Neupro

Country: Եվրոպական Միություն

language: անգլերեն

source: EMA (European Medicines Agency)

active_ingredient:

rotigotine

MAH:

UCB Pharma S.A.

ATC_code:

N04BC09

INN:

rotigotine

therapeutic_group:

Anti-Parkinson drugs

therapeutic_area:

Restless Legs Syndrome; Parkinson Disease

therapeutic_indication:

Parkinson's disease: Neupro is indicated for the treatment of the signs and symptoms of early-stage idiopathic Parkinson's disease as monotherapy (i.e. without levodopa) or in combination with levodopa, i.e. over the course of the disease, through to late stages when the effect of levodopa wears off or becomes inconsistent and fluctuations of the therapeutic effect occur (end of dose or 'on-off' fluctuations).Restless-legs syndrome: Neupro is indicated for the symptomatic treatment of moderate to severe idiopathic restless-legs syndrome in adults.

leaflet_short:

Revision: 31

authorization_status:

Authorised

authorization_date:

2006-02-15

PIL

124
B. PACKAGE LEAFLET
125
PACKAGE LEAFLET: INFORMATION FOR THE USER
NEUPRO 1 MG/24 H TRANSDERMAL PATCH
NEUPRO 3 MG/24 H TRANSDERMAL PATCH
Rotigotine
READ ALL OF THIS LEAFLET CAREFULLY BEFORE YOU START USING 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 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 or
nurse. This includes any possible
side effects not listed in this leaflet. See section 4.
WHAT IS IN THIS LEAFLET
1.
What Neupro is and what it is used for
2.
What you need to know before you use Neupro
3.
How to use Neupro
4.
Possible side effects
5.
How to store Neupro
6.
Contents of the pack and other information
1.
WHAT NEUPRO IS AND WHAT IT IS USED FOR
WHAT NEUPRO IS
Neupro contains the active substance rotigotine.
It belongs to a group of medicines called ‘dopamine agonists’.
Dopamine is a messenger in the brain
which is important for movement.
WHAT NEUPRO IS USED FOR
Neupro is used in adults to treat the signs and symptoms of:
•
RESTLESS LEGS SYNDROME (RLS) –
this can be associated with discomfort in your legs or arms,
urges to move around, sleep disturbance and feeling tired or sleepy
during the day. These
symptoms are either reduced or their duration is shortened with Neupro
treatment.
2.
WHAT YOU NEED TO KNOW BEFORE YOU USE NEUPRO
DO NOT USE NEUPRO IF:
•
you are
ALLERGIC
to
ROTIGOTINE
or any of the
OTHER INGREDIENTS
of this medicine (listed in
section 6)
•
you need to have a
MAGNETIC RESONANCE IMAGING
(MRI) scan (diagnostic pictures of the inside
of the body, created using magnetic rather than x-ray energy)
•
you need ‘
CARDIOVERSION
’ (specific treatment for abnormal heart beat).
You must take your Neupro patch off just before undergoing magnetic
resonance imaging (MR

SPC

1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE MEDICINAL PRODUCT
Neupro 1 mg/24 h transdermal patch
Neupro 3 mg/24 h transdermal patch
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Neupro 1 mg/24 h transdermal patch
Each patch releases 1 mg of rotigotine per 24 hours. Each patch of 5
cm
2
contains 2.25 mg of
rotigotine.
Neupro 3 mg/24 h transdermal patch
Each patch releases 3 mg of rotigotine per 24 hours. Each patch of 15
cm
2
contains 6.75 mg of
rotigotine.
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Transdermal patch.
Thin, matrix-type, square-shaped with rounded edges, consisting of
three layers.
Neupro 1 mg/24 h transdermal patch
The outside of the backing layer is tan-coloured and imprinted with
‘Neupro 1 mg/24 h’.
Neupro 3 mg/24 h transdermal patch
The outside of the backing layer is tan-coloured and imprinted with
‘Neupro 3 mg/24 h’.
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
Neupro is indicated for the symptomatic treatment of moderate to
severe idiopathic Restless Legs
Syndrome (RLS) in adults.
4.2
POSOLOGY AND METHOD OF ADMINISTRATION
Posology
The dose recommendations made are in nominal dose.
A single daily dose should be initiated at 1 mg/24 h. Depending on the
individual patient response, the
dose may be increased in weekly increments of 1 mg/24 h to a maximum
dose of 3 mg/24 h. The need
for treatment continuation should be reconsidered every 6 months.
Neupro is applied once a day. The patch should be applied at
approximately the same time every day.
The patch remains on the skin for 24 hours and will then be replaced
by a new one at a different site of
application.
If the patient forgets to apply the patch at the usual time of the day
or if the patch becomes detached,
another patch should be applied for the remainder of the day.
3
_Treatment discontinuation _
Neupro should be discontinued gradually. The daily dose should be
reduced in steps of 1 mg/24 h with
a dose reduction preferably every other day, until complete withdrawal
of Neupro (s