Revastad Filmuhúðuð tafla 20 mg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

revastad filmuhúðuð tafla 20 mg

stada arzneimittel ag - sildenafilum cítrat - filmuhúðuð tafla - 20 mg

Zoloft Filmuhúðuð tafla 100 mg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

zoloft filmuhúðuð tafla 100 mg

upjohn eesv - sertralinum hýdróklóríð - filmuhúðuð tafla - 100 mg

Zoloft Filmuhúðuð tafla 50 mg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

zoloft filmuhúðuð tafla 50 mg

upjohn eesv - sertralinum hýdróklóríð - filmuhúðuð tafla - 50 mg

Zydelig Evrópusambandið - íslenska - EMA (European Medicines Agency)

zydelig

gilead sciences ireland uc - idelalisib - lymphoma, non-hodgkin; leukemia, lymphocytic, chronic, b-cell - antineoplastic agents, other antineoplastic agents - zydelig is indicated in combination with an anti‑cd20 monoclonal antibody (rituximab or ofatumumab) for the treatment of adult patients with chronic lymphocytic leukaemia (cll):who have received at least one prior therapy, oras first line treatment in the presence of 17p deletion or tp53 mutation in patients who are not eligible for any other therapies. zydelig is indicated as monotherapy for the treatment of adult patients with follicular lymphoma (fl) that is refractory to two prior lines of treatment.

Viekirax Evrópusambandið - íslenska - EMA (European Medicines Agency)

viekirax

abbvie deutschland gmbh co. kg - ombitasvir, paritaprevir, rítónavír - lifrarbólga c, langvinn - veirueyðandi lyf til almennrar notkunar - viekirax er ætlað í samsettri meðferð með öðrum lyfjum til meðferðar við langvarandi lifrarbólgu c (chc) hjá fullorðnum. fyrir lifrarbólgu c veira (hcv) arfgerð ákveðna virkni.