Венгрия - венгерский - OGYÉI (Országos Gyógyszerészeti és Élelmezés-egészségügyi Intézetről)

menarini international operations luxembourg sa - olmesartan -

Венгрия - венгерский - OGYÉI (Országos Gyógyszerészeti és Élelmezés-egészségügyi Intézetről)

menarini international operations luxembourg sa - olmesartan -

Венгрия - венгерский - OGYÉI (Országos Gyógyszerészeti és Élelmezés-egészségügyi Intézetről)

menarini international operations luxembourg sa - olmesartan -

Европейский союз - венгерский - EMA (European Medicines Agency)

janssen-cilag international n.v.   - paliperidon-palmitát - skizofrénia - pszicholeptikumok - byannli (previously paliperidone janssen-cilag international) a 6 monthly injection, is indicated for the maintenance treatment of schizophrenia in adult patients who are clinically stable on 1 monthly or 3 monthly paliperidone palmitate injectable products (see section 5.

Венгрия - венгерский - OGYÉI (Országos Gyógyszerészeti és Élelmezés-egészségügyi Intézetről)

medicopus nonprofit kft. - 18f-fluoromethylcholin -

Венгрия - венгерский - OGYÉI (Országos Gyógyszerészeti és Élelmezés-egészségügyi Intézetről)

pfizer kft. - idarubicin -

Венгрия - венгерский - OGYÉI (Országos Gyógyszerészeti és Élelmezés-egészségügyi Intézetről)

pfizer kft. - idarubicin -

Европейский союз - венгерский - EMA (European Medicines Agency)

boehringer ingelheim international gmbh - telmisartan - magas vérnyomás - szív-és érrendszer - esszenciális hipertónia kezelése a felnőttek:add on therapyonduarp javallt felnőtteknél, akiknek vérnyomása nem megfelelően ellenőrzött a amlodipin. csere therapyadult részesülő betegeknél, a telmizartán, az amlodipin a különálló tabletta formájában lehet kapni, tabletta onduarp, amelyek ugyanezt a komponens adag.

Европейский союз - венгерский - EMA (European Medicines Agency)

janssen-cilag international nv - rilpivirine - hiv fertőzések - vírusellenes szerek szisztémás alkalmazásra - rekambys is indicated, in combination with cabotegravir injection, for the treatment of human immunodeficiency virus type 1 (hiv 1) infection in adults who are virologically suppressed (hiv-1 rna < 50 copies/ml) on a stable antiretroviral regimen without present or past evidence of viral resistance to, and no prior virological failure with, agents of the nnrti and ini class.

Европейский союз - венгерский - EMA (European Medicines Agency)

janssen-cilag international nv - darunavir - hiv fertőzések - vírusellenes szerek szisztémás alkalmazásra - 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.