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Reporte zur Charge UJ837AA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

5Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
AL 1 PA 1 MI 1 VA 1 CA 1

VAERS 2714055

SANOFI PASTEUR · HIB (ACTHIB) · Charge uj837aa

mild
Staat
AL
Alter
0,2
Geschlecht
M
Eingang
15.11.2023
Impfdatum
11.09.2023
Beginn
01.09.2023
Tage bis Beginn
-
Dosis
1
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Abnormal behaviour Agitation Crying Pain

Symptomtext

Mother reports patient was extremely agitated and unlike himself for 2 weeks following vaccination. She described as "near inconsolable" . Cried out in pain frequently.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pain
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
none
Vorgeschichte
-
Andere Medikamente
famotidine daily
Allergien
no known allergies
Vorherige Impfungen
-

VAERS 2671471

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ837AA

mild
Staat
PA
Alter
1,0
Geschlecht
F
Eingang
15.08.2023
Impfdatum
10.08.2023
Beginn
12.08.2023
Tage bis Beginn
2,0
Dosis
4
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Pyrexia

Symptomtext

Fever of 103

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pyrexia
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None
Allergien
None
Vorherige Impfungen
-

VAERS 2719043

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ837AA

gering
Staat
MI
Alter
0,6
Geschlecht
M
Eingang
29.11.2023
Impfdatum
29.11.2023
Beginn
29.11.2023
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Expired product administered No adverse event

Symptomtext

Immunization expired 10/30/2023 and was given by RMA today, 11/29/2023. Patient is not having any reaction per the mother. Mother was informed by RMA that the immunization given was expired and that a new dose can be given at anytime. Mother gave verbal understanding and plans to schedule an appointment to repeat the dose.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
none per last OV note.
Vorgeschichte
none per last OV note.
Andere Medikamente
none per last OV note.
Allergien
none per last OV note.
Vorherige Impfungen
-

VAERS 2715887

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ837AA

gering
Staat
VA
Alter
1,3
Geschlecht
F
Eingang
20.11.2023
Impfdatum
08.11.2023
Beginn
08.11.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered No adverse event

Symptomtext

once of their office has administered an expired dose of ACTHIB with no reported adverse event; Initial information received on 10-Nov-2023 regarding an unsolicited valid non-serious case received from a consumer/non-hcp. This case involves a 15 months and 14 days old female patient to whom once of their office has administered an expired dose of HIB (PRP/T) VACCINE [ACT-HIB] with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 08-Nov-2023, the patient once of their office has administered an expired dose of suspect HIB (PRP/T) VACCINE, Powder and solvent for solution for injection (lot UJ837AA; Expiry date: 30-Oct-2023) via intramuscular route in the Left anterior lateral thigh (left thigh) for Immunization with no reported adverse event (expired product administered) (latency: on same day). This dose was administered as a part of a 15-month wellness visit. Reporter stated that the Biohazard team did a pickup. Action taken : not applicable. 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 Directive and Regulatory Authority 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 2681119

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ837AA

gering
Staat
CA
Alter
0,2
Geschlecht
M
Eingang
12.09.2023
Impfdatum
29.08.2023
Beginn
29.08.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
OT / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Medication error No adverse event Product preparation error

Symptomtext

Sterile Water for Injection as the diluent of ACT-HIB instead of the 0.4% Sodium Chloride with no adverse event; Initial information received on 07-Sep-2023 regarding an unsolicited valid non-serious case received from other health professional. This case involves a 2-months-old male patient who had sterile water for injection as the diluent of HIB (PRP/T) vaccine [ACT-HIB] instead of the 0.4% sodium chloride with no adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. Concomitant medications included polio vaccine inact 3V (vero) (IPOL) for Immunisation. On 29-Aug-2023, the patient received 0.5 mL dose 1 of suspect HIB (PRP/T) vaccine, Powder and solvent for solution for injection (Strength: Standard; Frequency: Once) (batch number: UJ837AA; expiry date: unknown) via intramuscular route in the left vastus lateralis for Immunization with sterile water for injection as the diluent instead of the 0.4% sodium chloride with no adverse event (product preparation error) (same day latency). Action taken: not applicable. 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 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
Medication error
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
IPOL [POLIO VACCINE INACT 3V (VERO)]
Allergien
-
Vorherige Impfungen
-