VAERS Reports UJ523AA

VAERS 1403610

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ523AA

kritisch

Staat: CO
Alter: 0,2
Geschlecht: F
Eingang: 16.06.2021
Impfdatum: 14.06.2021
Beginn: 14.06.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LL

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

Death Respiratory arrest Resuscitation

Symptomtext

Patient was doing well until the evening of 6/14/21 when she suddenly stopped breathing while laying on side on father's chest. CPR attempted and was taken to hospital by EMS but unable to regain spontaneous circulation despite ACLS measures. Patient expired.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: -
Vorgeschichte: Congenital heart disease (VSD resolved, pulmonic stenosis), right renal agenesis, right inguinal hernia, right sensorineural hearing loss
Andere Medikamente: Pediatric multivitamin Ferrous sulfate
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 1231974

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ523AA

schwer

Staat: VA
Alter: 1,3
Geschlecht: M
Eingang: 20.04.2021
Impfdatum: 19.04.2021
Beginn: 19.04.2021
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LL

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

Pyrexia Seizure

Symptomtext

Mom reports seizure activity at home around 6 pm. Mom did not notice anything that stood out from his normal behavior. Paramedic's were called post seizure activity and child was checked out to be stable with a fever of 102.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: fever at the time the paramedics arrived was 102 per mom.
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: NKA
Vorherige Impfungen: -

VAERS 2177103

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ523AA

gering

Staat: PA
Alter: 74,0
Geschlecht: F
Eingang: 12.03.2022
Impfdatum: 03.03.2022
Beginn: 03.03.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / RA

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

Incorrect dose administered Medication error No adverse event Product administered to patient of inappropriate age Wrong product administered

Symptomtext

received the pentacel vaccine today instead of the tetanus shot with no reported adverse event; 74 years old took Pantacel vaccine with no reported adverse event; Initial information was received on 03-Mar-2022 regarding an unsolicited non-valid non-serious case received from a health professional via call center. This case involves a 74 years old female patient who reported that received the pentacel vaccine today instead of the tetanus shot with no reported adverse event while 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. On 03-Mar-2022, the patient received a dose of Diphtheria/Tetanus/5 Hybrid AC Pertussis/IPV(MRC5)/HIB(PRP/T) Vaccine suspension for injection(strength: unknown)at dose of 0.5ml (lot UJ523AA and expiry date:22-jul-2022) via intramuscular route in the right deltoid for immunization. On 03-MAR-2022, a 74years old patient reported that she received the pentacel vaccine today instead of the tetanus shot with no reported adverse event (incorrect dose administered)and (product administered to patient of inappropriate age) (latency: same day) 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 incorrect dose administration and product administered to patient of inappropriate age. 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: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -