Latvija - latviešu - Zāļu valsts aģentūra

unifarma, sia, latvia - sennas ekstrakts - tablete

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

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.

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

bial portela & companhia s.a. - opikapons - parkinsona slimība - anti-parkinsona zāles - ontilyv is indicated as adjunctive therapy to preparations of levodopa/ dopa decarboxylase inhibitors (ddci) in adult patients with parkinson’s disease and end-of-dose motor fluctuations who cannot be stabilised on those combinations.

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

accord healthcare s.l.u. - pleriksafors - multiple myeloma; hematopoietic stem cell transplantation - imunitātes stimulatori, - adult patientsplerixafor accord is indicated in combination with granulocyte-colony stimulating factor (g-csf) to enhance mobilisation of haematopoietic stem cells to the peripheral blood for collection and subsequent autologous transplantation in adult patients with lymphoma or multiple myeloma whose cells mobilise poorly (see section 4. paediatric patients (1 to less than 18 years)plerixafor accord is indicated in combination with g-csf to enhance mobilisation of haematopoietic stem cells to the peripheral blood for collection and subsequent autologous transplantation in children with lymphoma or solid malignant tumours, either:- pre-emptively, when circulating stem cell count on the predicted day of collection after adequate mobilization with g-csf (with or without chemotherapy) is expected to be insufficient with regards to desired hematopoietic stem cells yield, or- who previously failed to collect sufficient haematopoietic stem cells (see section 4.

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

janssen-cilag international n.v. - telaprevir - c hepatīts, hronisks - pretvīrusu līdzekļi sistēmiskai lietošanai - incivo, kopā ar peginterferon alfa un ribavirin, ir indicēts, lai ārstētu genotipa-1 hronisks c hepatīts pieaugušajiem pacientiem ar kompensēta aknu slimības, ieskaitot cirozi):kas ir ārstniecības naivs;kas jau iepriekš ir bijuši ārstēti ar interferonu alfa (pegylated vai ne-pegylated), atsevišķi vai kopā ar ribavirin, tostarp relapsers, daļēja glābējus un null glābējus.

Latvija - latviešu - Zāļu valsts aģentūra

hospira uk limited, united kingdom - meropenēms - pulveris injekciju vai infūziju šķīduma pagatavošanai - 1 g

Latvija - latviešu - Zāļu valsts aģentūra

hospira uk limited, united kingdom - meropenēms - pulveris injekciju vai infūziju šķīduma pagatavošanai - 500 mg

Latvija - latviešu - Zāļu valsts aģentūra

actavis group ptc ehf., iceland - meropenēms - pulveris injekciju vai infūziju šķīduma pagatavošanai - 1 g

Latvija - latviešu - Zāļu valsts aģentūra

accord healthcare b.v., netherlands - meropenēms - pulveris injekciju/infūziju šķīduma pagatavošanai - 1 g

Latvija - latviešu - Zāļu valsts aģentūra

fresenius kabi polska sp.z o.o., poland - meropenēms - pulveris injekciju/infūziju šķīduma pagatavošanai - 500 mg