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Reporte zur Charge U7788AA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

2Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
OH 1

VAERS 2715775

MSP VACCINE COMPANY · DTAP+IPV+HIB+HEPB (VAXELIS) · Charge U7788AA

moderat
Staat
-
Alter
0,5
Geschlecht
M
Eingang
20.11.2023
Impfdatum
08.11.2023
Beginn
15.11.2023
Tage bis Beginn
7,0
Dosis
2
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: unbekannt
Condition aggravated Dyskinesia Infantile spasms Laboratory test

Symptomtext

Patient previously healthy , started having episodes of abnormal movements later recognized as infantile spasms, that mom identifies they started after receiving Vaxelis vaccine at 2-month-old. Mother noticed that after his 2nd and 3rd dose of Vaxelis, the number of episodes intensified after the vaccination of this combination vaccine. The infantile spasms were witnessed by a nurse 1 week after receiving his 3rd dose of Vaxelis (dose given 11/08/2023), and there was an immediate workup and admission for diagnosis and treatment for this condition. Note that baby only received 1 type of vaccine per week per mother's preference, so she was able to identify the frequency of episodes was different when other vaccines were given.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Condition aggravated
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Epilepsy Spasm Not Intractable Without Status Epilepticus
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2727925

MSP VACCINE COMPANY · DTAP+IPV+HIB+HEPB (VAXELIS) · Charge U7788AA

mild
Staat
OH
Alter
-
Geschlecht
M
Eingang
28.12.2023
Impfdatum
16.08.2023
Beginn
-
Tage bis Beginn
-
Dosis
2
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Injection site nodule

Symptomtext

Pharmacy administrator called in to inform that they have 3 patients that was administered with VAXELIS and that they observed nodules at the injection site of these three patients.; This spontaneous safety report, with reference number 2023SA382063 (Inquiry number 01870351), was received by the partner on 07-DEC-2023 and forwarded to Agency on 08-DEC-2023, from a health professional. The reporter assessed the causality between the event "Pharmacy administrator called in to inform that they have 3 patients that was administered with VAXELIS and that they observed nodules at the injection site of these three patients." and Vaxelis as related. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site nodule
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
Prophylaxis
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-