Ribavirin BioPartners

Valsts: Eiropas Savienība

Valoda: angļu

Klimata pārmaiņas: EMA (European Medicines Agency)

Nopērc to tagad

Aktīvā sastāvdaļa:

Ribavirin

Pieejams no:

BioPartners GmbH

ATĶ kods:

J05AB04

SNN (starptautisko nepatentēto nosaukumu):

ribavirin

Ārstniecības grupa:

Antivirals for systemic use

Ārstniecības joma:

Hepatitis C, Chronic

Ārstēšanas norādes:

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).

Produktu pārskats:

Revision: 2

Autorizācija statuss:

Withdrawn

Autorizācija datums:

2010-04-06

Lietošanas instrukcija

                                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
                                
                                Izlasiet visu dokumentu
                                
                            

Produkta apraksts

                                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
                                
                                Izlasiet visu dokumentu
                                
                            

Dokumenti citās valodās

Lietošanas instrukcija Lietošanas instrukcija bulgāru 06-05-2013
Produkta apraksts Produkta apraksts bulgāru 06-05-2013
Publiskā novērtējuma ziņojums Publiskā novērtējuma ziņojums bulgāru 06-05-2013
Lietošanas instrukcija Lietošanas instrukcija spāņu 06-05-2013
Produkta apraksts Produkta apraksts spāņu 06-05-2013
Lietošanas instrukcija Lietošanas instrukcija čehu 06-05-2013
Produkta apraksts Produkta apraksts čehu 06-05-2013
Lietošanas instrukcija Lietošanas instrukcija dāņu 06-05-2013
Produkta apraksts Produkta apraksts dāņu 06-05-2013
Lietošanas instrukcija Lietošanas instrukcija vācu 06-05-2013
Produkta apraksts Produkta apraksts vācu 06-05-2013
Lietošanas instrukcija Lietošanas instrukcija igauņu 06-05-2013
Produkta apraksts Produkta apraksts igauņu 06-05-2013
Lietošanas instrukcija Lietošanas instrukcija grieķu 06-05-2013
Produkta apraksts Produkta apraksts grieķu 06-05-2013
Lietošanas instrukcija Lietošanas instrukcija franču 06-05-2013
Produkta apraksts Produkta apraksts franču 06-05-2013
Lietošanas instrukcija Lietošanas instrukcija itāļu 06-05-2013
Produkta apraksts Produkta apraksts itāļu 06-05-2013
Lietošanas instrukcija Lietošanas instrukcija latviešu 06-05-2013
Produkta apraksts Produkta apraksts latviešu 06-05-2013
Publiskā novērtējuma ziņojums Publiskā novērtējuma ziņojums latviešu 06-05-2013
Lietošanas instrukcija Lietošanas instrukcija lietuviešu 06-05-2013
Produkta apraksts Produkta apraksts lietuviešu 06-05-2013
Publiskā novērtējuma ziņojums Publiskā novērtējuma ziņojums lietuviešu 06-05-2013
Lietošanas instrukcija Lietošanas instrukcija ungāru 06-05-2013
Produkta apraksts Produkta apraksts ungāru 06-05-2013
Lietošanas instrukcija Lietošanas instrukcija maltiešu 06-05-2013
Produkta apraksts Produkta apraksts maltiešu 06-05-2013
Publiskā novērtējuma ziņojums Publiskā novērtējuma ziņojums maltiešu 06-05-2013
Lietošanas instrukcija Lietošanas instrukcija holandiešu 06-05-2013
Produkta apraksts Produkta apraksts holandiešu 06-05-2013
Publiskā novērtējuma ziņojums Publiskā novērtējuma ziņojums holandiešu 06-05-2013
Lietošanas instrukcija Lietošanas instrukcija poļu 06-05-2013
Produkta apraksts Produkta apraksts poļu 06-05-2013
Lietošanas instrukcija Lietošanas instrukcija portugāļu 06-05-2013
Produkta apraksts Produkta apraksts portugāļu 06-05-2013
Publiskā novērtējuma ziņojums Publiskā novērtējuma ziņojums portugāļu 06-05-2013
Lietošanas instrukcija Lietošanas instrukcija rumāņu 06-05-2013
Produkta apraksts Produkta apraksts rumāņu 06-05-2013
Publiskā novērtējuma ziņojums Publiskā novērtējuma ziņojums rumāņu 06-05-2013
Lietošanas instrukcija Lietošanas instrukcija slovāku 06-05-2013
Produkta apraksts Produkta apraksts slovāku 06-05-2013
Publiskā novērtējuma ziņojums Publiskā novērtējuma ziņojums slovāku 06-05-2013
Lietošanas instrukcija Lietošanas instrukcija slovēņu 06-05-2013
Produkta apraksts Produkta apraksts slovēņu 06-05-2013
Publiskā novērtējuma ziņojums Publiskā novērtējuma ziņojums slovēņu 06-05-2013
Lietošanas instrukcija Lietošanas instrukcija somu 06-05-2013
Produkta apraksts Produkta apraksts somu 06-05-2013
Lietošanas instrukcija Lietošanas instrukcija zviedru 06-05-2013
Produkta apraksts Produkta apraksts zviedru 06-05-2013
Lietošanas instrukcija Lietošanas instrukcija norvēģu 06-05-2013
Produkta apraksts Produkta apraksts norvēģu 06-05-2013
Lietošanas instrukcija Lietošanas instrukcija īslandiešu 06-05-2013
Produkta apraksts Produkta apraksts īslandiešu 06-05-2013

Meklēt brīdinājumus, kas saistīti ar šo produktu