Libmeldy Eiropas Savienība - horvātu - EMA (European Medicines Agency)

libmeldy

orchard therapeutics (netherlands) bv - atidarsagene autotemcel - leukodystrophy, metachromatic - ostali lijekovi protiv živčanog sustava - libmeldy is indicated for the treatment of metachromatic leukodystrophy (mld) characterized by biallelic mutations in the arysulfatase a (arsa) gene leading to a reduction of the arsa enzymatic activity:in children with late infantile or early juvenile forms, without clinical manifestations of the disease,in children with the early juvenile form, with early clinical manifestations of the disease, who still  have the ability to walk independently and before the onset of cognitive decline.

Zoledronic acid Teva Eiropas Savienība - horvātu - EMA (European Medicines Agency)

zoledronic acid teva

teva b.v. - zoledronske kiseline - fractures, bone; cancer - lijekovi za liječenje bolesti kostiju - prevencija skeletnih događaja i liječenje hiperkalcemije izazvane tumorom.

Adynovi Eiropas Savienība - horvātu - EMA (European Medicines Agency)

adynovi

baxalta innovations gmbh - rurioctocog alfa pegol - hemofilija a - antihemorrhagics - prevencija i liječenje krvarenja kod bolesnika 12 godina s гемофилией a (urođeni deficit faktora viii)u.

Xromi Eiropas Savienība - horvātu - EMA (European Medicines Agency)

xromi

nova laboratories ireland limited - hidroksikarbamid - anemija, sickle cell - antineoplastična sredstva - prevencija сосудисто-jamice komplikacija anemija srpastih stanica anemije u bolesnika starijih od 2 godine.

Monoclonal Mouse Anti-Human CD99 MIC2 Gene Product Ewing's Sarcoma Marker Clone 12E7 Ready-to-Use (Link) Melnkalne - horvātu - CInMED-Institut za ljekove i medicinska sredstva Crne Gore

monoclonal mouse anti-human cd99 mic2 gene product ewing's sarcoma marker clone 12e7 ready-to-use (link)

"medica" d.o.o. za proizvodnju, trgovinu na veliko i malo, export-import, podgorica - in vitro dijagnostička medicinska sredstva

Jayempi Eiropas Savienība - horvātu - EMA (European Medicines Agency)

jayempi

nova laboratories ireland limited - azathioprine - odbacivanje transplantata - imunosupresivi - jayempi is indicated in combination with other immunosuppressive agents for the prophylaxis of transplant rejection in patients receiving allogenic kidney, liver, heart, lung or pancreas transplants. azathioprine is indicated in immunosuppressive regimens as an adjunct to immunosuppressive agents that form the mainstay of treatment (basis immunosuppression). jayempi is used as an immunosuppressant antimetabolite either alone or, more commonly, in combination with other agents (usually corticosteroids) and/ or procedures which influence the immune response. jayempi is indicated in patients who are intolerant to glucocorticosteroids or if the therapeutic response is inadequate despite treatment with high doses of glucocorticosteroids, in the following diseases:severe active rheumatoid arthritis (chronic polyarthritis) that cannot be kept under control by less toxic agents (disease-modifying anti-rheumatic -medicinal products – dmards)auto-immune hepatitis systemic lupus erythematosusdermatomyositispolyarteritis nodosapemphigus vulgaris and bullous pemphigoidbehçet’s diseaserefractory auto-immune haemolytic anaemia, caused by warm igg antibodieschronic refractory idiopathic thrombocytopenic purpurajayempi is used for the treatment of moderately severe to severe forms of chronic inflammatory bowel disease (ibd) (crohn’s disease or ulcerative colitis) in patients in whom glucocorticosteroid therapy is necessary, but where glucocorticosteroids are not tolerated, or in whom the disease is untreatable with other common means of first choice. it is also indicated in adult patients in relapsing multiple sclerosis, if an immunomodulatory therapy is indicated but beta interferon therapy is not possible, or a stable course has been achieved with previous treatment with azathioprine. 3jayempi is indicated for the treatment of generalised myasthenia gravis. depending on the severity of the disease, jayempi should be given in combination with glucocorticosteroids because of slow onset of action at the beginning of treatment and the glucocorticosteroid dose should be gradually reduced after several months of treatment.

RHINOSTOP 251mg + 61.2mg + 2.54mg Tableta Melnkalne - horvātu - CInMED-Institut za ljekove i medicinska sredstva Crne Gore

rhinostop 251mg + 61.2mg + 2.54mg tableta

bosnalijek d.d. predstavniŠtvo crna gora - paracetamol, pseudoefedrin, hlorfenamin - tableta - 251mg + 61.2mg + 2.54mg

Ceprotin Eiropas Savienība - horvātu - EMA (European Medicines Agency)

ceprotin

takeda manufacturing austria ag - ljudski protein c - purpura fulminans; protein c deficiency - antitrombotska sredstva - ceprotin is indicated for prophylaxis and treatment of  purpura fulminans  coumarin-induced skin necrosis and venous thrombotic events in patients with severe congenital protein c deficiency.

Cervarix Eiropas Savienība - horvātu - EMA (European Medicines Agency)

cervarix

glaxosmithkline biologicals s.a. - tip osobe papillomavirus1 16 Л1 sirutke papilloma virus tipa 18 Л1 proteina - papillomavirus infections; uterine cervical dysplasia; immunization - cjepiva - cervarix je cjepivo namijenjeno u dobi od 9 godina za prevenciju premaligne ano-genitalnih lezija (vrata maternice, vulve, vaginalni i analni) i raka vrata maternice i analni uzročno povezan s određene onkogenih tipova humanog papiloma virusa (hpv). pogledajte odjeljke 4. 4 i 5. 1 za važne informacije o podacima koji podržavaju ovu oznaku. primjena Церварикс mora biti u skladu sa službenim preporukama.