VAERS Reports UJ090AA

VAERS 931513

SANOFI PASTEUR · YELLOW FEVER (YF-VAX) · Charge UJ090AA

mild

Staat: CA
Alter: 24,0
Geschlecht: M
Eingang: 09.01.2021
Impfdatum: 30.10.2020
Beginn: 30.10.2020
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SC / UN

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

Abdominal pain upper Influenza virus test Physical examination SARS-CoV-2 test

Symptomtext

Severe stomach pain (sharp)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain upper
Hospital-Tage: -
Labordaten: Physical exam to rule out appendicitis. Flu and COVID nasal swab.
Aktuelle Erkrankungen: Positive COVID-19 11/1/2020 Negative COVID-19 11/3/2020
Vorgeschichte: None
Andere Medikamente: None
Allergien: NKA
Vorherige Impfungen: -

VAERS 1068415

SANOFI PASTEUR · YELLOW FEVER (YF-VAX) · Charge UJ090AA

gering

Staat: -
Alter: -
Geschlecht: M
Eingang: 03.03.2021
Impfdatum: -
Beginn: 10.02.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: OT / LA

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

Expired product administered No adverse event

Symptomtext

patient ent was administered 0.5 ml of YF-Vax that had expired in the left upper arm with no reported adverse event; Initial information regarding an unsolicited valid non-serious case was received from a other health professional (nurse). This case involved a 40 year old male patient who received 0.5 mL dose of suspect YELLOW FEVER VACCINE - US [YF-VAX] [lot number: UJ090AA] via an unknown route at the left upper arm for prophylactic vaccination which was expired on 08-Jan-2021 (expired product administered). Medical history, medical treatment, vaccination, family history and concomitant medication were not reported. It was a case of actual medication error due to expired vaccine used. It was reported that, no other medications or vaccinations were given at that time. At the time of report, 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 in Directive 2001/83/EC and Module VI of the Good Pharmacovigilance Practices. 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 1068412

SANOFI PASTEUR · YELLOW FEVER (YF-VAX) · Charge UJ090AA

gering

Staat: -
Alter: -
Geschlecht: U
Eingang: 03.03.2021
Impfdatum: 10.02.2021
Beginn: 10.02.2021
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 No adverse event

Symptomtext

patient received expired YF-VAX vaccine/ NO AE; Initial information received on 12-Feb-2021 regarding an unsolicited valid non-serious case received from a other health professional. This case involves patient (unknown demographics) who received 0.5 mL YELLOW FEVER VACCINE - US [YF-VAX] (batch number: UJ090AA and expiry date: 08-Jan-2021 via an unknown at an unknown administration site) (expired product administered) on 10-Feb-2021 for prophylactic vaccination. The patient's medical history, past medical treatment, vaccination, concomitant medication and family history were not provided. It was an actual medication error case due to expired vaccine used (latency: same day). Caller would like to know if patient needs to revaccinate. The caller stated that he did not have time to provide additional adverse event details at the time of the call, as he was involved in patient care. He stated he would call back with the details. No Still using product. At the 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 in Directive 2001/83/EC and Module VI of the Good Pharmacovigilance Practices. 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: -