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Reporte zur Charge UJ603AAA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

5Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
PA 3 NY 1 MN 1

VAERS 2341830

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ603AAA

mild
Staat
PA
Alter
0,2
Geschlecht
F
Eingang
24.06.2022
Impfdatum
22.06.2022
Beginn
22.06.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Rash Rash macular

Symptomtext

* Patient developed blotchy rash on both legs. more on the left

Weitere VAERSDATA-Felder
Praegender Schweregrund
Rash
Hospital-Tage
-
Labordaten
N/A
Aktuelle Erkrankungen
none
Vorgeschichte
none
Andere Medikamente
Budesonide 0.25mg/2mL nebulizer (recently was on)
Allergien
-
Vorherige Impfungen
-

VAERS 2514897

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ603AAA

gering
Staat
PA
Alter
1,1
Geschlecht
F
Eingang
23.11.2022
Impfdatum
02.11.2022
Beginn
02.11.2022
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 Medication error No adverse event

Symptomtext

they administered an act-hib vaccine that was a couple of days out of date,with no reported adverse event; Initial information received on 16-Nov-2022 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 13 months old female patient and it was reported that they administered an act-hib vaccine that was a couple of days out of date, with no reported adverse event after receiving vaccine HIB (PRP/T) VACCINE [ACT-HIB]. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. Concomitant medications included varicella zoster vaccine (Varicella Vaccine) for Prophylactic vaccination; and hepatitis A vaccine(Hepatitis A) for Prophylactic vaccination. On 02-Nov-2022, the patient received a dose of suspect HIB (PRP/T) VACCINE powder and solvent for solution for injection (batch number: UJ603AAA) (strength and expiry date: unknown) via intramuscular route in the right thigh. On 02-Nov-2022, the patient developed a non-serious event they administered an act-hib vaccine that was a couple of days out of date, with no reported adverse event (expired product administered) (latency: same day) following the administration of HIB (PRP/T) VACCINE. Lab data not reported. Action taken with HAEMOPHILUS TYPE B (HIB) VACCINE (ACT-HIB) was not applicable. At time of reporting, the outcome was unknown for the event they administered an act-hib vaccine that was a couple of days out of date, 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
VARICELLA VACCINE; HEPATITIS A
Allergien
-
Vorherige Impfungen
-

VAERS 2497680

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ603AAA

gering
Staat
PA
Alter
1,0
Geschlecht
F
Eingang
03.11.2022
Impfdatum
02.11.2022
Beginn
02.11.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Expired product administered No adverse event

Symptomtext

no adverse reactions, administered expired vaccine. vaccine expired 10/29/22, administered 11/2/22

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

VAERS 2173368

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ603AAA

gering
Staat
NY
Alter
1,5
Geschlecht
F
Eingang
11.03.2022
Impfdatum
06.03.2022
Beginn
06.03.2022
Tage bis Beginn
0,0
Dosis
5
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Extra dose administered Inappropriate schedule of product administration Product administered to patient of inappropriate age Wrong product administered

Symptomtext

Patient received 2nd MMR and Varivax at 18 month check up on 3/6/22 instead of waiting until 4 years old. Patient also received a HIB vaccine dose #5 on 3/6/22. Patient had 15 month check up on 12/18/21 and received all of these vaccines at that time. MMR and Varivax are both valid for a second dose.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Extra dose administered
Hospital-Tage
-
Labordaten
N/A
Aktuelle Erkrankungen
N/A
Vorgeschichte
None
Andere Medikamente
N/A
Allergien
NKDA
Vorherige Impfungen
-

VAERS 2128213

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ603AAA

gering
Staat
MN
Alter
-
Geschlecht
U
Eingang
19.02.2022
Impfdatum
-
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Product storage error

Symptomtext

temperature excursion; Initial information received on 14-Feb-2022 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a patient with unknown demographics who had temperature excursion while receiving vaccines [ADACEL], [IPOL], DIPHTHERIA-15/TETANUS/5 AC PERTUSSIS VACCINE [DAPTACEL], DIPHTHERIA/TETANUS/5 HYBRID AC PERTUSSIS/IPV(MRC5)/HIB(PRP/T) VACCINE [PENTACEL], DIPHTHERIA-15/TETANUS/5 HYBRID AC PERTUSSIS/IPV (MRC5) VACCINE [QUADRACEL] and HIB (PRP/T) VACCINE [ACT-HIB] and while treated with TUBERCULIN TEST [TUBERSOL]. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On an unknown date, the patient started taking TUBERSOL (TUBERCULIN TEST) Solution for injection dosage unknown (lot - C582AA) for Product used for unknown indication. On an unknown date, the patient received a dose of suspect HIB (PRP/T) VACCINE lot UJ603AAA via unknown route in unknown administration site for immunization. On an unknown date, the patient received a dose of suspect DIPHTHERIA-15/TETANUS/5 HYBRID AC PERTUSSIS/IPV (MRC5) VACCINE lot C59700A via unknown route in unknown administration site immunization. On an unknown date, the patient received a dose of suspect DIPHTHERIA/TETANUS/5 HYBRID AC PERTUSSIS/IPV(MRC5)/HIB(PRP/T) VACCINE lot UJ597AAA via unknown route in unknown administration site immunization. On an unknown date, the patient received a dose of suspect DIPHTHERIA-15/TETANUS/5 AC PERTUSSIS VACCINE lot C5816AA via unknown route in unknown administration site. On an unknown date, the patient received a dose of suspect IPV (VERO) lot V1A011M via unknown route in unknown administration site immunization. On an unknown date, the patient received a dose of suspect DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS VACCINE lot U7093AA via unknown route in unknown administration site immunization. On an unknown date the patient had temperature excursion (product temperature excursion issue) (unknown latency) following the first dose intake and (unknown latency) following the last dose intake of DIPHTHERIA-15/TETANUS/5 HYBRID AC PERTUSSIS/IPV (MRC5) VACCINE. Action taken was not applicable. It was not reported if the patient received a corrective treatment for the event (temperature excursion). At time of reporting, the outcome was Unknown for the event temperature excursion.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Product storage error
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
TUBERSOL
Allergien
-
Vorherige Impfungen
-