Ísland -
íslenska -
LYFJASTOFNUN (Icelandic Medicines Agency)
centyl með kaliumklorid filmuhúðuð tafla 2,5 mg+573 mg
karo pharma ab* - bendroflumethiazidum inn; kalii chloridum - filmuhúðuð tafla - 2,5 mg+573 mg
Ísland -
íslenska -
LYFJASTOFNUN (Icelandic Medicines Agency)
centyl mite með kaliumklorid filmuhúðuð tafla 1,25 mg/573 mg
karo pharma ab* - kalii chloridum; bendroflumethiazidum inn - filmuhúðuð tafla - 1,25 mg/573 mg
Ísland -
íslenska -
LYFJASTOFNUN (Icelandic Medicines Agency)
darazíð tafla 20 mg/12,5 mg
actavis group ptc ehf. - enalaprilum maleat; hydrochlorothiazidum inn - tafla - 20 mg/12,5 mg
Evrópusambandið -
íslenska -
EMA (European Medicines Agency)
mekinist
novartis europharm limited - trametinib - melanoma - Æxlishemjandi lyf - melanomatrametinib as monotherapy or in combination with dabrafenib is indicated for the treatment of adult patients with unresectable or metastatic melanoma with a braf v600 mutation (see sections 4. 4 og 5. trametinib monotherapy has not demonstrated clinical activity in patients who have progressed on a prior braf inhibitor therapy (see section 5. adjuvant treatment of melanomatrametinib in combination with dabrafenib is indicated for the adjuvant treatment of adult patients with stage iii melanoma with a braf v600 mutation, following complete resection. ekki lítinn klefa lungnakrabbamein (nsclc)trametinib ásamt dabrafenib er ætlað fyrir meðferð fullorðinn sjúklinga með langt ekki lítið klefi lungnakrabbamein með meÐferÐ v600 stökkbreytingu.
Evrópusambandið -
íslenska -
EMA (European Medicines Agency)
koselugo
astrazeneca ab - selumetinib sulfate - neurofibromatosis 1 - Æxlishemjandi lyf - koselugo as monotherapy is indicated for the treatment of symptomatic, inoperable plexiform neurofibromas (pn) in paediatric patients with neurofibromatosis type 1 (nf1) aged 3 years and above.
Ísland -
íslenska -
LYFJASTOFNUN (Icelandic Medicines Agency)
metadon abcur (metadon novum abcur) tafla 40 mg
abcur ab* - methadonum hýdróklóríð - tafla - 40 mg
Ísland -
íslenska -
LYFJASTOFNUN (Icelandic Medicines Agency)
dexametason abcur tafla 1 mg
abcur ab - dexamethasonum fosfat - tafla - 1 mg
Ísland -
íslenska -
LYFJASTOFNUN (Icelandic Medicines Agency)
dexametason abcur tafla 4 mg
abcur ab - dexamethasonum fosfat - tafla - 4 mg
Ísland -
íslenska -
LYFJASTOFNUN (Icelandic Medicines Agency)
metadon abcur (metadon novum abcur) tafla 10 mg
abcur ab* - methadonum hýdróklóríð - tafla - 10 mg
Ísland -
íslenska -
LYFJASTOFNUN (Icelandic Medicines Agency)
metadon abcur (metadon novum abcur) tafla 20 mg
abcur ab* - methadonum hýdróklóríð - tafla - 20 mg