What is the recommended dosage of Namenda (memantine) for dementia?

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Recommended Dosage of Namenda (Memantine) for Dementia

The recommended dosage of Namenda (memantine) for dementia is 5 mg once daily initially, with gradual titration to a target dose of 20 mg/day (10 mg twice daily), increasing by 5 mg increments weekly. 1

Dosing Schedule and Titration

The FDA-approved dosing regimen for memantine follows a specific titration schedule:

  1. Initial dose: 5 mg once daily
  2. Week 2: Increase to 10 mg/day (5 mg twice daily)
  3. Week 3: Increase to 15 mg/day (5 mg and 10 mg as separate doses)
  4. Week 4 and beyond: Reach target dose of 20 mg/day (10 mg twice daily)

The minimum recommended interval between dose increases is one week, allowing for better tolerability 1.

Administration Considerations

  • Memantine can be taken with or without food
  • If doses are missed for several days, restart at a lower dose and retitrate
  • For oral solution formulation (2 mg/mL), use the provided dosing syringe and do not mix with other liquids 1

Special Populations

Renal Impairment

  • For patients with severe renal impairment (creatinine clearance 5-29 mL/min), the recommended target dose is reduced to 10 mg/day (5 mg twice daily) 1

Hepatic Impairment

  • Use with caution in patients with severe hepatic impairment 1

Extended-Release Formulation

An extended-release (ER) formulation is available as an alternative:

  • Namenda XR 28 mg once daily
  • Provides more convenient dosing and may improve adherence
  • Capsules can be opened and sprinkled on applesauce for patients with swallowing difficulties 2

Efficacy Considerations

Memantine is indicated specifically for moderate to severe Alzheimer's dementia 1. It works as an N-methyl-D-aspartate (NMDA) receptor antagonist that partially blocks glutamatergic neurotransmission in the central nervous system 3.

Clinical evidence shows that:

  • Memantine is not effective for mild Alzheimer's disease 4
  • Combination therapy with memantine plus a cholinesterase inhibitor (e.g., donepezil) is recommended for moderate to severe Alzheimer's disease 4, 5
  • Memantine should be deprescribed for individuals with mild cognitive impairment 6, 4

Monitoring and Discontinuation

Consider discontinuing memantine if:

  • Clinically meaningful worsening of dementia occurs over 6 months
  • No benefit is observed during treatment
  • Patient develops severe or end-stage dementia
  • Intolerable side effects develop (e.g., confusion, dizziness, falls)
  • Poor medication adherence 6, 4

When discontinuing memantine:

  • Reduce dose by 50% every 4 weeks until reaching the initial starting dose
  • After 4 weeks at the starting dose, discontinue completely
  • Monitor for worsening and consider reinitiating if clinically meaningful decline occurs 6, 4

Common Side Effects

The most common adverse events include:

  • Dizziness
  • Headache
  • Confusion
  • Constipation 1

Important Cautions

  • Conditions that raise urine pH may decrease urinary elimination of memantine, resulting in increased plasma levels 1
  • Do not discontinue memantine in patients with clinically meaningful psychotic symptoms, agitation, or aggression until these symptoms have stabilized 6, 4
  • Continue treatment in patients who have had meaningful reduction in neuropsychiatric symptoms even with cognitive/functional decline 6, 4

References

Research

Drug forecast: memantine, prototype of a new approach to treatment of dementia.

The Consultant pharmacist : the journal of the American Society of Consultant Pharmacists, 2003

Guideline

Dementia Management

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

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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