Neparvis

Țară: Uniunea Europeană

Limbă: engleză

Sursă: EMA (European Medicines Agency)

Cumpara asta acum

Prospect Prospect (PIL)
08-12-2023

Ingredient activ:

sacubitril, valsartan

Disponibil de la:

Novartis Europharm Limited

Codul ATC:

C09DX04

INN (nume internaţional):

sacubitril, valsartan

Grupul Terapeutică:

Agents acting on the renin-angiotensin system

Zonă Terapeutică:

Heart Failure

Indicații terapeutice:

Paediatric heart failureNeparvis is indicated in children and adolescents aged one year or older for treatment of symptomatic chronic heart failure with left ventricular systolic dysfunction (see section 5.1).Adult heart failureNeparvis is indicated in adult patients for treatment of symptomatic chronic heart failure with reduced ejection fraction (see section 5.1).

Rezumat produs:

Revision: 18

Statutul autorizaţiei:

Authorised

Data de autorizare:

2016-05-26

Prospect

                                75
B. PACKAGE LEAFLET
76
PACKAGE LEAFLET: INFORMATION FOR THE PATIENT
NEPARVIS 24 MG/26 MG FILM-COATED TABLETS
NEPARVIS 49 MG/51 MG FILM-COATED TABLETS
NEPARVIS 97 MG/103 MG FILM-COATED TABLETS
sacubitril/valsartan
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, pharmacist or
nurse.
-
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 Neparvis is and what it is used for
2.
What you need to know before you take Neparvis
3.
How to take Neparvis
4.
Possible side effects
5.
How to store Neparvis
6.
Contents of the pack and other information
1.
WHAT NEPARVIS IS AND WHAT IT IS USED FOR
Neparvis is a heart medicine containing an angiotensin receptor
neprilysin inhibitor. It delivers two
active substances, sacubitril and valsartan.
Neparvis is used to treat a type of long-term heart failure in adults,
children and adolescents (one year
and older).
This type of heart failure occurs when the heart is weak and cannot
pump enough blood to the lungs
and the rest of the body. The most common symptoms of heart failure
are breathlessness, fatigue,
tiredness and ankle swelling.
77
2.
WHAT YOU NEED TO KNOW BEFORE YOU TAKE
NEPARVIS
DO NOT TAKE NEPARVIS
•
if you are allergic to sacubitril, valsartan or any of the other
ingredients of this medicine (listed
in section 6).
•
if you are taking another type of medicine called an angiotensin
converting enzyme (ACE)
inhibitor (for example enalapril, lisinopril or ramipril), which is
used to treat high blood
pressure or heart failure. If you have been taking an ACE inhibitor,
wait for 36 hours after
taking the last dose before you sta
                                
                                Citiți documentul complet
                                
                            

Caracteristicilor produsului

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE MEDICINAL PRODUCT
Neparvis 24 mg/26 mg film-coated tablets
Neparvis 49 mg/51 mg film-coated tablets
Neparvis 97 mg/103 mg film-coated tablets
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Neparvis 24 mg/26 mg film-coated tablets
Each film-coated tablet contains 24.3 mg sacubitril and 25.7 mg
valsartan (as sacubitril valsartan
sodium salt complex).
Neparvis 49 mg/51 mg film-coated tablets
Each film-coated tablet contains 48.6 mg sacubitril and 51.4 mg
valsartan (as sacubitril valsartan
sodium salt complex).
Neparvis 97 mg/103 mg film-coated tablets
Each film-coated tablet contains 97.2 mg sacubitril and 102.8 mg
valsartan (as sacubitril valsartan
sodium salt complex).
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Film-coated tablet (tablet)
Neparvis 24 mg/26 mg film-coated tablets
Violet white ovaloid biconvex film-coated tablet with bevelled edges,
unscored, debossed with “NVR”
on one side and “LZ” on the other side. Approximate tablet
dimensions 13.1 mm x 5.2 mm.
Neparvis 49 mg/51 mg film-coated tablets
Pale yellow ovaloid biconvex film-coated tablet with bevelled edges,
unscored, debossed with “NVR”
on one side and “L1” on the other side. Approximate tablet
dimensions 13.1 mm x 5.2 mm.
Neparvis 97 mg/103 mg film-coated tablets
Light pink ovaloid biconvex film-coated tablet with bevelled edges,
unscored, debossed with “NVR”
on one side and “L11” on the other side. Approximate tablet
dimensions 15.1 mm x 6.0 mm.
3
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
Adult heart failure
Neparvis is indicated in adult patients for treatment of symptomatic
chronic heart failure with reduced
ejection fraction (see section 5.1).
Paediatric heart failure
Neparvis is indicated in children and adolescents aged one year or
older for treatment of symptomatic
chronic heart failure with left ventricular systolic dysfunction (see
section 5.1).
4.2
POSOLOGY AND METHOD OF ADMINISTRATION
Posology
_General considerations 
                                
                                Citiți documentul complet
                                
                            

Documente în alte limbi

Prospect Prospect bulgară 08-12-2023
Caracteristicilor produsului Caracteristicilor produsului bulgară 08-12-2023
Raport public de evaluare Raport public de evaluare bulgară 22-06-2023
Prospect Prospect spaniolă 08-12-2023
Caracteristicilor produsului Caracteristicilor produsului spaniolă 08-12-2023
Raport public de evaluare Raport public de evaluare spaniolă 22-06-2023
Prospect Prospect cehă 08-12-2023
Caracteristicilor produsului Caracteristicilor produsului cehă 08-12-2023
Raport public de evaluare Raport public de evaluare cehă 22-06-2023
Prospect Prospect daneză 08-12-2023
Caracteristicilor produsului Caracteristicilor produsului daneză 08-12-2023
Raport public de evaluare Raport public de evaluare daneză 22-06-2023
Prospect Prospect germană 08-12-2023
Caracteristicilor produsului Caracteristicilor produsului germană 08-12-2023
Raport public de evaluare Raport public de evaluare germană 22-06-2023
Prospect Prospect estoniană 08-12-2023
Caracteristicilor produsului Caracteristicilor produsului estoniană 08-12-2023
Raport public de evaluare Raport public de evaluare estoniană 22-06-2023
Prospect Prospect greacă 08-12-2023
Caracteristicilor produsului Caracteristicilor produsului greacă 08-12-2023
Raport public de evaluare Raport public de evaluare greacă 22-06-2023
Prospect Prospect franceză 08-12-2023
Caracteristicilor produsului Caracteristicilor produsului franceză 08-12-2023
Raport public de evaluare Raport public de evaluare franceză 22-06-2023
Prospect Prospect italiană 08-12-2023
Caracteristicilor produsului Caracteristicilor produsului italiană 08-12-2023
Raport public de evaluare Raport public de evaluare italiană 22-06-2023
Prospect Prospect letonă 08-12-2023
Caracteristicilor produsului Caracteristicilor produsului letonă 08-12-2023
Raport public de evaluare Raport public de evaluare letonă 22-06-2023
Prospect Prospect lituaniană 08-12-2023
Caracteristicilor produsului Caracteristicilor produsului lituaniană 08-12-2023
Raport public de evaluare Raport public de evaluare lituaniană 22-06-2023
Prospect Prospect maghiară 08-12-2023
Caracteristicilor produsului Caracteristicilor produsului maghiară 08-12-2023
Raport public de evaluare Raport public de evaluare maghiară 22-06-2023
Prospect Prospect malteză 08-12-2023
Caracteristicilor produsului Caracteristicilor produsului malteză 08-12-2023
Raport public de evaluare Raport public de evaluare malteză 22-06-2023
Prospect Prospect olandeză 08-12-2023
Caracteristicilor produsului Caracteristicilor produsului olandeză 08-12-2023
Raport public de evaluare Raport public de evaluare olandeză 22-06-2023
Prospect Prospect poloneză 08-12-2023
Caracteristicilor produsului Caracteristicilor produsului poloneză 08-12-2023
Raport public de evaluare Raport public de evaluare poloneză 22-06-2023
Prospect Prospect portugheză 08-12-2023
Caracteristicilor produsului Caracteristicilor produsului portugheză 08-12-2023
Raport public de evaluare Raport public de evaluare portugheză 22-06-2023
Prospect Prospect română 08-12-2023
Caracteristicilor produsului Caracteristicilor produsului română 08-12-2023
Raport public de evaluare Raport public de evaluare română 22-06-2023
Prospect Prospect slovacă 08-12-2023
Caracteristicilor produsului Caracteristicilor produsului slovacă 08-12-2023
Raport public de evaluare Raport public de evaluare slovacă 22-06-2023
Prospect Prospect slovenă 08-12-2023
Caracteristicilor produsului Caracteristicilor produsului slovenă 08-12-2023
Raport public de evaluare Raport public de evaluare slovenă 22-06-2023
Prospect Prospect finlandeză 08-12-2023
Caracteristicilor produsului Caracteristicilor produsului finlandeză 08-12-2023
Raport public de evaluare Raport public de evaluare finlandeză 22-06-2023
Prospect Prospect suedeză 08-12-2023
Caracteristicilor produsului Caracteristicilor produsului suedeză 08-12-2023
Raport public de evaluare Raport public de evaluare suedeză 22-06-2023
Prospect Prospect norvegiană 08-12-2023
Caracteristicilor produsului Caracteristicilor produsului norvegiană 08-12-2023
Prospect Prospect islandeză 08-12-2023
Caracteristicilor produsului Caracteristicilor produsului islandeză 08-12-2023
Prospect Prospect croată 08-12-2023
Caracteristicilor produsului Caracteristicilor produsului croată 08-12-2023
Raport public de evaluare Raport public de evaluare croată 22-06-2023

Căutați alerte legate de acest produs

Vizualizați istoricul documentelor