Plant Comparison

Tea vs Panax Ginseng

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 ATeaCamellia sinensisTheaceaeFull monograph →
Plant BPanax GinsengPanax ginsengAraliaceaeFull monograph →

At a glance

Tea and Panax Ginseng: they share 8 indicated uses (arthritis / joint pain, blood sugar / diabetes support, cardiovascular / heart health, …); 4 pharmacological actions in common.

TeaPanax Ginseng
Constituents33
Pharmacological actions66
Indicated uses1112
Safety notes22
Cited sources2121
Indicated uses
Only Tea
Cancer (anticancer research)Infection (general)Wounds
Shared (8)
Arthritis / joint painBlood sugar / diabetes supportCardiovascular / heart healthCognitive functionInflammation (general)MemoryMetabolic supportSkin irritation
Only Panax Ginseng
Cold & fluFatigue / low energyImmune supportMuscle soreness
Pharmacological actions
Only Tea
Anticancer (preclinical)Antimicrobial
Shared (4)
Anti-inflammatoryAntidiabetic (blood-sugar lowering)AntioxidantNeuroprotective / cognition support
Only Panax Ginseng
Physical performance / ergogenicImmunomodulator / immune support

Evidence face-off — shared uses

ConditionTeaPanax GinsengVerdict
Arthritis / joint pain1/105/10Stronger for Panax Ginseng
Blood sugar / diabetes support1/105/10Stronger for Panax Ginseng
Cardiovascular / heart health1/105/10Stronger for Panax Ginseng
Cognitive function1/109/10Stronger for Panax Ginseng
Inflammation (general)1/105/10Stronger for Panax Ginseng
Memory1/108/10Stronger for Panax Ginseng
Metabolic support1/105/10Stronger for Panax Ginseng
Skin irritation1/105/10Stronger for Panax Ginseng

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

Catechins (EGCG, ECG) and polyphenols[1, 15]

Principal antioxidant polyphenols, most concentrated in minimally oxidised green tea; epigallocatechin gallate (EGCG) is the best studied.

CatechinsPhenolic compounds
Caffeine and theanine[1]

Caffeine gives tea its mild stimulant effect; L-theanine, a unique amino acid, is associated with calm alertness and modulates caffeine's effects.

Caffeine
Theaflavins and thearubigins[15]

Oxidative polymerisation products of catechins formed during black tea processing, contributing to black tea's colour and its own antioxidant profile.

Ginsenosides (panaxosides)[3]

The principal bioactive triterpene saponins of the root, considered responsible for most of ginseng's adaptogenic, neuroprotective and immunomodulatory activity; the ratio of protopanaxadiol- to protopanaxatriol-type ginsenosides differs between fresh, white and red ginseng.

Ginsenosides / eleutherosides
Polysaccharides (panaxans)[7]

Contribute to the immunomodulatory activity of the root.

Polysaccharides
Volatile oil and phenolic compounds[7]

Minor constituents contributing to the aroma and antioxidant activity.

Essential (volatile) oilPhenolic compounds

Pharmacological Actions

Anti-inflammatory[15]
Anticancer (preclinical)[4, 5, 9, 15]
Antidiabetic (blood-sugar lowering)[15]
Antimicrobial[8, 11, 12, 15]
Antioxidant[4, 6, 10, 15]
Neuroprotective / cognition support[6, 15]
Anti-inflammatory[1, 7, 11, 12, 13]
Antidiabetic (blood-sugar lowering)[11, 12, 13]
Antioxidant[1, 7, 11, 12, 13]
Physical performance / ergogenic[6, 11, 12, 13]

Physical performance / strength improvement

Immunomodulator / immune support[1, 7, 11, 12, 13]
Neuroprotective / cognition support[1, 5, 9, 10, 11, 12, 13]

Traditional & Indicated Uses

Arthritis / joint pain[15]Traditional · 1/10

inferred from anti-inflammatory action

Evidence: 1
Label: Arthritis / joint pain
Blood sugar / diabetes support[15, 17]Traditional · 1/10

inferred from antidiabetic action

Evidence: 1
Label: Blood sugar / diabetes support
Cancer (anticancer research)[5, 9]Good · 8/10

inferred from anticancer action

Evidence: 8
Label: Cancer (anticancer research)
Cardiovascular / heart health[15, 17]Traditional · 1/10
Evidence: 1
Label: Cardiovascular / heart health
Cognitive function[15, 18]Traditional · 1/10

inferred from neuroprotective action

Evidence: 1
Label: Cognitive function
Infection (general)[15]Traditional · 1/10

inferred from antimicrobial action

Evidence: 1
Label: Infection (general)
Inflammation (general)[15]Traditional · 1/10

inferred from anti-inflammatory action

Evidence: 1
Label: Inflammation (general)
Memory[15, 18]Traditional · 1/10

inferred from neuroprotective action

Evidence: 1
Label: Memory
Metabolic support[15, 17]Traditional · 1/10
Evidence: 1
Label: Metabolic support
Skin irritation[15]Traditional · 1/10

inferred from anti-inflammatory action

Evidence: 1
Label: Skin irritation
Wounds[15]Traditional · 1/10

inferred from antimicrobial action

Evidence: 1
Label: Wounds
Arthritis / joint pain[11, 12, 13]Moderate · 5/10

inferred from anti-inflammatory action

Evidence: 5
Label: Arthritis / joint pain
Blood sugar / diabetes support[11, 12, 13]Moderate · 5/10

inferred from antidiabetic action

Evidence: 5
Label: Blood sugar / diabetes support
Cardiovascular / heart health[11, 12, 13]Moderate · 5/10
Evidence: 5
Label: Cardiovascular / heart health
Cognitive function[9, 10, 11, 12, 13]Strong · 9/10

inferred from neuroprotective action

Evidence: 9
Label: Cognitive function
Cold & flu[11, 12, 13]Moderate · 5/10

inferred from immunomodulator action

Evidence: 5
Label: Cold & flu
Fatigue / low energy[6, 11, 12, 13]Good · 8/10

inferred from ergogenic action

Evidence: 8
Label: Fatigue / low energy
Immune support[11, 12, 13]Moderate · 5/10
Evidence: 5
Label: Immune support
Inflammation (general)[11, 12, 13]Moderate · 5/10

inferred from anti-inflammatory action

Evidence: 5
Label: Inflammation (general)
Memory[9, 11, 12, 13]Good · 8/10

inferred from neuroprotective action

Evidence: 8
Label: Memory
Metabolic support[11, 12, 13]Moderate · 5/10
Evidence: 5
Label: Metabolic support
Muscle soreness[11, 12, 13]Moderate · 5/10

inferred from ergogenic action

Evidence: 5
Label: Muscle soreness
Skin irritation[11, 12, 13]Moderate · 5/10

inferred from anti-inflammatory action

Evidence: 5
Label: Skin irritation

Safety, Cautions & Contraindications

Safety note[15, 17, 18]Serious

Generally safe in moderate consumption. High caffeine intake may cause insomnia, anxiety, palpitations, or dependence. Large amounts of green tea extract supplements may be hepatotoxic (rare). May reduce iron absorption if consumed with meals. Avoid very high supplement doses during pregnancy.

Safety note[15, 17, 18, 19]Caution

Duke (2002) rates tea (Camellia sinensis) as ++ and notes anti-aggregant, antioxidant, anticariogenic, and antibacterial activities at the experimental level (score 1). The catechins (EGCG, ECG) and polyphenols are responsible for the antioxidant and anticancer properties under research investigation. Duke notes that green tea preserves more polyphenols than black tea due to less oxidation. Regular tea consumption is associated with reduced cardiovascular risk. Excess consumption (>10 cups daily) may cause fluoride-related bone changes. Caffeine content is relevant for sleep disturbance, anxiety, and interactions with cardiovascular medications (Duke, 2002).

Safety note[11, 12, 13]Caution

Generally well tolerated in short-term use (up to 3 months). May cause insomnia, headache, or gastrointestinal upset at high doses. Avoid during pregnancy and breastfeeding. May interact with warfarin, MAOIs, and diabetic medications. Not recommended for continuous use without breaks.

Safety note[11, 12, 13, 14]Caution

Duke (2002) rates Korean/Oriental ginseng (Panax ginseng) as highly active with clinical support for adaptogenic, immunostimulant, and performance-enhancing effects. Commission E approves standardized ginseng root extract (4–7% ginsenosides) as a tonic for fatigue and during convalescence. Dose: 200–600 mg standardized extract daily. Duke cautions about 'Ginseng Abuse Syndrome' (GAS) with overdose — symptoms include hypertension, insomnia, edema, and nervousness. Drug interactions are notable: ginseng potentiates MAOIs and may interact with warfarin, digoxin, and stimulants. Cycle use (2–3 weeks on, 2 weeks off) is recommended (Duke, 2002).

External Ids

Gbif: 3189635
Wikidata: Q101815
Gbif: 5372262
Wikidata: Q182881

Botanical Description

Evergreen shrub or small tree with glossy, dark green, leathery, finely toothed leaves. Small, fragrant, white flowers with a prominent central boss of yellow stamens are borne singly or in small clusters in the leaf axils. Commercial tea is made from the young leaves and unopened leaf buds ('sprouts'), processed differently to yield green, black, white or oolong tea from the same species.[15]

Height: 1-9 m (kept pruned to 1-1.5 m under cultivation)
Habit: Evergreen shrub or small tree, usually kept pruned as a shrub
Leaves: Glossy, dark green, leathery, finely toothed
Flowers: Small, fragrant, white, with a prominent boss of yellow stamens
Stem: Woody, branching, evergreen
Root: Deep taproot
Fruit: Woody capsule containing a few large seeds
Flowering Period: Autumn to winter

Slow-growing perennial herb (Araliaceae), 30-60 cm tall, harvested at 4 years of age or older. A single erect stem bears a whorl of palmately compound leaves, each with 3-5 toothed leaflets, at its top. Small greenish-white flowers are borne in a single terminal umbel, followed by small red berries. The fleshy, often forked or human-shaped taproot - the origin of the name 'ginseng' ('renshen', man-root) - is the medicinal part.[3]

Height: 30-60 cm
Habit: Slow-growing perennial herb, single erect stem
Leaves: Palmately compound, whorled at the stem top, 3-5 toothed leaflets per leaf
Flowers: Small, greenish-white, in a single terminal umbel
Stem: Single, erect
Root: Fleshy, often forked, human-shaped taproot - the medicinal part
Fruit: Small red berries
Flowering Period: May-June

Habitat

Native to the subtropical and tropical forests and hillsides of East and South Asia (China, India, Myanmar); cultivated extensively across Asia, Africa and elsewhere on well-drained, acidic upland soils.[15]

Native to the cool-temperate deciduous mountain forests of Manchuria, Korea and the Russian Far East. Historically wild-harvested, it is now predominantly cultivated, mainly in Korea and China, under artificial shade for several years before harvest.[1]

Harvesting

The youngest leaves and unopened leaf buds ('flush') are hand- or machine-picked repeatedly through the growing season; how the fresh leaf is subsequently processed (withered, rolled, oxidised, fixed and dried) determines whether it becomes green, black, white or oolong tea.[15]

Parts: Leaf, Young sprouts
Season: Repeated flushes through the growing season

The root is harvested after at least 4-6 years of growth, once its ginsenoside content is fully developed. Roots are either air-dried as 'white ginseng' or steamed and then dried as 'red ginseng', a processing step that alters the ginsenoside profile.[3]

Parts: Root
Season: After 4-6+ years of cultivation

Traditional Uses

Tea has an ancient East Asian tradition as both a beverage and a medicinal tonic, used for alertness, digestion and general wellbeing; green tea in particular has a long-standing reputation, now widely studied, as an antioxidant, cardiometabolic and cognitive-support beverage.[1, 15]

Ginseng is one of the most celebrated tonic herbs of East Asian traditional medicine, used for millennia as a general adaptogen to restore vitality, support recovery from illness and improve stamina and cognitive performance. Modern clinical research supports adaptogenic, immunomodulatory, antioxidant, neuroprotective and mild antidiabetic effects consistent with this traditional use.[1, 7]

Preparations

Infusion (green tea)[15]

Young leaf, minimally oxidised, infused in hot water; the least-processed and most-studied form for antioxidant polyphenol content.

Standardised extract[15]

Concentrated leaf extract standardised to catechin (e.g. EGCG) content, taken as capsules; used in some clinical studies, though high-dose extracts carry rare hepatotoxicity concerns.

Standardised root extract (capsule)[11, 12, 13]

Commission E-recognised standardised extract (4-7% ginsenosides), the most clinically studied preparation.

Red ginseng (steamed and dried root)[3]

Traditional processed form (steamed then dried), which alters and concentrates the ginsenoside profile compared with white (unprocessed) ginseng.

Dosage

Infusion[16]

The EU herbal monograph on green tea leaf (Camelliae sinensis non fermentatum folium) gives, for adults and elderly, 1.8-2.2 g of the whole or comminuted leaf in 100-150 mL of boiling water as an infusion, 3-5 times daily; a powdered herbal substance at 390 mg three times daily (up to 5 if necessary) is also listed. Contraindicated in gastric and duodenal ulcers, cardiovascular disorders such as hypertension and arrhythmia, and hyperthyroidism. Not recommended under 18 years. Educational reference only, not a prescription.

Standardised extract[11, 12, 13]

Duke (2002) and Commission E guidance: 200-600 mg of standardised extract (4-7% ginsenosides) daily, used cyclically (2-3 weeks on, 2 weeks off) rather than continuously. Educational reference only, not a prescription.

References

REF-0755, REF-0756, REF-0757, REF-1960, REF-1961, REF-1962, REF-1963, REF-1964, REF-1965, REF-1966, REF-1967, REF-1968, REF-1969, REF-1970
REF-1466, REF-1467, REF-1468, REF-1469, REF-1470, REF-1471, REF-1472, REF-1473, REF-1474, REF-1475

Drug Class Interactions

Safety note[20, 21]Caution
Drug Class: antihypertensives
Mechanism: Green tea catechins block an intestinal uptake transporter (OATP1A2) that some blood-pressure medicines rely on for absorption. In a controlled study, drinking green tea cut blood levels of the beta-blocker nadolol by about 85% and blunted its blood-pressure-lowering effect. If you take nadolol (or other OATP-transported medicines), separate green tea from the dose by several hours and keep intake consistent; watch that your blood pressure stays controlled.
Reviewed By: Omnia Sana (owner-authorized)
Reviewed Date: 2026-07-03
Safety note[15, 16]Caution
Drug Class: anticoagulants-antiplatelets
Mechanism: Ginseng may reduce the anticoagulant effect of warfarin (lower INR); a randomized trial of American ginseng showed a reduced INR. Monitor anticoagulation closely.
Reviewed By: Omnia Sana (owner-authorized)
Reviewed Date: 2026-07-03
Safety note[15]Caution
Drug Class: antidepressants-serotonergic
Mechanism: Case reports link ginseng with MAOI antidepressants (e.g. phenelzine) to headache, tremor and manic-like symptoms.
Reviewed By: Omnia Sana (owner-authorized)
Reviewed Date: 2026-07-03
Safety note[17, 18]Caution
Drug Class: antidiabetics
Mechanism: Ginseng can lower blood glucose - a controlled trial in type 2 diabetes reduced fasting glucose and HbA1c, and ginseng also lowers post-meal glucose. Combined with diabetes medicines it may add to blood-sugar lowering and risk hypoglycaemia, so monitor blood sugar.
Reviewed By: Omnia Sana (owner-authorized)
Reviewed Date: 2026-07-03

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

Pairings

Not documented

Ginseng and feverfew both reduce blood clotting/platelet stickiness, so taking them together may add up and raise the risk of bruising or bleeding — use caution, especially before surgery or alongside blood-thinning drugs.[19, 20]

Partner Id: tanacetum-parthenium
Type: caution
Reviewed By: Omnia Sana (owner-authorized)
Reviewed Date: 2026-07-03

Ginseng and ginger both reduce blood clotting/platelet stickiness, so taking them together may add up and raise the risk of bruising or bleeding — use caution, especially before surgery or alongside blood-thinning drugs.[19, 21]

Partner Id: zingiber-officinale
Type: caution
Reviewed By: Omnia Sana (owner-authorized)
Reviewed Date: 2026-07-03

References & Sources

  1. Mancini, E., Beglinger, C., Drewe, J., Zanchi, D. et al (2017) 'Green tea effects on cognition, mood and human brain function: A systematic review', Phytomedicine, 34, pp. 26-37. doi:10.1016/j.phymed.2017.07.008 Meta-analysis / review
    https://doi.org/10.1016/j.phymed.2017.07.008
  2. Musial, C., Kuban-Jankowska, A. and Gorska-Ponikowska, M (2020) 'Beneficial Properties of Green Tea Catechins', International Journal of Molecular Sciences, 21(5), pp. 1744. doi:10.3390/ijms21051744 Traditional / reference
    https://doi.org/10.3390/ijms21051744
  3. Ohishi, T., Goto, S., Monira, P., Isemura, M. and Nakamura, Y (2016) 'Anti-inflammatory Action of Green Tea', Anti-inflammatory & Anti-allergy Agents in Medicinal Chemistry, 15(2), pp. 74-90. doi:10.2174/1871523015666160915154443 Traditional / reference
    https://doi.org/10.2174/1871523015666160915154443
  4. Zhao, T., Li, C., Wang, S. and Song, X (2022) 'Green Tea (Camellia sinensis): A Review of Its Phytochemistry, Pharmacology, and Toxicology', Molecules, 27(12), pp. 3909. doi:10.3390/molecules27123909 Meta-analysis / review
    https://doi.org/10.3390/molecules27123909
  5. Filippini, T., Malavolti, M., Borrelli, F., Izzo, A.A., Fairweather-Tait, S.J., Horneber, M. and Vinceti, M (2020) 'Green tea (Camellia sinensis) for the prevention of cancer', Cochrane Database of Systematic Reviews, 3(3), pp. CD005004. doi:10.1002/14651858.CD005004.pub3 Meta-analysis / review
    https://doi.org/10.1002/14651858.CD005004.pub3
  6. Prasanth, M.I., Sivamaruthi, B.S., Chaiyasut, C. and Tencomnao, T (2019) 'A Review of the Role of Green Tea (Camellia sinensis) in Antiphotoaging, Stress Resistance, Neuroprotection, and Autophagy', Nutrients, 11(2), pp. 474. doi:10.3390/nu11020474 Meta-analysis / review
    https://doi.org/10.3390/nu11020474
  7. Bedrood, Z., Rameshrad, M. and Hosseinzadeh, H (2018) 'Toxicological effects of Camellia sinensis (green tea): A review', Phytotherapy Research, 32(7), pp. 1163-1180. doi:10.1002/ptr.6063 Meta-analysis / review
    https://doi.org/10.1002/ptr.6063
  8. Hamilton-Miller, J.M.T (2001) 'Anti-cariogenic properties of tea (Camellia sinensis)', Journal of Medical Microbiology, 50(4), pp. 299-302. doi:10.1099/0022-1317-50-4-299 Meta-analysis / review
    https://doi.org/10.1099/0022-1317-50-4-299
  9. Conde, V.R., Alves, M.G., Oliveira, P.F. and Silva, B.M (2015) 'Tea (Camellia sinensis (L.)): a putative anticancer agent in bladder carcinoma?', Anti-Cancer Agents in Medicinal Chemistry, 15(1), pp. 26-36. doi:10.2174/1566524014666141203143143 Meta-analysis / review
    https://doi.org/10.2174/1566524014666141203143143
  10. Moore, R.J., Jackson, K.G. and Minihane, A.M (2009) 'Green tea (Camellia sinensis) catechins and vascular function', British Journal of Nutrition, 102(12), pp. 1790-1802. doi:10.1017/S0007114509991218 Meta-analysis / review
    https://doi.org/10.1017/S0007114509991218
  11. Gaur, R. and Bao, G.H (2021) 'Chemistry and Pharmacology of Natural Catechins from Camellia sinensis as Anti-MRSA Agents', Current Topics in Medicinal Chemistry, 21(17), pp. 1519-1537. doi:10.2174/1568026621666210524100632 Meta-analysis / review
    https://doi.org/10.2174/1568026621666210524100632
  12. Tafazoli, A. and Tafazoli Moghadam, E (2020) 'Camellia Sinensis Mouthwashes in Oral Care: a Systematic Review', Journal of Dentistry (Shiraz), 21(4), pp. 249-262. doi:10.30476/DENTJODS.2020.83204.1045 Meta-analysis / review
    https://doi.org/10.30476/DENTJODS.2020.83204.1045
  13. Albassam, A.A. and Markowitz, J.S (2017) 'An Appraisal of Drug-Drug Interactions with Green Tea (Camellia sinensis)', Planta Medica, 83(6), pp. 496-508. doi:10.1055/s-0043-100934 Meta-analysis / review
    https://doi.org/10.1055/s-0043-100934
  14. Gramza-Michalowska, A (2014) 'Caffeine in tea Camellia sinensis - content, absorption, benefits and risks of consumption', Journal of Nutrition, Health & Aging, 18(2), pp. 143-149. doi:10.1007/s12603-013-0404-1 Meta-analysis / review
    https://doi.org/10.1007/s12603-013-0404-1
  15. Chacko, S.M. et al (2010) 'Beneficial effects of green tea: a literature review'. Traditional / reference
    https://scholar.google.com/scholar?q=Beneficial%20effects%20of%20green%20tea%3A%20a%20literature%20review
  16. European Medicines Agency (HMPC) (2013) 'Community herbal monograph on Camellia sinensis (L.) Kuntze, non fermentatum folium'. Available at: https://www.ema.europa.eu/en/documents/herbal-monograph/final-community-herbal-monograph-camellia-sinensis-l-kuntze-non-fermentatum-folium_en.pdf Traditional / reference
    https://www.ema.europa.eu/en/documents/herbal-monograph/final-community-herbal-monograph-camellia-sinensis-l-kuntze-non-fermentatum-folium_en.pdf
  17. Drake, V.J (2015) 'Tea catechins and cardiovascular disease risk', 74(1), pp. 39--46. Traditional / reference
    https://scholar.google.com/scholar?q=Tea%20catechins%20and%20cardiovascular%20disease%20risk
  18. Nobre, A.C., Rao, A. and Owen, G.N (2008) 'L-theanine, a natural constituent in tea, and its effect on mental state', pp. 167--168. Traditional / reference
    https://scholar.google.com/scholar?q=L-theanine%2C%20a%20natural%20constituent%20in%20tea%2C%20and%20its%20effect%20on%20mental%20state
  19. Duke, J.A (2002) 'Handbook of Medicinal Herbs, Second Edition'. Traditional / reference
    https://scholar.google.com/scholar?q=Handbook%20of%20Medicinal%20Herbs%2C%20Second%20Edition
  20. Misaka, S., Yatabe, J., Muller, F., Takano, K., Kawabe, K., Glaeser, H., Yatabe, M.S., Onoue, S., Werba, J.P., Watanabe, H., Yamada, S., Fromm, M.F. and Kimura, J (2014) 'Green tea ingestion greatly reduces plasma concentrations of nadolol in healthy subjects', Clinical Pharmacology and Therapeutics, 95(4), pp. 432-438. doi:10.1038/clpt.2013.241 Randomized trial
    https://doi.org/10.1038/clpt.2013.241
  21. Werba, J.P., Misaka, S., Giroli, M.G., Shimomura, K., Amato, M., Simonelli, N., Vigo, L. and Tremoli, E (2018) 'Update of green tea interactions with cardiovascular drugs and putative mechanisms', Journal of Food and Drug Analysis, 26(2S), pp. S72-S77. doi:10.1016/j.jfda.2018.01.008 Meta-analysis / review
    https://doi.org/10.1016/j.jfda.2018.01.008
  1. Mancuso, C. and Santangelo, R (2017) 'Panax ginseng and Panax quinquefolius: From pharmacology to toxicology', Food and Chemical Toxicology, 107(Pt A), pp. 362-372. doi:10.1016/j.fct.2017.07.019 Meta-analysis / review
    https://doi.org/10.1016/j.fct.2017.07.019
  2. Zhou, Z., Li, M., Zhang, Z., Song, Z. and others (2024) 'Overview of Panax ginseng and its active ingredients protective mechanism on cardiovascular diseases', Journal of Ethnopharmacology, 334, pp. 118506. doi:10.1016/j.jep.2024.118506 Meta-analysis / review
    https://doi.org/10.1016/j.jep.2024.118506
  3. Liu, H., Lu, X., Hu, Y. and Fan, X (2020) 'Chemical constituents of Panax ginseng and Panax notoginseng explain why they differ in therapeutic efficacy', Pharmacological Research, 161, pp. 105263. doi:10.1016/j.phrs.2020.105263 Meta-analysis / review
    https://doi.org/10.1016/j.phrs.2020.105263
  4. Fan, S., Zhang, Z., Su, H., Xu, P. and others (2020) 'Panax ginseng clinical trials: Current status and future perspectives', Biomedicine & Pharmacotherapy, 132, pp. 110832. doi:10.1016/j.biopha.2020.110832 Meta-analysis / review
    https://doi.org/10.1016/j.biopha.2020.110832
  5. Ni, X.C., Wang, H.F., Cai, Y.Y., Yang, D. and others (2022) 'Ginsenoside Rb1 inhibits astrocyte activation and promotes transfer of astrocytic mitochondria to neurons against ischemic stroke', Redox Biology, 54, pp. 102363. doi:10.1016/j.redox.2022.102363 Preclinical
    https://doi.org/10.1016/j.redox.2022.102363
  6. Arring, N.M., Millstine, D., Marks, L.A. and Nail, L.M (2018) 'Ginseng as a Treatment for Fatigue: A Systematic Review', Journal of Alternative and Complementary Medicine, 24(7), pp. 624-633. doi:10.1089/acm.2017.0361 Meta-analysis / review
    https://doi.org/10.1089/acm.2017.0361
  7. Zhou, G., Wang, C.Z., Mohammadi, S., Sawadogo, W.R. and others (2023) 'Pharmacological Effects of Ginseng: Multiple Constituents and Multiple Actions on Humans', The American Journal of Chinese Medicine, 51(5), pp. 1085-1104. doi:10.1142/S0192415X23500507 Meta-analysis / review
    https://doi.org/10.1142/S0192415X23500507
  8. Ramanathan, M.R. and Penzak, S.R (2017) 'Pharmacokinetic Drug Interactions with Panax ginseng', European Journal of Drug Metabolism and Pharmacokinetics, 42(4), pp. 545-557. doi:10.1007/s13318-016-0387-5 Meta-analysis / review
    https://doi.org/10.1007/s13318-016-0387-5
  9. Li, J., Huang, Q., Chen, J., Qi, H. and others (2021) 'Neuroprotective Potentials of Panax Ginseng Against Alzheimer's Disease: A Review of Preclinical and Clinical Evidences', Frontiers in Pharmacology, 12, pp. 688490. doi:10.3389/fphar.2021.688490 Meta-analysis / review
    https://doi.org/10.3389/fphar.2021.688490
  10. Geng, J., Dong, J., Ni, H., Lee, M.S. and others (2010) 'Ginseng for cognition', Cochrane Database of Systematic Reviews, (12), pp. CD007769. doi:10.1002/14651858.CD007769.pub2 Meta-analysis / review
    https://doi.org/10.1002/14651858.CD007769.pub2
  11. Attele, A.S., Wu, J.A. and Yuan, C.S (1999) 'Ginseng pharmacology: multiple constituents and multiple actions', 58(11), pp. 1685--1693. doi:10.1016/s0006-2952(99)00212-9 Traditional / reference
    https://doi.org/10.1016/s0006-2952(99)00212-9
  12. Kiefer, D. and Pantuso, T (2003) 'Panax ginseng', 68(8), pp. 1539--1542. Traditional / reference
    https://scholar.google.com/scholar?q=Panax%20ginseng
  13. Park, H.J., Kim, D.H. and Park, S.J (2014) 'Ginseng in traditional herbal prescriptions', 38(1), pp. 1--7. doi:10.5142/jgr.2012.36.3.225 Randomized trial
    https://doi.org/10.5142/jgr.2012.36.3.225
  14. Duke, J.A (2002) 'Handbook of Medicinal Herbs, Second Edition'. Traditional / reference
    https://scholar.google.com/scholar?q=Handbook%20of%20Medicinal%20Herbs%2C%20Second%20Edition
  15. Izzo, A.A. and Ernst, E (2009) 'Interactions between herbal medicines and prescribed drugs: an updated systematic review', Drugs, 69(13), pp. 1777-1798. doi:10.2165/11317010-000000000-00000 Meta-analysis / review
    https://doi.org/10.2165/11317010-000000000-00000
  16. Yuan, C.S., Wei, G., Dey, L., Karrison, T., Nahlik, L., Maleckar, S., Kasza, K., Ang-Lee, M. and Moss, J (2004) 'American ginseng reduces warfarin's effect in healthy patients: a randomized, controlled trial', Annals of Internal Medicine, 141(1), pp. 23-27. doi:10.7326/0003-4819-141-1-200407060-00011 Randomized trial
    https://doi.org/10.7326/0003-4819-141-1-200407060-00011
  17. Sotaniemi, E.A., Haapakoski, E. and Rautio, A (1995) 'Ginseng therapy in non-insulin-dependent diabetic patients', Diabetes Care, 18(10), pp. 1373-1375. doi:10.2337/diacare.18.10.1373 Randomized trial
    https://doi.org/10.2337/diacare.18.10.1373
  18. Vuksan, V., Sievenpiper, J.L., Koo, V.Y., Francis, T., Beljan-Zdravkovic, U., Xu, Z. and Vidgen, E (2000) 'American ginseng (Panax quinquefolius L) reduces postprandial glycemia in nondiabetic subjects and subjects with type 2 diabetes mellitus', Archives of Internal Medicine, 160(7), pp. 1009-1013. doi:10.1001/archinte.160.7.1009 Randomized trial
    https://doi.org/10.1001/archinte.160.7.1009
  19. Ang-Lee, M.K., Moss, J. and Yuan, C.S (2001) 'Herbal medicines and perioperative care', JAMA, 286(2), pp. 208-216. doi:10.1001/jama.286.2.208 Meta-analysis / review
    https://doi.org/10.1001/jama.286.2.208
  20. Groenewegen, W.A. and Heptinstall, S (1990) 'A comparison of the effects of an extract of feverfew and parthenolide, a component of feverfew, on human platelet activity in-vitro', Journal of Pharmacy and Pharmacology, 42(8), pp. 553-557. doi:10.1111/j.2042-7158.1990.tb07057.x Preclinical
    https://doi.org/10.1111/j.2042-7158.1990.tb07057.x
  21. Jiang, X., Williams, K.M., Liauw, W.S., Ammit, A.J., Roufogalis, B.D., Duke, C.C., Day, R.O. and McLachlan, A.J (2005) 'Effect of ginkgo and ginger on the pharmacokinetics and pharmacodynamics of warfarin in healthy subjects', British Journal of Clinical Pharmacology, 59(4), pp. 425-432. doi:10.1111/j.1365-2125.2005.02322.x Randomized trial
    https://doi.org/10.1111/j.1365-2125.2005.02322.x

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.