Ortiva Top Suspensionskoncentrat Danmark - dansk - SEGES Landbrug & Fødevarer

ortiva top suspensionskoncentrat

syngenta nordics a/s - difenoconazol, azoxystrobin - suspensionskoncentrat - 125 g/l difenoconazol ; 200 g/l azoxystrobin

Intrarosa Den Europæiske Union - dansk - EMA (European Medicines Agency)

intrarosa

endoceutics s.a. - prasterone - menopausen - andre kønshormoner og modulatorer af den genitale system - intrarosa er indiceret til behandling af vulvar og vaginal atrofi hos postmenopausale kvinder, der har moderate til svære symptomer.

Ortiva Suspensionskoncentrat Danmark - dansk - SEGES Landbrug & Fødevarer

ortiva suspensionskoncentrat

syngenta nordics a/s - azoxystrobin - suspensionskoncentrat - 250 g/l azoxystrobin

Bronchitol Den Europæiske Union - dansk - EMA (European Medicines Agency)

bronchitol

pharmaxis europe limited - mannitol - cystisk fibrose - hoste og kolde præparater - bronchitol er indiceret til behandling af cystisk fibrose (cf) hos voksne i alderen 18 år og derover som tillægsbehandling til den bedste plejestandard.

Coxevac Den Europæiske Union - dansk - EMA (European Medicines Agency)

coxevac

ceva santé animale - inaktiveret coxiella burnetii vaccine, stamme nine mile - immunologicals for bovidae, inactivated bacterial vaccines (including mycoplasma, toxoid and chlamydia) - goats; cattle - cattle: , for the active immunisation of cattle to lower the risk for non-infected animals vaccinated when non-pregnant to become shedder (5 times lower probability in comparison with animals receiving a placebo), and to reduce shedding of coxiella burnetii in these animals via milk and vaginal mucus. , onset of immunity: not established. , duration of immunity: 280 days after completion of the primary vaccination course. , goats: , for the active immunisation of goats to reduce abortion caused by coxiella burnetii and to reduce shedding of the organism via milk, vaginal mucus, faeces and placenta. , onset of immunity: not established. , duration of immunity: one year after completion of the primary vaccination course.

Oxervate Den Europæiske Union - dansk - EMA (European Medicines Agency)

oxervate

dompe farmaceutici s.p.a. - recombinant human nerve growth factor - keratitis - oftalmologiske - behandling af moderat (vedvarende epiteldefekt) eller alvorligt (hornhindeår) neurotrofisk keratitis hos voksne.