Európska únia - francúzština - EMA (European Medicines Agency)

abbvie deutschland gmbh co. kg - ombitasvir, paritaprevir, le ritonavir - hépatite c chronique - antiviraux à usage systémique - viekirax est indiqué en association avec d'autres médicaments pour le traitement de l'hépatite c chronique (chc) chez l'adulte. pour le virus de l'hépatite c (vhc) de génotype spécifique de l'activité.

Švajčiarsko - francúzština - Swissmedic (Swiss Agency for Therapeutic Products)

viatris pharma gmbh - emtricitabinum, tenofovirum disoproxilum - comprimés pelliculés - emtricitabinum 200 mg, tenofovirum disoproxilum 245 mg ut tenofoviri disoproxili maleas 300 mg, cellulosum microcristallinum, hydroxypropylcellulosum substitutum humile, silica colloidalis anhydrica, lactosum monohydricum 82.79 mg, magnesii stearas, e 172 (rubrum), Überzug: lactosum monohydricum 10.78 mg, hypromellosum, triacetinum, e 133, e 171, e 172 (flavum), pro compresso obducto. - l'infection à vih - synthetika

Švajčiarsko - francúzština - Swissmedic (Swiss Agency for Therapeutic Products)

viatris pharma gmbh - tenofovirum disoproxilum - comprimés pelliculés - tenofovirum disoproxilum 245 mg ut tenofoviri disoproxili maleas, cellulosum microcristallinum, lactosum monohydricum 150 mg, hydroxypropylcellulosum substitutum humile, silica colloidalis anhydrica, magnesii stearas, Überzug: hypromellosum, lactosum monohydricum 5.04 mg, triacetinum, e 171, e 132, pro compresso obducto. - le vih-infektion, l'hépatite b - synthetika

Európska únia - francúzština - EMA (European Medicines Agency)

abbvie deutschland gmbh & co. kg - risankizumab - psoriasis; arthritis, psoriatic - immunosuppresseurs - plaque psoriasisskyrizi is indicated for the treatment of moderate to severe plaque psoriasis in adults who are candidates for systemic therapy. psoriatic arthritisskyrizi, alone or in combination with methotrexate (mtx), is indicated for the treatment of active psoriatic arthritis in adults who have had an inadequate response or who have been intolerant to one or more disease-modifying antirheumatic drugs (dmards). crohn's diseaseskyrizi is indicated for the treatment of adult patients with moderately to severely active crohn's disease who have had an inadequate response to, lost response to, or were intolerant to conventional therapy or a biologic therapy.

Švajčiarsko - francúzština - Swissmedic (Swiss Agency for Therapeutic Products)

viatris pharma gmbh - efavirenzum, emtricitabinum, tenofovirum disoproxilum - comprimés pelliculés - efavirenzum 600 mg, emtricitabinum 200 mg, tenofovirum disoproxilum 245 mg ut tenofoviri disoproxili maleas, cellulosum microcristallinum, hydroxypropylcellulosum, carmellosum natricum conexum, magnesii stearas, lactosum monohydricum 105.5 mg, silica colloidalis anhydrica, e 172 (rubrum), e 223 7.5 mg, Überzug: poly(alcohol vinylicus), macrogolum 3350, talcum, e 171, e 172 (rubrum), e 172 (flavum), pro compresso obducto corresp. natrium 1.28 mg. - infection vih-1 - synthetika

Európska únia - francúzština - EMA (European Medicines Agency)

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

Belgicko - francúzština - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

eg sa-nv - rivaroxaban 2,5 mg - comprimé pelliculé - rivaroxaban

Európska únia - francúzština - EMA (European Medicines Agency)

bayer ag - rivaroxaban - arthroplasty, replacement; venous thromboembolism - agents antithrombotiques - xarelto, co-administré avec de l'acide acétylsalicylique (aas), seul ou à l'aspirine-clopidogrel ou de la ticlopidine, est indiqué pour la prévention de athérothrombotique événements chez les patients adultes après un syndrome coronarien aigu (sca) avec élévation des biomarqueurs cardiaques. 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. prévention de la thromboembolie veineuse (tev) chez les patients adultes subissant une chirurgie élective de remplacement de la hanche ou du genou. le traitement de la thrombose veineuse profonde (tvp) et l'embolie pulmonaire (ep) et prévention des récidives de tvp et l'ep chez les adultes. 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.

Kanada - francúzština - Health Canada

alexion pharma gmbh - sébélipase alfa - solution - 2mg - sébélipase alfa 2mg - enzymes

Švajčiarsko - francúzština - OFAG-BLW (Bundesamt für Landwirtschaft)

andermatt biogarten ag - huile de paraffine - alliquide destiné à être utilisé sans dilution - 1.2 %12 g/l; - insecticide ;