الاتحاد الأوروبي -
الأيسلاندية -
EMA (European Medicines Agency)
litfulo
pfizer europe ma eeig - ritlecitinib tosilate - alopecia areata - Ónæmisbælandi lyf - litfulo is indicated for the treatment of severe alopecia areata in adults and adolescents 12 years of age and older.
الاتحاد الأوروبي -
الأيسلاندية -
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.
الاتحاد الأوروبي -
الأيسلاندية -
EMA (European Medicines Agency)
olumiant
eli lilly nederland b.v. - baricitinib - liðagigt, liðagigt - Ónæmisbælandi lyf - rheumatoid arthritisbaricitinib is indicated for the treatment of moderate to severe active rheumatoid arthritis in adult patients who have responded inadequately to, or who are intolerant to one or more disease modifying anti rheumatic drugs (dmards). olumiant má nota sem einlyfjameðferð eða í samsettri meðferð með metotrexati. atopic dermatitisolumiant is indicated for the treatment of moderate to severe atopic dermatitis in adult and paediatric patients 2 years of age and older who are candidates for systemic therapy. alopecia areatabaricitinib is indicated for the treatment of severe alopecia areata in adult patients (see section 5. juvenile idiopathic arthritisbaricitinib is indicated for the treatment of active juvenile idiopathic arthritis in patients 2 years of age and older who have had an inadequate response or intolerance to one or more prior conventional synthetic or biologic dmards:- polyarticular juvenile idiopathic arthritis (polyarticular rheumatoid factor positive [rf+] or negative [rf-], extended oligoarticular),- enthesitis related arthritis, and- juvenile psoriatic arthritis. baricitinib may be used as monotherapy or in combination with methotrexate.
الاتحاد الأوروبي -
الأيسلاندية -
EMA (European Medicines Agency)
pirsue
zoetis belgium sa - pirlimycin - sýklalyf til notkunar í bláæð - nautgripir - fyrir meðferð vægur kvenna í mjólka kýr vegna gramm-jákvæð kokka næm pirlimycin þar á meðal völdum lífverur eins og Þegar sýkt merkið bit, bæði pensilínasa-jákvæð og pensilínasa-neikvæð, og kóagúlasa-neikvæð stafýlókokkar; streptókokka lífverur þar á meðal læknafélag agalactiae, læknafélag dysgalactiae og streptókokka uberis.
أيسلندا -
الأيسلاندية -
LYFJASTOFNUN (Icelandic Medicines Agency)
benestermycin vet. spenalyf, smyrsli
boehringer ingelheim vetmedica gmbh* - framycetinum súlfat; benethaminum penicillinum inn; penethamate hydroiodide ban - spenalyf, smyrsli
أيسلندا -
الأيسلاندية -
LYFJASTOFNUN (Icelandic Medicines Agency)
copaxone stungulyf, lausn í áfylltri sprautu 40 mg/ml
teva gmbh - glatiramer acetat - stungulyf, lausn í áfylltri sprautu - 40 mg/ml
أيسلندا -
الأيسلاندية -
LYFJASTOFNUN (Icelandic Medicines Agency)
copaxone stungulyf, lausn í áfylltri sprautu 20 mg/ml
teva gmbh - glatiramer acetat - stungulyf, lausn í áfylltri sprautu - 20 mg/ml
أيسلندا -
الأيسلاندية -
LYFJASTOFNUN (Icelandic Medicines Agency)
oxycodone/naloxone alvogen (oxycodone/naloxone ratiopharm) forðatafla 40 mg/20 mg
alvogen ehf. - oxycodonum hýdróklóríð; naloxonum hýdróklóríð - forðatafla - 40 mg/20 mg
أيسلندا -
الأيسلاندية -
LYFJASTOFNUN (Icelandic Medicines Agency)
remurel (brabio 20 mg/ml stungulyf, lausn í áfylltri sprautu) stungulyf, lausn í áfylltri sprautu 20 mg/ml
zentiva k.s.* - glatiramer acetat - stungulyf, lausn í áfylltri sprautu - 20 mg/ml
أيسلندا -
الأيسلاندية -
LYFJASTOFNUN (Icelandic Medicines Agency)
remurel stungulyf, lausn í áfylltri sprautu 40 mg/ml
zentiva k.s.* - glatiramer acetat - stungulyf, lausn í áfylltri sprautu - 40 mg/ml