यूरोपीय संघ - डेनिश - EMA (European Medicines Agency)

medac gesellschaft für klinische spezialpräparate mbh - pemetrexed - carcinoma, non-small-cell lung; mesothelioma - folic acid analogues, antineoplastic agents - malignt pleura mesotheliom pemetrexed medac i kombination med cisplatin er indiceret til behandling af kemoterapi-naive patienter med inoperabel malignt pleura mesotheliom. ikke-småcellet lungekræft pemetrexed medac i kombination med cisplatin er angivet for den første linje behandling af patienter med lokalt fremskreden eller metastatisk ikke-småcellet lungekræft andre end overvejende planocellulært histologi. pemetrexed medac er angivet som monoterapi til vedligeholdelse behandling af lokalt avanceret eller metastatisk ikke-småcellet lungekræft andre end overvejende planocellulært histologi hos patienter, hvis sygdom ikke har udviklet sig som følger umiddelbart efter platin-baseret kemoterapi. pemetrexed medac er angivet som monoterapi for den anden linje behandling af patienter med lokalt fremskreden eller metastatisk ikke-småcellet lungekræft andre end overvejende planocellulært histologi.

यूरोपीय संघ - डेनिश - EMA (European Medicines Agency)

sandoz gmbh - pemetrexed dinatriumhemipentahydrat - carcinoma, non-small-cell lung; mesothelioma - antineoplastiske midler - malignt pleura mesotheliom, pemetrexed, sandoz i kombination med cisplatin er indiceret til behandling af kemoterapi-naive patienter med inoperabel malignt pleura mesotheliom. ikke-småcellet lungekræft pemetrexed sandoz i kombination med cisplatin er angivet for den første linje behandling af patienter med lokalt fremskreden eller metastatisk ikke-småcellet lungekræft andre end overvejende planocellulært histologi. pemetrexed sandoz er angivet som monoterapi til vedligeholdelse behandling af lokalt avanceret eller metastatisk ikke-småcellet lungekræft andre end overvejende planocellulært histologi hos patienter, hvis sygdom ikke har udviklet sig som følger umiddelbart efter platin-baseret kemoterapi. pemetrexed sandoz er angivet som monoterapi for den anden linje behandling af patienter med lokalt fremskreden eller metastatisk ikke-småcellet lungekræft andre end overvejende planocellulært histologi.

यूरोपीय संघ - डेनिश - EMA (European Medicines Agency)

krka d.d. - pemetrexed dinatrium - carcinoma, non-small-cell lung; mesothelioma - antineoplastiske midler - malignt pleura mesotheliomapemetrexed krka i kombination med cisplatin er indiceret til behandling af kemoterapi-naive patienter med inoperabel malignt pleura mesotheliom. ikke-småcellet lungekræft cancerpemetrexed krka i kombination med cisplatin er angivet for den første linje behandling af patienter med lokalt fremskreden eller metastatisk ikke-småcellet lungekræft andre end overvejende planocellulært histologi. pemetrexed krka er angivet som monoterapi til vedligeholdelse behandling af lokalt avanceret eller metastatisk ikke-småcellet lungekræft andre end overvejende planocellulært histologi hos patienter, hvis sygdom ikke har udviklet sig som følger umiddelbart efter platin-baseret kemoterapi. pemetrexed krka er angivet som monoterapi for den anden linje behandling af patienter med lokalt fremskreden eller metastatisk ikke-småcellet lungekræft andre end overvejende planocellulært histologi.

डेनमार्क - डेनिश - Lægemiddelstyrelsen (Danish Medicines Agency)

filavie sas - kanin haemorrhagisk virus (rhdv2), variant stamme lp.sv.2012 (variant 2010, rhdv2) (inaktiveret) - injektionsvæske, suspension - små gnavere (f.eks. kaniner)

यूरोपीय संघ - डेनिश - EMA (European Medicines Agency)

intervet international b.v. - levende fugleinfektiøs bronkitisvirus, stamme d388 - live viral vaccines, domestic fowl - kylling - til aktiv immunisering af kyllinger for at reducere respiratoriske tegn på aviær infektiøs bronkitis forårsaget af qx-lignende varianter af infektiøs bronkitisvirus.

यूरोपीय संघ - डेनिश - EMA (European Medicines Agency)

orion corporation - levodopa, carbidopa, entakapon - parkinsons sygdom - anti-parkinson-lægemidler - corbilta er indiceret til behandling af voksne patienter med parkinsons sygdom og motoriske udsving i slutningen af ​​dosis, der ikke stabiliseres ved behandling med levodopa / dopa decarboxylase (ddc).

यूरोपीय संघ - डेनिश - EMA (European Medicines Agency)

orion corporation - levodopa, carbidopa, entakapon - parkinsons sygdom - nervesystem - levodopa/carbidopa/entacapone orion er indiceret til behandling af voksne patienter med parkinsons sygdom og slutningen af dosis motor udsving ikke stabiliseret på levodopa / dopa-decarboxylase (ddc)-inhibitor behandling.

यूरोपीय संघ - डेनिश - EMA (European Medicines Agency)

orion corporation - levodopa, carbidopa, entakapon - parkinsons sygdom - anti-parkinson-lægemidler - stalevo er indiceret til behandling af voksne patienter med parkinsons sygdom og motoriske udsving i slutningen af ​​dosis, der ikke stabiliseres ved behandling med levodopa / dopa-decarboxylase (ddc) -inhibitor.

यूरोपीय संघ - डेनिश - EMA (European Medicines Agency)

photonamic gmbh & co. kg - 5-aminolevulinsyrehydrochlorid - gliom - antineoplastiske midler - gliolan er indiceret hos voksne patienter til visualisering af malignt væv under operationen for malignt gliom (verdenssundhedsorganisation iii og iv).

यूरोपीय संघ - डेनिश - 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.