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Reporte zur Charge UJ668AAA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

3Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
TX 1 GA 1

VAERS 2634514

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge UJ668AAA

gering
Staat
-
Alter
0,2
Geschlecht
F
Eingang
20.05.2023
Impfdatum
15.05.2023
Beginn
15.05.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
OT / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered Medication error No adverse event

Symptomtext

product was administered to a patient and then they noticed that on the chart it says that the product has expired with no reported adverse event; Initial information received on 15-May-2023 regarding an unsolicited valid non-serious case received from a other health professional. This case involves 8 weeks old female patient who was administered Diphtheria/Tetanus/5 Hybrid AC Pertussis/IPV(VERO)/HIB(PRP/T) vaccine [Pentacel (VERO)] and then they noticed that on the chart it says that the product has expired 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 Rotavirus Vaccine, Pneumococcal Vaccine Conj (Pneumococcal Conjugate Vaccine) (PCV) and Hepatitis B vaccine (Hepatitis B vaccine) all for Immunisation. On 15-May-2023, the patient received a 0.5ml dose (dose 1) suspect Diphtheria/Tetanus/5 Hybrid AC Pertussis/IPV(VERO)/HIB(PRP/T) vaccine Suspension for injection of lot UJ668AAA and expiry: 13-May-2023 via intramuscular route in the right thigh for immunization. On 15-May-2023, the patient developed a non-serious event product was administered to a patient and then they noticed that on the chart it says that the product has expired with no reported adverse event (expired product administered) (latency: same day) following the administration of Diphtheria/Tetanus/5 Hybrid ac Pertussis/IPV(VERO)/HIB(PRP/T) vaccine. No lab data was reported. Action taken was not applicable. At time of reporting, the outcome was Unknown for the event product was administered to a patient and then they noticed that on the chart it says that the product has expired 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 2632748

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge UJ668AAA

gering
Staat
TX
Alter
0,4
Geschlecht
F
Eingang
17.05.2023
Impfdatum
15.05.2023
Beginn
15.05.2023
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 Medication error No adverse event

Symptomtext

Expired PENTACEL was inadvertently administered with no reported AE; Initial information received on 15-May-2023 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 5 months old female patient to whom diphtheria/tetanus/5 hybrid ac pertussis/IPV(VERO)/HIB(PRP/T) vaccine [pentacel (vero)] was inadvertently administered 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 PNEUMOCOCCAL VACCINE CONJ (PNEUMOCOCCAL CONJUGATE VACCINE) for Prophylactic vaccination; and ROTAVIRUS VACCINE (ROTAVIRUS VACCINE) for Prophylactic vaccination. On 15-May-2023, the patient received a expired 0.5 ml dose of suspect diphtheria/tetanus/5 hybrid ac pertussis/IPV(VERO)/HIB(PRP/T) vaccine Suspension for injection (lot UJ668AAA, expiry date: 13-MAY-2023 with unknown strength) via intramuscular route in the right thigh for immunization with no reported adverse event (expired product administered) (Latency: same day). Action taken: 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
Expired product administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
PNEUMOCOCCAL CONJUGATE VACCINE; ROTAVIRUS VACCINE
Allergien
-
Vorherige Impfungen
-

VAERS 2481265

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge UJ668AAA

gering
Staat
GA
Alter
1,5
Geschlecht
M
Eingang
18.10.2022
Impfdatum
10.10.2022
Beginn
10.10.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
OT / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Medication error No adverse event Product preparation error

Symptomtext

patient was administered pentacel DTAP-IPV component was administered, not the ACT-HIB portion with no reported adverse event; Initial information received on 10-Oct-2022 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 18 months old male patient was administered diphtheria/tetanus/5 hybrid AC pertussis/IPV(VERO)/HIB(PRP/T) vaccine [Pentacel (Vero)] onlyl DTAP-IPV component was administered, not the ACT-HIB portion 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 measles vaccine live (enders-edmonston), mumps vaccine live, rubella vaccine live (wistar ra 27/3), varicella zoster vaccine live (oka/merck) (Proquad); measles vaccine, mumps vaccine, rubella vaccine (MMR) and pneumococcal for Immunisation. On 10-Oct-2022, the patient received 0.5ml (dose 3) of suspect diphtheria/tetanus/5 hybrid AC pertussis/IPV(VERO)/HIB(PRP/T) vaccine, suspension for injection (lot UJ668AAA; Expiry date: 13-May-2023)via intramuscular route in the right leg (right thigh) for Immunization. On 10-OCT-2022 the patient was administered only dtap-ipv component was administered, not the act-hib portion with no reported adverse event (product preparation error) (latency; on same day). This situation is reported as a medication error due to the incorrect administration of PENTACEL. Only the liquid DTAP-IPV portion was administered to the patient 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 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
PROQUAD; MMR; PNEUMOCOCCAL VACCINE
Allergien
-
Vorherige Impfungen
-