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Reporte zur Charge UT8134MA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

7Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
NY 2 PA 2 MN 1 TX 1 WI 1

VAERS 2715725

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT8134MA

schwer
Staat
MN
Alter
12,0
Geschlecht
F
Eingang
20.11.2023
Impfdatum
19.11.2023
Beginn
19.11.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: unbekannt
Blood pressure decreased Cold sweat Injection site haemorrhage Loss of consciousness Pallor Vomiting

Symptomtext

A few minutes after vaccination, patient noticed blood leaking out of her bandage. As the pharmacist was cleaning up patient's arm and replacing the bandage, the patient lost consciousness for approximately 15-30 seconds. Patient regained consciousness and then was able to walk, then vomited. Patient was then seated by the pharmacy. Pharmacist attempted to check blood pressure, but got an error reading. Patient was given water per request. Patient vomited a second time. Patient seemed clammy and a bit pale. Per Pharmacist's best clinical judgment, EMS was called. Paramedics arrived about 1pm and decided to take patient to the hospital due to patient's low blood pressure readings and as a monitoring precaution.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Loss of consciousness
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2722235

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT8134MA

mild
Staat
NY
Alter
56,0
Geschlecht
F
Eingang
08.12.2023
Impfdatum
03.12.2023
Beginn
04.12.2023
Tage bis Beginn
1,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Injection site cellulitis Injection site erythema Injection site pain

Symptomtext

Patient described having a localized redness and tenderness at the injection site, which over the course of the 48 hours post-vaccination spread down her arm. At a routine primary care visit, her physician diagnosed her with cellulitis pertinent to the injection. The patient was treated by her physician and is recovering.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site cellulitis
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2719016

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT8134MA

mild
Staat
TX
Alter
62,0
Geschlecht
F
Eingang
29.11.2023
Impfdatum
29.11.2023
Beginn
29.11.2023
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Erythema Pruritus

Symptomtext

After Influenza Vaccine given, patient complain of feeling itching on the left arm and on the back. After inspection, notice mild redness . Dr. notified. Doctor assessed patient and order Diphenhydramine 50 mg/ml injection and given at 10:06. At 10:15 patient report relief.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pruritus
Hospital-Tage
-
Labordaten
NA
Aktuelle Erkrankungen
hypertension hyperlipidemia memory loss
Vorgeschichte
hypertension hyperlipidemia memory loss
Andere Medikamente
None
Allergien
Fish Containing Products, Iodine, Penicillin Alendronate
Vorherige Impfungen
-

VAERS 2707269

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT8134MA

mild
Staat
WI
Alter
51,0
Geschlecht
F
Eingang
31.10.2023
Impfdatum
19.10.2023
Beginn
19.10.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Rash Rash erythematous Rash pruritic

Symptomtext

About two hours post vaccine patient presented to nurse with a rash that presented on her right arm. rash was itchy and had a red and hive type appearance. Provider in the clinic advised 25 mg oral Benadryl.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Rash
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2725457

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT8134MA

gering
Staat
PA
Alter
2,0
Geschlecht
F
Eingang
19.12.2023
Impfdatum
12.12.2023
Beginn
12.12.2023
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Expired product administered

Symptomtext

THE HAVRIX VACCINE (HEPATITIS A) THAT WAS GIVEN ON 12/12/2023 HAD EXPIRED ON 12/07/2023.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
NONE
Aktuelle Erkrankungen
NONE
Vorgeschichte
NONE
Andere Medikamente
NONE
Allergien
NKA
Vorherige Impfungen
-

VAERS 2711218

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT8134MA

gering
Staat
NY
Alter
5,0
Geschlecht
F
Eingang
07.11.2023
Impfdatum
23.10.2023
Beginn
23.10.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
OT / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Extra dose administered No adverse event

Symptomtext

administration of multiple Flu vaccines in one flu season with no reported adverse event; Initial information received on 23-Oct-2023 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 5 years old female patient who was administered multiple flu vaccines in one flu season with no reported adverse event with influenza quadrival A-B vaccine [fluzone quadrivalent]. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 23-Oct-2023, the patient received a dose 1, 0.5 ml of suspect influenza quadrival A-B vaccine, Suspension for injection lot UT8134MA, expiry date: 30-Jun-2024 via intramuscular route in the left arm for immunization, was administered multiple flu vaccines in one flu season with no reported adverse event (inappropriate schedule of product administration) (latency same day). Action taken: not applicable. 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 2703701

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT8134MA

gering
Staat
PA
Alter
8,0
Geschlecht
F
Eingang
27.10.2023
Impfdatum
19.10.2023
Beginn
19.10.2023
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Incorrect dose administered

Symptomtext

Pt. given 0.5ml instead of 0.25ml - Covid Vaccine

Weitere VAERSDATA-Felder
Praegender Schweregrund
Incorrect dose administered
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
-
Allergien
Allergic to Amoxicillin and zithromax
Vorherige Impfungen
-