VAERS Reports UJ320AAA

VAERS 1105930

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ320AAA

mild

Staat: ID
Alter: 0,3
Geschlecht: F
Eingang: 16.03.2021
Impfdatum: 19.02.2021
Beginn: 19.02.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RL

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

Urticaria

Symptomtext

The patient developed hives on her trunk and both legs within 10 min after being vaccinated. The patient was kept in the office for over 30 min for observation, no additional symptoms developed and hives did not worsen or spread to other areas of her body. Patient's mother was given instructions to monitor for signs of anaphylaxis and instructed to call 911 if these symptoms developed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Urticaria
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none reported
Vorgeschichte: none
Andere Medikamente: Cholecalciferol 10 mcg/0.03 mL liquid
Allergien: none
Vorherige Impfungen: -

VAERS 2530634

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ320AAA

gering

Staat: WA
Alter: 2,0
Geschlecht: F
Eingang: 14.12.2022
Impfdatum: 08.12.2022
Beginn: 08.12.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: OT / -

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

Expired product administered No adverse event

Symptomtext

expired pentacel vaccine being administered with no reported adverse event; Initial information received on 09-Dec-2022 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 2 years old female patient who experienced expired pentacel vaccine being administered with no reported adverse event after receiving vaccine DIPHTHERIA/TETANUS/5 HYBRID AC PERTUSSIS/IPV(MRC5)/HIB(PRP/T) VACCINE [PENTACEL]. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. Concomitant medications included PNEUMOCOCCAL VACCINE CONJ 7V (CRM197) (PREVNAR) for Prophylactic vaccination; and HEPATITIS A VACCINE (HEPATITIS A) for Prophylactic vaccination. On 08-Dec-2022, the patient received 2 dose of suspect DIPHTHERIA/TETANUS/5 HYBRID AC PERTUSSIS/IPV(MRC5)/HIB(PRP/T) VACCINE at a dose of 0.5 ml (lot UJ320AAA)(unknown strength and expiry date) via intramuscular route at Vastus Lateralis for prophylactic immunisation(immunisation). On 08-Dec-2022 the patient had a non-serious event of expired pentacel vaccine being administered with no reported adverse event (expired product administered) following the administration of DIPHTHERIA/TETANUS/5 HYBRID AC PERTUSSIS/IPV(MRC5)/HIB(PRP/T) VACCINE. Action taken: not applicable. At time of reporting, the outcome was Unknown for the event expired pentacel vaccine being administered with no reported adverse 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: -