Mirapexin

Country: Evrópusambandið

Tungumál: enska

Heimild: EMA (European Medicines Agency)

Kauptu það núna

Vara einkenni Vara einkenni (SPC)
23-01-2024
Opinber matsskýrsla Opinber matsskýrsla (PAR)
06-01-2011

Virkt innihaldsefni:

pramipexole dihydrochloride monohydrate

Fáanlegur frá:

Boehringer Ingelheim International GmbH

ATC númer:

N04BC05

INN (Alþjóðlegt nafn):

pramipexole

Meðferðarhópur:

Anti-Parkinson drugs

Lækningarsvæði:

Restless Legs Syndrome; Parkinson Disease

Ábendingar:

Mirapexin is indicated for treatment of the signs and symptoms of idiopathic Parkinson's disease, alone (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).Mirapexin is indicated for symptomatic treatment of moderate to severe idiopathic restless-legs syndrome in dosages up to 0.54 mg of base (0.75 mg of salt).

Vörulýsing:

Revision: 40

Leyfisstaða:

Authorised

Leyfisdagur:

1998-02-23

Upplýsingar fylgiseðill

                                67
B. PACKAGE LEAFLET
68
PACKAGE LEAFLET: INFORMATION FOR THE USER
MIRAPEXIN 0.088 MG TABLETS
MIRAPEXIN 0.18 MG TABLETS
MIRAPEXIN 0.35 MG TABLETS
MIRAPEXIN 0.7 MG TABLETS
pramipexole
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 of the 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 MIRAPEXIN is and what it is used for
2.
What you need to know before you take MIRAPEXIN
3.
How to take MIRAPEXIN
4.
Possible side effects
5.
How to store MIRAPEXIN
6.
Contents of the pack and other information
1.
WHAT MIRAPEXIN IS AND WHAT IT IS USED FOR
MIRAPEXIN contains the active substance pramipexole and belongs to a
group of medicines known
as dopamine agonists, which stimulate dopamine receptors in the brain.
Stimulation of the dopamine
receptors triggers nerve impulses in the brain that help to control
body movements.
MIRAPEXIN IS USED TO:
-
treat the symptoms of primary Parkinson’s disease in adults. It can
be used alone or in
combination with levodopa (another medicine for Parkinson’s
disease).
-
treat the symptoms of moderate to severe primary Restless Legs
Syndrome in adults.
2.
WHAT YOU NEED TO KNOW BEFORE YOU TAKE MIRAPEXIN
DO NOT TAKE MIRAPEXIN
-
if you are allergic to pramipexole or to any of the other ingredients
of this medicine (listed in
section 6).
WARNINGS AND PRECAUTIONS
Talk to your doctor before taking MIRAPEXIN. Tell your doctor if you
have (had) or develop any
medical conditions or symptoms, especially any of the following:
-
Kidney disease
-
Hallucinations (seeing, hearing or feeling things that are not there).
Most hallucination
                                
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Vara einkenni

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE MEDICINAL PRODUCT
MIRAPEXIN 0.088 mg tablets
MIRAPEXIN 0.18 mg tablets
MIRAPEXIN 0.35 mg tablets
MIRAPEXIN 0.7 mg tablets
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
MIRAPEXIN 0.088 mg tablets
Each tablet contains 0.125 mg pramipexole dihydrochloride monohydrate
equivalent to 0.088 mg
pramipexole.
MIRAPEXIN 0.18 mg tablets
Each tablet contains 0.25 mg pramipexole dihydrochloride monohydrate
equivalent to 0.18 mg
pramipexole.
MIRAPEXIN 0.35 mg tablets
Each tablet contains 0.5 mg pramipexole dihydrochloride monohydrate
equivalent to 0.35 mg
pramipexole.
MIRAPEXIN 0.7 mg tablets
Each tablet contains 1.0 mg pramipexole dihydrochloride monohydrate
equivalent to 0.7 mg
pramipexole.
_Please note:_
Pramipexole doses as published in the literature refer to the salt
form.
Therefore, doses will be expressed in terms of both pramipexole base
and pramipexole salt (in
brackets).
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Tablet
MIRAPEXIN 0.088 mg tablets
The tablets are white, flat, of round shape, and have a code embossed
(one side with the code P6, and
one side with the Boehringer Ingelheim company symbol).
MIRAPEXIN 0.18 mg tablets
The tablets are white, flat, of oval shape, scored on both sides, and
have a code embossed (one side
with the code P7, and one side with the Boehringer Ingelheim company
symbol).
Tablets can be divided into equal halves.
MIRAPEXIN 0.35 mg tablets
The tablets are white, flat, of oval shape, scored on both sides, and
have a code embossed (one side
with the code P8, and one side with the Boehringer Ingelheim company
symbol).
Tablets can be divided into equal halves.
MIRAPEXIN 0.7 mg tablets
The tablets are white, flat, of round shape, scored on both sides, and
have a code embossed (one side
with the code P9, and one side with the Boehringer Ingelheim company
symbol).
Tablets can be divided into equal halves.
3
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
MIRAPEXIN is indicated in adults for treatment o
                                
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