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Reporte zur Charge UJ57AA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

2Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
TX 2

VAERS 2526272

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge UJ57AA

gering
Staat
TX
Alter
1,5
Geschlecht
F
Eingang
08.12.2022
Impfdatum
06.10.2022
Beginn
06.10.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered No adverse event

Symptomtext

expired PENTACEL was administered to one of their patients in October with no reported adverse event; Initial information was received on 05-Dec-2022 regarding an unsolicited valid non-serious case received from a healthcare professional. This case involves a 18 months old female patient who was administered expired Diphtheria/tetanus/5 hybrid AC pertussis/IPV(VERO)/HIB(PRP/T) vaccine [pentacel (VERO)] to one of their patients in october 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: Hepatitis A vaccine (Hepatitis A) and Pneumococcal vaccine CONJ 13V (CRM197) (Prevnar 13) for prophylactic vaccination. On 06-Oct-2022, the patient received expired Diphtheria/tetanus/5 hybrid AC pertussis/IPV(VERO)/HIB(PRP/T) vaccine at a dose of 0.5 ml (lot UJ57AA, expiration date: 11-Sep-2022) via intramuscular route in the right thigh for immunization to one of their patients in October with no reported adverse event (expired product administered) (unknown latency). Action taken: Not applicable. Corrective treatment: Not reported. 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
HEPATITIS A; PREVNAR 13
Allergien
-
Vorherige Impfungen
-

VAERS 2523077

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ57AA

gering
Staat
TX
Alter
1,5
Geschlecht
F
Eingang
05.12.2022
Impfdatum
06.10.2022
Beginn
06.10.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
No adverse event

Symptomtext

No reaction noted to patient, injection site clear and well , no symptoms noted or reported by parent.

Weitere VAERSDATA-Felder
Praegender Schweregrund
No adverse event
Hospital-Tage
-
Labordaten
No test done.
Aktuelle Erkrankungen
Possibility of constipation discussed at time of visit to the clinic. Provider recommended laxative, but mom declined at that moment, instead discussed using prune juice, increase fluids, fruits and veggies.
Vorgeschichte
None noted at the time of visit.
Andere Medikamente
Fluoride was an administered in clinic. No prescription medications sent at time of visit.
Allergien
NKA allergies to medications, food or other products.
Vorherige Impfungen
-