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Reporte zur Charge UJ633AAA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

4Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
CA 2 NJ 1 FL 1

VAERS 2593270

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ633AAA

gering
Staat
NJ
Alter
3,0
Geschlecht
F
Eingang
08.03.2023
Impfdatum
20.02.2023
Beginn
20.02.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Expired product administered No adverse event Vaccination error

Symptomtext

On 02/20/2023 patient received vaccine ActHIB that had expired 11/30/2022. Patient's mother informed of vaccine error by medical provider and was scheduled to come back for revaccination. Patient seen on 02/22/2023 and revaccinated with vaccine (not expired). Lot: UJ636AAA, IM on RD. Exp:02/26/2023. Patient did not report any adverse signs or symptoms.

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

VAERS 2539415

SANOFI PASTEUR · HIB (ACTHIB) · Charge uj633AAA

gering
Staat
FL
Alter
0,5
Geschlecht
M
Eingang
21.12.2022
Impfdatum
12.12.2022
Beginn
12.12.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered No adverse event

Symptomtext

Patient was administered a vaccine that had expired on 11/30/2022. No symptoms present at time of the vaccine

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

VAERS 2428183

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ633AAA

gering
Staat
CA
Alter
1,0
Geschlecht
M
Eingang
02.09.2022
Impfdatum
01.09.2022
Beginn
01.09.2022
Tage bis Beginn
0,0
Dosis
4
Route/Site
IM / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Incorrect route of product administration

Symptomtext

New MA inadvertently give MMR and Varicella IM rather than SQ

Weitere VAERSDATA-Felder
Praegender Schweregrund
Incorrect route of product administration
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
none
Vorgeschichte
none
Andere Medikamente
none
Allergien
none
Vorherige Impfungen
-

VAERS 2322988

SANOFI PASTEUR · HIB (ACTHIB) · Charge uj633aaa

gering
Staat
CA
Alter
0,8
Geschlecht
F
Eingang
17.06.2022
Impfdatum
08.06.2022
Beginn
08.06.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Product storage error

Symptomtext

temperature excursion due to refrigerator data logger malfunction low of 15.22 F 47 min with no ae; product being administered not suitable to use post temperature excursion with no adverse event; Initial information received on 09-Jun-2022 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 9-month-old female patient who reported HIB (PRP/T) VACCINE [ACT-HIB] product being administered not suitable to use post temperature excursion with no adverse event and temperature excursion due to refrigerator data logger malfunction low of 15.22 f 47 min with no adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. Concomitant medications included Diphtheria Vaccine Toxoid, Pertussis Vaccine Acellular, Tetanus Vaccine Toxoid (DTAP) for Immunization; Polio Vaccine Inactive (IPV) for Immunization; and Hepatitis B Vaccine (Hepatitis B Vaccine) for Immunization. On an unknown date, it was reported that temperature excursion occurred due to refrigerator data logger malfunction low temperature of 15.22 Fahrenheit and time 47 min with no ae (product storage error). On 08-Jun-2022, the patient received suspect ACT-HIB vaccine post temperature excursion at dose 0.5ml once intramuscular (lot uj633aaa, expiry date: 30-Nov-2022) via intramuscular route in unknown administration site for prophylactic vaccination (poor quality product administered, latency: same day). Action taken: Not applicable. At time of reporting, the outcome was Unknown for both the events. 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
Product storage error
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-