Latvija - latviešu - Zāļu valsts aģentūra

teva b.v., netherlands - pregabalīns - kapsula, cietā - 75 mg

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

glaxo group limited  - retigabine - epilepsija - antiepileptics, - trobalt, kas norādīts kā palīglīdzekļa attieksmi pret narkotiku rezistentu daļējo iestāšanās lēkmēm ar vai bez sekundārā vispārināšana pacientēm 18 gadus veciem vai vecākiem ar epilepsiju, kur citu atbilstīgu narkotiku kombinācijas, ir izrādījušies neatbilstīgi vai nav bijuši panes.

Latvija - latviešu - Zāļu valsts aģentūra

johnson & johnson, uab, lithuania - risperidons - pulveris un šķīdinātājs ilgstošas darbības injekciju suspensijas pagatavošanai - 50 mg/2 ml

Latvija - latviešu - Zāļu valsts aģentūra

johnson & johnson, uab, lithuania - risperidons - pulveris un šķīdinātājs ilgstošas darbības injekciju suspensijas pagatavošanai - 37,5 mg/2 ml

Latvija - latviešu - Zāļu valsts aģentūra

krka, d.d., novo mesto, slovenia - risperidons - mutē disperģējamās tabletes - 2 mg

Latvija - latviešu - Zāļu valsts aģentūra

johnson & johnson, uab, lithuania - risperidons - pulveris un šķīdinātājs ilgstošas darbības injekciju suspensijas pagatavošanai - 25 mg/2 ml

Latvija - latviešu - Zāļu valsts aģentūra

krka, d.d., novo mesto, slovenia - risperidons - mutē disperģējamās tabletes - 1 mg

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

janssen-cilag international nv - darunavir - hiv infekcijas - pretvīrusu līdzekļi sistēmiskai lietošanai - prezista, co administered with low dose ritonavir is indicated in combination with other antiretroviral medicinal products for the treatment of human immunodeficiency virus (hiv 1) infection in adult and paediatric patients from the age of 3 years and at least 15 kg body weight. prezista, co administered with cobicistat is indicated in combination with other antiretroviral medicinal products for the treatment of human immunodeficiency virus (hiv 1) infection in adults and adolescents (aged 12 years and older, weighing at least 40 kg). in deciding to initiate treatment with prezista co administered with cobicistat or low dose ritonavir, careful consideration should be given to the treatment history of the individual patient and the patterns of mutations associated with different agents. genotypic or phenotypic testing (when available) and treatment history should guide the use of prezista. prezista, co administered with low dose ritonavir is indicated in combination with other antiretroviral medicinal products for the treatment of patients with human immunodeficiency virus (hiv 1) infection. prezista 75 mg, 150 mg, and 600 mg tablets may be used to provide suitable dose regimens:for the treatment of hiv 1 infection in antiretroviral treatment (art) experienced adult patients, including those that have been highly pre treated. for the treatment of hiv 1 infection in paediatric patients from the age of 3 years and at least 15 kg body weight. in deciding to initiate treatment with prezista co administered with low dose ritonavir, careful consideration should be given to the treatment history of the individual patient and the patterns of mutations associated with different agents. genotypic or phenotypic testing (when available) and treatment history should guide the use of prezista. prezista, co administered with low dose ritonavir is indicated in combination with other antiretroviral medicinal products for the treatment of patients with human immunodeficiency virus (hiv 1) infection. prezista, co administered with cobicistat is indicated in combination with other antiretroviral medicinal products for the treatment of human immunodeficiency virus (hiv 1) infection in adults and adolescents (aged 12 years and older, weighing at least 40 kg). prezista 400 mg and 800 mg tablets may be used to provide suitable dose regimens for the treatment of hiv 1 infection in adult and paediatric patients from the age of 3 years and at least 40 kg body weight who are:antiretroviral therapy (art) naïve. art experienced with no darunavir resistance associated mutations (drv rams) and who have plasma hiv 1 rna < 100,000 copies/ml and cd4+ cell count ≥ 100 cells x 106/l. in deciding to initiate treatment with prezista in such art experienced patients, genotypic testing should guide the use of prezista.

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

eli lilly nederland b.v. - galcanezumab - migrēnas traucējumi - analgesics, galcanezumab - emgality ir norādīts migrēnas profilaksei pieaugušajiem, kam ir vismaz 4 migrēnas dienas mēnesī.

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

mérial - infekciozais katarālais drudzis-vīrusu serotipu-2 antigēnu, infekciozais katarālais drudzis-vīrusu serotipu-4 antigēnu - infekciozā katarālā drudža vīrusu, inaktivētu vīrusu vakcīnām, immunologicals par ovidae - aitas - aktīvās imunizācijas aitu, lai novērstu virēmija un samazināt klīniskās pazīmes, ko izraisa infekciozā katarālā drudža vīrusa serotipu 2. un 4..