Litva - litovčina - SMCA (Valstybinė vaistų kontrolės tarnyba)

alvogen malta operations (row) ltd. - vinorelbinas - minkštosios kapsulės - 20 mg - vinorelbine

Litva - litovčina - SMCA (Valstybinė vaistų kontrolės tarnyba)

alvogen malta operations (row) ltd. - vinorelbinas - minkštosios kapsulės - 30 mg - vinorelbine

Litva - litovčina - SMCA (Valstybinė vaistų kontrolės tarnyba)

alvogen malta operations (row) ltd. - vinorelbinas - minkštosios kapsulės - 80 mg - vinorelbine

Litva - litovčina - SMCA (Valstybinė vaistų kontrolės tarnyba)

as kalceks - furozemidas - injekcinis ar infuzinis tirpalas - 10 mg/ml - furosemide

Európska únia - litovčina - EMA (European Medicines Agency)

accord healthcare s.l.u. - rivaroksabanas - acute coronary syndrome; coronary artery disease; peripheral arterial disease; venous thromboembolism; stroke; atrial fibrillation; pulmonary embolism - antitromboziniai vaistai - venų tromboembolijos (vte) profilaktika suaugusiems pacientams, kuriems atliekama pasirinktinė klubo ar kelio sąnario pakeitimo operacija. gydant giliųjų venų trombozės (gvt) ir plaučių embolija (pe), prevencijos ir pasikartojančios gvt ir pe suaugusiems. (see section 4. 4 for haemodynamically unstable pe patients. gydant giliųjų venų trombozės (gvt) ir plaučių embolija (pe), prevencijos ir pasikartojančios gvt ir pe suaugusiems. (see section 4. 4 haemodynamically nestabili pe pacientų). 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. gydant giliųjų venų trombozės (gvt) ir plaučių embolija (pe), prevencijos ir pasikartojančios gvt ir pe suaugusiems. (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 ir 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. gydant giliųjų venų trombozės (gvt) ir plaučių embolija (pe), prevencijos ir pasikartojančios gvt ir pe suaugusiems. (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.

Litva - litovčina - SMCA (Valstybinė vaistų kontrolės tarnyba)

pharmsol europe limited - cefazolinas - milteliai injekciniam ar infuziniam tirpalui - 1000 mg - cefazolin

Litva - litovčina - SMCA (Valstybinė vaistų kontrolės tarnyba)

le vet b.v. (nyderlandai) - tabletės - 1 tabletėje yra: veikliosios (-iųjų) medžiagos (-ų): furozemido 10 mg; - hidrotorakso, hidroperikardo, ascito ir edemos, susijusios su širdies nepakankamumu ir inkstų funkcijos sutrikimu, gydymas.

Litva - litovčina - SMCA (Valstybinė vaistų kontrolės tarnyba)

le vet b.v. (nyderlandai) - tabletės - 1 tabletėje yra: veikliosios (-iųjų) medžiagos (-ų): furozemido 40 mg - hidrotorakso, hidroperikardo, ascito ir edemos, susijusios su širdies nepakankamumu ir inkstų funkcijos sutrikimu, gydymas.

Európska únia - litovčina - EMA (European Medicines Agency)

mylan ireland limited - rivaroksabanas - venous thromboembolism; pulmonary embolism; acute coronary syndrome; stroke; coronary artery disease; peripheral arterial disease; atrial fibrillation - antitromboziniai vaistai - rivaroxaban mylan co-administered with acetylsalicylic acid (asa) alone or with asa plus clopidogrel or ticlopidine, is indicated for the prevention of atherothrombotic events in adult patients after an acute coronary syndrome (acs) with elevated cardiac biomarkers.  rivaroxaban mylan 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.  ------prevention of venous thromboembolism (vte) in adult patients undergoing elective hip or knee replacement surgery.  treatment of deep vein thrombosis (dvt) and pulmonary embolism (pe), and prevention of recurrent dvt and pe in adults. -------adults prevention 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. paediatric population treatment 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. paediatric population treatment 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.

Európska únia - litovčina - EMA (European Medicines Agency)

eli lilly nederland b.v. - tirzepatide - cukrinis diabetas, 2 tipas - narkotikai, vartojami diabetu - mounjaro is indicated for the treatment of adults with insufficiently controlled type 2 diabetes mellitus as an adjunct to diet and exercise- as monotherapy when metformin is considered inappropriate due to intolerance or contraindications- in addition to other medicinal products for the treatment of diabetes. for study results with respect to combinations, effects on glycaemic control and the populations studied, see sections 4. 4, 4. 5 ir 5.