Примери за използване на Teratogenic in rats на Английски и техните преводи на Български
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Teriflunomide was embryotoxic and teratogenic in rats and rabbits at doses in the human therapeutic range.
Results of animal reproduction studies indicate that recombinant interferon alfa-2b was not teratogenic in rats.
It has been shown that nifedipine causes damage teratogenic in rats or rabbits, including digital anomalies.
In the reproduction studies, vinflunine appeared to be embryolethal and teratogenic in rabbits and teratogenic in rats.
Pramipexole was not teratogenic in rats and rabbits but was embryotoxic in the rat at maternally toxic doses.
Histamine dihydrochloride was not teratogenic in rats or rabbits at doses resulting in several hundredfold greater systemic exposures than the clinical exposure.
Fluticasone furoate was not teratogenic in rats or rabbits, but delayed development in rats
Alogliptin was not teratogenic in rats or rabbits with a systemic exposure at the NOAELs far above the human exposure at the recommended dose.
Memantine was not teratogenic in rats and rabbits, even at maternally toxic doses,
Histamine dihydrochloride was not teratogenic in rats or rabbits at doses resulting in several hundred- fold greater systemic exposures than the clinical exposure.
Tofacitinib has been shown to be teratogenic in rats and rabbits, and to affect parturition
Lurasidone was not teratogenic in rats or rabbits at an exposure similar to
Daclatasvir is embryotoxic and teratogenic in rats and rabbits at exposures at or above 4-fold(rat) and 16-fold(rabbit)
Upadacitinib was teratogenic in rats and rabbits with effects in bones in rat foetuses and in the heart in rabbit foetuses when exposed in utero.
Lomitapide was teratogenic in rats in the absence of maternal toxicity at an exposure(AUC)
Bosentan has been shown to be teratogenic in rats at plasma levels higher than 1.5 times the plasma concentrations achieved at the therapeutic dose in humans.
Mangafodipir is teratogenic in rats; it causes increased foetal skeletal abnormalities when given daily by intravenous injection to female rats at dosages slightly greater than clinical dosages.
Laropiprant was not teratogenic in rats or in rabbits at least 153