Examples of using Single dose study in English and their translations into Swedish
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The clinical relevance of results from this single dose study is unknown.
A single dose study was conducted in juvenile rats aged 14, 21, 24, 28, 31 or 36 days post-partum.
Pravafenix is bioequivalent to coadministered fenofibrate and pravastatin in a single dose study.
A single dose study in rabbits and a 13-week repeat dose toxicity study in Cynomolgus monkeys were conducted.
However, the bioavailability of ciprofloxacin was decreased by approximately 50% when co-administered with Renagel in a single dose study.
In a single dose study performed in adults, desloratadine 5 mg did not affect standard measures of flight performance including exacerbation of subjective sleepiness or tasks related to flying.
In interaction studies in healthy volunteers, sevelamer hydrochloride decreased the bioavailability of ciprofloxacin by approximately 50% when co-administered with Renagel in a single dose study.
In a open label, single dose study(n=31) various stages of renal impairment,
active moiety as Renvela, decreased the bioavailability of ciprofloxacin by approximately 50% when co-administered with sevelamer hydrochloride in a single dose study.
In a single dose study(1.0 microgram/kg)
Because nevirapine induces its own metabolism with multiple dosing, this single dose study may not reflect the impact of hepatic impairment on multiple dose pharmacokinetics see section 4.4.
Single dose study: After single doses of metformin hydrochloride 500 mg, paediatric patients have shown a similar pharmacokinetic profile to that observed in healthy adults.
In a single dose study performed in adults, desloratadine 5 mg did not affect standard
In a single dose study with Galafold in non-Fabry subjects with varying degrees of renal insufficiency,
In a single dose study the clearance of palifermin was approximately 30% lower in 8 healthy subjects aged 66-73 years after a dose of 90 micrograms/kg than in younger subjects(≤ 65 years) after a dose of 180 micrograms/kg.
In a open label, single dose study(n=31) various stages of renal impairment,
In a single dose study(6 subjects/ group),
Single dose studies demonstrate linearity of pharmacokinetics in the therapeutic dose range.
Single dose studies demonstrate linearity of pharmacokinetics in the therapeutic dose range.
Suggesting that meal content has less effect on nelfinavir exposures during multiple dosing than would be anticipated based on data from single dose studies.
Single dose studies in rodents indicate that the lethal dose is around 300 ppm nitric oxide or greater.
In separate single dose studies, at the recommended doses, paediatric patients had comparable AUC
A single dose pharmacokinetic study in volunteers indicated that hepatic impairment did not affect exposure to vandetanib.
Renagel is not absorbed from the gastrointestinal tract according to a single dose pharmacokinetic study in healthy volunteers.
A single dose pharmacokinetic study of insulin aspart was performed in 24 subjects with hepatic function ranging from normal to severely impaired.
A single dose pharmacokinetic study of insulin aspart in 18 subjects with renal function ranging from normal to severely impaired was performed.
Hepatic impairment A single dose pharmacokinetic study was performed in 24 subjects with various degrees of hepatic impairment and 12 healthy subjects as controls.
Potential for interaction following intramuscular injection In a single dose intramuscular study of olanzapine 5 mg, administered 1 hour before intramuscular lorazepam 2 mg(metabolised by glucuronidation), the pharmacokinetics of both medicines were unchanged.