What is it?
Devil’s claw is native to south Africa, including the Kalahari Desert, where it’s been used traditionally for many conditions. Devil’s claw contains chemicals that might decrease swelling. Because of this, it is often used to treat conditions that involve both pain and inflammation.
Devil’s claw is most commonly used for back pain and osteoarthritis. It is also used for rheumatoid arthritis (RA) and other conditions, but there is no good scientific evidence to support these uses. There is also no good evidence to support using devil’s claw for COVID-19.
How effective is it?
Natural Medicines Comprehensive Database rates effectiveness based on scientific evidence according to the following scale: Effective, Likely Effective, Possibly Effective, Possibly Ineffective, Likely Ineffective, Ineffective, and Insufficient Evidence to Rate.
The effectiveness ratings for DEVIL’S CLAW are as follows:
Possibly effective for…
- Back pain. Taking devil’s claw by mouth seems to reduce lower back pain. Devil’s claw seems to work about as well as some non-steroidal anti-inflammatory drugs (NSAIDs).
- Osteoarthritis. Taking devil’s claw by mouth alone, with other ingredients, or along with nonsteroidal anti-inflammatory drugs (NSAIDs) seems to help reduce osteoarthritis pain. Some people taking devil’s claw seem to be able to lower the dose of NSAIDs taken for pain relief.
There is interest in using devil’s claw for a number of other purposes, but there isn’t enough reliable information to say whether it might be helpful.
Is it safe?
When applied to the skin: There isn’t enough reliable information to know if devil’s claw is safe or what the side effects might be.
Special precautions & warnings:
Pregnancy: Devil’s claw is possibly unsafe when used during pregnancy. It might harm the developing fetus. Avoid use.
Breast-feeding: There isn’t enough reliable information to know if devil’s claw is safe to use when breast-feeding. Stay on the safe side and avoid use.
Heart and circulation problems: Devil’s claw may affect heart rate, heartbeat, and blood pressure. It might harm people with disorders of the heart and circulation. If you have one of these conditions, talk with your healthcare provider before starting devil’s claw.
Gallstones: Devil’s claw might increase bile production. This could be a problem for people with gallstones. Avoid using devil’s claw.
Low levels of sodium in the body: Devil’s claw might decrease levels of sodium in the body. This might worsen symptoms in people who already have low levels of sodium.
Peptic ulcer disease: Devil’s claw might increase the production of stomach acids, which might harm people with stomach ulcers. Avoid using devil’s claw.
Are there interactions with medications?
- Medications changed by the liver (Cytochrome P450 2C19 (CYP2C19) substrates)
- Some medications are changed and broken down by the liver. Devil’s claw might change how quickly the liver breaks down these medications. This could change the effects and side effects of these medications.
- Medications changed by the liver (Cytochrome P450 2C9 (CYP2C9) substrates)
- Some medications are changed and broken down by the liver. Devil’s claw might change how quickly the liver breaks down these medications. This could change the effects and side effects of these medications.
- Medications changed by the liver (Cytochrome P450 3A4 (CYP3A4) substrates)
- Some medications are changed and broken down by the liver. Devil’s claw might change how quickly the liver breaks down these medications. This could change the effects and side effects of these medications.
- Warfarin (Coumadin)
- Warfarin is used to slow blood clotting. Devil’s claw might increase its effects and the chances of bruising and bleeding. Be sure to have your blood checked regularly. The dose of your warfarin might need to be changed.
- Medications moved by pumps in cells (P-glycoprotein Substrates)
- Some medications are moved in and out of cells by pumps. Devil’s claw might change how these pumps work and change how much medication stays in the body. In some cases, this might change the effects and side effects of a medication.
- Medications that decrease stomach acid (H2-blockers)
- H2-blockers are used to decrease stomach acid. Devil’s claw can increase stomach acid. Taking Devil’s claw might decrease the effects of H2-blockers.
Some common H2-blockers include cimetidine (Tagamet), ranitidine (Zantac), and famotidine (Pepcid).
- Medications that decrease stomach acid (Proton pump inhibitors)
- Proton pump inhibitors are used to decrease stomach acid. Devil’s claw can increase stomach acid. Taking devil’s claw might decrease the effects of proton pump inhibitors.
Some common proton pump inhibitors include omeprazole (Prilosec), lansoprazole (Prevacid), rabeprazole (Aciphex), pantoprazole (Protonix), and esomeprazole (Nexium).
Are there interactions with herbs and supplements?
- There are no known interactions with herbs and supplements.
Are there interactions with foods?
- There are no known interactions with foods.
How is it typically used?
Other names
Methodology
To learn more about how this article was written, please see the Natural Medicines Comprehensive Database methodology.
References
- Diaz-Silveira GL, Deutsch J, Little DP. DNA Barcode Authentication of Devil’s Claw Herbal Dietary Supplements. Plants (Basel) 2021;10:2005. View abstract.
- Vu N, Nguyen TTT, Parmenter BH, Thouas GA. Safety, efficacy and tolerability of a combination micronutrient and polyherbal preparation (GoutFighter TM) for gout: a single-arm open-label pilot study. J Complement Integr Med 2020;18:113-21. View abstract.
- Zegota Z, Gozdzik J, Glogowska-Szelag J. Prospective, multicenter evaluation of a polyherbal supplement alongside standard-of-care treatment for mild knee osteoarthritis. Adv Orthop. 2021;2021:5589597. View abstract.
- Anon. Devil’s claw root: ulcers and gastrointestinal bleeding. Prescrire Int 2013;22:296. View abstract.
- Carvalho RR, Donadel CD, Cortez AF, Valviesse VR, Vianna PF, Correa BB. J Bras Nefrol. 2017 Mar;39:79-81. View abstract.
- More M, Gruenwald J, Pohl U, Uebelhack R. A Rosa canina – Urtica dioica – Harpagophytum procumbens/zeyheri combination significantly reduces gonarthritis symptoms in a randomized, placebo-controlled double-blind study. Planta Med. 2017 Dec;83:1384-91. View abstract.
- Mahomed IM, Ojewole JAO. Oxytocin-like effect of Harpagophytum procumbens [Pedaliacae] secondary root aqueous extract on rat isolated uterus. Afr J Trad CAM 2006;3:82-89.
- Cuspidi C, Sala C, Tadic M, et al. Systemic hypertension induced by Harpagophytum procumbens (devil’s claw): a case report. J Clin Hypertens (Greenwich) 2015;17:908-10. View abstract.
- Conrozier T, Mathieu P, Bonjean M, et al. A complex of three natural anti-inflammatory agents provides relief of osteoarthritis pain. Altern Ther Health Med. 2014;20 Suppl 1:32-7.View abstract.
- Chrubasik S, Sporer F, and Wink M. [Harpagoside content of different powdered dry extracts from Harpagophytum procumbens]. Forsch Komplmentarmed 1996;3:6-11.
- Chrubasik S, Schmidt A, Junck H, and et al. [Effectiveness and economy of Harpagophytum extract in the treatment of acute low back pain – first results of a therapeutic cohort study]. Forsch Komplementarmed 1997;4:332-336.
- Chrubasik S, Model A, Black A, and et al. A randomized double-blind pilot study comparing Doloteffin® and Vioxx® in the treatment of low back pain. Rheumatology 2003;42:141-148.
- Biller, A. Ergebnisse sweier randomisieter kontrollierter. Phyto-pharmaka 2002;7:86-88.
- Schendel, U. Arthritis treatment: Study with Devil Claw extract [in German]. Der Kassenarzt 2001;29/30:2-5.
- Usbeck, C. Teufelskralle: Devil claw: Treatment for chronic pain [in German]. Arzneimittel-Forum 2000;3:23-25.
- Rutten, S. and Schafer, I. Einsatz der afrikanischen Teufelskralle [Allya] bei Erkrankungen des Stutz unde Bewegungsapparates. Ergebnisse einer Anwendungscbeobachtung Acta Biol 2000;2:5-20.
- Pinget, M. and Lecomte, A. The effect of Harpagophytum Arkocaps in degenerative rheumatism [in German]. Naturheilpraxis 1997;50:267-269.
- Ribbat JM and Schakau D. Behandluing chronisch aktivierter Schmerzen am Bewegungsapparat. NaturaMed 2001;16:23-30.
- Loew D, Schuster O, and Möllerfeld J. Stabilität und biopharmazeutische Qualität. Voraussetzung für Bioverfügbarkeit von Harpagophytum procumbens. In: Loew D and Rietbrock N. Phytopharmaka II. Forschung und klinische Anwendung. Darmstadt: Forschung und klinische Anwendung;1996.
- Tunmann P and Bauersfeld HJ. Über weitere Inhaltsstoffe der Wurzel von Harpagophytum procumbens DC. Arch Pharm (Weinheim) 1975;308:655-657.
- Ficarra P, Ficarra R, Tommasini A, and et al. [HPLC analysis of a drug in traditional medicine: Harpagophytum procumbens DC. I]. Boll Chim Farm 1986;125:250-253.
- Tunmann P and Lux R. Zur Kenntnis der Inhaltsstoffe aus der Wurzel von Harpagophytum procumbens DC. DAZ 1962;102:1274-1275.
- Kikuchi T. New iridoid glucosides from Harpagophytum procumbens. Chem Pharm Bull 1983;31:2296-2301.
- Chrubasik S, Zimpfer C, Schutt U, and et al. Effectiveness of Harpagophytum procumbens in treatment of acute low back pain. Phytomedicine 1996;3:1-10.
- Chrubasik S, Sporer F, Wink M, and et al. Zum wirkstoffgehalt in arzneimitteln aus harpagophytum procumbens. Forsch Komplementärmed 1996;3:57-63.
- Chrubasik S, Sporer F, and Wink M. [Content of active substance in tea preparations from Harpagophytum procumbens]. Forsch Komplementarmed 1996;3:116-119.
- Langmead L, Dawson C, Hawkins C, and et al. Antioxidant effects of herbal therapies used by patients with inflammatory bowel disease: an in vitro study. Aliment Pharmacol Ther 2002;16:197-205.
- Bhattacharya A and Bhattacharya SK. Anti-oxidative activity of Harpagophytum procumbens. Br J Phytother 1998;72:68-71.
- Schmelz H, Haemmerle HD, and Springorum HW. Analgetische Wirksamkeit eines Teufels-krallenwurzel-Extraktes bei verschiedenen chronisch-degenerativen Gelenkerkrankungen. In: Chrubasik S and Wink M. Rheumatherapie mit Phytopharmaka. Stuttgart: Hippokrates;1997.
- Frerick H, Biller A, and Schmidt U. Stufenschema bei Coxarthrose. Der Kassenarzt 2001;5:41.
- Schrüffer H. Salus Teufelskralle-Tabletten. Ein Fortschritt in der nichtsteroidalen antirheumatischen Therapie. Die Medizinische Publikation 1980;1:1-8.
- Pinget M and Lecompte A. Etude des effets de I’harpagophytum en rhumatologie dégénérative. 37 Le magazine 1990;:1-10.
- Lecomte A and Costa JP. Harpagophytum dans l’arthrose: Etude en double insu contre placebo. Le Magazine 1992;15:27-30.
- Guyader M. Les plantes antirhumatismales. Etude historique et pharmacologique, et etude clinique du nebulisat d’Harpagohytum procumbens DC chez 50 patients arthrosiques suivis en service hospitalier [Dissertation]. Universite Pierre et Marie Curie, 1984.
- Belaiche P. Etude clinique de 630 cas d’artrose traites par le nebulisat aqueux d’Harpagophytum procumbens (Radix). Phytotherapy 1982;1:22-28.
- Chrubasik S, Fiebich B, Black A, and et al. Treating low back pain with an extract of Harpagophytum procumbens that inhibits cytokine release. Eur J Anaesthesiol 2002;19:209.
- Chrubasik S and Eisenberg E. Treatment of rheumatic pain with Kampo medicine in Europe. The Pain Clinic 1999;11:171.
- Jadot G and Lecomte A. Activite anti-inflammatoire d’Harpagophytum procumbens DC. Lyon Mediteranee Med Sud-Est 1992;28:833-835.
- Fontaine, J., Elchami, A. A., Vanhaelen, M., and Vanhaelen-Fastre, R. [Biological analysis of Harpagophytum procumbens D.C. II. Pharmacological analysis of the effects of harpagoside, harpagide and harpagogenine on the isolated guinea-pig ileum (author’s transl)]. J Pharm Belg. 1981;36:321-324. View abstract.
- Eichler, O. and Koch, C. [Antiphlogistic, analgesic and spasmolytic effect of harpagoside, a glycoside from the root of Harpagophytum procumbens DC]. Arzneimittelforschung. 1970;20:107-109. View abstract.
- Occhiuto, F., Circosta, C., Ragusa, S., Ficarra, P., and Costa, De Pasquale. A drug used in traditional medicine: Harpagophytum procumbens DC. IV. Effects on some isolated muscle preparations. J Ethnopharmacol. 1985;13:201-208. View abstract.
- Erdos, A., Fontaine, R., Friehe, H., Durand, R., and Poppinghaus, T. [Contribution to the pharmacology and toxicology of different extracts as well as the harpagosid from Harpagophytum procumbens DC]. Planta Med 1978;34:97-108. View abstract.
- Brien, S., Lewith, G. T., and McGregor, G. Devil’s Claw (Harpagophytum procumbens) as a treatment for osteoarthritis: a review of efficacy and safety. J Altern Complement Med 2006;12:981-993. View abstract.
- Grant, L., McBean, D. E., Fyfe, L., and Warnock, A. M. A review of the biological and potential therapeutic actions of Harpagophytum procumbens. Phytother Res 2007;21:199-209. View abstract.
- Ameye, L. G. and Chee, W. S. Osteoarthritis and nutrition. From nutraceuticals to functional foods: a systematic review of the scientific evidence. Arthritis Res Ther 2006;8:R127. View abstract.
- Teut, M. and Warning, A. [Bone metastases in breast carcinoma]. Forsch Komplement.Med 2006;13:46-48. View abstract.
- Kundu, J. K., Mossanda, K. S., Na, H. K., and Surh, Y. J. Inhibitory effects of the extracts of Sutherlandia frutescens (L.) R. Br. and Harpagophytum procumbens DC. on phorbol ester-induced COX-2 expression in mouse skin: AP-1 and CREB as potential upstream targets. Cancer Lett. 1-31-2005;218:21-31. View abstract.
- Chrubasik, S. Addendum to the ESCOP monograph on Harpagophytum procumbens. Phytomedicine. 2004;11(7-8):691-695. View abstract.
- Kaszkin, M., Beck, K. F., Koch, E., Erdelmeier, C., Kusch, S., Pfeilschifter, J., and Loew, D. Downregulation of iNOS expression in rat mesangial cells by special extracts of Harpagophytum procumbens derives from harpagoside-dependent and independent effects. Phytomedicine. 2004;11(7-8):585-595. View abstract.
- Na, H. K., Mossanda, K. S., Lee, J. Y., and Surh, Y. J. Inhibition of phorbol ester-induced COX-2 expression by some edible African plants. Biofactors 2004;21(1-4):149-153. View abstract.
- Chrubasik, S. [Devil’s claw extract as an example of the effectiveness of herbal analgesics]. Orthopade 2004;33:804-808. View abstract.
- Schulze-Tanzil, G., Hansen, C., and Shakibaei, M. [Effect of a Harpagophytum procumbens DC extract on matrix metalloproteinases in human chondrocytes in vitro]. Arzneimittelforschung. 2004;54:213-220.