Temozolomide Sandoz

Nchi: Umoja wa Ulaya

Lugha: Kiingereza

Chanzo: EMA (European Medicines Agency)

Nunua Sasa

Taarifa za kipeperushi Taarifa za kipeperushi (PIL)
27-02-2023
Tabia za bidhaa Tabia za bidhaa (SPC)
27-02-2023

Viambatanisho vya kazi:

temozolomide

Inapatikana kutoka:

Sandoz GmbH

ATC kanuni:

L01AX03

INN (Jina la Kimataifa):

temozolomide

Kundi la matibabu:

Antineoplastic agents

Eneo la matibabu:

Glioma; Glioblastoma

Matibabu dalili:

For the treatment of adult patients with newly diagnosed glioblastoma multiforme concomitantly with radiotherapy (RT) and subsequently as monotherapy treatment.For the treatment of children from the age of three years, adolescents and adult patients with malignant glioma, such as glioblastoma multiforme or anaplastic astrocytoma, showing recurrence or progression after standard therapy.

Bidhaa muhtasari:

Revision: 17

Idhini hali ya:

Withdrawn

Idhini ya tarehe:

2010-03-15

Taarifa za kipeperushi

                                132
B. PACKAGE LEAFLET
Medicinal product no longer authorised
133
PACKAGE LEAFLET: INFORMATION FOR THE USER
TEMOZOLOMIDE SANDOZ 5 MG HARD CAPSULES
TEMOZOLOMIDE SANDOZ 20 MG HARD CAPSULES
TEMOZOLOMIDE SANDOZ 100 MG HARD CAPSULES
TEMOZOLOMIDE SANDOZ 140 MG HARD CAPSULES
TEMOZOLOMIDE SANDOZ 180 MG HARD CAPSULES
TEMOZOLOMIDE SANDOZ 250 MG HARD CAPSULES
temozolomide
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 Temozolomide Sandoz is and what it is used for
2.
What you need to know before you take Temozolomide Sandoz
3.
How to take Temozolomide Sandoz
4.
Possible side effects
5.
How to store Temozolomide Sandoz
6.
Contents of the pack and other information
1.
WHAT TEMOZOLOMIDE SANDOZ IS AND WHAT IT IS USED FOR
Temozolomide Sandoz contains a medicine called temozolomide. This
medicine is an antitumour
agent.
Temozolomide Sandoz is used for the treatment of specific forms of
brain tumours:
•
in adults with newly-diagnosed glioblastoma multiforme. Temozolomide
Sandoz is first used
together with radiotherapy (concomitant phase of treatment) and after
that alone (monotherapy
phase of treatment).
•
in children 3 years and older and adult patients with malignant glioma
, such as glioblastoma
multiforme or anaplastic astrocytoma. Temozolomide Sandoz is used in
these tumours if they
return or get worse after standard treatment.
2.
WHAT YOU NEED TO KNOW BEFORE YOU TAKE TEMOZOLOMIDE SANDOZ
_ _
DO NOT TAKE TEMOZOLOMIDE SANDOZ
•
if you are allergic to temozolomide or any of the other ingredi
                                
                                Soma hati kamili
                                
                            

Tabia za bidhaa

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
Medicinal product no longer authorised
2
1.
NAME OF THE MEDICINAL PRODUCT
Temozolomide Sandoz 5 mg hard capsules
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Each hard capsule contains 5 mg of temozolomide.
Excipient with known effect:
Each hard capsule contains 168 mg of anhydrous lactose.
For the full list of excipients, see section 6.1.
_ _
3.
PHARMACEUTICAL FORM
Hard capsule (capsule).
_ _
The hard capsules have a white coloured body, a green coloured cap,
and are imprinted with black
ink. The cap is imprinted with “TMZ”. The body is imprinted with
“5”.
_ _
Each capsule is approximately 15.8 mm in length.
_ _
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
Temozolomide Sandoz is indicated for the treatment of:
-
adult patients with newly-diagnosed glioblastoma multiforme
concomitantly with radiotherapy
(RT) and subsequently as monotherapy treatment,
-
children from the age of three years, adolescents and adult patients
with malignant glioma, such
as glioblastoma multiforme or anaplastic astrocytoma, showing
recurrence or progression after
standard therapy.
4.2
POSOLOGY AND METHOD OF ADMINISTRATION
Temozolomide Sandoz should only be prescribed by physicians
experienced in the oncological
treatment of brain tumours.
Anti-emetic therapy may be administered (see section 4.4).
Posology
_ _
_Adult patients with newly-diagnosed glioblastoma multiforme _
Temozolomide Sandoz is administered in combination with focal
radiotherapy (concomitant phase)
followed by up to 6 cycles of temozolomide (TMZ) monotherapy
(monotherapy phase).
_ _
_Concomitant phase _
TMZ is administered orally at a dose of 75 mg/m
2
daily for 42 days concomitant with focal
radiotherapy (60 Gy administered in 30 fractions). No dose reductions
are recommended, but delay or
discontinuation of TMZ administration should be decided weekly
according to haematological and
non-haematological toxicity criteria. TMZ administration can be
continued throughout the 42 day
concomitant period (up to 49 days) 
                                
                                Soma hati kamili
                                
                            

Nyaraka katika lugha zingine

Taarifa za kipeperushi Taarifa za kipeperushi Kibulgaria 27-02-2023
Tabia za bidhaa Tabia za bidhaa Kibulgaria 27-02-2023
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kibulgaria 27-02-2023
Taarifa za kipeperushi Taarifa za kipeperushi Kihispania 27-02-2023
Tabia za bidhaa Tabia za bidhaa Kihispania 27-02-2023
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kihispania 27-02-2023
Taarifa za kipeperushi Taarifa za kipeperushi Kicheki 27-02-2023
Tabia za bidhaa Tabia za bidhaa Kicheki 27-02-2023
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kicheki 27-02-2023
Taarifa za kipeperushi Taarifa za kipeperushi Kidenmaki 27-02-2023
Tabia za bidhaa Tabia za bidhaa Kidenmaki 27-02-2023
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kidenmaki 27-02-2023
Taarifa za kipeperushi Taarifa za kipeperushi Kijerumani 27-02-2023
Tabia za bidhaa Tabia za bidhaa Kijerumani 27-02-2023
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kijerumani 27-02-2023
Taarifa za kipeperushi Taarifa za kipeperushi Kiestonia 27-02-2023
Tabia za bidhaa Tabia za bidhaa Kiestonia 27-02-2023
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kiestonia 27-02-2023
Taarifa za kipeperushi Taarifa za kipeperushi Kigiriki 27-02-2023
Tabia za bidhaa Tabia za bidhaa Kigiriki 27-02-2023
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kigiriki 27-02-2023
Taarifa za kipeperushi Taarifa za kipeperushi Kifaransa 27-02-2023
Tabia za bidhaa Tabia za bidhaa Kifaransa 27-02-2023
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kifaransa 27-02-2023
Taarifa za kipeperushi Taarifa za kipeperushi Kiitaliano 27-02-2023
Tabia za bidhaa Tabia za bidhaa Kiitaliano 27-02-2023
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kiitaliano 27-02-2023
Taarifa za kipeperushi Taarifa za kipeperushi Kilatvia 27-02-2023
Tabia za bidhaa Tabia za bidhaa Kilatvia 27-02-2023
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kilatvia 27-02-2023
Taarifa za kipeperushi Taarifa za kipeperushi Kilithuania 27-02-2023
Tabia za bidhaa Tabia za bidhaa Kilithuania 27-02-2023
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kilithuania 27-02-2023
Taarifa za kipeperushi Taarifa za kipeperushi Kihungari 27-02-2023
Tabia za bidhaa Tabia za bidhaa Kihungari 27-02-2023
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kihungari 27-02-2023
Taarifa za kipeperushi Taarifa za kipeperushi Kimalta 27-02-2023
Tabia za bidhaa Tabia za bidhaa Kimalta 27-02-2023
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kimalta 27-02-2023
Taarifa za kipeperushi Taarifa za kipeperushi Kiholanzi 27-02-2023
Tabia za bidhaa Tabia za bidhaa Kiholanzi 27-02-2023
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kiholanzi 27-02-2023
Taarifa za kipeperushi Taarifa za kipeperushi Kipolandi 27-02-2023
Tabia za bidhaa Tabia za bidhaa Kipolandi 27-02-2023
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kipolandi 27-02-2023
Taarifa za kipeperushi Taarifa za kipeperushi Kireno 27-02-2023
Tabia za bidhaa Tabia za bidhaa Kireno 27-02-2023
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kireno 27-02-2023
Taarifa za kipeperushi Taarifa za kipeperushi Kiromania 27-02-2023
Tabia za bidhaa Tabia za bidhaa Kiromania 27-02-2023
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kiromania 27-02-2023
Taarifa za kipeperushi Taarifa za kipeperushi Kislovakia 27-02-2023
Tabia za bidhaa Tabia za bidhaa Kislovakia 27-02-2023
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kislovakia 27-02-2023
Taarifa za kipeperushi Taarifa za kipeperushi Kislovenia 27-02-2023
Tabia za bidhaa Tabia za bidhaa Kislovenia 27-02-2023
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kislovenia 27-02-2023
Taarifa za kipeperushi Taarifa za kipeperushi Kifinlandi 27-02-2023
Tabia za bidhaa Tabia za bidhaa Kifinlandi 27-02-2023
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kifinlandi 27-02-2023
Taarifa za kipeperushi Taarifa za kipeperushi Kiswidi 27-02-2023
Tabia za bidhaa Tabia za bidhaa Kiswidi 27-02-2023
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kiswidi 27-02-2023
Taarifa za kipeperushi Taarifa za kipeperushi Kinorwe 27-02-2023
Tabia za bidhaa Tabia za bidhaa Kinorwe 27-02-2023
Taarifa za kipeperushi Taarifa za kipeperushi Kiaisilandi 27-02-2023
Tabia za bidhaa Tabia za bidhaa Kiaisilandi 27-02-2023
Taarifa za kipeperushi Taarifa za kipeperushi Kroeshia 27-02-2023
Tabia za bidhaa Tabia za bidhaa Kroeshia 27-02-2023
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kroeshia 27-02-2023

Tafuta arifu zinazohusiana na bidhaa hii