Liên Minh Châu Âu -
Tiếng Slovenia -
EMA (European Medicines Agency)
silgard
merck sharp dohme ltd - human papillomavirus tip 6 l1 beljakovin, human papillomavirus tip 11 l1 beljakovin, human papillomavirus tip 16 l1 beljakovin, human papillomavirus 18. vrsta beljakovine l1 - papillomavirus infections; uterine cervical dysplasia; condylomata acuminata; immunization - cepiva - silgard je cepivo za uporabo v starosti od 9 let, za preprečevanje:premalignant genitalni lezije (materničnega vratu, vulvar in nožnice), premalignant analni poškodb, raka materničnega vratu in analni raka vzročno povezane z določenimi oncogenic human papillomavirus (hpv) tipov;genitalni bradavice (condyloma acuminata) vzročno povezane s specifičnimi hpv tipov. glej poglavja 4. 4 in 5. 1 za pomembne podatke o podatkih, ki podpirajo to indikacijo. uporaba silgard je treba v skladu z uradnimi priporočili.
Liên Minh Châu Âu -
Tiếng Slovenia -
EMA (European Medicines Agency)
tritanrix hepb
glaxosmithkline biologicals s.a. - diphtheria toxoid, hepatitis b surface antigen, bordetella pertussis (inactivated), tetanus toxoid - hepatitis b; tetanus; immunization; whooping cough; diphtheria - cepiva - zdravilo tritanrix hepb je indicirano za aktivno imunizacijo proti davici, tetanusu, oslovskemu kašlju in hepatitisu b (hbv) pri dojenčkih šest tednov (glejte poglavje 4.
Liên Minh Châu Âu -
Tiếng Slovenia -
EMA (European Medicines Agency)
adynovi
baxalta innovations gmbh - rurioctocog alfa pegol - hemofilija a - antihemoragije - zdravljenje in preventivo za krvavitev pri bolnikih 12 let in zgoraj z hemofilija a (prirojeno faktor viii pomanjkljivost).
Liên Minh Châu Âu -
Tiếng Slovenia -
EMA (European Medicines Agency)
hemlibra
roche registration limited - emicizumab - hemofilija a - antihemoragije - hemlibra is indicated for routine prophylaxis of bleeding episodes in patients with haemophilia a (congenital factor viii deficiency):with factor viii inhibitorswithout factor viii inhibitors who have:severe disease (fviii < 1%)moderate disease (fviii ≥ 1% and ≤ 5%) with severe bleeding phenotype. hemlibra se lahko uporablja v vseh starostnih skupinah.
Liên Minh Châu Âu -
Tiếng Slovenia -
EMA (European Medicines Agency)
trecondi
medac gesellschaft für klinische spezialpräparate mbh - treosulfan - hematopoetična presaditev izvornih celic - antineoplastična sredstva - treosulfan in combination with fludarabine is indicated as part of conditioning treatment prior to allogeneic haematopoietic stem cell transplantation (allohsct) in adult patients and in paediatric patients older than one month with malignant and non-malignant diseases.
Liên Minh Châu Âu -
Tiếng Slovenia -
EMA (European Medicines Agency)
trodelvy
gilead sciences ireland uc - sacituzumab govitecan - breast neoplasms; triple negative breast neoplasms - antineoplastična sredstva - trodelvy as monotherapy is indicated for the treatment of adult patients with unresectable or metastatic triple-negative breast cancer (mtnbc) who have received two or more prior systemic therapies, including at least one of them for advanced disease.
Slovenia -
Tiếng Slovenia -
JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)
imigran sprint 50 mg disperzibilne tablete
gsk d.o.o., ljubljana - sumatriptan - disperzibilna tableta - sumatriptan 50 mg / 1 tableta - sumatriptan
Slovenia -
Tiếng Slovenia -
JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)
imigran 6 mg/0,5 ml raztopina za injiciranje
gsk d.o.o., ljubljana - sumatriptan - raztopina za injiciranje - sumatriptan 6 mg / 0,5 ml - sumatriptan
Slovenia -
Tiếng Slovenia -
JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)
imigran sprint 100 mg disperzibilne tablete
gsk d.o.o., ljubljana - sumatriptan - disperzibilna tableta - sumatriptan 100 mg / 1 tableta - sumatriptan
Slovenia -
Tiếng Slovenia -
JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)
imigran 20 mg/0,1 ml pršilo za nos, raztopina
gsk d.o.o., ljubljana - sumatriptan - pršilo za nos, raztopina - sumatriptan 20 mg / 0,1 ml - sumatriptan