Tenofovir disoproxil Mylan

Negara: Uni Eropa

Bahasa: Inggris

Sumber: EMA (European Medicines Agency)

Beli Sekarang

Selebaran informasi Selebaran informasi (PIL)
07-06-2023
Karakteristik produk Karakteristik produk (SPC)
07-06-2023

Bahan aktif:

tenofovir disoproxil

Tersedia dari:

Mylan Pharmaceuticals Limited

Kode ATC:

J05AF07

INN (Nama Internasional):

tenofovir disoproxil

Kelompok Terapi:

Antivirals for systemic use

Area terapi:

HIV Infections

Indikasi Terapi:

HIV-1 infectionTenofovir disoproxil 245 mg film-coated tablets are indicated in combination with other antiretroviral medicinal products for the treatment of HIV-1 infected adults.In adults, the demonstration of the benefit of tenofovir disoproxil in HIV-1 infection is based on results of one study in treatment-naïve patients, including patients with a high viral load (> 100,000 copies/ml) and studies in which tenofovir disoproxil was added to stable background therapy (mainly tritherapy) in antiretroviral pre-treated patients experiencing early virological failure (< 10,000 copies/ml, with the majority of patients having < 5,000 copies/ml).Tenofovir disoproxil 245 mg film-coated tablets are also indicated for the treatment of HIV-1 infected adolescents, with NRTI resistance or toxicities precluding the use of first line agents, aged 12 to < 18 years.The choice of tenofovir disoproxil to treat antiretroviral-experienced patients with HIV-1 infection should be based on individual viral resistance testing and/or treatment history of patients.Hepatitis B infectionTenofovir disoproxil 245 mg film-coated tablets are indicated for the treatment of chronic hepatitis B in adults with:compensated liver disease, with evidence of active viral replication, persistently elevated serum alanine aminotransferase (ALT) levels and histological evidence of active inflammation and/or fibrosis.evidence of lamivudine-resistant hepatitis B virus.decompensated liver disease.Tenofovir disoproxil 245 mg film-coated tablets are indicated for the treatment of chronic hepatitis B in adolescents 12 to < 18 years of age with:compensated liver disease and evidence of immune active disease, i.e. active viral replication, persistently elevated serum ALT levels and histological evidence of active inflammation and/or fibrosis.

Ringkasan produk:

Revision: 18

Status otorisasi:

Authorised

Tanggal Otorisasi:

2016-12-08

Selebaran informasi

                                62
B. PACKAGE LEAFLET
63
PACKAGE LEAFLET: INFORMATION FOR THE PATIENT
TENOFOVIR DISOPROXIL MYLAN 245 MG FILM-COATED TABLETS
tenofovir disoproxil
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 Tenofovir disoproxil Mylan is and what it is used for
2.
What you need to know before you take Tenofovir disoproxil Mylan
3.
How to take Tenofovir disoproxil Mylan
4.
Possible side effects
5.
How to store Tenofovir disoproxil Mylan
6.
Contents of the pack and other information
IF THIS MEDICINE 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 TENOFOVIR DISOPROXIL MYLAN IS AND WHAT IT IS USED FOR
Tenofovir disoproxil Mylan contains the active substance
_tenofovir disoproxil_
. This active substance
is an
_antiretroviral _
or antiviral medicine which is used to treat HIV or HBV infection or
both.
Tenofovir is a
_nucleotide reverse transcriptase inhibitor_
, generally known as an NRTI and works by
interfering with the normal working of enzymes (in HIV
_reverse transcriptase_
; in hepatitis B
_DNA _
_polymerase_
) that are essential for the viruses to reproduce themselves. In HIV
Tenofovir disoproxil
Mylan should always be used combined with other medicines to treat HIV
infection.
TENOFOVIR DISOPROXIL MYLAN 245 MG TABLETS ARE A TREATMENT FOR HIV
(Human Immunodeficiency
Virus) infection. The tablets are suitable for:
•
ADULTS
•
ADOLESCENTS AGED 12 TO LESS THAN 18 YEARS 
                                
                                Baca dokumen lengkapnya
                                
                            

Karakteristik produk

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE MEDICINAL PRODUCT
Tenofovir disoproxil Mylan 245 mg film-coated tablets
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Each film-coated tablet contains 245 mg of tenofovir disoproxil (as
maleate).
Excipient with known effect
Each tablet contains 155 mg lactose monohydrate.
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Film-coated tablet.
Light blue, round, biconvex, film-coated tablets, 12.20 ± 0.20 mm in
diameter, debossed with
‘TN245’ on one side and ‘M’ on other side.
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
HIV-1 infection
Tenofovir disoproxil 245 mg film-coated tablets are indicated in
combination with other
antiretroviral medicinal products for the treatment of HIV-1 infected
adults.
In adults, the demonstration of the benefit of tenofovir disoproxil in
HIV-1 infection is based on
results of one study in treatment-naïve patients, including patients
with a high viral load
(> 100,000 copies/ml) and studies in which tenofovir disoproxil was
added to stable background
therapy (mainly tritherapy) in antiretroviral pre-treated patients
experiencing early virological
failure (< 10,000 copies/ml, with the majority of patients having <
5,000 copies/ml).
Tenofovir disoproxil 245 mg film-coated tablets are also indicated for
the treatment of HIV-1
infected adolescents, with NRTI resistance or toxicities precluding
the use of first line agents, aged
12 to < 18 years.
The choice of tenofovir disoproxil to treat antiretroviral-experienced
patients with HIV-1 infection
should be based on individual viral resistance testing and/or
treatment history of patients.
Hepatitis B infection
Tenofovir disoproxil 245 mg film-coated tablets are indicated for the
treatment of chronic hepatitis B
in adults with:
•
compensated liver disease, with evidence of active viral replication,
persistently elevated serum
alanine aminotransferase (ALT) levels and histological evidence of
active inflammation and/or
fibrosis (see section 5.1)
                                
                                Baca dokumen lengkapnya
                                
                            

Dokumen dalam bahasa lain

Selebaran informasi Selebaran informasi Bulgar 07-06-2023
Karakteristik produk Karakteristik produk Bulgar 07-06-2023
Laporan Penilaian publik Laporan Penilaian publik Bulgar 19-12-2016
Selebaran informasi Selebaran informasi Spanyol 07-06-2023
Karakteristik produk Karakteristik produk Spanyol 07-06-2023
Laporan Penilaian publik Laporan Penilaian publik Spanyol 19-12-2016
Selebaran informasi Selebaran informasi Cheska 07-06-2023
Karakteristik produk Karakteristik produk Cheska 07-06-2023
Laporan Penilaian publik Laporan Penilaian publik Cheska 19-12-2016
Selebaran informasi Selebaran informasi Dansk 07-06-2023
Karakteristik produk Karakteristik produk Dansk 07-06-2023
Laporan Penilaian publik Laporan Penilaian publik Dansk 19-12-2016
Selebaran informasi Selebaran informasi Jerman 07-06-2023
Karakteristik produk Karakteristik produk Jerman 07-06-2023
Laporan Penilaian publik Laporan Penilaian publik Jerman 19-12-2016
Selebaran informasi Selebaran informasi Esti 07-06-2023
Karakteristik produk Karakteristik produk Esti 07-06-2023
Laporan Penilaian publik Laporan Penilaian publik Esti 19-12-2016
Selebaran informasi Selebaran informasi Yunani 07-06-2023
Karakteristik produk Karakteristik produk Yunani 07-06-2023
Laporan Penilaian publik Laporan Penilaian publik Yunani 19-12-2016
Selebaran informasi Selebaran informasi Prancis 07-06-2023
Karakteristik produk Karakteristik produk Prancis 07-06-2023
Laporan Penilaian publik Laporan Penilaian publik Prancis 19-12-2016
Selebaran informasi Selebaran informasi Italia 07-06-2023
Karakteristik produk Karakteristik produk Italia 07-06-2023
Laporan Penilaian publik Laporan Penilaian publik Italia 19-12-2016
Selebaran informasi Selebaran informasi Latvi 07-06-2023
Karakteristik produk Karakteristik produk Latvi 07-06-2023
Laporan Penilaian publik Laporan Penilaian publik Latvi 19-12-2016
Selebaran informasi Selebaran informasi Lituavi 07-06-2023
Karakteristik produk Karakteristik produk Lituavi 07-06-2023
Laporan Penilaian publik Laporan Penilaian publik Lituavi 19-12-2016
Selebaran informasi Selebaran informasi Hungaria 07-06-2023
Karakteristik produk Karakteristik produk Hungaria 07-06-2023
Laporan Penilaian publik Laporan Penilaian publik Hungaria 19-12-2016
Selebaran informasi Selebaran informasi Malta 07-06-2023
Karakteristik produk Karakteristik produk Malta 07-06-2023
Laporan Penilaian publik Laporan Penilaian publik Malta 19-12-2016
Selebaran informasi Selebaran informasi Belanda 07-06-2023
Karakteristik produk Karakteristik produk Belanda 07-06-2023
Laporan Penilaian publik Laporan Penilaian publik Belanda 19-12-2016
Selebaran informasi Selebaran informasi Polski 07-06-2023
Karakteristik produk Karakteristik produk Polski 07-06-2023
Laporan Penilaian publik Laporan Penilaian publik Polski 19-12-2016
Selebaran informasi Selebaran informasi Portugis 07-06-2023
Karakteristik produk Karakteristik produk Portugis 07-06-2023
Laporan Penilaian publik Laporan Penilaian publik Portugis 19-12-2016
Selebaran informasi Selebaran informasi Rumania 07-06-2023
Karakteristik produk Karakteristik produk Rumania 07-06-2023
Laporan Penilaian publik Laporan Penilaian publik Rumania 19-12-2016
Selebaran informasi Selebaran informasi Slovak 07-06-2023
Karakteristik produk Karakteristik produk Slovak 07-06-2023
Laporan Penilaian publik Laporan Penilaian publik Slovak 19-12-2016
Selebaran informasi Selebaran informasi Sloven 07-06-2023
Karakteristik produk Karakteristik produk Sloven 07-06-2023
Laporan Penilaian publik Laporan Penilaian publik Sloven 19-12-2016
Selebaran informasi Selebaran informasi Suomi 07-06-2023
Karakteristik produk Karakteristik produk Suomi 07-06-2023
Laporan Penilaian publik Laporan Penilaian publik Suomi 19-12-2016
Selebaran informasi Selebaran informasi Swedia 07-06-2023
Karakteristik produk Karakteristik produk Swedia 07-06-2023
Laporan Penilaian publik Laporan Penilaian publik Swedia 19-12-2016
Selebaran informasi Selebaran informasi Norwegia 07-06-2023
Karakteristik produk Karakteristik produk Norwegia 07-06-2023
Selebaran informasi Selebaran informasi Islandia 07-06-2023
Karakteristik produk Karakteristik produk Islandia 07-06-2023
Selebaran informasi Selebaran informasi Kroasia 07-06-2023
Karakteristik produk Karakteristik produk Kroasia 07-06-2023
Laporan Penilaian publik Laporan Penilaian publik Kroasia 19-12-2016

Peringatan pencarian terkait dengan produk ini