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Reporte zur Charge UT7330JA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

5Reporte angezeigt
0Todesfaelle
1Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
FL 2 TX 2 SC 1

VAERS 2014367

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7330JA

schwer
Staat
FL
Alter
19,0
Geschlecht
M
Eingang
07.01.2022
Impfdatum
30.12.2021
Beginn
30.12.2021
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja
Blood glucose Full blood count Laboratory test Metabolic function test Seizure

Symptomtext

Parent report shortly after leaving the physicians office, patient had a seizure in the car. Patient has a history of seizure disorder. Patient was taken to the emergency room for evaluation and was discharge later that same day in stable condition.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Seizure
Hospital-Tage
-
Labordaten
Lab work done (CBC, CMP, Glucose)
Aktuelle Erkrankungen
-
Vorgeschichte
Seizure Disorder Autism
Andere Medikamente
Lamictal 100mg Adderall XR 20mg Adderall 10mg
Allergien
None
Vorherige Impfungen
-

VAERS 1801431

SEQIRUS, INC. · INFLUENZA (SEASONAL) (FLUAD QUADRIVALENT) · Charge UT7330JA

moderat
Staat
FL
Alter
16,0
Geschlecht
F
Eingang
20.10.2021
Impfdatum
29.09.2021
Beginn
30.09.2021
Tage bis Beginn
1,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Chest X-ray normal Electrocardiogram T wave abnormal Sinus tachycardia Tachycardia

Symptomtext

Tachycardia for 24 hours after administration of vaccines. Patient went to ER following day.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Sinus tachycardia
Hospital-Tage
-
Labordaten
EKG 9/30/2021 - sinus tachycardia, nonspecific t-wave abnormality CXR 9/30/2021 - normal
Aktuelle Erkrankungen
NONE
Vorgeschichte
NONE
Andere Medikamente
NONE
Allergien
ANTS
Vorherige Impfungen
-

VAERS 1761388

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7330JA

moderat
Staat
SC
Alter
36,0
Geschlecht
F
Eingang
05.10.2021
Impfdatum
29.09.2021
Beginn
29.09.2021
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: ja
Activated partial thromboplastin time Blood thyroid stimulating hormone normal Brain natriuretic peptide normal Communication disorder Computerised tomogram head normal Full blood count normal Hypoaesthesia Influenza A virus test negative Influenza B virus test International normalised ratio normal Magnetic resonance imaging head normal Magnetic resonance imaging spinal normal Metabolic function test Mobility decreased Pregnancy test negative Prothrombin time normal SARS-CoV-2 test negative Troponin normal

Symptomtext

Symptoms: patient reported right arm numbness, difficulty moving right arm, blurred vision and difficulty speaking in full sentences - these occurred within 45 minutes of receiving the flu vaccine. Treatment: neurology consultation, CT of head, MRI of brain and spine, IV fluids, Benadryl IV, Compazine IV, lovenox subq., admission to hospital

Weitere VAERSDATA-Felder
Praegender Schweregrund
Mobility decreased
Hospital-Tage
2,0
Labordaten
CBC, PT, INT and PTT, troponin, BNP, pregnancy, TSH, CMP, UA and swabs for Flu, A & B, and COVID - all of these test were within normal range or negative. CT of head and MRI of brain and cervical spine- were both negative, within normal range. Within 24 hours there was significant improvement of symptoms. Patient reported no previous allergies to any vaccines; this was her first flu shot.
Aktuelle Erkrankungen
unknown
Vorgeschichte
Unknown
Andere Medikamente
Unknown
Allergien
None known
Vorherige Impfungen
-

VAERS 2606610

SEQIRUS, INC. · INFLUENZA (SEASONAL) (FLUAD QUADRIVALENT) · Charge UT7330JA

mild
Staat
TX
Alter
62,0
Geschlecht
F
Eingang
30.03.2023
Impfdatum
30.12.2021
Beginn
31.12.2021
Tage bis Beginn
1,0
Dosis
N/A
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Arthralgia Joint range of motion decreased Magnetic resonance imaging Pain in extremity

Symptomtext

Patient reported extreme pain in her shoulder and arm, decreased range of motion.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Arthralgia
Hospital-Tage
-
Labordaten
MRI - May 2022
Aktuelle Erkrankungen
-
Vorgeschichte
SCOLIOSIS OSTEOPENIA ESTROGEN DEFICIENCY
Andere Medikamente
MULTIVITAMINS CALCIUM WITH VIT D
Allergien
NKDA
Vorherige Impfungen
-

VAERS 1923109

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7330JA

gering
Staat
TX
Alter
-
Geschlecht
F
Eingang
04.12.2021
Impfdatum
22.11.2021
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
OT / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Medication error No adverse event Wrong product administered

Symptomtext

This case involves a 77-year-old female patient who received an INFLUENZA QUADRIVAL A-B VACCINE [FLUZONE QUADRIVALENT], intended vaccine was INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE [FLUZONE HIGH-DOSE QUADRIVALENT] (wrong product administered). The patient's medical history, medical treatment(s), vaccination(s) and family history were not provided. No other concomitant vaccines. On 22-Nov-2021, the patient received a dose of suspect FLUZONE QUADRIVALENT (0.5 ml, total, once, lot UT7330JA and expiration date: 30-Jun-2022) via intramuscular route in the left deltoid for prophylactic vaccination. It was an actual medication error due to wrong vaccine administered (same day latency). No adverse event reported. 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. 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
Medication error
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-