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Reporte zur Charge UT7407MA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

7Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
TN 4 TX 2 MO 1

VAERS 1967899

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7407MA

schwer
Staat
MO
Alter
2,0
Geschlecht
M
Eingang
21.12.2021
Impfdatum
20.12.2021
Beginn
20.12.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja
Febrile convulsion Pyrexia

Symptomtext

Patient developed a 103 F fever 30 minutes after vaccine and had a febrile seziure.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Febrile convulsion
Hospital-Tage
-
Labordaten
Patient was seen in the ER on 12/20/21.
Aktuelle Erkrankungen
Left ear infection on 12/07/21, treated with Amoxicillin
Vorgeschichte
N/A
Andere Medikamente
2.5 mL of Cetirizine Flonase
Allergien
NKDA
Vorherige Impfungen
-

VAERS 2460226

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7407MA

gering
Staat
TX
Alter
15,0
Geschlecht
M
Eingang
26.09.2022
Impfdatum
15.09.2022
Beginn
15.09.2022
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

administered FLUZONE QIV NP after the expiration date with no reported adverse event; Initial information received on 16-Sep-2022 regarding an unsolicited valid non-serious case received from a pediatrician. This case involves a 15-year-old male patient to whom INFLUENZA QUADRIVAL A-B VACCINE [FLUZONE QIV] np was administered after the expiration date with no reported adverse event while receiving vaccine. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 15-Sep-2022, the patient received suspect Fluzone QIV at dose 0.5ml once via intramuscular route in the left deltoid (lot: UT7407MA, expiry date: 30-Jun-2022) for prophylactic vaccination with no reported adverse event (expired product administered) at latency same day. Action taken: Not applicable. At time of reporting, the outcome was 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
-

VAERS 2459706

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7407MA

gering
Staat
TX
Alter
1,5
Geschlecht
F
Eingang
24.09.2022
Impfdatum
15.09.2022
Beginn
15.09.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered

Symptomtext

administered FLUZONE QIV NP after the expiration date with no reported adverse event; Initial information received fon 16-Sep-2022 regarding an unsolicited valid non-serious case received from a physician. This case involves 18 months old female patient who was administered INFLUENZA QUADRIVAL A-B VACCINE [FLUZONE QIV] after the expiration date with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. Concomitant medications included hepatitis A vaccine (hepatitis A) for Prophylactic vaccination. On 15-Sep-2022, the patient received suspect influenza quadrival A-B vaccine at a dose of 0.5 ml total (lot UT7407MA, expiry date: 30-Jun-2022) via intramuscular route in the left thigh for immunisation. On 15-Sep-2022 the patient was administered fluzone qiv np after the expiration date with no reported adverse event (expired product administered) following the administration of INFLUENZA QUADRIVAL A-B VACCINE. 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
HEPATITIS A
Allergien
-
Vorherige Impfungen
-

VAERS 2079215

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7407MA

gering
Staat
TN
Alter
9,0
Geschlecht
M
Eingang
01.02.2022
Impfdatum
25.01.2022
Beginn
25.01.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
No adverse event Product storage error

Symptomtext

Vaccine had expired 4 days prior. Miscalculated the expiration date. patient given vaccine but no signs or symptoms of any issues. Mom was advised to call with questions or concerns.

Weitere VAERSDATA-Felder
Praegender Schweregrund
No adverse event
Hospital-Tage
-
Labordaten
N/A
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
NKA
Vorherige Impfungen
-

VAERS 2079207

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7407MA

gering
Staat
TN
Alter
9,0
Geschlecht
F
Eingang
01.02.2022
Impfdatum
25.01.2022
Beginn
25.01.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Expired product administered No adverse event

Symptomtext

Vaccine given to patient and the vaccine had expired 4 days before. The vaccine expiration date was calculated incorrectly. The patient had no signs or symptoms and the mom was advised if any questions or concerns to call.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
N/A
Allergien
NKA
Vorherige Impfungen
-

VAERS 2079140

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7407MA

gering
Staat
TN
Alter
7,0
Geschlecht
M
Eingang
01.02.2022
Impfdatum
25.01.2022
Beginn
25.01.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
No adverse event Product storage error

Symptomtext

Expiration date expired. Dose given 4 days after expiration. Expiration date calculated incorrectly. Child tolerated well. No signs or symptoms and advised to call if questions or concerns.

Weitere VAERSDATA-Felder
Praegender Schweregrund
No adverse event
Hospital-Tage
-
Labordaten
N/A
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
N/A
Allergien
NKA
Vorherige Impfungen
-

VAERS 2079118

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7407MA

gering
Staat
TN
Alter
5,0
Geschlecht
F
Eingang
01.02.2022
Impfdatum
25.01.2022
Beginn
25.01.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Product storage error

Symptomtext

Dose of COVID 19 vaccine given 4 days after expiration. Incorrectly calculated expiration date.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Product storage error
Hospital-Tage
-
Labordaten
N/A
Aktuelle Erkrankungen
None
Vorgeschichte
-
Andere Medikamente
-
Allergien
NKA
Vorherige Impfungen
-