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Reporte zur Charge UJ578AAA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

6Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
MA 1 NM 1 WA 1 MI 1

VAERS 2058470

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ578AAA

mild
Staat
MA
Alter
0,3
Geschlecht
M
Eingang
24.01.2022
Impfdatum
18.01.2022
Beginn
18.01.2022
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Aggression Pyrexia

Symptomtext

Baby was fussy in the evening after the vaccines and woke up febrile @ 3:00 a.m,, temp 101.

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

VAERS 1843790

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ578AAA

mild
Staat
NM
Alter
0,3
Geschlecht
F
Eingang
04.11.2021
Impfdatum
04.11.2021
Beginn
04.11.2021
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Urticaria

Symptomtext

PATIENT DEVELOPED URTICARIA OF THE CHIN IN 15 MIN AFTER RECEIVING VACCINES. NO SWELLING OF LIPS, SHORTNESS OF BREATH, COUGH. LUNG SOUNDS ARE CLEAR BILATERALLY WITH OXYGEN LEVELS AT 100%. HIVES DID NOT SPREAD TO OTHER AREAS OF THE BODY. PATIENT WAS PROVIDED WITH DOSE OF PREDNISOLONE IN THE OFFICE. MOTHER WAS ADVISED TO PROVIDE 2 ADDITIONAL DAYS OF PREDNISOLONE STARTING TOMORROW. REVIEWED SIGNS OF ANAPHYLAXIS, MOTHER WAS ADVISED TO SEEK URGENT MEDICAL ATTENTION SOONER IF NEEDED FOR CONCERNING SIGNS AND SYMPTOMS. HIVES RESOLVED PRIOR TO PATIENT LEAVING OFFICE.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Urticaria
Hospital-Tage
-
Labordaten
PRELONE 15MG/5ML LIQUID TAKE 2 MLS PO ONCE DAILY X 2 DAYS
Aktuelle Erkrankungen
NONE
Vorgeschichte
NONE
Andere Medikamente
NONE
Allergien
NKDA
Vorherige Impfungen
-

VAERS 2455740

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ578AAA

gering
Staat
WA
Alter
1,0
Geschlecht
M
Eingang
23.09.2022
Impfdatum
14.09.2022
Beginn
14.09.2022
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 No adverse event

Symptomtext

a PENTACEL vaccine was administered, then noted to have expired a few days ago with no reported adverse event; Initial information received on 14-Sep-2022 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 1 years old male patient who was administered a pentacel vaccine , then noted to have expired a few days ago with no reported adverse event ,after receiving vaccine DIPHTHERIA/TETANUS/5 HYBRID AC PERTUSSIS/IPV(MRC5)/HIB(PRP/T) VACCINE [PENTACEL]. The patient's past medical history, medical treatment(s) and family history were not provided. Concomitant medications included MEASLES VACCINE, MUMPS VACCINE, RUBELLA VACCINE (MMR) for Immunisation; HEPATITIS A VACCINE (HEPATITIS A) for Immunisation; PNEUMOCOCCAL VACCINE CONJ (PNEUMOCOCCAL CONJUGATE VACCINE) for Immunisation; and VARICELLA ZOSTER VACCINE (VARICELLA VACCINE) for Immunisation. On 14-Sep-2022, the patient received a dose of suspect DIPHTHERIA/TETANUS/5 HYBRID AC PERTUSSIS/IPV(MRC5)/HIB(PRP/T) VACCINE( lot UJ578AAA and expiration date: 10-Sep-2022) at a dose of 0.5ml via intramuscular route in the right thigh for immunization. On 14-Sep-2022(latency: same day), the patient was administered a pentacel vaccine , then noted to have expired a few days ago with no reported adverse event (expired product administered) following the administration. Action taken :not applicable. It was not reported if the patient received a corrective treatment for the event . 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
Expired product administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2267194

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ578AAA

gering
Staat
-
Alter
1,0
Geschlecht
U
Eingang
09.05.2022
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

total time out of range is 2 days with a minimum of 9.2c and maximum of 28.3c, 30 minutes with a minimum of 12.3c and maximum of 15.6c, 1 hour with a minimum of negative 1.8c and maximum of 1.8c with no reported adverse event; Initial information received on 29-Apr-2022 regarding an unsolicited valid non-serious case received via other health professional. This case involves a 1 years old and unknown gender patient who was administered vaccine with reported total time out of range is 2 days with a minimum of 9.2c and maximum of 28.3c, 30 minutes with a minimum of 12.3c and maximum of 15.6c, 1 hour with a minimum of negative 1.8c and maximum of 1.8c with no reported adverse event while receiving vaccine diphtheria/tetanus/5 hybrid ac pertussis/ipv(mrc5)/hib(prp/t) vaccine (Pentacel). 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 diphtheria/tetanus/5 hybrid ac pertussis/ipv(mrc5)/hib(prp/t) vaccine with lot UJ578AAA and expiry date: 10-Sep-2022 (dose, route and administration site: unknown) for Immunization. On 17-Oct-2021, It was reported that temperature excursion of Pentacel vaccine occurred with total time out of range is 2 days with a minimum of 9.2c and maximum of 28.3c, on 19-Oct-2021, temperature excursion occurred with 30 minutes with a minimum of 12.3c and maximum of 15.6c, 1 hour with a minimum of negative 1.8c and maximum of 1.8c with no reported adverse event (product temperature excursion issue). Action taken: not applicable. At time of reporting, the outcome was Unknown for the event out of range for 2 days with a minimum of 9.2c and maximum of 28.3c 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
No adverse event
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2267192

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ578AAA

gering
Staat
-
Alter
0,3
Geschlecht
U
Eingang
09.05.2022
Impfdatum
30.03.2022
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

multiple temprature excursion with no adverse event; Initial information received on 29-Apr-2022 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 4 months old and unknown gender patient who experienced multiple temprature excursion with no adverse event while receiving vaccine diphtheria/tetanus/5 hybrid AC pertussis/IPV(MRC5)/HIB(PRP/T) vaccine [Pentacel]. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 30-Mar-2022, the patient received a dose of suspect diphtheria/tetanus/5 hybrid AC pertussis/IPV(MRC5)/HIB(PRP/T) vaccine suspension for injection (strength and formulation: unknown) (lot UJ578AAA, Expiration Date:09-Oct-2022) via unknown route in unknown administration site for prophylactic vaccination. On an unknown date it was reported multiple temprature excursion with no adverse event (intercepted product storage error) (unknown latency). Action taken : not applicable. At time of reporting, the outcome was Unknown for the event multiple temprature excursion with no 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
No adverse event
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2265766

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ578AAA

gering
Staat
MI
Alter
0,2
Geschlecht
U
Eingang
06.05.2022
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

total time out of range is 2 days with a minimum of 9.2C and maximum of 28.3C, 30 minutes with a minimum of 12.3C and maximum of 15.6C, 1 hour with a minimum of negative 1.8C and maximum of 1.8C with no reported adverse event; Initial information regarding an unsolicited valid non-serious case received from health professional received on 29-Apr-2022. This case involves a 2 months old patient of unknown gender who was administered vaccine with reported total time out of range is 2 days with a minimum of 9.2c and maximum of 28.3c, 30 minutes with a minimum of 12.3c and maximum of 15.6c, 1 hour with a minimum of negative 1.8c and maximum of 1.8c with no reported adverse event while receiving vaccine Diphtheria/Tetanus/5 Hybrid AC Pertussis/IPV(MRC5)/HIB(PRP/T) Vaccine [Pentacel]. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 17-Oct-2021, It was reported that temperature excursion of Pentacel vaccine occurred with total time out of range is 2 days with a minimum of 9.2c and maximum of 28.3c, on 19-Oct-2021, temperature excursion occurred with 30 minutes with a minimum of 12.3c and maximum of 15.6c, 1 hour with a minimum of negative 1.8c and maximum of 1.8c with no reported adverse event (product temperature excursion issue). On 15-MAR-2022, the patient received a dose of suspect Pentacel vaccine (lot UJ578AAA, expiry date: 10-Sep-2022) (formulation, strength, dose, lot number, expiration date, route of administration and administration site: unknown) as prophylactic vaccination (immunization). Action taken: Not applicable. At time of reporting, the outcome was Unknown for the event.

Weitere VAERSDATA-Felder
Praegender Schweregrund
No adverse event
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-