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Reporte zur Charge UJ542AAA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

3Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
IN 2 PA 1

VAERS 2387798

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge UJ542AAA

gering
Staat
IN
Alter
59,0
Geschlecht
F
Eingang
24.07.2022
Impfdatum
18.07.2022
Beginn
18.07.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered No adverse event

Symptomtext

product was expired at the time of administration with no reported adverse event; Initial information received on 18-Jul-2022 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 59 years old female patient who was administered vaccine expired at the time of administration with no reported adverse event after receiving vaccine DIPHTHERIA/TETANUS/5 HYBRID AC PERTUSSIS/IPV(VERO)/HIB(PRP/T) VACCINE [PENTACEL (VERO)]. 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 Prophylactic vaccination; and HEPATITIS B VACCINE (HEPATITIS B VACCINE) for Prophylactic vaccination. On 18-Jul-2022, the patient received a dose of suspect DIPHTHERIA/TETANUS/5 HYBRID AC PERTUSSIS/IPV(VERO)/HIB(PRP/T) VACCINE( lot UJ542AAAand expiration date: 10-Jul-2022) at a dose of 0.5ml via unknown route in the left deltoid for immunization. On 18-Jul-2022 (latency: same day),the patient was administered vaccine expired at the time of administration with no reported adverse event (expired product administered). The patient needed the vaccine for a stem cell transplant. 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 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
Expired product administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2289161

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ542AAA

gering
Staat
IN
Alter
0,5
Geschlecht
M
Eingang
21.05.2022
Impfdatum
12.05.2022
Beginn
12.05.2022
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 No adverse event

Symptomtext

Medical Assistant mistakenly gave a patient an IPOL vaccination in addition to their PENTACEL vaccination on 12MAY2022, causing the patient to receive an extra dose of IPV with no other reported adverse event; Initial information received on 13-May-2022 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 6 months old male patient to whom it was reported that medical assistant mistakenly gave a patient an IPV (VERO) [IPOL] vaccination in addition to their diphtheria/tetanus/5 HYBRID AC pertussis/IPV(MRC5)/HIB(PRP/T) vaccine [Pentacel] vaccination on 12may2022, causing the patient to receive an extra dose of ipv with no other reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. Concomitant medications included HEPATITIS B VACCINE (HEPATITIS B VACCINE) for Prophylactic vaccination. On 12-May-2022, the patient received 0.5 ml dose of suspect IPV (VERO) (lot U1C571M; expiry date 17-Jun-2023) along with 0.5 ml dose of suspect DIPHTHERIA/TETANUS/5 HYBRID AC PERTUSSIS/IPV(MRC5)/HIB(PRP/T) VACCINE (lot UJ542AAA, expiry date; 10-Jul-2022) via intramuscular route in unknown administration site for Prophylactic vaccination it was reported medical assistant mistakenly gave a patient an ipol vaccination in addition to their pentacel vaccination on 12may2022, causing the patient to receive an extra dose of ipv with no other reported adverse event (extra dose 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 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 1653312

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ542AAA

gering
Staat
PA
Alter
-
Geschlecht
F
Eingang
29.08.2021
Impfdatum
-
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
No adverse event Occupational exposure to product Product physical issue

Symptomtext

2 Pentacel vaccines that were broken and nurse was trying to draw out the vaccine for a patient and realized her hand was wet /No AE; Two Pentacel vaccines were broken and other vial had a crack in it as well/ No AE; Initial information was received on 02-Aug-2021 regarding an unsolicited valid non-serious case received from an other health care professional via phone (under Global Information Number Inquiry Number: 00706640). This case involves an unknown age female patient (nurse). This case involves two DIPHTHERIA/TETANUS/5 HYBRID AC PERTUSSIS/IPV(MRC5)/HIB(PRP/T) VACCINE [PENTACEL] which was broken and nurse was trying to draw out the vaccine for a patient and realized her hand was wet and other vial had a crack in it as well (occupational exposure to product and product physical issue) lot number: UJ542AAA and expiry date: 10-JUL-2022, indication: prophylactic vaccination. The patient's medical history, past medical treatments, concomitant medications vaccinations and family history were not provided. It was a case of occupational exposure via skin contact with product and cracked product (latency: same day). It was reported "Caller stated receiving two PENTACEL vaccines that were broken. Caller stated a nurse was trying to draw out the vaccine for a patient and realized her hand was wet. Caller stated the nurse noticed the bottom of the bottle was in the box and not attached to the vial. Caller stated the other vial had a crack in it as well. Caller reported she receives her shipments via FEDEX. Caller was requesting for a replacement of two PENTACEL vaccines. Resent due to possible Adverse Event (AE) vaccine got on a hand. Product used: Not Used, Still using product: No. Was Device Used: No, Product Technique Complain assessment medical/ Physical: Physical." 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 holders 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
-