Kyntheum Europese Unie - Nederlands - EMA (European Medicines Agency)

kyntheum

leo pharma a/s - brodalumab - psoriasis - immunosuppressiva - kyntheum is geïndiceerd voor de behandeling van matige tot ernstige plaque psoriasis bij volwassen patiënten die in aanmerking komen voor systemische therapie.

Spevigo Europese Unie - Nederlands - EMA (European Medicines Agency)

spevigo

boehringer ingelheim international gmbh - spesolimab - psoriasis - immunosuppressiva - spevigo is indicated for the treatment of flares in adult patients with generalised pustular psoriasis (gpp) as monotherapy.

VSM Schüssler zout No.14 Kalium bromatum D6 tabletten Nederland - Nederlands - CBG-MEB (College ter Beoordeling van Geneesmiddelen)

vsm schüssler zout no.14 kalium bromatum d6 tabletten

vsm geneesmiddelen b.v. berenkoog 35 1822 bh alkmaar - kalium bromatum d6 - tablet - , , , , , , , , , , , , , , , - datum verstrekking handelsvergunning:09 september 2003

Schüssler zout Nr. 14 Kalium bromatum D6 TS Products Nederland - Nederlands - CBG-MEB (College ter Beoordeling van Geneesmiddelen)

schüssler zout nr. 14 kalium bromatum d6 ts products

ts products gelreweg 9 3843 an harderwijk - kalium bromatum trit. d6 250 mg/stuk - tablet - , , , , , , , , , , , , , , , , , , , , , , , - datum verstrekking handelsvergunning:23 september 2011

Crysvita Europese Unie - Nederlands - EMA (European Medicines Agency)

crysvita

kyowa kirin holdings b.v. - burosumab - hypophosphatemia, familial; hypophosphatemic rickets, x-linked dominant; osteomalacia - geneesmiddelen voor de behandeling van botziekten - crysvita is indicated for the treatment of x-linked hypophosphataemia, in children and adolescents aged 1 to 17 years with radiographic evidence of bone disease, and in adults. crysvita is indicated for the treatment of fgf23-related hypophosphataemia in tumour-induced osteomalacia associated with phosphaturic mesenchymal tumours that cannot be curatively resected or localised in children and adolescents aged 1 to 17 years and in adults.

Imfinzi Europese Unie - Nederlands - EMA (European Medicines Agency)

imfinzi

astrazeneca ab - durvalumab - carcinoom, niet-kleincellige long - antineoplastische middelen - 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).