Komboglyze

Country: Evrópusambandið

Tungumál: enska

Heimild: EMA (European Medicines Agency)

Kauptu það núna

Vara einkenni Vara einkenni (SPC)
30-05-2023
Opinber matsskýrsla Opinber matsskýrsla (PAR)
02-08-2017

Virkt innihaldsefni:

metformin hydrochloride, saxagliptin hydrochloride

Fáanlegur frá:

AstraZeneca AB 

ATC númer:

A10BD10

INN (Alþjóðlegt nafn):

saxagliptin, metformin hydrochloride

Meðferðarhópur:

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

Lækningarsvæði:

Diabetes Mellitus, Type 2

Ábendingar:

Komboglyze is indicated as an adjunct to diet and exercise to improve glycaemic control in adult patients aged 18 years and older with type-2 diabetes mellitus inadequately controlled on their maximally tolerated dose of metformin alone or those already being treated with the combination of saxagliptin and metformin as separate tablets.Komboglyze is also indicated in combination with insulin (i.e. triple combination therapy) as an adjunct to diet and exercise to improve glycaemic control in adult patients aged 18 years and older with type-2 diabetes mellitus when insulin and metformin alone do not provide adequate glycaemic control.

Vörulýsing:

Revision: 20

Leyfisstaða:

Authorised

Leyfisdagur:

2011-11-24

Upplýsingar fylgiseðill

                                38
B. PACKAGE LEAFLET
39
PACKAGE LEAFLET: INFORMATION FOR THE PATIENT
KOMBOGLYZE 2.5 MG/850 MG FILM-COATED TABLETS
saxagliptin/metformin hydrochloride
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 Komboglyze is and what it is used for
2.
What you need to know before you take Komboglyze
3.
How to take Komboglyze
4.
Possible side effects
5.
How to store Komboglyze
6.
Contents of the pack and other information
1.
WHAT KOMBOGLYZE IS AND WHAT IT IS USED FOR
This medicine contains two different substances called:
saxagliptin, part of a class of medicines called DPP-4 inhibitors
(dipeptidyl peptidase-4 inhibitors),
and metformin, part of a class of medicines called biguanides.
Both belong to a group of medicines called oral anti-diabetics.
WHAT KOMBOGLYZE IS USED FOR
This medicine is used to treat a type of diabetes called ‘type 2
diabetes’.
HOW KOMBOGLYZE WORKS
Saxagliptin and metformin work together to control your blood sugar.
They increase the levels of
insulin after a meal. They also lower the amount of sugar made by your
body. Along with diet and
exercise, this helps lower your blood sugar. This medicine can be used
alone or together with other
antidiabetic medicines, including insulin.
To control your diabetes, you still need to diet and exercise, even
when you are taking this medicine.
So it is important to keep following the advice about diet and
exercise from your doctor or nurse.
2.
WHAT YOU NEED TO KNOW BEFORE YOU TAKE KOMBOGLYZE
DO NOT TAKE KOMBOGLYZE
-
If you are alle
                                
                                Lestu allt skjalið
                                
                            

Vara einkenni

                                ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE MEDICINAL PRODUCT
Komboglyze 2.5 mg/850 mg film-coated tablets
Komboglyze 2.5 mg/1,000 mg film-coated tablets
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Komboglyze 2.5 mg/850 mg film-coated tablets
Each tablet contains 2.5 mg of saxagliptin (as hydrochloride) and 850
mg of metformin hydrochloride.
Komboglyze 2.5 mg/1,000 mg film-coated tablets
Each tablet contains 2.5 mg of saxagliptin (as hydrochloride) and
1,000 mg of metformin
hydrochloride.
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Film-coated tablet (tablet).
Komboglyze 2.5 mg/850 mg film-coated tablets
Light brown to brown, biconvex, round, film-coated tablets, with
“2.5/850” printed on one side and
“4246” printed on the other side, in blue ink.
Komboglyze 2.5 mg/1,000 mg film-coated tablets
Pale yellow to light yellow, biconvex, oval shaped, film-coated
tablets, with “2.5/1000” printed on one
side and “4247” printed on the other side, in blue ink.
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
Komboglyze is indicated in adults with type 2 diabetes mellitus as an
adjunct to diet and exercise to
improve glycaemic control:

in patients inadequately controlled on their maximally tolerated dose
of metformin alone

in combination with other medicinal products for the treatment of
diabetes, including insulin, in
patients inadequately controlled with metformin and these medicinal
products (see sections 4.4,
4.5 and 5.1 for available data on different combinations)

in patients already being treated with the combination of saxagliptin
and metformin as separate
tablets.
4.2
POSOLOGY AND METHOD OF ADMINISTRATION
Posology
_Adults with normal renal function (GFR ≥ 90 mL/min)_
_For patients inadequately controlled on maximal tolerated dose of
metformin monotherapy_
Patients not adequately controlled on metformin alone should receive a
dose of this medicinal product
equivalent to the total daily dose of saxagliptin 5 mg, dosed as 2.5
mg twice daily,
                                
                                Lestu allt skjalið
                                
                            

Skjöl á öðrum tungumálum

Upplýsingar fylgiseðill Upplýsingar fylgiseðill búlgarska 30-05-2023
Vara einkenni Vara einkenni búlgarska 30-05-2023
Opinber matsskýrsla Opinber matsskýrsla búlgarska 02-08-2017
Upplýsingar fylgiseðill Upplýsingar fylgiseðill spænska 30-05-2023
Vara einkenni Vara einkenni spænska 30-05-2023
Opinber matsskýrsla Opinber matsskýrsla spænska 02-08-2017
Upplýsingar fylgiseðill Upplýsingar fylgiseðill tékkneska 30-05-2023
Vara einkenni Vara einkenni tékkneska 30-05-2023
Opinber matsskýrsla Opinber matsskýrsla tékkneska 02-08-2017
Upplýsingar fylgiseðill Upplýsingar fylgiseðill danska 30-05-2023
Vara einkenni Vara einkenni danska 30-05-2023
Opinber matsskýrsla Opinber matsskýrsla danska 02-08-2017
Upplýsingar fylgiseðill Upplýsingar fylgiseðill þýska 30-05-2023
Vara einkenni Vara einkenni þýska 30-05-2023
Opinber matsskýrsla Opinber matsskýrsla þýska 02-08-2017
Upplýsingar fylgiseðill Upplýsingar fylgiseðill eistneska 30-05-2023
Vara einkenni Vara einkenni eistneska 30-05-2023
Opinber matsskýrsla Opinber matsskýrsla eistneska 02-08-2017
Upplýsingar fylgiseðill Upplýsingar fylgiseðill gríska 30-05-2023
Vara einkenni Vara einkenni gríska 30-05-2023
Opinber matsskýrsla Opinber matsskýrsla gríska 02-08-2017
Upplýsingar fylgiseðill Upplýsingar fylgiseðill franska 30-05-2023
Vara einkenni Vara einkenni franska 30-05-2023
Opinber matsskýrsla Opinber matsskýrsla franska 02-08-2017
Upplýsingar fylgiseðill Upplýsingar fylgiseðill ítalska 30-05-2023
Vara einkenni Vara einkenni ítalska 30-05-2023
Opinber matsskýrsla Opinber matsskýrsla ítalska 02-08-2017
Upplýsingar fylgiseðill Upplýsingar fylgiseðill lettneska 30-05-2023
Vara einkenni Vara einkenni lettneska 30-05-2023
Opinber matsskýrsla Opinber matsskýrsla lettneska 02-08-2017
Upplýsingar fylgiseðill Upplýsingar fylgiseðill litháíska 30-05-2023
Vara einkenni Vara einkenni litháíska 30-05-2023
Opinber matsskýrsla Opinber matsskýrsla litháíska 02-08-2017
Upplýsingar fylgiseðill Upplýsingar fylgiseðill ungverska 30-05-2023
Vara einkenni Vara einkenni ungverska 30-05-2023
Opinber matsskýrsla Opinber matsskýrsla ungverska 02-08-2017
Upplýsingar fylgiseðill Upplýsingar fylgiseðill maltneska 30-05-2023
Vara einkenni Vara einkenni maltneska 30-05-2023
Opinber matsskýrsla Opinber matsskýrsla maltneska 02-08-2017
Upplýsingar fylgiseðill Upplýsingar fylgiseðill hollenska 30-05-2023
Vara einkenni Vara einkenni hollenska 30-05-2023
Opinber matsskýrsla Opinber matsskýrsla hollenska 02-08-2017
Upplýsingar fylgiseðill Upplýsingar fylgiseðill pólska 30-05-2023
Vara einkenni Vara einkenni pólska 30-05-2023
Opinber matsskýrsla Opinber matsskýrsla pólska 02-08-2017
Upplýsingar fylgiseðill Upplýsingar fylgiseðill portúgalska 30-05-2023
Vara einkenni Vara einkenni portúgalska 30-05-2023
Opinber matsskýrsla Opinber matsskýrsla portúgalska 02-08-2017
Upplýsingar fylgiseðill Upplýsingar fylgiseðill rúmenska 30-05-2023
Vara einkenni Vara einkenni rúmenska 30-05-2023
Opinber matsskýrsla Opinber matsskýrsla rúmenska 02-08-2017
Upplýsingar fylgiseðill Upplýsingar fylgiseðill slóvakíska 30-05-2023
Vara einkenni Vara einkenni slóvakíska 30-05-2023
Opinber matsskýrsla Opinber matsskýrsla slóvakíska 02-08-2017
Upplýsingar fylgiseðill Upplýsingar fylgiseðill slóvenska 30-05-2023
Vara einkenni Vara einkenni slóvenska 30-05-2023
Opinber matsskýrsla Opinber matsskýrsla slóvenska 02-08-2017
Upplýsingar fylgiseðill Upplýsingar fylgiseðill finnska 30-05-2023
Vara einkenni Vara einkenni finnska 30-05-2023
Opinber matsskýrsla Opinber matsskýrsla finnska 02-08-2017
Upplýsingar fylgiseðill Upplýsingar fylgiseðill sænska 30-05-2023
Vara einkenni Vara einkenni sænska 30-05-2023
Opinber matsskýrsla Opinber matsskýrsla sænska 02-08-2017
Upplýsingar fylgiseðill Upplýsingar fylgiseðill norska 30-05-2023
Vara einkenni Vara einkenni norska 30-05-2023
Upplýsingar fylgiseðill Upplýsingar fylgiseðill íslenska 30-05-2023
Vara einkenni Vara einkenni íslenska 30-05-2023
Upplýsingar fylgiseðill Upplýsingar fylgiseðill króatíska 30-05-2023
Vara einkenni Vara einkenni króatíska 30-05-2023
Opinber matsskýrsla Opinber matsskýrsla króatíska 02-08-2017

Skoða skjalasögu