Antidepressants, Anti-manic drugs & Mood Stabilizers Flashcards

1
Q

block 5HT pre-synaptic reuptake pump

A

• SSRIs:

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

block NE and 5-HT reuptake pumps

A

• SNRIs:

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

blocks 5-HT2A, 5-HT2C, 5-HT3, a-2-adrenergic receptors

A

• Mirtazapine:

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

increases whole-body NE, weakly blocks reuptake of DA

A

• Buproprion

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

most potent action is blockade of post-synaptic 5-HT2. Block reuptake of 5-HT and NE.

A

• Trazodone and nefazodone

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

block reuptake of 5-HT and NE, (and, to lesser extent, DA), as well as H1, muscarinic cholinergic receptors and a-1.

A

• Tricyclics:

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

irreversibly inhibit MAO-A and MAO-B, increasing levels of 5-HT and NE.

A

• MAOIs

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

a new antidepressant, is an SSRI + 5HT1A partial agonist.

A

• Vilazodone,

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q
  • Pluses: Time-tested, very effective, more effective in severe depression, can monitor blood levels. Newer TCAs (secondary amines such as desipramine and nortriptyline) have fewer side effects than older TCAs (tertiary amines, such as imipramine and amitryptyline)
  • Minuses: Hypotension, orthostasis, anticholinergic side effects, weight gain, sexual side effects, dangerous in overdose (10 day supply can be lethal)
A

TCAs

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q
  • Pluses: Can be very effective in non-responsive patients, especially atypical depression, time-tested.
  • Minuses: Hypotension, orthostasis, dry mouth, constipation, urinary retention, sexual side effects, weight gain, hypertensive crisis–Tyramine reaction
A

MAOIs

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q
  • Pluses: Safe, effective, multiple indications: Generalized Anxiety Disorder, social anxiety, panic, Obsessive Compulsive Disorder, Post Traumatic Stress Disorder, Premenstrual Dysphoric Disorder
  • Minuses: Diarrhea, nausea, jitteriness/anxiety, sexual side effects, drug interactions: P450 inhibition
A

SSRIs

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q
  • Pluses: Some evidence more effective than SSRIs, safe, better tolerated than TCAs, multiple indications
  • Minuses: Sexual side effects, sweating, increased diastolic blood pressure, withdrawal syndrome (flu-like, “electric shocks”)
A

SNRIs

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

TCAs

A
  • Pluses: Time-tested, very effective, more effective in severe depression, can monitor blood levels. Newer TCAs (secondary amines such as desipramine and nortriptyline) have fewer side effects than older TCAs (tertiary amines, such as imipramine and amitryptyline)
  • Minuses: Hypotension, orthostasis, anticholinergic side effects, weight gain, sexual side effects, dangerous in overdose (10 day supply can be lethal)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

SSRIs

A
  • Pluses: Safe, effective, multiple indications: Generalized Anxiety Disorder, social anxiety, panic, Obsessive Compulsive Disorder, Post Traumatic Stress Disorder, Premenstrual Dysphoric Disorder
  • Minuses: Diarrhea, nausea, jitteriness/anxiety, sexual side effects, drug interactions: P450 inhibition
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

MAOIs

A
  • Pluses: Can be very effective in non-responsive patients, especially atypical depression, time-tested.
  • Minuses: Hypotension, orthostasis, dry mouth, constipation, urinary retention, sexual side effects, weight gain, hypertensive crisis–Tyramine reaction
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

SNRIs

A
  • Pluses: Some evidence more effective than SSRIs, safe, better tolerated than TCAs, multiple indications
  • Minuses: Sexual side effects, sweating, increased diastolic blood pressure, withdrawal syndrome (flu-like, “electric shocks”)
17
Q
  • Pluses: No sexual side effects, weight neutral, activating.
  • Minuses: Increased anxiety, jitteriness, ineffective in panic disorder, insomnia, higher seizure risk (contraindicated in eating disorder patients and those with seizure disorder)
A

Bupropion

18
Q
  • Pluses: Helpful with insomnia, rapid anti-anxiety effect, low incidence of sexual side effects
  • Minuses: Daytime somnolence, weight gain
A

Mirtazapine

19
Q
  • Pluses: Best studied, best proven drug, effective anti-manic, reasonable preventative agent, some antidepressant effect, anti-suicidal properties, neuro-regenerative effects, inexpensive.
  • Minuses: Tremor, nausea, diarrhea, taste, thirst, cognitive dulling, narrow therapeutic window (0.6-1.2 mEq/l), toxic/lethal in overdose, renal effects, decreased urine concentration, diabetes insipidus, hypothyroidism.
A

Lithium

20
Q

Bupropion

A
  • Pluses: No sexual side effects, weight neutral, activating.
  • Minuses: Increased anxiety, jitteriness, ineffective in panic disorder, insomnia, higher seizure risk (contraindicated in eating disorder patients and those with seizure disorder)
21
Q

Mirtazapine

A
  • Pluses: Helpful with insomnia, rapid anti-anxiety effect, low incidence of sexual side effects
  • Minuses: Daytime somnolence, weight gain
22
Q

Lithium

A
  • Pluses: Best studied, best proven drug, effective anti-manic, reasonable preventative agent, some antidepressant effect, anti-suicidal properties, neuro-regenerative effects, inexpensive.
  • Minuses: Tremor, nausea, diarrhea, taste, thirst, cognitive dulling, narrow therapeutic window (0.6-1.2 mEq/l), toxic/lethal in overdose, renal effects, decreased urine concentration, diabetes insipidus, hypothyroidism.
23
Q
  • Pluses: Individualized treatment (based on weight), rapid loading (20-30 mg/kg), safe and effective.
  • Minuses: Not proven as preventative agent, weight gain, sedation, not effective in bipolar depression
A

Divalproex Sodium

24
Q
  • Pluses: All are anti-manic, reasonably safe & effective, different routes of administration (injection, dissolvable tabs), rapid dose titration
  • Minuses: Weight gain, risk of metabolic effects/diabetes, risk of increased cholesterol/lipids, expensive, are they any better than typical antipsychotics?
A

Atypical Antipsychotics

25
Q
  • No large, randomized, adequately controlled and powered studies have shown that antidepressants are effective in the treatment of bipolar depression. There is some evidence that antidepressants can worsen the course of bipolar disorder.
  • Best treatments for bipolar depression at present are (in descending order of efficacy): quetiapine, lamotrigine, Olanzapine/fluoxetine combination, lithium (unclear whether combined with antidepressant).
A

Bipolar Depression

26
Q

Divalproex Sodium

A
  • Pluses: Individualized treatment (based on weight), rapid loading (20-30 mg/kg), safe and effective.
  • Minuses: Not proven as preventative agent, weight gain, sedation, not effective in bipolar depression
27
Q

Bipolar Depression

A

• No large, randomized, adequately controlled and powered studies have shown that antidepressants are effective in the treatment of bipolar depression.

28
Q

Atypical Antipsychotics

A
  • Pluses: All are anti-manic, reasonably safe & effective, different routes of administration (injection, dissolvable tabs), rapid dose titration
  • Minuses: Weight gain, risk of metabolic effects/diabetes, risk of increased cholesterol/lipids, expensive, are they any better than typical antipsychotics?