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Reporte zur Charge U6576AB

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

2Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
MI 1 NY 1

VAERS 1381436

SANOFI PASTEUR · MENINGOCOCCAL CONJUGATE (MENACTRA) · Charge U6576AB

gering
Staat
MI
Alter
12,0
Geschlecht
F
Eingang
08.06.2021
Impfdatum
24.05.2021
Beginn
24.05.2021
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

12 year old patient was administered an expired Menactra, no AE; Initial information regarding an unsolicited valid non-serious case was received from the other healthcare professional via Medical Information inbound (reference number-00613470) and transmitted to Sanofi on 24-May-2021. This case involves a 12 year old female patient who was administered an expired 0.5 ml dose of suspect MENINGOCOCCAL A-C-Y-W135 (D CONJ) VACCINE [MENACTRA] (lot number: U6576AB; expiry date: 04-APR-2021) via intramuscular route in the left arm for prophylactic vaccination on 24-MAY-2021 (expired product administered). Medical history, medical treatment(s), past vaccination(s), and family history were not provided. Concomitant medications included DIPHTHERIA VACCINE TOXOID, PERTUSSIS VACCINE ACELLULAR 3-COMPONENT, TETANUS VACCINE TOXOID (BOOSTRIX) for prophylactic vaccination. It was a case of an actual medication error due to expired vaccine used (latency same day). The reporter was asking for appropriate follow up. 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
BOOSTRIX
Allergien
-
Vorherige Impfungen
-

VAERS 1255778

SANOFI PASTEUR · MENINGOCOCCAL CONJUGATE (MENACTRA) · Charge U6576AB

gering
Staat
NY
Alter
17,0
Geschlecht
F
Eingang
25.04.2021
Impfdatum
08.04.2021
Beginn
08.04.2021
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 No adverse event

Symptomtext

patient received an expired 0.5ml dose of Menactra in the left deltoid, with no AE; Initial information received on 08-Apr-2021 regarding an unsolicited valid non-serious case from a other health professional. This case involves a 17-year-old female patient who received an expired 0.5ml dose of MENINGOCOCCAL A-C-Y-W135 (D CONJ) VACCINE [MENACTRA] (lot U6576AB, expiry date- 04-Apr-2021) in the left deltoid via an unknown route for prophylactic vaccination on 08-Apr-2021 (expired product administered). Medical history, medical treatment(s), vaccination(s), concomitant medications and family history were not provided. It was an actual medication error due to expired vaccine used. (latency: same day). It was reported that, the Physician Assistant wanted to know if there is a grace period on the expiration date of a Menactra vaccine given? or do they need to call the patient back to revaccinate? 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
-