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Reporte zur Charge UJ614ABA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

6Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
MO 2 FL 2 NH 1 OH 1

VAERS 2452297

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ614ABA

gering
Staat
MO
Alter
-
Geschlecht
M
Eingang
28.12.2022
Impfdatum
25.07.2022
Beginn
25.07.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Extra dose administered No adverse event

Symptomtext

patient was given Vaxelis and Hib on the same day.; This case was retrieved during the Vaccines Adverse Event Reporting System (VAERS) monitoring on 12-OCT-2022 with the following VAERS Primary ID 2452297-1. The original narrative from the sender is the following: Patient was given Vaxelis and Hib on the same day. Patient had no adverse reaction or side effects. Dr. did speak with patient's mother regarding the event. The reporter did not provide an assessment of causal relationship between Vaxelis and the reported events "Patient was given Vaxelis and Hib on the same day". No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Extra dose administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
Prophylaxis
Vorgeschichte
-
Andere Medikamente
LACTULOSE
Allergien
-
Vorherige Impfungen
-

VAERS 2452297

UNKNOWN MANUFACTURER · HIB (NO BRAND NAME) · Charge UJ614ABA

gering
Staat
MO
Alter
-
Geschlecht
M
Eingang
28.12.2022
Impfdatum
25.07.2022
Beginn
25.07.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Extra dose administered No adverse event

Symptomtext

patient was given Vaxelis and Hib on the same day.; This case was retrieved during the Vaccines Adverse Event Reporting System (VAERS) monitoring on 12-OCT-2022 with the following VAERS Primary ID 2452297-1. The original narrative from the sender is the following: Patient was given Vaxelis and Hib on the same day. Patient had no adverse reaction or side effects. Dr. did speak with patient's mother regarding the event. The reporter did not provide an assessment of causal relationship between Vaxelis and the reported events "Patient was given Vaxelis and Hib on the same day". No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Extra dose administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
Prophylaxis
Vorgeschichte
-
Andere Medikamente
LACTULOSE
Allergien
-
Vorherige Impfungen
-

VAERS 2530631

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ614ABA

gering
Staat
FL
Alter
1,2
Geschlecht
M
Eingang
14.12.2022
Impfdatum
07.12.2022
Beginn
07.12.2022
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 Medication error No adverse event

Symptomtext

patient was administered expired acthib with no reported adverse event; Initial information received on 08-Dec-2022 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 14 months old male patient to whom expired HIB (PRP/T) vaccine [ACT-HIB] was 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 measles vaccine, mumps vaccine, rubella vaccine (MMR) for Prophylactic vaccination(immunization). On 07-Dec-2022, the patient received 0.5 ml(milliliter), 1x(once)(dose 4) of suspect HIB (PRP/T) vaccine, Powder and solvent for solution for injection (lot UJ614ABA)(expiry date: 30-Nov-2022) (with unknown dose) via intramuscular route in the left thigh for immunization. On 07-Dec-2022, patient received expired HIB (PRP/T) vaccine 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 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 2526641

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ614ABA

gering
Staat
FL
Alter
1,2
Geschlecht
M
Eingang
08.12.2022
Impfdatum
07.12.2022
Beginn
01.12.2022
Tage bis Beginn
-
Dosis
4
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Expired product administered

Symptomtext

DOSE EXP ON 11/30/2022 PRIOR TO ADMINISTRATION

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

VAERS 2258496

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ614ABA

gering
Staat
NH
Alter
4,0
Geschlecht
M
Eingang
29.04.2022
Impfdatum
29.04.2022
Beginn
-
Tage bis Beginn
-
Dosis
4
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Extra dose administered No adverse event

Symptomtext

pt was inadvertently given and extra IPV . no reaction at this time.

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

VAERS 2252179

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge UJ614ABA

gering
Staat
OH
Alter
0,8
Geschlecht
M
Eingang
26.04.2022
Impfdatum
25.04.2022
Beginn
-
Tage bis Beginn
-
Dosis
3
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Wrong product administered

Symptomtext

Typhim Vi (Typhoid injection) 0.5 ml was mistakenly given in the back of the left arm SQ instead of IPOL (polio). Tyhim Vi vaccine was in the state stock bin with other vaccines in mini fridge. Manufacturer and child's pediatrician were contacted and informed.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Wrong product administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
Fever 102 F, cough
Vorgeschichte
not known
Andere Medikamente
Amoxicillin, Ibuprofen
Allergien
nka
Vorherige Impfungen
-