Targin Forðatafla 40 mg/20 mg Islàndia - islandès - LYFJASTOFNUN (Icelandic Medicines Agency)

targin forðatafla 40 mg/20 mg

mundipharma a/s - oxycodonum hýdróklóríð; naloxonum hýdróklóríð - forðatafla - 40 mg/20 mg

Targin Forðatafla 5 mg/2,5 mg Islàndia - islandès - LYFJASTOFNUN (Icelandic Medicines Agency)

targin forðatafla 5 mg/2,5 mg

mundipharma a/s - oxycodonum hýdróklóríð; naloxonum hýdróklóríð - forðatafla - 5 mg/2,5 mg

Qaialdo Unió Europea - islandès - EMA (European Medicines Agency)

qaialdo

nova laboratories ireland limited - spironolactone - edema; heart failure; liver cirrhosis; ascites; nephrotic syndrome; hyperaldosteronism; essential hypertension - antihypertensives and diuretics in combination - in the management of refractory oedema associated with congestive cardiac failure; hepatic cirrhosis with ascites and oedema, malignant ascites, nephrotic syndrome, diagnosis and treatment of primary aldosteronism, essential hypertension. neonates, children and adolescents should only be treated under guidance of a paediatric specialist (see sections 5. 1 5.

Posatex Unió Europea - islandès - EMA (European Medicines Agency)

posatex

intervet international bv - orbifloxacin, mometasone furoate, posaconazole - otologicals - hundar - meðferð bráð bólgu í ytra og bráð tilvikum endurteknum bólgu í ytra, tengslum við bakteríum næm orbifloxacin og sveppi næm posaconazole, einkum malassezia pachydermatis.

SomaKit TOC Unió Europea - islandès - EMA (European Medicines Agency)

somakit toc

advanced accelerator applications - edotreótíð - neuroendocrine tumors; radionuclide imaging - greining geislavirkja - Þetta lyf er eingöngu ætlað til greiningar. eftir radiolabelling með gallín (68ga) i lausn, lausn gallín (68ga) edotreotide fæst er ætlað fyrir sneiðmyndatöku losun höfði (gÆludÝr) hugsanlegur somatostatini viðtaka yfirtjáningu í fullorðinn sjúklinga með staðfest eða grun vel þroskað maga-enteropancreatic taugakirtilsuppruna æxli (gep-hrein) fyrir localizing aðal æxli og þeirra meinvörp.

Ngenla Unió Europea - islandès - EMA (European Medicines Agency)

ngenla

pfizer europe ma eeig - somatrogon - growth and development - sterum og undirstÚku hormÓn og hliÐstÆÐum - indicated for the long-term treatment of paediatric patients with growth disturbance due to insufficient secretion of growth hormone.

Cortavance Unió Europea - islandès - EMA (European Medicines Agency)

cortavance

virbac s.a. - hydrocortisone aceponate - barksterar, húðsjúkdómar - hundar - til meðferðar við bólgu og kláða húðhúð hjá hundum. for alleviation of clinical signs associated with atopic dermatitis in dogs.

Easotic Unió Europea - islandès - EMA (European Medicines Agency)

easotic

virbac s.a. - gentamicin sulfate, hydrocortisone aceponate, miconazole nitrate - otologicals, krefur og antiinfectives í samsetning - hundar - meðferð bráð bólgu í ytra, og bráð versnað endurtekin bólgu í ytra tengslum við bakteríum næm gentamísín og sveppi næm miconazol, einkum malassezia pachydermatis.

Trimbow Unió Europea - islandès - EMA (European Medicines Agency)

trimbow

chiesi farmaceutici s.p.a. - beclometasone dipropionate, formóteróli fúmarat tvíhýdrat, Þannig brómíð - lungnasjúkdómur, langvarandi hindrandi - lyf til veikindi öndunarvegi sjúkdómum, - maintenance treatment of asthma, in adults not adequately controlled with a maintenance combination of a long-acting beta2-agonist and high dose of inhaled corticosteroid, and who experienced one or more asthma exacerbations in the previous year. copdmaintenance treatment in adult patients with moderate to severe chronic obstructive pulmonary disease (copd) who are not adequately treated by a combination of an inhaled corticosteroid and a long-acting beta2-agonist or a combination of a long-acting beta2-agonist and a long-acting muscarinic antagonist (for effects on symptoms control and prevention of exacerbations see section 5. asthmamaintenance treatment of asthma, in adults not adequately controlled with a maintenance combination of a long-acting beta2-agonist and medium dose of inhaled corticosteroid, and who experienced one or more asthma exacerbations in the previous year.

Alkindi Unió Europea - islandès - EMA (European Medicines Agency)

alkindi

diurnal europe b.v. - hýdrókortisón - skert nýrnastarfsemi - barksterar til almennrar notkunar - skipti meðferð skammta frekar í börn, börn og unglingar (frá fæðingu að < 18 ára).