Docetaxel Mylan

Riik: Euroopa Liit

keel: inglise

Allikas: EMA (European Medicines Agency)

Osta kohe

Infovoldik Infovoldik (PIL)
12-03-2015
Toote omadused Toote omadused (SPC)
12-03-2015
Avaliku hindamisaruande Avaliku hindamisaruande (PAR)
12-03-2015

Toimeaine:

docetaxel

Saadav alates:

Mylan S.A.S.

ATC kood:

L01CD02

INN (Rahvusvaheline Nimetus):

docetaxel

Terapeutiline rühm:

Antineoplastic agents

Terapeutiline ala:

Head and Neck Neoplasms; Carcinoma, Non-Small-Cell Lung; Adenocarcinoma; Prostatic Neoplasms; Breast Neoplasms

Näidustused:

Treatment of breast cancer, special forms of lung cancer (non-small-cell lung cancer), prostate cancer, gastric cancer, or head and neck cancer.

Toote kokkuvõte:

Revision: 6

Volitamisolek:

Withdrawn

Loa andmise kuupäev:

2012-01-31

Infovoldik

                                129
B. PACKAGE LEAFLET
Medicinal product no longer authorised
130
PACKAGE LEAFLET: INFORMATION FOR THE USER
DOCETAXEL MYLAN 20 MG/1 ML CONCENTRATE FOR SOLUTION FOR INFUSION
Docetaxel
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 hospital
pharmacist.
-
If you get any side effects, talk to your doctor, hospital pharmacist
or nurse. This includes any
possible side effects not listed in this leaflet. See section 4.
WHAT IS IN THIS LEAFLET:
1.
What Docetaxel Mylan 20 MG/1 ML is and what it is used for
2.
What you need to know before you use Docetaxel Mylan 20 MG/1 ML
3.
How to use Docetaxel Mylan 20 MG/1 ML
4.
Possible side effects
5.
How to store Docetaxel Mylan 20 MG/1 ML
6.
Contents of the pack and other information
1.
WHAT DOCETAXEL MYLAN 20 MG/1 ML IS AND WHAT IT IS USED FOR
Docetaxel is a substance derived from the needles of yew trees.
Docetaxel belongs to the group of anti-cancer medicines called
taxoids.
Docetaxel Mylan has been prescribed by your doctor for the treatment
of breast cancer, special forms
of lung cancer (non-small cell lung cancer), prostate cancer, gastric
cancer or head and neck cancer:
- For the treatment of advanced breast cancer, docetaxel could be
administered either alone or in
combination with doxorubicin, or trastuzumab, or capecitabine.
- For the treatment of early breast cancer with or without lymph node
involvement, docetaxel could be
administered in combination with doxorubicin and cyclophosphamide.
- For the treatment of lung cancer, docetaxel could be administered
either alone or in combination with
cisplatin.
- For the treatment of prostate cancer, docetaxel is administered in
combination with prednisone or
prednisolone.
- For the treatment of metastatic gastric cancer, docetaxel is
administered in combination with cisplatin
and 5-fluorouracil.
- For the treatment of head and neck cancer, docetaxe
                                
                                Lugege kogu dokumenti
                                
                            

Toote omadused

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
Medicinal product no longer authorised
2
1.
NAME OF THE MEDICINAL PRODUCT
Docetaxel Mylan 20 mg/1 ml concentrate for solution for infusion
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Each ml of concentrate for solution for infusion contains 20 mg of
docetaxel (anhydrous).
One vial of 1 ml of concentrate contains 20 mg of docetaxel.
Excipient with known effect:
Each ml of concentrate for solution for infusion contains 395 mg of
ethanol anhydrous.
One vial of 1 ml of concentrate contains 395 mg of ethanol anhydrous.
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Concentrate for solution for infusion (sterile concentrate).
The concentrate is pale yellow to brownish-yellow.
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
Breast cancer
Docetaxel Mylan in combination with doxorubicin and cyclophosphamide
is indicated for the adjuvant
treatment of patients with:

operable node-positive breast cancer

operable node-negative breast cancer
For patients with operable node-negative breast cancer, adjuvant
treatment should be restricted to
patients eligible to receive chemotherapy according to internationally
established criteria for primary
therapy of early breast cancer (see section 5.1).
Docetaxel Mylan in combination with doxorubicin is indicated for the
treatment of patients with
locally advanced or metastatic breast cancer who have not previously
received cytotoxic therapy for
this condition.
Docetaxel Mylan monotherapy is indicated for the treatment of patients
with locally advanced or
metastatic breast cancer after failure of cytotoxic therapy. Previous
chemotherapy should have
included an anthracycline or an alkylating agent.
Docetaxel Mylan in combination with trastuzumab is indicated for the
treatment of patients with
metastatic breast cancer whose tumours over express HER2 and who
previously have not received
chemotherapy for metastatic disease.
Docetaxel Mylan in combination with capecitabine is indicated for the
treatment of patient
                                
                                Lugege kogu dokumenti
                                
                            

Dokumendid teistes keeltes

Infovoldik Infovoldik bulgaaria 12-03-2015
Toote omadused Toote omadused bulgaaria 12-03-2015
Avaliku hindamisaruande Avaliku hindamisaruande bulgaaria 12-03-2015
Infovoldik Infovoldik hispaania 12-03-2015
Toote omadused Toote omadused hispaania 12-03-2015
Avaliku hindamisaruande Avaliku hindamisaruande hispaania 12-03-2015
Infovoldik Infovoldik tšehhi 12-03-2015
Toote omadused Toote omadused tšehhi 12-03-2015
Avaliku hindamisaruande Avaliku hindamisaruande tšehhi 12-03-2015
Infovoldik Infovoldik taani 12-03-2015
Toote omadused Toote omadused taani 12-03-2015
Avaliku hindamisaruande Avaliku hindamisaruande taani 12-03-2015
Infovoldik Infovoldik saksa 12-03-2015
Toote omadused Toote omadused saksa 12-03-2015
Avaliku hindamisaruande Avaliku hindamisaruande saksa 12-03-2015
Infovoldik Infovoldik eesti 12-03-2015
Toote omadused Toote omadused eesti 12-03-2015
Avaliku hindamisaruande Avaliku hindamisaruande eesti 12-03-2015
Infovoldik Infovoldik kreeka 12-03-2015
Toote omadused Toote omadused kreeka 12-03-2015
Avaliku hindamisaruande Avaliku hindamisaruande kreeka 12-03-2015
Infovoldik Infovoldik prantsuse 12-03-2015
Toote omadused Toote omadused prantsuse 12-03-2015
Avaliku hindamisaruande Avaliku hindamisaruande prantsuse 12-03-2015
Infovoldik Infovoldik itaalia 12-03-2015
Toote omadused Toote omadused itaalia 12-03-2015
Avaliku hindamisaruande Avaliku hindamisaruande itaalia 12-03-2015
Infovoldik Infovoldik läti 12-03-2015
Toote omadused Toote omadused läti 12-03-2015
Avaliku hindamisaruande Avaliku hindamisaruande läti 12-03-2015
Infovoldik Infovoldik leedu 12-03-2015
Toote omadused Toote omadused leedu 12-03-2015
Avaliku hindamisaruande Avaliku hindamisaruande leedu 12-03-2015
Infovoldik Infovoldik ungari 12-03-2015
Toote omadused Toote omadused ungari 12-03-2015
Avaliku hindamisaruande Avaliku hindamisaruande ungari 12-03-2015
Infovoldik Infovoldik malta 12-03-2015
Toote omadused Toote omadused malta 12-03-2015
Avaliku hindamisaruande Avaliku hindamisaruande malta 12-03-2015
Infovoldik Infovoldik hollandi 12-03-2015
Toote omadused Toote omadused hollandi 12-03-2015
Avaliku hindamisaruande Avaliku hindamisaruande hollandi 12-03-2015
Infovoldik Infovoldik poola 12-03-2015
Toote omadused Toote omadused poola 12-03-2015
Avaliku hindamisaruande Avaliku hindamisaruande poola 12-03-2015
Infovoldik Infovoldik portugali 12-03-2015
Toote omadused Toote omadused portugali 12-03-2015
Avaliku hindamisaruande Avaliku hindamisaruande portugali 12-03-2015
Infovoldik Infovoldik rumeenia 12-03-2015
Toote omadused Toote omadused rumeenia 12-03-2015
Avaliku hindamisaruande Avaliku hindamisaruande rumeenia 12-03-2015
Infovoldik Infovoldik slovaki 12-03-2015
Toote omadused Toote omadused slovaki 12-03-2015
Avaliku hindamisaruande Avaliku hindamisaruande slovaki 12-03-2015
Infovoldik Infovoldik sloveeni 12-03-2015
Toote omadused Toote omadused sloveeni 12-03-2015
Avaliku hindamisaruande Avaliku hindamisaruande sloveeni 12-03-2015
Infovoldik Infovoldik soome 12-03-2015
Toote omadused Toote omadused soome 12-03-2015
Avaliku hindamisaruande Avaliku hindamisaruande soome 12-03-2015
Infovoldik Infovoldik rootsi 12-03-2015
Toote omadused Toote omadused rootsi 12-03-2015
Avaliku hindamisaruande Avaliku hindamisaruande rootsi 12-03-2015
Infovoldik Infovoldik norra 12-03-2015
Toote omadused Toote omadused norra 12-03-2015
Infovoldik Infovoldik islandi 12-03-2015
Toote omadused Toote omadused islandi 12-03-2015
Infovoldik Infovoldik horvaadi 12-03-2015
Toote omadused Toote omadused horvaadi 12-03-2015

Otsige selle tootega seotud teateid

Vaadake dokumentide ajalugu