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Reporte zur Charge UJ575AAB

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

3Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
MA 2 ID 1

VAERS 2464252

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ575AAB

gering
Staat
ID
Alter
1,0
Geschlecht
M
Eingang
29.09.2022
Impfdatum
21.09.2022
Beginn
21.09.2022
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 Medication error No adverse event

Symptomtext

child received expired ACT-HIB/ liquid component of the ACT-HIB expired on 20Sep2022 with no reported AE; Initial information received on 22-Sep-2022 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 1 years old male patient who experienced child received expired act-hib/ liquid component of the act-hib expired on 20sep2022 with no reported adverse event while receiving vaccine HIB (PRP/T) VACCINE [ACT-HIB]. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. Concomitant medications included PNEUMOCOCCAL VACCINE (PNEUMOCOCCAL VACCINE) for Immunisation. On 21-Sep-2022, the patient received a 0.5ml dose of suspect HIB (PRP/T) VACCINE once ( lot UJ575AAB; expiry date; 20-SEP-2022) via intramuscular route in leg for immunization. On 21-SEP-2022 the patient developed a non-serious event child received expired act-hib/ liquid component of the act-hib expired on 20-Sep-2022 with no reported adverse event (expired product administered) following the administration of HIB (PRP/T) VACCINE. Action taken: not applicable. At time of reporting, the outcome was Unknown 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 guidelines. 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 2447852

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ575AAB

gering
Staat
MA
Alter
1,3
Geschlecht
F
Eingang
16.09.2022
Impfdatum
30.08.2022
Beginn
30.08.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
No adverse event Product preparation error

Symptomtext

Hib (ActHIB) was reconstituted with a single vial of sterile water instead of the 0.4% sodium chloride diluent that comes with the vaccine. No adverse effects, signs or symptoms were shown by patient.

Weitere VAERSDATA-Felder
Praegender Schweregrund
No adverse event
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None
Allergien
None
Vorherige Impfungen
-

VAERS 2447849

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ575AAB

gering
Staat
MA
Alter
1,3
Geschlecht
M
Eingang
16.09.2022
Impfdatum
29.08.2022
Beginn
29.08.2022
Tage bis Beginn
0,0
Dosis
4
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
No adverse event Product preparation error

Symptomtext

Hib (ActHIB) was reconstituted with a single vial of sterile water instead of the 0.4% sodium chloride diluent that comes with the vaccine. No adverse effects, signs or symptoms were shown by patient.

Weitere VAERSDATA-Felder
Praegender Schweregrund
No adverse event
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None
Allergien
NKA
Vorherige Impfungen
-