Inlyta Evrópusambandið - íslenska - EMA (European Medicines Agency)

inlyta

pfizer europe ma eeig  - axitinib - krabbamein, nýrnafrumur - prótín nt-hemlar - inlyta is indicated for the treatment of adult patients with advanced renal cell carcinoma (rcc) after failure of prior treatment with sunitinib or a cytokine.

Qinlock Evrópusambandið - íslenska - EMA (European Medicines Agency)

qinlock

deciphera pharmaceuticals (netherlands) b.v. - ripretinib - gastrointestinal stromal tumors - Æxlishemjandi lyf - qinlock is indicated for the treatment of adult patients with advanced gastrointestinal stromal tumour (gist) who have received prior treatment with three or more kinase inhibitors, including imatinib.

Duta Tamsaxiro Hart hylki 0,5/0,4 mg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

duta tamsaxiro hart hylki 0,5/0,4 mg

medical valley invest ab - dutasteridum inn; tamsulosinum hýdróklóríð - hart hylki - 0,5/0,4 mg

Zokinvy Evrópusambandið - íslenska - EMA (European Medicines Agency)

zokinvy

eigerbio europe limited - lonafarnib - progeria; laminopathies - Önnur meltingarvegi og efnaskipti vörur, - zokinvy is indicated for the treatment of patients 12 months of age and older with a genetically confirmed diagnosis of hutchinson-gilford progeria syndrome or a processing-deficient progeroid laminopathy associated with either a heterozygous lmna mutation with progerin-like protein accumulation or a homozygous or compound heterozygous zmpste24 mutation.

Spectrabactin Vet Tafla 200 mg/50 mg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

spectrabactin vet tafla 200 mg/50 mg

dechra regulatory b.v. - amoxicillinum tríhýdrat; acidum clavulanicum kalíum - tafla - 200 mg/50 mg

Spectrabactin Vet Tafla 40 mg/10 mg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

spectrabactin vet tafla 40 mg/10 mg

dechra regulatory b.v. - amoxicillinum tríhýdrat; acidum clavulanicum kalíum - tafla - 40 mg/10 mg

Duodart Hart hylki 0,5/0,4 mg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

duodart hart hylki 0,5/0,4 mg

glaxosmithkline pharma a/s - dutasteridum inn; tamsulosinum hýdróklóríð - hart hylki - 0,5/0,4 mg

Abilify Maintena Evrópusambandið - íslenska - EMA (European Medicines Agency)

abilify maintena

otsuka pharmaceutical netherlands b.v. - aripíprazól - geðklofa - psycholeptics - viðhald meðferð geðklofa í fullorðinn sjúklingar stöðug með inntöku sjúklingum.