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Reporte zur Charge UJ774AA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

12Reporte angezeigt
0Todesfaelle
2Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
MI 4 ME 3 PR 1 MD 1

VAERS 2390992

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ774AA

kritisch
Staat
MI
Alter
78,0
Geschlecht
F
Eingang
26.07.2022
Impfdatum
02.12.2021
Beginn
17.07.2022
Tage bis Beginn
227,0
Dosis
N/A
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja
Acute respiratory failure Bradycardia COVID-19 Cardiac pacemaker insertion Cardiac telemetry abnormal Dizziness SARS-CoV-2 test positive Syncope

Symptomtext

Discharge Provider: MD Primary Care Provider: DO Admission Date: 7/17/2022 Discharge Date: Jul 22, 2022 PRESENTING PROBLEM: COVID-19 [U07.1] HOSPITAL COURSE: 79-year-old patient with a past medical history of nonrheumatic aortic stenosis, chronic diastolic dysfunction, coronary artery disease presented to the emergency department after a syncopal episode and was found to have acute hypoxic respiratory failure. She was positive for COVID-19 A acquired 2 L of oxygen at the time of admission which was eventually weaned off to room air. Patient was placed on telemetry which showed persistent bradycardia along with associated dizziness because of his cardiology was involved. Patient underwent placement of dual-chamber permanent pacemaker on 07/21/2022 after which her symptoms significantly improved and resolved. Patient was discharged home in a stable condition.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Acute respiratory failure
Hospital-Tage
5,0
Labordaten
-
Aktuelle Erkrankungen
None
Vorgeschichte
Anxiety and depression Chronic pain Hypercholesteremia GERD (gastroesophageal reflux disease) Chronic, continuous use of opioids Adenocarcinoma of left lower lobe s/p lobecotmy 10/2013 Stage 1A (T1A N0 M0) Lung disease, restrictive History of histoplasmosis Multiple lung nodules Granulomatous lung disease (HCC) Iron deficiency anemia Leg edema, left Bronchitis Bronchiolitis Iron deficiency anemia Pneumonia due to infectious organism Shortness of breath ABLA (acute blood loss anemia) Anemia Coronary artery disease without angina pectoris Aortic stenosis Essential hypertension COVID-19
Andere Medikamente
albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler aspirin 81 MG chewable tablet citalopram (CELEXA) 10 MG tablet Cyanocobalamin (B-12) 1000 MCG CAPS diphenhydrAMINE (BANOPHEN) 50 MG capsule ferrous s
Allergien
IbuprofenGI Upset AspirinGI Upset Aspirin Clonazepam CodeineGI Upset Contrast Dye [Ivp Dye, Iodine Containing] Seroquel [Quetiapine]Agitation
Vorherige Impfungen
-

VAERS 2335780

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ774AA

moderat
Staat
MI
Alter
86,0
Geschlecht
F
Eingang
27.06.2022
Impfdatum
18.11.2021
Beginn
20.06.2022
Tage bis Beginn
214,0
Dosis
N/A
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja
Arthralgia Atrioventricular block first degree COVID-19 COVID-19 pneumonia Chest X-ray abnormal Confusional state Diet refusal Electrocardiogram abnormal Full blood count normal Hyponatraemia Hypophagia Hypovolaemia Lethargy Loss of personal independence in daily activities Metabolic function test Metabolic function test abnormal Procalcitonin normal Pterygium

Symptomtext

Discharge Provider: Private MD Primary Care Provider at Discharge: Private MD Admission Date: 6/20/2022 Discharge Date: 6/24/2022 PRESENTING PROBLEM: Hyponatremia [E87.1] Hip pain [M25.559] Fever, unspecified fever cause [R50.9] Pneumonia due to COVID-19 virus [U07.1, J12.82] HOSPITAL COURSE: Patient is a 87 y.o. female who presented to the emergency department with complaints of fever. She has a past medical history of asthma, CVA, glaucoma, and memory impairment. Per report from the patient's son, patient has been increasingly confused over the past week. He states that today, she has become increasingly lethargic and not performing daily activities as usual. She ate breakfast, however, she refused lunch and dinner. She was sent to the emergency department for further evaluation when it was noted by staff that she had a temperature of approximately 101.4? F. in the emergency department, patient was tachypneic, however, other vital signs were stable. She did not require supplemental oxygen. Complete blood count was unremarkable. CMP was remarkable for hyponatremia. Troponin was negative. Procalcitonin was negative. COVID-19 was positive. EKG showed sinus rhythm with a first-degree AV block. Chest x-ray showed findings consistent with COVID-19 pneumonia. Suspect presenting symptoms are secondary to COVID-19 pneumonia. Patient has been admitted for further evaluation and management of COVID-19 pneumonia and hyponatremia. 6/24: Patient did very well during this admission. Her hyponatremia has improved, it was felt to be in part due to hypovolemia. I will start her on salt tablets 2 times a day as well. Patient also was diagnosed with COVID, but steroids were stopped, she did not show any obvious respiratory involvement. Patient was seen by Physical therapy and has slowly improved, she will go back to the "Private". Patient will follow-up with Ophthalmology regarding a Pterygium. Patient is otherwise stable for discharge. She will need a repeat BMP on Monday June 27th.

Weitere VAERSDATA-Felder
Praegender Schweregrund
COVID-19 pneumonia
Hospital-Tage
4,0
Labordaten
-
Aktuelle Erkrankungen
None
Vorgeschichte
Asthma RSV (acute bronchiolitis due to respiratory syncytial virus) Cerebrovascular accident (CVA) due to embolism of left anterior cerebral artery (HCC) Hypokalemia Leukocytosis Atypical pneumonia Severe protein-calorie malnutrition (HCC) Physical deconditioning MCI (mild cognitive impairment) with memory loss Nodule of lower lobe of left lung--identified December 2019 Glaucoma Peripheral pterygium, stationary Urinary incontinence Pneumonia due to COVID-19 virus Hyponatremia
Andere Medikamente
acetaminophen (TYLENOL) 325 MG tablet albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler apixaban (ELIQUIS) 5 MG tab
Allergien
Cashews Peanut [Nuts] Sulfa Drugs
Vorherige Impfungen
-

VAERS 1905977

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ774AA

moderat
Staat
PR
Alter
81,0
Geschlecht
F
Eingang
29.11.2021
Impfdatum
29.11.2021
Beginn
29.11.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Chest pain Disorientation Dizziness Headache Malaise Resuscitation

Symptomtext

At around 3:03PM, patient came into the Pharmacy to request vaccination for flu. Paperwork was filled and at 3:14pm patient received Influenza vaccine (Fluzone HD) by Pharmacy Technician. After administration, the patient was walking with a relative and stated that she did not feel good, and was feeling faint. Family member was able to grab her and placed her on the ground in front of the Department. Health Ambassador came to the Pharmacy and notified that there was a person on the floor, she stated had received a vaccine. Pharmacist left the Pharmacy area to attend to the patient where the Store Co-Manager had already arrived at the scene and placed the patient on a chair. The patient was disoriented and stated she had chest pains and headache; Pharmacist felt for a radial pulse, and was able to feel it. Pharmacist instructed technicians to close the Pharmacy while calling 9-1-1 to request emergency personnel to come into the store. After that, pharmacist took oxygen tank and placed cannula in order to administer oxygen (at 3:26pm; 2L); meanwhile staff was helping with the code. Paramedic arrived at the scene at 3:32pm, and instructed the Pharmacist to accompany him to the ambulance with the oxygen tank in order to load her into the ambulance. Paramedics took the patient to nearest hospital at around 3:37pm; they mentioned were taking her to Hospital.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Chest pain
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
Patient's daughter stated Osteoporosis, Arthritis.
Vorgeschichte
-
Andere Medikamente
No
Allergien
None reported by the patient nor the relatives.
Vorherige Impfungen
-

VAERS 2462877

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ774AA

gering
Staat
ME
Alter
88,0
Geschlecht
F
Eingang
28.09.2022
Impfdatum
20.09.2022
Beginn
20.09.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered

Symptomtext

expired FLUZONE HIGH-DOSE QUADRIVALENT was administered to a patient with no reported adverse event; Initial information received on 21-Sep-2022 regarding an unsolicited valid non-serious case received from a pharmacist. This case involves a 88 years old female patient who experienced expired fluzone high-dose quadrivalent was administered to a patient with no reported adverse event while receiving vaccine INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE [FLUZONE HIGH-DOSE QUADRIVALENT]. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 20-Sep-2022, the patient received a 0.5 ml dose of suspect INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE once (lot UJ774AA; expiry date: 30-JUN-2022) via intramuscular route in the right deltoid for immunization. On 20-SEP-2022 the patient reported a non-serious event expired fluzone high-dose quadrivalent was administered to a patient with no reported adverse event (expired product administered) following the administration of INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE. Action taken: not applicable. At time of reporting, the outcome was Not Recovered / Not Resolved for the event. This suspected adverse reaction report is submitted and classified as a medication error solely and exclusively to ensure the marketing authorization holder's compliance with the requirements set out in the Directive 2001/83/EC and Module VI of the Good Pharmacovigilance Practices. The classification as a medical error is in no way intended, nor should it be interpreted or construed as an allegation or claim made by the marketing authorization holder that any third party has contributed to or is to be held liable for the occurrence of this medication error.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2453732

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ774AA

gering
Staat
-
Alter
88,0
Geschlecht
F
Eingang
21.09.2022
Impfdatum
20.09.2022
Beginn
20.09.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Expired product administered No adverse event

Symptomtext

Patient got 21/22 vaccine exp 6/30/22- no adverse event occured

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2453728

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ774AA

gering
Staat
-
Alter
66,0
Geschlecht
M
Eingang
21.09.2022
Impfdatum
20.09.2022
Beginn
20.09.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered No adverse event

Symptomtext

Patient received 21/22 vaccine exp 6/30/2022- no adverse event occured

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2453725

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ774AA

gering
Staat
-
Alter
65,0
Geschlecht
F
Eingang
21.09.2022
Impfdatum
20.09.2022
Beginn
01.09.2022
Tage bis Beginn
-
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered No adverse event

Symptomtext

Patient recieved 21/22 Fluzon eHD exp 6/30/2022- no reaction reported

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2453723

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ774AA

gering
Staat
ME
Alter
65,0
Geschlecht
F
Eingang
21.09.2022
Impfdatum
20.09.2022
Beginn
01.09.2022
Tage bis Beginn
-
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Expired product administered

Symptomtext

Patient received 21/22 fluzone HD exp 6/30/2022

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2308484

GLAXOSMITHKLINE BIOLOGICALS · INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) · Charge UJ774AA

gering
Staat
ME
Alter
21,0
Geschlecht
F
Eingang
03.06.2022
Impfdatum
02.06.2022
Beginn
02.06.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Incorrect dose administered

Symptomtext

I gave patient the high dose flu instead of the adult flu shot

Weitere VAERSDATA-Felder
Praegender Schweregrund
Incorrect dose administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
non know
Vorgeschichte
-
Andere Medikamente
Colace
Allergien
History Vaso-vagal reaction
Vorherige Impfungen
-

VAERS 1877740

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ774AA

gering
Staat
MI
Alter
61,0
Geschlecht
M
Eingang
17.11.2021
Impfdatum
17.11.2021
Beginn
17.11.2021
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Incorrect dose administered

Symptomtext

The 61 year old patient was given a high dose flu inadvertently. He was made aware of the occurrence at the time of the event.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Incorrect dose administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1866182

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ774AA

gering
Staat
MD
Alter
66,0
Geschlecht
F
Eingang
12.11.2021
Impfdatum
12.11.2021
Beginn
12.11.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Extra dose administered

Symptomtext

Patient accidently received fluzone hd. She said she already received the flu vaccine last week.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Extra dose administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1865513

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ774AA

gering
Staat
MI
Alter
68,0
Geschlecht
F
Eingang
12.11.2021
Impfdatum
12.11.2021
Beginn
12.11.2021
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Product preparation error

Symptomtext

PT was injected with 0.3 ml of undiluted pfizer booster shot, staff were immediately notified. Per protocol PT was informed of the issue and informed of reactions and told to seek medical attention if she feels she is having a reaction. She was watched for fifteen minutes and vitals were checked a second time vitals were still normal and were charted.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Product preparation error
Hospital-Tage
-
Labordaten
N/A
Aktuelle Erkrankungen
-
Vorgeschichte
legally blind Hypertension high cholesterol emphysema
Andere Medikamente
albertol anastrozole atrovastatin symbicort wellbutrin vitamin d3 and calcium felodipine metoprolol spiriva desyrl ibprofen
Allergien
apricot sulfamethoxazole-trimethoprim
Vorherige Impfungen
-