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Reporte zur Charge UJ709AB

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

4Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
PA 1 NJ 1 MI 1

VAERS 1675795

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge uj709ab

moderat
Staat
PA
Alter
67,0
Geschlecht
F
Eingang
06.09.2021
Impfdatum
04.09.2021
Beginn
04.09.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Blood pressure increased Condition aggravated Fatigue

Symptomtext

Patient got flu shot and started new BP med (coreg, replacing metoprolol) on the same day. That evening she became tired and felt as though she may pass out and has been feeling that way since. She has taken her BP several times since then and it is running higher than usual (diastolic number staying around 157). I advised her that her symptoms could be caused by her high blood pressure and that she should see a doctor today. I called her several hours later and she stated that she was feeling a little better and decided not to see a dr today but to wait and call either her doctor or nephrologist in the morning.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Condition aggravated
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
high blood pressure
Vorgeschichte
kidney disease, high blood pressure
Andere Medikamente
coreg, crestor, amlodipine, pentoxifylline, brilinta, slow mag
Allergien
no
Vorherige Impfungen
-

VAERS 1980878

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ709AB

gering
Staat
-
Alter
2,0
Geschlecht
M
Eingang
25.12.2021
Impfdatum
15.12.2021
Beginn
15.12.2021
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Medication error Product administered to patient of inappropriate age

Symptomtext

Pediatric patients were administered a dose of Fluzone HD with no reported adverse event; Initial information received on 15-Dec-2021 regarding an unsolicited valid non-serious case received from a other health professional via Regulatory Authority number: 00900069. This case is linked to case US-SA-2021SA422744(CLUSTER). This case involves a two years old male patient who was administered INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE [FLUZONE HIGH-DOSE QUADRIVALENT] (product administered to patient of inappropriate age). The patient's medical history, medical treatments, vaccinations, concomitant medications and family history were not provided. On 15-Dec-2021, the patient received a 0.7 ml dose of suspect INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE (lot number: UJ709AB and expiry date: 30-JUN-2022) via intramuscular route in the left thigh for prophylactic vaccination. It was case of an actual medication error due to inappropriate age at vaccine administration (latency: same day). At the time of reporting, 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
Medication error
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1974377

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ709AB

gering
Staat
NJ
Alter
-
Geschlecht
M
Eingang
23.12.2021
Impfdatum
15.12.2021
Beginn
15.12.2021
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Medication error Product administered to patient of inappropriate age

Symptomtext

This case is linked to cases US-SA-2021SA422716(CLUSTER). This case involves a Nine months old male patient who was administered a dose of INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE [FLUZONE HIGH-DOSE QUADRIVALENT] (product administered to patient of inappropriate age). The patient's medical history, medical treatments, vaccinations, concomitant medications and family history were not provided. On 15-Dec-2021, the patient received a 0.7 ml dose of suspect INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE lot number: UJ709AB and expiry date; 30-Jun-2022) via intramuscular route in the left thigh for prophylactic vaccination. It was case of an actual medication error due to inappropriate age at vaccine administration (latency: same day). At the time of reporting, 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
Medication error
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1731399

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ709AB

gering
Staat
MI
Alter
5,0
Geschlecht
F
Eingang
24.09.2021
Impfdatum
20.09.2021
Beginn
20.09.2021
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
No adverse event Product administered to patient of inappropriate age

Symptomtext

Patient was given the High Dose flu for 65 and older. No treatment needed. No reactions called to check on patient on 09/23/21 and mom states she was fine and had no reaction

Weitere VAERSDATA-Felder
Praegender Schweregrund
No adverse event
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None Takes Tylenol or Motrin as needed only
Allergien
NKDA
Vorherige Impfungen
-