Examples of using Postnatal development in English and their translations into German
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Political
Postnatal development disorder.
Studies in animals have shown toxicity with respect to postnatal development see section 5.3.
In studies on pre and postnatal development in rats the survival rate of offspring was significantly reduced at doses causing severe maternal toxicity.
However, animal studies have shown adverse effects on postnatal development see section 5.3.
In studies on pre and postnatal development in rats the survival rate of offspring was significantly reduced at doses causing severe maternal toxicity.
Animal studies with respect to effects on parturition and postnatal development have not been performed see section 5.3.
Animal studies do not indicate direct harmful effects with respect to pregnancy,parturition or postnatal development.
In a study on pre- and postnatal development the survival rate of offspring was significantly reduced at doses which slightly reduced maternal weight.
In monkeys, mepolizumab had no effect on pregnancy or on embryonic/fetal and postnatal development(including immune function) of the offspring.
The evaluation of the peri- and postnatal development study in rats is hampered due to subsequent administration of DPH, and therefore of limited relevance.
Increased mortality and morbidity were seen at all doses(1 mg/kg/day) in lactating females in mouse pre- and postnatal development studies.
In a study on pre- and postnatal development the survival rate of offspring was significantly reduced at doses which slightly reduced maternal weight.
Reproductive studies in animals with netupitant do not indicate direct or indirect harmful effects with respect to fertility,parturition or postnatal development.
In a pre- and postnatal development study limited changes in immune function were observed at 11-fold a human 10 mg/ kg dose based on AUC see section 5.3.
Animal studies do not indicate direct or indirect harmful effects with respect to pregnancy, embryonal/ foetal development, parturition or postnatal development.
Studies on embryofoetal development and pre-and postnatal development revealed eye malformations, skeletal anomalies, abortions, and an increased foetal death rate.
Animal studies with respect to effects on pregnancy, embryonal/ foetal development, parturition and postnatal development have not been conducted with Xigris.
Animal studies do not indicate direct or indirect harmful effects with respect to pregnancy, embryonal/ foetal development, parturition or postnatal development.
Animal studies showed reproductive toxicity, but did not indicate direct harmful effects with respect to pregnancy, embryonal/ foetal development, parturition or postnatal development see Section 5.3 Preclinical Safety Data.
Animal studies do not indicate direct or indirect harmful effects with respect to pregnancy, embryonal/ foetal development, birth or postnatal development.
Studies in animals do not indicate direct harmful effects with respect to pregnancy, embryonal/foetal development, parturition or postnatal development see section 5.3.
Animal studies with metformin do not indicate harmful effects with respect to pregnancy, embryonic or foetal development, parturition or postnatal development see section 5.3.
Animal studies do not indicate direct or indirect harmful effects with respect to pregnancy, embryonal/ foetal development, parturition or postnatal development see section 5.3.
In animal studies there was no indication of direct or indirect harmful effects with respect to pregnancy, embryonal/ foetal development, parturition or postnatal development see section 5.3.
Animal studies do not indicate direct or indirect harmful effects on pregnancy, embryonal/ foetal development, parturition and postnatal development see section 5.3.
Animal studies do not indicate direct or indirect harmful effects with respect to pregnancy, embryonal/foetal development, parturition, or postnatal development see section 5.3.
Animal studies do not indicate direct harmful effects with respect to pregnancy, embryonal/foetal development, parturition or postnatal development.
In non-clinical studies, Menveo had no direct or indirect harmful effects with respect to pregnancy, embryonal/foetal development, parturition or postnatal development.
Studies in animals do not indicate direct or indirect harmful effects with respect to pregnancy, embryonal/foetal development, parturition or postnatal development see section 5.3.
Animal studies with metformin do not indicate harmful effects with respect to pregnancy, embryonicor foetal development, parturition, or postnatal development see section 5.3.