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Reporte zur Charge UJ844AA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

6Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
AZ 2 NM 2 CA 1 WA 1

VAERS 2718455

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ844AA

mild
Staat
AZ
Alter
1,7
Geschlecht
M
Eingang
28.11.2023
Impfdatum
27.11.2023
Beginn
27.11.2023
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja
Cough Eye swelling Rash

Symptomtext

*note on PCV 15, pt had received 2 doses of Prevnar 13 in the past, this was the first time receiving prevnar 15. While driving home from doctor's office, mom noticed that pt was coughing and started to develop swelling around his eyes and began to develop a rash. Mom took pt to local ER where they administered benadryl and epinephrine. Pt's status improved and was discharged home with refills of benadryl and epi pen jr sent into pt's pharmacy. Pt doing well today. Seeing provider later this afternoon.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Rash
Hospital-Tage
-
Labordaten
n/a- referring to pediatric allergy
Aktuelle Erkrankungen
10/18/23- RSV+ with cough and Right otitis media. Prescribed: prednisolone 15mg/5ml 3ml PO qD x5 days Albuterol sulfate 1.25mg/3ml solution via nebulizer q4-6hrs as needed for wheeze Augmentin 400-57 mg/5ml suspension 2.75ml q12hrs
Vorgeschichte
n/a
Andere Medikamente
n/a
Allergien
NKDA
Vorherige Impfungen
-

VAERS 2692790

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ844AA

mild
Staat
CA
Alter
1,5
Geschlecht
M
Eingang
09.10.2023
Impfdatum
06.10.2023
Beginn
06.10.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Injection site discolouration Injection site erythema Injection site swelling

Symptomtext

10/07/23: Mother reports patient noted with redness on left thigh after vaccines. Patient received Pentacel yesterday, site noted with redness and swelling, no difficulty breathing, warmth, hives or severe swelling noted. Patient able to bear weight on left lower extremity. Explained to parent common vaccine SE usually lasting from 24-72 hrs, advised to apply cold compress, may give Ibuprofen if necessary and scheduled appointment on Monday 10/09/23. 10/09/23: Per provider's note, redness around site has increased and has some bluish discoloration noted to left thigh, able to ambulate. Return to clinic in 2 days, appointment scheduled on 10/11/23 for f/u.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site discolouration
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
10/07/23: Ibuprofen 10/09/23: Benadryl
Allergien
NKA
Vorherige Impfungen
-

VAERS 2721061

SANOFI PASTEUR · HIB (ACTHIB) · Charge uj844aa

gering
Staat
NM
Alter
0,3
Geschlecht
M
Eingang
05.12.2023
Impfdatum
04.12.2023
Beginn
04.12.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Product preparation error

Symptomtext

Patient was only given the diluent and it was not mixed with the powder.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Product preparation error
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2714004

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ844AA

gering
Staat
NM
Alter
5,0
Geschlecht
F
Eingang
14.11.2023
Impfdatum
27.10.2023
Beginn
27.10.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
No adverse event Product administered to patient of inappropriate age

Symptomtext

Extraneous IPV vaccine and out of range recommended age range with Pentacel (DtaP+Hib+IPV). Mother notified, no adverse effect/reaction reported.

Weitere VAERSDATA-Felder
Praegender Schweregrund
No adverse event
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None
Allergien
NKA
Vorherige Impfungen
-

VAERS 2713255

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ844AA

gering
Staat
WA
Alter
0,4
Geschlecht
M
Eingang
13.11.2023
Impfdatum
10.11.2023
Beginn
10.11.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Single component of a two-component product administered

Symptomtext

Only the liquid form was administered, I didn't realized there was also a powder form.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Single component of a two-component product administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2676334

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge UJ844AA

gering
Staat
AZ
Alter
5,0
Geschlecht
F
Eingang
24.08.2023
Impfdatum
05.08.2023
Beginn
05.08.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
OT / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
No adverse event Wrong product administered

Symptomtext

given a patient PENTACEL instead of PEDIARIX with no reported adverse event; Initial information received on 18-Aug-2023 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 5 years old female patient who was given diphtheria/tetanus/5 hybrid AC pertussis/IPV(vero)/hib(PRP/T) vaccine [Pentacel (Vero)] instead of pediarix 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) and HEPATITIS A VACCINE (HEPATITIS A) for Prophylactic vaccination. On 05-Aug-2023, the patient received a dose 1 Primary dose 0.5 ml of suspect Suspension for injection of diphtheria/tetanus/5 hybrid AC pertussis/IPV(vero)/hib(PRP/T) vaccine instead of pediarix (wrong product administered) (Latency: same day) (Batch number: UJ844AA, expiry date: 02-Mar-2024, strength: standard, Frequency: Once) via intramuscular route in the left arm as immunization. First time product used : Yes Still using product : No Action taken was 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
No adverse event
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
MMR; HEPATITIS A
Allergien
-
Vorherige Impfungen
-