Mood Med practice Flashcards

1
Q

SSRI MOA

A

decrease action of 5-HT reuptake pump which causes increased serotonin levels in the synapse

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2
Q

SSRI Dosing

A

Typically QAM can be halved if SE are bad. Metabolized mostly by the liver so caution in hepatic impairement.

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3
Q

SSRI SE

A

GI (N/D/anorexia) sleep change, headaches, dizziness, decreased libido, anorgasmia, ED, anxiety, increased suicide risk, prolonged QT, weight gain, bleeding, orthostatic hypotension, serotonin syndrome

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4
Q

SSRI CI

A

allergy to SSRI, use of MAOI within 2 weeks. Fluoxetine must wait 5 weeks.

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5
Q

SSRI drugs

A

fluvoxamine
fluoxetine
sertraline
Citalopram/Escitalopram
Paroxetine

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6
Q

SSRI with shortest half life, increased somnolence, DDIs

A

Fluvoxamine special notes

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7
Q

SSRI with Longest halft life, increased insomnia, DO NOT TAKE w Tamoxifen

A

Fluoxetine special notes

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8
Q

SSRI with increased GI upset mostly diarrhea, increased insomnia, decreased QT prolongation

A

sertraline special notes

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9
Q

SSRI with MOST associated with QT prolongation, least impact on liver!

A

Citalopram/Escitalopram special notes

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10
Q

SSRI with Only one to cause anticholinergic SE, orthostatis hypotension, weight gain, sexual dysfuntion are all increased. DO NOT TAKE w tamoxifen.

A

Paroxetine special notes

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11
Q

SNRIs MOA

A

Blocks reuptake of 5-HT and NE, increasing their levels in synapse.

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12
Q

SNRI Dosing

A

takes a few weeks to see full effects. Typically taken QD. Cleared through liver and kidneys.

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13
Q

SNRI SE

A

N/V/D constipation, dry mouth. Sleep changes, HA, dizziness, anorgasmia, anxiety, suicide, diaphoresis, hypertension, serotonin syndrome.

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14
Q

SNRI CI

A

allergy to SNRIs; use within 2 weeks of an MAOI, caution if using other serotonergic drugs, caution with angle closure glaucoma.

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15
Q

SNRIs drugs

A

duloxetine
Venlafaxine
Desvenlafaxine
Milnacipran/Levomilnacipran

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16
Q

Only SNRI with hepatic cytochrome inhibitors which leads to DDIs, LEAST associated w HTN, indicated for chronic pain relief

A

Duloxetine Special notes

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17
Q

SNRI with higher risk of SE than others. MOST associated w HTN

A

Venlafaxine special notes

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18
Q

SNRI with synthetic of venlafaxine, Less risk of HTN and other general SE than venlafaxine

A

Desvenlafaxine special notes

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19
Q

SNRI with Greater effects on NE. most likely to have Psuedo anticholinergic SE (UR, const, dry mouth).

A

Milnacipran/Levomilnacipran special notes

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20
Q

Bupropion MOA

A

acts as dopamine-NE reuptake inhibitor (also antagonizes nicotinic receptors)

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21
Q

patients with depression that may also want to quit smoking

22
Q

Weight loss, decreased appetite, Nausea, dry mouth, insomnia, seizures, suicide

A

Bupropion SE

23
Q

CI includes hepatic cytochrome inhibition causes DDIs
allergy
seizure disorder (HIGH RISK OF SEIZURE)
anorexia/bulemia ( causes weight loss and decreased appetite
use within 2 weeks of MAOI

24
Q

patients with depression who also have insomnia

A

mirtazapine

25
Mirtazapine MOA
antagonizes alpha-2 adrenergic receptors and 5-HT2 and 5-HT3 receptors which causes increased release of serotonin and NE.
26
Dry mouth, increased appetite, weight gain (more than SSRI/SNRI), drowsiness, sedation, sexual dysfunction (less than SSRI). LOWER HTN RISK NO HEPATIC CYTOCHROME INHIB.= FEW DDIs
Mirtazapine
27
Mirtazapine CI
Allergy MAOI w/i 2 weeks.
28
what are the atypical antidepressants
bupropion and mirtazapine
29
Serotonin Modulators MOA
blocks the reuptake of 5-HT = increased serotonin Nefazodone and trazodone also antagonize the 5-HT pump = increased serotonin Vilazodone and Vortioxetine partially antagonize 5-HT pump = mimic serotonergic effects
30
Serotonin Modulators Dosing
QD or BID, Cleared through liver
31
Serotonin Modulators SE
nausea, diarrhea, headache, suicide, serotonin syndrome.
32
Serotonin Modulators CI
allergy MAOI use W/I 2 weeks caution with other serotonergic drugs
33
What are the Serotonin Modulator medications
Nefazodone Trazodone Vilazodone Vortioxetine
34
SE: No sexual dysfunction, Less GI. increased Xerostomia, HA, Dizziness, insomnia or drowsiness, agitation, hypotension. Hepatic Cytochrome enzyme inhibition = MOST DDI RISK OF ALL 5-HT inhib. BBW = hepatotoxicity.
nefazadone
35
SE: nausea, constipation, dry mouth, sedation, fatigue, sexual dysfunction (less than SSRIs or SNRIs.) Rare: priapism and cardiac arrhythmias
Trazodone
36
SE: Nausea, Diarrhea, HA, sexual dysfunction (less than SSRIs or SNRIs)
Vilazodone
37
Ketamine/Esketamine MOA
opioid and glutamate agonist. NMDA antagonist. mechanism for antidepression is unknown
38
for severe, refractory depression w/o psychosis that is not respondant to ECT. short term use only!
Ketamine/Esketamine
39
ketamine/esketamine Dosing
ketamine - IV esketamine - Nasal rapid effects but effects end in about 2 weeks.
40
abuse potential becuase of euphoric/intoxicated effects N/V, HA, dizziness, neurotoxicity, hepatotoxicity, bladder toxicity, tachycardia, HTN and abuse/addiction
Ketamine/Esketamine
41
Ketamine/Esketamine CI
allergy aneurysmal disease or AV malformation hx of intracerebral hemorrhage inability to tolerate increase in BP
42
MAOIs Use
usually only for treatment-resistant or atypical depression. selegiline = low dose used for parkinsons
43
MAOI MOA
MOAa breaks down serotonin and NE MOAb works w MOAa to break down dopamine
44
hypotension, GI upset, urinary hesitancy, HA, myoclonic jerks, edema, suicidal ideation, hypertensive crisis w some foods (cheese, beer, tofu, cured meats)
MAOI
45
CI includes allergy, CVD, pheochromocytoma (adrenal gland tumor), hepatic/renal impairment, use w serotonergic drugs. LOTS OF DDIs
MAOI
46
what medications are the MAOIs
Tranylcypromine Phenelzine Isocarboxazid Selegiline
47
Tricyclic antidepressant MOA
inhibits reuptake of 5-HT and NE
48
SE includes: Anticholinergic, drowsiness, SD, Diaphoresis, tremor, weight gain, increased appetite, SI, prologned QT (cardiotoxicity), OD risk
tricyclic antidepressants
49
this tricyclics antidepressants MOA includes more potent blocking of 5-HT reuptake rather than NE reuptake
tertiary amines amitryptiline doxepin imipramine clomipramine trimipramine
50
SE includes: Anticholinergic (less than TCAs), drowsiness (more than TCAs), SD, Diaphoresis, tremor, weight gain, increased appetite, SI, prologned QT (cardiotoxicity), OD risk
Tetra cyclic antidepressants
51
this tetracyclic antidepressant blocks reuptake of NE and 5-HT
Maprotiline
52
this tetracyclic antidepressant blocks reuptake of NE and blocks dopamine receptors
Amoxapine