Europeiska unionen - svenska - EMA (European Medicines Agency)

astrazeneca ab - osimertinib mesilate - carcinom, non-small cell lung - andra antineoplastiska medel, protein kinas-hämmare - 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.

Europeiska unionen - svenska - EMA (European Medicines Agency)

glaxosmithkline (ireland) limited - niraparib (tosilate monohydrate) - fallopian tube neoplasms; peritoneal neoplasms; ovarian neoplasms - antineoplastiska medel - zejula is indicated: , as monotherapy for the maintenance treatment of adult patients with advanced epithelial (figo stages iii and iv) high-grade ovarian, fallopian tube or primary peritoneal cancer who are in response (complete or partial) following completion of first-line platinum-based chemotherapy. , as monotherapy for the maintenance treatment of adult patients with platinum sensitive relapsed high grade serous epithelial ovarian, fallopian tube, or primary peritoneal cancer who are in response (complete or partial) to platinum based chemotherapy.

Europeiska unionen - svenska - EMA (European Medicines Agency)

novartis europharm limited - trametinib - melanom - antineoplastiska medel - melanomatrametinib as monotherapy or in combination with dabrafenib is indicated for the treatment of adult patients with unresectable or metastatic melanoma with a braf v600 mutation (see sections 4. 4 och 5. trametinib monotherapy has not demonstrated clinical activity in patients who have progressed on a prior braf inhibitor therapy (see section 5. adjuvant treatment of melanomatrametinib in combination with dabrafenib is indicated for the adjuvant treatment of adult patients with stage iii melanoma with a braf v600 mutation, following complete resection. icke-småcellig lungcancer (nsclc)trametinib i kombination med dabrafenib är indicerat för behandling av vuxna patienter med avancerad icke-småcellig lungcancer med braf v600-mutation.

Europeiska unionen - svenska - EMA (European Medicines Agency)

roche registration gmbh - cobimetinibhemifumarat - melanom - antineoplastiska medel - cotellic är indicerat för användning i kombination med vemurafenib för behandling av vuxna patienter med oreceptabelt eller metastatiskt melanom med en braf v600-mutation.

Europeiska unionen - svenska - EMA (European Medicines Agency)

novartis europharm limited - dabrafenib mesilate - melanom - antineoplastiska medel - melanomadabrafenib as monotherapy or in combination with trametinib is indicated for the treatment of adult patients with unresectable or metastatic melanoma with a braf v600 mutation (see sections 4. 4 och 5. adjuvant behandling av melanomadabrafenib i kombination med trametinib är indicerat för adjuvant behandling av vuxna patienter med stadium iii melanom med braf v600-mutation, följande komplett resektion. non-small cell lung cancer (nsclc)dabrafenib in combination with trametinib is indicated for the treatment of adult patients with advanced non-small cell lung cancer with a braf v600 mutation.

Europeiska unionen - svenska - EMA (European Medicines Agency)

daiichi sankyo europe gmbh - quizartinib dihydrochloride - leukemi, myeloid, akut - antineoplastiska medel - behandling av akut myeloisk leukemi.

Europeiska unionen - svenska - EMA (European Medicines Agency)

daiichi sankyo europe gmbh - quizartinib dihydrochloride - leukemi, myeloid - antineoplastic agents, protein kinase inhibitors - vanflyta is indicated in combination with standard cytarabine and anthracycline induction and standard cytarabine consolidation chemotherapy, followed by vanflyta single-agent maintenance therapy for adult patients with newly diagnosed acute myeloid leukaemia (aml) that is flt3-itd positive.

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

ebb medical ab - itrakonazol - kapsel, hård - 100 mg - itrakonazol 100 mg aktiv substans; sockersfärer hjälpämne

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

janssen-cilag ab - itrakonazol - oral lösning - 10 mg/ml - hydroxipropylbetadex hjälpämne; itrakonazol 10 mg aktiv substans; sorbitol hjälpämne; propylenglykol hjälpämne - itrakonazol

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

janssen-cilag ab - itrakonazol - kapsel, hård - 100 mg - itrakonazol 100 mg aktiv substans; sockersfärer hjälpämne - itrakonazol