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

astrazeneca ab - osimertinib mesilate - karsinom, ikke-småcellet lunge - andre cytostatika, protein kinase hemmere - tagrisso as monotherapy is indicated for:- the adjuvant treatment after complete tumour resection in adult patients with stage ib-iiia non-small cell lung cancer (nsclc) whose tumours have epidermal growth factor receptor (egfr) exon 19 deletions or exon 21 (l858r) substitution mutations- the first-line treatment of adult patients nsclc with activating egfr mutations. - the treatment of adult patients with locally advanced or metastatic egfr t790m mutation-positive nsclc. tagrisso as monotherapy is indicated for:- the adjuvant treatment after complete tumour resection in adult patients with stage ib-iiia non-small cell lung cancer (nsclc) whose tumours have epidermal growth factor receptor (egfr) exon 19 deletions or exon 21 (l858r) substitution mutations. - the first-line treatment of adult patients with locally advanced or metastatic nsclc with activating egfr mutations. - the treatment of adult patients with locally advanced or metastatic egfr t790m mutation-positive nsclc.

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

eli lilly nederland b.v. - florbetapir (18f) - radionuklide bildebehandling - diagnostiske radiopharmaceuticals - dette legemidlet er kun til diagnostisk bruk. amyvid er en radiopharmaceutical indikert for positron emisjon tomografi (pet) avbildningen av β-amyloid neuritic plakk tetthet i hjernen hos voksne pasienter med kognitiv svikt som blir vurdert for alzheimers sykdom (ad) og andre årsaker til kognitiv svikt. amyvid skal brukes i forbindelse med en klinisk vurdering. en negativ søk angir sparsom eller ingen plakk, som ikke er forenlig med diagnosen ad.

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

merck sharp & dohme b.v. - tedizolid fosfat - soft tissue infections; skin diseases, bacterial - antibacterials for systemic use, , other antibacterials - sivextro is indicated for the treatment of acute bacterial skin and skin structure infections (absssi) in adults and adolescents 12 years of age and older.

Norge - norsk - Statens legemiddelverk

orifarm as - dimetylfumarat - enterokapsel, hard - 240 mg

Norge - norsk - Statens legemiddelverk

orifarm as - dimetylfumarat - enterokapsel, hard - 120 mg

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

biogen netherlands b.v. - diroximel fumarate (biib098) - multippel sklerose, relapsing-remitting - immunsuppressive - vumerity is indicated for the treatment of adult patients with relapsing remitting multiple sclerosis (see section 5. 1 for important information on the populations for which efficacy has been established).

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

biogen netherlands b.v. - dimetylfumarat - multippel sklerose - immunsuppressive - tecfidera is indicated for the treatment of adult and paediatric patients aged 13 years and older with relapsing remitting multiple sclerosis (rrms).

Norge - norsk - Statens legemiddelverk

orifarm as - pantoprazolnatriumsesquihydrat - enterotablett - 20 mg

Norge - norsk - Statens legemiddelverk

orifarm as - pantoprazolnatriumsesquihydrat - enterotablett - 20 mg

Norge - norsk - Statens legemiddelverk

orifarm as - pantoprazolnatriumsesquihydrat - enterotablett - 40 mg