Examples of using Developmental toxicity in English and their translations into Hungarian
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Medicine
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Colloquial
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Ecclesiastic
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Financial
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Official/political
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Computer
Developmental toxicity of trastuzumab has been identified in the clinical setting although it was not predicted in the non-clinical program.
Reproductive and developmental toxicity studies evaluating teduglutide have been carried out in rats
Conventional reproductive/ developmental toxicity studies with emtricitabine
embryotoxicity and developmental toxicity at dose above 30 mg/kg/day.
A reproductive and developmental toxicity study conducted in rabbits with HUMENZA showed no effects on embryo fetal development.
Conventional reproductive and developmental toxicity studies are not considered relevant, given the nature and the intended clinical use of the medicinal product.
In a developmental toxicity study conducted in monkeys, there was no indication of maternal toxicity,
however developmental toxicity has been observed(see section 5.3).
Developmental toxicity studies in rats and rabbits resulted in bone
Animal reproductive and developmental toxicity studies do not indicate direct
Embryo-foetal developmental toxicity studies conducted in rats
Developmental toxicity, including teratogenicity, was observed in rats and rabbits at dose levels of 150 mg/ kg and higher administered daily throughout organogenesis.
No evidence of reproductive or developmental toxicity was seen in a study where the human dose of Optaflu was administered prior to
Conventional non-clinical reproductive and developmental toxicity studies are not considered relevant,
In a developmental toxicity study conducted in mice following administration of the same analogous antibody, and in cynomolgus monkeys using golimumab, there was no indication of maternal toxicity,
foetal and developmental toxicity was seen in mice.
Embryo-foetal developmental toxicity studies conducted in rats and rabbits revealed no compound- induced malformations or developmental variations when
teratogenicity and developmental toxicity), undesirable effects observed were considered to be secondary to the hypoglycaemic effects induced by the compound in dams and in offspring.
birth defects or developmental toxicity were observed.
to amprenavir lower than therapeutic exposure in patients treated with Telzir, some developmental toxicity was observed(see section 5.3).