Zurueck zur Suche

Reporte zur Charge U6594AA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

5Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
NV 1 MA 1 MD 1 ME 1 MN 1

VAERS 1302877

SANOFI PASTEUR · MENINGOCOCCAL CONJUGATE (MENACTRA) · Charge U6594AA

schwer
Staat
NV
Alter
18,0
Geschlecht
F
Eingang
10.05.2021
Impfdatum
08.05.2021
Beginn
08.05.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Syncope Vital signs measurement

Symptomtext

Pt had a syncope episode lasted app 10 sec. Pt was placed on the exam table, provided with orange juice and glucose tabs. Pt mother was in the room with pt. VS sign were taken and document in EMR . Pt was able to walk out without any help, was AAo x 3 upon leaving office.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
Pt refused BS checked.
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1653372

SANOFI PASTEUR · MENINGOCOCCAL CONJUGATE (MENACTRA) · Charge U6594AA

gering
Staat
MA
Alter
17,0
Geschlecht
M
Eingang
29.08.2021
Impfdatum
13.08.2021
Beginn
13.08.2021
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 Medication error

Symptomtext

patient was given an expired vaccine/ no AE; Initial information regarding an unsolicited valid non-serious case was received on 13-Aug-2021 from a Pharmacist via Global Medical Information (Reference number- 00723727) and transmitted to Sanofi on 13-Aug-2021. This case involves a 17-year-old male patient reported that he was given an expired MENINGOCOCCAL A-C-Y-W135 (D CONJ) VACCINE [MENACTRA] (expired product administered). Medical history, medical treatment(s), vaccination(s), concomitant medications and family history were not provided. On 13-Aug-2021, the patient received 0.5 ml (total) dose of suspect MENINGOCOCCAL A-C-Y-W135 (D CONJ) VACCINE [lot U6594AA, expiry date 21-May-2021] via intramuscular route in deltoid (left or right) for prophylactic vaccination. It was reported that, "Pharmacist states that expired MENACTRA was given to a patient. Pharmacist states that a medical assistant was trying to scan MENACTRA into their system, but it would not let him; becoming frustrated, the medical assistant administered the MENACTRA to patient without first scanning MENACTRA into their system. After administering MENACTRA, the medical assistant went back to try to scan MENACTRA into their system again; the pharmacist tried to help him and realized that the system would not let him scan the MENACTRA because the MENACTRA had expired". It was a case of actual medication error due to expired vaccine used (latency was on same day). At the time of reporting, patient had 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 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 1483677

SANOFI PASTEUR · MENINGOCOCCAL CONJUGATE (MENACTRA) · Charge U6594AA

gering
Staat
MD
Alter
18,0
Geschlecht
F
Eingang
18.07.2021
Impfdatum
09.07.2021
Beginn
09.07.2021
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

18 year old female patient was given an expired dose of Menactra with no reported adverse event; Initial information received on 09-Jul-2021 regarding an unsolicited valid non-serious case received from a other health professional via physician in. This case involves a 18 year old female patient who was vaccinated with an expired dose of suspect MENINGOCOCCAL A-C-Y-W135 (D CONJ) VACCINE [MENACTRA]. Medical history, medical treatment, concomitant medication, vaccination and family history were not provided. On 09-Jul-2021, the patient received a 0.5 ml dose of suspect MENINGOCOCCAL A-C-Y-W135 (D CONJ) VACCINE (lot U6594AA and expiry date: 21-May-2021) (Frequency: once) via an intramuscular route in the left deltoid (expired product administered) for prophylactic vaccination. It was an actual medication error case due to expired vaccine used (latency: same day). It was reported that "Patient Information Patient age greater than 1 year enter as 2 month, 4 month, etc. Many pediatric vaccines need month for age. Dose 0.25 mL to 2 mL for vaccines or 0.1 mL for TB skin test- 0.5 ML Strength -standard except for Fluzone HD-STANDARD Pregnancy- no pregnancy, Last menstrual period-not applicable, Due date- not applicable. If baby was delivered: delivery date and if baby experienced an adverse event- not applicable Inform that they will be receiving a follow up questionnaire- not applicable If calling specifically about being added to the pregnancy registry: all pregnancy cases are added to the registry, it is an Drug Administration requirement.- not applicable. Reporter relationship: HCP (health care professional) Product used: Used First time product used: Yes Still using product: No". 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.

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

VAERS 1423206

SANOFI PASTEUR · MENINGOCOCCAL CONJUGATE (MENACTRA) · Charge U6594AA

gering
Staat
ME
Alter
64,0
Geschlecht
M
Eingang
24.06.2021
Impfdatum
15.06.2021
Beginn
15.06.2021
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 Product administered to patient of inappropriate age

Symptomtext

patient received an expired dose of Menactra, with no reported adverse event; 64 years old patient received a Menactra Vaccine with no AE; Initial information regarding an unsolicited valid non-serious case was received from other healthcare professional via Medical Information (Reference number- 00647494) and transmitted to Sanofi on 18-Jun-2021. This case involves a 64-year-old male patient who received an expired dose of MENINGOCOCCAL A-C-Y-W135 (D CONJ) VACCINE [MENACTRA] (Expired product administered,Product administered to patient of inappropriate age]. The patient medical history, medical treatment(s), vaccination(s) and family history were not provided. Concomitant medications included DIPHTHERIA VACCINE TOXOID, PERTUSSIS VACCINE ACELLULAR, TETANUS VACCINE TOXOID (TDAP). On 15-Jun-2021, the patient received a 0.5 mL dose of suspect MENINGOCOCCAL A-C-Y-W135 (D CONJ) VACCINE [lot U6594AA and expiry: 21-May2021] via an intramuscular route in the left deltoid for prophylactic vaccination. It was a case of actual medication error due to expired product administered and product administered to patient of inappropriate age [Latency: on the same day]. No laboratory test was reported. At the time of report no adverse event was reported. It was not reported if the patient received any corrective treatment for the events. 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
TDAP
Allergien
-
Vorherige Impfungen
-

VAERS 1376297

SANOFI PASTEUR · MENINGOCOCCAL CONJUGATE (MENACTRA) · Charge U6594AA

gering
Staat
MN
Alter
-
Geschlecht
M
Eingang
05.06.2021
Impfdatum
26.05.2021
Beginn
26.05.2021
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

administered a booster dose of Menactra that was expired by 5 days with no reported adverse event; Initial information regarding an unsolicited valid non-serious case from other health professional via A (Reference number- 00617105) and transmitted to Sanofi on 26-Apr-2021. This case involves a 20-year old male patient who administered a booster dose of MENINGOCOCCAL A-C-Y-W135 (D CONJ) VACCINE [MENACTRA] that was expired by 5 days (expired product administered) on 26-May-2021 (lot number: U6594AA and expiration date: 21-May-2021] at an booster dose of 0.5 ml once (total) via intramuscular route in the left deltoid for prophylactic vaccination. Medical history, past medical treatment(s), vaccination(s) and family history were not provided. Concomitant vaccination was not reported. It was an actual medication error due to expired vaccine used (latency: same day). At the time of report, no adverse event was reported. It was not reported if the patient received a corrective treatment. 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
Expired product administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-