Karvezide

Negara: Uni Eropa

Bahasa: Inggris

Sumber: EMA (European Medicines Agency)

Beli Sekarang

Selebaran informasi Selebaran informasi (PIL)
26-03-2024
Karakteristik produk Karakteristik produk (SPC)
26-03-2024

Bahan aktif:

irbesartan, hydrochlorothiazide

Tersedia dari:

Sanofi Winthrop Industrie

Kode ATC:

C09DA04

INN (Nama Internasional):

irbesartan, hydrochlorothiazide

Kelompok Terapi:

Agents acting on the renin-angiotensin system

Area terapi:

Hypertension

Indikasi Terapi:

Treatment of essential hypertension.This fixed-dose combination is indicated in adult patients whose blood pressure is not adequately controlled on irbesartan or hydrochlorothiazide alone.

Ringkasan produk:

Revision: 47

Status otorisasi:

Authorised

Tanggal Otorisasi:

1998-10-16

Selebaran informasi

                                109
B. PACKAGE LEAFLET
110
PACKAGE LEAFLET: INFORMATION FOR THE PATIENT
KARVEZIDE 150 MG/12.5 MG TABLETS
irbesartan/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 Karvezide is and what it is used for
2.
What you need to know before you take Karvezide
3.
How to take Karvezide
4.
Possible side effects
5.
How to store Karvezide
6.
Contents of the pack and other information
1.
WHAT KARVEZIDE IS AND WHAT IT IS USED FOR
Karvezide is a combination of two active substances, irbesartan and
hydrochlorothiazide.
Irbesartan belongs to a group of medicines known as angiotensin-II
receptor antagonists. Angiotensin-
II is a substance produced in the body that binds to receptors in
blood vessels causing them to tighten.
This results in an increase in blood pressure. Irbesartan prevents the
binding of angiotensin-II to these
receptors, causing the blood vessels to relax and the blood pressure
to lower.
Hydrochlorothiazide is one of a group of medicines (called thiazide
diuretics) that causes increased
urine output and so causes a lowering of blood pressure.
The two active ingredients in Karvezide work together to lower blood
pressure further than if either
was given alone.
KARVEZIDE IS USED TO TREAT HIGH BLOOD PRESSURE
, when treatment with irbesartan or
hydrochlorothiazide alone did not provide adequate control of your
blood pressure.
2.
WHAT YOU NEED TO KNOW BEFORE YOU TAKE KARVEZIDE
DO NOT TAKE KARVEZIDE
▪
if you are
ALLERGIC
to irbesartan or any of the other ingredients of this
                                
                                Baca dokumen lengkapnya
                                
                            

Karakteristik produk

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE MEDICINAL PRODUCT
Karvezide 150 mg/12.5 mg tablets.
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Each tablet contains 150 mg of irbesartan and 12.5 mg of
hydrochlorothiazide.
Excipient with known effect:
Each tablet contains 26.65 mg of lactose (as lactose monohydrate).
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Tablet.
Peach, biconvex, oval-shaped, with a heart debossed on one side and
the number 2775 engraved on the
other side.
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
Treatment of essential hypertension.
This fixed dose combination is indicated in adult patients whose blood
pressure is not adequately
controlled on irbesartan or hydrochlorothiazide alone (see section
5.1).
4.2
POSOLOGY AND METHOD OF ADMINISTRATION
Posology
Karvezide can be taken once daily, with or without food.
Dose titration with the individual components (i.e. irbesartan and
hydrochlorothiazide) may be
recommended.
When clinically appropriate direct change from monotherapy to the
fixed combinations may be
considered:
▪
Karvezide 150 mg/12.5 mg may be administered in patients whose blood
pressure is not
adequately controlled with hydrochlorothiazide or irbesartan 150 mg
alone.
▪
Karvezide 300 mg/12.5 mg may be administered in patients
insufficiently controlled by
irbesartan 300 mg or by Karvezide 150 mg/12.5 mg.
▪
Karvezide 300 mg/25 mg may be administered in patients insufficiently
controlled by
Karvezide 300 mg/12.5 mg.
Doses higher than 300 mg irbesartan/25 mg hydrochlorothiazide once
daily are not recommended.
When necessary, Karvezide may be administered with another
antihypertensive medicinal product (see
sections 4.3, 4.4, 4.5 and 5.1).
3
Special Populations
_Renal impairment_
Due to the hydrochlorothiazide component, Karvezide is not recommended
for patients with severe
renal dysfunction (creatinine clearance < 30 ml/min). Loop diuretics
are preferred to thiazides in this
population. No dosage adjustment is necessary in patients 
                                
                                Baca dokumen lengkapnya
                                
                            

Dokumen dalam bahasa lain

Selebaran informasi Selebaran informasi Bulgar 26-03-2024
Karakteristik produk Karakteristik produk Bulgar 26-03-2024
Laporan Penilaian publik Laporan Penilaian publik Bulgar 24-09-2013
Selebaran informasi Selebaran informasi Spanyol 26-03-2024
Karakteristik produk Karakteristik produk Spanyol 26-03-2024
Laporan Penilaian publik Laporan Penilaian publik Spanyol 24-09-2013
Selebaran informasi Selebaran informasi Cheska 26-03-2024
Karakteristik produk Karakteristik produk Cheska 26-03-2024
Laporan Penilaian publik Laporan Penilaian publik Cheska 24-09-2013
Selebaran informasi Selebaran informasi Dansk 26-03-2024
Karakteristik produk Karakteristik produk Dansk 26-03-2024
Laporan Penilaian publik Laporan Penilaian publik Dansk 24-09-2013
Selebaran informasi Selebaran informasi Jerman 26-03-2024
Karakteristik produk Karakteristik produk Jerman 26-03-2024
Laporan Penilaian publik Laporan Penilaian publik Jerman 24-09-2013
Selebaran informasi Selebaran informasi Esti 26-03-2024
Karakteristik produk Karakteristik produk Esti 26-03-2024
Laporan Penilaian publik Laporan Penilaian publik Esti 24-09-2013
Selebaran informasi Selebaran informasi Yunani 26-03-2024
Karakteristik produk Karakteristik produk Yunani 26-03-2024
Laporan Penilaian publik Laporan Penilaian publik Yunani 24-09-2013
Selebaran informasi Selebaran informasi Prancis 26-03-2024
Karakteristik produk Karakteristik produk Prancis 26-03-2024
Laporan Penilaian publik Laporan Penilaian publik Prancis 24-09-2013
Selebaran informasi Selebaran informasi Italia 26-03-2024
Karakteristik produk Karakteristik produk Italia 26-03-2024
Laporan Penilaian publik Laporan Penilaian publik Italia 24-09-2013
Selebaran informasi Selebaran informasi Latvi 26-03-2024
Karakteristik produk Karakteristik produk Latvi 26-03-2024
Laporan Penilaian publik Laporan Penilaian publik Latvi 24-09-2013
Selebaran informasi Selebaran informasi Lituavi 26-03-2024
Karakteristik produk Karakteristik produk Lituavi 26-03-2024
Laporan Penilaian publik Laporan Penilaian publik Lituavi 24-09-2013
Selebaran informasi Selebaran informasi Hungaria 26-03-2024
Karakteristik produk Karakteristik produk Hungaria 26-03-2024
Laporan Penilaian publik Laporan Penilaian publik Hungaria 24-09-2013
Selebaran informasi Selebaran informasi Malta 26-03-2024
Karakteristik produk Karakteristik produk Malta 26-03-2024
Laporan Penilaian publik Laporan Penilaian publik Malta 24-09-2013
Selebaran informasi Selebaran informasi Belanda 26-03-2024
Karakteristik produk Karakteristik produk Belanda 26-03-2024
Laporan Penilaian publik Laporan Penilaian publik Belanda 24-09-2013
Selebaran informasi Selebaran informasi Polski 26-03-2024
Karakteristik produk Karakteristik produk Polski 26-03-2024
Laporan Penilaian publik Laporan Penilaian publik Polski 24-09-2013
Selebaran informasi Selebaran informasi Portugis 26-03-2024
Karakteristik produk Karakteristik produk Portugis 26-03-2024
Laporan Penilaian publik Laporan Penilaian publik Portugis 24-09-2013
Selebaran informasi Selebaran informasi Rumania 26-03-2024
Karakteristik produk Karakteristik produk Rumania 26-03-2024
Laporan Penilaian publik Laporan Penilaian publik Rumania 24-09-2013
Selebaran informasi Selebaran informasi Slovak 26-03-2024
Karakteristik produk Karakteristik produk Slovak 26-03-2024
Laporan Penilaian publik Laporan Penilaian publik Slovak 24-09-2013
Selebaran informasi Selebaran informasi Sloven 26-03-2024
Karakteristik produk Karakteristik produk Sloven 26-03-2024
Laporan Penilaian publik Laporan Penilaian publik Sloven 24-09-2013
Selebaran informasi Selebaran informasi Suomi 26-03-2024
Karakteristik produk Karakteristik produk Suomi 26-03-2024
Laporan Penilaian publik Laporan Penilaian publik Suomi 24-09-2013
Selebaran informasi Selebaran informasi Swedia 26-03-2024
Karakteristik produk Karakteristik produk Swedia 26-03-2024
Laporan Penilaian publik Laporan Penilaian publik Swedia 24-09-2013
Selebaran informasi Selebaran informasi Norwegia 26-03-2024
Karakteristik produk Karakteristik produk Norwegia 26-03-2024
Selebaran informasi Selebaran informasi Islandia 26-03-2024
Karakteristik produk Karakteristik produk Islandia 26-03-2024
Selebaran informasi Selebaran informasi Kroasia 26-03-2024
Karakteristik produk Karakteristik produk Kroasia 26-03-2024
Laporan Penilaian publik Laporan Penilaian publik Kroasia 24-09-2013

Peringatan pencarian terkait dengan produk ini

Lihat riwayat dokumen