Zurueck zur Suche

Reporte zur Charge UT8072DA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

8Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
WI 4 ME 2 KS 1 MN 1

VAERS 2728124

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UT8072DA

gering
Staat
KS
Alter
63,0
Geschlecht
M
Eingang
28.12.2023
Impfdatum
13.12.2023
Beginn
13.12.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
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 63 years in age and received flu vaccine for >65 years. Hand written vaccine consent form had illegible age written. No adverse events noted at administration of vaccine or following. No adverse events reported by patient.

Weitere VAERSDATA-Felder
Praegender Schweregrund
No adverse event
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
none
Vorgeschichte
none
Andere Medikamente
None
Allergien
None
Vorherige Impfungen
-

VAERS 2713950

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UT8072DA

gering
Staat
ME
Alter
9,0
Geschlecht
M
Eingang
14.11.2023
Impfdatum
25.10.2023
Beginn
25.10.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
No adverse event Product administered to patient of inappropriate age

Symptomtext

FLUZONE HD QIV was administered to a 9 year old patient with no reported AE; Initial information received on 31-Oct-2023 regarding an unsolicited valid non-serious case received from other health professional. This case involves a 9-years-old male patient who was administered influenza quadrival A-B high dose HV vaccine [Fluzone High-Dose Quadrivalent] with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. Concomitant: no other vaccines On 25-Oct-2023, the 9-years-old patient received 0.7 mL dose of suspect influenza quadrival A-B high dose HV vaccine (unknown strength, formulation) (Batch number: UT8072DA; expiry date: 30-Jun-2024) via intramuscular route in the right deltoid for Immunization with no reported adverse event (product administered to patient of inappropriate age) (same day latency). Action taken : not applicable Outcome: 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
No adverse event
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2707317

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UT8072DA

gering
Staat
ME
Alter
9,0
Geschlecht
M
Eingang
31.10.2023
Impfdatum
25.10.2023
Beginn
01.10.2023
Tage bis Beginn
-
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
No adverse event Wrong product administered

Symptomtext

Patient had no adverse effects from taking this. The wrong flu vaccine was grabbed by mistake. 0.7ml was given instead of a 0.5ml. We called patients father and patient has had no effects to the shot. It has been one week today that it was given. We are just reporting for our records.

Weitere VAERSDATA-Felder
Praegender Schweregrund
No adverse event
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
NKDA
Vorgeschichte
none
Andere Medikamente
zyrtec flonase
Allergien
NKDA
Vorherige Impfungen
-

VAERS 2694024

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UT8072DA

gering
Staat
MN
Alter
31,0
Geschlecht
F
Eingang
11.10.2023
Impfdatum
10.10.2023
Beginn
10.10.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Wrong product administered

Symptomtext

Wrong vaccine was given.

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

VAERS 2685413

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UT8072DA

gering
Staat
WI
Alter
76,0
Geschlecht
U
Eingang
22.09.2023
Impfdatum
08.09.2023
Beginn
08.09.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Device connection issue No adverse event Syringe issue

Symptomtext

patient did not get a dose of FLUZONE HD after administration because the product leaked on the part where the needle meets the syringe when the administering staff injected the plunger with no adverse event; Initial information received on 12-Sep-2023 regarding an unsolicited valid non-serious case received from a Nurse. This case involves a 76 years old and unknown gender patient who did not get a dose of influenza quadrival A-B high dose HV vaccine [Fluzone High-Dose Quadrivalent] after administration because the product leaked on the part where the needle meets the syringe when the administering staff injected the plunger with no adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 08-Sep-2023 at 4:30 PM , the patient received a dose 0.5 ml of suspect influenza quadrival A-B high dose HV vaccine, injection, (lot UT8072DA; Expiration Date :30-Jun-2024: strength not reported) via intramuscular route in the deltoid nos (not otherwise specified) for Immunization and did not get a dose of Fluzone hd after administration because the product leaked on the part where the needle meets the syringe when the administering staff injected the plunger with no adverse event (incorrect dose administered) (latency: same day) It was reported by nurse from their department injected a patient with FLUZONE HD but it leaked on the part where the needle meets the syringe and patient was not able get any of the vaccine. Action taken : not applicable. Outcome : 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
Device connection issue
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2683966

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UT8072DA

gering
Staat
WI
Alter
39,0
Geschlecht
M
Eingang
20.09.2023
Impfdatum
19.09.2023
Beginn
19.09.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
No adverse event Product administered to patient of inappropriate age

Symptomtext

Patient was given High Dose Influenza and not the normal for his age. No adverse reaction noted. Patient and Provider were notified and no concerns reported.

Weitere VAERSDATA-Felder
Praegender Schweregrund
No adverse event
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2683139

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UT8072DA

gering
Staat
WI
Alter
60,0
Geschlecht
M
Eingang
18.09.2023
Impfdatum
18.09.2023
Beginn
18.09.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
No adverse event Product administered to patient of inappropriate age

Symptomtext

No adverse effect. High Dose was given when not indicated.

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

VAERS 2681271

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge UT8072DA

gering
Staat
WI
Alter
50,0
Geschlecht
F
Eingang
12.09.2023
Impfdatum
11.09.2023
Beginn
11.09.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Incorrect dose administered

Symptomtext

On 09/11/2023 patient was giving the wrong dose of flu vaccine. She received high dose and needed regular flu. Patient was called and notified of the incident and provider also notified. Was document and manager was notified.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Incorrect dose administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
No.
Vorgeschichte
Pulmonary Hypertension
Andere Medikamente
No.
Allergien
Seasonal Bactrim Sulfa Antibiotics
Vorherige Impfungen
-