Union européenne - français - EMA (European Medicines Agency)

sanofi b.v. - sevelamer - renal dialysis; hyperphosphatemia - tous les autres produits thérapeutiques - renagel is indicated for the control of hyperphosphataemia in adult patients receiving  haemodialysis or peritoneal dialysis. renagel should be used within the context of a multiple therapeutic approach, which could include calcium supplements, 1,25 - dihydroxy vitamin d3 or one of its analogues to control the development of renal bone disease.

Union européenne - français - EMA (European Medicines Agency)

sanofi winthrop industrie - dupilumab - dermatitis, atopic; prurigo; esophageal diseases; asthma; sinusitis - agents contre la dermatite, à l'exclusion des corticostéroïdes - atopic dermatitisadults and adolescentsdupixent is indicated for the treatment of moderate-to-severe atopic dermatitis in adults and adolescents 12 years and older who are candidates for systemic therapy. children 6 months to 11 years of agedupixent is indicated for the treatment of severe atopic dermatitis in children 6 months to 11 years old who are candidates for systemic therapy. asthmaadults and adolescentsdupixent is indicated in adults and adolescents 12 years and older as add-on maintenance treatment for severe asthma with type 2 inflammation characterised by raised blood eosinophils and/or raised fraction of exhaled nitric oxide (feno), see section 5. 1, who are inadequately controlled with high dose inhaled corticosteroids (ics) plus another medicinal product for maintenance treatment. children 6 to 11 years of agedupixent is indicated in children 6 to 11 years old as add-on maintenance treatment for severe asthma with type 2 inflammation characterised by raised blood eosinophils and/or raised fraction of exhaled nitric oxide (feno), who are inadequately controlled with medium to high dose inhaled corticosteroids (ics) plus another medicinal product for maintenance treatment. chronic rhinosinusitis with nasal polyposis (crswnp)dupixent is indicated as an add-on therapy with intranasal corticosteroids for the treatment of adults with severe crswnp for whom therapy with systemic corticosteroids and/or surgery do not provide adequate disease control. prurigo nodularis (pn)dupixent is indicated for the treatment of adults with moderate-to-severe prurigo nodularis (pn) who are candidates for systemic therapy. eosinophilic esophagitis (eoe)dupixent is indicated for the treatment of eosinophilic esophagitis in adults and adolescents 12 years and older, weighing at least 40 kg, who are inadequately controlled by, are intolerant to, or who are not candidates for conventional medicinal therapy.

Union européenne - français - EMA (European Medicines Agency)

sanofi b.v. - avalglucosidase alfa - maladie de stockage de glycogène type ii - d'autres tractus digestif et le métabolisme des produits, - nexviadyme (avalglucosidase alfa) is indicated for long-term enzyme replacement therapy for the treatment of patients with pompe disease (acid α-glucosidase deficiency).

Union européenne - français - EMA (European Medicines Agency)

sanofi b.v. - olipudase alfa - acid sphingomyelinase deficiency (asmd) type a/b or type b - d'autres tractus digestif et le métabolisme des produits, - xenpozyme is indicated as an enzyme replacement therapy for the treatment of non-central nervous system (cns) manifestations of acid sphingomyelinase deficiency (asmd) in paediatric and adult patients with type a/b or type b.

France - français - ANSM (Agence Nationale de Sécurité du Médicament et des Produits de Santé)

sanofi aventis france - paracétamol - poudre - 125 mg - composition pour un sachet-dose > paracétamol : 125 mg

Union européenne - français - EMA (European Medicines Agency)

sanofi winthrop industrie - tériflunomide - sclérose en plaque - immunosuppresseurs sélectifs - aubagio is indicated for the treatment of adult patients and paediatric patients aged 10 years and older with relapsing remitting multiple sclerosis (ms) (please refer to section 5. 1 for important information on the population for which efficacy has been established).

Union européenne - français - EMA (European Medicines Agency)

sanofi winthrop industrie - clopidogrel, acetylsalicylic acid - acute coronary syndrome; myocardial infarction - agents antithrombotiques - duoplavin est indiqué pour la prévention secondaire des événements athérothrombotiques chez les patients adultes qui prennent déjà du clopidogrel et de l'acide acétylsalicylique (aas). duoplavin is a fixed-dose combination medicinal product for continuation of therapy in: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 (pci);st segment elevation acute myocardial infarction (stemi) in patients undergoing a stent placement) or medically treated patients eligible for thrombolytic/fibrinolytic therapy. pour de plus amples informations, veuillez vous reporter à la section 5.

Union européenne - français - EMA (European Medicines Agency)

sanofi winthrop industrie - clopidogrel - stroke; peripheral vascular diseases; atrial fibrillation; myocardial infarction; acute coronary syndrome - agents antithrombotiques - la prévention secondaire de athérothrombotique eventsclopidogrel est indiqué pour le traitement:les patients adultes souffrant d'un infarctus du myocarde (de quelques jours jusqu'à moins de 35 jours), d'accident vasculaire cérébral ischémique (à partir de 7 jours jusqu'à moins de 6 mois) ou établis, la maladie artérielle périphérique. les patients adultes souffrant d'un syndrome coronaire aigu:non-élévation du segment st de syndrome coronaire aigu (angor instable ou sans onde q infarctus du myocarde), y compris les patients subissant une pose de l'endoprothèse suivant l'intervention coronarienne percutanée, en combinaison avec l'acide acétylsalicylique (aas). st segment elevation acute myocardial infarction, in combination with asa in patients undergoing percutaneous coronary intervention (including patients undergoing a stent placement) or medically treated patients eligible for thrombolytic/fibrinolytic therapy. in patients with moderate to high-risk transient ischemic attack (tia) or minor ischemic 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. la prévention de athérothrombotique et événements thromboemboliques dans la fibrillationin patients adultes atteints de fibrillation auriculaire qui ont au moins un facteur de risque d'événements vasculaires, ne sont pas appropriés pour un traitement par antagonistes de la vitamine k (vka) et qui ont un faible risque d'hémorragie, le clopidogrel est indiqué en association avec l'aspirine dans la prévention de athérothrombotique et des événements thromboemboliques, y compris les avc.

Union européenne - français - EMA (European Medicines Agency)

sanofi winthrop industrie - lixisénatide - diabète sucré, type 2 - drugs used in diabetes, glucagon-like peptide-1 (glp-1) analogues - lyxumia is indicated for the treatment of adults with type 2 diabetes mellitus to achieve glycaemic control in combination with oral glucose lowering medicinal products and/or basal insulin when these, together with diet and exercise, do not provide adequate glycaemic control.

Union européenne - français - EMA (European Medicines Agency)

sanofi winthrop industrie - sulfate d'hydrogène de clopidogrel - stroke; peripheral vascular diseases; atrial fibrillation; myocardial infarction; acute coronary syndrome - agents antithrombotiques - secondary prevention of atherothrombotic eventsclopidogrel is indicated in:adult patients suffering from myocardial infarction (from a few days until less than 35 days), ischaemic stroke (from seven days until less than six 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 patients undergoing percutaneous coronary intervention (including patients undergoing a stent replacement) or medically treated patients eligible for thrombolytic/fibrinolytic therapy. in patients with moderate to high-risk transient ischemic attack (tia) or minor ischemic 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. la prévention de athérothrombotique et événements thromboemboliques dans la fibrillationin patients adultes atteints de fibrillation auriculaire qui ont au moins un facteur de risque d'événements vasculaires, ne sont pas adaptés pour le traitement avec de la vitamine-k antagonistes et qui ont un faible risque d'hémorragie, le clopidogrel est indiqué en association avec l'aspirine dans la prévention de athérothrombotique et des événements thromboemboliques, y compris les avc.