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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 />

348

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