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Selective estrogen receptor modulators adverse effects

Xie, L., Wang, J. and Bourne, P.E. (2007) In silico elucidation of the molecular mechanism defining the adverse effect of selective estrogen receptor modulators. PLoS Computational Biology, 3 (11). [Pg.320]

Idoxifene is another of the newer selective estrogen receptor modulators (SERMs), and preclinical data show that it has greater antiestrogenic activity than tamoxifen but lower estrogenic activity. It is not yet clear whether this affects its degree of usefulness or safety when it is used, for example, in cases of metastatic breast cancer. In comparisons of the two drugs in such patients the desired effects were similar and the incidence of adverse effects was essentially the same (14). [Pg.297]

Selective Estrogen Receptor Modulators Raloxifene (EVISTa) acts as an estrogen agonist on bone and liver, is inactive on the uterus, and acts as an estrogen antagonist on the breast. In postmenopausal women, raloxifene modestly increases bone mineral density and has been shown to reduce the risk of vertebral compression fractures in this setting, it is approved for both the prevention and treatment of osteoporosis. The major adverse effect is worsened vasomotor symptoms the drug also increases the incidence of deep venous thrombosis. [Pg.1074]


See other pages where Selective estrogen receptor modulators adverse effects is mentioned: [Pg.330]    [Pg.862]    [Pg.912]    [Pg.962]    [Pg.962]    [Pg.1033]    [Pg.124]    [Pg.50]   
See also in sourсe #XX -- [ Pg.865 ]

See also in sourсe #XX -- [ Pg.1656 ]




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Adverse selection

Estrogen adverse effects

Estrogen receptor

Estrogen receptor (3-modulator

Estrogen receptor modulation

Estrogen receptor modulators

Estrogenic effects

Modulation effects

Selective estrogen receptor

Selective estrogen receptor modulator

Selective estrogen receptor modulators

Selective receptors

Selectivity effects

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