Examples of using Toxicity study in English and their translations into Hungarian
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Repeated Dose Toxicity Study.
Toxicity study with juvenile monkeys did not show any relevant toxicity. .
Long-term repeated toxicity study(≥ 12 months).
In the 14-week toxicity study etoricoxib caused gastrointestinal ulcers at exposures greater than those seen in man at the therapeutic dose.
A single dose study in rabbits anda 13-week repeat dose toxicity study in Cynomolgus monkeys were conducted.
The short-term toxicity study(28 days) does not need to be conducted if.
However, tenofovir disoproxil reduced the viability index and weight of pups in a peri and postnatal toxicity study at maternally toxic doses.
A pre- and postnatal toxicity study was not performed with reteplase.
However, a toxicity study conducted with Cynomolgus monkeys has shown that cladribine suppresses maturation of rapidly generating cells, including testicular cells.
Effects on endocrine active and reproductivesystem organs were not observed in a chronic cynomolgus monkey toxicity study and reproductive performance was not affected in IL-6 deficient mice.
The short-term toxicity study(28 days) does not need to be conducted if.
An acute intravenous toxicity study in mice up to 68 LDU/ kg.
Short-term repeated dose toxicity study(28 days), one species, male and female, most appropriate route of administration, having regard to the likely route of human exposure.
Sub-chronic repeated dose toxicity study(90 days), preferred species is rat.
In pre/postnatal toxicity study in the rat, duloxetine induced adverse behavioural effects in the offspring at systemic exposure levels below maximum clinical exposure(AUC).
The extended one generation reproductive toxicity study(OECD Test Guideline 443(19)) also provides for developmental neurotoxicity testing.
An embryo-foetal toxicity study in Cynomolgus monkeys revealed no signs of teratogenicity.
An enhanced pre and postnatal development(ePPND) toxicity study in pregnant cynomolgus monkeys showed no evidence of teratogenic effects.
In a 6-month repeated dose toxicity study in mice, using the same analogous antibody against mouse TNFα, crystalline deposits were observed on the lens capsule of some of the treated male mice.
A subcutaneous neonatal/juvenile toxicity study performed in rats 7-55 days of age resulted in a NOAEL of 10mg/kg/day.
A peri/ postnatal toxicity study in rats revealed no significant effects at therapeutically relevant doses.
The short-term toxicity study(28 days) does not need to be conducted if.
A reproductive and developmental toxicity study conducted in rabbits with HUMENZA showed no effects on embryo fetal development.
The long-term aquatic toxicity study on Daphnia(Tier II, section 7.1.5) shall be considered if the substance is poorly water soluble.
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.
In a four-month rat dermal toxicity study, significantly decreased body weight and increased spleen weight were observed at 0.5 and 2.5 mg/kg;
In a pre- and post-natal toxicity study in rats, the tauro-conjugate of obeticholic acid was found in pups nursing from dams dosed with obeticholic acid.
A reliable sub-chronic(90 days) or chronic toxicity study is available, provided that an appropriate species, dosage, solvent and route of administration were used, or.
In a reproductive and pre-/post-natal toxicity study, no vaccine-related effects were detected on reproduction, foetal weight, survival and development of the off-spring.
Reproductive and development toxicity study conducted with an anti-murine PDGFRα antibody in mice showed foetal malformations and skeletal alterations(see section 5.3).