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Reporte zur Charge UT7356NA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

2Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
OH 1 CO 1

VAERS 1843238

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7356NA

moderat
Staat
OH
Alter
53,0
Geschlecht
F
Eingang
04.11.2021
Impfdatum
13.10.2021
Beginn
20.10.2021
Tage bis Beginn
7,0
Dosis
1
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Injected limb mobility decreased Injection site pain Product administered at inappropriate site

Symptomtext

Worsening left should pain with subsequent decrease in range of motion, thought to be due to incorrect placement of the injection near or into the shoulder joint.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injected limb mobility decreased
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
heart failure, GERD, Hypertension, mitral valve prolapse
Andere Medikamente
Lasix, potassium, metoprolol
Allergien
sulfa drugs- causes rash
Vorherige Impfungen
-

VAERS 2489634

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7356NA

gering
Staat
CO
Alter
37,0
Geschlecht
F
Eingang
26.10.2022
Impfdatum
11.10.2022
Beginn
11.10.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered

Symptomtext

patient was accidentally administered an expired Fluzone Quadrivalent with no reported adverse event; Initial information received on 14-Oct-2022 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 37 years old female patient was accidentally administered an expired Influenza quadrival A-B vaccine [Fluzone Quadrivalent] with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 11-Oct-2022, the patient was accidentally administered an expired 0.5ml (total) dose of suspect Influenza quadrival A-B vaccine (lot UT7356NA;Expiration Date :30-Jun-2022) via intramuscular route in the left deltoid for Immunization with no reported adverse event (expired product administered). 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 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
-