Zurueck zur Suche

Reporte zur Charge UJ565AB

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

5Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
MN 1 MA 1 UT 1 FL 1 CT 1

VAERS 995945

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ565AB

moderat
Staat
MN
Alter
72,0
Geschlecht
F
Eingang
02.02.2021
Impfdatum
13.11.2020
Beginn
13.11.2020
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Dyspnoea Fatigue Hyperhidrosis Malaise Pyrexia Retching Tremor Vomiting

Symptomtext

4 HOURS AFTER VACCINE PT STARTED FEELING ILL. SHE THREW UP, WAS SHAKY AND SWEATY, FEVERISH FATIGUED. THEN STARTED HAVING SOME DIFFICULTY BREATHING AND DRY HEAVED A FEW TIMES. USED ALBUTERAL AND AFTER AN HOURS THINGS SETTLED AND SHE SLEPT A COUPLE HOURS. FELT BETTER AFTER 3 DAYS.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dyspnoea
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
COPD, hypothyroidism, osteoporosis, high cholesterol
Andere Medikamente
anoro, atorvastatin, alendronate, levothyroxine, albuterol
Allergien
aspirin, codeine
Vorherige Impfungen
PNEUMONIA VACCINE

VAERS 1259468

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UJ565AB

mild
Staat
MA
Alter
88,0
Geschlecht
M
Eingang
26.04.2021
Impfdatum
13.11.2020
Beginn
13.11.2020
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Pain in extremity

Symptomtext

4/26/2021 patient came in to inquire if people have been complaining about arm pain from the flu shot. He said his has hurt since the shot, and is still hurting.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pain in extremity
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
n/a
Vorgeschichte
n/a
Andere Medikamente
n/a
Allergien
Avalide, Benadryl, Diovan, Lisinopril, Minocycline, Omeprazole, Penicillin, Percocet
Vorherige Impfungen
-

VAERS 1774861

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ565AB

gering
Staat
UT
Alter
-
Geschlecht
U
Eingang
09.10.2021
Impfdatum
-
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered No adverse event

Symptomtext

Patient recieved expired vaccine with no reported adverse event; Initial information was received on 01-Oct-2021 regarding an unsolicited valid non-serious case received from a pharmacist via Regulatory authority (00794863). This case involves a patient of (unknown demographics) who was vaccinated with an expired dose of suspect INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE [FLUZONE HIGH-DOSE QUADRIVALENT] (expired product administered). The patient's medical history, medical treatment(s), vaccination(s) and family history were not provided. No other concomitant vaccines were not provided. On an unknown date, the patient received a dose of suspect INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE (lot number UJ565AB and expiry date not reported) via an unknown route at an unknown administration site for prophylactic vaccination. It was reported "Caller stated they administered vaccine to two patients and realized the vaccine expired 30Jun2021. Caller asking if there any safety issues and should the patients receive the updated version vaccine for this year? Caller declined to provide email." It was a case of an actual medication error due to expired vaccine used (latency was on same day). At the time of report, no adverse event reported. Event 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 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
Expired product administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 976985

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ565AB

gering
Staat
FL
Alter
65,0
Geschlecht
F
Eingang
27.01.2021
Impfdatum
08.01.2021
Beginn
08.01.2021
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

inadvertently administered Fluzone Quadrivalent instead of Prevnar with no AE; inadvertently administered Fluzone Quadrivalent High-Dose vaccine and Fluzone Quadrivalent instead on same day with no AE; Initial information regarding this unsolicited valid non-serious case was received from Pharmacist via The Agency (Reference number- 00422121) and transmitted to Sanofi on 08-Jan-2021. This case involves a 65 years old female patient who received a dose of INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE [FLUZONE HIGH-DOSE QUADRIVALENT] (prefilled syringe, lot UJ565AB, expiration date 30-Jun-2021) via intramuscular route in the left deltoid and then inadvertently received a 0.5ml dose of INFLUENZA QUADRIVAL A-B VACCINE [FLUZONE QUADRIVALENT] (prefilled syringe, lot UJ442AA, expiration 30 June 2021) via intramuscular route in the right deltoid both for prophylactic vaccination (extra dose administered) instead of PNEUMOCOCCAL VACCINE CONJ 7V (CRM197) [PREVENAR] on 08-Jan-2021 (wrong product administered). The patient's medical history, medical treatments, vaccinations and family history were not provided. Patient received no other concomitant vaccines. It was a actual medication error due to wrong vaccine administered and extra dose administered (latency-same day). At the time of reporting, no adverse event was reported. The reporter stated that she grabbed the Fluzone Quadrivalent prefilled syringe box instead of the Prevnar box because the boxes for the two vaccines look very similar. Prevnar was not administered. Repoert stated that doctor information not available since the vaccines were administered at a retail pharmacy. The reporter had been trying to reach the patient, but not spoken to the patient since the error. 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 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
-

VAERS 917372

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ565AB

gering
Staat
CT
Alter
66,0
Geschlecht
F
Eingang
02.01.2021
Impfdatum
13.11.2020
Beginn
13.11.2020
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / AR
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
No adverse event

Symptomtext

Patient received 3rd dose of Shingrix and 2nd flu shot on 11/13/20. She had no adverse reactions.

Weitere VAERSDATA-Felder
Praegender Schweregrund
No adverse event
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-