Symtuza

Country: Kesatuan Eropah

Bahasa: Inggeris

Sumber: EMA (European Medicines Agency)

Beli sekarang

Risalah maklumat Risalah maklumat (PIL)
21-03-2023
Ciri produk Ciri produk (SPC)
21-03-2023
Laporan Penilaian Awam Laporan Penilaian Awam (PAR)
11-10-2019

Bahan aktif:

darunavir, cobicistat, emtricitabine, tenofovir alafenamide

Boleh didapati daripada:

Janssen-Cilag International NV

Kod ATC:

J05

INN (Nama Antarabangsa):

darunavir, cobicistat, emtricitabine, tenofovir alafenamide

Kumpulan terapeutik:

Antivirals for systemic use, Antivirals for treatment of HIV infections, combinations

Kawasan terapeutik:

HIV Infections

Tanda-tanda terapeutik:

Symtuza is indicated for the treatment of human immunodeficiency virus type 1 (HIV‑1) infection in adults and adolescents (aged 12 years and older with body weight at least 40 kg).Genotypic testing should guide the use of Symtuza.

Ringkasan produk:

Revision: 17

Status kebenaran:

Authorised

Tarikh kebenaran:

2017-09-21

Risalah maklumat

                                42
B.
PACKAGE LEAFLET
43
PACKAGE LEAFLET: INFORMATION FOR THE USER
SYMTUZA 800 MG/150 MG/200 MG/10 MG - FILM-COATED TABLETS
darunavir/cobicistat/emtricitabine/tenofovir alafenamide
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, pharmacist or
nurse.
-
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, pharmacist or nurse.
This includes any possible
side effects not listed in this leaflet. See section 4.
WHAT IS IN THIS LEAFLET
1.
What Symtuza is and what it is used for
2.
What you need to know before you take Symtuza
3.
How to take Symtuza
4.
Possible side effects
5.
How to store Symtuza
6.
Contents of the pack and other information
1.
WHAT SYMTUZA IS AND WHAT IT IS USED FOR
Symtuza is an antiretroviral medicine used to treat infection with
human immunodeficiency virus 1
(HIV-1). It is used in adults and adolescents aged 12 years and older
who weigh at least 40 kg.
Symtuza contains four active substances:

darunavir, an anti-HIV medicine known as a protease inhibitor

cobicistat, a booster (enhancer) of darunavir

emtricitabine, an anti-HIV medicine known as a nucleoside reverse
transcriptase inhibitor

tenofovir alafenamide, an anti-HIV medicine known as a nucleotide
reverse transcriptase
inhibitor
Symtuza reduces HIV-1 in your body and this will improve your immune
system (your body’s natural
defences) and reduce the risk of developing illnesses linked to HIV
infection but Symtuza is not a cure
for HIV infection.
2.
WHAT YOU NEED TO KNOW BEFORE YOU TAKE SYMTUZA
DO NOT TAKE SYMTUZA
-
if you are ALLERGIC (hypersensitive) to darunavir, cobicistat,
emtricitabine, tenofovir
alafenamide, or any of the other ingredients of Symtuza (listed in
section 6).
-
if you have SEVERE LIVE
                                
                                Baca dokumen lengkap
                                
                            

Ciri produk

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE MEDICINAL PRODUCT
Symtuza 800 mg/150 mg/200 mg/10 mg film-coated tablets
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Each film-coated tablet contains 800 mg of darunavir (as ethanolate),
150 mg of cobicistat, 200 mg of
emtricitabine, and 10 mg of tenofovir alafenamide (as fumarate).
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Film-coated tablet (tablet).
Yellow to yellowish-brown capsule shaped tablet of 22 mm x 11 mm,
debossed with “8121” on one
side and “JG” on the other side.
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
Symtuza is indicated for the treatment of human immunodeficiency virus
type 1 (HIV-1) infection in
adults and adolescents (aged 12 years and older with body weight at
least 40 kg).
Genotypic testing should guide the use of Symtuza (see sections 4.2,
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-1 infection.
Posology
The recommended dose regimen in adults and adolescents aged 12 years
and older, weighing at least
40 kg, is one tablet taken once daily with food.
_Antiretroviral Therapy (ART)-naïve patients_
The recommended dose regimen is one film-coated tablet of Symtuza once
daily taken with food.
_ART-experienced patients_
One film-coated tablet of Symtuza once daily taken with food may be
used in patients with prior
exposure to antiretroviral medicinal products but without darunavir
resistance associated mutations
(DRV-RAMs)* and who have plasma HIV-1 RNA < 100 000 copies/mL and CD4+
cell count
≥ 100 cells x 10
6
/L (see section 5.1).
*
DRV-RAMs: V11I, V32I, L33F, I47V, I50V, I54M, I54L, T74P, L76V, I84V,
L89V.
_Advice on missed doses_
If a dose of Symtuza is missed within 12 hours of the time it is
usually taken, patients should be
instructed to take the prescribed dose of Symtuza with food as soon as
possible. If a missed dose is
noticed later than 12 hours of the time it is usually taken, it s
                                
                                Baca dokumen lengkap
                                
                            

Dokumen dalam bahasa lain

Risalah maklumat Risalah maklumat Bulgaria 21-03-2023
Ciri produk Ciri produk Bulgaria 21-03-2023
Laporan Penilaian Awam Laporan Penilaian Awam Bulgaria 11-10-2019
Risalah maklumat Risalah maklumat Sepanyol 21-03-2023
Ciri produk Ciri produk Sepanyol 21-03-2023
Laporan Penilaian Awam Laporan Penilaian Awam Sepanyol 11-10-2019
Risalah maklumat Risalah maklumat Czech 21-03-2023
Ciri produk Ciri produk Czech 21-03-2023
Laporan Penilaian Awam Laporan Penilaian Awam Czech 11-10-2019
Risalah maklumat Risalah maklumat Denmark 21-03-2023
Ciri produk Ciri produk Denmark 21-03-2023
Laporan Penilaian Awam Laporan Penilaian Awam Denmark 11-10-2019
Risalah maklumat Risalah maklumat Jerman 21-03-2023
Ciri produk Ciri produk Jerman 21-03-2023
Laporan Penilaian Awam Laporan Penilaian Awam Jerman 11-10-2019
Risalah maklumat Risalah maklumat Estonia 21-03-2023
Ciri produk Ciri produk Estonia 21-03-2023
Laporan Penilaian Awam Laporan Penilaian Awam Estonia 11-10-2019
Risalah maklumat Risalah maklumat Greek 21-03-2023
Ciri produk Ciri produk Greek 21-03-2023
Laporan Penilaian Awam Laporan Penilaian Awam Greek 11-10-2019
Risalah maklumat Risalah maklumat Perancis 21-03-2023
Ciri produk Ciri produk Perancis 21-03-2023
Laporan Penilaian Awam Laporan Penilaian Awam Perancis 11-10-2019
Risalah maklumat Risalah maklumat Itali 21-03-2023
Ciri produk Ciri produk Itali 21-03-2023
Laporan Penilaian Awam Laporan Penilaian Awam Itali 11-10-2019
Risalah maklumat Risalah maklumat Latvia 21-03-2023
Ciri produk Ciri produk Latvia 21-03-2023
Laporan Penilaian Awam Laporan Penilaian Awam Latvia 11-10-2019
Risalah maklumat Risalah maklumat Lithuania 21-03-2023
Ciri produk Ciri produk Lithuania 21-03-2023
Laporan Penilaian Awam Laporan Penilaian Awam Lithuania 11-10-2019
Risalah maklumat Risalah maklumat Hungary 21-03-2023
Ciri produk Ciri produk Hungary 21-03-2023
Laporan Penilaian Awam Laporan Penilaian Awam Hungary 11-10-2019
Risalah maklumat Risalah maklumat Malta 21-03-2023
Ciri produk Ciri produk Malta 21-03-2023
Laporan Penilaian Awam Laporan Penilaian Awam Malta 11-10-2019
Risalah maklumat Risalah maklumat Belanda 21-03-2023
Ciri produk Ciri produk Belanda 21-03-2023
Laporan Penilaian Awam Laporan Penilaian Awam Belanda 11-10-2019
Risalah maklumat Risalah maklumat Poland 21-03-2023
Ciri produk Ciri produk Poland 21-03-2023
Laporan Penilaian Awam Laporan Penilaian Awam Poland 11-10-2019
Risalah maklumat Risalah maklumat Portugis 21-03-2023
Ciri produk Ciri produk Portugis 21-03-2023
Laporan Penilaian Awam Laporan Penilaian Awam Portugis 11-10-2019
Risalah maklumat Risalah maklumat Romania 21-03-2023
Ciri produk Ciri produk Romania 21-03-2023
Laporan Penilaian Awam Laporan Penilaian Awam Romania 11-10-2019
Risalah maklumat Risalah maklumat Slovak 21-03-2023
Ciri produk Ciri produk Slovak 21-03-2023
Laporan Penilaian Awam Laporan Penilaian Awam Slovak 11-10-2019
Risalah maklumat Risalah maklumat Slovenia 21-03-2023
Ciri produk Ciri produk Slovenia 21-03-2023
Laporan Penilaian Awam Laporan Penilaian Awam Slovenia 11-10-2019
Risalah maklumat Risalah maklumat Finland 21-03-2023
Ciri produk Ciri produk Finland 21-03-2023
Laporan Penilaian Awam Laporan Penilaian Awam Finland 11-10-2019
Risalah maklumat Risalah maklumat Sweden 21-03-2023
Ciri produk Ciri produk Sweden 21-03-2023
Laporan Penilaian Awam Laporan Penilaian Awam Sweden 11-10-2019
Risalah maklumat Risalah maklumat Norway 21-03-2023
Ciri produk Ciri produk Norway 21-03-2023
Risalah maklumat Risalah maklumat Iceland 21-03-2023
Ciri produk Ciri produk Iceland 21-03-2023
Risalah maklumat Risalah maklumat Croat 21-03-2023
Ciri produk Ciri produk Croat 21-03-2023
Laporan Penilaian Awam Laporan Penilaian Awam Croat 11-10-2019

Lihat sejarah dokumen