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Reporte zur Charge UJ603AA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

4Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
MI 2 OR 1 PA 1

VAERS 2417299

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ603AA

moderat
Staat
MI
Alter
0,2
Geschlecht
M
Eingang
22.08.2022
Impfdatum
02.03.2022
Beginn
02.03.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Tremor

Symptomtext

Involuntary full body tremor that lasted until 03/25/2022. Tremor was spontaneous and was not correlated to any specific stimuli; occurred multiple times per day.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Tremor
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
Bronchiectasis
Vorgeschichte
Bronchiectasis
Andere Medikamente
Nebulized Budesonide, Ipratropium bromide, and Levalbuterol
Allergien
-
Vorherige Impfungen
-

VAERS 2561932

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ603AA

gering
Staat
OR
Alter
69,0
Geschlecht
M
Eingang
18.01.2023
Impfdatum
28.11.2022
Beginn
28.11.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered Medication error No adverse event

Symptomtext

HCP states that they accidentally gave a patient act-hib in which the diluent that came with it was expired, with no reported adverse event; Initial information received on 12-Jan-2023 regarding an unsolicited valid non-serious case received from a pharmacist. This case involves a 69 years old male patient whose hcp states that they accidentally gave a patient act-hib in which the diluent that came with it was expired, with no reported adverse event after receiving vaccine haemophilus type B (HIB) vaccine [ACT-HIB]. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. Concomitant medications included meningococcal vaccine A/C/Y/W CONJ (CRM197) (MENVEO) for Immunisation. On 28-Nov-2022, the patient received a standard 0.5 ml dose of suspect haemophilus type B (HIB) vaccine Powder and solvent for solution for injection (lot UJ603AA, expiry date: 29-Oct-2022) via intramuscular route in the deltoid nos not specified as immunization. On 28-NOV-2022 the patient developed hcp states that they accidentally gave a patient act-hib in which the diluent that came with it was expired, with no reported adverse event (expired product administered) on same day The HCP asks if the dose is valid and if they should revaccinate the patient Action taken was 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 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 2628797

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ603AA

gering
Staat
PA
Alter
0,3
Geschlecht
M
Eingang
11.11.2022
Impfdatum
07.11.2022
Beginn
-
Tage bis Beginn
-
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Unevaluable event

Symptomtext

None

Weitere VAERSDATA-Felder
Praegender Schweregrund
Unevaluable event
Hospital-Tage
-
Labordaten
N/A
Aktuelle Erkrankungen
N/A
Vorgeschichte
N/A
Andere Medikamente
N/A
Allergien
N/A
Vorherige Impfungen
-

VAERS 2497911

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ603AA

gering
Staat
MI
Alter
1,3
Geschlecht
F
Eingang
03.11.2022
Impfdatum
02.11.2022
Beginn
02.11.2022
Tage bis Beginn
0,0
Dosis
4
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered

Symptomtext

Patient was given expired vaccine. Vaccine was given 11/02/2022 and expired 10/29/2022. Patients parent/guardian was contacted and is now scheduled to receive replacing dose on 12/02/2022.

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