Examples of using Developmental toxicity in English and their translations into German
{-}
-
Medicine
-
Colloquial
-
Official
-
Ecclesiastic
-
Financial
-
Ecclesiastic
-
Political
-
Computer
-
Programming
-
Official/political
-
Political
Developmental toxicity studies were previously conducted in rabbits.
Animal studies have revealed minimal developmental toxicity see section 5.3.
Developmental toxicity studies in rats and rabbits have shown reproductive toxicity of riociguat.
Studies in animals have shown reproductive and developmental toxicity see section 5.3.
Developmental toxicity studies performed in cynomolgus monkeys revealed no evidence of embryotoxicity in utero.
Animal studies could not exclude potential developmental toxicity see section 5.3.
Developmental toxicity studies in rats and rabbits resulted in bone and tooth abnormalities(e.g. bent long bones and wavy ribs) in the offspring.
No carcinogenicity, mutagenicity or reproductive and developmental toxicity data are available.
In a developmental toxicity study in the rat, abiraterone acetate affected pregnancy including reduced foetal weight and survival.
Identification of novel molecular endpoints and studies on the role of miRNAs in developmental toxicity.
Do not use during pregnancy and lactation because developmental toxicity has been observed in laboratory species.
Developmental toxicity of trastuzumab has been identified in the clinical setting although it was not predicted in the non-clinical program.
In addition to this,ZEBET scientists are developing alternative methods for predicting developmental toxicity properties.
Developmental toxicity studies performed in rats and rabbits have revealed no evidence of harm to the foetus or neonatal rat due to etanercept.
Studies in animals(rats and rabbits) have shown developmental toxicity, including teratogenicity and embryo- lethality see section 5.3.
Developmental toxicity in rabbits(embryolethality, decreased litter size and decreased foetal weights) occurred at a maternally toxic dosage.
There are no exposure data in rabbits. The threshold for developmental toxicity was considered to be 6 mg/ m2/ day in rats and 1.2 mg/ m2/ day in rabbits.
In Europe, the Horizon 2020 to promote research into replacement methods toanimal use in the field of long-term toxicity and developmental toxicity is only 30 million euros.
Reproductive and developmental toxicity studies have not been performed, given the nature and the intended clinical use of the medicinal product.
The package contains summaries of the acute, subacute, and chronic toxicological properties of the technical material,including reproductive and developmental toxicity, genotoxicity, and carcinogenicity.
If a substance is known to cause developmental toxicity, meeting the criteria for classification as toxic for reproduction category 1A or 1B.
The SCAN adopted an opinion concerning Nifursol on 11 October 2001, which concluded that on the basis of the mutagenicity, genotoxicity and carcinogenicity studies provided by the person responsible for putting Nifursol into circulation,and because of the lack of data on developmental toxicity, it was not possible to derive an acceptable daily intake for the consumers.
There is therefore a high risk for developmental toxicity at clinical doses, primarily due to tegafur(5-FU) and to oteracil to a lesser extent.
Developmental toxicity studies in the rat and rabbit have shown embryo-fetal lethality at maternally toxic dosages, but no direct embryo-foetal toxicity below maternally toxic dosages.
The studies in earthworms and those on developmental toxicity were considered sufficient and adequate to support the risk assessments.
Additional developmental toxicity was limited to dose-related reductions in pup body weights, and observed only at doses≥ 15 mg/kg/day pup exposures≥ 29 times the human values at the MRHD.
The no observed adverse effect level(NOAEL) for developmental toxicity, the lowest dose tested, is associated with a maternal systemic exposure multiple that is approximately 19 times the human value at the maximum recommended human dose.
Developmental toxicity studies have been performed in rats and rabbits at daily doses up to 5 times the human daily dose and have revealed no evidence of harm to the foetus due to ivacaftor see section 5.3.
The reproductive and developmental toxicity studies conducted in rats and rabbits with AF03 did not show any effects on female fertility, pregnancy, embryofetal development or early postnatal development.
Additional developmental toxicity was limited to dose-related reductions in pup body weights, and observed only at doses≥ 15 mg/kg/day associated with pup exposures that are≥ 29 times the human values at the maximum recommended human dose.