Lotyšsko - lotyština - Zāļu valsts aģentūra

octapharma italy, italy - imūbnglobulīns, anti-d, cilvēka - Šķīdums injekcijām - 625 sv/ml

Lotyšsko - lotyština - Zāļu valsts aģentūra

octapharma (ip) sprl, belgium - imūbnglobulīns, anti-d, cilvēka - Šķīdums injekcijām - 625 sv/ml

Evropská unie - lotyština - EMA (European Medicines Agency)

baxalta innovations gmbh - imūbnglobulīns, normālais, cilvēka - imūndeficīta sindromi - un imūnglobulīni, - aizvietošanas terapija pieaugušajiem, bērniem un pusaudžiem (0 līdz 18 gadiem): primārā imūndeficīta sindromu ar ierobežotu antivielu ražošanas. hypogammaglobulinaemia un periodisko bakteriālas infekcijas pacientiem ar hronisku limfocītu leikēmija (cll), kuram, profilaktiskās antibiotikas nav vai tie nav norādīts. hypogammaglobulinaemia un periodisko bakteriālas infekcijas multiplā mieloma (mm) pacientiem. hypogammaglobulinaemia pacientiem pirms un pēc alogēnas asinsrades cilmes šūnu transplantācijas (hsct).

Evropská unie - lotyština - 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.

Evropská unie - lotyština - EMA (European Medicines Agency)

novartis europharm limited - eltrombopags - purpura, trombocitopēnija, idiopātija - other systemic hemostatics, antihemorrhagics - revolade is indicated for the treatment of adult patients with primary immune thrombocytopenia (itp) who are refractory to other treatments (e. corticosteroids, immunoglobulins) (see sections 4. 2 un 5. revolade is indicated for the treatment of paediatric patients aged 1 year and above with primary immune thrombocytopenia (itp) lasting 6 months or longer from diagnosis and who are refractory to other treatments (e. corticosteroids, immunoglobulins) (see sections 4. 2 un 5. revolade is indicated in adult patients with chronic hepatitis c virus (hcv) infection for the treatment of thrombocytopenia, where the degree of thrombocytopenia is the main factor preventing the initiation or limiting the ability to maintain optimal interferon-based therapy (see sections 4. 4 and 5. revolade is indicated in adult patients with acquired severe aplastic anaemia (saa) who were either refractory to prior immunosuppressive therapy or heavily pretreated and are unsuitable for haematopoietic stem cell transplantation (see section 5.

Lotyšsko - lotyština - Pārtikas un veterinārais dienests, Zemkopības ministrija

bellum, sia lv40003202289 artilērijas 13 k.2-20, rīga - cits, pulveris dzēriena pagatavošanai - cits - pārtikas produkts, kas paredzēts intensīvas muskuļu piepūles gadījumos, īpaši sportistiem, atbilstoši eiropas parlamenta un padomes 2009.gada 6.maija direktīvas 2009/39/ek par īpašas diētas pārtikas produktiem 1.pielikuma a daļas 5.apakšpunktam

Lotyšsko - lotyština - Pārtikas un veterinārais dienests, Zemkopības ministrija

spēka pasaule, biedrība 40008062117 raiņa ielā 3, valmiera, lv-4201, latvija - pulveris - cits - pārtikas produkts, kas paredzēts intensīvas muskuļu piepūles gadījumos, īpaši sportistiem

Lotyšsko - lotyština - Pārtikas un veterinārais dienests, Zemkopības ministrija

bellum, sia lv40003202289 artilērijas 13 k.2-20, rīga - cits, pulveris dzēriena pagatavošanai - cits - pārtikas produkts, kas paredzēts intensīvas muskuļu piepūles gadījumos, īpaši sportistiem

Lotyšsko - lotyština - Pārtikas un veterinārais dienests, Zemkopības ministrija

bellum, sia lv40003202289 artilērijas 13 k.2-20, rīga - pulveris - cits - pārtikas produkts, kas paredzēts intensīvas muskuļu piepūles gadījumos, īpaši sportistiem.

Lotyšsko - lotyština - Pārtikas un veterinārais dienests, Zemkopības ministrija

veselības pasaule, sia - pulveris