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Reporte zur Charge UJ659AAA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

4Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
NJ 1 CA 1 NV 1

VAERS 2404412

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ659AAA

mild
Staat
NJ
Alter
0,5
Geschlecht
F
Eingang
08.08.2022
Impfdatum
25.07.2022
Beginn
25.07.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Swelling face Urticaria

Symptomtext

Approximately 15 minutes after receiving vaccine, Mom saw that her left foot looked swollen and that she had small pink hives on her left lower leg. Injection site on left thigh did not have hives around it. Benadryl administered orally and hives cleared up as did swelling. No cough, oral swelling or trouble breathing.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Urticaria
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None
Allergien
None known
Vorherige Impfungen
-

VAERS 2581582

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ659AAA

gering
Staat
-
Alter
2,0
Geschlecht
M
Eingang
14.02.2023
Impfdatum
14.02.2023
Beginn
14.02.2023
Tage bis Beginn
0,0
Dosis
4
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Expired product administered No adverse event Product administration error

Symptomtext

Patient was administered Pentacel with an expiration date of 1/31/2023. Provider was notified immediately. Mother was contacted and advised of the error. Not other issues or reactions took place. The patient was in good health when he left the office and no other issues were reported.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
none
Vorgeschichte
none
Andere Medikamente
Greer's Goo and nystatin cream
Allergien
none
Vorherige Impfungen
-

VAERS 2576100

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge UJ659AAA

gering
Staat
CA
Alter
0,5
Geschlecht
M
Eingang
06.02.2023
Impfdatum
01.02.2023
Beginn
01.02.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered

Symptomtext

6-month-old patient was given a PENTACEL vaccine today (01Feb2023) but the vaccine expired yesterday; Initial information received on 01-Feb-2023 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 6 month old male patient who had taken DIPHTHERIA/TETANUS/5 HYBRID AC PERTUSSIS/IPV(MRC5)/HIB(PRP/T) VACCINE [PENTACEL] on 01-feb-2023 but the vaccine expired yesterday. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. Concomitant medications included Rotavirus Vaccine Live Reassort Oral 5v (Rotateq); Hepatitis B Vaccine (Hepatitis B Vaccine) and (Pneumococcal Vaccines). On 01-Feb-2023, the patient received a dose 1 of 0.5 ml of suspect DIPHTHERIA/TETANUS/5 HYBRID AC PERTUSSIS/IPV(MRC5)/HIB(PRP/T) VACCINE for Suspension for injection (Frequency: Once, lot: UJ659AAA, expiry date: 31-Jan-2023) via unknown route in unknown administration site for immunization. On 01-Feb-2023, (latency: same day) the patient was given a pentacel vaccine today but the vaccine expired yesterday (expired product administered). No lab data available. Action taken: not applicable. It was not reported if the patient received a corrective treatment for the event. 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
ROTATEQ; HEPATITIS B VACCINE; PNEUMOCOCCAL VACCINES
Allergien
-
Vorherige Impfungen
-

VAERS 2511950

GLAXOSMITHKLINE BIOLOGICALS · DTAP + HEPB + IPV (PEDIARIX) · Charge UJ659AAA

gering
Staat
NV
Alter
0,2
Geschlecht
F
Eingang
18.11.2022
Impfdatum
17.11.2022
Beginn
17.11.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Product administered to patient of inappropriate age Wrong product administered

Symptomtext

Patient in for her 2 month vaccines. Brother and sister were in for the flu vaccine and inadvertently given to the 2 month old. Mom was notified right away called manufacturer for any adverse side effects to watch out for. Mom said patient will be ok. Called today to check on patient. Mom stated doing well.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Product administered to patient of inappropriate age
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-