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Reporte zur Charge UT7741 LA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

14Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
CA 4 CO 3 IL 2 NY 1 NM 1 VA 1 WA 1

VAERS 2475754

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7741LA

schwer
Staat
CO
Alter
31,0
Geschlecht
F
Eingang
11.10.2022
Impfdatum
11.10.2022
Beginn
11.10.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Blood glucose normal Blood pressure increased Dizziness Heart rate increased Syncope Tremor

Symptomtext

Patient reported light headedness and a feeling of syncope soon after vaccination. Patient experienced shakiness. Blood pressure increased to 145/90, pulse increased to 135. After sitting pulse and blood pressure returned to normal. No injection site reaction no external signs of allergic reaction. No medication administered. Patient was given water, and transported to ER as requested by patient.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
Blood pressure = 145/90, returned to normal after sitting for about 30 minutes Pulse = 135 , returned to normal after sitting for 30 minutes Blood glucose within normal range
Aktuelle Erkrankungen
None reported
Vorgeschichte
None reported
Andere Medikamente
None reported
Allergien
Sulfa, tetracycline, IV iron, tree nuts
Vorherige Impfungen
-

VAERS 2499745

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE) · Charge UT7741 LA

moderat
Staat
CA
Alter
25,0
Geschlecht
F
Eingang
05.11.2022
Impfdatum
14.10.2022
Beginn
14.10.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Fatigue Heart rate increased Off label use Palpitations Product use issue Wrong product administered

Symptomtext

This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 25-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 14Oct2022 at 14:45 as dose 1, single (Lot number: GJ375) at the age of 25 years, in left arm for covid-19 immunisation; influenza vaccine (FLUZONE [INFLUENZA VACCINE]), on 14Oct2022 as dose 1, single (Lot number: UT7741 LA), in left arm. The patient didn't receive BNT162b2 (BNT162B2). The patient's relevant medical history included: "Asthma" (unspecified if ongoing); "ADHD" (unspecified if ongoing); "Known allergies: dairy" (unspecified if ongoing); "Covid" (unspecified if ongoing). Concomitant medication(s) included: CLARITIN [LORATADINE]; ADDERALL; XOPENEX; LORYNA. Past drug history included: Aspirin, reaction(s): "Known allergies". The following information was reported: OFF LABEL USE (non-serious), PRODUCT USE ISSUE (non-serious) all with onset 14Oct2022, outcome "unknown" and all described as "Other vaccine same date product: Fluzone"; WRONG PRODUCT ADMINISTERED (non-serious) with onset 14Oct2022 at 14:45, outcome "unknown", described as "Dose received: 1/ Is bivalent=True"; FATIGUE (non-serious) with onset 17Oct2022 at 07:15, outcome "recovering", described as "Extreme fatigue"; HEART RATE INCREASED (non-serious) with onset 17Oct2022 at 07:15, outcome "recovering", described as "Fast heart rate"; PALPITATIONS (non-serious) with onset 17Oct2022 at 07:15, outcome "recovering". The events "fast heart rate", "palpitations" and "extreme fatigue" required physician office visit and emergency room visit. Therapeutic measures were not taken as a result of heart rate increased, palpitations, fatigue. Additional information: Patient did not receive any other vaccines within 4 week prior vaccination and had not been tested for COVID-19 since vaccination. The information on the batch/lot number for BNT162b2 has been requested and will be submitted if and when received.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Palpitations
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: ADHD; Asthma; COVID-19; Milk allergy
Andere Medikamente
CLARITIN [LORATADINE]; ADDERALL; XOPENEX; LORYNA
Allergien
-
Vorherige Impfungen
-

VAERS 2487494

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge ut7741la

moderat
Staat
CA
Alter
34,0
Geschlecht
F
Eingang
24.10.2022
Impfdatum
24.10.2022
Beginn
24.10.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Cold sweat Nausea Paraesthesia Vomiting

Symptomtext

patient felt little nausea, tingling on both arms, cold sweat, vomiting.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Paraesthesia
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
no per patien
Vorgeschichte
gastritis per patient
Andere Medikamente
no prescription meds but take probiotic per patient
Allergien
allergic to mitrex and penicillin. per patient
Vorherige Impfungen
-

VAERS 2480356

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7741LA

mild
Staat
NY
Alter
3,0
Geschlecht
F
Eingang
17.10.2022
Impfdatum
14.10.2022
Beginn
14.10.2022
Tage bis Beginn
0,0
Dosis
4
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Injection site swelling Injection site urticaria Pyrexia Urticaria

Symptomtext

Friday night she had a 103 fever, mother administered Tylenol and fever resolved. She had started with hives around the shot site, raised welted hive at injection site that started to spread. Mother gave Benadryl and she woke up the next morning no fever but was covered in hives from head to toe. Mother gave her more Benadryl when she had woken up that morning. Hives would go away slightly but would come back when the Benadryl wore off. She went to an urgent care, they prescribed prednisolone for her. It helped with the hives but then it almost made the hives worse.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site swelling
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
She was sick with nasal congestion on and off up to one month prior. Most likely seasonal allergies
Vorgeschichte
No
Andere Medikamente
No
Allergien
Allergy to amoxicillin
Vorherige Impfungen
Her flu vaccine last year she had a reaction to as well

VAERS 2479863

SEQIRUS, INC. · INFLUENZA (SEASONAL) (FLUAD QUADRIVALENT) · Charge UT7741LA

mild
Staat
NM
Alter
64,0
Geschlecht
F
Eingang
16.10.2022
Impfdatum
14.10.2022
Beginn
14.10.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Contusion Erythema Pain in extremity Pruritus

Symptomtext

Pt received a flu immunization on 10-14-22 at 11 am in her left arm. Later that evening, her arm felt itchy , sore, and bruised. She has received yearly flu shots in the past with no incident. The red patch of skin seems to be growing. She had not taken anything to help with the pain or itching. I recommended benadryl. She can not take ibuprofen. Patient will follow up with her doctor tomorrow if there is no improvement.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pain in extremity
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
Nothing acute.
Vorgeschichte
Asthma, Arthritis, Renal Disease, Hypercholesterolemia
Andere Medikamente
Alendronate, Famotidine, Advair, Allopurinol, Oxybutynin, Atorvastatin, Montelukast,
Allergien
None reported.
Vorherige Impfungen
-

VAERS 2478603

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7741LA

mild
Staat
CA
Alter
63,0
Geschlecht
F
Eingang
14.10.2022
Impfdatum
11.10.2022
Beginn
11.10.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Cough Headache Pain Respiratory tract congestion Wheezing

Symptomtext

Patient calls on 10/14/2022 to report Rxn @ 5:30 PM same day as vaccination. Sudden onset HA 6/10 pain Congestion Wheezing (due to cough) Coughing ~2 hrs. persisted till midnight-1 am declines swelling/rash/itching took expired Sudafed before bed Some congestion the next day, then all sxs resolved.

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

VAERS 2466945

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7741LA

mild
Staat
-
Alter
58,0
Geschlecht
F
Eingang
02.10.2022
Impfdatum
02.10.2022
Beginn
02.10.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Rash Rash pruritic

Symptomtext

Itchy Rash on Left Forearm

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

VAERS 2631586

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7741LA

gering
Staat
CA
Alter
11,0
Geschlecht
M
Eingang
12.05.2023
Impfdatum
20.03.2023
Beginn
20.03.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Expired product administered No adverse event

Symptomtext

The Pfizer bivalent vaccine which was given on 3/20/23 had a before use date of 12/22/22. No symptoms were shown.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
n/a
Aktuelle Erkrankungen
N/a
Vorgeschichte
No
Andere Medikamente
N/A
Allergien
No know allergies
Vorherige Impfungen
-

VAERS 2622415

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7741LA

gering
Staat
IL
Alter
0,8
Geschlecht
F
Eingang
27.04.2023
Impfdatum
20.04.2023
Beginn
20.04.2023
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Incorrect product formulation administered

Symptomtext

Administered Moderna Bivalent Dark pink cap (yellow label) after being notified that monovalent covid vaccines were no longer authorized. Was administered prior to recommendation of using dark blue Moderna bivalent cap (gray label). Patient received one monovalent Moderna in the past and on this day received her 2nd dose as Moderna Dark Pink cap.

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

VAERS 2622402

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7741LA

gering
Staat
IL
Alter
0,8
Geschlecht
F
Eingang
27.04.2023
Impfdatum
18.04.2023
Beginn
18.04.2023
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Unevaluable event

Symptomtext

Administered Moderna Bivalent Dark pink cap (yellow label) after being notified that monovalent covid vaccines were no longer authorized. Was administered prior to recommendation of using dark blue Moderna bivalent cap (gray label)

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

VAERS 2525644

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7741LA

gering
Staat
VA
Alter
16,0
Geschlecht
M
Eingang
07.12.2022
Impfdatum
07.12.2022
Beginn
-
Tage bis Beginn
-
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Extra dose administered No adverse event

Symptomtext

Patient already received the flu shot on 11/7/22 and another dose again on 12/7/22 by accident. He was observed for 15min in the office and no adverse events were noted.

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 2481973

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7741LA

gering
Staat
CO
Alter
52,0
Geschlecht
F
Eingang
18.10.2022
Impfdatum
18.10.2022
Beginn
18.10.2022
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Extra dose administered No adverse event

Symptomtext

Patient received a second dose of influenza vaccine, she received first dose one week prior. NO adverse events reported, no treatment warranted.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Extra dose administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
Vertigo listed on consent form
Vorgeschichte
Vertigo
Andere Medikamente
-
Allergien
no
Vorherige Impfungen
-

VAERS 2476633

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7741LA

gering
Staat
CO
Alter
9,0
Geschlecht
F
Eingang
12.10.2022
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: unbekannt Erholt: nein
Expired product administered

Symptomtext

Vaccine was pulled from our fridge with a BUD date of 10/31 and administered. Later that day we received a notice from our corporate that the lot used was short-dated by the manufacturer and expired on 9/30 regardless of when it was placed in our fridge.

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

VAERS 2462536

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7741LA

gering
Staat
WA
Alter
52,0
Geschlecht
F
Eingang
27.09.2022
Impfdatum
27.09.2022
Beginn
27.09.2022
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
SC / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Incorrect route of product administration

Symptomtext

Both vaccines appeared to have been given subcutaneously as they were not near the patient's deltoid. Vaccines were re-administered. Patient appeared satisified with resolution.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Incorrect route of product administration
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
None known
Vorgeschichte
Asthma
Andere Medikamente
None known
Allergien
Yeast
Vorherige Impfungen
-