Femoxetine and amitriptyline in general practice: a randomized double-blind group comparison

Pharmacopsychiatry
|September 1, 1986
PubMed

Insights

This study found that femoxetine and amitriptyline showed similar effectiveness for major depressive disorder over six weeks. Amitriptyline had a faster initial effect on sleep symptoms, but both drugs had comparable dropout rates due to side effects.

Area of Science:

  • Psychiatry
  • Clinical Pharmacology

Background:

  • Major depressive disorder (MDD) is a prevalent mental health condition requiring effective treatment options.
  • Selective serotonin reuptake inhibitors (SSRIs) and tricyclic antidepressants (TCAs) are common pharmacological approaches.

Purpose of the Study:

  • To compare the efficacy and tolerability of femoxetine (an SSRI) versus amitriptyline (a TCA) in patients with definite major depressive disorder.
  • To assess treatment outcomes using the Hamilton Depression Scale (HDS) and clinical global assessment.

Main Methods:

  • A randomized, double-blind, group comparative study involving 81 patients diagnosed with definite major depressive disorder.
  • Patients received either 600 mg daily of femoxetine or 150 mg daily of amitriptyline for six weeks.
  • Efficacy was measured by HDS scores and global assessments; side effects and dropout rates were also recorded.

Main Results:

  • No statistically significant differences in overall efficacy were observed between femoxetine and amitriptyline after six weeks.
  • Amitriptyline demonstrated a significantly greater reduction in HDS sleep item scores at week 2.
  • Dropout rates due to side effects were similar (14-15%), though femoxetine had fewer reported side effects overall (38% vs. 14%).

Conclusions:

  • Femoxetine and amitriptyline exhibit comparable overall efficacy for major depressive disorder in general practice settings over a six-week period.
  • Amitriptyline may offer a faster onset of action, particularly concerning sleep disturbances.
  • Both treatments present distinct side effect profiles, with femoxetine associated with nausea and amitriptyline with anticholinergic effects; femoxetine did not cause weight gain.

Related Concept Videos

Peripherally and Centrally Acting Muscle Relaxants: A Comparison01:09

Peripherally and Centrally Acting Muscle Relaxants: A Comparison

Skeletal muscle relaxants can target the central nervous system [CNS] to reduce muscle tension or act directly at the neuromuscular junction to induce temporary paralysis. These two classes of muscle relaxants are called centrally acting muscle relaxants and peripherally acting muscle relaxants. They differ in their action, mechanism, administration route, and clinical uses.
Centrally acting muscle relaxants can be further divided into spasmolytic and antispasmodic drugs. Spasmolytic drugs,...
Antidepressant Drugs: Overview01:25

Antidepressant Drugs: Overview

Antidepressant drugs are a class of medications primarily used for treating various mood disorders, including major depression, anxiety disorders, and other related conditions. These medicines work by modulating the neurotransmitter balance within the brain, alleviating depressive symptoms. Antidepressants can be broadly categorized into several groups according to their mechanism of action and chemical structure: Selective Serotonin Reuptake Inhibitors (SSRIs), Serotonin-Norepinephrine...
Antidepressant Drugs: Tricyclics, SSRIs, and SNRIs01:28

Antidepressant Drugs: Tricyclics, SSRIs, and SNRIs

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...
Antidepressant Drugs: MAOIs and Other Agents01:23

Antidepressant Drugs: MAOIs and Other Agents

Atypical antidepressants, including bupropion (Wellbutrin), mirtazapine (Remeron), nefazodone (Serzone), trazodone (Desyrel), and vilazodone (Viibryd), offer unique mechanisms of action. Bupropion weakly inhibits dopamine and norepinephrine reuptake, aiding depression treatment and smoking cessation, with a low risk of sexual dysfunction. Mirtazapine enhances serotonin and norepinephrine neurotransmission, leading to sedation, increased appetite, and weight gain. As a result, it helps treat...
Sedatives and Hypnotics Drugs: Miscellaneous Agents01:17

Sedatives and Hypnotics Drugs: Miscellaneous Agents

Sedatives and hypnotics encompass a wide range of substances, each with its unique mechanism of action, uses, and potential adverse effects.
Melatonin congeners like ramelteon (Rozerem) and tasimelteon (Hetlioz) selectively bind to melatonin receptors (MT1 and MT2) and thus mimic the actions of melatonin, a hormone that regulates sleep-wake cycles. Tasimelteon is primarily used for non-24-hour sleep-wake disorder, common in blind patients. They are also used to treat conditions like insomnia...
Drugs Affecting GI Tract Motility: Serotonin Receptor Agonists01:23

Drugs Affecting GI Tract Motility: Serotonin Receptor Agonists

Serotonin, a crucial neurotransmitter synthesized by enterochromaffin cells, plays a cardinal role in regulating gastrointestinal (GI) motility. With over 90% of the body's total serotonin in the GI tract, its influence on digestive processes is profound. Serotonin is swiftly released upon various stimuli, such as food boluses or certain drugs, triggering intrinsic sensory neurons in the myenteric plexus and extrinsic vagal and spinal sensory neurons. This leads to the activation of the...