Potactasol

Country: Kesatuan Eropah

Bahasa: Inggeris

Sumber: EMA (European Medicines Agency)

Beli sekarang

Risalah maklumat Risalah maklumat (PIL)
01-06-2023
Ciri produk Ciri produk (SPC)
01-06-2023
Laporan Penilaian Awam Laporan Penilaian Awam (PAR)
10-11-2015

Bahan aktif:

topotecan

Boleh didapati daripada:

Actavis Group PTC ehf

Kod ATC:

L01CE01

INN (Nama Antarabangsa):

topotecan

Kumpulan terapeutik:

Antineoplastic agents

Kawasan terapeutik:

Uterine Cervical Neoplasms; Small Cell Lung Carcinoma

Tanda-tanda terapeutik:

Topotecan monotherapy is indicated for the treatment of:- patients with metastatic carcinoma of the ovary after failure of first-line or subsequent therapy- patients with relapsed small cell lung cancer (SCLC) for whom re-treatment with the first-line regimen is not considered appropriate (see section 5.1).Topotecan in combination with cisplatin is indicated for patients with carcinoma of the cervix recurrent after radiotherapy and for patients with Stage IVB disease. Patients with prior exposure to cisplatin require a sustained treatment free interval to justify treatment with the combination (see section 5.1).

Ringkasan produk:

Revision: 11

Status kebenaran:

Authorised

Tarikh kebenaran:

2011-01-06

Risalah maklumat

                                26
B. PACKAGE LEAFLET
27
PACKAGE LEAFLET: INFORMATION FOR THE USER
POTACTASOL 1 MG POWDER FOR CONCENTRATE FOR SOLUTION FOR INFUSION
POTACTASOL 4 MG POWDER FOR CONCENTRATE FOR SOLUTION FOR INFUSION
topotecan
READ ALL OF THIS LEAFLET CAREFULLY BEFORE YOU START USING 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 nurse.
-
If you get any side effects, talk to your doctor or nurse. This
includes any possible side effects
not listed in this leaflet. See section 4.
WHAT IS IN THIS LEAFLET
1.
What Potactasol is and what it is used for
2.
What you need to know before you use Potactasol
3.
How to use Potactasol
4.
Possible side effects
5.
How to store Potactasol
6.
Contents of the pack and other information
1.
WHAT POTACTASOL IS AND WHAT IT IS USED FOR
Potactasol contains the active substance topotecan which helps to kill
tumour cells.
Potactasol is used to treat:
-
ovarian cancer or small cell lung cancer that has come back after
chemotherapy
-
advanced cervical cancer if surgery or radiotherapy is not possible.
In this case Potactasol
treatment is combined with medicines containing cisplatin.
2.
WHAT YOU NEED TO KNOW BEFORE YOU USE POTACTASOL
DO NOT USE POTACTASOL
-
if you are allergic to topotecan or any of the other ingredients of
this medicine (listed in
section 6);
-
if you are breast-feeding.;
-
if your blood cell counts are too low. Your doctor will tell you
whether this is the case, based on
the results of your last blood test.
TELL YOU DOCTOR
if you think any of these could apply to you.
WARNINGS AND PRECAUTIONS
Talk to your doctor before using Potactasol:
-
if you have any kidney problems. Your dose of Potactasol may need to
be adjusted. Potactasol is
not recommended in case of severe kidney impairment;
-
if you have liver problems. Potactasol is not recommended in case of
severe liver impairment;
-
if you suffer from lung inflammation with signs such as cough, fever
and difficulties in

                                
                                Baca dokumen lengkap
                                
                            

Ciri produk

                                1
_ _
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE MEDICINAL PRODUCT
Potactasol 1 mg powder for concentrate for solution for infusion
Potactasol 4 mg powder for concentrate for solution for infusion
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Potactasol 1 mg powder for concentrate for solution for infusion
Each vial contains 1 mg topotecan (as hydrochloride).
After reconstitution, 1 ml concentrate contains 1 mg topotecan.
Excipient with known effect
Each vial contains 0.52 mg (0.0225 mmol) sodium.
Potactasol 4 mg powder for concentrate for solution for infusion
Each vial contains 4 mg topotecan (as hydrochloride).
After reconstitution, 1 ml concentrate contains 1 mg topotecan.
Excipient with known effect
Each vial contains 2.07 mg (0.09 mmol) sodium.
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Powder for concentrate for solution for infusion.
Yellow lyophilisate.
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
Topotecan monotherapy is indicated for the treatment of:
-
patients with metastatic carcinoma of the ovary after failure of
first-line or subsequent therapy
-
patients with relapsed small cell lung cancer (SCLC) for whom
re-treatment with the first-line
regimen is not considered appropriate (see section 5.1).
Topotecan in combination with cisplatin is indicated for patients with
carcinoma of the cervix
recurrent after radiotherapy and for patients with Stage IVB disease.
Patients with prior exposure to
cisplatin require a sustained treatment free interval to justify
treatment with the combination (see
section 5.1).
4.2
POSOLOGY AND METHOD OF ADMINISTRATION
The use of topotecan should be confined to units specialised in the
administration of cytotoxic
chemotherapy. Topotecan should only be administered under the
supervision of a physician
experienced in the use of chemotherapy (see section 6.6).
Posology
When topotecan is used in combination with cisplatin, the full
prescribing information for cisplatin
should be consulted.
3
Prior to administration of the firs
                                
                                Baca dokumen lengkap
                                
                            

Dokumen dalam bahasa lain

Risalah maklumat Risalah maklumat Bulgaria 01-06-2023
Ciri produk Ciri produk Bulgaria 01-06-2023
Laporan Penilaian Awam Laporan Penilaian Awam Bulgaria 10-11-2015
Risalah maklumat Risalah maklumat Sepanyol 01-06-2023
Ciri produk Ciri produk Sepanyol 01-06-2023
Laporan Penilaian Awam Laporan Penilaian Awam Sepanyol 10-11-2015
Risalah maklumat Risalah maklumat Czech 01-06-2023
Ciri produk Ciri produk Czech 01-06-2023
Laporan Penilaian Awam Laporan Penilaian Awam Czech 10-11-2015
Risalah maklumat Risalah maklumat Denmark 01-06-2023
Ciri produk Ciri produk Denmark 01-06-2023
Laporan Penilaian Awam Laporan Penilaian Awam Denmark 10-11-2015
Risalah maklumat Risalah maklumat Jerman 01-06-2023
Ciri produk Ciri produk Jerman 01-06-2023
Laporan Penilaian Awam Laporan Penilaian Awam Jerman 10-11-2015
Risalah maklumat Risalah maklumat Estonia 01-06-2023
Ciri produk Ciri produk Estonia 01-06-2023
Laporan Penilaian Awam Laporan Penilaian Awam Estonia 10-11-2015
Risalah maklumat Risalah maklumat Greek 01-06-2023
Ciri produk Ciri produk Greek 01-06-2023
Laporan Penilaian Awam Laporan Penilaian Awam Greek 10-11-2015
Risalah maklumat Risalah maklumat Perancis 01-06-2023
Ciri produk Ciri produk Perancis 01-06-2023
Laporan Penilaian Awam Laporan Penilaian Awam Perancis 10-11-2015
Risalah maklumat Risalah maklumat Itali 01-06-2023
Ciri produk Ciri produk Itali 01-06-2023
Laporan Penilaian Awam Laporan Penilaian Awam Itali 10-11-2015
Risalah maklumat Risalah maklumat Latvia 01-06-2023
Ciri produk Ciri produk Latvia 01-06-2023
Laporan Penilaian Awam Laporan Penilaian Awam Latvia 10-11-2015
Risalah maklumat Risalah maklumat Lithuania 01-06-2023
Ciri produk Ciri produk Lithuania 01-06-2023
Laporan Penilaian Awam Laporan Penilaian Awam Lithuania 10-11-2015
Risalah maklumat Risalah maklumat Hungary 01-06-2023
Ciri produk Ciri produk Hungary 01-06-2023
Laporan Penilaian Awam Laporan Penilaian Awam Hungary 10-11-2015
Risalah maklumat Risalah maklumat Malta 01-06-2023
Ciri produk Ciri produk Malta 01-06-2023
Laporan Penilaian Awam Laporan Penilaian Awam Malta 10-11-2015
Risalah maklumat Risalah maklumat Belanda 01-06-2023
Ciri produk Ciri produk Belanda 01-06-2023
Laporan Penilaian Awam Laporan Penilaian Awam Belanda 10-11-2015
Risalah maklumat Risalah maklumat Poland 01-06-2023
Ciri produk Ciri produk Poland 01-06-2023
Laporan Penilaian Awam Laporan Penilaian Awam Poland 10-11-2015
Risalah maklumat Risalah maklumat Portugis 01-06-2023
Ciri produk Ciri produk Portugis 01-06-2023
Laporan Penilaian Awam Laporan Penilaian Awam Portugis 10-11-2015
Risalah maklumat Risalah maklumat Romania 01-06-2023
Ciri produk Ciri produk Romania 01-06-2023
Laporan Penilaian Awam Laporan Penilaian Awam Romania 10-11-2015
Risalah maklumat Risalah maklumat Slovak 01-06-2023
Ciri produk Ciri produk Slovak 01-06-2023
Laporan Penilaian Awam Laporan Penilaian Awam Slovak 10-11-2015
Risalah maklumat Risalah maklumat Slovenia 01-06-2023
Ciri produk Ciri produk Slovenia 01-06-2023
Laporan Penilaian Awam Laporan Penilaian Awam Slovenia 10-11-2015
Risalah maklumat Risalah maklumat Finland 01-06-2023
Ciri produk Ciri produk Finland 01-06-2023
Laporan Penilaian Awam Laporan Penilaian Awam Finland 10-11-2015
Risalah maklumat Risalah maklumat Sweden 01-06-2023
Ciri produk Ciri produk Sweden 01-06-2023
Laporan Penilaian Awam Laporan Penilaian Awam Sweden 10-11-2015
Risalah maklumat Risalah maklumat Norway 01-06-2023
Ciri produk Ciri produk Norway 01-06-2023
Risalah maklumat Risalah maklumat Iceland 01-06-2023
Ciri produk Ciri produk Iceland 01-06-2023
Risalah maklumat Risalah maklumat Croat 01-06-2023
Ciri produk Ciri produk Croat 01-06-2023
Laporan Penilaian Awam Laporan Penilaian Awam Croat 10-11-2015

Cari amaran yang berkaitan dengan produk ini

Lihat sejarah dokumen