Busulfan Fresenius Kabi Uniunea Europeană - engleză - EMA (European Medicines Agency)

busulfan fresenius kabi

fresenius kabi deutschland gmbh - busulfan - hematopoietic stem cell transplantation - alkyl sulfonates - busulfan fresenius kabi followed by cyclophosphamide (bucy2) is indicated as conditioning treatment prior to conventional haematopoietic progenitor cell transplantation (hpct) in adult patients when the combination is considered the best available option.busulfan fresenius kabi followed by cyclophosphamide (bucy4) or melphalan (bumel) is indicated as conditioning treatment prior to conventional haematopoietic progenitor cell transplantation in paediatric patients.

Pemetrexed Fresenius Kabi Uniunea Europeană - engleză - EMA (European Medicines Agency)

pemetrexed fresenius kabi

fresenius kabi deutschland gmbh - pemetrexed - carcinoma, non-small-cell lung; mesothelioma - antineoplastic agents - malignant pleural mesotheliomapemetrexed fresenius kabi in combination with cisplatin is indicated for the treatment of chemotherapy naïve patients with unresectable malignant pleural mesothelioma.non-small cell lung cancerpemetrexed fresenius kabi in combination with cisplatin is indicated for the first line treatment of patients with locally advanced or metastatic non-small cell lung cancer other than predominantly squamous cell histology.pemetrexed fresenius kabi is indicated as monotherapy for the maintenance treatment of locally advanced or metastatic non-small cell lung cancer other than predominantly squamous cell histology in patients whose disease has not progressed immediately following platinum-based chemotherapy. pemetrexed fresenius kabi is indicated as monotherapy for the second line treatment of patients with locally advanced or metastatic non-small cell lung cancer other than predominantly squamous cell histology.

Lactulose Fresenius 670mg/ml oral solution Irlanda - engleză - HPRA (Health Products Regulatory Authority)

lactulose fresenius 670mg/ml oral solution

fresenius kabi austria gmbh - lactulose - oral solution - 670 milligram(s)/millilitre - osmotically acting laxatives; lactulose

FRESENIUS PROPOVEN 2%- propofol emulsion Statele Unite ale Americii - engleză - NLM (National Library of Medicine)

fresenius propoven 2%- propofol emulsion

fresenius kabi austria gmbh - propofol (unii: yi7vu623sf) (propofol - unii:yi7vu623sf) - the u.s. food and drug administration (fda) has issued an emergency use authorization (eua) to permit the emergency use of the unapproved product, fresenius propoven 2% (propofol 20 mg/ml) emulsion 100 ml, to maintain sedation via continuous infusion in patients greater than 16 years old who require mechanical ventilation in an intensive care unit (icu) setting. caution: there is a risk of unintentional overdose with this unapproved product. fresenius propoven 2% emulsion contains the same active ingredient, propofol, as fda-approved diprivan injectable emulsion usp 10 mg/ml, but contains double the concentration. because of this difference in concentration between this unapproved product and the fda-approved product, there is a risk of unintentional overdose. fresenius propoven 2% emulsion 100ml is not an fda-approved drug in the united states. however, fda has issued an eua permitting the emergency use of fresenius propoven 2% emulsion during the covid-19 pandemic. the scope of the eua is limited as follows

Bortezomib Fresenius Kabi Uniunea Europeană - engleză - EMA (European Medicines Agency)

bortezomib fresenius kabi

fresenius kabi deutschland gmbh - bortezomib - multiple myeloma - antineoplastic agents - bortezomib as monotherapy or in combination with pegylated liposomal doxorubicin or dexamethasone is indicated for the treatment of adult patients with progressive multiple myeloma who have received at least 1 prior therapy and who have already undergone or are unsuitable for haematopoietic stem cell transplantation.bortezomib in combination with melphalan and prednisone is indicated for the treatment of adult patients with previously untreated multiple myeloma who are not eligible for high-dose chemotherapy with haematopoietic stem cell transplantation.bortezomib in combination with dexamethasone, or with dexamethasone and thalidomide, is indicated for the induction treatment of adult patients with previously untreated multiple myeloma who are eligible for high-dose chemotherapy with haematopoietic stem cell transplantation.bortezomib in combination with rituximab, cyclophosphamide, doxorubicin and prednisone is indicated for the treatment of adult patients with previously untreated mantle cell lymphoma who are unsuitable for haematopoietic stem cell transplantation.

Sugammadex Fresenius Kabi Uniunea Europeană - engleză - EMA (European Medicines Agency)

sugammadex fresenius kabi

fresenius kabi deutschland gmbh - sugammadex sodium - neuromuscular blockade - all other therapeutic products - reversal of neuromuscular blockade induced by rocuronium or vecuronium in adults.for the paediatric population: sugammadex is only recommended for routine reversal of rocuronium induced blockade in children and adolescents aged 2 to 17 years.

Kabiven emulsion for infusion Irlanda - engleză - HPRA (Health Products Regulatory Authority)

kabiven emulsion for infusion

fresenius kabi deutschland gmbh - soya bean oil ; glucose monohydrate; alanine; arginine ; aspartic acid; glutamic acid ; glycine; histidine; isoleucine; leucine ; lysine hydrochloride; methionine; phenylalanine; proline; serine; threonine; tryptophan; tyrosine; valine; calcium chloride 2 h2o; sodium glycerophosphate anhydrous; magnesium sulphate 7h2o; potassium chloride; sodium acetate 3 h20 ; amino acids; nitrogen; fat; glucose; glucose (dextrose); sodium; potassium; magnesium; calcium; phosphate; sulphate; chloride; acetate - emulsion for infusion - solutions for parenteral nutrition; combinations

SmofKabiven Electrolyte Free Emulsion for Infusion Singapore - engleză - HSA (Health Sciences Authority)

smofkabiven electrolyte free emulsion for infusion

fresenius kabi (singapore) pte ltd - alanine; arginine; fish oil, rich in omega -3 acids; glucose monohydrate; glycine; histidine; isoleucine; leucine; lysine acetate; methionine; olive oil, refined; phenylalanine; proline; serine; soya bean oil, refined; taurine; threonine; triglycerides, medium chain; tryptophan; tyrosine; valine - injection, emulsion - 14.0g/1000ml - alanine 14.0g/1000ml; arginine 12.0g /1000ml; fish oil, rich in omega -3 acids 30g /1000ml; glucose monohydrate 462g /1000ml; glycine 11.0g /1000ml; histidine 3.0g /1000ml; isoleucine 5.0g /1000ml; leucine 7.4g /1000ml; lysine acetate 9.3g /1000ml; methionine 4.3g /1000ml; olive oil, refined 50g /1000ml; phenylalanine 5.1g /1000ml; proline 11.2g /1000ml; serine 6.5g /1000ml; soya bean oil, refined 60.0g /1000ml; taurine 1.0g /1000ml; threonine 4.4g /1000ml; triglycerides, medium chain 60g /1000ml; tryptophan 2.0g/1000ml; tyrosine 0.4g /1000ml; valine 6.2g /1000ml