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Feverfew |
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Feverfew (English) Tanacetum
parthenium/Chrysanthemum parthenium
(Botanical) Compositae (Plant Family) Tanaceti parthenii herba
(Pharmacopeial)
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Overview |
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A wealth of scientific evidence shows that feverfew is an effective treatment
and prophylactic for migraine headaches. Used for centuries in European folk
medicine, feverfew was traditionally utilized for headache, arthritis, and
fever. The word feverfew is a corruption of the Latin febrifuge, which literally
means fever-reducing.
In a survey conducted in Britain in the 1980s, 70% of migraine sufferers who
ate two to three fresh feverfew leaves daily experienced considerable relief
from their headaches. A clinical study later revealed that feverfew
significantly reduced the symptoms of migraine when compared with placebo.
Feverfew also lessened accompanying symptoms of nausea and vomiting. In 1997,
this medicinal herb ranked #19 on a list of the top herbs sold at health food
stores in the United States.
Feverfew's antimigraine activity comes from parthenolide, a sesquiterpene
lactone. Parthenolide is a spasmolytic that makes smooth muscle in the walls of
cerebral blood vessels less reactive to vasoconstrictors. Parthenolide helps
prevent migraines and lessen the severity of existing migraines by acting as an
antagonist to vasoconstrictors such as serotonin, prostaglandins, and
norepinephrine.
Parthenolide and standardized extracts of feverfew containing parthenolide
block the release of serotonin from blood vessels and prevent platelets from
over-aggregating. Parthenolide also inhibits the actions of compounds released
from cells that cause inflammation. |
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Macro Description |
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Native to southeastern Europe, feverfew is now widespread throughout Europe,
North America, and Australia. It is a short, herbaceous, composite perennial. It
is a member of the daisy family, and it blooms between July and October. This
aromatic plant gives off a strong and bitter odor. Its yellow-green leaves are
alternate and bipinnatifid. The small, daisy-like yellow flowers are arranged in
a dense corymb. |
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Part Used/Pharmaceutical
Designations |
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- Leaves (dried leaves)
- Dried aerial parts
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Constituents/Composition |
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Flavonoids, polyenes, volatile oil (camphor, borneol, terpenes, various
esters); sesquiterpene lactones (85% is parthenolide) (0.1% to 0.9% of plant);
sesquiterpenes, monoterpenes, spiroketal enol ether
polyenes. |
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Commercial
Preparations |
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Parthenolide content varies tremendously and depends on geographical origin.
Nearly 50% of feverfew products from Canada lacked parthenolide. And no
parthenolide could be detected in samples from Mexico and Eastern Serbia. It is
for this reason that feverfew preparations should be standardized for at least
0.2% parthenolide. |
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Medicinal
Uses/Indications |
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Traditional actions: relaxant, anti-inflammatory, vasodilator, digestive
bitter, emmenagogue. Historically, feverfew was used for intestinal parasites,
anemia, insect bites, irregular menses, stomachaches, and as an abortifacient,
although it is rarely used this way now.
Clinical applications: preventing and treating migraine, initial inflammatory
stages of arthritis, rheumatic diseases, allergies, congestive dysmenorrhea,
vertigo, and tinnitus.
Conditions: migraine, arthritis, rheumatic diseases,
allergies |
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Pharmacology |
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In vitro and in vivo studies show that feverfew has anti-inflammatory
activity and prophylactic action against migraines. The underlying cause of
migraine headaches presumably involves two primary mechanisms: (1)
over-aggregation of platelets; and (2) release of serotonin and inflammatory
compounds from platelets. In vivo and in vitro studies show unequivocally that
parthenolide disrupts both mechanisms.
Parthenolide apparently neutralizes sulfhydryl groups on enzymes crucial for
platelet aggregation. And it probably achieves its prophylactic effects by
suppressing the release of serotonin from platelets. In in vivo studies,
extracts of feverfew blocked the synthesis of prostaglandin, thromboxane, and
leukotriene.
In vitro findings indicate that feverfew may be beneficial for arthritis. The
anti-arthritic effects may be due to the ability of feverfew to destroy
peripheral blood mononuclear cells in the synovium.
The first human clinical study of feverfew involved a small sample of only 17
patients, but the results were dramatic. All patients enrolled in this study had
taken feverfew for several years. Nine patients were given a placebo and eight
were given 50 mg of feverfew daily. During the six-month study period, the
patients remaining on feverfew experienced continued relief. Migraines increased
almost threefold in the patients taking placebo. However, the increase in
symptoms in the placebo group may have actually been part of a
feverfew-withdrawal syndrome.
In a double-blind, placebo-controlled, crossover study of 72 migraine
sufferers, the treatment group received 70 to 114 mg of feverfew. They had a 24%
reduction in the number of migraines when compared with the placebo group. The
treatment group had fewer symptoms, although the length of each individual
migraine episode did not change.
In another investigation, feverfew showed no clear-cut clinical benefits for
rheumatoid arthritis. However, a low dosage of powdered leaf product was used
and the parthenolide content was not determined in this trial. Because of the
limitations of this study, the efficacy of feverfew for arthritis is
inconclusive. |
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Dosage Ranges and Duration of
Administration |
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Recommended dosage:
- Treatment and prevention of migraine: standardized feverfew extract
(minimum 0.25 mcg parthenolide) bid
- Acute migraine attack: 1 to 2 g parthenolide daily
- For other conditions: 1 to 2 ml bid of 1:1 fluid extract; 2 to 4 ml
bid of 1:5 tincture
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Side
Effects/Toxicology |
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There are no long-term studies on feverfew toxicology. Minor side effects of
nervousness and mild gastrointestinal irritation have been reported with use of
standardized feverfew tablets. Adverse side effects of abdominal pain,
indigestion, flatulence, diarrhea, nausea, and vomiting have also been observed.
Mouth ulcerations, loss of taste, and swelling of the lips, tongue, and mouth
occur in about 10% of individuals who chew the leaves.
In vivo studies revealed little evidence of negative reactions to feverfew in
daily doses 100 times the dose given to humans. A histological examination of
human lymphocytes showed that feverfew does not cause chromosomal abnormalities.
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Warnings/Contraindications/Precautions |
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Feverfew is indicated for migraine sufferers who do not respond to
conventional treatment. Because this herb can alter the menstrual cycle,
menstruating women should use it with caution. Pregnant and lactating women and
children under 2 years of age should not take feverfew. |
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Interactions |
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No specific interactions between feverfew and conventional medications have
been adequately researched to draw conclusions. However, a potential interaction
with non-steroidal anti-inflammatory drugs (NSAIDs) has been raised, because of
prostaglandin inhibition by NSAIDs, which may reduce the effectiveness of
feverfew (Miller 1998). Additionally, because of the platelet inhibitory effects
of feverfew, patients taking anticoagulants with feverfew should be monitored
closely for clinical signs of bleeding abnormalities. |
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Regulatory and Compendial
Status |
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The U.S. FDA classifies feverfew as a dietary supplement. Feverfew is used as
a nonprescription drug for migraine headache in Britain and
Germany. |
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References |
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Blumenthal M, ed. The Complete German Commission E Monographs: Therapeutic
Guide to Herbal Medicines. Boston, Mass: Integrative Medicine
Communications; 1998:12.
Bradley P, ed. British Herbal Compendium. Vol. 1. Dorset, England:
British Herbal Medicine Association; 1992:1:96-98.
Brown D. Herbal Prescriptions for Better Health. Rocklin, Calif: Prima
Publishing; 1996:91-95.
De Weerdt CJ, Bootsma HPR, Hendriks H. Herbal medicines in migraine
prevention. Randomized double-blind placebo controlled crossover trial of a
feverfew preparation. Phytomedicine. 1996;3:225-230.
Grieve M. A Modern Herbal. New York, NY: Dover; 1971:1:309-310.
Gruenwald J, Brendler T, Jaenicke C, et al., eds. PDR for Herbal
Medicines. Montvale, NJ: Medical Economics Co; 1998:1171-1173.
Heptinstall S, Groenewegen W, Spangenberg P, Lösche W. Inhibition of platelet
behavior by feverfew: a mechanism of action involving sulfhydryl groups.
Folia Haematol Int Mag Klin Morphol Blutforsch. 1988;43:447-449.
Johnson ES, Kadam NP, Hylands DM, Hylands PJ. Efficacy of feverfew as
prophylactic treatment of migraine. Br Med J. 1985;291:569-573.
Johnson ES. Patients who chew chrysanthemum leaves. MIMS Magazine May
15, 1983:32-35.
Miller LG. Herbal medicinals: selected clinical considerations focusing on
known or potential drug-herb interactions. Arch Intern Med.
1998;158(20):2200-2211.
Murphy JJ, Heptinstall S, Mitchell JR. Randomised double-blind
placebo-controlled trial of feverfew in migraine prevention. Lancet.
1988;2:189-192.
Murray MT. The Healing Power of Herbs: The Enlightened Person's Guide to
the Wonders of Medicinal Plants. 2nd ed. Rocklin, Calif: Prima Publishing;
1995.
Newall CA, Anderson LA, Phillipson JD. Herbal Medicines: A Guide for
Health-care Professionals. London: Pharmaceutical Press; 1996:119-120.
Palevitch D, Earon G, Carasso R. Feverfew (Tanacetum parthenium) as a
prophylactic treatment for migraine: a double-blind controlled study.
Phytotherapy Res. 1997;11:508-511.
Pattrick M, Heptinstall S, Doherty M. Feverfew in rheumatoid arthritis: a
double-blind, placebo controlled study. Ann Rheum Dis.
1989;48:547-549.
Tyler VE. Herbs of Choice: The Therapeutic Use of Phytomedicinals.
Binghamton, NY: Pharmaceutical Products Press; 1994:126-134.
Tyler VE. The Honest Herbal: A Sensible Guide to the Use of Herbs and
Related Remedies. 3rd ed. Binghamton, NY: Pharmaceutical Products Press;
1993. |
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Copyright © 2000 Integrative Medicine
Communications This publication contains
information relating to general principles
of medical care that should not in any event be construed as specific
instructions for individual patients. The publisher does not accept any
responsibility for the accuracy of the information or the consequences arising
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are made for any drugs or compounds currently marketed or in investigative use.
The reader is advised to check product information (including package inserts)
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interactions, and contraindications before administering any drug, herb, or
supplement discussed herein. | |