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Reporte zur Charge UJ404AA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

6Reporte angezeigt
0Todesfaelle
1Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
OH 1 AL 1 CA 1 NC 1 NY 1 PA 1

VAERS 1515534

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ404AA

schwer
Staat
OH
Alter
1,3
Geschlecht
F
Eingang
30.07.2021
Impfdatum
19.07.2021
Beginn
19.07.2021
Tage bis Beginn
0,0
Dosis
4
Route/Site
IM / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: ja
Athetosis Body temperature increased C-reactive protein Computerised tomogram head Electroencephalogram Eye movement disorder Foaming at mouth Full blood count Hyporesponsive to stimuli Metabolic function test Postictal paralysis Red blood cell sedimentation rate Seizure Vomiting

Symptomtext

7/29/21 Pt with 100F temporal temp at home post vaccines. Episode of emesis at 1800 after waking from nap. Less responsive and at 1830 started foaming at the mouth and looking up with writhing arm movements. Arrived at urgent care by car at 1850 still seizing. EMS arrived- placed on blowby, 2 mg versed given to abort seizure. Transported to ED and temp of 104.7F on arrival. +Todd's paralysis. Given fluids, tylenol and admitted for obs. Discharge 7/20/21.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Postictal paralysis
Hospital-Tage
2,0
Labordaten
CBC, Chem 7, ESR/CRP, CT head, EEG
Aktuelle Erkrankungen
not known
Vorgeschichte
none
Andere Medikamente
none
Allergien
nkda
Vorherige Impfungen
-

VAERS 1214790

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ404AA

schwer
Staat
AL
Alter
1,6
Geschlecht
F
Eingang
15.04.2021
Impfdatum
29.03.2021
Beginn
14.04.2021
Tage bis Beginn
16,0
Dosis
4
Route/Site
IM / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Febrile convulsion Pyrexia

Symptomtext

Fever to 102 x3 days starting on day 14 after vaccines; febrile seizure on day 16 after vaccines

Weitere VAERSDATA-Felder
Praegender Schweregrund
Febrile convulsion
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None
Vorgeschichte
Speech delay, possible thyroglossal duct cyst
Andere Medikamente
None
Allergien
Perfume
Vorherige Impfungen
-

VAERS 1354674

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ404AA

mild
Staat
CA
Alter
0,2
Geschlecht
F
Eingang
27.05.2021
Impfdatum
12.04.2021
Beginn
12.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Administration site indentation Injection site erythema Injection site nodule Injection site swelling

Symptomtext

Mom called on May 4th and states marble size lump right thigh. If she touches it; it will get red. Has dimple in the center now. Was really swollen the first day of injection.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site erythema
Hospital-Tage
-
Labordaten
NO
Aktuelle Erkrankungen
NO
Vorgeschichte
NO
Andere Medikamente
NO
Allergien
NO
Vorherige Impfungen
-

VAERS 2006057

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ404AA

gering
Staat
NC
Alter
5,0
Geschlecht
F
Eingang
05.01.2022
Impfdatum
25.10.2021
Beginn
01.10.2021
Tage bis Beginn
-
Dosis
UNK
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered No adverse event

Symptomtext

vaccine given on 10/25/2021, vaccine expiration on 10/1/2021. Patient has experienced no adverse reactions.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
n/a
Aktuelle Erkrankungen
n/a
Vorgeschichte
n/a
Andere Medikamente
n/a
Allergien
penicillin's
Vorherige Impfungen
-

VAERS 1794434

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ404AA

gering
Staat
NY
Alter
-
Geschlecht
F
Eingang
18.10.2021
Impfdatum
-
Beginn
12.10.2021
Tage bis Beginn
-
Dosis
UNK
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered No adverse event

Symptomtext

accidentally received an ACTHIB vaccine that expired on 04OCT2021 with no reported adverse event; Initial information received on 12-Oct-2021 regarding an unsolicited valid non-serious case received from a other health professional and consumer non health care professional via Medical Information (MI) number: 00809297. This case involves a one years old female patient who was administered an expired dose of HAEMOPHILUS TYPE B (HIB) VACCINE [ACT-HIB] (Expired product administered). The patient's medical history, medical treatments, vaccinations, and family history were not provided. Concomitant medications included MEASLES VACCINE, MUMPS VACCINE, RUBELLA VACCINE for Immunisation. On an unknown date, the patient received a 0.5 ml dose of suspect HIB (PRP/T) VACCINE lot number: UJ404AA and expiry date: 04-OCT-2021 via intramuscular route in unknown administration site for prophylactic vaccination. At the time of reporting, no adverse event was reported. 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
MMR
Allergien
-
Vorherige Impfungen
-

VAERS 1512077

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ404AA

gering
Staat
PA
Alter
11,0
Geschlecht
M
Eingang
29.07.2021
Impfdatum
20.07.2021
Beginn
-
Tage bis Beginn
-
Dosis
2
Route/Site
OT / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
No adverse event Product administered to patient of inappropriate age

Symptomtext

ACTHIB was administered to an 11 year old patient/ no AE; Initial information was received on 21-Jul-2021 regarding an unsolicited valid non-serious case received from an Other healthcare professional via Regulatory authority (Reference number- 00691458) and transmitted to Sanofi on 21-Jul-2021. This case involves a 11-year-old male patient reported that HIB (PRP/T) VACCINE [ACT-HIB] was administered to an 11-year-old patient with no adverse event (product administered to patient of inappropriate age). Medical history, medical treatment(s), vaccination(s), concomitant medications and family history were not provided. On 20-Jul-2021, the patient received 0.5 ml (total) second dose of suspect HIB (PRP/T) VACCINE [lot UJ404AA and expiry date 04-Oct-2021] via intramuscular route in right deltoid for prophylactic vaccination. It was reported that, "1st one was in 2010. Product used: Used. First time product used: No". It was a case of actual medication error due to inappropriate age at vaccine administration (latency was on same day). At the time of reporting, patient had no adverse 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 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
No adverse event
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-