Latvija - latviešu - Zāļu valsts aģentūra

grindeks, as, latvia - azitromicīns - apvalkotā tablete - 500 mg

Latvija - latviešu - Zāļu valsts aģentūra

zaklady farmaceutyczne polpharma s.a., poland - lenalidomīds - kapsula, cietā - 2,5 mg

Latvija - latviešu - Zāļu valsts aģentūra

zaklady farmaceutyczne polpharma s.a., poland - lenalidomīds - kapsula, cietā - 5 mg

Latvija - latviešu - Zāļu valsts aģentūra

zaklady farmaceutyczne polpharma s.a., poland - lenalidomīds - kapsula, cietā - 7,5 mg

Latvija - latviešu - Zāļu valsts aģentūra

zaklady farmaceutyczne polpharma s.a., poland - lenalidomīds - kapsula, cietā - 10 mg

Latvija - latviešu - Zāļu valsts aģentūra

zaklady farmaceutyczne polpharma s.a., poland - lenalidomīds - kapsula, cietā - 15 mg

Latvija - latviešu - Zāļu valsts aģentūra

zaklady farmaceutyczne polpharma s.a., poland - lenalidomīds - kapsula, cietā - 20 mg

Latvija - latviešu - Zāļu valsts aģentūra

zaklady farmaceutyczne polpharma s.a., poland - lenalidomīds - kapsula, cietā - 25 mg

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

amgen europe b.v. - carfilzomib - multiple mieloma - antineoplastiski līdzekļi - kyprolis in combination with daratumumab and dexamethasone, with lenalidomide and dexamethasone, or with dexamethasone alone is indicated for the treatment of adult patients with multiple myeloma who have received at least one prior therapy.

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

amgen europe b.v. - blinatumomab - prekursoru šūnu limfoblastiska leikēmija-limfoma - antineoplastiski līdzekļi - 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. blincyto is indicated as monotherapy for the treatment of paediatric patients aged 1 year or older with philadelphia chromosome negative cd19 positive b precursor all which is refractory or in relapse after receiving at least two prior therapies or in relapse after receiving prior allogeneic haematopoietic stem cell transplantation. blincyto is indicated as monotherapy for the treatment of paediatric 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 (see section 4.