Fluoxetin WH Hart hylki 20 mg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

fluoxetin wh hart hylki 20 mg

williams & halls ehf - fluoxetine hydrochloride - hart hylki - 20 mg

Elonva Evrópusambandið - íslenska - EMA (European Medicines Agency)

elonva

n.v. organon - corifollitropin alfa - reproductive techniques, assisted; ovulation induction; investigative techniques - hormón kynlíf og stillum kynfæri - controlled ovarian stimulation (cos) in combination with a gnrh antagonist for the development of multiple follicles in women participating in an assisted reproductive technology (art) program. elonva is indicated for the treatment of adolescent males (14 to less than 18 years and older) with hypogonadotropic hypogonadism, in combination with human chorionic gonadotropin (hcg).

Bimzelx Evrópusambandið - íslenska - EMA (European Medicines Agency)

bimzelx

ucb pharma s.a.   - bimekizumab - psoriasis - Ónæmisbælandi lyf - plaque psoriasisbimzelx is indicated for the treatment of moderate to severe plaque psoriasis in adults who are candidates for systemic therapy. psoriatic arthritisbimzelx, alone or in combination with methotrexate, is indicated for the treatment of active psoriatic arthritis in adults who have had an inadequate response or who have been intolerant to one or more disease-modifying antirheumatic drugs (dmards). axial spondyloarthritisnon-radiographic axial spondyloarthritis (nr-axspa)bimzelx is indicated for the treatment of adults with active non-radiographic axial spondyloarthritis with objective signs of inflammation as indicated by elevated c-reactive protein (crp) and/or magnetic resonance imaging (mri) who have responded inadequately or are intolerant to non-steroidal anti-inflammatory drugs (nsaids). ankylosing spondylitis (as, radiographic axial spondyloarthritis)bimzelx is indicated for the treatment of adults with active ankylosing spondylitis who have responded inadequately or are intolerant to conventional therapy.

Raplixa Evrópusambandið - íslenska - EMA (European Medicines Agency)

raplixa

mallinckrodt pharmaceuticals ireland limited - mannafíbrógen manna, trombín manna - hemostasis, skurðaðgerð - antihemorrhagics - stuðningsmeðferð þar sem venjulegar skurðaðgerðir eru ekki nægjanlegar til að bæta blóðflæði. raplixa verður að nota í ásamt samþykkt gelatín svampur. raplixa er ætlað í fullorðnir yfir 18 ára aldri.

Soolantra Krem 10 mg/g Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

soolantra krem 10 mg/g

galderma nordic ab - ivermectinum inn - krem - 10 mg/g

Daivobet Hlaup 50 míkróg/g /0,5 mg/g Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

daivobet hlaup 50 míkróg/g /0,5 mg/g

leo pharma a/s* - calcipotriolum inn; betamethasonum díprópíónat - hlaup - 50 míkróg/g /0,5 mg/g

Aklief Krem 50 míkróg/g Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

aklief krem 50 míkróg/g

galderma nordic ab - trifarotenum - krem - 50 míkróg/g

Elidel Krem 1 % Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

elidel krem 1 %

viatris aps - pimecrolimusum inn - krem - 1 %

Dexametason Abcur Tafla 1 mg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

dexametason abcur tafla 1 mg

abcur ab - dexamethasonum fosfat - tafla - 1 mg

Dexametason Abcur Tafla 4 mg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

dexametason abcur tafla 4 mg

abcur ab - dexamethasonum fosfat - tafla - 4 mg