TachoSil Europos Sąjunga - lietuvių - EMA (European Medicines Agency)

tachosil

corza medical gmbh - žmogaus fibrinogenas, žmogaus trombinas - hemostasas, chirurginis - antihemoraginiai - tachosil is indicated in adults and children from 1 month of age for supportive treatment in surgery for improvement of haemostasis, to promote tissue sealing and for suture support in vascular surgery where standard techniques are insufficient. tachosil is indicated in adults for supportive sealing of the dura mater to prevent postoperative cerebrospinal leakage following neurological surgery (see section 5.

Opgenra Europos Sąjunga - lietuvių - EMA (European Medicines Agency)

opgenra

olympus biotech international limited - eptoterminas alfa - spondilolistezė - narkotikai kaulų ligų gydymui - opgenra skiriamas posterolateralinei juosmens dalies stuburo suliejimui suaugusiems pacientams, sergantiems spondilolistezei, kai autograftas nesėkmingas arba yra kontraindikuotas.

Incivo Europos Sąjunga - lietuvių - EMA (European Medicines Agency)

incivo

janssen-cilag international n.v. - telapreviras - hepatitas c, lėtinis - antivirusiniai vaistai sisteminiam naudojimui - incivo, kartu su peginterferon alfa ir ribavirin, fluorouracilu ir folino genotipo-1 lėtinio hepatito c paplitimas tarp suaugusių pacientų su kompensuota kepenų liga (įskaitant kepenų cirozę):kas yra gydymo naivu;kas anksčiau buvo elgiamasi su interferonu alfa (pegylated ar ne pegylated) atskirai arba kartu su ribavirin, įskaitant relapsers, dalinis atsakas ir null gelbėtojai.

Zydelig Europos Sąjunga - lietuvių - EMA (European Medicines Agency)

zydelig

gilead sciences ireland uc - idelalisib - lymphoma, non-hodgkin; leukemia, lymphocytic, chronic, b-cell - antineoplastic agents, other antineoplastic agents - zydelig is indicated in combination with an anti‑cd20 monoclonal antibody (rituximab or ofatumumab) for the treatment of adult patients with chronic lymphocytic leukaemia (cll):who have received at least one prior therapy, oras first line treatment in the presence of 17p deletion or tp53 mutation in patients who are not eligible for any other therapies. zydelig is indicated as monotherapy for the treatment of adult patients with follicular lymphoma (fl) that is refractory to two prior lines of treatment.

Xtandi Europos Sąjunga - lietuvių - EMA (European Medicines Agency)

xtandi

astellas pharma europe b.v. - enzalutamidas - prostatos navikai - endokrininė terapija - xtandi is indicated for:the treatment of adult men with metastatic hormone-sensitive prostate cancer (mhspc) in combination with androgen deprivation therapy (see section 5. the treatment of adult men with high-risk non-metastatic castration-resistant prostate cancer (crpc) (see section 5. the treatment of adult men with metastatic crpc who are asymptomatic or mildly symptomatic after failure of androgen deprivation therapy in whom chemotherapy is not yet clinically indicated (see section 5. the treatment of adult men with metastatic crpc whose disease has progressed on or after docetaxel therapy.

Enzalutamide Norameda Lietuva - lietuvių - SMCA (Valstybinė vaistų kontrolės tarnyba)

enzalutamide norameda

norameda, uab - enzalutamidas - minkštosios kapsulės - 40 mg - enzalutamide

Enzalutamide Sandoz Lietuva - lietuvių - SMCA (Valstybinė vaistų kontrolės tarnyba)

enzalutamide sandoz

sandoz d.d. - enzalutamidas - plėvele dengtos tabletės - 40 mg - enzalutamide

Enzalutamide Sandoz Lietuva - lietuvių - SMCA (Valstybinė vaistų kontrolės tarnyba)

enzalutamide sandoz

sandoz d.d. - enzalutamidas - plėvele dengtos tabletės - 80 mg - enzalutamide