Zurueck zur Suche

Reporte zur Charge UJ184AA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

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

VAERS 1071185

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ184AA

gering
Staat
DC
Alter
-
Geschlecht
U
Eingang
04.03.2021
Impfdatum
23.02.2021
Beginn
23.02.2021
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

inadvertently administered expired ACTHIB to a patient because the diluent was still in date but the powered portion was expired; with no reported AE; Initial information was received on 23-Feb-2021 regarding an unsolicited valid non-serious case from a other healthcare professional in the United States. This case involves child patient (age and gender unknown) who inadvertently administered an expired dose of HIB (PRP/T) VACCINE [ACT-HIB] (lyophilized powder: lot number: UJ184AA, expiration date: 15-Feb-2021) via an unknown route at an unknown administration site on 23-Feb-2021 for prophylactic vaccination (expired product administered). Medical history, medical treatment, vaccination, concomitant medication and family history were not provided. It was reported that this occurred because diluent was still in date but the powered portion was expired [diluent: lot number: U6723AA, expiration date: 17-Sep-2021]. The agent asked caller if she can answer additional questions for a safety report. Caller stated that she cannot but if safety wants to send her the questions via email she can follow up that way. It was an actual medication error due to expired vaccine used (latency: same day). 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
-

VAERS 1050129

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ184AA

gering
Staat
OH
Alter
6,0
Geschlecht
F
Eingang
23.02.2021
Impfdatum
19.02.2021
Beginn
19.02.2021
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Expired product administered

Symptomtext

No adverse outcomes, but expired vaccine was given to the patient.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Diamond-Blackfan Anemia, s/p bone marrow transplant in 2018
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-