Examples of using Daptomycin in English and their translations into Hungarian
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Prescription drugs listed. Substance:"Daptomycin".
Daptomycin Hospira given as 30 or 60 minutes intravenous infusion.
Water should not be used for reconstitution of Daptomycin Hospira for intravenous injection.
Daptomycin Hospira is not physically or chemically compatible with glucose-containing solutions.
A total of 389 subjects weretreated in the study, including 256 subjects who received daptomycin and 133 subjects who received standard-of-care.
In in vitro studies, daptomycin was not metabolised by human liver microsomes.
Daptomycin may be administered intravenously as an infusion over 30 or 60 minutes or as an injection over 2 minutes.
The volume of distribution at steady state of daptomycin in healthy adult subjects was approximately 0.1 l/kg and was independent of dose.
Daptomycin, one of the most recent drugs, in 2003, and resistance to it just a year later in 2004.
Renal insufficiency Following administration of a single 4 mg/ kg or 6 mg/ kg dose of daptomycin to subjects with various degrees of renal insufficiency, daptomycin clearance(CL) was reduced and systemic exposure(AUC) was increased.
Daptomycin may be administered intravenously as an infusion over 30 or 60 minutes or as an injection over 2 minutes(see sections 4.2 and 5.2).
The findings of in vitro andsome in vivo studies designed to investigate the mechanism of daptomycin myotoxicity indicate that the plasma membrane of differentiated spontaneously contracting muscle cells is the target of toxicity.
Daptomycin(Cubicin), another IV medication, is effective against MSSA but is reserved for severe soft tissue or skin infections in adults.
In obese subjects with Body Mass Index(BMI)> 40 kg/m2 but with creatinine clearance> 70 ml/min,the AUC0-∞ daptomycin was significantly increased(mean 42% higher) compared with non-obese matched controls.
Daptomycin Hospira may be administered intravenously as an infusion over 30 or 60 minutes as an injection over 2 minutes(see sections 4.2 and 5.2).
In obese subjects with Body Mass Index(BMI)> 40 kg/ m2 but with creatinine clearance> 70 ml/ min,the AUC0-∞ daptomycin was significantly increased(mean 42% higher) compared with non-obese matched controls.
In addition, dose regimens of daptomycin that might be appropriate for the treatment of enterococcal infections, with or without bacteraemia, have not been identified.
Daptomycin administered as a 2-minute intravenous injection also exhibited dose proportional pharmacokinetics in the approved therapeutic dose range of 4 to 6 mg/kg.
In vitro studies have determined that daptomycin does not inhibit or induce the activities of clinically significant human CYP isoforms(1A2, 2A6, 2C9, 2C19, 2D6, 2E1, 3A4).
Daptomycin pharmacokinetics are generally linear and time-independent at doses of 4 to 12 mg/ kg administered as a single daily dose for up to 14 days in healthy volunteers.
Distribution The steady state volume of distribution of daptomycin was approximately 0.1 l/ kg in healthy adult volunteers, consistent with distribution primarily within the extracellular space.
Intravenous daptomycin doses of 5 to 10 mg/kg were administered and 256 children received daptomycin, from which pharmacokinetic sampling was performed on 45 children from across the age groups.
In vitro studies with human hepatocytes indicate that daptomycin does not inhibit or induce the activities of the following human cytochrome P450 isoforms: 1A2, 2A6, 2C9, 2C19, 2D6, 2E1 and 3A4.
Daptomycin is primarily cleared by renal filtration and so plasma levels may be increased during co-administration with medicinal products that reduce renal filtration(e.g. NSAIDs and COX-2 inhibitors).
Concomitant administration of probenecid and daptomycin has no effect on daptomycin pharmacokinetics in humans suggesting minimal to no active tubular secretion of daptomycin.
Based on pharmacokinetic data and modelling, the daptomycin AUC during the first day after administration of a 6 mg/kg dose to patients on HD or CAPD was 2-fold higher than that observed in patients with normal renal function who received the same dose.
If you take drugs that have been introduced since then-linezolid or daptomycin- those are significantly more expensive, so to a world that has been used to paying 10 cents a day for antibiotics, the idea of paying 180 dollars per day seems like a lot.
Following administration of a single 4 mg/kg or 6 mg/kg intravenous dose of daptomycin over a 30-minute period to subjects with various degrees of renal impairment, total daptomycin clearance(CL) decreased and systemic exposure(AUC) increased as renal function(creatinine clearance) decreased.
This should be taken into account when initiating daptomycin therapy and, if daptomycin is given, these patients should be monitored more frequently than once weekly.• CPK should be measured more frequently than once weekly in patients who are at higher risk of developing myopathy.