Den europeiske union - norsk - EMA (European Medicines Agency)

novartis europharm limited - vildagliptin, metformin hydrochloride - diabetes mellitus, type 2 - drugs used in diabetes, combinations of oral blood glucose lowering drugs - icandra is indicated as an adjunct to diet and exercise to improve glycaemic control in adults with type 2 diabetes mellitus:in patients who are inadequately controlled with metformin hydrochloride alone. in patients who are already being treated with the combination of vildagliptin and metformin hydrochloride, as separate tablets. in combination with other medicinal products for the treatment of diabetes, including insulin, when these do not provide adequate glycaemic control (see sections 4. 4, 4. 5 og 5. 1 for tilgjengelige data på forskjellige kombinasjoner).

Den europeiske union - norsk - EMA (European Medicines Agency)

glaxosmithkline biologicals s.a. - diphtheria toxoid, tetanus toxoid, bordetella pertussis antigens (pertussis toxoid, filamentous haemagglutinin, pertactin), hepatitis b surface antigen, poliovirus (inactivated) (type-1 (mahoney strain), type-2 (mef-1 strain), type-3 (saukett strain)), haemophilus influenzae type b polysaccharide - hepatitis b; tetanus; immunization; meningitis, haemophilus; whooping cough; poliomyelitis; diphtheria - vaksiner - infanrix hexa er angitt for primær og økte vaksinasjon av barn mot difteri, tetanus, kikhoste, hepatitt b, poliomyelitt og sykdom forårsaket av haemophilus influenzae type-b.

Den europeiske union - norsk - EMA (European Medicines Agency)

novartis europharm limited  - vildagliptin, metformin hydrochloride - diabetes mellitus, type 2 - legemidler som brukes i diabetes - zomarist is indicated as an adjunct to diet and exercise to improve glycaemic control in adults with type 2 diabetes mellitus:in patients who are inadequately controlled with metformin hydrochloride alone. in patients who are already being treated with the combination of vildagliptin and metformin hydrochloride, as separate tablets. in combination with other medicinal products for the treatment of diabetes, including insulin, when these do not provide adequate.

Norge - norsk - Statens legemiddelverk

aj vaccines a/s - difteritoksoid / clostridium tetani, toksoid - injeksjonsvæske, suspensjon i ferdigfylt sprøyte - 2 ie/ dose / 20 ie/ dose

Norge - norsk - Statens legemiddelverk

fresenius kabi norge as - halden - soyaolje, renset / glukosemonohydrat / alanin / arginin / aspartinsyre / glutaminsyre / glysin / histidin / isoleucin / leucin / lysinhydroklorid / metionin / fenylalanin / prolin / serin / treonin / tryptofan / tyrosin / valin / kalsiumkloriddihydrat / natriumglyserofosfat / magnesiumsulfatheptahydrat / kaliumklorid / natriumacetattrihydrat - infusjonsvæske, emulsjon

Norge - norsk - Statens legemiddelverk

merck sharp & dohme b.v. - pneumokokk-polysakkarid serotype 1 / pneumokokk-polysakkarid serotype 2 / pneumokokk-polysakkarid serotype 3 / pneumokokk-polysakkarid serotype 4 / pneumokokk-polysakkarid serotype 5 / pneumokokk-polysakkarid serotype 6b / pneumokokk-polysakkarid serotype 7f / pneumokokk-polysakkarid serotype 8 / pneumokokk-polysakkarid serotype 9n / pneumokokk-polysakkarid serotype 9v / pneumokokk-polysakkarid serotype 10a / pneumokokk-polysakkarid serotype 11a / pneumokokk-polysakkarid serotype 12f / pneumokokk-polysakkarid serotype 14 / pneumokokk-polysakkarid serotype 15b / pneumokokk-polysakkarid serotype 17f / pneumokokk-polysakkarid serotype 18c / pneumokokk-polysakkarid serotype 19f / pneumokokk-polysakkarid serotype 19a / pneumokokk-polysakkarid serotype 20 / pneumokokk-polysakkarid serotype 22f / pneumokokk-polysakkarid serotype 23f / pneumokokk-polysakkarid serotype 33f - injeksjonsvæske, oppløsning i ferdigfylt sprøyte - 25 mikrog/0.5 ml / 25 mikrog/0.5 ml / 25 mikrog/0.5 ml / 25 mikrog/0.5 ml / 25 mikrog/0.5 ml / 25 mikrog/0.5 ml / 25 mikrog/0.5 ml / 25 mikrog/0.5 ml / 25 mikrog/0.5 ml / 25 mikrog/0.5 ml / 25 mikrog/0.5 ml / 25 mikrog/0.5 ml / 25 mikrog/0.5 ml / 25 mikrog/0.5 ml / 25 mikrog/0.5 ml / 25 mikrog/0.5 ml / 25 mikrog/0.5 ml / 25 mikrog/0.5 ml / 25 mikrog/0.5 ml / 25 mikrog/0.5 ml / 25 mikrog/0.5 ml / 25 mikrog/0.5 ml / 25 mikrog/0.5 ml

Norge - norsk - Statens legemiddelverk

baxter medical ab - natriumklorid / kaliumklorid / kalsiumkloriddihydrat / magnesiumkloridheksahydrat / natriumacetattrihydrat - infusjonsvæske, oppløsning - 5.86 g/ l / 0.3 g/ l / 0.29 g/ l / 0.2 g/ l / 4.08 g/ l

Den europeiske union - norsk - EMA (European Medicines Agency)

advanced accelerator applications - lutetium (177lu) oksodotreotid - neuroendokrine tumorer - andre terapeutiske radiofarmaka - lutathera er angitt for de behandling av unresectable eller metastatisk, progressive, godt differensiert (g1 og g2), somatostatin reseptor positiv gastroenteropancreatic neuroendocrine svulster (gep‑nets) hos voksne.

Norge - norsk - Statens legemiddelverk

sanofi pasteur europe - clostridium tetani, toksoid - injeksjonsvæske, suspensjon - 40 ie/ dose

Norge - norsk - Statens legemiddelverk

sanofi pasteur europe - difteritoksoid / clostridium tetani, toksoid / pertussistoksoid / filamentøst hemagglutinin / poliovirus type 1, inaktivert / poliovirus type 2, inaktivert / poliovirus type 3, inaktivert - injeksjonsvæske, suspensjon - 30 ie/ sprøyte / 40 ie/ sprøyte / 25 mikrog/ sprøyte / 25 mikrog/ sprøyte / 40 d-antigen enheter/ sprøyte / 8 d-antigen enheter/