유럽 연합 - 라트비아어 - EMA (European Medicines Agency)

accord healthcare s.l.u. - fingolimod hidrohlorīds - multiplā skleroze, recidivējoši-pārskaitot - immunosuppressants, selektīvi immunosuppressants - norāda kā vienu slimību modificējošiem terapija ir ļoti aktīvs recidivējoši pārskaitot multiplo sklerozi, par šādu grupu pieaugušiem pacientiem un pediatrijas pacienti vecumā no 10 gadiem un vecāki:pacientiem ar ļoti aktīvu slimību, neskatoties uz pilnu un atbilstošu ārstēšanas kursu, ar vismaz vienu slimību modificējošiem therapyorpatients strauji attīstās smagas recidivējoši pārskaitot multiplā skleroze definēts 2 vai vairāk atspējošana recidīvu vienu gadu, un ar 1 vai vairāk gadolīnija uzlabot bojājumi uz smadzeņu mri vai ievērojami palielināt t2 bojājumu slodzes salīdzinājumā ar iepriekšējā pēdējo mr.

유럽 연합 - 라트비아어 - EMA (European Medicines Agency)

celltrion healthcare hungary kft. - bevacizumab - colorectal neoplasms; breast neoplasms; ovarian neoplasms; fallopian tube neoplasms; peritoneal neoplasms; carcinoma, non-small-cell lung; carcinoma, renal cell; uterine cervical neoplasms - antineoplastiski līdzekļi - vegzelma in combination with fluoropyrimidine based chemotherapy is indicated for treatment of adult patients with metastatic carcinoma of the colon or rectum. vegzelma in combination with paclitaxel is indicated for first line treatment of adult patients with metastatic breast cancer. papildinformāciju par cilvēka epidermas augšanas faktora 2 receptora (her2) statusu, lūdzu, skatiet 5. sadaļā. vegzelma 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 vegzelma in combination with capecitabine. sīkāku informāciju par her2 statusu, lūdzu, skatiet 5. sadaļā. vegzelma, 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 (nsclc) other than predominantly squamous cell histology. vegzelma, in combination with erlotinib, is indicated for first line treatment of adult patients with unresectable advanced, metastatic or recurrent nsclc with epidermal growth factor receptor (egfr) activating mutations (see section 5. vegzelma, in combination with interferon alfa 2a is indicated for first line treatment of adult patients with advanced and/or metastatic renal cell cancer. vegzelma, 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. vegzelma, 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 vascular endothelial growth factor (vegf) inhibitors or vegf receptor–targeted agents. vegzelma 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. vegzelma, 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.

라트비아 - 라트비아어 - Zāļu valsts aģentūra

sandoz d.d., slovenia - piperacillinum, tazobactamum - pulveris infūziju šķīduma pagatavošanai - 4000 mg/500 mg

라트비아 - 라트비아어 - Zāļu valsts aģentūra

aurobindo pharma (malta) limited, malta - piperacillinum, tazobactamum - pulveris infūziju šķīduma pagatavošanai - 2 g/0,25 g

라트비아 - 라트비아어 - Zāļu valsts aģentūra

eugia pharma (malta) limited, malta - piperacillinum, tazobactamum - pulveris infūziju šķīduma pagatavošanai - 4 g/0,5 g

유럽 연합 - 라트비아어 - EMA (European Medicines Agency)

bristol-myers squibb pharma eeig - azacitidine - myelodysplastic syndromes; leukemia, myelomonocytic, chronic; leukemia, myeloid, acute - antineoplastiski līdzekļi - vidaza is indicated for the treatment of adult patients who are not eligible for haematopoietic stem cell transplantation (hsct) with: intermediate 2 and high-risk myelodysplastic syndromes (mds) according to the international prognostic scoring system (ipss),chronic myelomonocytic leukaemia (cmml) with 10 29 % marrow blasts without myeloproliferative disorder,acute myeloid leukaemia (aml) with 20 30 % blasts and multi-lineage dysplasia, according to world health organisation (who) classification. vidaza is indicated for the treatment of adult patients aged 65 years or older who are not eligible for hsct with aml with >30% marrow blasts according to the who classification.

라트비아 - 라트비아어 - Zāļu valsts aģentūra

olainfarm, as, latvia - ciprofloksacīns - apvalkotā tablete - 250 mg

라트비아 - 라트비아어 - Zāļu valsts aģentūra

olainfarm, as, latvia - ciprofloksacīns - apvalkotā tablete - 500 mg

라트비아 - 라트비아어 - Zāļu valsts aģentūra

baxter holding b.v., netherlands - ciprofloksacīns - Šķīdums infūzijām - 2 mg/ml

라트비아 - 라트비아어 - Zāļu valsts aģentūra

unifarma, sia, latvia - ciprofloksacīns - Šķīdums infūzijām - 2 mg/ml