Anti-Psychotics Flashcards

(29 cards)

0
Q

Typical Mid Potency Anti-Psycotics

A

Perphenazine

Molindone

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1
Q

Typical Low Potency Anti-Psychotics

A

Chlorpromazine

Thioridazine

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2
Q

Typical High Potency Anti-Psychotics

A

Haloperidol
Fluphenazine
Trifluoperazine
Thiothixene

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3
Q

Typical Low Potency Side Effect Profile

A
Anticholinergic: increased temperature, decreased sweating, dry mouth, constipation, urinary retention, cognitive deficits, decreased seizure threshold, prolonged QT interval, blurred vision, closed angle glaucoma
Anti-alpha 1: orthostatic hypotension
Antihistaminic: sedation, weight gain
Tardive Dyskinesia
Neuroleptic Malignant syndrome
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4
Q

Typical High Potency Side Effect Profile

A
Extra pyramidal symptoms (EPS): acute dystonia, akathisia, parkinsonism, 
Tardive Dyskinesia
NMS
Hyperprolactinemia
Treat EPS with anticholinergics
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5
Q

Chlorpromazine

A

Typical AP: blocks D2 receptor
Low potency
Most sedation AP, retinal pigmentation

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6
Q

Thioridazine

A

Typical AP: blocks D2 receptor
Low potency
Worst QT prolongation, retinal pigmentation

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7
Q

Perphenazine

A

Typical AP

Mid potency

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8
Q

Molindone

A

Typical AP: blocks D2 receptor
Mid potency
Only typical AP that doesn’t cause weight gain

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9
Q

Haloperidol

A

Typical AP: blocks D2 receptor
High potency
Most common AP in emergency setting

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10
Q

Fluphenazine

A

Typical AP: blocks D2 receptor

High potency

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11
Q

Trifluoperazine

A

Typical AP: blocks D2 receptor

High potency

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12
Q

Thiothixene

A

Typical AP: blocks D2 receptor

High potency

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13
Q

Typical Anti-Psychotics

A

1st generation
TD, NMS
Block D2 receptor

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14
Q

Atypical Low Potency Anti-Psychotics

A

Clozapine

Quetiapine

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15
Q

Atypical Anti-Psychotics

A
2nd generation
Metabolic syndrome
Block a variety of receptors (less D2 activity)
1st line of treatment (except Clozapine)
Increased risk of stroke
16
Q

Atypical Mid Potency Anti-Psychotics

A

Olanzapine

Ziprazidone

17
Q

Atypical High Potency Anti-Psychotics

A
Risperidone
Aripiprazole (Abilify)
18
Q

*Clozapine

A
Atypical AP
Low potency
Many receptors: D2/3/4; 5HT1/2/3; M1; Alpha-1; H1
Most efficient AP
LAST RESORT
Worst side effects: metabolic syndrome, weight gain, sedation, orthostatic hypotension, AGRANULOCYTOSIS (blood tests every week for 6 months, 2 weeks forever), anticholinergic, antihistaminic, anti alpha-1, prolonged QT, myocarditis
Hyper salivation  
Short half life
19
Q

Quetiapine

A

Atypical AP
Low potency
Weight gain and moderate metabolic risk, less anticholinergic than clozapine
Cataracts in animals

20
Q

Ziprazidone

A

Atypical AP
Mid to low potency
No weight gain, LEAST RISK OF METABOLIC SYNDROME, low risk of QT prolongation
Sedation

21
Q

*Olanzapine

A

Atypical AP
Mid to high potency
Similar to clozapine molecularly
Significant weight gain, metabolic risk, increased liver enzymes, hypertriglyceridemia, bad lipid profile, decreased HDL, no agranulocytosis

22
Q

Risperidone

A

Atypical AP
High potency
High affinity for 5HT2 and D2
Most typical of atypical APs: EPS, TD, Hyperprolactinemia

23
Q

Aripiprazole (Abilify)

A
Atypical AP
High potency
D2, 5HT2, Partial D1 agonist
No weight gain, increased risk of akathisia (treat with beta blocker)
Activator, so only give in the morning
24
Anti-Cholinergics for psychotic disorders
Benzatropine/Atropine | Diphenhydramine (Benadryl)
25
Benzatropine/Atropine
Psychotic disorders and Alzheimer's disease Anticholinergic Treat EPS but not TD
26
Diphenhydramine (Benadryl)
Psychotic disorders, insomnia, anxiety disorders Anticholinergic, antihistamine Treat EPS, not TD Sedative
27
Cholinergics
Betachenol
29
Betachenol
Cholinergic Stimulates M1 receptor (CNS) Reduces anticholinergic effects