Intuniv

Negara: Uni Eropa

Bahasa: Inggris

Sumber: EMA (European Medicines Agency)

Beli Sekarang

Selebaran informasi Selebaran informasi (PIL)
16-02-2023
Karakteristik produk Karakteristik produk (SPC)
16-02-2023

Bahan aktif:

guanfacine hydrochloride

Tersedia dari:

Takeda Pharmaceuticals International AG Ireland Branch

Kode ATC:

C02AC02

INN (Nama Internasional):

guanfacine

Kelompok Terapi:

Antiadrenergic agents, centrally acting, Antihypertensives,

Area terapi:

Attention Deficit Disorder with Hyperactivity

Indikasi Terapi:

Intuniv is indicated for the treatment of attention deficit hyperactivity disorder (ADHD) in children and adolescents 6 17 years old for whom stimulants are not suitable, not tolerated or have been shown to be ineffective. Intuniv must be used as a part of a comprehensive ADHD treatment programme, typically including psychological, educational and social measures.,

Ringkasan produk:

Revision: 12

Status otorisasi:

Authorised

Tanggal Otorisasi:

2015-09-17

Selebaran informasi

                                36
B. PACKAGE LEAFLET
37
PACKAGE LEAFLET: INFORMATION FOR THE PATIENT
INTUNIV 1 MG PROLONGED-RELEASE TABLETS
INTUNIV 2 MG PROLONGED-RELEASE TABLETS
INTUNIV 3 MG PROLONGED-RELEASE TABLETS
INTUNIV 4 MG PROLONGED-RELEASE TABLETS
guanfacine
This medicine is subject to additional monitoring. This will allow
quick identification of new
safety information. You can help by reporting any side effects you may
get. See the end of section 4
for how to report side effects.
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 or pharmacist. This
includes any possible side
effects not listed in this leaflet. See section 4.

This leaflet has been written as though the person taking the medicine
is reading it. If you are
giving this medicine to your child, please replace “you” with
“your child” throughout.
WHAT IS IN THIS LEAFLET:
1.
What Intuniv is and what it is used for
2.
What you need to know before you take Intuniv
3.
How to take Intuniv
4.
Possible side effects
5.
How to store Intuniv
6.
Contents of the pack and other information
1.
WHAT INTUNIV IS AND WHAT IT IS USED FOR
WHAT INTUNIV IS
Intuniv contains the active substance guanfacine. This medicine
belongs to a group of medicines
which affects brain activity. This medicine can help improve your
attention, concentration and make
you less impulsive and hyperactive.
WHAT INTUNIV IS USED FOR
This medicine is used to treat ‘attention deficit hyperactivity
disorder’ (ADHD) in children and
adolescents 6-17 years old for whom current stimulant medication is
not appropriate and/or current
medication does not adequately control ADHD symptoms.
The medicine is given a
                                
                                Baca dokumen lengkapnya
                                
                            

Karakteristik produk

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
This medicinal product is subject to additional monitoring. This will
allow quick identification of
new safety information. Healthcare professionals are asked to report
any suspected adverse reactions.
See section 4.8 for how to report adverse reactions.
1.
NAME OF THE MEDICINAL PRODUCT
Intuniv 1 mg prolonged-release tablets
Intuniv 2 mg prolonged-release tablets
Intuniv 3 mg prolonged-release tablets
Intuniv 4 mg prolonged-release tablets
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Intuniv 1 mg prolonged-release tablet
Each tablet contains guanfacine hydrochloride equivalent to 1 mg of
guanfacine.
_Excipient(s) with known effect_
Each tablet contains 22.41 mg of lactose (as monohydrate).
Intuniv 2 mg prolonged-release tablet
Each tablet contains guanfacine hydrochloride equivalent to 2 mg of
guanfacine.
_Excipient(s) with known effect_
Each tablet contains 44.82 mg of lactose (as monohydrate).
Intuniv 3 mg prolonged-release tablet
Each tablet contains guanfacine hydrochloride equivalent to 3 mg of
guanfacine.
_Excipient(s) with known effect_
Each tablet contains 37.81 mg of lactose (as monohydrate).
Intuniv 4 mg prolonged-release tablet
Each tablet contains guanfacine hydrochloride equivalent to 4 mg of
guanfacine.
_Excipient(s) with known effect_
Each 4 mg tablet contains 50.42 mg of lactose (as monohydrate).
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Prolonged-release tablet
Intuniv 1 mg prolonged-release tablet
7.14 mm round, white to off-white tablets debossed with ‘1MG’ on
one side and ‘503’ on the other
side.
3
Intuniv 2 mg prolonged-release tablet
12.34 mm x 6.10 mm oblong shaped, white to off-white tablets debossed
with ‘2MG’ on one side and
“503” on the other side.
Intuniv 3 mg prolonged-release tablet
7.94 mm round, green tablets debossed with ‘3MG’ on one side and
‘503’ on the other side.
Intuniv 4 mg prolonged-release tablet
12.34 mm x 6.10 mm oblong shaped, green tablets debossed with
‘4MG’ on on
                                
                                Baca dokumen lengkapnya
                                
                            

Dokumen dalam bahasa lain

Selebaran informasi Selebaran informasi Bulgar 16-02-2023
Karakteristik produk Karakteristik produk Bulgar 16-02-2023
Laporan Penilaian publik Laporan Penilaian publik Bulgar 06-10-2015
Selebaran informasi Selebaran informasi Spanyol 16-02-2023
Karakteristik produk Karakteristik produk Spanyol 16-02-2023
Laporan Penilaian publik Laporan Penilaian publik Spanyol 06-10-2015
Selebaran informasi Selebaran informasi Cheska 16-02-2023
Karakteristik produk Karakteristik produk Cheska 16-02-2023
Laporan Penilaian publik Laporan Penilaian publik Cheska 06-10-2015
Selebaran informasi Selebaran informasi Dansk 16-02-2023
Karakteristik produk Karakteristik produk Dansk 16-02-2023
Laporan Penilaian publik Laporan Penilaian publik Dansk 06-10-2015
Selebaran informasi Selebaran informasi Jerman 16-02-2023
Karakteristik produk Karakteristik produk Jerman 16-02-2023
Laporan Penilaian publik Laporan Penilaian publik Jerman 06-10-2015
Selebaran informasi Selebaran informasi Esti 16-02-2023
Karakteristik produk Karakteristik produk Esti 16-02-2023
Laporan Penilaian publik Laporan Penilaian publik Esti 06-10-2015
Selebaran informasi Selebaran informasi Yunani 16-02-2023
Karakteristik produk Karakteristik produk Yunani 16-02-2023
Laporan Penilaian publik Laporan Penilaian publik Yunani 06-10-2015
Selebaran informasi Selebaran informasi Prancis 16-02-2023
Karakteristik produk Karakteristik produk Prancis 16-02-2023
Laporan Penilaian publik Laporan Penilaian publik Prancis 06-10-2015
Selebaran informasi Selebaran informasi Italia 16-02-2023
Karakteristik produk Karakteristik produk Italia 16-02-2023
Laporan Penilaian publik Laporan Penilaian publik Italia 06-10-2015
Selebaran informasi Selebaran informasi Latvi 16-02-2023
Karakteristik produk Karakteristik produk Latvi 16-02-2023
Laporan Penilaian publik Laporan Penilaian publik Latvi 06-10-2015
Selebaran informasi Selebaran informasi Lituavi 16-02-2023
Karakteristik produk Karakteristik produk Lituavi 16-02-2023
Laporan Penilaian publik Laporan Penilaian publik Lituavi 06-10-2015
Selebaran informasi Selebaran informasi Hungaria 16-02-2023
Karakteristik produk Karakteristik produk Hungaria 16-02-2023
Laporan Penilaian publik Laporan Penilaian publik Hungaria 06-10-2015
Selebaran informasi Selebaran informasi Malta 16-02-2023
Karakteristik produk Karakteristik produk Malta 16-02-2023
Laporan Penilaian publik Laporan Penilaian publik Malta 06-10-2015
Selebaran informasi Selebaran informasi Belanda 16-02-2023
Karakteristik produk Karakteristik produk Belanda 16-02-2023
Laporan Penilaian publik Laporan Penilaian publik Belanda 06-10-2015
Selebaran informasi Selebaran informasi Polski 16-02-2023
Karakteristik produk Karakteristik produk Polski 16-02-2023
Laporan Penilaian publik Laporan Penilaian publik Polski 06-10-2015
Selebaran informasi Selebaran informasi Portugis 16-02-2023
Karakteristik produk Karakteristik produk Portugis 16-02-2023
Laporan Penilaian publik Laporan Penilaian publik Portugis 06-10-2015
Selebaran informasi Selebaran informasi Rumania 16-02-2023
Karakteristik produk Karakteristik produk Rumania 16-02-2023
Laporan Penilaian publik Laporan Penilaian publik Rumania 06-10-2015
Selebaran informasi Selebaran informasi Slovak 16-02-2023
Karakteristik produk Karakteristik produk Slovak 16-02-2023
Laporan Penilaian publik Laporan Penilaian publik Slovak 06-10-2015
Selebaran informasi Selebaran informasi Sloven 16-02-2023
Karakteristik produk Karakteristik produk Sloven 16-02-2023
Laporan Penilaian publik Laporan Penilaian publik Sloven 06-10-2015
Selebaran informasi Selebaran informasi Suomi 16-02-2023
Karakteristik produk Karakteristik produk Suomi 16-02-2023
Laporan Penilaian publik Laporan Penilaian publik Suomi 06-10-2015
Selebaran informasi Selebaran informasi Swedia 16-02-2023
Karakteristik produk Karakteristik produk Swedia 16-02-2023
Laporan Penilaian publik Laporan Penilaian publik Swedia 06-10-2015
Selebaran informasi Selebaran informasi Norwegia 16-02-2023
Karakteristik produk Karakteristik produk Norwegia 16-02-2023
Selebaran informasi Selebaran informasi Islandia 16-02-2023
Karakteristik produk Karakteristik produk Islandia 16-02-2023
Selebaran informasi Selebaran informasi Kroasia 16-02-2023
Karakteristik produk Karakteristik produk Kroasia 16-02-2023
Laporan Penilaian publik Laporan Penilaian publik Kroasia 06-10-2015

Peringatan pencarian terkait dengan produk ini

Lihat riwayat dokumen