Zurueck zur Suche

Reporte zur Charge UT8040MA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

8Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
OH 3 TX 2 MA 1 TN 1 PA 1

VAERS 2702650

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT8040MA

mild
Staat
OH
Alter
4,0
Geschlecht
F
Eingang
26.10.2023
Impfdatum
25.10.2023
Beginn
26.10.2023
Tage bis Beginn
1,0
Dosis
6
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Injection site erythema Injection site swelling

Symptomtext

redness/swelling to sites

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site erythema
Hospital-Tage
-
Labordaten
n/a
Aktuelle Erkrankungen
none
Vorgeschichte
none
Andere Medikamente
none
Allergien
Latex
Vorherige Impfungen
-

VAERS 2701658

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT8040MA

mild
Staat
OH
Alter
2,0
Geschlecht
M
Eingang
25.10.2023
Impfdatum
23.10.2023
Beginn
24.10.2023
Tage bis Beginn
1,0
Dosis
4
Route/Site
IM / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Injection site erythema Injection site warmth

Symptomtext

redness/warmth to right upper thigh

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site erythema
Hospital-Tage
-
Labordaten
n/a
Aktuelle Erkrankungen
Hypertrophy of tonsil, Recurrent tonsillitis, Platelet function defect
Vorgeschichte
-
Andere Medikamente
Received several courses of oral antibiotics prior to appointment.
Allergien
Ragweed Pollen.
Vorherige Impfungen
-

VAERS 2715026

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT8040MA

gering
Staat
MA
Alter
15,0
Geschlecht
F
Eingang
17.11.2023
Impfdatum
15.11.2023
Beginn
15.11.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Extra dose administered

Symptomtext

This patient received 2 Flu vaccines in the month of November. One Flu vaccine was administered 11/02/2023 and the other Flu vaccine was administered 11/15/2023.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Extra dose administered
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
No
Vorgeschichte
Autism
Andere Medikamente
Benefiber, Culterelle, MVI, MOM
Allergien
Penicillin,
Vorherige Impfungen
-

VAERS 2714186

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT8040MA

gering
Staat
TN
Alter
12,0
Geschlecht
F
Eingang
15.11.2023
Impfdatum
14.11.2023
Beginn
14.11.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Wrong product administered

Symptomtext

Dad brought in daughter for vaccinations. He agreed to have her receive: MMR, Hep B, Flu, Polio, and Tdap. I inadvertently drew up and administered Dtap instead of Tdap vaccine, after administering all 5 vaccines, I then discovered the error and immediately notified my nursing supervisor. After reviewing protocol, I went and spoke with dad and daughter. I advised them of the error, and that the dose doesn't require repeat vaccination. Dad and daughter both verbalized understanding and they were both ok with it.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Wrong product administered
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
None reported
Vorgeschichte
None reported
Andere Medikamente
None reported
Allergien
None reported
Vorherige Impfungen
-

VAERS 2711229

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT8040MA

gering
Staat
TX
Alter
-
Geschlecht
U
Eingang
07.11.2023
Impfdatum
-
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Extra dose administered No adverse event

Symptomtext

given an extra dose of FLUZONE QIV-NP to a patient with no reported adverse event; Initial information received on 26-Oct-2023 regarding an unsolicited valid non-serious case received from a nurse. This case involves an unknown age and unknown gender patient who was given an extra dose of Influenza Quadrival A-B Vaccine [Fluzone Qiv] to a patient with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On an unknown date, the patient received an 0.5 ml total (1 X) of suspect Influenza Quadrival A-B Vaccine Suspension for injection (lot number: UT8040MA) (Expiry date: 30-Jun-2024) (strength: standard) (Frequency: once) via unknown route in unknown administration site for immunization. On an unknown date, the patient was given an extra dose of Influenza Quadrival A-B Vaccine to a patient with no reported adverse event (extra dose administered) (unknown latency). It was reported, Nurse called to inform that they have given an extra dose of FLUZONE QIV-NP to a patient. Licensed Vocational Nurse told that the patient received the vaccine 4 weeks ago from another facility and the patient came to their clinic and was injected an extra dose of the vaccine. Licensed Vocational Nurse informed that she cannot share any information on the patient and only provided the lot number, expiration date and NDC number of the vaccine. This situation is reported as a medication error due to vaccine double dosing. 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
Extra dose administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2710138

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT8040MA

gering
Staat
TX
Alter
1,2
Geschlecht
M
Eingang
06.11.2023
Impfdatum
03.11.2023
Beginn
03.11.2023
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
IM / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Extra dose administered

Symptomtext

the patient had flu vaccines 2/20/23 and 3/31/23 for 2022-2023 flu season. He also had flu vaccine 9/29/23 for 2023-2024 flu season. An extra dose of flu vaccines was given on 11/3/23 to the patient. No harm was caused to the patient. Incident report was filed. Parent was notified.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Extra dose administered
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
NONE
Vorgeschichte
NONE
Andere Medikamente
Flu vaccine, Fluzone
Allergien
NONE
Vorherige Impfungen
-

VAERS 2702602

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT8040MA

gering
Staat
OH
Alter
4,0
Geschlecht
F
Eingang
26.10.2023
Impfdatum
25.10.2023
Beginn
26.10.2023
Tage bis Beginn
1,0
Dosis
6
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Erythema Swelling

Symptomtext

Redness to area and swollen

Weitere VAERSDATA-Felder
Praegender Schweregrund
Erythema
Hospital-Tage
-
Labordaten
n/a
Aktuelle Erkrankungen
none
Vorgeschichte
none
Andere Medikamente
none
Allergien
Latex
Vorherige Impfungen
-

VAERS 2700873

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT8040MA

gering
Staat
PA
Alter
0,2
Geschlecht
M
Eingang
24.10.2023
Impfdatum
24.10.2023
Beginn
24.10.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Product administered to patient of inappropriate age

Symptomtext

Patient is 2 mo old and was inadvertently given influenza vaccine,-

Weitere VAERSDATA-Felder
Praegender Schweregrund
Product administered to patient of inappropriate age
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
none
Vorgeschichte
none
Andere Medikamente
none
Allergien
none
Vorherige Impfungen
-