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Reporte zur Charge UT8038MA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

6Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
TX 1 KY 1 CA 1 OH 1

VAERS 2685452

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT8038MA

schwer
Staat
TX
Alter
39,0
Geschlecht
F
Eingang
22.09.2023
Impfdatum
22.09.2023
Beginn
22.09.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Impaired driving ability Presyncope Slow response to stimuli

Symptomtext

Patient received 3 shots of vaccines. Boostrix in the left arm, Fluzone Quad and Engerix-B in the right arm. After the boostrix, patient started to pass out. I checked her pulse. She was breathing normally and conscious. She was responsive but not fully. I gave her 10 ml of benadryl (25mg). Patient stayed in the imz booth with a technician for 15 minutes. Patient relative came and picked her up because she did not fill comfortable to drive home. Called patient 4 hours later to check on her. She said she took a nap and was perfectly fine now.

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

VAERS 2691632

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT8038MA

mild
Staat
KY
Alter
50,0
Geschlecht
F
Eingang
05.10.2023
Impfdatum
22.09.2023
Beginn
24.09.2023
Tage bis Beginn
2,0
Dosis
UNK
Route/Site
OT / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Abdominal pain Diarrhoea Muscle spasms

Symptomtext

severe diarrhea; severe abdominal pain,still some cramping today; Initial information received on 26-Sep-2023 regarding an unsolicited valid non-serious case received from a consumer/non-healthcare professional. This case involves a 50 years old female patient who experienced severe diarrhea and severe abdominal pain,still some cramping today after receiving vaccine influenza quadrival A-B vaccine [Fluzone Quadrivalent]. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 22-Sep-2023, the patient received a dose of suspect Influenza Quadrival A-B Vaccine Suspension for injection expiry date: 30-Jun-2024 lot UT8038MA via unknown route in the left arm for Immunisation. On 24-SEP-2023 the patient developed severe diarrhea (diarrhoea) and severe abdominal pain,still some cramping today (abdominal pain) 2 days following the administration of Influenza Quadrival A-B Vaccine. Reportedly, she received on Friday, 22Sep2023 and by Sunday at 4 AM she had severe diarrhea and severe abdominal pain. She almost went to the Emergency Room but just ate a liquid diet. She had improvement yesterday but still some cramping today and can at least eat some solids today. Action taken was not applicable. It was not reported if the patient received a corrective treatment for the events severe diarrhea, severe abdominal pain,still some cramping today. At time of reporting, the outcome was Recovering / Resolving for the event severe diarrhea and severe abdominal pain,still some cramping today.

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

VAERS 2683120

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT8038MA

mild
Staat
CA
Alter
45,0
Geschlecht
F
Eingang
18.09.2023
Impfdatum
16.09.2023
Beginn
17.09.2023
Tage bis Beginn
1,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Injection site pruritus Injection site rash Injection site swelling Somnolence

Symptomtext

Pt reported swelling and itchy at injection site, feel sleepy than usual, reported rash only at injection site, reported no shortness of breath and chest pain. Pt has taken antihistamine at the morning of symptoms started next day. Reported the symptoms has getting better but not much.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site pruritus
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
none
Vorgeschichte
asthma
Andere Medikamente
Lansoprazole , Baclofen, Norethrindrone, Synthroid, Advair HFA
Allergien
demedrol, methadone, zantac
Vorherige Impfungen
-

VAERS 2696021

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT8038MA

gering
Staat
OH
Alter
-
Geschlecht
U
Eingang
14.10.2023
Impfdatum
-
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Circumstance or information capable of leading to medication error No adverse event Underdose

Symptomtext

patient pulled away and the full dose was not given. when the patient pulled away, the vaccine leaked out of the syringe and was not administered with no reported adverse event; Initial information received on 09-Oct-2023 regarding an unsolicited valid non-serious case received from a pharmacist. This case involves a patient of an unknown age and gender and reporter reported that the patient pulled away and the full dose was not given. when the patient pulled away, the Influenza Quadrival A-B Vaccine [Fluzone Qiv] leaked out of the syringe and was not administered 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 a unknown dose of suspect Influenza Quadrival A-B Vaccine Suspension for injection (strength: unknown, expiry date: Jun-2024 and lot UT8038MA) via unknown route in unknown administration site as Influenza and patient pulled away and the full dose was not given. when the patient pulled away, the vaccine leaked out of the syringe and was not administered with no reported adverse event (incorrect dose administered) (same day latency). 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.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Circumstance or information capable of leading to medication error
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2690321

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT8038MA

gering
Staat
-
Alter
7,0
Geschlecht
F
Eingang
03.10.2023
Impfdatum
30.09.2023
Beginn
30.09.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Extra dose administered No adverse event Wrong product administered

Symptomtext

administration error - 2 flu vaccines administered instead of 1 flu vaccine and 1 covid vaccine. No adverse events occurred due to the error.

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

VAERS 2690321

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT8038MA

gering
Staat
-
Alter
7,0
Geschlecht
F
Eingang
03.10.2023
Impfdatum
30.09.2023
Beginn
30.09.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Extra dose administered No adverse event Wrong product administered

Symptomtext

administration error - 2 flu vaccines administered instead of 1 flu vaccine and 1 covid vaccine. No adverse events occurred due to the error.

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