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:
- Initial dose: 5 mg once daily
- Week 2: Increase to 10 mg/day (5 mg twice daily)
- Week 3: Increase to 15 mg/day (5 mg and 10 mg as separate doses)
- 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