Zurueck zur Suche

Reporte zur Charge UJ802AA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

3Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
MO 1 TX 1 KS 1

VAERS 2683329

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ802AA

gering
Staat
MO
Alter
3,0
Geschlecht
M
Eingang
18.09.2023
Impfdatum
11.09.2023
Beginn
11.09.2023
Tage bis Beginn
0,0
Dosis
4
Route/Site
OT / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered Medication error No adverse event

Symptomtext

expired dose of acthib was inadvertently administered with no reported adverse event; Initial information received on 11-Sep-2023 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 3-year-old male patient for whom expired dose of HIB (PRP/T) vaccine [ACT-HIB] was inadvertently administered with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 11-Sep-2023, the patient received an expired dose inadvertently at dose 0.5 ml dose 4 (frequency: once) of suspect HIB (PRP/T) vaccine of standard strength (lot UJ802AA, Expiry date: 14-Aug-2023) via intramuscular route in the left vastus lateralis for Immunization with no reported adverse event (expired product administered) (latency: same day). Action taken: not applicable. At time of reporting, the outcome was Unknown. 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 2678775

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ802AA

gering
Staat
TX
Alter
1,3
Geschlecht
M
Eingang
01.09.2023
Impfdatum
28.08.2023
Beginn
28.08.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered Medication error No adverse event

Symptomtext

administered an expired ACT-HIB dose to a patient with no reported adverse event; Initial information received on 29-Aug-2023 regarding an unsolicited valid non-serious case received from an other health professional. This case involves a 15 month old male patient who was administered an expired HIB (PRP/T) VACCINE [ACT-HIB] dose to a patient with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. Concomitant medications included pneumococcal vaccine conj (Pneumococcal Conjugate Vaccine) for Prophylactic vaccination (immunization). On 28-Aug-2023, the patient received a dose 0.5 ml of suspect HIB (PRP/T) Vaccine Powder and solvent for solution for injection lot UJ802AA expiry date: 14-Aug-2023 via intramuscular route in the left thigh for immunization and was administered an expired act-hib dose to a patient with no reported adverse event (expired product administered) on the same day following the administration of HIB (PRP/T) Vaccine. Action taken was not applicable. At time of reporting, the outcome was Unknown for the event administered an expired act-hib dose to a patient with no reported adverse 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
PNEUMOCOCCAL CONJUGATE VACCINE
Allergien
-
Vorherige Impfungen
-

VAERS 2662663

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ802AA

gering
Staat
KS
Alter
4,0
Geschlecht
M
Eingang
28.07.2023
Impfdatum
25.07.2023
Beginn
25.07.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Expired product administered

Symptomtext

Patient?s parent called reporting that on 07/25/2023, the client received an expired vaccine. Parent states the client received four shots, and while checking out, the staff realized one vaccine expired on 07/08/2023. Patient was told that the clinic would be contacting the health department on what to do and if the vaccine was still viable after it expired. The Health Department did not receive a call. Parent was concerned for their child because this is not the first time something like this has happened, and so contacted the Health Department themselves. Patient?s record has the patient receiving MMR, Varicella, Hib, and Dtap-IPV on 07/25/2023. All vaccine information reported in this form is from system. The MMR, Varicella, and Hib are entered under the clinic, but the Dtap-IPV is entered as Historical without lot# and Expiration.

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