Donepezil
| Evidence Level: L5 | Predicted Indications: 8 |
Table of Contents
- Donepezil
- Pharmacist Assessment Report
- Donepezil: Acetylcholinesterase inhibitor → psychogenic movement disorders
- One-Sentence Summary
- Quick Overview
- Why is This Prediction Reasonable?
- Clinical Trial Evidence
- Literature Evidence
- Canada Market Information
- Safety Considerations
- Conclusion and Next Steps
- Disclaimer
Donepezil: Acetylcholinesterase inhibitor → psychogenic movement disorders
One-Sentence Summary
Donepezil is a cholinesterase inhibitor marketed in Canada under many licences. The TxGNN model predicts it may be effective for psychogenic movement disorders, but no clinical trials and no publications currently support this specific prediction, so it remains a model-only signal.
Quick Overview
| Item | Content |
|---|---|
| Original Indication | Not recorded in the local data |
| Predicted New Indication | Psychogenic movement disorders |
| TxGNN Prediction Score | 0.9923 |
| Evidence Level | L5 |
| Canada Market Status | Marketed (marketed DINs on record: at least 20) |
| Number of DINs | at least 20 |
| Recommended Decision | Hold |
Why is This Prediction Reasonable?
Detailed mechanism-of-action data for donepezil is not available in the data compiled for this report. Donepezil is generally known as an acetylcholinesterase inhibitor that raises cholinergic tone, and cholinergic signalling in the basal ganglia is involved in the control of movement.
That link is plausible but speculative for this condition. Psychogenic movement disorders are functional in origin, and no established pharmacological target for donepezil has been identified for them. The high model score is therefore not backed by any trial, case report or mechanistic study in the compiled data.
Clinical Trial Evidence
Currently no related clinical trials registered.
Literature Evidence
Currently no related literature available.
Canada Market Information
The data compiled for this report show 20 valid single-ingredient licences, with no cancelled licences. The list may be partial. Dosage form and approved-indication text are not recorded in the local data.
| DIN | Product Name | Dosage Form | Approved Indication |
|---|---|---|---|
| 02232044 | ARICEPT | Not recorded | Not recorded |
| 02232043 | ARICEPT | Not recorded | Not recorded |
| 02362279 | APO-DONEPEZIL | Not recorded | Not recorded |
| 02328682 | SANDOZ DONEPEZIL | Not recorded | Not recorded |
| 02340615 | TEVA-DONEPEZIL | Not recorded | Not recorded |
Safety Considerations
- Drug Interactions: 100 interactions were found in the interaction screening. The entries listed include:
- Major: Bupropion
- Moderate: Famotidine, Ranitidine, Cimetidine, Hyoscyamine, Atropine, Glycopyrronium, Clidinium, Dicyclomine, Dexamethasone, Metronidazole, Loperamide, Dolasetron, Picosulfuric acid
- Minor: Aprepitant, Acetylsalicylic acid, Lorcaserin, Clarithromycin
Many of the moderate entries are anticholinergic agents, which may oppose donepezil’s pharmacological action.
For warnings and contraindications, please refer to the package insert.
Conclusion and Next Steps
Decision: Hold
Rationale: The prediction score is high (0.9923), but no clinical trials or publications address psychogenic movement disorders. The mechanistic rationale is speculative, so the evidence level is L5.
To proceed, the following is needed:
- Any direct clinical or preclinical evidence in psychogenic (functional) movement disorders
- Detailed mechanism-of-action data for donepezil
- Package insert warnings and contraindications from Health Canada
- A safety review, since the interaction screening flagged a major interaction (bupropion) and several anticholinergic combinations, and the literature on cholinesterase inhibitors reports movement-disorder adverse effects in some patients
Disclaimer
This content is for research purposes only and does not constitute medical advice. Clinical validation is required before any clinical application.