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Reporte zur Charge UJ661AA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

6Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
GA 2 TX 1 MT 1 NV 1 MI 1

VAERS 2440318

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ661AA

gering
Staat
TX
Alter
2,0
Geschlecht
M
Eingang
12.09.2022
Impfdatum
03.09.2022
Beginn
03.09.2022
Tage bis Beginn
0,0
Dosis
4
Route/Site
OT / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered

Symptomtext

expired dose of acthib administered with no reported adverse event; Initial information received on 06-Sep-2022 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 2 years old male patient to whom experienced expired dose of HIB (PRP/T) VACCINE [ACT-HIB] administered with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. Concomitant medications included PNEUMOCOCCAL VACCINE CONJ 13V (CRM197) (PREVNAR 13) for Immunisation. On 03-Sep-2022, the patient received a 0.5 ml total, 4th dose of suspect HIB (PRP/T) VACCINE, unknown formulation, (lot UJ661AA, exp date: 06-May-2022) via intramuscular route in the left thigh as Immunization. On 03-Sep-2022 the patient got expired dose of acthib administered with no reported adverse event (expired product administered) (latency: same day). Action taken: not applicable. At time of reporting, the outcome was Unknown for the event. 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
Expired product administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
PREVNAR 13
Allergien
-
Vorherige Impfungen
-

VAERS 2309791

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ661AA

gering
Staat
GA
Alter
39,0
Geschlecht
M
Eingang
06.06.2022
Impfdatum
23.05.2022
Beginn
23.05.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered Medication error No adverse event

Symptomtext

expired ACTHIB being administered to a patient with no reported adverse event; Initial information received on 23-May-2022 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 39 years old male patient to whom expired acthib being administered to a patient with no reported adverse event while receiving vaccine HIB (PRP/T) vaccine [ACT-HIB]. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. Concomitant medications included pneumococcal vaccine polysacch 23V (Pneumovax) for Immunisation. On 23-May-2022, the patient received suspect HIB (PRP/T) vaccine at a dose of 0.5 ml total (lot UJ661AA , expiry date: 06-May-2022, form, strength: not reported) via intramuscular route in the left deltoid for immunisation. On 23-May-2022, expired acthib being administered to a patient with no reported adverse event (expired product administered, latency: same day) following the administration of HIB (PRP/T) 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 guidelines. 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 2290453

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ661AA

gering
Staat
GA
Alter
39,0
Geschlecht
M
Eingang
23.05.2022
Impfdatum
23.05.2022
Beginn
23.05.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Expired product administered No adverse event

Symptomtext

ActHIB vaccine was expired; Patient was informed. Patient not experiencing side effects of any kind.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
N/A
Aktuelle Erkrankungen
Hypertension, HIV
Vorgeschichte
Hypertension, HIV
Andere Medikamente
Amlodipine, Lisinopril, Biktarvy
Allergien
No Known Allergies
Vorherige Impfungen
-

VAERS 2275784

SANOFI PASTEUR · HIB (ACTHIB) · Charge uj661aa

gering
Staat
MT
Alter
1,0
Geschlecht
M
Eingang
13.05.2022
Impfdatum
12.05.2022
Beginn
12.05.2022
Tage bis Beginn
0,0
Dosis
4
Route/Site
IM / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Expired product administered No adverse event

Symptomtext

Patient was given a vaccine that had expired six days prior. There were no signs, symptoms, or events.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1683263

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ661AA

gering
Staat
NV
Alter
1,3
Geschlecht
M
Eingang
08.09.2021
Impfdatum
07.09.2021
Beginn
07.09.2021
Tage bis Beginn
0,0
Dosis
4
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Erythema Immune system disorder Peripheral swelling

Symptomtext

Swelling and redness left thigh started that night, spread the next day so pt came into the doctor's office. Skin only a light pink, so not concerned for infection, likely just the local immune response.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Erythema
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
none
Vorgeschichte
none
Andere Medikamente
none
Allergien
none
Vorherige Impfungen
-

VAERS 1641321

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ661AA

gering
Staat
MI
Alter
1,3
Geschlecht
F
Eingang
27.08.2021
Impfdatum
27.08.2021
Beginn
27.08.2021
Tage bis Beginn
0,0
Dosis
4
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Wrong product administered

Symptomtext

Prevnar 13 was to be given. Due to staff error Trumenba was given.

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