretic. 0.3 ml epinephrine administered. Left deltoid Symptoms resolved within minutes, patient returned to her desk
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia oral
- Hospital-Tage
- -
- Labordaten
- patient sought medical care in ER on 1/15/22. states her right side "locked up" severe muscle pain, given IM injection in buttocks and discharged home
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- Type 1 Diabetes
- Andere Medikamente
- Insulin for Type 1 Diabetes
- Allergien
- history of anaphylactic reaction to penicillin in 20's
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- Impfdatum
- 29.12.2021
- Beginn
- 29.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Injected limb mobility decreased
Injection site bruising
Injection site erythema
Injection site pain
Injection site swelling
Joint injury
Limb injury
Muscle haemorrhage
Skin discolouration
Symptomtext
Site: Bruising at Injection Site-Severe, Site: Pain at Injection Site-Severe, Site: Redness at Injection Site-Severe, Site: Swelling at Injection Site-Severe, Systemic: blood dispersed throughout and down arm; unable to use shoulder-Severe, Systemic: Joint Pain-Severe, Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)-, Additional Details: brusing at injection site; blood can be seen progressively moving down his arm (under the skin), arm is bright purple.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injected limb mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 18.01.2022
- Impfdatum
- 21.12.2021
- Beginn
- 27.12.2021
- Tage bis Beginn
- 6,0
- Dosis
- 3
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
Cough
Deafness bilateral
Dyspnoea
Malaise
Nausea
Palpitations
Rhinorrhoea
SARS-CoV-2 test positive
Tremor
Vertigo
Symptomtext
Patient went to bed and woke up with shortness of breath, shaking, heart racing, nausea and vertigo. Went to the bathroom. It lasted for about an hour. Drove to the emergency department in the early morning hours on 12/28/2021. It felt like her heart was beating out of her chest. This was the first time she had to seek emergency treatment at an ER. The ER told her to follow-up with an ENT for the vertigo. She had the first two Moderna injections on 5/6/2021, batch/lot# 003C21A and 2nd Moderna injection on 6/3/2021 batch/lot# 049C21A. She had knee pain on the front and back left of one knee starting about 30 days before this adverse event. She said she felt ill after those injections for about 5 hours. She felt continuing nausea and vertigo first week of January 2022. On January 6, 2022, she started to feel ill with COVID-19 symptoms (coughing and runny nose). This was 16 days after the booster shot. On January 10, 2022 she tested positive for COVID-19 (20 days after her Moderna booster shot).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Visit to ENT on 12/30/2021 for vertigo and nausea and to check ears. She said it was more than likely from the Moderna booster shot. ENT checked her ears and found some hearing loss in both ears. Told her to rest and to be cautious on airplane travel and any sudden movements. She prescribed prednisone steroid to reduce inflammation; ondansetron for nausea and vomiting and meclizine. She is to follow-up with the ENT.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Birth control pills
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 18.01.2022
- Impfdatum
- 13.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Cardiac stress test
Chest discomfort
Chest pain
Headache
Symptomtext
After receiving Moderna Booster, Pt felt chest pain 4/10 and headache. Per Pt she felt like "something is sitting on her chest". She felt the same type of chest pain after receiving her 1st dose of Moderna, she was sent to ED but was cleared to get her 2nd dose of Moderna vaccines. She was sent to ED after getting her 2nd dose due to chest pain again, they did stress test and was monitored then was sent home. Per Pt, she was cleared by her MD to get her booster vaccine. Pt BP 153/75, HR 107, RR 22 O2 Sat 98% RA T 97.8 F. Pt has Hx of Bypass surgery. Per Dr., send Pt to ED for further Eval and Tx. Called emergency immediately. EMS came @ 3:55pm and transported Pt to ED @ 4:01pm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- HEREDITARY SPHEROCYTOSIS DM 2 CAD (CORONARY ARTERY DISEASE) WO ANGINA DM 2 W HYPERLIPIDEMIA DM 2 W BILAT MILD NONPROLIFERATIVE RETINOPATHY HX OF CABG NEURALGIA NAUSEA ANEMIA IRON DEFICIENCY ANEMIA MYALGIA DUE TO STATIN
- Vorgeschichte
- HEREDITARY SPHEROCYTOSIS DM 2 CAD (CORONARY ARTERY DISEASE) WO ANGINA DM 2 W HYPERLIPIDEMIA DM 2 W BILAT MILD NONPROLIFERATIVE RETINOPATHY HX OF CABG NEURALGIA NAUSEA ANEMIA IRON DEFICIENCY ANEMIA MYALGIA DUE TO STATIN
- Andere Medikamente
- Propranolol (INDERAL) 10 mg Oral Tab traMADoL (ULTRAM) 50 mg Oral Tab Metoprolol Tartrate (LOPRESSOR) 25 mg Oral Tab Promethazine (PHENERGAN) 25 mg Oral Tab Gabapentin (NEURONTIN) 300 mg Oral Cap Glimepiride (AMARYL) 4 mg Oral Tab Empaglifl
- Allergien
- Crestor [Rosuvastatin Calcium] Lipitor [Atorvastatin] Nsaids, Non-selective [Non-steroidal Anti-inflammatory Agents] Penicillins Class Pravastatin Muscle Ache Reglan [Metoclopramide Hydrochloride]
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 14.01.2022
- Impfdatum
- 05.01.2022
- Beginn
- 06.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Condition aggravated
Dizziness
Fatigue
Headache
Impaired work ability
Pain in extremity
Pyrexia
SARS-CoV-2 test negative
Symptomtext
Developed severe headache/fever 36 hours later. Took 1000 mg Acetaminophen, That took care of fever/headache. Stayed home from work exhausted. 3rd day, still excessively fatigued. No energy. Stayed home from work. 4th day still extreme fatigue, no energy. Stayed home from work. 5th day extreme fatigue, no energy. Stayed home not working. 6th day stayed home, still tired, no energy, not working. 7th day went to work. Ran a fever at work, took 400 mg of Acetaminophen, fever was reduced. Stayed at work. 8th day went to work, almost fainted, weak, legs hurt. Tested negative for Covid-19. 9th day woke up dizzy, exhausted. Missed work.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Had mono as a teenager, lingering symptoms of fatigue. Also diagnosed with MS at the age of 34.
- Andere Medikamente
- Cognium Memory, (Silk Protein 100 mg), Folate 1,334 mg, Zinc, 50 mg, Thyroid support, Vitamin B-6 2mg, Vitamin B-12 1000 mcg
- Allergien
- Shrimp, Strawberries
- Vorherige Impfungen
- 68, 4/14/21, Moderna Covid-19.
- Staat
- NY
- Alter
- 37,0
- Geschlecht
- M
- Eingang
- 14.01.2022
- Impfdatum
- 23.12.2021
- Beginn
- 04.01.2022
- Tage bis Beginn
- 12,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Condition aggravated
Urticaria
Symptomtext
Hives on arm. Large skin welts on different parts of the body (back and arm). Sometimes on my rear neck. This also occurred since the second dose of Moderna approximately one month after the second dose. I do not have a history of hives or allergies. I have diabetes but have been on diabetes medication for about two years consistently with no side effects related to skin. My diabetes has been maintained under control. Since the second dose, I have intermittent hives. Since the booster, I have had daily hives after about one week.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- Medical appointment in April when symptoms first started.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Diabetes
- Andere Medikamente
- Metformin, 500mg 2x per day Ozempic, .05 once per week
- Allergien
- None
- Vorherige Impfungen
- 36 years, moderna vaccine March 18, 2021. Skin hives began to occur at least 4x per month in April 2021.
- Staat
- NY
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 13.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 6,0
- Dosis
- 2
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Heart rate increased
Hypertension
Irregular breathing
Symptomtext
I get even worse dizzy spells than before, irregular breathing, fast paced heart beat, and higher blood pressure that is normally controlled by hbp meds that ive been on for over a year
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypertension
- Hospital-Tage
- -
- Labordaten
- I have a cardiologist appointment on march 7th
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Obesity, high blood pressure, high cholesterol
- Andere Medikamente
- Labetelol, nifedipine
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 12.01.2022
- Impfdatum
- 22.12.2021
- Beginn
- 26.12.2021
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
Cough
Dyspnoea
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
Vaccinated with booster dose of Moderna on 12-22-21 Pt started having SOB, cough and chest congestion 12-26-21 12-29-21: presents to ED and tests positive for COVID-19 - symptomatic (note: booster given on 12-22-21, therefore did not have full protection form vaccine when tested positive) in ED pt was given 2L O2, remdesivir and steroids 12-30-2021:discharged home on room air, prednisone 1-6-21: pt returned to ED with worsening cough and SOB CXR showed improvement from 12-29-21 and patient was sent home with albuterol, benzonatate, guaifenesin and incentive spirometry
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- DM, COPD, CHF, HTN, HLD
- Andere Medikamente
- amiodarone, apixaban, aspirin, cetirizine, dapagliflozin propanediol, levothyroxine, metoprolol, rosuvastatin, sitagliptin/metformin
- Allergien
- penicillins
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 38,0
- Geschlecht
- M
- Eingang
- 10.01.2022
- Impfdatum
- 15.12.2021
- Beginn
- 29.12.2021
- Tage bis Beginn
- 14,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Atrial fibrillation
Chest X-ray normal
Electrocardiogram abnormal
Laboratory test normal
Palpitations
Sinus tachycardia
Symptomtext
Heart palpitations. Went to ER, and found to be in atrial fibrillation with RVR. I had to get a calcium-channel blocker to break rhythm to sinus tachycardia. Beta-blocker to convert the sinus tachycardia to normal sinus rhythm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- 12-lead EKG, chest X-ray and labs drawn. Labs normal, X-ray normal and the EKG revealed what I detailed in the prior answer.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Dextroamphetamine, Coffee, Multivitamin, Vitamin-B Complex, Magnesium bisglycinate, Fish oil, N-acetylcysteine
- Allergien
- Strattera
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 10.01.2022
- Impfdatum
- 17.12.2021
- Beginn
- 18.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Burning sensation
Discomfort
Dyspepsia
Heavy menstrual bleeding
Musculoskeletal chest pain
Nausea
Sleep disorder
Symptomtext
The medication that I am on called Latuda does have a side effect of heartburn, but that is why I was taking the Omeprazole to stop the heartburn that the Latuda medication caused. So, the heartburn was controlled and managed, but after getting the vaccine I had severe heart burn. I was struggling to drive when I had drove to the pharmacy to get the medication that my urgent treatment clinic doctor told me to get. I had pain under my ribcages that was just burning. It lasted all day and through the night. It made me stay awake till 1AM because of how uncomfortable it was. I took twice as much of the Famotidine medication than I was supposed to, but it did help relieve the heartburn. The next day it was still uncomfortable but not as bad. Also, 2 weeks later I had a super heavy period and extreme nausea. I still have lingering nausea, but it seems to be getting better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Musculoskeletal chest pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hidradenitis Suppurativa; PCOS; Bipolar Disorder
- Andere Medikamente
- Benztropine 1mg 2xday Spironolactone 25mg 1xday Norethindrone 0.35mg Omeprazole 40mg 1xday
- Allergien
- IV Contrast Dye
- Vorherige Impfungen
- Pfizer Vaccine (1st dose)- I had body aches. (4/9/2021)
- Staat
- FL
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 10.01.2022
- Impfdatum
- 30.12.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Chills
Dizziness
Dyspnoea
Injection site erythema
Injection site swelling
Pain
Pallor
Pyrexia
Symptomtext
swelling, redness at injection site, pain, fever, chills, dizziness, pale, hard to take deep bbreath
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- barratts, arthritis, bipolar, gerd, herpes, migraines, fibromyalgia, osteoarthritis, tmj, ulcerative collitis,
- Andere Medikamente
- clonazapam, cymbalta, depakote, entyvio, lasiks, hyoscamine, omeprazole, pregsatapin,
- Allergien
- cipro, penicillin, sulfa, aspirin, mascrobid, codeine, flagall , latex
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 48,0
- Geschlecht
- M
- Eingang
- 09.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 08.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Body temperature increased
Chills
Decreased appetite
Fatigue
Headache
Hypersomnia
Tremor
Symptomtext
On 1/8, extreme fatigue. Slept most of the day On 1/9, uncontrolled shaking, chills, temp 100.3, loss of appetite, headache
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- COPD, arthritis
- Andere Medikamente
- Ibuprofen, Atorvastatin, Benadryl,
- Allergien
- Ceclor
- Vorherige Impfungen
- 47. 2nd Moderna shot on 2/4/2021. Minor discomfort. Lasted 36 hours
- Staat
- IN
- Alter
- 42,0
- Geschlecht
- M
- Eingang
- 09.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 08.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dyspnoea
Flushing
Heart rate increased
Pain
Pyrexia
Symptomtext
I received the vaccine around 1:00 PM EST on 1/7/2022. Starting around 4:30 PM, I started feeling achy and flushed in my face. I also experienced a consistently increased heart rate. On 1/8/2022, around 4:30 AM, I experienced achiness which was extremely painful. I also had a fever at its highest of 105.0 degrees. My heart rate stayed elevated, along with my shortness of breath. I did take Ibprorin in regular doses, but my fever remained in the 100 range until the early morning of 1/9/2022. At this time, I have no fever but still feel a bit achy.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Clomiphene, Clonazepam, Vitamin D
- Allergien
- None
- Vorherige Impfungen
- Pfizer 2nd Dose Lot #EW0172. Similar to my experience from Moderna. My fever was not as high though.
- Staat
- CA
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 06.01.2022
- Impfdatum
- 30.12.2021
- Beginn
- 03.01.2022
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Back pain
Chills
Dizziness
Headache
Heart rate increased
Hot flush
Interchange of vaccine products
Lethargy
Musculoskeletal pain
Pain
Palpitations
Sleep disorder
Tremor
Symptomtext
Took Moderna booster shot on 12/30/2021. Prior shots were Pfizer on Jan 16, 2021 and Feb 6th, 2021. Same day: Dizzy spell - short term. Mild headache after 3 hours and into evening. Dec 31, 2021 - late morning - another momentary dizzy spell while walking. Lethargy sets in mid-day into evening. Pain in shoulder and down back to butt on left side. This subsides in next 36 hours. Jan 1st, 2022 - 1am PST, a significant chill hits me. Chattering and body shakes. I don ski-type undergarments, knit cap, and socks, and attempt sleep. In a hour I have a heat flash - removing all ski-garments I attempt cool down with cold wet cloths. The cycle continued with less severity the remainder of evening until about 4am. Jan 2, 2022. symptoms are mild - headache and lethargy. Jan 3, 2022 - 2am PST - racing heart that awakened me. I took up some yoga breathing techniques to combat and returned to sleep concerned. 3:30am - racing heart returns and I awake. I take pulse rate w/ is usually 80-90bpm and count 140+bpm. I take a dose of Eliquis (5 mg) which I have for use on long-flight and travel to avoid surface clotting. I walk about the house and use breathing techniques to bring down heart rate which was unsuccessful for an hour. I considered waking my wife to take me to emergency in SF, but resolved to text her instead. At 7am - we assessed my condition and did not seek medical treatment.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- On 12/20/2021 - had squmish cell successfully removed via NOSE from left temple.
- Vorgeschichte
- fat-ish currently. From 1/2006 to 6/2016 was susceptible to DVT's due to aneurysm in vein behind left knee related to a rugby injury two decades prior. Corrected by surgeon.
- Andere Medikamente
- Eliquis, Lamotrigine, Atomoxetine
- Allergien
- hayfever
- Vorherige Impfungen
- 02 6 2021, C19, Pfizer
- Staat
- IL
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 04.01.2022
- Impfdatum
- 29.12.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Heart rate irregular
Palpitations
Symptomtext
Heart palpitations, possibly premature arrhythmia, occurring approximately 6 times per minute. Regularly occurred over the course of approximately 20 hours. Issue first noticed 12/30/2021 at 8pm (the day after receiving the shot), and lasted until 12/31/2021 at 3pm. Symptoms included feeling one irregular heartbeat, repeating approximately 6x/minute. No chest pain, dizziness, shortness of breath. No other known contributing factors present, such as change in activity or ingestion of stimulants (caffeine, pseudoephedrine, etc.)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- Manual pulse check only.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypertension
- Andere Medikamente
- amlodipine 10mg, Vallarta 320mg
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 03.01.2022
- Impfdatum
- 28.12.2021
- Beginn
- 28.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest pain
Injection site erythema
Lymphadenopathy
Symptomtext
Site: Redness at Injection Site-Medium, Systemic: Lymph Node Swelling-Severe, Additional Details: chest pain
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 03.01.2022
- Impfdatum
- 29.12.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Discomfort
Headache
Hypoaesthesia
Nausea
Pain in extremity
Paraesthesia
Vaccination site pain
Symptomtext
It ran all the way down to my hand/ whole arm is hurting/fingers are hurting/left arm is the one that is hurting; My fingertips and my fingers are like tingling; It is very uncomfortable; Her hand is numb; Her wrist is hurting/ since her wrist was hurting so bad, is wondering if that is the joint pain; This time it is unbearably sore; She is also feeling a little nauseous; She is having headache; This spontaneous case was reported by a consumer and describes the occurrence of PAIN IN EXTREMITY (It ran all the way down to my hand/ whole arm is hurting/fingers are hurting/left arm is the one that is hurting), PARAESTHESIA (My fingertips and my fingers are like tingling), DISCOMFORT (It is very uncomfortable), HYPOAESTHESIA (Her hand is numb) and ARTHRALGIA (Her wrist is hurting/ since her wrist was hurting so bad, is wondering if that is the joint pain) in a 46-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 070H21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 29-Dec-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 30-Dec-2021, the patient experienced PAIN IN EXTREMITY (It ran all the way down to my hand/ whole arm is hurting/fingers are hurting/left arm is the one that is hurting), PARAESTHESIA (My fingertips and my fingers are like tingling), DISCOMFORT (It is very uncomfortable), HYPOAESTHESIA (Her hand is numb), ARTHRALGIA (Her wrist is hurting/ since her wrist was hurting so bad, is wondering if that is the joint pain), VACCINATION SITE PAIN (This time it is unbearably sore), NAUSEA (She is also feeling a little nauseous) and HEADACHE (She is having headache). At the time of the report, PAIN IN EXTREMITY (It ran all the way down to my hand/ whole arm is hurting/fingers are hurting/left arm is the one that is hurting), PARAESTHESIA (My fingertips and my fingers are like tingling), DISCOMFORT (It is very uncomfortable), HYPOAESTHESIA (Her hand is numb), ARTHRALGIA (Her wrist is hurting/ since her wrist was hurting so bad, is wondering if that is the joint pain), VACCINATION SITE PAIN (This time it is unbearably sore), NAUSEA (She is also feeling a little nauseous) and HEADACHE (She is having headache) outcome was unknown. No Concomitant medications were reported. No Treatment medications were reported. This case was linked to MOD-2021-435151, MOD-2021-435156 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- DC
- Alter
- 25,0
- Geschlecht
- M
- Eingang
- 01.01.2022
- Impfdatum
- 19.12.2021
- Beginn
- 29.12.2021
- Tage bis Beginn
- 10,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chest discomfort
Dyspnoea
Rash
Urticaria
Symptomtext
Hives and Rashes all over entire body 10 days after Moderna booster. Chest tightness and difficulty breathing.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 30.12.2021
- Impfdatum
- 11.04.2021
- Beginn
- 12.04.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: ja
Erholt: nein
Chest X-ray normal
Dyspnoea
Wheezing
Symptomtext
Shortness of breath and wheezing beginning the day after first dose and still present. The shortness of breath and wheezing was increased with the booster shot.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Chest x-ray 11/17/21 normal
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma
- Andere Medikamente
- Lithium geodon Ativan remeron
- Allergien
- Penicillin flagyl
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 30.12.2021
- Impfdatum
- 29.12.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest pain
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Risperidone; Fluoxetine; Low-ogesterol; Januvia; multi-vitamin
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 39,0
- Geschlecht
- M
- Eingang
- 30.12.2021
- Impfdatum
- 27.12.2021
- Beginn
- 28.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Muscle swelling
Musculoskeletal chest pain
Oedema peripheral
Skin swelling
Symptomtext
Diffuse swelling and tenderness over the left upper chest, axilla, and trapezius area
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Musculoskeletal chest pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 23.12.2021
- Impfdatum
- 23.12.2021
- Beginn
- 23.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chest pain
Dizziness
Moaning
Symptomtext
Client switched over to Moderna as a booster Lot#070H21A. Client stated to vaccinator that she had no reactions to the first two doses. Client received vaccine and walked over to observation area. At approximately 1242 Client was sitting with husband when, he alerted one of the vaccinators that his wife was feeling dizzy. RN was alerted about client. Client was placed in zero gravity chair for further assessment. Client was given water and denied having trouble swallowing. Client had sips of water. Client was AAOX3. Client was in no respiratory dress. No pallor was observed by RN. Client was grabbing her chest and nodded when asked by husband if she was having chest pain. EMS was activated at 1243 by RN. After grabbing her chest for a few seconds Client stated, ?I feel better?. Vitals taken at 1245 Client denies medical conditions or heart problems. Client denies any allergies. Client stated the chest pain was on and off. Client began grabbing her chest again and moaning. At 1248 02 sat 99%. Epi-pen 0.3ml was going to be administered when paramedics arrived and assumed care at 1250. Client had more water before standing up and walking over and laying on to the transport gurney. Client was taken via ambulance to hospital at 1255.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Unknown
- Aktuelle Erkrankungen
- none reported
- Vorgeschichte
- none reported
- Andere Medikamente
- unknown
- Allergien
- nka
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 21.12.2021
- Impfdatum
- 21.12.2021
- Beginn
- 21.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Chest discomfort
Palpitations
Symptomtext
Patient presented to the vaccination site on 12/21/21. Patient received first dose on 4/15/21 and second dose 5/13/21. Patient received booster Moderna dose (LOT#: 070H21A) on 12/21/21 at 1638. The client notified 2 EMTs that she felt her heart racing for about 10 minutes. RN arrived on scene and assessed patient. EMT took patients vital signs. BP: 140/84, HR: 70, RR: 16. Patient stated that she felt pressure in her chest. RN called 911 at 1604. EMS arrived on scene at 1615 and took over. EMS assessed patient. Patient signed AMA form. EMS left vaccination site at 1622. RN educated patient on adverse effects of COVID vaccine and when to seek EMS. RN recommended that patient go see PCP about her symptoms after booster dose. Patient verbalized understanding. Patient left vaccination site at 1630 unassisted with a steady gait with her son and husband.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 32,0
- Geschlecht
- M
- Eingang
- 20.12.2021
- Impfdatum
- 19.12.2021
- Beginn
- 19.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Hypoaesthesia
Paraesthesia
Symptomtext
Systemic: Dizziness / Lightheadness-Mild, Systemic: Tingling (specify: facial area, extemities)-Medium, Additional Details: Immediately after Moderna vaccination, patient reported numbness in his hands and arms. He then began to feel lightheaded. Numbness did not spread. Patient recovered after about 5 minutes and left the store.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 19.12.2021
- Impfdatum
- 18.12.2021
- Beginn
- 18.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Dyspnoea
Flushing
Headache
Hyperhidrosis
Symptomtext
Systemic: Allergic: Difficulty Breathing-Mild, Systemic: Chills-Mild, Systemic: Flushed / Sweating-Mild, Systemic: Headache-Mild, Additional Details: EMS called. Patient declined EMS transport as she felt symptoms improving.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 18.12.2021
- Impfdatum
- 16.12.2021
- Beginn
- 16.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / OT
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain
Asthenia
Chills
Eye swelling
Flushing
Heavy menstrual bleeding
Hyperhidrosis
Injection site pain
Lymphadenopathy
Mouth swelling
Pain
Paraesthesia
Swelling face
Swollen tongue
Symptomtext
Site: Pain at Injection Site-Severe, Systemic: Allergic: Swelling of Face / Eyes / Mouth / Tongue-Severe, Systemic: Abdominal Pain-Severe, Systemic: Body Aches Generalized-Severe, Systemic: Chills-Severe, Systemic: Flushed / Sweating-Severe, Systemic: Lymph Node Swelling-Severe, Systemic: Tingling (specify: facial area, extemities)-Severe, Systemic: Weakness-Severe, Additional Details: severe heavy mensustral bleeding
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 17.12.2021
- Impfdatum
- 16.12.2021
- Beginn
- 16.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cold sweat
Diarrhoea
Fatigue
Feeling of body temperature change
Hyperhidrosis
Nausea
Tremor
Vomiting projectile
Symptomtext
I received my booster of Moderna at 12:30pm. I went to bed at 8:30 because I was very tired. I woke up at 11:30pm and was very nauseous, clammy, hot/cold, sweating, shaky. I then began projectile vomiting. I also began having diarrhea simultaneously. This went on until 1:30am. I was finally able to settle around 2:30am and have not had any vomiting or diarrhea since.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- b12, optiferem, selenium
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 13.02.2023
- Impfdatum
- 10.02.2022
- Beginn
- 15.02.2022
- Tage bis Beginn
- 5,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain upper
Blood test normal
COVID-19
Symptomtext
About five days after receiving the vaccine I started having stomach pains it was persistent and nothing would help it so I knew it was the vaccine that caused my stomach problems. My doctor recommended to a Gastroenterologist. Nothing came of that so my regular medical doctor prescribe CYMBALTA and it got better but then I got COVID-19 and the stomach pains came back.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain upper
- Hospital-Tage
- -
- Labordaten
- Blood profile results normal.
- Aktuelle Erkrankungen
- Sinus infection
- Vorgeschichte
- Atrial Fibrillation; IC; Pacemaker; High Cholesterol; Hypertension
- Andere Medikamente
- DEXILANT; SYNTHROID; famciclovir; losartan; carvedilol; oxybutynin; lovastatin; LINZESS; famotidine; SINGULAIR; XARELTO; CYMBALTA
- Allergien
- Aspirin
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 09.01.2023
- Impfdatum
- 07.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Diarrhoea
Pyrexia
Vomiting
Symptomtext
01/07/2022, I got the vaccine in the morning and by the night, I had vomiting, diarrhea, fever, chills for 2 to 3 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Darifenacin; rosuvastatin; anastrozole; multivitamin women's vitamin; VIACTIV
- Allergien
- CT contrast
- Vorherige Impfungen
- Dose 1, Moderna, 01-27-2021 and dose 2, Moderna, 02-24-21, vomiting, diarrhea, fever, chills for 2 to 3 days
- Staat
- CA
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 30.12.2022
- Impfdatum
- 11.05.2021
- Beginn
- 20.12.2022
- Tage bis Beginn
- 588,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
COVID-19
Malaise
SARS-CoV-2 test positive
Symptomtext
COVID-19 Disease - Test positive 12/19/22 at SNF. mild symptoms. Remdesivir therapy completed. - end isolation 12/31/22 per ID rec
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 28.12.2022
- Impfdatum
- 27.12.2021
- Beginn
- 28.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Cough
Fatigue
Pain in extremity
Pyrexia
Vaccine positive rechallenge
Symptomtext
I experienced soreness in arm, fever, chills, fatigue, and, cough. I was not prescribed any medication for my symptoms. These symptoms persisted for 3 days before they resolved. I am fully recovered with no lingering symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Type II Diabetes
- Andere Medikamente
- Metformin
- Allergien
- N/A
- Vorherige Impfungen
- Moderna dose 1 & 2 experienced same symptoms.
- Staat
- MI
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 22.12.2022
- Impfdatum
- 04.01.2022
- Beginn
- 22.12.2022
- Tage bis Beginn
- 352,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Hyperhidrosis
Symptomtext
CHILLS, SWEATY
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 21.12.2022
- Impfdatum
- 19.12.2021
- Beginn
- 02.01.2022
- Tage bis Beginn
- 14,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Immediate post-injection reaction
Injection site erythema
Injection site induration
Injection site mass
Injection site warmth
Rash
Rash papular
Rash pruritic
Symptomtext
Immediately following vaccination I developed at the injection site a hard mass that was very red and hot to the touch. Mass dissipated over 7-10 days. Early January I began developing rashes all over my body. They were raised, very itchy, and painful at ties. Went to allergist/dermatologist on January 30th and he stated he had several patients present with the same thing following the Moderna booster. Put me on an acid reflux medicine and another medicine I can't recall. Symptoms lasted until mid May when it finally cleared and stayed clear.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- None
- Andere Medikamente
- Ca; mg; vitamin D; probiotic
- Allergien
- Minor food sensitivities
- Vorherige Impfungen
- Got very sick after flu shot in 2000-2001.
- Staat
- CA
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 18.11.2022
- Impfdatum
- 01.12.2021
- Beginn
- 18.11.2022
- Tage bis Beginn
- 352,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chest discomfort
Chills
Pyrexia
Symptomtext
within 24 hours of having the first booster, I experienced general tightness throughout chest area, developed fever and chills - took 1600mg acetaminophin ,,,went to bed and fever went away within 2 hours and I felt better ( I am an NP - didnt feel I was having a heart attack but wont take any more vaccines after this no radiating pain or shortness of breath
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- Did not go see a doctor as I got better and was able to travel next day
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- Levothyroxine .050 mcg
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 22,0
- Geschlecht
- M
- Eingang
- 29.09.2022
- Impfdatum
- 09.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 5,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Mechanical urticaria
Pruritus
Urticaria
Symptomtext
Dermatographic Urticaria: Hives, itching
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mechanical urticaria
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 24.09.2022
- Impfdatum
- 18.12.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Fatigue
Heart rate
Heart rate increased
Inappropriate schedule of product administration
Symptomtext
my heartrate is 175-180 BPM; have minimal energy; Fatigue; inappropriate schedule of vaccine administered; This spontaneous case was reported by a patient and describes the occurrence of FATIGUE (Fatigue), HEART RATE INCREASED (my heartrate is 175-180 BPM), ASTHENIA (have minimal energy) and INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (inappropriate schedule of vaccine administered) in a 22-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 070H21A) for COVID-19 prophylaxis. Co-suspect product included non-company product TOZINAMERAN (PFIZER BIONTECH COVID-19 VACCINE) for an unknown indication. Patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. patient received Estroidal within 2 weeks of vaccination. Patient was not diagnosed with COVID-19. Since the vaccination, the patient was not tested for COVID- 19. Device Date: 09Feb2022. Previously administered products included for Product used for unknown indication: PFIZER BIONTECH COVID-19 VACCINE (Dose Number: 1 Batch/Lot No: er8727 Location of injection: Arm Left) on 31-Mar-2021 and PFIZER BIONTECH COVID-19 VACCINE (Dose Number: 2 Batch/Lot No: ew0172 Location of injection: Arm Left) on 22-Apr-2021. Past adverse reactions to the above products included No adverse event with PFIZER BIONTECH COVID-19 VACCINE and PFIZER BIONTECH COVID-19 VACCINE. Concurrent medical conditions included Allergy NOS. On 18-Dec-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient received first dose of TOZINAMERAN (PFIZER BIONTECH COVID-19 VACCINE) (unknown route) 1 dosage form. On an unknown date, received second dose of TOZINAMERAN (PFIZER BIONTECH COVID-19 VACCINE) (unknown route) dosage was changed to 1 dosage form. On an unknown date, the patient experienced FATIGUE (Fatigue), HEART RATE INCREASED (my heartrate is 175-180 BPM), ASTHENIA (have minimal energy) and INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (inappropriate schedule of vaccine administered). At the time of the report, FATIGUE (Fatigue), HEART RATE INCREASED (my heartrate is 175-180 BPM) and ASTHENIA (have minimal energy) had not resolved and INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (inappropriate schedule of vaccine administered) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, Heart rate: 175-180 BPM. patient was collegiate runner capable to run 4min30sec miles at elevated heartbeats. Since having her shots she can barely run 7 min miles and her heartrate was 175-180 BPM. Patient had fatigued continuously when exercising. She found that she had minimal energy and seem to have lactic acid buildup in arms (very unusual) when trying to run. Her body was not recovering after a workout. She was 23 years old and should recover in same/next day as she had been for past 10-15 years while running track or swimming. She needs to have some testing performed to understand what was happening to her heart. to her recovery. Patient was world class athlete who had been trying to compete on TRiathalon team, with passion and drive, but with setback on stamina and intensity. No treatment details were reported. This case was identified as part of a retrospective clean-up activity where certain emails received in the Moderna mailbox were missed to be booked-in
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Test Name: Heart rate; Result Unstructured Data: 175-180 BPM
- Aktuelle Erkrankungen
- Allergy NOS
- Vorgeschichte
- Comments: Patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. patient received Estroidal within 2 weeks of vaccination. Patient was not diagnosed with COVID-19. Since the vaccination, the patient was not tested for COVID- 19. Device Date: 09Feb2022.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 14.09.2022
- Impfdatum
- 18.12.2021
- Beginn
- 30.08.2022
- Tage bis Beginn
- 255,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Pyrexia
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
COVID breakthrough. Presented to hospital on 8/30 for unrelated reason and tested positive for COVID on 8/30/22. Patient had fever of 100.8 on presentation to the hospital.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- COVID+ PCR on 8/30/22
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- COPD
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 77,0
- Geschlecht
- M
- Eingang
- 07.09.2022
- Impfdatum
- 03.03.2022
- Beginn
- 14.07.2022
- Tage bis Beginn
- 133,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood bilirubin
COVID-19
Cough
Diarrhoea
Glomerular filtration rate
Rhinorrhoea
SARS-CoV-2 test positive
Throat irritation
Symptomtext
I had my 4th vaccination on 03/03/2022. On 07/14/2022 I started to experience loose stool and diarrhea. I have had it for 8 weeks presently. On 07/15/2022 I started to have a runny nose and scratchy cough. I tested COVID-19 and tested positive. I contacted doctors office and prescribed Plaxovid. I am having an ultra sound 09/07/2022 to see if blocked duct causing the diarrhea and bilirubin.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- 07/15/2022 COVID-19 Positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- 2015 Bladder Cancer; Heart issues; Aneurysm; High Calcium in heart; 2018 Prostate Cancer
- Andere Medikamente
- Vitamin D; Flomax; Prozac; Pepcid; Pyridoxal; Toprol; Aspirin; Stool softener
- Allergien
- Nitroglycerin
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 01.08.2022
- Impfdatum
- 07.01.2022
- Beginn
- 30.07.2022
- Tage bis Beginn
- 204,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Chest X-ray normal
Fatigue
Nasal congestion
Oropharyngeal pain
SARS-CoV-2 test positive
Symptomtext
fatigue, nasal congestion, sore throat, tested positive for covid on 7/30/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- SARS-CoV-2 (COVID-19) by Nucleic Acid Amplification, POC detected on 7/30/22 cxr; lungs are clear
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- type 2 diabetes, hypertension, valvular heart disease, thrombocytopenia
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 18.07.2022
- Impfdatum
- 06.04.2022
- Beginn
- 17.06.2022
- Tage bis Beginn
- 72,0
- Dosis
- 4
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Chills
Fatigue
Headache
Pain
Pyrexia
SARS-CoV-2 test positive
Symptomtext
06/17/2022 I began to feel a terrible headache, chills, and a fever, and body aches that continued. I then reached out to my PCP and they provided me with Paxlovid, however the Paxlovid made me extremely nauseous and caused me to vomit frequently. Afterward I was given a anti nausea medication that helped out a lot but I did feel very tired and fatigued afterwards. I am just experiencing a small amount of tiredness however this is primarily it.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- Tested Positive COVID-19: 06/18/2022
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Asthma; Osteoporosis
- Andere Medikamente
- Montelukast; Symbicort; Albuterol; Multivitamin; Vitamin D3; Zinc; Allergy Pill
- Allergien
- Penicillin; Wheat; Corn; Dairy
- Vorherige Impfungen
- Moderna Dose #1 Date:01/12/2021 Lot: 026L20A Moderna Dose #2 Date: 02/11/2021 Lot: 030L20A Moderna Dose #3 Date: 11/04/2021 Lot:
- Staat
- OH
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 30.06.2022
- Impfdatum
- 30.03.2022
- Beginn
- 30.05.2022
- Tage bis Beginn
- 61,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Exposure to SARS-CoV-2
Headache
Malaise
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
My husband was exposed to a co-worker was positive for COVID-19, he developed symptoms. I tested four time and was negative until day 12 then I started getting symptoms. Runny nose, headaches, mild cough for maybe a day and a half. I waited to test again for another day it came back positive, I called to let my doctor know, they scheduled a telehealth visit where advised me to look for certain symptoms that may lead to long COVID-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- Home COVID-19 test.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Autoimmune Disease; dry eye; dry mouth
- Andere Medikamente
- Celecoxib; XIIDRA; progesterone; amitriptyline; sertraline; amlodipine; calcium; vitamin B-12; fluocinonide cream
- Allergien
- Ampicillin
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 27.06.2022
- Impfdatum
- 23.12.2021
- Beginn
- 26.05.2022
- Tage bis Beginn
- 154,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Body temperature fluctuation
COVID-19
Chills
Delivery
Exposure during pregnancy
Exposure to SARS-CoV-2
Malaise
Nasal congestion
Oropharyngeal pain
Pain
Pyrexia
SARS-CoV-2 test positive
Symptomtext
I tested positive in May 26. I got it from my husband. I had sore throat, nasal, congestion and body aches. I had alternating body temperature. I went from fever to chills. I was prescribed Paxlovid and took it for 5 days and I got better quickly. I tested negative a few days later. I got a few symptoms again in June, and I was sick again for two weeks. It was the same symptoms just more severe. It lasted two weeks. When I took the Paxlovid on June 1 and was negative. I believe the rebound happened after the Paxlovid. Delivery of child 01/22- at 6 lbs and 3 oz
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Over Weight
- Andere Medikamente
- Prenatal Vitamins and Baby Aspirin
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 22.06.2022
- Impfdatum
- 19.12.2021
- Beginn
- 29.05.2022
- Tage bis Beginn
- 161,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal pain
COVID-19
Cough
Diarrhoea
Fatigue
Feeling abnormal
Headache
Malaise
Nausea
Oropharyngeal pain
Pain
Pyrexia
SARS-CoV-2 test positive
Symptomtext
I contracted COVID-19 on 05/29/2022 with symptoms of sore throat, fever of 102 that lasted for 3 days, body aches, nausea, headache, fatigue, brain fog, abdominal pain, diarrhea, and cough. I went to the Clinic as was prescribed Paxlovid on 06/03/2022. I was ill for 5 days before my symptoms began to resolve. I became ill after a trip. I am fully recovered now with no lingering symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- -
- Labordaten
- COVID-19 rapid nasal swab home test was positive on 05/31/2022
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- Cardoval, Progesterone, Estrogen, Ambien
- Allergien
- Codeine
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 25.05.2022
- Impfdatum
- 18.02.2022
- Beginn
- 25.02.2022
- Tage bis Beginn
- 7,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood creatine phosphokinase
Lipids normal
Metabolic function test normal
Myalgia
Symptomtext
Intermittent muscle aches, episodes lasting 10-15 minutes, pain is worst 8/10, persisting from time of vaccination to present day (3 months), pain resolves spontaneously w/ deep breathing and light stretching.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myalgia
- Hospital-Tage
- -
- Labordaten
- Checking CK to rule out statin myopathy; CMP and lipids WNL; no other testing or lab results.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Hypertension, hyperlipidemia, acid reflux
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 06.05.2022
- Impfdatum
- 05.01.2022
- Beginn
- 27.04.2022
- Tage bis Beginn
- 112,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Chest discomfort
Cough
Diarrhoea
Fatigue
Headache
Malaise
Nasal congestion
Oropharyngeal pain
SARS-CoV-2 test positive
Symptomtext
COVID-19 symptoms started on 04/27/2022, tested positive on 04/30/2022. Symptoms were stuffiness, but not runny nose, sore throat, severe headache, and a little heaviness in chest. It was the sore throat that tipped me off to get tested. I've been fatigued but that's about it. Symptoms lasted for 6 days. I'm still fatigued but they put me on Paxlovid and I've had side effects. I also had a dry persistent cough for several days and diarrhea.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- COVID-19 04/29/22 Positive result on 04/30/22
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma.
- Andere Medikamente
- Asthma Medication
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 29.04.2022
- Impfdatum
- 27.12.2021
- Beginn
- 29.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Confusional state
Cough
Fatigue
Malaise
Symptomtext
On 12/29 I developed COVID-19 symptoms. I did a tele-health visit w/ my Dr. I was prescribed a Spiriva inhaler and Ventolin and a cough. I believe I have the symptom of occasional confusion as described w/ long COVID-19 and occasional fatigue.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma; Probable MS
- Andere Medikamente
- Baclofen, Carbamazepine, Omeprazole, Trazadone
- Allergien
- Penicillin; Seafood
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 19.04.2022
- Impfdatum
- 11.01.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Ageusia
Cough
Fatigue
Headache
Malaise
SARS-CoV-2 test negative
Sinus congestion
Symptomtext
I am reporting my COVID 19 symptoms after getting my booster dose 3 on 01/11/2022. I had a moderate to severe for the first two days and then after the 2nd day, it started getting mild. I had fatigue, cough, sinus congestion, headache and lost of taste. It last at least 10 days. I tested negative on 04/15/2022. I still have the cough. I called my doctor and they prescribe the cocktail that help shorten my days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- Rosuvastatin 20 mg.
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 13.04.2022
- Impfdatum
- 07.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 5,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain
Diarrhoea
Urticaria
Symptomtext
Abdominal cramps started 1/12 Diarrhea started 1/17 Hives all over body started 1/19 Symptoms still ongoing
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- levonorgestrel-ethinyl estradioL 0.1mg-20mcg
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 11.04.2022
- Impfdatum
- 17.02.2022
- Beginn
- 18.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Abdominal X-ray
Abdominal distension
Abdominal pain
Asthenia
Feeding disorder
Fluid intake reduced
Ileus
Ileus paralytic
Malaise
Therapeutic response unexpected
Symptomtext
Acute onset abdominal bloating and cramps, rapidly worsening. Inability to eat or drink for 6 days. Malaise, weakness. Attempted visit to urgent care center, was turned away, EMT came to the house to put in IV access, got several liters of saline. Had labs drawn at home. ABDOMINAL XR done. After 6 days abdominal distension and cramps started getting better. Started drinking. Careful solid foods after 7 days Noticed for about 10 days after recovery that I was free of chronic pain from tendinitis (probably due to overwhelming immune response - HAD EXTREMELY HIGH ANTIBODY TITERS AT THE TIME OF VACCINE WHICH WAS DISREGARDED BY MY EMPLOYER , QUOTING "MANDATE" TO VACCINATE)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- -
- Labordaten
- ABDOMINAL XR 2/21/22 confirmed clinical diagnosis of SMALL BOWEL ILEUS . CT scan discussed with radiologist, was deferred since PARALYTIC ILEUS more likely than obstruction
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Asthma HTN myopathy / tendinopathy (unspecified)
- Andere Medikamente
- Ramipril 5mg Flomax 0,4 mg ASA 81mg
- Allergien
- Latex
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 09.04.2022
- Impfdatum
- 21.12.2021
- Beginn
- 26.12.2021
- Tage bis Beginn
- 5,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site pruritus
Pruritus
Quality of life decreased
Rash
Rash pruritic
Rash vesicular
Symptomtext
Site: Itching at Injection Site-Severe, Systemic: Allergic: Itch (specify: facial area, extremeties)-Severe, Systemic: Allergic: Itch Generalized-Severe, Systemic: Allergic: Rash (specify: facial area, extremeties)-Severe, Systemic: Allergic: Rash Generalized-Severe, Systemic: Rash/lesions that is painful, itching, weaping-Severe, Additional Details: Rash started about 4 days after the shot. Initally rash started on back, but spread to sides, arms, legs. Rash was initally itchy. Became painful, itchy, 'ugly' and weaping lesions formed. Patient has tried antihistamines (hydroxyzine, allegra), creams (triamcinolone, mupirocin). Nothing has helped and he states that this shot has changed his life.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 08.04.2022
- Impfdatum
- 06.04.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Inappropriate schedule of product administration
Pain
Symptomtext
Patient received 1st Moderna Booster on 12/29/2021. Patient received 2nd Moderna Booster on 4/6/2022, but was not eligible for 2nd Moderna booster until 04/29/2022. Patient had no immediate adverse reaction after administration of 2nd Moderna Booster. Patient was contacted on 4/7/2022 and denied any adverse reactions. Patient reported that he had a "little less achiness than previous doses".
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- Unknown
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 05.04.2022
- Impfdatum
- 22.12.2021
- Beginn
- 24.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Allergy test positive
Anxiety
Arthralgia
COVID-19
Cataract operation
Depression
Extra dose administered
Hypersensitivity
Impaired work ability
Insomnia
Ocular discomfort
Pain
Rash
Rash erythematous
Rash pruritic
SARS-CoV-2 test positive
Symptomtext
Timeline o First two weeks in August 2021 (Post second Moderna vaccine) I experience severe shoulder pain. (unusual for me). It lasts for two weeks and then goes away. o October 23rd 2021 ? shoulder pain returns, and I start getting terrible rashes on the backs of my hands and between my fingers. They keep me awake at night (I've never had problems with rashes in my life). o November 2021 ? I see a dermatologist who prescribes a steroid cream. December 22nd - Receive the Moderna booster. Rash returns on December 24th, near my left eye, back of hands and between fingers. o December 30th I test positive for COVID via one of the home tests. o Dermatologist advises me to apply cortisone cream to my hands at night and wear plastic gloves for 10 nights. o January 4th My ophthalmologist tells me to stop using cortisone cream because my eye pressure is up. I have glaucoma. She tells me to ask the dermatologist to prescribe Tacrolimus. o January 6th Dermatologist calls in prescription. Walgreens finally has it in stock by January 8th. By then, the untreated rash spreads above my upper lip, below my bottom lip, neck and hands. It's beat red, stinging and itchy. Application of Tacrolimus is excruciating (like putting burn and itch on top of burn and itch. o February 20th My dermatologist does a patch test on me. It is discovered that I'm allergic to 18 different chemicals (all of sudden). Mind you, I've never been allergic to anything. The substances on this list are really ordinary daily chemicals and hard to avoid: polyester, wool, plastic, rubber, latex, fragrance, disperse blue dye, nickel. There's so many is overwhelming. o Ingredients in my glaucoma drops contain allergens that I'm now suddenly allergic to. I had received clearance to use them via a patch test with an allergist back in 2013. Now, my dermatologist and I have to scramble to find out what I can use to treat my glaucoma, literally. Once you lose vision cells, they're gone forever. Treatment is really damage control so that you don't go bling. My treatment during the month of February is inconsistent because we're now going through step therapy. There are very few options. I never had common allergies, but I had a hard time finding a drop that wouldn't give me blepharitis. o Now I'm on oral medication (acetazolamide) and that can compromise your kidney function and or give you kidney stones. This is a temporary drug as we are now talking eye surgery (many eye surgeries actually), and complications because there's a battery of eye drops that you must take after surgery. Drops that I can potentially be allergic to now. Cataract surgery afterwards is a given. Many follow up doctor visits will be required (so now there's a huge expense involved). On top of that, I will be out of work on disability for 12 plus weeks (6 weeks for each eye). I hope I have my job after that. This has to be a result of both the second Moderna shot and the booster. They were the only change in my life. After the vaccines, this happened to me. My life is pretty awful now. Try buying a winter coat when you're allergic to polyester. I'm anxious every day about surgery and being on a medication that can potentially hurt my healthy kidneys. I can't knit or crochet anymore because I'm allergic to almost all yarn. This condition is all consuming and draining. I've become very depressed and almost hopeless (not like me at all). I long for the life this horrible condition has taken from me. There is the potential for premature blindness and kidney failure if my Ophthalmologist and I can't find adequate treatment for my glaucoma, complicated by this new condition. I've gone to several doctors to treat this: Primary Care Physician, Ophthalmologist, 3 different Dermatologists and I'm scheduled to see a new Ophthalmologist for a second opinion this month. I'm also scheduled to see an allergist this month. I'm seeing my current Dermatologist tomorrow (second time this month).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- Patch test February 22nd 2022. Suddenly allergic to the following (never had allergies before): Gold Sodium Thiosulfate, Balsam of Peru, Fragrance Mix, Thiuriam mix, lanolin alcohol, lanolin alcohol, Melamine Formaldehyde Resin, Disperse Dye Blue 124, Bensophenone 4, Propylene Glycol (an ingredient in Latanoprost the glaucoma medication I took successfully for at least 10 years), DMDM Hydantion, Nickel Sulfate, 4-4 Dithiomorpholine, Amonium Persulfate, Benzoic Acid, Dodcyl gallate, Benazalkonium Chloride (chemical in my Azopt drops that an allergist patch tested my for in 2013 and gave me clearance to use it), Propolis, Limonene. I was never allergic to any of these substances prior to taking the Moderna vaccines.
- Aktuelle Erkrankungen
- Glaucoma
- Vorgeschichte
- Glaucoma
- Andere Medikamente
- Latanoprost and Azopt
- Allergien
- Before booster: many Glaucoma drops Cosopt, Timolol, Combigan.
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 31.03.2022
- Impfdatum
- 27.12.2021
- Beginn
- 13.01.2022
- Tage bis Beginn
- 17,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pruritus
Urticaria
Symptomtext
So on Jan. 13, I started developing severe itchiness all over my upper extremities, my back, arms, this happened back and forth for about two weeks I would say, I started using an over the counter steroid, it did not get any better, so started using Benadryl and topical Benadryl, as well, and like two week later it was not getting better but worse and I would get like whelps on my body from where I scratched at. Then the two weeks after it started is when I contacted my doctor. I sent him picture and he said it was hives and he seen a few cases where patients developed hives after the vaccine, so he prescribed me a prescription steroid cream for the neck down for two weeks, and Zyrtec once a day and Benadryl as needed which is like 4 times a day. I did all of that and I stopped taking the cream because I was only supposed to take it like for those two weeks. Since then, I now only take the Benadryl 2-3 times a day and it has gotten better but if I don't take it the hives began to spread down my legs and lower part or my body as well.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- High Cholesterol; Migraine; Rosacea
- Andere Medikamente
- Atorvastatin; 40mg Junel FE.
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 27.03.2022
- Impfdatum
- 25.03.2022
- Beginn
- 25.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Headache
Pyrexia
Symptomtext
Fever, chills, headache Fever and chills ended on 3/26 at 4:00 AM Headache is continuing. It isn?t debilitating, just constant.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- RA
- Andere Medikamente
- Methotrexate Simvastatin Montelukast Lexapro
- Allergien
- None
- Vorherige Impfungen
- Moderna
- Staat
- IN
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 23.03.2022
- Impfdatum
- 11.02.2022
- Beginn
- 13.02.2022
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cluster headache
Symptomtext
Diagnosed with episodic cluster headaches by general practitioner. Provided with care instructions and advised to report to VAERS by general practitioner.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cluster headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Systemic Lupus Erythematosus; Osteoporosis.
- Andere Medikamente
- Plaquenil; Actonel;Baby Aspirin;Calcium supplement;Multivitamin.
- Allergien
- Penicillin;Sulfa drugs (Bactrim);Leviquin/Levifloxacin;Nifedipine;Zoloft.
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 12.03.2022
- Impfdatum
- 22.12.2021
- Beginn
- 24.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Muscle rigidity
Musculoskeletal stiffness
Vomiting
Symptomtext
Per husband, patient had right-sided stiffness. Arm and hand rigid. She threw-up once, then napped for about 2 hours. She was back to normal after her nap. Patient encouraged to go to doctor. I am not sure if she went.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vomiting
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 41,0
- Geschlecht
- M
- Eingang
- 07.03.2022
- Impfdatum
- 04.03.2022
- Beginn
- 06.03.2022
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Rash erythematous
Rash pruritic
Urticaria
Symptomtext
Patient complained of an itchy rash on his left arm in the area of his elbow. Rash appears round and slightlyl red like a hive.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 07.03.2022
- Impfdatum
- 18.02.2022
- Beginn
- 01.03.2022
- Tage bis Beginn
- 11,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Ear swelling
Erythema
Pruritus
Swelling face
Swelling of eyelid
Urticaria
Symptomtext
Hives started on 3/1/22 behind ears then spread all over body. Unbearably itchy and red. On 3/3/22 hives led to swollen eyelids and earlobes and face. Still dealing with this.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- Started on prednisone 20mg 3/4. Increased to 40mg at ER. Then 60 mg on 3/6.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 07.03.2022
- Impfdatum
- 06.02.2022
- Beginn
- 07.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dry skin
Injection site bruising
Injection site pain
Injection site pruritus
Injection site reaction
Injection site swelling
Skin exfoliation
Symptomtext
Site: Bruising at Injection Site-Medium, Site: Itching at Injection Site-Mild, Site: Pain at Injection Site-Mild, Site: Swelling at Injection Site-Mild, Systemic: Dryness, skin peeling at sight of injection-Mild, Additional Details: Patient experienced a large bruise, dry skin peeling, and soreness at the site of injection. It has mostly resolved by the date of her second dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site bruising
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 01.03.2022
- Impfdatum
- 19.02.2022
- Beginn
- 19.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Incorrect dose administered
Pain
Symptomtext
Patient received full dose (0.5mL) for 4th dose instead of half dose (0.25mL). She was informed on the same date once the error was discovered. She reported no side effects outside of normal/expected first-second day side effects (tiredness, achiness, etc.). She reported no additional side effects after day 2.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- Sulfa antibiotics
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 01.03.2022
- Impfdatum
- 19.02.2022
- Beginn
- 19.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Fatigue
Pain
Symptomtext
Patient received full dose (0.5mL) for 4th dose instead of half dose (0.25mL). He was informed on the same date once the error was discovered. He reported no side effects outside of normal/expected first-second day side effects (tiredness, achiness, etc.). He reported no additional side effects after day 2.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- -
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 01.03.2022
- Impfdatum
- 20.12.2021
- Beginn
- 20.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Injection site pain
Pain in extremity
Symptomtext
Site: Pain at Injection Site-Medium, Additional Details: Patient is complaining of arm bicep pain that can extend into his shoulder and down to his forearm. It has been happening since he got his second dose. Patient did not receive his second dose at our facility and did not have his CDC card with him. But he said that it switched from pain in his left arm after the second dose to pain in his right arm after his booster dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 91,0
- Geschlecht
- F
- Eingang
- 25.02.2022
- Impfdatum
- 24.02.2022
- Beginn
- 25.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site pain
Injection site swelling
Pain
Sleep disorder
Symptomtext
My mom woke up at 5:30 this morning in pain. Her arm is swollen at the injection site, and very tender. She also received a tetanus shot right before her COVID-19 booster.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Chronic knee, shoulder and hip pain
- Vorgeschichte
- Alzheimer's, high blood pressure/cholesterol, hip replacement, chronic knee, shoulder and hip pain
- Andere Medikamente
- Pravastatin, Amlodipine, Donepezil, Glucosamine, Multivitamin, D3, Calcium, Fish oil, Fiber, Iron, Low-dose Aspirin
- Allergien
- Unknown
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 22.02.2022
- Impfdatum
- 23.12.2021
- Beginn
- 01.01.2022
- Tage bis Beginn
- 9,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lymphadenopathy
Mechanical urticaria
Pain
Peripheral swelling
Pruritus
Tongue pruritus
Urticaria
Symptomtext
Enlarged lymph node in right armpit began on 12/24/2021; painful, the size of a lime. Lasted 5 days. Then, full body hives began overnight on 1/1/2022; they started on my back and then spread to my chest/stomach/arms/legs; had extreme itching; swelling of left fingers to the point that fingers could not be bent. Full body hives lasted 3 days, took Benadryl daily during this time to manage the itching. Also had tongue itching. Have had daily bouts of less severe hives ever since, and have been diagnosed with dermatographia also. The hives/welts will appear at random all over my body, particularly concentrated on my inner forearms, abdomen, throat, and knees. They last 20-30 minutes.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mechanical urticaria
- Hospital-Tage
- -
- Labordaten
- none yet, seeing allergist on 3/10/2022
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- eczema
- Andere Medikamente
- none
- Allergien
- no known allergies
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 18.02.2022
- Impfdatum
- 28.01.2022
- Beginn
- 29.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Pruritus
Rash
Sleep disorder
Urticaria
Symptomtext
I first noticed I was really itchy when I was sleeping that night. When I got up in the middle of the night I noticed it on my arms, chest, and stomach. There were red bumps and some white bumps. I sprayed something on it. I don't remember what it was. I called my pharmacist and she told me to take Benadryl and Zyrtec. I was taking Zyrtec throughout the day and Benadryl at night. The bumps look red and the rash was in the form of lines. Always on my forearm, and sometimes on my neck, chest, face, and upper legs. When I take Zyrtec it seems to go away after an hour, but it comes back after about 4 hours, but its happening more often. I had a tele-visit with my doctor and he prescribed Urticaria and wanted my to see an allergist. I scheduled that appointment and I will see them in March 2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Lisinopril 20mg 1xday, Hydrochlorothiazide 25mg 1xday, Bupropion 150mg 1xday
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 18.02.2022
- Impfdatum
- 20.12.2021
- Beginn
- 22.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Pain in extremity
Pruritus
Skin discolouration
Swelling
Symptomtext
Left arm pain, swelling, itching and discoloration that started 2 days after receiving vaccine and has persisted to this day. All symptoms wax and wane, there appears to be no aggravating factors.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Moderate persistent asthma Migraine without aura Essential hypertension Hirsutism Obesity Vitamin D deficiency
- Andere Medikamente
- Labetolol 300mg 1 tab BID Sumatriptan 50mg 1 tab 2hrs between doses PRN q6hrs Topiramate 25mg 1 tab po daily Cetirizine 10mg 1 tab po once a day Breo ellipta 100-25 mcg/inh aerosol powder breath activate i puff inhalation qday Albuterol su
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 15.02.2022
- Impfdatum
- 31.01.2022
- Beginn
- 03.02.2022
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Erythema
Injection site rash
Pruritus
Skin warm
Symptomtext
Starting the morning of 02/03/2022, I noticed my arm was really hot and red. The rash extended from about an inch or two below the injection site, it was about 4-5 inches long and about 2 inches wide. For about 4-5 days, it stayed hot and red, and the same size. Starting 02/11/2022, it started itching and was itchy for about 2-3 days then stopped. After the initial 4-5 days, the size and heat/redness decreased daily. As of today, it still is present but barely and doesn't itch or bother me.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site rash
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Scoliosis
- Andere Medikamente
- Ibuprofen
- Allergien
- None
- Vorherige Impfungen
- For about 36 hours after the 2nd Pfizer dose, I felt fatigued and achy.
- Staat
- -
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 14.02.2022
- Impfdatum
- 20.01.2022
- Beginn
- 06.02.2022
- Tage bis Beginn
- 17,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Chills
Nausea
Pyrexia
Symptomtext
Chills, fever and nausea.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 13.02.2022
- Impfdatum
- 04.02.2022
- Beginn
- 05.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Symptomtext
On 2/8/2022, patient called pharmacy reporting a rash on right arm; worse on top of arm starting Saturday 2/5/2022 (after getting 2nd dose of Moderna on 2/4/2022). Patient asked if rash is a common side effect of Moderna shot. She stated rash is getting worse. I advised patient to call doctor especially if symptoms are not improving.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- N/A.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 11.02.2022
- Impfdatum
- 14.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Urticaria
Symptomtext
Patient came in for her second dose and upon filling out the checklist reported her prior reaction to her first dose of vaccine 4 weeks earlier. She reported hives that was treated with diphenhydramine at home, but she did not require treatment from a healthcare provider. The hives appeared within 6 hours of vaccination, but no other details were provided. I informed the patient she should contact her doctor about the reaction and that we aren't able to provide her second dose at our store.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- No allergies reported
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 10.02.2022
- Impfdatum
- 14.01.2022
- Beginn
- 21.01.2022
- Tage bis Beginn
- 7,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Symptomtext
Rashes came out after 7 days of booster dose. Rashes came out too after my second dose (Moderna)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- synthroid 100mcg
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 09.02.2022
- Impfdatum
- 02.02.2022
- Beginn
- 02.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cough
Influenza like illness
Oropharyngeal pain
Productive cough
Symptomtext
Minor dry cough began Saturday, got slowly worse Sunday, turned into sore throat with dry cough Monday, became bad flu like symptoms yesterday and this morning. I took robitussin starting Sunday night, Monday night, and last night and this morning. Also took aspirin Saturday and Sunday. The cough has become productive this morning, spitting up wads of flem.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- Have not been back to hospital.
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- no
- Andere Medikamente
- Levothyroxine
- Allergien
- no
- Vorherige Impfungen
- Covid-19 vaccine Moderna
- Staat
- NY
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 07.02.2022
- Impfdatum
- 21.12.2021
- Beginn
- 18.01.2022
- Tage bis Beginn
- 28,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Antinuclear antibody positive
Autoimmune haemolytic anaemia
Blood immunoglobulin G
Bone marrow myelogram normal
Chromaturia
Computerised tomogram abdomen normal
Computerised tomogram thorax normal
Coombs test positive
HIV test negative
Haematocrit decreased
Haemoglobin decreased
Influenza virus test negative
Jaundice
Lethargy
Mononucleosis heterophile test negative
Parasitic blood test negative
Pregnancy test negative
Respiratory syncytial virus test negative
Symptomtext
Patient self-observed lethargy, dark urine and jaundiced sclera on morning of 1/18. Vomited 1X on 1/19 . Went to out-patient urgent care in early afternoon of 1/19. Sent to Hospital. HCT @21% and hemoglobin of 7.3 upon admission. HCT 18.1% and hemo 6.2 on 1/20. Warm COOMBS (+) with POS IgG Abs; HCT fell to 17.5% with hemoglob at 5.9 on 1/21. Idiopathic AHIA suspected. Strong (good) RBC regenerative marrow response noted. Normal WBC count. High dose injectable corticosteroid given 1/20. Transfused with 1 unit RBCs on 1/21. Discharged on 1/22 PM with ORAL PRED 60 mg SID. First recheck on 1/25 showed PCV @25.8% (hemo 8.5); 2nd recheck on 2/2 showed PCV @33.9% (hemo 11.5).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vomiting
- Hospital-Tage
- 4,0
- Labordaten
- Abdom. ultrasound (-); SARs-Cov-2 (-); HIV (-); Influenza (-); Mono (-); Babesia (-); Preg (-); RSV (-); CT scans of chest, abdo, pelvis (-); ANA (+) with FANA Nucleated Dot @1:160 ANA Speckled Pattern 1:80 All above tests conducted between 1/19/22 and 1/22/22 except for the out-patient re-check blood draws on 1/25/22 and 2/2/22. Patient is responding to medication and is now in tapering dose phase of PRED therapy. But cannot yet determine with confidence for Q#20 that patient has recovered from this event.
- Aktuelle Erkrankungen
- Dermatographic urticaria (periodic not constant)
- Vorgeschichte
- -
- Andere Medikamente
- Ceterizine; methyphenidate, birth-control (IUD)
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 06.02.2022
- Impfdatum
- 14.01.2022
- Beginn
- 24.01.2022
- Tage bis Beginn
- 10,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Pruritus
Symptomtext
Started as general itchiness in hands and feet, no rash at first has progressed to general itchiness all over body mainly arms, back, face with redness around neck. Has been going on for 2 weeks now
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- -
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 04.02.2022
- Impfdatum
- 20.01.2021
- Beginn
- 20.01.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Ear pain
Headache
Insomnia
Musculoskeletal stiffness
Neck pain
Vaccination site pain
Symptomtext
Sore left arm after 1st dose; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION SITE PAIN (Sore left arm after 1st dose) in a 57-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 028L20A, 011M20A and 070H21A) for COVID-19 vaccination. Concomitant products included MELOXICAM for Arthritis, METFORMIN for Diabetes. On 20-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 17-Feb-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 14-Jan-2022, received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 20-Jan-2021, the patient experienced VACCINATION SITE PAIN (Sore left arm after 1st dose). On 22-Jan-2021, VACCINATION SITE PAIN (Sore left arm after 1st dose) 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. It was reported that patient had no treatment been given. It was reported that there was no product complaint associated. This case was linked to MOD-2022-465155, MOD-2022-465201 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Ear pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- MELOXICAM; METFORMIN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 02.02.2022
- Impfdatum
- 25.01.2022
- Beginn
- 25.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Body temperature
Chills
Fatigue
Fibrin D dimer normal
Inflammation
Pain
Pain in extremity
Symptomtext
chills, temp, fatigue inflammation of right arm with severe pain that radiates down the arm. Has lasted over a week. Medical treatment was sought. Doctor ordered Motrin and Ketorolac and also Tylenol with codeine ordered for pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- d-dimer test done to rule out blood clot and this was negative
- Aktuelle Erkrankungen
- NO
- Vorgeschichte
- No
- Andere Medikamente
- No
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 31.01.2022
- Impfdatum
- 10.01.2022
- Beginn
- 21.01.2022
- Tage bis Beginn
- 11,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acoustic stimulation tests
Deafness unilateral
Pruritus
Rash
Tinnitus
Symptomtext
Full body rash started Friday 1/21/22 which was itchy and in patches from head to toe. It comes goes and moves locations. Went to the doctor starting Monday 1/24/22. I was informed that this rash is the same as that seen in patients 2 weeks post booster repeatedly. With this rash came a ringing in my left ear. By Wednesday 1/26/22 I am deaf. in my left ear from tinnitus caused by the COVID moderna booster.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- The course of prednisone was started on 1/25/22 to control rash, Hearing test was conducted on Friday 1/28/22, ENT and MRI conducted tomorrow 2/1/22.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Asthma
- Andere Medikamente
- N/A
- Allergien
- Zithromax
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 31.01.2022
- Impfdatum
- 31.01.2022
- Beginn
- 31.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Dizziness
Symptomtext
reported feeling lightheaded after vaccine. she reports feeling this way frequently after getting vaccines. placed in supine position. symptoms resolved upon discharge.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 31.01.2022
- Impfdatum
- 29.01.2022
- Beginn
- 29.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cold sweat
Dizziness
Symptomtext
Almost immediately after vaccine, patient reports feeling light headed and clammy. BP 120/78, HR70, RR20, O2 Sat 96% on room air. Pt given water and placed in supine position with feet elevated. Pt recovered after 30 minutes of observation
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Finast Bactrim
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 27.01.2022
- Impfdatum
- 27.01.2022
- Beginn
- 27.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Dizziness
Symptomtext
Pt received Moderna Booster at 0948 and went to sit to be observed for 15 mins. While being observed vaccinator noticed patient was rubbing his eyes and shaking his head. When asked how patient was feeling, he stated ?he felt a little light headed.? Vaccinator had patient sit on the ground with back against wall and offered water. Clinic lead was notified. Patient stated that he worked at night and just got off work and didn?t have a chance to eat dinner or breakfast. When asked what happened, patient said he felt lightheaded, a little dizzy, and hot. Offered chips and took BP at 10:05am; 139/81. Continued to keep patient on ground to be observed. Patient?s affect was polite and pleasant, patient was very talkative. At 10:10am patient stated he wanted to sit on chair, helped patient move to chair and monitored signs of syncope and dizziness. Retook vitals at 10:20am; BP 138/83, HR 80, Temp 97.1F, RR 18. Patient stated that he didn?t feel lightheaded anymore and wanted to leave. Patient appeared stable and was walked to his vehicle by accompanied by a volunteer.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 27.01.2022
- Impfdatum
- 04.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 8,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Axillary pain
Dermatitis
Pain
Rash
Rash pruritic
Symptomtext
1/5/22: full body aches, temperature 1/6/22: slight body ache 1/7/22: left armpit hurt for 2 days Itchy rash 1/12/22 : rash on right hip 1/13/22: rash on left hip 1/14/22: rash on left and right forearms 1/15/22: rash on the front of my left and right thighs 1/16/22- 1/26/22 present day: rash continues to spread on body. right ankle, behind left & right knees, left & right upper arms, scattered areas of bumps on lower legs. new areas continue to pop up on forearms, and hips. Dermatologist appt via telehealth diagnosed as Dermatitis. recommended cerave lotion and prescribed Clobetasol Propionate. zyrtech and benadryl also recommended but does not relieve the itching.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- Sulfa
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 26.01.2022
- Impfdatum
- 01.01.2022
- Beginn
- 11.01.2022
- Tage bis Beginn
- 10,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Angioedema
Antinuclear antibody negative
Mechanical urticaria
Urticaria
Symptomtext
spontaneous urticaria all over body, angioedema of the face, eyelids, lips. dermatographia. symptoms began 10 days after Moderna booster (1/11/22). Began PO prednisone 60mg x 7 days, 40mg x 7 days, 20 mg x 7 days. currently tapering.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mechanical urticaria
- Hospital-Tage
- -
- Labordaten
- ANA: negative (1/18/22)
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 82,0
- Geschlecht
- F
- Eingang
- 24.01.2022
- Impfdatum
- 20.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site pruritus
Pain in extremity
Pruritus
Symptomtext
Symptoms started with soreness to left arm. Then progressed redness and itching from injection site to 6" down arm and around arm at injection site. Itching to chest and back.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- -
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 20,0
- Geschlecht
- M
- Eingang
- 22.01.2022
- Impfdatum
- 19.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lymph node pain
Lymphadenopathy
Symptomtext
Moderna COVID-19 Vaccine EUA. Swollen lymph node on armpit of injection, started taken ibuprofen to limit pain, pain reduced two days after first noticing, haven't given enough time to see swelling reduce
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lymph node pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- whey protein, pre-workout
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 21.01.2022
- Impfdatum
- 11.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Discomfort
Injection site erythema
Injection site rash
Symptomtext
Patient called pharmacy to report a rash and erythema at and around injection site. I thought that she may have been experiencing Covid Arm. I suggested that patient use OTC pain reliever/fever reducer to help with the discomfort as well as oral Benadryl. Patient presented back into the pharmacy 6 days after vaccination; She had drawn a circle around the rash area and it had continued to spread beyond the margins defined by patient. At this time, I recommended that the patient visit an urgent care/ER so that a physician could take a look at it as it had still not improved even after OTC remedies and time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 20.01.2022
- Impfdatum
- 27.12.2021
- Beginn
- 04.01.2022
- Tage bis Beginn
- 8,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Urticaria
Vaccine positive rechallenge
Symptomtext
Hives on back, stomach, arms, back of hands and fingers, palms, neck, face and scalp. Would appear after the slightest touch on my skin, even just from touching my face to wash my face with soap and water, or on my palms after holding a bag. Skin creams find not work particularly well but helped a bit, but the rash would keep coming back. Tried both Benadryl and Zyrtec and they would help to calm hives when they were really bad, but didn?t stop the hives from returning. This reaction occurred after my second does of Moderna in April 2020, and again after my booster (Moderna again) in December 2021. Both times the hives started around a week after the shot, and it took around 2 full weeks for the hives to go away. I currently still get hives occasionally, but they seem to have mostly gone away.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Vitamin D, B12
- Allergien
- Penicillin, spring and fall hayfever
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 20.01.2022
- Impfdatum
- 17.12.2021
- Beginn
- 19.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dizziness
Symptomtext
Patient states that after receiving the 1st dose of Moderna 12/17/2021, started experiencing symptoms 12/19/2021 of extreme dizziness. Emergency Room visit 12/28/2021, no recommendations. Patient still experiencing symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 20.01.2022
- Impfdatum
- 14.01.2021
- Beginn
- 14.01.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Pain in extremity
Pyrexia
Rash erythematous
Skin burning sensation
Symptomtext
I experienced sore arm, fever, burning sensation on my skin, red rash on my left leg, and extreme fatigue.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Lupus
- Andere Medikamente
- -
- Allergien
- I am allergic to Penicillin and Sulfa
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 20.01.2022
- Impfdatum
- 12.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test
Feeling abnormal
Hypoaesthesia
Muscle spasms
Musculoskeletal stiffness
Neck pain
Symptomtext
That night when I left vaccination location, started experiencing numbing in the right arm down to the right leg. During bed time, began having sharp muscle spasms. stiffness on left side of neck and sharp pain. Spasms still continue till this day. Still documenting for doctors records. Weird feeling in toes and fingers.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Neck pain
- Hospital-Tage
- -
- Labordaten
- bloodwork, follow up with specialist.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- No not the day of vaccination
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 40,0
- Geschlecht
- M
- Eingang
- 20.01.2022
- Impfdatum
- 18.01.2022
- Beginn
- 18.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site pain
Insomnia
Pain
Pain in extremity
Restlessness
Symptomtext
Arm soreness above a server for vaccination. Next day increased X2, increase tenderness at shot site. Body aches, uneasy sleeping, restless. Arm still sore and body aches to this day (48hrs+) after injection.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- None yet.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- N/a
- Allergien
- Cellibex
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 20.01.2022
- Impfdatum
- 05.01.2022
- Beginn
- 16.01.2022
- Tage bis Beginn
- 11,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Angioedema
Urticaria
Symptomtext
urticaria and angioedema of the palms of hands.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- No allergies
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 23,0
- Geschlecht
- M
- Eingang
- 19.01.2022
- Impfdatum
- 22.12.2021
- Beginn
- 02.01.2022
- Tage bis Beginn
- 11,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Mechanical urticaria
Oropharyngeal discomfort
Pruritus
Urticaria
Symptomtext
Extreme itching; hives; dermatographia and feeling of a bubble in the throat.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mechanical urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VT
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- Impfdatum
- 06.01.2022
- Beginn
- 09.01.2022
- Tage bis Beginn
- 3,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Fatigue
Vertigo
Symptomtext
Waves of dizziness, wooziness, vertigo and fatigue. Beginning 3 days post-injection, lasting about 4 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- I had a week-long cold about 4 weeks before vaccination.
- Vorgeschichte
- Depression, anxiety, migraines
- Andere Medikamente
- Bupropion, Fluoxetine, Estrogen, Progesterone, Vitamin B, Vitamin D, CoQ10, Magnesium
- Allergien
- Morphine
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- Impfdatum
- 19.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain upper
Diarrhoea
Dizziness
Fatigue
Feeling hot
Pruritus
Symptomtext
The patient confirmed 2nd dose of Moderna was given on 2/5/21, is allergic to shrimp, and has Asthma. 3rd dose of Moderna was administered today at 9:15 am. The patient was monitored for 30 mins. 9;29 am, the patient-reported symptoms of light-headed, stomach cramp, face and back feeling hot and itchy, and lastly had diarrhea and fatigue. The patient also stated that she did not have anything to eat prior to taking the vaccine. Upon assessment, the patient is A&O. V/S was taken at 9:40 am BP 142/65, HR 61, O2SAT 100. The patient was asked to stay for an additional hour for observation and when she was stable she was picked up by her friend.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain upper
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Asthma
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- Shrimp
- Vorherige Impfungen
- Moderna S/S nausea and fatigue
- Staat
- MD
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- Impfdatum
- 19.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Feeling hot
Headache
Hyperhidrosis
Interchange of vaccine products
Pruritus
Symptomtext
The patient confirmed 1st dose of J&J on 6/26/21, NKDA. 2nd dose Pfizer 0.3ml administered 1/19/22 to LA. The patient was vaccinated at 12:15 pm, at 12:30 patient reported feeling left palm itching, body hot and sweaty, no SOB, some dizziness, some headache. BP130/80 pulse 72, respiration 20, O2sat 97%. The patient says she has a history of allergy to seafood, migraines, and takes medication for migraines and for allergies. The patient asked to wait another 30 minutes for monitoring. 12:49 patient reports feeling a little dizzy and vitals stable pulse 64/ min, 18/min, O2 SAT 99%, B/P 132/75. The patient was released at 1:05 pm stable, alert, and oriented. The patient stated feeling okay and was going home to take her medication.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- H/O Migraines and Asthma
- Vorgeschichte
- -
- Andere Medikamente
- Allergy and Migraine Medication
- Allergien
- Shellfish
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 18.01.2022
- Impfdatum
- 26.12.2021
- Beginn
- 08.01.2022
- Tage bis Beginn
- 13,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood immunoglobulin E
C-reactive protein increased
Erythema
Mechanical urticaria
Pain of skin
Pruritus
Urticaria
Symptomtext
Diagnosed with Dermatographia 10 days after receiving my booster shot (extreme hives, itching, red ears, uncomfortable scalp).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mechanical urticaria
- Hospital-Tage
- -
- Labordaten
- C-Reactive Protein (High ) 1/13/22 Immunoglobulin E (High) 1/13/22
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- - Zyrtec - Kyleena (IUD) - Celexa (20mg)
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 18.01.2022
- Impfdatum
- 17.01.2022
- Beginn
- 17.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Discomfort
Erythema
Pain
Peripheral swelling
Pruritus
Skin exfoliation
Symptomtext
The patient reported that her arm was very swollen (more than expected). She also reported that her fingertips and palms of her hands were red, and that the skin had started peeling. She said it was itchy and painful, and generally very uncomfortable. The skin peeling started on her fingertips in the evening (on the day the vaccine was administered), and spread to her palms the next morning. This was her second dose, and she did not have any problems with the first.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 18.01.2022
- Impfdatum
- 22.12.2021
- Beginn
- 01.01.2022
- Tage bis Beginn
- 10,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal discomfort
Abdominal pain upper
COVID-19
Dyspepsia
Fatigue
Nausea
Oesophageal pain
Pruritus
SARS-CoV-2 test positive
Urticaria
Symptomtext
Dose 1: slight nausea for 24hrs Dose 2: slight stomach upset/heartburn/tired Dose 3: intense hives and itching began 10 days after shot. Hives and dermatographia continue to occur multiple times daily/still have not resolved. intense esophageal pain and stomach pain believed to be heart burn or indigestion occurred on days 2-4/5.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain upper
- Hospital-Tage
- -
- Labordaten
- Covid positive test result on 1/5/22
- Aktuelle Erkrankungen
- Spontaneous hive outbreaks post Moderna booster, extreme itching, and dermatographia (skin writing) began 1/1 along with intense esophageal/heart burn sensation and pain that resolved by 1/6. Felt like something was stuck deep in throat for many days and pain with swallowing.
- Vorgeschichte
- Continuous spontaneous hive outbreaks, dermatographia and heartburn. All symptoms worsen at night.
- Andere Medikamente
- Natures Bounty daily gummy vitamins with collagen and biotin
- Allergien
- Gadolinium/ IV Contrast - rash Chloropyramine - extreme dizziness/out of body experience
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 17.01.2022
- Impfdatum
- 15.12.2021
- Beginn
- 28.12.2021
- Tage bis Beginn
- 13,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pruritus
Urticaria
Symptomtext
On Decemeber 28th, severe itching and hives started on hands and feet. This continued for days and then started in other parts of the body: armpits, neck, scalp, forearms, backs of arms, backs of legs. Itching is severe, random, and worsens if scratched and worsens at night. I have no allergies, contact or seasonal. Used hydrocortisone, no relief. Used steroid cream, Clobetesol - no relief. Used Benedryl - no relief. Tried numerous lotions and anti itch, no relief. Found others on the internet with same issues and was suggested to try Zyrtec. The itching only stopped after using Zyrtec. If Zyrtec is discontinued, itching comes back. I continue to take Zyrtec every 24 hours.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Diabetes type 2, PCOS
- Andere Medikamente
- Metformin, Trulicity, Losartan, Vitamin D
- Allergien
- No know allergies
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 16.01.2022
- Impfdatum
- 04.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Headache
Heavy menstrual bleeding
Menstruation irregular
Pyrexia
Symptomtext
1/4/22 Moderna 3 rd shot booster (2 shots Pfizer in the previous year) 1/5-1/6: fever, fatigue, headache 1/6-1/11 period came - abnormally long bleeding cycle (6 days instead of normal 3days); twice as much blood flow . Will monitor and report if there are further events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- NA
- Andere Medikamente
- No
- Allergien
- Penicillin
- Vorherige Impfungen
- Fever, headache with the first 2 Pfizer shots done on 4/16/21 and 5/14/21. The 2nd Pfizer shot reaction was much stronger than t
- Staat
- IA
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 14.01.2022
- Impfdatum
- 04.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 10,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pain
Pain in extremity
Shoulder injury related to vaccine administration
Symptomtext
Patient states she has had shooting arm pain since the injection which was on 1/4/22. She believes she has SIRVA (Shoulder Injury Related to Vaccine Administration)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 14.01.2022
- Impfdatum
- 14.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pruritus
Rash
Urticaria
Symptomtext
rash/hive/itching on neck, facial, ears, and upper arms
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Jannsen caused rash/hive
- Vorherige Impfungen
- JJ cause rash/hive/itching also
- Staat
- MD
- Alter
- 26,0
- Geschlecht
- M
- Eingang
- 14.01.2022
- Impfdatum
- 14.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Symptomtext
Patient felt dizzy after receiving vaccine, vitals signs checked and stable, BP 134/84, HR 80, RR 18, Temp 98.0, SPo2 98%. He drank water and was monitored for 30minutes. No acute ditress noted. He stated he was ok after 30minutes observation and ready to leave. Accompained by Mom.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Asthma and heart condition at birth which has resolved
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 14.01.2022
- Impfdatum
- 12.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Mass
Pain
Skin warm
Tenderness
Symptomtext
Woke up with a big lump, pain, tenderness, skin in red and warm to touch
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- Returned to clinic site and showed them my arm. They drew a circle around it on 1/14/22 at approximately noontime and said if the redness continues outside the circle than to seek treatment at an urgent care facility
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- NA
- Andere Medikamente
- Biotin, sertraline, losartan, hydrochlorothiazide, clonazapam
- Allergien
- Numerous medicines
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 14.01.2022
- Impfdatum
- 03.01.2022
- Beginn
- 04.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fibrin D dimer
Herpes zoster
Pain in extremity
Rash vesicular
Symptomtext
Patient received her 3rd Moderna vaccine on 1/3/21. The next day, 1/4/21, she developed a "deep, achy pain" in her right upper thigh. After a few days, she was concerned, and was evaluated at an Urgent Care on 1/7/21. Due to her personal concern for blood clot, d-dimer was sent, and result was normal (<0.270 ugFEU/mL). Pain continued, and a few days later she developed a blistering rash in the area of pain, on approximately 1/10/21 or 1/11/21. She was then evaluated by this provider in clinic on 1/14/21, and diagnosed with herpes zoster.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- See Item 18
- Aktuelle Erkrankungen
- None known
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 14.01.2022
- Impfdatum
- 18.12.2021
- Beginn
- 10.01.2022
- Tage bis Beginn
- 23,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Breast mass
Breast pain
Breast swelling
Symptomtext
I have fibrocystic breasts, with many cysts and 3 fibroadenoma tumors. I occasionally experience mild soreness before my period. After receiving the Moderna booster (my previous vaccine on 5/2/2021 was J&J) within a few days I noticed a little bit on f breast pain and noted that it was uncommon to have pain in my left breast which has fewer/smaller cysts. I assumed my period was coming and there must just be more swelling this time. I took Tylenol a few days to alleviate the pain. On January 5 my period did start. It came and went and the pain did not go away as it normally would. On January 11 I noticed that I could see a slightly raised area of skin below the nipple of my right breast, and when I touched it I felt a hard lump right below the surface that feels about an inch long and is similar in feeling to my fibroadenomas. However, it is in the same area where I have a cluster of large cysts that span 60mm at my last ultrasound in October 2020. This lump is either new or an existing one that moved or grew. I am still waiting on a referral for another ultrasound and having to take daily Aleve for the pain. In the meantime the pain has become constant in the right breast. It is sharp pains behind and around the nipple. The left breast experiences less sever zaps of pain. I?ve talked to several other women in the Facebook group for women with Fibrocystic breast and many are reporting the same issue; pain after receiving an mRNA vaccine, growing or changing of fibroadenomas, swelling of breast. One said it mostly went away after a couple of months, while others have reported no changes even months after their last vaccine. There seems to be a correlation between the vaccine and fibrocystic breasts and I think this needs to be researched ASAP!
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Breast pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Eczema Allergic contact dermatitis High cholesterol Fibrocystic breast changes/fibroadenomas Seasonal allergies/hay fever POTS and/or Supraventricular Tachycardia
- Vorgeschichte
- Eczema Allergic contact dermatitis High cholesterol Fibrocystic breast changes/fibroadenomas Seasonal allergies/hay fever POTS and/or Supraventricular Tachycardia
- Andere Medikamente
- Lorazepam 1mg
- Allergien
- Penicillin Contact allergies to: Cobalt Chloride Alpha-Tocopherol (Vitamin E) Dodecyl Gallate Ethyl Cyanoacrylate Monoethanolamine (PPD-derivatives, aminophenol dimethylamine) Hydroperoxides of Linalool (all fragrance) Carba Mix/Diphenylguanidine Thiuram Mix
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 14.01.2022
- Impfdatum
- 10.01.2022
- Beginn
- 10.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Maternal exposure during breast feeding
Pain in extremity
Symptomtext
Pain in the left arm with 2nd shot; Patient concern about 2nd dose administered 2 weeks before indicated schedule; Patient breastfeeding administered with first 2 shots; This spontaneous case was reported by a consumer and describes the occurrence of PAIN IN EXTREMITY (Pain in the left arm with 2nd shot), INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Patient concern about 2nd dose administered 2 weeks before indicated schedule) and MATERNAL EXPOSURE DURING BREAST FEEDING (Patient breastfeeding administered with first 2 shots) in a 29-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 070H21A) for COVID-19 vaccination. Concomitant products included MAGNESIUM and ZINC for Supplementation therapy. On 10-Jan-2022, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 10-Jan-2022, the patient experienced INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Patient concern about 2nd dose administered 2 weeks before indicated schedule) and MATERNAL EXPOSURE DURING BREAST FEEDING (Patient breastfeeding administered with first 2 shots). On 11-Jan-2022, the patient experienced PAIN IN EXTREMITY (Pain in the left arm with 2nd shot). On 10-Jan-2022, INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Patient concern about 2nd dose administered 2 weeks before indicated schedule) and MATERNAL EXPOSURE DURING BREAST FEEDING (Patient breastfeeding administered with first 2 shots) had resolved. On 12-Jan-2022, PAIN IN EXTREMITY (Pain in the left arm with 2nd shot) had resolved. No Treatment information was reported. This case was linked to MOD-2022-449528 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- MAGNESIUM; ZINC
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 39,0
- Geschlecht
- M
- Eingang
- 12.01.2022
- Impfdatum
- 04.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Injection site pain
Myalgia
Vomiting
Symptomtext
Immunocompromised (AIDS) patient received a dose of Moderna which is not currently authorized by written Agency/CDC guidelines as of 1/6/22. Janssen Dose #1 in April 2021. Janssen Dose #2 in November 2021. Received a full dose (0.5mL) of Moderna with Team on 01/04/2022. Current guideline for Janssen schedule is 1 dose only for Primary Schedule, no immunocompromised dose, and a booster dose 2 months from Primary Dose. Moderna Dose given by Team falls outside of this current guideline. I telephoned patient in the afternoon of 1/6/22, and he reported only moderate side effects. Soreness at injection site, myalgia, & vomiting. Did not have to visit PCP, UC, or ED. Otherwise felt decent.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- AIDS
- Vorgeschichte
- AIDS
- Andere Medikamente
- HIV Anti-Virals
- Allergien
- None disclosed at time of assessment.
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 12.01.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Diarrhoea
Injection site pain
Injection site swelling
Malaise
Myalgia
Nausea
Symptomtext
Swelling of injection site and pain in muscle from injection, unwell feeling for two days, nausea for two days and diarrhea for one day, muscular aches and pains .
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 11.01.2022
- Impfdatum
- 27.12.2021
- Beginn
- 06.01.2022
- Tage bis Beginn
- 10,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pruritus
Sleep disorder
Symptomtext
Itching all over, especially bottom of my feet, underarms and groin area. The more I scratch my the more I itch, but it feels so good to scratch it. It wakes me up at night.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- No
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 10.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 08.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Diarrhoea
Headache
Nausea
Symptomtext
diarrhea, headache, nausea, chills
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 09.01.2022
- Impfdatum
- 22.12.2021
- Beginn
- 07.01.2022
- Tage bis Beginn
- 16,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Urticaria
Symptomtext
Experienced rash all over upper body one day after receiving booster, no itch, which went away in a couple of days. About 2 weeks later I am now experiencing chronic migrating urticaria. Very itchy.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 08.01.2022
- Impfdatum
- 06.01.2022
- Beginn
- 06.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Burning sensation
Lymphadenopathy
Rash
Rash erythematous
Symptomtext
Swollen lymph node on left side of neck doubled in size within a few hours of booster. Also developed a red burning rash on both sides of my neck between my should and my neck and between/under both breasts.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma
- Andere Medikamente
- Albuterol; Zyrtec; Nasacort; Estradiol; Medroxyprogesterone; Natures Bounty hair skin & nail gummies; Natures Bounty Womens multivitamin gummies
- Allergien
- None
- Vorherige Impfungen
- Same as described for booster. 2nd Covid vaccine shot; age 46; 4/22/21; Moderna
- Staat
- OK
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 08.01.2022
- Impfdatum
- 29.12.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Urticaria
Vaccination site mass
Symptomtext
hives in left arm are really bad; Big knot in the left arm/knot went down; This spontaneous case was reported by a consumer and describes the occurrence of URTICARIA (hives in left arm are really bad) and VACCINATION SITE MASS (Big knot in the left arm/knot went down) in a 78-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 070H21A) for COVID-19 vaccination. No Medical History information was reported. On 29-Dec-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 30-Dec-2021, the patient experienced VACCINATION SITE MASS (Big knot in the left arm/knot went down). On an unknown date, the patient experienced URTICARIA (hives in left arm are really bad). At the time of the report, URTICARIA (hives in left arm are really bad) outcome was unknown and VACCINATION SITE MASS (Big knot in the left arm/knot went down) was resolving. After the booster dose, patient had a big knot in the left arm that appeared on 30-dec-2021 and it went down on 01-jan-2022 but was still there. It was reported that concomitant medication included 7 or 8 of them. No treatment medication were reported. This case was linked to MOD-2022-437506 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 08.01.2022
- Impfdatum
- 06.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Pruritus
Somnolence
Symptomtext
Extreme fatigue, sleeping 22 hours per day. Up briefly twice daily for food. Severe itching over 75% of skin area unrelieved by oral antihistamines or topical aloe Vera gel application
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Type II diabetes, plaque psoriasis.
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- Moderna COVID 19 vaccine 1/4/2021 and 2/2/21. Same fatigue reaction but no itching
- Staat
- CA
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 07.01.2022
- Impfdatum
- 05.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Fatigue
Insomnia
Pain
Pyrexia
Symptomtext
Fatigue, body aches, fever, chills, insomnia
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 07.01.2022
- Impfdatum
- 05.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Body temperature increased
Chills
Headache
Hyperhidrosis
Neck pain
Pain in extremity
Pyrexia
Symptomtext
Approximately 8 pm on January 5,2022, the day I received my first vaccine, I started chilling, took 2 , 200mg of Ibuprofen, temperature 102. Headache most of the day. Following morning, headache continues, neck pain, sore arm, no fever. Approximately 4:30, chills begin. Not as bad, slept for 2 hours, felt better. Back in bed by 8 pm, no temp taken, sometime during the night, fever broke with sweats, feeling much better. Slight headache today, no other complaints.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Hydrochlorothiazide Citalopram Hydrobromide Levothyroxin Low dose Aspirin Losartan Potassium Ibuprofen
- Allergien
- Minocycline Keflex
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 22,0
- Geschlecht
- M
- Eingang
- 06.01.2022
- Impfdatum
- 14.12.2021
- Beginn
- 24.12.2021
- Tage bis Beginn
- 10,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Mechanical urticaria
Pruritus
Urticaria
Symptomtext
Dermatographia of the entire skin appeared 10 days after receiving the COVID-19 booster shot. It has persisted so far for at least 2 weeks. Hives appear on the skin when itched or rubbed, and remain for around 30 minutes before subsiding.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mechanical urticaria
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Acne
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 42,0
- Geschlecht
- M
- Eingang
- 06.01.2022
- Impfdatum
- 04.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Asthenia
Chills
Fatigue
Headache
Pain in extremity
Pyrexia
Symptomtext
It started with weakness, fatigue, and joint pain. By the afternoon on the day following the shot I had severe chills and my feet hurt as if cramping but there were no cramps. I also had a fever of 103? F and a severe headache.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 06.01.2022
- Impfdatum
- 15.12.2021
- Beginn
- 16.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Influenza like illness
Lymphadenopathy
Pyrexia
Rash
Symptomtext
I started off with a fever of 101.8, developed a rash on my torso, neck, face, ears, scalp. Experienced flu-like symptoms. I felt run down, tired. Lymph node swollen under the arm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- No
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Diabetes type 2, Thyroid cancer (remission), Migraines, Chronic Kidney Disease, Autoimmune disease, Limbal Cell Dysfunction
- Andere Medikamente
- Metformin, Minocycline, Methotrexate, Folic Acid, Fluorometholone, Dexamethasone Ointment, Ziozis, Zinc, Ambien CR, Levothyroxine, Fenofibrate, Topiramate
- Allergien
- Sulfa, IVC contrast
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 05.01.2022
- Impfdatum
- 01.12.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 29,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Fatigue
Headache
Injection site rash
Peripheral swelling
Pruritus
Symptomtext
Severe headache onset at 9pm. Chills, rigors overnight. Severe fatigue the following day. R arm significant swelling, redness, and pain which worsened over 48 hrs. Arm also became very itchy. Continues to be itchy on 1/5 and rash present near injection site. Headaches daily since injection.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- Fish oil, vitamin c, vitamin d
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 05.01.2022
- Impfdatum
- 04.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Nausea
Pain
Pain in extremity
Pyrexia
Symptomtext
Fever, chills, aches, nausea, intense arm pain. All started 12 hours after the dose
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Non
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 38,0
- Geschlecht
- M
- Eingang
- 04.01.2022
- Impfdatum
- 20.12.2021
- Beginn
- 31.12.2021
- Tage bis Beginn
- 11,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pruritus
Rash
Urticaria
Symptomtext
Started having Rash and Hives about 10 days after vaccine. It is aggressive and I got hives all over my body and it is very itchy. It's been 5 days and I am not getting any relief from over the counter Benadryl or Zyrtec. Been applying ointments and also took steroids but none are working.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- Had a virtual visit online. Dr. did not ask about any vaccine info but prescribed steroids for hives. I later realized it is due to Covid vaccine as my sister who got vaccine around the same time who lives in another state and took same vaccine started having the same symptoms. I think doctors should also be educated on these side effects and should enquire about vaccine during the visit.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Dutasteride 0.5 mg for hair loss.
- Allergien
- Pollen Allergy
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 04.01.2022
- Impfdatum
- 21.12.2021
- Beginn
- 02.01.2022
- Tage bis Beginn
- 12,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Rash pruritic
Urticaria
Symptomtext
Experiencing itchy hives/rashes throughout my body that started on 01/02/2022. Started below my knee and has slowly gone up to groin area, back, and neck. I have taken Fexofenadine which has helped a little bit and hydrocortisone cream which prevents me from itching. Will try Claritin and Benadryl next,
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Junel 1.5/30
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 04.01.2022
- Impfdatum
- 29.12.2021
- Beginn
- 29.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Cellulitis
Erythema
Injection site pruritus
Injection site swelling
Symptomtext
Patient received her vaccination and by that evening her injection side was slightly raised and itchy. She used benadryl spray to try to alleviate the itching. The redness spread down her arm and when she was seeing her heart doctor they recommended getting seen by her primary doctor and letting the pharmacy know of the reaction. Her primary doctor didn't have any availability to see her so on 1/3/21 she went to the urgent care center. They prescribed her Duricef 500mg. They diagnosed her with cellulitis. Her first dose was at 1pm on 1/4/22. So far she hasn't not experienced any fever.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- pepcid 40mg, prilosec 20mg, zoloft 25mg, klor con 20meq, requip 0.25mg, zoloft 50mg, eliquis 5mg, lipitor 10mg, aspirin 81mg, torsemide 20mg, trelegy, synthroid 150mcg, toprol xl 100mg.
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 04.01.2022
- Impfdatum
- 03.01.2022
- Beginn
- 03.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Urticaria
Symptomtext
Pt. developed HIVES.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Asthma, Seasonal Allergies, Hypertension
- Andere Medikamente
- Lisinopril, Adderall,
- Allergien
- Seafood, Kiwi, Latex, Coconut, Ambien, Ultraset
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 03.01.2022
- Impfdatum
- 24.12.2021
- Beginn
- 26.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Ear discomfort
Lymph node palpable
Lymphadenitis
Lymphadenopathy
Pyrexia
Tinnitus
Symptomtext
about 24 to 36 hours after vaccination, after a low grade fever and some chills, I developed a large lump under my left armpit. This large swelling remained for about a week, and once it diminished, there is still palpable inflamation of lymphnodes and tissues under arm. Additionally, about 1 week after vaccine, significant Tinnitus and a feeling of pressure in the left ear started, and is still continuing
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Thyroid Cancer, currently.
- Andere Medikamente
- Vitamin D3, Probiotics, Beef Liver supplement
- Allergien
- none known
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 03.01.2022
- Impfdatum
- 29.12.2021
- Beginn
- 29.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Nausea
Symptomtext
Client received her booster dose COVID Moderna vaccine on 12/29/2021 at approximately 1100 in the L deltoid. At 1110, the client reported to EMT in the observation area that she was feeling nauseous. EMT notified Lead RN offered client emesis bag, water, and saltine crackers and assessed the client while EMT took vitals. Clients vitals at 1114 were BP 114/78, HR 72, SPO2 99%, and RR 16. Client denied SOB, dizziness, pain, and altered vision. Client reported that her last intake was a smoothie in the morning. Client reported her nausea onset was approximately 5 minutes after receiving the vaccine and denied experiencing nausea prior to receiving the vaccine. Client denied experiencing an adverse reaction after her 1st dose COVID Pfizer vaccine on 04/15/2021 and 2nd dose COVID Pfizer vaccine on 08/06/2021. At 1124 the client reported to EMT that she wanted fresh air and stated she was going to take a walk in the hallway of the building. EMT advised the client to remain in observation but client declined recommendation. The client returned to observation after approximately 5 minutes later. Client reported to EMT that her nausea had subsided and she "feels fine now". Client stated her husband will drive her home. RN educated on ER precautions and when to follow up with her PCP. Client left vaccine site at approximately 1135.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 02.01.2022
- Impfdatum
- 18.12.2021
- Beginn
- 28.12.2021
- Tage bis Beginn
- 10,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lip swelling
Maternal exposure during breast feeding
Pruritus
Swelling of eyelid
Urticaria
Symptomtext
Generalized urticaria began 10 days after Moderna booster. Also experienced swollen lip and eyelids. Still experiencing extremely itchy hives all over body. Not yet resolved. Treating with Zyrtec and a short course of prednisone
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Cold
- Vorgeschichte
- None (But currently breastfeeding)
- Andere Medikamente
- Daily multivitamin
- Allergien
- Allergic to penicillin
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 34,0
- Geschlecht
- M
- Eingang
- 02.01.2022
- Impfdatum
- 21.12.2021
- Beginn
- 01.01.2022
- Tage bis Beginn
- 11,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash pruritic
Symptomtext
Broke out in itchy skin rash at various parts of my body. Mostly upper body / head and neck area. No remedy yet.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash pruritic
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 02.01.2022
- Impfdatum
- 29.12.2021
- Beginn
- 31.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dysgeusia
Headache
Lymph node pain
Symptomtext
lymph nodes in left underarm quite tender and painful - this is the most disturbing and uncomfortable side effect bad taste in mouth (like I've smoked a cigar), no amount of tooth brushing will eliminate it slight headache
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- recovering from a lingering sinus infection; had completed a course of augmentin the week of Christmas
- Vorgeschichte
- arthritis
- Andere Medikamente
- n/a
- Allergien
- Sulfa
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 02.01.2022
- Impfdatum
- 29.12.2021
- Beginn
- 29.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Heart rate increased
Symptomtext
Patient reported feeling dizzy and short of breath 15 minutes after vaccine was given while sitting in the observation area. SHe was placed in an anti gravity chair, given a bottle of water, and vitals were taken. Her HR was slightly increased HR: 101, BP: 133/77, O2: 98%. Patient has a history of panic and anxiety disorder. She stated she felt better at 12:10 PM. She was alert and oriented times 4 the entire time while in the observation area. Vitals were taken at 12:10 PM and were as follows: HR: 97, BP: 119/80, and O2: 98%. She left the observation area with a steady gait and was advised to follow up her primary care provider. She did not have any reaction with her first 2 doses of Moderna.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Birth Control and Fluoxetine
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 01.01.2022
- Impfdatum
- 29.12.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain upper
Diarrhoea
Fatigue
Headache
Injection site pain
Injection site swelling
Pain
Pyrexia
Symptomtext
Started with aches, pain at injection site, and fatigue. 2nd day fatigue, diarrhea, stomach pain and noticeable swelling at injection site, third day fever and slight headache.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain upper
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- COPD, EMPHEZMA
- Andere Medikamente
- Zoloft, omneprazole
- Allergien
- Cipron
- Vorherige Impfungen
- Moderna covid 2
- Staat
- TN
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 31.12.2021
- Impfdatum
- 28.12.2021
- Beginn
- 28.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Body temperature
Eye pain
Myalgia
Pyrexia
Symptomtext
My eyes hurt; Aching in my hand/aching in my elbow/aching in my back/I felt achy all over/I felt achy in my joints/I felt achy in my muscles; Fever of 101F for 1 day; This spontaneous case was reported by a consumer and describes the occurrence of EYE PAIN (My eyes hurt), PYREXIA (Fever of 101F for 1 day) and MYALGIA (Aching in my hand/aching in my elbow/aching in my back/I felt achy all over/I felt achy in my joints/I felt achy in my muscles) in a 59-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 070H21A) for COVID-19 vaccination. Previously administered products included for COVID-19 vaccination: Pfizer Covid-19 vaccine (Patient had doses of the Pfizer Covid-19 vaccine) in April 2020. Past adverse reactions to the above products included No adverse event with Pfizer Covid-19 vaccine. On 28-Dec-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 28-Dec-2021, the patient experienced PYREXIA (Fever of 101F for 1 day). On 29-Dec-2021, the patient experienced EYE PAIN (My eyes hurt) and MYALGIA (Aching in my hand/aching in my elbow/aching in my back/I felt achy all over/I felt achy in my joints/I felt achy in my muscles). The patient was treated with PARACETAMOL (TYLENOL [PARACETAMOL]) for Fever, at an unspecified dose and frequency and IBUPROFEN (ADVIL [IBUPROFEN]) at an unspecified dose and frequency. On 29-Dec-2021, PYREXIA (Fever of 101F for 1 day) had resolved. At the time of the report, EYE PAIN (My eyes hurt) and MYALGIA (Aching in my hand/aching in my elbow/aching in my back/I felt achy all over/I felt achy in my joints/I felt achy in my muscles) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 28-Dec-2021, Body temperature: 101f (High) fever of 101F. No Concomitant Products were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Eye pain
- Hospital-Tage
- -
- Labordaten
- Test Date: 20211228; Test Name: Body temperature; Result Unstructured Data: fever of 101F
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 31.12.2021
- Impfdatum
- 21.12.2021
- Beginn
- 21.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Diplopia
Eye swelling
Pain in extremity
Peripheral swelling
Rash
Skin warm
Symptomtext
Day 1 Sore arm, Day 2 sore, hot, swollen, spread to armpit that continues to day 10, 4th day rash on forehead that spread to both eyes and made them swollen almost shut, Day 8 double vision in right eye
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- escitalopram, spiriva, nystatin, trazodone
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 31.12.2021
- Impfdatum
- 17.12.2021
- Beginn
- 28.12.2021
- Tage bis Beginn
- 11,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Pruritus
Swelling
Urticaria
Symptomtext
As happened with my 2nd Moderna vaccine, I developed hives a little over a week after the shot. Last time it was on my torso and feet with intense itching usually around 7-8 pm (I thought that the timing thing was really strange). This time around it manifested on my head, forearms, buttocks and, now, clavicle area. The itching was even more intense and then came the swelling of my head. I woke on the second day of this with swelling around my head, from the temple area, behind the ears and around the back of my head. It felt like the reaction I get to a bee sting, like a thick pad of something forming beneath my skin. I had taken a Benadryl before bed, then a Zyrtec in the morning to keep the itching at bay (with varying results). I iced the swollen area and the swelling subsided after an hour, but the temple are remained swollen. The swelling was moving too close to my eye for comfort, so I went to the local clinic to be examined. I was prescribed a steroid, which seems to have helped. The only itching and hives are now around my neck/clavicle area.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Levaquin
- Vorherige Impfungen
- 02/03/21 Moderna 010M20A (Mall Site), age 56, Itching/hives - torso and feet, no swelling lasting more than 1 week, but bearable
- Staat
- CA
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 31.12.2021
- Impfdatum
- 27.12.2021
- Beginn
- 27.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site bruising
Injection site erythema
Injection site swelling
Symptomtext
Site: Bruising at Injection Site-Mild, Site: Redness at Injection Site-Mild, Site: Swelling at Injection Site-Mild
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site bruising
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 31.12.2021
- Impfdatum
- 26.12.2021
- Beginn
- 27.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Eye swelling
Mouth swelling
Pruritus
Rash
Swelling face
Symptomtext
Systemic: Allergic: Itch (specify: facial area, extremeties)-Severe, Systemic: Allergic: Itch Generalized-Severe, Systemic: Allergic: Rash (specify: facial area, extremeties)-Severe, Systemic: Allergic: Rash Generalized-Severe, Systemic: Allergic: Swelling of Face / Eyes / Mouth / Tongue-Medium, Additional Details: Patient has received booster shot on 12/26/2021. Patient called on 12/29/21 stating that he expereinced severe swelling and itch of his whole body and face on morning of 12/27/2021. Pt stated that he has been using cortisone and eczema creams to help with the itch and swelling since that time and symtoms did get better by 12/29/21, but there still was moderate swelling and onstatnt itch. I did advise patient to see a dr and go to the ER if symtoms get worse. Symptoms are better on 12/30/21.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 30.12.2021
- Impfdatum
- 20.12.2021
- Beginn
- 21.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Burning sensation
Pruritus
Rash
Urticaria
Symptomtext
Eight days following my booster shot, (the evening of Tuesday, December 20) I experienced a break out of hives and rashes in various spots around my body. These breakouts itched badly. Since that evening, I have experienced continual breakouts of rashes and/or hives that itch and/or burn. They appear in large patches or as streaks across my skin. They can appear anywhere, but mostly appear around my scalp, ears, neck, shoulders, and back. I've also experienced them on my arms, hands, legs, stomach, and face. I can tell when a new rash will appear because I feel a slight burning that increases as time goes on. Since they've appeared, I have been using Zyrtec or Benadryl to keep symptoms at bay. These help but do not fully relieve symptoms. I am also using anti-itch lotion and ice to help control the uncomfortable symptoms. I have been in contact with my doctor via e-mail and she has prescribed me hydroxyzine and prednisone, but I have yet to take them.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- I have not been seen yet, but will visit with my doctor on Monday, if symptoms have not improved.
- Aktuelle Erkrankungen
- I had a cold about 4 weeks prior.
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 46,0
- Geschlecht
- M
- Eingang
- 30.12.2021
- Impfdatum
- 21.12.2021
- Beginn
- 23.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pruritus
Rash
Rash erythematous
Symptomtext
Systemic: Allergic: Itch (specify: facial area, extremeties)-Mild, Systemic: Allergic: Rash (specify: facial area, extremeties)-Mild, Additional Details: Patient complains of red, and itchy rashes on his left arm extending above and below is elbow. Patient states that the rashes appeared 2 days after Moderna booster was administered and has not gone away. I counseled patient to take OTC antihistamine and topical steroid (hydrocortisone) and to refer to doctor if symptoms don't improve in the next couple days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 29.12.2021
- Impfdatum
- 29.12.2021
- Beginn
- 29.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Symptomtext
PATIENT FELT DIZZINESS POST VACCINATION
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 29.12.2021
- Impfdatum
- 27.12.2021
- Beginn
- 27.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Dizziness
Feeling cold
Nervousness
Vision blurred
Symptomtext
Client received the Booster COVID vaccine (Moderna, Lot #070H21A, exp 4/7/2022) at approximately 1220. At 1259, re-entered the observation room after leaving notifying Observation RN, and Co-Lead that when she left the building she started feeling dizzy and having some blurry vision. At 1300 Client was seated in the anti-gravity chair and vitals assessed (BP 122/67, P 60, color wnl). Client reports she had not eaten breakfast or lunch today. Client was provided water and snacks. Client has hypothyroidism and takes 44 mg synthroid daily. Client denies any allergies. At 1309 Client states she's feeling shaky/chills and lightheaded but no longer experiencing blurry vision. Client provided juice and tolerating. At 1317 vitals assessed (BP 114/77, P 62, color wnl). Client feels cold but no other symptoms at this time. At 1327 Client reports feeling better and ready to leave. Vitals assessed (BP116/69, P 63, color wnl). Client educated on signs/symptoms when to seek medical care and to follow-up with primary care provider. Client left with steady gait and with mother present.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- hypothyroidsim
- Andere Medikamente
- Synthroid 44mg
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 29.12.2021
- Impfdatum
- 29.12.2021
- Beginn
- 29.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Rash pruritic
Symptomtext
Approximately thirty minutes post vaccination, pt reported feeling an itchy rash on the back of her neck and palm of her hands. After approximately 20 minutes, with no resolution in symptoms, the decision was made to administer a 25 mg tablet of PO Benadryl. Approximately 20 minutes later, pt reported relief in itchy rash as well as observation of resolution of rash on the neck.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Pt reports history of atopic dermatitis
- Andere Medikamente
- -
- Allergien
- Pt reports allergy to doxycycline, pollen, dust mites, shellfish, cockroaches.
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 28.12.2021
- Impfdatum
- 20.12.2021
- Beginn
- 20.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Asthenia
Feeling abnormal
Hyperhidrosis
Pain
Pyrexia
Speech disorder
Vomiting
Symptomtext
Patient called on 12/21/2021 and reported that she developed fever and bodyache on 12/20/2021 after receiving Moderna full dose (dose # 3) yesterday (had J&J vaccine previously), also started vomiting. Woke up on 12/21/2021 morning, not feeling better. Still feels feverish, profuse sweating, severe bodyache and weakness. No chest pain or SOB but unable to speak in fluid sentences, sounds out of breath.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 25.12.2021
- Impfdatum
- 16.12.2021
- Beginn
- 23.12.2021
- Tage bis Beginn
- 7,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Headache
Lymphadenopathy
Pyrexia
Rash
Symptomtext
Chills, several nights Fever: 100.4 3 days Rash on arm (left) Swollen glands on left side if body since vaccine Headache
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- PCN, sulfa
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 25.12.2021
- Impfdatum
- 23.12.2021
- Beginn
- 24.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Blood pressure increased
Fatigue
Headache
Injection site pain
Myalgia
Pyrexia
Symptomtext
Systemic muscle aches Systemic joint pain Fever 99.4 degrees Mild headache Fatigue Elevated blood pressure 145/85 Injection site soreness Symptoms began within 24 hours and peaked at 30 hours. Muscle and joint pain continues at 40 hours.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Advil Vitamin D Zyrtec
- Allergien
- None
- Vorherige Impfungen
- Injection site soreness
- Staat
- NY
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 24.12.2021
- Impfdatum
- 21.12.2021
- Beginn
- 22.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Breast swelling
Chills
Lymphadenopathy
Nausea
Pain
Pyrexia
Rash
Symptomtext
I had nausea, 102 degree fever, chills, aches and my lymph nodes on my right-side swelled up significantly. I also have a rash at the top of my shoulder and upper arm. My lymph nodes in my chest area have swelled significantly as well. My right breast is also swollen. The pharmacy recorded the shot being placed in my left arm but that is not correct, it was my right arm. After my 2nd shot of the Moderna vaccine, I had all of these symptoms as well but the swelling of the lymph nodes is much more significant. After the 2nd shot, my lymph nodes remained swollen for 4-6 weeks.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Stage 1 breast cancer survivor (2011). Had lumpectomy and radiation.
- Andere Medikamente
- Tamoxifen 20mg, OTC multivitamin and calcium supplement
- Allergien
- None
- Vorherige Impfungen
- Moderna shot #2. Same as current AEs but lymph nodes swelling was much less significant.
- Staat
- IN
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 24.12.2021
- Impfdatum
- 22.12.2021
- Beginn
- 23.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site indentation
Injection site swelling
Injection site warmth
Symptomtext
Stolen hard arm at injection site. Pinkish and warm to the touch
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- IPF
- Andere Medikamente
- Esbrie Eliquis Pravastatin
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 23.12.2021
- Impfdatum
- 21.12.2021
- Beginn
- 22.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site pain
Injection site pruritus
Injection site reaction
Injection site swelling
Injection site warmth
Urticaria
Symptomtext
A welt about 4inches from top to bottom and about 6 inches from side to side on my arm at injection site. Swelling, hot to touch, tight extremely itchy and painful.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma
- Andere Medikamente
- 40mg Nexium daily 75mg Diclofenac daily 50,000mg Vitamin D every 7 days 10ml Sucralfate oral suspension before lunch and dinner
- Allergien
- None
- Vorherige Impfungen
- 2nd covid vaccine same reaction that lasts about 2 weeks.
- Staat
- NJ
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 23.12.2021
- Impfdatum
- 19.12.2021
- Beginn
- 19.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site warmth
Pruritus
Rash
Symptomtext
Systemic: Allergic: Itch Generalized-Severe, Systemic: Allergic: Rash (specify: facial area, extremeties)-Severe, Systemic: skin is hot to touch around injection site-Severe, Additional Details: mom (NAME) called about daughter (NAME) . Mom cell is (PRIVACY). Pt's ph# (PRIVACY). I advised mom pt. is over 18 years old and may be point of contact. Pt got rash on arm and injection site is hot to touch. Advised mom to follow up with primary care doctor.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site warmth
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 23.12.2021
- Impfdatum
- 20.12.2021
- Beginn
- 21.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site pruritus
Injection site swelling
Pain
Rash
Swelling
Symptomtext
Site: Itching at Injection Site-Mild, Site: Redness at Injection Site-Mild, Site: Swelling at Injection Site-Mild, Systemic: Allergic: Rash Generalized-Mild, Additional Details: Rash swelling local pain
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 23.12.2021
- Impfdatum
- 21.12.2021
- Beginn
- 21.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Chills
Injection site pain
Malaise
Myalgia
Pyrexia
Vaccine positive rechallenge
Vertigo
Symptomtext
Symptoms began approximately 8 hours after the injection. Injection site pain, fever, chills, vertigo, headache, joint pain, muscle aches. Now 43 hours post injection & still very sick feeling.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- possible auto-immune disease (cutaneous Lupus) - I'm being tested to rule out other issues
- Andere Medikamente
- none
- Allergien
- latex, sulfa drugs
- Vorherige Impfungen
- covid shot #2 - same reactions & symptoms, age 40. Varicella zoster vaccine - reaction- swollen arm, rash, fever, pain, age 39
- Staat
- CA
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 22.12.2021
- Impfdatum
- 22.12.2021
- Beginn
- 22.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Flushing
Pruritus
Symptomtext
Pt received her Moderna 0.25 ml booster shot today at 0954. Pt began to experience flushing to neck and chest area, coupled with severe itching within ten mins of receiving injection. Pt was brought to triage area. Vital signs were taken and WNL. No c/o of SOB or dizzyness. Notified Dr and recvd verbal order for Zyrtec 10mg dissolvable tab PO x 1. Admin medication at 1014 and Vitals retaken 15mins later. Vitals retaken at 1045,VSS, redness and itching resolved. Pt D/Cd home and advised to monitor to a return of symptoms or SOB and act accordingly.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- na
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 22.12.2021
- Impfdatum
- 17.12.2021
- Beginn
- 17.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Ageusia
Anosmia
Chills
Cough
Injection site reaction
Nasopharyngitis
Pyrexia
Rash macular
Skin warm
Wheezing
Symptomtext
Cold chills and fever starting Friday night by saturday afternoon had red blotches on arm at injection site.. cold symptoms came on along with a cough arm became hot to the touch it is Wednesday now and fever broke yesterday but red and heated arm is still there as are the cough and wheezing . Sense of taste and smell are off.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- -
- Andere Medikamente
- None
- Allergien
- Morphine
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 22.12.2021
- Impfdatum
- 20.12.2021
- Beginn
- 20.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Interchange of vaccine products
Symptomtext
Site: Redness at Injection Site-Mild, Additional Details: Pt got the Moderna booster shot 0.25ml on 12/20/21. Pt was suppose to get Pfizer booster shot 0.3ml. Pt received 2 COVID SHIELD vaccines. The 2nd covid shot was on 7/17/21. Pt was scheduled to have a Moderna booster shot at Pharmacy. There was a miscommunication from Pharmacy side to store side on what vaccine to give patients. *Pt did not have any side effects at injection sites. * Only side effects listed above.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 22.12.2021
- Impfdatum
- 20.12.2021
- Beginn
- 20.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Interchange of vaccine products
Symptomtext
Site: Redness at Injection Site-Mild, Additional Details: Pt got the Moderna booster shot 0.25ml on 12/20/21. Pt was suppose to get Pfizer booster shot 0.3ml. Pt received 2 COVID SHIELD vaccines. The 2nd covid shot was on 7/17/21. Pt was scheduled to have a Moderna booster shot at Pharmacy. There was a miscommunication from Pharmacy side to store side on what vaccine to give patients. *Pt did NOT have any side effects at injection sites. * Only side effects listed above.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 21.12.2021
- Impfdatum
- 19.12.2021
- Beginn
- 20.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Chills
Fatigue
Hyperhidrosis
Hypersomnia
Pyrexia
Symptomtext
I received a vaccination as it was the soonest available. 12-13 hours after the booster, I awoke to fever, sweats and chills. It was more mild than my second dose of Pfizer but persisted longer. I awoke to a fever of 101.5 at 4 am, which is when I took Tylenol. For most of the day, I had a low-grade fever, sweating and general fatigue. I took the day off. I felt generally weak/tired. I slept most of the morning and afternoon. Around 6 pm, I felt back to normal but still a bit weak.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Vitamin D, Multivitamin, Omega-3
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 21.12.2021
- Impfdatum
- 17.12.2021
- Beginn
- 17.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Eye swelling
Injection site pruritus
Lymphadenopathy
Mouth swelling
Pain
Swelling face
Swollen tongue
Symptomtext
Site: Itching at Injection Site-Medium, Systemic: Allergic: Swelling of Face / Eyes / Mouth / Tongue-Medium, Systemic: Body Aches Generalized-Medium, Systemic: Lymph Node Swelling-Medium, Additional Details: PT SEEING DR 12/21/2021
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 21.12.2021
- Impfdatum
- 17.12.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Feeding disorder
Feeling cold
Headache
Myalgia
Pyrexia
Thirst
Symptomtext
unable to eat after booster; feeling cold after booster; Feeling thirsty all the time after booster; after the booster dose: fever 102.8?F; headache persistent after Tylenol after booster; body ache persistent after Tylenol after booster; chills after booster; This spontaneous case was reported by a consumer and describes the occurrence of FEEDING DISORDER (unable to eat after booster), FEELING COLD (feeling cold after booster), THIRST (Feeling thirsty all the time after booster), PYREXIA (after the booster dose: fever 102.8?F) and HEADACHE (headache persistent after Tylenol after booster) in a 39-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 070H21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concurrent medical conditions included Constipation. Concomitant products included MACROGOL 3350 (MIRALAX) for Constipation. On 17-Dec-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced FEEDING DISORDER (unable to eat after booster), FEELING COLD (feeling cold after booster), THIRST (Feeling thirsty all the time after booster), PYREXIA (after the booster dose: fever 102.8?F), HEADACHE (headache persistent after Tylenol after booster), MYALGIA (body ache persistent after Tylenol after booster) and CHILLS (chills after booster). The patient was treated with PARACETAMOL (TYLENOL [PARACETAMOL]) for Fever, at an unspecified dose and frequency. At the time of the report, FEEDING DISORDER (unable to eat after booster), FEELING COLD (feeling cold after booster), THIRST (Feeling thirsty all the time after booster), PYREXIA (after the booster dose: fever 102.8?F), HEADACHE (headache persistent after Tylenol after booster), MYALGIA (body ache persistent after Tylenol after booster) and CHILLS (chills after booster) outcome was unknown. No concomitant medications were reported. Patient also states that she has constipation issues, that in October it was very serious and started taking Miralax. She even saw a doctor a couple of times due to this. This case was linked to MOD-2021-418185 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Constipation
- Vorgeschichte
- -
- Andere Medikamente
- MIRALAX
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 20.12.2021
- Impfdatum
- 20.12.2021
- Beginn
- 20.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Hypoaesthesia oral
Impaired work ability
Lip swelling
Pruritus
Swollen tongue
Vaccine positive rechallenge
Symptomtext
Patient presented to clinic for booster dose of Moderna vaccine. Patient successfully vaccinated. Post waiting period patient reports itchiness, numbness and swelling in her tongue and upper lip. Rapid Response activated. Patient denies difficulty breathing, respiratory distress or any other symptoms. Patient is otherwise stable and oriented to person, place, and time. Provider Dr notified and assessment complete. 1:30 vitals 124/80 HR 63. 02 98%. Patient reports that she can feel her tongue. Vitals at 1:37pm. BP 147/90 HR 62. 02 98% (elevated by reading most likely due to patient talking and moving during this reading). Vitals at 1:52pm 125/80. HR 60. 02 95%. Temp 97.9. Patient reports resolution of itchiness stating "I just feel a little itchy on my back and no where else". Patients resolution of symptoms is reassuring. Hx: Patient experienced same symptoms after her 1 dose of Moderna vaccine in January. Per patient symptoms lasted 3 days. 2nd dose in Feb no adverse symptoms, Booster dose today symptomatic. Patient is stable at this time. Walking, talking, and laughed with RN. Ok for discharge at this time per provider. Patient released to her son who will take her home and monitor. Patient excused for X2 days from work due to return 12/22/2021. Son and patient advised If itchiness/swelling persist patient can take OTC Benadryl. If symptoms worsen or patient develops difficulty breathing or respiratory distress to head straight to the ER. Son and patient verbalized understanding. No other questions or concerns.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- HTN
- Andere Medikamente
- Losartan Levothyroxine Cholesterol medication
- Allergien
- Penecillins, Eggs, dust, pets, seasonal allergies, fish, Sun
- Vorherige Impfungen
- Per patient , she experienced tongue and lip swelling as well as itching at first dose of vaccination with Moderna Vaccine.
- Staat
- -
- Alter
- 42,0
- Geschlecht
- M
- Eingang
- 20.12.2021
- Impfdatum
- 13.12.2021
- Beginn
- 13.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Dizziness
Symptomtext
2mins post vaccination pt reported feeling faint. Vitals: 109/61, 65, 19, 98% -- > 14:40 119/73, 68, 18, 98% By 14:40 pt's symptoms improved. Pt stable and released from the vaccination site. Pt was escorted to the exit door @14:51.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Pt denies any significant PMH
- Andere Medikamente
- None
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 19.12.2021
- Impfdatum
- 18.12.2021
- Beginn
- 19.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site pain
Injection site pruritus
Injection site rash
Injection site swelling
Symptomtext
Swelling and rash at the injection site. Also sore, itchy and pain. Itchiness started a few hours after injection, other symptoms a day after injection. Took Tylenol the day after for pain
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- birth control
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 17.12.2021
- Impfdatum
- 16.12.2021
- Beginn
- 17.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest discomfort
Feeling cold
Pain
Pain in extremity
Symptomtext
Per patient she was in the third floor in the dentist office and decided to come to second floor and report it to the nurse. Per patient she has body ache, feels very cold, left arm is very sore, and pressure in the chest rated it at 6/10. Vital Signs Temperature 98.0, Pulse 97, Respiration 20, Blood Pressure 130/89, Oxygen saturation 97%. Patient is alert x4 and verbally responsive. No shortness of breath noted. No complain of nausea, vomiting, diarrhea. Reported to Dr, and to let patient know it is okay for patient to wait as a walk in to be seen by a provider in the afternoon session or go home and monitor, give ER precautions, and okay to take Tylenol. Per patient, decline to wait for the afternoon session as she had other obligations/appointments to attend this afternoon already. I gave patient paperwork information about Moderna vaccine and VAERS paperwork. ER precautions strongly advise the patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- Epilepsy, Severe Depression, panic Disorder, mammography Abnormal, Benign Neoplasm of Kidney, fatty Liver, Hyperlipidemia, Gastroduodenitis, Migraine without Aura, Dysfuntional Uterine Bleeding, Lichenification of vulva, Carpal Tunnel syndrome, BMIA 30+, back strain of thorasic region, cervical radiculopathy,, degeneration of cervical intervertebral disc, history of covid-19 infection
- Andere Medikamente
- N/A
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 17.12.2021
- Impfdatum
- 13.12.2021
- Beginn
- 14.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Headache
Influenza
Nodule
Pain
Pain in extremity
Tenderness
Symptomtext
12/13 6:00pm received my Maderna Booster at Pharmacy in left arm 12/13 9:00pm left arm started hurting badly and felt pain all night while trying to sleep 12/14 All day had very bad flu symptoms of chills, head ache and body ache; by late evening around 9pm I was finally feeling better; Even my arm wasn't as sore but I had pain travel to my left clavicle and felt a "large blueberry" size nodule on my clavicle about 1 inch from the end of my clavicle nearest my shoulder. The pain on my clavicle was tender to touch. 12/17 The nodule remains on my clavicle and is tender to touch. Arm pain gone.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- allergies to dust and pollen causing nasal drip causes dry cough
- Andere Medikamente
- metoprolol tartrate 50mg linsinopril 10mg Bayer low dose asprin
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 17.12.2021
- Impfdatum
- 15.12.2021
- Beginn
- 15.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Axillary pain
Chills
Headache
Nausea
Pain in extremity
Pyrexia
Symptomtext
Left arm , leg, armpit pain. Headache nauseated. dec 16 feel most of joints pain, mild chill headache and nauseated, Fever 102.5. Tylenol 1000 mg rapids relief. Cold pack one hour go down to 101.x. Couple hours later go to 100.1 Dec 17. Temp 99.5 this morning. Still headache.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Hypertension
- Andere Medikamente
- No
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 87,0
- Geschlecht
- M
- Eingang
- 15.09.2023
- Impfdatum
- 12.01.2022
- Beginn
- 11.09.2023
- Tage bis Beginn
- 607,0
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Asthenia
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- F
- Eingang
- 12.09.2023
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Product storage error
Symptomtext
VACCINE GIVEN AFTER EXPIRATION DATE DUE TO TEMPERATURE CHANGE IN STORAGE; VACCINE GIVEN AFTER EXPIRATION DATE DUE TO TEMPERATURE CHANGE IN STORAGE; no adverse event; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (VACCINE GIVEN AFTER EXPIRATION DATE DUE TO TEMPERATURE CHANGE IN STORAGE), PRODUCT STORAGE ERROR (VACCINE GIVEN AFTER EXPIRATION DATE DUE TO TEMPERATURE CHANGE IN STORAGE) and NO ADVERSE EVENT (no adverse event) in a female patient of an unknown age who received mRNA-1273 (Spikevax) (batch no. 070H21A) for COVID-19 prophylaxis. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Spikevax) (Intramuscular use) 1 dosage form. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (VACCINE GIVEN AFTER EXPIRATION DATE DUE TO TEMPERATURE CHANGE IN STORAGE), PRODUCT STORAGE ERROR (VACCINE GIVEN AFTER EXPIRATION DATE DUE TO TEMPERATURE CHANGE IN STORAGE) and NO ADVERSE EVENT (no adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (VACCINE GIVEN AFTER EXPIRATION DATE DUE TO TEMPERATURE CHANGE IN STORAGE), PRODUCT STORAGE ERROR (VACCINE GIVEN AFTER EXPIRATION DATE DUE TO TEMPERATURE CHANGE IN STORAGE) and NO ADVERSE EVENT (no adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Intramuscular use), the reporter considered NO ADVERSE EVENT (no adverse event) to be not related. No further causality assessments were provided for EXPIRED PRODUCT ADMINISTERED (VACCINE GIVEN AFTER EXPIRATION DATE DUE TO TEMPERATURE CHANGE IN STORAGE) and PRODUCT STORAGE ERROR (VACCINE GIVEN AFTER EXPIRATION DATE DUE TO TEMPERATURE CHANGE IN STORAGE). Concomitant product use was not provided by the reporter. It was unknown if the patient experienced any additional symptoms/events. Treatment information was not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- -
- Geschlecht
- U
- Eingang
- 11.09.2023
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No Adverse event; HCP states that they administered 16 shots to patients after their expiration date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (HCP states that they administered 16 shots to patients after their expiration date) and NO ADVERSE EVENT (No Adverse event) in a patient of an unknown age and gender who received mRNA-1273 (Spikevax) (batch no. 070H21A) for COVID-19 prophylaxis. No Medical History information was reported. In 2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) .5 milliliter. In 2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (HCP states that they administered 16 shots to patients after their expiration date). On an unknown date, the patient experienced NO ADVERSE EVENT (No Adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (HCP states that they administered 16 shots to patients after their expiration date) and NO ADVERSE EVENT (No Adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter considered NO ADVERSE EVENT (No Adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (HCP states that they administered 16 shots to patients after their expiration date). No concomitant medication was reported. Suspect product dosage text was reported as unknown. The intact cartons of 0.5 ml of were initially stored in the refrigerator and the thaw dates were the same as administration dates as 01-Sep-2022 ,25-Aug-2022, 04-Aug-2022, 26-Jul-2022 and 19-Jul-2022. The vial did not undergo any temperature excursions. No treatment medication was reported. It was unknown if patient received any other vaccines in the 4 weeks prior to COVID-19 vaccine. It was unknown if patient had any relevant medical history conditions, allergy, concomitant diseases and risk factor. This case contains information for patient 16 out of 16. This case was linked to US-MODERNATX, INC.-MOD-2023-739796 (E2B Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2023-739796:Master case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 82,0
- Geschlecht
- F
- Eingang
- 06.09.2023
- Impfdatum
- 01.04.2022
- Beginn
- 01.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
VACCINE GIVEN AFTER EXPIRATION DATE DUE TO TEMPERATURE CHANGE IN STORAGE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 14.08.2023
- Impfdatum
- 20.12.2021
- Beginn
- 12.03.2022
- Tage bis Beginn
- 82,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Obstructive sleep apnoea syndrome
Symptom recurrence
Symptomtext
ADULT OBSTRUCTIVE SLEEP APNEA 3/13/2022 & 4/15/2022 -- RECURRENCE OF HOSPITALIZATION WITH SAME SYMPTOMS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Obstructive sleep apnoea syndrome
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 09.08.2023
- Impfdatum
- 12.01.2022
- Beginn
- 02.06.2022
- Tage bis Beginn
- 141,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Hypersensitivity
Neuropathy peripheral
Symptomtext
NEUROPATHY HYPERSENSITIVITY REACTION, SUBSEQ
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypersensitivity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 08.08.2023
- Impfdatum
- 01.02.2022
- Beginn
- 18.01.2023
- Tage bis Beginn
- 351,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Epilepsy
Symptomtext
EPILEPSY, UNSPECIFIED
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Epilepsy
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 91,0
- Geschlecht
- F
- Eingang
- 31.05.2023
- Impfdatum
- 14.12.2021
- Beginn
- 12.04.2023
- Tage bis Beginn
- 484,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case admission after 3 vaccines ; Pfizer 3/17/21 lot# EN6207; Pfizer 4/7/21 lot# EW0150; Moderna 12/14/21 lot# 070H21A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 28.02.2023
- Impfdatum
- 22.12.2021
- Beginn
- 24.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case admission after 3 vaccines Moderna 3/15/21 Lot#030A21A; Moderna 4/12/21 Lot# 018B21A; Moderna 12/22/21 Lot# 070H21A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 23.02.2023
- Impfdatum
- 15.12.2022
- Beginn
- 15.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 23.02.2023
- Impfdatum
- 08.12.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 23.02.2023
- Impfdatum
- 21.11.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 32,0
- Geschlecht
- M
- Eingang
- 23.02.2023
- Impfdatum
- 21.11.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 14,0
- Geschlecht
- F
- Eingang
- 23.02.2023
- Impfdatum
- 08.11.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 23.02.2023
- Impfdatum
- 22.09.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 23.02.2023
- Impfdatum
- 05.09.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 23.02.2023
- Impfdatum
- 25.08.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 23.02.2023
- Impfdatum
- 24.08.2022
- Beginn
- 24.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 37,0
- Geschlecht
- M
- Eingang
- 23.02.2023
- Impfdatum
- 23.08.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 18,0
- Geschlecht
- M
- Eingang
- 23.02.2023
- Impfdatum
- 22.08.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 18,0
- Geschlecht
- M
- Eingang
- 23.02.2023
- Impfdatum
- 22.08.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 23.02.2023
- Impfdatum
- 22.08.2022
- Beginn
- 22.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 81,0
- Geschlecht
- M
- Eingang
- 23.02.2023
- Impfdatum
- 22.08.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 23.02.2023
- Impfdatum
- 18.08.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 23.02.2023
- Impfdatum
- 18.08.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 23.02.2023
- Impfdatum
- 17.08.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 23.02.2023
- Impfdatum
- 16.08.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 96,0
- Geschlecht
- M
- Eingang
- 23.02.2023
- Impfdatum
- 16.08.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 23.02.2023
- Impfdatum
- 15.08.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 23.02.2023
- Impfdatum
- 15.08.2022
- Beginn
- 15.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 40,0
- Geschlecht
- M
- Eingang
- 23.02.2023
- Impfdatum
- 11.08.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 23.02.2023
- Impfdatum
- 10.08.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 23.02.2023
- Impfdatum
- 08.08.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 23.02.2023
- Impfdatum
- 04.08.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 94,0
- Geschlecht
- M
- Eingang
- 23.02.2023
- Impfdatum
- 02.08.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 90,0
- Geschlecht
- F
- Eingang
- 23.02.2023
- Impfdatum
- 02.08.2022
- Beginn
- 02.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 23.02.2023
- Impfdatum
- 01.08.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 23.02.2023
- Impfdatum
- 01.08.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 23.02.2023
- Impfdatum
- 01.08.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 23.02.2023
- Impfdatum
- 26.07.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 23.02.2023
- Impfdatum
- 26.07.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 23,0
- Geschlecht
- M
- Eingang
- 23.02.2023
- Impfdatum
- 25.07.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 23.02.2023
- Impfdatum
- 25.07.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 23.02.2023
- Impfdatum
- 25.07.2022
- Beginn
- 25.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 23.02.2023
- Impfdatum
- 21.07.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 23.02.2023
- Impfdatum
- 21.07.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 18,0
- Geschlecht
- M
- Eingang
- 23.02.2023
- Impfdatum
- 20.07.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 23.02.2023
- Impfdatum
- 20.07.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 20,0
- Geschlecht
- M
- Eingang
- 23.02.2023
- Impfdatum
- 20.07.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 23.02.2023
- Impfdatum
- 19.07.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 23.02.2023
- Impfdatum
- 19.07.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 23.02.2023
- Impfdatum
- 19.07.2022
- Beginn
- 19.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 23.02.2023
- Impfdatum
- 19.07.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 23.02.2023
- Impfdatum
- 12.07.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 19,0
- Geschlecht
- M
- Eingang
- 23.02.2023
- Impfdatum
- 12.07.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 23.02.2023
- Impfdatum
- 12.07.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 23.02.2023
- Impfdatum
- 11.07.2022
- Beginn
- 11.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 45,0
- Geschlecht
- M
- Eingang
- 23.02.2023
- Impfdatum
- 11.07.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 23.02.2023
- Impfdatum
- 11.07.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 91,0
- Geschlecht
- F
- Eingang
- 23.02.2023
- Impfdatum
- 07.07.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 23.02.2023
- Impfdatum
- 07.07.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 23.02.2023
- Impfdatum
- 07.07.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 23.02.2023
- Impfdatum
- 07.07.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 23.02.2023
- Impfdatum
- 07.07.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 34,0
- Geschlecht
- M
- Eingang
- 23.02.2023
- Impfdatum
- 07.07.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 23.02.2023
- Impfdatum
- 07.07.2022
- Beginn
- 07.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 23.02.2023
- Impfdatum
- 07.07.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 23.02.2023
- Impfdatum
- 30.06.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 23.02.2023
- Impfdatum
- 30.06.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 23.02.2023
- Impfdatum
- 30.06.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 34,0
- Geschlecht
- M
- Eingang
- 23.02.2023
- Impfdatum
- 30.06.2022
- Beginn
- 30.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 23.02.2023
- Impfdatum
- 30.06.2022
- Beginn
- 30.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 23.02.2023
- Impfdatum
- 23.06.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 23.02.2023
- Impfdatum
- 16.06.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 23.02.2023
- Impfdatum
- 16.06.2022
- Beginn
- 16.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 23.02.2023
- Impfdatum
- 16.06.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 23.02.2023
- Impfdatum
- 28.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 23.02.2023
- Impfdatum
- 28.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 23.02.2023
- Impfdatum
- 28.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 23.02.2023
- Impfdatum
- 28.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 23.02.2023
- Impfdatum
- 28.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 23.02.2023
- Impfdatum
- 28.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 23.02.2023
- Impfdatum
- 28.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 39,0
- Geschlecht
- M
- Eingang
- 23.02.2023
- Impfdatum
- 28.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 23.02.2023
- Impfdatum
- 28.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 23.02.2023
- Impfdatum
- 14.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 23.02.2023
- Impfdatum
- 14.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 23.02.2023
- Impfdatum
- 14.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 14.02.2023
- Impfdatum
- 29.09.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 18,0
- Geschlecht
- M
- Eingang
- 14.02.2023
- Impfdatum
- 22.09.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
It was discovered on 12/20/2022 that the Moderna vaccine that was administered was expired. Contacted Moderna and was advised that the vaccine was still viable at this time, therefore the vaccine was considered a valid dose, and patient does not need to be re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 14.02.2023
- Impfdatum
- 14.01.2022
- Beginn
- 13.02.2023
- Tage bis Beginn
- 395,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Symptomtext
Patient vaccinated against then tested positive for COVID-19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 09.02.2023
- Impfdatum
- 07.02.2022
- Beginn
- 07.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Symptomtext
No adverse event, vaccine may have been expired
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 09.02.2023
- Impfdatum
- 18.02.2022
- Beginn
- 18.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Product storage error
Unevaluable event
Symptomtext
No adverse event, vaccine may have been expired
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 09.02.2023
- Impfdatum
- 18.02.2022
- Beginn
- 18.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Product storage error
Unevaluable event
Symptomtext
No adverse event, vaccine may have been expired
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 07.02.2023
- Impfdatum
- 31.01.2022
- Beginn
- 31.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Symptomtext
No adverse event, vaccine may have been expired
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 06.02.2023
- Impfdatum
- 05.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Symptomtext
No adverse event, vaccine may have been expired
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 30.01.2023
- Impfdatum
- 11.02.2022
- Beginn
- 11.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Product storage error
Symptomtext
No Adverse effect, expired vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 30.01.2023
- Impfdatum
- 11.02.2022
- Beginn
- 11.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Product storage error
Symptomtext
No Adverse effect, expired vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 26.12.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; Expired vaccine used; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vaccine used) and NO ADVERSE EVENT (No adverse event) in a 67-year-old male patient who received mRNA-1273 (Spikevax) (batch no. 070H21A) for COVID-19 prophylaxis. No Medical History information was reported. In 2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. In 2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vaccine used). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired vaccine used) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Expired vaccine used). The patients age was reported as 67 Year 7 Month. No concomitant medications were reported. The vaccine was administered to patient between 08-Apr-2022 and 15-Dec-2022. NDC ID: 80777027399 Treatment information was not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 26.12.2022
- Impfdatum
- 07.07.2022
- Beginn
- 07.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; Patient received the vaccine from an expired lot; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient received the vaccine from an expired lot) and NO ADVERSE EVENT (No adverse event) in a 35-year-old male patient who received mRNA-1273 (Spikevax) (batch no. 070H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 07-Jul-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 07-Jul-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient received the vaccine from an expired lot). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient received the vaccine from an expired lot) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Patient received the vaccine from an expired lot). No concomitant medication information was reported. The patient age was reported as 35 Year 0 Month. Patients at the facility received vaccine between 08Apr2022 and 15Dec2022. No treatment medication information was reported. NDC ID: 80777027399
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 26.12.2022
- Impfdatum
- 30.06.2022
- Beginn
- 30.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Past lot that had also been expired that was administered to patient) and NO ADVERSE EVENT (No adverse event) in a 68-year-old male patient who received mRNA-1273 (Spikevax) (batch no. 070H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 30-Jun-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 30-Jun-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Past lot that had also been expired that was administered to patient). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Past lot that had also been expired that was administered to patient) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Past lot that had also been expired that was administered to patient). No concomitant medications were reported. Treatment information was not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 18,0
- Geschlecht
- M
- Eingang
- 24.12.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
no adverse event; expired vaccine used/ Patients received this Moderna vaccine (lot 070H21A) between 8-Apr-2022 and 15-Dec-2022; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (expired vaccine used/ Patients received this Moderna vaccine (lot 070H21A) between 8-Apr-2022 and 15-Dec-2022) and NO ADVERSE EVENT (no adverse event) in an 18-year-old male patient who received mRNA-1273 (Spikevax) (batch no. 070H21A) for COVID-19 prophylaxis. No Medical History information was reported. In 2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. In 2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (expired vaccine used/ Patients received this Moderna vaccine (lot 070H21A) between 8-Apr-2022 and 15-Dec-2022). On an unknown date, the patient experienced NO ADVERSE EVENT (no adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (expired vaccine used/ Patients received this Moderna vaccine (lot 070H21A) between 8-Apr-2022 and 15-Dec-2022) and NO ADVERSE EVENT (no adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter considered NO ADVERSE EVENT (no adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (expired vaccine used/ Patients received this Moderna vaccine (lot 070H21A) between 8-Apr-2022 and 15-Dec-2022). Patient age was reported as 18 Year 11 Month. It was reported that lot 070H21A, that has an expiration date of 7-Apr-2022. Patients received this Moderna vaccine between 8-Apr-2022 and 15-Dec-2022. No concomitant medication were reported. No treatment medication were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 24.12.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
no adverse event; expired vaccine used/ Patients received this Moderna vaccine (lot 070H21A) between 8-Apr-2022 and 15-Dec-2022; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (expired vaccine used/ Patients received this Moderna vaccine (lot 070H21A) between 8-Apr-2022 and 15-Dec-2022) and NO ADVERSE EVENT (no adverse event) in a 65-year-old male patient who received mRNA-1273 (Spikevax) (batch no. 070H21A) for COVID-19 prophylaxis. No Medical History information was reported. In 2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. In 2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (expired vaccine used/ Patients received this Moderna vaccine (lot 070H21A) between 8-Apr-2022 and 15-Dec-2022). On an unknown date, the patient experienced NO ADVERSE EVENT (no adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (expired vaccine used/ Patients received this Moderna vaccine (lot 070H21A) between 8-Apr-2022 and 15-Dec-2022) and NO ADVERSE EVENT (no adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter considered NO ADVERSE EVENT (no adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (expired vaccine used/ Patients received this Moderna vaccine (lot 070H21A) between 8-Apr-2022 and 15-Dec-2022). Patient age was reported as 65 Year 05 Month. It was reported that lot 070H21A, that has an expiration date of 7-Apr-2022. Patients received this Moderna vaccine between 8-Apr-2022 and 15-Dec-2022. No concomitant medication were reported. No treatment medication were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 24.12.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
expired vaccine used/ Patients received this Moderna vaccine (lot 070H21A) between 8-Apr-2022 and 15-Dec-2022; no adverse event; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (expired vaccine used/ Patients received this Moderna vaccine (lot 070H21A) between 8-Apr-2022 and 15-Dec-2022) and NO ADVERSE EVENT (no adverse event) in a 69-year-old male patient who received mRNA-1273 (Spikevax) (batch no. 070H21A) for COVID-19 prophylaxis. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (expired vaccine used/ Patients received this Moderna vaccine (lot 070H21A) between 8-Apr-2022 and 15-Dec-2022) and NO ADVERSE EVENT (no adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (expired vaccine used/ Patients received this Moderna vaccine (lot 070H21A) between 8-Apr-2022 and 15-Dec-2022) and NO ADVERSE EVENT (no adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter considered NO ADVERSE EVENT (no adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (expired vaccine used/ Patients received this Moderna vaccine (lot 070H21A) between 8-Apr-2022 and 15-Dec-2022). Patient age was reported as 69 Year 6 Month. It was reported that lot 070H21A, that has an expiration date of 7-Apr-2022. Patients received this Moderna vaccine between 8-Apr-2022 and 15-Dec-2022. No concomitant medication were reported. No treatment medication were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 24.12.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; Expired vaccine used; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vaccine used) and NO ADVERSE EVENT (No adverse event) in a 67-year-old male patient who received mRNA-1273 (Spikevax) (batch no. 070H21A) for COVID-19 prophylaxis. No Medical History information was reported. In 2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. In 2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vaccine used). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired vaccine used) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Expired vaccine used). No concomitant medication information was reported. The patient age was reported as 67 Year 9 Month. Patients at the facility received vaccine between 08Apr2022 and 15Dec2022. No treatment medication information was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 24.12.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
no adverse event; expired vaccine used; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (expired vaccine used) and NO ADVERSE EVENT (no adverse event) in a 76-year-old female patient who received mRNA-1273 (Spikevax) (batch no. 070H21A) for COVID-19 prophylaxis. No Medical History information was reported. In 2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. In 2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (expired vaccine used). On an unknown date, the patient experienced NO ADVERSE EVENT (no adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (expired vaccine used) and NO ADVERSE EVENT (no adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter considered NO ADVERSE EVENT (no adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (expired vaccine used). Patient age was reported as 76 Year 10 Month. Concomitant medications details were not reported by the reporter. Reportedly, the number of patients at facility that received this Moderna vaccine between 08-Apr-2022 and 15-Dec-2022. Completion date provided as 21-Jul-2022 Treatment details were not reported by the reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 18,0
- Geschlecht
- M
- Eingang
- 24.12.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; Expired vaccine used; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vaccine used) and NO ADVERSE EVENT (No adverse event) in an 18-year-old male patient who received mRNA-1273 (Spikevax) (batch no. 070H21A) for COVID-19 prophylaxis. No Medical History information was reported. In 2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. In 2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vaccine used). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired vaccine used) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Expired vaccine used). No concomitant medications were reported. Treatment information was not provided. ID: 80777027399
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 34,0
- Geschlecht
- M
- Eingang
- 24.12.2022
- Impfdatum
- 30.06.2022
- Beginn
- 30.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; Expired vaccine used/ Patients received this Moderna vaccine between 8-Apr-2022 and 15-Dec-2022, expiration date was 07 Apr 2022; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vaccine used/ Patients received this Moderna vaccine between 8-Apr-2022 and 15-Dec-2022, expiration date was 07 Apr 2022) and NO ADVERSE EVENT (No adverse event) in a 34-year-old male patient who received mRNA-1273 (Spikevax) (batch no. 070H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 30-Jun-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 30-Jun-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vaccine used/ Patients received this Moderna vaccine between 8-Apr-2022 and 15-Dec-2022, expiration date was 07 Apr 2022). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired vaccine used/ Patients received this Moderna vaccine between 8-Apr-2022 and 15-Dec-2022, expiration date was 07 Apr 2022) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Expired vaccine used/ Patients received this Moderna vaccine between 8-Apr-2022 and 15-Dec-2022, expiration date was 07 Apr 2022). Patient age was reported as 34 years 2 months. No concomitant medication were reported. It was reported that lot 070H21A, that has an expiration date of 7-Apr-2022. Patients received this Moderna vaccine between 8-Apr-2022 and 15-Dec-2022. No treatment medication were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 24.12.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; Patient received expired vaccine; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient received expired vaccine) and NO ADVERSE EVENT (No adverse event) in a 21-year-old male patient who received mRNA-1273 (Spikevax) (batch no. 070H21A) for COVID-19 prophylaxis. No Medical History information was reported. In 2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. In 2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient received expired vaccine). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient received expired vaccine) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Patient received expired vaccine). Patient's age was reported as 21 Year 1 Month. No concomitant medications were reported. completion date was reported as 18-Aug-2022. The vaccine from the vial with lot number O70H21A was administered to the patient in between a period of 08-Apr-2022 to 15-Dec-2022. No treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 24.12.2022
- Impfdatum
- 07.07.2022
- Beginn
- 07.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; Expired vaccine used/ Patients received this Moderna vaccine expiration date was 07 Apr 2022; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vaccine used/ Patients received this Moderna vaccine expiration date was 07 Apr 2022) and NO ADVERSE EVENT (No adverse event) in a 68-year-old female patient who received mRNA-1273 (Spikevax) (batch no. 070H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 07-Jul-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 07-Jul-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vaccine used/ Patients received this Moderna vaccine expiration date was 07 Apr 2022). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired vaccine used/ Patients received this Moderna vaccine expiration date was 07 Apr 2022) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Expired vaccine used/ Patients received this Moderna vaccine expiration date was 07 Apr 2022). Patient age was reported as 68 years 10 months. It was reported that lot 070H21A, that has an expiration date of 7-Apr-2022. Patients received this Moderna vaccine between 8-Apr-2022 and 15-Dec-2022. No concomitant medication were reported. No treatment medication were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 07.12.2022
- Impfdatum
- 20.12.2021
- Beginn
- 20.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Vaccine was stored post puncture past the recommended manufactures time (stored up to 28 days)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 42,0
- Geschlecht
- M
- Eingang
- 16.11.2022
- Impfdatum
- 16.11.2022
- Beginn
- 16.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Vaccine Expired
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 02.11.2022
- Impfdatum
- 02.02.2022
- Beginn
- 02.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
Vaccine vial store for longer than recommended post puncture of vial (potentially up to 28 days) no adverse reaction
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Amox, PCN, Latex, Lisinopril, Cephalosporins
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 31.10.2022
- Impfdatum
- -
- Beginn
- 17.08.2022
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Biopsy skin
Blood test
Central venous catheterisation
Chemotherapy
Computerised tomogram
Hodgkin's disease
Hodgkin's disease nodular sclerosis stage III
Multiple gated acquisition scan
Neck mass
Positron emission tomogram
Symptomtext
Hodgkin Lymphoma, Lump on L side of neck Nodular Sclerosis. lymph nodes of head, face neck C81.11 Chemotherapy CT Scan, postiron Emission tomography (PET SCAN) biopsy L side of neck, MUGA Scan IV Port Placed
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Biopsy skin
- Hospital-Tage
- -
- Labordaten
- Blood work x5, CT SCAN, PET SCAN, MUGA SCAN countless Doctor Appts
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 14.09.2022
- Impfdatum
- 18.12.2021
- Beginn
- 30.08.2022
- Tage bis Beginn
- 255,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
COVID breakthrough. Patient presented to the ED on 8/30 for reason unrelated to COVID but was tested and resulted positive. Infectious disease consult considered him asymptomatic.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID+ by PCR on 8/30/22
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 19.08.2022
- Impfdatum
- 16.01.2022
- Beginn
- 09.08.2022
- Tage bis Beginn
- 205,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Symptomtext
Pt tested positive for COVID on 08/09/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ME
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 16.08.2022
- Impfdatum
- 04.03.2021
- Beginn
- 13.01.2022
- Tage bis Beginn
- 315,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Symptomtext
Patient hospitalized with COVID after being vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- 76,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 26,0
- Geschlecht
- M
- Eingang
- 04.08.2022
- Impfdatum
- 26.02.2022
- Beginn
- 26.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Our office had a temperature excursion as per the department of health we have to submit this to VAERS, As per patient no adverse side affect on vaccine date till present day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NO PAST MEDICAL HISTORY
- Vorgeschichte
- NO PAST MEDICAL HISTORY
- Andere Medikamente
- NONE
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 01.08.2022
- Impfdatum
- 31.01.2022
- Beginn
- 30.07.2022
- Tage bis Beginn
- 180,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Asymptomatic COVID-19
Inappropriate schedule of product administration
SARS-CoV-2 test positive
Symptomtext
positive covid test in asymptomatic vaccinated pt
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Asymptomatic COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 13.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 13.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 13.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 13.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 13.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 13.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 13.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 13.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 13.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 13.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 82,0
- Geschlecht
- M
- Eingang
- 13.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 13.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 13.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 13.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 13.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 13.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 13.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 13.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 13.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 13.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 13.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 13.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 13.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 13.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 13.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 13.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 40,0
- Geschlecht
- M
- Eingang
- 13.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 13.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 87,0
- Geschlecht
- M
- Eingang
- 12.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 12.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 12.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 12.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 12.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 12.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 12.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 12.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 12.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 12.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 12.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 12.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 12.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 12.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 12.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 12.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 12.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 84,0
- Geschlecht
- M
- Eingang
- 12.07.2022
- Impfdatum
- 10.11.2021
- Beginn
- 10.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 07.07.2022
- Impfdatum
- 14.04.2022
- Beginn
- 14.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Symptomtext
Vaccine given when expired, no adverse reaction
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- DM type II, HTN, Hypothyrodism, Vitamin D deficiency, HLD
- Andere Medikamente
- Amlodipine, Atorvastatin, Caltrate, Ozempic, Levothyroxine, Losartan, Metoprolol, Niacin, Pioglitazone
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 07.07.2022
- Impfdatum
- 25.04.2022
- Beginn
- 25.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Symptomtext
Vaccine was given when expired, no adverse reaction
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Adjustment Disorder, Anxiety/depression
- Andere Medikamente
- Aripiprazole, Buproion, Cetirizine, Hydroxyzine
- Allergien
- Seasonal
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 07.07.2022
- Impfdatum
- 25.04.2022
- Beginn
- 25.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Symptomtext
Vaccine was given when it was expired, no adverse reaction
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- HTN, GERD, Vitamin D deficiency, HLD, Afib
- Andere Medikamente
- Amlodipine, ASA, Crestor, HCTZ, Lcosapent Ethyl, Losartan Potassium, Metoprolol, Nitro, Pantoprazole, Vitamin D
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 07.07.2022
- Impfdatum
- 25.04.2022
- Beginn
- 25.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Symptomtext
Vaccine given when it was expired, no adverse reaction
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- HLD, Osteoporosis, GERD, Anxiety/depression, Vitamin D deficiency, RA
- Andere Medikamente
- Airborne, Alprazolam, Citalopram, Estradiol, Gabapentin, Krill Oil, Vitamin D
- Allergien
- Amitriptyline, Sulfa Drugs
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 07.07.2022
- Impfdatum
- 25.04.2022
- Beginn
- 25.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Symptomtext
Vaccine was expired when given, no adverse reaction
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- HLD, Vitamin D deficiency, Anxiety/depression
- Andere Medikamente
- Calcium, Escitalopram, Glucosamine, Magnesium, Vitamin D, Biotin
- Allergien
- Bisphosphonates, gabapentin, risedronate
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 07.07.2022
- Impfdatum
- 25.04.2022
- Beginn
- 25.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Symptomtext
Vaccine given when expired, no adverse reaction
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Afib, HLD, GERD, Dementia, HTN
- Andere Medikamente
- carbidopa-Levodopa, Donepezil, escitalopram, furosemide, lisinopril, magnesium, melatonin, metoprolol, sildenafil, vitamin b12, voltaren gel
- Allergien
- terbinafine, amoxicillin, verapamil
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 07.07.2022
- Impfdatum
- 25.04.2022
- Beginn
- 25.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Symptomtext
Patient was given expire vaccine. No Adverse reaction.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- HTN, Afib, HLD, hypothyrodism
- Andere Medikamente
- Atorvastatin, HCTZ, Levothyroxine, Multivit, Calcium, Eliquis, Metoprolol, Vitamin D
- Allergien
- IV contrast, shell fish
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 85,0
- Geschlecht
- M
- Eingang
- 07.07.2022
- Impfdatum
- 25.04.2022
- Beginn
- 25.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Symptomtext
Vaccine was expired when given. There were no adverse reactions.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Afib, GERD, HTN, HLD, hypothyroidism
- Andere Medikamente
- Atorvastatin, Krill Oil, Levothyroxine, Multivit, Eliquis, Finasteride
- Allergien
- Keflex
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 03.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 03.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 03.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 03.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 03.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 03.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 03.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 03.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 03.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 03.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 03.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 20,0
- Geschlecht
- M
- Eingang
- 03.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 03.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 03.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 03.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 03.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 03.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 03.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 03.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 03.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 86,0
- Geschlecht
- F
- Eingang
- 03.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 93,0
- Geschlecht
- M
- Eingang
- 03.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 03.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 03.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 03.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 03.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 03.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 03.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 90,0
- Geschlecht
- M
- Eingang
- 03.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 03.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 03.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 03.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 03.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 03.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 03.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 03.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 03.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 03.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 03.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 82,0
- Geschlecht
- M
- Eingang
- 03.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 82,0
- Geschlecht
- M
- Eingang
- 03.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 03.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 03.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 03.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 03.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 03.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 63,0
- Geschlecht
- U
- Eingang
- 03.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 03.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 84,0
- Geschlecht
- F
- Eingang
- 03.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 03.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 03.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 03.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 03.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 03.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 03.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 03.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 03.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 81,0
- Geschlecht
- M
- Eingang
- 03.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 03.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 03.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 03.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 03.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 03.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 82,0
- Geschlecht
- M
- Eingang
- 03.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 03.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 03.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 03.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 03.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 01.04.2022
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 03.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 03.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 03.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 03.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 03.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 03.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 62,0
- Geschlecht
- U
- Eingang
- 03.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 03.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 03.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 03.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 03.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 83,0
- Geschlecht
- M
- Eingang
- 03.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 03.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 03.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 03.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 03.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 03.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 83,0
- Geschlecht
- F
- Eingang
- 03.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 03.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 86,0
- Geschlecht
- F
- Eingang
- 03.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
patient received expired medication. confirmed with manufacturer that dose maintained its efficacy. no follow-up needed. no adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -