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Reporte zur Charge U6428AA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

5Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
VA 5

VAERS 1839366

SANOFI PASTEUR · YELLOW FEVER (YF-VAX) · Charge U6428AA

gering
Staat
VA
Alter
-
Geschlecht
F
Eingang
03.11.2021
Impfdatum
-
Beginn
-
Tage bis Beginn
-
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

YF-VAX was administered using an expired diluent with no reported adverse event; Initial information received on 25-Oct-2021 regarding an unsolicited valid non-serious case received from a other health professional and non health care professional via Medical Information number: 00826516. This case involves 58 years old female patient was administered expired YELLOW FEVER VACCINE - US [YF-VAX] (expired product administered). This case is linked to cases US-SA-2021SA356051, 2021SA357534 and 2021SA356051(CLUSTER). The patient's medical history, past medical treatments, vaccinations, and family history were not provided. Concomitant medications included TYPHOID VACCINE (TYPHIM). On an unknown date, the patient received a 0.5 ml dose of suspect YELLOW FEVER VACCINE - US (lot number: U6428AA and expiry date: 30-SEP-2021) via intramuscular route in the left deltoid 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. 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.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-2021SA354616: US-SA-2021SA356701: US-SA-2021SA354618:

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

VAERS 1839365

SANOFI PASTEUR · YELLOW FEVER (YF-VAX) · Charge U6428AA

gering
Staat
VA
Alter
46,0
Geschlecht
F
Eingang
03.11.2021
Impfdatum
-
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
OT / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered

Symptomtext

YF-VAX was administered to 5 patients using an expired diluent with no reported adverse event; Initial information was received on 25-Oct-2021 regarding an unsolicited valid non-serious case from a other healthcare professional via Medical Information (under reference:00826473). This case involves a 46-year-old female patient who was administered YELLOW FEVER VACCINE - US [YF-VAX] using an expired diluent (expired product administered). The patient's medical history, past medical treatment(s), vaccination(s), concomitant medication(s) and family history were not provided. On an unknown date, the patient received a (dose of suspect YELLOW FEVER VACCINE - US (0.5ml, once, total, lot U6428AA, expiry date: 30-Sep-2021) via intramuscular route in the right deltoid for prophylactic vaccination. It was a case of actual medication error due to expired vaccine used (latency same day) It was reported "Operations manager is following-up, providing additional information on expired YF-VAX administered to 5 patients." 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.; Sender's Comments: 00824899: US-SA-2021SA354618: US-SA-2021SA356701: US-SA-2021SA354616:

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

VAERS 1835794

SANOFI PASTEUR · YELLOW FEVER (YF-VAX) · Charge U6428AA

gering
Staat
VA
Alter
32,0
Geschlecht
M
Eingang
02.11.2021
Impfdatum
-
Beginn
-
Tage bis Beginn
-
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

YF-VAX was administered to patient using an expired diluent with no reported adverse event; Initial information was received on 25-Oct-2021 regarding an unsolicited valid non-serious case received from a other healthcare professional via information (under the reference:00826342). This case is linked to cases 2021SA356701 and 2021SA356051 (same reporter). This case involves a 32-year-old male patient who was administered YELLOW FEVER VACCINE - US [YF-VAX] using an expired diluent (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) for prophylactic vaccination. On an unknown date, the patient received a dose of suspect YELLOW FEVER VACCINE - US (0.5mL, lot U6428AA, expiry date: 30-Sep-2021) via intramuscular route in the left deltoid for prophylactic vaccination. It was a case of actual medication error due to expired vaccine used. (latency: same day) It was reported "Operations manager is following-up, providing additional information on expired YF-VAX administered to 5 patients." At time of reporting, the 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.; Sender's Comments: US-SA-2021SA354616: US-SA-2021SA354618:

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

VAERS 1831434

SANOFI PASTEUR · YELLOW FEVER (YF-VAX) · Charge U6428AA

gering
Staat
VA
Alter
32,0
Geschlecht
M
Eingang
30.10.2021
Impfdatum
-
Beginn
-
Tage bis Beginn
-
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

expired dose of YF-VAX was administered with no adverse event reported; Initial information received on 25-Oct-2021 regarding an unsolicited valid non-serious case from other health professional via Media information (under the reference: 00826503). This case involves a 32-year-old male patient receiving expired dose of YELLOW FEVER VACCINE - US [YF-VAX] (expired product administered). On an unknown date, the patient received a 0.5mL dosage form total dose of suspect YELLOW FEVER VACCINE - US [Frequency: once, strength: standard, lot U6428AA,Expiration Date :30-Sep-2021] via intramuscular route in the left deltoid for prophylactic vaccination. It was a case of actual medication error due to expired vaccine use. (latency: same day) It was reported "expired YF-VAX administered to 5 patients." 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 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-2021SA356701: US-SA-2021SA354618: US-SA-2021SA355405: US-SA-2021SA357534: US-SA-2021SA356051: US-SA-2021SA354618: US-SA-2021SA354616:

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
TWINRIX; TYPHIM; TDAP
Allergien
-
Vorherige Impfungen
-

VAERS 1831433

SANOFI PASTEUR · YELLOW FEVER (YF-VAX) · Charge U6428AA

gering
Staat
VA
Alter
29,0
Geschlecht
F
Eingang
30.10.2021
Impfdatum
-
Beginn
-
Tage bis Beginn
-
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

expired dose of YF-VAX was administered with no adverse event reported; Initial information received on 25-Oct-2021 regarding an unsolicited valid non-serious case from other health professional via Global Media information (under the reference: 00826494) This case involved a 29-year-old female patient receiving expired dose of YELLOW FEVER VACCINE - US [YF-VAX] (expired product administered). On an unknown date, the patient received a 0.5mL dosage form total dose of suspect YELLOW FEVER VACCINE - US [Frequency: once, Strength: standard lot U6428AA, expiry date: 30-Sep-2021] via intramuscular route in the left deltoid for prophylactic vaccination. It was a case of actual medication error due to expired vaccine use. (latency: same day) It was reported "expired YF-VAX administered to 5 patients." At the time of report, no adverse event reported. This suspected adverse reaction report was 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 was 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 had contributed to or is to be held liable for the occurrence of this medication error.; Sender's Comments: US-SA-2021SA356701: US-SA-2021SA354618: US-SA-2021SA355405: US-SA-2021SA357534: US-SA-2021SA356051:

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