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Reporte zur Charge UJ784AAA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

5Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
VT 2 OR 1 VA 1 TN 1

VAERS 2673561

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ784AAA

mild
Staat
OR
Alter
1,3
Geschlecht
F
Eingang
18.08.2023
Impfdatum
15.08.2023
Beginn
17.08.2023
Tage bis Beginn
2,0
Dosis
4
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Discomfort Irritability Rash Urticaria

Symptomtext

2 days after immunization pt developed an urticarial rash on her right thigh, trunk, and face. She was otherwise well. Overnight, she was fussy and seemed uncomfortable, so parents gave a dose of Zyrtec. The following day the urticaria were resolve.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Rash
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
Respiratory viral illness with conjunctivitis.
Vorgeschichte
None
Andere Medikamente
None
Allergien
None
Vorherige Impfungen
-

VAERS 2698864

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ784AAA

gering
Staat
VT
Alter
1,3
Geschlecht
U
Eingang
19.10.2023
Impfdatum
09.10.2023
Beginn
09.10.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered Medication error No adverse event

Symptomtext

a practice that i oversee gave a act-hib vaccination after the expiration date with no reported adverse event; Initial information received on 10-Oct-2023 regarding an unsolicited valid non-serious case received from other health professional. This case involves a 15-months-old and unknown gender patient who got a HIB (PRP/T) vaccine [ACT-HIB] vaccination after the expiration date with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 09-Oct-2023, the patient received unknown expired dose of suspect HIB (PRP/T) vaccine, Powder and solvent for solution for injection (batch number: UJ784AAA; expiry date: 07-Oct-2023) via unknown route in unknown administration site for immunization with no reported adverse event (expired product administered) (same day latency). Reportedly, A practice that reporter oversee gave a Hib vaccination after the expiration date and reporter was hoping you could tell me if the dose should be repeated or if it will count as valid Action taken: not applicable. At time of reporting, the outcome was Unknown for the event. No additional details. 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
-
Allergien
-
Vorherige Impfungen
-

VAERS 2692888

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ784AAA

gering
Staat
VT
Alter
1,3
Geschlecht
M
Eingang
09.10.2023
Impfdatum
09.10.2023
Beginn
09.10.2023
Tage bis Beginn
0,0
Dosis
4
Route/Site
IM / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Expired product administered

Symptomtext

Patient was given a dose of expired ActHIB. Dose expired 10/7/23 and was administered 10/09/23

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
N/A
Aktuelle Erkrankungen
N/A
Vorgeschichte
asthma
Andere Medikamente
albuterol, Fluoride
Allergien
NKA
Vorherige Impfungen
-

VAERS 2634212

MERCK & CO. INC. · HIB (PEDVAXHIB) · Charge UJ784AAA

gering
Staat
VA
Alter
0,5
Geschlecht
F
Eingang
19.05.2023
Impfdatum
18.05.2023
Beginn
18.05.2023
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Product dose omission issue Vaccination error

Symptomtext

A MEDICAL ASSISTANT ADMINISTERED A PRESYRINGED VACCINE TO THIS PATIENT, THEREAFTER PICKED THE EMPTY SYRINGE SHE HAD JUST ADMIN ISTERED TO THE PATIENT AND INSERTED THE NEEDLE WITH NO VACCINE IN IT AGAIN THINKING SHE WAS PICKING UP PREVNAR THEN REALISED IT WAS EMPTY. SHE THEN BROUGHT OUT THNEEDLE WITHOUT INJECTING ANYTHING. MOM REALISED IT AT SAME TIME GOT UPSET AND REFUSED TO CONTINUE TO GIVE THE PREVNER.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Product dose omission issue
Hospital-Tage
-
Labordaten
NONE
Aktuelle Erkrankungen
SKIN RASH ON FACE
Vorgeschichte
NONE
Andere Medikamente
NONE
Allergien
NONE
Vorherige Impfungen
-

VAERS 2633005

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ784AAA

gering
Staat
TN
Alter
1,0
Geschlecht
M
Eingang
17.05.2023
Impfdatum
12.05.2023
Beginn
12.05.2023
Tage bis Beginn
0,0
Dosis
4
Route/Site
IM / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Inappropriate schedule of product administration

Symptomtext

Varicella vaccine was given prior to the 28 day interval mark after the MMR vaccine was administered.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Inappropriate schedule of product administration
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
no other illnesses at the time of vaccination
Vorgeschichte
no chronic or long-standing health conditions
Andere Medikamente
Patient does not take daily medications, over-ther-counter medications, supplements, or herbal remedies.
Allergien
No known allergies
Vorherige Impfungen
-