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Reporte zur Charge U7584AD

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

1Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
WA 1

VAERS 2647605

UNKNOWN MANUFACTURER · MENINGOCOCCAL (NO BRAND NAME) · Charge U7584AD

gering
Staat
WA
Alter
-
Geschlecht
U
Eingang
21.06.2023
Impfdatum
-
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Accidental exposure to product Medication error No adverse event

Symptomtext

the vial cut finger of staff member when removing from carton with no repoted adverse event; Initial information was received on 15-Jun-2023 regarding an unsolicited valid non-serious case received from a other health professional. This case involves an unknown age and unknown gender patient who reported that the vial cut finger of staff member when removing from carton with no repoted adverse event after receiving vaccine meningococcal a-c-y-w135 (t conj) vaccine [Menquadfi]. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On an unknown date, the patient received a unknown dose of suspect meningococcal a-c-y-w135 (t conj) vaccine (Solution for injection) (lot U7584AD) (strength, expiry date unknown) via unknown route in unknown administration site for prophylactic vaccination(Immunization). On an unknown date the patient developed a non-serious event of the vial cut finger of staff member when removing from carton with no repoted adverse event (accidental exposure to product) (unknown latency) following the administration of meningococcal a-c-y-w135 (t conj) vaccine. Action taken with meningococcal vaccine (Menquadfi) was not applicable. At time of reporting, the outcome was Unknown for the event the vial cut finger of staff member when removing from carton with no repoted adverse 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
Accidental exposure to product
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
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Andere Medikamente
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Allergien
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Vorherige Impfungen
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