Zurueck zur Suche

Reporte zur Charge UT7316NA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

5Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
WA 2 CA 1 NJ 1 RI 1

VAERS 1825538

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7316NA

schwer
Staat
CA
Alter
11,0
Geschlecht
F
Eingang
28.10.2021
Impfdatum
28.10.2021
Beginn
28.10.2021
Tage bis Beginn
0,0
Dosis
7+
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Muscle twitching Presyncope

Symptomtext

Per mother's report, Near syncopal and minor twitching

Weitere VAERSDATA-Felder
Praegender Schweregrund
Presyncope
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
none
Vorgeschichte
none
Andere Medikamente
none
Allergien
none
Vorherige Impfungen
-

VAERS 2039135

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7316NA

mild
Staat
WA
Alter
1,3
Geschlecht
F
Eingang
12.01.2022
Impfdatum
14.12.2021
Beginn
28.12.2021
Tage bis Beginn
14,0
Dosis
1
Route/Site
IM / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Rash erythematous Rash papular Swelling

Symptomtext

Patient developed red, swollen, raised rash on Tuesday 12/28/21, 2 weeks after her Varicella vaccine. Parent's presented to the Clinic for concerns. Patient is well appearing and has no other symptoms. Rash does not seem to bother patient. Doctor educated parents that "1-3 percent of patients who receive varicella vaccine develop a localized rash consisting of two to five lesions at the injection site, and another 3-5 percent develop a generalized varicella-like rash within one month of immunization. Most of the vesticular rashes that occur within the first two weeks after varicella immunization are caused by wild-type VZV. People with rash should refrain from physical contact with people who are susceptible.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Rash erythematous
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
no
Vorgeschichte
None
Andere Medikamente
Vitamin D
Allergien
Unknown
Vorherige Impfungen
-

VAERS 1731146

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7316NA

mild
Staat
NJ
Alter
29,0
Geschlecht
F
Eingang
24.09.2021
Impfdatum
20.09.2021
Beginn
20.09.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja
Asthenia Malaise Urticaria

Symptomtext

pt reported a few hours after vaccine was administered, she developed hives. Also felt sick and weak.

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

VAERS 2513684

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE) · Charge UT7316NA

gering
Staat
RI
Alter
57,0
Geschlecht
M
Eingang
22.11.2022
Impfdatum
12.10.2022
Beginn
12.10.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered No adverse event

Symptomtext

Patient received an expired dose of fluzone QIV with no reported adverse event; Initial information was received on 14-Nov-2022 regarding an unsolicited valid non-serious case received from a other health professional. This case involves 57 years old male patient received an expired dose of fluzone qiv with no reported adverse event after receiving influenza quadrival a-b multidose vaccine preserved [Fluzone]. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 12-Oct-2022, the patient received a dose of 0.5 ml suspect influenza quadrival a-b multidose vaccine preserved (suspection for injection) (Frequency: once) (lot number: UT7316NA,Expiration date:30-Jun-2022)(strength: unknown) via unknown route in unknown administration site for prophylactic vaccination (immunization) . On 12-Oct-2022 the patient received an expired dose of fluzone qiv with no reported adverse event (expired product administered) (latency: same day) following the administration of influenza quadrival a-b multidose vaccine preserved. Action taken : not applicable. At time of reporting, the outcome was Unknown for the event patient received an expired dose of fluzone qiv with no reported adverse event. 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 1894808

SEQIRUS, INC. · INFLUENZA (SEASONAL) (FLUAD QUADRIVALENT) · Charge UT7316NA

gering
Staat
WA
Alter
13,0
Geschlecht
F
Eingang
23.11.2021
Impfdatum
19.11.2021
Beginn
21.11.2021
Tage bis Beginn
2,0
Dosis
UNK
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: unbekannt
Dermatitis Periorbital cellulitis

Symptomtext

Patient was seen and evaluated at urgent care for periorbital cellulitis of right eye and dermatitis. Given prednisone and Keflex.

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