01 Identity and provenance
- Accepted binomial
- Harpagophytum procumbens
- Common names
- Devil's Claw
- Family (APG IV)
- Pedaliaceae
- Part used
- Tuber
- Verification tier
- Tier 2 · Verified Clinical columns reviewed and a source is on record.
- Reviewer note (2026 audit)
- Drugs.com NPP Devil’s Claw monograph | VERIFIED 2026 - synthetic analogue, application, interactions, side effects and references populated from retrieved primary/regulatory sources (see References). Interaction entries are labelled CLINICAL (case reports or trials in humans) vs THEORETICAL (in-vitro or animal only). Marketed-formulation column intentionally left blank. | HOST FACTOR
02 Constituent chemistry
| Chemical class | Marker compound | Synthetic analogue in use |
|---|---|---|
| Iridoid glycosides | Harpagoside
Tuber
|
NSAIDs - diclofenac, ibuprofen (FUNCTIONAL anti-inflammatory). No structural analogue. |
The analogue column is what makes the interaction reasoning tractable: where a constituent has a marketed structural counterpart, the counterpart's interaction profile is the starting hypothesis for the plant.
03 Stated application
- Reported activity
- Osteoarthritis (knee and hip) and low back pain; adjuvant in degenerative rheumatism and tendinitis per Commission E and ESCOP. Dose matters: little evidence below 30 mg/day harpagoside; >50 mg/day used in knee/hip OA.
- Reported adverse effects
- Gastrointestinal upset. CONTRAINDICATED in gastric or duodenal ulcer - the bitter principle increases gastric acid secretion. Caution in gallstones or bile-duct obstruction. Avoid in pregnancy (possible oxytocic effect).
04 Interaction matrix
Source column, verbatim: CLINICAL: purpura reported in a patient taking warfarin - caution with anticoagulants and antiplatelets. Drugs.com NPP advises against use with antiarrhythmic, chronotropic or inotropic medicines (negative chronotropic and inotropic properties reported). May reduce required NSAID dose.
Normalised onto 4 canonical drug classes below.
Curated from the reviewed source
| Drug class | Severity | Mechanism type | Provenance | Expected effect | |
|---|---|---|---|---|---|
|
Antiarrhythmics
Cardiovascular
|
4Contraindicated | PD-additive + electrolyte-mediated | curated A | Proarrhythmia, QT prolongation, torsade de pointes, ventricular arrhythmi… | why ▾ |
Class mechanism. Botanicals that shift potassium or magnesium, block sodium or potassium channels, or prolong repolarisation add to class I and class III antiarrhythmic effects on an already unstable myocardium.
| |||||
|
Anticoagulants (vitamin-K antagonists, DOACs)
Haemostasis
|
3Major | PD-additive + PK-CYP2C9 | curated A | INR destabilisation in either direction; ecchymosis, epistaxis, gum bleed… | why ▾ |
Class mechanism. Coumarin-, salicylate- and coumestan-bearing botanicals add to vitamin-K-antagonist effect; several also compete for CYP2C9 and CYP3A4, raising S-warfarin exposure. Botanicals rich in vitamin K1 act in the opposite direction and blunt anticoagulation.
| |||||
|
Antiplatelet agents
Haemostasis
|
3Major | PD-additive | curated A | Prolonged bleeding time, surgical and post-procedural bleeding, bruising,… | why ▾ |
Class mechanism. Organosulfur compounds, gingerols, salicylates, ginkgolides and eugenol inhibit thromboxane A2 synthesis, platelet aggregation and PAF-mediated activation, duplicating the pharmacology of aspirin and P2Y12 blockers.
| |||||
|
NSAIDs
Analgesia
|
3Major | PD-additive | curated A | Peptic ulceration, upper GI bleeding, acute kidney injury in volume-deple… | why ▾ |
Class mechanism. Salicylate-, coumarin- and eugenol-bearing botanicals add both antiplatelet activity and direct gastric mucosal irritation to cyclo-oxygenase inhibition; several also reduce renal prostaglandin-dependent perfusion.
| |||||
05 Hazard register
06 Confusable material
No same-genus or shared-common-name entry in the corpus.
07 Mechanism map
Chemistry sorts to the left, pharmacology to the right. Dashed edges are predicted. Drag nodes, scroll to zoom, export at 3× for a figure.
08 Open literature
Abstract-scoped query built from this binomial, its common names and its marker compounds, run live against Europe PMC, PubMed and OpenAlex, then ranked locally against an evidence hierarchy.
09 Isomechanistic neighbours
Species whose interaction profile overlaps this one, ranked by shared severity weight rather than by count — a shared contraindication counts for more than a shared minor signal. Practical use: these are the plants you should not stack with this one, because the mechanisms summate.
| Species | Family | Shared classes | Weight | Jaccard |
|---|---|---|---|---|
| Camellia sinensis
Green Tea |
Theaceae | 3 | 0.25 | |
| Trachyspermum ammi
Ajwain |
Apiaceae | 3 | 0.60 | |
| Kaempferia galanga
Chandramula |
Zingiberaceae | 3 | 0.60 | |
| Gaultheria fragrantissima
Wintergreen |
Ericaceae | 3 | 0.75 | |
| Salix alba
White Willow |
Salicaceae | 3 | 0.75 | |
| Filipendula ulmaria
Meadowsweet |
Rosaceae | 3 | 0.75 |
10 References and notes
Source column: Brien S et al. J Altern Complement Med 2006;12:981-93. PubMed 17212570
Brien S et al. J Altern Complement Med 2006
12:981-93. PubMed 17212570
BibTeX for all 2 records
@article{BrienSeta2006,
title = {Brien S et al. J Altern Complement Med 2006},
author = {Brien S et al.},
journal = {J Altern Complement Med},
year = {2006},
}
@article{anon,
title = {12:981-93. PubMed 17212570},
}
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