01 Identity and provenance
- Accepted binomial
- Salix alba
- Common names
- White Willow
- Family (APG IV)
- Salicaceae
- Part used
- Bark
- Verification tier
- Tier 2 · Verified Clinical columns reviewed and a source is on record.
- Reviewer note (2026 audit)
- USP Safety Review of Willow Bark: PubMed 31604354 | VERIFIED 2026 - synthetic analogue, application, interactions, side effects and references populated from retrieved primary/regulatory sources (see References). Interaction entries are labelled CLINICAL (case reports or trials in humans) vs THEORETICAL (in-vitro or animal only). Marketed-formulation column intentionally left blank. | HOST FACTOR
02 Constituent chemistry
| Chemical class | Marker compound | Synthetic analogue in use |
|---|---|---|
| Phenolic glycosides | Salicin
Bark
|
Aspirin, Salicylic acid (TRUE STRUCTURAL relationship - salicin is a natural prodrug metabolised to salicylate). |
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
- Low back pain, osteoarthritis, rheumatic complaints, headache and fever. Approved by German Commission E. Note the salicin dose alone is likely insufficient for analgesia - flavonoids and polyphenols contribute.
- Reported adverse effects
- CONTRAINDICATED in salicylate/aspirin hypersensitivity, G6PD deficiency (haemolytic anaemia), active peptic ulcer, third-trimester pregnancy, and in children (Reye syndrome concern). 240 mg salicin can yield approx. 113 mg salicylic acid. Less gastric mucosal damage than aspirin in comparative work.
04 Interaction matrix
Source column, verbatim: CLINICAL: anticoagulants, antiplatelets, other salicylates and NSAIDs - EMA monograph recommends an explicit warning on concomitant anticoagulant use. High tannin content may impair nutrient absorption on prolonged use.
Normalised onto 3 canonical drug classes 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 ▾ |
Chemistry of this pair. Salicylate esters hydrolyse to salicylic acid, giving irreversible platelet COX-1 acetylation equivalent to low-dose aspirin. 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.
| |||||
|
Antiplatelet agents
Haemostasis
|
3Major | PD-additive | curated A | Prolonged bleeding time, surgical and post-procedural bleeding, bruising,… | why ▾ |
Chemistry of this pair. Salicylate esters hydrolyse to salicylic acid, giving irreversible platelet COX-1 acetylation equivalent to low-dose aspirin. Class mechanism. Organosulfur compounds, gingerols, salicylates, ginkgolides and eugenol inhibit thromboxane A2 synthesis, platelet aggregation and PAF-mediated activation, duplicating the pharmacology of aspirin and P2Y12 blockers.
| |||||
|
NSAIDs
Analgesia
|
3Major | PD-additive | curated A | Peptic ulceration, upper GI bleeding, acute kidney injury in volume-deple… | why ▾ |
Chemistry of this pair. Salicylate esters hydrolyse to salicylic acid, giving irreversible platelet COX-1 acetylation equivalent to low-dose aspirin. Class mechanism. Salicylate-, coumarin- and eugenol-bearing botanicals add both antiplatelet activity and direct gastric mucosal irritation to cyclo-oxygenase inhibition; several also reduce renal prostaglandin-dependent perfusion.
| |||||
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.
| Veratrum album
White Hellebore |
Melanthiaceae | Shares the common name "white" |
| Epilobium parviflorum
Small-flowered Willowherb |
Onagraceae | Shares the common name "willow" |
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 |
|---|---|---|---|---|
| Trachyspermum ammi
Ajwain |
Apiaceae | 3 | 0.75 | |
| Kaempferia galanga
Chandramula |
Zingiberaceae | 3 | 0.75 | |
| Alpinia galanga
Greater Galangal |
Zingiberaceae | 3 | 0.75 | |
| Gaultheria fragrantissima
Wintergreen |
Ericaceae | 3 | 1.00 | |
| Filipendula ulmaria
Meadowsweet |
Rosaceae | 3 | 1.00 | |
| Harpagophytum procumbens
Devil's Claw |
Pedaliaceae | 3 | 0.75 |
10 References and notes
Source column: EMA/HMPC Assessment report on Salix cortex
EMA/HMPC Assessment report on Salix cortex
BibTeX for all 1 records
@article{anon,
title = {EMA/HMPC Assessment report on Salix cortex},
}
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