Valganciclovir Medical Valley 450 mg Norge - norsk - Statens legemiddelverk

valganciclovir medical valley 450 mg

medical valley invest ab - valganciklovirhydroklorid - tablett, filmdrasjert - 450 mg

Valganciclovir Accord 450 mg Norge - norsk - Statens legemiddelverk

valganciclovir accord 450 mg

accord healthcare b.v. - valganciklovirhydroklorid - tablett, filmdrasjert - 450 mg

Valganciclovir Sandoz 450 mg Norge - norsk - Statens legemiddelverk

valganciclovir sandoz 450 mg

sandoz - københavn - valganciklovirhydroklorid - tablett, filmdrasjert - 450 mg

Ganciclovir Oresund Pharma 500 mg Norge - norsk - Statens legemiddelverk

ganciclovir oresund pharma 500 mg

oresund pharma aps - ganciklovirnatrium - pulver til konsentrat til infusjonsvæske, oppløsning - 500 mg

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

livtencity

takeda pharmaceuticals international ag ireland branch - maribavir - cytomegalovirusinfeksjoner - antivirale midler til systemisk bruk - livtencity is indicated for the treatment of cytomegalovirus (cmv) infection and/or disease that are refractory (with or without resistance) to one or more prior therapies, including ganciclovir, valganciclovir, cidofovir or foscarnet in adult patients who have undergone a haematopoietic stem cell transplant (hsct) or solid organ transplant (sot). det bør vurderes å offisielle retningslinjer for riktig bruk av antivirale midler.

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

purevax rcpch

boehringer ingelheim vetmedica gmbh - attenuated feline rhinotracheitis herpesvirus (fhv f2 strain), inactivated feline calicivirosis antigens (fcv 431 and g1 strains), attenuated chlamydophila felis (905 strain), attenuated feline panleucopenia virus (pli iv) - immunologicals for felidae, - katter - active immunisation of cats aged eight weeks and older:• against feline viral rhinotracheitis to reduce clinical signs;• against calicivirus infection to reduce clinical signs;• against chlamydophila felis infection to reduce clinical signs;• against feline panleucopenia to prevent mortality and clinical signs. immunitetstrinn har blitt vist en uke etter primær vaksinasjonskurs for rhinotrakeitt, calicivirus, chlamydophila felis og panleukopeni-komponenter. the duration of immunity is one year after the last re-vaccination for the chlamydiosis component, and oneyear after primary vaccination and three years after the last re-vaccination for the rhinotracheitis, calicivirosis and panleucopenia components.

Purevax RCPCh FeLV Den europeiske union - norsk - EMA (European Medicines Agency)

purevax rcpch felv

boehringer ingelheim vetmedica gmbh - attenuated feline rhinotracheitis herpesvirus (fhv f2 strain), inactivated feline calicivirosis antigens (fcv 431 and g1 strains), attenuated feline panleucopenia virus (pli iv), felv recombinant canarypox virus (vcp97), attenuated chlamydophila felis (905 strain) - immunologicals for felidae, - katter - active immunisation of cats aged 8 weeks and older:against feline viral rhinotracheitis to reduce clinical signs;against calicivirus infection to reduce clinical signs;against chlamydophila felis infection to reduce clinical signs;against feline panleucopenia to prevent mortality and clinical signs;against leukaemia to prevent persistent viraemia and clinical signs of the related disease. onsets of immunity are 1 week after primary vaccination course for rhinotracheitis, calicivirus, chlamydophila felis and panleucopenia components, and 2 weeks after primary vaccination course for feline leukaemia component. the duration of immunity is one year after the last re-vaccination for the chlamydiosis and feline leukaemia components, and one year after primary vaccination course and three years after the last re-vaccination for the rhinotracheitis, calicivirosis and panleucopenia components.

Ezetimibe Orion 10 mg Norge - norsk - Statens legemiddelverk

ezetimibe orion 10 mg

orion corporation - espoo - ezetimib - tablett - 10 mg

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

striascan

cis bio international - ioflupan (123l) - radionuclide imaging; dementia; movement disorders - diagnostiske radiopharmaceuticals - dette legemidlet er kun til diagnostisk bruk. striascan er indikert for å påvise tap av funksjonelle dopaminerge nevron terminaler i striatum:hos voksne pasienter med klinisk usikker parkinsonian syndromer, for eksempel de med tidlige symptomer, for å kunne skille mellom essensielle tremor fra parkinsonian syndromer i slekt å parkinsons sykdom, multippel system atrofi og progressive supranuclear parese. striascan er i stand til å diskriminere mellom parkinsons sykdom, multippel system atrofi og progressive supranuclear parese. hos voksne pasienter, for å kunne skille mellom sannsynlig demens med lewy legemer fra alzheimers sykdom. striascan er i stand til å skille mellom demens med lewy legemer og parkinson ' s sykdom demens.