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Reporte zur Charge UJ521AAA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

4Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
PA 1 CA 1 OH 1 WA 1

VAERS 1689677

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ521AAA

kritisch
Staat
PA
Alter
0,2
Geschlecht
F
Eingang
10.09.2021
Impfdatum
10.09.2021
Beginn
10.09.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Cardio-respiratory arrest Dyspnoea Oxygen saturation decreased

Symptomtext

1:55pm, Shortness of Breath, O2 desaturated to 89%. Code called. Epinephrine 1.5mg x 2 (1:58pm, and 2:15pm). HR 110s-200s. 0xygen 1 Liter via Ambu bag with infant mask. O2 100% HR 125. EMT arrived 2:20pm. taken to hospital ED.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Cardio-respiratory arrest
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
hemangioma
Vorgeschichte
-
Andere Medikamente
n/a, unknown.
Allergien
No known allegy
Vorherige Impfungen
-

VAERS 2440302

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ521AAA

gering
Staat
CA
Alter
0,5
Geschlecht
F
Eingang
12.09.2022
Impfdatum
31.08.2022
Beginn
31.08.2022
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

Symptomtext

an expired ACTHIB was given to patient with no reported adverse event; Initial information received from on 31-Aug-2022 regarding an unsolicited valid non-serious case received from a physician. This case involves a 6 months old female patient to whom an expired HIB (PRP/T) VACCINE [ACT-HIB] was given with no reported adverse event. Concomitant medications included DIPHTHERIA, TETANUS AND ACELLULAR PERTUSSIS VACCINE (DAPTACEL), PNEUMOCOCCAL VACCINE CONJ 7V (CRM197) (PREVNAR) ; POLIO VACCINE (POLIO) and ROTAVIRUS VACCINE (ROTAVIRUS VACCINE) all for Immunisation. On 31-Aug-2022, the patient received an expired dose 3 (0.5ml) of suspect HIB (PRP/T) VACCINE, powder and solvent for solution for injection, (Strength; Unknown) (lot UJ521AAA: expiry date 11-Jul-2022) via intramuscular route in the right thigh for immunization with no reported adverse event (expired product administered) (latency: same day). Reporter wants to know if they need to revaccinate and if there are adverse effects that they should look out for. 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 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
DAPTACEL; PREVNAR; POLIO; ROTAVIRUS VACCINE
Allergien
-
Vorherige Impfungen
-

VAERS 2404220

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ521AAA

gering
Staat
OH
Alter
0,6
Geschlecht
F
Eingang
08.08.2022
Impfdatum
29.07.2022
Beginn
29.07.2022
Tage bis Beginn
0,0
Dosis
2
Route/Site
OT / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered Medication error No adverse event

Symptomtext

ACT-HIB vaccine which had expired on 11-Jul-2022 was administered to a patient with no reported adverse event; Initial information received on 29-Jul-2022 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 7 months old female patient and it was reported that HIB (PRP/T) VACCINE [ACT-HIB] vaccine which had expired on 11-Jul-2022 was administered to a patient with no reported adverse event The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. Concomitant medications included DIPHTHERIA VACCINE TOXOID, PERTUSSIS VACCINE ACELLULAR 3-COMPONENT, TETANUS VACCINE TOXOID (INFANRIX). On 29-Jul-2022, the patient received a dose of 0.5 ml of suspect HIB (PRP/T) VACCINE, (frequency: once), with an unknown formulation and strength ( lot: UJ521AAA ; expiry date: 11-Jul-2022) (diluent lot: U6999AB ; expiry date: 11-Jul-2022) via intramuscular route in the left vastus lateralis for immunization. It was reported that an Act-hib vaccine which had expired on 11-Jul-2022 was administered to a patient with no reported adverse event (Expired product administered) (onset date: 29-Jul-2022; latency: same day) 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 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
INFANRIX
Allergien
-
Vorherige Impfungen
-

VAERS 1879711

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ521AAA

gering
Staat
WA
Alter
-
Geschlecht
U
Eingang
18.11.2021
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

no adverse event; This case was considered as non-case as temperature excursion reported without stability data.

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