Venezuela - español - Instituto Nacional de Higiene

laboratorios leti, s.a.v. - ticlopidina clorhidrato - gragea - 250 mg

Venezuela - español - Instituto Nacional de Higiene

laboratorios giempi, c.a - ticlopidina clorhidrato - comprimido recubierto - 250 mg

Venezuela - español - Instituto Nacional de Higiene

laboratorios klinos, c.a. - ticlopidina clorhidrato - comprimido - 250 mg

Unión Europea - español - EMA (European Medicines Agency)

bayer ag - rivaroxaban - arthroplasty, replacement; venous thromboembolism - agentes antitrombóticos - xarelto, co-administrado con ácido acetilsalicílico (aas), solos o con aas más clopidogrel o ticlopidina, está indicado para la prevención de eventos aterotrombóticos en pacientes adultos después de un síndrome coronario agudo (sca) con elevación de biomarcadores cardiacos. xarelto, 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. prevención del tromboembolismo venoso (tev) en pacientes adultos sometidos a cirugía electiva de reemplazo de cadera o rodilla. tratamiento de la trombosis venosa profunda (tvp) y embolia pulmonar (pe), y la prevención de la recurrencia de la tvp y de la ep en los adultos. 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. 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.