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Reporte zur Charge UJ637AA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

2Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
NJ 1 OH 1

VAERS 2267669

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ637AA

mild
Staat
NJ
Alter
1,3
Geschlecht
F
Eingang
09.05.2022
Impfdatum
04.05.2022
Beginn
04.05.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Extra dose administered Fatigue

Symptomtext

patients mother states her child went to this clinic and was given a dose of the ActHIB vaccine, however the pt had previously been given 3 doses of PedvaxHIB vaccine, which was the full dose series. This was doctor insisted that the patient receive the 4th dose of the HIB vaccine even though she completed the entire PedvaxHIB series (series of 3 to complete) . She tried to explain to the doctor that the patient had already completed this vaccine but he did not check the state website or obtain previous medical records prior to administering this. Patient was extremely tired after receiving this shot.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Fatigue
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
pt has to have one vaccine at a time due to having issues when receiving more than one

VAERS 2524925

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ637AA

gering
Staat
OH
Alter
1,3
Geschlecht
F
Eingang
07.12.2022
Impfdatum
-
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered Medication error No adverse event

Symptomtext

administered ACTHIB to a patient wherein the diluent is expired by one day with no reported adverse event; Initial information received on 01-Dec-2022 regarding an unsolicited valid non-serious case via other health professional. This case involves a 16-month-old female patient who was administered ACTHIB to a patient wherein the diluent is expired by one day with no reported adverse event after receiving vaccine HIB (PRP/T) vaccine [ACT-HIB]. The patient's past medical history, medical treatment(s), vaccination(s), concomitant(s) and family history were not provided. Concomitant medications included diphtheria vaccine toxoid, pertussis vaccine acellular, tetanus vaccine toxoid (DTAP). On an unknown date, the patient received a 0.5 ml dose of suspect HIB (PRP/T) vaccine (batch lot number: UJ637AA) (strength, form: unknown) (expiry date: 27-Feb-2022) via unknown route in unknown administration site for Immunization. On an unknown date the patient had a non-serious event of administered ACTHIB to a patient wherein the diluent is expired by one day with no reported adverse event (expired product administered) (latency: same day) following the administration of HIB (PRP/T) vaccine. Action taken with haemophilus type B (HIB) vaccine (ACT-HIB) was not applicable. 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 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
-