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Reporte zur Charge UJ571AAA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

3Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
OR 1 ME 1 TN 1

VAERS 2459709

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge UJ571AAA

gering
Staat
OR
Alter
-
Geschlecht
F
Eingang
24.09.2022
Impfdatum
15.09.2022
Beginn
15.09.2022
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

Symptomtext

pentacel administered today expired on 09/11/2022, with no reported adverse event; Initial information received on 15-Sep-2022 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 1 months old female patient and it was reported that DIPHTHERIA/TETANUS/5 HYBRID AC PERTUSSIS/IPV(VERO)/HIB(PRP/T) VACCINE [PENTACEL (VERO)] administered today expired on 09/11/2022, with no reported adverse event . The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 15-Sep-2022, the patient received a dose of 0.5 ml of suspect DIPHTHERIA/TETANUS/5 HYBRID AC PERTUSSIS/IPV(VERO)/HIB(PRP/T) VACCINE , once (lot : UJ571AAA; expiry date: 11-Sep-2022) via intramuscular route in unknown administration site for immunization. t was reported that Pentacel administered was administered on 15-Sep-2022 and it expired on 09/11/2022, with no reported adverse event" (expired product administered) (latency: same day) Action taken : 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
Expired product administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2455752

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ571AAA

gering
Staat
ME
Alter
0,3
Geschlecht
F
Eingang
23.09.2022
Impfdatum
16.09.2022
Beginn
16.09.2022
Tage bis Beginn
0,0
Dosis
2
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 PENTACEL was administered to a patient today with no reported adverse event; Initial information regarding an unsolicited valid non-serious case via health professional on 16-Sep-2022. Agency number: 01282761 This case involves a 4-month-old female patient to whom expired dose of Diphtheria/Tetanus/5 Hybrid AC Pertussis/IPV(MRC5)/HIB(PRP/T) Vaccine [Pentacel] was administered to a patient today 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 13V (CRM197) (Prevnar 13) for Prophylactic vaccination; and Rotavirus Vaccine Live Reassort Oral 5V (Rotateq) for Prophylactic vaccination. On 16-Sep-2022, the patient received expired 2nd dose of suspect Pentacel at dose 0.5ml once via intramuscular route in the left thigh (lot: UJ571AAA, expiry date: 11-Sep-2022) for Immunization with no reported adverse event (expired product administered) at same day latency. 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
PREVNAR 13; ROTATEQ
Allergien
-
Vorherige Impfungen
-

VAERS 2445017

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ571AAA

gering
Staat
TN
Alter
1,6
Geschlecht
F
Eingang
14.09.2022
Impfdatum
14.09.2022
Beginn
14.09.2022
Tage bis Beginn
0,0
Dosis
4
Route/Site
IM / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Circumstance or information capable of leading to medication error Expired product administered

Symptomtext

Pentacel Vaccine Lot # UJ571AAA Exp. date 09112011 was give by RN. He scanned Pentacel vaccine in system, administered vaccine, and attempted to put administration documentation and it would not pull vaccine with lot # and he realized he did not check expiration prior to administration and had administered an expired vaccine. LPN who manages vaccine inventory had Pentacel written on Monthly Expiration Date calendar and also on calendar at desk with other vaccine that was due to expire 09092022. She checks this calendar daily for vaccines that are due to expire and removes them. She removed other vaccine from vaccine refrigerator on 09092022 but failed to remove the Pentacel vaccine on 09092011 that expired 09112022. She put a check mark by vaccines on Monthly Expiration Date calendar and desk calendar indicating both had been removed. They immediately came to Nursing Supervisor and notified her of error.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Circumstance or information capable of leading to medication error
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-