Norwegia - Norwegia - Statens legemiddelverk

ratiopharm gmbh - lovastatin - tablett - 40 mg

Norwegia - Norwegia - Statens legemiddelverk

teva gmbh - fingolimodhydroklorid - kapsel, hard - 0.5 mg

Norwegia - Norwegia - Statens legemiddelverk

teva gmbh - sapropterindihydroklorid - oppløselig tablett - 100 mg

Uni Eropa - Norwegia - EMA (European Medicines Agency)

otsuka pharmaceutical netherlands b.v. - aripiprazol - schizophrenia; bipolar disorder - psykoleptiske - abilify er indisert for behandling av schizofreni hos voksne og hos ungdom i alderen 15 år og eldre. abilify er angitt for behandling av moderate til alvorlige maniske episoder i bipolar jeg uorden og for forebygging av en ny manisk episode i voksne som har opplevd hovedsakelig maniske episoder og som maniske episoder svarte til aripiprazole behandling. abilify er angitt for behandling i inntil 12 uker av moderate til alvorlige maniske episoder i bipolar jeg uorden i ungdom i alderen 13 år og eldre.

Uni Eropa - Norwegia - EMA (European Medicines Agency)

h. lundbeck a/s - nalmefene hydrochloride dihydrat - alkoholrelaterte lidelser - legemidler som brukes i alkoholavhengighet - selincro er indikert for reduksjon av alkoholkonsumet hos voksne pasienter med alkoholavhengighet som har et høyt drikkerisikonivå (se avsnitt 5. 1), uten fysiske tilbakeslagssymptomer, og som ikke krever umiddelbar avgiftning. selincro bør bare forskrives sammen med kontinuerlig psykososial støtte fokusert på behandling tilslutning og redusere alkoholforbruket. selincro bør initieres bare hos pasienter som fortsetter å ha en høy drikke risiko nivå to uker etter den første vurderingen.

Uni Eropa - Norwegia - EMA (European Medicines Agency)

otsuka pharmaceutical netherlands b.v. - brexpiprazole - schizofreni - psykoleptiske - behandling av schizofreni.

Uni Eropa - Norwegia - EMA (European Medicines Agency)

stada arzneimittel ag - teriparatide - osteoporose - kalsiumhomeostase - movymia er indisert hos voksne. behandling av osteoporose hos postmenopausale kvinner og hos menn med økt risiko for brudd. hos postmenopausale kvinner er det vist en signifikant reduksjon i forekomsten av vertebrale og ikke vertebrale frakturer, men ikke hoftefrakturer. behandling av osteoporose assosiert med vedvarende systemisk glukokortikoid terapi hos kvinner og menn med økt risiko for brudd.

Uni Eropa - Norwegia - EMA (European Medicines Agency)

mundipharma corporation (ireland) limited - pegfilgrastim - nøytropeni - immunostimulants, - reduksjon i varigheten av nøytropeni og forekomsten av febril nøytropeni hos voksne pasienter behandlet med cytotoksiske kjemoterapi for kreft (med unntak av kronisk myelogen leukemi og aml syndromer).

Uni Eropa - Norwegia - EMA (European Medicines Agency)

stada arzneimittel ag - bevacizumab - colorectal neoplasms; breast neoplasms; ovarian neoplasms; fallopian tube neoplasms; peritoneal neoplasms; carcinoma, non-small-cell lung; carcinoma, renal cell; uterine cervical neoplasms - antineoplastiske midler - oyavas in combination with fluoropyrimidine based chemotherapy is indicated for treatment of adult patients with metastatic carcinoma of the colon or rectum. oyavas in combination with paclitaxel is indicated for first line treatment of adult patients with metastatic breast cancer. for ytterligere informasjon om human epidermal growth factor receptor 2 (her2) status, se avsnitt 5. oyavas in combination with capecitabine is indicated for first line treatment of adult patients with metastatic breast cancer in whom treatment with other chemotherapy options including taxanes or anthracyclines is not considered appropriate. patients who have received taxane and anthracycline containing regimens in the adjuvant setting within the last 12 months should be excluded from treatment with oyavas in combination with capecitabine. for ytterligere informasjon om her2-status, se avsnitt 5. oyavas, in addition to platinum based chemotherapy, is indicated for first line treatment of adult patients with unresectable advanced, metastatic or recurrent non small cell lung cancer other than predominantly squamous cell histology. oyavas, in combination with erlotinib, is indicated for first line treatment of adult patients with unresectable advanced, metastatic or recurrent non squamous non small cell lung cancer with epidermal growth factor receptor (egfr) activating mutations (see section 5. oyavas in combination with interferon alfa 2a is indicated for first line treatment of adult patients with advanced and/or metastatic renal cell cancer. oyavas, in combination with carboplatin and paclitaxel is indicated for the front line treatment of adult patients with advanced (international federation of gynecology and obstetrics (figo) stages iii b, iii c and iv) epithelial ovarian, fallopian tube, or primary peritoneal cancer (see section 5. oyavas, in combination with carboplatin and gemcitabine or in combination with carboplatin and paclitaxel, is indicated for treatment of adult patients with first recurrence of platinum sensitive epithelial ovarian, fallopian tube or primary peritoneal cancer who have not received prior therapy with bevacizumab or other vegf inhibitors or vegf receptor–targeted agents. oyavas, in combination with topotecan, or pegylated liposomal doxorubicin is indicated for the treatment of adult patients with platinum resistant recurrent epithelial ovarian, fallopian tube, or primary peritoneal cancer who received no more than two prior chemotherapy regimens and who have not received prior therapy with bevacizumab or other vegf inhibitors or vegf receptor targeted agents (see section 5. oyavas, in combination with paclitaxel and cisplatin or, alternatively, paclitaxel and topotecan in patients who cannot receive platinum therapy, is indicated for the treatment of adult patients with persistent, recurrent, or metastatic carcinoma of the cervix (see section 5.

Uni Eropa - Norwegia - EMA (European Medicines Agency)

stada arzneimittel ag - budesonide, micronised - glomerulonephritis, iga - antidiarrheals, intestinal betennelsesdempende / antiinfective agents - kinpeygo is indicated for the treatment of primary immunoglobulin a (iga) nephropathy (igan) in adults at risk of rapid disease progression with a urine protein-to-creatinine ratio (upcr) ≥1. 5 g/gram.