Rasilez HCT

Negara: Uni Eropa

Bahasa: Inggris

Sumber: EMA (European Medicines Agency)

Beli Sekarang

Selebaran informasi Selebaran informasi (PIL)
20-05-2022
Karakteristik produk Karakteristik produk (SPC)
20-05-2022

Bahan aktif:

aliskiren, hydrochlorothiazide

Tersedia dari:

Noden Pharma DAC

Kode ATC:

C09XA52

INN (Nama Internasional):

aliskiren, hydrochlorothiazide

Kelompok Terapi:

Agents acting on the renin-angiotensin system

Area terapi:

Hypertension

Indikasi Terapi:

Treatment of essential hypertension in adults.Rasilez HCT is indicated in patients whose blood pressure is not adequately controlled on aliskiren or hydrochlorothiazide used alone.Rasilez HCT is indicated as substitution therapy in patients adequately controlled with aliskiren and hydrochlorothiazide, given concurrently, at the same dose level as in the combination.

Ringkasan produk:

Revision: 17

Status otorisasi:

Withdrawn

Tanggal Otorisasi:

2009-01-16

Selebaran informasi

                                92
B. PACKAGE LEAFLET
Medicinal Product no longer authorised
93
PACKAGE LEAFLET: INFORMATION FOR THE USER
RASILEZ HCT 150 MG/12.5 MG FILM-COATED TABLETS
RASILEZ HCT 150 MG/25 MG FILM-COATED TABLETS
RASILEZ HCT 300 MG/12.5 MG FILM-COATED TABLETS
RASILEZ HCT 300 MG/25 MG FILM-COATED TABLETS
Aliskiren/hydrochlorothiazide
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 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 Rasilez HCT is and what it is used for
2.
What you need to know before you take Rasilez HCT
3.
How to take Rasilez HCT
4.
Possible side effects
5.
How to store Rasilez HCT
6.
Contents of the pack and other information
1.
WHAT RASILEZ HCT IS AND WHAT IS IT USED FOR
WHAT RASILEZ HCT IS
This medicine contains two active substances, called aliskiren and
hydrochlorothiazide. Both of these
active substances help to control high blood pressure (hypertension).
Aliskiren is a renin inhibitor. It reduces the amount of angiotensin
II the body can make.
Angiotensin II causes blood vessels to tighten, which makes blood
pressure higher. Lowering the
amount of angiotensin II allows the blood vessels to relax; this
lowers blood pressure.
Hydrochlorothiazide belongs to a group of medicines called thiazide
diuretics. Hydrochlorothiazide
increases urine output, which also lowers blood pressure.
This helps to lower high blood pressure in adult patients. High blood
pressure increases the workload
of the heart and arteries. If this continues for a long time, it can
damage the blood vessels of the brain,
heart and kidneys, and may result in a stroke, heart 
                                
                                Baca dokumen lengkapnya
                                
                            

Karakteristik produk

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
Medicinal Product no longer authorised
2
1.
NAME OF THE MEDICINAL PRODUCT
Rasilez HCT 150 mg/12.5 mg film-coated tablets
Rasilez HCT 150 mg/25 mg film-coated tablets
Rasilez HCT 300 mg/12.5 mg film-coated tablets
Rasilez HCT 300 mg/25 mg film-coated tablets
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Rasilez HCT 150 mg/12.5 mg film-coated tablets
Each film-coated tablet contains 150 mg aliskiren (as hemifumarate)
and 12.5 mg hydrochlorothiazide.
_Excipients with known effect: _
Each tablet contains 25 mg lactose (as monohydrate) and 24.5 mg wheat
starch.
Rasilez HCT 150 mg/25 mg film-coated tablets
Each film-coated tablet contains 150 mg aliskiren (as hemifumarate)
and 25 mg hydrochlorothiazide.
_Excipients with known effect: _
Each tablet contains 50 mg lactose (as monohydrate) and 49 mg wheat
starch.
Rasilez HCT 300 mg/12.5 mg film-coated tablets
Each film-coated tablet contains 300 mg aliskiren (as hemifumarate)
and 12.5 mg hydrochlorothiazide.
_Excipients with known effect: _
Each tablet contains 25 mg lactose (as monohydrate) and 24.5 mg wheat
starch.
Rasilez HCT 300 mg/25 mg film-coated tablets
Each film-coated tablet contains 300 mg aliskiren (as hemifumarate)
and 25 mg hydrochlorothiazide.
_Excipients with known effect: _
Each tablet contains 50 mg lactose (as monohydrate) and 49 mg wheat
starch.
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Film-coated tablet.
Rasilez HCT 150 mg/12.5 mg film-coated tablets
White, biconvex, ovaloid film-coated tablet imprinted with “LCI”
on one side and “NVR” on the
other.
Rasilez HCT 150 mg/25 mg film-coated tablets
Pale yellow, biconvex, ovaloid film-coated tablet imprinted with
“CLL” on one side and “NVR” on
the other.
Rasilez HCT 300 mg/12.5 mg film-coated tablets
Violet white, biconvex, ovaloid film-coated tablet imprinted with
“CVI” on one side and “NVR” on
the other.
Rasilez HCT 300 mg/25 mg film-coated tablets
Light yellow, biconvex, ovaloid film-coated tablet imprinted
                                
                                Baca dokumen lengkapnya
                                
                            

Dokumen dalam bahasa lain

Selebaran informasi Selebaran informasi Bulgar 20-05-2022
Karakteristik produk Karakteristik produk Bulgar 20-05-2022
Laporan Penilaian publik Laporan Penilaian publik Bulgar 20-05-2022
Selebaran informasi Selebaran informasi Spanyol 20-05-2022
Karakteristik produk Karakteristik produk Spanyol 20-05-2022
Laporan Penilaian publik Laporan Penilaian publik Spanyol 20-05-2022
Selebaran informasi Selebaran informasi Cheska 20-05-2022
Karakteristik produk Karakteristik produk Cheska 20-05-2022
Laporan Penilaian publik Laporan Penilaian publik Cheska 20-05-2022
Selebaran informasi Selebaran informasi Dansk 20-05-2022
Karakteristik produk Karakteristik produk Dansk 20-05-2022
Laporan Penilaian publik Laporan Penilaian publik Dansk 20-05-2022
Selebaran informasi Selebaran informasi Jerman 20-05-2022
Karakteristik produk Karakteristik produk Jerman 20-05-2022
Laporan Penilaian publik Laporan Penilaian publik Jerman 20-05-2022
Selebaran informasi Selebaran informasi Esti 20-05-2022
Karakteristik produk Karakteristik produk Esti 20-05-2022
Laporan Penilaian publik Laporan Penilaian publik Esti 20-05-2022
Selebaran informasi Selebaran informasi Yunani 20-05-2022
Karakteristik produk Karakteristik produk Yunani 20-05-2022
Laporan Penilaian publik Laporan Penilaian publik Yunani 20-05-2022
Selebaran informasi Selebaran informasi Prancis 20-05-2022
Karakteristik produk Karakteristik produk Prancis 20-05-2022
Laporan Penilaian publik Laporan Penilaian publik Prancis 20-05-2022
Selebaran informasi Selebaran informasi Italia 20-05-2022
Karakteristik produk Karakteristik produk Italia 20-05-2022
Laporan Penilaian publik Laporan Penilaian publik Italia 20-05-2022
Selebaran informasi Selebaran informasi Latvi 20-05-2022
Karakteristik produk Karakteristik produk Latvi 20-05-2022
Laporan Penilaian publik Laporan Penilaian publik Latvi 20-05-2022
Selebaran informasi Selebaran informasi Lituavi 20-05-2022
Karakteristik produk Karakteristik produk Lituavi 20-05-2022
Laporan Penilaian publik Laporan Penilaian publik Lituavi 20-05-2022
Selebaran informasi Selebaran informasi Hungaria 20-05-2022
Karakteristik produk Karakteristik produk Hungaria 20-05-2022
Laporan Penilaian publik Laporan Penilaian publik Hungaria 20-05-2022
Selebaran informasi Selebaran informasi Malta 20-05-2022
Karakteristik produk Karakteristik produk Malta 20-05-2022
Laporan Penilaian publik Laporan Penilaian publik Malta 20-05-2022
Selebaran informasi Selebaran informasi Belanda 20-05-2022
Karakteristik produk Karakteristik produk Belanda 20-05-2022
Laporan Penilaian publik Laporan Penilaian publik Belanda 20-05-2022
Selebaran informasi Selebaran informasi Polski 20-05-2022
Karakteristik produk Karakteristik produk Polski 20-05-2022
Laporan Penilaian publik Laporan Penilaian publik Polski 20-05-2022
Selebaran informasi Selebaran informasi Portugis 20-05-2022
Karakteristik produk Karakteristik produk Portugis 20-05-2022
Laporan Penilaian publik Laporan Penilaian publik Portugis 20-05-2022
Selebaran informasi Selebaran informasi Rumania 26-08-2020
Karakteristik produk Karakteristik produk Rumania 26-08-2020
Laporan Penilaian publik Laporan Penilaian publik Rumania 20-05-2022
Selebaran informasi Selebaran informasi Slovak 26-08-2020
Karakteristik produk Karakteristik produk Slovak 26-08-2020
Laporan Penilaian publik Laporan Penilaian publik Slovak 20-05-2022
Selebaran informasi Selebaran informasi Sloven 26-08-2020
Karakteristik produk Karakteristik produk Sloven 26-08-2020
Laporan Penilaian publik Laporan Penilaian publik Sloven 20-05-2022
Selebaran informasi Selebaran informasi Suomi 20-05-2022
Karakteristik produk Karakteristik produk Suomi 20-05-2022
Laporan Penilaian publik Laporan Penilaian publik Suomi 20-05-2022
Selebaran informasi Selebaran informasi Swedia 26-08-2020
Karakteristik produk Karakteristik produk Swedia 26-08-2020
Laporan Penilaian publik Laporan Penilaian publik Swedia 20-05-2022
Selebaran informasi Selebaran informasi Norwegia 20-05-2022
Karakteristik produk Karakteristik produk Norwegia 20-05-2022
Selebaran informasi Selebaran informasi Islandia 20-05-2022
Karakteristik produk Karakteristik produk Islandia 20-05-2022
Selebaran informasi Selebaran informasi Kroasia 20-05-2022
Karakteristik produk Karakteristik produk Kroasia 20-05-2022
Laporan Penilaian publik Laporan Penilaian publik Kroasia 20-05-2022

Peringatan pencarian terkait dengan produk ini

Lihat riwayat dokumen