Latvija - latviešu - Zāļu valsts aģentūra

g.l. pharma gmbh, austria - risperidons - apvalkotā tablete - 2 mg

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

laboratorios farmacéuticos rovi, s.a. - risperidons - Šizofrēnija - psihoterapija - treatment of schizophrenia in adults for whom tolerability and effectiveness has been established with oral risperidone.

Latvija - latviešu - Zāļu valsts aģentūra

cto lt uab, lithuania - ibuprofēns - suspensija iekšķīgai lietošanai - 20 mg/ml

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

accord healthcare s.l.u. - rivaroxaban - acute coronary syndrome; coronary artery disease; peripheral arterial disease; venous thromboembolism; stroke; atrial fibrillation; pulmonary embolism - antitrombotiskie līdzekļi - venozās trombembolijas (vte) profilakse pieaugušiem pacientiem, kuriem tiek veikta gēnu vai ceļa locītavas locītavas operācija. Ārstēšana ar dziļo vēnu tromboze (dvt) un plaušu embolija (pe), un novērst atkārtotu dvt un pe pieaugušajiem. (see section 4. 4 for haemodynamically unstable pe patients. Ārstēšana ar dziļo vēnu tromboze (dvt) un plaušu embolija (pe), un novērst atkārtotu dvt un pe pieaugušajiem. (see section 4. 4 haemodynamically nestabila pe pacientiem). adultsprevention of stroke and systemic embolism in adult patients with non valvular atrial fibrillation with one or more risk factors, such as congestive heart failure, hypertension, age ≥ 75 years, diabetes mellitus, prior stroke or transient ischaemic attack. Ārstēšana ar dziļo vēnu tromboze (dvt) un plaušu embolija (pe), un novērst atkārtotu dvt un pe pieaugušajiem. (see section 4. 4 for haemodynamically unstable pe patients. )paediatric populationtreatment of venous thromboembolism (vte) and prevention of vte recurrence in children and adolescents aged less than 18 years and weighing from 30 kg to 50 kg after at least 5 days of initial parenteral anticoagulation treatment. rivaroxaban accord, co administered with acetylsalicylic acid (asa) alone or with asa plus ticlopidine, is indicated for the prevention of atherothrombotic events in adult patients after an acute coronary syndrome (acs) with elevated cardiac biomarkers (see sections 4. 3, 4. 4 un 5. rivaroxaban accord, co administered with acetylsalicylic acid (asa), is indicated for the prevention of atherothrombotic events in adult patients with coronary artery disease (cad) or symptomatic peripheral artery disease (pad) at high risk of ischaemic events. adultsprevention of stroke and systemic embolism in adult patients with non-valvular atrial fibrillation with one or more risk factors, such as congestive heart failure, hypertension, age ≥ 75 years, diabetes mellitus, prior stroke or transient ischaemic attack. Ārstēšana ar dziļo vēnu tromboze (dvt) un plaušu embolija (pe), un novērst atkārtotu dvt un pe pieaugušajiem. (see section 4. 4 for haemodynamically unstable pe patients. )paediatric populationtreatment of venous thromboembolism (vte) and prevention of vte recurrence in children and adolescents aged less than 18 years and weighing more than 50 kg after at least 5 days of initial parenteral anticoagulation treatment.

Latvija - latviešu - Adama

adama - emulsijas koncentrāts - fenpropidīns - fungicīdi

Latvija - latviešu - Adama

adama - emulsijas koncentrāts - fenpropidīns + prohlorazs + tebukonazols - fungicīdi

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

roche registration ltd. - daclizumab - graft rejection; kidney transplantation - imūnsupresanti - zenapax ir indicēts orgānu akūtu atteikuma de novo allogenic nieru transplantācijas profilaksei un ir jālieto kopā ar imunitāti nomācošu režīms, ieskaitot cyclosporine un kortikosteroīdi pacientiem, kuriem nav imunizēti augsti.

Latvija - latviešu - Zāļu valsts aģentūra

aurobindo pharma (malta) limited, malta - gabapentīns - kapsula, cietā - 400 mg

Latvija - latviešu - Zāļu valsts aģentūra

aurobindo pharma (malta) limited, malta - gabapentīns - kapsula, cietā - 300 mg

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

esteve pharmaceuticals gmbh - thiotepa - hematopoietic stem cell transplantation; neoplasms - antineoplastiski līdzekļi - thiotepa riemser is indicated, in combination with other chemotherapy medicinal products:with or without total body irradiation (tbi), as conditioning treatment prior to allogeneic or autologous haematopoietic progenitor cell transplantation (hpct) in haematological diseases in adult and paediatric patients;when high dose chemotherapy with hpct support is appropriate for the treatment of solid tumours in adult and paediatric patients. thiotepa riemser is indicated, in combination with other chemotherapy medicinal products:with or without total body irradiation (tbi), as conditioning treatment prior to allogeneic or autologous haematopoietic progenitor cell transplantation (hpct) in haematological diseases in adult and paediatric patients;when high dose chemotherapy with hpct support is appropriate for the treatment of solid tumours in adult and paediatric patients.