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Reporte zur Charge UJ571AA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

2Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
MI 1 MD 1

VAERS 2147467

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ571AA

gering
Staat
MI
Alter
0,2
Geschlecht
M
Eingang
27.02.2022
Impfdatum
12.10.2021
Beginn
12.10.2021
Tage bis Beginn
0,0
Dosis
2
Route/Site
OT / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Underdose

Symptomtext

incomplete dose administered; Initial information received on 21-Feb-2022 regarding an unsolicited valid non-serious case received from a other health professional via call center. This case involves a 2 months old male patient who experienced incomplete dose administered 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 pneumococcal vaccine CONJ 7V (CRM197) (Prevnar) and rotavirus vaccine (Rotavirus vaccine) for Immunization. On 12-Oct-2021, the patient received a first 0.5 ml dose of suspect diphtheria/tetanus/5 hybrid ac pertussis/IPV(MRC5)/HIB(PRP/T) vaccine lot UJ571AA via unknown route in the left thigh (dosage form, strength, formulation and expiry date: unknown). On 21-Feb-2022 he also received a second 0.5 ml dose of the same vaccine lot UJ527AA via unknown route in the left thigh (dosage form, strength, formulation and expiry date: unknown) for immunization. On 12-OCT-2021, the patient developed a non-serious event incomplete dose administered (incorrect dose administered) (latency: same day) following the administration of diphtheria/tetanus/5 hybrid ac pertussis/IPV(MRC5)/HIB(PRP/T) vaccine. Action taken: Not applicable. It was not reported if the patient received a corrective treatment for the event (incomplete dose administered). At time of reporting, the outcome was Unknown for the event incomplete dose administered. 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
Underdose
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2109252

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ571AA

gering
Staat
MD
Alter
0,2
Geschlecht
M
Eingang
12.02.2022
Impfdatum
01.02.2022
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
No adverse event Wrong product administered

Symptomtext

patient received a dose of pentacle but the nurse made an error and used saline diluent for the hib component instead of using the dtap/ipv as the diluent, with no reported adverse event'; Initial information received on 02-Feb-2022 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 2 months old male patient who received a dose of pentacle but the nurse made an error and used saline diluent for the hib component instead of using the dtap ipv as the diluent, with no reported adverse event while receiving 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 13V (CRM197) (PREVNAR 13), and ROTAVIRUS VACCINE (ROTAVIRUS VACCINE). On 01-Feb-2022, the patient received a dose of suspect DIPHTHERIA/TETANUS/5 HYBRID AC PERTUSSIS/IPV(MRC5)/HIB(PRP/T) VACCINE lot UJ571AA via intramuscular route in unknown administration site. On an unknown date the patient received a dose of pentacle but the nurse made an error and used saline diluent for the hib component instead of using the dtap ipv as the diluent, with no reported adverse event (wrong product administered) (unknown latency) following the administration of DIPHTHERIA/TETANUS/5 HYBRID AC PERTUSSIS/IPV(MRC5)/HIB(PRP/T) VACCINE. Action taken was not applicable. It was not reported if the patient received a corrective treatment for the event (patient received a dose of pentacle but the nurse made an error and used saline diluent for the hib component instead of using the dtap/ipv as the diluent, with no reported adverse event). At time of reporting, the outcome was Unknown for the event patient received a dose of pentacle but the nurse made an error and used saline diluent for the hib component instead of using the dtap ipv as the diluent, 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 holders 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
-