Examples of using Post-natal development in English and their translations into Polish
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Medicine
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Colloquial
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Ecclesiastic
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Ecclesiastic
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Official/political
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Computer
Post-natal development.
Effects on post-natal development.
No studies have been conducted with respect to parturition or peri/ post-natal development.
Animal studies on pre- and post-natal development have not been conducted.
Animal studies performed in rats did not indicateharmful effects on parturition, embryonal/foetal and post-natal development.
No effects were detected in the post-natal development of rat pups.
In a study of peri- and post-natal development in rats, retigabine was associated with increased perinatal mortality following administration during pregnancy.
No effects were detected in the post-natal development of rat pups.
In a pre- and post-natal development study in rats, an increase in stillborn pups and reduced embryo/ fetal survival was seen at maternally toxic doses≥ 3 mg/ kg.
Dedicated studies to assess the potential of vismodegib to affect post-natal development have not been performed.
No adverse effects on female reproduction and post-natal development in rats were seen at systemic exposures up to 2,300 times human exposures at the maximum recommended intrathecal dose.
Neither fluticasone furoate norvilanterol trifenatate had any adverse effects on fertility or pre- and post-natal development in rats.
Effects of rimonabant on pre- and post-natal development were assessed in the rat at doses up to 10 mg/ kg/ day.
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.
Overall, no adverse effects on fertility or post-natal development were observed in the rat at up to 5 times the observed clinical exposure.
Animal studies do not indicate direct or indirect harmful effects with respect to fertility, pregnancy, embryonic/fetal development, parturition or post-natal development see section 5.3.
No studies on fertility,early embryonic and post-natal development, or carcinogenicity studies were conducted because chronic dosing in animals would be expected to be associated with development of neutralising antibodies to the human protein.
The potential effects of plerixafor on male and female fertility and post-natal development have not been evaluated in non-clinical studies.
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. .
In peri and post-natal studies in rats,dystocia, increased foetal deaths in utero and toxicity to post-natal development(pup body weight and development land marks) were observed at systemic exposure levels up to 11 times the AUC0-24h of free plasma concentration at MRHD.
Animal studies do not indicate direct or indirect harmful effects with respect to fertility, pregnancy, embryonal/foetal development, parturition or post-natal development see section 5.3.
Non-clinical data reveal no special hazard for humans based on conventional studies of safety pharmacology, repeated dose toxicity, genotoxicity, carcinogenic potential andtoxicity to fertility and post-natal development.
Preclinical data reveal no special hazard for humans based on conventional studies of genotoxicity, fertility, embryo/ foetal development, parturition or post-natal development, and local tolerance.
Experimental animal studies are insufficient to assess the safety with respect to fertility, reproduction, development of the embryo or foetus, the course of gestation,and peri- and post-natal development.
However, irreversible defects in growing teeth and premature closure of the femoral epiphyseal plate, observed in rat toxicity studies at clinically relevant exposures,represent risks to post-natal development.
Preclinical data revealed no special hazard for humans based on conventional studies of safety pharmacology,repeated dose toxicity, genotoxicity, carcinogenic potential and toxicity to fertility and post-natal development.
Animal 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 fertility, pregnancy, embryonal/fetal development, parturition or post-natal development see section 5.3.
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.