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Reporte zur Charge U6576AA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

4Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
ME 1 TX 1 FL 1 CA 1

VAERS 1653357

SANOFI PASTEUR · MENINGOCOCCAL CONJUGATE (MENACTRA) · Charge U6576AA

gering
Staat
ME
Alter
-
Geschlecht
U
Eingang
29.08.2021
Impfdatum
10.08.2021
Beginn
10.08.2021
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

Symptomtext

Expired Menactra vaccine was accidentally given with no reported adverse event; Initial information received on 11-Aug-2021 regarding an unsolicited valid non-serious case from a other health care professional via Global Medical Information (Reference number- 00719410). This case involves a patient (unknown demographics) who was vaccinated with the expired dose of suspect 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. On 10-Aug-2021, the patient received a dose of suspect MENINGOCOCCAL A-C-Y-W135 (D CONJ) VACCINE (lot U6576AA and expiry date: 04-Apr-2021) via an unknown route at an unknown administration site for prophylactic vaccination. It was an actual medication error case due to expired vaccine used (latency on same day). It was reported that "Caller with provider office stated that an expired Menactra vaccine was accidentally given yesterday. Caller asked if there are any concerns or what should be done next. She would like to know if they should wait a week before administering a second vaccine. She would like to know if there might be any side effects expected by giving two vaccines". At 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 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 1376298

SANOFI PASTEUR · MENINGOCOCCAL CONJUGATE (MENACTRA) · Charge U6576AA

gering
Staat
TX
Alter
-
Geschlecht
F
Eingang
05.06.2021
Impfdatum
26.05.2021
Beginn
26.05.2021
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

administered an expired dose of Menactra with no reported adverse event; Initial information regarding an unsolicited valid non-serious case from consumer /non-health professional via Medical Information (Reference number- 00617311) and transmitted to Sanofi on 26-Apr-2021. This case involves a 24-year old female patient who administered an expired dose of MENINGOCOCCAL A-C-Y-W135 (D CONJ) VACCINE [MENACTRA] (expired product administered) on 26-May-2021 (lot number: U6576AA and expiration date: 04-Apr-2021] at an 0.5 ml once (total) dose via intramuscular route in the left deltoid for prophylactic vaccination. Medical history, past medical treatment(s), vaccination(s) and family history were not provided. Concomitant vaccination was not reported. It was an actual medication error due to expired vaccine used (latency: same day). At the time of report, no adverse event was reported. It was not reported if the patient received a corrective treatment. Disclaimer: 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 1357372

SANOFI PASTEUR · MENINGOCOCCAL CONJUGATE (MENACTRA) · Charge U6576AA

gering
Staat
FL
Alter
11,0
Geschlecht
M
Eingang
28.05.2021
Impfdatum
21.04.2021
Beginn
21.04.2021
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 Product storage error

Symptomtext

11 year old male patient administered expired dose of menactra with no reported adverse event; Initial information received on 18-May-2021 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 11 year old male patient who was administered an 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 HPV VACCINE VLP RL1 9V (YEAST) (GARDASIL 9) for Immunisation; and DIPHTHERIA VACCINE TOXOID, PERTUSSIS VACCINE ACELLULAR, TETANUS VACCINE TOXOID (TDAP) for Immunisation. On 21-Apr-2021, the patient received a 0.5 ml dose of suspect MENINGOCOCCAL A-C-Y-W135 (D CONJ) VACCINE (lot U6576AA and expiry date: 04-Apr-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 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 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 1320386

SANOFI PASTEUR · MENINGOCOCCAL CONJUGATE (MENACTRA) · Charge U6576AA

gering
Staat
CA
Alter
-
Geschlecht
F
Eingang
15.05.2021
Impfdatum
06.05.2021
Beginn
06.05.2021
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

Symptomtext

nurse asks if expired Menactra dose that she administered needs to be repeated with no reported adverse event; Initial information regarding an unsolicited valid non-serious case from other health professional via Medical Information (GMI) (Reference number- 00594513) and transmitted to Sanofi on 10-May-2021. This case involves a 20-year old female patient for whom nurse asked if expired MENINGOCOCCAL A-C-Y-W135 (D CONJ) VACCINE [MENACTRA] dose that she administered needs to be repeated (expired product administered) on 06-May-2021 (lot number: U6576AA and expiration date: 04-Apr-2021] at an 0.5 ml once dose via intramuscular route in the left deltoid for prophylactic vaccination. Medical history, past medical treatment(s), vaccination(s) and family history were not provided. Concomitant vaccination was not reported, and concomitant vaccination included INFLUENZA VACCINE (FLUZONE [INFLUENZA VACCINE]). It was an actual medication error due to expired vaccine used (latency: same day). At the time of report, no adverse event was reported. It was not reported if the patient received a corrective treatment. Disclaimer: 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
FLUZONE [INFLUENZA VACCINE]
Allergien
-
Vorherige Impfungen
-