Примери за използване на Toxicity study на Английски и техните преводи на Български
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In the 53- and 106-week toxicity study, gastrointestinal ulcers were also seen at exposures comparable to those seen in man at the therapeutic dose.
An enhanced pre and postnatal development(ePPND) toxicity study in pregnant cynomolgus monkeys showed no evidence of teratogenic effects.
Histologically, testicular degeneration was only seen in one male monkey in a 1-year subcutaneous toxicity study.
Additionally, proliferative lesions were not observed in a 6-month chronic toxicity study in cynomolgus monkeys
in liver enzymes and calcium levels in a repeat dose toxicity study in rats.
A single dose study in rabbits and a 13-week repeat dose toxicity study in Cynomolgus monkeys were conducted.
In the 14-week toxicity study etoricoxib caused gastrointestinal ulcers at exposures greater than those seen in man at the therapeutic dose.
in the 13 weeks repeated dose toxicity study in rats(without recovery).
A non-clinical reproduction toxicity study with daclizumab has shown an increased risk of early prenatal loss in cynomolgus monkeys compared to placebo.
In a single dose toxicity study a dose of 125 mg/kg was administered intravenously to mice
In a repeated-dose toxicity study in rabbits there was no evidence of systemic toxicity
In a repeated-dose toxicity study in rabbits there was no evidence of systemic toxicity and the vaccine was locally well tolerated.
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.
In a four-month rat dermal toxicity study, significantly decreased body weight
In another juvenile toxicity study in 14-day-old rats, aliskiren administration at 300 mg/kg/day(8.5-fold the maximum recommended human dose)
In the rabbit embryo-foetal toxicity study, findings including embryo-foetal death,
At Gestational Day 29, in rabbit embryo-foetal development toxicity study skull anomaly was found in one male foetus from mother treated with galcanezumab at an exposure approximately 33 times the human exposure at 240 mg.
organs which would possibly remain undetected in a short term toxicity study but which are liable to result in adverse effects after prolonged exposure.
In a pre- and postnatal development toxicity study in rats, abnormal delivery
In a pre- and postnatal development toxicity study in monkeys, no related increase in pregnancy loss was observed at exposures up to 85 times the human exposure at the recommended dose.