Zurueck zur Suche

Reporte zur Charge UJ563AA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

15Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
CA 6 CO 1 IN 1 SC 1 AZ 1 KY 1 MD 1 OR 1 NJ 1 MN 1

VAERS 2314560

SANOFI PASTEUR · YELLOW FEVER (YF-VAX) · Charge UJ563AA

moderat
Staat
CO
Alter
47,0
Geschlecht
F
Eingang
09.06.2022
Impfdatum
07.06.2022
Beginn
07.06.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Dyspepsia Dyspnoea Ear discomfort Eustachian tube dysfunction Hypersensitivity Hypoacusis Nasal congestion Paranasal sinus inflammation Tympanic membrane disorder

Symptomtext

within 10 minutes nasal stuffiness began, and was unable to take full breaths through nose but was able to breathe normally through mouth; used Asmanex inhaler and felt some relief, figured it was an anxiety response, given history; woke next morning with ear pressure and inability to hear clearly; call to allergist indicated need to visit urgent care; urgent care physician confirmed allergic response to something and diagnosed "1. Allergic reaction, initial encounter T78.40XA and 2. Dysfunction of both eustachian tubes H69.83 tube dysfunction and mentioned in notes "TM clear. White. Air-fluid level noted. Somewhat bulging. Immobile to Valsalva", prescribed a return to oral prednisone already on hand for allergic reactions, an increase to double of normal dose of xyzal, add zantac, and add Astelin spray; next morning (~36 hours after vax) ear pressure had not decreased, and gastric distress (reminiscent of the worst case experienced when my entire body was inflamed before getting under the care of an allergist) had begun. At this time, ~50 hours post vax, inflammation in sinuses, nasal cavity, ear canals remain and are same or worse than when began meds to control, digestive is decreasing with use of H2 blocker, anti-inflammatory diet, and quality probiotic

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dyspnoea
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
none
Vorgeschichte
lifetime history of reactions to medications before PEG allergy diagnosis, and to those listed above which do not contain PEG, none to vaccines in past; history of chronic episodic systemic inflammation in multiple systems for past 5 years, avoidance of diagnosed allergens has made recurrence of inflammation less frequent, but has not eliminated unexplained episodes, and has not lessened their severity; inflammation was fully under control and zero symptoms in advance of this vaccine, by design, and in fact appointment was previously postponed twice until such a time as zero symptoms were present
Andere Medikamente
xyzal
Allergien
Phenergan, Demerol, polyethylene glycol (PEG), "fragrance mix", chocolate, almonds
Vorherige Impfungen
-

VAERS 2522059

SANOFI PASTEUR · YELLOW FEVER (YF-VAX) · Charge UJ563AA

mild
Staat
IN
Alter
45,0
Geschlecht
F
Eingang
02.12.2022
Impfdatum
17.11.2022
Beginn
30.11.2022
Tage bis Beginn
13,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Headache Muscle twitching Musculoskeletal stiffness Nausea

Symptomtext

neck stiffness, mild nausea, slight headache and occasional slight twitching in both hands

Weitere VAERSDATA-Felder
Praegender Schweregrund
Headache
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
none known
Vorgeschichte
Asthma
Andere Medikamente
Albuterol
Allergien
-
Vorherige Impfungen
-

VAERS 2469728

SANOFI PASTEUR · YELLOW FEVER (YF-VAX) · Charge UJ563AA

mild
Staat
SC
Alter
25,0
Geschlecht
M
Eingang
05.10.2022
Impfdatum
29.09.2022
Beginn
01.10.2022
Tage bis Beginn
2,0
Dosis
1
Route/Site
SC / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Injection site pruritus Injection site rash

Symptomtext

Per patient, he has had a rash at the injection site since 9/26 and complains of it itching. Denies any fever, night sweats, chills, loss of appetite, diarrhea, or nausea and vomiting.

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

VAERS 2414894

SANOFI PASTEUR · YELLOW FEVER (YF-VAX) · Charge UJ563AA

mild
Staat
AZ
Alter
25,0
Geschlecht
F
Eingang
18.08.2022
Impfdatum
09.08.2022
Beginn
09.08.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
SC / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Inflammation Injection site erythema Injection site pain Oropharyngeal discomfort Pain Pharyngeal swelling Pyrexia

Symptomtext

Client called office 8/11/22 to review adverse reactions of vaccines received 8/9/22. Reports throat swelling 75 min after vaccine administration. Treated at home with benadryl and inhaler. States there is improvement but throat still feels a little "funny" also reports low grade fever and achiness with reddness/tenderness at YF injection site. Encouraged to call PCP that day to let them know what happened so she could have a physical examination and see if they'd like to do anything else. Discussed immune responses vs allergic reactions. Client speaking in complete sentences and doesn't sound to have any difficulty breathing over the phone. Called client to follow up 8/18/22, she did get into see PCP, monitoring at this time, slight inflammation noted per MD. No further inventions at this time as well. Will go back 8/19/22.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site erythema
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None reported
Vorgeschichte
None reported
Andere Medikamente
adderall 5mg TID daysee 90 day birth control once daily zofran 4mg PRN
Allergien
Childhood food allergies noted but pt states that she has grown out of and can consume all food now without difficulty
Vorherige Impfungen
-

VAERS 2405926

SANOFI PASTEUR · YELLOW FEVER (YF-VAX) · Charge UJ563AA

mild
Staat
KY
Alter
72,0
Geschlecht
F
Eingang
09.08.2022
Impfdatum
04.08.2022
Beginn
05.08.2022
Tage bis Beginn
1,0
Dosis
1
Route/Site
SC / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Feeling hot Injection site discomfort Injection site erythema Injection site warmth

Symptomtext

"The day after, I noticed a little red cluster of red dots at the site, the next day it got bigger, the next day it got bigger and it continued to get bigger each day. Now it looks like a raspberry stain with redness around the edges, longer than it is wide and not uniform, it is irregularly shaped. I have minor discomfort at site of injection that comes and goes. The area is not hot to touch. Today I felt warm, my temperature was 98.6 however my normal temperature is 97.6. More air conditioning for comfort than usual." No treatment at this time. Outcome- will monitor the injection site and contact us of any changes or new concerning signs/symptoms.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site discomfort
Hospital-Tage
-
Labordaten
None at this time.
Aktuelle Erkrankungen
None
Vorgeschichte
Asthma Rosaceaa Vitamin D deficiency Pre-diabetic
Andere Medikamente
Zyrtec pm Montelukast pm Glucosamine with Chrondroitin am Vitamin D 10,000IU am Vitamin B12 am Azelaic acid gel 15% for rosacea on nose Symbicort in am 80 for asthma Fluticasone nasal spray in am Weekly allergy shot- had injection 2 days pr
Allergien
Sulfa- "rash/abdominal skin blotches" Breo Inhaler "pharyngitis and infection in throat"
Vorherige Impfungen
Typhoid oral- wheezing requiring nebulizer treatment

VAERS 2396537

SANOFI PASTEUR · YELLOW FEVER (YF-VAX) · Charge UJ563AA

mild
Staat
MD
Alter
33,0
Geschlecht
F
Eingang
29.07.2022
Impfdatum
20.07.2022
Beginn
29.07.2022
Tage bis Beginn
9,0
Dosis
1
Route/Site
SC / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Rash Rash erythematous

Symptomtext

She states she has developed a small non-pustule rash on her arms, legs, torso. She describes the rash as pale pink edges with white color in the middle. She states her injection site at YF developed same presentation several days after vaccination. She denies any itching, shortness of breath, hives, chest pain, swelling

Weitere VAERSDATA-Felder
Praegender Schweregrund
Rash
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
LO LOESTRIN FE (ETHINYL ESTRADIOL; NORETHINDRONE ACETATE) ESCITALOPRAM (ESCITALOPRAM OXALATE)
Allergien
NKA
Vorherige Impfungen
-

VAERS 2586015

SANOFI PASTEUR · YELLOW FEVER (YF-VAX) · Charge UJ563AA

gering
Staat
OR
Alter
-
Geschlecht
U
Eingang
23.02.2023
Impfdatum
27.01.2023
Beginn
27.01.2023
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 No adverse event Product preparation error

Symptomtext

yellow fever vaccine was mixed with a sterile diluent instead of the diluent that came with the vaccine with no reported adverse event; Initial information received on 27-Jan-2023 regarding an unsolicited valid non-serious case received from a other health professional. This case involves an unknown age and unknown gender patient to whom who given yellow fever vaccine - [YF-VAX] that was mixed with a sterile diluent instead of the diluent that came with the vaccine with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. Concomitant medications included typhoid vaccine (TYPHIM) for Immunisation. On 27-Jan-2023, the patient received 0.5 ml once (1X) (total) dose of suspect yellow fever vaccine, solution for injection (strength; not reported; lot UJ563AA; ,Expiration Date :23-May-2023) via subcutaneous route in the left arm for Immunization was mixed with a sterile diluent instead of the diluent that came with the vaccine with no reported adverse event (product preparation error) (latency; same day). 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
Medication error
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
TYPHIM
Allergien
-
Vorherige Impfungen
-

VAERS 2450443

SANOFI PASTEUR · YELLOW FEVER (YF-VAX) · Charge UJ563AA

gering
Staat
NJ
Alter
0,8
Geschlecht
M
Eingang
17.09.2022
Impfdatum
07.09.2022
Beginn
07.09.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Medication error No adverse event Poor quality product administered Product storage error

Symptomtext

YF-VAX had an excursion and were administered to a patient, with no reported adverse event; YF-VAX had an excursion and were administered to a patient, with no reported adverse event; Initial information received on 08-Sep-2022 regarding an unsolicited valid non-serious case received from a nurse. GMI number: 01270287 This case involves a 9-month-old male patient who had YELLOW FEVER VACCINE - [YF-VAX] after excursion 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, nurse reported yf-vax had an excursion (product storage error). On 07-Sep-2022, the patient received suspect YF-VAX vaccine post excursion at dose 0.5 ml once via subcutaneous route in the left leg (lot UJ563AA, expiry date: 23-May-2023) for prophylactic vaccination with no reported adverse event (poor quality product administered) same day latency. It was not the first time of product use. At time of report, product was not in use. It was reported that "Nurse called to report that her YF-VAX had an excursion and were administered to a patient. Nurse also wants to know if they need to revaccinate and if they could return or reimburse the vaccines. Nurse also confirmed stability information just to make sure she has right info. Agent advised nurse to contact customer service with regards to replacement and reimbursement. Agent provided contact details." Action taken: Not applicable. At time of reporting, the outcome was Unknown for both events. 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
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2408279

SANOFI PASTEUR · YELLOW FEVER (YF-VAX) · Charge UJ563AA

gering
Staat
CA
Alter
-
Geschlecht
M
Eingang
11.08.2022
Impfdatum
15.07.2022
Beginn
15.07.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Product preparation issue

Symptomtext

dose of YF-Vax that was incorrectly reconstituted with sterile water instead of the sodium chloride diluent provided with the product with no reporter; Initial information received on 04-Aug-2022 regarding an unsolicited valid non-serious case received from health professional. Agency number: 01222412 This case involves a 43-year-old male patient to whom dose of YELLOW FEVER VACCINE - [YF-VAX] was administered that was incorrectly reconstituted with sterile water instead of the sodium chloride diluent provided with the product with no reported. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. Concomitant medications included TYPHOID VACCINE (TYPHOID VACCINE) for Prophylactic vaccination; and RABIES VACCINE (RABIES VACCINE) for Prophylactic vaccination. On 15-Jul-2022, the patient received dose of yf-vax that was incorrectly reconstituted with sterile water instead of the sodium chloride diluent provided at dose 0.5 ml once (lot UJ563AA) via unknown route in right arm for Immunization with no reported (product preparation error, latency same day). A medical assistant administered the vaccine. A staff member accidently combined it. First time product used : Yes 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 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 issue
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
TYPHOID VACCINE; RABIES VACCINE
Allergien
-
Vorherige Impfungen
-

VAERS 2408300

SANOFI PASTEUR · YELLOW FEVER (YF-VAX) · Charge UJ563AA

gering
Staat
CA
Alter
27,0
Geschlecht
M
Eingang
10.08.2022
Impfdatum
21.07.2022
Beginn
21.07.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Product preparation issue

Symptomtext

Yellow fever vaccine was reconstituted using the incorrect diluent (sterile water) and administered to patient. Sanofi Pasteur (manufacturer) was consulted and notified.

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

VAERS 2403069

SANOFI PASTEUR · YELLOW FEVER (YF-VAX) · Charge UJ563AA

gering
Staat
CA
Alter
27,0
Geschlecht
M
Eingang
05.08.2022
Impfdatum
21.07.2022
Beginn
21.07.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Product preparation error

Symptomtext

The Yellow Fever vaccine was reconstituted with the incorrect diluent (sterile water) and administered to the patient.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Product preparation error
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None
Allergien
Sulfa antibiotics
Vorherige Impfungen
-

VAERS 2372133

SANOFI PASTEUR · YELLOW FEVER (YF-VAX) · Charge UJ563AA

gering
Staat
CA
Alter
-
Geschlecht
U
Eingang
18.07.2022
Impfdatum
-
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
No adverse event Wrong product administered

Symptomtext

received a dose of saline instead of the yellow fever vaccine with no reported adverse event; Initial information received on 11-Jul-2022 regarding an unsolicited valid non-serious case received from a physician. GMI number: 01184725 This case involves an unknown age and unknown gender patient who experienced received a dose of SALINE [SODIUM CHLORIDE] instead of the YELLOW FEVER VACCINE - [YF-VAX] vaccine with no reported adverse event. The patient's past medical history, medical treatment(s), concomitant medication, vaccination(s) and family history were not provided. This case is linked to cases 2022SA279048, 2022SA276277 and 2022SA278093. On an unknown date, the patient took Saline [Sodium Chloride] at (unknown: strength, formulation, dose, frequency, batch number and expiry date) for unknown indication. On an unknown date, the patient received a dose of suspect YELLOW FEVER VACCINE - (with an unknown strength, formulation, frequency, batch number and expiry date) via unknown route in unknown administration site for Immunization. On an unknown date, the patient developed a non-serious event of received a dose of saline instead of the yellow fever vaccine with no reported adverse event (wrong product administered) (latency: unknown). 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 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
No adverse event
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2371893

SANOFI PASTEUR · YELLOW FEVER (YF-VAX) · Charge UJ563AA

gering
Staat
CA
Alter
-
Geschlecht
U
Eingang
16.07.2022
Impfdatum
-
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
No adverse event Wrong product administered

Symptomtext

a single family member of 4 that received a dose of saline instead of the yellow fever vaccine with no reported Adverse event; Initial information received on 11-Jul-2022 regarding an unsolicited valid non-serious case received from a physician. Agency number: 01184696 This case involves an unknown age and unknown gender patient who experienced received a dose of SALINE [SODIUM CHLORIDE] instead of the YELLOW FEVER VACCINE - [YF-VAX] vaccine with no reported adverse event. The patient's past medical history, medical treatment(s), concomitant medication, vaccination(s) and family history were not provided. This case is linked to cases 2022SA278536, 2022SA278093 and 2022SA276277. On an unknown date, the patient took Saline [Sodium Chloride] at (unknown: strength, formulation, dose, frequency, batch number and expiry date) for unknown indication. On an unknown date, the patient received a dose of suspect YELLOW FEVER VACCINE at lot: UJ563AA, expiry: 23-May-2023 (with an unknown strength, formulation, frequency) via unknown route in unknown administration site for Immunization. On an unknown date, the patient developed a non-serious event of received a dose of saline instead of the yellow fever vaccine with no reported adverse event (wrong product administered) (latency: unknown). 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
No adverse event
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
SODIUM CHLORIDE
Allergien
-
Vorherige Impfungen
-

VAERS 2371892

SANOFI PASTEUR · YELLOW FEVER (YF-VAX) · Charge UJ563AA

gering
Staat
CA
Alter
-
Geschlecht
U
Eingang
16.07.2022
Impfdatum
-
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Wrong product administered

Symptomtext

has a problem with a single family member of 4 that received a dose of saline instead of the yellow fever vaccine with no reported adverse event; Initial information received on 10-Jul-2022 regarding an unsolicited valid non-serious case received from a physician. This case involves an unknown age and unknown gender patient, reportedly has a problem with a single family member of 4 that received a dose of sodium chloride (Saline) instead of the YELLOW FEVER VACCINE - [YF-VAX] 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 unknown dose of suspect YELLOW FEVER VACCINE (strength, formulation, route, frequency: unknown) (lot: UJ563AA and expiry date: 23-May-2023) in unknown administration site for Immunization. On an unknown date, the patient started taking sodium chloride (strength, formulation, route, frequency, dose: unknown) (with an unknown batch number and expiry date). On an unknown date the patient developed a non-serious event, has a problem with a single family member of 4 that received a dose of saline instead of the yellow fever vaccine with no reported adverse event (wrong product administered) (unknown latency). It was reported, after hours call received at 12:10pm on 10jul2022. Doctor states that he has a problem with a single family member of 4 that received a dose of saline instead of the yellow fever vaccine. "Do I need to give a dose to every family member?" After hours call returned at 12:30pm on 10jul2022. Caller states that a family of 4 came in and introspect he counted the vials and determined that probably they gave one of the 4-member saline only and not the yellow fever vaccine. "Do I need to repeat the dose for all 4?" Do you know where they can receive a yellow fever titer?" What happens if they receive an extra dose?" Action taken with YELLOW FEVER VACCINE (YF-VAX) and SODIUM CHLORIDE (SODIUM CHLORIDE) was 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 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
Wrong product administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
SODIUM CHLORIDE
Allergien
-
Vorherige Impfungen
-

VAERS 2309808

SANOFI PASTEUR · YELLOW FEVER (YF-VAX) · Charge uj563aa

gering
Staat
MN
Alter
-
Geschlecht
M
Eingang
06.06.2022
Impfdatum
26.05.2022
Beginn
26.05.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Incorrect route of product administration No adverse event

Symptomtext

administered the YF-VAX intramuscularly instead of subcutaneously with no reported adverse event; Initial information received on 26-May-2022 regarding an unsolicited valid non-serious case received from a other health professional via call center. This case involves a 42 years old male patient who reported administered the yf-vax intramuscularly instead of subcutaneously 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. Concomitant medications included Typhoid Vaccine (Typhoid) for Immunisation. On 26-May-2022, the patient received a 0.5 ml dose of suspect yellow fever vaccine - US lot uj563aa, expiry date: 23-May-2023, unknown strength and formulation, frequency: once, via intramuscular route in the left deltoid for prophylactic vaccination. On 26-MAY-2022 the patient developed a non-serious event administered the yf-vax intramuscularly instead of subcutaneously with no reported adverse event (incorrect route of product administration) (latency: same day) following the administration of yellow fever vaccine. Action taken was not applicable. It was not reported if the patient received a corrective treatment for the event (incorrect route of product administration). At time of reporting, the outcome was Unknown for the event incorrect route of product administration. 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 regulatory agency. 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
-