Примери за използване на Teratogenic in rats and rabbits на Английски и техните преводи на Български
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Baricitinib was teratogenic in rats and rabbits.
Methylphenidate is not considered to be teratogenic in rats and rabbits.
Darifenacin was not teratogenic in rats and rabbits at doses up to 50 and 30 mg/kg/day, respectively.
Ambrisentan has been shown to be teratogenic in rats and rabbits.
Ziconotide was not teratogenic in rats and rabbits at exposures< 100 times human plasma levels.
Sufentanil was not teratogenic in rats and rabbits.
Pramipexole was not teratogenic in rats and rabbits, but was embryotoxic in the rat at maternotoxic doses(see section 5.3).
Clofarabine was teratogenic in rats and rabbits.
Memantine was not teratogenic in rats and rabbits, even at maternally toxic doses,and no adverse effects of memantine were noted on fertility.
Non-liposomal irinotecan was teratogenic in rats and rabbits at doses below the human therapeutic dose.
Upadacitinib was teratogenic in rats and rabbits with effects in bones in rat foetusesand in the heart in rabbit foetuses when exposed in utero.
Teriflunomide was embryotoxic and teratogenic in rats and rabbits at doses in the human therapeutic range.
Selexipag was not teratogenic in rats and rabbits(exposure margins above therapeutic exposure of 13-fold for selexipag and 43-fold for the active metabolite, based on total exposure).
Tofacitinib has been shown to be teratogenic in rats and rabbits, and to affect parturitionand peri/postnatal development(see section 5.3).
Nicotinic acid was not teratogenic in rats and rabbits up to exposure levels approximately 253and 104 times the human AUC of nicotinic acid at the recommended daily human dose, respectively.
Pramipexole was not teratogenic in rats and rabbits but was embryotoxic in the rat at maternally toxic doses.
Daclatasvir is embryotoxic and teratogenic in rats and rabbits at exposures at or above 4-fold(rat) and 16-fold(rabbit) the clinical AUC exposure.
Leflunomide was embryotoxic and teratogenic in rats and rabbits at doses in the human therapeutic range and exerted adverse effects on male reproductive organs in repeated dose toxicity studies.
Leflunomide was embryotoxic and teratogenic in rats and rabbits at doses in the human therapeutic range and exerted adverse effects on male reproductive organs in repeated dose toxicity studies.
Tofacitinib was shown to be teratogenic in rats and rabbits, and have effects in rats on female fertility(decreased pregnancy rate; decreases in the numbers of corpora lutea, implantation sites, and viable foetuses; and an increase in early resorptions), parturition, and peri/postnatal development.
Paliperidone was not teratogenic in rat and rabbit.
Sofosbuvir had no effects on embryo-foetal viability or on fertility in rat and was not teratogenic in rat and rabbit development studies.
There was no evidence of a teratogenic effect in rats and rabbits.
Because mycophenolate mofetil has demonstrated teratogenic effects in rats and rabbits, CellCept tablets should not be crushed.
Because mycophenolate mofetil has demonstrated teratogenic effects in rats and rabbits, CellCept capsules should not be opened or crushed.
Carmustine is embryotoxic in rats and rabbits and teratogenic in rats when given in doses equivalent to the human dose.
Because mycophenolate mofetil has demonstrated teratogenic effects in rats and rabbits, Myclausen film-coated tablets should not be broken or crushed.
The related razoxane has been demonstrated to be embryotoxic in mice, rats and rabbits and teratogenic in rats and mice.
Carmustine was embryotoxic and teratogenic in rats and embryotoxic in rabbits at dose levels equivalent to the human dose.
Mifamurtide was not mutagenic and did not cause teratogenic effects in rats and rabbits.