Miglustat Dipharma Evropská unie - španělština - EMA (European Medicines Agency)

miglustat dipharma

dipharma arzneimittel gmbh - miglustat - enfermedad de gaucher - otros productos del metabolismo y del tracto alimentario - miglustat dipharma está indicado para el tratamiento oral de pacientes adultos con insuficiencia renal leve a moderado de la enfermedad de gaucher de tipo 1. miglustat dipharma sólo puede ser utilizado en el tratamiento de pacientes en quienes la terapia de reemplazo enzimático no es adecuado. miglustat dipharma está indicado para el tratamiento de la progresiva manifestaciones neurológicas en pacientes adultos y pacientes pediátricos con enfermedad de niemann-pick tipo c de la enfermedad.

Sapropterin Dipharma Evropská unie - španělština - EMA (European Medicines Agency)

sapropterin dipharma

dipharma arzneimittel gmbh - dihidrocloruro de sapropterina - fenilcetonurias - otros tracto alimentario y metabolismo de los productos, - sapropterin dipharma is indicated for the treatment of hyperphenylalaninaemia (hpa) in adults and paediatric patients of all ages with phenylketonuria (pku) who have been shown to be responsive to such treatment. sapropterin dipharma is also indicated for the treatment of hyperphenylalaninaemia (hpa) in adults and paediatric patients of all ages with tetrahydrobiopterin (bh4) deficiency who have been shown to be responsive to such treatment.

CLOPIDOGREL PHARMACIA 75 mg COMPRIMIDOS RECUBIERTOS CON PELICULA EFG Španělsko - španělština - AEMPS (Agencia Española de Medicamentos y Productos Sanitarios)

clopidogrel pharmacia 75 mg comprimidos recubiertos con pelicula efg

pharmacia grupo pfizer, s.l. - clopidogrel - comprimido recubierto con pelÍcula - 75 mg - clopidogrel 75 mg - clopidogrel

ROPINIROL PHARMACIA 1 MG COMPRIMIDOS RECUBIERTOS CON PELICULA EFG Španělsko - španělština - AEMPS (Agencia Española de Medicamentos y Productos Sanitarios)

ropinirol pharmacia 1 mg comprimidos recubiertos con pelicula efg

pharmacia grupo pfizer, s.l. - ropinirol hidrocloruro - excipientes: lactosa monohidrato,croscarmelosa sodica,croscarmelosa sodica - agentes dopaminÉrgicos - agonistas dopaminérgicos - ropinirol

Budesonide/Formoterol Teva Pharma B.V. Evropská unie - španělština - EMA (European Medicines Agency)

budesonide/formoterol teva pharma b.v.

teva pharma b.v. - budesonide, formoterol - asma - medicamentos para la enfermedad obstructiva de las vías respiratorias enfermedades, - budesonida / formoterol teva pharma b. está indicado únicamente en adultos de 18 años de edad o mayores. asthmabudesonide/formoterol teva pharma b. is indicated in the regular treatment of asthma, where use of a combination (inhaled corticosteroid and long-acting β2 adrenoceptor agonist) is appropriate: orin patients not adequately controlled with inhaled corticosteroids and “as needed” inhaled short-acting β2 adrenoceptor agonists. in patients already adequately controlled on both inhaled corticosteroids and long-acting β2 adrenoceptor agonists.

Clopidogrel Taw Pharma (previously Clopidogrel Mylan) Evropská unie - španělština - EMA (European Medicines Agency)

clopidogrel taw pharma (previously clopidogrel mylan)

taw pharma (ireland) limited - clorhidrato de clopidogrel - peripheral vascular diseases; stroke; myocardial infarction; acute coronary syndrome - 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), ischaemic 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). ,     - st segment elevation acute myocardial infarction, in combination with asa in medically treated patients eligible for thrombolytic therapy. , , 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. , , for further information please refer to section 5. , , ,.

Pregabalin Mylan Pharma Evropská unie - španělština - EMA (European Medicines Agency)

pregabalin mylan pharma

mylan s.a.s. - pregabalina - anxiety disorders; neuralgia; epilepsy - los antiepilépticos, - epilepsypregabalin mylan pharma está indicado como terapia adyuvante en pacientes adultos con crisis parciales con o sin generalización secundaria. de ansiedad generalizada disorderpregabalin mylan pharma está indicado para el tratamiento del trastorno de ansiedad generalizada (tag) en adultos.

LEVETIRACETAM KERN PHARMA 100 MG/ML CONCENTRADO SOLUCION PARA PERFUSION EFG Španělsko - španělština - AEMPS (Agencia Española de Medicamentos y Productos Sanitarios)

levetiracetam kern pharma 100 mg/ml concentrado solucion para perfusion efg

kern pharma s.l. - levetiracetam - concentrado para soluciÓn para perfusiÓn - 100 mg/ml - levetiracetam 100 mg - levetiracetam