Tysabri Den europeiske union - norsk - EMA (European Medicines Agency)

tysabri

biogen netherlands b.v. - natalizumab - multippel sklerose - selektive immunosuppressiva - tysabri is indicated as single disease modifying therapy in adults with highly active relapsing remitting multiple sclerosis for the following patient groups: , patients with highly active disease activity despite a full and adequate course of treatment with at least one disease modifying therapy (dmt) (for exceptions and information about washout periods see sections 4. 4 og 5. 1), , or, patients with rapidly evolving severe relapsing remitting multiple sclerosis defined by 2 or more disabling relapses in one year, and with 1 or more gadolinium enhancing lesions on brain mri or a significant increase in t2 lesion load as compared to a previous recent mri.

Lumeblue (previously known as Methylthioninium chloride Cosmo) Den europeiske union - norsk - EMA (European Medicines Agency)

lumeblue (previously known as methylthioninium chloride cosmo)

alfasigma s.p.a. - metyltioniniumklorid - colorectal neoplasms; colonoscopy - other diagnostic agents - lumeblue is indicated as a diagnostic agent enhancing visualisation of colorectal lesions in adult patients undergoing screening or surveillance colonoscopy.

Fingolimod Mylan Den europeiske union - norsk - EMA (European Medicines Agency)

fingolimod mylan

mylan ireland limited - fingolimod hydrochloride - multippel sklerose, relapsing-remitting - immunsuppressive - indicated as single disease modifying therapy in highly active relapsing remitting multiple sclerosis for the following groups of adult and paediatric patients aged 10 years and older: patients with highly active disease despite a full and adequate course of treatment with at least one disease modifying therapy (for exceptions and information about washout periods see sections 4. 4 og 5. 1) or patients with rapidly evolving severe relapsing remitting multiple sclerosis defined by 2 or more disabling relapses in one year, and with 1 or more gadolinium enhancing lesions on brain mri or a significant increase in t2 lesion load as compared to a previous recent mri.

Tyruko Den europeiske union - norsk - EMA (European Medicines Agency)

tyruko

sandoz gmbh - natalizumab - multiple sclerosis, relapsing-remitting; multiple sclerosis - immunsuppressive - tyruko is indicated as single disease modifying therapy in adults with highly active relapsing remitting multiple sclerosis (rrms) for the following patient groups: patients with highly active disease despite a full and adequate course of treatment with at least one disease modifying therapy (dmt) (for exceptions and information about washout periods see sections 4. 4 og 5. 1), or, patients with rapidly evolving severe rrms defined by 2 or more disabling relapses in one year, and with 1 or more gadolinium enhancing lesions on brain magnetic resonance imaging (mri) or a significant increase in t2 lesion load as compared to a previous recent mri.

Rosuvastatin Xiromed 20 mg Norge - norsk - Statens legemiddelverk

rosuvastatin xiromed 20 mg

medical valley invest ab - rosuvastatinkalsium - tablett, filmdrasjert - 20 mg

Rosuvastatin Xiromed 5 mg Norge - norsk - Statens legemiddelverk

rosuvastatin xiromed 5 mg

medical valley invest ab - rosuvastatinkalsium - tablett, filmdrasjert - 5 mg

Rosuvastatin Xiromed 10 mg Norge - norsk - Statens legemiddelverk

rosuvastatin xiromed 10 mg

medical valley invest ab - rosuvastatinkalsium - tablett, filmdrasjert - 10 mg

Rosuvastatin Xiromed 40 mg Norge - norsk - Statens legemiddelverk

rosuvastatin xiromed 40 mg

medical valley invest ab - rosuvastatinkalsium - tablett, filmdrasjert - 40 mg

Simvastatin Bluefish 10 mg Norge - norsk - Statens legemiddelverk

simvastatin bluefish 10 mg

bluefish pharmaceuticals ab - simvastatin - tablett, filmdrasjert - 10 mg

Simvastatin Bluefish 20 mg Norge - norsk - Statens legemiddelverk

simvastatin bluefish 20 mg

bluefish pharmaceuticals ab - simvastatin - tablett, filmdrasjert - 20 mg