Fotil 5 mg/ ml / 20 mg/ ml Norge - norsk - Statens legemiddelverk

fotil 5 mg/ ml / 20 mg/ ml

santen oy - timololmaleat / pilokarpinhydroklorid - Øyedråper, oppløsning - 5 mg/ ml / 20 mg/ ml

Fotil Forte 5 mg/ ml / 40 mg/ ml Norge - norsk - Statens legemiddelverk

fotil forte 5 mg/ ml / 40 mg/ ml

santen oy - timololmaleat / pilokarpinhydroklorid - Øyedråper, oppløsning - 5 mg/ ml / 40 mg/ ml

Fotil Forte 5 mg/ ml / 40 mg/ ml Norge - norsk - Statens legemiddelverk

fotil forte 5 mg/ ml / 40 mg/ ml

santen oy - timololmaleat / pilokarpinhydroklorid - Øyedråper, oppløsning i endosebeholder - 5 mg/ ml / 40 mg/ ml

Mannitol Baxter Viaflo 150 mg/ ml Norge - norsk - Statens legemiddelverk

mannitol baxter viaflo 150 mg/ ml

baxter medical ab - mannitol - infusjonsvæske, oppløsning - 150 mg/ ml

Robinul-Neostigmin 0.5 mg/ ml / 2.5 mg/ ml Norge - norsk - Statens legemiddelverk

robinul-neostigmin 0.5 mg/ ml / 2.5 mg/ ml

viatris as - glykopyrroniumbromid / neostigminmetylsulfat - injeksjonsvæske, oppløsning - 0.5 mg/ ml / 2.5 mg/ ml

Tetravac Norge - norsk - Statens legemiddelverk

tetravac

sanofi pasteur europe - difteritoksoid / clostridium tetani, toksoid / pertussistoksoid / filamentøst hemagglutinin / poliovirus type 1, inaktivert / poliovirus type 2, inaktivert / poliovirus type 3, inaktivert - injeksjonsvæske, suspensjon - 30 ie/ sprøyte / 40 ie/ sprøyte / 25 mikrog/ sprøyte / 25 mikrog/ sprøyte / 40 d-antigen enheter/ sprøyte / 8 d-antigen enheter/

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

imfinzi

astrazeneca ab - durvalumab - karsinom, ikke-småcellet lunge - antineoplastiske midler - non-small cell lung cancer (nsclc)imfinzi as monotherapy is indicated for the treatment of locally advanced, unresectable non small cell lung cancer (nsclc) in adults whose tumours express pd-l1 on ≥ 1% of tumour cells and whose disease has not progressed following platinum based chemoradiation therapy (see section 5. imfinzi in combination with tremelimumab and platinum-based chemotherapy is indicated for the first-line treatment of adults with metastatic nsclc with no sensitising egfr mutations or alk positive mutations. small cell lung cancer (sclc)imfinzi in combination with etoposide and either carboplatin or cisplatin is indicated for the first-line treatment of adults with extensive-stage small cell lung cancer (es-sclc). biliary tract cancer (btc)imfinzi in combination with gemcitabine and cisplatin is indicated for the first line treatment of adults with unresectable or metastatic biliary tract cancer (btc). hepatocellular carcinoma (hcc)imfinzi in combination with tremelimumab is indicated for the first line treatment of adults with advanced or unresectable hepatocellular carcinoma (hcc).

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

portrazza

eli lilly nederland b.v. - necitumumab - karsinom, ikke-småcellet lunge - antineoplastiske midler - portrazza i kombinasjon med gemcitabine og cisplatin kjemoterapi er indisert for behandling av voksne pasienter med lokalt avansert eller metastatisk epidermal vekstfaktor reseptor (egfr) uttrykker squamous ikke-småcellet lungekreft som ikke har mottatt før kjemoterapi for denne tilstanden.

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

imjudo

astrazeneca ab - tremelimumab - carcinoma, hepatocellular - antineoplastiske midler - imjudo in combination with durvalumab is indicated for the first line treatment of adults with advanced or unresectable hepatocellular carcinoma (hcc). imjudo in combination with durvalumab and platinum-based chemotherapy is indicated for the first-line treatment of adults with metastatic non-small cell lung cancer (nsclc) with no sensitising egfr mutations or alk positive mutations.

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

tremelimumab astrazeneca

astrazeneca ab - tremelimumab - karsinom, ikke-småcellet lunge - antineoplastiske midler - tremelimumab astrazeneca in combination with durvalumab and platinum-based chemotherapy is indicated for the first-line treatment of adults with metastatic non-small cell lung cancer (nsclc) with no sensitising egfr mutations or alk positive mutations.