Europeiska unionen - svenska - EMA (European Medicines Agency)

bristol-myers squibb pharma eeig - cobicistat, atazanavir - hiv-infektioner - antivirala medel för systemisk användning - evotaz is indicated in combination with other antiretroviral medicinal products for the treatment of hiv-1 infected adults and adolescents (aged 12 years and older weighing at least 35 kg) without known mutations associated with resistance to atazanavir (see sections 4. 4 och 5.

Europeiska unionen - svenska - EMA (European Medicines Agency)

actavis group ptc ehf - topotekan - uterine cervical neoplasms; small cell lung carcinoma - antineoplastiska medel - topotecan monotherapy is indicated for the treatment of:- patients with metastatic carcinoma of the ovary after failure of first-line or subsequent therapy- patients with relapsed small cell lung cancer (sclc) for whom re-treatment with the first-line regimen is not considered appropriate (see section 5. topotecan i kombination med cisplatin är indicerat för patienter med cancer i livmoderhalsen återkommande efter strålbehandling för patienter med stadium ivb sjukdom. patients with prior exposure to cisplatin require a sustained treatment free interval to justify treatment with the combination (see section 5.

Europeiska unionen - svenska - EMA (European Medicines Agency)

adienne s.r.l. s.u. - melphalan hydrochloride - multiple myeloma; hodgkin disease; lymphoma, non-hodgkin; precursor cell lymphoblastic leukemia-lymphoma; leukemia, myeloid, acute; neuroblastoma; ovarian neoplasms; hematopoietic stem cell transplantation - antineoplastiska medel - high-dose of phelinun used alone or in combination with other cytotoxic medicinal products and/or total body irradiation is indicated in the treatment of:multiple myeloma,malignant lymphoma (hodgkin, non-hodgkin lymphoma),acute lymphoblastic and myeloblastic leukemia,childhood neuroblastoma,ovarian cancer,mammary adenocarcinoma. phelinun in combination with other cytotoxic medicinal products is indicated as reduced intensity conditioning (ric) treatment prior to allogeneic haematopoietic stem cell transplantation (allo-hsct) in malignant haematological diseases in adults. phelinun in combination with other cytotoxic medicinal products is indicated as conditioning regimen prior to allogeneic haematopoietic stem cell transplantation in haematological diseases in the paediatric population as:myeloablative conditioning (mac) treatment in case of malignant haematological diseasesric treatment in case of non-malignant haematological diseases.

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

2care4 aps - testosteron - gel - 2 % - etanol, vattenfri hjälpämne; propylenglykol hjälpämne; testosteron 20 mg aktiv substans; butylhydroxitoluen hjälpämne

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

orifarm ab - testosteron - gel - 2 % - testosteron 20 mg aktiv substans; etanol, vattenfri hjälpämne; butylhydroxitoluen hjälpämne; propylenglykol hjälpämne

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

medartuum ab - testosteron - gel - 2 % - butylhydroxitoluen hjälpämne; etanol, vattenfri hjälpämne; propylenglykol hjälpämne; testosteron 20 mg aktiv substans

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

stragen nordic a/s - ceftriaxonnatrium (hemiheptahydrat) - pulver till injektionsvätska, lösning - 1 g - ceftriaxonnatrium (hemiheptahydrat) 1193 mg aktiv substans - ceftriaxon

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

stragen nordic a/s - ceftriaxonnatrium (hemiheptahydrat) - pulver till injektions-/infusionsvätska, lösning - 1 g - ceftriaxonnatrium (hemiheptahydrat) 1193 mg aktiv substans - ceftriaxon

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

fresenius kabi ab - ceftriaxonnatrium (hemiheptahydrat) - pulver till injektions-/infusionsvätska, lösning - 1 g - ceftriaxonnatrium (hemiheptahydrat) 1,193 g aktiv substans - ceftriaxon

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

stragen nordic a/s - ceftriaxonnatrium (hemiheptahydrat) - pulver till infusionsvätska, lösning - 2 g - ceftriaxonnatrium (hemiheptahydrat) 2380 mg aktiv substans - ceftriaxon