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Reporte zur Charge UT7065MA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

3Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
OH 1 IN 1

VAERS 917932

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7065MA

mild
Staat
OH
Alter
35,0
Geschlecht
F
Eingang
03.01.2021
Impfdatum
12.10.2020
Beginn
12.10.2020
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Arthralgia

Symptomtext

PATIENT REPORTS EXPERIENCING SHOOTING PAIN ALL OVER HER ELBOW. PATIENT VISITED FAMILY PHYSICIAN WHO RECOMMENDED PHYSICAL THERAPY. SHE STATES THAT SHE THINKS SHOT WAS GIVEN TOO HIGH. (PHARMACIST WHO ADMINISTERED SHOT WAS CAREFUL AND BELIEVES SHOT PLACEMENT WAS CORRECT (2-3 FINGERS BELOW SHOULDER), HOWEVER, PATIENT IS STILL HAVING PAIN.)

Weitere VAERSDATA-Felder
Praegender Schweregrund
Arthralgia
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
NO KNOWN HEALTH CONDITIONS
Vorgeschichte
NO KNOWN HEALTH CONDITIONS
Andere Medikamente
NO KNOWN MEDICATIONS
Allergien
PENICILLIN
Vorherige Impfungen
-

VAERS 2128206

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7065MA

gering
Staat
IN
Alter
21,0
Geschlecht
F
Eingang
19.02.2022
Impfdatum
01.02.2022
Beginn
01.02.2022
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 Exposure during pregnancy No adverse event

Symptomtext

pregnant female received expired Fluzone with no reported adverse event.; pregnant female received expired Fluzone with no reported adverse event.; Initial information received on 10-Feb-2022 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 21 years old female patient who was exposed to vaccine INFLUENZA QUADRIVAL A-B VACCINE [FLUZONE QIV] in and pregnant female received expired fluzone with no reported adverse event at unknown gestation period<<the gestation period at onset and gestation period at exposure data needs to be populated, if available. The date of last menstrual period was not reported. The estimated due date was not reported. The actual date of delivery was not reported. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. The patient had unknown previous pregnancy/ies. On an unknown date of February 2022, the patient received a dose of suspect INFLUENZA QUADRIVAL A-B VACCINE Suspension for injection (lot UT7065MA and expiration date: 30-Jun-2021) once via unknown route in unknown administration site a prophylactic vaccination. In FEB-2022, the patient developed a non-serious event "pregnant female received expired fluzone with no reported adverse event" (exposure during pregnancy)(expired product administered) (latency: same day) following the administration of INFLUENZA QUADRIVAL A-B VACCINE. Action taken with QUADRIVALENT INFLUENZA VACCINE (FLUZONE QIV) was not applicable. It was not reported if the patient received a corrective treatment for the events (pregnant female received expired Fluzone with no reported adverse event., pregnant female received expired Fluzone with no reported adverse event.). At time of reporting, the outcome was Unknown for the event pregnant female received expired fluzone with no reported adverse event. and was Unknown for the event pregnant female received expired fluzone with no reported adverse event.. Additionally, at time of reporting, the outcome of the pregnancy is unknown.

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

VAERS 1337142

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7065MA

gering
Staat
-
Alter
0,5
Geschlecht
M
Eingang
21.05.2021
Impfdatum
21.05.2021
Beginn
21.05.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
No adverse event Product administered to patient of inappropriate age Wrong product administered

Symptomtext

no adverse reaction, pt was given the wrong vaccine pt was given PPV 23 and pt was supposed to be given PCV 13

Weitere VAERSDATA-Felder
Praegender Schweregrund
No adverse event
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
administered the wrong vaccination but no harm to pt
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-