Norwegia - Norwegia - Statens legemiddelverk

krka sverige ab - ropinirolhydroklorid - depottablett - 4 mg

Norwegia - Norwegia - Statens legemiddelverk

ratiopharm gmbh - tamsulosinhydroklorid - depottablett - 0.4 mg

Uni Eropa - Norwegia - EMA (European Medicines Agency)

boehringer ingelheim vetmedica gmbh - svin parvovirus, belastning 27a, viral protein 2 - immunologicals for suidae - griser - for aktive vaksinering av statsobligasjoner og sår fra fylte 5 måneder for å beskytte avkom mot transplacental infeksjon forårsaket av svin parvovirus.

Uni Eropa - Norwegia - EMA (European Medicines Agency)

koanaa healthcare gmbh - imatinib mesilate - leukemia, myelogenous, chronic, bcr-abl positive; precursor cell lymphoblastic leukemia-lymphoma; myelodysplastic-myeloproliferative diseases; hypereosinophilic syndrome; dermatofibrosarcoma; gastrointestinal stromal tumors - antineoplastiske midler - imatinib koanaa is indicated for the treatment ofadult and paediatric patients with newly diagnosed philadelphia chromosome (bcr-abl) positive (ph+) chronic myeloid leukaemia (cml) for whom bone marrow transplantation is not considered as the first line of treatment. adult and paediatric patients with ph+ cml in chronic phase after failure of interferon-alpha therapy, or in accelerated phase or blast crisis. adult and paediatric patients with newly diagnosed philadelphia chromosome positive acute lymphoblastic leukaemia (ph+ all) integrated with chemotherapy. adult patients with relapsed or refractory ph+ all as monotherapy. adult patients with myelodysplastic/myeloproliferative diseases (mds/mpd) associated with platelet-derived growth factor receptor (pdgfr) gene re-arrangements. adult patients with advanced hypereosinophilic syndrome (hes) and/or chronic eosinophilic leukaemia (cel) with fip1l1-pdgfrα rearrangement. the effect of imatinib on the outcome of bone marrow transplantation has not been determined. imatinib koanaa is indicated forthe treatment of adult patients with kit (cd 117) positive unresectable and/or metastatic malignant gastrointestinal stromal tumours (gist). the adjuvant treatment of adult patients who are at significant risk of relapse following resection of kit (cd117)-positive gist. pasienter som har en lav eller svært lav risiko for tilbakefall bør ikke får adjuvant behandling. the treatment of adult patients with unresectable dermatofibrosarcoma protuberans (dfsp) and adult patients with recurrent and/or metastatic dfsp who are not eligible for surgery. in adult and paediatric patients, the effectiveness of imatinib is based on overall haematological and cytogenetic response rates and progression-free survival in cml, on haematological and cytogenetic response rates in ph+ all, mds/mpd, on haematological response rates in hes/cel and on objective response rates in adult patients with unresectable and/or metastatic gist and dfsp and on recurrence-free survival in adjuvant gist. the experience with imatinib in patients with mds/mpd associated with pdgfr gene re-arrangements is very limited (see section 5. bortsett fra i nydiagnostisert kronisk fase kml, det er ingen kontrollerte studier som viser en klinisk nytte eller økt overlevelse for disse sykdommer.

Uni Eropa - Norwegia - EMA (European Medicines Agency)

novartis europharm limited - brinzolamid - glaucoma, open-angle; ocular hypertension - Øyemidler - azopt er indisert for å redusere forhøyet intraokulært trykk i:okulær hypertensjon;åpen vinkel glaucomaas monoterapi hos voksne pasienter som ikke svarer til beta-blokkere eller hos voksne pasienter som beta-blokkere er kontraindisert, eller som tilleggsbehandling til beta-blokkere eller prostaglandin analoger.

Uni Eropa - Norwegia - EMA (European Medicines Agency)

galderma international - brimonidintartrat - hudsykdommer - andre dermatologiske preparater - mirvaso er indisert for symptomatisk behandling av rosace ansikts erytem hos voksne pasienter.

Uni Eropa - Norwegia - EMA (European Medicines Agency)

novartis europharm limited - nepafenak - pain, postoperative; ophthalmologic surgical procedures - Øyemidler - nevanac is indicated for: , prevention and treatment of postoperative pain and inflammation associated with cataract surgery;, reduction in the risk of postoperative macular oedema associated with cataract surgery in diabetic patients.

Uni Eropa - Norwegia - EMA (European Medicines Agency)

grunenthal gmbh - capsaicin - nervesmerter - anestetika - qutenza er indisert for behandling av perifer neuropatisk smerte hos voksne, enten alene eller i kombinasjon med andre legemidler for smerte.

Norwegia - Norwegia - Statens legemiddelverk

glaxosmithkline as - betametasonvalerat - liniment, oppløsning - 1 mg/ ml

Norwegia - Norwegia - Statens legemiddelverk

immedica pharma ab - betaksololhydroklorid - Øyedråper, suspensjon - 2.5 mg/ ml