Sutent

Țară: Uniunea Europeană

Limbă: engleză

Sursă: EMA (European Medicines Agency)

Cumpara asta acum

Prospect Prospect (PIL)
02-04-2024

Ingredient activ:

sunitinib

Disponibil de la:

Pfizer Limited

Codul ATC:

L01EX01

INN (nume internaţional):

sunitinib

Grupul Terapeutică:

Antineoplastic agents

Zonă Terapeutică:

Gastrointestinal Stromal Tumors; Carcinoma, Renal Cell; Neuroendocrine Tumors

Indicații terapeutice:

Gastrointestinal stromal tumour (GIST)Sutent is indicated for the treatment of unresectable and/or metastatic malignant gastrointestinal stromal tumour (GIST) in adults after failure of imatinib mesilate treatment due to resistance or intolerance.Metastatic renal cell carcinoma (MRCC)Sutent is indicated for the treatment of advanced/metastatic renal cell carcinoma (MRCC) in adults.Pancreatic neuroendocrine tumours (pNET)Sutent is indicated for the treatment of unresectable or metastatic, well-differentiated pancreatic neuroendocrine tumours with disease progression in adults.Experience with Sutent as first-line treatment is limited (see section 5.1).

Rezumat produs:

Revision: 39

Statutul autorizaţiei:

Authorised

Data de autorizare:

2006-07-19

Prospect

                                59
B. PACKAGE LEAFLET
60
PACKAGE LEAFLET: INFORMATION FOR THE USER
SUTENT 12.5 MG HARD CAPSULES
SUTENT 25 MG HARD CAPSULES
SUTENT 37.5 MG HARD CAPSULES
SUTENT 50 MG HARD CAPSULES
sunitinib
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. This includes any
possible side effects not listed
in this leaflet. See section 4.
WHAT IS IN THIS LEAFLET
1.
What Sutent is and what it is used for
2.
What you need to know before you take Sutent
3.
How to take Sutent
4.
Possible side effects
5.
How to store Sutent
6.
Contents of the pack and other information
1.
WHAT SUTENT IS AND WHAT IT IS USED FOR
Sutent contains the active substance sunitinib, which is a protein
kinase inhibitor. It is
used to treat
cancer by preventing the activity of a special group of proteins which
are known to be involved in the
growth and spread of cancer cells.
Sutent is used to treat adults with the following types of cancer:
-
Gastrointestinal stromal tumour (GIST), a type of cancer of the
stomach and bowel, where
imatinib (another anticancer medicine) no longer works or you cannot
take imatinib.
-
Metastatic renal cell carcinoma (MRCC), a type of kidney cancer that
has spread to other parts
of the body.
-
Pancreatic neuroendocrine tumours (pNET) (tumours of the
hormone-producing cells in the
pancreas) that have progressed or cannot be removed with surgery.
If you have any questions about how Sutent works or why this medicine
has been prescribed for you,
ask your doctor.
2.
WHAT YOU NEED TO KNOW BEFORE YOU TAKE SUTENT
DO NOT TAKE SUTENT
-
If you are allergic to sunitinib or any of the other ingredients of
Sutent (listed in section 6).
61
WARNINGS AND PRECAUT
                                
                                Citiți documentul complet
                                
                            

Caracteristicilor produsului

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
_ _
2
1.
NAME OF THE MEDICINAL PRODUCT
Sutent 12.5 mg hard capsules
Sutent 25 mg hard capsules
Sutent 37.5 mg hard capsules
Sutent 50 mg hard capsules
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
12.5 mg hard capsules
Each capsule contains sunitinib malate, equivalent to 12.5 mg of
sunitinib.
25 mg hard capsules
Each capsule contains sunitinib malate, equivalent to 25 mg of
sunitinib.
37.5 mg hard capsules
Each capsule contains sunitinib malate, equivalent to 37.5 mg of
sunitinib.
50 mg hard capsules
Each capsule contains sunitinib malate, equivalent to 50 mg of
sunitinib.
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Hard capsule.
Sutent 12.5 mg hard capsules
Gelatin capsules with orange cap and orange body, printed with white
ink “Pfizer” on the cap,
“STN 12.5 mg” on the body, and containing yellow to orange
granules.
Sutent 25 mg hard capsules
Gelatin capsules with caramel cap and orange body, printed with white
ink “Pfizer” on the cap,
“STN 25 mg” on the body, and containing yellow to orange granules.
Sutent 37.5 mg hard capsules
Gelatin capsules with yellow cap and yellow body, printed with black
ink “Pfizer” on the cap,
“STN 37.5 mg” on the body, and containing yellow to orange
granules.
Sutent 50 mg hard capsules
Gelatin capsule with caramel cap and caramel body, printed with white
ink “Pfizer” on the cap,
“STN 50 mg” on the body, and containing yellow to orange granules.
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
Gastrointestinal stromal tumour (GIST)
Sutent is indicated for the treatment of unresectable and/or
metastatic malignant
gastrointestinal
stromal tumour (GIST) in adults after failure of imatinib treatment
due to resistance or intolerance.
Metastatic renal cell carcinoma (MRCC)
Sutent is indicated for the treatment of advanced/metastatic renal
cell carcinoma (MRCC) in adults.
3
Pancreatic neuroendocrine tumours (pNET)
Sutent is indicated for the treatment of unresectable or metastatic,

                                
                                Citiți documentul complet
                                
                            

Documente în alte limbi

Prospect Prospect bulgară 02-04-2024
Caracteristicilor produsului Caracteristicilor produsului bulgară 02-04-2024
Raport public de evaluare Raport public de evaluare bulgară 03-10-2014
Prospect Prospect spaniolă 02-04-2024
Caracteristicilor produsului Caracteristicilor produsului spaniolă 02-04-2024
Raport public de evaluare Raport public de evaluare spaniolă 03-10-2014
Prospect Prospect cehă 02-04-2024
Caracteristicilor produsului Caracteristicilor produsului cehă 02-04-2024
Raport public de evaluare Raport public de evaluare cehă 03-10-2014
Prospect Prospect daneză 02-04-2024
Caracteristicilor produsului Caracteristicilor produsului daneză 02-04-2024
Raport public de evaluare Raport public de evaluare daneză 03-10-2014
Prospect Prospect germană 02-04-2024
Caracteristicilor produsului Caracteristicilor produsului germană 02-04-2024
Raport public de evaluare Raport public de evaluare germană 03-10-2014
Prospect Prospect estoniană 02-04-2024
Caracteristicilor produsului Caracteristicilor produsului estoniană 02-04-2024
Raport public de evaluare Raport public de evaluare estoniană 03-10-2014
Prospect Prospect greacă 02-04-2024
Caracteristicilor produsului Caracteristicilor produsului greacă 02-04-2024
Raport public de evaluare Raport public de evaluare greacă 03-10-2014
Prospect Prospect franceză 02-04-2024
Caracteristicilor produsului Caracteristicilor produsului franceză 02-04-2024
Raport public de evaluare Raport public de evaluare franceză 03-10-2014
Prospect Prospect italiană 02-04-2024
Caracteristicilor produsului Caracteristicilor produsului italiană 02-04-2024
Raport public de evaluare Raport public de evaluare italiană 03-10-2014
Prospect Prospect letonă 02-04-2024
Caracteristicilor produsului Caracteristicilor produsului letonă 02-04-2024
Raport public de evaluare Raport public de evaluare letonă 03-10-2014
Prospect Prospect lituaniană 02-04-2024
Caracteristicilor produsului Caracteristicilor produsului lituaniană 02-04-2024
Raport public de evaluare Raport public de evaluare lituaniană 03-10-2014
Prospect Prospect maghiară 02-04-2024
Caracteristicilor produsului Caracteristicilor produsului maghiară 02-04-2024
Raport public de evaluare Raport public de evaluare maghiară 03-10-2014
Prospect Prospect malteză 02-04-2024
Caracteristicilor produsului Caracteristicilor produsului malteză 02-04-2024
Raport public de evaluare Raport public de evaluare malteză 03-10-2014
Prospect Prospect olandeză 02-04-2024
Caracteristicilor produsului Caracteristicilor produsului olandeză 02-04-2024
Raport public de evaluare Raport public de evaluare olandeză 03-10-2014
Prospect Prospect poloneză 02-04-2024
Caracteristicilor produsului Caracteristicilor produsului poloneză 02-04-2024
Raport public de evaluare Raport public de evaluare poloneză 03-10-2014
Prospect Prospect portugheză 02-04-2024
Caracteristicilor produsului Caracteristicilor produsului portugheză 02-04-2024
Raport public de evaluare Raport public de evaluare portugheză 03-10-2014
Prospect Prospect română 02-04-2024
Caracteristicilor produsului Caracteristicilor produsului română 02-04-2024
Raport public de evaluare Raport public de evaluare română 03-10-2014
Prospect Prospect slovacă 02-04-2024
Caracteristicilor produsului Caracteristicilor produsului slovacă 02-04-2024
Raport public de evaluare Raport public de evaluare slovacă 03-10-2014
Prospect Prospect slovenă 02-04-2024
Caracteristicilor produsului Caracteristicilor produsului slovenă 02-04-2024
Raport public de evaluare Raport public de evaluare slovenă 03-10-2014
Prospect Prospect finlandeză 02-04-2024
Caracteristicilor produsului Caracteristicilor produsului finlandeză 02-04-2024
Raport public de evaluare Raport public de evaluare finlandeză 03-10-2014
Prospect Prospect suedeză 02-04-2024
Caracteristicilor produsului Caracteristicilor produsului suedeză 02-04-2024
Raport public de evaluare Raport public de evaluare suedeză 03-10-2014
Prospect Prospect norvegiană 02-04-2024
Caracteristicilor produsului Caracteristicilor produsului norvegiană 02-04-2024
Prospect Prospect islandeză 02-04-2024
Caracteristicilor produsului Caracteristicilor produsului islandeză 02-04-2024
Prospect Prospect croată 02-04-2024
Caracteristicilor produsului Caracteristicilor produsului croată 02-04-2024
Raport public de evaluare Raport public de evaluare croată 03-10-2014

Căutați alerte legate de acest produs

Vizualizați istoricul documentelor