Evotaz

Țară: Uniunea Europeană

Limbă: engleză

Sursă: EMA (European Medicines Agency)

Cumpara asta acum

Prospect Prospect (PIL)
25-04-2023

Ingredient activ:

cobicistat, atazanavir

Disponibil de la:

Bristol-Myers Squibb Pharma EEIG

Codul ATC:

J05AR15

INN (nume internaţional):

atazanavir, cobicistat

Grupul Terapeutică:

Antivirals for systemic use

Zonă Terapeutică:

HIV Infections

Indicații terapeutice:

EVOTAZ is indicated in combination with other antiretroviral medicinal products for the treatment of HIV-1 infected adults and adolescents (aged 12 years and older weighing at least 35 kg) without known mutations associated with resistance to atazanavir (see sections 4.4 and 5.1).

Rezumat produs:

Revision: 14

Statutul autorizaţiei:

Authorised

Data de autorizare:

2015-07-13

Prospect

                                52
B. PACKAGE LEAFLET
53
PACKAGE LEAFLET: INFORMATION FOR THE USER
EVOTAZ 300 MG/150 MG FILM-COATED TABLETS
atazanavir/cobicistat
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 EVOTAZ is and what it is used for
2.
What you need to know before you take EVOTAZ
3.
How to take EVOTAZ
4.
Possible side effects
5.
How to store EVOTAZ
6.
Contents of the pack and other information
1.
WHAT EVOTAZ IS AND WHAT IT IS USED FOR
EVOTAZ contains two active substances:

ATAZANAVIR, AN ANTIVIRAL (OR ANTIRETROVIRAL) MEDICINE.
It is one of a group called
_protease _
_inhibitors_
. These medicines control human immunodeficiency virus (HIV) infection
by stopping
production of a protein that HIV needs for its multiplication. They
work by reducing the amount
of HIV in your body and this in turn, strengthens your immune system.
In this way atazanavir
reduces the risk of developing illnesses linked to HIV infection.

COBICISTAT, A BOOSTER (PHARMACOKINETIC ENHANCER) TO HELP IMPROVE THE
EFFECTS OF ATAZANAVIR
.
Cobicistat, does not directly treat your HIV, but boosts the levels of
atazanavir in the blood. It
does this by slowing down the breakdown of atazanavir which will make
it stay in the body for
longer.
EVOTAZ may be used by adults and adolescents (aged 12 years and older
weighing at least 35 kg),
who are infected with HIV, the virus that causes acquired
immunodeficiency syndrome (AIDS). It is
used in combination with other anti-HIV medicines to help control your
HIV infection. Your doctor
will discuss wi
                                
                                Citiți documentul complet
                                
                            

Caracteristicilor produsului

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE MEDICINAL PRODUCT
EVOTAZ 300 mg/150 mg film-coated tablets
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Each film-coated tablet contains atazanavir sulphate corresponding to
300 mg atazanavir and 150 mg
of cobicistat.
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Film-coated tablet
Pink, oval, biconvex, film-coated tablet of approximate dimensions of
19 mm x 10.4 mm, debossed
with "3641" on one side and plain on the other side.
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
EVOTAZ is indicated in combination with other antiretroviral medicinal
products for the treatment of
HIV-1 infected adults and adolescents (aged 12 years and older
weighing at least 35 kg) without
known mutations associated with resistance to atazanavir (see sections
4.4 and 5.1).
4.2
POSOLOGY AND METHOD OF ADMINISTRATION
Therapy should be initiated by a physician experienced in the
management of HIV infection.
Posology
_ _
The recommended dose of EVOTAZ for adults and adolescents (aged 12
years and older weighing at
least 35 kg) is one tablet once daily taken orally with food (see
section 5.2).
_Advice on missed doses_
If EVOTAZ is missed within 12 hours of the time it is usually taken,
patients should be instructed to
take the prescribed dose of EVOTAZ with food as soon as possible. If
this is noticed later than
12 hours of the time it is usually taken, the missed dose should not
be taken and the patient should
resume the usual dosing schedule.
Special populations
_ _
_Renal impairment _
Based on the very limited renal elimination of cobicistat and
atazanavir, no special precautions or dose
adjustments of EVOTAZ are required for patients with renal impairment.
EVOTAZ is not recommended for patients undergoing haemodialysis (see
sections 4.4 and 5.2).
Cobicistat has been shown to decrease estimated creatinine clearance
due to inhibition of tubular
secretion of creatinine without affecting actual renal glomerular
function. EVOTAZ should not be
initiate
                                
                                Citiți documentul complet
                                
                            

Documente în alte limbi

Prospect Prospect bulgară 25-04-2023
Caracteristicilor produsului Caracteristicilor produsului bulgară 25-04-2023
Raport public de evaluare Raport public de evaluare bulgară 07-10-2023
Prospect Prospect spaniolă 25-04-2023
Caracteristicilor produsului Caracteristicilor produsului spaniolă 25-04-2023
Raport public de evaluare Raport public de evaluare spaniolă 07-10-2023
Prospect Prospect cehă 25-04-2023
Caracteristicilor produsului Caracteristicilor produsului cehă 25-04-2023
Raport public de evaluare Raport public de evaluare cehă 07-10-2023
Prospect Prospect daneză 25-04-2023
Caracteristicilor produsului Caracteristicilor produsului daneză 25-04-2023
Raport public de evaluare Raport public de evaluare daneză 07-10-2023
Prospect Prospect germană 25-04-2023
Caracteristicilor produsului Caracteristicilor produsului germană 25-04-2023
Raport public de evaluare Raport public de evaluare germană 07-10-2023
Prospect Prospect estoniană 25-04-2023
Caracteristicilor produsului Caracteristicilor produsului estoniană 25-04-2023
Raport public de evaluare Raport public de evaluare estoniană 07-10-2023
Prospect Prospect greacă 25-04-2023
Caracteristicilor produsului Caracteristicilor produsului greacă 25-04-2023
Raport public de evaluare Raport public de evaluare greacă 07-10-2023
Prospect Prospect franceză 25-04-2023
Caracteristicilor produsului Caracteristicilor produsului franceză 25-04-2023
Raport public de evaluare Raport public de evaluare franceză 07-10-2023
Prospect Prospect italiană 25-04-2023
Caracteristicilor produsului Caracteristicilor produsului italiană 25-04-2023
Raport public de evaluare Raport public de evaluare italiană 07-10-2023
Prospect Prospect letonă 25-04-2023
Caracteristicilor produsului Caracteristicilor produsului letonă 25-04-2023
Raport public de evaluare Raport public de evaluare letonă 07-10-2023
Prospect Prospect lituaniană 25-04-2023
Caracteristicilor produsului Caracteristicilor produsului lituaniană 25-04-2023
Raport public de evaluare Raport public de evaluare lituaniană 07-10-2023
Prospect Prospect maghiară 25-04-2023
Caracteristicilor produsului Caracteristicilor produsului maghiară 25-04-2023
Raport public de evaluare Raport public de evaluare maghiară 07-10-2023
Prospect Prospect malteză 25-04-2023
Caracteristicilor produsului Caracteristicilor produsului malteză 25-04-2023
Raport public de evaluare Raport public de evaluare malteză 07-10-2023
Prospect Prospect olandeză 25-04-2023
Caracteristicilor produsului Caracteristicilor produsului olandeză 25-04-2023
Raport public de evaluare Raport public de evaluare olandeză 07-10-2023
Prospect Prospect poloneză 25-04-2023
Caracteristicilor produsului Caracteristicilor produsului poloneză 25-04-2023
Raport public de evaluare Raport public de evaluare poloneză 07-10-2023
Prospect Prospect portugheză 25-04-2023
Caracteristicilor produsului Caracteristicilor produsului portugheză 25-04-2023
Raport public de evaluare Raport public de evaluare portugheză 07-10-2023
Prospect Prospect română 25-04-2023
Caracteristicilor produsului Caracteristicilor produsului română 25-04-2023
Raport public de evaluare Raport public de evaluare română 07-10-2023
Prospect Prospect slovacă 25-04-2023
Caracteristicilor produsului Caracteristicilor produsului slovacă 25-04-2023
Raport public de evaluare Raport public de evaluare slovacă 07-10-2023
Prospect Prospect slovenă 25-04-2023
Caracteristicilor produsului Caracteristicilor produsului slovenă 25-04-2023
Raport public de evaluare Raport public de evaluare slovenă 07-10-2023
Prospect Prospect finlandeză 25-04-2023
Caracteristicilor produsului Caracteristicilor produsului finlandeză 25-04-2023
Raport public de evaluare Raport public de evaluare finlandeză 07-10-2023
Prospect Prospect suedeză 25-04-2023
Caracteristicilor produsului Caracteristicilor produsului suedeză 25-04-2023
Raport public de evaluare Raport public de evaluare suedeză 07-10-2023
Prospect Prospect norvegiană 25-04-2023
Caracteristicilor produsului Caracteristicilor produsului norvegiană 25-04-2023
Prospect Prospect islandeză 25-04-2023
Caracteristicilor produsului Caracteristicilor produsului islandeză 25-04-2023
Prospect Prospect croată 25-04-2023
Caracteristicilor produsului Caracteristicilor produsului croată 25-04-2023
Raport public de evaluare Raport public de evaluare croată 07-10-2023

Căutați alerte legate de acest produs

Vizualizați istoricul documentelor