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Reporte zur Charge U7576AD

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

10Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
NH 2 OR 1 GA 1 UT 1 HI 1 WA 1 MI 1 VA 1 OH 1

VAERS 2585617

SANOFI PASTEUR · MENINGOCOCCAL CONJUGATE (MENQUADFI) · Charge U7576AD

mild
Staat
NH
Alter
16,0
Geschlecht
F
Eingang
22.02.2023
Impfdatum
22.02.2023
Beginn
22.02.2023
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Urticaria

Symptomtext

urticaria within 10 min of vaccine.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Urticaria
Hospital-Tage
-
Labordaten
n/a
Aktuelle Erkrankungen
n/a
Vorgeschichte
asthma, food allergies, eczema, seasonal allergies
Andere Medikamente
cetirizine 10 mg . monteleukast 10 mg
Allergien
flaxseed, mupirocin, pine nuts
Vorherige Impfungen
-

VAERS 2714467

SANOFI PASTEUR · MENINGOCOCCAL CONJUGATE (MENQUADFI) · Charge U7576AD

gering
Staat
OR
Alter
9,0
Geschlecht
M
Eingang
16.11.2023
Impfdatum
26.09.2023
Beginn
26.09.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Extra dose administered No adverse event

Symptomtext

Vaccine Meningococcal MCV4 Menquadfi was administered to patient before mentioned. For no known reason, the vaccine was showing in health maintenance when administered it showed as an error in ALERT. Provider on site was notified as well as the patient. Patient was in observation for over 40 minutes and no reactions were presented.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Extra dose administered
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None
Allergien
None
Vorherige Impfungen
-

VAERS 2669420

SANOFI PASTEUR · MENINGOCOCCAL CONJUGATE (MENQUADFI) · Charge U7576AD

gering
Staat
GA
Alter
16,0
Geschlecht
F
Eingang
10.08.2023
Impfdatum
04.08.2023
Beginn
04.08.2023
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Exposure during pregnancy No adverse event Pregnancy test positive

Symptomtext

Patient was unaware of pregnancy and presented to clinic for back to school immunizations on 8/4/2023. Screening questionnaire completed by patient's father and no was marked to the question regarding any concern or risk for pregnancy now or within the next month. Patient returned to the clinic 6 days later on 8/10/2023 requesting pregnancy test and it was confirmed patient is indeed pregnant and is estimated to be 8 1/2 weeks gestation, which indicates she was pregnant at time of administration of MenQuadfi and Gardasil vaccines on 8/4/2023 visit. Patient states she hasn't had any reactions to vaccines and is just concerned about receiving them since she is pregnant.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Exposure during pregnancy
Hospital-Tage
-
Labordaten
Pregnancy test performed on 8/10/2023 = positive test, client estimated to be 8 1/2 weeks gestation
Aktuelle Erkrankungen
none
Vorgeschichte
None
Andere Medikamente
None
Allergien
Penicillin and Amoxicillin causes swelling of entire body, face and tongue
Vorherige Impfungen
-

VAERS 2656564

SANOFI PASTEUR · MENINGOCOCCAL CONJUGATE (MENQUADFI) · Charge U7576AD

gering
Staat
UT
Alter
17,0
Geschlecht
M
Eingang
14.07.2023
Impfdatum
10.07.2023
Beginn
-
Tage bis Beginn
-
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Tuberculin test positive

Symptomtext

No symptoms have been reported

Weitere VAERSDATA-Felder
Praegender Schweregrund
Tuberculin test positive
Hospital-Tage
-
Labordaten
Patient also had a PPD test done at the time of vaccine administration. Patient came back after 48 hours for a PPD reading and came back positive. Pt was ordered a chest X-ray.
Aktuelle Erkrankungen
N/A
Vorgeschichte
N/a
Andere Medikamente
N/A
Allergien
N/A
Vorherige Impfungen
-

VAERS 2649678

UNKNOWN MANUFACTURER · MENINGOCOCCAL (NO BRAND NAME) · Charge U7576AD

gering
Staat
HI
Alter
1,7
Geschlecht
F
Eingang
27.06.2023
Impfdatum
24.05.2023
Beginn
24.05.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Medication error No adverse event Product administered to patient of inappropriate age

Symptomtext

menquadfi to a patient under 2 years of age with no reported adverse event; Initial information received on 16-Jun-2023 regarding an unsolicited valid non-serious case received from a physician. This case involves a 20 months old female patient who was under 2 years of age was administered Meningococcal A-C-Y-W135 (T CONJ) vaccine [Menquadfi] with no reported adverse event. The patient's past medical history included Cancer with patient who had cancer and was successfully treated and cleared and Acute myeloid leukaemia in remission. The patient's past medical treatment(s), vaccination(s) and family history were not provided. Concomitant medications included Hepatitis A Vaccine (Hepatitis A) and Hepatitis B Vaccine (Hepatitis B Vaccine) in the left leg for Prophylactic vaccination. On 24-May-2023, the patient received a dose of 0.5 ml of suspect Meningococcal A-C-Y-W135 (T CONJ) vaccine solution for injection (lot: U7576AD) with unknown strength & expiry date via intramuscular route into the right quadriceps muscle for Immunization with no reported adverse event (product use issue) (latency: same day). Action taken: not applicable. At time of reporting, the outcome was Unknown. 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
Medication error
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Acute myeloid leukaemia in remission; Cancer (patient who had cancer and was successfully treated and cleared)
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2630638

SANOFI PASTEUR · MENINGOCOCCAL CONJUGATE (MENQUADFI) · Charge U7576AD

gering
Staat
WA
Alter
10,0
Geschlecht
M
Eingang
11.05.2023
Impfdatum
11.05.2023
Beginn
11.05.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Product administered to patient of inappropriate age

Symptomtext

Patient received Menquad at age 10 instead of age 11

Weitere VAERSDATA-Felder
Praegender Schweregrund
Product administered to patient of inappropriate age
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
N/A
Vorgeschichte
N/A
Andere Medikamente
N/A
Allergien
N/A
Vorherige Impfungen
-

VAERS 2624090

NOVARTIS VACCINES AND DIAGNOSTICS · MENINGOCOCCAL B (BEXSERO) · Charge U7576AD

gering
Staat
NH
Alter
16,0
Geschlecht
M
Eingang
01.05.2023
Impfdatum
12.04.2023
Beginn
14.04.2023
Tage bis Beginn
2,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Cellulitis Peripheral swelling

Symptomtext

Swollen left arm that worsened almost a week after the event. Was treated for cellulitis of his left upper arm.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Cellulitis
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None
Vorgeschichte
Asthma
Andere Medikamente
Flovent Inhaler, Pro-Air Inhaler, as needed. Epi-Pen PRN for tree nut allergy.
Allergien
Tree Nuts
Vorherige Impfungen
-

VAERS 2594715

SANOFI PASTEUR · MENINGOCOCCAL CONJUGATE (MENQUADFI) · Charge U7576AD

gering
Staat
MI
Alter
4,0
Geschlecht
M
Eingang
10.03.2023
Impfdatum
22.02.2023
Beginn
10.03.2023
Tage bis Beginn
16,0
Dosis
1
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
No adverse event Wrong product administered

Symptomtext

Dr prescribed by accident and given, no adverse event

Weitere VAERSDATA-Felder
Praegender Schweregrund
No adverse event
Hospital-Tage
-
Labordaten
N/A
Aktuelle Erkrankungen
-
Vorgeschichte
Autistic Disorder
Andere Medikamente
Clonidine HCL 0.1mg tablet
Allergien
NKA
Vorherige Impfungen
-

VAERS 2592364

SANOFI PASTEUR · MENINGOCOCCAL CONJUGATE (MENQUADFI) · Charge U7576AD

gering
Staat
VA
Alter
18,0
Geschlecht
F
Eingang
07.03.2023
Impfdatum
07.03.2023
Beginn
01.03.2023
Tage bis Beginn
-
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Wrong product administered

Symptomtext

MMRV Vaccine given in error when MMR vaccine should have been given. Patient received Varicella vaccine in the other arm at the same time.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Wrong product administered
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
n/a
Vorgeschichte
Asthma
Andere Medikamente
N/A
Allergien
N/A
Vorherige Impfungen
-

VAERS 2552829

SANOFI PASTEUR · MENINGOCOCCAL CONJUGATE (MENQUADFI) · Charge U7576AD

gering
Staat
OH
Alter
-
Geschlecht
U
Eingang
07.01.2023
Impfdatum
-
Beginn
30.12.2022
Tage bis Beginn
-
Dosis
UNK
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Product storage error

Symptomtext

excursion was due to the door being ajar. The temperature of the refrigerator reached 41.0-62.0 degrees Fahrenheit with no adverse event; Initial information received on 03-Jan-2023 regarding an unsolicited valid serious case received from a other health professional. This case involves an event of product storage error of MENINGOCOCCAL A-C-Y-W135 (T CONJ) VACCINE [MENQUADFI], DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS VACCINE [ADACEL] and DIPHTHERIA/TETANUS/5 HYBRID AC PERTUSSIS/IPV(MRC5)/HIB(PRP/T) VACCINE [PENTACEL] (excursion was due to the door being ajar. the temperature of the refrigerator reached 41.0-62.0 degrees fahrenheit with no adverse event). On 30-Dec-2022, it was reported DIPHTHERIA/TETANUS/5 HYBRID AC PERTUSSIS/IPV(MRC5)/HIB(PRP/T) VACCINE (lot UJ680ABA), DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS VACCINE (lot U7561AA) and MENINGOCOCCAL A-C-Y-W135 (T CONJ) VACCINE lot (U7576AD) (strength, formulation, dose, route and expiry date: unknown) to be used for immunization was exposed to excursion due to the door being ajar. the temperature of the refrigerator reached 41.0-62.0 degrees fahrenheit with no adverse event (product storage error) (unknown latency). Action taken: not applicable. It was not reported if the patient received a corrective treatment for the events. Outcome: Unknown. 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
Product storage error
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-