Vafseo

Țară: Uniunea Europeană

Limbă: engleză

Sursă: EMA (European Medicines Agency)

Cumpara asta acum

Descarcare Prospect (PIL)
05-03-2024

Ingredient activ:

Vadadustat

Disponibil de la:

Akebia Europe Limited

INN (nume internaţional):

vadadustat

Grupul Terapeutică:

Antianemic preparations

Zonă Terapeutică:

Renal Insufficiency, Chronic; Anemia

Indicații terapeutice:

Vafseo is indicated for the treatment of symptomatic anaemia associated with chronic kidney disease (CKD) in adults on chronic maintenance dialysis.

Statutul autorizaţiei:

Authorised

Data de autorizare:

2023-04-24

Prospect

                                31
B. PACKAGE LEAFLET
32
PACKAGE LEAFLET: INFORMATION FOR THE PATIENT
VAFSEO
150 MG FILM-COATED TABLETS
VAFSEO 300 MG FILM-COATED TABLETS
VAFSEO 450 MG FILM-COATED TABLETS
vadadustat
This medicine is subject to additional monitoring. This will allow
quick identification of new
safety information. You can help by reporting any side effects you may
get. See the end of section 4
for how to report side effects.
READ ALL OF THIS LEAFLET CAREFULLY BEFORE YOU START TAKING THIS
MEDICINE BECAUSE IT CONTAINS
IMPORTANT INFORMATION FOR YOU.
-
Keep this leaflet. You may need to read it again.
-
If you have any further questions, ask your doctor, or pharmacist.
-
This medicine has been prescribed for you only. Do not pass it on to
others. It may harm them,
even if their signs of illness are the same as yours.
-
If you get any side effects, talk to your doctor or pharmacist. This
includes any possible side
effects not listed in this leaflet. See section 4.
WHAT IS IN THIS LEAFLET
1.
What Vafseo is and what it is used for
2.
What you need to know before you take Vafseo
3.
How to take Vafseo
4.
Possible side effects
5.
How to store Vafseo
6.
Contents of the pack and other information
1.
WHAT VAFSEO IS AND WHAT IT IS USED FOR
Vafseo is a medicine that increases the amount of haemoglobin (the
protein in your red blood cells
that carries oxygen around the body) and the number of red blood cells
in your blood. It contains the
active substance vadadustat.
Vafseo is used to treat symptomatic anaemia (low levels of red blood
cells or haemoglobin in your
blood) that is associated with chronic kidney disease (CKD) in adults
on chronic maintenance dialysis.
When the amount of haemoglobin or the number of red blood cells is
low, the cells in your body might
not receive enough oxygen. Anaemia can cause symptoms such as
tiredness, weakness, or shortness of
breath.
HOW VAFSEO WORKS
Vafseo increases the level of a substance called “Hypoxia-Inducible
Factor” (HIF), which increases
the production of red blood cells when oxygen levels are low.
                                
                                Citiți documentul complet
                                
                            

Caracteristicilor produsului

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
This medicinal product is subject to additional monitoring. This will
allow quick identification of
new safety information. Healthcare professionals are asked to report
any suspected adverse reactions.
See section 4.8 for how to report adverse reactions.
1.
NAME OF THE MEDICINAL PRODUCT
Vafseo 150 mg film-coated tablets
Vafseo 300 mg film-coated tablets
Vafseo 450 mg film-coated tablets
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Vafseo
150 mg film-coated tablets
Each 150 mg film-coated tablet contains 150 mg of vadadustat
Vafseo
300 mg film-coated tablets
Each 300 mg film-coated tablet contains 300 mg of vadadustat
Vafseo
450 mg film-coated tablets
Each 450 mg film-coated tablet contains 450 mg of vadadustat
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Film-coated tablet
Vafseo
150 mg film-coated tablets
Round, white tablets 8 mm in diameter, debossed with “VDT” on one
side and “150” on the other
side.
Vafseo 300 mg film-coated tablets
Oval, yellow tablets 8 mm in width, 13 mm in length, debossed with
“VDT” on one side and “300” on
the other side.
Vafseo 450 mg film-coated tablets
Oval, pink tablets 9 mm in width, 15 mm in length debossed with
“VDT” on one side and “450” on
the other side.
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
Vafseo is indicated for the treatment of symptomatic anaemia
associated with chronic kidney disease
(CKD) in adults on chronic maintenance dialysis.
4.2
POSOLOGY AND METHOD OF ADMINISTRATION
3
Vadadustat should be initiated by a physician experienced in the
management of anaemia. All other
causes of anaemia should be evaluated prior to initiating therapy with
Vafseo, and when deciding to
increase the dose.
Anaemia symptoms and sequelae may vary with age, gender, and overall
burden of disease; a
physician’s evaluation of the individual patient’s clinical course
and condition is necessary. In addition
to the presence of symptoms of anaemia, criteria such as rate of fall
of hae
                                
                                Citiți documentul complet
                                
                            

Documente în alte limbi

Prospect Prospect bulgară 05-03-2024
Caracteristicilor produsului Caracteristicilor produsului bulgară 05-03-2024
Raport public de evaluare Raport public de evaluare bulgară 31-05-2023
Prospect Prospect spaniolă 05-03-2024
Caracteristicilor produsului Caracteristicilor produsului spaniolă 05-03-2024
Raport public de evaluare Raport public de evaluare spaniolă 31-05-2023
Prospect Prospect cehă 05-03-2024
Caracteristicilor produsului Caracteristicilor produsului cehă 05-03-2024
Raport public de evaluare Raport public de evaluare cehă 31-05-2023
Prospect Prospect daneză 05-03-2024
Caracteristicilor produsului Caracteristicilor produsului daneză 05-03-2024
Raport public de evaluare Raport public de evaluare daneză 31-05-2023
Prospect Prospect germană 05-03-2024
Caracteristicilor produsului Caracteristicilor produsului germană 05-03-2024
Raport public de evaluare Raport public de evaluare germană 31-05-2023
Prospect Prospect estoniană 05-03-2024
Caracteristicilor produsului Caracteristicilor produsului estoniană 05-03-2024
Raport public de evaluare Raport public de evaluare estoniană 31-05-2023
Prospect Prospect greacă 05-03-2024
Caracteristicilor produsului Caracteristicilor produsului greacă 05-03-2024
Raport public de evaluare Raport public de evaluare greacă 31-05-2023
Prospect Prospect franceză 05-03-2024
Caracteristicilor produsului Caracteristicilor produsului franceză 05-03-2024
Raport public de evaluare Raport public de evaluare franceză 31-05-2023
Prospect Prospect italiană 05-03-2024
Caracteristicilor produsului Caracteristicilor produsului italiană 05-03-2024
Raport public de evaluare Raport public de evaluare italiană 31-05-2023
Prospect Prospect letonă 05-03-2024
Caracteristicilor produsului Caracteristicilor produsului letonă 05-03-2024
Raport public de evaluare Raport public de evaluare letonă 31-05-2023
Prospect Prospect lituaniană 05-03-2024
Caracteristicilor produsului Caracteristicilor produsului lituaniană 05-03-2024
Raport public de evaluare Raport public de evaluare lituaniană 31-05-2023
Prospect Prospect maghiară 05-03-2024
Caracteristicilor produsului Caracteristicilor produsului maghiară 05-03-2024
Raport public de evaluare Raport public de evaluare maghiară 31-05-2023
Prospect Prospect malteză 05-03-2024
Caracteristicilor produsului Caracteristicilor produsului malteză 05-03-2024
Raport public de evaluare Raport public de evaluare malteză 31-05-2023
Prospect Prospect olandeză 05-03-2024
Caracteristicilor produsului Caracteristicilor produsului olandeză 05-03-2024
Raport public de evaluare Raport public de evaluare olandeză 31-05-2023
Prospect Prospect poloneză 05-03-2024
Caracteristicilor produsului Caracteristicilor produsului poloneză 05-03-2024
Raport public de evaluare Raport public de evaluare poloneză 31-05-2023
Prospect Prospect portugheză 05-03-2024
Caracteristicilor produsului Caracteristicilor produsului portugheză 05-03-2024
Raport public de evaluare Raport public de evaluare portugheză 31-05-2023
Prospect Prospect română 05-03-2024
Caracteristicilor produsului Caracteristicilor produsului română 05-03-2024
Raport public de evaluare Raport public de evaluare română 31-05-2023
Prospect Prospect slovacă 05-03-2024
Caracteristicilor produsului Caracteristicilor produsului slovacă 05-03-2024
Raport public de evaluare Raport public de evaluare slovacă 31-05-2023
Prospect Prospect slovenă 05-03-2024
Caracteristicilor produsului Caracteristicilor produsului slovenă 05-03-2024
Raport public de evaluare Raport public de evaluare slovenă 31-05-2023
Prospect Prospect finlandeză 05-03-2024
Caracteristicilor produsului Caracteristicilor produsului finlandeză 05-03-2024
Raport public de evaluare Raport public de evaluare finlandeză 31-05-2023
Prospect Prospect suedeză 05-03-2024
Caracteristicilor produsului Caracteristicilor produsului suedeză 05-03-2024
Raport public de evaluare Raport public de evaluare suedeză 31-05-2023
Prospect Prospect norvegiană 05-03-2024
Caracteristicilor produsului Caracteristicilor produsului norvegiană 05-03-2024
Prospect Prospect islandeză 05-03-2024
Caracteristicilor produsului Caracteristicilor produsului islandeză 05-03-2024
Prospect Prospect croată 05-03-2024
Caracteristicilor produsului Caracteristicilor produsului croată 05-03-2024
Raport public de evaluare Raport public de evaluare croată 31-05-2023

Căutați alerte legate de acest produs

Vizualizați istoricul documentelor