Karvea

Country: Kesatuan Eropah

Bahasa: Inggeris

Sumber: EMA (European Medicines Agency)

Beli sekarang

Risalah maklumat Risalah maklumat (PIL)
07-07-2023
Ciri produk Ciri produk (SPC)
07-07-2023
Laporan Penilaian Awam Laporan Penilaian Awam (PAR)
23-09-2013

Bahan aktif:

irbesartan

Boleh didapati daripada:

Sanofi Winthrop Industrie

Kod ATC:

C09CA04

INN (Nama Antarabangsa):

irbesartan

Kumpulan terapeutik:

Agents acting on the renin-angiotensin system

Kawasan terapeutik:

Hypertension

Tanda-tanda terapeutik:

Treatment of essential hypertension.Treatment of renal disease in patients with hypertension and type-2 diabetes mellitus as part of an antihypertensive medicinal product regimen.

Ringkasan produk:

Revision: 46

Status kebenaran:

Authorised

Tarikh kebenaran:

1997-08-26

Risalah maklumat

                                103
B. PACKAGE LEAFLET
104
PACKAGE LEAFLET: INFORMATION FOR THE USER
KARVEA 75 MG TABLETS
irbesartan
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 Karvea is and what it is used for
2.
What you need to know before you take Karvea
3.
How to take Karvea
4.
Possible side effects
5.
How to store Karvea
6.
Contents of the pack and other information
1.
WHAT KARVEA IS AND WHAT IT IS USED FOR
Karvea belongs to a group of medicines known as angiotensin-II
receptor antagonists. Angiotensin-II
is a substance produced in the body which binds to receptors in blood
vessels causing them to tighten.
This results in an increase in blood pressure. Karvea prevents the
binding of angiotensin-II to these
receptors, causing the blood vessels to relax and the blood pressure
to lower. Karvea slows the
decrease of kidney function in patients with high blood pressure and
type 2 diabetes.
Karvea is used in adult patients

to treat high blood pressure (
_essential hypertension_
)

to protect the kidney in patients with high blood pressure, type 2
diabetes and laboratory
evidence of impaired kidney function.
2.
WHAT YOU NEED TO KNOW BEFORE YOU TAKE KARVEA
DO NOT TAKE KARVEA

if you are
ALLERGIC
to irbesartan or any other ingredients of this medicine (listed in
section 6)

if you are
MORE THAN 3 MONTHS PREGNANT
. (It is also better to avoid Karvea in early pregnancy –
see pregnancy section)

IF YOU HAVE DIABETES OR IMPAIRED KIDNEY FUNCTION
and you are treated with a blood pressure
lowering medicine 
                                
                                Baca dokumen lengkap
                                
                            

Ciri produk

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE MEDICINAL PRODUCT
Karvea 75 mg tablets.
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Each tablet contains 75 mg of irbesartan.
Excipient with known effect: 15.37 mg of lactose monohydrate per
tablet.
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Tablet.
White to off-white, biconvex, and oval-shaped with a heart debossed on
one side and the number 2771
engraved on the other side.
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
Karvea is indicated in adults for the treatment of essential
hypertension.
It is also indicated for the treatment of renal disease in adult
patients with hypertension and type 2
diabetes mellitus as part of an antihypertensive medicinal product
regimen (see sections 4.3, 4.4, 4.5
and 5.1).
4.2
POSOLOGY AND METHOD OF ADMINISTRATION
Posology
The usual recommended initial and maintenance dose is 150 mg once
daily, with or without food.
Karvea at a dose of 150 mg once daily generally provides a better
24-hour blood pressure control than
75 mg. However, initiation of therapy with 75 mg could be considered,
particularly in haemodialyzed
patients and in the elderly over 75 years.
In patients insufficiently controlled with 150 mg once daily, the dose
of Karvea can be increased to
300 mg, or other antihypertensive agents can be added (see sections
4.3, 4.4, 4.5 and 5.1). In
particular, the addition of a diuretic such as hydrochlorothiazide has
been shown to have an additive
effect with Karvea (see section 4.5).
In hypertensive type 2 diabetic patients, therapy should be initiated
at 150 mg irbesartan once daily
and titrated up to 300 mg once daily as the preferred maintenance dose
for treatment of renal disease.
The demonstration of renal benefit of Karvea in hypertensive type 2
diabetic patients is based on
studies where irbesartan was used in addition to other
antihypertensive agents, as needed, to reach
target blood pressure (see sections 4.3, 4.4, 4.5 and 5.1).
Special Populations
_Renal impairment_
No dos
                                
                                Baca dokumen lengkap
                                
                            

Dokumen dalam bahasa lain

Risalah maklumat Risalah maklumat Bulgaria 07-07-2023
Ciri produk Ciri produk Bulgaria 07-07-2023
Laporan Penilaian Awam Laporan Penilaian Awam Bulgaria 23-09-2013
Risalah maklumat Risalah maklumat Sepanyol 07-07-2023
Ciri produk Ciri produk Sepanyol 07-07-2023
Laporan Penilaian Awam Laporan Penilaian Awam Sepanyol 23-09-2013
Risalah maklumat Risalah maklumat Czech 07-07-2023
Ciri produk Ciri produk Czech 07-07-2023
Laporan Penilaian Awam Laporan Penilaian Awam Czech 23-09-2013
Risalah maklumat Risalah maklumat Denmark 07-07-2023
Ciri produk Ciri produk Denmark 07-07-2023
Laporan Penilaian Awam Laporan Penilaian Awam Denmark 23-09-2013
Risalah maklumat Risalah maklumat Jerman 07-07-2023
Ciri produk Ciri produk Jerman 07-07-2023
Laporan Penilaian Awam Laporan Penilaian Awam Jerman 23-09-2013
Risalah maklumat Risalah maklumat Estonia 07-07-2023
Ciri produk Ciri produk Estonia 07-07-2023
Laporan Penilaian Awam Laporan Penilaian Awam Estonia 23-09-2013
Risalah maklumat Risalah maklumat Greek 07-07-2023
Ciri produk Ciri produk Greek 07-07-2023
Laporan Penilaian Awam Laporan Penilaian Awam Greek 23-09-2013
Risalah maklumat Risalah maklumat Perancis 07-07-2023
Ciri produk Ciri produk Perancis 07-07-2023
Laporan Penilaian Awam Laporan Penilaian Awam Perancis 23-09-2013
Risalah maklumat Risalah maklumat Itali 07-07-2023
Ciri produk Ciri produk Itali 07-07-2023
Laporan Penilaian Awam Laporan Penilaian Awam Itali 23-09-2013
Risalah maklumat Risalah maklumat Latvia 07-07-2023
Ciri produk Ciri produk Latvia 07-07-2023
Laporan Penilaian Awam Laporan Penilaian Awam Latvia 23-09-2013
Risalah maklumat Risalah maklumat Lithuania 07-07-2023
Ciri produk Ciri produk Lithuania 07-07-2023
Laporan Penilaian Awam Laporan Penilaian Awam Lithuania 23-09-2013
Risalah maklumat Risalah maklumat Hungary 07-07-2023
Ciri produk Ciri produk Hungary 07-07-2023
Laporan Penilaian Awam Laporan Penilaian Awam Hungary 23-09-2013
Risalah maklumat Risalah maklumat Malta 07-07-2023
Ciri produk Ciri produk Malta 07-07-2023
Laporan Penilaian Awam Laporan Penilaian Awam Malta 23-09-2013
Risalah maklumat Risalah maklumat Belanda 07-07-2023
Ciri produk Ciri produk Belanda 07-07-2023
Laporan Penilaian Awam Laporan Penilaian Awam Belanda 23-09-2013
Risalah maklumat Risalah maklumat Poland 07-07-2023
Ciri produk Ciri produk Poland 07-07-2023
Laporan Penilaian Awam Laporan Penilaian Awam Poland 23-09-2013
Risalah maklumat Risalah maklumat Portugis 07-07-2023
Ciri produk Ciri produk Portugis 07-07-2023
Laporan Penilaian Awam Laporan Penilaian Awam Portugis 23-09-2013
Risalah maklumat Risalah maklumat Romania 07-07-2023
Ciri produk Ciri produk Romania 07-07-2023
Laporan Penilaian Awam Laporan Penilaian Awam Romania 23-09-2013
Risalah maklumat Risalah maklumat Slovak 07-07-2023
Ciri produk Ciri produk Slovak 07-07-2023
Laporan Penilaian Awam Laporan Penilaian Awam Slovak 23-09-2013
Risalah maklumat Risalah maklumat Slovenia 07-07-2023
Ciri produk Ciri produk Slovenia 07-07-2023
Laporan Penilaian Awam Laporan Penilaian Awam Slovenia 23-09-2013
Risalah maklumat Risalah maklumat Finland 07-07-2023
Ciri produk Ciri produk Finland 07-07-2023
Laporan Penilaian Awam Laporan Penilaian Awam Finland 23-09-2013
Risalah maklumat Risalah maklumat Sweden 07-07-2023
Ciri produk Ciri produk Sweden 07-07-2023
Laporan Penilaian Awam Laporan Penilaian Awam Sweden 23-09-2013
Risalah maklumat Risalah maklumat Norway 07-07-2023
Ciri produk Ciri produk Norway 07-07-2023
Risalah maklumat Risalah maklumat Iceland 07-07-2023
Ciri produk Ciri produk Iceland 07-07-2023
Risalah maklumat Risalah maklumat Croat 07-07-2023
Ciri produk Ciri produk Croat 07-07-2023
Laporan Penilaian Awam Laporan Penilaian Awam Croat 23-09-2013

Cari amaran yang berkaitan dengan produk ini

Lihat sejarah dokumen