Avaglim

Riik: Euroopa Liit

keel: inglise

Allikas: EMA (European Medicines Agency)

Osta kohe

Infovoldik Infovoldik (PIL)
17-01-2011
Toote omadused Toote omadused (SPC)
17-01-2011
Avaliku hindamisaruande Avaliku hindamisaruande (PAR)
17-01-2011

Toimeaine:

rosiglitazone, glimepiride

Saadav alates:

SmithKline Beecham Ltd

ATC kood:

A10BD04

INN (Rahvusvaheline Nimetus):

rosiglitazone, glimepiride

Terapeutiline rühm:

Drugs used in diabetes

Terapeutiline ala:

Diabetes Mellitus, Type 2

Näidustused:

AVAGLIM is indicated in the treatment of type 2 diabetes mellitus patients who are unable to achieve sufficient glycaemic control on optimal dosage of sulphonylurea monotherapy, and for whom metformin is inappropriate because of contraindication or intolerance.

Toote kokkuvõte:

Revision: 11

Volitamisolek:

Withdrawn

Loa andmise kuupäev:

2006-06-27

Infovoldik

                                Medicinal product no longer authorised
46
B. PACKAGE LEAFLET
Medicinal product no longer authorised
47
PACKAGE LEAFLET: INFORMATION FOR THE USER
AVAGLIM 4 MG/4 MG FILM-COATED TABLETS
AVAGLIM 8 MG/4 MG FILM-COATED TABLETS
rosiglitazone/glimepiride
READ ALL OF THIS LEAFLET CAREFULLY BEFORE YOU START TAKING THIS
MEDICINE.
-
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. Do not pass it on to
others. It may harm them, even
if their symptoms are the same as yours.
-
IF ANY OF THE SIDE EFFECTS GETS SERIOUS, OR IF YOU NOTICE ANY SIDE
EFFECTS NOT LISTED IN THIS
LEAFLET, TELL YOUR DOCTOR OR PHARMACIST.
IN THIS LEAFLET
:
1.
WHAT AVAGLIM IS AND WHAT IT IS USED FOR
2.
BEFORE YOU TAKE AVAGLIM
3.
HOW TO TAKE AVAGLIM
4.
POSSIBLE SIDE EFFECTS
5
HOW TO STORE AVAGLIM
6.
FURTHER INFORMATION
1.
WHAT AVAGLIM IS AND WHAT IT IS USED FOR
AVAGLIM TABLETS ARE A COMBINATION OF TWO DIFFERENT MEDICINES
called
_rosiglitazone_
and
_glimepiride. _
These two medicines are used to treat
TYPE 2 DIABETES.
People with type 2 diabetes either don’t make enough insulin (a
hormone that controls blood sugar
levels), or don’t respond normally to the insulin their body makes.
Rosiglitazone and glimepiride work
together so your body makes better use of the insulin it produces, and
this helps reduce your blood
sugar to a normal level.
2.
BEFORE YOU TAKE AVAGLIM
To help manage your diabetes, it is important that you follow any diet
and lifestyle advice from your
doctor as well as taking Avaglim.
DON’T TAKE AVAGLIM:
•
IF YOU ARE ALLERGIC
(
_hypersensitive_
) to rosiglitazone, glimepiride, or any of the other
ingredients of Avaglim (
_listed in Section 6), _
or to
_ _
other medicines called sulphonylureas
(like
_glibenclamide_
) or sulphonamides
•
IF YOU HAVE HAD A HEART ATTACK OR SEVERE ANGINA,
that’s being treated in hospital
•
IF YOU HAVE HEART FAILURE,
or have had heart failure in the past
•
IF YOU HAVE LIVER DISEASE
•
IF YOU 
                                
                                Lugege kogu dokumenti
                                
                            

Toote omadused

                                Medicinal product no longer authorised
1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
Medicinal product no longer authorised
2
1.
NAME OF THE MEDICINAL PRODUCT
AVAGLIM 4 mg/4 mg film-coated tablets.
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
_ _
Each tablet contains rosiglitazone maleate corresponding to 4 mg
rosiglitazone and 4 mg glimepiride.
Excipient
-
contains lactose (approximately 104 mg)
For a full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Film-coated tablet.
Pink, rounded triangular tablet with “gsk” debossed on one side
and “4/4” on the other side.
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
AVAGLIM is indicated in the treatment of type 2 diabetes mellitus
patients who are unable to achieve
sufficient glycaemic control on optimal dosage of
sulphonylurea monotherapy, and for whom
metformin is inappropriate because of contraindication or intolerance.
4.2
POSOLOGY AND METHOD OF ADMINISTRATION
AVAGLIM therapy should be individualised for each patient. Before
therapy is initiated with
AVAGLIM appropriate clinical evaluation should be made to assess the
patient’s risk of developing
hypoglycaemia (see section 4.4).
AVAGLIM should be taken once daily shortly before or during a meal
(usually the first main meal of
the day). If a dose is forgotten, the following dose must not be
increased.
_For patients inadequately controlled on glimepiride monotherapy
(typically 4 mg)._
Concomitant
administration should be considered before the patient is switched to
AVAGLIM. Where clinically
appropriate, direct change from glimepiride monotherapy to AVAGLIM may
be considered
.
The
starting dose is 4 mg/day rosiglitazone plus 4 mg/day glimepiride
(given as one tablet AVAGLIM
4 mg/4 mg).
_Patients unable to achieve glycaemic control on at least half-maximum
dose of other sulphonylurea _
_monotherapy (except chlorpropamide, see section 4.4)._
Rosiglitazone 4 mg should be administered
concomitantly with the dose of sulphonylurea already being taken. Once
glycaemic control is stable at
these doses
                                
                                Lugege kogu dokumenti
                                
                            

Dokumendid teistes keeltes

Infovoldik Infovoldik bulgaaria 17-01-2011
Toote omadused Toote omadused bulgaaria 17-01-2011
Avaliku hindamisaruande Avaliku hindamisaruande bulgaaria 17-01-2011
Infovoldik Infovoldik hispaania 17-01-2011
Toote omadused Toote omadused hispaania 17-01-2011
Avaliku hindamisaruande Avaliku hindamisaruande hispaania 17-01-2011
Infovoldik Infovoldik tšehhi 17-01-2011
Toote omadused Toote omadused tšehhi 17-01-2011
Avaliku hindamisaruande Avaliku hindamisaruande tšehhi 17-01-2011
Infovoldik Infovoldik taani 17-01-2011
Toote omadused Toote omadused taani 17-01-2011
Avaliku hindamisaruande Avaliku hindamisaruande taani 17-01-2011
Infovoldik Infovoldik saksa 17-01-2011
Toote omadused Toote omadused saksa 17-01-2011
Avaliku hindamisaruande Avaliku hindamisaruande saksa 17-01-2011
Infovoldik Infovoldik eesti 17-01-2011
Toote omadused Toote omadused eesti 17-01-2011
Avaliku hindamisaruande Avaliku hindamisaruande eesti 17-01-2011
Infovoldik Infovoldik kreeka 17-01-2011
Toote omadused Toote omadused kreeka 17-01-2011
Avaliku hindamisaruande Avaliku hindamisaruande kreeka 17-01-2011
Infovoldik Infovoldik prantsuse 17-01-2011
Toote omadused Toote omadused prantsuse 17-01-2011
Avaliku hindamisaruande Avaliku hindamisaruande prantsuse 17-01-2011
Infovoldik Infovoldik itaalia 17-01-2011
Toote omadused Toote omadused itaalia 17-01-2011
Avaliku hindamisaruande Avaliku hindamisaruande itaalia 17-01-2011
Infovoldik Infovoldik läti 17-01-2011
Toote omadused Toote omadused läti 17-01-2011
Avaliku hindamisaruande Avaliku hindamisaruande läti 17-01-2011
Infovoldik Infovoldik leedu 17-01-2011
Toote omadused Toote omadused leedu 17-01-2011
Avaliku hindamisaruande Avaliku hindamisaruande leedu 17-01-2011
Infovoldik Infovoldik ungari 17-01-2011
Toote omadused Toote omadused ungari 17-01-2011
Avaliku hindamisaruande Avaliku hindamisaruande ungari 17-01-2011
Infovoldik Infovoldik malta 17-01-2011
Toote omadused Toote omadused malta 17-01-2011
Avaliku hindamisaruande Avaliku hindamisaruande malta 17-01-2011
Infovoldik Infovoldik hollandi 17-01-2011
Toote omadused Toote omadused hollandi 17-01-2011
Avaliku hindamisaruande Avaliku hindamisaruande hollandi 17-01-2011
Infovoldik Infovoldik poola 17-01-2011
Toote omadused Toote omadused poola 17-01-2011
Avaliku hindamisaruande Avaliku hindamisaruande poola 17-01-2011
Infovoldik Infovoldik portugali 17-01-2011
Toote omadused Toote omadused portugali 17-01-2011
Avaliku hindamisaruande Avaliku hindamisaruande portugali 17-01-2011
Infovoldik Infovoldik rumeenia 17-01-2011
Toote omadused Toote omadused rumeenia 17-01-2011
Avaliku hindamisaruande Avaliku hindamisaruande rumeenia 17-01-2011
Infovoldik Infovoldik slovaki 17-01-2011
Toote omadused Toote omadused slovaki 17-01-2011
Avaliku hindamisaruande Avaliku hindamisaruande slovaki 17-01-2011
Infovoldik Infovoldik sloveeni 17-01-2011
Toote omadused Toote omadused sloveeni 17-01-2011
Avaliku hindamisaruande Avaliku hindamisaruande sloveeni 17-01-2011
Infovoldik Infovoldik soome 17-01-2011
Toote omadused Toote omadused soome 17-01-2011
Avaliku hindamisaruande Avaliku hindamisaruande soome 17-01-2011
Infovoldik Infovoldik rootsi 17-01-2011
Toote omadused Toote omadused rootsi 17-01-2011
Avaliku hindamisaruande Avaliku hindamisaruande rootsi 17-01-2011

Otsige selle tootega seotud teateid

Vaadake dokumentide ajalugu