Eiropas Savienība - latviešu - EMA (European Medicines Agency)

ceva-phylaxia veterinary biologicals co. ltd - turkey herpes virus, strain rhvt/nd/ibd, expressing the fusion protein of newcastle disease virus and the vp2 protein of infectious bursal disease virus, live recombinant - imunoloģisks aves - embryonated chicken eggs; chicken - for the active immunisation of one-day-old chicks or 18-day-old chicken embryonated eggs to reduce mortality, clinical signs and lesions caused by newcastle disease virus (ndv) and to reduce virus shedding; to reduce mortality, clinical signs and bursa lesions caused by very virulent infectious bursal disease virus (ibdv); to reduce mortality, clinical signs and lesions caused by classical marek’s disease virus (mdv).

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

zoetis belgium - inactivated mycoplasma hyopneumoniae, strain p-5722-3, inactivated recombinant chimeric porcine circovirus type 1 containing the porcine circovirus type 2a open reading frame 2 (orf2) protein, inactivated recombinant chimeric porcine circovirus type 1 containing the porcine circovirus type 2b orf2 protein - imunoloģiskie līdzekļi suidae - cūkas (nobarošanas) - active immunisation of pigs against porcine circovirus type 2 to reduce viral load in blood and lymphoid tissues, fecal shedding and the lesions in lymphoid tissues associated with pcv2 infection. protection was demonstrated against porcine circovirus types 2a, 2b and 2d. active immunisation of pigs against mycoplasma hyopneumoniae to reduce the lung lesions associated with mycoplasma hyopneumoniae infection.  onset of immunity (both vaccination schedules): 3 weeks after (the last) vaccination.  duration of immunity (both vaccination schedules): 23 weeks after (the last) vaccination.  in addition, vaccination has been shown to reduce body weight gain losses under field conditions.

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

laboratoire francais du fractionnement et des biotechnologies - eptacog beta (activated) - hemophilia a; hemophilia b - antihemorāģija - cevenfacta is indicated in adults and adolescents (12 years of age and older) for the treatment of bleeding episodes and for the prevention of bleeding in those undergoing surgery or invasive procedures in the following patient groups:in patients with congenital haemophilia with high-responding inhibitors to coagulation factors viii or ix (i. ≥5 bethesda units (bu)); in patients with congenital haemophilia with low titre inhibitors (bu.

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

pfizer ireland pharmaceuticals - ceftarolīna fosamils - community-acquired infections; skin diseases, infectious; pneumonia - antibakteriālas līdzekļi sistēmiskai lietošanai, - zinforo is indicated for the treatment of the following infections in neonates, infants, children, adolescents and adults: , complicated skin and soft tissue infections (cssti), community-acquired pneumonia (cap) , consideration should be given to official guidance on the appropriate use of antibacterial agents.

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

merck sharp & dohme b.v. - ertugliflozin l-pyroglutamic acid, metformin hydrochloride - cukura diabēts, 2. tips - drugs used in diabetes, combinations of oral blood glucose lowering drugs - segluromet is indicated in adults aged 18 years and older with type 2 diabetes mellitus as an adjunct to diet and exercise to improve glycaemic control:in patients not adequately controlled on their maximally tolerated dose of metformin alonein patients on their maximally tolerated doses of metformin in addition to other medicinal products for the treatment of diabetesin patients already being treated with the combination of ertugliflozin and metformin as separate tablets.

Latvija - latviešu - Zāļu valsts aģentūra

zentiva, k.s., czech republic - dienogestum, ethinylestradiolum - apvalkotā tablete - 2 mg/0,03 mg

Latvija - latviešu - Zāļu valsts aģentūra

accord healthcare b.v., netherlands - meropenēms - pulveris injekciju/infūziju šķīduma pagatavošanai - 1 g

Latvija - latviešu - Zāļu valsts aģentūra

sandoz d.d., slovenia - ethinylestradiolum, drospirenonum - apvalkotā tablete - 0,03 mg/3 mg

Latvija - latviešu - Zāļu valsts aģentūra

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

Latvija - latviešu - Zāļu valsts aģentūra

teva pharma b.v., netherlands - piperacillinum, tazobactamum - pulveris infūziju šķīduma pagatavošanai - 4000 mg/500 mg