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Reporte zur Charge UJ622AAA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

4Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
PA 1 GA 1 IL 1 AL 1

VAERS 2547634

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ622AAA

gering
Staat
PA
Alter
0,4
Geschlecht
M
Eingang
31.12.2022
Impfdatum
27.12.2022
Beginn
27.12.2022
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

an expired dose of PENTACEL was administered today, to a 5 month-old boy,with no reported adverse event; Initial information received on 27-Dec-2022 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 5 months old male patient for whom an expired dose of diphtheria/tetanus/5 hybrid AC pertussis/IPV(MRC5)/HIB(PRP/T) vaccine [Pentacel] was administered today. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 27-Dec-2022, the patient received a 0.5 ml dose of suspect diphtheria/tetanus/5 hybrid AC pertussis/IPV(MRC5)/HIB(PRP/T) vaccine suspension for injection (lot number: UJ622AAA, expiry date: 07-Dec-2022) via intramuscular route in unknown administration site for immunization, which is an expired dose of pentacel administered with no reported adverse event (expired product administered) (latency: same day). Action taken was 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 2542686

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge UJ622AAA

gering
Staat
GA
Alter
1,0
Geschlecht
M
Eingang
24.12.2022
Impfdatum
20.12.2022
Beginn
20.12.2022
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

child was given expired product with no reported adverse event; Initial information received on 20-Dec-2022 regarding an unsolicited valid non-serious case received from a healthcare professional. This case involves a 1-year-old male patient who was given expired product, DIPHTHERIA/TETANUS/5 HYBRID AC PERTUSSIS/IPV(VERO)/HIB(PRP/T) VACCINE [PENTACEL (VERO)] 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 INFLUENZA VACCINE for Prophylactic vaccination and Pneumonia vaccine. On 20-Dec-2022, the patient received dose 4 (0.5ml total) of suspect DIPHTHERIA/TETANUS/5 HYBRID AC PERTUSSIS/IPV(VERO)/HIB(PRP/T) VACCINE (Strength: standard, formulation: unknown) (lot number: UJ622AAA and expiry date: 07-Dec-2022) via intramuscular route in the left thigh (left leg) for Immunization and on the same day child was given expired product with no reported adverse event (expired product administered). Reporter wanted to know next steps. Action taken with DIPHTHERIA, TETANUS, AC PERTUSSIS, IPV AND HIB VACCINE (PENTACEL (VERO)) was 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
INFLUENZA VACCINE
Allergien
-
Vorherige Impfungen
-

VAERS 2440257

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge UJ622AAA

gering
Staat
IL
Alter
-
Geschlecht
F
Eingang
12.09.2022
Impfdatum
18.07.2022
Beginn
18.07.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Product preparation error

Symptomtext

products not being mixed together before administration with no reported adverse event; receiving the liquid portion DTap-IPV and not the powder portion HIB due to the products not being mixed together before administration with no reported adverse event; Initial information received on 22-Aug-2022 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 1 years old female patient and reported that products not being mixed together before administration with no reported adverse event and receiving the liquid portion dtap-ipv and not the powder portion hib due to the products not being mixed together before administration with no reported adverse event , for the vaccine DIPHTHERIA/TETANUS/5 HYBRID AC PERTUSSIS/IPV(VERO)/HIB(PRP/T) VACCINE [PENTACEL (VERO)]. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. Concomitant medications included HEPATITIS A VACCINE (HEPATITIS A) for Immunisation. On 18-Jul-2022, the patient received a dose of 0.5 ml of suspect DIPHTHERIA/TETANUS/5 HYBRID AC PERTUSSIS/IPV(VERO)/HIB(PRP/T) VACCINE , with an unknown formulation and strength , (lot: UJ622AAA ; expiry date: 07-Dec-2022) (frequency: once) via intramuscular route in the left thigh for immunization. The clinic reported on behalf of a consumer having a medication error with PENTACEL described as the patent only receiving the liquid portion DTap-IPV and not the powder portion HIB due to the products not being mixed together before administration with no reported adverse event (product preparation error) (single component of a two-component product administered) (onset date: 18-Jul-2022; latency: same day) Action taken : not applicable for both the events. Outcome: unknown for both the events 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
Product preparation error
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
HEPATITIS A
Allergien
-
Vorherige Impfungen
-

VAERS 2329442

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ622AAA

gering
Staat
AL
Alter
4,0
Geschlecht
M
Eingang
23.06.2022
Impfdatum
23.05.2022
Beginn
23.05.2022
Tage bis Beginn
0,0
Dosis
5
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
No adverse event Wrong product administered

Symptomtext

4 year old in clinic for preschool immunizations. Due Kinrix and Proquad. Nurse inadvertently administered Pentacel and Proquad. Child experienced no adverse reactions. Nursing Director instructed clinic to complete VAERS report due to wrong vaccine being given.

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