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Reporte zur Charge UJ349AA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

3Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
TN 1 FL 1 AR 1

VAERS 2262150

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ349AA

gering
Staat
TN
Alter
3,0
Geschlecht
M
Eingang
03.05.2022
Impfdatum
31.03.2021
Beginn
31.03.2021
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Eye swelling Oedema peripheral Pharyngeal swelling Swelling face Swelling of eyelid

Symptomtext

AFTER VACCINES, PT AND MOTHER LEFT TO GO TO STORE. MOM CALLED AND REPORTED THAT PT HAD SUDDEN SWELLING OF BOTH EYES AND THROAT CLEARING APPROX. 20 MINS AFTER VACCINES ADMINISTERED. PARENT WAS ADVISED TO RETURN TO CLINIC. UPON EXAMINATION, PT WAS FOUND TO HAVE MODERATE EDEMA BIL. UPPER AND LOWER EYELIDS AND MILD FACIAL SWELLING. NO RESPIRATORY SYMPTOMS OR RASHES NOTED. BENADRYL AND PREDNISOLONE ADMINISTERED IMMEDIATLEY UPON PT'S RETURN AND PT OBSERVED IN OFFICE X 45 MINS. PT WAS SIGNIFICANTLY IMPROVED PRIOR TO D/C HOME. MOM WAS INSTRUCTED TO CONTINUE BENADRYL AND PRED. X 3 DAYS RTC

Weitere VAERSDATA-Felder
Praegender Schweregrund
Eye swelling
Hospital-Tage
-
Labordaten
ALLERGY PANEL FOR FOOD AND RESPIRATORY ORDERED, MOM NEVER COMPLETED LAB WORK.
Aktuelle Erkrankungen
COUGH DX ON 3/12/21 AND WAS INST TO TAKE OTC MUCINEX PRN
Vorgeschichte
NONE
Andere Medikamente
NONE
Allergien
NKA, NKDA
Vorherige Impfungen
-

VAERS 1678035

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge UJ349AA

gering
Staat
FL
Alter
-
Geschlecht
U
Eingang
07.09.2021
Impfdatum
29.07.2021
Beginn
29.07.2021
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered No adverse event

Symptomtext

expired PENTACEL vaccine was given with no reported adverse event; Initial information was received on 31-Aug-2021 regarding an unsolicited valid non-serious case from a nurse. This case involves an unknown age and gender patient who received expired DIPHTHERIA/TETANUS/5 HYBRID AC PERTUSSIS/IPV(VERO)/HIB(PRP/T) VACCINE [PENTACEL (VERO)] (expired product administered). The patient's medical history, past medical treatment(s), vaccination(s) and family history were not provided. On 29-Jul-2021, the patient received a dose of 0.5 ml suspect DIPHTHERIA/TETANUS/5 HYBRID AC PERTUSSIS/IPV(VERO)/HIB(PRP/T) VACCINE (lot number-UJ349AA, expiry date-22-Jun-2022) via an unknown route in unknown administration site for prophylactic vaccination (expired product administered). It was reported that, "Caller stated that a 2-month-old patient was given the Ipol and dtap portion of product and not the Acthib. Caller wanted to know if the ActHIB can be given separately. She also wanted to know if there was any concerns of not given the product with Act-Hib". It was a case of actual medication error due to expired vaccine used (latency-same day). 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
-
Allergien
-
Vorherige Impfungen
-

VAERS 1403717

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ349AA

gering
Staat
AR
Alter
16,0
Geschlecht
F
Eingang
16.06.2021
Impfdatum
15.06.2021
Beginn
15.06.2021
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Product administered to patient of inappropriate age Wrong product administered

Symptomtext

The patient presented to the clinic needing a Tdap vaccination. When the vaccination was taken out of the fridge, Pentacel was taken out and administered instead of regular Tdap. Staff with Department of Health was notified. She got back in contact with our office to let us know that the patient will not need to come back in for a regular tdap, as the pentacel covers as well as regular tdap. Actions to be taken are to report the incident to VAERS and to notify the patient's mother.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Product administered to patient of inappropriate age
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
none
Vorgeschichte
none
Andere Medikamente
Albuterol HFA, loratadine, mupirocin ointment, flonase, montelukast
Allergien
iodine
Vorherige Impfungen
-