Examples of using Repeat-dose toxicity in English and their translations into Polish
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Depletion of lymphoid organs was observed in repeat-dose toxicity studies in rats and cynomolgus monkeys.
In the dog, foamy macrophages were observed in lymphoid tissue of various organs during repeat-dose toxicity studies.
Effects observed in the repeat-dose toxicity studies were due to the exaggerated pharmacodynamic effect of dabigatran.
Including range-finding studies that cannot appropriately be included under repeat-dose toxicity or pharmacokinetics.
Effects observed in repeat-dose toxicity studies were mainly due to the exaggerated pharmacodynamic activity of rivaroxaban.
female reproductive organs were observed in repeat-dose toxicity studies in cynomolgus monkeys see section 5.3.
Repeat-dose toxicity studies in rabbits revealed an inhibitory effect of delamanid and/or its metabolites on vitamin K-dependent blood clotting.
Non-clinical data reveal no special hazards for humans based on conventional studies of safety pharmacology, repeat-dose toxicity, or genotoxicity.
Only very limited data are available from repeat-dose toxicity studies with respect to the risk for adverse effects on the male reproductive system.
Non-clinical data reveal no special hazards for humans based on conventional studies of safety pharmacology or repeat-dose toxicity.
In a repeat-dose toxicity study in rats, there was a decrease in the number of corpora lutea in the ovaries of rats given vandetanib for 1 month.
Iclusig has been evaluated in safety pharmacology, repeat-dose toxicity, genotoxicity, reproductive toxicity,
A repeat-dose toxicity study was conducted in juvenile rats 8 days post-partum for 4 weeks with aliskiren dosing at 30, 100 or 300 mg/kg/day.
In cynomolgus monkeys, thyroid gland follicular atrophy mostly accompanied by a reduction in T3 levels and a tendency toward increased TSH levels were observed in the 4-week repeat-dose toxicity study in cynomolgus monkeys.
In repeat-dose toxicity studies in cynomolgus monkeys obinutuzumab had no adverse effects on male
Non-clinical data reveal no special hazard for humans based on conventional studies of safety pharmacology, repeat-dose toxicity, genotoxicity, carcinogenic potential,
However, in repeat-dose toxicity studies in rats
Ponatinib-related microscopic findings in the ovaries(increased follicular atresia) and testes(minimal germ cell degeneration) in animals treated with 5 mg/kg ponatinib were noted in repeat-dose toxicity studies in cynomolgus monkeys.
Effects observed in repeat-dose toxicity studies were mainly due to the exaggerated pharmacodynamic activity of riociguat haemodynamic
fertility in humans based on findings in repeat-dose toxicity studies in the rat.
Major findings in repeat-dose toxicity studies of lurasidone were centrally-mediated endocrine changes resulting from serum prolactin elevations in rats,
however there were no findings in the repeat-dose toxicity studies to indicate any vaccine-related changes to the tissues of the male reproductive tract.
Repeat-dose toxicity studies have shown that primary target organs were tissues that undergo rapid cell division:
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
Multi-cycle repeat-dose toxicity studies in rats
seen in rats during repeat-dose toxicity studies at exposure levels higher than clinical exposure levels
In repeat-dose toxicity studies boceprevir showed testicular degeneration in rats at systemic exposures lower than those in humans at the recommended human therapeutic dose.
Other liver-related changes in repeat-dose toxicity studies in rats and dogs included increased serum aminotransferases,
In a repeat-dose toxicity studies in rats and dogs, effects on the central
In general, the tolerability of Erivedge in repeat-dose toxicity studies in rats and dogs was limited by nonspecific manifestations of toxicity