Alymsys Eiropas Savienība - latviešu - EMA (European Medicines Agency)

alymsys

mabxience research sl - bevacizumab - colorectal neoplasms; breast neoplasms; ovarian neoplasms; peritoneal neoplasms; carcinoma, non-small-cell lung; carcinoma, renal cell; uterine cervical neoplasms - antineoplastiski līdzekļi - alymsys in combination with fluoropyrimidine based chemotherapy is indicated for treatment of adult patients with metastatic carcinoma of the colon or rectum. alymsys in combination with paclitaxel is indicated for first line treatment of adult patients with metastatic breast cancer. alymsys 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 alymsys in combination with capecitabine. alymsys, 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. alymsys, 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. alymsys in combination with interferon alfa 2a is indicated for first line treatment of adult patients with advanced and/or metastatic renal cell cancer. alymsys, 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. alymsys, 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. alymsys, in combination with 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. alymsys, 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.

Miglustat Gen.Orph Eiropas Savienība - latviešu - EMA (European Medicines Agency)

miglustat gen.orph

gen.orph - miglustat - gošē slimība - citas gremošanas trakta un metabolisma produkti, - miglustat gen. orph indicēts iekšķīgo ārstēšanu pieaugušiem pacientiem ar vieglas līdz vidēji tipa 1 gošē slimība. miglustat gen. orph var izmantot tikai attieksmi pret pacientiem, par kuriem enzīma aizstājterapija ir nepiemērots. miglustat gen. orph ir indicēts, lai ārstētu progresējošu neiroloģiskas izpausmes pieaugušiem pacientiem un pediatrijā, pacientiem ar niemann-pick c tipa slimības.

Rilonacept Regeneron (previously Arcalyst) Eiropas Savienība - latviešu - EMA (European Medicines Agency)

rilonacept regeneron (previously arcalyst)

regeneron uk limited - rilonacepts - cryopyrin saistītie periodiskie sindromi - imūnsupresanti - rilonacept regeneron tiek norādīts cryopyrin saistīto periodisku sindromi (caps) ārstēšanai ar smagi simptomi, ieskaitot ģimenisko aukstā auto iekaisuma sindroms (fcas) un muckle wells sindroms (mws) pieaugušajiem un bērniem vecumā no 12 gadiem un vecāki.

Vamadrid 40 mg apvalkotās tabletes Latvija - latviešu - Zāļu valsts aģentūra

vamadrid 40 mg apvalkotās tabletes

laboratorios liconsa, s.a., spain - valsartāns - apvalkotā tablete - 40 mg

Vamadrid 80 mg apvalkotās tabletes Latvija - latviešu - Zāļu valsts aģentūra

vamadrid 80 mg apvalkotās tabletes

laboratorios liconsa, s.a., spain - valsartāns - apvalkotā tablete - 80 mg

Vamadrid 160 mg apvalkotās tabletes Latvija - latviešu - Zāļu valsts aģentūra

vamadrid 160 mg apvalkotās tabletes

laboratorios liconsa, s.a., spain - valsartāns - apvalkotā tablete - 160 mg

Vamadrid 320 mg apvalkotās tabletes Latvija - latviešu - Zāļu valsts aģentūra

vamadrid 320 mg apvalkotās tabletes

laboratorios liconsa, s.a., spain - valsartāns - apvalkotā tablete - 320 mg

Co-Codamol 500 mg/8 mg tabletes Latvija - latviešu - Zāļu valsts aģentūra

co-codamol 500 mg/8 mg tabletes

actavis group ptc ehf., iceland - paracetamolum, codeini phosphas hemihydricus - tablete - 500 mg/8 mg