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NEWSLETTER 4 : The Interactions between Nutraceuticals and
between Nutraceuticals and
Pharmaceuticals. (Updated November 2002)
Introduction
Sumary
Purpose
This text is derived from the abstract of the publication
by Lucinda G. Miller: "Herbal Medicinals" In the Archives of Internal Medicine/Vol. 158, Nov. 9, 1998, and from original
research.
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SUMMARY :
Echinacea can cause hepatotoxicity and therefore should not be used with other known hepatotoxic drugs, such
as anabolic steroids, amiodarone, methotrexate, and ketoconazole.
Nonsteroidal anti-inflammatory drugs may negate the usefulness of feverfew in the treatment of migraine
headaches.
Fever few, garlic, Ginkgo, ginger, and ginseng may alter bleeding time and should not be used concomitantly
with warfarin sodium.
Ginseng may cause headache, tremulousness, and manic episodes in patients treated with phenelzine sulfate.
Ginseng should also not be used with estrogens or corticosteroids because of possible additive effects.
St John wort: Not to use with MAO inhibitors and serotonin reuptake inhibitors.
Valerian should not be used with barbiturates because of excessive sedation.
Kyushin, licorice, plantain, uzara root, hawthorn, and ginseng may interfere with digoxin pharmacodynamically
and with digoxin monitoring.
Evening primrose oil and borage should not be used with anticonvulsants because they may lower the seizure
threshold.
Kava when used with alprazolam has resulted in coma.
Immunostimulants (eg, Echinacea and zinc) should not be given with immunosuppressants (eg, corticosteroids
and cyclosporine).
Tannic acids present in some herbs (eg, St John's wort and saw palmetto) may inhibit the absorption of
iron.
Kelp as a source of iodine may interfere with thyroid replacement therapies.
Licorice can offset the pharmacological effect of spironolactone.
Numerous herbs (eg, karela and ginseng) may affect blood glucose levels and should not be used in patients
with diabetes mellitus.
Ginseng and Ginkgo Biloba have opposed activity and should not be used together
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