Actos

Nazione: Unione Europea

Lingua: inglese

Fonte: EMA (European Medicines Agency)

Compra

Foglio illustrativo Foglio illustrativo (PIL)
28-08-2023
Scheda tecnica Scheda tecnica (SPC)
28-08-2023

Principio attivo:

pioglitazone hydrochloride

Commercializzato da:

CHEPLAPHARM Arzneimittel GmbH

Codice ATC:

A10BG03

INN (Nome Internazionale):

pioglitazone

Gruppo terapeutico:

Drugs used in diabetes

Area terapeutica:

Diabetes Mellitus, Type 2

Indicazioni terapeutiche:

Pioglitazone is indicated in the treatment of type-2 diabetes mellitus:as monotherapy:in patients (particularly overweight patients) inadequately controlled by diet and exercise for whom metformin is inappropriate because of contraindications or intolerance;as dual oral therapy in combination with:metformin, in patients (particularly overweight patients) with insufficient glycaemic control despite maximal tolerated dose of monotherapy with metformin;a sulphonylurea, only in patients who show intolerance to metformin or for whom metformin is contraindicated, with insufficient glycaemic control despite maximal tolerated dose of monotherapy with a sulphonylurea;as triple oral therapy in combination with:metformin and a sulphonylurea, in patients (particularly overweight patients) with insufficient glycaemic control despite dual oral therapy.Pioglitazone is also indicated for combination with insulin in type-2 diabetes mellitus patients with insufficient glycaemic control on insulin for whom metformin is inappropriate because of contraindications or intolerance.

Dettagli prodotto:

Revision: 30

Stato dell'autorizzazione:

Authorised

Data dell'autorizzazione:

2000-10-13

Foglio illustrativo

                                28
B. PACKAGE LEAFLET
29
PACKAGE LEAFLET: INFORMATION FOR THE PATIENT
ACTOS 15 MG TABLETS
ACTOS 30 MG TABLETS
ACTOS 45 MG TABLETS
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 Actos is and what it is used for
2.
What you need to know before you take Actos
3.
How to take Actos
4.
Possible side effects
5.
How to store Actos
6.
Contents of the pack and other information
1.
WHAT ACTOS IS AND WHAT IT IS USED FOR
Actos contains pioglitazone. It is an anti-diabetic medicine used to
treat type 2 (non-insulin dependent)
diabetes mellitus in adults, when metformin is not suitable or has
failed to work adequately. This is the
diabetes that usually develops in adulthood.
Actos helps control the level of sugar in your blood when you have
type 2 diabetes by helping your
body make better use of the insulin it produces. Your doctor will
check whether Actos is working 3 to
6 months after you start taking it.
Actos may be used on its own in patients who are unable to take
metformin, and where treatment with
diet and exercise has failed to control blood sugar or may be added to
other therapies (such as
metformin, sulphonylurea or insulin) which have failed to provide
sufficient control of blood sugar.
2.
WHAT YOU NEED TO KNOW BEFORE YOU TAKE ACTOS
DO NOT TAKE ACTOS
-
if you are allergic to pioglitazone or any of the other ingredients of
this medicine (listed in
section 6).
-
if you have heart failure or have had heart failure in the past.
-
if you have liver disease.
-
if you have had diabetic ketoa
                                
                                Leggi il documento completo
                                
                            

Scheda tecnica

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE MEDICINAL PRODUCT
Actos 15 mg tablets
Actos 30 mg tablets
Actos 45 mg tablets
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Actos 15 mg tablets
Each tablet contains 15 mg of pioglitazone (as hydrochloride).
_Excipient with known effect_
Each tablet contains 92.87 mg of lactose monohydrate (see section
4.4).
Actos 30 mg tablets
Each tablet contains 30 mg of pioglitazone (as hydrochloride).
_Excipient with known effect_
Each tablet contains 76.34 mg of lactose monohydrate (see section
4.4).
Actos 45 mg tablets
Each tablet contains 45 mg of pioglitazone (as hydrochloride).
_Excipient with known effect_
Each tablet contains 114.51 mg of lactose monohydrate (see section
4.4).
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Tablet
Actos 15 mg tablets
The tablets are white to off-white, round, convex and marked ‘15’
on one face and ‘ACTOS’ on the
other face.
Actos 30 mg tablets
The tablets are white to off-white, round, flat and marked ‘30’ on
one face and ‘ACTOS’ on the other
face.
Actos 45 mg tablets
The tablets are white to off-white, round, flat and marked ‘45’ on
one face and ‘ACTOS’ on the other
face.
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
Pioglitazone is indicated as second or third line treatment of type 2
diabetes mellitus as described
below:
3
as
MONOTHERAPY
-
in adult patients (particularly overweight patients) inadequately
controlled by diet and
exercise for whom metformin is inappropriate because of
contraindications or
intolerance
as
DUAL ORAL THERAPY
in combination with
-
metformin, in adult patients (particularly overweight patients) with
insufficient
glycaemic control despite maximal tolerated dose of monotherapy with
metformin
-
a sulphonylurea, only in adult patients who show intolerance to
metformin or for
whom metformin is contraindicated, with insufficient glycaemic control
despite
maximal tolerated dose of monotherapy with a sulphonylurea.
as
TRIPLE ORAL THERAPY
in combination 
                                
                                Leggi il documento completo
                                
                            

Documenti in altre lingue

Foglio illustrativo Foglio illustrativo bulgaro 28-08-2023
Scheda tecnica Scheda tecnica bulgaro 28-08-2023
Foglio illustrativo Foglio illustrativo spagnolo 28-08-2023
Scheda tecnica Scheda tecnica spagnolo 28-08-2023
Relazione pubblica di valutazione Relazione pubblica di valutazione spagnolo 29-09-2016
Foglio illustrativo Foglio illustrativo ceco 28-08-2023
Scheda tecnica Scheda tecnica ceco 28-08-2023
Foglio illustrativo Foglio illustrativo danese 28-08-2023
Scheda tecnica Scheda tecnica danese 28-08-2023
Foglio illustrativo Foglio illustrativo tedesco 28-08-2023
Scheda tecnica Scheda tecnica tedesco 28-08-2023
Foglio illustrativo Foglio illustrativo estone 28-08-2023
Scheda tecnica Scheda tecnica estone 28-08-2023
Foglio illustrativo Foglio illustrativo greco 28-08-2023
Scheda tecnica Scheda tecnica greco 28-08-2023
Foglio illustrativo Foglio illustrativo francese 28-08-2023
Scheda tecnica Scheda tecnica francese 28-08-2023
Relazione pubblica di valutazione Relazione pubblica di valutazione francese 29-09-2016
Foglio illustrativo Foglio illustrativo italiano 28-08-2023
Scheda tecnica Scheda tecnica italiano 28-08-2023
Relazione pubblica di valutazione Relazione pubblica di valutazione italiano 29-09-2016
Foglio illustrativo Foglio illustrativo lettone 28-08-2023
Scheda tecnica Scheda tecnica lettone 28-08-2023
Foglio illustrativo Foglio illustrativo lituano 28-08-2023
Scheda tecnica Scheda tecnica lituano 28-08-2023
Foglio illustrativo Foglio illustrativo ungherese 28-08-2023
Scheda tecnica Scheda tecnica ungherese 28-08-2023
Relazione pubblica di valutazione Relazione pubblica di valutazione ungherese 29-09-2016
Foglio illustrativo Foglio illustrativo maltese 28-08-2023
Scheda tecnica Scheda tecnica maltese 28-08-2023
Foglio illustrativo Foglio illustrativo olandese 28-08-2023
Scheda tecnica Scheda tecnica olandese 28-08-2023
Relazione pubblica di valutazione Relazione pubblica di valutazione olandese 29-09-2016
Foglio illustrativo Foglio illustrativo polacco 28-08-2023
Scheda tecnica Scheda tecnica polacco 28-08-2023
Foglio illustrativo Foglio illustrativo portoghese 28-08-2023
Scheda tecnica Scheda tecnica portoghese 28-08-2023
Relazione pubblica di valutazione Relazione pubblica di valutazione portoghese 29-09-2016
Foglio illustrativo Foglio illustrativo rumeno 28-08-2023
Scheda tecnica Scheda tecnica rumeno 28-08-2023
Foglio illustrativo Foglio illustrativo slovacco 28-08-2023
Scheda tecnica Scheda tecnica slovacco 28-08-2023
Relazione pubblica di valutazione Relazione pubblica di valutazione slovacco 29-09-2016
Foglio illustrativo Foglio illustrativo sloveno 28-08-2023
Scheda tecnica Scheda tecnica sloveno 28-08-2023
Foglio illustrativo Foglio illustrativo finlandese 28-08-2023
Scheda tecnica Scheda tecnica finlandese 28-08-2023
Relazione pubblica di valutazione Relazione pubblica di valutazione finlandese 29-09-2016
Foglio illustrativo Foglio illustrativo svedese 28-08-2023
Scheda tecnica Scheda tecnica svedese 28-08-2023
Foglio illustrativo Foglio illustrativo norvegese 28-08-2023
Scheda tecnica Scheda tecnica norvegese 28-08-2023
Foglio illustrativo Foglio illustrativo islandese 28-08-2023
Scheda tecnica Scheda tecnica islandese 28-08-2023
Foglio illustrativo Foglio illustrativo croato 28-08-2023
Scheda tecnica Scheda tecnica croato 28-08-2023

Cerca alert relativi a questo prodotto

Visualizza cronologia documenti