Rankings / Cognitive

Memantine

Cognitive · NMDA antagonist

Tier A

nmda-modulatorprescription
8 / 10
Tier A
Ev 8 Bn 5 Sf 9

Bottom line

Read Off Label grades Memantine as A (8.0/10) based on strong evidence, med benefit magnitude, and a low-risk safety profile.

Approved for moderate-to-severe AD; modest effect sizes on ADCS-ADL.

Studied, labeled, or reported-use context: 5-20 mg/day PO titrated — Rx; not individualized guidance.

What the evidence says

Approved for moderate-to-severe AD; modest effect sizes on ADCS-ADL. Off-label uses include augmentation in OCD and neuropathic pain. Healthy-person nootropic use is poorly studied and is not an approved indication; higher doses may produce cognitive blunting.

Mechanism

Low-affinity, uncompetitive NMDA receptor antagonist; blocks pathologic tonic glutamate activation while preserving physiologic bursts; also 5-HT3 and nicotinic antagonism

Studied, labeled, or reported dose & route

5-20 mg/day PO titrated

This records doses and routes described in studies, approved labeling, clinical practice, or documented use. It is not individualized guidance and does not establish safety; context changes with indication, formulation, health history, monitoring, and other medicines.

Citations

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Common questions

What does the evidence show about Memantine's effects?
Read Off Label rates the evidence for Memantine as Strong and the benefit magnitude as med, producing an overall grade of A (8.0/10). Approved for moderate-to-severe AD; modest effect sizes on ADCS-ADL.
What safety findings are reported for Memantine?
Memantine has a low risk profile in the database. Low (well-tolerated; dizziness, headache) Legal status: Rx.
What doses or routes are reported for Memantine?
5-20 mg/day PO titrated This is context from studies, approved labeling, clinical practice, or documented use; it is not individualized guidance and does not establish safety.
How does Memantine work?
Low-affinity, uncompetitive NMDA receptor antagonist; blocks pathologic tonic glutamate activation while preserving physiologic bursts; also 5-HT3 and nicotinic antagonism

This is an independent synthesis of published research by a non-clinician. Scores are opinions supported by citations, not prescriptions. See the full disclaimer and methodology for how this score was produced and what it does and doesn't mean.