Plant Comparison

Devil's Claw vs Common coltsfoot

A side-by-side comparison of two medicinal plants — every documented constituent, action, use, safety note and cited source, assembled automatically from the Omnia Sana database.

First plant
Second plant
Show:
Plant ADevil's ClawHarpagophytum procumbensPedaliaceaeFull monograph →
Plant BCommon coltsfootTussilago farfaraAsteraceaeFull monograph →

At a glance

Devil's Claw and Common coltsfoot: they share 3 indicated uses (arthritis / joint pain, inflammation (general), skin irritation); 1 pharmacological action in common.

Devil's ClawCommon coltsfoot
Constituents23
Pharmacological actions22
Indicated uses64
Safety notes37
Cited sources1515
Indicated uses
Only Devil's Claw
Back painHeadachePain (general)
Shared (3)
Arthritis / joint painInflammation (general)Skin irritation
Only Common coltsfoot
Insomnia / sleeplessness
Pharmacological actions
Only Devil's Claw
Analgesic (pain relief)
Shared (1)
Anti-inflammatory
Only Common coltsfoot
Sedative / sleep support

Evidence face-off — shared uses

ConditionDevil's ClawCommon coltsfootVerdict
Arthritis / joint pain8/101/10Stronger for Devil's Claw
Inflammation (general)8/102/10Stronger for Devil's Claw
Skin irritation8/101/10Stronger for Devil's Claw

Evidence scores (1–10) are computed from the tier of each cited source. “Comparable” means the two scores are within one point. Follow a score to its detailed sources.

Key Constituents

Iridoid glycosides (harpagoside, harpagide, procumbide)[12, 13, 14]

Harpagoside is the main marker compound and anti-inflammatory principle; effective extracts are standardised to it, with the better-quality clinical evidence using preparations delivering roughly 50-60 mg harpagoside per day.

Iridoid glycosidesHarpagosideGlycosides
Phenylethanoids (acteoside/verbascoside) and flavonoids[13]

Antioxidant supporting constituents.

Verbascoside (acteoside)Flavonoids
Pyrrolizidine alkaloids (senkirkine, senecionine-type)[12]

Hepatotoxic constituents that are the central safety concern for this plant; regulatory limits and PA-controlled/PA-reduced products exist specifically because of these compounds.

Alkaloids
Mucilage[1, 2]

Demulcent polysaccharide contributing to the traditional soothing action on irritated airways.

Mucilage
Flavonoids and tannins[1, 2]

Contribute to anti-inflammatory and astringent activity.

FlavonoidsTannins

Pharmacological Actions

Analgesic (pain relief)[1, 2, 4, 6, 7, 9, 10, 12, 13]

Anti-inflammatory and analgesic for osteoarthritis (hip and knee) pain

Anti-inflammatory[1, 3, 4, 5, 6, 8, 9, 11, 12, 13]

Anti-inflammatory and analgesic for osteoarthritis (hip and knee) pain

Anti-inflammatory[1, 2, 10, 11, 12]
Sedative / sleep support[2, 11, 12]

Traditional & Indicated Uses

Arthritis / joint pain[12, 13]Good · 8/10

Anti-inflammatory and analgesic for osteoarthritis (hip and knee) pain; General joint pain and arthritis support

Evidence: 8
Label: Arthritis / joint pain
Back pain[12, 13, 14, 15]Strong · 9/10

Effective at standardised doses (~50-60 mg harpagoside/day); an aqueous extract was non-inferior to rofecoxib for short-term chronic low back pain; Relief of chronic non-specific low back pain

Evidence: 9
Label: Back pain
Headache[12, 13]Good · 8/10

inferred from analgesic action

Evidence: 8
Label: Headache
Inflammation (general)[12, 13]Good · 8/10

inferred from anti-inflammatory action

Evidence: 8
Label: Inflammation (general)
Pain (general)[12, 13, 14, 15]Strong · 9/10

Anti-inflammatory and analgesic for osteoarthritis (hip and knee) pain; Effective at standardised doses (~50-60 mg harpagoside/day); an aqueous extract was non-inferior to rofecoxib for short-term chronic low back pain; General joint pain and arthritis support; Relief of chronic non-specific low back pain

Evidence: 9
Label: Pain (general)
Skin irritation[12, 13]Good · 8/10

inferred from anti-inflammatory action

Evidence: 8
Label: Skin irritation
Arthritis / joint pain[2, 11, 12]Traditional · 1/10

inferred from anti-inflammatory action

Evidence: 1
Label: Arthritis / joint pain
Inflammation (general)[2, 10, 11, 12]Traditional · 2/10

inferred from anti-inflammatory action

Evidence: 2
Label: Inflammation (general)
Insomnia / sleeplessness[2, 11, 12]Traditional · 1/10

inferred from sedative action

Evidence: 1
Label: Insomnia / sleeplessness
Skin irritation[2, 11, 12]Traditional · 1/10

inferred from anti-inflammatory action

Evidence: 1
Label: Skin irritation

Safety, Cautions & Contraindications

Safety note[13]Caution

Because it is a bitter that increases stomach-acid and bile secretion, it is contraindicated in active peptic ulcer, gastritis and (without medical supervision) gallstones.

Safety note[13]Caution

May add to the effect of anticoagulants (e.g. warfarin) and may influence blood sugar, blood pressure and heart rhythm; use caution with these medicines.

Safety note[13]Caution

Avoid during pregnancy (oxytocic/uterine effect) and while breastfeeding.

Safety note[5, 11, 12, 13]Caution

Safety notes (contraindications, interactions, pregnancy/lactation notes, adverse effects, dose-duration cautions) Important: Coltsfoot naturally contains pyrrolizidine alkaloids (PAs)—plant chemicals that can damage the liver and may increase cancer risk with enough exposure (EMA, 2021; Kopp et al., 2020).

Safety note[5, 11, 12, 13]Info

Because of this, European regulators set very strict limits for PA exposure from herbal products (EMA, 2021).

Safety note[5, 11, 12, 13]Caution

Many safety-focused herbal references recommend avoiding homemade/internal coltsfoot use, unless the product is specifically made to be PA-controlled / PA-reduced (EMA, 2021).

Safety note[5, 11, 12, 13]Caution

Avoid internal use if you are pregnant or breastfeeding, have liver disease, or for children—these groups are treated as “sensitive” in PA risk guidance (EMA, 2021).

Safety note[5, 11, 12, 13]Caution

Medication caution: if you take medicines that stress the liver (some prescription drugs can), it’s extra important to avoid unregulated PA exposure (general PA risk logic; consult a clinician) (EMA, 2021).

Safety note[5, 11, 12, 13]Info

Topical use may still carry PA considerations; EMA discusses limits and recommends use only on intact skin for PA-containing products (EMA, 2021).

Safety note[5, 11, 12, 13, 14]Serious

Duke (2002) provides clinical support (score 2) for coltsfoot's anti-inflammatory and expectorant effects, explaining its traditional use in bronchitis and coughs. However, the plant contains hepatotoxic pyrrolizidine alkaloids (PAs), and Duke notes a carcinogenic score (1) — a critical safety concern. Commission E has placed restrictions on coltsfoot use, recommending maximum internal use of 4–6 weeks per year and avoiding use in pregnancy, lactation, and in children under 12. Duke rates its overall safety as low (+) and emphasizes that preparations free of PAs are preferred (Duke, 2002).

External Ids

Gbif: 3585335
Powo: urn:lsid:ipni.org:names:675824-1
Wikidata: Q386675
Gbif: 3149879
Wikidata: Q26302

Botanical Description

Low-growing, sprawling perennial herb with trailing stems and deeply lobed, greyish-green leaves arising from a large, fleshy primary taproot bearing smaller secondary storage tubers (the part used medicinally). Striking funnel-shaped, purplish-pink to violet flowers give way to a distinctive woody fruit covered in long, hooked spines - the origin of the common name.[13]

Height: Trailing stems to 1.5 m, low-growing
Habit: Low-growing, sprawling perennial herb
Leaves: Deeply lobed, greyish-green
Flowers: Funnel-shaped, purplish-pink to violet
Stem: Trailing, sprawling stems
Root: Large primary taproot with smaller secondary storage tubers (the medicinal part)
Fruit: Woody capsule covered in long, hooked spines ('devil's claw')
Flowering Period: Summer (during the rainy season)

Low perennial herb notable for flowering before its leaves appear: solitary, bright yellow, dandelion-like flower heads emerge on scaly pinkish stalks in very early spring, followed later by large, hoof-shaped (heart-shaped with angular teeth), white-woolly-backed leaves arising directly from the creeping rhizome.[11]

Height: 10-30 cm (flowering stalks); leaves slightly taller once expanded
Habit: Low perennial herb spreading by a creeping rhizome, flowers before leaves appear
Leaves: Hoof-shaped (heart-shaped with angular teeth), white-woolly underneath, appearing after flowering
Flowers: Solitary, bright yellow, dandelion-like heads on scaly pinkish stalks
Stem: Scaly, pinkish flowering stalks appearing before the leaves
Root: Creeping rhizome
Fruit: Small achene with a fluffy white pappus (like a small dandelion clock)
Flowering Period: February-April, before the leaves appear

Habitat

Native to the dry savannas and semi-desert regions of southern Africa, particularly the Kalahari Desert region of Namibia, Botswana and South Africa.[13]

Grows on disturbed, damp or clay-rich waste ground, riverbanks, railway embankments and bare soil; native to Europe, North Africa and temperate Asia and naturalised in North America.[11]

Harvesting

The secondary root tubers are dug by hand, sliced and dried in the sun, traditionally by local harvesters in southern Africa; sustainable wild-harvesting practices are important given the plant's slow growth and habitat sensitivity.

Parts: Secondary root tuber

Flowers are gathered in very early spring before the leaves appear; leaves are gathered later in the season once expanded. Given the plant's pyrrolizidine alkaloid content, harvesting from a positively confirmed patch (not a look-alike) and preferring PA-tested commercial material for internal use is strongly advised.[2]

Parts: Flower, Leaf
Season: Flower in very early spring; leaf later in the growing season

Traditional Uses

Devil's claw has a long southern African traditional-medicine history as a remedy for fever, pain and digestive complaints, and is now one of the most clinically studied herbal analgesics for osteoarthritis and chronic low back pain, with standardised extracts showing efficacy comparable to some conventional analgesics in trials.[13]

Coltsfoot has an ancient European and Chinese tradition, reflected in its Latin name (tussis = cough), as an expectorant and demulcent remedy for coughs, bronchitis and irritated airways; because of its pyrrolizidine alkaloid content, contemporary use is restricted to short courses of PA-controlled preparations under regulatory limits (see contraindications).[1, 2, 12]

Preparations

Standardised extract[13, 14]

Root tuber extract standardised to harpagoside content, taken as capsules or tablets; the best-studied clinical form for osteoarthritis and back pain.

PA-controlled commercial extract[2, 13]

Commercially prepared, pyrrolizidine-alkaloid-tested extract or syrup, the only form recommended for internal use given the plant's natural PA content.

Infusion (short-term, traditional)[2]

Dried flower or leaf infused in hot water; traditional but subject to strict duration/PA-content limits under EU herbal regulation.

Topical preparation[2, 13]

Leaf used topically (e.g. poultice) on intact skin; EMA guidance still notes PA-exposure limits apply to topical products.

Dosage

Standardised extract[14]

Clinical trials for osteoarthritis and back pain commonly use extracts providing around 50-60 mg harpagoside daily. Educational reference only, not a prescription.

PA-controlled internal use[13]

EU regulatory guidance restricts internal use to PA-controlled preparations. The EMA public statement on unsaturated pyrrolizidine alkaloids records a maximum daily intake for internal use of 1 microgram of PAs for at most 6 weeks per year, or 0.1 microgram per day with no duration limit; for cutaneous use the limits are 100 micrograms for at most 6 weeks per year, or 10 micrograms without a duration limit. Not for use in pregnancy, breastfeeding, or children. Note that these are limits on PA intake, not a herb dose — no EMA monograph exists for Tussilago farfara, so there is no official posology for the herb itself. Educational reference only, not a prescription — consult a qualified practitioner and prefer tested commercial products.

References

REF-1829, REF-1830, REF-1831, REF-1832, REF-1833, REF-1834, REF-1835, REF-1836, REF-1837, REF-1838, REF-1839
REF-0910, REF-0911, REF-0912, REF-0913, REF-0914, REF-0915, REF-0916, REF-0917, REF-0918, REF-0919

Lookalikes Review

Outcome: none-known
Reviewed By: Omnia Sana (owner-authorized)
Reviewed Date: 2026-07-07
Outcome: has-lookalikes
Reviewed By: Omnia Sana (owner-authorized)
Reviewed Date: 2026-07-07

Dangerous Lookalikes

Not documented

Safety note[15]Dangerous
Dangerous Plant: adenostyles-alliariae
Confused Part: Broad leaves gathered and brewed as coltsfoot tea; alpendost (and butterbur) have similar rounded leaves and grow in the same damp ground.
Confusion Context: Coltsfoot (Tussilago farfara) leaves are gathered for herbal tea. Alpendost (Adenostyles alliariae) has similar large, rounded leaves and grows in damp woodland and mountain ground; the two are easily confused, especially after the flowering period. Alpendost contains hepatotoxic pyrrolizidine alkaloids: a peer-reviewed case (Sperl et al., 1995) describes an infant who developed liver veno-occlusive disease after long-term 'coltsfoot' tea that was actually alpendost. Butterbur (Petasites) is a similar large-leaved confusion with the same kind of toxicity. Because dried leaf material is especially hard to tell apart, unverified coltsfoot is a real hazard.
Distinguishing Features: Leaf shape: coltsfoot leaves are hoof-shaped (heart-shaped with angular teeth) and white-woolly underneath, usually no more than about 20 cm across. Alpendost leaves are larger, more rounded/kidney-shaped and coarsely toothed., Timing: coltsfoot flowers (yellow dandelion-like heads on scaly stalks) appear BEFORE the leaves, in very early spring; by summer only leaves remain, which is when confusion is greatest., Best practice: because leaves (and dried material) are hard to separate, use coltsfoot only if an expert has confirmed the plant, or buy authenticated, pyrrolizidine-tested material.
Key Test: Do not gather broad heart- or kidney-shaped leaves for 'coltsfoot' tea unless an expert has confirmed the species - alpendost and butterbur leaves look very similar and contain liver-damaging pyrrolizidine alkaloids. Confirm coltsfoot by its early-spring yellow flowers and hoof-shaped white-woolly-backed leaves, or use authenticated material.
Reviewed By: Omnia Sana (owner-authorized)
Reviewed Date: 2026-07-07

References & Sources

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  4. Gxaba, N. and Manganyi, M.C (2022) 'The Fight against Infection and Pain: Devil's Claw (Harpagophytum procumbens) a Rich Source of Anti-Inflammatory Activity: 2011-2022', Molecules, 27(11), pp. 3637. doi:10.3390/molecules27113637 Meta-analysis / review
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  5. Menghini, L., Recinella, L., Leone, S., Chiavaroli, A., Cicala, C., Brunetti, L., Vladimir-Knezevic, S., Orlando, G. and Ferrante, C (2019) 'Devil's claw (Harpagophytum procumbens) and chronic inflammatory diseases: A concise overview on preclinical and clinical data', Phytotherapy Research, 33(9), pp. 2152-2162. doi:10.1002/ptr.6395 Meta-analysis / review
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  6. Brien, S., Lewith, G.T. and McGregor, G (2006) 'Devil's Claw (Harpagophytum procumbens) as a treatment for osteoarthritis: a review of efficacy and safety', Journal of Alternative and Complementary Medicine, 12(10), pp. 981-993. doi:10.1089/acm.2006.12.981 Meta-analysis / review
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  8. Recinella, L., Chiavaroli, A., Ronci, M., Menghini, L., Brunetti, L., Leone, S., Tirillini, B., Angelini, P., Covino, S., Venanzoni, R., Zengin, G., Di Simone, S., Ciferri, M.C., di Giacomo, V., Cataldi, A., Rapino, M., Valerio, V.D., Orlando, G. and Ferrante, C (2020) 'Multidirectional Pharma-Toxicological Study on Harpagophytum procumbens DC. ex Meisn.: An IBD-Focused Investigation', Antioxidants, 9(2), pp. 168. doi:10.3390/antiox9020168 Preclinical
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  9. Baghdikian, B., Lanhers, M.C., Fleurentin, J., Ollivier, E., Maillard, C., Balansard, G. and Mortier, F (1997) 'An analytical study, anti-inflammatory and analgesic effects of Harpagophytum procumbens and Harpagophytum zeyheri', Planta Medica, 63(2), pp. 171-176. doi:10.1055/s-2006-957638 Preclinical
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  11. Jang, M., Lim, S., Han, S., Park, H., Shin, I., Kim, J., Kim, N., Lee, J., Kim, K. and Kim, C (2003) 'Harpagophytum procumbens suppresses lipopolysaccharide-stimulated expressions of cyclooxygenase-2 and inducible nitric oxide synthase in fibroblast cell line L929', Journal of Pharmacological Sciences, 93(3), pp. 367-371. doi:10.1254/jphs.93.367 Preclinical
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  12. Chrubasik, S (2004) 'Devil's claw extract as an example of the effectiveness of herbal analgesics', Der Orthopade. doi:10.1007/s00132-004-0675-7 Clinical study
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  13. Brendler, T., Gruenwald, J., Ulbricht, C. and Basch, E (2006) 'Devil's Claw (Harpagophytum procumbens DC): an evidence-based systematic review by the Natural Standard Research Collaboration', Journal of Herbal Pharmacotherapy. doi:10.1080/j157v06n01_09 Meta-analysis / review
    https://doi.org/10.1080/j157v06n01_09
  14. Chrubasik, S., Conradt, C. and Roufogalis, B.D (2004) 'Effectiveness of Harpagophytum extracts and clinical efficacy', Phytotherapy Research, 18(2), pp. 187--189. doi:10.1002/ptr.1416 Preclinical
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    https://doi.org/10.1186/1472-6882-4-13
  1. Ahmad, I., Kudaibergenova, B., Ahmad, M. and others (2025) 'Coltsfoot (Tussilago farfara L.; Asteraceae): modern methods of extraction, phytochemistry, nanoparticles synthesis, ethnopharmacology, and biological activities', Natural Product Research, pp. 1-20. doi:10.1080/14786419.2025.2548616 Traditional / reference
    https://doi.org/10.1080/14786419.2025.2548616
  2. Chen, S., Dong, L., Quan, H., Zhou, X. and others (2020) 'A review of the ethnobotanical value, phytochemistry, pharmacology, toxicity and quality control of Tussilago farfara L. (coltsfoot)', Journal of Ethnopharmacology, 267, pp. 113478. doi:10.1016/j.jep.2020.113478 Traditional / reference
    https://doi.org/10.1016/j.jep.2020.113478
  3. Feng, J., Zhang, Y., Qin, X., Gao, T. and others (2022) 'Novel Quinic Acid Glycerates from Tussilago farfara Inhibit Polypeptide GalNAc-Transferase', ChemBioChem, 23(3), pp. e202100539. doi:10.1002/cbic.202100539 Preclinical
    https://doi.org/10.1002/cbic.202100539
  4. Zhao, J., Evangelopoulos, D., Bhakta, S., Gray, A.I. and Seidel, V (2014) 'Antitubercular activity of Arctium lappa and Tussilago farfara extracts and constituents', Journal of Ethnopharmacology, 155(1), pp. 796-800. doi:10.1016/j.jep.2014.06.034 Preclinical
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  5. Avila, C., Breakspear, I., Hawrelak, J., Salmond, S. and Evans, S (2020) 'A systematic review and quality assessment of case reports of adverse events for borage (Borago officinalis), coltsfoot (Tussilago farfara) and comfrey (Symphytum officinale)', Fitoterapia, 142, pp. 104519. doi:10.1016/j.fitote.2020.104519 Meta-analysis / review
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  6. Lee, J., Park, S., Kim, M.J., Kwon, S.J. and others (2019) 'Sesquiterpenoids from Tussilago farfara Flower Bud Extract for the Eco-Friendly Synthesis of Silver and Gold Nanoparticles Possessing Antibacterial and Anticancer Activities', Nanomaterials (Basel), 9(6), pp. 819. doi:10.3390/nano9060819 Preclinical
    https://doi.org/10.3390/nano9060819
  7. Bota, V.B., Neamtu, A.A., Olah, N.K., Chiselita, O. and others (2022) 'A Comparative Analysis of the Anatomy, Phenolic Profile, and Antioxidant Capacity of Tussilago farfara L. Vegetative Organs', Plants (Basel), 11(13), pp. 1663. doi:10.3390/plants11131663 Preclinical
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  8. Boucher, M.A., Cote, H., Pichette, A., Ripoll, L. and Legault, J (2020) 'Chemical composition and antibacterial activity of Tussilago farfara (L.) essential oil from Quebec, Canada', Natural Product Research, 34(4), pp. 545-548. doi:10.1080/14786419.2018.1489384 Preclinical
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  9. Li, Z.Y., Zhang, J., Zhang, Y.B., Yang, X.W. and others (2022) 'Polyhydroxylated eudesmane sesquiterpenoids and sesquiterpenoid glucoside from the flower buds of Tussilago farfara', Chinese Journal of Natural Medicines, 20(4), pp. 301-308. doi:10.1016/S1875-5364(21)60120-6 Preclinical
    https://doi.org/10.1016/S1875-5364(21)60120-6
  10. Jang, H., Lee, J.W., Lee, C., Jin, Q. and others (2016) 'Sesquiterpenoids from Tussilago farfara inhibit LPS-induced nitric oxide production in macrophage RAW 264.7 cells', Archives of Pharmacal Research, 39(1), pp. 127-132. doi:10.1007/s12272-015-0667-7 Preclinical
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  11. Royal Botanic Gardens, Kew (n.d.). Available at: https://powo.science.kew.org Traditional / reference
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  12. Westendorf, J., Czok, G., Marquardt, R., Nausner, M., Krauer, B. and Paul, H.L (1988) 'Pyrrolizidine alkaloid content of Tussilago farfara plants from different regions and preparations', pp. 903--909. Traditional / reference
    https://scholar.google.com/scholar?q=Pyrrolizidine%20alkaloid%20content%20of%20Tussilago%20farfara%20plants%20from%20different%20regions%20and%20preparations
  13. European Medicines Agency (HMPC) (2021) 'Public statement on the use of herbal medicinal products containing toxic, unsaturated pyrrolizidine alkaloids (PAs), including recommendations regarding contamination of herbal medicinal products with PAs, Revision 1'. Available at: https://www.ema.europa.eu/en/documents/public-statement/public-statement-use-herbal-medicinal-products-containing-toxic-unsaturated-pyrrolizidine-alkaloids-pas-including-recommendations-regarding-contamination-herbal-medicinal-products-pyrrolizidine_en.pdf Traditional / reference
    https://www.ema.europa.eu/en/documents/public-statement/public-statement-use-herbal-medicinal-products-containing-toxic-unsaturated-pyrrolizidine-alkaloids-pas-including-recommendations-regarding-contamination-herbal-medicinal-products-pyrrolizidine_en.pdf
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  15. Sperl, W. and Stuppner, H. and Gassner, I. and Judmaier, W. and Dietze, O. and Vogel, W (1995) 'Reversible hepatic veno-occlusive disease in an infant after consumption of pyrrolizidine-containing herbal tea', European Journal of Pediatrics, 154(2), pp. 112-6. doi:10.1007/BF01991912 Clinical study
    https://doi.org/10.1007/BF01991912

Generated automatically from the Omnia Sana plant database and its cited sources. For educational purposes only — not medical advice. Always consult a qualified practitioner before using medicinal plants.