Mirapexin

Country: European Union

Language: Icelandic

Source: EMA (European Medicines Agency)

Active ingredient:

pramipexól tvíhýdróklóríð einhýdrat

Available from:

Boehringer Ingelheim International GmbH

ATC code:

N04BC05

INN (International Name):

pramipexole

Therapeutic group:

Anti-Parkinsonslyf

Therapeutic area:

Restless Legs Syndrome; Parkinson Disease

Therapeutic indications:

Mirapexin er ætlað til meðferðar á einkennum einkenna Parkinsonsveiki, ein og sér (án levodopa) eða í samsettri meðferð með levodopa, ég. á meðan á sjúkdómnum stendur, í gegnum seint stig þegar áhrif levódópa berast eða verða ósamræmi og sveiflur á meðferðaráhrifum eiga sér stað (lokaskammtur eða "á-burt" sveiflur). Mirapexin er ætlað fyrir einkennum meðferð í meðallagi til alvarlega sjálfvakin eirðarlaus-fætur heilkenni í skammtar upp að 0. 54 mg af stöð (0. 75 mg af salti).

Product summary:

Revision: 40

Authorization status:

Leyfilegt

Authorization date:

1998-02-23

Patient Information leaflet

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Summary of Product characteristics

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Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 23-01-2024
Summary of Product characteristics Summary of Product characteristics Bulgarian 23-01-2024
Public Assessment Report Public Assessment Report Bulgarian 06-01-2011
Patient Information leaflet Patient Information leaflet Spanish 23-01-2024
Public Assessment Report Public Assessment Report Spanish 06-01-2011
Patient Information leaflet Patient Information leaflet Czech 23-01-2024
Public Assessment Report Public Assessment Report Czech 06-01-2011
Patient Information leaflet Patient Information leaflet Danish 23-01-2024
Public Assessment Report Public Assessment Report Danish 06-01-2011
Patient Information leaflet Patient Information leaflet German 23-01-2024
Public Assessment Report Public Assessment Report German 06-01-2011
Patient Information leaflet Patient Information leaflet Estonian 23-01-2024
Public Assessment Report Public Assessment Report Estonian 06-01-2011
Patient Information leaflet Patient Information leaflet Greek 23-01-2024
Public Assessment Report Public Assessment Report Greek 06-01-2011
Patient Information leaflet Patient Information leaflet English 23-01-2024
Public Assessment Report Public Assessment Report English 06-01-2011
Patient Information leaflet Patient Information leaflet French 23-01-2024
Public Assessment Report Public Assessment Report French 06-01-2011
Patient Information leaflet Patient Information leaflet Italian 23-01-2024
Public Assessment Report Public Assessment Report Italian 06-01-2011
Patient Information leaflet Patient Information leaflet Latvian 23-01-2024
Public Assessment Report Public Assessment Report Latvian 06-01-2011
Patient Information leaflet Patient Information leaflet Lithuanian 23-01-2024
Summary of Product characteristics Summary of Product characteristics Lithuanian 23-01-2024
Public Assessment Report Public Assessment Report Lithuanian 06-01-2011
Patient Information leaflet Patient Information leaflet Hungarian 23-01-2024
Summary of Product characteristics Summary of Product characteristics Hungarian 23-01-2024
Public Assessment Report Public Assessment Report Hungarian 06-01-2011
Patient Information leaflet Patient Information leaflet Maltese 23-01-2024
Public Assessment Report Public Assessment Report Maltese 06-01-2011
Patient Information leaflet Patient Information leaflet Dutch 23-01-2024
Public Assessment Report Public Assessment Report Dutch 06-01-2011
Patient Information leaflet Patient Information leaflet Polish 23-01-2024
Public Assessment Report Public Assessment Report Polish 06-01-2011
Patient Information leaflet Patient Information leaflet Portuguese 23-01-2024
Summary of Product characteristics Summary of Product characteristics Portuguese 23-01-2024
Public Assessment Report Public Assessment Report Portuguese 06-01-2011
Patient Information leaflet Patient Information leaflet Romanian 23-01-2024
Public Assessment Report Public Assessment Report Romanian 06-01-2011
Patient Information leaflet Patient Information leaflet Slovak 23-01-2024
Public Assessment Report Public Assessment Report Slovak 06-01-2011
Patient Information leaflet Patient Information leaflet Slovenian 23-01-2024
Summary of Product characteristics Summary of Product characteristics Slovenian 23-01-2024
Public Assessment Report Public Assessment Report Slovenian 06-01-2011
Patient Information leaflet Patient Information leaflet Finnish 23-01-2024
Public Assessment Report Public Assessment Report Finnish 06-01-2011
Patient Information leaflet Patient Information leaflet Swedish 23-01-2024
Public Assessment Report Public Assessment Report Swedish 06-01-2011
Patient Information leaflet Patient Information leaflet Norwegian 23-01-2024
Summary of Product characteristics Summary of Product characteristics Norwegian 23-01-2024
Patient Information leaflet Patient Information leaflet Croatian 23-01-2024

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