WHO monographs on selected medicinal plants - travolekar.ru
WHO monographs on selected medicinal plants - travolekar.ru
WHO monographs on selected medicinal plants - travolekar.ru
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<str<strong>on</strong>g>WHO</str<strong>on</strong>g> <str<strong>on</strong>g>m<strong>on</strong>ographs</str<strong>on</strong>g> <strong>on</strong> <strong>selected</strong> <strong>medicinal</strong> <strong>plants</strong><br />
Adverse reacti<strong>on</strong>s<br />
Ingesti<strong>on</strong> of large amounts of clover in animal feed has been associated<br />
with a number of adverse effects in sheep in Australia. A publicati<strong>on</strong> <strong>on</strong><br />
“clover disease” described symptoms of infertility, abnormal lactati<strong>on</strong>,<br />
dystocia and prolapsed ute<strong>ru</strong>s, all of which were hypothetically attributed<br />
to the estrogenic effects of isoflav<strong>on</strong>es (42). N<strong>on</strong>e of the c<strong>on</strong>trolled, clinical<br />
trials has reported adverse effects at doses up to 160 mg of isoflav<strong>on</strong>es<br />
per day. Trifolium pratense does not c<strong>on</strong>tain coumarins, and therefore the<br />
c<strong>on</strong>cerns about blood coagulati<strong>on</strong> are unfounded (43, 44).<br />
C<strong>on</strong>traindicati<strong>on</strong>s<br />
Flos Trifolii is c<strong>on</strong>traindicated in cases of hypersensitivity or allergy to<br />
the c<strong>ru</strong>de d<strong>ru</strong>g. It is also c<strong>on</strong>traindicated during pregnancy, breastfeeding<br />
and for children under the age of 12 years, and in cases of horm<strong>on</strong>eassociated<br />
diseases, due to the potential horm<strong>on</strong>al effects.<br />
Warnings<br />
Due to the potential estrogenic effects of the c<strong>ru</strong>de d<strong>ru</strong>g, patients with<br />
horm<strong>on</strong>e-related disorders, estrogen-dependent cancers or a familial history<br />
of estrogen-dependent cancers should c<strong>on</strong>tact a health care provider<br />
before use.<br />
Precauti<strong>on</strong>s<br />
Carcinogenesis, mutagenesis, impairment of fertility<br />
No informati<strong>on</strong> was found.<br />
D<strong>ru</strong>g interacti<strong>on</strong>s<br />
There are c<strong>on</strong>flicting data c<strong>on</strong>cerning an interacti<strong>on</strong> of the c<strong>ru</strong>de d<strong>ru</strong>g<br />
with tamoxifen and other antiestrogenic d<strong>ru</strong>gs. Some studies suggest that<br />
specific isoflav<strong>on</strong>es may enhance the ability of tamoxifen to inhibit the<br />
growth of estrogen-receptor-positive breast cancer cells (45–47). In rodent<br />
models, genistein has been shown to inhibit the efficacy of tamoxifen<br />
<strong>on</strong> the growth of estrogen-receptor-positive breast cancer cells implanted<br />
in ovariectomized mice, while other research shows that specific isoflav<strong>on</strong>es<br />
may be additive and work in a synergistic manner to prevent the<br />
development of chemically induced tumours and the growth of existing<br />
tumours (48–50). Therefore, the use of the c<strong>ru</strong>de d<strong>ru</strong>g or its preparati<strong>on</strong>s<br />
is not recommended in those being treated with tamoxifen and other antiestrogenic<br />
d<strong>ru</strong>gs until further research has been d<strong>on</strong>e.<br />
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