Lacosamide Krka Filmuhúðuð tafla 100 mg Izland - izlandi - LYFJASTOFNUN (Icelandic Medicines Agency)

lacosamide krka filmuhúðuð tafla 100 mg

krka, d.d., novo mesto - lacosamidum inn - filmuhúðuð tafla - 100 mg

Lacosamide Krka Filmuhúðuð tafla 200 mg Izland - izlandi - LYFJASTOFNUN (Icelandic Medicines Agency)

lacosamide krka filmuhúðuð tafla 200 mg

krka, d.d., novo mesto - lacosamidum inn - filmuhúðuð tafla - 200 mg

Lacosamide Krka Filmuhúðuð tafla 50 mg Izland - izlandi - LYFJASTOFNUN (Icelandic Medicines Agency)

lacosamide krka filmuhúðuð tafla 50 mg

krka, d.d., novo mesto - lacosamidum inn - filmuhúðuð tafla - 50 mg

Adcetris Európai Unió - izlandi - EMA (European Medicines Agency)

adcetris

takeda pharma a/s - brentuximab vedotin - lymphoma, non-hodgkin; hodgkin disease - Æxlishemjandi lyf - hodgkin lymphomaadcetris is indicated for adult patients with previously untreated cd30+ stage iv hodgkin lymphoma (hl) in combination with doxorubicin, vinblastine and dacarbazine (avd). adcetris is indicated for the treatment of adult patients with cd30+ hl at increased risk of relapse or progression following autologous stem cell transplant (asct). adcetris is indicated for the treatment of adult patients with relapsed or refractory cd30+ hodgkin lymphoma (hl):following asct, orfollowing at least two prior therapies when asct or multi-agent chemotherapy is not a treatment option. systemic anaplastic large cell lymphomaadcetris in combination with cyclophosphamide, doxorubicin and prednisone (chp) is indicated for adult patients with previously untreated systemic anaplastic large cell lymphoma (salcl). adcetris is indicated for the treatment of adult patients with relapsed or refractory salcl. cutaneous t cell lymphomaadcetris is indicated for the treatment of adult patients with cd30+ cutaneous t cell lymphoma (ctcl) after at least 1 prior systemic therapy.

Bronchitol Európai Unió - izlandi - EMA (European Medicines Agency)

bronchitol

pharmaxis europe limited - mannitól - cystic fibrosis - hósti og kuldablöndur - bronchitol er ætlað til meðferðar við blöðrubólgu (cf) hjá fullorðnum 18 ára og eldri sem viðbótarmeðferð við bestu umönnun.

Nulojix Európai Unió - izlandi - EMA (European Medicines Agency)

nulojix

bristol-myers squibb pharma eeig - belatacept - graft rejection; kidney transplantation - Ónæmisbælandi lyf - nulojix, in combination with corticosteroids and a mycophenolic acid (mpa), is indicated for prophylaxis of graft rejection in adult recipients of a renal transplant.

Nerfasin vet. Stungulyf, lausn 100 mg/ml Izland - izlandi - LYFJASTOFNUN (Icelandic Medicines Agency)

nerfasin vet. stungulyf, lausn 100 mg/ml

le vet b.v.* - xylazinum hýdróklóríð - stungulyf, lausn - 100 mg/ml

Symbicort forte Turbuhaler Innöndunarduft 320/9 míkróg/skammt Izland - izlandi - LYFJASTOFNUN (Icelandic Medicines Agency)

symbicort forte turbuhaler innöndunarduft 320/9 míkróg/skammt

astrazeneca a/s - budesonidum inn; formoterolum fúmarat - innöndunarduft - 320/9 míkróg/skammt

Symbicort mite Turbuhaler Innöndunarduft 80/4,5 míkróg/skammt Izland - izlandi - LYFJASTOFNUN (Icelandic Medicines Agency)

symbicort mite turbuhaler innöndunarduft 80/4,5 míkróg/skammt

astrazeneca a/s - budesonidum inn; formoterolum fúmarat - innöndunarduft - 80/4,5 míkróg/skammt

Symbicort Turbuhaler Innöndunarduft 160/4,5 míkróg/skammt Izland - izlandi - LYFJASTOFNUN (Icelandic Medicines Agency)

symbicort turbuhaler innöndunarduft 160/4,5 míkróg/skammt

astrazeneca a/s - budesonidum inn; formoterolum fúmarat - innöndunarduft - 160/4,5 míkróg/skammt