Euroopan unioni - islanti - EMA (European Medicines Agency)

novartis ireland ltd - ofatumumab - heila-og mænusigg, köstum tilkynnt - immunosuppressant - kesimpta is indicated for the treatment of adult patients with relapsing forms of multiple sclerosis (rms) with active disease defined by clinical or imaging features (see section 5.

Euroopan unioni - islanti - EMA (European Medicines Agency)

novartis europharm limited  - capmatinib dihydrochloride monohydrate - krabbamein, lungnakrabbamein - Æxlishemjandi lyf - tabrecta as monotherapy is indicated for the treatment of adult patients with advanced non small cell lung cancer (nsclc) harbouring alterations leading to mesenchymal epithelial transition factor gene exon 14 (metex14) skipping, who require systemic therapy following prior treatment with immunotherapy and/or platinum based chemotherapy.

Euroopan unioni - islanti - EMA (European Medicines Agency)

novartis europharm limited  - gozetotide - radionuclide imaging - greining geislavirkja - Þetta lyf er eingöngu ætlað til greiningar. locametz, after radiolabelling with gallium 68, is indicated for the detection of prostate specific membrane antigen (psma) positive lesions with positron emission tomography (pet) in adults with prostate cancer (pca) in the following clinical settings:primary staging of patients with high risk pca prior to primary curative therapy,suspected pca recurrence in patients with increasing levels of serum prostate specific antigen (psa) after primary curative therapy,identification of patients with psma positive progressive metastatic castration resistant prostate cancer (mcrpc) for whom psma targeted therapy is indicated (see section 4.

Euroopan unioni - islanti - EMA (European Medicines Agency)

novartis europharm limited  - lutetium (177lu) vipivotide tetraxetan - stækkun Æxli, gelding-Þola - heilsueyðandi lyf - pluvicto in combination with androgen deprivation therapy (adt) with or without androgen receptor (ar) pathway inhibition is indicated for the treatment of adult patients with progressive prostate-specific membrane antigen (psma)-positive metastatic castration-resistant prostate cancer (mcrpc) who have been treated with ar pathway inhibition and taxane based chemotherapy.

Islanti - islanti - LYFJASTOFNUN (Icelandic Medicines Agency)

novartis healthcare a/s - moxifloxacinum hýdróklóríð - augndropar, lausn - 5 mg/ml

Islanti - islanti - LYFJASTOFNUN (Icelandic Medicines Agency)

novartis healthcare a/s - ciprofloxacinum hýdróklóríð; hydrocortisonum inn - eyrnadropar, dreifa - 2 mg + 10 mg/ml

Islanti - islanti - LYFJASTOFNUN (Icelandic Medicines Agency)

novartis healthcare a/s - dexamethasonum fosfat - augndropar, dreifa - 1 mg/ml

Islanti - islanti - LYFJASTOFNUN (Icelandic Medicines Agency)

novartis healthcare a/s - neomycinum súlfat; polymyxinum b súlfat; dexamethasonum fosfat - augndropar, dreifa

Islanti - islanti - LYFJASTOFNUN (Icelandic Medicines Agency)

novartis healthcare a/s - mycophenolatum natríum - magasýruþolin tafla - 180 mg

Islanti - islanti - LYFJASTOFNUN (Icelandic Medicines Agency)

novartis healthcare a/s - mycophenolatum natríum - magasýruþolin tafla - 360 mg