Zurueck zur Suche

Reporte zur Charge UT8079AA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

5Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
NJ 1 KS 1 AL 1 GA 1 AR 1

VAERS 2698078

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UT8079AA

schwer
Staat
NJ
Alter
79,0
Geschlecht
M
Eingang
18.10.2023
Impfdatum
06.10.2023
Beginn
16.10.2023
Tage bis Beginn
10,0
Dosis
UNK
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
CSF protein increased Guillain-Barre syndrome Immunoglobulin therapy

Symptomtext

? Guillain-Barr? syndrome (GBS) Commenced on IVIG

Weitere VAERSDATA-Felder
Praegender Schweregrund
Guillain-Barre syndrome
Hospital-Tage
-
Labordaten
CSF showing albuminocytologic dissociation
Aktuelle Erkrankungen
N/A
Vorgeschichte
End state renal disease on maintenance Hemodialysis, T2DM, HTN, Atrial Fibrillation, prior TIA, Secondary Hyperparathyroidism, Chronic anemia
Andere Medikamente
N/A
Allergien
NKDA
Vorherige Impfungen
-

VAERS 2708877

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UT8079AA

moderat
Staat
KS
Alter
57,0
Geschlecht
F
Eingang
02.11.2023
Impfdatum
24.10.2023
Beginn
27.10.2023
Tage bis Beginn
3,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Hypoaesthesia Mobility decreased Peripheral swelling Product administered to patient of inappropriate age

Symptomtext

On 10/24/23 was in for a Fluzone vaccine a High dose Fluzone was given. On 10/27/23 patient called in to the Health Department to report that her Flu shot that she received on 10/14/23, made her right arm start to go numb and swell about 3 hours after she received her shot. States that her arm and hand was swollen so bad that she couldn't bend her arm or her and for several days. 10/27/23 today the swelling was down and she could move her arm and hand. Had no other problems. She wanted to report it to us. This is when I realized that I gave her a High dose Fluzone when she should of had a regular Fluzone due to her age. Her age was 57 years old.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Mobility decreased
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None reported
Vorgeschichte
None reported
Andere Medikamente
None
Allergien
Metform
Vorherige Impfungen
-

VAERS 2697569

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UT8079AA

mild
Staat
AL
Alter
77,0
Geschlecht
F
Eingang
18.10.2023
Impfdatum
09.10.2023
Beginn
10.10.2023
Tage bis Beginn
1,0
Dosis
UNK
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Chills Fatigue Sleep disorder Urinary incontinence

Symptomtext

It woke me up around 12-2 am with a cold shiver and chills. I got up and got another shirt on over my nightgown and another blanket and went to bed. I felt the need to urinate and before I could get there it was like a balloon popped and it went everywhere. I had no control over it at all. It felt like a balloon popped and it all gushed out. Not at all like the feeling when you normally use the bathroom. My chills went away shortly after that. Lingering fatigue. Its been 6 days and I'm starting to feel better. I also believe there was an error in my vaccination. The person who gave me the shot had just been in a disagreement with a coworker and I believe they were distracted and gave me an overdose.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Chills
Hospital-Tage
-
Labordaten
No
Aktuelle Erkrankungen
No
Vorgeschichte
Acid reflux, high blood pressure-its under control.
Andere Medikamente
Losartan, ezmaprozol, simvastatin, famotidine, and several more.
Allergien
No
Vorherige Impfungen
-

VAERS 2686975

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UT8079AA

gering
Staat
GA
Alter
48,0
Geschlecht
F
Eingang
27.09.2023
Impfdatum
26.09.2023
Beginn
26.09.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Product administered to patient of inappropriate age Wrong product administered

Symptomtext

Note from client that administered vaccine: THIS PATIENT GIVEN HIGH DOSE FLU VACCINE BY ME TODAY. I HAVE CALLED EMPLOYEE IN BILLING DEPARTMENT TO ADJUST THE AGE PARAMETERS SO I CAN PUT THE VACCINE IN FOR THIS PATIENT AS I WAS NOT ABLE TO BECAUSE OF AGE PARAMETERS. ALSO, THE BILLING WAS REMOVED SO THIS PATIENT WILL NOT BE CHARGED FOR THIS VACCINE. HER INSURANCE WILL DENY PAYMENT DUE TO HER AGE. I CALLED THE PATIENT TO NOTIFY HER OF THE MEDICATION ERROR. I APOLOGIZED AND INFORMED HER THAT SHE WILL NOT BE CHARGED FOR THE VACCINE NOR WILL HER INSURANCE BE BILLED. PATIENT UNDERSTOOD ALL. I WILL PUT AN INCIDENT REPORT IN FILE CABINET AND UPDATE PROGRESS NOTE AS NEEDED.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Product administered to patient of inappropriate age
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
No
Vorgeschichte
No
Andere Medikamente
No
Allergien
NKA
Vorherige Impfungen
-

VAERS 2684855

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UT8079AA

gering
Staat
AR
Alter
69,0
Geschlecht
F
Eingang
21.09.2023
Impfdatum
06.09.2023
Beginn
06.09.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Extra dose administered No adverse event

Symptomtext

mistakenly gave (2) injections with no reported adverse event; Initial information received on 06-Sep-2023 regarding an unsolicited valid non-serious case received from a pharmacist. This case involves a 69-year-old female patient who mistakenly taken (2) injections with no reported adverse event while receiving vaccine Influenza Quadrival A-B High Dose HV Vaccine [Fluzone High-Dose Quadrivalent]. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. Concomitant medications included VARICELLA ZOSTER VACCINE RGE (CHO) (SHINGRIX) and SHINGLES VACCINE for Prophylactic vaccination. On 06-Sep-2023, the patient received a dose and strength of 0.7 ml (Frequency = once) suspect Influenza Quadrival A-B High Dose HV vaccine injection (lot: UT8079AA, Expiry date: 30-Jun-2024) via intramuscular route in the left deltoid for Immunization and patient had mistakenly (2) injections with no reported adverse event (extra dose 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 06-Sep-2023 from a physician. Concomitant medication (SHINGRIX) added, CO updated, however no significant information received, text amended accordingly.

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