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Reporte zur Charge UJ397AA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

17Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
PA 5 NV 2 SC 2 AZ 1 MI 1 MS 1 LA 1 WA 1 DC 1 IL 1 TX 1

VAERS 2198870

SANOFI PASTEUR · YELLOW FEVER (YF-VAX) · Charge UJ397AA

schwer
Staat
AZ
Alter
32,0
Geschlecht
F
Eingang
25.03.2022
Impfdatum
24.03.2022
Beginn
24.03.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
SC / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja
Anaphylactic reaction Chest pain Dyspnoea Odynophagia Urticaria

Symptomtext

Anaphylaxis about 15 minutes after the injections. Chest pain, shortness of breath, hives, pain with swallowing. She was given an EpiPen, put on oxygen, vital signs monitored and were stable. Patient was transported to a local emergency room. Recovered. Referred to allergist for further evaluation

Weitere VAERSDATA-Felder
Praegender Schweregrund
Anaphylactic reaction
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Anxiety, asthma, depression, GERD, hypothyroidism, IBS, migraine, osteopenia, Hashimoto's
Andere Medikamente
-
Allergien
Avocado, barley, Cabbage, codeine, cucumber, fish, grapefruit, Vicodin, milk, nuts, pair, pineapple, rye, shellfish, wheat, latex, see the med if in
Vorherige Impfungen
-

VAERS 2119699

SANOFI PASTEUR · YELLOW FEVER (YF-VAX) · Charge UJ397AA

mild
Staat
NV
Alter
-
Geschlecht
F
Eingang
09.07.2022
Impfdatum
10.02.2022
Beginn
11.02.2022
Tage bis Beginn
1,0
Dosis
1
Route/Site
SC / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Injection site erythema Injection site pruritus Injection site swelling Wrong technique in product usage process

Symptomtext

Menactra and YF-Vax administered on the same day in the same site as RabAvert; Redness; Swelling; Itchiness around injection site; Injection site erythema; injection site swelling; Case reference number US-BN-2022-000225, initially downloaded from Vaccine Adverse Event Reporting System (VAERS) on 07-Mar-2022, is a spontaneous case received from other health professional via health authority VAERS (Worldwide Unique Identifier 2119699-1) and concerns a 28-year-old female patient. The patient's medical history and concomitant medication details were not provided. On 10-Feb-2022, the patient was vaccinated with the first dose of RabAvert (inactivated rabies virus vaccine, batch number: ARBA911D), at an unknown dose, administered intramuscularly in the left arm and for unknown indication, with co-suspects Menactra (meningococcal vaccine, batch number: U7207AA) administered intramuscularly and YF-Vax (yellow fever vaccine, batch number: UJ397AA) administered subcutaneously, both at an unknown dose, administered in the left arm and for unknown indication (explicitly coded as 'Vaccination error'). On 11-Feb-2022, one day after the first dose, the patient experienced redness, swelling, itchiness around the injection site, injection site erythema and injection site swelling. At the time of this report, the patient was recovering from the events of 'redness', 'swelling', 'injection site erythema', 'injection site swelling' and 'injection site itching', reported as improving and only mildly itchy. The reporter assessed all the events as non-serious. Causality assessment was not provided. No further information was provided.; Reporter's Comments: A 28-year-old female patient was vaccinated with the first dose of RabAvert administered intramuscularly in the left arm along with co-suspects Menactra, administered intramuscularly and YF-Vax, administered subcutaneously, both administered at the same site, which is considered as vaccination error. One day after the first dose, the patient experienced erythema, swelling, injection site pruritus, injection site erythema and injection site swelling. Erythema, swelling, injection site pruritus, injection site erythema and injection site swelling are all listed for Rabipur according to Datasheet, whilst vaccination error is listed per company convention. The patient's medical history and concomitant medication details were not provided. Co-suspect vaccines Menactra and YF-Vax may have contributed to all reported events. However, having in mind the plausible temporal relationship and well known product safety profile, the causality for all reported events is assessed as related to Rabipur. Vaccination error is not related to Rabipur, but to a human factor. The case is non-serious.; Sender's Comments: A 28-year-old female patient was vaccinated with the first dose of RabAvert administered intramuscularly in the left arm along with co-suspects Menactra, administered intramuscularly and YF-Vax, administered subcutaneously, both administered at the same site, which is considered as vaccination error. One day after the first dose, the patient experienced erythema, swelling, injection site pruritus, injection site erythema and injection site swelling. Erythema, swelling, injection site pruritus, injection site erythema and injection site swelling are all listed for Rabipur according to Datasheet, whilst vaccination error is listed per company convention. The patient's medical history and concomitant medication details were not provided. Co-suspect vaccines Menactra and YF-Vax may have contributed to all reported events. However, having in mind the plausible temporal relationship and well known product safety profile, the causality for all reported events is assessed as related to Rabipur. Vaccination error is not related to Rabipur, but to a human factor. The case is non-serious.

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

VAERS 2119699

SANOFI PASTEUR · YELLOW FEVER (YF-VAX) · Charge UJ397AA

mild
Staat
NV
Alter
-
Geschlecht
F
Eingang
09.07.2022
Impfdatum
10.02.2022
Beginn
11.02.2022
Tage bis Beginn
1,0
Dosis
UNK
Route/Site
OT / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Injection site erythema Injection site pruritus Injection site swelling Wrong technique in product usage process

Symptomtext

Menactra and YF-Vax administered on the same day in the same site as RabAvert; Redness; Swelling; Itchiness around injection site; Injection site erythema; injection site swelling; Case reference number US-BN-2022-000225, initially downloaded from Vaccine Adverse Event Reporting System (VAERS) on 07-Mar-2022, is a spontaneous case received from other health professional via health authority VAERS (Worldwide Unique Identifier 2119699-1) and concerns a 28-year-old female patient. The patient's medical history and concomitant medication details were not provided. On 10-Feb-2022, the patient was vaccinated with the first dose of RabAvert (inactivated rabies virus vaccine, batch number: ARBA911D), at an unknown dose, administered intramuscularly in the left arm and for unknown indication, with co-suspects Menactra (meningococcal vaccine, batch number: U7207AA) administered intramuscularly and YF-Vax (yellow fever vaccine, batch number: UJ397AA) administered subcutaneously, both at an unknown dose, administered in the left arm and for unknown indication (explicitly coded as 'Vaccination error'). On 11-Feb-2022, one day after the first dose, the patient experienced redness, swelling, itchiness around the injection site, injection site erythema and injection site swelling. At the time of this report, the patient was recovering from the events of 'redness', 'swelling', 'injection site erythema', 'injection site swelling' and 'injection site itching', reported as improving and only mildly itchy. The reporter assessed all the events as non-serious. Causality assessment was not provided. No further information was provided.; Reporter's Comments: A 28-year-old female patient was vaccinated with the first dose of RabAvert administered intramuscularly in the left arm along with co-suspects Menactra, administered intramuscularly and YF-Vax, administered subcutaneously, both administered at the same site, which is considered as vaccination error. One day after the first dose, the patient experienced erythema, swelling, injection site pruritus, injection site erythema and injection site swelling. Erythema, swelling, injection site pruritus, injection site erythema and injection site swelling are all listed for Rabipur according to Datasheet, whilst vaccination error is listed per company convention. The patient's medical history and concomitant medication details were not provided. Co-suspect vaccines Menactra and YF-Vax may have contributed to all reported events. However, having in mind the plausible temporal relationship and well known product safety profile, the causality for all reported events is assessed as related to Rabipur. Vaccination error is not related to Rabipur, but to a human factor. The case is non-serious.; Sender's Comments: A 28-year-old female patient was vaccinated with the first dose of RabAvert administered intramuscularly in the left arm along with co-suspects Menactra, administered intramuscularly and YF-Vax, administered subcutaneously, both administered at the same site, which is considered as vaccination error. One day after the first dose, the patient experienced erythema, swelling, injection site pruritus, injection site erythema and injection site swelling. Erythema, swelling, injection site pruritus, injection site erythema and injection site swelling are all listed for Rabipur according to Datasheet, whilst vaccination error is listed per company convention. The patient's medical history and concomitant medication details were not provided. Co-suspect vaccines Menactra and YF-Vax may have contributed to all reported events. However, having in mind the plausible temporal relationship and well known product safety profile, the causality for all reported events is assessed as related to Rabipur. Vaccination error is not related to Rabipur, but to a human factor. The case is non-serious.

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

VAERS 2165473

SANOFI PASTEUR · YELLOW FEVER (YF-VAX) · Charge UJ397AA

mild
Staat
MI
Alter
6,0
Geschlecht
M
Eingang
08.03.2022
Impfdatum
04.03.2022
Beginn
04.03.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
SC / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja
Eye swelling Lip swelling Urticaria

Symptomtext

Father reported that child developed hives on neck and torso and mild swelling of lips and right eye at approximately 11:36am while shopping at a store. Father reported no breathing difficulties. Father reported that child was evaluated at the Emergency Room and was given medication and discharged home with a plan to follow-up with the Primary Care Physician.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Urticaria
Hospital-Tage
-
Labordaten
Per Father done through the Emergency Department.
Aktuelle Erkrankungen
None reported.
Vorgeschichte
None reported.
Andere Medikamente
None reported.
Allergien
None reported.
Vorherige Impfungen
-

VAERS 2128589

SANOFI PASTEUR · YELLOW FEVER (YF-VAX) · Charge UJ397AA

mild
Staat
MS
Alter
47,0
Geschlecht
F
Eingang
20.02.2022
Impfdatum
10.02.2022
Beginn
16.02.2022
Tage bis Beginn
6,0
Dosis
1
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Injection site erythema Injection site pruritus Injection site reaction Pyrexia Rash vesicular

Symptomtext

On Day of vaccine I felt fine. The next day my arm itches a little where vaccine was given. By the following week I went ahead and had my covid vaccine on Monday evening and developed a fever on Tuesday and by Wednesday where my yellow fever vaccine was given my arm had a bright red , very itchy and bubbly rash. I became nervous and took precautions by using cortizone10 otc cream and taking Benadryl. It itched worse and looked worse by Thursday.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site erythema
Hospital-Tage
-
Labordaten
None-
Aktuelle Erkrankungen
Had covid 3 weeks prior to shot
Vorgeschichte
Dm hypertension
Andere Medikamente
Met formin Bystolic Trulicity Alvorstorin Lisinopril Vitamin d Multi vitamin etc
Allergien
Latex
Vorherige Impfungen
-

VAERS 2028392

SANOFI PASTEUR · YELLOW FEVER (YF-VAX) · Charge uj397aa

mild
Staat
SC
Alter
21,0
Geschlecht
F
Eingang
12.01.2022
Impfdatum
05.01.2022
Beginn
07.01.2022
Tage bis Beginn
2,0
Dosis
1
Route/Site
SC / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Rash Urticaria

Symptomtext

Rash and urticaria covering arms, axilla, thighs and groin. Went to urgent care and received steroid taper and epi pen. Instructed to take benadryl at bedtime and allegra in the am. 1 week later rash improving but still present.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Rash
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
no
Vorgeschichte
no
Andere Medikamente
Adderal, Prozac, Ativan
Allergien
Latex, strawberries
Vorherige Impfungen
-

VAERS 1865338

SANOFI PASTEUR · YELLOW FEVER (YF-VAX) · Charge UJ397AA

mild
Staat
SC
Alter
1,1
Geschlecht
M
Eingang
12.11.2021
Impfdatum
12.11.2021
Beginn
12.11.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
SC / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Urticaria

Symptomtext

Father called clinic stating the child had hives all over his body. Stated there was no swelling on face/lips/or near airway and that child was not having difficulty breathing. Advised to contact child's pediatrician for guidance on if and how much BENADRYL is safe for the child, and to call 911 if he notices any of the aforementioned swelling or difficulty breathing.

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

VAERS 1821351

SANOFI PASTEUR · YELLOW FEVER (YF-VAX) · Charge UJ397AA

mild
Staat
PA
Alter
24,0
Geschlecht
F
Eingang
27.10.2021
Impfdatum
21.10.2021
Beginn
27.10.2021
Tage bis Beginn
6,0
Dosis
N/A
Route/Site
SC / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Erythema Pruritus Swelling

Symptomtext

Itchy, Raised reddened area 3 cm x 2.5 cm .

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pruritus
Hospital-Tage
-
Labordaten
n/a
Aktuelle Erkrankungen
denies
Vorgeschichte
denies
Andere Medikamente
denies
Allergien
denies
Vorherige Impfungen
-

VAERS 2465317

SANOFI PASTEUR · YELLOW FEVER (YF-VAX) · Charge UJ397AA

gering
Staat
LA
Alter
-
Geschlecht
U
Eingang
30.09.2022
Impfdatum
01.09.2022
Beginn
01.09.2022
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 Medication error No adverse event

Symptomtext

receiving expired YF-VAX, with no reported adverse event; Initial information received on 22-Sep-2022 regarding an unsolicited valid non-serious case received from a pharmacist. This case involves 3 patients of unknown age and unknown gender who was receiving expired YELLOW FEVER VACCINE - [YF-VAX], with no reported adverse event. The patient's past medical history, medical treatment(s), Concomitant medication, vaccination(s) and family history were not provided. Patients received the vaccine between 20-Sep-2022 and 21-Sep-2022, with an unknown dose of suspect YELLOW FEVER VACCINE - (strength, formulation was unknown, lot UJ397AA and expiry date: 22-Sep-2022) via unknown route in unknown administration site for Immunization. On 20-Sep-2022 and 21-Sep-2022 the patient developed a non-serious event of receiving expired yf-vax, with no reported adverse event (expired product administered) (latency: same day or 1 day) following the administration of YELLOW FEVER VACCINE - . Reporter was asking if the patients needed to be re-vaccinated and when they should be re-vaccinated. 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 2440271

SANOFI PASTEUR · YELLOW FEVER (YF-VAX) · Charge UJ397AA

gering
Staat
WA
Alter
-
Geschlecht
U
Eingang
12.09.2022
Impfdatum
24.08.2022
Beginn
24.08.2022
Tage bis Beginn
0,0
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

This situation is reported as a medication error due to giving an expired product with no reported adverse event; Initial information received on 25-Aug-2022 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a patient of unknown demographics who was treated with YELLOW FEVER VACCINE - [YF-VAX] and it was reported that this situation is reported as a medication error due to giving an expired product with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 24-Aug-2022, the patient received an unknown dose of suspect YELLOW FEVER VACCINE (formulation, strength, route: unknown) lot UJ397AA, expiration date:22-Aug-2022, in unknown administration site as Immunization. On 24-AUG-2022 this situation is reported as a medication error due to giving an expired product with no reported adverse event (expired product administered) same day following the administration of YELLOW FEVER VACCINE. Nurse manager was calling to find out if an expired dose of YF-VAX was given to a patient would that count as a valid dose? The nurse did not have any patient information available at this time. Action taken was not applicable. It was not reported if the patient received a corrective treatment for the event (This situation is reported as a medication error due to giving an expired product with no reported adverse event). 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 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
Expired product administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2375273

SANOFI PASTEUR · YELLOW FEVER (YF-VAX) · Charge UJ397AA

gering
Staat
DC
Alter
5,0
Geschlecht
M
Eingang
21.07.2022
Impfdatum
20.07.2022
Beginn
20.07.2022
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

Symptomtext

Patient was given Yellow Fever vaccine on 07/20/2022 but a later search of his vaccine record showed that he had received the Yellow Fever vaccine on 03/3/2020. There are no symptoms being reported yet by the parents. However, wanted to be informed about what to do next if possible.

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 2020332

SANOFI PASTEUR · YELLOW FEVER (YF-VAX) · Charge UJ397AA

gering
Staat
IL
Alter
20,0
Geschlecht
F
Eingang
10.01.2022
Impfdatum
-
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
No adverse event Product preparation error

Symptomtext

This case involves a 20 years old female patient who was administered with wrong diluent was used for the yellow fever vaccine/used sterile water rather than sodium chloride with no reported adverse event while receiving vaccine YELLOW FEVER VACCINE - US [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 a dose of 0.5 ml once of suspect YELLOW FEVER VACCINE - US (of unknown formulation, strength) lot UJ397AA, expiration date: 22-Oct-2022), in unknown administration site. On an unknown date the patient developed a non-serious event "wrong diluent was used for the yellow fever vaccine/used sterile water rather than sodium chloride and administered to a patient with no reported adverse event" (product reconstitution quality issue) same day following the administration of YELLOW FEVER VACCINE - US. It was reported" Caller reported the wrong diluent was used for the YELLOW FEVER VACCINE. Caller reported they used sterile water rather than sodium chloride and administered to a patient. Caller wanted to know if there are any repercussions or if they need to re-vaccinate the patient." Action taken with YELLOW FEVER VACCINE (YF-VAX) was not applicable. It was not reported if the patient received a corrective treatment for the event (wrong diluent was used for the Yellow Fever Vaccine/used sterile water rather than sodium chloride and administered to a patient with no reported adverse event). At time of reporting, the outcome was Unknown for the event wrong diluent was used for the yellow fever vaccine/used sterile water rather than sodium chloride and administered to a patient with no reported adverse event.

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

VAERS 1887859

SANOFI PASTEUR · YELLOW FEVER (YF-VAX) · Charge UJ397AA

gering
Staat
TX
Alter
42,0
Geschlecht
F
Eingang
20.11.2021
Impfdatum
-
Beginn
05.11.2021
Tage bis Beginn
-
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

she gave the vaccine to a patient when it was mixed with sterile water instead of the diluent that was needed with no reported AE; Initial information received on 05-Nov-2021 regarding an unsolicited valid non-serious case received from a physician via Medical Information number: 00845695. This case involves a 42 years old female patient who received YELLOW FEVER VACCINE - US [YF-VAX] mixed with sterile water instead of the diluent that was needed (product preparation error). The patient's medical history, medical treatments, vaccinations, concomitant medications and family history were not provided. On an unknown date, the patient received a 0.5 ml dose of suspect YELLOW FEVER VACCINE - US lot number: UJ397AA and expiry date not reported via subcutaneous route in the left arm for prophylactic vaccination. It was case of an actual medication error due to Wrong solution used in drug reconstitution (latency: 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
Medication error
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1761653

SANOFI PASTEUR · YELLOW FEVER (YF-VAX) · Charge UJ397AA

gering
Staat
PA
Alter
27,0
Geschlecht
M
Eingang
05.10.2021
Impfdatum
01.10.2021
Beginn
01.10.2021
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
SC / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
No adverse event Product preparation error

Symptomtext

This was a vaccine error, not an adverse reaction. The nurse reconstituted yellow fever with sterile water instead of sodium chloride. According to the CDC and Sanofi Pasteur this error renders the vaccine ineffective. Patient notified and made aware.

Weitere VAERSDATA-Felder
Praegender Schweregrund
No adverse event
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
Allopurinol, Sildenafil Citrate
Allergien
None
Vorherige Impfungen
-

VAERS 1761591

SANOFI PASTEUR · YELLOW FEVER (YF-VAX) · Charge UJ397AA

gering
Staat
PA
Alter
27,0
Geschlecht
F
Eingang
05.10.2021
Impfdatum
01.10.2021
Beginn
01.10.2021
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
SC / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Drug ineffective No adverse event Product preparation error Vaccination error

Symptomtext

This was a vaccine error, not an adverse event. The nurse reconstituted yellow fever with sterile water instead of the sodium chloride. According to CDC and Sanofi Pasteur this renders the vaccine ineffective. Patient notified and aware.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Drug ineffective
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None
Allergien
None
Vorherige Impfungen
-

VAERS 1761523

SANOFI PASTEUR · YELLOW FEVER (YF-VAX) · Charge UJ397AA

gering
Staat
PA
Alter
28,0
Geschlecht
F
Eingang
05.10.2021
Impfdatum
01.10.2021
Beginn
01.10.2021
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
SC / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Product preparation error

Symptomtext

This was a vaccine error, not an adverse event. The nurse reconstituted yellow fever with sterile water instead of sodium chloride. According to CDC and Sanofi Pasteur this renders the vaccine ineffective. Patient notified and aware.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Product preparation error
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None
Allergien
Food allergy= shellfish (onset 2019)
Vorherige Impfungen
-

VAERS 1761469

SANOFI PASTEUR · YELLOW FEVER (YF-VAX) · Charge UJ397AA

gering
Staat
PA
Alter
28,0
Geschlecht
M
Eingang
05.10.2021
Impfdatum
01.10.2021
Beginn
01.10.2021
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
SC / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Drug ineffective No adverse event Product preparation error

Symptomtext

This was a vaccine error. The nurse reconstituted yellow fever with sterile water instead of sodium chloride. According to CDC and Sanofi Pasteur there are no side effects. The vaccine is now ineffective. Patient notified and aware.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Drug ineffective
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None
Allergien
None
Vorherige Impfungen
-