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Reporte zur Charge UJ769AA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

10Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
FL 4 SC 1 CA 1 OR 1 IL 1 PA 1 MI 1

VAERS 2122892

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ769AA

mild
Staat
FL
Alter
67,0
Geschlecht
M
Eingang
18.02.2022
Impfdatum
08.02.2022
Beginn
08.02.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Arthralgia Asthenia Chills Headache Pain

Symptomtext

Weak, Aches, Chills, Joint Pain, Headache

Weitere VAERSDATA-Felder
Praegender Schweregrund
Arthralgia
Hospital-Tage
-
Labordaten
N/A
Aktuelle Erkrankungen
benign prostatic hyperplasia Benign prostatic hyperplasia (disorder) displacement of lumbar intervertebral disc without myelopathy epigastric pain Epigastric pain erectile dysfunction due to arterial disease Erectile dysfunction due to arterial disease (disorder) gastroparesis syndrome Gastroparesis (disorder) generalized anxiety disorder ICD-10: F41.1 - Generalized anxiety disorder (disorder) hyperlipidemia ICD-10: E78.5 - Hyperlipidemia (disorder) increased body mass index Increased body mass index (finding) low back pain neoplasm of uncertain behavior of skin pain in right lower limb pain of right thigh primary insomnia Primary insomnia (disorder) raised prostate specific antigen Elevated prostate specific antigen [PSA] varicose veins of lower extremity (Right)
Vorgeschichte
same as above
Andere Medikamente
Xanax, Zolpidem Tartrate, Pantoprazole, Venlafaxine, Gas X, Tramadol, Domperidone, Fish Oil, Aspirin, Atorvastatin, Butalbital Acetaminophen, Cyclobenzaprine.
Allergien
Banana, Iodine, Peanut
Vorherige Impfungen
Influenza Vaccine

VAERS 1921152

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ769AA

mild
Staat
SC
Alter
62,0
Geschlecht
F
Eingang
03.12.2021
Impfdatum
19.10.2021
Beginn
20.10.2021
Tage bis Beginn
1,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Erythema Rash Swelling

Symptomtext

Patient had redness, swelling, rash

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

VAERS 1876062

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ769AA

mild
Staat
CA
Alter
87,0
Geschlecht
M
Eingang
16.11.2021
Impfdatum
15.11.2021
Beginn
15.11.2021
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 bruising

Symptomtext

patient came back today concerned about the 1.5 inch bruise surrounding the bandaid from his flu shot, it was not uncomfortable and he says he was on no blood thinner or asprin like product. The Pfizer vaccine on the left arm had no discomfort or brusing at all

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site bruising
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
none known
Vorgeschichte
not known.
Andere Medikamente
unknown
Allergien
none mentioned
Vorherige Impfungen
-

VAERS 1894435

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ769AA

gering
Staat
OR
Alter
82,0
Geschlecht
M
Eingang
23.11.2021
Impfdatum
18.11.2021
Beginn
18.11.2021
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Extra dose administered

Symptomtext

Patient received 2nd flu vaccine. Not realizing he had already had a flu vaccine this flu season. So far no reactions reported.

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

VAERS 1843773

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ769AA

gering
Staat
IL
Alter
62,0
Geschlecht
M
Eingang
04.11.2021
Impfdatum
04.11.2021
Beginn
04.11.2021
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Product administered to patient of inappropriate age

Symptomtext

VACCINE ERROR: FLUZONE HIGH DOSE ADMINISTERED ACCIDENTALLY WHEN PATIENT NOT ELIGIBLE BECAUSE OF HIS AGE.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Product administered to patient of inappropriate age
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1839364

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ769AA

gering
Staat
FL
Alter
60,0
Geschlecht
F
Eingang
03.11.2021
Impfdatum
22.10.2021
Beginn
22.10.2021
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Extra dose administered Medication error Product administered to patient of inappropriate age

Symptomtext

A 60-year-old patient received flu zone high-dose no AE; A 60-year-old patient received flu zone high-dose no AE; Initial information regarding an unsolicited valid non-serious case was received from a pharmacist via a consumer/non-health care professional via (Reference number- 00824766) and transmitted on 22-OCT-2021. This case is linked to cases 2021SA356392 and 2021SA355376 (same reporter). This case involves a 60-year-old female patient who received INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE [FLUZONE HIGH-DOSE QUADRIVALENT] (product administered to patient of inappropriate age and overdose). At the time of the event, the patient had ongoing medical history of Chronic obstructive pulmonary disease (COPD) and Neoplasm malignant (unspecified cancer). The patient's past medical treatment(s), vaccination(s) and family history were not provided. The patient had no other concomitant vaccine. On 22-Oct-2021, the patient received a 0.7 mL dose of suspect INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE (lot UJ769AA, expiry: 30-Jun-2022) via intramuscular route in the left arm for prophylactic vaccination. It was a case of an actual medication error due to inappropriate age at vaccine administration and overdose (latency same day). It was reported "Pharmacist states that during a flu-shot clinic, three of the patients who received FLUZONE QUADRIVALENT HIGH-DOSE, after attesting to be less than 65 years of age, were found to be younger. Two of the women were 60 and one was 45 years old. Caller asking what should be done." No other 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. 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
Extra dose administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
Cancer (NOS); COPD
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1831431

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ769AA

gering
Staat
FL
Alter
45,0
Geschlecht
F
Eingang
30.10.2021
Impfdatum
22.10.2021
Beginn
22.10.2021
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Incorrect dose administered No adverse event Product administered to patient of inappropriate age

Symptomtext

A 45 years old patient received FLUZONE QUADRIVALENT HIGH-DOSE with no reported adverse event; A 45 years old patient received FLUZONE QUADRIVALENT HIGH-DOSE with no reported adverse event; Initial information received on 22-Oct-2021 regarding an unsolicited valid non-serious case from pharmacist and consumer/ non health care professional via Media Information (under reference 00824871) in the . This case is linked to cases 2021SA356620 and 2021SA355376 (same reporter). This case involves a 45 years old female patient who received INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE [FLUZONE HIGH-DOSE QUADRIVALENT] (product administered to patient of inappropriate age and overdose). The patient's medical history, medical treatment(s), vaccination(s) and family history were not provided. The patient had no other concomitant vaccines. On 22-Oct-2021, the patient received a 0.7 mL dose of suspect INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE (Total, lot UJ769AA and expiration date: 30-Jun-2022) via intramuscular route in the left arm for prophylactic vaccination. It was a case of an actual medication error due to inappropriate age at vaccine administration and overdose (same day latency). It was reported "Pharmacist states that today, during a flu-shot clinic, 3 of the patients who received FLUZONE QUADRIVALENT HIGH-DOSE, after attesting to be less than 65 years of age, were found to be younger. Two of the women were 60 and one was 45 years old. Caller asking what should be done." At time of reporting, no adverse event 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
Incorrect dose administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1831430

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ769AA

gering
Staat
FL
Alter
60,0
Geschlecht
F
Eingang
30.10.2021
Impfdatum
22.10.2021
Beginn
22.10.2021
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 Product administered to patient of inappropriate age

Symptomtext

A 60-year-old patient received fluzone high-dose with no adverse event; A 60-year-old patient received fluzone high-dose with no adverse event; Initial information received on 22-Oct-2021 regarding an unsolicited valid non-serious case from pharmacist and consumer/ non health care professional via Media Information (under reference 00824838) in a specific country. This case is linked to cases 2021SA356620 and 2021SA356392 (same reporter). This case involves a 60 years old female patient who received INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE [FLUZONE HIGH-DOSE QUADRIVALENT] (product administered to patient of inappropriate age and overdose). The patient's medical history, medical treatment(s), vaccination(s) and family history were not provided. The patient had no other concomitant vaccines. On 22-Oct-2021, the patient received a 0.7 mL dose of suspect INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE (Total, lot UJ769AA and expiration date: 30-6-2022) via intramuscular route in the left arm for prophylactic vaccination. It was case of an actual medication error due to inappropriate age at vaccine administration and overdose (same day latency). It was reported "Pharmacist states that today, during a flu-shot clinic, 3 of the patients who received FLUZONE QUADRIVALENT HIGH-DOSE, after attesting to be less than 65 years of age, were found to be younger. Two of the women were 60 and one was 45 years old. Caller asking what should be done." At time of reporting, no adverse event 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 1776319

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ769AA

gering
Staat
PA
Alter
75,0
Geschlecht
F
Eingang
11.10.2021
Impfdatum
08.10.2021
Beginn
09.10.2021
Tage bis Beginn
1,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Cellulitis

Symptomtext

Pt went to ER with cellulitis in right arm. Was given cephalexin 500mg 1 bid x7days

Weitere VAERSDATA-Felder
Praegender Schweregrund
Cellulitis
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
none
Vorgeschichte
diabetes, hypertension
Andere Medikamente
albuterol MDI, allopurinol 100mg, tramadol 50mg, metformin er 500mg, carvediolol 3.125, montelukast 10mg,
Allergien
none
Vorherige Impfungen
-

VAERS 1765391

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ769AA

gering
Staat
MI
Alter
64,0
Geschlecht
F
Eingang
06.10.2021
Impfdatum
05.10.2021
Beginn
05.10.2021
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Incorrect dose administered

Symptomtext

Client asked for high dose influenza vaccine and was given it. RN verified her DOB but not her exact age at time of vaccination. Client was not eligible for the high dose as she is not yet 65 years of age.

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