Примери за използване на Fertility in rats на Английски и техните преводи на Български
{-}
-
Medicine
-
Colloquial
-
Official
-
Ecclesiastic
-
Ecclesiastic
-
Computer
There were no effects on female fertility in rats.
Fertility In rats, vandetanib had no effect on male fertility but impaired female fertility(see section 5.3).
Budesonide had no effect on fertility in rats.
Bimatoprost did not impair fertility in rats up to doses of 0.6 mg/kg/day(at least 103-times the intended human exposure).
Semaglutide did not affect male fertility in rats.
Bimatoprost did not impair fertility in rats up to doses of 0.6 mg/ kg/ day(approximately 103-times the intended human exposure).
Cilazapril had no effect on male or female fertility in rats.
Lamivudine Lamivudine did not affect male or female fertility in rats.
Ivacaftor had an effect on fertility in rats(see section 5.3).
Glycopyrronium did not cause any adverse effects on fertility in rats.
Ivacaftor had an effect on fertility in rats(see section 5.3).
Subcutaneous injections of RELISTOR at 150 mg/ kg/ day decreased fertility in rats.
In a study on male and female fertility in rats no effects were seen(see section 5.3).
Subcutaneous injections of Relistor at 150 mg/kg/day decreased fertility in rats.
Intravenously administered chlormethine impaired male fertility in rats at a daily dose of≥ 0.25 mg/kg for 2 weeks.
Paclitaxel was shown to be embryo andfeto-toxic in rabbits and to decrease fertility in rats.
Tigecycline did not affect mating or fertility in rats at exposures up to 4.7 times the human daily dose based on AUC.
Consequently, no adequate assessment of potential effects on male fertility in rats can be made.
Darifenacin had no effect on male or female fertility in rats or any effect in the reproductive organs of either sex in rats and dogs(for details, see section 5.3).
Tofacitinib impaired female fertility butnot male fertility in rats(see section 5.3).
Lusutrombopag did not affect male or female fertility in rats at doses up to 176 and 252 times the human clinical exposures in adults based on AUC in males and females, respectively(see section 5.3).
Paclitaxel has been shown to be embryotoxic and foetotoxic in rabbits,and to decrease fertility in rats.
There was a possible association with an effect on fertility in rats, namely a lower pregnancy rate.
Animal studies did not indicate direct harmful effects with respect to male and female fertility in rats.
There were no effects on oestrous cycle(female rats) or mating and fertility in rats(male or female)in nonclinical reproductive studies.
Fluticasone furoate, umeclidinium andvilanterol did not have any adverse effects on male or female fertility in rats.
Voriconazole administration induced no impairment of male or female fertility in rats at exposures similar to those obtained in humans at therapeutic doses.
Docetaxel has been shown to be both embryotoxic and foetotoxic in rabbits and rats, and to reduce fertility in rats.
Amifampridine had no adverse reaction on male or female fertility in rats at doses up to 75 mg/kg/day, and no effect on post-natal development or fertility was observed in the offspring of the treated animals.