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Reporte zur Charge UJ820AB

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

10Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
NY 2 AR 1 NC 1 MT 1 KY 1 TX 1 MD 1

VAERS 2694141

SANOFI PASTEUR · YELLOW FEVER (YF-VAX) · Charge UJ820AB

schwer
Staat
AR
Alter
17,0
Geschlecht
M
Eingang
11.10.2023
Impfdatum
11.10.2023
Beginn
11.10.2023
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
SC / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Feeling hot Hyperhidrosis Hypertonia Loss of consciousness Nausea Pallor Skin discolouration Skin warm Thirst

Symptomtext

After completion of vaccination, patient lost consciousness and went limp. Patient was supported is seated position - did not fall or hit head/body. Patient remained unconscious for approximately 15 seconds with eyes remaining open, but unfocused. Additional pharmacy staff was immediately alerted and called EMS. When patient regained consciousness, he was pale/green in the face, sweating, and warm to the touch. He reported feeling "normal" but shortly stated he was thirsty, hot, and nauseous. Patient was wearing an Smart Watch that reported his heart rate at 63 bpm and regular rate and rhythm.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Loss of consciousness
Hospital-Tage
-
Labordaten
EMS arrived on scene at approximately 12:25 pm. They evaluated vital signs and verified hate rate, blood pressure, heart function and electrical activity- which was all found to be within normal limits. Patient's mother was given a written copy of vitals and declined further medical attention and transport from EMS.
Aktuelle Erkrankungen
No known illnesses
Vorgeschichte
No know chronic or long-standing health conditions
Andere Medikamente
No prescriptions, OTC, herbals, or supplements
Allergien
No known allergies
Vorherige Impfungen
-

VAERS 2723139

SANOFI PASTEUR · YELLOW FEVER (YF-VAX) · Charge UJ820AB

mild
Staat
NC
Alter
42,0
Geschlecht
F
Eingang
12.12.2023
Impfdatum
19.09.2023
Beginn
25.09.2023
Tage bis Beginn
6,0
Dosis
UNK
Route/Site
SC / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Erythema Injection site pruritus Injection site swelling Myalgia Nausea Pyrexia Skin exfoliation

Symptomtext

Developed erythema, swelling and pealing of the skin around the injection site. This improved but remained pruritic. Then she developed fevers, nausea and myalgias. Took motrin and benadryl with resolution of symptoms

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site pruritus
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
-
Vorgeschichte
GERD, HSV
Andere Medikamente
Bentyl 10mg prn, benadryl q6h PRN, flonase 2 sprays daily, claritin, pantoprazole, valtrex
Allergien
latex, tizanidine, orange juice, vicodin
Vorherige Impfungen
-

VAERS 2720314

SANOFI PASTEUR · YELLOW FEVER (YF-VAX) · Charge UJ820AB

mild
Staat
NY
Alter
47,0
Geschlecht
F
Eingang
02.12.2023
Impfdatum
06.09.2023
Beginn
07.09.2023
Tage bis Beginn
1,0
Dosis
UNK
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Abdominal distension Abdominal pain Cholelithiasis Cold sweat Fatigue Headache Helicobacter test positive Hepatic enzyme increased Hepatitis A virus test positive Immobile Inflammation Liver disorder Pruritus Pyrexia Ultrasound liver abnormal Vomiting

Symptomtext

Cold sweats, fever, headache, abdominal pain, exhaustion and fatigue, immobile for 2 hours, vomiting. itchy skin, inflamed and swollen midsection

Weitere VAERSDATA-Felder
Praegender Schweregrund
Abdominal pain
Hospital-Tage
-
Labordaten
blood test showed hepatitis A/ elevated liver ultrasound of liver showed elevated signs of liver disease and gallstones H. Pirolyi positive
Aktuelle Erkrankungen
sciatic nerve pain
Vorgeschichte
none
Andere Medikamente
iron supplement, probiotic, meloxicam
Allergien
none
Vorherige Impfungen
-

VAERS 2696118

SANOFI PASTEUR · YELLOW FEVER (YF-VAX) · Charge UJ820AB

mild
Staat
NY
Alter
31,0
Geschlecht
F
Eingang
14.10.2023
Impfdatum
13.10.2023
Beginn
14.10.2023
Tage bis Beginn
1,0
Dosis
1
Route/Site
SC / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Urticaria

Symptomtext

Patient states her arm initially broke out in hives and the spread to her legs. She noticed this on the morning after the vaccination. She called the pharmacy at 1:30pm to report the reaction, stating the hives were already fading from this morning. I suggested she take a dose of benadryl and reach out to her primary care provider. She reported not other issues.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Urticaria
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
NONE
Vorgeschichte
NONE
Andere Medikamente
NONE
Allergien
NKA
Vorherige Impfungen
-

VAERS 2680452

SANOFI PASTEUR · YELLOW FEVER (YF-VAX) · Charge UJ820AB

mild
Staat
-
Alter
30,0
Geschlecht
M
Eingang
08.09.2023
Impfdatum
30.08.2023
Beginn
07.09.2023
Tage bis Beginn
8,0
Dosis
UNK
Route/Site
SC / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Inflammation Rash erythematous Rash papular

Symptomtext

red, inflamed, raised rash to left tricep

Weitere VAERSDATA-Felder
Praegender Schweregrund
Rash erythematous
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
no known allergies
Vorherige Impfungen
-

VAERS 2674238

SANOFI PASTEUR · YELLOW FEVER (YF-VAX) · Charge UJ820AB

mild
Staat
MT
Alter
18,0
Geschlecht
M
Eingang
21.08.2023
Impfdatum
26.07.2023
Beginn
10.08.2023
Tage bis Beginn
15,0
Dosis
UNK
Route/Site
SC / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Urticaria

Symptomtext

Patient with uriticaria on August 10, 2023. He did see his Health Care Provider and was prescribed a cream to put on the hives. Utiricaria resolving on August 18, 2023 when PHN call Patient.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Urticaria
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
none
Vorgeschichte
none
Andere Medikamente
none
Allergien
none
Vorherige Impfungen
-

VAERS 2717098

SANOFI PASTEUR · YELLOW FEVER (YF-VAX) · Charge UJ820AB

gering
Staat
KY
Alter
-
Geschlecht
U
Eingang
23.11.2023
Impfdatum
14.11.2023
Beginn
14.11.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Incorrect route of product administration No adverse event

Symptomtext

administration of yf-vax intramuscularly instead of subcutaneously with no reported adverse event; Initial information received on 15-Nov-2023 regarding an unsolicited valid non-serious case received from a pharmacist. This case involves an unknown age and gender patient to whom administration of yellow fever vaccine [YF-VAX] intramuscularly instead of subcutaneously with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On an 14-Nov-2023, the patient received 0.5 ml dose of suspect yellow fever vaccine, Solution for injection (lot UJ820AB; strength and expiry date not reported) via intramuscular route in unknown administration site for Immunization instead of subcutaneously with no reported adverse event (incorrect route of product administration) (latency: on same day). Caller reported that her did not have any patient information because he just ask to gather information for the physician but the event occurred yesterday. Action taken: not applicable. 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 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
Incorrect route of product administration
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2663810

SANOFI PASTEUR · YELLOW FEVER (YF-VAX) · Charge UJ820AB

gering
Staat
-
Alter
73,0
Geschlecht
U
Eingang
01.08.2023
Impfdatum
19.05.2023
Beginn
19.05.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
No adverse event Product colour issue Product preparation error

Symptomtext

used sterile water instead of the sterile diluent (normal saline solution) that comes with the Stamaril/color turned into rose-tinge color upon dilution/ was administered to a patient with no reported adverse event; Initial information was received on 26-May-2023 regarding an unsolicited valid non-serious case received from a nurse. This case involves 73 years old and unknown gender patient for whom sterile water was used instead of the sterile diluent (normal saline solution) that comes with the stamaril/color turned into rose-tinge color upon dilution/ was administered to a patient with no reported adverse event for yellow fever vaccine [YF-VAX]. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 19-May-2023 at 03:16 PM, the patient received a dose of 0.5 ml of suspect yellow fever vaccine (Solution for injection) (lot UJ820AB) (with an unknown strength and expiry date) via subcutaneous route in the left arm for Travel for which the sterile water was used instead of the sterile diluent (normal saline solution) that comes with the stamaril/color turned into rose-tinge color upon dilution/ was administered to a patient with no reported adverse event (product preparation error) (latency- same day). Reportedly, there were no harmful effects and patient was revaccinated as advised 28 days later. Action taken: not applicable. At time of reporting, the outcome was Unknown for the 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. Additional information was received on 25-Jul-2023 from other healthcare professional: age of the patient was added, vaccine administration details were added, product coding (trade name) was updated. Narrative amended accordingly.

Weitere VAERSDATA-Felder
Praegender Schweregrund
No adverse event
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2656653

SANOFI PASTEUR · YELLOW FEVER (YF-VAX) · Charge UJ820AB

gering
Staat
TX
Alter
-
Geschlecht
U
Eingang
14.07.2023
Impfdatum
-
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Incorrect route of product administration

Symptomtext

YF-VAX administered IM instead of Subcutaneous with no reported adverse event; Initial information received on 11-Jul-2023 regarding an unsolicited valid non-serious case received from a pharmacist. This case involves an unknown age and unknown gender patient and Yellow Fever Vaccine [Yf-Vax] administered im (Intramuscularly) instead of subcutaneous with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On an unknown date, the patient received an unknown dose of suspect Yellow Fever Vaccine Solution for injection (lot number: UJ820AB, Expiry date: 28-May-2024) (with an unknown strength) via intramuscular route in unknown administration site for Immunization. On an unknown date, the patient received Yellow Fever Vaccine -vax im (Intramuscularly) instead of subcutaneous with no reported adverse event (incorrect route of product administration) (latency: same day). It was reported, reports YF-VAX administered IM instead of Subcutaneous. She would like to know if there are any anticipated side effects and if the pt needs to be re-immunized." The pharmacist states that she doesn't have time right now to provide additional AE information but if e-mails her a form with specific questions she would be happy to fill it out. This is all the additional information she provided at the time of her call. Action taken: not applicable. 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 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
Incorrect route of product administration
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2650150

SANOFI PASTEUR · YELLOW FEVER (YF-VAX) · Charge UJ820AB

gering
Staat
MD
Alter
10,0
Geschlecht
M
Eingang
28.06.2023
Impfdatum
27.06.2023
Beginn
27.06.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
SC / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
No adverse event Product administration error

Symptomtext

vaccine was given to patient on hydroxyurea. no adverse reaction reported.

Weitere VAERSDATA-Felder
Praegender Schweregrund
No adverse event
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
none
Vorgeschichte
sickle cell anemia
Andere Medikamente
none
Allergien
none
Vorherige Impfungen
-