VAERS Reports U6586BA

VAERS 974800

SANOFI PASTEUR · MENINGOCOCCAL CONJUGATE (MENACTRA) · Charge U6586BA

mild

Staat: AL
Alter: 22,0
Geschlecht: F
Eingang: 26.01.2021
Impfdatum: 19.01.2021
Beginn: 21.01.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / RA

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

Headache Injection site swelling Pyrexia Urticaria

Symptomtext

48-72hours after the patient had low grade fever, headache, swollen arm at injection site, and welps on upper back and shoulder

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1908672

SANOFI PASTEUR · MENINGOCOCCAL CONJUGATE (MENACTRA) · Charge U6586BA

gering

Staat: NV
Alter: 13,0
Geschlecht: F
Eingang: 30.11.2021
Impfdatum: 16.11.2021
Beginn: 16.11.2021
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

Symptomtext

expired MENACTRA was administered to a patient with no AE; Initial information was received on 19-Nov-2021 regarding an unsolicited valid non-serious case from a pharmacist via Global Medical Information (GMI) (under reference: 00866702). This case involves a 13-year-old female patient who was administered expired MENINGOCOCCAL A-C-Y-W135 (D CONJ) VACCINE [MENACTRA] (expired product administered). The patient's medical history, past medical treatment(s), vaccination(s), concomitant medication(s) and family history were not provided. On 16-Nov-2021, the patient received a dose of suspect MENINGOCOCCAL A-C-Y-W135 (D CONJ) VACCINE (0.5mL, lot U6586BA, expiry date Apr-2021) via intramuscular route at an unknown administration site for prophylactic vaccination. It was a case of actual medication error due to expired vaccine used (latency: same day). It was reported "An expired MENACTRA was administered to a patient. Pharmacist wants to know what to do?" At time of reporting, no adverse event was 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 by the regulatory authority. 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: -