Ribavirin BioPartners

Land: Europeiska unionen

Språk: engelska

Källa: EMA (European Medicines Agency)

Köp det nu

Bipacksedel Bipacksedel (PIL)
06-05-2013
Produktens egenskaper Produktens egenskaper (SPC)
06-05-2013

Aktiva substanser:

Ribavirin

Tillgänglig från:

BioPartners GmbH

ATC-kod:

J05AB04

INN (International namn):

ribavirin

Terapeutisk grupp:

Antivirals for systemic use

Terapiområde:

Hepatitis C, Chronic

Terapeutiska indikationer:

Ribavirin BioPartners is indicated for the treatment of chronic hepatitis-C-virus (HCV) infection in adults, children three years of age and older and adolescents and must only be used as part of a combination regimen with interferon alfa-2b. Ribavirin monotherapy must not be used. There is no safety or efficacy information on the use of ribavirin with other forms of interferon (i.e. not alfa-2b).Naïve patientsAdult patientsRibavirin BioPartners is indicated, in combination with interferon alfa-2b, for the treatment of adult patients with all types of chronic hepatitis C except genotype 1, not previously treated, without liver decompensation, with elevated alanine aminotransferase (ALT), who are positive for hepatitis C viral ribonucleic acid (HCV-RNA) (see section 4.4)Children three years of age and older and adolescentsRibavirin BioPartners is intended for use, in a combination regimen with interferon alfa-2b, for the treatment of children three years of age and older and adolescents, who have all types of chronic hepatitis C except genotype 1, not previously treated, without liver decompensation, and who are positive for HCV-RNA.When deciding to not to defer treatment until adulthood, it is important to consider that the combination therapy induced a growth inhibition. The reversibility of growth inhibition is uncertain. The decision to treat should be made on a case by case basis (see section 4.4).Previous-treatment-failure patientsAdult patientsRibavirin BioPartners is indicated, in combination with interferon alfa-2b, for the treatment of adult patients with chronic hepatitis C who have previously responded (with normalisation of ALT at the end of treatment) to interferon alfa monotherapy but who have subsequently relapsed (see section 5.1).

Produktsammanfattning:

Revision: 2

Bemyndigande status:

Withdrawn

Tillstånd datum:

2010-04-06

Bipacksedel

                                33
B. PACKAGE LEAFLET
Medicinal product no longer authorised
34
PACKAGE LEAFLET: INFORMATION FOR THE USER
RIBAVIRIN BIOPARTNERS 200 MG FILM-COATED TABLETS
ribavirin
READ ALL OF THIS LEAFLET CAREFULLY BEFORE YOU START TAKING THIS
MEDICINE
-
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. Do not pass it on to
others. It may harm them, even
if their symptoms are the same as yours.
-
If any of the side effects gets serious, or if you notice any side
effects not listed in this leaflet,
please tell your doctor or pharmacist.
IN THIS LEAFLET:
1.
What Ribavirin BioPartners is and what it is used for
2.
Before you take Ribavirin BioPartners
3.
How to take Ribavirin BioPartners
4.
Possible side effects
5.
How to store Ribavirin BioPartners
6.
Further information
1.
WHAT RIBAVIRIN BIOPARTNERS IS AND WHAT IT IS USED FOR
Ribavirin BioPartners contains the active ingredient ribavirin.
Ribavirin BioPartners stops the
multiplication of many types of viruses, including hepatitis C virus.
Ribavirin BioPartners must not be
used without interferon alfa-2b, i.e. Ribavirin BioPartners must not
be used alone.
_Previously untreated patients_
:
The combination of Ribavirin BioPartners with interferon alfa-2b is
used to treat patients 3 years of
age and older who have chronic hepatitis C (HCV) infection, except
genotype 1. For children and
adolescents weighing less than 47 kg a solution formulation is
available.
_Previously treated adult patients_
:
The combination of Ribavirin BioPartners with interferon alfa-2b is
used to treat adult patients with
chronic hepatitis C, who have previously responded to a treatment with
an alpha interferon alone, but
whose condition has recurred.
There is no safety or efficacy information on the use of ribavirin
with other forms of interferon (i.e.,
not alfa-2b).
2.
BEFORE YOU TAKE RIBAVIRIN BIOPARTNERS
Ribavirin BioPartners is not recommended for use in patients under the
age of 3 years.
DO N
                                
                                Läs hela dokumentet
                                
                            

Produktens egenskaper

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
Medicinal product no longer authorised
2
1.
NAME OF THE MEDICINAL PRODUCT
Ribavirin BioPartners 200 mg film-coated tablets
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Each Ribavirin BioPartners film-coated tablet contains 200 mg of
ribavirin.
For a full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Film-coated tablet.
Round, white, biconvex film-coated tablet.
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
Ribavirin BioPartners is indicated for the treatment of chronic
hepatitis C virus (HCV) infection in
adults, children 3 years of age and older and adolescents and must
only be used as part of a
combination regimen with interferon alfa-2b. Ribavirin monotherapy
must not be used.
There is no safety or efficacy information on the use of Ribavirin
with other forms of interferon (i.e.,
not alfa-2b).
Naïve patients
_Adult patients: _
Ribavirin BioPartners is indicated, in combination with interferon
alfa-2b, for the
treatment of adult patients with all types of chronic hepatitis C
except genotype 1, not previously
treated, without liver decompensation, with elevated alanine
aminotransferase (ALT), who are positive
for hepatitis C viral ribonucleic acid HCV-RNA (see section 4.4).
_Children 3 years of age and older and adolescents:_
Ribavirin BioPartners is intended for use, in a
combination regimen with interferon alfa-2b, for the treatment of
children 3 years of age and older and
adolescents, who have all types of chronic hepatitis C except genotype
1, not previously treated,
without liver decompensation, and who are positive for HCV-RNA.
When deciding to not to defer treatment until adulthood, it is
important to consider that the
combination therapy induced a growth inhibition. The reversibility of
growth inhibition is uncertain.
The decision to treat should be made on a case by case basis (see
section 4.4).
Previous treatment failure patients
_Adult patients:_
Ribavirin BioPartners is indicated, in combination with interferon
alfa-2b, for the
treatmen
                                
                                Läs hela dokumentet
                                
                            

Dokument på andra språk

Bipacksedel Bipacksedel bulgariska 06-05-2013
Produktens egenskaper Produktens egenskaper bulgariska 06-05-2013
Offentlig bedömningsrapport Offentlig bedömningsrapport bulgariska 06-05-2013
Bipacksedel Bipacksedel spanska 06-05-2013
Produktens egenskaper Produktens egenskaper spanska 06-05-2013
Offentlig bedömningsrapport Offentlig bedömningsrapport spanska 06-05-2013
Bipacksedel Bipacksedel tjeckiska 06-05-2013
Produktens egenskaper Produktens egenskaper tjeckiska 06-05-2013
Offentlig bedömningsrapport Offentlig bedömningsrapport tjeckiska 06-05-2013
Bipacksedel Bipacksedel danska 06-05-2013
Produktens egenskaper Produktens egenskaper danska 06-05-2013
Offentlig bedömningsrapport Offentlig bedömningsrapport danska 06-05-2013
Bipacksedel Bipacksedel tyska 06-05-2013
Produktens egenskaper Produktens egenskaper tyska 06-05-2013
Offentlig bedömningsrapport Offentlig bedömningsrapport tyska 06-05-2013
Bipacksedel Bipacksedel estniska 06-05-2013
Produktens egenskaper Produktens egenskaper estniska 06-05-2013
Offentlig bedömningsrapport Offentlig bedömningsrapport estniska 06-05-2013
Bipacksedel Bipacksedel grekiska 06-05-2013
Produktens egenskaper Produktens egenskaper grekiska 06-05-2013
Offentlig bedömningsrapport Offentlig bedömningsrapport grekiska 06-05-2013
Bipacksedel Bipacksedel franska 06-05-2013
Produktens egenskaper Produktens egenskaper franska 06-05-2013
Offentlig bedömningsrapport Offentlig bedömningsrapport franska 06-05-2013
Bipacksedel Bipacksedel italienska 06-05-2013
Produktens egenskaper Produktens egenskaper italienska 06-05-2013
Offentlig bedömningsrapport Offentlig bedömningsrapport italienska 06-05-2013
Bipacksedel Bipacksedel lettiska 06-05-2013
Produktens egenskaper Produktens egenskaper lettiska 06-05-2013
Offentlig bedömningsrapport Offentlig bedömningsrapport lettiska 06-05-2013
Bipacksedel Bipacksedel litauiska 06-05-2013
Produktens egenskaper Produktens egenskaper litauiska 06-05-2013
Offentlig bedömningsrapport Offentlig bedömningsrapport litauiska 06-05-2013
Bipacksedel Bipacksedel ungerska 06-05-2013
Produktens egenskaper Produktens egenskaper ungerska 06-05-2013
Offentlig bedömningsrapport Offentlig bedömningsrapport ungerska 06-05-2013
Bipacksedel Bipacksedel maltesiska 06-05-2013
Produktens egenskaper Produktens egenskaper maltesiska 06-05-2013
Offentlig bedömningsrapport Offentlig bedömningsrapport maltesiska 06-05-2013
Bipacksedel Bipacksedel nederländska 06-05-2013
Produktens egenskaper Produktens egenskaper nederländska 06-05-2013
Offentlig bedömningsrapport Offentlig bedömningsrapport nederländska 06-05-2013
Bipacksedel Bipacksedel polska 06-05-2013
Produktens egenskaper Produktens egenskaper polska 06-05-2013
Offentlig bedömningsrapport Offentlig bedömningsrapport polska 06-05-2013
Bipacksedel Bipacksedel portugisiska 06-05-2013
Produktens egenskaper Produktens egenskaper portugisiska 06-05-2013
Offentlig bedömningsrapport Offentlig bedömningsrapport portugisiska 06-05-2013
Bipacksedel Bipacksedel rumänska 06-05-2013
Produktens egenskaper Produktens egenskaper rumänska 06-05-2013
Offentlig bedömningsrapport Offentlig bedömningsrapport rumänska 06-05-2013
Bipacksedel Bipacksedel slovakiska 06-05-2013
Produktens egenskaper Produktens egenskaper slovakiska 06-05-2013
Offentlig bedömningsrapport Offentlig bedömningsrapport slovakiska 06-05-2013
Bipacksedel Bipacksedel slovenska 06-05-2013
Produktens egenskaper Produktens egenskaper slovenska 06-05-2013
Offentlig bedömningsrapport Offentlig bedömningsrapport slovenska 06-05-2013
Bipacksedel Bipacksedel finska 06-05-2013
Produktens egenskaper Produktens egenskaper finska 06-05-2013
Offentlig bedömningsrapport Offentlig bedömningsrapport finska 06-05-2013
Bipacksedel Bipacksedel svenska 06-05-2013
Produktens egenskaper Produktens egenskaper svenska 06-05-2013
Offentlig bedömningsrapport Offentlig bedömningsrapport svenska 06-05-2013
Bipacksedel Bipacksedel norska 06-05-2013
Produktens egenskaper Produktens egenskaper norska 06-05-2013
Bipacksedel Bipacksedel isländska 06-05-2013
Produktens egenskaper Produktens egenskaper isländska 06-05-2013

Sök varningar relaterade till denna produkt