OxyNorm Dispersa (OxyNorm) Munndreifitafla 20 mg Islande - islandais - LYFJASTOFNUN (Icelandic Medicines Agency)

oxynorm dispersa (oxynorm) munndreifitafla 20 mg

mundipharma a/s - oxycodonum hýdróklóríð - munndreifitafla - 20 mg

OxyNorm Dispersa (OxyNorm) Munndreifitafla 5 mg Islande - islandais - LYFJASTOFNUN (Icelandic Medicines Agency)

oxynorm dispersa (oxynorm) munndreifitafla 5 mg

mundipharma a/s - oxycodonum hýdróklóríð - munndreifitafla - 5 mg

Targin Forðatafla 10 mg /5 mg Islande - islandais - LYFJASTOFNUN (Icelandic Medicines Agency)

targin forðatafla 10 mg /5 mg

mundipharma a/s - oxycodonum hýdróklóríð; naloxonum hýdróklóríð - forðatafla - 10 mg /5 mg

Targin Forðatafla 20 mg /10 mg Islande - islandais - LYFJASTOFNUN (Icelandic Medicines Agency)

targin forðatafla 20 mg /10 mg

mundipharma a/s - oxycodonum hýdróklóríð; naloxonum hýdróklóríð - forðatafla - 20 mg /10 mg

Targin Forðatafla 40 mg/20 mg Islande - islandais - 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 Islande - islandais - LYFJASTOFNUN (Icelandic Medicines Agency)

targin forðatafla 5 mg/2,5 mg

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

Quadramet Union européenne - islandais - EMA (European Medicines Agency)

quadramet

cis bio international - samarium (153sm) lexidronam pentasodium - pain; cancer - heilsueyðandi lyf - quadramet er ætlað til léttir á bein sársauka í sjúklinga með mörgum sársaukafullt beinmyndun beinagrind meinvörp sem taka upp teknetín [99mtc]-merkt biphosphonates á bein skanna. nærveru beinmyndun meinvörp sem taka upp teknetín [99mtc]-merkt biphosphonates ætti að vera staðfest áður en meðferð.

Ytracis Union européenne - islandais - 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.

Lutetium (177Lu) chloride Billev (previously Illuzyce) Union européenne - islandais - EMA (European Medicines Agency)

lutetium (177lu) chloride billev (previously illuzyce)

billev pharma aps - lutetium (177lu) chloride - radionuclide imaging - heilsueyðandi lyf - lutetium (177lu) chloride billev is a radiopharmaceutical precursor, and it is not intended for direct use in patients. it is to be used only for the radiolabelling of carrier molecules that have been specifically developed and authorised for radiolabelling with lutetium (177lu) chloride.

Synthadon vet. Stungulyf, lausn 10 mg/ml Islande - islandais - LYFJASTOFNUN (Icelandic Medicines Agency)

synthadon vet. stungulyf, lausn 10 mg/ml

le vet beheer b.v. - methadonum hýdróklóríð - stungulyf, lausn - 10 mg/ml