Eksempler på brug af Rats and rabbits på Engelsk og deres oversættelser til Dansk
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embryolethality was seen in both rat and rabbit studies see section 5.3.
Embryo-foetal development studies were conducted with abatacept in mice, rats, and rabbits at doses up to 20 to 30 times a human 10 mg/ kg dose and no undesirable effects were observed in the offspring.
Embryofoetal toxicity was evaluated in rats and rabbits.
Abatacept was shown to cross the placenta in rats and rabbits.
Studies in rats and rabbits were inconclusive with respect to potential.
Developmental Toxicity Raltegravir was not teratogenic in developmental toxicity studies in rats and rabbits.
Topotecan was also shown to cause embryo-foetal lethality when given to rats and rabbits.
There is no evidence from studies in rats and rabbits that filgrastim is teratogenic.
Etoricoxib crosses the placenta in rats and rabbits, and the blood-brain barrier in rats. .
There is no evidence from studies in rats and rabbits that filgrastim is teratogenic.
Foetal toxicity in rats and rabbits occurred only at exposures sufficiently above human exposure.
Reproductive function was not affected and no teratogenic potential was noted in rats and rabbits.
Embryo-foetal developmental toxicology studies in rats and rabbits showed no evidence of malformations due to prasugrel.
Development studies in rats and rabbits have shown no evidence of foetal malformations
In rats and rabbits, no effects on embryonic/ foetal survival or foetal weights were observed.
Renal toxicity has been observed with even lower single doses of doxorubicin HCl in rats and rabbits.
Laboratory studies in rats and rabbits have not produced any evidence of teratogenic,
In rats and rabbits, tacrolimus caused embryofoetal toxicity at doses which demonstrated maternal toxicity see section 5.3.
Laboratory studies in rats and rabbits with pimobendan have not shown any effect on fertility.
Laboratory studies in rats and rabbits with pimobendan have shown foetotoxic effects at maternotoxic doses.