Примери за използване на Effects were observed на Английски и техните преводи на Български
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No effects were observed in dogs;
In atosiban clinical trials no effects were observed on breast-feeding.
No effects were observed at 3times the human therapeutic exposure.
Consistent with the pharmacological action of ketaconazole, effects were observed on adrenal and gonads in rats and dogs.
Similar effects were observed in sedated pigs.
In repeated dose toxicity studies in rats andmonkeys CNS effects were observed, including hypoactivity, hyperactivity and ataxia.
No effects were observed on males and females fertility in animal studies.
However, testicular effects were observed in mice and monkeys(see section 5.3).
No effects were observed on pup development or fertility in the two generation study in rats.
In addition, similar effects were observed on other lung function endpoints e.g.
Best effects were observed in infertility with oligospermia and correlated with astenospermia.
Embryotoxic effects were observed only at maternal toxic levels.
These effects were observed within several hours post-dose and generally resolved within 48 hours.
Reversible cardiotoxic effects were observed in rabbits following intravenous administration of tacrolimus.
Adverse effects were observed in intake of inorganic sulfur, because it is toxic.
Vitamin D and its anti-inflammatory effects were observed in a wide range of diseases, including hypertension, diabetes mellitus type 1 and psoriasis.
These effects were observed only at exposures sufficiently in excess of maximum human exposure to indicate little relevance to clinical use.
Embryotoxic effects were observed at doses in the range of maternal toxicity.
These effects were observed at exposures of 14 and 3 times the human daily dose based on the AUC in rats and dogs respectively.
No undesirable effects were observed after the administration of 10 times the recommended dose.
These effects were observed at exposure levels in excess of the maximum human exposure indicating little relevance to clinical use.
These beneficial effects were observed as early as the second day of therapy and maintained for up to 52 weeks.
Cardiac effects were observed in rats consistent with cardiomyopathy and contributed to signs of cardiac failure after repeated cycles of treatment.
In monkeys, no renal effects were observed after single use even at a dose 100-times higher than the clinical dose.
Cardiac effects were observed in some non-clinical studies in canines(prolongation of action potentials in Purkinje fibers or prolongation of the QTc interval).
After repeated dosing to mice, rats anddogs, adverse effects were observed in a number of organs, primarily in the kidneys, liver, digestive tract, thyroid gland, lympho-/haematopoietic system, endocrine system, reproductive system and skin.
No QTc prolonging effects were observed after administration of 160 mg regorafenib at steady state in a dedicated QT study in male and female cancer patients.
Inhibitory effects were observed on the humoral and T-cell dependent immune responses.
No undesirable effects were observed after the administration of 10 times the recommended dose of selamectin.
Gastrointestinal effects were observed in the dog at systemic exposure levels equivalent to or less than the clinical exposure at the recommended doses.