Etoricoxib Stada 30 mg tabletti, kalvopäällysteinen Suomi - suomi - Fimea (Suomen lääkevirasto)

etoricoxib stada 30 mg tabletti, kalvopäällysteinen

stada arzneimittel ag - etoricoxib - tabletti, kalvopäällysteinen - 30 mg - etorikoksibi

Etoricoxib Stada 60 mg tabletti, kalvopäällysteinen Suomi - suomi - Fimea (Suomen lääkevirasto)

etoricoxib stada 60 mg tabletti, kalvopäällysteinen

stada arzneimittel ag - etoricoxib - tabletti, kalvopäällysteinen - 60 mg - etorikoksibi

Etoricoxib Stada 90 mg tabletti, kalvopäällysteinen Suomi - suomi - Fimea (Suomen lääkevirasto)

etoricoxib stada 90 mg tabletti, kalvopäällysteinen

stada arzneimittel ag - etoricoxib - tabletti, kalvopäällysteinen - 90 mg - etorikoksibi

Etoricoxib Stada 120 mg tabletti, kalvopäällysteinen Suomi - suomi - Fimea (Suomen lääkevirasto)

etoricoxib stada 120 mg tabletti, kalvopäällysteinen

stada arzneimittel ag - etoricoxib - tabletti, kalvopäällysteinen - 120 mg - etorikoksibi

Trulicity Euroopan unioni - suomi - EMA (European Medicines Agency)

trulicity

eli lilly nederland b.v. - dulaglutide - diabetes mellitus, tyyppi 2 - drugs used in diabetes, blood glucose lowering drugs, excl. insulins - trulicity is indicated for the treatment of patients 10 years and above with insufficiently controlled type 2 diabetes mellitus as an adjunct to diet and exerciseas monotherapy when metformin is considered inappropriate due to intolerance or contraindicationsin addition to other medicinal products for the treatment of diabetes. tutkimuksen tuloksia suhteessa yhdistelmiä, vaikutuksia verensokeritasapainoon ja sydän-ja verisuonitapahtumien, ja väestön tutkittu, ks. kohdat 4. 4, 4. 5 ja 5.

Candemox Comp 16 mg / 12,5 mg tabletti Suomi - suomi - Fimea (Suomen lääkevirasto)

candemox comp 16 mg / 12,5 mg tabletti

sandoz a/s - hydrochlorothiazide, candesartan cilexetil - tabletti - 16 mg / 12,5 mg - kandesartaani ja diureetit

Budesonide/Formoterol Teva Pharma B.V. Euroopan unioni - suomi - EMA (European Medicines Agency)

budesonide/formoterol teva pharma b.v.

teva pharma b.v. - budesonide, formoterol - astma - obstruktiivisten hengitystiesairauksien lääkkeet, - budesonidi / formoterol teva pharma b. on tarkoitettu aikuisille vain 18-vuotiaille ja vanhemmille. asthmabudesonide/formoterol teva pharma b. is indicated in the regular treatment of asthma, where use of a combination (inhaled corticosteroid and long-acting β2 adrenoceptor agonist) is appropriate: orin patients not adequately controlled with inhaled corticosteroids and “as needed” inhaled short-acting β2 adrenoceptor agonists. in patients already adequately controlled on both inhaled corticosteroids and long-acting β2 adrenoceptor agonists.

Imoxat Euroopan unioni - suomi - EMA (European Medicines Agency)

imoxat

chanelle pharmaceuticals manufacturing ltd - imidaklopridi, moksidektiini - antiparasitic products, insecticides and repellents, macrocyclic lactones, milbemycins - cats; dogs; ferrets - for cats suffering from, or at risk from, mixed parasitic infections:• the treatment and prevention of flea infestation (ctenocephalides felis),• the treatment of ear mite infestation (otodectes cynotis),• the treatment of notoedric mange (notoedres cati),• the treatment of the lungworm eucoleus aerophilus (syn. capillaria aerophila) (adults),• the prevention of lungworm disease (l3/l4 larvae of aelurostrongylus abstrusus),• the treatment of the lungworm aelurostrongylus abstrusus (adults),• the treatment of the eye worm thelazia callipaeda (adults),• the prevention of heartworm disease (l3 and l4 larvae of dirofilaria immitis),• the treatment of infections with gastrointestinal nematodes (l4 larvae, immature adults and adults of toxocara cati and ancylostoma tubaeforme). eläinlääkevalmistetta voidaan käyttää osana kirppu allergiadermatiitin (fad) hoitostrategiaa,.  for ferrets suffering from, or at risk from, mixed parasitic infections:• the treatment and prevention of flea infestation (ctenocephalides felis),• the prevention of heartworm disease (l3 and l4 larvae of dirofilaria immitis).  for dogs suffering from, or at risk from, mixed parasitic infections:• the treatment and prevention of flea infestation (ctenocephalides felis),• the treatment of biting lice (trichodectes canis),• the treatment of ear mite infestation (otodectes cynotis), sarcoptic mange (caused by sarcoptes scabiei var. canis), demodicosis (caused by demodex canis),• the prevention of heartworm disease (l3 and l4 larvae of dirofilaria immitis),• the treatment of circulating microfilariae (dirofilaria immitis),• the treatment of cutaneous dirofilariosis (adult stages of dirofilaria repens)• the prevention of cutaneous dirofilariosis (l3 larvae of dirofilaria repens),• the reduction of circulating microfilariae (dirofilaria repens),• the prevention of angiostrongylosis (l4 larvae and immature adults of angiostrongylus vasorum),• the treatment of angiostrongylus vasorum and crenosoma vulpis,• the prevention of spirocercosis (spirocerca lupi),• the treatment of eucoleus (syn. capillaria) boehmi (adults),• the treatment of the eye worm thelazia callipaeda (adults),• the treatment of infections with gastrointestinal nematodes (l4 larvae, immature adults and adults of toxocara canis, ancylostoma caninum and uncinaria stenocephala, adults of toxascaris leonina and trichuris vulpis). eläinlääkevalmistetta voidaan käyttää osana kirppu allergiadermatiitin (fad) hoitostrategiaa,.

Amlodipin Essential Pharmaceuticals 1 mg/ml oraalisuspensio Suomi - suomi - Fimea (Suomen lääkevirasto)

amlodipin essential pharmaceuticals 1 mg/ml oraalisuspensio

essential pharmaceuticals ltd - amlodipine besylate - oraalisuspensio - 1 mg/ml - amlodipiini

Sitagliptin / Metformin hydrochloride Mylan Euroopan unioni - suomi - EMA (European Medicines Agency)

sitagliptin / metformin hydrochloride mylan

mylan ireland limited - sitagliptin hydrochloride monohydrate, metformin hydrochloride - diabetes mellitus, tyyppi 2 - diabeetilla käytettävät lääkkeet - for adult patients with type 2 diabetes mellitus:sitagliptin/metformin hydrochloride mylan is indicated as an adjunct to diet and exercise to improve glycaemic control in patients inadequately controlled on their maximal tolerated dose of metformin alone or those already being treated with the combination of sitagliptin and metformin. sitagliptin/metformin hydrochloride mylan is indicated in combination with a sulphonylurea (i. kolmen lääkkeen yhdistelmähoito) lisänä ruokavalion ja liikunnan ohella potilaille riittävästi hallinnassa heidän maksimaalinen siedetty annos metformiinia ja sulfonyyliureaa. sitagliptin/metformin hydrochloride mylan is indicated as triple combination therapy with a peroxisome proliferator-activated receptor gamma (pparg) agonist (i. , a thiazolidinedione) as an adjunct to diet and exercise in patients inadequately controlled on their maximal tolerated dose of metformin and a pparg agonist. sitagliptin/metformin hydrochloride mylan is also indicated as add-on to insulin (i. , triple combination therapy) as an adjunct to diet and exercise to improve glycaemic control in patients when stable dose of insulin and metformin alone do not provide adequate glycaemic control.