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Reporte zur Charge U6612AA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

2Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
CA 1 KS 1

VAERS 2356773

SANOFI PASTEUR · TDAP (ADACEL) · Charge U6612AA

gering
Staat
CA
Alter
22,0
Geschlecht
F
Eingang
03.07.2022
Impfdatum
27.06.2022
Beginn
-
Tage bis Beginn
-
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

administer an expired ADACEL to a patient, with no reproted adverse event; Initial information received on 27-Jun-2022 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 22 years old female patient who was administered an expired diphtheria-2/tetanus/5 AC pertussis vaccine [Adacel], with no reproted adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 27-Jun-2022, the patient received 0.5 mL dose of suspect diphtheria-2/tetanus/5 AC pertussis vaccine (lot: U6612AA, expiry date: 19-Mar-2022; formulation and strength not reported) via intramuscular route for immunization. On an unknown date, the patient was administered an expired diphtheria-2/tetanus/5 AC pertussis vaccine, with no reproted adverse event (expired product administered). Action taken 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
Expired product administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2203577

SANOFI PASTEUR · TDAP (ADACEL) · Charge U6612AA

gering
Staat
KS
Alter
11,0
Geschlecht
M
Eingang
29.03.2022
Impfdatum
21.03.2022
Beginn
21.03.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered Medication error No adverse event

Symptomtext

11 year-old boy received an ADACEL vaccine that was then noted to have expired with no reported adverse event; Initial information received on 21-Mar-2022 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 11 years old male patient who experienced 11 year-old boy received an adacel vaccine that was then noted to have expired with no reported adverse event while receiving vaccine diphtheria-2/tetanus/5 ac pertussis vaccine [Adacel]. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. Concomitant medications included meningococcal vaccine a/c/y/w conj (dip tox) (Menactra) for Prophylactic vaccination. On 21-Mar-2022, the patient received 0.5 ml dose of suspect diphtheria-2/tetanus/5 ac pertussis vaccine (batch lot :U6612AA) (unknown strength and expiry date) via intramuscular route in the right deltoid for immunisation On 21-Mar-2022 (latency: same day)the patient developed a non-serious event of 11 year-old boy received an adacel vaccine that was then noted to have expired with no reported adverse event (expired product administered) following the administration of diphtheria-2/tetanus/5 ac pertussis vaccine. Action taken : not applicable. It was not reported if the patient received a corrective treatment for the event . 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
-