01 Identity and provenance
- Accepted binomial
- Aloe barbadensis Mill
- Common names
- Aloe Vera
- Family (APG IV)
- Asphodelaceae
- Part used
- Leaves
- Verification tier
- Tier 2 · Verified Clinical columns reviewed and a source is on record.
- Reviewer note (2026 audit)
- CORRECTED - Chemical composition / class: Lupeol is a pentacyclic triterpenoid, not a phytosterol.
Reference not supplied - claim unverified against primary literature.
02 Constituent chemistry
| Chemical class | Marker compound | Synthetic analogue in use |
|---|---|---|
| polysaccharide | Acemannan, glucomannan
Leaves
|
carboxymethyl cellulose, HPMC, PVA, PEG, Hyaluronic acid |
| Triterpenoid | Lupeol
Leaves
|
none |
| Anthraquinone | Aloe-emodin
Leaves
|
none |
| Anthraquinone Glycoside | Aloin (Barbaloin)
Leaves
|
none |
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
- Topical creams and ointments, oral drug delivery
Anti-inflammatory, wound healing, bowel disease, anti cancer
laxative, antioxidant - Marketed in
- Topical gel : patanjali, Himalya Oral juice: Kapiva, Dabur, Forever
capsule, tablet - Reported adverse effects
- hypoglycemia, fall in blood pressure,dizziness
hypokalemia, dehydration, muscle weakness, diarrhea
04 Interaction matrix
Source column, verbatim: Antidiabetic drugs, antihypertensive
diuretics
Normalised onto 3 canonical drug classes below.
Curated from the reviewed source
| Drug class | Severity | Mechanism type | Provenance | Expected effect | |
|---|---|---|---|---|---|
|
Antidiabetic drugs (insulin, sulfonylureas, biguanides, GLP-1, SGLT2)
Endocrine
|
3Major | PD-additive | curated B | 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.
| |||||
|
Diuretics
Renal
|
3Major | PD-additive + electrolyte-mediated | curated B | Hypokalaemia, hyponatraemia, dehydration, muscle weakness, cramps, arrhyt… | why ▾ |
Chemistry of this pair. Hydroxyanthracene derivatives are colonic prokinetics activated by gut flora; chronic use produces potassium loss through the colon. Class mechanism. Aquaretic and saluretic botanicals add to renal potassium and sodium loss. Anthraquinone laxatives compound this through colonic potassium loss, and glycyrrhizin causes mineralocorticoid-like retention of sodium with kaliuresis.
| |||||
|
Antihypertensives
Cardiovascular
|
2Moderate | PD-additive | curated B | Orthostatic hypotension, dizziness, syncope and falls; or loss of blood-p… | why ▾ |
Class mechanism. Vasodilator, diuretic, ACE-inhibitory and calcium-antagonist activity in botanical extracts adds to prescribed blood-pressure lowering. A minority (ephedrine-, glycyrrhizin- and caffeine-bearing) act in the opposite direction and antagonise control.
| |||||
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. Hydroxyanthracene derivatives are colonic prokinetics activated by gut flora; chronic use produces potassium loss through the colon. 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.
| |||||
|
Corticosteroids
Endocrine
|
3Major | PD-additive + PK-CYP3A4 | predicted D | Pseudohyperaldosteronism: hypertension, hypokalaemia, oedema, myopathy; C… | why ▾ |
Chemistry of this pair. Hydroxyanthracene derivatives are colonic prokinetics activated by gut flora; chronic use produces potassium loss through the colon. Class mechanism. Glycyrrhizin inhibits 11-beta-hydroxysteroid dehydrogenase type 2 and prolongs cortisol half-life, potentiating mineralocorticoid effect. Anthraquinone laxatives compound steroid-driven potassium loss, and CYP3A4 inhibition raises systemic corticosteroid exposure.
| |||||
|
Laxatives and antidiarrhoeals
Gastrointestinal
|
3Major | PD-additive | predicted D | Cramping, diarrhoea, electrolyte loss, melanosis coli with chronic anthra… | why ▾ |
Chemistry of this pair. Hydroxyanthracene derivatives are colonic prokinetics activated by gut flora; chronic use produces potassium loss through the colon. Class mechanism. Anthraquinone and mucilage botanicals add to stimulant and bulk laxative action; tannin-rich astringents oppose it.
| |||||
|
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
The audit recorded no hazard beyond the interaction profile. The controlled-vocabulary field reads not assessed, which means the assessment has not been done rather than that it came back clear.
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.
| Aloe ferox
Cape Aloe |
Asphodelaceae | Same genus (Aloe) |
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 |
|---|---|---|---|---|
| Rubia cordifolia
Manjistha |
Rubiaceae | 6 | 0.43 | |
| Senna alexandrina
Senna |
Fabaceae | 6 | 0.40 | |
| Echinacea purpurea
Echinacea |
Asteraceae | 6 | 0.40 | |
| Panax ginseng
Ginseng |
Araliaceae | 6 | 0.46 | |
| Senegalia senegal
Gum Acacia |
Fabaceae | 5 | 0.56 | |
| Salvia hispanica
Chia |
Lamiaceae | 5 | 0.56 |
10 References and notes
No citation is on record for this entry. That is itself the finding: the audit flagged it, and it is why the entry does not carry an A evidence grade.
Curator notes
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