What is the classification of amisulpride?

Medical Advisory BoardAll articles are reviewed for accuracy by our Medical Advisory Board
Educational purpose only • Exercise caution as content is pending human review
Article Review Status
Submitted
Under Review
Approved

Last updated: September 30, 2025View editorial policy

Personalize

Help us tailor your experience

Which best describes you? Your choice helps us use language that's most understandable for you.

Amisulpride Drug Classification

Amisulpride is classified as an atypical (second-generation) antipsychotic that selectively blocks dopamine D2 and D3 receptors. 1, 2

Pharmacological Profile

Amisulpride has a unique pharmacological profile that distinguishes it from other antipsychotics:

  • Receptor Selectivity: Highly selective for dopamine D2/D3 receptor subtypes 3
  • Dose-Dependent Action:
    • At low doses (50-300 mg/day): Preferentially blocks presynaptic dopamine D2/D3 autoreceptors, enhancing dopaminergic neurotransmission 2, 4
    • At higher doses (400-800 mg/day): Antagonizes postsynaptic dopamine D2/D3 receptors, primarily in the limbic system rather than the striatum 2

Clinical Applications

Amisulpride's unique pharmacological profile allows for different therapeutic applications based on dosage:

  • Positive Symptoms: 400-800 mg/day for acute exacerbations of schizophrenia with predominantly positive symptoms 2
  • Negative Symptoms: 50-300 mg/day for predominantly negative symptoms of schizophrenia 2, 4
  • Maintenance Therapy: Effective for long-term treatment in chronic schizophrenia 2
  • Clozapine Augmentation: May be particularly suitable for augmenting clozapine in treatment-resistant schizophrenia 1

Safety Profile

According to cardiac safety classifications, amisulpride is categorized as follows:

  • Listed as a Class B drug in cardiac safety guidelines, indicating it has "a propensity of inducing QT prolongation" 5
  • This classification places it in an intermediate risk category for cardiac arrhythmias compared to Class A (no risk) and Class B* (pronounced QT prolongation) drugs 5

Comparative Efficacy

  • As effective as haloperidol, flupenthixol, and risperidone in controlling positive symptoms 2
  • More effective than haloperidol in controlling negative symptoms 2
  • More effective than haloperidol, risperidone, and flupenthixol in controlling affective symptoms 2
  • One of the few antipsychotics with demonstrated efficacy in patients with predominantly negative symptoms 6

Tolerability Advantages

  • Superior neurological tolerability profile compared to conventional antipsychotics 2
  • Lower incidence of extrapyramidal symptoms than typical antipsychotics 1, 2
  • Significantly less weight gain than olanzapine and risperidone 1
  • Favorable influence on lipid profiles 1

Clinical Considerations

  • Amisulpride is included in treatment guidelines for schizophrenia as a second-line option for positive symptoms when D2 partial agonists (like aripiprazole) have failed 5
  • It has been shown to improve quality of life and social functioning in long-term treatment 2
  • The drug has a low risk of drug-drug interactions, making it suitable for combination therapies 1

Amisulpride represents a unique member of the atypical antipsychotic class with its selective dopamine receptor activity and dose-dependent effects, allowing it to be tailored to different symptom profiles in schizophrenia.

References

Research

Is amisulpride an 'atypical' atypical antipsychotic agent?

International clinical psychopharmacology, 2000

Research

Clinical update on amisulpride in deficit schizophrenia.

International clinical psychopharmacology, 1997

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Amisulpride: progress and outcomes.

Current medical research and opinion, 2002

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.

Have a follow-up question?

Our Medical A.I. is used by practicing medical doctors at top research institutions around the world. Ask any follow up question and get world-class guideline-backed answers instantly.