Mulpleo (previously Lusutrombopag Shionogi) 유럽 연합 - 라트비아어 - EMA (European Medicines Agency)

mulpleo (previously lusutrombopag shionogi)

shionogi b.v. - lusutrombopag - trombocitopēnija - antihemorāģija - mulpleo ir indicēts, lai ārstētu smaga trombocitopēnija pieaugušiem pacientiem ar hronisku aknu slimību pārcieš invazīvās procedūras,.

Delstrigo 유럽 연합 - 라트비아어 - EMA (European Medicines Agency)

delstrigo

merck sharp & dohme b.v. - doravirine, lamivudīnu, tenofovir disoproxil fumarate - hiv infekcijas - antivirals for treatment of hiv infections, combinations - delstrigo ir indicēts, lai ārstētu pieaugušos ar hiv inficēti 1 bez pagātnes vai tagadnes pierādījumus par pretestību nnrti klases, lamivudīnu, vai tenofovir. delstrigo is also indicated for the treatment of adolescents aged 12 years and older weighing at least 35 kg who are infected with hiv-1 without past or present evidence of resistance to the nnrti class, lamivudine, or tenofovir and who have experienced toxicities which preclude the use of other regimens that do not contain tenofovir disoproxil.

Tamisten 5 mg apvalkotās tabletes 라트비아 - 라트비아어 - Zāļu valsts aģentūra

tamisten 5 mg apvalkotās tabletes

medochemie ltd., cyprus - solifencīna sukcināts - apvalkotā tablete - 5 mg

Milurit 150 mg tabletes 라트비아 - 라트비아어 - Zāļu valsts aģentūra

milurit 150 mg tabletes

egis pharmaceuticals plc, hungary - allopurinols - tablete - 150 mg

Milurit 200 mg tabletes 라트비아 - 라트비아어 - Zāļu valsts aģentūra

milurit 200 mg tabletes

egis pharmaceuticals plc, hungary - allopurinols - tablete - 200 mg

Allopurinol Accord 100 mg tabletes 라트비아 - 라트비아어 - Zāļu valsts aģentūra

allopurinol accord 100 mg tabletes

accord healthcare b.v., netherlands - allopurinols - tablete - 100 mg

Allopurinol Accord 300 mg tabletes 라트비아 - 라트비아어 - Zāļu valsts aģentūra

allopurinol accord 300 mg tabletes

accord healthcare b.v., netherlands - allopurinols - tablete - 300 mg

Increxxa 유럽 연합 - 라트비아어 - EMA (European Medicines Agency)

increxxa

elanco gmbh - tulatromicīns - antibakteriālie līdzekļi sistēmiskai lietošanai - cattle; pigs; sheep - cattle: treatment and metaphylaxis of bovine respiratory disease (brd) associated with mannheimia haemolytica, pasteurella multocida, histophilus somni and mycoplasma bovis susceptible to tulathromycin. slimības klātbūtne ganāmpulkā jānosaka pirms metapigaktiskas apstrādes. treatment of infectious bovine keratoconjunctivitis (ibk) associated with moraxella bovis susceptible to tulathromycin. pigs: treatment and metaphylaxis of swine respiratory disease (srd) associated with actinobacillus pleuropneumoniae, pasteurella multocida, mycoplasma hyopneumoniae, haemophilus parasuis and bordetella bronchiseptica susceptible to tulathromycin. slimības klātbūtne ganāmpulkā jānosaka pirms metapigaktiskas apstrādes. the product should only be used if pigs are expected to develop the disease within 2–3 days. aitas: Ārstēšana agrīnā stadijā infekcijas pododermatitis (pamatnes puve), kas saistīts ar bīstamu dichelobacter nodosus nepieciešama sistēmiska ārstēšana.

Jayempi 유럽 연합 - 라트비아어 - EMA (European Medicines Agency)

jayempi

nova laboratories ireland limited - azatioprīns - transplanta noraidīšana - imūnsupresanti - jayempi is indicated in combination with other immunosuppressive agents for the prophylaxis of transplant rejection in patients receiving allogenic kidney, liver, heart, lung or pancreas transplants. azathioprine is indicated in immunosuppressive regimens as an adjunct to immunosuppressive agents that form the mainstay of treatment (basis immunosuppression). jayempi is used as an immunosuppressant antimetabolite either alone or, more commonly, in combination with other agents (usually corticosteroids) and/ or procedures which influence the immune response. jayempi is indicated in patients who are intolerant to glucocorticosteroids or if the therapeutic response is inadequate despite treatment with high doses of glucocorticosteroids, in the following diseases:severe active rheumatoid arthritis (chronic polyarthritis) that cannot be kept under control by less toxic agents (disease-modifying anti-rheumatic -medicinal products – dmards)auto-immune hepatitis systemic lupus erythematosusdermatomyositispolyarteritis nodosapemphigus vulgaris and bullous pemphigoidbehçet’s diseaserefractory auto-immune haemolytic anaemia, caused by warm igg antibodieschronic refractory idiopathic thrombocytopenic purpurajayempi is used for the treatment of moderately severe to severe forms of chronic inflammatory bowel disease (ibd) (crohn’s disease or ulcerative colitis) in patients in whom glucocorticosteroid therapy is necessary, but where glucocorticosteroids are not tolerated, or in whom the disease is untreatable with other common means of first choice. it is also indicated in adult patients in relapsing multiple sclerosis, if an immunomodulatory therapy is indicated but beta interferon therapy is not possible, or a stable course has been achieved with previous treatment with azathioprine. 3jayempi is indicated for the treatment of generalised myasthenia gravis. depending on the severity of the disease, jayempi should be given in combination with glucocorticosteroids because of slow onset of action at the beginning of treatment and the glucocorticosteroid dose should be gradually reduced after several months of treatment.

Gliolan 유럽 연합 - 라트비아어 - EMA (European Medicines Agency)

gliolan

photonamic gmbh & co. kg - 5-aminolevulinic acid hydrochloride - glioma - antineoplastiski līdzekļi - gliolan ir indicēts pieaugušiem pacientiem ļaundabīgo audu vizualizēšanai ļaundabīgās gliomas ķirurģiskās iejaukšanās laikā (pasaules veselības organizācijas iii un iv pakāpe).