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Reporte zur Charge UJ671AAA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

2Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
CT 1 CO 1

VAERS 2662177

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge UJ671AAA

gering
Staat
CT
Alter
0,6
Geschlecht
F
Eingang
27.07.2023
Impfdatum
20.07.2023
Beginn
20.07.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered No adverse event

Symptomtext

administered an expired pentacel vaccine to a patient today with no reported adverse event; Initial information was received on 20-Jul-2023 regarding an unsolicited valid non-serious case received from other health professional. Live follow up information was processed together. This case involves a 7 months old female patient who received an expired diphtheria/tetanus/5 hybrid ac pertussis/ipv(vero)/hib(prp/t) vaccine [Pentacel (vero)] vaccine to a patient today 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 7v (crm197) (Prevnar) for Prophylactic vaccination (immunisation); and hepatitis b vaccine for Prophylactic vaccination (immunisation). On 20-Jul-2023, the patient received a dose of suspect diphtheria/tetanus/5 hybrid ac pertussis/ipv(vero)/hib(prp/t) vaccine Suspension for injection (strength: standard) at dose of 0.5 ml once (1x) (lot number: UJ671AAA, expiration date: 13-May-2023, administration site: Unknown) via intramuscular route for Immunization (immunisation) with no reported adverse event (expired product administered) (latency: same day). No lab data reported. Action taken: not applicable. At time of reporting, the outcome was Unknown for the event administered an expired pentacel vaccine to a patient today 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
Expired product administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
PREVNAR; HEPATITIS B VACCINE
Allergien
-
Vorherige Impfungen
-

VAERS 2637012

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge UJ671AAA

gering
Staat
CO
Alter
-
Geschlecht
M
Eingang
26.05.2023
Impfdatum
16.05.2023
Beginn
16.05.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered Medication error No adverse event

Symptomtext

administering expired PENTACEL with no reported AE; Initial information received on 23-May-2023 regarding an unsolicited valid non-serious case received from a other health professional. This case involves an unknown age male patient who was administered expired vaccine DIPHTHERIA/TETANUS/5 HYBRID AC PERTUSSIS/IPV(VERO)/HIB(PRP/T) VACCINE [PENTACEL (VERO)] 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 and PNEUMOCOCCAL VACCINE CONJ (PNEUMOCOCCAL CONJUGATE VACCINE) for prophylactic vaccination (Immunization). On 16-May-2023, the patient received 0.25 ml 1x (total) dose of suspect DIPHTHERIA/TETANUS/5 HYBRID AC PERTUSSIS/IPV(VERO)/HIB(PRP/T) VACCINE (Suspension for injection) Frequency = once, Strength = standard (lot UJ671AAA and expiry date: 13-May-2023) via unknown route in Left Vastus Lateralis administration site for immunization. On 16-May-2023, the patient was administered expired DIPHTHERIA/TETANUS/5 HYBRID AC PERTUSSIS/IPV(VERO)/HIB(PRP/T) VACCINE with no reported adverse event (expired product administered) (latency: same day). It was reported that"Nurse is asking if there's any side effects that go along with administering expired PENTACEL to a 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 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
-