Mechanism of action: Quetiapine XR balliculeVisual mnemonic: Quetiapine XR mascot “Sera, Quit typing!” Spooky mascot → antipsychotic Crown → antihistamine Polka dots on pink → α1 blocker → syncope if titrated too quickly (hit the floor) QT prolongation For mania (typing all night)
What it isExtended-release D2 and 5-HT2A antagonist with strong H1 and alpha-1 blockade; schizophrenia and adjunctive depression.
Why this oneIt offers once-daily evening dosing; the XR label carries the MDD-adjunct indication (2009).
What limits itTake without food or with a light meal (<300 kcal). Sedation, orthostasis, and metabolic disease limit use; strong CYP3A4 modifiers alter exposure.
BOXED WARNING Increased mortality in elderly patients with dementia-related psychosis treated with antipsychotics (not approved for this use). Increased risk of suicidal thoughts and behaviors in children, adolescents, and young adults taking antidepressants; monitor closely. Not approved for pediatric patients under 10 years of age.
FDA dosing
Population
Start
Target
Max
Schizophrenia
Adults
300 mg/day (Day 1)
400-800 mg/day
800 mg/day
Schizophrenia
Adolescents 13-17 y
50 mg/day, titrate 100/200/300/400 over Days 2-5
400-800 mg/day
800 mg/day
Bipolar I disorder, manic or mixed (monotherapy or adjunct to lithium/divalproex)
Adults
300 mg/day Day 1, 600 mg/day Day 2
400-800 mg/day
800 mg/day
Bipolar I disorder, manic (acute monotherapy)
Children/adolescents 10-17 y
50 mg/day, titrate 100/200/300/400 over Days 2-5
400-600 mg/day
600 mg/day
Bipolar disorder, depressive episodes
Adults
50 mg/day, titrate 100/200/300 over Days 2-4
300 mg/day
300 mg/day
Bipolar I disorder maintenance (adjunct to lithium/divalproex)
Adults
Continue effective dose
400-800 mg/day
800 mg/day
Major depressive disorder (adjunct to antidepressants)
Adults
50 mg/day Days 1-2, 150 mg/day Day 3
150-300 mg/day
300 mg/day
Titration Schizophrenia (adults): dose increases at intervals as short as 1 day (increments up to 300 mg/day)
Increased blood pressure in children and adolescents
Leukopenia, neutropenia, agranulocytosis
Cataracts (lens changes)
Anticholinergic (antimuscarinic) effects
Adverse reactions
Somnolence
Dry mouth
Dizziness
Constipation
Dyspepsia
Weight gain
Increased appetite
Fatigue
Pregnancy Third-trimester exposure risks extrapyramidal and/or withdrawal symptoms in neonates; epidemiologic data have not established increased risk of major birth defects
Lactation Present in human milk (relative infant dose <1%); consider benefits vs risk