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Reporte zur Charge UT7695MA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

12Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
NY 3 PR 1 SC 1 MO 1 IL 1 RI 1 MI 1 NC 1 OH 1 TX 1

VAERS 2538992

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7695MA

schwer
Staat
PR
Alter
92,0
Geschlecht
M
Eingang
21.12.2022
Impfdatum
14.10.2022
Beginn
31.10.2022
Tage bis Beginn
17,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Guillain-Barre syndrome Malaise

Symptomtext

Patient reports that approximately 15 days he attended his primary doctor because he did not feel well and received a diagnosis from Guillain-Barr?.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Guillain-Barre syndrome
Hospital-Tage
-
Labordaten
Not available.
Aktuelle Erkrankungen
Patient refers does not suffer from any health condition.
Vorgeschichte
Refers patient does not suffer from any condition.
Andere Medikamente
Patient did not report medication at time of interview.
Allergien
Patient refers no allergies.
Vorherige Impfungen
-

VAERS 2502602

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7695MA

moderat
Staat
SC
Alter
41,0
Geschlecht
F
Eingang
09.11.2022
Impfdatum
07.11.2022
Beginn
07.11.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Condition aggravated Restless legs syndrome

Symptomtext

Severe RLS triggered in legs and arms

Weitere VAERSDATA-Felder
Praegender Schweregrund
Condition aggravated
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
Hypothyroidism
Vorgeschichte
RLS
Andere Medikamente
Tirosint 88mcg
Allergien
No
Vorherige Impfungen
-

VAERS 2505493

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7695MA

mild
Staat
MO
Alter
17,0
Geschlecht
F
Eingang
10.11.2022
Impfdatum
07.11.2022
Beginn
08.11.2022
Tage bis Beginn
1,0
Dosis
UNK
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Erythema Pain in extremity Peripheral swelling Pruritus

Symptomtext

red raised area on arm about 4 x 4 inches sore to the touch, arm was itchy

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pain in extremity
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None
Vorgeschichte
Diabetes hypothyroidism
Andere Medikamente
None
Allergien
No Known
Vorherige Impfungen
-

VAERS 2502066

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7695MA

mild
Staat
IL
Alter
11,0
Geschlecht
M
Eingang
08.11.2022
Impfdatum
08.11.2022
Beginn
08.11.2022
Tage bis Beginn
0,0
Dosis
6
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Fatigue Malaise

Symptomtext

The patient was present at the school base center for his 11-year-old well exam. MCV4 and TDaP given. Patient did not feel well. Positioned patient supine with HOB slightly elevated and legs up. Patient able to respond verbally. Patient feeling well and states normal within few minutes. Able to drink water and snack. Patient and mother reviewed risks and occurrence. Consented to continue vaccines. Positioned in supine, HOB up, talking throughout vaccines, HPV and Flu given. Felt tired. Legs up again. Symptoms resolved after few minutes. Maintained position HOB slightly elevated and supine for 15 minutes. No orthostatic hypotension with BP checks positionally. Pulse and pulse ox remained stable.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Fatigue
Hospital-Tage
-
Labordaten
BP, pulse, pulse ox normal
Aktuelle Erkrankungen
None - Mother reported the child was not sick and feeling well prior to receiving the vaccines.
Vorgeschichte
Learning disability
Andere Medikamente
None
Allergien
Fish containing products
Vorherige Impfungen
-

VAERS 2500507

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7695MA

mild
Staat
NY
Alter
7,0
Geschlecht
F
Eingang
07.11.2022
Impfdatum
25.10.2022
Beginn
25.10.2022
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Injection site reaction Local reaction No reaction on previous exposure to drug Urticaria

Symptomtext

Several hours after vaccine administered, patient developed local reaction at site and diffuse hives. Was given dose of Benadryl at home and hives resolved. No other symptoms developed and had no residual hives the following day. Of note, patient has received Quadrivalent Influenza vaccine several times in past (2021, 2017, 2016) without any reaction.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site reaction
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
Upper respiratory symptoms for 2-3 days - runny nose, congestion and cough; possible wheezing
Vorgeschichte
Asthma, food allergies, eczema, alopecia areata
Andere Medikamente
Asmanex, albuterol
Allergien
Egg, milk, soy, peanut, dog, cat; note, has never eaten eggs before so reaction unknown (has avoided since positive blood test at age 2)
Vorherige Impfungen
-

VAERS 2496983

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7695MA

mild
Staat
RI
Alter
30,0
Geschlecht
F
Eingang
02.11.2022
Impfdatum
24.10.2022
Beginn
24.10.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Dizziness

Symptomtext

Patient received vaccine while sitting and leaned over stating she felt lightheaded. No fainting occured BP 86/54 P-70. Rapid response team took over and checked vitals.

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

VAERS 2496763

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7695MA

mild
Staat
MI
Alter
9,0
Geschlecht
F
Eingang
02.11.2022
Impfdatum
31.10.2022
Beginn
01.11.2022
Tage bis Beginn
1,0
Dosis
UNK
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Vaccination site erythema Vaccination site pain Vaccination site pruritus Vaccination site warmth

Symptomtext

Starting 11/1/2022, child developed an increasing area of redness around the vaccination site, to 10 x 12 cm circular area with intense redness, warmth, no induration. This progressed despite starting Amoxicillin for her right otitis media on the same day the redness started. The area was itchy, only painful if prodded. It was treated with a combination of Benadryl orally and topical antibiotic.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Vaccination site pain
Hospital-Tage
-
Labordaten
None.
Aktuelle Erkrankungen
URI and right otitis media
Vorgeschichte
Obesity, esotropia, allergic rhinitis
Andere Medikamente
None
Allergien
None known
Vorherige Impfungen
local vaccine reaction to something as a baby

VAERS 2477288

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge UT7695MA

mild
Staat
NY
Alter
13,0
Geschlecht
F
Eingang
17.10.2022
Impfdatum
12.10.2022
Beginn
12.10.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja
Erythema Injection site rash Pruritus Urticaria Hypersensitivity Rash pruritic

Symptomtext

Per pt / mother child Started having itching rash( hives) in thigh 3 hrs after office visit Rash was spreading : mother gave benadryl with no improvement . Mother call EMS The rash spread to most parts of body leading to ER visit No other symptoms : no itchy/ tingly throat/ no chest pain or SOB no palpitations , no dizziness no other symptoms per pt In ER per mother child was observed : found to have rash Around The injection site for flu. She was given an injection ( probably epinephrine) with good resolution Of rash . She was observed for another > 1 hr and then discharged. Discharge diagnosis : allergic reaction etio ? Per mother possibly to flu vaccine ( no discharge notes/ papers available in

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

VAERS 2539435

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7695MA

gering
Staat
NC
Alter
2,0
Geschlecht
M
Eingang
21.12.2022
Impfdatum
07.12.2022
Beginn
07.12.2022
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Extra dose administered No adverse event

Symptomtext

Per the report, the patient was due for this year's flu vaccine. Consent was obtained from the parent and the form was signed. I drew up the Fluzone vaccine and upon entry to the room, obtained the patient's name and date of birth and verified the vaccine. When I went to enter the administered vaccine to our EMR, I observed that a flu vaccine was administered on 11/8/2022 but was not documented in system. However, signed consent for that date was present in the patient's EHR. I informed the provider and my immediate supervisors. I spoke with RN from our Immunizations Department...who advised that the patient was at risk to develop a high fever and that ibuprofen was recommended to be used every 6-8 hours, at least three times. I informed the parent of the error and how it occurred. The patient was kept for approximately 30 minutes after the vaccine and showed no noticeable signs of a reaction. Patient was alert, oriented, had a good demeanor, was breathing and playing well and skin appeared within normal limits. I relayed the recommmendations for ibuprofen use for the next 24 hours, parent demonstrated understanding. I called and followed up with parent on 12/8/22 who stated that she did not use ibuprofen since the patient did not develop a fever and the injection site looked fine, the patient was also playing and acting well.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Extra dose administered
Hospital-Tage
-
Labordaten
NONE
Aktuelle Erkrankungen
FEBRILE SEIZURE, RIGHT EAR AOM, AND INFLUENZA ON 11/2/2022
Vorgeschichte
ABNORMAL HIGH LEAD LEVEL IN BLOOD, BRADYCARDIA
Andere Medikamente
NONE
Allergien
NKDA
Vorherige Impfungen
-

VAERS 2524123

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7695MA

gering
Staat
OH
Alter
9,0
Geschlecht
F
Eingang
06.12.2022
Impfdatum
02.12.2022
Beginn
02.12.2022
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Expired product administered No adverse event

Symptomtext

The vaccination given was expired by 2 days. Given on 12/2/2022 and expired on 11/30/2022. No adverse reaction occurred. Reported to Pfizer and waiting to hear back if vaccination needs to be repeated.

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

VAERS 2513682

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7695MA

gering
Staat
TX
Alter
0,8
Geschlecht
F
Eingang
22.11.2022
Impfdatum
10.11.2022
Beginn
10.11.2022
Tage bis Beginn
0,0
Dosis
2
Route/Site
OT / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Inappropriate schedule of product administration No adverse event

Symptomtext

Patient received the FLUZONE QIV NP vaccine 3 weeks apart instead of 4 weeks apart, with no reported adverse event; Initial information received on 14-Nov-2022 regarding an unsolicited valid non-serious case received from an other health professional. This case involves a 10 months old female patient who received the influenza quadrival A-B [Fluzone Quadrivalent] vaccine 3 weeks apart instead of 4 weeks apart, with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s), concomitant disease or risk factor and family history were not provided. On 10-Nov-2022, the patient received dose 2 of suspect influenza quadrival A-B Vaccine suspension for injection with unknown strength (lot: UT7695MA, expiry date: 30-Jun-2023) via intramuscular route in the right vastus lateralis for Immunization, 3 weeks apart instead of 4 weeks apart with no reported adverse event (inappropriate schedule of product administration). Action taken was 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
Inappropriate schedule of product administration
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2500516

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7695MA

gering
Staat
NY
Alter
5,0
Geschlecht
M
Eingang
07.11.2022
Impfdatum
27.10.2022
Beginn
27.10.2022
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Underdose

Symptomtext

None; dose given was for younger age group than recommended based on patient's age

Weitere VAERSDATA-Felder
Praegender Schweregrund
Underdose
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
Cold symptoms within 2 weeks prior to vaccination
Vorgeschichte
None
Andere Medikamente
Zyrtec
Allergien
Dog, cat, dust
Vorherige Impfungen
-