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Reporte zur Charge UJ577AA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

3Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
HI 1 KS 1 MI 1

VAERS 2404198

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge UJ577AA

gering
Staat
HI
Alter
0,7
Geschlecht
M
Eingang
08.08.2022
Impfdatum
25.07.2022
Beginn
25.07.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Product preparation error

Symptomtext

a medication error with PENTACEL described as only the liquid DTap-IPV portion was given and not the Hib portion due to the products not being mixed with no reported adverse event; Initial information received on 27-Jul-2022 regarding an unsolicited valid non-serious case received from a nurse . This case involves a 8 months old male patient and it reported a medication error with Pentacel described as only the liquid Dtap-ipv portion was given and not the hib portion due to the products not being mixed with no reported adverse event , for receiving vaccine DIPHTHERIA/TETANUS/5 HYBRID AC PERTUSSIS/IPV(MRC5)/HIB(PRP/T) VACCINE [PENTACEL]. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. Concomitant medications included PNEUMOCOCCAL VACCINE CONJ (PNEUMOCOCCAL CONJUGATE VACCINE). On 25-Jul-2022, the patient received a dose of 0.5 ml (once) of suspect DIPHTHERIA/TETANUS/5 HYBRID AC PERTUSSIS/IPV(MRC5)/HIB(PRP/T) VACCINE , (lot: UJ577AA ; expiry date: 10-Sep-2022) in unknown administration site for immunization. It was reported that a medication error with Pentacel described as only the liquid dtap-ipv portion was given and not the hib portion due to the products not being mixed with no reported adverse event (product preparation error) following the administration of DIPHTHERIA/TETANUS/5 HYBRID AC PERTUSSIS/IPV(MRC5)/HIB(PRP/T) VACCINE. Action taken: not applicable. Outcome: unknown 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 preparation error
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2109240

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ577AA

gering
Staat
KS
Alter
1,0
Geschlecht
M
Eingang
12.02.2022
Impfdatum
25.01.2022
Beginn
25.01.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
No adverse event Product preparation issue

Symptomtext

gave a patient the Hib component of PENTACEL that was reconstituted with sterile water with no reported adverse event; Initial information received on 27-Jan-2022 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 1 years old male patient who experienced gave a patient the hib component of pentacel that was reconstituted with sterile water with no reported adverse event while receiving vaccine DIPHTHERIA/TETANUS/5 HYBRID AC PERTUSSIS/IPV(MRC5)/HIB(PRP/T) VACCINE [PENTACEL]. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. Concomitant medications included HEPATITIS A VACCINE INACT (VAQTA) for Prophylactic vaccination. On 25-Jan-2022, the patient received a dose of suspect DIPHTHERIA/TETANUS/5 HYBRID AC PERTUSSIS/IPV(MRC5)/HIB(PRP/T) VACCINE lot UJ577AA (Strength and expiry date was unknow) via intramuscular route in unknown administration site for prophylactic vaccination. On 25-JAN-2022 the patient developed a non-serious gave a patient the hib component of pentacel that was reconstituted with sterile water with no reported adverse event (product preparation error) following the administration of DIPHTHERIA/TETANUS/5 HYBRID AC PERTUSSIS/IPV(MRC5)/HIB(PRP/T) VACCINE. Action taken with DIPHTHERIA, TETANUS, AC PERTUSSIS, IPV AND HIB VACCINE (PENTACEL) was not applicable. It was not reported if the patient received a corrective treatment for the event (gave a patient the Hib component of PENTACEL that was reconstituted with sterile water with no reported adverse event). At time of reporting, the outcome was Unknown for the event gave a patient the hib component of pentacel that was reconstituted with sterile water 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 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
No adverse event
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1921122

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ577AA

gering
Staat
MI
Alter
0,2
Geschlecht
F
Eingang
03.12.2021
Impfdatum
02.12.2021
Beginn
02.12.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Wrong product administered

Symptomtext

Medical Assistant mistakenly given Hep A vaccine dose to patient. The doctor ordered Hep B to be given to the patient.

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