Примери за използване на The clinical exposure на Английски и техните преводи на Български
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rabbits at doses resulting in several hundred- fold greater systemic exposures than the clinical exposure.
19 times the clinical exposure level at 5 mg or 10 mg twice daily.
94 times the clinical exposure level at 5 mg or 10 mg twice daily.
Significant increased pre-implantation losses were observed at 4.1-fold the clinical exposure at MRHD.
less than 0.5 times the clinical exposure at the recommended clinical dose of 2 g/day(see section 4.6).
No interaction with MRP2 or MRP3 was observed in vitro at the clinical exposure of rucaparib, however,
Adverse reactions observed in animal studies occurred at exposure levels appreciably lower than the clinical exposure levels to eslicarbazepine(the principal and pharmacologically active metabolite of eslicarbazepine acetate).
Adverse affects observed in animal studies occurred at exposure levels appreciably lower than the clinical exposure levels to eslicarbazepine(the principal and pharmacologically active metabolite of eslicarbazepine acetate).
In the 10-month study decreases in bone mineral content, bone area and/or bone mineral density in lumbar vertebrae and/or femur were observed in high-dose female animals at exposure levels lower than the clinical exposure levels to eslicarbazepine in children.
Incisor teeth abnormalities were observed in rats at exposure levels 67 times the clinical exposure level; the no- effect level for this finding was 58-fold based on the 14-week rat study.
moderately higher than the clinical exposure level were: changes in lymphoid organs in all species tested,
for the lymphomas was approximately 1 or 0.5 times the clinical exposure level of 5 mg or 10 mg twice daily.
41 times the clinical exposure level at 5 mg or 10 mg twice daily.
levels similar to or moderately higher than the clinical exposure level were: changes in lymphoid.
50 mg/kg(2-5 times the clinical exposure based on Cmax and AUC).
less than 0.5 times the clinical exposure at the recommended clinical dose of 2 g/ day for renal transplant patients and approximately 0.3 times the clinical exposure at the recommended clinical dose of 3 g/ day for cardiac transplant patients.
moderately higher than the clinical exposure level were: changes in lymphoid organs in all species tested,
In a 26-week chronic toxicology study in cynomolgus monkeys at doses of up to 50 mg/kg/week(about 70 times the clinical exposure at the MRHD), there were no pre-neoplastic
skeletal alterations(including retarded ossification) were reported in rats receiving doses which produced approximately 2 to 3 fold the clinical exposure(54 mg/m2/day) and in rabbits receiving 12 mg/m 2/day clofarabine.
decreased activity, and/or hunched posture were observed in dogs at exposure levels approximately 23 times the clinical exposure level.