Euroopa Liit - eesti - EMA (European Medicines Agency)

takeda pharma a/s - brentuximab vedotin - lymphoma, non-hodgkin; hodgkin disease - antineoplastilised ained - hodgkin lymphomaadcetris is indicated for adult patients with previously untreated cd30+ stage iv hodgkin lymphoma (hl) in combination with doxorubicin, vinblastine and dacarbazine (avd). adcetris is indicated for the treatment of adult patients with cd30+ hl at increased risk of relapse or progression following autologous stem cell transplant (asct). adcetris on näidustatud ravi täiskasvanud patsientidel, kellel on taastekkinud või tulekindlad cd30+ hodgkini lümfoom (hl):pärast asct, orfollowing vähemalt kaks enne ravi kui asct või multi-agent keemiaravi ei ole ravi valik. süsteemne anaplastic suur kärje lymphomaadcetris koos tsüklofosfamiidi, doxorubicin ja prednisoon (chp) on näidustatud täiskasvanud patsientidel, kellel on varem ravimata süsteemne anaplastic suur raku lümfoom (salcl). adcetris on näidustatud ravi täiskasvanud patsientidel, kellel on taastekkinud või tulekindlad salcl. naha t-rakkude lymphomaadcetris on näidustatud ravi täiskasvanud patsientidel, kellel cd30+ naha t-raku lümfoom (ctcl) pärast vähemalt 1 enne süsteemset ravi.

Euroopa Liit - eesti - EMA (European Medicines Agency)

virbac s.a. - kasside päritolu rekombinantne oomega interferoon - immunostimulants, - dogs; cats - dogsreduction of mortality and clinical signs of parvovirosis (enteric form) in dogs from one month of age. catstreatment of cats infected with feline leukaemia virus (felv) and / or feline immunodeficiency virus (fiv), in non-terminal clinical stages, from the age of nine weeks. in a field study conducted, it was observed that there was:a reduction of clinical signs during the symptomatic phase (four months);a reduction of mortality:in anaemic cats, mortality rate of about 60% at four, six, nine and 12 months was reduced by approximately 30% following treatment with interferon;in non-anaemic cats, mortality rate of 50% in cats infected by felv was reduced by 20% following treatment with interferon. fiv-i nakatunud kassides oli suremus madal (5%) ja ravi ei mõjutanud.

Euroopa Liit - eesti - EMA (European Medicines Agency)

a. menarini industrie farmaceutiche riunite s.r.l. - delafloxacin meglumine - Ühenduse omandatud infektsioonid - antibacterials süsteemseks kasutamiseks, - quofenix is indicated for the treatment of the following infections in adults:acute bacterial skin and skin structure infections (absssi),community-acquired pneumonia (cap), when it is considered inappropriate to use other antibacterial agents that are commonly recommended for the initial treatment of these infections (see sections 4. 4 ja 5. tuleks arvesse võtta ametlikke juhiseid sobiva kasutada antibakteriaalseid aineid.

Euroopa Liit - eesti - EMA (European Medicines Agency)

laboratoire francais du fractionnement et des biotechnologies - eptacog beta (activated) - hemophilia a; hemophilia b - antihemorraagilised ained - cevenfacta is indicated in adults and adolescents (12 years of age and older) for the treatment of bleeding episodes and for the prevention of bleeding in those undergoing surgery or invasive procedures in the following patient groups:in patients with congenital haemophilia with high-responding inhibitors to coagulation factors viii or ix (i. ≥5 bethesda units (bu)); in patients with congenital haemophilia with low titre inhibitors (bu.

Euroopa Liit - eesti - EMA (European Medicines Agency)

daiichi sankyo europe gmbh - trastuzumab deruxtecan - rinnanäärmed - antineoplastilised ained - breast cancerher2-positive breast cancerenhertu as monotherapy is indicated for the treatment of adult patients with unresectable or metastatic her2-positive breast cancer who have received one or more prior anti-her2-based regimens. her2-low breast cancerenhertu as monotherapy is indicated for the treatment of adult patients with unresectable or metastatic her2-low breast cancer who have received prior chemotherapy in the metastatic setting or developed disease recurrence during or within 6 months of completing adjuvant chemotherapy (see section 4. non-small cell lung cancer (nsclc)enhertu as monotherapy is indicated for the treatment of adult patients with advanced nsclc whose tumours have an activating her2 (erbb2) mutation and who require systemic therapy following platinum-based chemotherapy with or without immunotherapy. gastric cancerenhertu as monotherapy is indicated for the treatment of adult patients with advanced her2-positive gastric or gastroesophageal junction (gej) adenocarcinoma who have received a prior trastuzumab-based regimen.

Euroopa Liit - eesti - EMA (European Medicines Agency)

pfizer europe ma eeig - pemetrexed disodium, pemetrexed disodium hemipentahydrate - carcinoma, non-small-cell lung; mesothelioma - antineoplastilised ained - malignant pleural mesotheliomapemetrexed pfizer in combination with cisplatin is indicated for the treatment of chemotherapy naïve patients with unresectable malignant pleural mesothelioma. non-small cell lung cancerpemetrexed pfizer in combination with cisplatin is indicated for the first-line treatment of patients with locally advanced or metastatic non-small cell lung cancer other than predominantly squamous cell histology. pemetrexed pfizer is indicated as monotherapy for the maintenance treatment of locally advanced or metastatic non-small cell lung cancer other than predominantly squamous cell histology in patients whose disease has not progressed immediately following platinum-based chemotherapy. pemetrexed pfizer is indicated as monotherapy for the second-line treatment of patients with locally advanced or metastatic non-small cell lung cancer other than predominantly squamous cell histology.

Euroopa Liit - eesti - EMA (European Medicines Agency)

boehringer ingelheim international gmbh - tenekteplaas - müokardi infarkt - antitrombootilised ained - metalyse on näidustatud trombolüütiliseks raviks ägeda müokardiinfarkti kahtluse korral püsiv st tõus või tehtud vasakule hisi kimbu blokaad kuue jooksul pärast sümptomite teket äge-müokardi-infarkt.

Euroopa Liit - eesti - EMA (European Medicines Agency)

pharma mar s.a. - trabektediin - ovarian neoplasms; sarcoma - antineoplastilised ained - yondelis on näidustatud arenenud pehmete kudede sarkoomiga patsientide raviks pärast antratsükliinide ja ifosfamiidi ebaõnnestumist või kes ei sobi neid aineid võtma. efektiivsusandmed põhinevad peamiselt liposarkoomil ja leiomüosarkoomiga patsientidel. yondelis koos pegylated liposomal doxorubicin (pld) on näidustatud ravi patsientidel, kellel on taastekkinud plaatina-tundlik munasarja vähk.

Euroopa Liit - eesti - EMA (European Medicines Agency)

gilead sciences ireland uc - astreonaami lüsiin - cystic fibrosis; respiratory tract infections - antibacterials süsteemseks kasutamiseks, - cayston on näidustatud pseudomonas aeruginosa põhjustatud krooniliste kopsuinfektsioonide surpressava raviks 6-aastastel ja vanematel tsüstilise fibroosi (cf) patsientidel. tuleks arvesse võtta ametlikke juhiseid sobiva kasutada antibakteriaalseid aineid.

Euroopa Liit - eesti - EMA (European Medicines Agency)

chiesi farmaceutici s.p.a - levofloksatsiin - cystic fibrosis; respiratory tract infections - antibacterials süsteemseks kasutamiseks, - quinsair on näidustatud krooniliste kopsu-nakkuste pseudomonas aeruginosa täiskasvanud patsientidel, kellel on tsüstiline fibroos. tuleks arvesse võtta ametlikke juhiseid sobiva kasutada antibakteriaalseid aineid.