Ristaben

Country: Kesatuan Eropah

Bahasa: Inggeris

Sumber: EMA (European Medicines Agency)

Beli sekarang

Risalah maklumat Risalah maklumat (PIL)
21-09-2023
Ciri produk Ciri produk (SPC)
21-09-2023
Laporan Penilaian Awam Laporan Penilaian Awam (PAR)
09-03-2015

Bahan aktif:

sitagliptin

Boleh didapati daripada:

Merck Sharp & Dohme B.V.

Kod ATC:

A10BH01

INN (Nama Antarabangsa):

sitagliptin

Kumpulan terapeutik:

Drugs used in diabetes

Kawasan terapeutik:

Diabetes Mellitus, Type 2

Tanda-tanda terapeutik:

For adult patients with type-2 diabetes mellitus, Ristaben is indicated to improve glycaemic control:as monotherapy:in patients inadequately controlled by diet and exercise alone and for whom metformin is inappropriate due to contraindications or intolerance;as dual oral therapy in combination with:metformin when diet and exercise plus metformin alone do not provide adequate glycaemic control;a sulphonylurea when diet and exercise plus maximal tolerated dose of a sulphonylurea alone do not provide adequate glycaemic control and when metformin is inappropriate due to contraindications or intolerance;a peroxisome proliferator-activated-receptor-gamma (PPARγ) agonist (i.e. a thiazolidinedione) when use of a PPARγ agonist is appropriate and when diet and exercise plus the PPARγ agonist alone do not provide adequate glycaemic control;as triple oral therapy in combination with:a sulphonylurea and metformin when diet and exercise plus dual therapy with these medicinal products do not provide adequate glycaemic control;a PPARγ agonist and metformin when use of a PPARγ agonist is appropriate and when diet and exercise plus dual therapy with these medicinal products do not provide adequate glycaemic control.Ristaben is also indicated as add-on to insulin (with or without metformin) when diet and exercise plus stable dose of insulin do not provide adequate glycaemic control.

Ringkasan produk:

Revision: 27

Status kebenaran:

Authorised

Tarikh kebenaran:

2010-03-15

Risalah maklumat

                                32
B. PACKAGE LEAFLET
33
PACKAGE LEAFLET: I
NFO
RMATION FOR THE PATIENT
RISTABEN 25 MG FILM-
COATED TABLETS
RISTABEN 50 MG FILM-COATED TABLETS
RISTABEN 100 MG FILM-
COATED TABLETS
sitagliptin
READ ALL OF THIS LEAFLET CAREFULLY BEFORE YOU START TAKING THIS
MEDICINE
BECAUSE IT CONTAINS
IMPORTANT INFORM
ATION FOR YOU.
-
Keep t
his leaflet. You may need to read it again.
-
If you ha
ve any furth
er questions, ask your
doctor,
pharmacist
, or nurse.
-
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, phar
macist, or nurse. This
includes any possible
side effects not listed in this leaflet.
See section 4.
WHAT IS I
N THIS LEAFLET
1.
What Ristaben is and what it is used for
2.
What you need to know b
efore you take Ristaben
3.
How to take Ristaben
4.
Possible
side effects
5.
How t
o store Ristaben
6.
Contents of the pack and other
information
1.
WHAT RISTABEN IS AND WHAT IT IS USED FOR
Ristaben contains the active substance
sitagliptin which is
a member of a class of medicines called
DPP-4 inhibi
tors (dipept
idyl peptidase
-4 inhib
itors) that lowers blood sugar levels in adult patients
with type 2 diabetes mellitus.
This medicine helps to increase the levels of insulin produc
ed after a meal and d
ecreases the amount
of sugar made by the body.
Your
doctor has p
rescribed this medicine
to help lower your blood sugar, which is too high because of
your type 2 diabetes.
This medicine
can be used alone or in combination with certain
oth
er medicine
s
(insu
lin, metformin, sulphonylureas, or glitazones) that l
ower blood s
ugar, which you may al
ready be
taking for your diabetes together with a food and exercise plan.
What is type 2 diabetes?
Type 2 diabetes is a condition in which your bod
y d
oes not mak
e enoug
h insulin, and the insulin that
your body produces do
es not work
as well as it should.
Your body can also make too much sugar.
When this happens, sugar (glucose)
                                
                                Baca dokumen lengkap
                                
                            

Ciri produk

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE MEDICINAL PRODUCT
Ristaben 25 mg film-
coated tablets
Ristaben 50 mg film-
coated tablets
Ristaben 100 mg film-
coated tablets
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Ristaben 25 mg film-
coated tablets
Each tablet contains sitagliptin phosphate monohydrate, equivalent to
2
5
mg sitagliptin.
Ristaben 50 mg film-
coated tablets
Each tablet contains sitagliptin phosphate monohydrate, equivalent to
50
mg sitagliptin.
Ristaben 100 mg film-
coated tablets
Each tablet contains sitagliptin phosphate monohydrate, equivalent to
100
mg sitagliptin.
For the
full list of excipients, see section
6.1.
3.
PHARMACEUTICAL
FORM
Film-
coated tablet (tablet)
.
Ristaben 25 mg film-coated tablets
Round, pink film
-
coated tablet with “221” on one side.
Ritaben 50 mg film-
coated tablets
Round, light beige film
-
coated table
t with “112” on one side
.
Ristaben 100 mg film-
coated tablets
Round, beige f
ilm-
coated tablet with “277” on one side.
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
For adult patients w
ith type 2 diabetes mellitus, Ristaben is indicated to improve
glycaemic control:
as
monotherapy
:
•
in patients inadequately controlled by diet and exercise alone and for
whom metfo
rmin is
inappropriate due to contraindications or intolerance.
as dual oral
therapy in combination with
:
•
metformin when diet and exercise plus metformin alone do not provide
adequate glycaemic
control.
•
a sulphonylurea when diet and exercise plus maximal
t
olerated dose of a sulphonylurea alone do
not provide adequate glycaemic
co
ntrol and when metformin is inappropriate due to
contraindications or intolerance.
3
•
a
peroxisome proliferator
-
activated receptor gamma (PPAR

)
agonist (i.e. a thiazolidinedione)
whe
n use of a PPAR

agonist is appropriate and when diet and exercise plus t
he PPAR

agonist
alone do not provide adequate glycaemic control.
as triple oral therapy in combination with
:
•
a sulphonylurea and metformin when diet and ex
                                
                                Baca dokumen lengkap
                                
                            

Dokumen dalam bahasa lain

Risalah maklumat Risalah maklumat Bulgaria 21-09-2023
Ciri produk Ciri produk Bulgaria 21-09-2023
Laporan Penilaian Awam Laporan Penilaian Awam Bulgaria 09-03-2015
Risalah maklumat Risalah maklumat Sepanyol 21-09-2023
Ciri produk Ciri produk Sepanyol 21-09-2023
Laporan Penilaian Awam Laporan Penilaian Awam Sepanyol 09-03-2015
Risalah maklumat Risalah maklumat Czech 21-09-2023
Ciri produk Ciri produk Czech 21-09-2023
Laporan Penilaian Awam Laporan Penilaian Awam Czech 09-03-2015
Risalah maklumat Risalah maklumat Denmark 21-09-2023
Ciri produk Ciri produk Denmark 21-09-2023
Laporan Penilaian Awam Laporan Penilaian Awam Denmark 09-03-2015
Risalah maklumat Risalah maklumat Jerman 21-09-2023
Ciri produk Ciri produk Jerman 21-09-2023
Laporan Penilaian Awam Laporan Penilaian Awam Jerman 09-03-2015
Risalah maklumat Risalah maklumat Estonia 21-09-2023
Ciri produk Ciri produk Estonia 21-09-2023
Laporan Penilaian Awam Laporan Penilaian Awam Estonia 09-03-2015
Risalah maklumat Risalah maklumat Greek 21-09-2023
Ciri produk Ciri produk Greek 21-09-2023
Laporan Penilaian Awam Laporan Penilaian Awam Greek 09-03-2015
Risalah maklumat Risalah maklumat Perancis 21-09-2023
Ciri produk Ciri produk Perancis 21-09-2023
Laporan Penilaian Awam Laporan Penilaian Awam Perancis 09-03-2015
Risalah maklumat Risalah maklumat Itali 21-09-2023
Ciri produk Ciri produk Itali 21-09-2023
Laporan Penilaian Awam Laporan Penilaian Awam Itali 09-03-2015
Risalah maklumat Risalah maklumat Latvia 21-09-2023
Ciri produk Ciri produk Latvia 21-09-2023
Laporan Penilaian Awam Laporan Penilaian Awam Latvia 09-03-2015
Risalah maklumat Risalah maklumat Lithuania 21-09-2023
Ciri produk Ciri produk Lithuania 21-09-2023
Laporan Penilaian Awam Laporan Penilaian Awam Lithuania 09-03-2015
Risalah maklumat Risalah maklumat Hungary 21-09-2023
Ciri produk Ciri produk Hungary 21-09-2023
Laporan Penilaian Awam Laporan Penilaian Awam Hungary 09-03-2015
Risalah maklumat Risalah maklumat Malta 21-09-2023
Ciri produk Ciri produk Malta 21-09-2023
Laporan Penilaian Awam Laporan Penilaian Awam Malta 09-03-2015
Risalah maklumat Risalah maklumat Belanda 21-09-2023
Ciri produk Ciri produk Belanda 21-09-2023
Laporan Penilaian Awam Laporan Penilaian Awam Belanda 09-03-2015
Risalah maklumat Risalah maklumat Poland 21-09-2023
Ciri produk Ciri produk Poland 21-09-2023
Laporan Penilaian Awam Laporan Penilaian Awam Poland 09-03-2015
Risalah maklumat Risalah maklumat Portugis 21-09-2023
Ciri produk Ciri produk Portugis 21-09-2023
Laporan Penilaian Awam Laporan Penilaian Awam Portugis 09-03-2015
Risalah maklumat Risalah maklumat Romania 21-09-2023
Ciri produk Ciri produk Romania 21-09-2023
Laporan Penilaian Awam Laporan Penilaian Awam Romania 09-03-2015
Risalah maklumat Risalah maklumat Slovak 21-09-2023
Ciri produk Ciri produk Slovak 21-09-2023
Laporan Penilaian Awam Laporan Penilaian Awam Slovak 09-03-2015
Risalah maklumat Risalah maklumat Slovenia 21-09-2023
Ciri produk Ciri produk Slovenia 21-09-2023
Laporan Penilaian Awam Laporan Penilaian Awam Slovenia 09-03-2015
Risalah maklumat Risalah maklumat Finland 21-09-2023
Ciri produk Ciri produk Finland 21-09-2023
Laporan Penilaian Awam Laporan Penilaian Awam Finland 09-03-2015
Risalah maklumat Risalah maklumat Sweden 21-09-2023
Ciri produk Ciri produk Sweden 21-09-2023
Laporan Penilaian Awam Laporan Penilaian Awam Sweden 09-03-2015
Risalah maklumat Risalah maklumat Norway 21-09-2023
Ciri produk Ciri produk Norway 21-09-2023
Risalah maklumat Risalah maklumat Iceland 21-09-2023
Ciri produk Ciri produk Iceland 21-09-2023
Risalah maklumat Risalah maklumat Croat 21-09-2023
Ciri produk Ciri produk Croat 21-09-2023
Laporan Penilaian Awam Laporan Penilaian Awam Croat 09-03-2015

Cari amaran yang berkaitan dengan produk ini

Lihat sejarah dokumen