Incresync

Land: Europäische Union

Sprache: Englisch

Quelle: EMA (European Medicines Agency)

Kaufe es jetzt

Wirkstoff:

alogliptin, pioglitazone

Verfügbar ab:

Takeda Pharma A/S

ATC-Code:

A10BD09

INN (Internationale Bezeichnung):

alogliptin, pioglitazone

Therapiegruppe:

Drugs used in diabetes, Combinations of oral blood glucose lowering drugs

Therapiebereich:

Diabetes Mellitus, Type 2

Anwendungsgebiete:

Incresync is indicated as a second- or third-line treatment in adult patients aged 18 years and older with type-2 diabetes mellitus: , as an adjunct to diet and exercise to improve glycaemic control in adult patients (particularly overweight patients) inadequately controlled on pioglitazone alone, and for whom metformin is inappropriate due to contraindications or intolerance;, in combination with metformin (i.e. triple combination therapy) as an adjunct to diet and exercise to improve glycaemic control in adult patients (particularly overweight patients) inadequately controlled on their maximal tolerated dose of metformin and pioglitazone. , In addition, Incresync can be used to replace separate tablets of alogliptin and pioglitazone in those adult patients aged 18 years and older with type-2 diabetes mellitus already being treated with this combination. After initiation of therapy with Incresync, patients should be reviewed after three to six months to assess adequacy of response to treatment (e.g. reduction in HbA1c). In patients who fail to show an adequate response, Incresync should be discontinued. In light of potential risks with prolonged pioglitazone therapy, prescribers should confirm at subsequent routine reviews that the benefit of Incresync is maintained (see section 4.4).,

Produktbesonderheiten:

Revision: 13

Berechtigungsstatus:

Authorised

Berechtigungsdatum:

2013-09-19

Gebrauchsinformation

                                42
B. PACKAGE LEAFLET
43
PACKAGE LEAFLET: INFORMATION FOR THE PATIENT
INCRESYNC 12.5 MG/30 MG FILM-COATED TABLETS
INCRESYNC 25 MG/30 MG FILM-COATED TABLETS
INCRESYNC 25 MG/45 MG FILM-COATED TABLETS
alogliptin/pioglitazone
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 Incresync is and what it is used for
2.
What you need to know before you take Incresync
3.
How to take Incresync
4.
Possible side effects
5.
How to store Incresync
6.
Contents of the pack and other information
1.
WHAT INCRESYNC IS AND WHAT IT IS USED FOR
WHAT INCRESYNC IS
Incresync contains two different medicines called alogliptin and
pioglitazone in one tablet:
-
alogliptin belongs to a group of medicines called DPP-4 inhibitors
(dipeptidyl peptidase-4
inhibitors). Alogliptin works to increase the levels of insulin in the
body after a meal and
decrease the amount of sugar in the body.
-
pioglitazone belongs to a group of medicines called
thiazolidinediones. It helps your body make
better use of the insulin it produces.
Both of these groups of medicines are “oral anti-diabetics”.
WHAT INCRESYNC IS USED FOR
Incresync is used to lower blood sugar levels in adults with type 2
diabetes. Type 2 diabetes is also
called non-insulin-dependent diabetes mellitus or NIDDM.
Incresync is taken when your blood sugar cannot be adequately
controlled by diet, exercise and other
oral anti-diabetic medicines such as pioglitazone; or pioglitazone and
metformin taken together. Your
doctor will check whether Incresync is working 3 to 6 months afte
                                
                                Lesen Sie das vollständige Dokument
                                
                            

Fachinformation

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE MEDICINAL PRODUCT
Incresync 12.5 mg/30 mg film-coated tablets
Incresync 25 mg/30 mg film-coated tablets
Incresync 25 mg/45 mg film-coated tablets
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Incresync 12.5 mg/30 mg film-coated tablets
Each tablet contains alogliptin benzoate and pioglitazone
hydrochloride equivalent to 12.5 mg
alogliptin and 30 mg pioglitazone.
_Excipient(s) with known effect_
Each tablet contains 121 mg of lactose (as monohydrate).
Incresync 25 mg/30 mg film-coated tablets
Each tablet contains alogliptin benzoate and pioglitazone
hydrochloride equivalent to 25 mg alogliptin
and 30 mg pioglitazone.
_Excipient(s) with known effect_
Each tablet contains 121 mg of lactose (as monohydrate).
Incresync 25 mg/45 mg film-coated tablets
Each tablet contains alogliptin benzoate and pioglitazone
hydrochloride equivalent to 25 mg alogliptin
and 45 mg pioglitazone.
_Excipient(s) with known effect_
Each tablet contains 105 mg of lactose (as monohydrate).
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Film-coated tablet (tablet).
Incresync 12.5 mg/30 mg film-coated tablets
Pale peach, round (approximately 8.7 mm in diameter), biconvex,
film-coated tablets with both “A/P”
and “12.5/30” printed in red ink on one side.
Incresync 25 mg/30 mg film-coated tablets
Peach, round (approximately 8.7 mm in diameter), biconvex, film-coated
tablets with both “A/P” and
“25/30” printed in grey ink on one side.
Incresync 25 mg/45 mg film-coated tablets
Red, round (approximately 8.7 mm in diameter), biconvex, film-coated
tablets with both “A/P” and
“25/45” printed in grey ink on one side.
3
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
Incresync is indicated as a second or third line treatment in adult
patients aged 18 years and older with
type 2 diabetes mellitus:

as an adjunct to diet and exercise to improve glycaemic control in
adult patients (particularly
overweight patients) inadequately controlled on pio
                                
                                Lesen Sie das vollständige Dokument
                                
                            

Dokumente in anderen Sprachen

Gebrauchsinformation Gebrauchsinformation Bulgarisch 09-09-2022
Fachinformation Fachinformation Bulgarisch 09-09-2022
Öffentlichen Beurteilungsberichts Öffentlichen Beurteilungsberichts Bulgarisch 04-10-2021
Gebrauchsinformation Gebrauchsinformation Spanisch 09-09-2022
Fachinformation Fachinformation Spanisch 09-09-2022
Gebrauchsinformation Gebrauchsinformation Tschechisch 09-09-2022
Fachinformation Fachinformation Tschechisch 09-09-2022
Öffentlichen Beurteilungsberichts Öffentlichen Beurteilungsberichts Tschechisch 04-10-2021
Gebrauchsinformation Gebrauchsinformation Dänisch 09-09-2022
Fachinformation Fachinformation Dänisch 09-09-2022
Gebrauchsinformation Gebrauchsinformation Deutsch 09-09-2022
Fachinformation Fachinformation Deutsch 09-09-2022
Gebrauchsinformation Gebrauchsinformation Estnisch 09-09-2022
Fachinformation Fachinformation Estnisch 09-09-2022
Gebrauchsinformation Gebrauchsinformation Griechisch 09-09-2022
Fachinformation Fachinformation Griechisch 09-09-2022
Öffentlichen Beurteilungsberichts Öffentlichen Beurteilungsberichts Griechisch 04-10-2021
Gebrauchsinformation Gebrauchsinformation Französisch 09-09-2022
Fachinformation Fachinformation Französisch 09-09-2022
Öffentlichen Beurteilungsberichts Öffentlichen Beurteilungsberichts Französisch 04-10-2021
Gebrauchsinformation Gebrauchsinformation Italienisch 09-09-2022
Fachinformation Fachinformation Italienisch 09-09-2022
Öffentlichen Beurteilungsberichts Öffentlichen Beurteilungsberichts Italienisch 04-10-2021
Gebrauchsinformation Gebrauchsinformation Lettisch 09-09-2022
Fachinformation Fachinformation Lettisch 09-09-2022
Gebrauchsinformation Gebrauchsinformation Litauisch 09-09-2022
Fachinformation Fachinformation Litauisch 09-09-2022
Öffentlichen Beurteilungsberichts Öffentlichen Beurteilungsberichts Litauisch 04-10-2021
Gebrauchsinformation Gebrauchsinformation Ungarisch 09-09-2022
Fachinformation Fachinformation Ungarisch 09-09-2022
Öffentlichen Beurteilungsberichts Öffentlichen Beurteilungsberichts Ungarisch 04-10-2021
Gebrauchsinformation Gebrauchsinformation Maltesisch 09-09-2022
Fachinformation Fachinformation Maltesisch 09-09-2022
Öffentlichen Beurteilungsberichts Öffentlichen Beurteilungsberichts Maltesisch 04-10-2021
Gebrauchsinformation Gebrauchsinformation Niederländisch 09-09-2022
Fachinformation Fachinformation Niederländisch 09-09-2022
Öffentlichen Beurteilungsberichts Öffentlichen Beurteilungsberichts Niederländisch 04-10-2021
Gebrauchsinformation Gebrauchsinformation Polnisch 09-09-2022
Fachinformation Fachinformation Polnisch 09-09-2022
Gebrauchsinformation Gebrauchsinformation Portugiesisch 09-09-2022
Fachinformation Fachinformation Portugiesisch 09-09-2022
Öffentlichen Beurteilungsberichts Öffentlichen Beurteilungsberichts Portugiesisch 04-10-2021
Gebrauchsinformation Gebrauchsinformation Rumänisch 09-09-2022
Fachinformation Fachinformation Rumänisch 09-09-2022
Öffentlichen Beurteilungsberichts Öffentlichen Beurteilungsberichts Rumänisch 04-10-2021
Gebrauchsinformation Gebrauchsinformation Slowakisch 09-09-2022
Fachinformation Fachinformation Slowakisch 09-09-2022
Öffentlichen Beurteilungsberichts Öffentlichen Beurteilungsberichts Slowakisch 04-10-2021
Gebrauchsinformation Gebrauchsinformation Slowenisch 09-09-2022
Fachinformation Fachinformation Slowenisch 09-09-2022
Öffentlichen Beurteilungsberichts Öffentlichen Beurteilungsberichts Slowenisch 04-10-2021
Gebrauchsinformation Gebrauchsinformation Finnisch 09-09-2022
Fachinformation Fachinformation Finnisch 09-09-2022
Gebrauchsinformation Gebrauchsinformation Schwedisch 09-09-2022
Fachinformation Fachinformation Schwedisch 09-09-2022
Öffentlichen Beurteilungsberichts Öffentlichen Beurteilungsberichts Schwedisch 04-10-2021
Gebrauchsinformation Gebrauchsinformation Norwegisch 09-09-2022
Fachinformation Fachinformation Norwegisch 09-09-2022
Gebrauchsinformation Gebrauchsinformation Isländisch 09-09-2022
Fachinformation Fachinformation Isländisch 09-09-2022
Gebrauchsinformation Gebrauchsinformation Kroatisch 09-09-2022
Fachinformation Fachinformation Kroatisch 09-09-2022
Öffentlichen Beurteilungsberichts Öffentlichen Beurteilungsberichts Kroatisch 04-10-2021

Suchen Sie nach Benachrichtigungen zu diesem Produkt

Dokumentverlauf anzeigen