Memantine: Difference between revisions

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NCLEX nursing pharmacology monographs — batch import
 
Add medication infobox (Drugbox) to monographs
 
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{{Drugbox
| name = Memantine
| brand = Namenda
| therapeutic = Anti-Alzheimer
| pharmacologic = NMDA receptor antagonist
| onset = Effect over weeks; ER once daily.
| halflife = Half-life 60 to 80 hours; level not routine.
| routes = PO (oral)
| highalert = No
| blackbox = None
| antidote = None.
| pregnancy = Not typically used.
}}
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''Nursing pharmacology study reference (NCLEX-style monograph). Numeric values are standard teaching ranges for study and '''must be verified against current manufacturer labeling before clinical use'''. This is educational content, not prescribing guidance.''
''Nursing pharmacology study reference (NCLEX-style monograph). Numeric values are standard teaching ranges for study and '''must be verified against current manufacturer labeling before clinical use'''. This is educational content, not prescribing guidance.''

Latest revision as of 16:09, 17 June 2026

Memantine
Drug monograph · NCLEX study reference
Trade namesNamenda
Therapeutic classAnti-Alzheimer
Pharmacologic classNMDA receptor antagonist
Onset / peak / durationEffect over weeks; ER once daily.
Half-life / levelHalf-life 60 to 80 hours; level not routine.
RoutesPO (oral)
High-alert (ISMP)No
Black box warningNone
Antidote / reversalNone.
Pregnancy / lactationNot typically used.

Nursing pharmacology study reference (NCLEX-style monograph). Numeric values are standard teaching ranges for study and must be verified against current manufacturer labeling before clinical use. This is educational content, not prescribing guidance.

Memantine (brand name Namenda) — Anti-Alzheimer; NMDA receptor antagonist.

Identification

  • Therapeutic class: Anti-Alzheimer.
  • Pharmacologic class: NMDA receptor antagonist.

Pharmacology

  • Mechanism of action: Blocks excess glutamate at NMDA receptors to limit excitotoxicity.
  • Onset / peak / duration: Effect over weeks; ER once daily.
  • Half-life / therapeutic level: Half-life 60 to 80 hours; level not routine.

Clinical use

  • Indications: Moderate to severe Alzheimer dementia, often with a cholinesterase inhibitor.
  • Usual dose, route, frequency: Titrated PO; ER once daily.
  • Maximum dose / adjustments: Reduce in severe renal impairment.

Safety

  • Contraindications: Hypersensitivity.
  • Black box warning: None.
  • Interactions: Urinary alkalinizers raise levels, other NMDA antagonists.
  • Pregnancy / lactation: Not typically used.
  • High-alert: No.

Adverse effects

  • Common side effects: Dizziness, headache, confusion, constipation.
  • Serious effects to report: Worsening confusion, severe dizziness.
  • Antidote / reversal: None.

Nursing process

  • Assessment before administration: Renal function, cognitive baseline.
  • Interventions during therapy: Titrate slowly.
  • Monitor: Cognition, renal function.
  • Evaluation / expected outcome: Slowed decline.

Patient teaching

  • Patient teaching: Effects are gradual; can pair with donepezil.
  • Notify provider if: Marked confusion, severe dizziness.
  • Administration tips: With or without food.