Clindamycin Navamedic 600 mg নরওয়ে - নরওয়েজীয় - Statens legemiddelverk

clindamycin navamedic 600 mg

navamedic asa - klindamycinfosfat - infusjonsvæske, oppløsning - 600 mg

Sorafenib Accord ইউরোপীয় ইউনিয়ন - নরওয়েজীয় - EMA (European Medicines Agency)

sorafenib accord

accord healthcare s.l.u. - sorafenib tosilate - carcinoma, hepatocellular; carcinoma, renal cell - antineoplastiske midler - hepatocellular carcinomasorafenib accord is indicated for the treatment of hepatocellular carcinoma (see section 5. renal cell carcinomasorafenib accord is indicated for the treatment of patients with advanced renal cell carcinoma who have failed prior interferon-alpha or interleukin-2 based therapy or are considered unsuitable for such therapy.

Carbaglu ইউরোপীয় ইউনিয়ন - নরওয়েজীয় - EMA (European Medicines Agency)

carbaglu

recordati rare diseases - cargluminsyre - amino acid metabolism, inborn errors; propionic acidemia - andre alimentary tract and metabolism products, - carbaglu er angitt i behandling av:hyperammonaemia på grunn av n-acetylglutamate-syntase primær mangel;hyperammonaemia på grunn av isovaleric acidaemia;hyperammonaemia på grunn av methymalonic acidaemia;hyperammonaemia på grunn av propionsyre acidaemia.

Nordimet ইউরোপীয় ইউনিয়ন - নরওয়েজীয় - EMA (European Medicines Agency)

nordimet

nordic group b.v. - methotrexate - arthritis, psoriatic; psoriasis; arthritis, juvenile rheumatoid; arthritis, rheumatoid - antineoplastiske midler - nordimet is indicated for the treatment of:active rheumatoid arthritis in adult patients,polyarthritic forms of severe, active juvenile idiopathic arthritis (jia), when the response to nonsteroidal anti-inflammatory drugs (nsaids) has been inadequate,moderate to severe plaque psoriasis in adults who are candidates for systemic therapy, and severe psoriatic arthritis in adult patients, induction of remission in moderate steroid-dependent crohn's disease in adult patients, in combination with corticosteroids and for maintenance of remission, as monotherapy, in patients who have responded to methotrexate.

Sivextro ইউরোপীয় ইউনিয়ন - নরওয়েজীয় - EMA (European Medicines Agency)

sivextro

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.

Stivarga ইউরোপীয় ইউনিয়ন - নরওয়েজীয় - EMA (European Medicines Agency)

stivarga

bayer pharma ag - regorafenib - colorektale neoplasmer - antineoplastic agents, protein kinase inhibitors - stivarga er indisert som monoterapi for behandling av voksne pasienter med metastatisk kolorektal cancer (crc) som tidligere har blitt behandlet med, eller er ikke vurdert som kandidater for, er tilgjengelige behandlingsformer - disse inkluderer fluoropyrimidine-basert kjemoterapi, en anti-vegf terapi og en anti-egfr terapi;inoperabel eller metastatisk gastrointestinal stromal svulster (gist) som har kommet på eller er intolerante til tidligere behandling med imatinib og sunitinib;hepatocellulært karsinom (hcc) som tidligere har blitt behandlet med sorafenib.

Jylamvo ইউরোপীয় ইউনিয়ন - নরওয়েজীয় - EMA (European Medicines Agency)

jylamvo

therakind (europe) limited - methotrexate - arthritis, psoriatic; precursor cell lymphoblastic leukemia-lymphoma; psoriasis; arthritis, rheumatoid; arthritis - antineoplastiske midler - i rheumatological og dermatologiske diseasesactive revmatoid artritt hos voksne pasienter. polyarthritic former for aktiv, alvorlig juvenil idiopatisk artritt (jia) i ungdom og barn i alderen 3 år og over når respons til ikke-steroidal anti-inflammatorisk legemidler (nsaids) har vært mangelfull. alvorlige, behandling-ildfaste, invalidiserende psoriasis som ikke responderer tilstrekkelig til andre former for behandling, for eksempel lysbehandling, psoralen og uv-a stråling (puva) terapi og retinoider, og alvorlig psoriasis artritt hos voksne pasienter. i oncologymaintenance behandling av akutt lymfoblastisk leukemi (all) hos voksne, ungdom og barn i alderen 3 år og over.

Ucedane ইউরোপীয় ইউনিয়ন - নরওয়েজীয় - EMA (European Medicines Agency)

ucedane

eurocept international bv - cargluminsyre - hyperammonemia; amino acid metabolism, inborn errors - andre alimentary tract and metabolism products, - ucedane is indicated in treatment of:hyperammonaemia due to n-acetylglutamate synthase primary deficiency;hyperammonaemia due to isovaleric acidaemia;hyperammonaemia due to methymalonic acidaemia;hyperammonaemia due to propionic acidaemia.

Apocillin 330 mg নরওয়ে - নরওয়েজীয় - Statens legemiddelverk

apocillin 330 mg

actavis group ptc ehf (1) - fenoksymetylpenicillinkalium - tablett, filmdrasjert - 330 mg

Apocillin 250 mg/ ml নরওয়ে - নরওয়েজীয় - Statens legemiddelverk

apocillin 250 mg/ ml

actavis group ptc ehf (1) - fenoksymetylpenicillinkalium - granulat til dråper, oppløsning - 250 mg/ ml