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Tricyclic Antidepressants (TCAs), including Desipramine (Norpramin), Imipramine (Tofranil), Clomipramine (Anafranil), and Amitriptyline (Elavil), inhibit serotonin and norepinephrine reuptake and also block other receptors. They are used for depression, pain conditions, and insomnia. Common adverse effects include anticholinergic effects, sedation, orthostatic hypotension, and weight gain. They have a narrow therapeutic window and so require plasma-level monitoring. Abrupt discontinuation can...
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The Forced Swim Test as a Model of Depressive-like Behavior
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Fluoxetine induced extrapyramidal symptoms : case reports.

S H Nizamie1, P N Suresh Kumar

  • 1S. HAQUE NIZAMIE, M.D., D.P.M., Professor of Psychiatry, Central Institute of Psychiatry, Ranchi -834006.

Indian Journal of Psychiatry
|April 16, 2011
PubMed
Summary

Fluoxetine can rarely cause extrapyramidal symptoms, such as movement disorders. This may occur due to serotonin affecting dopamine pathways in the brain.

Keywords:
Fluoxetineextrapyramidal symptoms

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Area of Science:

  • Neuroscience
  • Pharmacology
  • Clinical Medicine

Background:

  • Fluoxetine is a widely prescribed selective serotonin reuptake inhibitor (SSRI).
  • Extrapyramidal symptoms (EPS) are movement disorders typically associated with dopamine pathway dysfunction.
  • While SSRIs are generally not associated with EPS, rare cases have been reported.

Purpose of the Study:

  • To report a rare case of extrapyramidal symptoms induced by fluoxetine.
  • To explore the potential mechanism underlying fluoxetine-induced EPS.

Main Methods:

  • This is a case report detailing a patient's experience with fluoxetine.
  • Clinical observations and pharmacological principles were used to analyze the event.

Main Results:

  • The patient developed extrapyramidal symptoms after initiating fluoxetine treatment.
  • A proposed mechanism involves serotonin's influence on dopamine blockade at the nigrostriatal level.

Conclusions:

  • Fluoxetine can, in rare instances, induce extrapyramidal symptoms.
  • Serotonin-mediated dopamine blockade is a plausible mechanism for this adverse effect.