dailiport hart forðahylki 5 mg
sandoz a/s - tacrolimus monohydrate; tacrolimus - hart forðahylki - 5 mg
dailiport hart forðahylki 0,5 mg
sandoz a/s - tacrolimus monohydrate; tacrolimus - hart forðahylki - 0,5 mg
dailiport hart forðahylki 1 mg
sandoz a/s - tacrolimus monohydrate; tacrolimus - hart forðahylki - 1 mg
dailiport hart forðahylki 2 mg
sandoz a/s - tacrolimus; tacrolimus monohydrate - hart forðahylki - 2 mg
dailiport hart forðahylki 3 mg
sandoz a/s - tacrolimus monohydrate; tacrolimus - hart forðahylki - 3 mg
veraloc retard forðatafla 200 mg
orion corporation - verapamilum hýdróklóríð - forðatafla - 200 mg
isoptin retard forðatafla 120 mg
viatris aps - verapamilum hýdróklóríð - forðatafla - 120 mg
bosulif
pfizer europe ma eeig - bosutinib (sem einhýdrat) - kyrningahvítblæði, mergbólga - antineoplastic agents, protein kinase inhibitors - bosulif er ætlað fyrir meðferð fullorðinn sjúklinga með:nýlega‑greind langvarandi áfanga (aÐili) philadelphia litning-jákvæð langvarandi myelogenous hvítblæði (ph+ cml). aÐili, flýta áfanga (ap), og sprengja áfanga (bp) ph+ cml áður meðhöndluð með einn eða fleiri týrósín nt hemil(s) [tki(s)] og fyrir hvern imatinib, nilotinib og dasatinib eru ekki talin viðeigandi meðferð valkosti.
dronedarone stada (verodron) filmuhúðuð tafla 400 mg
stada arzneimittel ag - dronedaronum hýdróklóríð - filmuhúðuð tafla - 400 mg
venclyxto
abbvie deutschland gmbh co. kg - venetoclax - kyrningahvítblæði, eitilfrumnafæð, langvarandi, b-frumur - Æxlishemjandi lyf - venclyxto in combination with obinutuzumab is indicated for the treatment of adult patients with previously untreated chronic lymphocytic leukaemia (cll) (see section 5. venclyxto in combination with rituximab is indicated for the treatment of adult patients with cll who have received at least one prior therapy. venclyxto monotherapy is indicated for the treatment of cll:- in the presence of 17p deletion or tp53 mutation in adult patients who are unsuitable for or have failed a b cell receptor pathway inhibitor, or- in the absence of 17p deletion or tp53 mutation in adult patients who have failed both chemoimmunotherapy and a b-cell receptor pathway inhibitor. venclyxto in combination with a hypomethylating agent is indicated for the treatment of adult patients with newly diagnosed acute myeloid leukaemia (aml) who are ineligible for intensive chemotherapy.