Neparvis

Nchi: Umoja wa Ulaya

Lugha: Kiingereza

Chanzo: EMA (European Medicines Agency)

Nunua Sasa

Taarifa za kipeperushi Taarifa za kipeperushi (PIL)
08-12-2023
Tabia za bidhaa Tabia za bidhaa (SPC)
08-12-2023

Viambatanisho vya kazi:

sacubitril, valsartan

Inapatikana kutoka:

Novartis Europharm Limited

ATC kanuni:

C09DX04

INN (Jina la Kimataifa):

sacubitril, valsartan

Kundi la matibabu:

Agents acting on the renin-angiotensin system

Eneo la matibabu:

Heart Failure

Matibabu dalili:

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).

Bidhaa muhtasari:

Revision: 18

Idhini hali ya:

Authorised

Idhini ya tarehe:

2016-05-26

Taarifa za kipeperushi

                                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
                                
                                Soma hati kamili
                                
                            

Tabia za bidhaa

                                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 
                                
                                Soma hati kamili
                                
                            

Nyaraka katika lugha zingine

Taarifa za kipeperushi Taarifa za kipeperushi Kibulgaria 08-12-2023
Tabia za bidhaa Tabia za bidhaa Kibulgaria 08-12-2023
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kibulgaria 22-06-2023
Taarifa za kipeperushi Taarifa za kipeperushi Kihispania 08-12-2023
Tabia za bidhaa Tabia za bidhaa Kihispania 08-12-2023
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kihispania 22-06-2023
Taarifa za kipeperushi Taarifa za kipeperushi Kicheki 08-12-2023
Tabia za bidhaa Tabia za bidhaa Kicheki 08-12-2023
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kicheki 22-06-2023
Taarifa za kipeperushi Taarifa za kipeperushi Kidenmaki 08-12-2023
Tabia za bidhaa Tabia za bidhaa Kidenmaki 08-12-2023
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kidenmaki 22-06-2023
Taarifa za kipeperushi Taarifa za kipeperushi Kijerumani 08-12-2023
Tabia za bidhaa Tabia za bidhaa Kijerumani 08-12-2023
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kijerumani 22-06-2023
Taarifa za kipeperushi Taarifa za kipeperushi Kiestonia 08-12-2023
Tabia za bidhaa Tabia za bidhaa Kiestonia 08-12-2023
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kiestonia 22-06-2023
Taarifa za kipeperushi Taarifa za kipeperushi Kigiriki 08-12-2023
Tabia za bidhaa Tabia za bidhaa Kigiriki 08-12-2023
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kigiriki 22-06-2023
Taarifa za kipeperushi Taarifa za kipeperushi Kifaransa 08-12-2023
Tabia za bidhaa Tabia za bidhaa Kifaransa 08-12-2023
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kifaransa 22-06-2023
Taarifa za kipeperushi Taarifa za kipeperushi Kiitaliano 08-12-2023
Tabia za bidhaa Tabia za bidhaa Kiitaliano 08-12-2023
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kiitaliano 22-06-2023
Taarifa za kipeperushi Taarifa za kipeperushi Kilatvia 08-12-2023
Tabia za bidhaa Tabia za bidhaa Kilatvia 08-12-2023
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kilatvia 22-06-2023
Taarifa za kipeperushi Taarifa za kipeperushi Kilithuania 08-12-2023
Tabia za bidhaa Tabia za bidhaa Kilithuania 08-12-2023
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kilithuania 22-06-2023
Taarifa za kipeperushi Taarifa za kipeperushi Kihungari 08-12-2023
Tabia za bidhaa Tabia za bidhaa Kihungari 08-12-2023
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kihungari 22-06-2023
Taarifa za kipeperushi Taarifa za kipeperushi Kimalta 08-12-2023
Tabia za bidhaa Tabia za bidhaa Kimalta 08-12-2023
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kimalta 22-06-2023
Taarifa za kipeperushi Taarifa za kipeperushi Kiholanzi 08-12-2023
Tabia za bidhaa Tabia za bidhaa Kiholanzi 08-12-2023
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kiholanzi 22-06-2023
Taarifa za kipeperushi Taarifa za kipeperushi Kipolandi 08-12-2023
Tabia za bidhaa Tabia za bidhaa Kipolandi 08-12-2023
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kipolandi 22-06-2023
Taarifa za kipeperushi Taarifa za kipeperushi Kireno 08-12-2023
Tabia za bidhaa Tabia za bidhaa Kireno 08-12-2023
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kireno 22-06-2023
Taarifa za kipeperushi Taarifa za kipeperushi Kiromania 08-12-2023
Tabia za bidhaa Tabia za bidhaa Kiromania 08-12-2023
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kiromania 22-06-2023
Taarifa za kipeperushi Taarifa za kipeperushi Kislovakia 08-12-2023
Tabia za bidhaa Tabia za bidhaa Kislovakia 08-12-2023
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kislovakia 22-06-2023
Taarifa za kipeperushi Taarifa za kipeperushi Kislovenia 08-12-2023
Tabia za bidhaa Tabia za bidhaa Kislovenia 08-12-2023
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kislovenia 22-06-2023
Taarifa za kipeperushi Taarifa za kipeperushi Kifinlandi 08-12-2023
Tabia za bidhaa Tabia za bidhaa Kifinlandi 08-12-2023
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kifinlandi 22-06-2023
Taarifa za kipeperushi Taarifa za kipeperushi Kiswidi 08-12-2023
Tabia za bidhaa Tabia za bidhaa Kiswidi 08-12-2023
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kiswidi 22-06-2023
Taarifa za kipeperushi Taarifa za kipeperushi Kinorwe 08-12-2023
Tabia za bidhaa Tabia za bidhaa Kinorwe 08-12-2023
Taarifa za kipeperushi Taarifa za kipeperushi Kiaisilandi 08-12-2023
Tabia za bidhaa Tabia za bidhaa Kiaisilandi 08-12-2023
Taarifa za kipeperushi Taarifa za kipeperushi Kroeshia 08-12-2023
Tabia za bidhaa Tabia za bidhaa Kroeshia 08-12-2023
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kroeshia 22-06-2023

Tafuta arifu zinazohusiana na bidhaa hii

Tazama historia ya hati