Pirfenidone Viatris União Europeia - português - EMA (European Medicines Agency)

pirfenidone viatris

viatris limited - pirfenidone - idiopathic pulmonary fibrosis; lung diseases; respiratory tract diseases - imunossupressores - pirfenidone viatris is indicated in adults for the treatment of mild to moderate idiopathic pulmonary fibrosis (ipf).

Dapagliflozin Viatris União Europeia - português - EMA (European Medicines Agency)

dapagliflozin viatris

viatris limited - dapagliflozin - diabetes mellitus, type 2; heart failure, systolic; heart failure; renal insufficiency, chronic - drogas usadas em diabetes - type 2 diabetes mellitusdapagliflozin viatris is indicated in adults and children aged 10 years and above for the treatment of insufficiently controlled type 2 diabetes mellitus as an adjunct to diet and exercise- as monotherapy when metformin is considered inappropriate due to intolerance. - in addition to other medicinal products for the treatment of type 2 diabetes. for study results with respect to combination of therapies, effects on glycaemic control, cardiovascular and renal events, and the populations studied, see sections 4. 4, 4. 5 e 5. heart failuredapagliflozin viatris is indicated in adults for the treatment of symptomatic chronic heart failure with reduced ejection fraction. chronic kidney diseasedapagliflozin viatris is indicated in adults for the treatment of chronic kidney disease.

Clopidogrel Viatris (previously Clopidogrel Taw Pharma) União Europeia - português - EMA (European Medicines Agency)

clopidogrel viatris (previously clopidogrel taw pharma)

viatris limited - clopidogrel besilate - peripheral vascular diseases; stroke; myocardial infarction - agentes antitrombóticos - secondary prevention of atherothrombotic events clopidogrel is indicated in:adult patients suffering from myocardial infarction (from a few days until less than 35 days), ischemic stroke (from 7 days until less than 6 months) or established peripheral arterial disease. adult patients suffering from acute coronary syndrome. 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). segmento st elevação infarto agudo do miocárdio, em combinação com asa em medicamente tratados os pacientes elegíveis para terapia trombolítica. in patients with moderate to high-risk transient ischaemic attack (tia) or minor ischaemic stroke (is) clopidogrel in combination with asa is indicated in:adult patients with moderate to high-risk tia (abcd2 score ≥4) or minor is (nihss ≤3) within 24 hours of either the tia or is event. prevention of atherothrombotic and thromboembolic events in atrial fibrillation:in adult patients with atrial fibrillation who have at least one risk factor for vascular events, are not suitable for treatment with vitamin k antagonists (vka) and who have a low bleeding risk, clopidogrel is indicated in combination with asa for the prevention of atherothrombotic and thromboembolic events, including stroke. para mais informações, por favor consulte a secção 5.

Rivaroxaban Viatris (previously Rivaroxaban Mylan) União Europeia - português - EMA (European Medicines Agency)

rivaroxaban viatris (previously rivaroxaban mylan)

mylan ireland limited - rivaroxaban - venous thromboembolism; pulmonary embolism; acute coronary syndrome; stroke; coronary artery disease; peripheral arterial disease; atrial fibrillation - agentes antitrombóticos - 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.

Aldara União Europeia - português - EMA (European Medicines Agency)

aldara

viatris healthcare limited - imiquimod - condylomata acuminata; keratosis; keratosis, actinic; carcinoma, basal cell - antibióticos e quimioterápicos para uso dermatológico - imiquimod cream is indicated for the topical treatment of :external genital and perianal warts (condylomata acuminata) in adults. small superficial basal cell carcinomas (sbccs) in adults. clinically typical, nonhyperkeratotic, nonhypertrophic actinic keratoses (aks) on the face or scalp in immunocompetent adult patients when size or number of lesions limit the efficacy and/or acceptability of cryotherapy and other topical treatment options are contraindicated or less appropriate.

Cholib União Europeia - português - EMA (European Medicines Agency)

cholib

viatris healthcare limited - fenofibrate, sinvastatina - deslipidemias - agentes modificadores de lipídios - o cholib é indicado como terapia adjuvante para dieta e exercício em pacientes com alto risco cardiovascular em pacientes adultos com dislipidemia mista para reduzir os triglicerídeos e aumentar os níveis de hdl c quando os níveis de ldl c são adequadamente controlados com a dose correspondente de monoterapia com simvastatina.

Mysildecard União Europeia - português - EMA (European Medicines Agency)

mysildecard

viatris limited - citrato de sildenafil - hipertensão, pulmonar - urologia - adultstreatment de pacientes adultos com hipertensão arterial pulmonar classificados como classe funcional ii e iii, para melhorar a capacidade de exercício. a eficácia foi demonstrada na hipertensão pulmonar primária e hipertensão pulmonar associada à doença do tecido conjuntivo. pediátrica populationtreatment de pacientes pediátricos com idades entre 1 ano a 17 anos de idade com hipertensão arterial pulmonar. a eficácia em termos de melhoria da capacidade de exercício ou hemodinâmica pulmonar tem sido demonstrada na hipertensão pulmonar primária e hipertensão pulmonar associada à doença cardíaca congênita (ver seção 5.

Tobi Podhaler União Europeia - português - EMA (European Medicines Agency)

tobi podhaler

viatris healthcare limited - tobramicina - cystic fibrosis; respiratory tract infections - antibacterianos para uso sistémico, - tobi podhaler está indicado para a terapia supressiva de infecção pulmonar crônica por pseudomonas aeruginosa em adultos e crianças com idade igual ou superior a 6 anos com fibrose cística. veja as seções 4. 4 e 5. 1 em relação a diferentes faixas etárias. deve ser tido em consideração a orientação oficial sobre o uso apropriado de agentes antibacterianos..

Talmanco (previously Tadalafil Generics) União Europeia - português - EMA (European Medicines Agency)

talmanco (previously tadalafil generics)

viatris limited - tadalafil - hipertensão, pulmonar - urologia - talmanco é indicado em adultos para o tratamento da hipertensão arterial pulmonar (hap) classificada como classe funcional ii e iii da oms, para melhorar a capacidade de exercício. a eficácia foi demonstrada na pah idiopática (ipah) e na pah relacionada à doença vascular do colágeno.

Tasmar União Europeia - português - EMA (European Medicines Agency)

tasmar

viatris healthcare limited - tolcapone - doença de parkinson - anti-parkinson drogas, outros agentes dopaminérgicos - tasmar é indicado em combinação com levodopa / benserazida ou levodopa / carbidopa para uso em pacientes com doença de parkinson idiopática responsiva com levodopa e flutuações motoras, que não responderam ou são intolerantes a outros inibidores de catecol-o-metiltransferase (comt). devido ao risco de, potencialmente fatal, aguda, lesão hepática, tasmar não deve ser considerado como uma primeira linha de coadjuvante a terapia com levodopa / benserazide ou levodopa / carbidopa. desde tasmar deve ser usado somente em combinação com levodopa / benserazide e levodopa / carbidopa, a informação de prescrição para essas preparações de levodopa também é aplicável para o seu uso concomitante com tasmar.