Italia - italiano - Ministero della Salute

so.se.pharm srl -

Italia - italiano - Ministero della Salute

coswell spa -

Italia - italiano - AIFA (Agenzia Italiana del Farmaco)

viatris pharma s.r.l. - venlafaxina - venlafaxina

Italia - italiano - AIFA (Agenzia Italiana del Farmaco)

sandoz s.p.a. - venlafaxina - venlafaxina

Italia - italiano - AIFA (Agenzia Italiana del Farmaco)

italfarmaco s.p.a. - venlafaxina - venlafaxina

Unione Europea - italiano - EMA (European Medicines Agency)

zoetis belgium sa - synthetic peptide analogue of gnrf conjugated to diptheria toxoid - immunologici per suidi - male pigs (from 8 weeks of age); female pigs (from 14 weeks of age) - male pigs:induction of antibodies against gnrf to produce a temporary immunological suppression of testicular function. for use as an alternative to physical castration for the reduction of boar taint caused by the key boar taint compound androstenone, in entire male pigs following the onset of puberty. un altro fattore chiave per la contaminazione del verro, lo skatole, può anche essere ridotto come effetto indiretto. anche i comportamenti aggressivi e sessuali (di montaggio) sono ridotti. female pigs:induction of antibodies against gnrf to produce a temporary immunological suppression of ovarian function (suppression of oestrus) in order to reduce the incidence of unwanted pregnancies in gilts intended for slaughter, and to reduce the associated sexual behaviour (standing oestrus).

Unione Europea - italiano - EMA (European Medicines Agency)

viiv healthcare bv - dolutegravir - infezioni da hiv - antivirali per uso sistemico - tivicay is indicated in combination with other anti-retroviral medicinal products for the treatment of human immunodeficiency virus (hiv) infected adults, adolescents and children of at least 6 years of age or older and weighing at least 14 kg. tivicay is indicated in combination with other anti-retroviral medicinal products for the treatment of human immunodeficiency virus (hiv) infected adults, adolescents and children of at least 4 weeks of age or older and weighing at least 3 kg.

Unione Europea - italiano - EMA (European Medicines Agency)

abbvie deutschland gmbh & co. kg - risankizumab - psoriasis; arthritis, psoriatic - immunosoppressori - plaque psoriasisskyrizi is indicated for the treatment of moderate to severe plaque psoriasis in adults who are candidates for systemic therapy. psoriatic arthritisskyrizi, alone or in combination with methotrexate (mtx), is indicated for the treatment of active psoriatic arthritis in adults who have had an inadequate response or who have been intolerant to one or more disease-modifying antirheumatic drugs (dmards). crohn's diseaseskyrizi is indicated for the treatment of adult patients with moderately to severely active crohn's disease who have had an inadequate response to, lost response to, or were intolerant to conventional therapy or a biologic therapy.

Unione Europea - italiano - EMA (European Medicines Agency)

ucb pharma s.a. - romosozumab - osteoporosi - farmaci per il trattamento delle malattie ossee - evenity è indicato nel trattamento della grave osteoporosi nelle donne in postmenopausa ad alto rischio di frattura.

Unione Europea - italiano - EMA (European Medicines Agency)

boehringer ingelheim international gmbh - spesolimab - psoriasi - immunosoppressori - spevigo is indicated for the treatment of flares in adult patients with generalised pustular psoriasis (gpp) as monotherapy.