Sifrol

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)
05-01-2011

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:

Sifrol 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, though 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).Sifrol 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: 37

Leyfisstaða:

Authorised

Leyfisdagur:

1997-10-13

Upplýsingar fylgiseðill

                                67
B. PACKAGE LEAFLET
68
PACKAGE LEAFLET: INFORMATION FOR THE USER
SIFROL 0.088 MG TABLETS
SIFROL 0.18 MG TABLETS
SIFROL 0.35 MG TABLETS
SIFROL 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 SIFROL is and what it is used for
2.
What you need to know before you take SIFROL
3.
How to take SIFROL
4.
Possible side effects
5.
How to store SIFROL
6.
Contents of the pack and other information
1.
WHAT SIFROL IS AND WHAT IT IS USED FOR
SIFROL 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.
SIFROL 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 SIFROL
DO NOT TAKE SIFROL
-
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 SIFROL. 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 hallucinations are visual.
-
Dyskinesia (e.g. abnormal
                                
                                Lestu allt skjalið
                                
                            

Vara einkenni

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE MEDICINAL PRODUCT
SIFROL 0.088 mg tablets
SIFROL 0.18 mg tablets
SIFROL 0.35 mg tablets
SIFROL 0.7 mg tablets
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
SIFROL 0.088 mg tablets
Each tablet contains 0.125 mg pramipexole dihydrochloride monohydrate
equivalent to 0.088 mg
pramipexole.
SIFROL 0.18 mg tablets
Each tablet contains 0.25 mg pramipexole dihydrochloride monohydrate
equivalent to 0.18 mg
pramipexole.
SIFROL 0.35 mg tablets
Each tablet contains 0.5 mg pramipexole dihydrochloride monohydrate
equivalent to 0.35 mg
pramipexole.
SIFROL 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
SIFROL 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).
SIFROL 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.
SIFROL 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.
SIFROL 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
SIFROL is indicated in adults for treatment of the signs and symptoms
of idiopathic 
                                
                                Lestu allt skjalið
                                
                            

Skjöl á öðrum tungumálum

Upplýsingar fylgiseðill Upplýsingar fylgiseðill búlgarska 23-01-2024
Vara einkenni Vara einkenni búlgarska 23-01-2024
Opinber matsskýrsla Opinber matsskýrsla búlgarska 05-01-2011
Upplýsingar fylgiseðill Upplýsingar fylgiseðill spænska 23-01-2024
Vara einkenni Vara einkenni spænska 23-01-2024
Opinber matsskýrsla Opinber matsskýrsla spænska 05-01-2011
Upplýsingar fylgiseðill Upplýsingar fylgiseðill tékkneska 23-01-2024
Vara einkenni Vara einkenni tékkneska 23-01-2024
Opinber matsskýrsla Opinber matsskýrsla tékkneska 05-01-2011
Upplýsingar fylgiseðill Upplýsingar fylgiseðill danska 23-01-2024
Vara einkenni Vara einkenni danska 23-01-2024
Opinber matsskýrsla Opinber matsskýrsla danska 05-01-2011
Upplýsingar fylgiseðill Upplýsingar fylgiseðill þýska 23-01-2024
Vara einkenni Vara einkenni þýska 23-01-2024
Opinber matsskýrsla Opinber matsskýrsla þýska 05-01-2011
Upplýsingar fylgiseðill Upplýsingar fylgiseðill eistneska 23-01-2024
Vara einkenni Vara einkenni eistneska 23-01-2024
Opinber matsskýrsla Opinber matsskýrsla eistneska 05-01-2011
Upplýsingar fylgiseðill Upplýsingar fylgiseðill gríska 23-01-2024
Vara einkenni Vara einkenni gríska 23-01-2024
Opinber matsskýrsla Opinber matsskýrsla gríska 05-01-2011
Upplýsingar fylgiseðill Upplýsingar fylgiseðill franska 23-01-2024
Vara einkenni Vara einkenni franska 23-01-2024
Opinber matsskýrsla Opinber matsskýrsla franska 05-01-2011
Upplýsingar fylgiseðill Upplýsingar fylgiseðill ítalska 23-01-2024
Vara einkenni Vara einkenni ítalska 23-01-2024
Opinber matsskýrsla Opinber matsskýrsla ítalska 05-01-2011
Upplýsingar fylgiseðill Upplýsingar fylgiseðill lettneska 23-01-2024
Vara einkenni Vara einkenni lettneska 23-01-2024
Opinber matsskýrsla Opinber matsskýrsla lettneska 05-01-2011
Upplýsingar fylgiseðill Upplýsingar fylgiseðill litháíska 23-01-2024
Vara einkenni Vara einkenni litháíska 23-01-2024
Opinber matsskýrsla Opinber matsskýrsla litháíska 05-01-2011
Upplýsingar fylgiseðill Upplýsingar fylgiseðill ungverska 23-01-2024
Vara einkenni Vara einkenni ungverska 23-01-2024
Opinber matsskýrsla Opinber matsskýrsla ungverska 05-01-2011
Upplýsingar fylgiseðill Upplýsingar fylgiseðill maltneska 23-01-2024
Vara einkenni Vara einkenni maltneska 23-01-2024
Opinber matsskýrsla Opinber matsskýrsla maltneska 05-01-2011
Upplýsingar fylgiseðill Upplýsingar fylgiseðill hollenska 23-01-2024
Vara einkenni Vara einkenni hollenska 23-01-2024
Opinber matsskýrsla Opinber matsskýrsla hollenska 05-01-2011
Upplýsingar fylgiseðill Upplýsingar fylgiseðill pólska 23-01-2024
Vara einkenni Vara einkenni pólska 23-01-2024
Opinber matsskýrsla Opinber matsskýrsla pólska 05-01-2011
Upplýsingar fylgiseðill Upplýsingar fylgiseðill portúgalska 23-01-2024
Vara einkenni Vara einkenni portúgalska 23-01-2024
Opinber matsskýrsla Opinber matsskýrsla portúgalska 05-01-2011
Upplýsingar fylgiseðill Upplýsingar fylgiseðill rúmenska 23-01-2024
Vara einkenni Vara einkenni rúmenska 23-01-2024
Opinber matsskýrsla Opinber matsskýrsla rúmenska 05-01-2011
Upplýsingar fylgiseðill Upplýsingar fylgiseðill slóvakíska 23-01-2024
Vara einkenni Vara einkenni slóvakíska 23-01-2024
Opinber matsskýrsla Opinber matsskýrsla slóvakíska 05-01-2011
Upplýsingar fylgiseðill Upplýsingar fylgiseðill slóvenska 23-01-2024
Vara einkenni Vara einkenni slóvenska 23-01-2024
Opinber matsskýrsla Opinber matsskýrsla slóvenska 05-01-2011
Upplýsingar fylgiseðill Upplýsingar fylgiseðill finnska 23-01-2024
Vara einkenni Vara einkenni finnska 23-01-2024
Opinber matsskýrsla Opinber matsskýrsla finnska 05-01-2011
Upplýsingar fylgiseðill Upplýsingar fylgiseðill sænska 23-01-2024
Vara einkenni Vara einkenni sænska 23-01-2024
Opinber matsskýrsla Opinber matsskýrsla sænska 05-01-2011
Upplýsingar fylgiseðill Upplýsingar fylgiseðill norska 23-01-2024
Vara einkenni Vara einkenni norska 23-01-2024
Upplýsingar fylgiseðill Upplýsingar fylgiseðill íslenska 23-01-2024
Vara einkenni Vara einkenni íslenska 23-01-2024
Upplýsingar fylgiseðill Upplýsingar fylgiseðill króatíska 23-01-2024
Vara einkenni Vara einkenni króatíska 23-01-2024

Leitaðu viðvaranir sem tengjast þessari vöru

Skoða skjalasögu