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Reporte zur Charge UT7751JA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

11Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
OH 3 NY 3 MI 2 IL 2 WI 1

VAERS 2485607

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7751JA

moderat
Staat
OH
Alter
63,0
Geschlecht
M
Eingang
21.10.2022
Impfdatum
20.10.2022
Beginn
21.10.2022
Tage bis Beginn
1,0
Dosis
UNK
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Dyspnoea Influenza like illness Speech disorder

Symptomtext

Pt called office 10/21 around 12:40pm reporting flu like sx, was advised to go to ER or call doctor. RN called pt around 3pm, pt was struggling to speak and seemed very short of breath. RN asked if pt was having trouble breathing, pt stated yes. Pt was advised to call 911 and go to the hospital.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dyspnoea
Hospital-Tage
-
Labordaten
unknown
Aktuelle Erkrankungen
unknown
Vorgeschichte
Diabetes type 1
Andere Medikamente
unknown
Allergien
denies
Vorherige Impfungen
-

VAERS 2551589

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7751JA

mild
Staat
OH
Alter
16,0
Geschlecht
F
Eingang
05.01.2023
Impfdatum
05.01.2023
Beginn
05.01.2023
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Axillary pain Cold sweat Dizziness Injection site rash Injection site reaction Nervousness Oedema peripheral Pain in extremity Rash macular

Symptomtext

15 minutes following administration, the patient came back to the pharmacy with arm pain. Upon further discussion, she noted feeling dizzy with pain under the armpit (scale 6/10). I observed a red splotchy rash at the injection site. She indicated she had swelling under the armpit and the pain was stabbing from the inside out. She did not have hives or feel like her throat was closing. She was nervous about the vaccine and felt clammy. I recommended she speak with the Clinic before leaving the pharmacy or calling her primary care provider to discuss the reaction. For nonpharmacologic care, I recommended she ice the area, rest, and stay hydrated. She could use ibuprofen or acetaminophen for pain. Her mother was driving her home and I advised her on what to watch for and to seek emergent medical care if the situation got worse. I also advised her to monitor her closely and follow up with her primary care if it did not resolve. The patient left the pharmacy with her mother and the pharmacy will follow up tomorrow.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Axillary pain
Hospital-Tage
-
Labordaten
N/A
Aktuelle Erkrankungen
Migraine headaches
Vorgeschichte
History of seizure in July 2022 (unknown origin, under care of neurologist), COVID-19 infection three months ago (~October 2022)
Andere Medikamente
Routine medications: norethindrone 0.35mg daily, vitamin d3 2000 units daily, coenzyme Q-10 100mg daily, fluoxetine 20mg daily, dicyclomine 10mg three times daily, rizatriptan 10mg as needed
Allergien
No known allergies
Vorherige Impfungen
-

VAERS 2517950

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7751JA

mild
Staat
WI
Alter
15,0
Geschlecht
F
Eingang
28.11.2022
Impfdatum
28.11.2022
Beginn
28.11.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Dizziness

Symptomtext

After vaccination patient reported dizziness while waiting in the waiting area. Patient laid on bench and had some water. After 10 - 15 minutes she felt better and left the pharmacy with her parents.

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

VAERS 2499810

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7751JA

mild
Staat
MI
Alter
5,0
Geschlecht
F
Eingang
04.11.2022
Impfdatum
04.11.2022
Beginn
04.11.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Injection site erythema Injection site swelling

Symptomtext

POST VACCINATION ONE HOUR LATER PARENT CALLED AND INDICATED THAT PATIENT HAS REDNESS AND SWELLING AT INJECTION SITE.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site erythema
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
UNKNOWN
Vorgeschichte
UNKNOWN
Andere Medikamente
n/a
Allergien
NO
Vorherige Impfungen
-

VAERS 2492745

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7751JA

mild
Staat
IL
Alter
22,0
Geschlecht
F
Eingang
28.10.2022
Impfdatum
05.10.2022
Beginn
05.10.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Urticaria

Symptomtext

broke out in hives after receiving the flu vaccine

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

VAERS 2726086

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7751JA

gering
Staat
NY
Alter
63,0
Geschlecht
F
Eingang
20.12.2023
Impfdatum
18.11.2022
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
OT / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Adverse reaction

Symptomtext

had a reaction from it last year; Initial information received on 13-Dec-2023 regarding an unsolicited valid non-serious case received from a consumer/non-hcp. This case involves a 64 years old female patient who had a reaction from it last year after receiving INFLUENZA QUADRIVAL A-B VACCINE [FLUZONE QIV]. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 18-Nov-2022, the patient received suspect INFLUENZA QUADRIVAL A-B VACCINE, Suspension for injection lot UT7751JA, expiry date- 30-JUN-2023 via intramuscular route in the left arm for immunization (strength, dose: unknown). On an unknown date the patient had a reaction from it last year (immunisation reaction) (unknown latency). Action taken: not applicable. It was not reported if the patient received a corrective treatment for the event At time of reporting, the outcome was Recovered / Resolved on an unknown date for the event

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

VAERS 2711743

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7751JA

gering
Staat
NY
Alter
62,0
Geschlecht
M
Eingang
08.11.2023
Impfdatum
27.10.2023
Beginn
27.10.2023
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 No adverse event

Symptomtext

states that a staff administered a patient with expired fluzone qiv with no reported adverse event; Initial information was received on 27-Oct-2023 regarding an unsolicited valid non-serious case received from a other health professional. This case involves 62 years old male patient who states that a staff administered a patient with expired influenza quadrival a-b vaccine [Fluzone QIV] with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 27-Oct-2023, the patient received a dose of 0.5 ml of suspect influenza quadrival a-b vaccine (Suspension for injection) (lot UT7751JA, Expiry date : 30-Jun-2023, strength was unknown) via intramuscular route in the left arm for Immunization and states that a staff administered a patient with expired fluzone qiv with no reported adverse event (expired product administered) (latency : same day). Action taken with QUADRIVALENT influenza vaccine (Fluzone QIV) was not applicable. At time of reporting, the outcome was Unknown for the event states that a staff administered a patient with expired 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 2575164

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7751JA

gering
Staat
IL
Alter
14,0
Geschlecht
M
Eingang
03.02.2023
Impfdatum
31.01.2023
Beginn
31.01.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
No adverse event Underdose

Symptomtext

Pt was given the Pfizer Covid Bivalent booster for the 5-11 year age group rather than the >12 year age group. Parent was contacted. No known physical adverse reaction. Plan reviewed to follow up with age appropriate booster dose.

Weitere VAERSDATA-Felder
Praegender Schweregrund
No adverse event
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
None known
Vorgeschichte
ADHD, anxiety
Andere Medikamente
Adderall Xr 15 mg
Allergien
none
Vorherige Impfungen
-

VAERS 2551948

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7751JA

gering
Staat
NY
Alter
71,0
Geschlecht
M
Eingang
06.01.2023
Impfdatum
-
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
OT / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
No adverse event Wrong product administered

Symptomtext

the patient received the fluzone quad instead of fluzone hd with no reported adverse event; Initial information received on 03-Jan-2023 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 71 years old male patient who received the influenza quadrival a-b vaccine [fluzone qiv] instead of fluzone hd 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 a dose of 0.5 ml total of suspect influenza quadrival a-b vaccine (Suspension for injection) (lot: UT7751JA ; expiry date: 30-Jun-2023) via intramuscular route in right deltoid for Immunization. On an unknown date the patient received the fluzone quad instead of fluzone hd with no reported adverse event (wrong product administered) (latency: same day). Action taken was 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
No adverse event
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2493998

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7751JA

gering
Staat
MI
Alter
59,0
Geschlecht
F
Eingang
31.10.2022
Impfdatum
25.10.2022
Beginn
25.10.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
No adverse event

Symptomtext

Patient had no adverse reactions to the vaccine.

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

VAERS 2490157

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7751JA

gering
Staat
OH
Alter
17,0
Geschlecht
M
Eingang
26.10.2022
Impfdatum
22.10.2022
Beginn
22.10.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Wrong product administered

Symptomtext

Patient presented w/ mother to receive meningitis vaccination series and flu vaccination. Menveo vaccination was provided. Upon further conversation it was noted an clarified with the patient and mother that they desired the Men B vaccination series. They were informed wrong vaccine had been provided and reported no symptoms at that time.

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