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Reporte zur Charge UJ579AA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

4Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
PA 1 VT 1 LA 1 TX 1

VAERS 2109261

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ579AA

gering
Staat
PA
Alter
-
Geschlecht
U
Eingang
12.02.2022
Impfdatum
-
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Medication error No adverse event Product storage error

Symptomtext

Temperature excursion at a high of 66F for 27 minutes due to the refrigerator being accidentally left opened with no reported adverse event; Initial information received on 08-Feb-2022 regarding an unsolicited valid non-serious case received from a other health professional. This case involves patient with unknown demographics who had temperature excursion at a high of 66f for 27 minutes due to the refrigerator being accidentally left opened with no reported adverse event while receiving vaccines [ACT-HIB], [IPOL],[ADACEL],[DAPTACEL]. 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 HIB (PRP/T) VACCINE with lot UJ579AA via unknown route in unknown administration site with(unknown dosage form, strength, frequency)for immunization. On an unknown date, the patient received a dose of suspect DIPHTHERIA-15/TETANUS/5 AC PERTUSSIS VACCINE lot C5829BA via unknown route in unknown administration site with(unknown dosage form, strength, frequency)for immunization. On an unknown date, the patient received a dose of suspect ACTHIB not produced by Sanofi Pasteur lot UJ579AA via unknown route in unknown administration site with(unknown dosage form, strength, frequency)for immunization. On an unknown date, the patient received a dose of suspect DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS VACCINE lot U7055AA via unknown route in unknown administration site with(unknown dosage form, strength, frequency)for immunization. On an unknown date, the patient received a dose of suspect IPV (VERO) lot T1E87 via unknown route in unknown administration site with(unknown dosage form, strength, frequency)for immunization. On an unknown date the patient had temperature excursion at a high of 66f for 27 minutes due to the refrigerator being accidentally left opened with no reported adverse event (product storage error) (unknown latency) following the administration of DIPHTHERIA-15/TETANUS/5 AC PERTUSSIS VACCINE. Action taken was not applicable. It was not reported if the patient received a corrective treatment for the event (Temperature excursion at a high of 66F for 27 minutes due to the refrigerator being accidentally left opened with no reported adverse event). At time of reporting, the outcome was Unknown for the event temperature excursion at a high of 66f for 27 minutes due to the refrigerator being accidentally left opened 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 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 2104805

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ579AA

gering
Staat
VT
Alter
0,3
Geschlecht
F
Eingang
11.02.2022
Impfdatum
11.02.2022
Beginn
11.02.2022
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Product administered to patient of inappropriate age

Symptomtext

Patient was given Kinrix combination vaccine; patient is only 4 months of age.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Product administered to patient of inappropriate age
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
none
Vorgeschichte
none
Andere Medikamente
Vitamin D
Allergien
NKDA
Vorherige Impfungen
-

VAERS 1985208

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ579AA

gering
Staat
LA
Alter
0,5
Geschlecht
F
Eingang
28.12.2021
Impfdatum
28.12.2021
Beginn
28.12.2021
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Inappropriate schedule of product administration No adverse event

Symptomtext

Pt was given the HPV vaccine outside of the schedule recommendations. Pt has shown no adverse effects from receiving this vaccine.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Inappropriate schedule of product administration
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
ACTHIB, PEDIARIX, ROTATEQ.
Vorgeschichte
NONE
Andere Medikamente
FAMOTIDINE PO
Allergien
NKDA
Vorherige Impfungen
-

VAERS 1856902

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ579AA

gering
Staat
TX
Alter
0,6
Geschlecht
F
Eingang
10.11.2021
Impfdatum
01.11.2021
Beginn
01.11.2021
Tage bis Beginn
0,0
Dosis
4
Route/Site
OT / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Product preparation error

Symptomtext

administering ACTHIB on saline diluent for ACTHIB was not used for reconstitution; diluent from MMR was used with no adverse event; Initial information regarding an unsolicited non-valid non serious case was received from other health professional via Medical Information (MI) (Reference number: 00838515) and transmitted to Sanofi on 02-Nov-2021. This case involves a 7-month-old female patient administering HIB (PRP/T) VACCINE [ACT-HIB] on saline diluent for HIB (PRP/T) VACCINE [ACT-HIB] was not used for reconstitution; diluent from MEASLES VACCINE, MUMPS VACCINE, RUBELLA VACCINE [MMR VACCINE] with the use of medical device FLUZONE QUADRIVALENT PRE-FILLED SYRINGE (Product preparation error). The patient medical history, medical treatment(s), vaccination(s) and family history were not provided. Concomitant medications included QUADRIVALENT INFLUENZA VACCINE (FLUZONE QUADRIVALENT). On 01-Nov-2021, the patient received a fourth dose of 0.5 mL total dose of suspect HIB (PRP/T) VACCINE [lot UJ579AA, expiry date 09-Oct-2021] via intramuscular route in the left thigh for prophylactic vaccination. On an unknown date, the patient started using MEASLES VACCINE, MUMPS VACCINE, RUBELLA VACCINE (MMR VACCIN) [lot number and expiry date not reported] via unknown route at an unknown administration site for prophylactic vaccination. This was actual medication error case due to wrong solution used in drug reconstitution (latency same day). It was reporter "Caller reports administering ACTHIB on 01Nov2021; saline diluent for ACTHIB was not used for reconstitution; diluent from MEASLES VACCINE, MUMPS VACCINE, RUBELLA VACCINE was used." At the time of reporting, no adverse event was reported. This suspected adverse reaction report was 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 was 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 had contributed to or is to be held liable for the occurrence of this medication error. There will be no information available on the batch number for this FLUZONE QUADRIVALENT.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Product preparation error
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
FLUZONE QUADRIVALENT
Allergien
-
Vorherige Impfungen
-