Emtricitabine/Tenofovir disoproxil Mylan Den Europæiske Union - dansk - EMA (European Medicines Agency)

emtricitabine/tenofovir disoproxil mylan

mylan pharmaceuticals limited - emtricitabine, tenofovir disoproxil maleate - hiv infektioner - antivirale midler til systemisk anvendelse - treatment of hiv-1 infection:emtricitabine/tenofovir disoproxil mylan is indicated in antiretroviral combination therapy for the treatment of hiv-1 infected adults (see section 5. emtricitabine/tenofovir disoproxil mylan is also indicated for the treatment of hiv-1 infected adolescents, with nrti resistance or toxicities precluding the use of first line agents, (see sections 4. 2, 4. 4 og 5. pre-exposure prophylaxis (prep):emtricitabine/tenofovir disoproxil mylan is indicated in combination with safer sex practices for pre-exposure prophylaxis to reduce the risk of sexually acquired hiv-1 infection in adults and adolescents at high risk (see sections 4. 2, 4. 4 og 5.

Meropenem "SUN" 500 mg pulver til injektions-/infusionsvæske, opløsning Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

meropenem "sun" 500 mg pulver til injektions-/infusionsvæske, opløsning

sun pharmaceutical industries europe bv - meropenem (trihydrat) - pulver til injektions-/infusionsvæske, opløsning - 500 mg

Anagrelide Mylan Den Europæiske Union - dansk - EMA (European Medicines Agency)

anagrelide mylan

mylan pharmaceuticals limited - anagrelide hydrochlorid - trombocytæmi, essentiel - antineoplastiske midler - anagrelide er indiceret til reduktion af forhøjede blodplader tæller i risiko afgørende thrombocythaemia (et) patienter, der er intolerante over for deres igangværende behandling, eller hvis forhøjede blodplader tæller ikke reduceres til et acceptabelt niveau med deres nuværende behandling. an at-risk patientan at-risk essential thrombocythaemia patient is defined by one or more of the following features:>60 years of age ora platelet count >1,000 x 10⁹/l ora history of thrombo-haemorrhagic events.

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

rxulti

otsuka pharmaceutical netherlands b.v. - brexpiprazole - skizofreni - psykoleptika - behandlingen af skizofreni.

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

imcivree

rhythm pharmaceuticals netherlands b.v. - setmelanotide - fedme - antiobesity preparations, excl. diætprodukter - imcivree is indicated for the treatment of obesity and the control of hunger associated with genetically confirmed bardet biedl syndrome (bbs), loss-of-function biallelic pro-opiomelanocortin (pomc), including pcsk1, deficiency or biallelic leptin receptor (lepr) deficiency in adults and children 6 years of age and above.

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

briumvi

neuraxpharm pharmaceuticals s.l. - ublituximab - multiple sclerosis, relapsing-remitting; multiple sclerosis - immunosuppressiva - briumvi is indicated for the treatment of adult patients with relapsing forms of multiple sclerosis (rms) with active disease defined by clinical or imaging features.

MS-H Vaccine Den Europæiske Union - dansk - EMA (European Medicines Agency)

ms-h vaccine

pharmsure veterinary products europe ltd - mycoplasma synoviae stamme ms-h - immunologicals for aves, live bakterielle vacciner - kylling - til aktiv immunisering af fremtidige slagtekyllinger, kyllinger fra fremtidige lagdeltagere og fremtidige lagkyllinger for at reducere lungerne og reducere antallet af æg med unormal skaldannelse forårsaget af mycoplasma synoviae.

Vyxeos liposomal (previously known as Vyxeos) Den Europæiske Union - dansk - EMA (European Medicines Agency)

vyxeos liposomal (previously known as vyxeos)

jazz pharmaceuticals ireland limited - daunorubicin hydrochloride, cytarabine - leukæmi, myeloid, akut - antineoplastiske midler - vyxeos liposomal er indiceret til behandling af voksne med nyligt diagnosticeret, terapi-relateret akut myeloid leukæmi (t-aml) eller aml med myelodysplastisk-relaterede ændringer (aml-mrc).

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

livmarli

mirum pharmaceuticals international b.v. - maralixibat chloride - alagille syndrome - other drugs for bile therapy - livmarli is indicated for the treatment of cholestatic pruritus in patients with alagille syndrome (algs) 2 months of age and older.

Trimaxx Emulsionskoncentrat Danmark - dansk - SEGES Landbrug & Fødevarer

trimaxx emulsionskoncentrat

adama northern europe b.v. - trinexapac-ethyl, trinexapac - emulsionskoncentrat - 175 g/l trinexapac-ethyl ; (~ 156 g/l trinexapac