Zurueck zur Suche

Reporte zur Charge UJ806AA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

6Reporte angezeigt
0Todesfaelle
1Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
MI 2 SC 1 NJ 1 PA 1 KY 1

VAERS 2674334

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ806AA

mild
Staat
SC
Alter
0,3
Geschlecht
M
Eingang
21.08.2023
Impfdatum
25.07.2023
Beginn
18.08.2023
Tage bis Beginn
24,0
Dosis
UNK
Route/Site
SYR / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: ja
Abdominal pain Crying Dyskinesia Enema administration Infant irritability Intussusception Small intestinal intussusception reduction Ultrasound abdomen abnormal Urinary tract imaging abnormal X-ray

Symptomtext

Patient had increased fussiness and abdominal pain with significantly increased crying and leg raising. He came to the emergency department at the Hospital, where he had a KUB (showed increased stool burden), ultrasound (showed target sign with small bowel to small bowel intussusception, but couldn't rule out ileocolonic), and a fluoroscopic intussusception reduction enema which revealed that there was no intussusception, so presumably it self resolved.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Abdominal pain
Hospital-Tage
1,0
Labordaten
8/20 ultrasound: target sign suspicious for ileo-ileal intussusception 8/20-KUB: increased stool burden 8/20- fluoroscopic intussusception reduction enema- no intussusception
Aktuelle Erkrankungen
Unkown
Vorgeschichte
None
Andere Medikamente
Unknown
Allergien
Unknown
Vorherige Impfungen
-

VAERS 2695494

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ806AA

gering
Staat
MI
Alter
1,6
Geschlecht
F
Eingang
13.10.2023
Impfdatum
16.09.2023
Beginn
16.09.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Wrong product administered

Symptomtext

Pentacel administered instead of DTaP.

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

VAERS 2675982

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge UJ806AA

gering
Staat
NJ
Alter
-
Geschlecht
U
Eingang
24.08.2023
Impfdatum
10.06.2023
Beginn
10.06.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Medication error No adverse event Poor quality product administered

Symptomtext

inappropriate administration of PENTACEL to a patient that was no longer suitable for use post excursion with no reported adverse event; Initial information received on 14-Aug-2023 regarding an unsolicited valid non-serious case received from other health professional. This case involves an unknown age and unknown gender patient who had inappropriate administration of diphtheria/tetanus/5 hybrid AC pertussis/IPV(VERO)/HIB(PRP/T) vaccine [Pentacel (Vero)] that was no longer suitable for use post excursion with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 10-Jun-2023, the patient had inappropriate administration of suspect diphtheria/tetanus/5 hybrid AC pertussis/IPV(VERO)/HIB(PRP/T) vaccine Suspension for injection (lot UJ806AA, expiry date- 18-FEB-2024) via unknown route in unknown administration site for Immunization that was no longer suitable for use post excursion with no reported adverse event (poor quality product administered) (latency- same day). Reportedly, Caller reported a temperature excursion due to an unknown cause. The excursion occurred on 06JUN2023. The lowest temperature reached negative 0.92 C and the total excursion lasted 1 hour and 15 minutes. Pentacel was administered on 10JUN2023 after being exposed to NEGATIVE 0.92 C. 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 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
Medication error
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2653946

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ806AA

gering
Staat
MI
Alter
0,2
Geschlecht
F
Eingang
07.07.2023
Impfdatum
28.06.2023
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
IM / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Product preparation error

Symptomtext

Pentacel powder (HIB) never mixed with diluent (dtap-IPV) so pt did not receive HIB portion of vaccine

Weitere VAERSDATA-Felder
Praegender Schweregrund
Product preparation error
Hospital-Tage
-
Labordaten
N/A
Aktuelle Erkrankungen
-
Vorgeschichte
Umbilical hernia
Andere Medikamente
Vitamin D3 drops
Allergien
NKA
Vorherige Impfungen
-

VAERS 2644608

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ806AA

gering
Staat
PA
Alter
0,5
Geschlecht
F
Eingang
13.06.2023
Impfdatum
13.06.2023
Beginn
13.06.2023
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
No adverse event Product administered to patient of inappropriate age

Symptomtext

No known adverse event. Age inappropriate vaccine given.

Weitere VAERSDATA-Felder
Praegender Schweregrund
No adverse event
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
Unknown
Allergien
NKDA
Vorherige Impfungen
-

VAERS 2629479

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ806AA

gering
Staat
KY
Alter
5,0
Geschlecht
F
Eingang
10.05.2023
Impfdatum
02.05.2023
Beginn
02.05.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered No adverse event Product administered to patient of inappropriate age

Symptomtext

5 year old patient was given pentacel in error (with no reported adverse event); pentacel vaccine code 242 with batch number UJ806AA was administered (with no reported adverse event); Initial information received on 02-May-2023 regarding an unsolicited valid non-serious case received from a physician. This case involves a 5 years old female patient who was given diphtheria/tetanus/5 hybrid AC pertussis/IPV(MRC5)/HIB(PRP/T) vaccine [Pentacel] of code 242 with batch number UJ806AA in error (with no reported adverse event). The patient's past medical history, medical treatment(s), vaccination(s), concomitant(s) and family history were not provided. Concomitant medications included Pneumococcal Vaccine CONJ 7V (CRM197) (Prevnar) and Measles Vaccine, Mumps Vaccine, Rubella Vaccine (MMR), both for Prophylactic vaccination. On 02-May-2023, The Physician misread the birthdate and thought that the patient was 4 and the patient of age 5 received a dose of suspect Diphtheria/Tetanus/5 hybrid AC pertussis/IPV(MRC5)/HIB(PRP/T) vaccine of standard strength at 0.5 ml dose, suspension for injection of code 242 with lot: UJ806AA via intramuscular route in the right deltoid for prophylactic vaccination (Immunization) with no reported adverse event (product administered to patient of inappropriate age) and (expired 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
Expired product administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-