Examples of using Post-natal development in English and their translations into Finnish
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Pre- and post-natal development.
Dedicated studies to assess the potential of vismodegib to affect post-natal development have not been performed.
Pre- and post-natal development studies have not been performed.
Neither fluticasone furoate norvilanterol trifenatate had any adverse effects on fertility or pre- and post-natal development in rats.
Peri- and Post-Natal Development.
Animal studies do not indicate direct or indirect harmful effects with respect to pregnancy, embryo/foetal development, parturition or post-natal development see section 5.3.
It caused a delay in post-natal development safety margin of 1.
Data from the literature also indicate that decitabine has adverse effects on all aspects of the reproductive cycle, including fertility,embryo-foetal development and post-natal development.
Animal studies on pre- and post-natal development have not been conducted.
Pre- and post-natal development of Sprague-Dawley rats was not affected at exposures of about 135-times the human exposure based on Cmax.
The potential effects of plerixafor on male andfemale fertility and post-natal development have not been evaluated in non-clinical studies.
No pre- and post-natal development animal studies have been conducted with panitumumab.
All patients should be advised regarding the potential risk of panitumumab on pre- and post-natal development prior to initiation of Vectibix therapy.
A peri- and post-natal development study was performed in rats with levetiracetam doses of 70, 350 and 1,800 mg/kg/day.
In a pre- and postnatal development study in rats, effects on pre- and post-natal development were seen at an exposure below the MRHD.
In the rat pre-/post-natal development study, selexipag induced no effects on maternal and pup reproductive function.
Animal reproductive and developmental toxicity studies with H5N1 strain vaccines(A/Vietnam/1203/2004 and A/Indonesia/05/2005) do not indicate direct or indirect harmful effects with respect to female fertility, pregnancy, embryonal/foetal development, parturition or post-natal development see section 5.3.
Fertility and pre- and post-natal development were not affected in rats.
Animal reproductive and developmental toxicity studies with H5N1 strain vaccines(A/Vietnam/1203/2004 and A/Indonesia/05/2005) do not indicate direct or indirect harmful effects with respect to female fertility, pregnancy, embryonal/foetal development, parturition or post-natal development see section 5.3.
Daclizumab had no effect on peri- and post-natal development from birth to up to 6 months in the offspring.
In the pre- and post-natal development study in rats, there were no undesirable effects on pregnancy, parturition or lactation of F0 female rats at maternally non-toxic doses(10 and 20 mg/kg/day) and no effects on the growth, development, neurobehavioral or reproductive function of the offspring F1.
Studies carried out in rats did not reveal significant findings on fertility,embryo-fetal development or pre- and post-natal development at any of the tested doses corresponding to a systemic exposure in rats similar or lower than that observed in humans at the recommended dose of 150 mg once daily.
In a pre- and post-natal development study, a slightly prolonged gestation period, reduced number of implantation sites, and reduced number of pups delivered were observed.
Effects of rimonabant on pre- and post-natal development were assessed in the rat at doses up to 10 mg/ kg/ day.
In pre- and post-natal development studies with tipranavir in rats, growth inhibition of pups was observed at maternally toxic doses approximating 0.8-fold human exposure.
Fertility, pre-natal development and post-natal development were unaffected in rats at doses up to 250 mg/ kg/ day.
In a rat pre- and post-natal development study, at doses producing maternal toxicity during gestation and/or lactation, vandetanib increased pre-birth loss and reduced post-natal pup growth.
Overall, no adverse effects on fertility or post-natal development were observed in the rat at up to 5 times the observed clinical exposure.
In the rat peri- and post-natal development study with tafamidis, decreased pup survival and reduced pup weights were noted following maternal treatment during pregnancy and lactation at doses of 15 and 30 mg/kg.
Fertility, pre-natal development and post-natal development were unaffected in rats at doses up to 250 mg/ kg/ day.