Zurueck zur Suche

Reporte zur Charge UJ249AA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

2Reporte angezeigt
1Todesfaelle
1Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
OH 1 MN 1

VAERS 972898

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ249AA

kritisch
Staat
OH
Alter
68,0
Geschlecht
M
Eingang
25.01.2021
Impfdatum
30.09.2019
Beginn
05.10.2019
Tage bis Beginn
5,0
Dosis
1
Route/Site
IM / LA
Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein
Death Encephalopathy Haemophagocytic lymphohistiocytosis Laboratory test Malaise Septic shock

Symptomtext

5 days after receiving the vaccination the patient developed generalized malaise progressing to encephalopathy. He was admitted to the hospital with presumed septic shock, and work-up revealed hemophagocytic lymphohistiocytosis. He died from the disease process 9 days after vaccination.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Death
Hospital-Tage
3,0
Labordaten
Many tests performed during hospitalization 10/06/2019 through 10/09/2019
Aktuelle Erkrankungen
-
Vorgeschichte
HTN, high cholesterol, BPH, meniere's
Andere Medikamente
pred forte right eye, zaditor right eye, finasteride 5 mg daily, aspirin 81 mg daily, MVI, xyzal 5 mg daily, saw palmetto, antivert 25 mg TID PRN, pantoprazole 40 mg daily, lisinopril 20 mg daily, verapamil 180 mg daily, atorvastatin 20 mg
Allergien
NKDA
Vorherige Impfungen
-

VAERS 996749

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ249AA

gering
Staat
MN
Alter
57,0
Geschlecht
F
Eingang
03.02.2021
Impfdatum
21.01.2021
Beginn
21.01.2021
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

patient had received an expired Fluzone HD vaccine/ No AE; Initial information received on 21-Jan-2021 regarding an unsolicited valid non-serious case received from a pharmacist. This case involves a 57 year old female patient who vaccinated with an expired dose of INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE [FLUZONE HIGH-DOSE QUADRIVALENT] inadvertently (expired product administered). Medical history, medical treatment, vaccination, concomitant medications and family history were not provided. On 21-Jan-2021, the patient received a dose of suspect INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE (lot UJ249AA and expiry date: 30-Apr-2020) via unknown route in unknown administration site. It was a case of actual medication error due to expired vaccine used. At the time of report, no adverse event was reported. 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 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
-