Antipsychotics Flashcards

1
Q

Chlorpromazine

A
  • Phenothiazine, aiphatic typical.

- Low-medium potency, sedative, with pronounced anticholinergic side effects.

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2
Q

Clozapine

A
  • Atypical; blocks D4 and 5-HT2 receptors, with litte effect on D2. Also muscarinic antagonist.
  • Improves positive symptoms even in patients not helped by other drugs; most efficacious.
  • Improves negative symptoms.
  • Lowers seizure thresholds more than other antipsychotics.
  • Can cause fatal agranulocytosis, so requires monitoring.
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3
Q

Thioridazine

A
  • Phenothiazine; peridine typical.

- Low potency, sedative, with fewer extrapyramidal and anticholinergic actions

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4
Q

Olanzapine

A
  • Related to clozapine; potent 5-HT2 antagonist, with some D1 and D2 antagonist action, and some D4 action. –Less seizure incidence than clozapine and no risk of agranulocytosis.
  • Weight gain and diabetes-related adverse events.
  • There have been reports of olanzapine abuse.
  • Can also be used for augmentation during depression.
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5
Q

Thiothixene

A
  • Thioxanthine typical.

- Non-nitrogen containing analogs of the phenothiazines; pharm is similar.

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6
Q

Haloperidol

A

-Butyrophenone derivative; not chemically related to phenothiazines but pharm. similar to high-potency piperazine derivatives.

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7
Q

Pimozide

A
  • Potent neuroleptic; many side effects.

- Approved for treatment of Tourette’s in patients where haloperidol doesn’t work.

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8
Q

Risperidone

A
  • Atypical; combined D2 and 5-HT2 antagonist.
  • Greater reductions in negative symptoms and less EPS than traditional psychotics.
  • Less seizure activity and less antimuscarinic activity than clozapine.
  • Active metabolite is paliperidone; both available as IM depot prep.
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9
Q

Quetiapine

A
  • Structurally related to clozapine; similar to risperidone and olanzapine in effects on schizophrenia symptoms and side effects, with shorter half-life.
  • Approved for augmentation in depression. Some reports of abuse.
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10
Q

Ziprasidone

A
  • Atypical.
  • 5-HT2 and D2 antagonist; may have 5-HT1a agonist activity.
  • No weight gain.
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11
Q

Aripiprazole

A
  • Atypical.
  • A partial D2 agonist and 5-HT2 antagonist.
  • Also approved for augmentation/adjunct therapy for depression.
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12
Q

Clonazepam

A

-Used for initial control of manic symptoms.

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13
Q

Lithium Carbonate

A
  • Monovalent of the lightest alkali metal.
  • One of the few psychotherapeutic drugs that has no behavior effects in normals. Blocks manic behavior.
  • Sodium levels affect lithium levels; increases Na excretion causes clinically significant increase in lithium levels (watch out for thiazide diuretics, losses of fluid/electrolytes). ACEI and ARBs also can raise lithium levels.
  • Side effects: fatigue, muscle weakness, tremor, GI symptoms, slurred speech and ataxia, serious toxicity (impaired consciousness, rigidity and hyperactive deep reflexes, coma).
  • Narrow therapeutic window.
  • Should be used with caution in pregnant women.
  • Used to treat mania and prevent bipolar recurrence. May be useful in preventing recurrences of unipolar depression in some patients. Also used for schizoaffective disorder and cluster headaches.
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14
Q

Valproic Acid

A
  • Lithium alternative.

- Used as first line drug in bipolar disorder; sedating.

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15
Q

Actions of antipsychotic drugs

A
  • Decrease psychotic behavior
  • Sedation
  • Extrapyramidal effects (dystonia, akathisia, parkinsonism have early onset, tardive dyskinesia develops later)
  • Anticholinergic activity (dry mouth, blurred vision, urinary retention)
  • Orthostatic hypotension
  • Neuroendocrine effects due to DA receptor blockade
  • Allergic effects
  • Decreased seizure threshold
  • Weight gain.
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16
Q

Neuroleptic Malignant Syndrome

A
  • Potential lethal hypodopaminergic side effect:
  • Hypothermia
  • Parkinson-like symptoms
  • Mutism
  • Possible death
  • Treat with cooling, hydration, bromocriptine and dantrolene.
17
Q

Advantages of Atypicals

A
  • Lower incidence of EPS and possible lower incidence of tardive dyskinesia.
  • May improve negative symptoms; improve positive symptoms in many antipsychotic-resistant or refractory patients.
  • Less impact on cognitive functioning.