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Reporte zur Charge UJ496AAA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

2Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
CA 1 NY 1

VAERS 2648189

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge UJ496AAA

mild
Staat
CA
Alter
0,8
Geschlecht
M
Eingang
22.06.2023
Impfdatum
29.09.2022
Beginn
29.09.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
OT / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered Medication error Pyrexia

Symptomtext

fever; patient received a dose of pentacel that expired; Initial information received on 30-Sep-2022 regarding an unsolicited valid non-serious case received from a physician. This case involves a 10 months old male patient who was having fever and patient received a dose of pentacel (DIPHTHERIA/TETANUS/5 HYBRID AC PERTUSSIS/IPV(VERO)/HIB(PRP/T) VACCINE [PENTACEL (VERO)] that expired. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 29-Sep-2022, the patient received 0.5 ml third dose of suspect DIPHTHERIA/TETANUS/5 HYBRID AC PERTUSSIS/IPV(VERO)/HIB(PRP/T) VACCINE (formulation, strength: unknown) lot number: UJ496AAA, expiration date: 09-Jul-2022, via intramuscular route in right vastus lateralis as Immunization On 29-Sep-2022 the patient received a dose of pentacel that expired (expired product administered) (same day) following the administration of DIPHTHERIA/TETANUS/5 HYBRID AC PERTUSSIS/IPV(VERO)/HIB(PRP/T) VACCINE. On an unknown date the patient had fever (pyrexia) (unknown latency) following the administration of DIPHTHERIA/TETANUS/5 HYBRID AC PERTUSSIS/IPV(VERO)/HIB(PRP/T) VACCINE. Action taken was not applicable. It was not reported if the patient received a corrective treatment for the events (fever, patient received a dose of pentacel that expired). At time of reporting, the outcome was Unknown for all. 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. Additional information received on 30-Sep-2022 from other health care professional: therapy details, therapy start date, batch number and expiry date updated for the suspect, event onset date updated for expired product administered, text amended accordingly

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pyrexia
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1980866

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ496AAA

gering
Staat
NY
Alter
-
Geschlecht
U
Eingang
25.12.2021
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 storage error

Symptomtext

The products were exposed to highest temperature of 54.9 degrees Fahrenheit (12.72 degrees Celsius) and lowest temperature of 40.5 degrees Fahrenheit (4.72 degrees Celsius) with no AE; Initial information received on 14-Dec-2021 regarding an unsolicited valid non-serious case received from an other health professional. This case involves unknown gender patient for whom it was reported the products were exposed to highest temperature of 54.9 degrees Fahrenheit (12.72 degrees Celsius) and lowest temperature of 40.5 degrees Fahrenheit (4.72 degrees Celsius) after receiving DIPHTHERIA-15/TETANUS/5 AC PERTUSSIS VACCINE [DAPTACEL], MENINGOCOCCAL A-C-Y-W135 (D CONJ) VACCINE [MENACTRA], HIB (PRP/T) VACCINE [ActHIB], DIPHTHERIA/TETANUS/5 HYBRID AC PERTUSSIS/IPV(VERO)/HIB(PRP/T) VACCINE [PENTACEL (VERO)] and INFLUENZA QUADRIVAL A-B VACCINE [FLUZONE QUADRIVALENT] (Product storage error). The patient medical history, medical treatment(s), vaccination(s),concomitant medication and family history were not provided. On an unknown date, the patient received a dose of suspect INFLUENZA QUADRIVAL A-B VACCINE [lot U7328AA, expiry date: 30-Jun-2022] via an unknown route in unknown administration site for prophylactic vaccination. On an unknown date, the patient received a dose of suspect DIPHTHERIA/TETANUS/5 HYBRID AC PERTUSSIS/IPV(VERO)/HIB(PRP/T) VACCINE [lot UJ496AAA, expiry date:09-Jul-2022] via an unknown route in unknown administration site for prophylactic vaccination. On an unknown date, the patient received a dose of suspect HIB (PRP/T) VACCINE [lot UJ426AAA and expiry date:07-Mar-20222] via an unknown route in unknown administration site for prophylactic vaccination. On an unknown date, the patient received a dose of suspect MENINGOCOCCAL A-C-Y-W135 (D CONJ) VACCINE [lot U6828AB, expiry date: 09-Jan-2022] via an unknown route in unknown administration site for prophylactic vaccination. On an unknown date, the patient received a dose of suspect DIPHTHERIA-15/TETANUS/5 AC PERTUSSIS VACCINE [lot C5765BA and expiry date: 28-Aug-2022] via an unknown route in unknown administration site for prophylactic vaccination. It was case of actual medication error due to product storage error [Latency: on the same day]. At the time of report, 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 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
No adverse event
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-