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Reporte zur Charge UT7701LA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

6Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
MI 1 ND 1 OH 1 IL 1 WV 1 MA 1

VAERS 2504566

GLAXOSMITHKLINE BIOLOGICALS · INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) · Charge UT7701LA

moderat
Staat
MI
Alter
54,0
Geschlecht
F
Eingang
10.11.2022
Impfdatum
18.10.2022
Beginn
18.10.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
SYR / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Chest X-ray Cough Dyspnoea Fatigue Nasal congestion Oropharyngeal pain Pyrexia Respiratory tract infection Rhinorrhoea

Symptomtext

Fever, chronic cough, fatigue, trouble breathing, runny nose, stuffy nose, sore throat, . Went to the Dr was reported I had a respiratory infection.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dyspnoea
Hospital-Tage
-
Labordaten
chest x ray
Aktuelle Erkrankungen
none
Vorgeschichte
-
Andere Medikamente
Multi vitamin Vitamin C Zinc
Allergien
none known
Vorherige Impfungen
-

VAERS 2497660

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7701LA

mild
Staat
ND
Alter
41,0
Geschlecht
F
Eingang
03.11.2022
Impfdatum
28.09.2022
Beginn
29.10.2022
Tage bis Beginn
31,0
Dosis
UNK
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Acne Ear pain Erythema Eye swelling Headache Parotitis Skin warm Swelling face

Symptomtext

24 hours after vaccination swelling began on the right jawline. It started a roll under the skin. It progressed to ear and ear was painful. Client went to the clinic 10/31/22 for the ear pain. She also had a acne breakout on forehead on her right forehead on the day of vaccination too. FNP thought it was swelling due to vaccine and recommended watchful waiting. 11/1/22 client developed sever HA for whole head which OTC analgesics did not help. 11/2/22 swelling increased to include all of right face including eye. No swelling to L side noted. Went back in to clinic 11/2/22 and was started on metronidazole and levofloxacin for paroditis. Swelling continued and client returned to Health facility later the same day and got a steroid injection. Swelling has not improved. Redness is noted on the forehead area since 10/28/22 and at the jawline on 10/31/22.Client has no fever,. Skin is warm where the redness is.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Ear pain
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
cold symptoms 2 week prior to vaccination
Vorgeschichte
Diabetic, HTN, PCLS,
Andere Medikamente
victoza 0.6 u, 20 insulin glargine, 1,000 mg Metformin, procardia 30 mg, gabapentin 100 mg, zinc,
Allergien
sulfa, pcn, starlex
Vorherige Impfungen
-

VAERS 2586390

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge ut7701la

gering
Staat
OH
Alter
10,0
Geschlecht
M
Eingang
23.02.2023
Impfdatum
13.10.2022
Beginn
13.10.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Product administered to patient of inappropriate age

Symptomtext

dtap vaccine was inadvertently given to a 10 year old

Weitere VAERSDATA-Felder
Praegender Schweregrund
Product administered to patient of inappropriate age
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
unknown
Vorgeschichte
denies
Andere Medikamente
Unknown
Allergien
denies
Vorherige Impfungen
-

VAERS 2548890

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7701LA

gering
Staat
IL
Alter
38,0
Geschlecht
F
Eingang
03.01.2023
Impfdatum
17.10.2022
Beginn
17.10.2022
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Bursitis

Symptomtext

Patient began experiencing anterior right deltoid pain 2 hours after receiving the flu vaccine. The pain continued in the following days with certain movements and she had symptom improvement with NSAID use. She was diagnosed with post-injection bursitis two weeks post-injection and prescribed methylprednisolone along with modified activity with some improvement. An MRI 2 months post-injection showed bursitis and partial rotator cuff wear and tear. Physical therapy was recommended.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Bursitis
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
No known allergies.
Vorherige Impfungen
-

VAERS 2526270

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7701LA

gering
Staat
WV
Alter
16,0
Geschlecht
M
Eingang
08.12.2022
Impfdatum
29.11.2022
Beginn
29.11.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Extra dose administered No adverse event

Symptomtext

Patient received 2 doses of the product FLUZONE QIV NP in a span of 5 weeks with no adverse event; Initial information was received on 01-Dec-2022 regarding an unsolicited valid non-serious case received from a other health professional. This case involves 16 years old male patient who stated received 2 doses of the product fluzone qiv np in a span of 5 weeks with no adverse event after receiving influenza quadrival A-B vaccine [Fluzone QIV]. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 29-Nov-2022, the patient received 0.5 ml dose of suspect influenza quadrival A-B vaccine (Suspension for injection) (lot: UT7701LA, expiry date: 30-Jun-2023, strength: standard frequency: total) via intramuscular route in right deltoid for Immunization. On 29-Nov-2022 the patient developed a non-serious event of event patient received 2 doses of the product fluzone qiv np in a span of 5 weeks with no adverse event (extra dose administered) (Latency: same day) following the administration of influenza quadrival A-B vaccine. Action taken: not applicable. It was not reported if the patient received a corrective treatment for the 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 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. Additional information was received on 02-Dec-2022 from other health professional: Classification, Therapy start date, frequency, Dose, Location, Route, New event (extra dose administered) were updated. Text amended accordingly.

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

VAERS 2462008

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7701LA

gering
Staat
MA
Alter
70,0
Geschlecht
F
Eingang
27.09.2022
Impfdatum
22.09.2022
Beginn
01.09.2022
Tage bis Beginn
-
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Wrong product administered

Symptomtext

Patient received Fluzone Quadrivalent vaccine instead of Fluzone High-Dose Quadrivalent. Patient was notified on 9/27/22 after the error had been discovered. Patient was directed to consult with her healthcare provider to determine whether an additional vaccine would be recommended. Patient reported that she felt fine following the vaccination and didn't have any ill effects.

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