Europeiska unionen - svenska - EMA (European Medicines Agency)

sanofi winthrop industrie - insulin aspart - diabetes mellitus - läkemedel som används vid diabetes - insulin aspart sanofi is indicated for the treatment of diabetes mellitus in adults, adolescents and children aged 1 year and above.

Europeiska unionen - svenska - EMA (European Medicines Agency)

janssen-cilag international nv - darunavir - hiv-infektioner - antivirala medel för systemisk användning - 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.

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

sun pharmaceutical industries europe b.v. - terlipressinacetat - injektionsvätska, lösning - 1 mg - terlipressinacetat 1 mg aktiv substans - terlipressin

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

baxter medical ab - alanin; arginin; asparaginsyra; fenylalanin; glukosmonohydrat; glutaminsyra; glycin; histidin; isoleucin; kalciumkloriddihydrat; kaliumklorid; leucin; lysinacetat; magnesiumkloridhexahydrat; metionin; natriumacetattrihydrat; natriumglycerofosfat, hydratiserat; olivolja, raffinerad; prolin; serin; sojaolja, raffinerad; treonin; tryptofan; tyrosin; valin - infusionsvätska, emulsion - fenylalanin 5,7 g aktiv substans; metionin 4,11 g aktiv substans; valin 5,26 g aktiv substans; tyrosin 0,21 g aktiv substans; tryptofan 1,37 g aktiv substans; treonin 4,11 g aktiv substans; alanin 11,9 g aktiv substans; natriumglycerofosfat, hydratiserat 9,18 g aktiv substans; magnesiumkloridhexahydrat 2,03 g aktiv substans; kaliumklorid 5,59 g aktiv substans; natriumacetattrihydrat 3,74 g aktiv substans; prolin 4,91 g aktiv substans; leucin 5,7 g aktiv substans; isoleucin 4,11 g aktiv substans; histidin 4,91 g aktiv substans; glycin 5,7 g aktiv substans; glutaminsyra 4,11 g aktiv substans; asparaginsyra 2,38 g aktiv substans; arginin 8,06 g aktiv substans; serin 3,25 g aktiv substans; glycerol hjälpämne; sojaolja, raffinerad 40 g aktiv substans; olivolja, raffinerad 160 g aktiv substans; glukosmonohydrat 316,25 g aktiv substans; kalciumkloriddihydrat 1,29 g aktiv substans; lysinacetat 9,13 g aktiv substans - kombinationer

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

sanofi ab - levofloxacinhemihydrat - infusionsvätska, lösning - 5 mg/ml - levofloxacinhemihydrat 5,125 mg aktiv substans - levofloxacin

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

orifarm ab - levofloxacinhemihydrat - infusionsvätska, lösning - 5 mg/ml - levofloxacinhemihydrat 5,125 mg aktiv substans

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

orifarm ab - levofloxacinhemihydrat - infusionsvätska, lösning - 5 mg/ml - levofloxacinhemihydrat 5,125 mg aktiv substans

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

noridem enterprises ltd - alanin; arginin; asparaginsyra; fenylalanin; glukosmonohydrat; glutaminsyra; glycin; histidin; isoleucin; kalciumkloriddihydrat; kaliumklorid; leucin; lysinacetat; magnesiumkloridhexahydrat; metionin; natriumacetattrihydrat; natriumglycerofosfat, hydratiserat; olivolja, raffinerad; prolin; serin; sojaolja, raffinerad; treonin; tryptofan; tyrosin; valin - infusionsvätska, emulsion - olivolja, raffinerad 160 g aktiv substans; sojaolja, raffinerad 40 g aktiv substans; glycerol hjälpämne; kalciumkloriddihydrat 1,3 g aktiv substans; glukosmonohydrat 316,25 g aktiv substans; metionin 4,11 g aktiv substans; fenylalanin 5,7 g aktiv substans; valin 5,26 g aktiv substans; tyrosin 0,21 g aktiv substans; tryptofan 1,37 g aktiv substans; treonin 4,11 g aktiv substans; alanin 11,9 g aktiv substans; lysinacetat 9,13 g aktiv substans; leucin 5,7 g aktiv substans; isoleucin 4,11 g aktiv substans; histidin 4,91 g aktiv substans; glycin 5,7 g aktiv substans; glutaminsyra 4,11 g aktiv substans; asparaginsyra 2,38 g aktiv substans; arginin 8,06 g aktiv substans; serin 3,25 g aktiv substans; prolin 4,91 g aktiv substans; natriumacetattrihydrat 3,74 g aktiv substans; kaliumklorid 5,59 g aktiv substans; magnesiumkloridhexahydrat 2,03 g aktiv substans; natriumglycerofosfat, hydratiserat 9,18 g aktiv substans

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

noridem enterprises ltd - alanin; arginin; asparaginsyra; fenylalanin; glukosmonohydrat; glutaminsyra; glycin; histidin; isoleucin; kalciumkloriddihydrat; kaliumklorid; leucin; lysinacetat; magnesiumkloridhexahydrat; metionin; natriumacetattrihydrat; natriumglycerofosfat, hydratiserat; olivolja, raffinerad; prolin; serin; sojaolja, raffinerad; treonin; tryptofan; tyrosin; valin - infusionsvätska, emulsion - tyrosin 0,28 g aktiv substans; kalciumkloriddihydrat 1,3 g aktiv substans; glukosmonohydrat 385 g aktiv substans; glycerol hjälpämne; sojaolja, raffinerad 40 g aktiv substans; olivolja, raffinerad 160 g aktiv substans; natriumglycerofosfat, hydratiserat 9,18 g aktiv substans; magnesiumkloridhexahydrat 2,03 g aktiv substans; kaliumklorid 5,59 g aktiv substans; natriumacetattrihydrat 3,74 g aktiv substans; treonin 5,53 g aktiv substans; serin 4,37 g aktiv substans; tryptofan 1,84 g aktiv substans; valin 7,08 g aktiv substans; alanin 16,02 g aktiv substans; arginin 10,85 g aktiv substans; asparaginsyra 3,2 g aktiv substans; glutaminsyra 5,53 g aktiv substans; glycin 7,67 g aktiv substans; histidin 6,61 g aktiv substans; isoleucin 5,53 g aktiv substans; leucin 7,67 g aktiv substans; lysinacetat 12,19 g aktiv substans; metionin 5,53 g aktiv substans; fenylalanin 7,67 g aktiv substans; prolin 6,61 g aktiv substans

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

noridem enterprises ltd - alanin; arginin; asparaginsyra; fenylalanin; glukosmonohydrat; glutaminsyra; glycin; histidin; isoleucin; kalciumkloriddihydrat; kaliumklorid; leucin; lysinacetat; magnesiumkloridhexahydrat; metionin; natriumacetattrihydrat; natriumglycerofosfat, hydratiserat; olivolja, raffinerad; prolin; serin; sojaolja, raffinerad; treonin; tryptofan; tyrosin; valin - infusionsvätska, emulsion - lysinacetat 15,8 g aktiv substans; natriumacetattrihydrat 3,74 g aktiv substans; kaliumklorid 5,59 g aktiv substans; magnesiumkloridhexahydrat 2,03 g aktiv substans; natriumglycerofosfat, hydratiserat 9,18 g aktiv substans; kalciumkloriddihydrat 1,3 g aktiv substans; glukosmonohydrat 302,5 g aktiv substans; olivolja, raffinerad 160 g aktiv substans; sojaolja, raffinerad 40 g aktiv substans; glycerol hjälpämne; metionin 7,11 g aktiv substans; fenylalanin 9,87 g aktiv substans; prolin 8,49 g aktiv substans; serin 5,62 g aktiv substans; treonin 7,11 g aktiv substans; tryptofan 2,37 g aktiv substans; tyrosin 0,37 g aktiv substans; valin 9,11 g aktiv substans; alanin 20,6 g aktiv substans; arginin 13,95 g aktiv substans; asparaginsyra 4,12 g aktiv substans; glutaminsyra 7,11 g aktiv substans; glycin 9,87 g aktiv substans; histidin 8,49 g aktiv substans; isoleucin 7,11 g aktiv substans; leucin 9,87 g aktiv substans