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Reporte zur Charge U6521AA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

6Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
NM 1 TX 1 NH 1 MS 1 MA 1 IL 1

VAERS 1653329

SANOFI PASTEUR · MENINGOCOCCAL CONJUGATE (MENACTRA) · Charge U6521AA

gering
Staat
NM
Alter
11,0
Geschlecht
F
Eingang
29.08.2021
Impfdatum
29.07.2021
Beginn
29.07.2021
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered No adverse event

Symptomtext

A patient received an expired vaccine, no AE; Initial information regarding an unsolicited valid non-serious case was received from consumer/non-healthcare professional via Global Medical Information (GMI) (Reference number- 00710335) and transmitted to Sanofi on 04-Aug-2021. This case involves a 11-year-old female patient received an expired MENINGOCOCCAL A-C-Y-W135 (D CONJ) VACCINE [MENACTRA] (expired product administered). The patient's medical history, past medical treatment(s), vaccination(s) and family history were not provided. Concomitant medications included DIPHTHERIA VACCINE TOXOID, PERTUSSIS VACCINE ACELLULAR, TETANUS VACCINE TOXOID (TDAP) and HPV VACCINE for prophylactic vaccination. On 29-Jul-2021, the patient received a dose of expired suspect MENINGOCOCCAL A-C-Y-W135 (D CONJ) VACCINE (lot U6521AA and expiry date: 26-Jan-2021) via an unknown route in the right deltoid for prophylactic vaccination (expired product administered). It was reported that "It was realized afterwards that the Menactra dose had expired on 26-Jan-2021. The pharmacist had incorrectly entered the expiry in the facility's electronic system as 21-Jan-2026, and that is why their system did not alert that the product should not have been used. The nurse stated that despite the pharmacist's error, the nurse who administered Menactra should have checked the label at the time, but that was not done and therefore the fact that the product was expired was overlooked prior to administration." This was a case of actual medication error due to Expired vaccine used (latency same day). At time of reporting, no adverse events were reported. 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 by the regulatory authority. 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
TDAP; HPV VACCINE
Allergien
-
Vorherige Impfungen
-

VAERS 1113970

SANOFI PASTEUR · MENINGOCOCCAL CONJUGATE (MENACTRA) · Charge U6521AA

gering
Staat
TX
Alter
11,0
Geschlecht
M
Eingang
19.03.2021
Impfdatum
17.02.2021
Beginn
17.02.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
OT / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered

Symptomtext

The patient was inadvertently administered an expired dose of vaccine, no AE; Initial information regarding an unsolicited valid non-serious case was received from a Nurse via Global Medical Information (GMI) (Reference number- 00509255) and transmitted to Sanofi on 08-Mar-2021. This case involves an 11 year old male patient who was inadvertently administered a 0.5 ml first dose of suspect MENINGOCOCCAL A-C-Y-W135 (D CONJ) VACCINE [MENACTRA] (lot U6521AA, expiry date: 26-Jan-2021) via unknown route in the right deltoid on 17-Feb-2021 for prophylactic vaccination (Expired product administered) Medical history, medical treatment(s), vaccination(s) and family history were not provided. The patient received no concomitant vaccines. It was a case of an actual medication error due to Expired vaccine used (latency same day). The reporter had a question on the expiration date for Menactra as it was given to a patient past the expiration date At the time of report, 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 holder's 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
Expired product administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1107271

SANOFI PASTEUR · MENINGOCOCCAL CONJUGATE (MENACTRA) · Charge U6521AA

gering
Staat
NH
Alter
38,0
Geschlecht
F
Eingang
17.03.2021
Impfdatum
03.03.2021
Beginn
03.03.2021
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered No adverse event

Symptomtext

the patient received an expired dose of Menactra/no AE; Initial information regarding an unsolicited valid non-serious case was received on 04-Mar-2021, from Physician and Other Health Care Professional via Global Medical Information (GMI) (Reference number- 00503940) and transmitted to Sanofi on 04-Mar-2021. This case involves a 38 year-old female patient who was inadvertently vaccinated with 0.5 mL expired dose of MENINGOCOCCAL A-C-Y-W135 (D CONJ) VACCINE [MENACTRA] (batch number U6521AA and expiry date 26-Jan-2021) via an intramuscular route at the right deltoid for prophylactic vaccination (Expired product administered). The patient's medical history, past medical treatment(s), vaccination(s) and family history were not provided. Concomitant medications included MENINGOCOCCAL VACCINE B RFHBP/NADA/NHBA OMV (BEXSERO) at left deltoid for prophylactic vaccination. Reporter asked if it would still be effective or if the patient needed to be revaccinated. It was reported that practice would plan to re-schedule the patient to administer an unexpired dose of Menactra. Product used : Used Still using product : No It was a case of actual medication error due to expired vaccine used (latency was on same day). At the time of report, no adverse event reported. 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 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
BEXSERO
Allergien
-
Vorherige Impfungen
-

VAERS 1030230

SANOFI PASTEUR · MENINGOCOCCAL CONJUGATE (MENACTRA) · Charge U6521AA

gering
Staat
MS
Alter
12,0
Geschlecht
M
Eingang
15.02.2021
Impfdatum
01.02.2021
Beginn
01.02.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
OT / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered No adverse event

Symptomtext

12 year old male patient administered expired dose of Menactra, no AE; Initial information received on 02-Feb-2021 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 12 year old male patient who was vaccinated with expired dose of MENINGOCOCCAL A-C-Y-W135 (D CONJ) VACCINE [MENACTRA] (expired product administered). Medical history, medical treatment, vaccination and family history were not provided. Concomitant medications included DIPHTHERIA VACCINE TOXOID, PERTUSSIS VACCINE ACELLULAR, TETANUS VACCINE TOXOID (TDAP) for Immunisation. On 01-Feb-2021, the patient received a 0.5 ml first dose of suspect MENINGOCOCCAL A-C-Y-W135 (D CONJ) VACCINE (lot U6521AA and expiry date: 26-Jan-2021) (frequency once) via an intramuscular route in the left deltoid for prophylactic vaccination. It was a case of actual medication error due to expired product administered (latency on same day). It was also reported that patient was administered Menactra that was expired for 3 days. Reporter relationship: Self Product used: Used, first time product used: yes Still using product: no At the time of reporting, patient had no 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 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
TDAP
Allergien
-
Vorherige Impfungen
-

VAERS 1022318

SANOFI PASTEUR · MENINGOCOCCAL CONJUGATE (MENACTRA) · Charge U6521AA

gering
Staat
MA
Alter
45,0
Geschlecht
F
Eingang
11.02.2021
Impfdatum
08.02.2021
Beginn
08.02.2021
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered No adverse event

Symptomtext

Patient given expired vaccine on 2/8/21 vaccine expired on 1/26/21. Patient reports no adverse event or outcome.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Splenectomy
Andere Medikamente
-
Allergien
Pneumococcal vaccine
Vorherige Impfungen
-

VAERS 1011559

SANOFI PASTEUR · MENINGOCOCCAL CONJUGATE (MENACTRA) · Charge U6521AA

gering
Staat
IL
Alter
-
Geschlecht
U
Eingang
08.02.2021
Impfdatum
01.02.2021
Beginn
01.02.2021
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

patient was received expired dose of MENACTRA, no AE; Initial information received on 01-Feb-2021 regarding an unsolicited valid non-serious case received from a pharmacist. This case involves patient (unknown demographics) who was vaccinated with an expired dose of MENINGOCOCCAL A-C-Y-W135 (D CONJ) VACCINE [MENACTRA] (expired product administered). Medical history, medical treatment, concomitant medication, vaccination and family history were not provided. Patient did not received other vaccines. On 01-Feb-2021, the patient received a 0.5 ml dose of suspect MENINGOCOCCAL A-C-Y-W135 (D CONJ) VACCINE (lot U6521AA and expiry date: 26-Jan-2021) via an intramuscular route at an unknown administration site for prophylactic vaccination. It was a case of actual medication error due to expired vaccine used (latency on same day). At the time of report, 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 holder's 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
Expired product administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-