Verzenios

Country: Kesatuan Eropah

Bahasa: Inggeris

Sumber: EMA (European Medicines Agency)

Beli sekarang

Risalah maklumat Risalah maklumat (PIL)
12-03-2024
Ciri produk Ciri produk (SPC)
12-03-2024
Laporan Penilaian Awam Laporan Penilaian Awam (PAR)
21-04-2022

Bahan aktif:

abemaciclib

Boleh didapati daripada:

Eli Lilly Nederland B.V.

Kod ATC:

L01EF03

INN (Nama Antarabangsa):

abemaciclib

Kumpulan terapeutik:

Antineoplastic agents

Kawasan terapeutik:

Breast Neoplasms

Tanda-tanda terapeutik:

Early Breast CancerVerzenios in combination with endocrine therapy is indicated for the adjuvant treatment of adult patients with hormone receptor (HR) positive, human epidermal growth factor receptor 2 (HER2) negative, node positive early breast cancer at high risk of recurrence (see section 5.1).In pre or perimenopausal women, aromatase inhibitor endocrine therapy should be combined with a luteinising hormone-releasing hormone (LHRH) agonist.Advanced or Metastatic Breast CancerVerzenios is indicated for the treatment of women with hormone receptor (HR) positive, human epidermal growth factor receptor 2 (HER2) negative locally advanced or metastatic breast cancer in combination with an aromatase inhibitor or fulvestrant as initial endocrine-based therapy, or in women who have received prior endocrine therapy.In pre- or perimenopausal women, the endocrine therapy should be combined with a LHRH agonist.

Ringkasan produk:

Revision: 10

Status kebenaran:

Authorised

Tarikh kebenaran:

2018-09-26

Risalah maklumat

                                42
B. PACKAGE LEAFLET
43
PACKAGE LEAFLET: INFORMATION FOR THE PATIENT
VERZENIOS 50 MG FILM-COATED TABLETS
VERZENIOS 100 MG FILM-COATED TABLETS
VERZENIOS 150 MG FILM-COATED TABLETS
abemaciclib
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 Verzenios is and what it is used for
2.
What you need to know before you take Verzenios
3.
How to take Verzenios
4.
Possible side effects
5.
How to store Verzenios
6.
Contents of the pack and other information
1.
WHAT VERZENIOS IS AND WHAT IT IS USED FOR
Verzenios is a cancer medicine containing the active substance
abemaciclib.
Abemaciclib blocks the effects of proteins called cyclin-dependent
kinase 4 and 6. These proteins are
abnormally active in some cancer cells and make them grow out of
control. Blocking the action of
these proteins can slow down growth of cancer cells, shrink the tumour
and delay progression of the
cancer.
Verzenios is used to treat certain types of breast cancer (hormone
receptor-positive (HR+), human
epidermal growth factor receptor 2-negative (HER2-)) which have:
-
spread to the lymph nodes of the armpit, with no detectable spread to
other parts of the body,
been surgically removed, and have certain characteristics that
increase the risk of the cancer
returning. Treatment is given in combination with hormonal therapy,
such as aromatase
inhibitors or tamoxifen, to prevent the cancer from coming back after
surgery (treatment after
surgery is called adjuvant therapy)
-
spread beyond the original tumour and/or to other orga
                                
                                Baca dokumen lengkap
                                
                            

Ciri produk

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE MEDICINAL PRODUCT
Verzenios 50 mg film-coated tablets
Verzenios 100 mg film-coated tablets
Verzenios 150 mg film-coated tablets
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Verzenios 50 mg film-coated tablets
Each film-coated tablet contains 50 mg abemaciclib.
_Excipients with known effect _
Each film-coated tablet contains 14 mg of lactose monohydrate.
Verzenios 100 mg film-coated tablets
Each film-coated tablet contains 100 mg abemaciclib.
_Excipients with known effect _
Each film-coated tablet contains 28 mg of lactose monohydrate.
Verzenios 150 mg film-coated tablets
Each film-coated tablet contains 150 mg abemaciclib.
_Excipients with known effect _
Each film-coated tablet contains 42 mg of lactose monohydrate.
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Film-coated tablet (tablet).
Verzenios 50 mg film-coated tablets
Beige, oval tablet of 5.2 x 9.5 mm, debossed with “Lilly” on one
side and “50” on the other.
Verzenios 100 mg film-coated tablets
White, oval tablet of 6.6 x 12.0 mm, debossed with “Lilly” on one
side and “100” on the other.
Verzenios 150 mg film-coated tablets
Yellow, oval tablet of 7.5 x 13.7 mm, debossed with “Lilly” on one
side and “150” on the other.
3
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
Early breast cancer
Verzenios in combination with endocrine therapy is indicated for the
adjuvant treatment of adult
patients with hormone receptor (HR)-positive, human epidermal growth
factor receptor 2
(HER2)-negative, node-positive early breast cancer at high risk of
recurrence (see section 5.1).
In pre- or perimenopausal women, aromatase inhibitor endocrine therapy
should be combined with a
luteinising hormone-releasing hormone (LHRH) agonist.
Advanced or metastatic breast cancer
Verzenios is indicated for the treatment of women with hormone
receptor (HR)-positive, human
epidermal growth factor receptor 2 (HER2)-negative locally advanced or
metastatic breast cancer in
combin
                                
                                Baca dokumen lengkap
                                
                            

Dokumen dalam bahasa lain

Risalah maklumat Risalah maklumat Bulgaria 12-03-2024
Ciri produk Ciri produk Bulgaria 12-03-2024
Laporan Penilaian Awam Laporan Penilaian Awam Bulgaria 21-04-2022
Risalah maklumat Risalah maklumat Sepanyol 12-03-2024
Ciri produk Ciri produk Sepanyol 12-03-2024
Laporan Penilaian Awam Laporan Penilaian Awam Sepanyol 21-04-2022
Risalah maklumat Risalah maklumat Czech 12-03-2024
Ciri produk Ciri produk Czech 12-03-2024
Laporan Penilaian Awam Laporan Penilaian Awam Czech 21-04-2022
Risalah maklumat Risalah maklumat Denmark 12-03-2024
Ciri produk Ciri produk Denmark 12-03-2024
Laporan Penilaian Awam Laporan Penilaian Awam Denmark 21-04-2022
Risalah maklumat Risalah maklumat Jerman 12-03-2024
Ciri produk Ciri produk Jerman 12-03-2024
Laporan Penilaian Awam Laporan Penilaian Awam Jerman 21-04-2022
Risalah maklumat Risalah maklumat Estonia 12-03-2024
Ciri produk Ciri produk Estonia 12-03-2024
Laporan Penilaian Awam Laporan Penilaian Awam Estonia 21-04-2022
Risalah maklumat Risalah maklumat Greek 12-03-2024
Ciri produk Ciri produk Greek 12-03-2024
Laporan Penilaian Awam Laporan Penilaian Awam Greek 21-04-2022
Risalah maklumat Risalah maklumat Perancis 12-03-2024
Ciri produk Ciri produk Perancis 12-03-2024
Laporan Penilaian Awam Laporan Penilaian Awam Perancis 21-04-2022
Risalah maklumat Risalah maklumat Itali 12-03-2024
Ciri produk Ciri produk Itali 12-03-2024
Laporan Penilaian Awam Laporan Penilaian Awam Itali 21-04-2022
Risalah maklumat Risalah maklumat Latvia 12-03-2024
Ciri produk Ciri produk Latvia 12-03-2024
Laporan Penilaian Awam Laporan Penilaian Awam Latvia 21-04-2022
Risalah maklumat Risalah maklumat Lithuania 12-03-2024
Ciri produk Ciri produk Lithuania 12-03-2024
Laporan Penilaian Awam Laporan Penilaian Awam Lithuania 21-04-2022
Risalah maklumat Risalah maklumat Hungary 12-03-2024
Ciri produk Ciri produk Hungary 12-03-2024
Laporan Penilaian Awam Laporan Penilaian Awam Hungary 21-04-2022
Risalah maklumat Risalah maklumat Malta 12-03-2024
Ciri produk Ciri produk Malta 12-03-2024
Laporan Penilaian Awam Laporan Penilaian Awam Malta 21-04-2022
Risalah maklumat Risalah maklumat Belanda 12-03-2024
Ciri produk Ciri produk Belanda 12-03-2024
Laporan Penilaian Awam Laporan Penilaian Awam Belanda 21-04-2022
Risalah maklumat Risalah maklumat Poland 12-03-2024
Ciri produk Ciri produk Poland 12-03-2024
Laporan Penilaian Awam Laporan Penilaian Awam Poland 21-04-2022
Risalah maklumat Risalah maklumat Portugis 12-03-2024
Ciri produk Ciri produk Portugis 12-03-2024
Laporan Penilaian Awam Laporan Penilaian Awam Portugis 21-04-2022
Risalah maklumat Risalah maklumat Romania 12-03-2024
Ciri produk Ciri produk Romania 12-03-2024
Laporan Penilaian Awam Laporan Penilaian Awam Romania 21-04-2022
Risalah maklumat Risalah maklumat Slovak 12-03-2024
Ciri produk Ciri produk Slovak 12-03-2024
Laporan Penilaian Awam Laporan Penilaian Awam Slovak 21-04-2022
Risalah maklumat Risalah maklumat Slovenia 12-03-2024
Ciri produk Ciri produk Slovenia 12-03-2024
Laporan Penilaian Awam Laporan Penilaian Awam Slovenia 21-04-2022
Risalah maklumat Risalah maklumat Finland 12-03-2024
Ciri produk Ciri produk Finland 12-03-2024
Laporan Penilaian Awam Laporan Penilaian Awam Finland 21-04-2022
Risalah maklumat Risalah maklumat Sweden 12-03-2024
Ciri produk Ciri produk Sweden 12-03-2024
Laporan Penilaian Awam Laporan Penilaian Awam Sweden 21-04-2022
Risalah maklumat Risalah maklumat Norway 12-03-2024
Ciri produk Ciri produk Norway 12-03-2024
Risalah maklumat Risalah maklumat Iceland 12-03-2024
Ciri produk Ciri produk Iceland 12-03-2024
Risalah maklumat Risalah maklumat Croat 12-03-2024
Ciri produk Ciri produk Croat 12-03-2024
Laporan Penilaian Awam Laporan Penilaian Awam Croat 21-04-2022

Cari amaran yang berkaitan dengan produk ini

Lihat sejarah dokumen