Examples of using Repeat-dose in English and their translations into Swedish
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Repeat-dose toxicology studies.
In monkeys, pomalidomide was evaluated in repeat-dose studies of up to 9 months in duration.
In a 1 year repeat-dose study in dogs there were no microscopic changes in the liver although serum AST was minimally increased in females.
No alogliptin-related effects were observed in juvenile rats following repeat-dose administration for 4 and 8 weeks.
In intravenous repeat-dose toxicology studies in monkeys, ipilimumab was generally well tolerated.
Including range-finding studies that cannot appropriately be included under repeat-dose toxicity or pharmacokinetics.
However, in single and repeat-dose general toxicity studies no adverse reactions at the injection sites were reported.
A slightly increased incidence of thickening of the atrioventricular valves of the heart was seen in the 26 week repeat-dose toxicity study in rats.
Caecal lesions observed in some repeat-dose studies with rats, but not in monkeys, are not relevant for humans under normal conditions of administration.
Short- or medium-term studies including range-finding studies that cannot appropriately be included under repeat-dose toxicity or pharmacokinetics.
In a long-term dog repeat-dose study, high serum prolactin levels were associated with effects on male
exposure of carfilzomib following single or repeat-dose administration at doses up to 20 mg/m2 see section 4.2.
In repeat-dose studies the effects seen after trametinib exposure are found mainly in the skin, gastrointestinal tract, haematological system, bone and liver.
No effects on reproductive tissues were noted during 28-day repeat-dose rat and monkey toxicity studies or in 6-month rat and 9-month monkey chronic toxicity studies.
Repeat-dose toxicity studies involving the co-administration of lumacaftor
Mean metabolite to parent AUC ratios following repeat-dose administration were 0.9, 11 and 0.7 for hydroxy-, carboxy-, and desmethyl-dabrafenib, respectively.
dogs in single- or repeat-dose regimens that exceed the dose that is used clinically.
High serum prolactin levels in long-term repeat-dose studies in female rats were associated with effects on bones, adrenal glands, and reproductive tissues.
at doses above those inducing analgesia and in two repeat-dose studies with sufentanil sublingual tablets administered buccally in Golden Syrian hamster.
Single and repeat-dose toxicity studies in mice,
Non-clinical data reveal no special hazards for humans based on conventional studies of safety pharmacology, repeat-dose toxicity, or genotoxicity conducted with immediate-release exenatide
Other liver-related changes in repeat-dose toxicity studies in rats and dogs included increased serum aminotransferases, subacute inflammation(rats only), and single-cell necrosis.
its metabolites extrapolated from Day 90 exposures at 100 mg/kg/day in the 6-month repeat-dose toxicity study in this species.
In rat and dog repeat-dose toxicity studies up to 6 months duration, target organs for toxicity were GI tract,
Non-clinical studies suggest no specific hazard for humans on the basis of single-and repeat-dose studies, with the exception of transient
In repeat-dose studies in juvenile rats and dogs, the toxicity profile of aripiprazole was comparable to that observed in adult animals,
female fertility can however be expected because repeat-dose studies in animals have shown changes in male
Repeat-dose toxicity studies performed in rats
The plasma amprenavir pharmacokinetics were evaluated in a 14 day repeat-dose study in HIV-1 infected adult subjects with mild, moderate, or severe hepatic impairment receiving fosamprenavir with ritonavir compared to matched control subjects with normal hepatic function.