Aspirin-C 리투아니아 - 리투아니아어 - SMCA (Valstybinė vaistų kontrolės tarnyba)

aspirin-c

limedika, uab - acetilsalicilo rūgštis/askorbo rūgštis - šnypščiosios tabletės - 400 mg/240 mg - acetylsalicylic acid

Agranin 리투아니아 - 리투아니아어 - SMCA (Valstybinė vaistų kontrolės tarnyba)

agranin

ibe pharma, uab - acetilsalicilo rūgštis/paracetamolis/kofeinas - tabletės - 250 mg/250 mg/65 mg - acetylsalicylic acid, comb. with psycholeptics

Aggrenox 리투아니아 - 리투아니아어 - SMCA (Valstybinė vaistų kontrolės tarnyba)

aggrenox

boehringer ingelheim international gmbh - dipiridamolis/acetilsalicilo rūgštis - modifikuoto atpalaidavimo kietosios kapsulės - 200 mg/25 mg - combinations

Citramon phs 리투아니아 - 리투아니아어 - SMCA (Valstybinė vaistų kontrolės tarnyba)

citramon phs

corpus medica, uab - acetilsalicilo rūgštis/paracetamolis/kofeinas - tabletės - 240 mg/180 mg/30 mg - salicylic acid and derivatives

Citramonas forte L 리투아니아 - 리투아니아어 - SMCA (Valstybinė vaistų kontrolės tarnyba)

citramonas forte l

pharmaswiss Česká republika s.r.o. - acetilsalicilo rūgštis/paracetamolis/kofeinas - tabletės - 240 mg/300 mg/27,46 mg; 240 mg/180 mg/27,46 mg - salicylic acid and derivatives

Febrisan 리투아니아 - 리투아니아어 - SMCA (Valstybinė vaistų kontrolės tarnyba)

febrisan

takeda pharma as - paracetamolis/askorbo rūgštis/fenilefrinas - šnypštieji milteliai - 750 mg/60 mg/10 mg - acetylsalicylic acid, comb. excl. psycholeptics

Possia 유럽 연합 - 리투아니아어 - EMA (European Medicines Agency)

possia

astrazeneca ab - ticagrelor - peripheral vascular diseases; acute coronary syndrome - antitromboziniai vaistai - possia vartojant kartu su acetilsalicilo rūgštimi (asr), vartojamas aterotrombozės reiškinių profilaktikai suaugusiems pacientams, sergantiems ūminių koronarinių sindromų (nestabilios krūtinės anginos, miokardo infarkto st pakilimo [nstemi] arba st-pakilimo prevencija miokardo infarkto [stemi]); pacientų valdomos mediciniškai, ir tie, kurie yra tvarkomi su perkutaninė koronarinė intervencija (pki) arba vainikinių arterijų apylankos persodinimas (cabg).

Rivaroxaban Accord 유럽 연합 - 리투아니아어 - EMA (European Medicines Agency)

rivaroxaban accord

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.

Rivaroxaban Viatris (previously Rivaroxaban Mylan) 유럽 연합 - 리투아니아어 - EMA (European Medicines Agency)

rivaroxaban viatris (previously rivaroxaban mylan)

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.

Clopidogrel Acino 유럽 연합 - 리투아니아어 - EMA (European Medicines Agency)

clopidogrel acino

acino ag - klopidogrelis - peripheral vascular diseases; acute coronary syndrome; myocardial infarction; stroke - antitromboziniai vaistai - clopidogrel is indicated in adults for the prevention of atherothrombotic events in: , , , patients suffering from myocardial infarction (from a few days until less than 35 days), ischaemic stroke (from 7 days until less than 6 months) or established peripheral arterial disease, non-st segment elevation acute coronary syndrome (unstable angina or non-q-wave myocardial infarction), including patients undergoing a stent placement following percutaneous coronary intervention, in combination with acetylsalicylic acid (asa), st segment elevation acute myocardial infarction, in combination with asa in medically treated patients eligible for thrombolytic therapy, patients suffering from acute coronary syndrome. , ,.