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Reporte zur Charge UJ730AB

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

6Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
ID 1 AZ 1 WA 1 NH 1 CA 1 PA 1

VAERS 1844025

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ730AB

schwer
Staat
ID
Alter
88,0
Geschlecht
M
Eingang
04.11.2021
Impfdatum
04.11.2021
Beginn
04.11.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Fall Haematocrit decreased Head injury Loss of consciousness Syncope Vomiting

Symptomtext

ABOUT 45 MINUTES AFTER THE SHOT PATIENT WAS SHOPPING IN STORE AND HAD A SYNCOPAL EPISODE WITH LOSS OF CONSCIENCENESS AND VOMITING

Weitere VAERSDATA-Felder
Praegender Schweregrund
Loss of consciousness
Hospital-Tage
-
Labordaten
TAKEN VIA AMBULANCE DUE TO AGE AND HITTING HEAD WHEN FALLING.. FOUND TO HAVE A LOW HEMATOCRIT BUT OTHERWISE FINE
Aktuelle Erkrankungen
NONE LISTED ON FORM NOR MENTIONED WHEN UPON INTERVIEW, HOWEVER HAD A LOW HEMATOCRIT UPON ADMISSION TO HOSPITAL
Vorgeschichte
-
Andere Medikamente
-
Allergien
NO KNOWN DRUG ALLERGIES LISTED , AND PATEINT STATES NONE UPON INTERVIEW
Vorherige Impfungen
-

VAERS 1733254

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ730AB

mild
Staat
AZ
Alter
71,0
Geschlecht
F
Eingang
24.09.2021
Impfdatum
20.09.2021
Beginn
21.09.2021
Tage bis Beginn
1,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Injection site erythema Injection site pain Injection site pruritus Injection site swelling

Symptomtext

Patient complained of Redness and swelling around injection site with Itching and pain. All symptoms resolved by 9/23/2021

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

VAERS 1722919

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge uj730ab

mild
Staat
WA
Alter
65,0
Geschlecht
F
Eingang
22.09.2021
Impfdatum
07.09.2021
Beginn
22.09.2021
Tage bis Beginn
15,0
Dosis
UNK
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Arthralgia Pain in extremity

Symptomtext

pt states having arm/shoulder pain that seems to be worsening 15 days following injection

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

VAERS 2324273

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ730AB

gering
Staat
NH
Alter
15,0
Geschlecht
F
Eingang
20.06.2022
Impfdatum
20.06.2022
Beginn
20.06.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Product administered to patient of inappropriate age Wrong product administered

Symptomtext

Patient is only 15 years old and received the 65 and over flu vaccine. She should have received the 65 and under flu vaccine. patient has not had any reported events from receiving this vaccine, but it is a medication error as she received the wrong flu vaccine based on her age.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Product administered to patient of inappropriate age
Hospital-Tage
-
Labordaten
N/A
Aktuelle Erkrankungen
Nothing
Vorgeschichte
N/A
Andere Medikamente
Retin-A, Romycin, Omeprazole, Multivitamin
Allergien
Penicillin- Rash
Vorherige Impfungen
-

VAERS 1891219

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ730AB

gering
Staat
CA
Alter
50,0
Geschlecht
F
Eingang
22.11.2021
Impfdatum
22.11.2021
Beginn
22.11.2021
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Product administered to patient of inappropriate age Wrong product administered

Symptomtext

Patient came to pharmacy only for moderna booster vaccination. Patient received flu vaccination intended for another patient. Patient confirmed their name multiple times before entering and after entering immunization booth. Patient was well informed in the booth prior to receiving vaccination that two vaccinations were prepared, flu and moderna booster, and confirmed with patient if they wanted both shots in one arm or one shot in each arm. Pt confirmed to have both shots in one arm. When patient was presented with their immunization card, they stated that that was not their name. Patient received an apology. The patient then stated they were sorry, that they were OK and did not appear to be upset. The patient only wanted their COVID vaccination card and left upon receipt of their card. Patient was not charged cost of flu HD vaccination

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

VAERS 1813080

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ730AB

gering
Staat
PA
Alter
74,0
Geschlecht
M
Eingang
23.10.2021
Impfdatum
14.10.2021
Beginn
14.10.2021
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

Symptomtext

was given the fluzone high dose quadrivalent with no reported adverse event; Initial information was regarding an unsolicited valid non serious case was received from a other health professional via Agency (Reference number- 00813036) and transmitted to Sanofi on 14-Oct-2021. This case involves a 74-year-old male patient who received FLUZONE HIGH-DOSE QUADRIVALENT (extra dose administered). The patient's medical history, past medical treatment(s), vaccination(s), concomitant medication and family history were not provided. On 14-Oct-2021, the patient received a 0.7 mL dose of suspect INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE (lot UJ730AB, expiry date: 30-Jun-2022) via intramuscular route in the left deltoid for prophylactic vaccination. It was an actual medication error due to extra dose administered. (latency: same day). It was reported "a patient was given the FLUZONE HIGH DOSE QUADRIVALENT on 07-Oct-2021 and then 14-Oct-2021 in error". At the time of report, no 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 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
Extra dose administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-