VAERS Reports UT7035NA

VAERS 978200

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7035NA

moderat

Staat: IN
Alter: 25,0
Geschlecht: F
Eingang: 27.01.2021
Impfdatum: 13.10.2020
Beginn: 13.10.2020
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Paraesthesia oral Pharyngeal paraesthesia Pruritus Throat tightness

Symptomtext

10/13/20/ pm - Received FLU vaccine. About 3pm facial itching, lips tingling, throat itching/tight feeling. 5:30 pm took Allegra which resolved symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia oral
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: birth control - seasonique, multivitamin
Allergien: sulfa's (Antibiotic)
Vorherige Impfungen: -

VAERS 1931698

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7035NA

gering

Staat: GA
Alter: -
Geschlecht: U
Eingang: 08.12.2021
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

Symptomtext

This case involves patients with an unknown age and gender who received an expired dose of INFLUENZA QUADRIVAL A-B VACCINE [FLUZONE QUADRIVALENT] with no reported adverse event (expired product administered). The patient's medical history, past medical treatments, concomitant medications, vaccinations, and family history were not provided. On an unknown date, the patients received a dose of suspect INFLUENZA QUADRIVAL A-B VACCINE (lot number: UT7035NA and expiry date: 30-Jun-2021) via unknown route in unknown administration site for prophylactic vaccination. It was case of an actual medication error due to expired vaccine used (latency: same day). It was reported "The caller stated that there were several employees that received the expired dose of FLUZONE QUADRIVALENT Prefilled syringe (PFS). The caller estimated about NINE employees, but did not have any patient specific information to provide. The caller did not know the date of administration." 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 the Directive 2001/83/EC and Module VI. 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 1821031

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge UT7035NA

gering

Staat: MN
Alter: 28,0
Geschlecht: F
Eingang: 27.10.2021
Impfdatum: 18.01.2021
Beginn: 24.10.2021
Tage bis Beginn: 279,0
Dosis: 2
Route/Site: IM / LA

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

COVID-19 SARS-CoV-2 test positive

Symptomtext

Covid symptoms (mild)

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Positive Covid-19 PCR test on 10/16/21
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -