Pirfenidone Viatris

Land: Europeiska unionen

Språk: engelska

Källa: EMA (European Medicines Agency)

Köp det nu

Ladda ner Bipacksedel (PIL)
28-11-2023
Ladda ner Produktens egenskaper (SPC)
28-11-2023

Aktiva substanser:

Pirfenidone

Tillgänglig från:

Viatris Limited

ATC-kod:

L04AX05

INN (International namn):

pirfenidone

Terapeutisk grupp:

Immunosuppressants

Terapiområde:

Idiopathic Pulmonary Fibrosis; Lung Diseases; Respiratory Tract Diseases

Terapeutiska indikationer:

Pirfenidone Viatris is indicated in adults for the treatment of mild to moderate idiopathic pulmonary fibrosis (IPF).

Produktsammanfattning:

Revision: 1

Bemyndigande status:

Authorised

Tillstånd datum:

2023-01-10

Bipacksedel

                                32
B. PACKAGE LEAFLET
33
PACKAGE LEAFLET: INFORMATION FOR THE USER
PIRFENIDONE VIATRIS 267 MG FILM-COATED TABLETS
PIRFENIDONE VIATRIS 534 MG FILM-COATED TABLETS
PIRFENIDONE VIATRIS 801 MG FILM-COATED TABLETS
pirfenidone
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 Pirfenidone Viatris is and what it is used for
2.
What you need to know before you take Pirfenidone Viatris
3.
How to take Pirfenidone Viatris
4.
Possible side effects
5.
How to store Pirfenidone Viatris
6.
Contents of the pack and other information
1.
WHAT PIRFENIDONE VIATRIS
IS AND WHAT IT IS USED FOR
Pirfenidone Viatris contains the active substance pirfenidone and it
is used for the treatment of
Idiopathic Pulmonary Fibrosis (IPF) in adults.
IPF is a condition in which the tissues in your lungs become swollen
and scarred over time, and as a
result makes it difficult to breathe deeply. This makes it hard for
your lungs to work properly.
Pirfenidone Viatris helps to reduce scarring and swelling in the
lungs, and helps you breathe better.
2.
WHAT YOU NEED TO KNOW BEFORE YOU TAKE PIRFENIDONE VIATRIS
DO NOT TAKE PIRFENIDONE VIATRIS
•
if you are allergic to pirfenidone or any of the other ingredients of
this medicine (listed in
section 6)
•
if you have previously expe
rienced angioedema with pirfenidone, including symptoms such as
swelling of the face, lips and/or tongue which may be associated with
difficulty breathing or
wheezing
•
if you are taking a medicine called fluvoxamine (used to treat
depression and obsessive
comp
                                
                                Läs hela dokumentet
                                
                            

Produktens egenskaper

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE MEDICINAL PRODUCT
Pirfenidone Viatris 267 mg film-coated tablets
Pirfenidone Viatris 534 mg film-coated tablets
Pirfenidone Viatris 801 mg film-coated tablets
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Pirfenidone Viatris 267 mg film-coated tablets
Each tablet contains 267 mg of pirfenidone.
Pirfenidone Viatris 534 mg film-coated tablets
Each tablet contains 534 mg of pirfenidone.
Pirfenidone Viatris 801 mg film-coated tablets
Each tablet contains 801 mg of pirfenidone.
3.
PHARMACEUTICAL FORM
Film-coated tablet
Pirfenidone Viatris 267 mg film-coated tablets
Pirfenidone Viatris 267 mg film-coated tablets are yellow, oval
shaped, approximately 13 x 6 mm
biconvex film-coated tablets, plain on both sides.
Pirfenidone Viatris 534 mg film-coated tablets
Pirfenidone Viatris 534 mg film-coated tablets are orange, oval
shaped, approximately 16 x 8 mm
biconvex film-coated tablets, plain on both sides.
Pirfenidone Viatris 801 mg film-coated tablets
Pirfenidone Viatris 801 mg film-coated tablets are brown, oval shaped,
approximately 20 x 9 mm
biconvex film-coated tablets, plain on both sides.
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
Pirfenidone Viatris is indicated in adults for the treatment of
idiopathic pulmonary fibrosis (IPF).
4.2
POSOLOGY AND METHOD OF ADMINISTRATION
Treatment with Pirfenidone Viatris should be initiated and supervised
by specialist physicians
experienced in the diagnosis and treatment of IPF.
3
Posology
_Adults _
Upon initiating treatment, the dose should be titrated to the
recommended daily dose of 2 403 mg/day
over a 14-day period as follows:
•
Days 1 to 7: a dose of 267 mg administered three times a day (801
mg/day)
•
Days 8 to 14: a dose of 534 mg administered three times a day (1 602
mg/day)
•
Day 15 onward: a dose of 801 mg administered three times a day (2 403
mg/day)
The recommended maintenance daily dose of Pirfenidone Viatris is 801
mg three times a day
with
food for a total of 2 403 mg/day.
Doses above 2 403 mg/
                                
                                Läs hela dokumentet
                                
                            

Dokument på andra språk

Bipacksedel Bipacksedel bulgariska 28-11-2023
Produktens egenskaper Produktens egenskaper bulgariska 28-11-2023
Offentlig bedömningsrapport Offentlig bedömningsrapport bulgariska 17-01-2023
Bipacksedel Bipacksedel spanska 28-11-2023
Produktens egenskaper Produktens egenskaper spanska 28-11-2023
Offentlig bedömningsrapport Offentlig bedömningsrapport spanska 17-01-2023
Bipacksedel Bipacksedel tjeckiska 28-11-2023
Produktens egenskaper Produktens egenskaper tjeckiska 28-11-2023
Offentlig bedömningsrapport Offentlig bedömningsrapport tjeckiska 17-01-2023
Bipacksedel Bipacksedel danska 28-11-2023
Produktens egenskaper Produktens egenskaper danska 28-11-2023
Offentlig bedömningsrapport Offentlig bedömningsrapport danska 17-01-2023
Bipacksedel Bipacksedel tyska 28-11-2023
Produktens egenskaper Produktens egenskaper tyska 28-11-2023
Offentlig bedömningsrapport Offentlig bedömningsrapport tyska 17-01-2023
Bipacksedel Bipacksedel estniska 28-11-2023
Produktens egenskaper Produktens egenskaper estniska 28-11-2023
Offentlig bedömningsrapport Offentlig bedömningsrapport estniska 17-01-2023
Bipacksedel Bipacksedel grekiska 28-11-2023
Produktens egenskaper Produktens egenskaper grekiska 28-11-2023
Offentlig bedömningsrapport Offentlig bedömningsrapport grekiska 17-01-2023
Bipacksedel Bipacksedel franska 28-11-2023
Produktens egenskaper Produktens egenskaper franska 28-11-2023
Offentlig bedömningsrapport Offentlig bedömningsrapport franska 17-01-2023
Bipacksedel Bipacksedel italienska 28-11-2023
Produktens egenskaper Produktens egenskaper italienska 28-11-2023
Offentlig bedömningsrapport Offentlig bedömningsrapport italienska 17-01-2023
Bipacksedel Bipacksedel lettiska 28-11-2023
Produktens egenskaper Produktens egenskaper lettiska 28-11-2023
Offentlig bedömningsrapport Offentlig bedömningsrapport lettiska 17-01-2023
Bipacksedel Bipacksedel litauiska 28-11-2023
Produktens egenskaper Produktens egenskaper litauiska 28-11-2023
Offentlig bedömningsrapport Offentlig bedömningsrapport litauiska 17-01-2023
Bipacksedel Bipacksedel ungerska 28-11-2023
Produktens egenskaper Produktens egenskaper ungerska 28-11-2023
Offentlig bedömningsrapport Offentlig bedömningsrapport ungerska 17-01-2023
Bipacksedel Bipacksedel maltesiska 28-11-2023
Produktens egenskaper Produktens egenskaper maltesiska 28-11-2023
Offentlig bedömningsrapport Offentlig bedömningsrapport maltesiska 17-01-2023
Bipacksedel Bipacksedel nederländska 28-11-2023
Produktens egenskaper Produktens egenskaper nederländska 28-11-2023
Offentlig bedömningsrapport Offentlig bedömningsrapport nederländska 17-01-2023
Bipacksedel Bipacksedel polska 28-11-2023
Produktens egenskaper Produktens egenskaper polska 28-11-2023
Offentlig bedömningsrapport Offentlig bedömningsrapport polska 17-01-2023
Bipacksedel Bipacksedel portugisiska 28-11-2023
Produktens egenskaper Produktens egenskaper portugisiska 28-11-2023
Offentlig bedömningsrapport Offentlig bedömningsrapport portugisiska 17-01-2023
Bipacksedel Bipacksedel rumänska 28-11-2023
Produktens egenskaper Produktens egenskaper rumänska 28-11-2023
Offentlig bedömningsrapport Offentlig bedömningsrapport rumänska 17-01-2023
Bipacksedel Bipacksedel slovakiska 28-11-2023
Produktens egenskaper Produktens egenskaper slovakiska 28-11-2023
Offentlig bedömningsrapport Offentlig bedömningsrapport slovakiska 17-01-2023
Bipacksedel Bipacksedel slovenska 28-11-2023
Produktens egenskaper Produktens egenskaper slovenska 28-11-2023
Offentlig bedömningsrapport Offentlig bedömningsrapport slovenska 17-01-2023
Bipacksedel Bipacksedel finska 28-11-2023
Produktens egenskaper Produktens egenskaper finska 28-11-2023
Offentlig bedömningsrapport Offentlig bedömningsrapport finska 17-01-2023
Bipacksedel Bipacksedel svenska 28-11-2023
Produktens egenskaper Produktens egenskaper svenska 28-11-2023
Offentlig bedömningsrapport Offentlig bedömningsrapport svenska 17-01-2023
Bipacksedel Bipacksedel norska 28-11-2023
Produktens egenskaper Produktens egenskaper norska 28-11-2023
Bipacksedel Bipacksedel isländska 28-11-2023
Produktens egenskaper Produktens egenskaper isländska 28-11-2023
Bipacksedel Bipacksedel kroatiska 28-11-2023
Produktens egenskaper Produktens egenskaper kroatiska 28-11-2023
Offentlig bedömningsrapport Offentlig bedömningsrapport kroatiska 17-01-2023

Sök varningar relaterade till denna produkt