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Reporte zur Charge UJ680ABA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

6Reporte angezeigt
1Todesfaelle
1Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
MA 1 NY 1 GA 1 ME 1 OH 1 CA 1

VAERS 2638438

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ680ABA

kritisch
Staat
MA
Alter
0,3
Geschlecht
M
Eingang
30.05.2023
Impfdatum
20.01.2023
Beginn
22.01.2023
Tage bis Beginn
2,0
Dosis
2
Route/Site
IM / RL
Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Death

Symptomtext

Patient received vaccines 01/20/23, died 01/22/23. Diagnosed with Influenza A 1/2/23- Asymptomatic at time of vaccines. Do not suspect vaccines contributed to death of patient.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Death
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
Influenza A (dx 1/2/23)
Vorgeschichte
-
Andere Medikamente
-
Allergien
NKDA
Vorherige Impfungen
-

VAERS 2582246

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ680ABA

kritisch
Staat
NY
Alter
0,1
Geschlecht
M
Eingang
15.02.2023
Impfdatum
07.02.2023
Beginn
11.02.2023
Tage bis Beginn
4,0
Dosis
1
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: unbekannt
Musculoskeletal stiffness Pallor Respiratory arrest Skin discolouration

Symptomtext

ON 2/11/23, child taken to ED by parents. Per ED documentation, patient presented to the ED "for 3 episodes lasting 10 seconds, with 10 seconds of resolution in between, where the patient stopped breathing and became stiff, was initially pale and then turned purple around his face."

Weitere VAERSDATA-Felder
Praegender Schweregrund
Respiratory arrest
Hospital-Tage
2,0
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
no known allergies
Vorherige Impfungen
-

VAERS 2686447

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ680ABA

gering
Staat
GA
Alter
0,9
Geschlecht
F
Eingang
26.09.2023
Impfdatum
27.07.2023
Beginn
27.07.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / LG
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
No adverse event Product preparation error

Symptomtext

INFANT WAS NOT ADMINISTERED THE HIB COMPONENT OF THE PENTACEL VACCINE AT THE TIME OF VACCINATION. NO ADVERSE REACTIONS NOTED.

Weitere VAERSDATA-Felder
Praegender Schweregrund
No adverse event
Hospital-Tage
-
Labordaten
NONE
Aktuelle Erkrankungen
NONE
Vorgeschichte
NONE
Andere Medikamente
NONE
Allergien
NKA
Vorherige Impfungen
-

VAERS 2621520

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ680ABA

gering
Staat
ME
Alter
1,6
Geschlecht
F
Eingang
26.04.2023
Impfdatum
19.04.2023
Beginn
19.04.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
No adverse event Wrong product administered

Symptomtext

Pentacel was given when DTaP was ordered. Provider, and parent notified. Patient suffered no adverse reaction.

Weitere VAERSDATA-Felder
Praegender Schweregrund
No adverse event
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
none
Vorgeschichte
none
Andere Medikamente
none
Allergien
none
Vorherige Impfungen
-

VAERS 2552829

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ680ABA

gering
Staat
OH
Alter
-
Geschlecht
U
Eingang
07.01.2023
Impfdatum
-
Beginn
30.12.2022
Tage bis Beginn
-
Dosis
UNK
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Product storage error

Symptomtext

excursion was due to the door being ajar. The temperature of the refrigerator reached 41.0-62.0 degrees Fahrenheit with no adverse event; Initial information received on 03-Jan-2023 regarding an unsolicited valid serious case received from a other health professional. This case involves an event of product storage error of MENINGOCOCCAL A-C-Y-W135 (T CONJ) VACCINE [MENQUADFI], DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS VACCINE [ADACEL] and DIPHTHERIA/TETANUS/5 HYBRID AC PERTUSSIS/IPV(MRC5)/HIB(PRP/T) VACCINE [PENTACEL] (excursion was due to the door being ajar. the temperature of the refrigerator reached 41.0-62.0 degrees fahrenheit with no adverse event). On 30-Dec-2022, it was reported DIPHTHERIA/TETANUS/5 HYBRID AC PERTUSSIS/IPV(MRC5)/HIB(PRP/T) VACCINE (lot UJ680ABA), DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS VACCINE (lot U7561AA) and MENINGOCOCCAL A-C-Y-W135 (T CONJ) VACCINE lot (U7576AD) (strength, formulation, dose, route and expiry date: unknown) to be used for immunization was exposed to excursion due to the door being ajar. the temperature of the refrigerator reached 41.0-62.0 degrees fahrenheit with no adverse event (product storage error) (unknown latency). Action taken: not applicable. It was not reported if the patient received a corrective treatment for the events. 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
Product storage error
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2521588

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ680ABA

gering
Staat
CA
Alter
0,3
Geschlecht
M
Eingang
02.12.2022
Impfdatum
30.11.2022
Beginn
30.11.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
OT / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
No adverse event Product preparation issue

Symptomtext

patient was administered with the product PENTACEL but with sterile diluent with no reported adverse event; Initial information received on 30-Nov-2022 regarding an unsolicited valid non-serious case received from a other health professional. This case involves 3 months old male patient who was administered with the product Pentacel (DIPHTHERIA/TETANUS/5 HYBRID AC PERTUSSIS/IPV(MRC5)/HIB(PRP/T) VACCINE) but with sterile diluent with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 30-Nov-2022, the patient received a one dose of suspect DIPHTHERIA/TETANUS/5 HYBRID AC PERTUSSIS/IPV(MRC5)/HIB(PRP/T) VACCINE (formulation, strength: unknown) lot UJ680ABA, expiration date: 16-Sep-2023 via intramuscular route in the right thigh as Immunization. On 30-Nov-2022 the patient was administered with the product pentacel but with sterile diluent with no reported adverse event (product preparation error) (same day) following the administration of DIPHTHERIA/TETANUS/5 HYBRID AC PERTUSSIS/IPV(MRC5)/HIB(PRP/T) VACCINE. Caller was asking some guidance with regards to Pentacel that was administered to a patient separately. The lyophilized portion was diluted with a different diluent instead of the diluent supplied with the vaccine thus wanted to know if that would count as a valid dose. Action taken was not applicable. It was not reported if the patient received a corrective treatment for the event (patient was administered with the product Pentacel but with sterile diluent with no reported adverse event). At time of reporting, the outcome was Unknown for the 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
No adverse event
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-