Caspofungin Lorien 70 mg Νορβηγία - Νορβηγικά - Statens legemiddelverk

caspofungin lorien 70 mg

laboratorios lorien s.l - kaspofunginacetat - pulver til konsentrat til infusjonsvæske, oppløsning - 70 mg

Caspofungin Lorien 50 mg Νορβηγία - Νορβηγικά - Statens legemiddelverk

caspofungin lorien 50 mg

laboratorios lorien s.l - kaspofunginacetat - pulver til konsentrat til infusjonsvæske, oppløsning - 50 mg

Lakrimont 2 mg/ g Νορβηγία - Νορβηγικά - Statens legemiddelverk

lakrimont 2 mg/ g

laboratoires théa s.a.s (1) - karbomer - Øyegel - 2 mg/ g

Mhyosphere PCV ID Ευρωπαϊκή Ένωση - Νορβηγικά - EMA (European Medicines Agency)

mhyosphere pcv id

laboratorios hipra, s.a. - mycoplasma hyopneumoniae, strain 7304 (nexhyon), expressing the capsid protein of porcine circovirus type 2a, inactivated - immunologicals for suidae, inactivated viral and inactivated bacterial vaccines - griser - for the active immunisation of pigs:to reduce lung lesions associated with porcine enzootic pneumonia caused by mycoplasma hyopneumoniae. also, to reduce the incidence of these lesions (as observed in field studies). to reduce viraemia, virus load in lungs and lymphoid tissues and the duration of the viraemic period associated with diseases caused by porcine circovirus type 2 (pcv2). efficacy against pcv2 genotypes a, b and d has been demonstrated in field studies. to reduce culling rate and the loss of daily weight gain caused by mycoplasma hyopneumoniae and/or pcv2 related diseases (as observed at 6 months of age in field studies). mycoplasma hyopneumoniae: onset of immunity: 3 weeks after vaccinationduration of immunity: 23 weeks after vaccinationporcine circovirus type 2:onset of immunity: 2 weeks after vaccinationduration of immunity: 22 weeks after vaccinationin addition, a reduction in nasal and faecal shedding and the duration of nasal excretion of pcv2 was demonstrated in animals challenged at 4 weeks and at 22 weeks after vaccination.

Suiseng Diff/A Ευρωπαϊκή Ένωση - Νορβηγικά - EMA (European Medicines Agency)

suiseng diff/a

laboratorios hipra, s.a. - clostridioides difficile toxoid a, clostridioides difficile toxoid b, clostridium perfringens, type a, alpha toxoid - immunologicals for suidae, inactivated bacterial vaccines for pigs, clostridium - griser - for the passive immunisation of neonatal piglets by means of the active immunisation of breeding sows and gilts:- to prevent mortality and reduce clinical signs and macroscopic lesions caused by clostridioides difficile toxins a and b. - to reduce clinical signs and macroscopic lesions caused by clostridium perfringens type a, alpha toxin.

Thiamine Sterop 50 mg/ ml Νορβηγία - Νορβηγικά - Statens legemiddelverk

thiamine sterop 50 mg/ ml

laboratoires sterop nv - tiaminhydroklorid - injeksjonsvæske, oppløsning - 50 mg/ ml

Thiamine Sterop 125 mg/ ml Νορβηγία - Νορβηγικά - Statens legemiddelverk

thiamine sterop 125 mg/ ml

laboratoires sterop nv - tiaminhydroklorid - injeksjonsvæske, oppløsning - 125 mg/ ml

Dienogest Besins 2 mg Νορβηγία - Νορβηγικά - Statens legemiddelverk

dienogest besins 2 mg

laboratoires besins international s.a.s. - dienogest - tablett - 2 mg

Osseor Ευρωπαϊκή Ένωση - Νορβηγικά - EMA (European Medicines Agency)

osseor

les laboratoires servier - strontiumranelat - osteoporose, postmenopausale - legemidler til behandling av bein sykdommer - behandling av alvorlig osteoporose hos postmenopausale kvinner med høy risiko for brudd for å redusere risikoen for vertebrale og hoftefrakturer. behandling av alvorlig osteoporose hos voksne menn med økt risiko for brudd. beslutningen om å forskrive strontium ranelate bør være basert på en vurdering av den enkelte pasients samlede risiko.

Protelos Ευρωπαϊκή Ένωση - Νορβηγικά - EMA (European Medicines Agency)

protelos

les laboratoires servier - strontiumranelat - osteoporose, postmenopausale - legemidler til behandling av bein sykdommer - behandling av alvorlig osteoporose hos postmenopausale kvinner med høy risiko for brudd for å redusere risikoen for vertebrale og hoftefrakturer. behandling av alvorlig osteoporose hos voksne menn med økt risiko for brudd. beslutningen om å forskrive strontium ranelate bør være basert på en vurdering av den enkelte pasients samlede risiko.