Estonia - Tiếng Estonia - Ravimiamet

bayer ag - levonorgestreel - intrauteriinne ravivahend - 52mg 1tk

Estonia - Tiếng Estonia - Ravimiamet

sun pharmaceutical industries europe b.v. - lopinaviir+ritonaviir - õhukese polümeerikattega tablett - 200mg+50mg 120tk; 200mg+50mg 360tk

Estonia - Tiếng Estonia - Ravimiamet

accord healthcare b.v. - lopinaviir+ritonaviir - õhukese polümeerikattega tablett - 200mg+50mg 120tk; 200mg+50mg 60tk; 200mg+50mg 360tk

Estonia - Tiếng Estonia - Ravimiamet

ranbaxy (u.k.) limited - lopinaviir+ritonaviir - õhukese polümeerikattega tablett - 100mg+25mg 60tk

Liên Minh Châu Âu - Tiếng Estonia - EMA (European Medicines Agency)

biosimilar collaborations ireland limited - bevatsizumab - colorectal neoplasms; breast neoplasms; ovarian neoplasms; fallopian tube neoplasms; peritoneal neoplasms; carcinoma, non-small-cell lung; carcinoma, renal cell; uterine cervical neoplasms - antineoplastilised ained - abevmy in combination with fluoropyrimidine-based chemotherapy is indicated for treatment of adult patients with metastatic carcinoma of the colon or rectum. abevmy in combination with paclitaxel is indicated for first-line treatment of adult patients with metastatic breast cancer. lisateavet inimese epidermaalse kasvufaktori retseptori 2 (her2) seisundi kohta vt palun 5. jaotisest. abevmy in combination with capecitabine is indicated for first-line treatment of adult patients with metastatic breast cancer in whom treatment with other chemotherapy options including taxanes or anthracyclines is not considered appropriate. patients who have received taxane and anthracycline containing regimens in the adjuvant setting within the last 12 months should be excluded from treatment with abevmy in combination with capecitabine. her2 staatuse kohta lisateabe saamiseks lugege palun 5. jaotist. abevmy, in addition to platinum-based chemotherapy, is indicated for first-line treatment of adult patients with unresectable advanced, metastatic or recurrent non-small cell lung cancer other than predominantly squamous cell histology. abevmy, in combination with erlotinib, is indicated for first-line treatment of adult patients with unresectable advanced, metastatic or recurrent non-squamous non-small cell lung cancer with epidermal growth factor receptor (egfr) activating mutations (see section 5. abevmy in combination with interferon alfa-2a is indicated for first line treatment of adult patients with advanced and/or metastatic renal cell cancer. abevmy, in combination with carboplatin and paclitaxel is indicated for the front-line treatment of adult patients with advanced (international federation of gynecology and obstetrics [figo] stages iii b, iii c and iv) epithelial ovarian, fallopian tube, or primary peritoneal cancer (see section 5. abevmy, in combination with carboplatin and gemcitabine or in combination with carboplatin and paclitaxel, is indicated for treatment of adult patients with first recurrence of platinum-sensitive epithelial ovarian, fallopian tube or primary peritoneal cancer who have not received prior therapy with bevacizumab or other vegf inhibitors or vegf receptor–targeted agents. abevmy in combination with paclitaxel, topotecan, or pegylated liposomal doxorubicin is indicated for the treatment of adult patients with platinum-resistant recurrent epithelial ovarian, fallopian tube, or primary peritoneal cancer who received no more than two prior chemotherapy regimens and who have not received prior therapy with bevacizumab or other vegf inhibitors or vegf receptor–targeted agents (see section 5. abevmy, in combination with paclitaxel and cisplatin or, alternatively, paclitaxel and topotecan in patients who cannot receive platinum therapy, is indicated for the treatment of adult patients with persistent, recurrent, or metastatic carcinoma of the cervix (see section 5.

Liên Minh Châu Âu - Tiếng Estonia - EMA (European Medicines Agency)

mylan ire healthcare limited - bevatsizumab - colorectal neoplasms; breast neoplasms; ovarian neoplasms; fallopian tube neoplasms; peritoneal neoplasms; carcinoma, non-small-cell lung; carcinoma, renal cell; uterine cervical neoplasms - antineoplastilised ained - treatment of carcinoma of the colon or rectum, breast cancer, non-small cell lung cancer, renal cell cancer, epithelial ovarian, fallopian tube or primary peritoneal cancer, and carcinoma of the cervix.

Liên Minh Châu Âu - Tiếng Estonia - EMA (European Medicines Agency)

sun pharmaceutical industries europe b.v. - kapetsitabiin - stomach neoplasms; breast neoplasms; colonic neoplasms; colorectal neoplasms - kapetsitabiin - kapetsitabiini on näidustatud käärsoolevähi adjuvantravina operatsiooni kasvaja iii staadium (dukes´i etapp-c). capecitabine on näidustatud ravi metastaatilise kolorektaalse vähi. capecitabine on näidustatud esimese rea ravi arenenud mao-vähi koos plaatina baasil raviskeemi. capecitabine koos docetaxel on näidustatud ravi patsientidel, kellel on lokaalselt kaugelearenenud või metastaatilise rinnavähi pärast rikke tsütotoksilist keemiaravi. eelnev ravi peaks sisaldama antratsükliini. capecitabine on ka märgitud, et monotherapy raviks patsientidel, kellel on lokaalselt kaugelearenenud või metastaatilise rinnavähi pärast rikke taxanes ja anthracycline-sisaldava keemiaravi raviskeemi või kelle jaoks veelgi anthracycline ravi ei ole näidustatud.

Liên Minh Châu Âu - Tiếng Estonia - EMA (European Medicines Agency)

gilead sciences ireland uc - elvitegravir, cobicistat, emtricitabine, tenofovir alafenamide - hiv-nakkused - viirusevastased ravimid süsteemseks kasutamiseks - genvoya on näidustatud täiskasvanutel ja noorukitel (vanuses 12 aastat ja vanemad koos kehakaalu vähemalt 35 kg) nakatunud inimese immuunpuudulikkuse viiruse (hiv-1) 1 ilma mis tahes teadaolevate resistentsus integraasi inhibiitorit koos emtritsitabiini või tenofoviiri.

Liên Minh Châu Âu - Tiếng Estonia - EMA (European Medicines Agency)

vetoquinol s.a. - emodepside, toltrazuril - antibakteriaalsed tooted, insektitsiidid ja repellendid - koerad - koertele, kui on segatud parasiitide poolt põhjustatud infektsioonide ümarussid ja coccidia järgmiste liikide puhul kahtlustatakse või on näidanud:Ümarussid (ümarusse)toxocara canis (küps täiskasvanu, ebaküps täiskasvanud, l4);uncinaria stenocephala (mature adult);ancylostoma caninum (täiskasvanud täiskasvanud). coccidiaisospora ohioensis keeruline;isospora canis. procox on efektiivne isospora replikatsiooni ja ootsüstide leviku vastu. kuigi ravi vähendab infektsiooni levikut, ei ole see juba nakatunud loomade nakkuse kliiniliste tunnuste suhtes tõhus.

Liên Minh Châu Âu - Tiếng Estonia - EMA (European Medicines Agency)

zoetis belgium sa - dibotermiin alfa - luu morfogeneetilised valgud - koerad - osteoinduktiivne aine, mida kasutatakse pikkade luumurdude raviks standardse kirurgilise hoolduse lisana, kasutades koertel avatud luumurdude vähenemist.