Invokana

Country: Unjoni Ewropea

Lingwa: Ingliż

Sors: EMA (European Medicines Agency)

Ixtrih issa

Ingredjent attiv:

canagliflozin

Disponibbli minn:

Janssen-Cilag International NV

Kodiċi ATC:

A10BK02

INN (Isem Internazzjonali):

canagliflozin

Grupp terapewtiku:

Drugs used in diabetes

Żona terapewtika:

Diabetes Mellitus, Type 2

Indikazzjonijiet terapewtiċi:

Invokana is indicated for the treatment of adults with insufficiently controlled type 2 diabetes mellitus as an adjunct to diet and exercise:as monotherapy when metformin is considered inappropriate due to intolerance or contraindicationsin addition to other medicinal products for the treatment of diabetes.For study results with respect to combination of therapies, effects on glycaemic control, cardiovascular and renal events, and the populations studied, see sections 4.4, 4.5 and 5.1.

Sommarju tal-prodott:

Revision: 23

L-istatus ta 'awtorizzazzjoni:

Authorised

Data ta 'l-awtorizzazzjoni:

2013-11-15

Fuljett ta 'informazzjoni

                                39
B. PACKAGE LEAFLET
40
PACKAGE LEAFLET: INFORMATION FOR THE PATIENT
INVOKANA 100 MG FILM-COATED TABLETS
INVOKANA 300 MG FILM-COATED TABLETS
canagliflozin
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 Invokana is and what it is used for
2.
What you need to know before you take Invokana
3.
How to take Invokana
4.
Possible side effects
5.
How to store Invokana
6.
Contents of the pack and other information
1.
WHAT INVOKANA IS AND WHAT IT IS USED FOR
Invokana contains the active substance canagliflozin which belongs to
a group of medicines called
“blood-glucose lowering drugs.”
Invokana is used:

to treat adults with type 2 diabetes.
This medicine works by increasing the amount of sugar removed from
your body in your urine. This
reduces the amount of sugar in your blood and can help prevent heart
disease in patients with type 2
diabetes mellitus (T2DM). It also helps to slow down deterioration of
kidney function in patients with
T2DM by a mechanism beyond blood glucose lowering.
Invokana can be used by itself or along with other medicines you may
be using to treat your type 2
diabetes (such as metformin, insulin, a DPP-4 inhibitor [such as
sitagliptin, saxagliptin, or linagliptin],
a sulphonylurea [such as glimepiride or glipizide], or pioglitazone)
that lower blood sugar levels. You
may already be taking one or more of these to treat your type 2
diabetes.
It is also important to keep following advice about diet and exercise
given by your doctor or nurse.
WHAT IS TYPE 2 DIABE
                                
                                Aqra d-dokument sħiħ
                                
                            

Karatteristiċi tal-prodott

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE MEDICINAL PRODUCT
Invokana 100 mg film-coated tablets
Invokana 300 mg film-coated tablets
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Invokana 100 mg film-coated tablets
Each tablet contains canagliflozin hemihydrate, equivalent to 100 mg
canagliflozin.
_Excipient(s) with known effect_
Each tablet contains 39.2 mg lactose.
Invokana 300 mg film-coated tablets
Each tablet contains canagliflozin hemihydrate, equivalent to 300 mg
canagliflozin.
_Excipient(s) with known effect_
Each tablet contains 117.78 mg lactose.
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Film-coated tablet (tablet).
Invokana 100 mg film-coated tablets
The tablet is yellow, capsule-shaped, approximately 11 mm in length,
immediate-release and
film-coated, with “CFZ” on one side and “100” on the other
side.
Invokana 300 mg film-coated tablets
The tablet is white, capsule-shaped, approximately 17 mm in length,
immediate-release and
film-coated, with “CFZ” on one side and “300” on the other
side.
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
Invokana is indicated for the treatment of adults with insufficiently
controlled type 2 diabetes mellitus
as an adjunct to diet and exercise:
-
as monotherapy when metformin is considered inappropriate due to
intolerance or
contraindications
-
in addition to other medicinal products for the treatment of diabetes.
For study results with respect to combination of therapies, effects on
glycaemic control, cardiovascular
and renal events, and the populations studied, see sections 4.4, 4.5
and 5.1.
3
4.2
POSOLOGY AND METHOD OF ADMINISTRATION
Posology
The recommended starting dose of canagliflozin is 100 mg once daily.
In patients tolerating
canagliflozin 100 mg once daily who have an estimated glomerular
filtration rate
(eGFR) ≥ 60 mL/min/1.73 m
2
or CrCl ≥ 60 mL/min and need tighter glycaemic control, the dose can
be increased to 300 mg once daily (see section 4.4). For dose
adjustment recommendations a
                                
                                Aqra d-dokument sħiħ
                                
                            

Dokumenti f'lingwi oħra

Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Bulgaru 27-07-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Bulgaru 27-07-2023
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Spanjol 27-07-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Spanjol 27-07-2023
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Ċek 27-07-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Ċek 27-07-2023
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Daniż 27-07-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Daniż 27-07-2023
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Ġermaniż 27-07-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Ġermaniż 27-07-2023
Rapport ta 'Valutazzjoni Pubblika Rapport ta 'Valutazzjoni Pubblika Ġermaniż 06-08-2020
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Estonjan 27-07-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Estonjan 27-07-2023
Rapport ta 'Valutazzjoni Pubblika Rapport ta 'Valutazzjoni Pubblika Estonjan 06-08-2020
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Grieg 27-07-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Grieg 27-07-2023
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Franċiż 27-07-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Franċiż 27-07-2023
Rapport ta 'Valutazzjoni Pubblika Rapport ta 'Valutazzjoni Pubblika Franċiż 06-08-2020
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Taljan 27-07-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Taljan 27-07-2023
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Latvjan 27-07-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Latvjan 27-07-2023
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Litwanjan 27-07-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Litwanjan 27-07-2023
Rapport ta 'Valutazzjoni Pubblika Rapport ta 'Valutazzjoni Pubblika Litwanjan 06-08-2020
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Ungeriż 27-07-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Ungeriż 27-07-2023
Rapport ta 'Valutazzjoni Pubblika Rapport ta 'Valutazzjoni Pubblika Ungeriż 06-08-2020
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Malti 27-07-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Malti 27-07-2023
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Olandiż 27-07-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Olandiż 27-07-2023
Rapport ta 'Valutazzjoni Pubblika Rapport ta 'Valutazzjoni Pubblika Olandiż 06-08-2020
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Pollakk 27-07-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Pollakk 27-07-2023
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Portugiż 27-07-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Portugiż 27-07-2023
Rapport ta 'Valutazzjoni Pubblika Rapport ta 'Valutazzjoni Pubblika Portugiż 06-08-2020
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Rumen 27-07-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Rumen 27-07-2023
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Slovakk 27-07-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Slovakk 27-07-2023
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Sloven 27-07-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Sloven 27-07-2023
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Finlandiż 27-07-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Finlandiż 27-07-2023
Rapport ta 'Valutazzjoni Pubblika Rapport ta 'Valutazzjoni Pubblika Finlandiż 06-08-2020
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Svediż 27-07-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Svediż 27-07-2023
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Norveġiż 27-07-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Norveġiż 27-07-2023
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Iżlandiż 27-07-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Iżlandiż 27-07-2023
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Kroat 27-07-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Kroat 27-07-2023

Fittex twissijiet relatati ma 'dan il-prodott

Ara l-istorja tad-dokumenti