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Reporte zur Charge U6486AC

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

4Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
CO 2 IL 1 CA 1

VAERS 1182775

SANOFI PASTEUR · MENINGOCOCCAL CONJUGATE (MENACTRA) · Charge U6486AC

gering
Staat
IL
Alter
16,0
Geschlecht
F
Eingang
08.04.2021
Impfdatum
24.03.2021
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered

Symptomtext

expired Menactra was administered to a patient (with no reported adverse event); Initial information regarding an unsolicited valid non-serious case was received from Other Health Care Professional via Agency (Reference number- 00533762) and transmitted to Sanofi on 24-Mar-2021. This case involves a 16 years old female patient who received 0.5 mL expired dose of MENINGOCOCCAL A-C-Y-W135 (D CONJ) VACCINE [MENACTRA] lot number lot U6486AC expiry date- 10-Jan-2021 via intramuscular route in unknown administration site for prophylactic vaccination on 24-Mar-2021. Medical history, medical treatment(s), vaccination(s), concomitant medication and family history were not provided. It was a case of actual medication error due to expired vaccine used (latency same day). The caller would like to know if the patient must be revaccinated. At the time of report there was 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
-
Allergien
-
Vorherige Impfungen
-

VAERS 1019183

SANOFI PASTEUR · MENINGOCOCCAL CONJUGATE (MENACTRA) · Charge U6486AC

gering
Staat
CO
Alter
51,0
Geschlecht
M
Eingang
10.02.2021
Impfdatum
12.01.2021
Beginn
12.01.2021
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 Medication error

Symptomtext

patient received an expired dose of Menactra with no adverse event; Initial information received on 27-Jan-2021 regarding an unsolicited valid non-serious case received from the other health care professional (Medical Assistant) via Global Medical Information (Reference number-00448383). This case involves a 51 years old male patient who received an expired dose of MENINGOCOCCAL A-C-Y-W135 (D CONJ) VACCINE [MENACTRA] (batch number: U6486AC, expiration date: 10-JAN-2021, strength: standard) via intramuscular route in the left arm for prophylactic vaccination on 12-Jan-2021 (expired product administered). The patient's medical history, medical treatments, vaccinations and family history were not provided. No concomitant medication given. It was an actual medication error due to expired vaccine used (latency: same day). Description: A Medical Assistant wanting to know how to proceed after a consumer received an expired dose of Menactra. Product used and still using product: yes. 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 holders 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 1016639

SANOFI PASTEUR · MENINGOCOCCAL CONJUGATE (MENACTRA) · Charge U6486AC

gering
Staat
CA
Alter
18,0
Geschlecht
F
Eingang
09.02.2021
Impfdatum
25.01.2021
Beginn
25.01.2021
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 was inadvertently administered an expired dose of Menactra, no AE; Initial information received on 26-Jan-2021 regarding an unsolicited valid non-serious case from a other health professional. This case involves a 18 years old female patient who was inadvertently administered an expired booster dose of MENINGOCOCCAL A-C-Y-W135 (D CONJ) VACCINE [MENACTRA] (lot U6486AC and expiration date :10-Jan-2021) via intramuscular route in the left deltoid for prophylactic vaccination on 25-Jan-2021. Patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. Concomitant medications included HPV VACCINE VLP RL1 4V (YEAST) (GARDASIL). It was a case of actual medication error due to expired vaccine used (expired product administered, latency on same day). And they wants to find out if the medication needs to be re-administered No adverse event were reported at the time of reporting. 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
GARDASIL
Allergien
-
Vorherige Impfungen
-

VAERS 1006915

SANOFI PASTEUR · MENINGOCOCCAL CONJUGATE (MENACTRA) · Charge U6486AC

gering
Staat
CO
Alter
51,0
Geschlecht
F
Eingang
05.02.2021
Impfdatum
12.01.2021
Beginn
12.01.2021
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Expired product administered

Symptomtext

MEDICAL ASSISTANT INJECTED VACCINE IN THE LEFT ARM. AFTER ADMINISTRATION MEDICAL ASSISTANT FOLLOWED UP WITH DOCUMENTATION AND NOTICED THAT THE VACCINE WAS EXPIRED. SHE QUICKLY LET PROVIDER KNOW, PATIENT WAS INSTRUCTED TO STAY FOR OBSERVATION FOR 15 MIN. AFTER 15 MIN PT DID NOT REPORT/EXPRESS ANY SYMPTOMS OR RACTION TO THE VACCINE.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
HIV+
Andere Medikamente
YES
Allergien
AMITRIPTYLIE AND CYCLOBENZAPRINE CAUSES INSOMNIA
Vorherige Impfungen
-