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

imlygic

amgen europe b.v. - talimogene laherparepvec - melanoma - antineoplastiski līdzekļi - imlygic apzīmē pieaugušajiem ar unresectable melanomas, kas ir reģionāli vai attāli metastātisku (posms iiib, iiic un ivm1a) ārstēšanai nav kaulu, smadzeņu, plaušu vai citu iekšējo orgānu slimības.

Euthanimal 20% Latvija - latviešu - Pārtikas un veterinārais dienests, Zemkopības ministrija

euthanimal 20%

alfasan nederland bv, nīderlande - pentobarbitāla nātrija sāls - šķīdums injekcijām - 200 mg/ml - aitas; cūkas; kazas; kaķi; liellopi; suņi; zirgi

Streptomycine Panpharma 1 g pulveris injekciju šķīduma pagatavošanai Latvija - latviešu - Zāļu valsts aģentūra

streptomycine panpharma 1 g pulveris injekciju šķīduma pagatavošanai

panpharma, france - streptomicīns - pulveris injekciju šķīduma pagatavošanai - 1 g

CircoMax Myco Eiropas Savienība - latviešu - EMA (European Medicines Agency)

circomax myco

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.

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

daronrix

glaxosmithkline biologicals s.a. - visu virion, inaktivēta, kas satur antigēnu*:/vjetnama/1194/2004 (h5n1)* ražots olas - influenza, human; immunization; disease outbreaks - vakcīnas - gripas profilakse oficiāli paziņotajā pandēmijas situācijā. pandēmiskās gripas vakcīna jāizmanto saskaņā ar oficiālajām vadlīnijām.

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

elzonris

stemline therapeutics b.v. - tagraxofusp - lymphoma - antineoplastiski līdzekļi - elzonris is indicated as monotherapy for the first-line treatment of adult patients with blastic plasmacytoid dendritic cell neoplasm (bpdcn).

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

bylvay

albireo - odevixibat - cholestasis, intrahepatic - Žults un aknu terapija - bylvay is indicated for the treatment of progressive familial intrahepatic cholestasis (pfic) in patients aged 6 months or older (see sections 4. 4 un 5.

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

nexpovio

stemline therapeutics b.v. - selinexor - multiple mieloma - antineoplastiski līdzekļi - nexpovio is indicatedin combination with bortezomib and dexamethasone for the treatment of adult patients with multiple myeloma who have received at least one prior therapy. in combination with dexamethasone for the treatment of multiple myeloma in adult patients who have received at least four prior therapies and whose disease is refractory to at least two proteasome inhibitors, two immunomodulatory agents and an anti-cd38 monoclonal antibody, and who have demonstrated disease progression on the last therapy.

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

orserdu

stemline therapeutics b.v. - elacestrant - krūts audzējs - endokrīnā terapija - orserdu monotherapy is indicated for the treatment of postmenopausal women, and men, with estrogen receptor (er) positive, her2-negative, locally advanced or metastatic breast cancer with an activating esr1 mutation who have disease progression following at least one line of endocrine therapy including a cdk 4/6 inhibitor.

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

palladia

zoetis belgium sa - toceranibs - antineoplastiski līdzekļi - suņi - Ārstnieciski izmantojamu neatgriezenisku patnaik ii pakāpi (vidējā pakāpe) vai -iii (augstas kvalitātes), recidivējošus, ādas mastocelozes audzējus suņiem.