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Reporte zur Charge UJ386AA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

18Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
1Bleibende Schaeden
NY 3 UT 2 PA 2 VA 2 IL 1 OR 1 MN 1 DC 1 FL 1 AL 1 TX 1

VAERS 1821099

SANOFI PASTEUR · YELLOW FEVER (YF-VAX) · Charge UJ386AA

schwer
Staat
IL
Alter
28,0
Geschlecht
M
Eingang
27.10.2021
Impfdatum
26.10.2021
Beginn
26.10.2021
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
SC / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja
Asthenia Confusional state Dizziness Dyspnoea Headache Hyperhidrosis Seizure Unresponsive to stimuli

Symptomtext

Pt felt a headache, diaphoretic, and short of breath approximately 30 minutes after receiving vaccines, then got dizzy and felt weak; while his friend was getting a wheelchair he convulsed and became unresponsive then confused. Was taken to ED after this episode.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Seizure
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
none
Vorgeschichte
Anxiety/depression
Andere Medikamente
Buproprion; Finasteride
Allergien
Cefaclor
Vorherige Impfungen
-

VAERS 1421289

SANOFI PASTEUR · YELLOW FEVER (YF-VAX) · Charge UJ386AA

schwer
Staat
OR
Alter
17,0
Geschlecht
F
Eingang
23.06.2021
Impfdatum
23.06.2021
Beginn
23.06.2021
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
SC / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Breath holding Dizziness Dyskinesia Hyperhidrosis Pallor Presyncope Syncope

Symptomtext

17 yo Client here for vaccines prior to travel with organized travel company. Vaccine record obtained and downloaded, consent obtained from MOC. Reviewed all travel vaccine information, TD, YF/Malaria, Rabies PEP, possible side effects, etc. Client and MOC voiced understanding, all questions answered. MOC very anxious about vaccines and kept asking client, "Are you okay?" and stated that she, herself may pass out. Client stated that she was not nervous and denied any issues with prior vaccines. Upon receiving vaccines, MOC was complimentary of child, client stated she felt like she was "going to pass out". Pt had vasovagal response to stress of injections, syncope occurred x approx 30-40 seconds with breath holding, involuntary movements, pale, slightly diaphoretic skin. Moved to floor with RN holding pt at side for safety, with resp and head support. MOC very anxious and stating "Do something, help her". I assured MOC client would be fine and would become alert and awake shortly. MOC dialed 911 but hung up as client awakened, answered questions and was appropriate. Pt moved to recliner, provided water and fanned with cool air. MOC sitting on floor, pale and nervous, provided water to MOC also. Pt observed for 10 additional minutes. MOC stated that she needed to get child something to eat. MOC & client to car, both walking well, stating they feel fine at this point. Grandfather in car waiting for family. Event reported to RN at the Nurse Hotline and form completed and sent to corp for documentation per policy.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Presyncope
Hospital-Tage
-
Labordaten
Injections X 3
Aktuelle Erkrankungen
None reported or observed
Vorgeschichte
None reported
Andere Medikamente
None reported
Allergien
None reported
Vorherige Impfungen
-

VAERS 1750261

SANOFI PASTEUR · YELLOW FEVER (YF-VAX) · Charge UJ386AA

mild
Staat
MN
Alter
44,0
Geschlecht
F
Eingang
30.09.2021
Impfdatum
31.08.2021
Beginn
31.08.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
SC / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Anxiety Blood thyroid stimulating hormone normal Dizziness Flushing Full blood count normal Headache Metabolic function test normal Nausea SARS-CoV-2 test negative Thyroxine free normal

Symptomtext

Patient reports the following symptoms: 8/31/21-9/2/21 mild headache, nausea, flushed, and anxious feeling. 09/03/21 onset of 'woozy' feeling (like on a boat), Headache improved. 09/04/21-09/16/2021 onset of tinnitus, continued woozy feeling /dizziness. Treatment: Prednisone, Meclizine, referral to ENT 09/18-09/28 Woozy feeling improved with prednisone, tinnitus persists. 09/28/21 increased fatigue and headache x2 days, persistent tinnitus. Follow up scheduled for 10/1/021 tomorrow for next steps.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dizziness
Hospital-Tage
-
Labordaten
Covid test negative patient initiated, unknown date. 09/17/2021 TSH, Free T4, and Metabolic profile all normal, Glucose 131 HGB A1c: 5.1 09/17/2021 CBC normal
Aktuelle Erkrankungen
None known
Vorgeschichte
Intermittent palpitations/PVC's; Covid-19 10/2020. For 2 months after diagnosis of Covid-19 she experienced tinnitus, fatigue (similar to current symptoms) Symptoms eventually resolved.
Andere Medikamente
MULTIVITAMINS
Allergien
COMPAZINE
Vorherige Impfungen
-

VAERS 1693131

SANOFI PASTEUR · YELLOW FEVER (YF-VAX) · Charge UJ386AA

mild
Staat
-
Alter
30,0
Geschlecht
M
Eingang
11.09.2021
Impfdatum
11.09.2021
Beginn
11.09.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
SC / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Cold sweat Dizziness Mydriasis Pallor

Symptomtext

Received three vaccines while in clinic. After the third vaccine, began to feel lightheaded. No loss of consciousness. Dilated pupils, clammy and pale. Vitals obtained, initial BP: 96/57, HR 39. Feet elevated and felt better after a few minutes. Final vitals: BP- 116/66, HR 58. Refused further medical treatment and was escorted back to unit.

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

VAERS 1689646

SANOFI PASTEUR · YELLOW FEVER (YF-VAX) · Charge UJ386AA

mild
Staat
UT
Alter
66,0
Geschlecht
M
Eingang
10.09.2021
Impfdatum
21.07.2021
Beginn
21.07.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
SYR / AR
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: unbekannt Erholt: nein
Immediate post-injection reaction Incorrect route of product administration Injection site pain Limb injury

Symptomtext

I had 5 injections at the same time. The Yellow Fever was only one of the 5. The above field did not allow me to report all 5 vaccines. When the injection was given in each arm I felt more pain that previous vaccinations that I have had in the past. Over the next hours, days and weeks, the pain has increased and not gone away. Today is September 10 and I still have a lot of pain. It is my opinion that I suffered shoulder injuries 'due to improper injection into my Bursa not my deltoid mussel or to long of needle or both. I did see my primary health care provider and I was given an oral anti-inflammatory medicine called Prednisone. to treat the problem. The medicine has helped but the intense pain continues.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site pain
Hospital-Tage
-
Labordaten
I visited Dr. and he is currently treating me from both of my shoulder injuries.
Aktuelle Erkrankungen
none
Vorgeschichte
none
Andere Medikamente
none
Allergien
none
Vorherige Impfungen
-

VAERS 1661885

SANOFI PASTEUR · YELLOW FEVER (YF-VAX) · Charge UJ386AA

mild
Staat
-
Alter
29,0
Geschlecht
F
Eingang
01.09.2021
Impfdatum
18.08.2021
Beginn
18.08.2021
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Headache Incorrect route of product administration Medication error Pain

Symptomtext

body ache that are worse at night; headache and body ache that are worse at night; patient received YF-VAX intramuscularly instead of subcutaneously; Initial information was received on 20-Aug-2021 regarding an unsolicited valid non-serious case received from a consumer (patient). This case involves a 29 year-old female patient who experienced body ache and headache that are worse at night (pain), (headache), after receiving vaccine YELLOW FEVER VACCINE [YF-VAX] (Incorrect route of product administration). The patient's medical history, medical treatment(s), vaccination(s) and family history were not provided. No concomitant therapy was given. Reporter stated she was not pregnant On 18-Aug-2021, the patient received (once) dose of suspect YELLOW FEVER VACCINE (Solution; lot UJ386AA and expiry date not reported) via an intramuscular route in the right deltoid for prophylactic vaccination. On 18-Aug-2021, the patient developed non-serious body ache and headache that are worse at night (pain), (headache) on the same day following the administration of YELLOW FEVER VACCINE. It was also a case of actual medication error due to in appropriate route of vaccination (latency was on same day). It was reported "Caller states she received YF-VAX intramuscularly instead of subcutaneously. Caller asking for safety and efficacy information regarding YF-VAX given intramuscularly. Caller also asking for clinical studies of YF-VAX given intramuscularly vs. subcutaneously. States she received YF-VAX because she will be traveling soon. Details of laboratory data were not reported. Caller reported she had not taken anything or gone to doctor for headache and body aches. At time of reporting, outcome of the events 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 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
Headache
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1637105

SANOFI PASTEUR · YELLOW FEVER (YF-VAX) · Charge UJ386AA

mild
Staat
PA
Alter
46,0
Geschlecht
M
Eingang
26.08.2021
Impfdatum
18.08.2021
Beginn
25.08.2021
Tage bis Beginn
7,0
Dosis
1
Route/Site
SC / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Injection site erythema Injection site swelling

Symptomtext

Injection site developed localized redness, slightly raised. No itching or pain noted.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site erythema
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
Claritin 1 tab daily
Allergien
None
Vorherige Impfungen
-

VAERS 1525618

SANOFI PASTEUR · YELLOW FEVER (YF-VAX) · Charge UJ386AA

mild
Staat
VA
Alter
31,0
Geschlecht
F
Eingang
04.08.2021
Impfdatum
04.08.2021
Beginn
04.08.2021
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
SC / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Dysphagia Erythema Injection site erythema Injection site swelling Pruritus Throat irritation

Symptomtext

Patient arrived back to clinic about an hour and half (1600) after vaccine administration c/o itching, redness/flush on face, itchy/scratchy throat, redness and swelling at YF injection site, and difficulty swallowing. Administered 50mg IM Benadryl on right arm at 1604. Called husband to come pick her up. Client waited in our office for symptoms to subside. Client still had some symptoms upon leaving our office at 1700 but symptoms have not worsened. Informed her to call 911 if she were to develop difficulty breathing. Instructed to take another dose of po Benadryl in 4-6 hours.

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

VAERS 2322970

SANOFI PASTEUR · YELLOW FEVER (YF-VAX) · Charge UJ386AA

gering
Staat
NY
Alter
-
Geschlecht
U
Eingang
17.06.2022
Impfdatum
-
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered Medication error No adverse event

Symptomtext

administered a YF-Vax for which the diluent had expired with no reported adverse event; Initial information received on 03-Jun-2022 regarding an unsolicited valid non-serious case received from a physician. This case involves a patient of an unknown age and gender patient who was administered a YF-Vax for which the diluent had expired with no reported adverse event while receiving vaccine YELLOW FEVER VACCINE [YF-VAX]. 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 , ( lot : UJ386AA ; expiry date : 22-Aug-2022) and diluent (lot: U6627AB ; expiry date: 20-May-2022) in unknown administration site for immunization. On an unknown date the patient was administered a YF-Vax for which the diluent had expired with no reported adverse event (expired product administered) (unknown latency). The diluent expired in May 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
Expired product administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1937028

SANOFI PASTEUR · YELLOW FEVER (YF-VAX) · Charge UJ386AA

gering
Staat
UT
Alter
12,0
Geschlecht
M
Eingang
09.12.2021
Impfdatum
02.12.2021
Beginn
02.12.2021
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
SC / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Extra dose administered No adverse event Product administration error

Symptomtext

Vaccine administration error. Patient had a Meningococcal ACWY vaccine 10/19/2021. Another dose was inadvertently administered on 12/2/2021. No adverse reaction to vaccine was reported.

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

VAERS 1793483

SANOFI PASTEUR · YELLOW FEVER (YF-VAX) · Charge UJ386AA

gering
Staat
NY
Alter
1,3
Geschlecht
F
Eingang
16.10.2021
Impfdatum
05.10.2021
Beginn
05.10.2021
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Product preparation error

Symptomtext

was improperly reconstituted with sterile water instead of the supplied diluent; Initial information received on 11-Oct-2021 regarding an unsolicited valid non-serious case from a physician via Media Information (under the reference 00806397). This case involves a 15 months old female patient who was vaccinated with YELLOW FEVER VACCINE [YF-VAX] and STERILE WATER which improperly reconstituted with sterile water instead of the supplied diluent (product preparation error). The patient's medical history, medical treatment(s), concomitant medication(s) and family history were not provided. Patient had no other vaccines. On 05-Oct-2021, the patient received a dose of suspect YF-VAX (0.5 ml, total, lot UJ386AA and expiration date: 22-aug-2022) via unknown route in an unknown administration site for prophylactic vaccination. On an unknown date, the patient received a dose of suspect STERILE WATER not produced by Sanofi Pasteur (lot number and expiration date not reported) via unknown route in an unknown administration site for prophylactic vaccination. It was an actual medication error due to Wrong solution used in drug reconstitution. No adverse event reported. It was reported "Caller wants to know if there are any issues with administering another dose. MD (Doctor of Medicine) is a pediatric infectious disease specialist, consulting as to how to manage the above situation. How do I approach properly vaccinating this child so she can go visit her family? When information was shared from the "Use of Alternate Diluents" SRD (system requirement document), he then asked, since it is a live vaccine, should there be an interval between the time of the improperly-reconstituted dose and a re-dose, such as 28 days?" 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.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Product preparation error
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
STERILE WATER
Allergien
-
Vorherige Impfungen
-

VAERS 1793474

SANOFI PASTEUR · YELLOW FEVER (YF-VAX) · Charge UJ386AA

gering
Staat
NY
Alter
1,3
Geschlecht
F
Eingang
16.10.2021
Impfdatum
05.10.2021
Beginn
05.10.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Product preparation error

Symptomtext

patient received the YF-VAX but the diluent that was used to reconstitute it was a sterile diluent which was taken from an MMR vaccine, with no adverse event;Initial information received on 07-Oct-2021 regarding an unsolicited valid non-serious case from a consumer/non-healthcare professional and physician via Media Information (under reference 00803170). This case involves a 1 years old female patient who received YELLOW FEVER VACCINE (YF-VAX) but the diluent that was used to reconstitute it was a sterile diluent which was taken from an MMR vaccine (product preparation error). Patient received no other vaccines as concomitant medication(s). The patient's medical history, medical treatment(s), past vaccination(s) and family history were not provided. On 05-Oct-2021, the patient received a 0.5 mL first dose of suspect YF-VAX (Total, lot UJ386AA and expiration date: 22-AUG-2022) via unknown route in an unknown administration site for prophylactic vaccination. It was an actual medication error due to Wrong diluent used (same day latency). It was reported "Caller states that a patient received the YF-VAX in her office on 05OCT2021 but the diluent that was used to reconstitute it was a sterile diluent which was taken from an MMR vaccine and not the diluent supplied with the YF-VAX. Caller wanted to know if that dose counted and how to proceed." At time of reporting, no adverse event 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
Product preparation error
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1719202

SANOFI PASTEUR · YELLOW FEVER (YF-VAX) · Charge uj386aa

gering
Staat
PA
Alter
29,0
Geschlecht
F
Eingang
21.09.2021
Impfdatum
18.08.2021
Beginn
18.08.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Incorrect route of product administration

Symptomtext

Vaccine should be administered subcutaneously, the vaccine was administered intramuscularly in error.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Incorrect route of product administration
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1663060

SANOFI PASTEUR · YELLOW FEVER (YF-VAX) · Charge UJ386AA

gering
Staat
DC
Alter
42,0
Geschlecht
F
Eingang
01.09.2021
Impfdatum
17.08.2021
Beginn
01.09.2021
Tage bis Beginn
15,0
Dosis
N/A
Route/Site
SC / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Medication error No adverse event

Symptomtext

No adverse advent, however reporting as a medication error due to other medications patient was on at the time of vaccination. Client states she has had no adverse events or side effects due to vaccination at the time of this report.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Medication error
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None noted
Vorgeschichte
Rheumatoid Arthritis
Andere Medikamente
Prednisone, Folic Acid, Estradiol, Medroxyprogesterone, Amitriptyline, Calcium, Vit. D, Rituxan
Allergien
Shellfish, sensitivity to Aspirin
Vorherige Impfungen
-

VAERS 1653404

SANOFI PASTEUR · YELLOW FEVER (YF-VAX) · Charge UJ386AA

gering
Staat
FL
Alter
-
Geschlecht
U
Eingang
29.08.2021
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 No adverse event

Symptomtext

Patient received a yellow fever vaccine intramuscular instead of subcutaneous with no adverse event; Initial information regarding an unsolicited valid non-serious case was received from other Health Professional. This case involves patient with unknown demography who received YELLOW FEVER VACCINE - US [YF-VAX] intramuscular instead of subcutaneous (incorrect route of product administration). The patient's medical history, past medical treatment(s), vaccination(s), concomitant medication and family history were not provided. On an unknown date, the patient received a dose of suspect YELLOW FEVER VACCINE - US (lot UJ386AA and expiry date was not reported) via intramuscular route at an unknown administration site instead of subcutaneous route for prophylactic vaccination (incorrect route of product administration). It was reported "Caller asked what, if anything, needed to be done". It was an actual medication error case due to inappropriate route of vaccination (latency: same day). At the time of reporting, the patient experienced 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 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 1641453

SANOFI PASTEUR · YELLOW FEVER (YF-VAX) · Charge UJ386AA

gering
Staat
AL
Alter
27,0
Geschlecht
M
Eingang
27.08.2021
Impfdatum
26.08.2021
Beginn
26.08.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
SC / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: unbekannt
Eye swelling Lip swelling

Symptomtext

-UNIT REPORTED LIPS SWOLLEN & EYES SWOLLEN TO MDG -SM DROVE TO URGENT CARE- GIVEN STERIOD SHOTS TOLD TO RETURN IN 1 HR IF SYMPTOMS CONTINUE CALLED SERVICE MEMBER AT 1214 TO CONFIRM IF HE WAS HAVING ADDITIONAL SYMPTOMS. URGENT CARE GAVE HIM FAST ACTING STERIOD AND INSTRUCTED HIM TO TAKE ZYRTEC THEN BENEDRYL EVERY 6 HRS

Weitere VAERSDATA-Felder
Praegender Schweregrund
Eye swelling
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
N/A
Vorgeschichte
N/A
Andere Medikamente
WORKOUT SUPPLEMENTS
Allergien
PCN, SULFA DRUGS
Vorherige Impfungen
-

VAERS 1532135

SANOFI PASTEUR · YELLOW FEVER (YF-VAX) · Charge UJ386AA

gering
Staat
VA
Alter
24,0
Geschlecht
F
Eingang
06.08.2021
Impfdatum
06.08.2021
Beginn
06.08.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Food allergy Gastrooesophageal reflux disease

Symptomtext

Client received typhoid and yellow fever vaccine. Client reports allergy to egg with "acid reflux" reaction. Client stated that she had received "egg based vaccines in the past without reaction". Client was made aware that she still could have reaction with yellow fever vaccine. Client wished to proceed with vaccination. Client telephoned clinic to report "severe acid reflux" "worst she has ever had" approximately 30 min after vaccine. Client was advised to report to nearest ER for evaluation and treatment. Client verbalizes understanding to this.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Food allergy
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
Allergy to eggs-causes acid reflux. Client states she is not treated routinely for this allergy
Vorherige Impfungen
-

VAERS 1489866

SANOFI PASTEUR · YELLOW FEVER (YF-VAX) · Charge UJ386AA

gering
Staat
TX
Alter
40,0
Geschlecht
M
Eingang
21.07.2021
Impfdatum
13.07.2021
Beginn
13.07.2021
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 Medication error No adverse event

Symptomtext

40 year old male patient administered expired diluent with no adverse event; Initial information received on 13-Jul-2021 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 40 year old male patient who was vaccinated with an expired diluent dose of suspect YELLOW FEVER VACCINE - US [YF-VAX]. Medical history, medical treatment, concomitant medication, vaccination and family history were not provided. On 13-Jul-2021, the patient received a 0.5 ml dose of suspect YELLOW FEVER VACCINE - US (lot number: UJ386AA and expiry date: 22-Aug-2022, Diluent Lot number: U6309AA and expiry date: 30-Jun-2021) (Frequency: once) via an subcutaneous route in the left arm (Expired product administered) for prophylactic vaccination. It was an actual medication error case due to Expired medical agent used (latency on same day). 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
-