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Reporte zur Charge UT8040KA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

6Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
ID 2 VA 2 AZ 1 UT 1

VAERS 2695602

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UT8040KA

moderat
Staat
AZ
Alter
52,0
Geschlecht
F
Eingang
13.10.2023
Impfdatum
04.10.2023
Beginn
04.10.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Injected limb mobility decreased Pain

Symptomtext

Patient reports that she was given the flu vaccine to upper right arm (about less than 1 finger below the acromion process and off to the side), and 6 to 7 hours experienced significant pain to the point that she could not raise her arm above the lower clavicle areas. She trying to do range of motion with right arm and took NSAIDS around to clock since 10/4/23.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injected limb mobility decreased
Hospital-Tage
-
Labordaten
No tests at this point.
Aktuelle Erkrankungen
None
Vorgeschichte
Rheumatoid Arthritis and Migraines.
Andere Medikamente
Omeprazole 40 mg QD, Folic Acid 1mg QD, Methotrexate 25 mg Q week, Plaquenil 200mg QD, Topamax 300 mg BID, Qulipta 60 mg QD, Modafinil 200mg QD, Orencia 500mg IV Q month, Boniva IV Q 3 months, Gabapentin 300 mg Q HS, Amitriptyline 30 mg QHS
Allergien
Erythromycin Tetracycline Sulfa
Vorherige Impfungen
-

VAERS 2721056

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge ut8040ka

mild
Staat
UT
Alter
64,0
Geschlecht
F
Eingang
05.12.2023
Impfdatum
27.09.2023
Beginn
28.09.2023
Tage bis Beginn
1,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Arthralgia Asthenia

Symptomtext

Pt reports shoulder pain/weakness shortly after receiving vaccination which continued for several days

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

VAERS 2708303

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT8040KA

mild
Staat
ID
Alter
29,0
Geschlecht
F
Eingang
01.11.2023
Impfdatum
31.10.2023
Beginn
01.11.2023
Tage bis Beginn
1,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Erythema Nausea Pruritus Skin erosion Swelling face Urticaria

Symptomtext

hives on neck, cheeks, behind ears and on scalp. itching on areas described before plus arms, legs, chest and back. Face also appeared reddeded and puffy. My scalp is somewhat raw from scratching in my sleep. nausea when i got up in the morning.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Nausea
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
I had a on and off again cold, but I have 3 toddlers and a cold is part of my life
Vorgeschichte
pcos
Andere Medikamente
Metformin topirimate valcyclovir vit d vit c alov
Allergien
allergic to poison ivy nkda
Vorherige Impfungen
I felt like I had a more mild reaction than this last year., but when i tried to address it with a healthcare professional with

VAERS 2712659

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT8040KA

gering
Staat
ID
Alter
60,0
Geschlecht
M
Eingang
10.11.2023
Impfdatum
10.11.2023
Beginn
10.11.2023
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Extra dose administered Wrong product administered

Symptomtext

2 doses were accidentally given instead of 1 flu and 1 comirnaty

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

VAERS 2682747

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT8040KA

gering
Staat
VA
Alter
0,8
Geschlecht
F
Eingang
16.09.2023
Impfdatum
-
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
No adverse event Product distribution issue

Symptomtext

Flu Vaccines received were in transit too long due to delayed delivery with no adverse event; Initial information received on 08-Sep-2023 regarding an unsolicited valid non-serious case received from an other health professional. This case involves a 9 months old female patient and the flu vaccines received were in transit too long due to delayed delivery with no adverse event for influenza quadrival A-B vaccine [Fluzone Quadrivalent]. The patient had no medical history, concomitant disease or risk factor.The patient's medical treatment(s), vaccination(s) and family history were not provided. On an unknown date, the patient received 0.5 ml of suspect influenza quadrival A-B vaccine, single dose pre-filled syringe lot UT8040KA via intramuscular route in unknown administration site for flu prevention(strength, expiry date: unknown), flu vaccines received were in transit too long due to delayed delivery with no adverse event (poor quality product administered) (latency same day). There were no lab data/results available. Reportedly, the Flu Vaccines received were in transit too long due to delayed delivery therefore they were considered ineffective. Vaccine had been administered prior to getting this information. There have been no signs or symptoms of any type of reaction to the adverse event Action taken: not applicable. At time of reporting, the outcome was Unknown for the event poor quality product administered 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 2681819

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT8040KA

gering
Staat
VA
Alter
1,8
Geschlecht
F
Eingang
14.09.2023
Impfdatum
29.08.2023
Beginn
29.08.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Medication error No adverse event Poor quality product administered

Symptomtext

vaccines being in transit too long as vaccines were sent on 26Aug2023, and it should have been at the office, yesterday (28Aug2023), vaccines already being administered with no reported adverse event; Initial information received on 29-Aug-2023 regarding an unsolicited valid non-serious case received from a other health professional (nurse). This case involves a 21-month-old female patient who experienced vaccines being in transit too long as vaccines were sent on 26aug2023, and it should have been at the office, yesterday (28aug2023), vaccines already being administered with no reported adverse event while receiving vaccine 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 26-Aug-2023, the vaccines being in transit too long as vaccines were sent, and it should have been at the office, yesterday (28aug2023). On 29-Aug-2023, the patient received a dose of 0.5 ml suspect Influenza Quadrival A-B Vaccine Suspension for injection in pre-filled syringe (lot: UT8040KA, expiration date: 30-Jun-2024) via intramuscular route in unknown administration site for flu prevention (Antiviral prophylaxis) & Immunization with no reported adverse event (poor quality product administered) (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. Additional information was received on 08-Sep-2023 from Other health professional. Case has become non valid to valid. Patient information added, clinical course updated and text amended accordingly.

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