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Reporte zur Charge UJ662AA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

6Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
KY 3 SD 1 WA 1 TN 1

VAERS 2222974

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ662AA

schwer
Staat
SD
Alter
0,3
Geschlecht
M
Eingang
08.04.2022
Impfdatum
05.04.2022
Beginn
05.04.2022
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja
Febrile convulsion Laboratory test Lethargy Viral infection

Symptomtext

patient was seen at an outside ER organization. My medical documentation is limited. -Patient reported to the ER due to lethargy. -does not appear that any treatment was completed while in the ER, it is possible that patient may have been given Tylenol in the ER, but I am unable to verify that for sure. -exam and lab work completed -Diagnosed with: Febrile seizure Acute viral syndrome

Weitere VAERSDATA-Felder
Praegender Schweregrund
Febrile convulsion
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None
Allergien
None
Vorherige Impfungen
-

VAERS 2635780

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge UJ662AA

gering
Staat
KY
Alter
-
Geschlecht
U
Eingang
24.05.2023
Impfdatum
17.05.2023
Beginn
17.05.2023
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

vaccine was administered 13 days expired with no reported adverse event; Initial information was received on 18-May-2023 regarding an unsolicited valid non-serious case received from a other health professional. This case involves an unknown age and gender patient to whom diphtheria/tetanus/5 hybrid ac pertussis/ipv(vero)/hib(prp/t) vaccine [Pentacel (VERO)] was administered 13 days expired with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 17-May-2023, the patient received an unknown dose of suspect diphtheria/tetanus/5 hybrid ac pertussis/ipv(vero)/hib(prp/t) vaccine Suspension for injection (lot UJ662AA, expiry date: 04-May-2023), strength, was unknown) via unknown route in unknown administration site for Immunization. On 17-May-2023 the patient was administered 13 days 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. 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
-
Allergien
-
Vorherige Impfungen
-

VAERS 2635216

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge UJ662AA

gering
Staat
KY
Alter
4,0
Geschlecht
M
Eingang
23.05.2023
Impfdatum
17.05.2023
Beginn
17.05.2023
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

pentacel product expired on 5/4, but was administered on 5/17 with no reported adverse event; Initial information received on 18-May-2023 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 4 years old male patient who was administered expired DIPHTHERIA/TETANUS/5 HYBRID AC PERTUSSIS/IPV(VERO)/HIB(PRP/T) VACCINE [PENTACEL (VERO)] vaccine which expired on 04-May-2023, but was administered on 17-May-2023 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 (JERYL LYNN), RUBELLA VACCINE LIVE (WISTAR RA 27/3), VARICELLA ZOSTER VACCINE LIVE (OKA/MERCK) (PROQUAD) and HEPATITIS A VACCINE (HEPATITIS A VACCINE) both for Prophylactic vaccination (Immunization). On 17-May-2023, the patient received a dose of 0.5 ml once of suspect DIPHTHERIA/TETANUS/5 HYBRID AC PERTUSSIS/IPV(VERO)/HIB(PRP/T) VACCINE (Suspension for injection) (lot: UJ662AA; expiry date: 04-MAY-2023; strength: standard) via intramuscular route in unknown administration site for Immunization. On 17-May-2023 the patient was administered expired pentacel vaccine which expired on 04-May-2023 with no reported adverse event (expired product administered) (latency: same day). It was reported, "Caller wanted to know if patient need to be re-vaccinated." Action taken was 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 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 2633623

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ662AA

gering
Staat
KY
Alter
4,0
Geschlecht
M
Eingang
18.05.2023
Impfdatum
17.05.2023
Beginn
17.05.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Expired product administered Poor quality product administered

Symptomtext

Pentacel (DTaP,IPV,Hib) vaccine given 5-17-23, vaccine expired on 5-4-23. Called and spoke with Medical Information and was advised to repeat vaccine asap, vaccine not valid. Called and informed patient mother of incident and rescheduled patient for repeat vaccination of Pentacel. Mom verbalized understanding.

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

VAERS 2630744

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge UJ662AA

gering
Staat
WA
Alter
2,0
Geschlecht
M
Eingang
11.05.2023
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 No adverse event

Symptomtext

they had administered an expired vaccine to a patient, with no reported adverse event; Initial information received on 09-May-2023 regarding an unsolicited valid non-serious case received from a health professional. This case involves a 27 months old male patient administered an 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 a dose of suspect Diphtheria/Tetanus/5 Hybrid Ac Pertussis/Ipv(Vero)/Hib(Prp/T) Vaccine, Suspension for injection (strength, dose: unknown) (lot: UJ662AA, Expiry date: 04-May-2023) via unknown route in unknown administration site for prophylactic vaccination (immunization). On an unknown date the patient had administered an 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 to report that they had administered an expired vaccine to a patient." Action taken with Diphtheria, Tetanus, Ac Pertussis, Ipv And Hib Vaccine was not applicable. It was not reported if the patient received a corrective treatment for the event. 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 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 2427567

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ662AA

gering
Staat
TN
Alter
0,5
Geschlecht
M
Eingang
02.09.2022
Impfdatum
25.08.2022
Beginn
26.08.2022
Tage bis Beginn
1,0
Dosis
3
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja
Unevaluable event

Symptomtext

See attached ER visit note.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Unevaluable event
Hospital-Tage
-
Labordaten
See attached ER visit note
Aktuelle Erkrankungen
-
Vorgeschichte
Dx with seizures after 4 month vaccines
Andere Medikamente
Keppra, famotidine
Allergien
NKA
Vorherige Impfungen
Seizures after 4 month vaccines