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Reporte zur Charge UJ794AB

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

7Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
TX 3 WY 1 MO 1 DC 1

VAERS 2712272

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge UJ794AB

gering
Staat
TX
Alter
0,6
Geschlecht
F
Eingang
09.11.2023
Impfdatum
30.10.2023
Beginn
30.10.2023
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 No adverse event

Symptomtext

an expired dose of Pentacel was accidentally administered to a 7 month-old child with no reported adverse event; Initial information received on 30-Oct-2023 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 7 months old female patient to whom an expired dose of pentacel was accidentally 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 POLYSACCH (PNEUMOVAX VACCIN) for Prophylactic vaccination. On 30-Oct-2023, the patient received a 0.5 ml dose of suspect DIPHTHERIA/TETANUS/5 HYBRID AC PERTUSSIS/IPV(VERO)/HIB(PRP/T) VACCINE, Suspension for injection lot UJ794AB, expiry- 08-Oct-2023 via intramuscular route in the right thigh for immunization with no reported adverse event (expired product administered) (latency same day). Action taken: not applicable. 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
PNEUMOVAX VACCIN
Allergien
-
Vorherige Impfungen
-

VAERS 2705294

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge UJ794AB

gering
Staat
TX
Alter
0,8
Geschlecht
F
Eingang
28.10.2023
Impfdatum
-
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered Medication error No adverse event

Symptomtext

she administered a one-day old expired PENTACEL vaccine to a patient with no reported adverse event; Initial information received on 19-Oct-2023 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 9 months old female patient who was administered a one-day old expired Diphtheria/Tetanus/5 Hybrid Ac Pertussis/Ipv(Vero)/Hib(Prp/T) Vaccine [Pentacel (Vero)] vaccine with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On an unknown date, the patient received an unknown dose of suspect Diphtheria/Tetanus/5 Hybrid Ac Pertussis/Ipv(Vero)/Hib(Prp/T) Vaccine Suspension for injection (lot number: UJ794AB) (Expiry date: 08-Oct-2023) (with an unknown strength) via unknown route in unknown administration site for immunization. On an unknown date, the patient was administered a one-day old 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, Medical assistant called stating that she administered a one-day old expired PENTACEL vaccine to a patient. She is calling to inquire if she needs to revaccinate. 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
-
Allergien
-
Vorherige Impfungen
-

VAERS 2702477

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ794AB

gering
Staat
WY
Alter
0,5
Geschlecht
F
Eingang
26.10.2023
Impfdatum
24.10.2023
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
IM / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered

Symptomtext

Expired Vaccine given on 10/24/23, expiration date of 10/08/2023

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

VAERS 2698899

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge UJ794AB

gering
Staat
MO
Alter
-
Geschlecht
U
Eingang
20.10.2023
Impfdatum
11.10.2023
Beginn
11.10.2023
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 Medication error No adverse event

Symptomtext

administering an expired pentacel to a patient with no reported adverse event; Initial information received on 12-Oct-2023 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a patient of an unknown age and gender, reporter reported that the an expired diphtheria/tetanus/5 Hybrid Ac Pertussis/IPV(Vero)/HIB(PRP/T) Vaccine [Pentacel (Vero)] administering to a patient with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 11-Oct-2023, the patient received a expired dose of 0.5 ml of suspect diphtheria/tetanus/5 Hybrid Ac Pertussis/IPV(Vero)/HIB(PRP/T) Vaccine Suspension for injection (strength: standard, frequency: once, expiry date: 08-Oct-2023 and lot UJ794AB) via unknown route in unknown administration site as immunization (expired product administered) (same day latency). 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. No additional information available at time of call; caller declined to respond to questions and refuses future follow-up.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2696320

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge UJ794AB

gering
Staat
-
Alter
0,3
Geschlecht
F
Eingang
16.10.2023
Impfdatum
09.10.2023
Beginn
09.10.2023
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

expired PENTACEL vaccine was inadvertently administered with no reported adverse event; Initial information received on 10-Oct-2023 regarding an unsolicited valid non-serious case received from a consumer/non-hcp (Non-healthcare professional). This case involves a 4 months old female patient who received expired Diphtheria/Tetanus/5 Hybrid Ac Pertussis/Ipv(Vero)/Hib(Prp/T) Vaccine [Pentacel (Vero)] inadvertently 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 live reassort oral 5v (rotateq) for immunisation; and pneumococcal vaccine conj 15v (crm197) (vaxneuvance) for immunisation. On 09-Oct-2023, the patient received 0.5 ml Total (1 X) of suspect Diphtheria/Tetanus/5 Hybrid Ac Pertussis/Ipv(Vero)/Hib(Prp/T) Vaccine Suspension for injection (lot number: UJ794AB) (Expiry date: 08-Oct-2023) (Strength: Standard) (Frequency: Once) via intramuscular route in unknown administration site for immunization. On 09-Oct-2023, the patient received expired Diphtheria/Tetanus/5 Hybrid Ac Pertussis/Ipv(Vero)/Hib(Prp/T) vaccine inadvertently with no reported adverse event (expired product administered) (latency: same day). It was reported, Office manager reports an expired PENTACEL vaccine was inadvertently administered yesterday, 09Oct2023 and that the product expired a day earlier on 08Oct2023. This situation is reported as a medication error due to the administration of an expired 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 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
ROTATEQ; VAXNEUVANCE
Allergien
-
Vorherige Impfungen
-

VAERS 2693035

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ794AB

gering
Staat
TX
Alter
0,8
Geschlecht
F
Eingang
09.10.2023
Impfdatum
09.10.2023
Beginn
09.10.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Unevaluable event

Symptomtext

N/A

Weitere VAERSDATA-Felder
Praegender Schweregrund
Unevaluable event
Hospital-Tage
-
Labordaten
N/A
Aktuelle Erkrankungen
N/A
Vorgeschichte
N/A
Andere Medikamente
N/A
Allergien
N\A
Vorherige Impfungen
-

VAERS 2610190

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ794AB

gering
Staat
DC
Alter
1,3
Geschlecht
F
Eingang
05.04.2023
Impfdatum
03.04.2023
Beginn
03.04.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
No adverse event Product preparation issue

Symptomtext

Pentacel was not reconstituted. No adverse reaction just did not receive complete dose. Will repeat vaccination for full protection.

Weitere VAERSDATA-Felder
Praegender Schweregrund
No adverse event
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None
Vorgeschichte
-
Andere Medikamente
none
Allergien
none
Vorherige Impfungen
-