Plant Comparison

Greater Celandine vs Wild Yam

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 AGreater CelandineChelidonium majusPapaveraceaeFull monograph →
Plant BWild YamDioscorea villosaDioscoreaceaeFull monograph →

At a glance

Greater Celandine and Wild Yam: they share 9 indicated uses (arthritis / joint pain, back pain, cancer (anticancer research), …); 4 pharmacological actions in common.

Greater CelandineWild Yam
Constituents32
Pharmacological actions64
Indicated uses1510
Safety notes22
Cited sources1415
Indicated uses
Only Greater Celandine
BloatingIndigestionInfection (general)Liver supportWartsWounds
Shared (9)
Arthritis / joint painBack painCancer (anticancer research)HeadacheInflammation (general)Menstrual crampsMuscle spasmPain (general)Skin irritation
Only Wild Yam
Menopause
Pharmacological actions
Only Greater Celandine
AntimicrobialCholeretic / cholagogue (bile flow)
Shared (4)
Analgesic (pain relief)Anti-inflammatoryAnticancer (preclinical)Antispasmodic
Only Wild Yam
none

Evidence face-off — shared uses

ConditionGreater CelandineWild YamVerdict
Arthritis / joint pain1/102/10Comparable evidence
Back pain1/102/10Comparable evidence
Cancer (anticancer research)2/102/10Comparable evidence
Headache1/102/10Comparable evidence
Inflammation (general)1/102/10Comparable evidence
Menstrual cramps1/102/10Comparable evidence
Muscle spasm1/102/10Comparable evidence
Pain (general)1/102/10Comparable evidence
Skin irritation1/102/10Comparable evidence

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

Isoquinoline alkaloids (chelidonine, coptisine, berberine, sanguinarine, chelerythrine)[4]

The biologically active and toxicologically important constituents.

AlkaloidsBerberine
Flavonoids and phenolic acids[4]

Antioxidant constituents.

Phenolic acidsFlavonoids
Orange latex (alkaloid-rich sap)[4]

The caustic sap used traditionally on warts.

Alkaloids
Steroidal saponins yielding diosgenin[5, 8, 9, 10, 11, 13, 14]

Diosgenin is an industrial precursor for making steroid hormones in the laboratory, but it is NOT converted into hormones in the human body. Oral bioavailability of diosgenin is low; in animal studies orally administered diosgenin restored skin thickness in ovariectomised mice and lowered blood lipids.

Saponins
Phytosterols and alkaloids[4, 10]

Supporting constituents of the root.

PhytosterolsAlkaloids

Pharmacological Actions

Analgesic (pain relief)[4]

Anti-inflammatory, antimicrobial and analgesic (preclinical)

Anti-inflammatory[1, 4, 8]

Anti-inflammatory, antimicrobial and analgesic (preclinical)

Anticancer (preclinical)[6, 7, 12]
Antimicrobial[1, 3, 4, 10]

Anti-inflammatory, antimicrobial and analgesic (preclinical)

Antispasmodic[4]

Antispasmodic / choleretic bitter for upper-abdominal and biliary dyspepsia (indigestion, bloating, cramping) - oral use now restricted for safety

Choleretic / cholagogue (bile flow)[4]

Antispasmodic / choleretic bitter for upper-abdominal and biliary dyspepsia (indigestion, bloating, cramping) - oral use now restricted for safety

Analgesic (pain relief)[10]

Antispasmodic / analgesic for menstrual cramps and muscle spasm (antinociceptive in animal models)

Anti-inflammatory[10]

Anti-inflammatory for joint and inflammatory pain

Anticancer (preclinical)[7]
Antispasmodic[10]

Antispasmodic / analgesic for menstrual cramps and muscle spasm (antinociceptive in animal models)

Traditional & Indicated Uses

Arthritis / joint pain[4]Traditional · 1/10

inferred from anti-inflammatory action

Evidence: 1
Label: Arthritis / joint pain
Back pain[4]Traditional · 1/10

inferred from analgesic action

Evidence: 1
Label: Back pain
Bloating[4]Traditional · 1/10

Antispasmodic / choleretic bitter for upper-abdominal and biliary dyspepsia (indigestion, bloating, cramping) - oral use now restricted for safety

Evidence: 1
Label: Bloating
Cancer (anticancer research)[6, 7, 12]Traditional · 2/10

inferred from anticancer action

Evidence: 2
Label: Cancer (anticancer research)
Headache[4]Traditional · 1/10

inferred from analgesic action

Evidence: 1
Label: Headache
Indigestion[4]Traditional · 1/10

Antispasmodic / choleretic bitter for upper-abdominal and biliary dyspepsia (indigestion, bloating, cramping) - oral use now restricted for safety

Evidence: 1
Label: Indigestion
Infection (general)[4]Traditional · 1/10

inferred from antimicrobial action

Evidence: 1
Label: Infection (general)
Inflammation (general)[4]Traditional · 1/10

inferred from anti-inflammatory action

Evidence: 1
Label: Inflammation (general)
Liver support[4]Traditional · 1/10

inferred from choleretic action

Evidence: 1
Label: Liver support
Menstrual cramps[4]Traditional · 1/10

inferred from antispasmodic action

Evidence: 1
Label: Menstrual cramps
Muscle spasm[4]Traditional · 1/10

inferred from antispasmodic action

Evidence: 1
Label: Muscle spasm
Pain (general)[4]Traditional · 1/10

inferred from analgesic action

Evidence: 1
Label: Pain (general)
Skin irritation[4]Traditional · 1/10

inferred from anti-inflammatory action

Evidence: 1
Label: Skin irritation
Warts[4]Traditional · 1/10

Fresh orange latex traditionally dabbed on warts

Evidence: 1
Label: Warts
Wounds[4]Traditional · 1/10

inferred from antimicrobial action

Evidence: 1
Label: Wounds
Arthritis / joint pain[10]Traditional · 2/10

inferred from anti-inflammatory action

Evidence: 2
Label: Arthritis / joint pain
Back pain[10]Traditional · 2/10

inferred from analgesic action

Evidence: 2
Label: Back pain
Cancer (anticancer research)[7]Traditional · 2/10

inferred from anticancer action

Evidence: 2
Label: Cancer (anticancer research)
Headache[10]Traditional · 2/10

inferred from analgesic action

Evidence: 2
Label: Headache
Inflammation (general)[10]Traditional · 2/10

inferred from anti-inflammatory action

Evidence: 2
Label: Inflammation (general)
Menopause[10, 15]Moderate · 5/10

Traditional support for menopausal symptoms (see safety note - it does NOT act as a natural progesterone) - a placebo-controlled crossover RCT of topical wild yam cream found little effect on menopausal symptoms, lipids or hormones

Evidence: 5
Label: Menopause
Menstrual cramps[10]Traditional · 2/10

Antispasmodic / analgesic for menstrual cramps and muscle spasm (antinociceptive in animal models)

Evidence: 2
Label: Menstrual cramps
Muscle spasm[10]Traditional · 2/10

Antispasmodic / analgesic for menstrual cramps and muscle spasm (antinociceptive in animal models)

Evidence: 2
Label: Muscle spasm
Pain (general)[10]Traditional · 2/10

Anti-inflammatory for joint and inflammatory pain

Evidence: 2
Label: Pain (general)
Skin irritation[10]Traditional · 2/10

inferred from anti-inflammatory action

Evidence: 2
Label: Skin irritation

Safety, Cautions & Contraindications

Safety note[13, 14]Serious

SERIOUS: oral greater celandine can cause acute idiosyncratic liver injury (hepatocellular hepatotoxicity with jaundice). Multiple reported cases - dozens of herb-induced liver injury reports in the literature, with continuing recent case reports - led regulators to restrict or suspend oral products. Do not take internally if you have any liver disease, and stop immediately and seek care at any sign of liver problems (jaundice, dark urine, upper-abdominal pain).

Safety note[4, 13]Caution

Avoid in pregnancy and breastfeeding. The fresh orange latex is irritant and caustic - keep it away from the eyes and broken skin.

Safety note[10, 15]Info

IMPORTANT myth-bust: wild yam / diosgenin is NOT converted into progesterone or DHEA in the body, so it does not work as a 'natural progesterone' - claims to that effect are incorrect. Consistent with this, a randomized placebo-controlled crossover trial of topical wild yam cream found no significant change in symptoms, serum/salivary progesterone, oestradiol, FSH or lipids.

Safety note[10]Caution

Generally well tolerated orally (no acute or subchronic toxicity in animal studies); large doses may cause nausea or vomiting. Avoid medicinal doses in pregnancy and breastfeeding and in hormone-sensitive conditions as a precaution.

External Ids

Gbif: 5334186
Wikidata: Q156807
Gbif: 2754553
Wikidata: Q309632

Botanical Description

Branching perennial herb with soft, brittle, hairy stems that exude a distinctive bright orange-yellow latex (sap) when cut or broken. The leaves are deeply lobed, pale bluish-green beneath, giving a delicate, almost fern-like appearance. Small, four-petalled, bright yellow flowers are borne in loose umbel-like clusters.[4]

Height: 30-90 cm
Habit: Branching, brittle-stemmed perennial herb
Leaves: Deeply lobed, pale bluish-green beneath
Flowers: Small, four-petalled, bright yellow, in loose umbel-like clusters
Stem: Soft, brittle, hairy, exuding bright orange-yellow latex when broken
Root: Branching taproot, also exuding orange latex
Fruit: Slender, curved capsule
Flowering Period: April-September

Twining, herbaceous perennial vine with heart-shaped leaves arising from a knotty, woody, cinnamon-brown rhizome ('root'). Small, inconspicuous greenish-yellow flowers are borne on separate male and female plants, followed on female plants by small three-winged seed capsules.[10]

Height: Vine to several metres, twining over support
Habit: Twining, herbaceous perennial vine
Leaves: Heart-shaped, alternate
Flowers: Small, inconspicuous, greenish-yellow, on separate male and female plants
Stem: Slender, twining
Root: Knotty, woody, cinnamon-brown rhizome
Fruit: Small three-winged seed capsule (female plants)
Flowering Period: Summer

Habitat

Grows in shaded, nutrient-rich ground - hedgerows, walls, waste ground and woodland edges, often near old buildings; native to Europe and Western Asia and naturalised in North America.[4]

Native to woodland edges, thickets and fence rows of eastern North America, growing over shrubs and fences in moist, rich soil.[10]

Harvesting

The flowering aerial parts are cut in spring to summer; the fresh orange latex is collected by breaking a stem or leaf as needed for topical (wart) use. Given the documented hepatotoxicity of oral preparations, harvesting for internal use is not recommended.[4]

Parts: Aerial parts (and fresh orange latex)
Season: Spring to summer, while flowering

The knotty rhizome is dug in autumn once the aerial vine has died back, then cleaned and dried.

Parts: Root and rhizome
Season: Autumn

Traditional Uses

Greater celandine has a long European folk history, reflected in its name 'tetterwort', as a topical remedy for warts and skin blemishes (the fresh orange latex dabbed directly on), and internally as a bitter choleretic digestive remedy for biliary and upper-abdominal dyspepsia - though oral use is now medically restricted because of documented liver injury.[4]

Wild yam root has a Native American and Eclectic-medicine history as an antispasmodic remedy for colic, menstrual cramps and rheumatic joint pain (reflected in the old names 'colic root' and 'rheumatism root'); despite a persistent modern myth, its diosgenin content is not converted into progesterone or other hormones in the human body.[10]

Preparations

Fresh latex (topical, warts only)[4]

Fresh orange latex from a broken stem dabbed directly onto warts, the classic external folk use; kept well away from eyes, mucous membranes and broken skin.

Infusion/tincture (historical, oral - restricted)[13]

Historically taken as an infusion or tincture for biliary dyspepsia, but oral use is now restricted in several jurisdictions due to hepatotoxicity risk and should only be considered under professional supervision, if at all.

Decoction[10]

Dried root and rhizome simmered in water as a traditional antispasmodic remedy for colic and cramping.

Topical cream[15]

Root extract formulated into topical creams, historically marketed (without good supporting evidence) for menopausal symptoms.

Dosage

All internal preparations[13, 14]

Because of a documented risk of acute liver injury, no internal dose is given here; oral use should be avoided, especially by anyone with liver disease, and any sign of jaundice, dark urine or upper-abdominal pain warrants immediate medical attention. Educational reference only, not a prescription.

Not documented

References

REF-0770, REF-0771, REF-0772, REF-0460, REF-2264, REF-2265, REF-2266, REF-2267, REF-2268, REF-2269, REF-2270, REF-2271
REF-0794, REF-0795, REF-0796, REF-2281, REF-2282, REF-2283, REF-2284, REF-2285, REF-2286, REF-0528, REF-2287, REF-2288, REF-2289

Lookalikes Review

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

References & Sources

  1. Li, X.L., Sun, Y.P., Wang, M., Wang, Z.B. and Kuang, H.X (2024) 'Alkaloids in Chelidonium majus L.: a review of its phytochemistry, pharmacology and toxicology', Frontiers in Pharmacology, 15, pp. 1440979. doi:10.3389/fphar.2024.1440979 Traditional / reference
    https://doi.org/10.3389/fphar.2024.1440979
  2. Koriem, K.M.M., Arbid, M.S. and Asaad, G.F (2012) 'Chelidonium majus leaves methanol extract and its chelidonine alkaloid ingredient reduce cadmium-induced nephrotoxicity in rats', Journal of Natural Medicines, 67(1), pp. 159-167. doi:10.1007/s11418-012-0667-6 Preclinical
    https://doi.org/10.1007/s11418-012-0667-6
  3. Nawrot, R (2017) 'Defense-related Proteins from Chelidonium majus L. as Important Components of its Latex', Current Protein & Peptide Science, 18(8), pp. 864-880. doi:10.2174/1389203718666170406124013 Traditional / reference
    https://doi.org/10.2174/1389203718666170406124013
  4. Gilca, M., Gaman, L., Panait, E., Stoian, I. and Atanasiu, V (2010) 'Chelidonium majus - an integrative review: traditional knowledge versus modern findings', Forschende Komplementarmedizin. doi:10.1159/000321397 Traditional / reference
    https://doi.org/10.1159/000321397
  5. Popovic, A., Deljanin, M., Popovic, S., Todorovic, D., Djurdjevic, P., Matic, S., Stankovic, M., Avramovic, D. and Baskic, D (2021) 'Chelidonium majus crude extract induces activation of peripheral blood mononuclear cells and enhances their cytotoxic effect toward HeLa cells', International Journal of Environmental Health Research, 32(7), pp. 1554-1566. doi:10.1080/09603123.2021.1897534 Preclinical
    https://doi.org/10.1080/09603123.2021.1897534
  6. Shen, L., Lee, S.A., Joo, J.C., Hong, E., Cui, Z.Y., Jo, E., Park, S.J. and Jang, H.J (2022) 'Chelidonium majus induces apoptosis of human ovarian cancer cells via ATF3-mediated regulation of Foxo3a by Tip60', Journal of Microbiology and Biotechnology, 32(4), pp. 493-503. doi:10.4014/jmb.2109.09030 Preclinical
    https://doi.org/10.4014/jmb.2109.09030
  7. Deljanin, M., Nikolic, M., Baskic, D., Todorovic, D., Djurdjevic, P., Zaric, M., Stankovic, M., Todorovic, M., Avramovic, D. and Popovic, S (2016) 'Chelidonium majus crude extract inhibits migration and induces cell cycle arrest and apoptosis in tumor cell lines', Journal of Ethnopharmacology, 190, pp. 362-371. doi:10.1016/j.jep.2016.06.056 Preclinical
    https://doi.org/10.1016/j.jep.2016.06.056
  8. Warowicka, A., Qasem, B., Dera-Szymanowska, A., Wolun-Cholewa, M., Florczak, P., Horst, N., Napierala, M., Szymanowski, K., Popenda, L., Bartkowiak, G., Florek, E., Gozdzicka-Jozefiak, A. and Mlynarz, P (2021) 'Effect of protoberberine-rich fraction of Chelidonium majus L. on endometriosis regression', Pharmaceutics, 13(7), pp. 931. doi:10.3390/pharmaceutics13070931 Preclinical
    https://doi.org/10.3390/pharmaceutics13070931
  9. Kadan, G., Gozler, T. and Hesse, M (1992) '(+)-Norchelidonine from Chelidonium majus', Planta Medica, 58(5), pp. 477. doi:10.1055/s-2006-961523 Preclinical
    https://doi.org/10.1055/s-2006-961523
  10. Musidlak, O., Warowicka, A., Broniarczyk, J., Adamczyk, D., Gozdzicka-Jozefiak, A. and Nawrot, R (2022) 'The activity of Chelidonium majus L. latex and its components on HPV reveal insights into the antiviral molecular mechanism', International Journal of Molecular Sciences, 23(16), pp. 9241. doi:10.3390/ijms23169241 Preclinical
    https://doi.org/10.3390/ijms23169241
  11. Zhang, W., You, C., Wang, C., Fan, L., Wang, Y., Su, Y., Deng, Z. and Du, S (2014) 'One new alkaloid from Chelidonium majus L', Natural Product Research, 28(21), pp. 1873-1878. doi:10.1080/14786419.2014.953497 Preclinical
    https://doi.org/10.1080/14786419.2014.953497
  12. Capistrano I, R., Wouters, A., Lardon, F., Gravekamp, C., Apers, S. and Pieters, L (2015) 'In vitro and in vivo investigations on the antitumour activity of Chelidonium majus', Phytomedicine, 22(14), pp. 1279-1287. doi:10.1016/j.phymed.2015.10.013 Preclinical
    https://doi.org/10.1016/j.phymed.2015.10.013
  13. Teschke, R., Frenzel, C., Glass, X., Schulze, J. and Eickhoff, A (2012) 'Greater Celandine hepatotoxicity: a clinical review', Annals of Hepatology. doi:10.1016/s1665-2681(19)31408-5 Clinical study
    https://doi.org/10.1016/s1665-2681(19)31408-5
  14. Ciornolutchii, V., Ismaiel, A., Sabo, C.M., Al Hajjar, N., Seicean, A. and Dumitrascu, D.L (2024) 'A Hidden Cause of Hypertransaminasemia: Liver Toxicity Caused by Chelidonium Majus L. Report of Two Cases of Herb-Induced Liver Injury and Literature Review', American Journal of Therapeutics, 31(4), pp. e382--e387. doi:10.1097/MJT.0000000000001708 Clinical study
    https://doi.org/10.1097/MJT.0000000000001708
  1. Depypere, H.T. and Comhaire, F.H (2013) 'Herbal preparations for the menopause: beyond isoflavones and black cohosh', Maturitas, 77(2), pp. 191-194. doi:10.1016/j.maturitas.2013.11.001 Traditional / reference
    https://doi.org/10.1016/j.maturitas.2013.11.001
  2. Cai, B., Zhang, Y., Wang, Z., Xu, D. et al (2020) 'Therapeutic Potential of Diosgenin and Its Major Derivatives against Neurological Diseases: Recent Advances', Oxidative Medicine and Cellular Longevity, 2020, pp. 3153082. doi:10.1155/2020/3153082 Traditional / reference
    https://doi.org/10.1155/2020/3153082
  3. Raj, P.S., Bergfeld, W.F., Belsito, D.V., Cohen, D.E. et al (2023) 'Safety Assessment of Dioscorea Villosa (Wild Yam) Root Extract as Used in Cosmetics', International Journal of Toxicology, 42(3_suppl), pp. 29S-31S. doi:10.1177/10915818231204230 Traditional / reference
    https://doi.org/10.1177/10915818231204230
  4. Dong, S., Nikolic, D., Simmler, C., Qiu, F., van Breemen, R.B., Soejarto, D.D., Pauli, G.F. and Chen, S (2012) 'Diarylheptanoids from Dioscorea villosa (wild yam)', Journal of Natural Products, 75(12), pp. 2168-2177. doi:10.1021/np300603z Preclinical
    https://doi.org/10.1021/np300603z
  5. Dong, S., Cai, G., Napolitano, J.G., Nikolic, D., Lankin, D.C., McAlpine, J.B., van Breemen, R.B., Soejarto, D.D., Pauli, G.F. and Chen, S (2013) 'Lipidated steroid saponins from Dioscorea villosa (wild yam)', Fitoterapia, 91, pp. 113-124. doi:10.1016/j.fitote.2013.07.018 Preclinical
    https://doi.org/10.1016/j.fitote.2013.07.018
  6. Wojcikowski, K., Wohlmuth, H., Johnson, D.W. and Gobe, G (2008) 'Dioscorea villosa (wild yam) induces chronic kidney injury via pro-fibrotic pathways', Food and Chemical Toxicology, 46(9), pp. 3122-3131. doi:10.1016/j.fct.2008.06.090 Preclinical
    https://doi.org/10.1016/j.fct.2008.06.090
  7. Mazzio, E., Almalki, A., Darling-Reed, S.F. and Soliman, K.F.A (2021) 'Effects of wild yam root (Dioscorea villosa) extract on the gene expression profile of triple-negative breast cancer cells', Cancer Genomics & Proteomics, 18(6), pp. 735-755. doi:10.21873/cgp.20294 Preclinical
    https://doi.org/10.21873/cgp.20294
  8. Ali, Z., Smillie, T.J. and Khan, I.A (2013) 'Cholestane steroid glycosides from the rhizomes of Dioscorea villosa (wild yam)', Carbohydrate Research, 370, pp. 86-91. doi:10.1016/j.carres.2012.12.022 Preclinical
    https://doi.org/10.1016/j.carres.2012.12.022
  9. Manda, V.K., Avula, B., Ali, Z., Wong, Y., Smillie, T.J., Khan, I.A. and Khan, S.I (2013) 'Characterization of in vitro ADME properties of diosgenin and dioscin from Dioscorea villosa', Planta Medica, 79(15), pp. 1421-1428. doi:10.1055/s-0033-1350699 Preclinical
    https://doi.org/10.1055/s-0033-1350699
  10. Lima, C.M., Lima, A.K., Melo, M.G.D., Serafini, M.R., Oliveira, D.L., de Almeida, E.B., Barreto, R.S.S., Nogueira, P.C., Moraes, V.R.S., Oliveira, E.R.A., de Albuquerque, R.L.C., Quintans-Junior, L.J. and Araujo, A.A.S (2013) 'Bioassay-guided evaluation of Dioscorea villosa - an acute and subchronic toxicity, antinociceptive and anti-inflammatory approach', BMC Complementary and Alternative Medicine. doi:10.1186/1472-6882-13-195 Preclinical
    https://doi.org/10.1186/1472-6882-13-195
  11. Avula, B., Wang, Y., Wang, M., Ali, Z., Smillie, T.J., Zweigenbaum, J. and Khan, I.A (2014) 'Characterization of steroidal saponins from Dioscorea villosa and D. cayenensis using ultrahigh performance liquid chromatography/electrospray ionization quadrupole time-of-flight mass spectrometry', Planta Medica, 80(4), pp. 321-329. doi:10.1055/s-0033-1360330 Preclinical
    https://doi.org/10.1055/s-0033-1360330
  12. Siddiqui, M.A., Ali, Z., Chittiboyina, A.G. and Khan, I.A (2018) 'Hepatoprotective effect of steroidal glycosides from Dioscorea villosa on hydrogen peroxide-induced hepatotoxicity in HepG2 cells', Frontiers in Pharmacology, 9, pp. 797. doi:10.3389/fphar.2018.00797 Preclinical
    https://doi.org/10.3389/fphar.2018.00797
  13. Hayes, P.Y., Lambert, L.K., Lehmann, R., Penman, K., Kitching, W. and De Voss, J.J (2007) 'Complete 1H and 13C assignments of the four major saponins from Dioscorea villosa (wild yam)', Magnetic Resonance in Chemistry, 45(11), pp. 1001-1005. doi:10.1002/mrc.2071 Preclinical
    https://doi.org/10.1002/mrc.2071
  14. Okawara, M. and Tokudome, Y. and Todo, H. and Sugibayashi, K. and Hashimoto, F (2013) 'Enhancement of diosgenin distribution in the skin by cyclodextrin complexation following oral administration', Biological & Pharmaceutical Bulletin, 36(1), pp. 36--40. doi:10.1248/bpb.b12-00467 Preclinical
    https://doi.org/10.1248/bpb.b12-00467
  15. Komesaroff, P.A., Black, C.V., Cable, V. and Sudhir, K (2001) 'Effects of wild yam extract on menopausal symptoms, lipids and sex hormones in healthy menopausal women', Climacteric, 4(2), pp. 144--150. doi:10.1080/cmt.4.2.144.150 Randomized trial
    https://doi.org/10.1080/cmt.4.2.144.150

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.