Israel - English - Ministry of Health

amgen europe b.v. - apremilast - film coated tablets - apremilast 20 mg - apremilast - otezla is indicated:- for treatment of adult patients with active psoriatic arthritis (psa).- for adult patients with moderate to severe plaque psoriasis who are candidates for phototherapy or systemic therapy (psor).- for the treatment of adult patients with oral ulcers associated with behçet’s disease (bd).

Israel - English - Ministry of Health

amgen europe b.v. - apremilast - film coated tablets - apremilast 20 mg - apremilast - otezla is indicated:- for treatment of adult patients with active psoriatic arthritis (psa).- for adult patients with moderate to severe plaque psoriasis who are candidates for phototherapy or systemic therapy (psor).- for the treatment of adult patients with oral ulcers associated with behçet’s disease (bd).

Israel - English - Ministry of Health

amgen europe b.v. - apremilast - film coated tablets - apremilast 20 mg - apremilast - otezla is indicated:- for treatment of adult patients with active psoriatic arthritis (psa).- for adult patients with moderate to severe plaque psoriasis who are candidates for phototherapy or systemic therapy (psor).- for the treatment of adult patients with oral ulcers associated with behçet’s disease (bd).

Israel - English - Ministry of Health

amgen europe b.v. - apremilast - film coated tablets - apremilast 30 mg - apremilast - otezla is indicated:- for treatment of adult patients with active psoriatic arthritis (psa).- for adult patients with moderate to severe plaque psoriasis who are candidates for phototherapy or systemic therapy (psor).- for the treatment of adult patients with oral ulcers associated with behçet’s disease (bd).

Israel - English - Ministry of Health

amgen europe b.v. - apremilast - film coated tablets - apremilast 30 mg - apremilast - otezla is indicated:- for treatment of adult patients with active psoriatic arthritis (psa).- for adult patients with moderate to severe plaque psoriasis who are candidates for phototherapy or systemic therapy (psor).- for the treatment of adult patients with oral ulcers associated with behçet’s disease (bd).

Israel - English - Ministry of Health

amgen europe b.v. - apremilast - film coated tablets - apremilast 30 mg - apremilast - otezla is indicated:- for treatment of adult patients with active psoriatic arthritis (psa).- for adult patients with moderate to severe plaque psoriasis who are candidates for phototherapy or systemic therapy (psor).- for the treatment of adult patients with oral ulcers associated with behçet’s disease (bd).

Israel - English - Ministry of Health

amgen europe b.v. - apremilast - film coated tablets - apremilast 30 mg - apremilast - otezla is indicated:- for treatment of adult patients with active psoriatic arthritis (psa).- for adult patients with moderate to severe plaque psoriasis who are candidates for phototherapy or systemic therapy (psor).- for the treatment of adult patients with oral ulcers associated with behçet’s disease (bd).

Israel - English - Ministry of Health

amgen europe b.v. - apremilast - film coated tablets - apremilast 30 mg - apremilast - otezla is indicated:- for treatment of adult patients with active psoriatic arthritis (psa).- for adult patients with moderate to severe plaque psoriasis who are candidates for phototherapy or systemic therapy (psor).- for the treatment of adult patients with oral ulcers associated with behçet’s disease (bd).

Israel - English - Ministry of Health

amgen europe b.v. - apremilast - film coated tablets - apremilast 30 mg - apremilast - otezla is indicated:- for treatment of adult patients with active psoriatic arthritis (psa).- for adult patients with moderate to severe plaque psoriasis who are candidates for phototherapy or systemic therapy (psor).- for the treatment of adult patients with oral ulcers associated with behçet’s disease (bd).

Israel - English - Ministry of Health

amgen europe b.v. - blinatumomab - powder for concentrate for solution for infusion - blinatumomab 35 mcg / 1 vial - blinatumomab - • blincyto is indicated as monotherapy for the treatment of adults with cd19 positive relapsed or refractory b- precursor acute lymphoblastic leukaemia (all). patients with philadelphia chromosome positive b-precursor all should have failed treatment with at least 2 tyrosine kinase inhibitors (tkis) and have no alternative treatment options.• blincyto is indicated as monotherapy for the treatment of adults with philadelphia chromosome negative cd19 positive b-precursor all in first or second complete remission with minimal residual disease (mrd) greater than or equal to 0.1%.• blincyto is indicated as monotherapy for the treatment of pediatric patients aged 1 year or older with philadelphia chromosome negative cd19 positive b-cell precursor all which is refractory or in relapse after receiving at least two prior therapies or in relapse after receiving prior allogeneic hematopoietic stem cell transplantation.• blincyto is indicated as monotherapy for the treatment of pediatric patients aged 1 year or older with high-risk first relapsed philadelphia chromosome negative cd19 positive b precursor all as part of the consolidation therapy.limitations of use: after failure of two previous treatments and with no cns involvement.