Γαλλία - Γαλλικά - ANSM (Agence Nationale de Sécurité du Médicament et des Produits de Santé)

accord healthcare france sas - silodosine - gélule - 4 mg - composition pour une gélule > silodosine : 4 mg - médicaments urologiques, alpha-bloquants

Γαλλία - Γαλλικά - ANSM (Agence Nationale de Sécurité du Médicament et des Produits de Santé)

accord healthcare france sas - silodosine - gélule - 8 mg - composition pour une gélule > silodosine : 8 mg - médicaments urologiques, alpha-bloquants

Βέλγιο - Γαλλικά - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

accord healthcare b.v. - lopinavir 200 mg; ritonavir 50 mg - comprimé pelliculé - lopinavir and ritonavir

Βέλγιο - Γαλλικά - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

accord healthcare b.v. - névirapine anhydre 400 mg - comprimé à libération prolongée - nevirapine

Βέλγιο - Γαλλικά - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

accord healthcare b.v. - ritonavir 100 mg - comprimé pelliculé - ritonavir

Ευρωπαϊκή Ένωση - Γαλλικά - EMA (European Medicines Agency)

accord healthcare s.l.u. - dasatinib - precursor cell lymphoblastic leukemia-lymphoma; leukemia, myelogenous, chronic, bcr-abl positive - agents antinéoplasiques - dasatinib accordpharma is indicated for the treatment of adult patients with: newly diagnosed philadelphia chromosome positive (ph+) chronic myelogenous leukaemia (cml) in the chronic phase.  chronic, accelerated or blast phase cml with resistance or intolerance to prior therapy including imatinib.  ph+ acute lymphoblastic leukaemia (all) and lymphoid blast cml with resistance or intolerance to prior therapy. dasatinib accordpharma is indicated for the treatment of paediatric patients with: newly diagnosed ph+ cml in chronic phase (ph+ cml-cp) or ph+ cml-cp resistant or intolerant to prior therapy including imatinib.  newly diagnosed ph+ all in combination with chemotherapy.

Ευρωπαϊκή Ένωση - Γαλλικά - EMA (European Medicines Agency)

accord healthcare s.l.u. - la tigécycline - soft tissue infections; intraabdominal infections; bacterial infections; skin diseases, infectious - les antibactériens à usage systémique, - tygecycline accord est indiqué chez les adultes et chez les enfants dès l'âge de huit ans pour le traitement des infections suivantes (voir les sections 4. 4 et 5. 1):compliquées de la peau et des tissus mous (cssti), à l'exclusion des infections du pied diabétique (voir la section 4. 4)compliquées intra-abdominales, infections (ciia)tygecycline accord doit être utilisé uniquement dans des situations où d'autres alternatives antibiotiques ne sont pas adaptés (voir les sections 4. 4, 4. 8 et 5. la considération devrait être donnée à des recommandations officielles concernant l'utilisation appropriée des antibactériens.

Ευρωπαϊκή Ένωση - Γαλλικά - EMA (European Medicines Agency)

accord healthcare s.l.u. - rivaroxaban - acute coronary syndrome; coronary artery disease; peripheral arterial disease; venous thromboembolism; stroke; atrial fibrillation; pulmonary embolism - agents antithrombotiques - 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. (see section 4. 4 for haemodynamically unstable pe patients. 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. (see section 4. 4 pour en présentant des répercussions hémodynamiques instables pe malades). 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. 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. (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 et 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. 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. (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.

Ευρωπαϊκή Ένωση - Γαλλικά - EMA (European Medicines Agency)

accord healthcare s.l.u. - icatibant acetate - angioedèmes, héréditaires - other hematological agents - icatibant accord is indicated for symptomatic treatment of acute attacks of hereditary angioedema (hae) in adults, adolescents and children aged 2 years and older, with c1 esterase inhibitor deficiency.

Ευρωπαϊκή Ένωση - Γαλλικά - EMA (European Medicines Agency)

accord healthcare s.l.u. - sitagliptin hydrochloride - diabète sucré, type 2 - les médicaments utilisés dans le diabète - for adult patients with type 2 diabetes mellitus, sitagliptin accord is indicated to improve glycaemic control:as monotherapy:- in patients inadequately controlled by diet and exercise alone and for whom metformin is inappropriate due to contraindications or intolerance. as dual oral therapy in combination with:- metformin when diet and exercise plus metformin alone do not provide adequate glycaemic control. - a sulphonylurea when diet and exercise plus maximal tolerated dose of a sulphonylurea alone do not provide adequate glycaemic control and when metformin is inappropriate due to contraindications or intolerance. - a peroxisome proliferator-activated receptor gamma (ppary) agonist (i. a thiazolidinedione) when use of a ppary agonist is appropriate and when diet and exercise plus the ppary agonist alone do not provide adequate glycaemic control. as triple oral therapy in combination with:- a sulphonylurea and metformin when diet and exercise plus dual therapy with these medicinal products do not provide adequate glycaemic control. - a ppary agonist and metformin when use of a ppary agonist is appropriate and when diet and exercise plus dual therapy with these medicinal products do not provide adequate glycaemic control. sitagliptin accord is also indicated as add-on to insulin (with or without metformin) when diet and exercise plus stable dose of insulin do not provide adequate glycaemic control.