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Reporte zur Charge UJ649AA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

3Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
MO 1 LA 1 UT 1

VAERS 2541936

SANOFI PASTEUR · HIB (ACTHIB) · Charge uj649aa

gering
Staat
MO
Alter
0,4
Geschlecht
M
Eingang
23.12.2022
Impfdatum
16.12.2022
Beginn
16.12.2022
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Aspartate aminotransferase increased Blood potassium normal Cyanosis Differential white blood cell count Electroencephalogram Full blood count Haemoglobin decreased Hyporesponsive to stimuli Hypotonia Irritability Metabolic function test Pallor Platelet count increased Respiratory rate decreased

Symptomtext

Pt became slightly fussy after vaccines but about 4 hours later had an episode where mom feels that he was fairly limp in the limbs with eyes open but less responsive and decreased respirations. He became more pale and some bluing of the lips. No shaking or tremors or lip smacking or eye movements. Episode lasted about 10 minutes and then he slowly improved over the following 20 min. He was taken to the ED where he was back to his normal self and took bottle. He was admitted overnight to the hospital and had normal asleep and awake EEG. He also had blood work drawn in the ED.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Aspartate aminotransferase increased
Hospital-Tage
-
Labordaten
normal EEG, Hemoglobin 10.3, platelets 518,000, potassium 4.4, AST 48 otherwise CBC w/diff was normal and remainder of CMP was normal
Aktuelle Erkrankungen
none
Vorgeschichte
none
Andere Medikamente
famotadine
Allergien
none
Vorherige Impfungen
-

VAERS 2520002

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ649AA

gering
Staat
LA
Alter
1,0
Geschlecht
M
Eingang
30.11.2022
Impfdatum
26.11.2022
Beginn
26.11.2022
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Extra dose administered No adverse event

Symptomtext

Pt received Vaxelis and Hib vaccine on same day, No treatment, no adverse reactions noted.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Extra dose administered
Hospital-Tage
-
Labordaten
None.
Aktuelle Erkrankungen
none- well child
Vorgeschichte
None
Andere Medikamente
-
Allergien
NKA
Vorherige Impfungen
-

VAERS 2387800

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ649AA

gering
Staat
UT
Alter
1,2
Geschlecht
F
Eingang
24.07.2022
Impfdatum
19.07.2022
Beginn
19.07.2022
Tage bis Beginn
0,0
Dosis
4
Route/Site
OT / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Extra dose administered Medication error No adverse event

Symptomtext

patient was given ACTHIB and PENTACEL on the same day medication error due to patient receiving an extra dose of HIB vaccine with no reported adverse event; Initial information received on 19-Jul-2022 regarding an unsolicited valid non-serious case received from a other health professional. This case is linked to case 2022SA295304(CLUSTER) for same patient. This case involves a 14 months old female patient who was given HIB (PRP/T) VACCINE [ACT-HIB] and Pentacel on the same day medication error due to patient receiving an extra dose of HIB vaccine 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 MEASLES VACCINE, MUMPS VACCINE, RUBELLA VACCINE (MMR), VARICELLA ZOSTER VACCINE (VARICELLA VACCINE) and HEPATITIS A VACCINE (HEPATITIS A) for Prophylactic vaccination. On 19-Jul-2022, the patient received 0.5 ml (dose 4) of suspect HIB (PRP/T) VACCINE, powder and solvent for solution for injection (lot UJ649AA; strength and expiry date not provided) via intramuscular route in the right thigh for prophylactic vaccination On 19-JUL-2022 on same day it was reported that patient was given acthib and pentacel on the same day medication error due to patient receiving an extra dose of hib vaccine with no reported adverse event (extra dose administered). Reporter asked if there were any concerns about the patient receiving two doses of HIB in the 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
Extra dose administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
MMR; VARICELLA VACCINE; HEPATITIS A
Allergien
-
Vorherige Impfungen
-