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Reporte zur Charge UJ422AA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

3Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
IL 1 VA 1 NH 1

VAERS 1176315

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ422AA

mild
Staat
IL
Alter
0,4
Geschlecht
F
Eingang
07.04.2021
Impfdatum
25.03.2021
Beginn
27.03.2021
Tage bis Beginn
2,0
Dosis
UNK
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Injection site rash Rash Rash erythematous Rash papular

Symptomtext

1-2 days after administration patient developed a erythematous papular rash all over left thigh (site of injection). rash did not extend to diaper area or below knee, was not pruritic. no other systemic signs such as full body hives, no swelling, no airway involvement, no trouble breathing. no fevers. no n/v/d. no changes in appetite, sleep, play patterns. Appears patient had received dtap/hib/hepb/polio prior on 12/7/20 but was not completed at our clinic so exact formulation (pentacel vs pediarix vs separate?) is unknown

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site rash
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
none; patient had normal physical exam and no other prior complaints
Vorgeschichte
none
Andere Medikamente
none
Allergien
none prior
Vorherige Impfungen
-

VAERS 1110325

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ422AA

mild
Staat
VA
Alter
3,0
Geschlecht
M
Eingang
18.03.2021
Impfdatum
17.03.2021
Beginn
17.03.2021
Tage bis Beginn
0,0
Dosis
4
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Diarrhoea Nausea Pyrexia Skin warm Vomiting

Symptomtext

Mom reports possible fever; states that patient feels warm. Nausea and vomiting X4, diarrhea X2 on the way home from getting vaccines.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Diarrhoea
Hospital-Tage
-
Labordaten
N/A
Aktuelle Erkrankungen
n/a
Vorgeschichte
n/a
Andere Medikamente
n/a
Allergien
No known allergies
Vorherige Impfungen
-

VAERS 1756431

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge UJ422AA

gering
Staat
NH
Alter
-
Geschlecht
F
Eingang
02.10.2021
Impfdatum
-
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
No adverse event Product preparation issue

Symptomtext

Act-hib component with sterile diluent; Initial information received on 24-Sep-2021 regarding an unsolicited valid non-serious case received from a other health professional and consumer non health care professional via Medical Information number: 00784569. This case involves an unknown age female patient who was received DIPHTHERIA/TETANUS/5 HYBRID AC PERTUSSIS/IPV(VERO)/HIB(PRP/T) VACCINE [PENTACEL (VERO)] (product preparation issue). The patient's medical history, medical treatments, vaccinations, concomitant medications 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 (lot number: UJ422AA and expiry date not reported) via unknown route in unknown administration site for prophylactic vaccination. It was case of an actual medication error due to Inappropriate reconstitution technique (latency: same day). It was reported that nurse who states she doesn't have any information other than what was provided in initial contact. Caller isn't sure what diluent the medical assistant mixed the Act-HIB powder with. Caller states it "like what comes with Varicella" and informed her that is not our product. At the time of reporting, no adverse event was reported. 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
No adverse event
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-