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Reporte zur Charge UJ668AA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

5Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
CT 1 GA 1 MA 1 MI 1 VA 1

VAERS 2633328

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge UJ668AA

gering
Staat
CT
Alter
0,3
Geschlecht
F
Eingang
18.05.2023
Impfdatum
23.03.2023
Beginn
15.05.2023
Tage bis Beginn
53,0
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

administered PENTACEL to a pediatric patient that expired with no reported AE; Initial information received on 16-May-2023 regarding an unsolicited valid non-serious case received from a Nurse. This case involves a 3 months old female patient who was administered diphtheria/tetanus/5 hybrid AC pertussis/IPV(VERO)/HIB(PRP/T) vaccine [Pentacel (Vero)] that expired with no reported ae (adverse event). The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 23-Mar-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: UJ668AA; expiry date: 13-May-2023) via intramuscular route in unknown administration site for immunisation. On 15-May-2023, the patient received an unknown expired 0.5 ml dose of suspect diphtheria/tetanus/5 hybrid AC pertussis/IPV(VERO)/HIB(PRP/T) vaccine, Suspension for injection (lot: UJ668AA; expiry date: 13-May-2023) via intramuscular route in unknown administration site for immunisation with no reported ae (expired product administered) (same day latency). It was reported that The patient did not experience anything and is still under the care and monitoring of the said physician. 3 vaccines were administered prior to PENTACEL but the reporter did not disclose the information about this. Action taken: not applicable. At time of reporting, the outcome was Unknown for the event administered pentacel to a pediatric patient that expired with no reported ae. 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 2615045

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge UJ668AA

gering
Staat
GA
Alter
0,3
Geschlecht
F
Eingang
14.04.2023
Impfdatum
10.04.2023
Beginn
10.04.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Incorrect dose administered No adverse event Product preparation issue

Symptomtext

patient being administered PENTACEL after the liquid and lyophilized components were not properly reconstituted together and some of the lyophilized vaccine component was still left in the vial after administration with no reported adverse event; patient being administered PENTACEL after the liquid and lyophilized components were not properly reconstituted together and some of the lyophilized vaccine component was still left in the vial after administration with no reported adverse event; Initial information received on 10-Apr-2023 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 4 months old female patient who was administered diphtheria/tetanus/5 hybrid AC pertussis/IPV(VERO)/HIB(PRP/T) vaccine [Pentacel (Vero)] after the liquid and lyophilized components were not properly reconstituted together and some of the lyophilized vaccine component was still left in the vial after administration 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 13V (CRM197) (Prevnar 13) for Prophylactic vaccination. On 10-Apr-2023, the patient was administered 0.5ml dose of suspect diphtheria/tetanus/5 hybrid AC pertussis/IPV(VERO)/HIB(PRP/T) vaccine, Suspension for injection (strength; not reported) (lot UJ668AA; Expiry Date: 13-May-2023) via unknown route in the right vastus lateralis (Rt thigh) for Immunization after the liquid and lyophilized components were not properly reconstituted together and some of the lyophilized vaccine component was still left in the vial after administration with no reported adverse event (product preparation issue) (incorrect dose administered) (latency; on same day). It was reported that she reconstituted the liquid component (DTAP-IPV) of vaccine with the powder component (lyophilized ACTHIB vaccine) and after they were mixed it was some powder component still stuck to the bottom of the vial once she withdrew the vaccine into a syringe. It was hard to dissolve the powder into the solution even after shaking for about 1 minute and tapping on her hand. The vaccine was administered 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
Incorrect dose administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2463088

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ668AA

gering
Staat
MA
Alter
0,3
Geschlecht
M
Eingang
28.09.2022
Impfdatum
26.09.2022
Beginn
26.09.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / UN
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
No adverse event Product preparation issue

Symptomtext

Information per RN Well child appointment 4:30 PM 09/26/2022 Due for 4 month vaccines: Pentacel (DTaP, IPV, Hib), Prevnar, Rota Child up to date on vaccinations according to system RN ordered immunizations due in system w/provider as cosigner RN prepared vaccines to be administered at 4:55 pm RN opened new box of Pentacel (Lot: RN took out 1 vial of DTap-IPV RN did not take out vial of Hib to be mixed w/DTap-IPV component of combination vaccine This RN administered DTAP-IPV component of Pentacel to patient at 5:05 pm Pt did not receive Hib vaccine RN went to document administration of vaccinations 5:15 pm RN then realized she did not provide Hib component of combination vaccine to child RN was only person in clinic RN found the below documentation: LPN notified 09/27/2022 8:30 AM notified 8:45 AM Provider notified 09/27/2022 9:30 AM RN notified 11 AM 9/27/22 The parents were not notified No adverse effects reported by patient's parents

Weitere VAERSDATA-Felder
Praegender Schweregrund
No adverse event
Hospital-Tage
-
Labordaten
N/A
Aktuelle Erkrankungen
N/A
Vorgeschichte
N/A - This was a well child visit on 9/26/22
Andere Medikamente
None reported but the RN
Allergien
No known allergies
Vorherige Impfungen
-

VAERS 2371895

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ668AA

gering
Staat
MI
Alter
0,5
Geschlecht
M
Eingang
16.07.2022
Impfdatum
06.07.2022
Beginn
06.07.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Medication error No adverse event Poor quality product administered Product storage error

Symptomtext

Temperature excursion of the vaccine with no reported adverse event; medication error due to product being administered post excursion with no reported adverse events; Initial information received on 11-Jul-2022 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 6 months old male patient who was administered diphtheria/tetanus/5 hybrid AC pertussis/IPV(MRC5)/HIB(PRP/T) vaccine [Pentacel] post temperature excursion with no reported adverse events. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. Concomitant medications included hepatitis B vaccine. On an unknown date the suspect diphtheria/tetanus/5 hybrid AC pertussis/IPV(MRC5)/HIB(PRP/T) vaccine was exposed to a temperature excursion with no reported adverse event (product storage error). On 06-Jul-2022, the patient received 0.5 mL dose of suspect diphtheria/tetanus/5 hybrid AC pertussis/IPV(MRC5)/HIB(PRP/T) vaccine Injection (lot UJ668AA; expiry date: 13-May-2023) via intramuscular route in the left thigh for prophylactic immunization. On 06-Jul-2022, the patient was administered diphtheria/tetanus/5 hybrid AC pertussis/IPV(MRC5)/HIB(PRP/T) vaccine [Pentacel] post temperature excursion with no reported adverse events (poor quality product administered) (latency: same day). Action taken was not applicable. Outcome: Unknown for both the 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
Medication error
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2307014

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ668AA

gering
Staat
VA
Alter
1,9
Geschlecht
F
Eingang
02.06.2022
Impfdatum
01.06.2022
Beginn
02.06.2022
Tage bis Beginn
1,0
Dosis
4
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Extra dose administered

Symptomtext

Pt received extra dose of Varicella, MMR, and PCV13

Weitere VAERSDATA-Felder
Praegender Schweregrund
Extra dose administered
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
UNKNOWN
Vorgeschichte
NONE
Andere Medikamente
UKNOWN
Allergien
NKA
Vorherige Impfungen
-