Irbesartan Zentiva (previously Irbesartan Winthrop)

Nchi: Umoja wa Ulaya

Lugha: Kiingereza

Chanzo: EMA (European Medicines Agency)

Nunua Sasa

Taarifa za kipeperushi Taarifa za kipeperushi (PIL)
28-09-2022
Tabia za bidhaa Tabia za bidhaa (SPC)
28-09-2022

Viambatanisho vya kazi:

irbesartan

Inapatikana kutoka:

Zentiva k.s.

ATC kanuni:

C09CA04

INN (Jina la Kimataifa):

irbesartan

Kundi la matibabu:

Agents acting on the renin-angiotensin system

Eneo la matibabu:

Hypertension

Matibabu dalili:

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.

Bidhaa muhtasari:

Revision: 28

Idhini hali ya:

Authorised

Idhini ya tarehe:

2007-01-19

Taarifa za kipeperushi

                                104
B. PACKAGE LEAFLET
105
PACKAGE LEAFLET: INFORMATION FOR THE USER
IRBESARTAN ZENTIVA 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 Irbesartan Zentiva is and what it is used for
2.
What you need to know before you take Irbesartan Zentiva
3.
How to take Irbesartan Zentiva
4.
Possible side effects
5.
How to store Irbesartan Zentiva
6.
Contents of the pack and other information
1.
WHAT IRBESARTAN ZENTIVA IS AND WHAT IT IS USED FOR
Irbesartan Zentiva 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.
Irbesartan Zentiva prevents the binding
of angiotensin-II to these receptors, causing the blood vessels to
relax and the blood pressure to lower.
Irbesartan Zentiva slows the decrease of kidney function in patients
with high blood pressure and
type 2 diabetes.
Irbesartan Zentiva 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 IRBESARTAN ZENTIVA
DO NOT TAKE IRBESARTAN ZENTIVA
▪
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
Irbesartan Zentiva in e
                                
                                Soma hati kamili
                                
                            

Tabia za bidhaa

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE MEDICINAL PRODUCT
Irbesartan Zentiva 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
Irbesartan Zentiva 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.
Irbesartan Zentiva 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
haemodialysed patients and in the elderly over 75 years.
In patients insufficiently controlled with 150 mg once daily, the dose
of Irbesartan Zentiva 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 Irbesartan Zentiva (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 Irbesartan Zentiva 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 sectio
                                
                                Soma hati kamili
                                
                            

Nyaraka katika lugha zingine

Taarifa za kipeperushi Taarifa za kipeperushi Kibulgaria 28-09-2022
Tabia za bidhaa Tabia za bidhaa Kibulgaria 28-09-2022
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kibulgaria 23-09-2013
Taarifa za kipeperushi Taarifa za kipeperushi Kihispania 28-09-2022
Tabia za bidhaa Tabia za bidhaa Kihispania 28-09-2022
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kihispania 23-09-2013
Taarifa za kipeperushi Taarifa za kipeperushi Kicheki 28-09-2022
Tabia za bidhaa Tabia za bidhaa Kicheki 28-09-2022
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kicheki 23-09-2013
Taarifa za kipeperushi Taarifa za kipeperushi Kidenmaki 28-09-2022
Tabia za bidhaa Tabia za bidhaa Kidenmaki 28-09-2022
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kidenmaki 23-09-2013
Taarifa za kipeperushi Taarifa za kipeperushi Kijerumani 28-09-2022
Tabia za bidhaa Tabia za bidhaa Kijerumani 28-09-2022
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kijerumani 23-09-2013
Taarifa za kipeperushi Taarifa za kipeperushi Kiestonia 28-09-2022
Tabia za bidhaa Tabia za bidhaa Kiestonia 28-09-2022
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kiestonia 23-09-2013
Taarifa za kipeperushi Taarifa za kipeperushi Kigiriki 28-09-2022
Tabia za bidhaa Tabia za bidhaa Kigiriki 28-09-2022
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kigiriki 23-09-2013
Taarifa za kipeperushi Taarifa za kipeperushi Kifaransa 28-09-2022
Tabia za bidhaa Tabia za bidhaa Kifaransa 28-09-2022
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kifaransa 23-09-2013
Taarifa za kipeperushi Taarifa za kipeperushi Kiitaliano 28-09-2022
Tabia za bidhaa Tabia za bidhaa Kiitaliano 28-09-2022
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kiitaliano 23-09-2013
Taarifa za kipeperushi Taarifa za kipeperushi Kilatvia 28-09-2022
Tabia za bidhaa Tabia za bidhaa Kilatvia 28-09-2022
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kilatvia 23-09-2013
Taarifa za kipeperushi Taarifa za kipeperushi Kilithuania 28-09-2022
Tabia za bidhaa Tabia za bidhaa Kilithuania 28-09-2022
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kilithuania 23-09-2013
Taarifa za kipeperushi Taarifa za kipeperushi Kihungari 28-09-2022
Tabia za bidhaa Tabia za bidhaa Kihungari 28-09-2022
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kihungari 23-09-2013
Taarifa za kipeperushi Taarifa za kipeperushi Kimalta 28-09-2022
Tabia za bidhaa Tabia za bidhaa Kimalta 28-09-2022
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kimalta 23-09-2013
Taarifa za kipeperushi Taarifa za kipeperushi Kiholanzi 28-09-2022
Tabia za bidhaa Tabia za bidhaa Kiholanzi 28-09-2022
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kiholanzi 23-09-2013
Taarifa za kipeperushi Taarifa za kipeperushi Kipolandi 28-09-2022
Tabia za bidhaa Tabia za bidhaa Kipolandi 28-09-2022
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kipolandi 23-09-2013
Taarifa za kipeperushi Taarifa za kipeperushi Kireno 28-09-2022
Tabia za bidhaa Tabia za bidhaa Kireno 28-09-2022
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kireno 23-09-2013
Taarifa za kipeperushi Taarifa za kipeperushi Kiromania 28-09-2022
Tabia za bidhaa Tabia za bidhaa Kiromania 28-09-2022
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kiromania 23-09-2013
Taarifa za kipeperushi Taarifa za kipeperushi Kislovakia 28-09-2022
Tabia za bidhaa Tabia za bidhaa Kislovakia 28-09-2022
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kislovakia 23-09-2013
Taarifa za kipeperushi Taarifa za kipeperushi Kislovenia 28-09-2022
Tabia za bidhaa Tabia za bidhaa Kislovenia 28-09-2022
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kislovenia 23-09-2013
Taarifa za kipeperushi Taarifa za kipeperushi Kifinlandi 28-09-2022
Tabia za bidhaa Tabia za bidhaa Kifinlandi 28-09-2022
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kifinlandi 23-09-2013
Taarifa za kipeperushi Taarifa za kipeperushi Kiswidi 28-09-2022
Tabia za bidhaa Tabia za bidhaa Kiswidi 28-09-2022
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kiswidi 23-09-2013
Taarifa za kipeperushi Taarifa za kipeperushi Kinorwe 28-09-2022
Tabia za bidhaa Tabia za bidhaa Kinorwe 28-09-2022
Taarifa za kipeperushi Taarifa za kipeperushi Kiaisilandi 28-09-2022
Tabia za bidhaa Tabia za bidhaa Kiaisilandi 28-09-2022
Taarifa za kipeperushi Taarifa za kipeperushi Kroeshia 28-09-2022
Tabia za bidhaa Tabia za bidhaa Kroeshia 28-09-2022
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kroeshia 23-09-2013

Tafuta arifu zinazohusiana na bidhaa hii