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Reporte zur Charge U6575AA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

4Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
PA 1 ND 1 NY 1 FL 1

VAERS 1392011

SANOFI PASTEUR · MENINGOCOCCAL CONJUGATE (MENACTRA) · Charge U6575AA

mild
Staat
PA
Alter
16,0
Geschlecht
M
Eingang
10.06.2021
Impfdatum
20.08.2020
Beginn
20.08.2020
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Chills Dizziness Eczema Fatigue Headache Injection site pain Injection site reaction Keratosis pilaris Malaise Molluscum contagiosum Pain in extremity Pyrexia SARS-CoV-2 test Skin lesion removal

Symptomtext

Within office visit felt like he was going to pass out when came to stand, drank some water and continued to feel light headed before leaving office, Chilled during that night did not feel well tired and fatigued, He felt like he was going to pass out in the shower that night. Called the dr that night and todl them something was wrong. Arms ached for a week could feel injection site as tender. A headache that came and went over 2 week and had low grade fever 99-100 until Sept fever increased to 103.4 with urgent care visit. skin conditions occured of Kelartosis Pilaris at in jection sites. and eczema on anterior neck with molluscum contaglosum diagnosis and removal of lesions.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Chills
Hospital-Tage
-
Labordaten
Tested for COvid, eczema with molluscum contagiosum removals in April and May of 2021, still monitoring progress.
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1440128

SANOFI PASTEUR · MENINGOCOCCAL CONJUGATE (MENACTRA) · Charge U6575AA

gering
Staat
ND
Alter
16,0
Geschlecht
F
Eingang
01.07.2021
Impfdatum
23.06.2021
Beginn
23.06.2021
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 MENACTRA was administered to a patient, no AE; Initial information received on 23-Jun-2021 regarding an unsolicited valid non-serious case from a pharmacist and physician via Regulatory Authority (under reference number: 00653585). This case involves a 16 years old female patient who was administered with 0.5 ml expired MENINGOCOCCAL A-C-Y-W135 (D CONJ) VACCINE [MENACTRA] (Total, lot U6575AA and expiration date: 08-May-2021) via unknown route in unknown administration site for prophylactic vaccination on 23-Jun-202 (expired product administered). The patient's past medical history, medical treatment(s), vaccination(s), concomitant medication(s) and family history were not provided. It was a case of an actual medication error due to expired vaccine used (same day latency). Reported that the caller would like to know what to do next regarding matter. At time of reporting, the outcome was unknown for the reported 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 1419967

SANOFI PASTEUR · MENINGOCOCCAL CONJUGATE (MENACTRA) · Charge U6575AA

gering
Staat
NY
Alter
20,0
Geschlecht
U
Eingang
23.06.2021
Impfdatum
17.06.2021
Beginn
17.06.2021
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

Symptomtext

given an vaccine that expired a month ago/ no AE; Initial information was received on 17-Jun-2021 regarding an unsolicited valid non-serious case received from a Other health care professional via regulatory authority (Reference number- 00646123) and transmitted to Sanofi on 17-Jun-2021. This case involves a 20-year-old patient (unknown gender) who was vaccinated with 0.5 mL dose of MENINGOCOCCAL A-C-Y-W135 (D CONJ) VACCINE [MENACTRA] (total) (lot number U6575AA, expiry date 08-May-2021) via intramuscular route in left deltoid on 17-Jun-2021 for prophylactic vaccination (expired product administered). Medical history, medical treatment(s), vaccination(s), concomitant medications 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 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 970174

SANOFI PASTEUR · MENINGOCOCCAL CONJUGATE (MENACTRA) · Charge U6575AA

gering
Staat
FL
Alter
-
Geschlecht
M
Eingang
25.01.2021
Impfdatum
07.01.2021
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
OT / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Infant Wrong product administered

Symptomtext

gave a Menactra instead of an MMR yesterday with no AE; Initial information regarding this unsolicited valid non-serious case from Regulatory Authority (Reference number- 00421820) was received from Pharmacist and transmitted to Sanofi on 08-Jan-2021. This case involved a 7 months old male patient who received a 0.5 ml dose of MENINGOCOCCAL A-C-Y-W135 (D CONJ) VACCINE [MENACTRA] instead of MEASLES VACCINE, MUMPS VACCINE, RUBELLA VACCINE [MMR] (lot: U6575AA, expiration date: 08-May-2021), gave a Menactra instead of an MMR yesterday with no AE (Wrong vaccine administered). The dose was given in the left deltoid via intramuscular route. Past vaccination included meningococcal vaccine(unknown brand) 2 years ago. The patient's medical history, medical treatments, vaccinations, concomitant medications and family history were not provided. It was a actual medication error due to wrong vaccine administered (Wrong product administered). 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 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
Infant
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-