VAERS Reports UJ507AC

VAERS 1876130

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UJ507AC

gering

Staat: NY
Alter: 95,0
Geschlecht: F
Eingang: 17.11.2021
Impfdatum: -
Beginn: 03.11.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered No adverse event

Symptomtext

in their shipment of 2021-2022 product they received vials of 2020-2021, with no reported adverse event; 20-staff members and 7-Residents received expired doses, with no reported adverse event; Initial information received on 04-Nov-2021 regarding an unsolicited valid non-serious case received from a other health professional, physician and non health care professional via Agency number: 00842649. This case is linked to cases 2021SA371630, 2021SA369738, US-SA-2021SA370183, US-SA-2021SA371632, US-SA-2021SA369738, US-SA-2021SA370183, US-SA-2021SA371632, 2021SA370209 and 2021SA369789 (CLUSTER). This case involves a 95 years old female patient who experienced in their shipment of 2021-2022 product they received vials of 2020-2021, with no reported adverse event administered an expired dose of INFLUENZA QUADRIVAL A-B MULTIDOSE VACCINE PRESERVED [FLUZONE QUADRIVALENT MULTIDOSE] (expired product administered). The patient's medical history, past medical treatments, vaccinations, concomitant medications and family history were not provided. On 03-Nov-2021, the patient received a dose of suspect INFLUENZA QUADRIVAL A-B MULTIDOSE VACCINE PRESERVED lot number: UJ507AC and expiry date: 30-JUN-2021via unknown route in unknown administration site for prophylactic vaccination. It was case of an actual medication error due to expired vaccine used (latency: same day). At the time of reporting, no adverse event was reported. It was reported 'The Nurse reported that the doses came shipped to their central supply; that then the vaccines were distributed and placed in the vaccine refrigerators through the facility; that she is not the person that receives the vaccines from shipping and that she does not have the packaging slips or boxes due to it is handled with central supply; that when their staff is administering a vaccine the expiration date is not noted prior to administration; that the expiration date is not documented but just the LOT number; that the staff is not looking at the expiration date when administering; and that a nurse, yesterday, saw the expiration date to be expired after vaccinating residents." At time of reporting, the outcome of the event was reported as unknown 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.; Sender's Comments: US-SA-2021SA369738:

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1876110

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UJ507AC

gering

Staat: NY
Alter: 83,0
Geschlecht: M
Eingang: 17.11.2021
Impfdatum: 03.11.2021
Beginn: 03.11.2021
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

received expired dose of FLUZONE QUADRIVALENT with no reported adverse event; Initial information regarding an unsolicited valid non-serious case was received from nurse, physician and consumer/non-health care professional via Agency (Reference number- 00842655) and transmitted to Sanofi on 04-Nov-2021. This case is linked to cases 2021SA371630, 2021SA369738, 2021SA370209, 2021SA369789, 2021SA369806 and 2021SA370183 (same reporter). This case involves 83-year-old male patient received expired dose of INFLUENZA QUADRIVAL A-B MULTIDOSE VACCINE PRESERVED [FLUZONE QUADRIVALENT MULTIDOSE] (expired product administered) Relevant medical history, medical treatment(s), vaccination(s) concomitant medication and family history were not provided. On 03-Nov-2021, the patient received 0.5ml total dose of suspect INFLUENZA QUADRIVAL A-B MULTIDOSE VACCINE PRESERVED (Frequency = once) (Strength = standard) (lot: UJ507AC and expiry date: 30-Jun-2021) via unknown route in an unknown administration site for prophylactic vaccination (expired product administered). It was reported "The Medical Information agent confirmed the spelling of demographics with the caller for accuracy. The caller reported that her facility orders Fluzone Quad directly from Sanofi and in their shipment of 2021-2022 product they received vials of 2020-2021. The caller reported that some staff and residents were administered the expired product and she wants to know what to do. A Nurse reporting a medication error described as 20-staff members and 7-Residents received expired doses of FLUZONE QUADRIVALENT MDV from 2020-2021 year after receiving these 6-vials of the FLUZONE QUADRIVALENT MDV in the current years flu vaccine shipment. The Nurse reported that the 20-staff members received the dose since the end of Oct2021; that the information on the staff members are not known, at the time of this report; that the staff has had no reports of adverse issues since dosing; that the 6-Residents received their dose on 03Nov2021; that the information for the residents is known to the reporter; that the residents have had no reports of adverse issues since dosing. The Nurse reported that the doses came shipped to their central supply; that then the vaccines were distributed and placed in the vaccine refrigerators through the facility; that she is not the person that receives the vaccines from shipping and that she does not have the packaging slips or boxes due to it is handled with central supply; that when their staff is administering a vaccine the expiration date is not noted prior to administration; that the expiration date is not documented but just the lot number; that the staff is not looking at the expiration date when administering; and that a nurse, yesterday, saw the expiration date to be expired after vaccinating residents". This case was an actual medication error due to expired vaccine used (latency: same day). At the time of reporting, 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 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 1876109

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UJ507AC

gering

Staat: NY
Alter: 77,0
Geschlecht: M
Eingang: 17.11.2021
Impfdatum: 03.11.2021
Beginn: 03.11.2021
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

This case involves a 77-years-old male patient who received an expired INFLUENZA QUADRIVAL A-B MULTIDOSE VACCINE PRESERVED [FLUZONE QUADRIVALENT MULTIDOSE] (expired product administered). The patient's medical history, past medical treatment(s), vaccination(s) and family history were not provided. No concomitant medications were given to the patient. On 03-Nov-2021, the patient received a 0.5 mL dose of suspect INFLUENZA QUADRIVAL A-B MULTIDOSE VACCINE PRESERVED (once), (suspension for injection, lot UJ507AC, expiry date: 30-Jun-2021) via an unknown route at an unknown administration site for prophylactic vaccination. It was an actual medication error due to expired vaccine used (latency: same day). It was reported "The medical Information agent confirmed the spelling of demographics with the caller for accuracy. The caller reported that her facility orders Fluzone Quad directly from Sanofi and in their shipment of 2021-2022 product they received vials of 2020-2021. The caller reported that some staff and residents were administered the expired product and she wants to know what to do. A nurse reporting a medication error described as 20-staff members and 7-Residents received expired doses of FLUZONE QUADRIVALENT MDV from 2020-2021 year after receiving these 6-vials of the FLUZONE QUADRIVALENT MDV in the current years flu vaccine shipment. The nurse reported that the 20-staff members received the dose since the end of Oct2021; that the information on the staff members are not known, at the time of this report; that the staff has had no reports of adverse issues since dosing; that the 6-Residents received their dose on 03Nov2021; that the information for the residents is known to the reporter; that the residents have had no reports of adverse issues since dosing. The nurse reported that the doses came shipped to their central supply; that then the vaccines were distributed and placed in the vaccine refrigerators through the facility; that she is not the person that receives the vaccines from shipping and that she does not have the packaging slips or boxes due to it is handled with central supply; that when their staff is administering a vaccine the expiration date is not noted prior to administration; that the expiration date is not documented but just the LOT number; that the staff is not looking at the expiration date when administering; and that a nurse, yesterday, saw the expiration date to be expired after vaccinating residents." At time of reporting, 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 the Directive 2001/83/EC and Module 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. This case is linked to cases 2021SA369738, 2021SA369789, 2021SA370183, 2021SA370209, 2021SA369806 and 2021SA371632 (CLUSTERS).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1876107

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE) · Charge UJ507AC

gering

Staat: NY
Alter: 71,0
Geschlecht: F
Eingang: 17.11.2021
Impfdatum: 03.11.2021
Beginn: 03.11.2021
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

Administered the expired product with no reported adverse event; Initial information regarding an unsolicited valid non-serious case was received from nurse, physician and consumer/non-health care professional via Medical Information (Reference number- 00842654) and transmitted to Sanofi on 04-Nov-2021. This case is linked to cases 2021SA371630, 2021SA369738, 2021SA370209, 2021SA369789, 2021SA369789, 2021SA369806, 2021SA369806 and 2021SA371632 (same reporter). This case involves a 71 year old female patient who received expired dose of INFLUENZA QUADRIVAL A-B MULTIDOSE VACCINE PRESERVED [FLUZONE] (expired product administered) The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 03-Nov-2021, the patient received a 0.5ml dose of suspect INFLUENZA QUADRIVAL A-B MULTIDOSE VACCINE PRESERVED (Frequency = once) (Strength = standard) (lot: UJ507AC and expiry date: 30-Jun-2021) via unknown route in an unknown administration site for prophylactic vaccination (expired product administered). It was reported "The Medical Information agent confirmed the spelling of demographics with the caller for accuracy. The caller reported that her facility orders Fluzone Quad directly from Sanofi and in their shipment of 2021-2022 product they received vials of 2020-2021. The caller reported that some staff and residents were administered the expired product and she wants to know what to do. A Nurse reporting a medication error described as 20-staff members and 7-Residents received expired doses of FLUZONE QUADRIVALENT MDV from 2020-2021 year after receiving these 6-vials of the FLUZONE QUADRIVALENT MDV in the current years flu vaccine shipment. The Nurse reported that the 20-staff members received the dose since the end of Oct2021; that the information on the staff members are not known, at the time of this report; that the staff has had no reports of adverse issues since dosing; that the 6-Residents received their dose on 03Nov2021; that the information for the residents is known to the reporter; that the residents have had no reports of adverse issues since dosing. The Nurse reported that the doses came shipped to their central supply; that then the vaccines were distributed and placed in the vaccine refrigerators through the facility; that she is not the person that receives the vaccines from shipping and that she does not have the packaging slips or boxes due to it is handled with central supply; that when their staff is administering a vaccine the expiration date is not noted prior to administration; that the expiration date is not documented but just the lot number; that the staff is not looking at the expiration date when administering; and that a nurse, yesterday, saw the expiration date to be expired after vaccinating residents". This case was an actual medication error due to expired vaccine used (latency: same day). At the time of reporting, 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 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 1872398

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UJ507AC

gering

Staat: NY
Alter: 89,0
Geschlecht: F
Eingang: 16.11.2021
Impfdatum: 03.11.2021
Beginn: 03.11.2021
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

in their shipment of 2021-2022 product they received vials of 2020-2021, with no reported adverse event; 20-staff members and 7-Residents received expired doses, with no reported adverse event; Initial information received on 04-Nov-2021 regarding an unsolicited valid non-serious case received from a other health professional and non-health care Regulatory Authority (RA) number: 00842648. This case is linked to cases US-SA-2021SA370183(CLUSTER), US-SA-2021SA369806, US-SA-2021SA371632, US-SA-2021SA369738, US-SA-2021SA370183, US-SA-2021SA369789, US-SA-2021SA369738, 2021SA371630, 2021SA369738, 2021SA370209 and 2021SA369789 (CLUSTER). This case involves a 89 years old female patient who experienced in their shipment of 2021-2022 product they received vials of 2020-2021, with no reported adverse event administered an expired dose of INFLUENZA QUADRIVAL A-B MULTIDOSE VACCINE PRESERVED [FLUZONE QUADRIVALENT MULTIDOSE] (expired product administered). The patient's medical history, past medical treatments, vaccinations, concomitant medications and family history were not provided. On 03-Nov-2021, the patient received a dose of suspect INFLUENZA QUADRIVAL A-B MULTIDOSE VACCINE PRESERVED lot number: UJ507AC and expiry date not reported via unknown route in unknown administration site for prophylactic vaccination. It was case of an actual medication error due to expired vaccine used (latency: same day). At the time of reporting, no adverse event was reported. At time of reporting, the outcome of the event was reported as unknown 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 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: -
Allergien: -
Vorherige Impfungen: -

VAERS 1867465

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE) · Charge UJ507AC

gering

Staat: NY
Alter: 87,0
Geschlecht: F
Eingang: 13.11.2021
Impfdatum: 03.11.2021
Beginn: 03.11.2021
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

This case is linked to cases 2021SA371630 and 2021SA369738 (same reporter). This case involves an 87-year-old female patient who received expired dose INFLUENZA QUADRIVAL A-B MULTIDOSE VACCINE PRESERVED [FLUZONE] (Expired vaccine used). The patient's medical history, concomitant therapy, medical treatment(s), vaccination(s) and family history were not provided. On 03-Nov-2021, the patient received a dose of suspect INFLUENZA QUADRIVAL A-B MULTIDOSE VACCINE PRESERVED (lot UJ507AC and expiry date not reported) via unknown route in unknown administration site for prophylactic vaccination. It was reported "A Nurse reporting a medication error described as 20-staff members and 7-Residents received expired doses of FLUZONE QUADRIVALENT MDV from 2020-2021 year after receiving these 6-vials of the FLUZONE QUADRIVALENT MDV in the current years flu vaccine shipment". It was a case of an actual medication error due to expired vaccine used (latency was on same day). At the time of report, no adverse event reported. Outcome of event was unknown. 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 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: -
Allergien: -
Vorherige Impfungen: -

VAERS 1867464

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UJ507AC

gering

Staat: NY
Alter: -
Geschlecht: U
Eingang: 13.11.2021
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: UNK
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered No adverse event

Symptomtext

Administered the expired product with no received expired dose of FLUZONE QUADRIVALENT with no reported adverse event; Initial information was regarding an unsolicited valid non serious case was received from other health professional via Medical Information (Reference number- 00842588) and transmitted to Sanofi on 04-Nov-2021. This case is linked to cases 2021SA371630(CLUSTER), 2021SA369789(CLUSTER), 2021SA370183(CLUSTER), 2021SA370209(CLUSTER), 2021SA371632(CLUSTER) and 2021SA369806(CLUSTER). This case involves a patient (unknown demographic) receiving expired dose of INFLUENZA QUADRIVAL A-B VACCINE [FLUZONE QIV] (expired product administered). The patient medical history, medical treatment(s), vaccination(s) and family history were not provided. On 03-Nov-2021, the patient received a 0.5 mL dose of suspect INFLUENZA QUADRIVAL A-B VACCINE (once), (suspension for injection, lot UJ507AC, expiry date: 30-Jun-2021) via an unknown route at an unknown administration site for prophylactic vaccination. It was an actual medication error due to expired vaccine used. (latency: same day). It was reported "A Nurse reporting a medication error described as 20-staff members and 7-Residents received expired doses of FLUZONE QUADRIVALENT MDV from 2020-2021 year after receiving these 6-vials of the FLUZONE QUADRIVALENT MDV in the current years flu vaccine shipment. The Nurse reported that the 20-staff members received the dose since the end of Oct-2021; that the information on the staff members are not known, at the time of this report; that the staff has had no reports of adverse issues since dosing; that the 6-Residents received their dose on 03-Nov-2021; that the information for the residents is known to the reporter; that the residents have had no reports of adverse issues since dosing." At time of reporting, 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 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: -