What is the starting dose of Exelon (Rivastigmine) patch for mild to moderate dementia?

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Last updated: November 3, 2025View editorial policy

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Exelon Patch Starting Dose for Mild to Moderate Dementia

The starting dose of the Exelon (rivastigmine) transdermal patch is 4.6 mg/24 hours (5 cm² patch), applied once daily. 1, 2

Initial Dosing Protocol

  • Begin with the 4.6 mg/24 hours patch applied to clean, dry, hairless skin on the upper or lower back, upper arm, or chest, rotating application sites daily. 1, 2

  • Maintain the starting dose for a minimum of 4 weeks before considering dose escalation to allow assessment of tolerability and initial therapeutic response. 3, 4

  • The 4.6 mg/24 hours starting dose applies to both treatment-naïve patients and those transitioning from other cholinesterase inhibitors. 5

Dose Titration Strategy

  • After at least 4 weeks on the starting dose, increase to 9.5 mg/24 hours (10 cm² patch) if the patient tolerates the initial dose well and requires higher dosing based on clinical response. 3, 1

  • The 9.5 mg/24 hours patch is considered the recommended maintenance dose for most patients with mild to moderate Alzheimer's disease. 1, 2

  • For patients experiencing continued functional and cognitive decline on the 9.5 mg/24 hours patch, escalation to 13.3 mg/24 hours (15 cm² patch) can be considered after adequate trial duration. 4, 1

Evidence Supporting This Approach

  • The rivastigmine transdermal patch formulation provides continuous drug delivery with improved tolerability compared to oral capsules, particularly regarding gastrointestinal side effects like nausea and vomiting. 2, 5

  • In clinical trials, rivastigmine at doses of 6-12 mg daily orally or 9.5 mg daily transdermally demonstrated statistically significant benefits on cognitive function (ADAS-Cog improvement of -2.1 points), activities of daily living, and clinician-rated global assessment compared to placebo. 2

  • Real-world effectiveness data from 1204 patients showed that the rivastigmine patch maintained cognitive function over 18 months with 88.2% of caregivers preferring the transdermal patch to oral medications. 5

Critical Dosing Considerations

  • Abrupt switching from oral rivastigmine to patch without proper dose conversion creates effective underdosing, which can precipitate cholinergic withdrawal manifesting as acute cognitive decline and hallucinations. 3

  • When converting from oral rivastigmine, patients on 6 mg oral twice daily should transition to the 9.5 mg/24 hours patch, not the 4.6 mg/24 hours starting dose, to maintain therapeutic equivalence. 3

  • Allow 6-12 months to assess full therapeutic response after reaching maintenance dosing, as cognitive benefits may take time to manifest. 3, 4

Monitoring for Adverse Effects

  • The most common adverse events are nausea, vomiting, diarrhea, anorexia, and dizziness, consistent with cholinergic effects. 2, 6

  • These side effects can be managed by ensuring the patch is applied after meals and monitoring for skin reactions at application sites. 3

  • Patients receiving rivastigmine are approximately twice as likely to withdraw from treatment compared to placebo (OR 2.01), primarily due to gastrointestinal adverse events. 2

References

Research

Rivastigmine for Alzheimer's disease.

The Cochrane database of systematic reviews, 2015

Guideline

Management of Cognitive Decline and Hallucinations

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Transitioning from Oral to Transdermal Rivastigmine

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Rivastigmine for Alzheimer's disease.

The Cochrane database of systematic reviews, 2000

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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