Relifex 1 g apvalkotās tabletes Latvija - latvių - Zāļu valsts aģentūra

relifex 1 g apvalkotās tabletes

meda ab, sweden - nabumetons - apvalkotā tablete - 1 g

Relifex 500 mg apvalkotās tabletes Latvija - latvių - Zāļu valsts aģentūra

relifex 500 mg apvalkotās tabletes

meda ab, sweden - nabumetons - apvalkotās tabletes - 500 mg

Tetraciklīns „Ņižfarm” 30 mg/g ziede Latvija - latvių - Zāļu valsts aģentūra

tetraciklīns „Ņižfarm” 30 mg/g ziede

as Ņižfarm pārstāvniecība, latvija - tetraciklīna hidrohlorīds - ziede - 30 mg/g

Brimonal 2 mg/ml acu pilieni, šķīdums Latvija - latvių - Zāļu valsts aģentūra

brimonal 2 mg/ml acu pilieni, šķīdums

unimed pharma spol. s r.o., slovakia - brimonidīna tartrāts - acu pilieni, šķīdums - 2 mg/ml

Cordarone 50 mg/ml koncentrāts injekciju/infūziju šķīduma pagatavošanai Latvija - latvių - Zāļu valsts aģentūra

cordarone 50 mg/ml koncentrāts injekciju/infūziju šķīduma pagatavošanai

sanofi-aventis latvia, sia, latvija - amiodarona hidrohlorīds - koncentrāts injekciju/infūziju šķīduma pagatavošanai - 50 mg/ml

Alunbrig Europos Sąjunga - latvių - EMA (European Medicines Agency)

alunbrig

takeda pharma a/s - brigatinib - karcinoma, nesīkšūnu plaušas - antineoplastiski līdzekļi - alunbrig is indicated as monotherapy for the treatment of adult patients with anaplastic lymphoma kinase (alk)‑positive advanced non‑small cell lung cancer (nsclc) previously not treated with an alk inhibitor. alunbrig is indicated as monotherapy for the treatment of adult patients with anaplastic lymphoma kinase alkpositive advanced nsclc previously treated with crizotinib.

Dovprela (previously Pretomanid FGK) Europos Sąjunga - latvių - EMA (European Medicines Agency)

dovprela (previously pretomanid fgk)

mylan ire healthcare limited - pretomanid - tuberkuloze, pret multidrugiem izturīga - antimikobaktērijas - dovprela is indicated in combination with bedaquiline and linezolid, in adults, for the treatment of pulmonary extensively drug resistant (xdr), or treatment-intolerant or nonresponsive multidrug-resistant (mdr) tuberculosis (tb). jāņem vērā oficiālās vadlīnijas par piemērotu izmantot antibakteriālas vielas.

Koselugo Europos Sąjunga - latvių - EMA (European Medicines Agency)

koselugo

astrazeneca ab - selumetinib sulfate - neurofibromatosis 1 - antineoplastiski līdzekļi - koselugo as monotherapy is indicated for the treatment of symptomatic, inoperable plexiform neurofibromas (pn) in paediatric patients with neurofibromatosis type 1 (nf1) aged 3 years and above.

Imoxat Europos Sąjunga - latvių - EMA (European Medicines Agency)

imoxat

chanelle pharmaceuticals manufacturing ltd - imidakloprīdu, moksidektīns - antiparasitic products, insecticides and repellents, macrocyclic lactones, milbemycins - cats; dogs; ferrets - for cats suffering from, or at risk from, mixed parasitic infections:• the treatment and prevention of flea infestation (ctenocephalides felis),• the treatment of ear mite infestation (otodectes cynotis),• the treatment of notoedric mange (notoedres cati),• the treatment of the lungworm eucoleus aerophilus (syn. capillaria aerophila) (adults),• the prevention of lungworm disease (l3/l4 larvae of aelurostrongylus abstrusus),• the treatment of the lungworm aelurostrongylus abstrusus (adults),• the treatment of the eye worm thelazia callipaeda (adults),• the prevention of heartworm disease (l3 and l4 larvae of dirofilaria immitis),• the treatment of infections with gastrointestinal nematodes (l4 larvae, immature adults and adults of toxocara cati and ancylostoma tubaeforme). Šīs veterinārās zāles var izmantot kā daļu no blusu alerģiskā dermatīta (fad) terapijas stratēģijas..  for ferrets suffering from, or at risk from, mixed parasitic infections:• the treatment and prevention of flea infestation (ctenocephalides felis),• the prevention of heartworm disease (l3 and l4 larvae of dirofilaria immitis).  for dogs suffering from, or at risk from, mixed parasitic infections:• the treatment and prevention of flea infestation (ctenocephalides felis),• the treatment of biting lice (trichodectes canis),• the treatment of ear mite infestation (otodectes cynotis), sarcoptic mange (caused by sarcoptes scabiei var. canis), demodicosis (caused by demodex canis),• the prevention of heartworm disease (l3 and l4 larvae of dirofilaria immitis),• the treatment of circulating microfilariae (dirofilaria immitis),• the treatment of cutaneous dirofilariosis (adult stages of dirofilaria repens)• the prevention of cutaneous dirofilariosis (l3 larvae of dirofilaria repens),• the reduction of circulating microfilariae (dirofilaria repens),• the prevention of angiostrongylosis (l4 larvae and immature adults of angiostrongylus vasorum),• the treatment of angiostrongylus vasorum and crenosoma vulpis,• the prevention of spirocercosis (spirocerca lupi),• the treatment of eucoleus (syn. capillaria) boehmi (adults),• the treatment of the eye worm thelazia callipaeda (adults),• the treatment of infections with gastrointestinal nematodes (l4 larvae, immature adults and adults of toxocara canis, ancylostoma caninum and uncinaria stenocephala, adults of toxascaris leonina and trichuris vulpis). Šīs veterinārās zāles var izmantot kā daļu no blusu alerģiskā dermatīta (fad) terapijas stratēģijas..

Amvuttra Europos Sąjunga - latvių - EMA (European Medicines Agency)

amvuttra

alnylam netherlands b.v. - vutrisiran sodium - amyloid neuropathies, familial - other nervous system drugs - treatment of hereditary transthyretin-mediated amyloidosis (hattr amyloidosis) in adult patients with stage 1 or stage 2 polyneuropathy.