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Reporte zur Charge UJ735AAB

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

6Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
AR 2 GA 2 MO 1 WA 1

VAERS 2609164

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ735AAB

mild
Staat
AR
Alter
1,1
Geschlecht
F
Eingang
04.04.2023
Impfdatum
16.03.2023
Beginn
25.03.2023
Tage bis Beginn
9,0
Dosis
4
Route/Site
IM / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Decreased appetite Fatigue Poor quality sleep Pyrexia

Symptomtext

Mother called and reported that on PM of 03/25 patient started running fever, by 03/26 at approximately 0400 the fever had gotten up to 104.2. Mother was able to get fever to break with luke warm bath and tylenol. Mother states fever has been running between 99-101 since 03/25 (03/25-03/28). Child also had fatigue, poor appetite, and did not sleep well. Mother took child to clinic and was told that child looked good no problems, and to continue to treat fever with tylenol and ibuprofen.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Fatigue
Hospital-Tage
-
Labordaten
N/A
Aktuelle Erkrankungen
none
Vorgeschichte
none
Andere Medikamente
none
Allergien
pears
Vorherige Impfungen
-

VAERS 2673747

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ735AAB

gering
Staat
MO
Alter
4,0
Geschlecht
F
Eingang
19.08.2023
Impfdatum
15.08.2023
Beginn
15.08.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered No adverse event

Symptomtext

patient had an ActHIB vaccine on 15Aug2023, however the vaccine had expired on 07Aug2023 with no reported adverse event; Initial information received on 15-Aug-2023 regarding an unsolicited valid non-serious case received from other health professional. This case involves a 4 years old female patient who had an HIB (PRP/T) vaccine [ACT-HIB] on 15aug2023, however the vaccine had expired on 07aug2023 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 hepatitis A vaccine inact (Havrix); measles vaccine, mumps vaccine, rubella vaccine (MMR); pneumococcal vaccine conj 13V (CRM197) (Prevnar 13); varicella zoster vaccine live (OKA/MERCK) (Varivax); and diphtheria vaccine toxoid, pertussis vaccine acellular 3-component, polio vaccine inact 3V (vero), tetanus vaccine toxoid (Kinrix) all for prophylactic vaccination (Immunisation). On 15-Aug-2023, the patient received 0.5 mL dose of expired suspect HIB (PRP/T) vaccine, powder and solvent for solution for injection (batch number: UJ735AAB; expiry date: 07-Aug-2023) via intramuscular route in the right thigh for immunization with no reported adverse event (expired product administered) (same day latency). Action taken: not applicable. At time of reporting, the outcome was Unknown for the event patient had an acthib vaccine on 15aug2023, however the vaccine had expired on 07aug2023 with no reported adverse 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 2671549

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ735AAB

gering
Staat
AR
Alter
1,0
Geschlecht
F
Eingang
15.08.2023
Impfdatum
17.07.2023
Beginn
17.07.2023
Tage bis Beginn
0,0
Dosis
4
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Wrong product administered

Symptomtext

On 7/27/23, during immunization reconciliation, the counts for specific lots of Pediatric MMR vaccine and Pediatric MMRV vaccine in system were noted to be discrepant from the physical Count of inventory in the clinic. MMRV (Lot: X007087 Exp: 9/4/24) was showing in system as having 10 doses in inventory with no doses having been administered, however, the physical count revealed only 9 doses in clinic. MMR (Lot: W007041 Exp: 02/29/2024) was showing in system as having 6 doses remaining, however, physical count of the vaccine in the unit was 7 doses. All other inventory counts were correct. 4 patients had documentation in system showing vaccination with this lot of MMR, since last reconciliation. All 4 patients were also vaccinated with Varicella vaccine during each of their visits. Documentation for each of the 4 patients also noted the MMR (and Varicella) vaccinations. Due to the discrepancies in count, however, it can be presumed that one of these children (although we cannot determine which child) were vaccinated with MMRV in the place of MMR and therefore received MMRV and Varicella on the same day inadvertently. RN reported findings to supervisor. Immunization Program Nurse and Regional Director were notified by RN. Dr. was also noted of above information. PHN contacted parents of all 4 minor patients and notified them of the possibility of vaccination error. Mom denies any reaction of any kind after receiving the vaccine. Child is currently doing fine.

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

VAERS 2643760

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ735AAB

gering
Staat
WA
Alter
1,0
Geschlecht
M
Eingang
09.06.2023
Impfdatum
28.04.2023
Beginn
-
Tage bis Beginn
-
Dosis
4
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Discontinued product administered No adverse event

Symptomtext

no side effects noted per mom

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

VAERS 2589290

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ735AAB

gering
Staat
GA
Alter
1,4
Geschlecht
F
Eingang
01.03.2023
Impfdatum
28.02.2023
Beginn
28.02.2023
Tage bis Beginn
0,0
Dosis
4
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Product storage error

Symptomtext

Pt was given a non viable vaccine that was in an excursion the night prior. The excursion was not caught before this pt got vaccine. The patients parent was called and rescheduled to come back in the office to repeat vaccine.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Product storage error
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2589287

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ735AAB

gering
Staat
GA
Alter
1,3
Geschlecht
M
Eingang
01.03.2023
Impfdatum
28.02.2023
Beginn
28.02.2023
Tage bis Beginn
0,0
Dosis
4
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Product storage error

Symptomtext

Pt was given a non viable vaccine that was in an excursion the night prior. The excursion was not caught before this pt got vaccine. The patients parent was called and rescheduled to come back in the office to repeat vaccine.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Product storage error
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-