Sitagliptin SUN Uniunea Europeană - norvegiană - EMA (European Medicines Agency)

sitagliptin sun

sun pharmaceutical industries europe b.v. - sitagliptin fumarate - diabetes mellitus, type 2 - legemidler som brukes i diabetes - for adult patients with type 2 diabetes mellitus, sitagliptin sun 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 (pparγ) agonist (i. a thiazolidinedione) when use of a pparγ agonist is appropriate and when diet and exercise plus the pparγ 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 pparγ agonist and metformin when use of a pparγ agonist is appropriate and when diet and exercise plus dual therapy with these medicinal products do not provide adequate glycaemic control. sitagliptin sun 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.

Riltrava Aerosphere Uniunea Europeană - norvegiană - EMA (European Medicines Agency)

riltrava aerosphere

astrazeneca ab - budesonide, formoterol fumarate dihydrate, glycopyrronium bromide - lungesykdom, kronisk obstruktiv - legemidler for obstruktive sykdommer i luftveiene, - riltrava aerosphere is indicated as a maintenance treatment in adult patients with moderate to severe chronic obstructive pulmonary disease (copd) who are not adequately treated by a combination of an inhaled corticosteroid and a long-acting beta2 agonist or combination of a long-acting beta2 agonist and a long-acting muscarinic antagonist (for effects on symptoms control and prevention of exacerbations see section 5.

Xylocain Dental Adrenalin 20 mg/ ml / 12.5 mikrog/ ml Norvegia - norvegiană - Statens legemiddelverk

xylocain dental adrenalin 20 mg/ ml / 12.5 mikrog/ ml

dentsply detrey gmbh - lidokainhydroklorid / adrenalintartrat - injeksjonsvæske, oppløsning - 20 mg/ ml / 12.5 mikrog/ ml

Xeomin 100 E Norvegia - norvegiană - Statens legemiddelverk

xeomin 100 e

merz pharmaceuticals gmbh, frankfurt, tyskland - botulinumtoksin type a - pulver til injeksjonsvæske, oppløsning - 100 e

Xeomin 50 E Norvegia - norvegiană - Statens legemiddelverk

xeomin 50 e

merz pharmaceuticals gmbh, frankfurt, tyskland - botulinumtoksin type a - pulver til injeksjonsvæske, oppløsning - 50 e

Xeomin 200 E Norvegia - norvegiană - Statens legemiddelverk

xeomin 200 e

merz pharmaceuticals gmbh - botulinumtoksin type a - pulver til injeksjonsvæske, oppløsning - 200 e

Skilarence Uniunea Europeană - norvegiană - EMA (European Medicines Agency)

skilarence

almirall s.a - dimetylfumarat - psoriasis - immunsuppressive - skilarens er indisert for behandling av moderat til alvorlig plakspsoriasis hos voksne som har behov for systemisk medisinsk terapi.

Tiogiva 18 mikrog Norvegia - norvegiană - Statens legemiddelverk

tiogiva 18 mikrog

glenmark pharmaceuticals nordic ab - tiotropiumbromid - inhalasjonspulver, hard kapsel - 18 mikrog

Crysvita Uniunea Europeană - norvegiană - EMA (European Medicines Agency)

crysvita

kyowa kirin holdings b.v. - burosumab - hypophosphatemia, familial; hypophosphatemic rickets, x-linked dominant; osteomalacia - legemidler til behandling av bein sykdommer - crysvita is indicated for the treatment of x-linked hypophosphataemia, in children and adolescents aged 1 to 17 years with radiographic evidence of bone disease, and in adults. crysvita is indicated for the treatment of fgf23-related hypophosphataemia in tumour-induced osteomalacia associated with phosphaturic mesenchymal tumours that cannot be curatively resected or localised in children and adolescents aged 1 to 17 years and in adults.

Enurev Breezhaler Uniunea Europeană - norvegiană - EMA (European Medicines Agency)

enurev breezhaler

novartis europharm ltd - glycopyrronium bromide - lungesykdom, kronisk obstruktiv - legemidler for obstruktive sykdommer i luftveiene, - enurev breezhaler er indisert som en vedlikeholdsbronkodilatorbehandling for å lindre symptomer hos voksne pasienter med kronisk obstruktiv lungesykdom (kol).