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Reporte zur Charge UT7336LA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

10Reporte angezeigt
1Todesfaelle
1Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
MI 3 PA 2 MN 1 MA 1 AR 1 WI 1

VAERS 2157679

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UT7336LA

kritisch
Staat
-
Alter
62,0
Geschlecht
M
Eingang
04.03.2022
Impfdatum
28.09.2021
Beginn
11.10.2021
Tage bis Beginn
13,0
Dosis
1
Route/Site
IM / LA
Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: unbekannt
Death Dehydration Lung cancer metastatic Lung neoplasm malignant Sepsis

Symptomtext

ED visit for dehydration, treated and discharged. ED to hospital for Severe sepsis; Primary malignant neoplasm of left lung metastatic to other site Treated and discharged to skilled nursing facility. Patient died on 11/7/2021. ED visit and hospital admission within 6 weeks of receiving the COVID vaccine.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Death
Hospital-Tage
14,0
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2092652

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7336LA

schwer
Staat
PA
Alter
10,0
Geschlecht
M
Eingang
07.02.2022
Impfdatum
07.02.2022
Beginn
07.02.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Dizziness Loss of consciousness Pallor Urinary incontinence

Symptomtext

Child showed signs of anxiety prior to vaccines so he sat on his guardian's lap, child nervous during vaccines but allowing vaccines without verbal protest. After last vaccine to be given ( Pediatric Pfizer) child in guardians arms lost consciousness for less than 5 seconds, child slumped in guardians arms, turned pale, loss control of bladder, then came around and began to lift head and stand in guardians arms. Child was able to assist with sitting and laying on stirrup medical bed in room with use of step and assistance of nurse and guardian, child laid down and rested for 10 minutes, was given sips of water and instructed on breathing and after 10 minutes given bite to eat of fruit breakfast bar, child laid back down, instructed to and able to follow commands to pumping hands for increased circulation for approximately 3 minutes. Child stated he was feeling better, child sat up on bed with guardian and nurse present for approximately 10 minutes used distraction conversation with guardian about family child participated and smiled and laughed with conversation, child displayed signs of improvement with conversation, self supporting bodily movements, improved pallor and hands warm to touch.

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

VAERS 1864750

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7336LA

mild
Staat
MN
Alter
37,0
Geschlecht
F
Eingang
12.11.2021
Impfdatum
10.11.2021
Beginn
11.11.2021
Tage bis Beginn
1,0
Dosis
UNK
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Rash Rash pruritic

Symptomtext

Rash bilateral arms and truck, itchy.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Rash
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None.
Vorgeschichte
Migraines.
Andere Medikamente
Allergy medication.
Allergien
Allergies to Medication: Depakote, Reglan, Topamax, Zofran, Demerol, Sulfa
Vorherige Impfungen
-

VAERS 1832944

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7336LA

mild
Staat
MA
Alter
1,2
Geschlecht
F
Eingang
01.11.2021
Impfdatum
23.10.2021
Beginn
23.10.2021
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Decreased appetite Irritability Pyrexia

Symptomtext

Patient received flu vaccine in the morning and had a 103.8 temp by the evening, temp lasted for three days; patient also had a decreased appetite and increased fussiness.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pyrexia
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None
Allergien
None Known
Vorherige Impfungen
-

VAERS 2465319

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7336LA

gering
Staat
PA
Alter
-
Geschlecht
F
Eingang
30.09.2022
Impfdatum
-
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered No adverse event

Symptomtext

administration of an expired dose of FLUZONE QIV NP to a patient who was pregnant with no reported adverse event; administration of an expired dose of FLUZONE QIV NP to a patient who was pregnant with no reported adverse event; Initial information received on 23-Sep-2022 regarding an unsolicited valid non-serious case received from a other health professional. This case involves an unknown age female patient who was exposed to vaccine INFLUENZA QUADRIVAL A-B VACCINE [FLUZONE QIV] in context of administration of an expired dose of FLUZONE QIVNP to a patient who was pregnant with no reported adverse event. Data regarding this pregnancy were received prospectively, i.e. before pregnancy outcome was known. The reported adverse event occurred at unknown gestation period. The date of last menstrual period was not reported. The estimated due date was not reported. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. The patient had unknown previous pregnancy/ies. On an unknown date nurse reporting the administration of an expired dose of FLUZONE QIV (lot UT7336LA,30-Jun-2022) to patient who was pregnant (exposure during pregnancy) (expired product administered) (latency: same day). This situation is reported as a medication error due to a pregnant patient being administered FLUZONE QIV NP after the expiration date. Action taken: not applicable. At time of reporting, the outcome was Unknown for the 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 2282989

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7336LA

gering
Staat
MI
Alter
1,3
Geschlecht
M
Eingang
18.05.2022
Impfdatum
23.12.2021
Beginn
01.12.2021
Tage bis Beginn
-
Dosis
2
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Extra dose administered No adverse event

Symptomtext

patient is 15 months old and received 2 dose series of flu second year in a row. no adverse effects noted, patient was notified immediately by provider and advised to follow up if any adverse effects.

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

VAERS 2101781

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7336LA

gering
Staat
AR
Alter
4,0
Geschlecht
M
Eingang
10.02.2022
Impfdatum
30.12.2021
Beginn
10.02.2022
Tage bis Beginn
42,0
Dosis
2
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Inappropriate schedule of product administration No adverse event

Symptomtext

Patient received second dose of flu shot at 3 weeks instead of 4 weeks. No adverse reaction noted per mother

Weitere VAERSDATA-Felder
Praegender Schweregrund
Inappropriate schedule of product administration
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1877354

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7336LA

gering
Staat
MI
Alter
12,0
Geschlecht
F
Eingang
17.11.2021
Impfdatum
17.11.2021
Beginn
17.11.2021
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Underdose

Symptomtext

Peds Pfizer dose given to 12 year old. I notified the mom of the incident and she was ok.

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

VAERS 1828067

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7336LA

gering
Staat
WI
Alter
66,0
Geschlecht
M
Eingang
29.10.2021
Impfdatum
21.10.2021
Beginn
21.10.2021
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
No adverse event Wrong product administered

Symptomtext

they accidentally administered FLUZONE QUADRIVALENT instead of FLUZONE HIGH DOSE with no reported adverse event; Initial information received on 22-Oct-2021 regarding an unsolicited valid non-serious case from a other health professional and consumer/ non health care professional via Agency (reference number 00824877). This case involves a 66-year-old male patient who was by mistakenly given dose of suspect and INFLUENZA QUADRIVAL A-B VACCINE [FLUZONE QIV] instead of INFLUENZA USP TRIVAL A-B HIGH DOSE SUBVIRION VACCINE [FLUZONE HIGH DOSE] (wrong product administered). Medical history, medical treatment, concomitant medication, vaccination and family history were not provided. On 21-Oct-2021, the patient received a dose of suspect INFLUENZA QUADRIVAL A-B VACCINE (lot UT7336LA and expire vaccine: 21-Oct-2022) (Frequency Once) via intramuscular route in the left deltoid for prophylactic vaccination. It was an actual medication error case due to wrong vaccine administered (latency: same day). It was reported "Nurse practitioner asks what the proper next steps would be; asks if the patient should still receive FLUZONE HIGH DOSE in addition to the FLUZONE QUADRIVALENT that was already administered." At the time of reporting, no adverse event was reported. 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
No adverse event
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1782219

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7336LA

gering
Staat
MI
Alter
9,0
Geschlecht
M
Eingang
13.10.2021
Impfdatum
12.10.2021
Beginn
-
Tage bis Beginn
-
Dosis
N/A
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
No adverse event

Symptomtext

No adverse events witnessed while in office.

Weitere VAERSDATA-Felder
Praegender Schweregrund
No adverse event
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
Quillichew ER 20mg
Allergien
NKDA
Vorherige Impfungen
-