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Reporte zur Charge UJ735AA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

4Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
IL 1 NY 1 ME 1 PA 1

VAERS 2450857

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ735AA

mild
Staat
IL
Alter
41,0
Geschlecht
F
Eingang
19.09.2022
Impfdatum
16.09.2022
Beginn
16.09.2022
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Injection site cellulitis Injection site discolouration Injection site erythema Injection site swelling

Symptomtext

Left deltoid became swollen and red, for a few days, now improving but still slightly red and yellow. According to pt, looked similar to cellulitis.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site cellulitis
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
post stem cell transplant in 2018 for Hemophagocytic Lymphohistiocytosis, avascular necrosis
Vorgeschichte
HLH/MAS
Andere Medikamente
Prolia, Tums, Vitamin D, Estradiol, Toprol XL, Prednisone, Ursodiol, Valcyclovir
Allergien
Vancomycin, adhesive tape
Vorherige Impfungen
-

VAERS 2671028

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ735AA

gering
Staat
NY
Alter
1,0
Geschlecht
M
Eingang
14.08.2023
Impfdatum
09.08.2023
Beginn
09.08.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered

Symptomtext

ACTHIB vial that expired was inadvertently administered to a patient with no reported adverse event; Initial information received on 10-Aug-2023 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 1 years old male patient who experienced HIB (PRP/T) vaccine [ACT-HIB] vial that expired 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 09-Aug-2023, the patient inadvertently received an expired dose of 0.5 ml (frequency: once) suspect of standard strength HIB (PRP/T) vaccine powder and solvent for solution for injection (lot: UJ735AA, Expiry date: 07-Aug-2023) via intramuscular route in the left deltoid 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 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 2663050

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ735AA

gering
Staat
ME
Alter
1,0
Geschlecht
M
Eingang
31.07.2023
Impfdatum
20.07.2023
Beginn
20.07.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
No adverse event Product preparation issue

Symptomtext

ACTHIB was reconstituted with 0.9% sodium chloride instead of using the 0.4% sodium chloride ACTHIB diluent, with no reported adverse event; Initial information received on 24-Jul-2023 regarding an unsolicited valid non-serious case received from a nurse. This case involves a 1-year-old male patient, HIB (PRP/T) VACCINE [ACT-HIB] was reconstituted with 0.9% sodium chloride instead of using the 0.4% sodium chloride acthib diluent, 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 MEASLES VACCINE LIVE (ENDERS-EDMONSTON), MUMPS VACCINE LIVE, RUBELLA VACCINE LIVE (WISTAR RA 27/3) (MMR II); PNEUMOCOCCAL VACCINE CONJ (PNEUMOCOCCAL CONJUGATE VACCINE) and HEPATITIS A VACCINE (HEPATITIS A) for Prophylactic vaccination. On 20-Jul-2023, the patient received an unknown dose of suspect HIB (PRP/T) VACCINE Powder and solvent for solution for injection (strength: unknown) (lot: UJ735AA, expiry date: 07-Aug-2023) via intramuscular route in unknown administration site for immunization. On 20-Jul-2023 the patient had an event of acthib was reconstituted with 0.9% sodium chloride instead of using the 0.4% sodium chloride acthib diluent, with no reported adverse event (product preparation error) (latency: same day) following the administration of HIB (PRP/T) VACCINE. It was unknown if any lab data/tests available. Action taken with HAEMOPHILUS TYPE B (HIB) VACCINE (ACT-HIB) was not applicable. Outcome: 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
No adverse event
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
MMR II; PNEUMOCOCCAL CONJUGATE VACCINE; HEPATITIS A
Allergien
-
Vorherige Impfungen
-

VAERS 2593916

SANOFI PASTEUR · HIB (ACTHIB) · Charge uj735aa

gering
Staat
PA
Alter
2,0
Geschlecht
F
Eingang
09.03.2023
Impfdatum
07.03.2023
Beginn
09.03.2023
Tage bis Beginn
2,0
Dosis
1
Route/Site
IM / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Wrong product administered

Symptomtext

working in a Family Practice been so busy and having multiple well child visits a wrong vaccine was given. Provider order DTAP and was given Pentacel. Per provider patient will not be harm and provider will communicate with parents.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Wrong product administered
Hospital-Tage
-
Labordaten
None.
Aktuelle Erkrankungen
None.
Vorgeschichte
None.
Andere Medikamente
None.
Allergien
Amoxicillin.
Vorherige Impfungen
-