ATOMOXETINE

Kraj: Irlandia

Język: angielski

Źródło: HPRA (Health Products Regulatory Authority)

Kup teraz

Ulotka dla pacjenta Ulotka dla pacjenta (PIL)
13-12-2017

Składnik aktywny:

ATOMOXETINE HYDROCHLORIDE

Dostępny od:

Generics (UK) Limited

Kod ATC:

N06BA09

INN (International Nazwa):

ATOMOXETINE HYDROCHLORIDE

Dawkowanie:

25 Milligram

Forma farmaceutyczna:

Capsules Hard

Typ recepty:

Product subject to prescription which may not be renewed (A)

Dziedzina terapeutyczna:

atomoxetine

Status autoryzacji:

Not Marketed

Data autoryzacji:

2017-11-24

Ulotka dla pacjenta

                                Page 1 of 11
PACKAGE LEAFLET: INFORMATION FOR THE PATIENT
ATOMOXETINE 10 MG HARD CAPSULES
ATOMOXETINE 18 MG HARD CAPSULES
ATOMOXETINE 25 MG HARD CAPSULES
ATOMOXETINE 40 MG HARD CAPSULES
ATOMOXETINE 60 MG HARD CAPSULES
ATOMOXETINE 80 MG HARD CAPSULES
ATOMOXETINE 100 MG HARD CAPSULES
atomoxetine
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 Atomoxetine is and what it is used for
2.
What you need to know before you take Atomoxetine
3.
How to take Atomoxetine
4.
Possible side effects
5.
How to store Atomoxetine
6.
Contents of the pack and other information
1.
WHAT ATOMOXETINE IS AND WHAT IT IS USED FOR
Atomoxetine hard capsules contains the active substance atomoxetine,
which is used to treat
attention-deficit and hyperactivity disorder (ADHD). It is used:
-
in children over six years of age
-
in adolescents
-
in adults
Atomoxetine is used only as a part of the total treatment of the
disease which also requires
treatments which do not involve medicines, such as counselling and
behavioural therapy.
Atomoxetine is not for use as a treatment for ADHD in children under 6
years of age as it is
not known if the medicine works or is safe in these people.
In adults, atomoxetine is used to treat ADHD when the symptoms are
very troublesome and
affect your work or social life and when you have had symptoms of the
disease as a child.
HOW IT WORKS
Page 2 of 11
Atomoxetine increases the amount of noradrenaline in the brain. This
is a chemical that is
produced naturally, and increases attention and decreases
impu
                                
                                Przeczytaj cały dokument
                                
                            

Charakterystyka produktu

                                SUMMARY OF PRODUCT CHARACTERISTICS
1 NAME OF THE MEDICINAL PRODUCT
Atomoxetine 25 mg hard capsules
2 QUALITATIVE AND QUANTITATIVE COMPOSITION
Each hard capsule contains atomoxetine hydrochloride equivalent to 25
mg atomoxetine.
For the full list of excipients, see section 6.1.
3 PHARMACEUTICAL FORM
Hard capsule
25 mg Hard Capsules are hard gelatine capsules with blue opaque cap
and white opaque body, approximately 16 mm in
length, printed with “A925” on the cap and body in black ink.
4 CLINICAL PARTICULARS
4.1 THERAPEUTIC INDICATIONS
Atomoxetine is indicated for the treatment of
Attention-Deficit/Hyperactivity Disorder (ADHD) in children aged 6
years and older, in adolescents and in adults as part of a
comprehensive treatment programme. Treatment must be
initiated by a specialist in the treatment of ADHD, such as a
paediatrician, child/adolescent psychiatrist, or psychiatrist.
Diagnosis should be made according to current DSM criteria or the
guidelines in ICD.
In adults, the presence of symptoms of ADHD that were pre-existing in
childhood should be confirmed. Third-party
corroboration is desirable and atomoxetine should not be initiated
when the verification of childhood ADHD symptoms
is uncertain. Diagnosis cannot be made solely on the presence of one
or more symptoms of ADHD. Based on clinical
judgment, patients should have ADHD of at least moderate severity as
indicated by at least moderate functional
impairment in 2 or more settings (for example, social, academic,
and/or occupational functioning), affecting several
aspects of an individual's life.
Additional information for the safe use of this product: A
comprehensive treatment programme typically includes
psychological, educational and social measures and is aimed at
stabilising patients with a behavioural syndrome
characterised by symptoms which may include chronic history of short
attention span, distractibility, emotional lability,
impulsivity, moderate to severe hyperactivity, minor neurological
signs and abnormal EEG. Learning may or may not
be imp
                                
                                Przeczytaj cały dokument
                                
                            

Wyszukaj powiadomienia związane z tym produktem

Zobacz historię dokumentów