Latvija - latviešu - Pārtikas un veterinārais dienests, Zemkopības ministrija

laboratories calier s.a., spānija - vitamīns b 12,caseine peptīdi,kalcija phosphorylcholine - šķīdums injekcijām - aitas; cūkas; kazas; kaķi; liellopi; suņi; zirgi

Latvija - latviešu - Pārtikas un veterinārais dienests, Zemkopības ministrija

laboratories calier s.a., spānija - carbetocin - šķīdums injekcijām - 0.05 mg/ml - cūkas; liellopi

Latvija - latviešu - Pārtikas un veterinārais dienests, Zemkopības ministrija

dopharma research b.v., nīderlande - toltrazurils - šķīdums lietošanai ar dzeramo ūdeni - 25 mg/ml - vistas

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

stada arzneimittel ag - 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 - oyavas in combination with fluoropyrimidine based chemotherapy is indicated for treatment of adult patients with metastatic carcinoma of the colon or rectum. oyavas 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. oyavas 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 oyavas in combination with capecitabine. sīkāku informāciju par her2 statusu, lūdzu, skatiet 5. sadaļā. oyavas, 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. oyavas, 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. oyavas in combination with interferon alfa 2a is indicated for first line treatment of adult patients with advanced and/or metastatic renal cell cancer. oyavas, 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. oyavas, 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. oyavas, 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 (see section 5. oyavas, 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.

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

janssen-cilag international nv - rilpivirīns - hiv infekcijas - pretvīrusu līdzekļi sistēmiskai lietošanai - rekambys is indicated, in combination with cabotegravir injection, for the treatment of human immunodeficiency virus type 1 (hiv 1) infection in adults who are virologically suppressed (hiv-1 rna < 50 copies/ml) on a stable antiretroviral regimen without present or past evidence of viral resistance to, and no prior virological failure with, agents of the nnrti and ini class.

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

janssen-cilag international nv - canagliflozin - cukura diabēts, 2. tips - cukura diabēts - invokana is indicated for the treatment of adults with insufficiently controlled type 2 diabetes mellitus as an adjunct to diet and exercise:as monotherapy when metformin is considered inappropriate due to intolerance or contraindicationsin addition to other medicinal products for the treatment of diabetes. for study results with respect to combination of therapies, effects on glycaemic control, cardiovascular and renal events, and the populations studied, see sections 4. 4, 4. 5 un 5.

Latvija - latviešu - Pārtikas un veterinārais dienests, Zemkopības ministrija

laboratorios calier, s.a., spānija - fenilbutazons - šķīdums injekcijām - 200 mg/ml - zirgi

Latvija - latviešu - Pārtikas un veterinārais dienests, Zemkopības ministrija

laboratorios calier, s.a., spānija - inaktivēta šūnas propionibacterium aknes,lipopolysaccharide e. coli šūnas - suspensija iekšķīgai lietošanai - vistas

Latvija - latviešu - Pārtikas un veterinārais dienests, Zemkopības ministrija

laboratorios liconsa, s.a. - kapsula

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

laboratorios hipra, s.a. - dzīvas novājinātas infekcijas bursal sērgas vīrusu (ibdv), celms 1052 - immunologicals par aves, vistas, dzīvu vīrusu vakcīnas, putnu infekcijas bursal sērgas vīrusu (gumboro slimība) - chicken; embryonated chicken eggs - aktīvās imunizācijas 1 dienu vecus broileru cāļus un embryonated broileru vistas olas, lai samazinātu klīniskās pazīmes un bojājumu bursa fabricius, ko izraisa ļoti bīstamu putnu infekcijas bursal slimības vīrusa infekcija.