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Reporte zur Charge U6970BB

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

3Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
GA 1 CA 1 ME 1

VAERS 2589431

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge U6970BB

gering
Staat
GA
Alter
0,3
Geschlecht
F
Eingang
01.03.2023
Impfdatum
01.03.2023
Beginn
01.03.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Expired product administered No adverse event

Symptomtext

The patient was accidentally administered an expired dose of Pentacel by the Medical Assistant. There was no immediate adverse effect witnessed. This was discovered during charting of the vaccine into patient's chart. The family was immediately notified via phone by Dr.; the family reported the patient, 4 hours later, continues to have no witnessed adverse effect. An incident report will be filed by the Practice Manager.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
Vitamin D oral supplement
Allergien
No known
Vorherige Impfungen
-

VAERS 2404218

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge U6970bb

gering
Staat
CA
Alter
0,3
Geschlecht
F
Eingang
08.08.2022
Impfdatum
20.07.2022
Beginn
20.07.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Product preparation error

Symptomtext

patient was only given the liquid component of Pentacel, it was not reconstituted with Acthib with no reported adverse event; patient was only given the liquid component of Pentacel, it was not reconstituted with Acthib with no reported adverse event; Initial information received on 29-Jul-2022 regarding an unsolicited valid non-serious case received from a consumer/non-hcp. (GMI number: 01213528) This case involves a 3-month-old female patient was only given the liquid component of Diphtheria/Tetanus/5 Hybrid AC Pertussis/IPV(MRC5)/HIB(PRP/T) Vaccine [Pentacel], it was not reconstituted with acthib 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 B vaccine for Prophylactic vaccination; Rotavirus Vaccine for Prophylactic vaccination; and Pneumococcal Vaccine CONJ (pcv 13) for Prophylactic vaccination. On 20-Jul-2022, the patient received suspect Pentacel vaccine only liquid component at dose 0.5ml once (lot U6970bb) via intramuscular route in the left thigh for Immunization no reported adverse event (product preparation error, single component of a two-component product administered, same day latency). It was reported that "Caller states that a patient was only given the liquid component of Pentacel. It was not reconstituted with Acthib. Do we give a repeat dose or just give Acthib?" Action taken: Not applicable. At time of reporting, the outcome was Unknown for both 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 preparation error
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2376772

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge U6970BB

gering
Staat
ME
Alter
0,3
Geschlecht
M
Eingang
21.07.2022
Impfdatum
15.07.2022
Beginn
15.07.2022
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Incorrect dose administered No adverse event

Symptomtext

Pt was given 0.4 mL of pentacel vaccine instead of 0.5 mL. Pt did not have any adverse reactions or symptoms.

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