Zoledronic acid Teva Generics 유럽 연합 - 슬로베니아어 - EMA (European Medicines Agency)

zoledronic acid teva generics

teva generics b.v - monohidrat zoledronske kisline - osteoporosis; osteitis deformans - bisfosfonati - zdravljenje osteoporosisin post-menopavzi womenin odraslih menat povečano tveganje za zlome, vključno s tistimi z zadnjih nizko travme, zlom kolka. zdravljenje osteoporoze, povezane z dolgoročno sistemsko glukokortikoidnih therapyin post-menopavzi womenin odraslih menat povečano tveganje za zlome. zdravljenje paget je bolezen kosti v odrasli.

Zoledronic acid Teva Pharma 유럽 연합 - 슬로베니아어 - EMA (European Medicines Agency)

zoledronic acid teva pharma

teva b.v. - zoledronska kislina - osteoporosis; osteitis deformans; osteoporosis, postmenopausal - zdravila za zdravljenje bolezni kosti - treatment of osteoporosis: , in post-menopausal women;, in men; , at increased risk of fracture including those with a recent low-trauma hip fracture. treatment of osteoporosis associated with long-term systemic glucocorticoid therapy: , in post-menopausal women;, in men; , at increased risk of fracture. zdravljenje paget je bolezen kosti v odrasli.

Vaxelis 유럽 연합 - 슬로베니아어 - EMA (European Medicines Agency)

vaxelis

mcm vaccine b.v. - davica toxoid, tetanus toxoid, bordetella oslovskemu kašlju antigenov: oslovskemu kašlju toxoid, nitastih haemagglutinin, pertactin, fimbriae vrste 2 in 3, hepatitis b surface antigen, proizvedene v kvas celice, poliovirus (inaktivirano): tip 1 (mahoney), tip 2 (mef-1), tip 3 (saukett), ki v chicagu celic/ haemophilus influenzae tipa b polysaccharide (polyribosylribitol fosfat) konjugiran na meningococcal beljakovin. - meningitis, haemophilus; poliomyelitis; tetanus; diphtheria; whooping cough; hepatitis b - cepiva - vaxelis (dtap-hb-ipv-hib) je indicirano za osnovno in obnovitveno cepljenje pri dojenčkih in malčkih od starosti 6 tednov, proti davici, tetanus, oslovski kašelj, hepatitis b, otroški ohromelosti in invazivnih bolezni, ki povzroča haemophilus influenzae tipa b (hib). uporaba zdravila vaxelis mora biti v skladu z uradnimi priporočili.

Duavive 유럽 연합 - 슬로베니아어 - EMA (European Medicines Agency)

duavive

pfizer europe ma eeig - oestrogens konjugiran, bazedoxifene - postmenopavza - konjugiran estrogenov in bazedoxifene - duavive je indicirano za:zdravljenje oestrogen pomanjkljivost simptomi pri ženskah po menopavzi z maternico (z najmanj 12 mesecev od zadnjega menses), za katere zdravljenje z progestin, ki vsebujejo terapija ni primerna,. izkušnje zdravljenju žensk, starejših od 65 let, je omejeno.

Xydalba 유럽 연합 - 슬로베니아어 - EMA (European Medicines Agency)

xydalba

abbvie deutschland gmbh & co. kg - dalbavancin hydrochloride - soft tissue infections; skin diseases, bacterial - antibacterials za sistemsko uporabo, - zdravljenje, akutna bakterijska kože in strukturo kožo okužb (absssi) pri odraslih.

Sotyktu 유럽 연합 - 슬로베니아어 - EMA (European Medicines Agency)

sotyktu

bristol-myers squibb pharma eeig - deucravacitinib - psoriaza - imunosupresivi - treatment of moderate-to-severe plaque psoriasis in adults.

Iressa 유럽 연합 - 슬로베니아어 - EMA (European Medicines Agency)

iressa

astrazeneca ab - gefitinib - karcinom, pljučni pljuč - antineoplastična sredstva - iressa je indiciran za zdravljenje odraslih bolnikov z lokalno napredno ali metastatskim non-small-cell lung cancer z aktiviranjem mutacije od epidermalna-rast-faktor-receptor tirozin kinaza.

Saphnelo 유럽 연합 - 슬로베니아어 - EMA (European Medicines Agency)

saphnelo

astrazeneca ab - anifrolumab - lupus erythematosus, sistemski - imunosupresivi - saphnelo is indicated as an add-on therapy for the treatment of adult patients with moderate to severe, active autoantibody-positive systemic lupus erythematosus (sle), despite standard therapy.

Mirena 20 mikrogramov/24 ur intrauterini dostavni sistem 슬로베니아 - 슬로베니아어 - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

mirena 20 mikrogramov/24 ur intrauterini dostavni sistem

bayer d.o.o. - levonorgestrel - intrauterini dostavni sistem - levonorgestrel 52 mg / 1 vložek - plastični maternični vložki z dodatkom progestogenov

Purevax RCP FeLV 유럽 연합 - 슬로베니아어 - EMA (European Medicines Agency)

purevax rcp 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) - immunologicals za skupin felidae, - mačke - 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 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 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 feline leukaemia component, and one year after primary vaccination course and three years after the last re-vaccination for the rhinotracheitis, calicivirosis and panleucopenia components.