Antidepressant Poisoning
Basics
Basics
Basics
Description
Description
- Antidepressants are the most commonly prescribed psychiatric medications in U.S.
- Patients who overdose on antidepressants may be on various antidepressants, divided into SSRIs, SNRIs, and atypical. Concomitant usage of atypical antipsychotics and mood-stabilizing medications, some of which are FDA approved for the treatment of depressive disorders, is common
- Antidepressants may be prescribed for multiple other indications, including chronic pain syndromes, anxiety, eating disorders, substance abuse, and sleep disorders
- Tricyclic antidepressants (TCAs) are covered in a separate chapter
Etiology
Etiology
Mechanism
- SSRIs:
- Increase serotonin at the synapse by preventing the reuptake of serotonin by the presynaptic neuron
- SSRIs include paroxetine, fluoxetine, sertraline, citalopram, and escitalopram
- SNRIs:
- Similar to SSRIs, but also inhibit reuptake of norepinephrine
- Developed because said to have fewer side effects than SSRIs at therapeutic dose, although not true for toxicity
- SNRIs include venlafaxine, desvenlafaxine, and duloxetine
- Atypical antidepressants:
- Have variable effects on serotonin, norepinephrine, and dopamine
- Include mirtazapine, trazodone, and bupropion
- Atypical antipsychotics:
- Most antipsychotics have activity at dopamine receptors, although variable agonism/antagonism depending on medication and dopamine receptor
- Additional activity at serotonin, α-adrenergic, histamine, and muscarinic receptors
- Psychiatric medications also have variable potassium and sodium channel blockade, leading to cardiotoxicity (QT and QRS prolongation, respectively)
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