01 Identity and provenance
- Accepted binomial
- Lycium barbarum
- Common names
- Goji Berry
- Family (APG IV)
- Solanaceae
- Part used
- Fruit
- Verification tier
- Tier 2 · Verified Clinical columns reviewed and a source is on record.
- Reviewer note (2026 audit)
- Lam AY & Elmer GW. Ann Pharmacother 2001;35:1199-201. PubMed 11675844 | Leung H & El-Kadiki S. Am J Health Syst Pharm 2009;66:2225-7 | PMC5598317 (gouqizi wine case) | VERIFIED 2026 (batch 7) - synthetic analogue, application, interactions, side effects and references populated from retrieved primary/regulatory sources. Interactions labelled CLINICAL vs THEORETICAL. Marketed-formulation column intentionally blank. | INTERACTION
02 Constituent chemistry
| Chemical class | Marker compound | Synthetic analogue in use |
|---|---|---|
| Polysaccharides, carotenoids | Zeaxanthin dipalmitate
Fruit
|
No analogue. Lycium barbarum polysaccharides and zeaxanthin dipalmitate are the marker constituents. |
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
- Chinese Pharmacopoeia drug (Gouqizi) at 6-12 g daily; traditional tonic for vision, immunity and liver. Widely sold as juice and dried fruit outside Asia, where consumers do not regard it as a medicine.
- Reported adverse effects
- Generally well tolerated as food. The risk profile is dominated by the warfarin interaction rather than intrinsic toxicity.
04 Interaction matrix
Source column, verbatim: WARFARIN - FOUR INDEPENDENT PUBLISHED CASES, WHICH IS UNUSUALLY STRONG FOR A FOOD. A 71-year-old on warfarin after knee surgery drank goji juice for four days and presented with epistaxis, bruising and rectal bleeding at an indeterminate INR (PT > 120 s), resolving to 2.6 with phytonadione; Naranjo score 6 (probable). A 61-year-old woman reached INR 4.1 after four days of concentrated L. barbarum tea. A 65-year-old man bled after gouqizi wine at more than 6-12 g. MECHANISM IS NOT SETTLED: in-vitro CYP2C9 inhibition of S-warfarin metabolism is WEAK (Ki 3.4 mg/mL), so something other than CYP450 is probably contributing. Treat as a real clinical interaction with an unexplained mechanism - increase INR monitoring, and ask about goji explicitly, since patients classify juice as food, not herbal medicine.
Normalised onto 1 canonical drug class below.
Curated from the reviewed source
| Drug class | Severity | Mechanism type | Provenance | Expected effect | |
|---|---|---|---|---|---|
|
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.
| |||||
Predicted from constituent chemistry
| Drug class | Severity | Mechanism type | Provenance | Expected effect | |
|---|---|---|---|---|---|
|
Cardiac glycosides (digoxin, digitoxin)
Cardiovascular
|
4Contraindicated | PD-additive + PK-transporter + assay interference | predicted D | Nausea, xanthopsia, bradyarrhythmia, AV block, ventricular tachycardia an… | why ▾ |
Chemistry of this pair. Hydrocolloids raise luminal viscosity and physically entrap co-administered drug molecules, delaying and reducing absorption. Class mechanism. Cardenolide- and bufadienolide-bearing plants are themselves Na+/K+-ATPase inhibitors, so co-administration is pharmacological overdose. Several also inhibit intestinal P-glycoprotein, raising digoxin exposure, and cross-react with digoxin immunoassays so that serum levels become uninterpretable.
| |||||
|
Antidiabetic drugs (insulin, sulfonylureas, biguanides, GLP-1, SGLT2)
Endocrine
|
3Major | PD-additive | predicted D | Symptomatic hypoglycaemia, sweating, tremor, confusion; severe events rep… | why ▾ |
Chemistry of this pair. Hydrocolloids raise luminal viscosity and physically entrap co-administered drug molecules, delaying and reducing absorption. Class mechanism. Hypoglycaemic botanicals act through insulin secretagogue, insulin-sensitising, alpha-glucosidase-inhibiting or glucose-transport routes. Added to a titrated pharmacological regimen the effects summate rather than plateau.
| |||||
|
Antibacterials and anthelmintics
Infection
|
2Moderate | PK-chelation + PK-CYP | predicted D | Treatment failure from subtherapeutic antibiotic concentrations, or raise… | why ▾ |
Chemistry of this pair. Hydrocolloids raise luminal viscosity and physically entrap co-administered drug molecules, delaying and reducing absorption. Class mechanism. Cation- and tannin-rich botanicals chelate tetracyclines and fluoroquinolones; efflux-pump-inhibiting and CYP-modulating constituents alter macrolide, rifamycin and azole exposure. Anthelmintic botanicals add to praziquantel and albendazole effect.
| |||||
|
Iron, calcium and mineral supplements
Nutrition
|
2Moderate | PK-chelation | predicted D | Failure of iron-deficiency correction, unexplained non-response to oral i… | why ▾ |
Chemistry of this pair. Hydrocolloids raise luminal viscosity and physically entrap co-administered drug molecules, delaying and reducing absorption. Class mechanism. Tannins, phytates, oxalates and mucilage form insoluble complexes with divalent and trivalent cations in the gut lumen, reducing absorption of both the mineral and any co-administered chelating drug.
| |||||
|
Thyroid hormones and antithyroid drugs
Endocrine
|
2Moderate | PK-absorption + PD-modulation | predicted D | Iatrogenic hyper- or hypothyroidism, unexplained TSH drift, loss of euthy… | why ▾ |
Chemistry of this pair. Hydrocolloids raise luminal viscosity and physically entrap co-administered drug molecules, delaying and reducing absorption. Class mechanism. Guggulsterone stimulates thyroid function and T4-to-T3 conversion; goitrogenic glucosinolates and lithospermic acid suppress it; high-fibre and cation-rich botanicals bind levothyroxine in the gut and reduce absorption.
| |||||
05 Hazard register
06 Confusable material
These entries could be mistaken for this one in trade, in the herbarium, or in a prescription. Powdered material is often indistinguishable, so the check is macroscopic, microscopic and chromatographic rather than nominal.
| Vaccinium macrocarpon
Cranberry |
Ericaceae | Shares the common name "berry" |
| Vaccinium myrtillus
Bilberry |
Ericaceae | Shares the common name "berry" |
| Morus alba
Mulberry |
Moraceae | Shares the common name "berry" |
| Berberis vulgaris
Barberry |
Berberidaceae | Shares the common name "berry" |
| Anamirta cocculus
Fish Berry |
Menispermaceae | Shares the common name "berry" |
| Sambucus nigra
Elderberry |
Adoxaceae | Shares the common name "berry" |
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 |
|---|---|---|---|---|
| Panax ginseng
Ginseng |
Araliaceae | 6 | 0.60 | |
| Plantago ovata
Isabgol |
Plantaginaceae | 5 | 0.71 | |
| Senegalia senegal
Gum Acacia |
Fabaceae | 5 | 0.83 | |
| Salvia hispanica
Chia |
Lamiaceae | 5 | 0.83 | |
| Cyamopsis tetragonoloba
Guar |
Fabaceae | 5 | 0.83 | |
| Astragalus gummifer
Tragacanth |
Fabaceae | 5 | 0.83 |
10 References and notes
Source column: Rivera CA et al. Pharmacotherapy 2012;32:e50-3. PubMed 22392461
Rivera CA et al. Pharmacotherapy 2012
32:e50-3. PubMed 22392461
BibTeX for all 2 records
@article{RiveraCAet2012,
title = {Rivera CA et al. Pharmacotherapy 2012},
author = {Rivera CA et al.},
journal = {Pharmacotherapy},
year = {2012},
}
@article{anon,
title = {32:e50-3. PubMed 22392461},
}
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