ישראל -
עברית -
Ministry of Health
נוכסקורן
dexxon ltd - benzocaine 2.1 %; salicylic acid 10.5 % - liquid - benzocaine - for removal of corns and callouses.
ישראל -
עברית -
Ministry of Health
נוכסקורן
dexxon ltd - benzocaine 2.1 %; salicylic acid 10.5 % - liquid - benzocaine - for removal of corns and callouses.
ישראל -
עברית -
Ministry of Health
דבק להדבקת ריסים - לכל סוגי הריסים
לאון מזרחי - זיוה מזרחי - דבק להדבקת ריסים
ישראל -
עברית -
Ministry of Health
פרזיסטה 75 מג
j-c health care ltd - darunavir as ethanolate - טבליות מצופות פילם - darunavir as ethanolate 75 mg - darunavir - darunavir - adult patients : prezista, co-administered with ritonavir (prezista/rtv), and with other antiretroviral agents, is indicated for the treatment of human immunodeficiency virus (hiv -1) infection. this indication is based on analyses of plasma hiv rna levels and cd4+ cell counts from 2 controlled phase 3 trials of 48 weeks duration in antiretroviral treatment - naive and treatment -experienced patients and 2 controlled phase 2 trials of 96 weeks duration in clinically advanced, treatment -experienced adult patients .pediatric patients :prezista, co-administered with ritonavir (prezista/rtv), and with other antiretroviral agents, is indicated for the treatment of hiv in pediatric patients 6 years of age and older. this indication is based on week 24 analyses of plasma hiv rna levels and cd4+ cell counts from an open-label phase 2 trial in antiretroviral treatment -experienced pediatric patients 6 to < 18 years of age. in treatment-experienced adult and pediatric the following points should be considered when ini
ישראל -
עברית -
Ministry of Health
פרזיסטה 150 מג
j-c health care ltd - darunavir as ethanolate - טבליות מצופות פילם - darunavir as ethanolate 150 mg - darunavir - darunavir - adult patients : prezista, co-administered with ritonavir (prezista/rtv), and with other antiretroviral agents, is indicated for the treatment of human immunodeficiency virus (hiv -1) infection. this indication is based on analyses of plasma hiv rna levels and cd4+ cell counts from 2 controlled phase 3 trials of 48 weeks duration in antiretroviral treatment - naive and treatment -experienced patients and 2 controlled phase 2 trials of 96 weeks duration in clinically advanced, treatment -experienced adult patients .pediatric patients :prezista, co-administered with ritonavir (prezista/rtv), and with other antiretroviral agents, is indicated for the treatment of hiv in pediatric patients 6 years of age and older. this indication is based on week 24 analyses of plasma hiv rna levels and cd4+ cell counts from an open-label phase 2 trial in antiretroviral treatment -experienced pediatric patients 6 to < 18 years of age. in treatment-experienced adult and pediatric the following points should be considered when ini
ישראל -
עברית -
Ministry of Health
סילדנאפיל טבע 100 מג
abic marketing ltd, israel - sildenafil as citrate - טבליות מצופות פילם - sildenafil as citrate 100 mg - sildenafil
ישראל -
עברית -
Ministry of Health
סילדנאפיל טבע 25 מג
abic marketing ltd, israel - sildenafil as citrate - טבליות מצופות פילם - sildenafil as citrate 25 mg - sildenafil
ישראל -
עברית -
Ministry of Health
סילדנאפיל טבע 50 מג
abic marketing ltd, israel - sildenafil as citrate - טבליות מצופות פילם - sildenafil as citrate 50 mg - sildenafil