PDR for Herbal Medicines

(Barré) #1
308 /FEVERFEW PDR FOR HERBAL MEDICINES

Skin: There are reports of allergic dermatitis on exposure to
the leaves and petals of Feverfew (Schmidt, 1986). Two
elderly individuals suffering from acute recurrent photoder-
matitis were shown to be allergic to Feverfew (Mensing,
1985). Eczema was reported in greenhouse workers exposed
to various members of the Compositae family, including
Feverfew (Paulsen, 1998). A recent investigation does not
support the theory of airborne sesquiterpine lactone-contain-
ing plant parts, or of direct release of sesquiterpene lactones
from living plants as the only explanations for airborne
Compositae dermatitis (Christensen, 1999).

Musculoskeletal: Feverfew contains sesquiterpenes (parthe-
nolide and cynaropicrin), which have been shown to induce
toxic and irreversible inhibition of smooth muscle contractil-
ity when there are high concentrations in the tissue (Hay,
1994).

Drug Interactions: Although reports are sketchy, and most
involve animal subjects and in vitro research, there is a
strong possibility that Feverfew may interact with thrombo-
lytics, anticoagulants and platelet aggregation. The mecha-
nism of action is believed to be inhibition of arachidonic
acid, which is a precursor for prostaglandins that are
involved in the clotting mechanism.

DOSAGE
Mode of Administration: Feverfew preparations are used
both internally and externally.

How Supplied:
Capsules — 80 mg, 380 mg, 384 mg, 400 mg, 500 mg, 1000
mg

Tablets — 12mg (standardized to 600 meg sesuiterpine
lactone content)

Preparation: To make an infusion, use 2 teaspoonfuls of the
drug per cup, allow to draw for 15 minutes. To make a
strong infusion, double the amount and allow to draw for 25
minutes.

Daily Dosage:
Capsules — 200 to 250 mg daily for the treatment of
migraines; the usual standardization level is 0.2% partheno-
lide content (Brown, 1996). Freshly dried powdered Fever-
few of 25 mg is approximately equal to 0.1 mg of
sesquiterpine lactones (SL) (Mervyn,1986).

Fresh leaf — 1 to 3 leaves (25 to 75 mg) once or twice daily
has been recommended (Johnson et al, 1985; O'Hara, 1998).

Unproven uses — 3 cups of the infusion are taken per day.
The stronger infusions are used for washes.


Storage: Store the herb in sealed containers.


LITERATURE
Abad MJ, Berjemo P, Villar A, Phytother Res 9:79-92. 1995.
Anderson D, Jenkinson PC, Dewdney RS, Blower SD, Johnson
ES, Kadam NP, Human Toxicol 7:145-152. 1988.
Anonym, Naturmedizin: Mutterkraut gegen Migrane. In: DAZ
137(28):2424. 1997.
Awang DVC, Dawson BA, Kindack DG, Crompton CW,
Heptinstall S, JNP 54:1516-1521. 1991.
Barsby RW, Knight DW, McFadzean I, A chloroform extract of
the herb Feverfew blocks voltage-dependent potassium currents
recorded from single smooth muscle cells. J Pharm Pharmacol
1993 Jul;45(7):641-5.
Berry MI, (1984) Pharm J 232:611.
Bohlmann F, Arndt C, Bomowski H, Kleine KM, Herbst P,
Chem Ber 97, 1179-1192. 1964.
Bohlmann F, Zdero C, (1982) Phytochemistry 21(10):2543.
Brown AMG et al., Inhibition of human neutrophils by aqueous
and organic extracts of Tanacetum ssp. In: PM 62, Abstracts of
the 44th Ann Congress of GA, 66. 1996.
Brown AM, Edwards CM, Davey MR et al., Pharmacological
activity of Feverfew (Tanacetum parthenium (L.) Schultz-Bip):
assessment by inhibition of human polymorphnuclear leukocyte
chemiluminescence in-vitro. J Pharm Pharmacol 1997
May;49(5):558-61.
Christensen LP; Jakobsen HB; Paulsen E et al. Airborne
Compositae dermatitis: monoterpenes and no parthenolide are
released from flowering Tanacetum parthenium (feverfew)
plants. Arch Dermatol Res 1999 Jul-Aug;291(7-8):425-31.
Collier HOJ et al., (1980) Lancet 11:922.
Deweerdt CJ, Bootsma HPR, Hendricks H, Herbal medicines in
migraine prevention. In: Phytomedicine 3(3):225-230. 1996.
Govindachari TR et al., (1964) Tetrahedron 21(6): 1509.
Groenewegen WA, Heptinstall S, A comparison of the effects
of an extract of Feverfew and parthenolide, a component of
Feverfew, on human platelet activity in-vitro. J Pharm
Pharmacol 1990 Aug;42(8):553-557.
Groenewegen WA, Heptinstall S, Lancet, No 8471, 44-45.
1986.
Groenewegen WA, Knight DW, Heptinstall S. J Pharm
Pharmacol 1986 Sep;38(9):709-712.
Groenewegen WA, Knight DW, Heptinstall S, Progr Med Chem
29:217-238. 1992.
Guin JD, Skidmore G, Arch Derm 123:500-503. 1987.
Hay AJ, Hamburger M, Hostettmann K et al., Toxic inhibition
of smooth muscle contractility by plant-derived sesquiterpenes
caused by their chemically reactive alpha-
methylenebutyrolactone functions. Br J Pharmacol 1994; 112:9-
12.
Hayes NA, Foreman JC, J Pharm Pharmacol 1987
Jun;39(6):466-70.
Heptinstall S et al., (1985) Lancet 1:1071.
Free download pdf