Fablyn

Country: Kesatuan Eropah

Bahasa: Inggeris

Sumber: EMA (European Medicines Agency)

Beli sekarang

Risalah maklumat Risalah maklumat (PIL)
21-06-2012
Ciri produk Ciri produk (SPC)
21-06-2012
Laporan Penilaian Awam Laporan Penilaian Awam (PAR)
22-06-2012

Bahan aktif:

Lasofoxifene tartrate

Boleh didapati daripada:

Dr. Friedrich Eberth Arzneimittel GmbH

Kod ATC:

G03

INN (Nama Antarabangsa):

lasofoxifene

Kumpulan terapeutik:

Sex hormones and modulators of the genital system,

Kawasan terapeutik:

Osteoporosis, Postmenopausal

Tanda-tanda terapeutik:

Fablyn is indicated for the treatment of osteoporosis in postmenopausal women at increased risk of fracture. A significant reduction in the incidence of vertebral and non-vertebral fractures but not hip fractures has been demonstrated (see section 5.1).When determining the choice of Fablyn or other therapies, including oestrogens, for a postmenopausal woman, consideration should be given to menopausal symptoms, effects on uterine and breast tissues, and cardiovascular risks and benefits (see section 5.1).

Ringkasan produk:

Revision: 2

Status kebenaran:

Withdrawn

Tarikh kebenaran:

2009-02-24

Risalah maklumat

                                34
B. PACKAGE LEAFLET
Medicinal product no longer authorised
35
PACKAGE LEAFLET: INFORMATION FOR THE USER
FABLYN 500 MICROGRAM FILM-COATED TABLETS
lasofoxifene
READ ALL OF THIS LEAFLET CAREFULLY BEFORE YOU START TAKING THIS
MEDICINE.

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. Do not pass it on to
others. It may harm them, even
if their symptoms are the same as yours.

If any of the side effects gets serious, or if you notice any side
effects not listed in this leaflet,
please tell your doctor or pharmacist.
WHAT IS IN THIS LEAFLET
1.
What FABLYN is and what it is used for
2.
Before you take FABLYN
3.
How to FABLYN
4.
Possible side effects
5.
How to store FABLYN
6.
Further information
1.
WHAT FABLYN IS AND WHAT IT IS USED FOR
FABLYN is used to treat osteoporosis in women after the menopause
(postmenopausal osteoporosis)
who are likely to break bones, especially in the spine, hips and
wrists. It belongs to a group of
medicines called Selective Estrogen Receptor Modulators (SERM).
In women with postmenopausal osteoporosis, FABLYN reduces the risk of
both fractures of the spine
(vertebral fractures) and non-spine fractures (non-vertebral
fractures), but not hip fractures.
2.
BEFORE YOU TAKE FABLYN
_ _
DO NOT TAKE FABLYN

if you are allergic (hypersensitive) to lasofoxifene or any of the
other ingredients of FABLYN.

if you currently have or previously had blood clots, for example in
your veins, lungs or eyes
(deep vein thrombosis, pulmonary embolism or retinal vein thrombosis).

if you have any vaginal bleeding. This must be investigated by your
doctor BEFORE STARTING
TREATMENT.

if you could still become pregnant.

if you are pregnant or breast-feeding.
Medicinal product no longer authorised
36
TAKE SPECIAL CARE WITH FABLYN

IF YOU ARE IMMOBILE FOR SOME TIME
, such as, needing to be admitted to a hospital or having to
stay in bed while recovering from an operation or an
                                
                                Baca dokumen lengkap
                                
                            

Ciri produk

                                1
_ _
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
Medicinal product no longer authorised
2
1.
NAME OF THE MEDICINAL PRODUCT
FABLYN 500 microgram film-coated tablets.
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Each film-coated tablet contains lasofoxifene tartrate, equivalent to
500 micrograms lasofoxifene.
Excipient: Each film-coated tablet contains 71.34 mg lactose.
For a full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Film-coated tablet.
Triangular, peach-coloured, film-coated tablets debossed with
“Pfizer” on one side and “OPR 05” on
the other side.
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
FABLYN is indicated for the treatment of osteoporosis in
postmenopausal women at increased risk of
fracture. A significant reduction in the incidence of vertebral and
non-vertebral fractures but not hip
fractures has been demonstrated (see section 5.1).
When determining the choice of FABLYN or other therapies, including
estrogens, for a
postmenopausal woman, consideration should be given to menopausal
symptoms, effects on uterine
and breast tissues, and cardiovascular risks and benefits (see section
5.1).
4.2
POSOLOGY AND METHOD OF ADMINISTRATION
_ _
Adult (postmenopausal women):
The recommended dose is one 500 microgram tablet daily.
The tablet may be taken any time of day without regard to food and
beverage intake.
Supplemental calcium and/or vitamin D should be added to the diet if
daily intake is inadequate.
Postmenopausal women require an average of 1,500 mg/day of elemental
calcium. The recommended
intake of vitamin D is 400-800 IU daily.
Children and adolescents below 18 years of age:
There is no indication for FABLYN in children and adolescents below 18
years of age since the medicinal
product is for use in postmenopausal women only. Therefore safety and
efficacy have not been studied (see
section 5.2).
Elderly women (65 years and older):
No dose adjustment is necessary in elderly female patients (see
section 5.2).
Medicinal product no longer authorised
3
Hepatic insufficiency:
No 
                                
                                Baca dokumen lengkap
                                
                            

Dokumen dalam bahasa lain

Risalah maklumat Risalah maklumat Bulgaria 21-06-2012
Ciri produk Ciri produk Bulgaria 21-06-2012
Laporan Penilaian Awam Laporan Penilaian Awam Bulgaria 22-06-2012
Risalah maklumat Risalah maklumat Sepanyol 21-06-2012
Ciri produk Ciri produk Sepanyol 21-06-2012
Laporan Penilaian Awam Laporan Penilaian Awam Sepanyol 22-06-2012
Risalah maklumat Risalah maklumat Czech 21-06-2012
Ciri produk Ciri produk Czech 21-06-2012
Laporan Penilaian Awam Laporan Penilaian Awam Czech 22-06-2012
Risalah maklumat Risalah maklumat Denmark 21-06-2012
Ciri produk Ciri produk Denmark 21-06-2012
Laporan Penilaian Awam Laporan Penilaian Awam Denmark 22-06-2012
Risalah maklumat Risalah maklumat Jerman 21-06-2012
Ciri produk Ciri produk Jerman 21-06-2012
Laporan Penilaian Awam Laporan Penilaian Awam Jerman 22-06-2012
Risalah maklumat Risalah maklumat Estonia 21-06-2012
Ciri produk Ciri produk Estonia 21-06-2012
Laporan Penilaian Awam Laporan Penilaian Awam Estonia 22-06-2012
Risalah maklumat Risalah maklumat Greek 21-06-2012
Ciri produk Ciri produk Greek 21-06-2012
Laporan Penilaian Awam Laporan Penilaian Awam Greek 22-06-2012
Risalah maklumat Risalah maklumat Perancis 21-06-2012
Ciri produk Ciri produk Perancis 21-06-2012
Laporan Penilaian Awam Laporan Penilaian Awam Perancis 22-06-2012
Risalah maklumat Risalah maklumat Itali 21-06-2012
Ciri produk Ciri produk Itali 21-06-2012
Laporan Penilaian Awam Laporan Penilaian Awam Itali 22-06-2012
Risalah maklumat Risalah maklumat Latvia 21-06-2012
Ciri produk Ciri produk Latvia 21-06-2012
Laporan Penilaian Awam Laporan Penilaian Awam Latvia 22-06-2012
Risalah maklumat Risalah maklumat Lithuania 21-06-2012
Ciri produk Ciri produk Lithuania 21-06-2012
Laporan Penilaian Awam Laporan Penilaian Awam Lithuania 22-06-2012
Risalah maklumat Risalah maklumat Hungary 21-06-2012
Ciri produk Ciri produk Hungary 21-06-2012
Laporan Penilaian Awam Laporan Penilaian Awam Hungary 22-06-2012
Risalah maklumat Risalah maklumat Malta 21-06-2012
Ciri produk Ciri produk Malta 21-06-2012
Laporan Penilaian Awam Laporan Penilaian Awam Malta 22-06-2012
Risalah maklumat Risalah maklumat Belanda 21-06-2012
Ciri produk Ciri produk Belanda 21-06-2012
Laporan Penilaian Awam Laporan Penilaian Awam Belanda 22-06-2012
Risalah maklumat Risalah maklumat Poland 21-06-2012
Ciri produk Ciri produk Poland 21-06-2012
Laporan Penilaian Awam Laporan Penilaian Awam Poland 22-06-2012
Risalah maklumat Risalah maklumat Portugis 21-06-2012
Ciri produk Ciri produk Portugis 21-06-2012
Laporan Penilaian Awam Laporan Penilaian Awam Portugis 22-06-2012
Risalah maklumat Risalah maklumat Romania 21-06-2012
Ciri produk Ciri produk Romania 21-06-2012
Laporan Penilaian Awam Laporan Penilaian Awam Romania 22-06-2012
Risalah maklumat Risalah maklumat Slovak 21-06-2012
Ciri produk Ciri produk Slovak 21-06-2012
Laporan Penilaian Awam Laporan Penilaian Awam Slovak 22-06-2012
Risalah maklumat Risalah maklumat Slovenia 21-06-2012
Ciri produk Ciri produk Slovenia 21-06-2012
Laporan Penilaian Awam Laporan Penilaian Awam Slovenia 22-06-2012
Risalah maklumat Risalah maklumat Finland 21-06-2012
Ciri produk Ciri produk Finland 21-06-2012
Laporan Penilaian Awam Laporan Penilaian Awam Finland 22-06-2012
Risalah maklumat Risalah maklumat Sweden 21-06-2012
Ciri produk Ciri produk Sweden 21-06-2012
Laporan Penilaian Awam Laporan Penilaian Awam Sweden 22-06-2012
Risalah maklumat Risalah maklumat Norway 21-06-2012
Ciri produk Ciri produk Norway 21-06-2012
Risalah maklumat Risalah maklumat Iceland 21-06-2012
Ciri produk Ciri produk Iceland 21-06-2012

Cari amaran yang berkaitan dengan produk ini

Lihat sejarah dokumen