ইউরোপীয় ইউনিয়ন - এস্তোনীয় - EMA (European Medicines Agency)

zoetis belgium sa - muudetud elusate sigade hingamisteede ja reproduktiivne sündroom viirus - immunologicals for suidae, live viral vaccines - sead - aktiivse immuniseerimise kliiniliselt tervete sigade alates 1. päev vanuse sigade hingamisteede ja reproduktiivne sündroom (prrs) viirusega saastunud keskkond, vähendada viraemia ja nina kadumas põhjustatud infektsioon koos euroopa liinide prrs viirus (genotüüp 1). täiskasvanud sigad: lisaks näidati, et seronegatiivsete 1-päevaste põrsaste vaktsineerimine vähendas kopsukahjustusi 26 nädala jooksul pärast vaktsineerimist. näidati, et seronegatiivsete 2-nädalaste põrsaste vaktsineerimine vähendas kopsukahjustusi ja suukaudset levikut 28 päeva ja 16 nädalat pärast vaktsineerimist. nooremiste ja emiste puhul: lisaks eel-raseduse ajal vaktsineerimine kliiniliselt terve nooremiste ja emiste puhul, kas seropositive või seronegative, näitas, et vähendada transplatsentaarse nakatumise põhjustatud prrs viirus raseduse kolmandal trimestril raseduse ja vähendada nendega seotud negatiivne mõju paljunemine (vähendada esinemise stillbirths, põrsa viraemia sünnil ja võõrutamine, kopsu kahjustused ja viirusliku koormus kopse põrsad kell võõrutamiseni).

ইউরোপীয় ইউনিয়ন - এস্তোনীয় - EMA (European Medicines Agency)

glaxosmithkline (ireland) limited - niraparib (tosilate monohydrate) - fallopian tube neoplasms; peritoneal neoplasms; ovarian neoplasms - antineoplastilised ained - zejula is indicated: , as monotherapy for the maintenance treatment of adult patients with advanced epithelial (figo stages iii and iv) high-grade ovarian, fallopian tube or primary peritoneal cancer who are in response (complete or partial) following completion of first-line platinum-based chemotherapy. , as monotherapy for the maintenance treatment of adult patients with platinum sensitive relapsed high grade serous epithelial ovarian, fallopian tube, or primary peritoneal cancer who are in response (complete or partial) to platinum based chemotherapy.

ইউরোপীয় ইউনিয়ন - এস্তোনীয় - EMA (European Medicines Agency)

pharmaand gmbh - rucaparib camsylate - munasarjade kasvajad - antineoplastilised ained - rubraca is indicated as monotherapy for the maintenance treatment of adult patients with advanced (figo stages iii and iv) high-grade epithelial ovarian, fallopian tube, or primary peritoneal cancer who are in response (complete or partial) following completion of first-line platinum-based chemotherapy. rubraca on näidustatud monotherapy hooldus-ravi täiskasvanud patsientidel, kellel on plaatina-tundlik taastekkinud kõrge kvaliteediga epiteeli munasarja -, munajuha-või esmase peritoneaaldialüüsi vähi, kes on vastuseks (täielik või osaline) platinum põhineva keemiaravi.

ইউরোপীয় ইউনিয়ন - এস্তোনীয় - EMA (European Medicines Agency)

astrazeneca ab - durvalumab - kartsinoom, mitteväikerakk-kopsu - antineoplastilised ained - non-small cell lung cancer (nsclc)imfinzi as monotherapy is indicated for the treatment of locally advanced, unresectable non small cell lung cancer (nsclc) in adults whose tumours express pd-l1 on ≥ 1% of tumour cells and whose disease has not progressed following platinum based chemoradiation therapy (see section 5. imfinzi in combination with tremelimumab and platinum-based chemotherapy is indicated for the first-line treatment of adults with metastatic nsclc with no sensitising egfr mutations or alk positive mutations. small cell lung cancer (sclc)imfinzi in combination with etoposide and either carboplatin or cisplatin is indicated for the first-line treatment of adults with extensive-stage small cell lung cancer (es-sclc). biliary tract cancer (btc)imfinzi in combination with gemcitabine and cisplatin is indicated for the first line treatment of adults with unresectable or metastatic biliary tract cancer (btc). hepatocellular carcinoma (hcc)imfinzi in combination with tremelimumab is indicated for the first line treatment of adults with advanced or unresectable hepatocellular carcinoma (hcc).

ইউরোপীয় ইউনিয়ন - এস্তোনীয় - EMA (European Medicines Agency)

regeneron ireland designated activity company (dac) - cemiplimab - kartsinoom, squamous cell - antineoplastilised ained - cutaneous squamous cell carcinomalibtayo as monotherapy is indicated for the treatment of adult patients with metastatic or locally advanced cutaneous squamous cell carcinoma (mcscc or lacscc) who are not candidates for curative surgery or curative radiation. basal cell carcinomalibtayo as monotherapy is indicated for the treatment of adult patients with locally advanced or metastatic basal cell carcinoma (labcc or mbcc) who have progressed on or are intolerant to a hedgehog pathway inhibitor (hhi). non-small cell lung cancerlibtayo as monotherapy is indicated for the first-line treatment of adult patients with non-small cell lung cancer (nsclc) expressing pd-l1 (in ≥ 50% tumour cells), with no egfr, alk or ros1 aberrations, who have:locally advanced nsclc who are not candidates for definitive chemoradiation, ormetastatic nsclc. libtayo in combination with platinum‐based chemotherapy is indicated for the first‐line treatment of adult patients with nsclc expressing pd-l1 (in ≥ 1% of tumour cells), with no egfr, alk or ros1 aberrations, who have:locally advanced nsclc who are not candidates for definitive chemoradiation, ormetastatic nsclc. cervical cancerlibtayo as monotherapy is indicated for the treatment of adult patients with recurrent or metastatic cervical cancer and disease progression on or after platinum-based chemotherapy.

ইউরোপীয় ইউনিয়ন - এস্তোনীয় - EMA (European Medicines Agency)

elanco gmbh - pegbovigrastim - koloonia stimuleerivaid faktoreid, immunostimulants, antineoplastilised ained - cattle (cows and heifers); cattle - haigekassa juhtimisprogrammina antav abi kliinilise mastiidi ohu vähendamiseks periparturulistes piimalehmades ja mullikatel 30 päeva jooksul pärast poegimist.

ইউরোপীয় ইউনিয়ন - এস্তোনীয় - EMA (European Medicines Agency)

intervet international bv - clostridium perfringens tüüp c / escherichia coli f4ab / e. coli f4ac / e. coli f5 / e. coli f6 / e. coli lt - immunoloogilised vahendid - sead - on passiivse immuniseerimise kohta järglaskonna aktiivse immuniseerimise emiste ja nooremiste vähendada suremust ja kliinilisi tunnuseid esimeste päevade jooksul elu, mis on põhjustatud nende escherichia coli tüved, mis väljendavad adhesins f4ab (k88ab), f4ac (k88ac), f5 (k99) või f6 (987p) ja põhjustatud clostridium perfringens tüüp c.

ইউরোপীয় ইউনিয়ন - এস্তোনীয় - EMA (European Medicines Agency)

zoetis belgium sa - live nõrgenenud aujeszky haiguse viirus - immunoloogilised vahendid - sead - sigade aktiivne immuniseerimine alates 10 nädala vanusest, et vältida aujeszky haiguse suremust ja kliinilisi tunnuseid ning vähendada aujeszky haiguse väliuuringu viiruse. vaktsineeritud noorte ja emiste järglaste passiivne immuniseerimine, et vähendada aujeszky haiguse suremust ja kliinilisi tunnuseid ning vähendada aujeszky haiguse põldviiruse eritumist.

ইউরোপীয় ইউনিয়ন - এস্তোনীয় - EMA (European Medicines Agency)

bristol-myers squibb pharma eeig - ipilimumab - melanoma; carcinoma, renal cell; carcinoma, non-small-cell lung; mesothelioma, malignant; colorectal neoplasms - antineoplastilised ained - melanomayervoy as monotherapy or combination with nivolumab is indicated for the treatment of advanced (unresectable or metastatic) melanoma in adults and adolescents 12 years of age and older (see section 4.  yervoy in combination with nivolumab is indicated for the treatment of advanced (unresectable or metastatic) melanoma in adults. relative to nivolumab monotherapy, an increase in progression-free survival (pfs) and overall survival (os) for the combination of nivolumab with ipilimumab is established only in patients with low tumour pd-l1 expression (see sections 4. 4 ja 5. renal cell carcinoma (rcc)yervoy in combination with nivolumab is indicated for the first-line treatment of adult patients with intermediate/poor-risk advanced renal cell carcinoma (see section 5. non-small cell lung cancer (nsclc)yervoy in combination with nivolumab and 2 cycles of platinum-based chemotherapy is indicated for the first-line treatment of metastatic non-small cell lung cancer in adults whose tumours have no sensitising egfr mutation or alk translocation. malignant pleural mesothelioma (mpm)yervoy in combination with nivolumab is indicated for the first-line treatment of adult patients with unresectable malignant pleural mesothelioma. mismatch repair deficient (dmmr) or microsatellite instability-high (msi-h) colorectal cancer (crc)yervoy in combination with nivolumab is indicated for the treatment of adult patients with mismatch repair deficient or microsatellite instability-high metastatic colorectal cancer after prior fluoropyrimidine based combination chemotherapy (see section 5. oesophageal squamous cell carcinoma (oscc)yervoy in combination with nivolumab is indicated for the first-line treatment of adult patients with unresectable advanced, recurrent or metastatic oesophageal squamous cell carcinoma with tumour cell pd-l1 expression ≥ 1%.

ইউরোপীয় ইউনিয়ন - এস্তোনীয় - 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.