GEMCITABINE STRIDES infusioonilahuse pulber 에스토니아 - 에스토니아어 - Ravimiamet

gemcitabine strides infusioonilahuse pulber

strides arcolab international limited - gemtsitabiin - infusioonilahuse pulber - 38mg 1ml 200mg 1tk; 38mg 1ml 1000mg 1tk

DICLOFENAC MYLAN ravimplaaster 에스토니아 - 에스토니아어 - Ravimiamet

diclofenac mylan ravimplaaster

mylan ireland limited - diklofenak - ravimplaaster - 180mg 5tk; 180mg 10tk

Abevmy 유럽 연합 - 에스토니아어 - EMA (European Medicines Agency)

abevmy

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.

Scenesse 유럽 연합 - 에스토니아어 - EMA (European Medicines Agency)

scenesse

clinuvel europe limited - afamelanotiid - protoporfüüria, erütropoeetiline - moodustavad ja kaitsevad - fototoksilisuse ennetamine erütropoeetilise protoporforüüriaga (epp) täiskasvanud patsientidel.

Spotinor täpilahus 에스토니아 - 에스토니아어 - Ravimiamet

spotinor täpilahus

norbrook laboratories (ireland) limited - deltametriin - täpilahus - 10mg 1ml 250ml 1tk; 10mg 1ml 1000ml 1tk; 10mg 1ml 500ml 2tk; 10mg 1ml 500ml 1tk

Dectospot kriipsulahus 에스토니아 - 에스토니아어 - Ravimiamet

dectospot kriipsulahus

bimeda animal health limited - deltametriin - kriipsulahus - 10mg 1ml 1000ml 1tk; 10mg 1ml 2500ml 1tk; 10mg 1ml 500ml 1tk; 10mg 1ml 250ml 1tk

Betafuse geel 에스토니아 - 에스토니아어 - Ravimiamet

betafuse geel

norbrook laboratories (ireland) limited - beetametasoon+fusidiinhape - geel - 1mg+5mg 1g 15g 1tk; 1mg+5mg 1g 30g 1tk

Lextemy 유럽 연합 - 에스토니아어 - EMA (European Medicines Agency)

lextemy

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.

Ogivri 유럽 연합 - 에스토니아어 - EMA (European Medicines Agency)

ogivri

biosimilar collaborations ireland limited - trastuzumab - stomach neoplasms; breast neoplasms - antineoplastilised ained - rindade cancermetastatic rindade cancerogivri on näidustatud ravi täiskasvanud patsientidel, kellel her2 positiivse metastaatilise rinnavähi (mbc):monotherapy raviks nendel patsientidel, kes on saanud vähemalt kaks keemiaravi raviskeemi oma metastaatilise haiguse. eelnev keemiaravi peab olema kantud vähemalt anthracycline ja taxane välja arvatud juhul, kui patsientidele ei sobi nende ravi. hormooni retseptori positiivne patsientidel peab olema ebaõnnestunud hormoonravi, välja arvatud juhul, kui patsientidele ei sobi need treatmentsin koos paclitaxel raviks nendel patsientidel, kes ei ole saanud keemiaravi oma metastaatilise haiguse ja kelle jaoks on anthracycline ei suitablein koos docetaxel raviks nendel patsientidel, kes ei ole saanud keemiaravi oma metastaatilise diseasein koos aromataasi inhibiitoriga ravi postmenopausis patsientidel hormoon-retseptor positiivne mbc, mis ei ole varem ravitud trastuzumab. varajase rinnavähi ogivri on näidustatud ravi täiskasvanud patsientidel, kellel her2 positiivse varajase rinnavähi (ebc):pärast operatsiooni, kemoteraapiat (neoadjuvant-või abiaine) ja kiiritusravi (kui on kohaldatav)pärast abiaine keemiaravi koos doxorubicin ja tsüklofosfamiidiga kombinatsioonis paclitaxel või docetaxelin koos abiaine keemiaravi, mis koosneb docetaxel ja carboplatin. koos neoadjuvant kemoteraapiat, millele järgneb abiaine ogivri ravi, lokaalselt kaugelearenenud (sh põletikuline) haiguse või kasvajate > 2 cm läbimõõduga. ogivri tuleks kasutada ainult metastaatilise või ebc, kelle kasvajad on kas her2 overexpression või her2 geeni amplifikatsiooni mis on kindlaks määratud täpse ja valideeritud analüüs. metastaatilise mao cancerogivri koos capecitabine või 5-fluorouratsiili ja cisplatin on näidustatud ravi täiskasvanud patsientidel, kellel her2 positiivse metastaatilise adenocarcinoma kõhus või gastroesophageal ristmikul, kes ei ole eelnevalt saanud anti-vähi ravi oma metastaatilise haiguse. ogivri tuleks kasutada ainult metastaatilise mao vähk (mgc), kelle kasvajad on her2 overexpression määratletud ihc2+ ja kinnitavat sish või fish tulemus, või ihc 3+ tulemuse. täpseid ja valideeritud analüüsi meetodeid tuleks kasutada.

LERCARIL õhukese polümeerikattega tablett 에스토니아 - 에스토니아어 - Ravimiamet

lercaril õhukese polümeerikattega tablett

recordati ireland limited - enalapriil+lerkanidipiin - õhukese polümeerikattega tablett - 20mg+10mg 14tk; 20mg+10mg 30tk; 20mg+10mg 50tk; 20mg+10mg 56tk; 20mg+10mg 98tk; 20mg+10mg 7tk; 20mg+10mg 90tk; 20mg+10mg 35tk; 20mg+10mg 100tk