Galvus

Land: Europeiska unionen

Språk: engelska

Källa: EMA (European Medicines Agency)

Köp det nu

Bipacksedel Bipacksedel (PIL)
17-08-2023
Produktens egenskaper Produktens egenskaper (SPC)
17-08-2023

Aktiva substanser:

vildagliptin

Tillgänglig från:

Novartis Europharm Limited

ATC-kod:

A10BH02

INN (International namn):

vildagliptin

Terapeutisk grupp:

Drugs used in diabetes

Terapiområde:

Diabetes Mellitus, Type 2

Terapeutiska indikationer:

Vildagliptin is indicated as an adjunct to diet and exercise to improve glycaemic control in adults with type 2 diabetes mellitus:as monotherapy in patients in whom metformin is inappropriate due to contraindications or intolerance.in combination with other medicinal products for the treatment of diabetes, including insulin, when these do not provide adequate glycaemic control

Produktsammanfattning:

Revision: 23

Bemyndigande status:

Authorised

Tillstånd datum:

2007-09-25

Bipacksedel

                                30
B. PACKAGE LEAFLET
31
PACKAGE LEAFLET: INFORMATION FOR THE USER
GALVUS 50 MG TABLETS
vildagliptin
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, 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, pharmacist or nurse.
This includes any possible
side effects not listed in this leaflet. See section 4.
WHAT IS IN THIS LEAFLET
1.
What Galvus is and what it is used for
2.
What you need to know before you take Galvus
3.
How to take Galvus
4.
Possible side effects
5.
How to store Galvus
6.
Contents of the pack and other information
1.
WHAT GALVUS IS AND WHAT IT IS USED FOR
The active substance of Galvus, vildagliptin, belongs to a group of
medicines called “oral
antidiabetics”.
Galvus is used to treat adult patients with type 2 diabetes. It is
used when diabetes cannot be
controlled by diet and exercise alone. It helps to control the level
of sugar in the blood. Your doctor
will prescribe Galvus either alone or together with certain other
antidiabetic medicines which you will
already be taking, if these have not proved sufficiently effective to
control diabetes.
Type 2 diabetes develops if the body does not make enough insulin or
if the insulin that the body
makes does not work as well as it should. It can also develop if the
body produces too much glucagon.
Insulin is a substance which helps to lower the level of sugar in the
blood, especially after meals.
Glucagon is a substance which triggers the production of sugar by the
liver, causing the blood sugar
level to rise. The pancreas makes both of these substances.
HOW GALVUS WORKS
Galvus works by making the pancreas produce more insulin and less
glucagon. This helps to control
the blood sugar level. This medicine 
                                
                                Läs hela dokumentet
                                
                            

Produktens egenskaper

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE MEDICINAL PRODUCT
Galvus 50 mg tablets
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Each tablet contains 50 mg of vildagliptin.
Excipient with known effect: Each tablet contains 47.82 mg lactose
(anhydrous).
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Tablet.
White to light yellowish, round (8 mm diameter), flat-faced,
bevelled-edge tablet. One side is
debossed with “NVR”, and the other side with “FB”.
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
Vildagliptin is indicated as an adjunct to diet and exercise to
improve glycaemic control in adults with
type 2 diabetes mellitus:
•
as monotherapy in patients in whom metformin is inappropriate due to
contraindications or
intolerance.
•
in combination with other medicinal products for the treatment of
diabetes, including insulin,
when these do not provide adequate glycaemic control (see sections
4.4, 4.5 and 5.1 for
available data on different combinations).
4.2
POSOLOGY AND METHOD OF ADMINISTRATION
Posology
_Adults _
When used as monotherapy, in combination with metformin, in
combination with thiazolidinedione, in
combination with metformin and a sulphonylurea, or in combination with
insulin (with or without
metformin), the recommended daily dose of vildagliptin is 100 mg,
administered as one dose of 50 mg
in the morning and one dose of 50 mg in the evening.
When used in dual combination with a sulphonylurea, the recommended
dose of vildagliptin is 50 mg
once daily administered in the morning. In this patient population,
vildagliptin 100 mg daily was no
more effective than vildagliptin 50 mg once daily.
When used in combination with a sulphonylurea, a lower dose of the
sulphonylurea may be considered
to reduce the risk of hypoglycaemia.
Doses higher than 100 mg are not recommended.
3
If a dose of Galvus is missed, it should be taken as soon as the
patient remembers. A double dose
should not be taken on the same day.
The safety and efficacy of vildagliptin as tri
                                
                                Läs hela dokumentet
                                
                            

Dokument på andra språk

Bipacksedel Bipacksedel bulgariska 17-08-2023
Produktens egenskaper Produktens egenskaper bulgariska 17-08-2023
Offentlig bedömningsrapport Offentlig bedömningsrapport bulgariska 24-08-2021
Bipacksedel Bipacksedel spanska 17-08-2023
Produktens egenskaper Produktens egenskaper spanska 17-08-2023
Offentlig bedömningsrapport Offentlig bedömningsrapport spanska 24-08-2021
Bipacksedel Bipacksedel tjeckiska 17-08-2023
Produktens egenskaper Produktens egenskaper tjeckiska 17-08-2023
Offentlig bedömningsrapport Offentlig bedömningsrapport tjeckiska 24-08-2021
Bipacksedel Bipacksedel danska 17-08-2023
Produktens egenskaper Produktens egenskaper danska 17-08-2023
Offentlig bedömningsrapport Offentlig bedömningsrapport danska 24-08-2021
Bipacksedel Bipacksedel tyska 17-08-2023
Produktens egenskaper Produktens egenskaper tyska 17-08-2023
Offentlig bedömningsrapport Offentlig bedömningsrapport tyska 24-08-2021
Bipacksedel Bipacksedel estniska 17-08-2023
Produktens egenskaper Produktens egenskaper estniska 17-08-2023
Offentlig bedömningsrapport Offentlig bedömningsrapport estniska 24-08-2021
Bipacksedel Bipacksedel grekiska 17-08-2023
Produktens egenskaper Produktens egenskaper grekiska 17-08-2023
Offentlig bedömningsrapport Offentlig bedömningsrapport grekiska 24-08-2021
Bipacksedel Bipacksedel franska 17-08-2023
Produktens egenskaper Produktens egenskaper franska 17-08-2023
Offentlig bedömningsrapport Offentlig bedömningsrapport franska 24-08-2021
Bipacksedel Bipacksedel italienska 17-08-2023
Produktens egenskaper Produktens egenskaper italienska 17-08-2023
Offentlig bedömningsrapport Offentlig bedömningsrapport italienska 24-08-2021
Bipacksedel Bipacksedel lettiska 17-08-2023
Produktens egenskaper Produktens egenskaper lettiska 17-08-2023
Offentlig bedömningsrapport Offentlig bedömningsrapport lettiska 24-08-2021
Bipacksedel Bipacksedel litauiska 17-08-2023
Produktens egenskaper Produktens egenskaper litauiska 17-08-2023
Offentlig bedömningsrapport Offentlig bedömningsrapport litauiska 24-08-2021
Bipacksedel Bipacksedel ungerska 17-08-2023
Produktens egenskaper Produktens egenskaper ungerska 17-08-2023
Offentlig bedömningsrapport Offentlig bedömningsrapport ungerska 24-08-2021
Bipacksedel Bipacksedel maltesiska 17-08-2023
Produktens egenskaper Produktens egenskaper maltesiska 17-08-2023
Offentlig bedömningsrapport Offentlig bedömningsrapport maltesiska 24-08-2021
Bipacksedel Bipacksedel nederländska 17-08-2023
Produktens egenskaper Produktens egenskaper nederländska 17-08-2023
Offentlig bedömningsrapport Offentlig bedömningsrapport nederländska 24-08-2021
Bipacksedel Bipacksedel polska 17-08-2023
Produktens egenskaper Produktens egenskaper polska 17-08-2023
Offentlig bedömningsrapport Offentlig bedömningsrapport polska 24-08-2021
Bipacksedel Bipacksedel portugisiska 17-08-2023
Produktens egenskaper Produktens egenskaper portugisiska 17-08-2023
Offentlig bedömningsrapport Offentlig bedömningsrapport portugisiska 24-08-2021
Bipacksedel Bipacksedel rumänska 17-08-2023
Produktens egenskaper Produktens egenskaper rumänska 17-08-2023
Offentlig bedömningsrapport Offentlig bedömningsrapport rumänska 24-08-2021
Bipacksedel Bipacksedel slovakiska 17-08-2023
Produktens egenskaper Produktens egenskaper slovakiska 17-08-2023
Offentlig bedömningsrapport Offentlig bedömningsrapport slovakiska 24-08-2021
Bipacksedel Bipacksedel slovenska 17-08-2023
Produktens egenskaper Produktens egenskaper slovenska 17-08-2023
Offentlig bedömningsrapport Offentlig bedömningsrapport slovenska 24-08-2021
Bipacksedel Bipacksedel finska 17-08-2023
Produktens egenskaper Produktens egenskaper finska 17-08-2023
Offentlig bedömningsrapport Offentlig bedömningsrapport finska 24-08-2021
Bipacksedel Bipacksedel svenska 17-08-2023
Produktens egenskaper Produktens egenskaper svenska 17-08-2023
Offentlig bedömningsrapport Offentlig bedömningsrapport svenska 24-08-2021
Bipacksedel Bipacksedel norska 17-08-2023
Produktens egenskaper Produktens egenskaper norska 17-08-2023
Bipacksedel Bipacksedel isländska 17-08-2023
Produktens egenskaper Produktens egenskaper isländska 17-08-2023
Bipacksedel Bipacksedel kroatiska 17-08-2023
Produktens egenskaper Produktens egenskaper kroatiska 17-08-2023
Offentlig bedömningsrapport Offentlig bedömningsrapport kroatiska 24-08-2021

Sök varningar relaterade till denna produkt

Visa dokumenthistorik