Europäische Union - Deutsch - EMA (European Medicines Agency)

sanofi b.v. - plerixafor - multiple myeloma; hematopoietic stem cell transplantation; lymphoma - immunostimulants, - mozobil wird in kombination mit granulozyten-kolonie-stimulierende faktor zur mobilisierung von hämatopoetischen stammzellen in das periphere blut für sammlung und anschließende autologe transplantation bei patienten mit lymphom und multiple verbesserung angegeben. myelom, deren zellen schlecht zu mobilisieren.

Europäische Union - Deutsch - EMA (European Medicines Agency)

sanofi-aventis deutschland gmbh - insulin glargin - diabetes mellitus - drogen bei diabetes verwendet - behandlung von diabetes mellitus bei erwachsenen, jugendlichen und kindern ab dem alter von 6 jahren.

Europäische Union - Deutsch - EMA (European Medicines Agency)

sanofi winthrop industrie - insulin glargine, lixisenatide - diabetes mellitus, typ 2 - drogen bei diabetes verwendet - suliqua is indicated for the treatment of adults with insufficiently controlled type 2 diabetes mellitus to improve glycaemic control as an adjunct to diet and exercise in addition to metformin with or without sglt-2 inhibitors.

Europäische Union - Deutsch - EMA (European Medicines Agency)

sanofi pasteur - influenza a virus subtype h1n1 haemagglutinin, recombinant, influenza a virus subtype h3n2 haemagglutinin, recombinant, influenza b virus victoria lineage haemagglutinin, recombinant, influenza b virus yamagata lineage haemagglutinin, recombinant - influenza, mensch - impfstoffe - supemtek is indicated for active immunization for the prevention of influenza disease in adults. supemtek should be used in accordance with official recommendations.

Europäische Union - Deutsch - EMA (European Medicines Agency)

sanofi b.v. - sutimlimab - hemolysis; anemia, hemolytic, autoimmune - immunsuppressiva - enjaymo is indicated for the treatment of haemolytic anaemia in adult patients with cold agglutinin disease (cad).

Europäische Union - Deutsch - EMA (European Medicines Agency)

sanofi pasteur - neisseria meningitidis group c polysaccharide conjugated to tetanus toxoid, neisseria meningitidis group a polysaccharide conjugated to tetanus toxoid, neisseria meningitidis group y polysaccharide conjugated to tetanus toxoid, neisseria meningitidis group w-135 polysaccharide conjugated to tetanus toxoid - meningitis, meningokokken - impfstoffe - menquadfi is indicated for active immunisation of individuals from the age of 12 months and older against invasive meningococcal disease caused by neisseria meningitidis serogroups a, c, w, and y. the use of this vaccine should be in accordance with available official recommendations.

Europäische Union - Deutsch - EMA (European Medicines Agency)

sanofi pasteur - sars-cov-2 prefusion spike delta tm protein, recombinant (b.1.351 strain) - covid-19 virus infection - impfstoffe - vidprevtyn beta is indicated as a booster for active immunisation to prevent covid-19 in adults who have previously received an mrna or adenoviral vector covid-19 vaccine (see sections 4. 2 und 5. 1 in product information document). der einsatz dieses impfstoffs sollte in übereinstimmung mit den offiziellen empfehlungen.

Schweiz - Deutsch - Swissmedic (Swiss Agency for Therapeutic Products)

sanofi-aventis (suisse) sa - sarilumabum - lösung zur injektion in fertigspritze - sarilumabum 150 mg, histidinum aut histidini hydrochloridum monohydricum, arginini hydrochloridum, saccharum, polysorbatum 20, aqua ad iniectabile q.s. ad solutionem pro 1.14 ml. - rheumatoide arthritis - biotechnologika

Schweiz - Deutsch - Swissmedic (Swiss Agency for Therapeutic Products)

sanofi-aventis (suisse) sa - sarilumabum - lösung zur injektion in fertigspritze - sarilumabum 200 mg, histidinum aut histidini hydrochloridum monohydricum, arginini hydrochloridum, saccharum, polysorbatum 20, aqua ad iniectabile q.s. ad solutionem pro 1.14 ml. - rheumatoide arthritis - biotechnologika

Schweiz - Deutsch - Swissmedic (Swiss Agency for Therapeutic Products)

sanofi-aventis (suisse) sa - sarilumabum - lösung zur injektion in einen stift ausgefüllt - sarilumabum 150 mg, histidinum aut histidini hydrochloridum monohydricum, arginini hydrochloridum, saccharum, polysorbatum 20, aqua ad iniectabile q.s. ad solutionem pro 1.14 ml. - rheumatoide arthritis - biotechnologika