VAERS Reports UJ738AA

VAERS 2260080

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ738AA

mild

Staat: UT
Alter: 0,5
Geschlecht: M
Eingang: 01.05.2022
Impfdatum: 26.04.2022
Beginn: 29.04.2022
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / LL

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Pyrexia Rash

Symptomtext

2 days of fever, rash on 3rd day treated with nystatin

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: fluoride 0.5mg
Allergien: -
Vorherige Impfungen: -

VAERS 2635783

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ738AA

gering

Staat: AZ
Alter: 60,0
Geschlecht: M
Eingang: 24.05.2023
Impfdatum: 17.05.2023
Beginn: 17.05.2023
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 No adverse event

Symptomtext

60 years patient received expired ACT-HIB with no reported adverse event; Initial information was received on 19-May-2023 regarding an unsolicited valid non-serious case received from a nurse. This case involves 60 years old male patient who received expired hib (prp/t) vaccine [ACT-HIB] with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 17-May-2023, the patient received 0.5 ml, total dose of suspect hib (prp/t) vaccine Powder and solvent for solution for injection (lot UJ738AA, expiry date:29-Apr-2023) of unknown strength via intramuscular route in the left deltoid for prophylactic vaccination (Immunization). On 17-May-2023 the patient received expired act-hib with no reported adverse event (expired product administered) (Latency:same day) following the administration of hib (prp/t) vaccine. Action taken: not applicable. At time of reporting, the outcome was Unknown for 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 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: -