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Reporte zur Charge UJ716AB

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

8Reporte angezeigt
1Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
PA 2 FL 2 CA 1 IL 1 GA 1 CO 1

VAERS 2570684

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ716AB

kritisch
Staat
PA
Alter
80,0
Geschlecht
M
Eingang
30.01.2023
Impfdatum
15.10.2021
Beginn
16.10.2021
Tage bis Beginn
1,0
Dosis
UNK
Route/Site
SYR / LA
Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Death Facial paralysis General physical condition abnormal

Symptomtext

My father died in his sleep the night he got this shot. I did not find the paperwork regarding this vaccine until April 2022. He never told me he got the flu shot the day he got it.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Death
Hospital-Tage
-
Labordaten
He told me when he was alive that he did not want to have an autopsy so I had to honor his wishes. The undertaker said they had a heck of a time making the left side of his face look like the right side because e the left side was droopy. He said it looked like he had a massive stroke.
Aktuelle Erkrankungen
-
Vorgeschichte
Coronary artery disease
Andere Medikamente
Aspirin, Vitamin D3, Avodart, Ferrex, Lisinapril, Metroprolol, Xerelto, Crestor, Mucinex
Allergien
-
Vorherige Impfungen
-

VAERS 2072187

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ716AB

mild
Staat
FL
Alter
68,0
Geschlecht
F
Eingang
28.01.2022
Impfdatum
15.10.2021
Beginn
16.10.2021
Tage bis Beginn
1,0
Dosis
UNK
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Hypoaesthesia Injection site pain Insomnia Myalgia Neuralgia Pain Sleep disorder

Symptomtext

Pain in muscle trying to lift the arm. Tenderness at site of shot. 2 " circle. seems like nerve pain back of upper arm. Numbness in pinky finger. On 11/14pain so severe it woke me up and then I couldn't sleep. continuously from 10/16 to 11/19/2021. 12-10 Reports pain a little better.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site pain
Hospital-Tage
-
Labordaten
NA
Aktuelle Erkrankungen
none
Vorgeschichte
thyroid
Andere Medikamente
NP , Thyroid AREDS2, Calcium, Vitamin D, Viviscal, Finesteride
Allergien
Band-Aid, glue
Vorherige Impfungen
-

VAERS 1736962

GLAXOSMITHKLINE BIOLOGICALS · INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) · Charge UJ716AB

mild
Staat
PA
Alter
71,0
Geschlecht
M
Eingang
27.09.2021
Impfdatum
23.09.2021
Beginn
24.09.2021
Tage bis Beginn
1,0
Dosis
UNK
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Chills Nausea Pyrexia Vomiting

Symptomtext

Low-grade fever, chills, nausea/vomiting

Weitere VAERSDATA-Felder
Praegender Schweregrund
Chills
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None known
Vorgeschichte
Coronary artery disease, carotid artery stenosis, type 2 diabetes mellitus, essential hypertension, hyperlipidemia
Andere Medikamente
Aspirin, Atorvastatin, HCTZ, Lisinopril, Metformin, Metoprolol tartrate
Allergien
NKA
Vorherige Impfungen
-

VAERS 1939108

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ716AB

mild
Staat
CA
Alter
66,0
Geschlecht
F
Eingang
14.09.2021
Impfdatum
13.09.2021
Beginn
13.09.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Arthralgia Injection site erythema Injection site hypersensitivity Injection site pain Injection site rash Neck pain

Symptomtext

red rash at about 2x4 inch dimension at site of injection. pt stated painful and sensetive to the touch Also experiencing Left side of neck and Left Shoulder pain. Symptoms started 9-13-2021 at night advised pt to apply cold pack at site monitor and if symptoms get worse, seek medical care.

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

VAERS 1984404

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ716AB

gering
Staat
IL
Alter
-
Geschlecht
U
Eingang
27.12.2021
Impfdatum
17.11.2021
Beginn
17.11.2021
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Device breakage

Symptomtext

Preparing to administer a flu vaccine with Fluzone high dose lot # UJ716AB. When taking off the cap to the needle the glass vial snapped in half. A new fluzone vaccine was given to the patient with same lot# and expiration with no problems.

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

VAERS 1836578

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ716AB

gering
Staat
FL
Alter
87,0
Geschlecht
M
Eingang
02.11.2021
Impfdatum
02.11.2021
Beginn
02.11.2021
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Extra dose administered No adverse event

Symptomtext

Received high dose 1 month ago. Patient denied receiving it. No adverse reactions noted.

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

VAERS 1788616

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge Uj716ab

gering
Staat
GA
Alter
72,0
Geschlecht
F
Eingang
15.10.2021
Impfdatum
15.10.2021
Beginn
15.10.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Extra dose administered No adverse event

Symptomtext

Client given an additional dose of the vaccine. No apparent side effects and then left the site. Upon attempting to enter information in database it was discovered she already received the seasonal vaccine.

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

VAERS 1734346

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ716AB

gering
Staat
CO
Alter
-
Geschlecht
F
Eingang
25.09.2021
Impfdatum
-
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Medication error No adverse event Product storage error

Symptomtext

multiple excurion occured during shiping time with no adverse event; Initial information received on 16-Sep-2021 regarding an unsolicited valid non-serious case received from a other health care profession and non-healthcare professional via Medical Information under reference - 00773210. This case involves a unknown age of 13 female patient's were vaccinated INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE [FLUZONE HIGH-DOSE QUADRIVALENT] which went on multiple temperature excursions (product storage error). The patient's medical history, medical treatment(s), vaccination(s) and family history were not provided. No concomitant therapy was given. On an unknown date, the patient's received a 0.7 mL (total) dose of INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE (lot - UJ716AB and expiry date 30-06-2022) via an unknown route at an unknown administration site for prophylactic vaccination. It was reported "The caller stated that she was contacted by a Sanofi Rep who advised her that her recent shipment of FLUZONE HIGH DOSE QUADRIVALENT was not viable. The caller stated that she has already contacted Sanofi regarding a product replacement, as directed by her Sanofi Rep. The caller stated that the product was shipped on 02 SEP 2021 and received on 07 SEP 2021. The caller stated that 13 patients have received the vaccine since delivery. At this time, the caller is requesting medical information for the proper care for the 13 patients who received the vaccine. Note from Agent; At the time of the call back the clinic did not have the information for the patients that received the vaccines." It was a case of a actual medication error due to incorrect product storage. At the time of reporting, no adverse event reported. Outcome of event 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.

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