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Reporte zur Charge U6641AB

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

6Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
IN 5 MD 1

VAERS 1653334

SANOFI PASTEUR · MENINGOCOCCAL CONJUGATE (MENACTRA) · Charge U6641AB

gering
Staat
IN
Alter
12,0
Geschlecht
F
Eingang
29.08.2021
Impfdatum
02.08.2021
Beginn
02.08.2021
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 No adverse event

Symptomtext

the vaccine MENACTRA had expired on 31-Jul-2021 and was administered with no reported adverse event;Initial information regarding an unsolicited valid non-serious case from a consumer/ non-health care professional via Medical Information (Reference number- 00711805) and transmitted to Sanofi on 05-Aug-2021 and live follow up received on 03-Aug-2021. This case was linked with GMI ID 00707969 and ARTEMIS ID SAD20210803001152. This case involves a 12-year-old female patient for whom it was reported that the vaccine MENINGOCOCCAL A-C-Y-W135 (D CONJ) VACCINE, solution for injection [MENACTRA] had expired on 31-Jul-2021 and was administered (expired product administered) (lot number: U6641AB) at 0.5 ml dose via unknown route in an unknown site for prophylactic vaccination on 02-Aug-2021. Medical history, past medical treatments, past vaccinations and family history were not provided. Concomitant medications were not reported. It was an actual medication error case due to expired vaccine used (latency: same day). At the time of reporting, the patient experienced 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 1653331

SANOFI PASTEUR · MENINGOCOCCAL CONJUGATE (MENACTRA) · Charge U6641AB

gering
Staat
MD
Alter
18,0
Geschlecht
F
Eingang
29.08.2021
Impfdatum
-
Beginn
04.08.2021
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

Patient was administered expired dose of MENACTRA not realizing it was expired on 30-Jul-2021 with no AE; Initial information regarding an unsolicited valid non-serious case was received from other healthcare professional via Global Medical Information (Reference number- 00710629) and transmitted to Sanofi on 04-Aug-2021. This case involves a 18 year old female patient who experienced patient was administered expired dose of menactra not realizing it was expired on 30-Jul-2021 (expired product administered) while receiving MENINGOCOCCAL A-C-Y-W135 (D CONJ) VACCINE [MENACTRA]. The patient past medical history, medical treatment(s), vaccination(s) concomitant medication and family history were not provided. On 04-Aug-2021, the patient received a dose of suspect MENINGOCOCCAL A-C-Y-W135 (D CONJ) VACCINE [lot U6641AB and expiry date: 30-Jul-2021] via an intramuscular route in the right arm for prophylactic vaccination. It was case of actual medication error due to expired product administered. (Latency: on the same day). Details of laboratory data not reported. It was not reported if the patient received any 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 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 1653313

SANOFI PASTEUR · MENINGOCOCCAL CONJUGATE (MENACTRA) · Charge U6641AB

gering
Staat
IN
Alter
12,0
Geschlecht
F
Eingang
29.08.2021
Impfdatum
02.08.2021
Beginn
02.08.2021
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

expired MENACTRA was given yesterday with no adverse event; Initial information regarding an unsolicited valid non-serious case was received from other health care professional via Global Medical Information (GMI) (Reference number- 00707969) and transmitted to Sanofi on 03-Aug-2021. This case involves a 12-year-old female patient who was given expired MENINGOCOCCAL A-C-Y-W135 (D CONJ) VACCINE [MENACTRA] yesterday (expired product administered) Relevant medical history, medical treatment(s), vaccination(s) concomitant medication and family history were not provided. On 02-Aug-2021, the patient received 0.5ml dose of suspect MENINGOCOCCAL A-C-Y-W135 (D CONJ) VACCINE (lot: U6641AB and expiry date: 31-Jul-2021) (Frequency = once) (Strength = standard) via unknown route in the right deltoid for prophylactic vaccination (expired product administered) This was an actual medication error case 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 1520494

SANOFI PASTEUR · MENINGOCOCCAL CONJUGATE (MENACTRA) · Charge U6641AB

gering
Staat
IN
Alter
12,0
Geschlecht
F
Eingang
02.08.2021
Impfdatum
02.08.2021
Beginn
02.08.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Expired product administered

Symptomtext

Vaccine administered on 8/02/21 and was expired on 7/31/21

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
na
Aktuelle Erkrankungen
none
Vorgeschichte
unknown
Andere Medikamente
NA
Allergien
None
Vorherige Impfungen
-

VAERS 1520462

SANOFI PASTEUR · MENINGOCOCCAL CONJUGATE (MENACTRA) · Charge U6641AB

gering
Staat
IN
Alter
12,0
Geschlecht
F
Eingang
02.08.2021
Impfdatum
02.08.2021
Beginn
02.08.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Expired product administered

Symptomtext

Medication expired 7/31/21 and was administered on 8/02/21

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
NA
Aktuelle Erkrankungen
unknown
Vorgeschichte
unknown
Andere Medikamente
none
Allergien
none
Vorherige Impfungen
-

VAERS 918159

SANOFI PASTEUR · MENINGOCOCCAL CONJUGATE (MENACTRA) · Charge U6641AB

gering
Staat
IN
Alter
-
Geschlecht
F
Eingang
04.01.2021
Impfdatum
21.12.2020
Beginn
21.12.2020
Tage bis Beginn
0,0
Dosis
3
Route/Site
OT / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Wrong product administered

Symptomtext

a dose of MENACTRA was inadvertently administered instead of Meningitis B with no adverse event; Initial information received on 21-Dec-2020 regarding an unsolicited valid non-serious case from a other health professional. This case involves a 17 years old female patient who received a dose of Menactra was inadvertently administered instead of Meningitis B (wrong product administered), while she received vaccine MENINGOCOCCAL A-C-Y-W135 (D CONJ) VACCINE [MENACTRA]. On 21-Dec-2020, the patient received a dose of 0.5 mL suspect MENINGOCOCCAL A-C-Y-W135 (D CONJ) VACCINE (lot number: U6641AB and expiry date: 30-Jul-2021) via intramuscular route in the left deltoid. Reporter stated patient had already received both (two) doses of MENACTRA, the second dose was administered 18-Jun-2020. Medical history, past medical treatment, vaccination, concomitant medication and family history were not provided. This was an actual medication error case due to the event wrong vaccine administered (latency: same day). At the time of reporting, no adverse event was reported. No laboratory data was reported. 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
Wrong product administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-