Tepadina Evropska unija - hrvaščina - EMA (European Medicines Agency)

tepadina

adienne s.r.l. s.u. - thiotepa - transplantacija hematopoetskih matičnih stanica - antineoplastična sredstva - u kombinaciji s drugim kemoterapije lijekova:sa ili bez ukupne izloženosti (tbi), kao i tretmani klima ispred аллогенной ili autologne transplantacije гемопоэтических stanica prethodnika (hpct) u гематологических bolesti kod odraslih i pedijatrijska bolesnika;kada высокодозной kemoterapije s hpct podršku pogodan za liječenje uglednih tumora kod odraslih i pedijatrijska bolesnika. pretpostavlja se da tepadina moraju biti propisani iskusni liječnici tretman kose do гемопоэтических прогениторных stanica transplantacija .

Axumin Evropska unija - hrvaščina - EMA (European Medicines Agency)

axumin

blue earth diagnostics ireland ltd - fluciclovine (18f) - prostatic neoplasms; radionuclide imaging - dijagnostički radiofarmaceutici - ovaj je lijek samo za dijagnostičku uporabu. axumin indiciran za pozitronska emisijska tomografija (pet) ct za otkrivanje recidiva raka prostate kod odraslih muškaraca sumnja na recidiv, na temelju povišeni krvni razine specifičnog antigena prostate (psa) nakon primarnog liječenja.

Refixia Evropska unija - hrvaščina - EMA (European Medicines Agency)

refixia

novo nordisk a/s - beta nonacog pegol - hemofilija b - antihemorrhagics - liječenje i profilaksu krvarenja u bolesnika s hemofilijom b (nedostatak prirođenog faktora ix). , refixia can be used for all age groups.

Spherox Evropska unija - hrvaščina - EMA (European Medicines Agency)

spherox

co.don gmbh - sferoidi humanih autolognih matriksa povezanih hondrocita - bolesti hrskavice - ostali lijekovi za poremećaje mišićno-koštanog sustava - popravak oštećenja simptomatskih zglobnih zglobova femoralnog kondila i patele koljena (međunarodna klasifikacija ictr-a iii ili iv) s veličinom kvara do 10 cm2 u odraslih osoba.

Fingolimod Accord Evropska unija - hrvaščina - EMA (European Medicines Agency)

fingolimod accord

accord healthcare s.l.u. - финголимод hidroklorid - multipla skleroza, Рецидивно-Ремиттирующее - imunosupresivima selektivni imunosupresivima - istaknuo kao jedan bolest модифицирующей terapije kod visoke aktivnosti relapsing ublažavanje multiplom sklerozom za sljedećih skupina odraslih pacijenata i pedijatrijska bolesnika u dobi od 10 godina i stariji:pacijenti sa visokom aktivnošću bolesti, unatoč potpun i adekvatan tretman sa najmanje jednim bolest дорабатывая therapyorpatients s brzo razvija težak relapsing ublažavanje multiplom sklerozom određuje se 2 ili više teških recidiva u roku od jedne godine, s 1 ili više gadolinij revitalizacije lezija na mr mozga ili značajno povećanje u t2 leglo opterećenja u usporedbi s posljednjim mr.

Exparel liposomal Evropska unija - hrvaščina - EMA (European Medicines Agency)

exparel liposomal

pacira ireland limited - bupivacaine - acute pain - amides, anesthetics, local - exparel liposomal is indicated:in adults as a brachial plexus block or femoral nerve block for treatment of post-operative pain. in adults and children aged 6 years or older as a field block for treatment of somatic post-operative pain from small- to medium-sized surgical wounds.

Thiotepa Riemser Evropska unija - hrvaščina - EMA (European Medicines Agency)

thiotepa riemser

esteve pharmaceuticals gmbh - thiotepa - hematopoietic stem cell transplantation; neoplasms - antineoplastična sredstva - thiotepa riemser is indicated, in combination with other chemotherapy medicinal products:with or without total body irradiation (tbi), as conditioning treatment prior to allogeneic or autologous haematopoietic progenitor cell transplantation (hpct) in haematological diseases in adult and paediatric patients;when high dose chemotherapy with hpct support is appropriate for the treatment of solid tumours in adult and paediatric patients. thiotepa riemser is indicated, in combination with other chemotherapy medicinal products:with or without total body irradiation (tbi), as conditioning treatment prior to allogeneic or autologous haematopoietic progenitor cell transplantation (hpct) in haematological diseases in adult and paediatric patients;when high dose chemotherapy with hpct support is appropriate for the treatment of solid tumours in adult and paediatric patients.

Fingolimod Mylan Evropska unija - hrvaščina - EMA (European Medicines Agency)

fingolimod mylan

mylan ireland limited - финголимод hidroklorid - multipla skleroza, Рецидивно-Ремиттирующее - imunosupresivi - indicated as single disease modifying therapy in highly active relapsing remitting multiple sclerosis for the following groups of adult and paediatric patients aged 10 years and older:patients with highly active disease despite a full and adequate course of treatment with at least one disease modifying therapy (for exceptions and information about washout periods see sections 4. 4 i 5. 1)orpatients s brzo razvija težak relapsing ublažavanje multiplom sklerozom određuje se 2 ili više teških recidiva u roku od jedne godine, s 1 ili više gadolinij revitalizacije lezija na mr mozga ili značajno povećanje opterećenja t2 lezija u odnosu na najnoviji mri.

Fingolimod Mylan Evropska unija - hrvaščina - EMA (European Medicines Agency)

fingolimod mylan

mylan ireland limited - финголимод hidroklorid - multipla skleroza, Рецидивно-Ремиттирующее - imunosupresivi - indicated as single disease modifying therapy in highly active relapsing remitting multiple sclerosis for the following groups of adult and paediatric patients aged 10 years and older: patients with highly active disease despite a full and adequate course of treatment with at least one disease modifying therapy (for exceptions and information about washout periods see sections 4. 4 i 5. 1) or patients with rapidly evolving severe relapsing remitting multiple sclerosis defined by 2 or more disabling relapses in one year, and with 1 or more gadolinium enhancing lesions on brain mri or a significant increase in t2 lesion load as compared to a previous recent mri.

Thalidomide Lipomed Evropska unija - hrvaščina - EMA (European Medicines Agency)

thalidomide lipomed

lipomed gmbh - Талидомид - multipli mijelom - imunosupresivi - thalidomide lipomed in combination with melphalan and prednisone is indicated as first line treatment of patients with untreated multiple myeloma, aged ≥ 65 years or ineligible for high dose chemotherapy. thalidomide lipomed is prescribed and dispensed in accordance with the thalidomide lipomed pregnancy prevention programme (see section 4.