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

zomarist

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.

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

prezista

janssen-cilag international nv - darunavir - hiv-infeksjoner - antivirale midler til systemisk bruk - prezista, co administered with low dose ritonavir is indicated in combination with other antiretroviral medicinal products for the treatment of human immunodeficiency virus (hiv 1) infection in adult and paediatric patients from the age of 3 years and at least 15 kg body weight. prezista, co administered with cobicistat is indicated in combination with other antiretroviral medicinal products for the treatment of human immunodeficiency virus (hiv 1) infection in adults and adolescents (aged 12 years and older, weighing at least 40 kg). in deciding to initiate treatment with prezista co administered with cobicistat or low dose ritonavir, careful consideration should be given to the treatment history of the individual patient and the patterns of mutations associated with different agents. genotypic or phenotypic testing (when available) and treatment history should guide the use of prezista. prezista, co administered with low dose ritonavir is indicated in combination with other antiretroviral medicinal products for the treatment of patients with human immunodeficiency virus (hiv 1) infection. prezista 75 mg, 150 mg, and 600 mg tablets may be used to provide suitable dose regimens:for the treatment of hiv 1 infection in antiretroviral treatment (art) experienced adult patients, including those that have been highly pre treated. for the treatment of hiv 1 infection in paediatric patients from the age of 3 years and at least 15 kg body weight. in deciding to initiate treatment with prezista co administered with low dose ritonavir, careful consideration should be given to the treatment history of the individual patient and the patterns of mutations associated with different agents. genotypic or phenotypic testing (when available) and treatment history should guide the use of prezista. prezista, co administered with low dose ritonavir is indicated in combination with other antiretroviral medicinal products for the treatment of patients with human immunodeficiency virus (hiv 1) infection. prezista, co administered with cobicistat is indicated in combination with other antiretroviral medicinal products for the treatment of human immunodeficiency virus (hiv 1) infection in adults and adolescents (aged 12 years and older, weighing at least 40 kg). prezista 400 mg and 800 mg tablets may be used to provide suitable dose regimens for the treatment of hiv 1 infection in adult and paediatric patients from the age of 3 years and at least 40 kg body weight who are:antiretroviral therapy (art) naïve. art experienced with no darunavir resistance associated mutations (drv rams) and who have plasma hiv 1 rna < 100,000 copies/ml and cd4+ cell count ≥ 100 cells x 106/l. in deciding to initiate treatment with prezista in such art experienced patients, genotypic testing should guide the use of prezista.

Nemona 49.5 % w/w Norge - norsk - Statens legemiddelverk

nemona 49.5 % w/w

nouryon pulp and performance chemicals ab - hydrogenperoksid - konsentrat til behandlingsoppløsning til fisk - 49.5 % w/w

Azasure Vet 500 mg/ g Norge - norsk - Statens legemiddelverk

azasure vet 500 mg/ g

sunrise animal health company limited - azametifos - pulver til behandlingssuspensjon til fisk - 500 mg/ g

Alpha Max 10 mg/ ml Norge - norsk - Statens legemiddelverk

alpha max 10 mg/ ml

pharmaq as - deltametrin - konsentrat til behandlingsoppløsning til fisk - 10 mg/ ml

Betamax vet 50 mg/ ml Norge - norsk - Statens legemiddelverk

betamax vet 50 mg/ ml

elanco europe ltd - cypermetrin - konsentrat til behandlingsoppløsning til fisk - 50 mg/ ml

Ivomec Comp 15.5 mg/ g / 77.5 mg/ g Norge - norsk - Statens legemiddelverk

ivomec comp 15.5 mg/ g / 77.5 mg/ g

boehringer ingelheim animal health nordics a/s - ivermektin / prazikvantel - oralpasta - 15.5 mg/ g / 77.5 mg/ g

Frontline Comp 50 mg / 60 mg Norge - norsk - Statens legemiddelverk

frontline comp 50 mg / 60 mg

boehringer ingelheim animal health nordics a/s - fipronil / metopren - påflekkingsvæske, oppløsning - 50 mg / 60 mg

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

nexgard spectra

boehringer ingelheim vetmedica gmbh - afoxolaner, milbemycin oxime - endectocides, antiparasitic products, insektmidler og repellents, milbemycin oxime, kombinasjoner - hunder - for behandling av loppemarked og hake infestations i hunder når den samtidige forebygging av hjerteorm sykdom (dirofilaria immitis larver), angiostrongylosis (reduksjon i nivået av umodne voksne (l5) og voksne i angiostrongylus vasorum), thelaziosis (voksen thelazia callipaeda) og/eller behandling av gastrointestinale nematode infestations er angitt. behandling av flea " (ctenocephalides felis og c. canis) i hunder for 5 uker. behandling av kryss infestations (dermacentor reticulatus, ixodes ricinus, ixodes hexagonus, rhipicephalus sanguineus) i hunder for 4 uker. lopper og flått må feste til verten og påbegynne fôring for å bli utsatt for det aktive stoffet. behandling av infestations med voksne gastrointestinale nematoder av følgende arter: roundworms (toxocara canis og toxascaris leonina), hookworms (ancylostoma caninum, ancylostoma braziliense og ancylostoma ceylanicum) og whipworm (trichuris vulpis). behandling av demodicosis (forårsaket av demodexkvalster canis). behandling av sarcoptic skabb (forårsaket av sarcoptes scabiei var. canis -). forebygging av hjerteorm sykdom (dirofilaria immitis larver) med månedlige administrasjon. forebygging av angiostrongylosis (ved reduksjon av nivået av infeksjon med umoden voksen (l5) og voksne stadier av angiostrongylus vasorum) med månedlige administrasjon. forebygging av etablering av thelaziosis (voksen thelazia callipaeda eyeworm infeksjon) med månedlige administrasjon.

Frontline Comp 67 mg / 60.3 mg Norge - norsk - Statens legemiddelverk

frontline comp 67 mg / 60.3 mg

boehringer ingelheim animal health nordics a/s - fipronil / metopren - påflekkingsvæske, oppløsning - 67 mg / 60.3 mg