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Reporte zur Charge UJ583AB

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

9Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
NH 2 IL 2 NY 1 PR 1 PA 1 TX 1 MI 1

VAERS 2113131

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ583AB

mild
Staat
NY
Alter
0,8
Geschlecht
M
Eingang
15.02.2022
Impfdatum
18.01.2022
Beginn
18.01.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Fatigue Hypotonia Neurological examination Petit mal epilepsy

Symptomtext

Immediately following the vaccines pt. became very hypotonic and acted as he had an absence seizure. Vitals obtained and all normal. After a couple of minutes he did start to interact with his mom. MD called into the room. Physical exam completed with all normal neurological assessments. He did continueto act "very tired". He raimed in the office for 40 minutes after the episode. He was then cleared to go home by the MD.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Fatigue
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
mild cold symptoms
Vorgeschichte
none
Andere Medikamente
Vitamin d
Allergien
none
Vorherige Impfungen
-

VAERS 2085152

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ583AB

mild
Staat
PR
Alter
2,0
Geschlecht
F
Eingang
03.02.2022
Impfdatum
25.01.2022
Beginn
26.01.2022
Tage bis Beginn
1,0
Dosis
4
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja
Injection site erythema Injection site rash Injection site swelling

Symptomtext

Right arm deltoid area red, swelling and skin rashes.

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

VAERS 2495928

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ583AB

gering
Staat
PA
Alter
0,6
Geschlecht
F
Eingang
02.11.2022
Impfdatum
21.10.2022
Beginn
21.10.2022
Tage bis Beginn
0,0
Dosis
3
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

received an expired dose of ACT-HIB with no reported adverse event; Initial information received on 21-Oct-2022 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 7 months old female patient who received an expired dose of (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. Concomitant medications included PNEUMOCOCCAL VACCINE CONJ 7V (CRM197) (PREVNAR) for Immunisation. On 21-Oct-2022, the patient received expired 0.5 ml, third dose of suspect HIB (PRP/T) VACCINE with unknown formulation (lot UJ583AB, expiry date:15-Oct-2022) via intramuscular route in the left thigh for Immunization with no reported adverse event (expired product administered) (latency: same day). 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
Expired product administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
PREVNAR
Allergien
-
Vorherige Impfungen
-

VAERS 2493211

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ583AB

gering
Staat
TX
Alter
1,0
Geschlecht
F
Eingang
29.10.2022
Impfdatum
17.10.2022
Beginn
17.10.2022
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 Medication error No adverse event

Symptomtext

expired dose of acthib was administered with no reported adverse event; Initial information received on 17-Oct-2022 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 1 years old female patient to whom experienced expired dose of acthib was administered 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 LIVE (ENDERS-EDMONSTON), MUMPS VACCINE LIVE (JERYL LYNN), RUBELLA VACCINE LIVE (WISTAR RA 27/3), VARICELLA ZOSTER VACCINE LIVE (OKA/MERCK) (PROQUAD) for Immunisation; HEPATITIS A VACCINE (HEPATITIS A) for Immunisation; and VARICELLA ZOSTER VACCINE (VARICELLA VACCINE) for Immunisation. On 17-Oct-2022, the patient received 0.5 ml of suspect HIB (PRP/T) VACCINE (lot UJ583AB and expiry-15-10-22) (strength and formulation: unknown) via intramuscular route in the left thigh for immunization. On 17-OCT-2022 the patient developed a non-serious expired dose of acthib was administered with no reported adverse event (expired product administered) (latency same day). Action taken with HAEMOPHILUS TYPE B (HIB) VACCINE (ACT-HIB) was not applicable. At time of reporting, the outcome was Unknown for the event expired dose of acthib was administered with no reported 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 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
PROQUAD; HEPATITIS A; VARICELLA VACCINE
Allergien
-
Vorherige Impfungen
-

VAERS 2455745

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ583AB

gering
Staat
IL
Alter
0,2
Geschlecht
M
Eingang
23.09.2022
Impfdatum
15.09.2022
Beginn
15.09.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Extra dose administered Medication error No adverse event

Symptomtext

medication error due to the extra dose of acthib given since it was concomitantly administered with pentacel with no reported adverse event; Initial information received on 15-Sep-2022 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 2 months old male patient who experienced medication error due to the extra dose of acthib given since it was concomitantly administered with pentacel with no reported adverse event while receiving vaccine HIB (PRP/T) VACCINE [ACT-HIB]. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. Concomitant medications included DIPHTHERIA VACCINE TOXOID, HIB VACCINE CONJ (TET TOX), PERTUSSIS VACCINE ACELLULAR 5-COMPONENT, POLIO VACCINE INACT 3V (MRC 5), TETANUS VACCINE TOXOID (PENTACEL); PNEUMOCOCCAL VACCINE CONJ 13V (CRM197) (PREVNAR 13); and ROTAVIRUS VACCINE LIVE REASSORT ORAL 5V (ROTATEQ). On 15-Sep-2022, the patient received a 0.5 ml dose of suspect HIB (PRP/T) VACCINE once ( lot UJ583AB; expiry date: 15-Oct-2022) via unknown route in unknown administration site for immunization. On 15-SEP-2022 the patient reported a non-serious event medication error due to the extra dose of acthib given since it was concomitantly administered with pentacel with no reported adverse event (extra dose administered) following the administration of HIB (PRP/T) VACCINE. Action taken: not applicable. At time of reporting, the outcome was Unknown for the event extra dose administered. 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 guidelines. 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
-
Allergien
-
Vorherige Impfungen
-

VAERS 2447706

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ583AB

gering
Staat
IL
Alter
0,2
Geschlecht
M
Eingang
16.09.2022
Impfdatum
15.09.2022
Beginn
15.09.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Extra dose administered No adverse event Vaccination error

Symptomtext

Vaccine Error- patient received a duplicate dose of HIB. Manufacture contacted, adverse effects and management relayed to parents by provider. Patient doing well with no concerning symptoms.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Extra dose administered
Hospital-Tage
-
Labordaten
NONE
Aktuelle Erkrankungen
NONE
Vorgeschichte
NONE
Andere Medikamente
NONE
Allergien
NONE
Vorherige Impfungen
-

VAERS 2275692

MERCK & CO. INC. · HIB (PEDVAXHIB) · Charge UJ583AB

gering
Staat
MI
Alter
1,0
Geschlecht
M
Eingang
13.05.2022
Impfdatum
11.05.2022
Beginn
11.05.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Extra dose administered

Symptomtext

Parents were notified by physician

Weitere VAERSDATA-Felder
Praegender Schweregrund
Extra dose administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2112760

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ583AB

gering
Staat
NH
Alter
1,0
Geschlecht
M
Eingang
15.02.2022
Impfdatum
03.02.2022
Beginn
03.02.2022
Tage bis Beginn
0,0
Dosis
4
Route/Site
IM / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Extra dose administered Wrong product administered

Symptomtext

Gave this patient MMR-V (Proquad) in error, instead of giving M-M-R. Also gave varicella. This resulted in a double dose of varicella.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Extra dose administered
Hospital-Tage
-
Labordaten
N/A
Aktuelle Erkrankungen
N/A
Vorgeschichte
N/A
Andere Medikamente
N/A
Allergien
N/A
Vorherige Impfungen
-

VAERS 2039146

SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ583AB

gering
Staat
NH
Alter
1,1
Geschlecht
M
Eingang
13.01.2022
Impfdatum
05.01.2022
Beginn
05.01.2022
Tage bis Beginn
0,0
Dosis
4
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
No adverse event

Symptomtext

No adverse reaction reported

Weitere VAERSDATA-Felder
Praegender Schweregrund
No adverse event
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
Cold symptoms
Vorgeschichte
None
Andere Medikamente
none
Allergien
No know Allergies
Vorherige Impfungen
-