CoAprovel

Riik: Euroopa Liit

keel: inglise

Allikas: EMA (European Medicines Agency)

Osta kohe

Infovoldik Infovoldik (PIL)
26-03-2024
Toote omadused Toote omadused (SPC)
26-03-2024
Avaliku hindamisaruande Avaliku hindamisaruande (PAR)
23-09-2013

Toimeaine:

irbesartan, hydrochlorothiazide

Saadav alates:

Sanofi Winthrop Industrie

ATC kood:

C09DA04

INN (Rahvusvaheline Nimetus):

irbesartan, hydrochlorothiazide

Terapeutiline rühm:

Agents acting on the renin-angiotensin system

Terapeutiline ala:

Hypertension

Näidustused:

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.

Toote kokkuvõte:

Revision: 49

Volitamisolek:

Authorised

Loa andmise kuupäev:

1998-10-14

Infovoldik

                                109
B. PACKAGE LEAFLET
110
PACKAGE LEAFLET: INFORMATION FOR THE PATIENT
COAPROVEL 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 CoAprovel is and what it is used for
2.
What you need to know before you take CoAprovel
3.
How to take CoAprovel
4.
Possible side effects
5.
How to store CoAprovel
6.
Contents of the pack and other information
1.
WHAT COAPROVEL IS AND WHAT IT IS USED FOR
CoAprovel 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 CoAprovel work together to lower blood
pressure further than if either
was given alone.
COAPROVEL 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 COAPROVEL
DO NOT TAKE COAPROVEL
▪
if you are
ALLERGIC
to irbesartan or any of the other ingredients of this
                                
                                Lugege kogu dokumenti
                                
                            

Toote omadused

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE MEDICINAL PRODUCT
CoAprovel 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
CoAprovel 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:
▪
CoAprovel 150 mg/12.5 mg may be administered in patients whose blood
pressure is not
adequately controlled with hydrochlorothiazide or irbesartan 150 mg
alone.
▪
CoAprovel 300 mg/12.5 mg may be administered in patients
insufficiently controlled by
irbesartan 300 mg or by CoAprovel 150 mg/12.5 mg.
▪
CoAprovel 300 mg/25 mg may be administered in patients insufficiently
controlled by
CoAprovel 300 mg/12.5 mg.
Doses higher than 300 mg irbesartan/25 mg hydrochlorothiazide once
daily are not recommended.
When necessary, CoAprovel 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, CoAprovel 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 
                                
                                Lugege kogu dokumenti
                                
                            

Dokumendid teistes keeltes

Infovoldik Infovoldik bulgaaria 26-03-2024
Toote omadused Toote omadused bulgaaria 26-03-2024
Avaliku hindamisaruande Avaliku hindamisaruande bulgaaria 23-09-2013
Infovoldik Infovoldik hispaania 26-03-2024
Toote omadused Toote omadused hispaania 26-03-2024
Avaliku hindamisaruande Avaliku hindamisaruande hispaania 23-09-2013
Infovoldik Infovoldik tšehhi 26-03-2024
Toote omadused Toote omadused tšehhi 26-03-2024
Avaliku hindamisaruande Avaliku hindamisaruande tšehhi 23-09-2013
Infovoldik Infovoldik taani 26-03-2024
Toote omadused Toote omadused taani 26-03-2024
Avaliku hindamisaruande Avaliku hindamisaruande taani 23-09-2013
Infovoldik Infovoldik saksa 26-03-2024
Toote omadused Toote omadused saksa 26-03-2024
Avaliku hindamisaruande Avaliku hindamisaruande saksa 23-09-2013
Infovoldik Infovoldik eesti 26-03-2024
Toote omadused Toote omadused eesti 26-03-2024
Avaliku hindamisaruande Avaliku hindamisaruande eesti 23-09-2013
Infovoldik Infovoldik kreeka 26-03-2024
Toote omadused Toote omadused kreeka 26-03-2024
Avaliku hindamisaruande Avaliku hindamisaruande kreeka 23-09-2013
Infovoldik Infovoldik prantsuse 26-03-2024
Toote omadused Toote omadused prantsuse 26-03-2024
Avaliku hindamisaruande Avaliku hindamisaruande prantsuse 23-09-2013
Infovoldik Infovoldik itaalia 26-03-2024
Toote omadused Toote omadused itaalia 26-03-2024
Avaliku hindamisaruande Avaliku hindamisaruande itaalia 23-09-2013
Infovoldik Infovoldik läti 26-03-2024
Toote omadused Toote omadused läti 26-03-2024
Avaliku hindamisaruande Avaliku hindamisaruande läti 23-09-2013
Infovoldik Infovoldik leedu 26-03-2024
Toote omadused Toote omadused leedu 26-03-2024
Avaliku hindamisaruande Avaliku hindamisaruande leedu 23-09-2013
Infovoldik Infovoldik ungari 26-03-2024
Toote omadused Toote omadused ungari 26-03-2024
Avaliku hindamisaruande Avaliku hindamisaruande ungari 23-09-2013
Infovoldik Infovoldik malta 26-03-2024
Toote omadused Toote omadused malta 26-03-2024
Avaliku hindamisaruande Avaliku hindamisaruande malta 23-09-2013
Infovoldik Infovoldik hollandi 26-03-2024
Toote omadused Toote omadused hollandi 26-03-2024
Avaliku hindamisaruande Avaliku hindamisaruande hollandi 23-09-2013
Infovoldik Infovoldik poola 26-03-2024
Toote omadused Toote omadused poola 26-03-2024
Avaliku hindamisaruande Avaliku hindamisaruande poola 23-09-2013
Infovoldik Infovoldik portugali 26-03-2024
Toote omadused Toote omadused portugali 26-03-2024
Avaliku hindamisaruande Avaliku hindamisaruande portugali 23-09-2013
Infovoldik Infovoldik rumeenia 26-03-2024
Toote omadused Toote omadused rumeenia 26-03-2024
Avaliku hindamisaruande Avaliku hindamisaruande rumeenia 23-09-2013
Infovoldik Infovoldik slovaki 26-03-2024
Toote omadused Toote omadused slovaki 26-03-2024
Avaliku hindamisaruande Avaliku hindamisaruande slovaki 23-09-2013
Infovoldik Infovoldik sloveeni 26-03-2024
Toote omadused Toote omadused sloveeni 26-03-2024
Avaliku hindamisaruande Avaliku hindamisaruande sloveeni 23-09-2013
Infovoldik Infovoldik soome 26-03-2024
Toote omadused Toote omadused soome 26-03-2024
Avaliku hindamisaruande Avaliku hindamisaruande soome 23-09-2013
Infovoldik Infovoldik rootsi 26-03-2024
Toote omadused Toote omadused rootsi 26-03-2024
Avaliku hindamisaruande Avaliku hindamisaruande rootsi 23-09-2013
Infovoldik Infovoldik norra 26-03-2024
Toote omadused Toote omadused norra 26-03-2024
Infovoldik Infovoldik islandi 26-03-2024
Toote omadused Toote omadused islandi 26-03-2024
Infovoldik Infovoldik horvaadi 26-03-2024
Toote omadused Toote omadused horvaadi 26-03-2024
Avaliku hindamisaruande Avaliku hindamisaruande horvaadi 23-09-2013

Vaadake dokumentide ajalugu