Caelyx pegylated liposomal

Riik: Euroopa Liit

keel: inglise

Allikas: EMA (European Medicines Agency)

Osta kohe

Infovoldik Infovoldik (PIL)
05-09-2023
Toote omadused Toote omadused (SPC)
05-09-2023
Avaliku hindamisaruande Avaliku hindamisaruande (PAR)
02-04-2020

Toimeaine:

doxorubicin hydrochloride

Saadav alates:

Baxter Holding B.V.

ATC kood:

L01DB

INN (Rahvusvaheline Nimetus):

doxorubicin

Terapeutiline rühm:

Antineoplastic agents

Terapeutiline ala:

Sarcoma, Kaposi; Multiple Myeloma; Ovarian Neoplasms; Breast Neoplasms

Näidustused:

Caelyx pegylated liposomal is indicated:as monotherapy for patients with metastatic breast cancer, where there is an increased cardiac risk;for treatment of advanced ovarian cancer in women who have failed a first-line platinum-based chemotherapy regimen;in combination with bortezomib for the treatment of progressive multiple myeloma in patients who have received at least one prior therapy and who have already undergone or are unsuitable for bone marrow transplant;for treatment of AIDS-related Kaposi’s sarcoma (KS) in patients with low CD4 counts (

Toote kokkuvõte:

Revision: 36

Volitamisolek:

Authorised

Loa andmise kuupäev:

1996-06-20

Infovoldik

                                31
B. PACKAGE LEAFLET
32
PACKAGE LEAFLET: INFORMATION FOR THE USER
CAELYX PEGYLATED LIPOSOMAL 2 MG/ML CONCENTRATE FOR SOLUTION FOR
INFUSION
doxorubicin hydrochloride
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 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 Caelyx pegylated liposomal is and what it is used for
2.
What you need to know before you use Caelyx pegylated liposomal
3.
How to use Caelyx pegylated liposomal
4.
Possible side effects
5
How to store Caelyx pegylated liposomal
6.
Contents of the pack and other information
1.
WHAT CAELYX PEGYLATED LIPOSOMAL IS AND WHAT IT IS USED FOR
Caelyx pegylated liposomal is an antitumour agent.
Caelyx pegylated liposomal is used to treat cancer of the breast in
patients at risk for heart problems.
Caelyx pegylated liposomal is also used to treat cancer of the ovary.
It is used to kill cancer cells,
shrink the size of the tumour, delay the growth of the tumour, and
extend your survival.
Caelyx pegylated liposomal is also used in combination with another
medicine, bortezomib, to treat
multiple myeloma (a cancer of the blood) in patients who have received
at least 1 prior therapy.
Caelyx pegylated liposomal is also used to produce an improvement in
your Kaposi’s sarcoma
including flattening, lightening and even shrinkage of the cancer.
Other symptoms of Kaposi’s
sarcoma, such as swelling around the tumour, may also improve or
disappear.
Caelyx pegylated liposomal contains a medicine which is able to
interact with cells in such a way as to
selectively kill cancer cells. The doxorubicin hydrochlor
                                
                                Lugege kogu dokumenti
                                
                            

Toote omadused

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE MEDICINAL PRODUCT
Caelyx pegylated liposomal 2 mg/ml concentrate for solution for
infusion
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
One ml of Caelyx pegylated liposomal contains 2 mg doxorubicin
hydrochloride in a pegylated
liposomal formulation.
Caelyx pegylated liposomal is doxorubicin hydrochloride encapsulated
in liposomes with
surface-bound methoxypolyethylene glycol (MPEG). This process is known
as pegylation and protects
liposomes from detection by the mononuclear phagocyte system (MPS),
which increases blood
circulation time.
Excipients with known effect
Contains fully hydrogenated soy phosphatidylcholine (from soyabean)
– see section 4.3.
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Concentrate for solution for infusion (sterile concentrate)
The dispersion is sterile, translucent and red.
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
Caelyx pegylated liposomal is indicated:
-
As monotherapy for patients with metastatic breast cancer, where there
is an increased cardiac
risk.
-
For treatment of advanced ovarian cancer in women who have failed a
first-line platinum-based
chemotherapy regimen.
-
In combination with bortezomib for the treatment of progressive
multiple myeloma in patients
who have received at least one prior therapy and who have already
undergone or are unsuitable
for bone marrow transplant.
-
For treatment of
AIDS-related Kaposi’s sarcoma (KS) in patients with low CD4
counts
(< 200 CD4 lymphocytes/mm
3
) and extensive mucocutaneous or visceral disease.
Caelyx pegylated liposomal may be used as first-line systemic
chemotherapy, or as second line
chemotherapy in AIDS-KS patients with disease that has progressed
with, or in patients intolerant to,
prior combination systemic chemotherapy comprising at least two of the
following agents: a vinca
alkaloid, bleomycin and standard
_ _
doxorubicin (or other anthracycline).
4.2
POSOLOGY AND METHOD OF ADMINISTRATION
Caelyx pegylated liposomal should on
                                
                                Lugege kogu dokumenti
                                
                            

Dokumendid teistes keeltes

Infovoldik Infovoldik bulgaaria 05-09-2023
Toote omadused Toote omadused bulgaaria 05-09-2023
Avaliku hindamisaruande Avaliku hindamisaruande bulgaaria 02-04-2020
Infovoldik Infovoldik hispaania 05-09-2023
Toote omadused Toote omadused hispaania 05-09-2023
Avaliku hindamisaruande Avaliku hindamisaruande hispaania 02-04-2020
Infovoldik Infovoldik tšehhi 05-09-2023
Toote omadused Toote omadused tšehhi 05-09-2023
Avaliku hindamisaruande Avaliku hindamisaruande tšehhi 02-04-2020
Infovoldik Infovoldik taani 05-09-2023
Toote omadused Toote omadused taani 05-09-2023
Avaliku hindamisaruande Avaliku hindamisaruande taani 02-04-2020
Infovoldik Infovoldik saksa 05-09-2023
Toote omadused Toote omadused saksa 05-09-2023
Avaliku hindamisaruande Avaliku hindamisaruande saksa 02-04-2020
Infovoldik Infovoldik eesti 05-09-2023
Toote omadused Toote omadused eesti 05-09-2023
Avaliku hindamisaruande Avaliku hindamisaruande eesti 02-04-2020
Infovoldik Infovoldik kreeka 05-09-2023
Toote omadused Toote omadused kreeka 05-09-2023
Avaliku hindamisaruande Avaliku hindamisaruande kreeka 02-04-2020
Infovoldik Infovoldik prantsuse 05-09-2023
Toote omadused Toote omadused prantsuse 05-09-2023
Avaliku hindamisaruande Avaliku hindamisaruande prantsuse 02-04-2020
Infovoldik Infovoldik itaalia 05-09-2023
Toote omadused Toote omadused itaalia 05-09-2023
Avaliku hindamisaruande Avaliku hindamisaruande itaalia 02-04-2020
Infovoldik Infovoldik läti 05-09-2023
Toote omadused Toote omadused läti 05-09-2023
Avaliku hindamisaruande Avaliku hindamisaruande läti 02-04-2020
Infovoldik Infovoldik leedu 05-09-2023
Toote omadused Toote omadused leedu 05-09-2023
Avaliku hindamisaruande Avaliku hindamisaruande leedu 02-04-2020
Infovoldik Infovoldik ungari 05-09-2023
Toote omadused Toote omadused ungari 05-09-2023
Avaliku hindamisaruande Avaliku hindamisaruande ungari 02-04-2020
Infovoldik Infovoldik malta 05-09-2023
Toote omadused Toote omadused malta 05-09-2023
Avaliku hindamisaruande Avaliku hindamisaruande malta 02-04-2020
Infovoldik Infovoldik hollandi 05-09-2023
Toote omadused Toote omadused hollandi 05-09-2023
Avaliku hindamisaruande Avaliku hindamisaruande hollandi 02-04-2020
Infovoldik Infovoldik poola 05-09-2023
Toote omadused Toote omadused poola 05-09-2023
Avaliku hindamisaruande Avaliku hindamisaruande poola 02-04-2020
Infovoldik Infovoldik portugali 05-09-2023
Toote omadused Toote omadused portugali 05-09-2023
Avaliku hindamisaruande Avaliku hindamisaruande portugali 02-04-2020
Infovoldik Infovoldik rumeenia 05-09-2023
Toote omadused Toote omadused rumeenia 05-09-2023
Avaliku hindamisaruande Avaliku hindamisaruande rumeenia 02-04-2020
Infovoldik Infovoldik slovaki 05-09-2023
Toote omadused Toote omadused slovaki 05-09-2023
Avaliku hindamisaruande Avaliku hindamisaruande slovaki 02-04-2020
Infovoldik Infovoldik sloveeni 05-09-2023
Toote omadused Toote omadused sloveeni 05-09-2023
Avaliku hindamisaruande Avaliku hindamisaruande sloveeni 02-04-2020
Infovoldik Infovoldik soome 05-09-2023
Toote omadused Toote omadused soome 05-09-2023
Avaliku hindamisaruande Avaliku hindamisaruande soome 02-04-2020
Infovoldik Infovoldik rootsi 05-09-2023
Toote omadused Toote omadused rootsi 05-09-2023
Avaliku hindamisaruande Avaliku hindamisaruande rootsi 02-04-2020
Infovoldik Infovoldik norra 05-09-2023
Toote omadused Toote omadused norra 05-09-2023
Infovoldik Infovoldik islandi 05-09-2023
Toote omadused Toote omadused islandi 05-09-2023
Infovoldik Infovoldik horvaadi 05-09-2023
Toote omadused Toote omadused horvaadi 05-09-2023
Avaliku hindamisaruande Avaliku hindamisaruande horvaadi 02-04-2020