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Reporte zur Charge UJ679AAA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

2Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
TX 1 CA 1

VAERS 2627817

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ679AAA

gering
Staat
TX
Alter
1,0
Geschlecht
U
Eingang
06.05.2023
Impfdatum
07.04.2023
Beginn
07.04.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered No adverse event

Symptomtext

expired ACTHIB vaccine was given, with no reported adverse event; Initial information received on 01-May-2023 regarding an unsolicited valid non-serious case received from a consumer/non-healthcare professional. This case involves a 1 years old and unknown gender patient where expired acthib vaccine was given, with no reported adverse event while receiving vaccine hib (prp/t) vaccine [act-HIB]. The patient's past medical history, medical treatment(s), concomitant medication(s) and family history were not provided. On 07-Apr-2023, the patient received a dose of suspect hib (prp/t) vaccine (batch number- UJ679AAA) via unknown route in unknown administration site (dose, frequency, route, formulation, strength and expiration date: not provided) for Immunization. On 07-Apr-2023 expired acthib vaccine was given, with no reported adverse event (expired product administered) (latency- same day) following the administration of hib (prp/t) vaccine. It was reported asking guidance on giving an expired ACTHIB to a patient on Friday, 07Apr2023. Product used : Used Action taken- Not applicable. At time of reporting, the outcome was Unknown for the 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
-

VAERS 2574700

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ679AAA

gering
Staat
CA
Alter
3,0
Geschlecht
F
Eingang
03.02.2023
Impfdatum
27.01.2023
Beginn
27.01.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
OT / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Medication error No adverse event Product preparation error Product storage error

Symptomtext

using an alternate diluent from an MMR vaccine that had been kept at room temperature with no reported adverse event; using an alternate diluent from an MMR vaccine with no reported adverse event; Initial information received on 30-Jan-2023 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 3 years old female patient who received HIB (PRP/T) Vaccine [ACT-HIB] using an alternate diluent from an mmr vaccine that had been kept at room temperature with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. Concomitant medications included Hepatitis B Vaccine (Hepatitis B [Hepatitis B Vaccine]) for Prophylactic vaccination. On 27-Jan-2023, the patient received a dose of 0.5 ml Total dose 1 of suspect HIB (PRP/T) Vaccine using an alternate diluent from an mmr vaccine that had been kept at room temperature with no reported adverse event (product storage error), (product preparation error) Powder and solvent for solution for injection: form (lot: UJ679AAA) via intramuscular route in the left thigh for immunization with expiry date: 07-Apr-2023 with unknown strength. Action taken: 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
Medication error
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-