Den Europæiske Union - dansk - EMA (European Medicines Agency)

amgen europe b.v. - talimogen laherparepvec - melanom - antineoplastiske midler - imlygic er indiceret til behandling af voksne med inoperabel modermærkekræft, regionalt eller fjernt metastatisk (stadie iiib, iiic og ivm1a) med ingen ben, hjerne, lunge eller andre visceral sygdom.

Den Europæiske Union - dansk - EMA (European Medicines Agency)

clinuvel europe limited - afamelanotide - protoporphyria, erytropoietisk - emollients og protectives - forebyggelse af fototoksicitet hos voksne patienter med erytropoietisk protoporphyria (epp).

Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

novartis healthcare a/s - aldesleukin - pulver til injektions-/infusionsvæske, opløsning - 18 mill. ie

Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

aristo pharma gmbh - lamotrigin - tabletter - 25 mg

Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

jubilant pharmaceuticals nv - losartankalium - filmovertrukne tabletter - 100 mg

Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

jubilant pharmaceuticals nv - losartankalium - filmovertrukne tabletter - 50 mg

Den Europæiske Union - dansk - EMA (European Medicines Agency)

pfizer europe ma eeig - ritlecitinib tosilate - alopecia areata - immunosuppressiva - litfulo is indicated for the treatment of severe alopecia areata in adults and adolescents 12 years of age and older.

Danmark - dansk - SEGES Landbrug & Fødevarer

adama northern europe b.v. - tebuconazol, fludioxonil - suspensionskoncentrat - 10 g/l tebuconazol ; 50 g/l fludioxonil

Danmark - dansk - Adama

adama - fludioxonil 50g/l + tebuconacol 10 g/l - bejdsemidler

Den Europæiske Union - dansk - EMA (European Medicines Agency)

bristol-myers squibb pharma eeig - ipilimumab - melanoma; carcinoma, renal cell; carcinoma, non-small-cell lung; mesothelioma, malignant; colorectal neoplasms - antineoplastiske midler - melanomayervoy as monotherapy or combination with nivolumab is indicated for the treatment of advanced (unresectable or metastatic) melanoma in adults and adolescents 12 years of age and older (see section 4.  yervoy in combination with nivolumab is indicated for the treatment of advanced (unresectable or metastatic) melanoma in adults. 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 (see sections 4. 4 og 5. renal cell carcinoma (rcc)yervoy in combination with nivolumab is indicated for the first-line treatment of adult patients with intermediate/poor-risk advanced renal cell carcinoma (see section 5. non-small cell lung cancer (nsclc)yervoy in combination with nivolumab 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. malignant pleural mesothelioma (mpm)yervoy in combination with nivolumab is indicated for the first-line treatment of adult patients with unresectable malignant pleural mesothelioma. mismatch repair deficient (dmmr) or microsatellite instability-high (msi-h) colorectal cancer (crc)yervoy in combination with nivolumab 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 (see section 5. oesophageal squamous cell carcinoma (oscc)yervoy in combination with nivolumab 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%.