Last edited by Academic Press
28.07.2021 | History

4 edition of Drugs and pregnancy found in the catalog.

Drugs and pregnancy

maternal drug handling--fetal drug exposure

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  • 946 Currently reading

Published by Administrator in Academic Press

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      • Includes bibliographies and index.Proceedings of the symposium, drugs and pregnancy, maternal drug handling--fetal exposure, Geneva, Switzerland, Oct. 6-7, 1983.

        StatementAcademic Press
        PublishersAcademic Press
        Classifications
        LC Classifications1984
        The Physical Object
        Paginationxvi, 134 p. :
        Number of Pages79
        ID Numbers
        ISBN 10012425960X
        Series
        1nodata
        2
        3

        nodata File Size: 4MB.


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Interestingly, this effect was absent when subjects were allowed to smoke freely, indicating that the deficit was withdrawal-induced and that smoking was a means to compensate for this deficit.

Pegcetacoplan (Empaveli) Use During Pregnancy

Naltrexone Naltrexone is a long-acting, nonselective opioid receptor antagonist used more commonly outside of the United States to prevent relapse in opiate addicts due to its ability to block the euphoric effects of opioid agonists, low tolerance and abuse potential, and modest adverse effects.

All medication should be taken as instructed on the pack or as prescribed by a doctor or midwife. It may not be safe for you. Alterations in the fetal development of the monoaminergic system can affect short- and long-term attention and cognitive development.

Belcheva MM, Bohn LM, Ho MT, Johnson FE, Yanai J, Barron S et al 1998. Warfarin is a common example. In addition to the aforementioned deficits, prenatally exposed children are more likely to develop substance use disorders.

Drug Use During Pregnancy

Many women need to take medicines when they are pregnant. Endogenous opioids regulate dendritic growth and spine formation in developing rat brain. Fried PA, Watkinson B, Gray R 2003. Organization of cortico-cortical associative projections in rats exposed to ethanol during early postnatal life.

Jones LB, Stanwood GD, Reinoso BS, Washington RA, Wang HY, Friedman E et al 2000. Additional disruptions in monoamine oxidase B levelsMETH sensitizationand startle response ; also have implications for cognition and addiction vulnerability.