Camcevi Evrópusambandið - íslenska - EMA (European Medicines Agency)

camcevi

accord healthcare s.l.u. - leuprorelin mesilate - blöðruhálskirtli - innkirtla meðferð - camcevi is indicated for the treatment of hormone dependent advanced prostate cancer and for the treatment of high-risk localised and locally advanced hormone dependent prostate cancer in combination with radiotherapy.

Firmagon Evrópusambandið - íslenska - EMA (European Medicines Agency)

firmagon

ferring pharmaceuticals a/s - degarelix - blöðruhálskirtli - innkirtla meðferð - firmagon is a gonadotrophin releasing hormone (gnrh) antagonist indicated:- for treatment of adult male patients with advanced hormone-dependent prostate cancer. - for treatment of high-risk localised and locally advanced hormone dependent prostate cancer in combination with radiotherapy. - as neo-adjuvant treatment prior to radiotherapy in patients with high-risk localised or locally advanced hormone dependent prostate cancer.

Degarelix Accord Evrópusambandið - íslenska - EMA (European Medicines Agency)

degarelix accord

accord healthcare s.l.u. - degarelix acetate - blöðruhálskirtli - other hormone antagonists and related agents - degarelix accord is a gonadotrophin releasing hormone (gnrh) antagonist indicated:for treatment of adult male patients with advanced hormone-dependent prostate cancer. for treatment of high-risk localised and locally advanced hormone dependent prostate cancer in combination with radiotherapy. as neo-adjuvant treatment prior to radiotherapy in patients with high-risk localised or locally advanced hormone dependent prostate cancer.

Cuprymina Evrópusambandið - íslenska - EMA (European Medicines Agency)

cuprymina

a.c.o.m. - advanced center oncology - kopar (64cu) klóríð - radionuclide imaging - various diagnostic radiopharmaceuticals - cuprymina er geislavirka forvera. Það er ekki ætlað til beinnar notkunar hjá sjúklingum. Þetta lyf verður einungis notað fyrir geislamerktu flutningsameindir, sem hafa verið sérstaklega þróaðir og leyfð til geislamerktar með þessu radionuklíði.

Pylclari Evrópusambandið - íslenska - EMA (European Medicines Agency)

pylclari

curium pet france - piflufolastat (18f) - blöðruhálskirtli - greining geislavirkja - Þetta lyf er eingöngu ætlað til greiningar. pylclari is indicated for the detection of prostate-specific membrane antigen (psma) positive lesions with positron emission tomography (pet) in adults with prostate cancer (pca) in the following clinical settings:primary staging of patients with high-risk pca prior to initial curative therapy,to localize recurrence of pca in patients with a suspected recurrence based on increasing serum prostate-specific antigen (psa) levels after primary treatment with curative intent. pylclari is indicated for use with positron emission tomography (pet).

Adasuve Evrópusambandið - íslenska - EMA (European Medicines Agency)

adasuve

ferrer internacional s.a. - loxapín - schizophrenia; bipolar disorder - taugakerfi - adasuve er ætlað til að stjórna hraðri stjórn á væga til í meðallagi æsing hjá fullorðnum sjúklingum með geðklofa eða geðhvarfasýki. sjúklingar ættu að fá reglulega meðferð strax eftir að hafa fengið bráða æsandi einkenni.

Crysvita Evrópusambandið - íslenska - EMA (European Medicines Agency)

crysvita

kyowa kirin holdings b.v. - burosumab - hypophosphatemia, familial; hypophosphatemic rickets, x-linked dominant; osteomalacia - lyf til að meðhöndla beinsjúkdóma - 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.

Remodulin Innrennslislyf, lausn 1 mg/ml Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

remodulin innrennslislyf, lausn 1 mg/ml

ferrer internacional s.a. - treprostinilum natríum - innrennslislyf, lausn - 1 mg/ml

Remodulin Innrennslislyf, lausn 10,0 mg/ml Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

remodulin innrennslislyf, lausn 10,0 mg/ml

ferrer internacional s.a. - treprostinilum natríum - innrennslislyf, lausn - 10,0 mg/ml

Remodulin Innrennslislyf, lausn 2,5 mg/ml Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

remodulin innrennslislyf, lausn 2,5 mg/ml

ferrer internacional s.a. - treprostinilum natríum - innrennslislyf, lausn - 2,5 mg/ml