Norge - norsk - Statens legemiddelverk

ebewe pharma ges.m.b.h nfg. kg - vinorelbintartrat - konsentrat til infusjonsvæske, oppløsning - 10 mg/ ml

Norge - norsk - Statens legemiddelverk

evolan pharma ab - diklofenakdietylamin - gel - 11.6 mg/ g

Norge - norsk - Statens legemiddelverk

evolan pharma ab - diklofenakdietylamin - gel - 23.2 mg/ g

Norge - norsk - myHealthbox

bayer ag -

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

ucb pharma s.a.   - rotigotin - restless legs syndrome; parkinson disease - anti-parkinson medisiner - leganto er indisert for symptomatisk behandling av moderat til alvorlig idiopatisk restless-legs syndrom hos voksne. leganto er angitt for behandling av tegn og symptomer på et tidlig stadium idiopatisk parkinsons sykdom, som monoterapi (jeg. uten levodopa) eller i kombinasjon med levodopa, i. i løpet av sykdommen, gjennom til slutten stadier når effekten av levodopa avtar eller blir ustabil og fluktuasjoner i terapeutisk effekt oppstår (slutten av dose eller "on-off" - fluktuasjoner).

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

ucb pharma s.a. - rotigotin - restless legs syndrome; parkinson disease - anti-parkinson medisiner - parkinsons sykdom: neupro er indisert for behandling av tegn og symptomer på idiopatisk parkinsons sykdom i tidlig stadium som monoterapi (jeg. uten levodopa) eller i kombinasjon med levodopa, i. i løpet av sykdommen, gjennom til sent stadier når effekten av levodopa slites av eller blir inkonsekvent og fluktuasjoner av den terapeutiske effekten oppstår (slutten av dosen eller "on-off" fluktuasjoner). rastløs-bein-syndromet: neupro er indikert for symptomatisk behandling av moderat til alvorlig idiopatisk rastløs-legs syndrom hos voksne.

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

bristol-myers squibb pharma eeig - nivolumab - melanoma; hodgkin disease; carcinoma, renal cell; carcinoma, non-small-cell lung; carcinoma, transitional cell; squamous cell carcinoma of head and neck; urologic neoplasms; mesothelioma; colorectal neoplasms - antineoplastiske midler - melanomaopdivo as monotherapy or in combination with ipilimumab is indicated for the treatment of advanced (unresectable or metastatic) melanoma in adults and adolescents 12 years of age and older. relative to nivolumab monotherapy, an increase in progression free survival (pfs) and overall survival (os) for the combination of nivolumab with ipilimumab is established only in patients with low tumour pd-l1 expression. adjuvant treatment of melanomaopdivo as monotherapy is indicated for the adjuvant treatment of adults and adolescents 12 years of age and older with melanoma with involvement of lymph nodes or metastatic disease who have undergone complete resection. non-small cell lung cancer (nsclc)opdivo in combination with ipilimumab and 2 cycles of platinum-based chemotherapy is indicated for the first-line treatment of metastatic non-small cell lung cancer in adults whose tumours have no sensitising egfr mutation or alk translocation. opdivo as monotherapy is indicated for the treatment of locally advanced or metastatic non-small cell lung cancer after prior chemotherapy in adults. neoadjuvant treatment of nsclcopdivo in combination with platinum-based chemotherapy is indicated for the neoadjuvant treatment of resectable non-small cell lung cancer at high risk of recurrence in adult patients whose tumours have pd-l1 expression ≥ 1%. malignant pleural mesothelioma (mpm)opdivo in combination with ipilimumab is indicated for the first-line treatment of adult patients with unresectable malignant pleural mesothelioma. neoadjuvant treatment of nsclcopdivo in combination with platinum-based chemotherapy is indicated for the neoadjuvant treatment of resectable non-small cell lung cancer at high risk of recurrence in adult patients whose tumours have pd-l1 expression ≥ 1%. renal cell carcinoma (rcc)opdivo as monotherapy is indicated for the treatment of advanced renal cell carcinoma after prior therapy in adults. opdivo in combination with ipilimumab is indicated for the first-line treatment of adult patients with intermediate/poor risk advanced renal cell carcinoma. opdivo in combination with cabozantinib is indicated for the first-line treatment of adult patients with advanced renal cell carcinoma. classical hodgkin lymphoma (chl)opdivo as monotherapy is indicated for the treatment of adult patients with relapsed or refractory classical hodgkin lymphoma after autologous stem cell transplant (asct) and treatment with brentuximab vedotin. squamous cell cancer of the head and neck (scchn)opdivo as monotherapy is indicated for the treatment of recurrent or metastatic squamous cell cancer of the head and neck in adults progressing on or after platinum based therapy. urothelial carcinomaopdivo as monotherapy is indicated for the treatment of locally advanced unresectable or metastatic urothelial carcinoma in adults after failure of prior platinum containing therapy. adjuvant treatment of urothelial carcinomaopdivo as monotherapy is indicated for the adjuvant treatment of adults with muscle invasive urothelial carcinoma (miuc) with tumour cell pd-l1 expression ≥ 1%, who are at high risk of recurrence after undergoing radical resection of miuc. mismatch repair deficient (dmmr) or microsatellite instability-high (msi-h) colorectal cancer (crc)opdivo in combination with ipilimumab is indicated for the treatment of adult patients with mismatch repair deficient or microsatellite instability-high metastatic colorectal cancer after prior fluoropyrimidine based combination chemotherapy. oesophageal squamous cell carcinoma (oscc)opdivo in combination with ipilimumab is indicated for the first-line treatment of adult patients with unresectable advanced, recurrent or metastatic oesophageal squamous cell carcinoma with tumour cell pd-l1 expression ≥ 1%. opdivo in combination with fluoropyrimidine- and platinum-based combination chemotherapy is indicated for the first-line treatment of adult patients with unresectable advanced, recurrent or metastatic oesophageal squamous cell carcinoma with tumour cell pd-l1 expression ≥ 1%. opdivo as monotherapy is indicated for the treatment of adult patients with unresectable advanced, recurrent or metastatic oesophageal squamous cell carcinoma after prior fluoropyrimidine- and platinum-based combination chemotherapy. adjuvant treatment of oesophageal or gastro-oesophageal junction cancer (oc or gejc)opdivo as monotherapy is indicated for the adjuvant treatment of adult patients with oesophageal or gastro-oesophageal junction cancer who have residual pathologic disease following prior neoadjuvant chemoradiotherapy. gastric, gastro‑oesophageal junction (gej) or oesophageal adenocarcinomaopdivo in combination with fluoropyrimidine- and platinum-based combination chemotherapy is indicated for the first‑line treatment of adult patients with her2‑negative advanced or metastatic gastric, gastro‑oesophageal junction or oesophageal adenocarcinoma whose tumours express pd-l1 with a combined positive score (cps) ≥ 5.

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

leo pharma a/s - takrolimus - dermatitt, atopisk - andre dermatologiske preparater - flare treatmentadults and adolescents (16 years of age and above)treatment of moderate to severe atopic dermatitis in adults who are not adequately responsive to or are intolerant of conventional therapies such as topical corticosteroids. children (two years of age and above)treatment of moderate to severe atopic dermatitis in children (two years of age and above) who failed to respond adequately to conventional therapies such as topical corticosteroids. maintenance treatmentmaintenance treatment of moderate to severe atopic dermatitis for the prevention of flares and the prolongation of flare-free intervals in patients experiencing a high frequency of disease exacerbations (i. forekommer fire ganger eller mer per år) som har hatt et første svar til maksimalt seks uker behandling av to ganger daglig takrolimus salve (lesjoner ryddet, nesten ryddet eller mildt rammet).

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

immedica pharma ab - glycerolfenylbutyrat - ureasyklusforstyrrelser, innfødte - andre alimentary tract and metabolism products, - ravicti er indikert for bruk som adjunctive therapy for kronisk behandling av pasienter med urea-syklus lidelser (ucds) inkludert svekkelse av carbamoyl fosfat-syntase-jeg (cps), ornithine carbamoyltransferase (otc), argininosuccinate synthetase (ass), argininosuccinate lyase (asl), arginase jeg (arg) og ornithine translocase mangel hyperornithinaemia-hyperammonaemia homocitrullinuria syndrom (hhh) som ikke er administrert av kosttilskudd protein begrensning og/eller aminosyre kosttilskudd alene. ravicti må brukes med kosttilskudd protein begrensning og, i noen tilfeller, kosttilskudd (e. , essensielle aminosyrer, arginin, citrullin, proteinfri kalori kosttilskudd).

Norge - norsk - Statens legemiddelverk

leo pharma (2) - kalsipotriolmonohydrat / betametasondipropionat - gel - 50 mikrog/ g / 0.5 mg/ g