Zytiga

Riik: Euroopa Liit

keel: inglise

Allikas: EMA (European Medicines Agency)

Osta kohe

Infovoldik Infovoldik (PIL)
29-06-2022
Toote omadused Toote omadused (SPC)
29-06-2022
Avaliku hindamisaruande Avaliku hindamisaruande (PAR)
12-01-2018

Toimeaine:

abiraterone acetate

Saadav alates:

Janssen-Cilag International N.V.

ATC kood:

L02BX03

INN (Rahvusvaheline Nimetus):

abiraterone

Terapeutiline rühm:

Endocrine therapy

Terapeutiline ala:

Prostatic Neoplasms

Näidustused:

Zytiga is indicated with prednisone or prednisolone for:the treatment of metastatic castration resistant prostate cancer in adult men who are asymptomatic or mildly symptomatic after failure of androgen deprivation therapy in whom chemotherapy is not yet clinically indicatedthe treatment of metastatic castration resistant prostate cancer in adult men whose disease has progressed on or after a docetaxel based chemotherapy regimen.

Toote kokkuvõte:

Revision: 26

Volitamisolek:

Authorised

Loa andmise kuupäev:

2011-09-05

Infovoldik

                                63
B. PACKAGE LEAFLET
64
PACKAGE LEAFLET: INFORMATION FOR THE USER
ZYTIGA 250 MG TABLETS
abiraterone acetate
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 ZYTIGA is and what it is used for
2.
What you need to know before you take ZYTIGA
3.
How to take ZYTIGA
4.
Possible side effects
5.
How to store ZYTIGA
6.
Contents of the pack and other information
1.
WHAT ZYTIGA IS AND WHAT IT IS USED FOR
ZYTIGA contains a medicine called abiraterone acetate. It is used to
treat prostate cancer in adult men
that has spread to other parts of the body. ZYTIGA stops your body
from making testosterone; this can
slow the growth of prostate cancer.
When ZYTIGA is prescribed for the early stage of disease where it is
still responding to hormone
therapy, it is used with a treatment that lowers testosterone
(androgen deprivation therapy).
When you take this medicine your doctor will also prescribe another
medicine called prednisone or
prednisolone. This is to lower your chances of getting high blood
pressure, having too much water in
your body (fluid retention), or having reduced levels of a chemical
known as potassium in your blood.
2.
WHAT YOU NEED TO KNOW BEFORE YOU TAKE ZYTIGA
DO NOT TAKE ZYTIGA
-
if you are allergic to abiraterone acetate or any of the other
ingredients of this medicine (listed
in section 6).
-
if you are a woman, especially if pregnant. ZYTIGA is for use in male
patients only.
-
if you have severe liver damage.
-
in combination with Ra-223 (which is used to treat prostate cancer).
Do not take 
                                
                                Lugege kogu dokumenti
                                
                            

Toote omadused

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE MEDICINAL PRODUCT
ZYTIGA 250 mg tablets
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Each tablet contains 250 mg of abiraterone acetate equivalent to 223
mg of abiraterone.
Excipients with known effect
Each tablet contains 198.65 mg of lactose monohydrate and 6.8 mg of
sodium.
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Tablet
White to off-white oval tablets (15.9 mm long x 9.5 mm wide), debossed
with AA250 on one side.
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
ZYTIGA is indicated with prednisone or prednisolone for:

the treatment of newly diagnosed high risk metastatic hormone
sensitive prostate cancer
(mHSPC) in adult men in combination with androgen deprivation therapy
(ADT) (see section
5.1)

the treatment of metastatic castration resistant prostate cancer
(mCRPC) in adult men who are
asymptomatic or mildly symptomatic after failure of androgen
deprivation therapy in whom
chemotherapy is not yet clinically indicated (see section 5.1)

the treatment of mCRPC in adult men whose disease has progressed on or
after a
docetaxel-based chemotherapy regimen.
4.2
POSOLOGY AND METHOD OF ADMINISTRATION
This medicinal product should be prescribed by an appropriate
healthcare professional.
Posology
The recommended dose is 1 000 mg (four 250 mg tablets) as a single
daily dose that must not be taken
with food (see “Method of administration” below). Taking the
tablets with food increases systemic
exposure to abiraterone (see sections 4.5 and 5.2).
_Dosage of prednisone or prednisolone_
For mHSPC, ZYTIGA is used with 5 mg prednisone or prednisolone daily.
For mCRPC, ZYTIGA is used with 10 mg prednisone or prednisolone daily.
Medical castration with luteinising hormone releasing hormone (LHRH)
analogue should be continued
during treatment in patients not surgically castrated.
_Recommended monitoring_
Serum transaminases should be measured prior to starting treatment,
every two weeks for the first
three months of tre
                                
                                Lugege kogu dokumenti
                                
                            

Dokumendid teistes keeltes

Infovoldik Infovoldik bulgaaria 29-06-2022
Toote omadused Toote omadused bulgaaria 29-06-2022
Avaliku hindamisaruande Avaliku hindamisaruande bulgaaria 12-01-2018
Infovoldik Infovoldik hispaania 29-06-2022
Toote omadused Toote omadused hispaania 29-06-2022
Avaliku hindamisaruande Avaliku hindamisaruande hispaania 12-01-2018
Infovoldik Infovoldik tšehhi 29-06-2022
Toote omadused Toote omadused tšehhi 29-06-2022
Avaliku hindamisaruande Avaliku hindamisaruande tšehhi 12-01-2018
Infovoldik Infovoldik taani 29-06-2022
Toote omadused Toote omadused taani 29-06-2022
Avaliku hindamisaruande Avaliku hindamisaruande taani 12-01-2018
Infovoldik Infovoldik saksa 29-06-2022
Toote omadused Toote omadused saksa 29-06-2022
Avaliku hindamisaruande Avaliku hindamisaruande saksa 12-01-2018
Infovoldik Infovoldik eesti 29-06-2022
Toote omadused Toote omadused eesti 29-06-2022
Avaliku hindamisaruande Avaliku hindamisaruande eesti 12-01-2018
Infovoldik Infovoldik kreeka 29-06-2022
Toote omadused Toote omadused kreeka 29-06-2022
Avaliku hindamisaruande Avaliku hindamisaruande kreeka 12-01-2018
Infovoldik Infovoldik prantsuse 29-06-2022
Toote omadused Toote omadused prantsuse 29-06-2022
Avaliku hindamisaruande Avaliku hindamisaruande prantsuse 12-01-2018
Infovoldik Infovoldik itaalia 29-06-2022
Toote omadused Toote omadused itaalia 29-06-2022
Avaliku hindamisaruande Avaliku hindamisaruande itaalia 12-01-2018
Infovoldik Infovoldik läti 29-06-2022
Toote omadused Toote omadused läti 29-06-2022
Avaliku hindamisaruande Avaliku hindamisaruande läti 12-01-2018
Infovoldik Infovoldik leedu 29-06-2022
Toote omadused Toote omadused leedu 29-06-2022
Avaliku hindamisaruande Avaliku hindamisaruande leedu 12-01-2018
Infovoldik Infovoldik ungari 29-06-2022
Toote omadused Toote omadused ungari 29-06-2022
Avaliku hindamisaruande Avaliku hindamisaruande ungari 12-01-2018
Infovoldik Infovoldik malta 29-06-2022
Toote omadused Toote omadused malta 29-06-2022
Avaliku hindamisaruande Avaliku hindamisaruande malta 12-01-2018
Infovoldik Infovoldik hollandi 29-06-2022
Toote omadused Toote omadused hollandi 29-06-2022
Avaliku hindamisaruande Avaliku hindamisaruande hollandi 12-01-2018
Infovoldik Infovoldik poola 29-06-2022
Toote omadused Toote omadused poola 29-06-2022
Avaliku hindamisaruande Avaliku hindamisaruande poola 12-01-2018
Infovoldik Infovoldik portugali 29-06-2022
Toote omadused Toote omadused portugali 29-06-2022
Avaliku hindamisaruande Avaliku hindamisaruande portugali 12-01-2018
Infovoldik Infovoldik rumeenia 29-06-2022
Toote omadused Toote omadused rumeenia 29-06-2022
Avaliku hindamisaruande Avaliku hindamisaruande rumeenia 12-01-2018
Infovoldik Infovoldik slovaki 29-06-2022
Toote omadused Toote omadused slovaki 29-06-2022
Avaliku hindamisaruande Avaliku hindamisaruande slovaki 12-01-2018
Infovoldik Infovoldik sloveeni 29-06-2022
Toote omadused Toote omadused sloveeni 29-06-2022
Avaliku hindamisaruande Avaliku hindamisaruande sloveeni 12-01-2018
Infovoldik Infovoldik soome 29-06-2022
Toote omadused Toote omadused soome 29-06-2022
Avaliku hindamisaruande Avaliku hindamisaruande soome 12-01-2018
Infovoldik Infovoldik rootsi 29-06-2022
Toote omadused Toote omadused rootsi 29-06-2022
Avaliku hindamisaruande Avaliku hindamisaruande rootsi 12-01-2018
Infovoldik Infovoldik norra 29-06-2022
Toote omadused Toote omadused norra 29-06-2022
Infovoldik Infovoldik islandi 29-06-2022
Toote omadused Toote omadused islandi 29-06-2022
Infovoldik Infovoldik horvaadi 29-06-2022
Toote omadused Toote omadused horvaadi 29-06-2022
Avaliku hindamisaruande Avaliku hindamisaruande horvaadi 12-01-2018

Otsige selle tootega seotud teateid

Vaadake dokumentide ajalugu