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Examen

NR 546 Week 3: Antipsychotic Medications Comparison Table – Chamberlain University

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This professionally formatted table provides a comprehensive comparison of key antipsychotic medications covered in Week 3 of NR 546 at Chamberlain University. It includes detailed information on drug names, classifications (typical vs atypical), mechanisms of action, indications, side effects, black box warnings, monitoring parameters, and prescribing considerations. Designed for psychiatric nurse practitioner students, this resource supports clinical decision-making, exam preparation, and psychopharmacology mastery. Ideal for midterm and final review, case study support, and certification prep.

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NR 546
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NR 546

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Subido en
5 de noviembre de 2025
Número de páginas
29
Escrito en
2025/2026
Tipo
Examen
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NR 546 Week 3 Assignment; Antipsychotic Medications Table

Antipsychotic Medications
Kristin Reddy NR 546 September 2022

Drug name Indication (Bold = FDA approved) Half-life Notable side effects (associate to pathway or NT)
Target symptoms: state if positive or negative effect (T1/2),
Potency (if noted. receptor occupancy if noted) metabolism
Neurotransmitter(s) affected (CYP 450
enzyme)
Typical antipsychotics (conventional)

,Haloperidol Indication: Half Life ▪ Neuroleptic-induced deficit syndrome – Blocking of
▪ Manifestations of psychotic disorders (oral, Oral: dopamine two receptors excessively in the
immediate-release injection) Approximatel mesocortical and mesolimbic dopamine pathways,
▪ Tics and vocal utterances in Tourette’s syndrome (oral, y 12-38 specially at high doses, it can cause worsening of
immediate-release injection) hours negative and cognitive symptoms
▪ Second-line treatment of severe behavior problems in ▪ Akathisia - Acute blockade of dopamine 2 receptors
children of combative, explosive hyperexcitability Decanoate: in the striatum
(oral) approximatel ▪ Drug-induced parkinsonism - Acute blockade of
▪ Second-line short-term treatment of hyperactive y 3 weeks dopamine 2 receptors in the striatum
children (oral) ▪ Tardive dyskinesia, tardive dystonia – Chronic and
▪ Treatment of schizophrenic patients who require acute blockade of dopamine 2 receptors in the
prolonged parenteral antipsychotic therapy (depot striatum
Metabolized
intramuscular decanoate) ▪ Risk of potentially irreversible involuntary
by CYP450 -
▪ Bipolar disorder dyskinetic movements may increase with
2D6, 3A4,
▪ Behavioral disturbances in dementias cumulative dose and treatment duration
3A5
▪ Delirium (with lorazepam) ▪ Galactorrhea, amenorrhea – Blocking of dopamine
Target symptoms: 2 receptors in the pituitary can cause elevations in
▪ Positive symptoms of psychosis prolactin
▪ Violent or aggressive behavior ▪ Dizziness, sedation – Blocking of alpha 1 adrenergic
Potency: High receptors
Neurotransmitter(s) affected: ▪ Dry mouth, constipation, urinary retention,
▪ Blocks dopamine 2 receptors, reducing positive blurred vision, decreased sweating – Blockade of
symptoms of psychosis and possibly combative, muscarinic cholinergic receptors
explosive, and hyperactive behaviors ▪ Hypotension, tachycardia, hypertension – Blocking
of alpha 1 adrenergic receptors
▪ Blocks dopamine 2 receptors in the nigrostriatal
pathway, improving tics and other symptoms in ▪ Weight gain - Mechanism of weight gain and any
Tourette’s syndrome possible increased incidence of diabetes or
dyslipidemia with unconventional antipsychotics is
currently unknown

Thioridazine Indication: Half Life ▪ Neuroleptic-induced deficit syndrome – Blocking of

, ▪ Schizophrenic patients who fail to respond to 21–24 hours dopamine 2 receptors excessively in the
treatment with other antipsychotic drugs mesocortical and mesolimbic dopamine pathways,
Target symptoms: especially at high doses, it can cause worsening of
▪ Positive symptoms of psychosis in patients who fail to Metabolized negative and cognitive symptoms
respond to treatment with other antipsychotics Primarily by ▪ Akathisia - Acute blockade of dopamine 2 receptors
▪ Motor and autonomic hyperactivity in patients who fail CYP450 - 2D6 in the striatum
to respond to treatment with other antipsychotics ▪ Priapism – Blocking of alpha 1 adrenergic receptors
Potency: Low ▪ Drug-induced parkinsonism - Acute blockade of
Neurotransmitter(s) affected: dopamine 2 receptors in the striatum
▪ Blocks dopamine 2 receptors, reducing positive ▪ Tardive dyskinesia - Chronic blockade of dopamine
symptoms of psychosis 2 receptors in the striatum
▪ Risk of potentially irreversible involuntary
dyskinetic movements may increase with
cumulative dose and treatment duration
▪ Galactorrhea, amenorrhea - Blocking of dopamine
2 receptors in the pituitary
▪ Pigmentary retinopathy at high doses – may be
due to blockade of retinal D2/D4 receptors
▪ Dizziness, sedation - Antihistaminic actions,
blocking of alpha 1 adrenergic receptors
▪ Dry mouth, constipation, blurred vision, decreased
sweating, paralytic ileus – Blocking of muscarinic
cholinergic receptors
▪ Sexual dysfunction - Blockade of dopamine D2
receptors in the tuberoinfundibular pathway
▪ Hypotension – Blocking of alpha 1 adrenergic
receptors
▪ Weight gain - Antihistaminic actions
▪ Mechanism of weight gain and any possible
increased incidence of diabetes or dyslipidemia
with conventional antipsychotics is unknown
▪ Mechanism of potentially dangerous QTc
prolongation may be related to actions at ion
channels

Thiothixene Indication: Half Life: ▪ Neuroleptic-induced deficit syndrome - Blocking of
▪ Schizophrenia Initial dopamine 2 receptors excessively in the
▪ Other psychotic disorders elimination: mesocortical and mesolimbic dopamine pathways,
▪ Bipolar disorder approximatel especially at high doses, can cause worsening of
Target symptoms: y 3.4 hours negative and cognitive symptoms

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