الاتحاد الأوروبي -
الأيسلاندية -
EMA (European Medicines Agency)
lokelma
astrazeneca ab - járn sirkon cyclosilicate - blóðkalíumlækkun - Öll önnur lækningavörur - lokelma er ætlað fyrir meðferð hyperkalaemia í fullorðinn sjúklingar.
الاتحاد الأوروبي -
الأيسلاندية -
EMA (European Medicines Agency)
ytracis
cis bio international - yttrium (90y) chloride - radionuclide imaging - greining geislavirkja - aðeins má nota til geislamerktar flutningsfrumeindanna sem hafa verið sérstaklega þróuð og leyfð til geislamerktar með þessu radionuklíði. radiopharmaceutical precursor - not intended for direct application to patients.
أيسلندا -
الأيسلاندية -
LYFJASTOFNUN (Icelandic Medicines Agency)
norspan forðaplástur 10 míkróg/klst.
mundipharma a/s - buprenorphinum inn - forðaplástur - 10 míkróg/klst.
أيسلندا -
الأيسلاندية -
LYFJASTOFNUN (Icelandic Medicines Agency)
norspan forðaplástur 20 míkróg/klst.
mundipharma a/s - buprenorphinum inn - forðaplástur - 20 míkróg/klst.
أيسلندا -
الأيسلاندية -
LYFJASTOFNUN (Icelandic Medicines Agency)
norspan forðaplástur 5 míkróg/klst.
mundipharma a/s - buprenorphinum inn - forðaplástur - 5 míkróg/klst.
الاتحاد الأوروبي -
الأيسلاندية -
EMA (European Medicines Agency)
bevespi aerosphere
astrazeneca ab - glycopyrronium, formoterol fumarate dihydrate - lungnasjúkdómur, langvarandi hindrandi - formóteróli og þannig brómíð - bevespi aerosphere er ætlað sem viðhald berkjuvíkkandi meðferð til að létta einkenni í fullorðinn sjúklinga með langvinn veikindi í lungum (llt).
أيسلندا -
الأيسلاندية -
LYFJASTOFNUN (Icelandic Medicines Agency)
dropizol (dropium) dropar til inntöku, lausn 10 mg/ml
pharmanovia a/s - opium - dropar til inntöku, lausn - 10 mg/ml
الاتحاد الأوروبي -
الأيسلاندية -
EMA (European Medicines Agency)
zimbus breezhaler
novartis europharm limited - glycopyrronium bromide, indacaterol (acetate), mometasone furoate - astma - lyf til veikindi öndunarvegi sjúkdómum, - maintenance treatment of asthma in adults whose disease is not adequately controlled.
الاتحاد الأوروبي -
الأيسلاندية -
EMA (European Medicines Agency)
pedmarqsi
fennec pharmaceuticals (eu) limited - sodium thiosulfate - ear diseases; ototoxicity - Öll önnur lækningavörur - pedmarqsi is indicated for the prevention of ototoxicity induced by cisplatin chemotherapy in patients 1 month to < 18 years of age with localised, non-metastatic, solid tumours.
الاتحاد الأوروبي -
الأيسلاندية -
EMA (European Medicines Agency)
sugammadex mylan
mylan ireland limited - sugammadex sodium - taugakerfi - Öll önnur lækningavörur - reversal of neuromuscular blockade induced by rocuronium or vecuronium in adults. for the paediatric population: sugammadex is only recommended for routine reversal of rocuronium induced blockade in children and adolescents aged 2 to 17 years.