VAERS Reports UJ670AAA

VAERS 2470833

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ670AAA

mild

Staat: NY
Alter: 0,2
Geschlecht: M
Eingang: 06.10.2022
Impfdatum: 23.09.2022
Beginn: 28.09.2022
Tage bis Beginn: 5,0
Dosis: 1
Route/Site: IM / LL

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

Crying Fatigue Gastrointestinal wall thickening Haematochezia Intussusception Ultrasound abdomen abnormal

Symptomtext

On 9/28, 5 days after receiving rotateq, infant presented with crying episodes, followed by fatigue and blood in his stool. Abdominal Ultrasound confirmed an ileocolic intussusception. Intussusception self reduced without medical intervention on repeat ultrasound that was done upon transfer to another institution.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 9/29/22, 1:22 am: Abdominal Ultrasound: ileocolic intussusception 9/29/22, 6:53am: Intussusception resolved, wall thickening of terminal ileum and cecum, likely sequela of prior intussusception
Aktuelle Erkrankungen: None
Vorgeschichte: none
Andere Medikamente: -
Allergien: None
Vorherige Impfungen: -

VAERS 2641858

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge UJ670AAA

gering

Staat: NC
Alter: 0,3
Geschlecht: M
Eingang: 06.06.2023
Impfdatum: 22.05.2023
Beginn: 22.05.2023
Tage bis Beginn: 0,0
Dosis: UNK
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

child was administered expired pentacel in the left thigh with no adverse event reported; Initial information received on 22-May-2023 regarding an unsolicited valid non-serious case received from other health professional. This case involves a 4 months old male patient who was administered expired diphtheria/tetanus/5 hybrid AC pertussis/IPV(VERO)/HIB(PRP/T) vaccine [Pentacel (Vero)] in the left thigh with no adverse event reported. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. Concomitant medications included pneumococcal vaccine polysacch 23V (Pneumovax) and Rotavirus Vaccine for Prophylactic vaccination (immunization). On 22-May-2023, the patient received 0.5ml expired dose of suspect diphtheria/tetanus/5 hybrid AC pertussis/ IPV (vero)/HIB (PRP/T) vaccine (batch number: UJ670AAA; expiry date: 13-May-2023) via unknown route in the left thigh for immunization with no adverse event reported (expired product administered) (same day latency). Action taken: not applicable. At time of reporting, the outcome was Unknown for the event child was administered expired pentacel in the left thigh with no adverse event reported. 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: PNEUMOVAX; ROTAVIRUS VACCINE
Allergien: -
Vorherige Impfungen: -