Antidepressants and Antipsychotics Flashcards
(21 cards)
SSRIs
Sertraline,
Citalopram,
Escitalopram, Fluoxetine, Paroxetine
SNRIs
Venlafaxine,
Desvenlafaxine, Duloxetine
atypical antidepressants
Bupropion,
Mirtazapine
serotonin modulators
Trazodone and Vilazodone
tricyclic antidepressants (TCA)
Amitriptyline, Nortriptyline
MAOI
- Phenelzine (Nardil; generic)
- Tranylcypromine (Parnate; generic)
- Isocarboxazid (Marplan)
Selegiline
FGA
Chlorpromazine (Thorazine)
Promethazine (Phenergan)
Prochlorperazine (Compazine)
Haloperidol (Haldol)
Droperidol -
SGA - atypical
Olanzapine (Zyprexa)
Ziprasidone (Geodon)
Risperidone (Risperdal)
Quetiapine (Seroquel)
SGA - DA Stabilizer
SSRI MOA
Inhibition of 5-HT reuptake transporter (SERT)***
SNRI MOA
Blocks SERT and NET activity
* NET blockade associated with effectiveness in treating multiple pain syndromes
MOA - Atypical Antidepressants: Bupropion (Wellbutrin)
Increase synaptic NE and DA activity (Block NET and dopamine reuptake transporter/DAT and increase their release) and noncompetitive antagonist of nicotinic receptors.
Bupropion (Wellbutrin) AEs?
CNS stimulation (agitation, insomnia, tremor), decreases seizure threshold (but not sexual dysfunction)
MOA - * Mirtazapine (Remeron)
a2 adrenergic antagonist blocks presynaptic receptors to elevate both NE and 5-HT in brain synapses. Also blocks postsynaptic 5-HT2 receptors.
AE- * Mirtazapine (Remeron)
weight gain and sedation
DI with Mirtazapine
pharmacodynamic interactions with MAO-Is, other 5-HT agents with potential for Serotonin Syndrome; Diminishes effects of Clonidine (used for hypertension and ADHD).
MOA of Trazadone
o Blocks 5-HT2 receptors, histamine1 and a1 adrenergic receptors, and inhibit SERT at high doses
o Sedating effects at low doses – mainly used as hypnotic (sleep aid)
AE of trazadone
include priapism (persistent erection), postural hypotension
MOA of vilazadone
o Inhibitor of SERT and is a 5-HT1A partial agonist (anxiety). Both activities of Vilazodone may contribute to anti-depressant and anxiolytic potential.
vilazadone DI
o Primarily metabolized by CYP3A4; not significant source of drug interactions in vivo.
vilazadone AEs
GI: N/V, diarrhea (most common AEs), withdrawal symptoms, platelet dysfunction (bleeding risk).