Zurueck zur Suche

Reporte zur Charge U6690AA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

8Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
PA 2 NH 2 TX 1 NC 1 OK 1 CO 1

VAERS 2134542

SANOFI PASTEUR · MENINGOCOCCAL CONJUGATE (MENACTRA) · Charge u6690aa

gering
Staat
TX
Alter
17,0
Geschlecht
F
Eingang
23.02.2022
Impfdatum
21.02.2022
Beginn
21.02.2022
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered No adverse event

Symptomtext

Patient came to get menectra vaccine but was administered expired vaccine, after it was realized that the vaccine was expired , the patient contacted and no adverse effects were reported.

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

VAERS 1756418

SANOFI PASTEUR · MENINGOCOCCAL CONJUGATE (MENACTRA) · Charge U6690AA

gering
Staat
PA
Alter
17,0
Geschlecht
M
Eingang
02.10.2021
Impfdatum
22.09.2021
Beginn
22.09.2021
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

MENACTRA was expired and administered to a patient, with no reported adverse event; Initial information was received on 22-Sep-2021 regarding an unsolicited valid non-serious case received from an other health professional. This case involves a 17- years old male patient who experienced menactra was expired and administered to a patient, with no reported adverse event while receiving vaccine MENINGOCOCCAL A-C-Y-W135 (D CONJ) VACCINE [MENACTRA]. This case involves a 17 years old male patient who received an expired MENINGOCOCCAL A-C-Y-W135 (D CONJ) VACCINE [MENACTRA] (expired product administered). The patient's medical history, past medical treatments, vaccinations and family history were not provided. On 22-Sep-2021, the patient received a 0.5 mL dose of suspect MENACTRA (lot number: U6690AA and expiration date: 23-Aug-2021) via intramuscular route in the arm for prophylactic vaccination. It was an actual medication error due to expired vaccine used (same day latency). It was reported "What do we need to do next office manager asking if there is any grace period. Reporter was not sure if the patient had MENACTRA in the past or not. That was a new patient to them. Office manager stated that the patient may have gotten the flu vaccine as well that day, but she was not sure." 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 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 1674440

SANOFI PASTEUR · MENINGOCOCCAL CONJUGATE (MENACTRA) · Charge U6690AA

gering
Staat
NH
Alter
35,0
Geschlecht
F
Eingang
04.09.2021
Impfdatum
30.08.2021
Beginn
30.08.2021
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

The patient was administered with an expired menactra vaccine with no adverse event reported; Initial information regarding an unsolicited valid non-serious case was received from the pharmacist via Medical Information (Reference number- 00747873) and transmitted to Sanofi on 31-Aug-2021. This case involves a 35-year-old female patient received an dose of MENINGOCOCCAL A-C-Y-W135 (D CONJ) VACCINE [MENACTRA] which was expired in 23-Aug-2021 (expired product administered). Medical history, past medical treatment, vaccination and family history were not provided. Concomitant medications included INFLUENZA VACCINE INACT SAG 3V (FLUCELVAX). On 30-Aug-2021, the patient received an expired 0.5 mL total dose of suspect MENINGOCOCCAL A-C-Y-W135 (D CONJ) VACCINE [Drug Interval Dosage : once, lot U6690AA, expiry date: 23-Aug-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). The reporter reported " would like to know did they need let the patient know about adverse reactions and if they need to re-administer the dose as the patient received the vaccine yesterday". 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 in the Directive 2001/83/EC and Module VI of the Good Pharmacovigilance Practices. 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.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Comments: Patient age <1 year enter as 2m, 4m, etc. Many pediatric vaccines need month for age. patient date of birth: 2-JUN-1986
Andere Medikamente
FLUCELVAX
Allergien
-
Vorherige Impfungen
-

VAERS 1919914

SANOFI PASTEUR · MENINGOCOCCAL CONJUGATE (MENACTRA) · Charge U6690AA

gering
Staat
NH
Alter
35,0
Geschlecht
F
Eingang
01.09.2021
Impfdatum
30.08.2021
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Expired product administered No adverse event

Symptomtext

Rph found that the given Vaccine has expired a week before the administration. Pt Contacted, and confirmed no adverse event occured.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
N/A
Aktuelle Erkrankungen
-
Vorgeschichte
No health Condition
Andere Medikamente
-
Allergien
No Known allergy
Vorherige Impfungen
-

VAERS 1657926

SANOFI PASTEUR · MENINGOCOCCAL CONJUGATE (MENACTRA) · Charge U6690AA

gering
Staat
NC
Alter
-
Geschlecht
M
Eingang
31.08.2021
Impfdatum
24.08.2021
Beginn
24.08.2021
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

expired dose of Menactra was given with no reported adverse event; Initial information regarding an unsolicited valid non-serious case was received from other health professional via Global Medical Information (Reference number- 00737725) and transmitted to Sanofi on 24-Aug-2021. This case involves an unknown age male patient who vaccinated with a 0.5mL (total) dose of an expired MENINGOCOCCAL A-C-Y-W135 (D CONJ) VACCINE [MENACTRA] (solution for injection) [lot U6690AA and expiry date 23-Aug-2021] via intramuscular route at an unknown administration site on 24-Aug-2021 for prophylactic vaccination (expired product administered). Medical history, medical treatment, past vaccination, concomitant medication and family history were not provided. It was a case of actual medication error due to expired vaccine used (latency was on same day). At the time of report, no adverse event reported. Reporter would like to know what is to be done in such a scenario. 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 1512977

SANOFI PASTEUR · MENINGOCOCCAL CONJUGATE (MENACTRA) · Charge U6690AA

gering
Staat
OK
Alter
15,0
Geschlecht
M
Eingang
29.07.2021
Impfdatum
10.06.2021
Beginn
10.06.2021
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Extra dose administered

Symptomtext

Administered the listed vaccines that were due on 6/10/2021. Upon chart auditing noted that client's record that had been under the name and had additional vaccines added to it which invalidated several vaccines given on 06/10/2021. The client is in therapy and upon calling the client's medical case manager she reported she did not correctly report the client's name at the appointment on 06/10/2021 and that the name had been corrected. Advised medical case manager that client had received additional doses of Tdap, Hep A, Hep B, Varicella, and Menactra since full shot record was not available at appointment in June. Medical case manager reported the client had no reactions after vaccine administration.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Extra dose administered
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None.
Vorgeschichte
Psychiatric diagnosis.
Andere Medikamente
Unknown medications for psychiatric diagnosis.
Allergien
None.
Vorherige Impfungen
-

VAERS 1483675

SANOFI PASTEUR · MENINGOCOCCAL CONJUGATE (MENACTRA) · Charge U6690AA

gering
Staat
PA
Alter
18,0
Geschlecht
M
Eingang
18.07.2021
Impfdatum
08.07.2021
Beginn
08.07.2021
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Medication error Wrong product administered

Symptomtext

patient was given Menactra in the left deltoid in error, instead of the intended meningococcal B vaccine, with no reported adverse event; Initial information was received on 09-Jul-2021 regarding an unsolicited valid non-serious case from other health professional (GMI Inquiry number: 00675660). This case involves 18-year-old male patient who was given MENINGOCOCCAL A-C-Y-W135 (D CONJ) VACCINE [MENACTRA] in the left deltoid in error, instead of the intended meningococcal b vaccine (wrong product administered). It was a case of actual medication error due to wrong vaccine administered. On an unknown date, the patient received a 0.5 mL dose of suspect MENINGOCOCCAL A-C-Y-W135 (D CONJ) VACCINE [lot number: U6690AA, expiry date: 23-Aug-2021] via an unknown route at left deltoid for prophylactic vaccination. At the time of report, no adverse event reported. Description: Yesterday, 08Jul2021, a patient was given Menactra in the left deltoid in error, instead of the intended meningococcal B vaccine. o Treatment NA o Dose # if series Yesterday's dose was an accidental, extra third dose of Menactra. The patient's two prior doses of MCV4 vaccine were in 2014 and Jun2020. 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
Medication error
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1427955

SANOFI PASTEUR · MENINGOCOCCAL CONJUGATE (MENACTRA) · Charge U6690AA

gering
Staat
CO
Alter
19,0
Geschlecht
F
Eingang
25.06.2021
Impfdatum
23.06.2021
Beginn
23.06.2021
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Extra dose administered No adverse event

Symptomtext

The patient was scheduled to come in for her 2nd series of the Trunemba. She had already completed the 2 doses of Menactra on June 20, 2013 (1st dose) and May 18, 2020 (2nd dose). She was given her 2nd series dose of Trunemba and what was thought to be the 2nd dose of Menactra during the office visit on 6/23/2021. She was not supposed to have a 3rd series dose of the Menactra. Patient did not have any signs or symptoms of a reaction, but was concerned due to the extra series dose of Menactra. Dr. spoke with the patient's mother regarding their concerns.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Extra dose administered
Hospital-Tage
-
Labordaten
N/A
Aktuelle Erkrankungen
None
Vorgeschichte
Eosinophilic esophagitis Acne Vulgaris
Andere Medikamente
Azelex 20% Cream Clindamycin Phos-Benzoyl Perox 1.2-5% Gel Omeprazole 10 mg Capsule
Allergien
N.K.D.A
Vorherige Impfungen
-