Словения - словенски - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

gsk d.o.o., ljubljana - paracetamol - prašek za peroralno raztopino - paracetamol 500 mg / 1 vrečica - paracetamol

Словения - словенски - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

gsk d.o.o., ljubljana - paracetamol - prašek za peroralno raztopino - paracetamol 500 mg / 1 vrečica - paracetamol

Словения - словенски - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

gsk d.o.o., ljubljana - paracetamol - prašek za peroralno raztopino - paracetamol 500 mg / 1 vrečica - paracetamol

Словения - словенски - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

gsk d.o.o., ljubljana - paracetamol - prašek za peroralno raztopino - paracetamol 500 mg / 1 vrečica - paracetamol

Европейски съюз - словенски - EMA (European Medicines Agency)

takeda pharma a/s - darvadstrocel - rektalna fistula - imunosupresivi - alofisel je primerna za zdravljenje kompleksnih perianalnih fistulas pri odraslih bolnikih z ne-aktivna/lahko aktivno luminal crohnova bolezen, ko fistulas so pokazale, nezadosten odgovor na vsaj eno konvencionalne ali biološke terapije. alofisel je treba uporabiti po kondicioniranje fistula.

Европейски съюз - словенски - EMA (European Medicines Agency)

ucb pharma sa - certolizumab pegol - crohnova bolezen - imunosupresivi - cimzia, in combination with methotrexate (mtx), is indicated for the treatment of moderate to severe, active rheumatoid arthritis (ra) in adult patients when the response to disease-modifying antirheumatic drugs (dmard) including methotrexate, has been inadequate. cimzia lahko podana kot monotherapy v primeru nestrpnost do metotreksatom ali ko nadaljnje zdravljenje z metotreksatom ni primerno. cimzia has been shown to reduce the rate of progression of joint damage as measured by x-ray and to improve physical function, when given in combination with methotrexate.

Европейски съюз - словенски - EMA (European Medicines Agency)

elan pharma international ltd. - natalizumab - crohnova bolezen - immunostimulants, - zdravljenje zmerno do hudo aktivno crohnovo boleznijo za zmanjšanje znakov in simptomov, in uvajanja in vzdrževanja trajno odziva in odpust, pri bolnikih, ki se niso odzvali, kljub temu polno in ustrezni tečaj zdravljenja s kortikosteroidi in immunosuppressant; ali ne prenašajo ali imajo medicinske kontraindikacije za take terapije.

Европейски съюз - словенски - EMA (European Medicines Agency)

abbvie deutschland gmbh & co. kg - upadacitinib - artritis, revmatoidni - imunosupresivi - rheumatoid arthritisrinvoq is indicated for the treatment of moderate to severe active rheumatoid arthritis in adult patients who have responded inadequately to, or who are intolerant to one or more disease-modifying anti-rheumatic drugs (dmards). rinvoq may be used as monotherapy or in combination with methotrexate. psoriatic arthritisrinvoq is indicated for the treatment of active psoriatic arthritis in adult patients who have responded inadequately to, or who are intolerant to one or more dmards. rinvoq may be used as monotherapy or in combination with methotrexate. axial spondyloarthritisnon-radiographic axial spondyloarthritis (nr-axspa)rinvoq is indicated for the treatment of active non-radiographic axial spondyloarthritis in adult patients with objective signs of inflammation as indicated by elevated c-reactive protein (crp) and/or magnetic resonance imaging (mri), who have responded inadequately to nonsteroidal anti-inflammatory drugs (nsaids). ankylosing spondylitis (as, radiographic axial spondyloarthritis)rinvoq is indicated for the treatment of active ankylosing spondylitis in adult patients who have responded inadequately to conventional therapy. atopic dermatitisrinvoq is indicated for the treatment of moderate to severe atopic dermatitis in adults and adolescents 12 years and older who are candidates for systemic therapy. ulcerative colitisrinvoq is indicated for the treatment of adult patients with moderately to severely active ulcerative colitis who have had an inadequate response, lost response or were intolerant to either conventional therapy or a biologic agent.  crohn’s diseaserinvoq is indicated for the treatment of adult patients with moderately to severely active crohn’s disease who have had an inadequate response, lost response or were intolerant to either conventional therapy or a biologic agent.

Европейски съюз - словенски - EMA (European Medicines Agency)

abbvie deutschland gmbh & co. kg - risankizumab - psoriasis; arthritis, psoriatic - imunosupresivi - 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.