Which of the following is NOT a general characteristic of second‑generation antipsychotics?

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Second-Generation Antipsychotics: Identifying the Incorrect Characteristic

The statement "Has effects limited to positive symptoms, with no effect on negative symptoms" is NOT a general characteristic of second-generation antipsychotics—this is the incorrect option.

Understanding Second-Generation Antipsychotic Properties

The question asks you to identify which characteristic does NOT apply to second-generation antipsychotics. Let me break down each option:

Effects on Positive vs. Negative Symptoms

  • Second-generation antipsychotics DO have effects on negative symptoms, contrary to the first option 1, 2
  • A 2009 meta-analysis of 150 studies with 21,533 participants found that several second-generation antipsychotics (amisulpride, clozapine, olanzapine, risperidone) showed efficacy for overall symptoms, though the effect on negative symptoms specifically was not consistently superior across all agents 1
  • Second-generation antipsychotics provide "at least modest promise of reduction of negative symptoms and enhancement of some aspects of cognition," unlike first-generation agents which "had little or no effect on the most disabling, core symptoms associated with withdrawal of interests and interpersonal relationships" 2
  • This makes the first statement FALSE and therefore the correct answer to identify

Lower Incidence of Extrapyramidal Symptoms (EPS)

  • Second-generation antipsychotics ARE associated with lower EPS compared to high-potency first-generation agents 1, 3, 4
  • The 2009 meta-analysis confirmed that second-generation drugs "induced fewer extrapyramidal side-effects than did haloperidol (even at low doses)" 1
  • A 2017 review stated that "the incidence of treatment-emergent extrapyramidal side effects is lower" with second-generation agents 3
  • This statement is TRUE about second-generation antipsychotics

Better Tolerability

  • Second-generation antipsychotics ARE generally more easily tolerated than first-generation agents 3, 2
  • Evidence indicates that second-generation drugs "show an improved safety and tolerability profile compared with FGAs" with "less impairment of cognitive function and treatment-related negative symptoms" 3
  • They have "strikingly less morbidity, contributing little or no EPS" 2
  • This statement is TRUE about second-generation antipsychotics

Cognitive Improvement

  • Second-generation antipsychotics HAVE been found to improve cognition 3, 2
  • They provide "enhancement of some aspects of cognition" 2
  • There is "less impairment of cognitive function" compared to first-generation agents 3
  • This statement is TRUE about second-generation antipsychotics

Critical Clinical Context

Important caveat: The traditional classification system distinguishing first- from second-generation antipsychotics is "clinically misleading and should not guide treatment selection" according to current guidelines 5, 6. Treatment decisions should be based on individual drug pharmacodynamic profiles, side-effect profiles, and patient-specific factors rather than generational labels 5, 6.

References

Research

Extrapyramidal motor side-effects of first- and second-generation antipsychotic drugs.

The British journal of psychiatry : the journal of mental science, 2012

Guideline

Antipsychotic Medication Classification and Treatment

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Antipsychotic Medication Selection and Management

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 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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