Vosevi

Pays: Union européenne

Langue: anglais

Source: EMA (European Medicines Agency)

Achète-le

Ingrédients actifs:

Sofosbuvir, velpatasvir, voxilaprevi

Disponible depuis:

Gilead Sciences Ireland UC

Code ATC:

J05A

DCI (Dénomination commune internationale):

sofosbuvir, velpatasvir, voxilaprevi

Groupe thérapeutique:

Antivirals for systemic use

Domaine thérapeutique:

Hepatitis C, Chronic

indications thérapeutiques:

Vosevi is indicated for the treatment of chronic hepatitis C virus (HCV) infection in patients aged 12 years and older and weighing at least 30 kg. (see sections 4.2, 4.4 and 5.1).

Descriptif du produit:

Revision: 16

Statut de autorisation:

Authorised

Date de l'autorisation:

2017-07-26

Notice patient

                                43
B. PACKAGE LEAFLET
44
PACKAGE LEAFLET: INFORMATION FOR THE USER
VOSEVI 400 MG/100 MG/100 MG FILM-COATED TABLETS
VOSEVI 200 MG/50 MG/50 MG FILM-COATED TABLETS
sofosbuvir/velpatasvir/voxilaprevir
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 Vosevi is and what it is used for
2.
What you need to know before you take Vosevi
3.
How to take Vosevi
4.
Possible side effects
5.
How to store Vosevi
6.
Contents of the pack and other information
IF VOSEVI HAS BEEN PRESCRIBED FOR YOUR CHILD, PLEASE NOTE THAT ALL THE
INFORMATION IN THIS LEAFLET IS
ADDRESSED TO YOUR CHILD (IN THIS CASE PLEASE READ “YOUR CHILD”
INSTEAD OF “YOU”).
1.
WHAT VOSEVI IS AND WHAT IT IS USED FOR
Vosevi is a medicine that contains the active substances sofosbuvir,
velpatasvir and voxilaprevir in a
single tablet. It is given to treat a chronic (long-term) viral
infection of the liver called hepatitis C in
patients aged 12 years and older and weighing at least 30 kg.
The active substances in this medicine work together by blocking three
different proteins that the
hepatitis C virus needs to grow and reproduce itself, causing the
infection to be eliminated from the
body.
2.
WHAT YOU NEED TO KNOW BEFORE YOU TAKE VOSEVI
DO NOT TAKE VOSEVI
•
IF YOU ARE ALLERGIC
to sofosbuvir, velpatasvir, voxilaprevir or any of the other
ingredients of this
medicine (listed in section 6 of this leaflet).

If this applies to you,
DO NOT TAKE VOSEVI AND TELL YOUR DOCTOR IMMEDIATELY.
•
IF YOU ARE CURRENTLY TAKING ANY OF THE FOLLOWING MEDICINES
                                
                                Lire le document complet
                                
                            

Résumé des caractéristiques du produit

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE MEDICINAL PRODUCT
Vosevi 400 mg/100 mg/100 mg film-coated tablets
Vosevi 200 mg/50 mg/50 mg film-coated tablets
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Vosevi 400 mg/100 mg/100 mg film-coated tablets
Each film-coated tablet contains 400 mg sofosbuvir, 100 mg velpatasvir
and 100 mg voxilaprevir.
Excipients with known effect
Each film-coated tablet contains 111 mg of lactose (as monohydrate).
Vosevi 200 mg/50 mg/50 mg film-coated tablets
Each film-coated tablet contains 200 mg sofosbuvir, 50 mg velpatasvir
and 50 mg voxilaprevir.
Excipients with known effect
Each film-coated tablet contains 55 mg of lactose (as monohydrate).
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Film-coated tablet.
Vosevi 400 mg/100 mg/100 mg film-coated tablets
Beige, capsule-shaped, film-coated tablet of dimensions 10 mm x 20 mm,
debossed with “GSI” on one
side and “3” on the other side.
Vosevi 200 mg/50 mg/50 mg film-coated tablets
Beige, oval-shaped, film-coated tablet of dimensions 8 mm x 15 mm,
debossed with “GSI” on one
side and “SVV” on the other side.
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
Vosevi is indicated for the treatment of chronic hepatitis C virus
(HCV) infection in patients aged
12 years and older and weighing at least 30 kg (see sections 4.2, 4.4
and 5.1).
3
4.2
POSOLOGY AND METHOD OF ADMINISTRATION
Vosevi treatment should be initiated and monitored by a physician
experienced in the management of
patients with HCV infection.
Posology
The recommended dose of Vosevi in patients aged 12 years and older and
weighing at least 30 kg is
one 400 mg/100 mg/100 mg tablet or two 200 mg/50 mg/50 mg tablets,
taken orally, once daily with
food (see section 5.2).
The recommended durations of treatment applicable to all HCV genotypes
are shown in Table 1.
TABLE 1: RECOMMENDED TREATMENT DURATIONS FOR VOSEVI FOR ALL HCV
GENOTYPES IN PATIENTS
12 YEARS AND OLDER AND WEIGHING AT LEAST 30 KG
PATIENT POPULATION
TREATMENT DUR
                                
                                Lire le document complet
                                
                            

Documents dans d'autres langues

Notice patient Notice patient bulgare 14-08-2023
Rapport public d'évaluation Rapport public d'évaluation bulgare 04-11-2021
Notice patient Notice patient espagnol 14-08-2023
Rapport public d'évaluation Rapport public d'évaluation espagnol 04-11-2021
Notice patient Notice patient tchèque 14-08-2023
Rapport public d'évaluation Rapport public d'évaluation tchèque 04-11-2021
Notice patient Notice patient danois 14-08-2023
Rapport public d'évaluation Rapport public d'évaluation danois 04-11-2021
Notice patient Notice patient allemand 14-08-2023
Rapport public d'évaluation Rapport public d'évaluation allemand 04-11-2021
Notice patient Notice patient estonien 14-08-2023
Rapport public d'évaluation Rapport public d'évaluation estonien 04-11-2021
Notice patient Notice patient grec 14-08-2023
Notice patient Notice patient français 14-08-2023
Rapport public d'évaluation Rapport public d'évaluation français 04-11-2021
Notice patient Notice patient italien 14-08-2023
Rapport public d'évaluation Rapport public d'évaluation italien 04-11-2021
Notice patient Notice patient letton 14-08-2023
Rapport public d'évaluation Rapport public d'évaluation letton 04-11-2021
Notice patient Notice patient lituanien 14-08-2023
Rapport public d'évaluation Rapport public d'évaluation lituanien 04-11-2021
Notice patient Notice patient hongrois 14-08-2023
Rapport public d'évaluation Rapport public d'évaluation hongrois 04-11-2021
Notice patient Notice patient maltais 14-08-2023
Rapport public d'évaluation Rapport public d'évaluation maltais 04-11-2021
Notice patient Notice patient néerlandais 14-08-2023
Rapport public d'évaluation Rapport public d'évaluation néerlandais 04-11-2021
Notice patient Notice patient polonais 14-08-2023
Rapport public d'évaluation Rapport public d'évaluation polonais 04-11-2021
Notice patient Notice patient portugais 14-08-2023
Rapport public d'évaluation Rapport public d'évaluation portugais 04-11-2021
Notice patient Notice patient roumain 14-08-2023
Rapport public d'évaluation Rapport public d'évaluation roumain 04-11-2021
Notice patient Notice patient slovaque 14-08-2023
Rapport public d'évaluation Rapport public d'évaluation slovaque 04-11-2021
Notice patient Notice patient slovène 14-08-2023
Rapport public d'évaluation Rapport public d'évaluation slovène 04-11-2021
Notice patient Notice patient finnois 14-08-2023
Rapport public d'évaluation Rapport public d'évaluation finnois 04-11-2021
Notice patient Notice patient suédois 14-08-2023
Rapport public d'évaluation Rapport public d'évaluation suédois 04-11-2021
Notice patient Notice patient norvégien 14-08-2023
Notice patient Notice patient islandais 14-08-2023
Notice patient Notice patient croate 14-08-2023
Rapport public d'évaluation Rapport public d'évaluation croate 04-11-2021

Rechercher des alertes liées à ce produit

Afficher l'historique des documents