Unjoni Ewropea - Estonjan - EMA (European Medicines Agency)

pfizer europe ma eeig  - aksitiniib - kartsinoom, neerurakk - protein kinase inhibiitorid - inlyta is indicated for the treatment of adult patients with advanced renal cell carcinoma (rcc) after failure of prior treatment with sunitinib or a cytokine.

Unjoni Ewropea - Estonjan - 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.

Unjoni Ewropea - Estonjan - EMA (European Medicines Agency)

bayer pharma ag - regorafenib - kolorektaalne kasvaja - antineoplastic agents, protein kinase inhibitors - stivarga on näidustatud monotherapy raviks täiskasvanud patsientidel, kellel on:metastaatilise kolorektaalse vähi (crc), kes on olnud varem ravitud, või ei peeta kandidaadid, kättesaadav ravi - nende hulka kuuluvad fluoropyrimidine põhineva keemiaravi, anti-vegf ravi ja anti-egfr-ravi;unresectable või metastaatilise gastrointestinaalne stromaalne tuumor (pÕhilised), kes edenenud või on talumatus eelneva ravi imatinib ja sunitinib;hepatotsellulaarne kartsinoom (hcc), kes on olnud varem ravitud sorafenib.

Unjoni Ewropea - Estonjan - 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.

Unjoni Ewropea - Estonjan - EMA (European Medicines Agency)

forte healthcare limited - fluoksetiin - psühhoanaleptikumid - koerad - kui abi ravi eraldamine seotud häired koertel avaldub hävitamine ja sobimatu käitumise (vocalisation ja sobimatu roojamine ja / või urineerimine) ja ainult koos käitumis-muutmise tehnikad.

Unjoni Ewropea - Estonjan - EMA (European Medicines Agency)

biosimilar collaborations ireland limited - adalimumab - hidradenitis suppurativa; psoriasis; uveitis; arthritis, rheumatoid; spondylitis, ankylosing; crohn disease; colitis, ulcerative; arthritis, psoriatic - immunosuppressants, tuumornekroosifaktor alfa (tnf-α) inhibiitorid

Estonja - Estonjan - Ravimiamet

mylan ire healthcare limited - gripiviirus, inaktiveeritud, tükeldatud viirus või pinnaantigeen - süstesuspensioon - 1annus 0.5ml 1tk; 1annus 0.5ml 10tk

Unjoni Ewropea - Estonjan - EMA (European Medicines Agency)

pfizer europe ma eeig - pneumococcal polysaccharide serotype 1, pneumococcal polysaccharide serotype 3, pneumococcal polysaccharide serotype 4, pneumococcal polysaccharide serotype 5, pneumococcal polysaccharide serotype 6a, pneumococcal polysaccharide serotype 6b, pneumococcal polysaccharide serotype 7f, pneumococcal polysaccharide serotype 9v, pneumococcal polysaccharide serotype 14, pneumococcal polysaccharide serotype 18c, pneumococcal polysaccharide serotype 19a, pneumococcal polysaccharide serotype 19f, pneumococcal polysaccharide serotype 23f - pneumococcal infections; immunization - vaktsiinid - aktiivseks immuniseerimiseks invasiivse haiguse, kopsupõletiku ja ägeda keskkõrvapõletiku põhjustatud streptococcus pneumoniae imikutel, lastel ja noorukitel 6 nädalat kuni 17 aastat vältimiseks. aktiivse immuniseerimise ennetamise invasiivne haigus, mis on põhjustatud streptococcus pneumoniae täiskasvanud ≥18-aastased ja eakad. vt lõigud 4. 4 ja 5. 1, mis käsitleb kaitset spetsiifiliste pneumokokkide serotüüpide eest. kasutada prevenar 13 peaks olema põhjal kindlaks määratud euroopa liidu soovitusi arvesse võttes risk invasiivsete haiguste erinevas vanuses, aluseks comorbidities samuti varieeruvust ja serotüübi epidemioloogiat erinevates geograafilistes piirkondades.

Unjoni Ewropea - Estonjan - EMA (European Medicines Agency)

roche registration ltd. - daklüsumab - graft rejection; kidney transplantation - immunosupressandid - zenapax on näidustatud ägeda äratõukereaktsiooni de novo allogenic neerutransplantatsiooni profülaktikaks ja kasutatakse samaaegselt immunosupressiivset ravi, sh tsüklosporiini ja kortikosteroididega tugevasti immuniseeritud patsientidel.

Estonja - Estonjan - Ravimiamet

viatris healthcare limited - gripiviirus, inaktiveeritud, tükeldatud viirus või pinnaantigeen - süstesuspensioon süstlis - 1annus 0.5ml 0.5ml 1tk