• Schizophrenia:
    • Immediate release:
      • Adult: Initially PO 25mg BD then increased daily in increments of 25-50mg divided BD/TDS to 300-400mg by day 4
        • Can be further increased by 25-50mg BD at intervals ≥2 days
        • Maintenance: 150-750mg/day
      • Children 13-17 years: PO 25mg BD *1/7, then 50mg BD *1/7, then increased by 100mg/day up to 200mg BD by day 5, then may be increased by 50-100mg/day PRN
        • Maintenance: 400-800mg/day
        • Max: 800mg/day
    • Extended release:
      • Adult: Initially PO 300mg nocte, then increased up to 300mg/day PRN
        • Maintenance: 400-800mg/day
        • Max: 800mg/day
      • Children 13-17 years: Initially 50mg nocte*1, then 100mg *1, then increased by 100mg/day
      • Maintenance: 400-800mg/day
      • Max: 800mg/day
  • Manic bipolar I disorder as monotherapy or as an adjunct to lithium or divalproex:
    • Immediate release:
      • Adults: Initially PO 50mg BD, then increased by 100mg/day up to 200mg BD by day 4, then may increase by 200mg/day PRN
        • Maintenance: 200-400mg BD
        • Max: 800mg/day
      • Children 10-17 years: 25mg BD *1, then 50mg BD *1, then increased by 100mg/day up to 200mg BD by day 5, then may increased by 50-100mg/day PRN
      • Maintenance: 400-600mg/day divided BD/TDS
      • Max: 600mg/day
    • Extended release:
      • Adults: Initially PO 300mg nocte *1, then 600mg *1, then may adjust by 200mg/day PRN
        • Maintenance: 400-800mg/day
        • Max: 800mg/day
      • Children 10-17 years: PO 50mg *1, then 100mg *1, then increased by 100mg/day
        • Maintenance: 400-600mg OD
        • Max: 600mg/day
  • Acute depressive bipolar disorder:
    • Immediate release: PO 50mg nocte *1, then 100mg *1, then 200mg *1, then 300mg *1
      • Maintenance: 300mg
      • Max: 600 mg/day
    • Extended release: PO 50mg nocte *1, then 100mg *1, then 200mg *1, then 300mg
      • Maintenance: 300mg
      • Max: 300mg/day
  • Maintenance in bipolar I disorder as an adjunct to lithium or divalproex:
    • Immediate release: PO 400-800mg/day divided BD
    • Extended release: PO 400-800 mg/day in single dose
  • Major depressive disorder as adjunct to antidepressants:
    • Initially PO 50mg nocte *2/7 then may be increased to 150mg
      • Maintenance: 150-300 mg/day
  • Alcohol dependence (Off-label):
    • PO 25-50mg nocte
    • Max 300mg
  • Insomnia (Off-label):
    • Initially 25mg/day nocte
  • Treatment-resistant anxiety disorder (Off-label):
    • Immediate release: Initially 25mg OD, then increased by 25-50mg/day
      • Maintenance: 50-150mg/day
      • Max: 300mg/day
    • Extended release: Initially 50mg OD, then may be increased by 50mg/day
      • Maintenance: 50-150mg/day
      • Max: 300mg/day
  • Tablet:
    • 50mg
    • 100mg
    • 150mg
    • 200mg
    • 300mg

Preferably to be taken in evening without food or with a light meal

2nd generation atypical antipsychotic

It is thought to reduce positive and negative symptoms of psychotic disorders via antagonism of multiple neurotransmitter receptors in brain, including dopamine D1 and D2, histamine H1, alpha1- and alpha2-adrenergic and serotonin types 1 and 2 (5-HT1A, 5-HT2)

  • Somnolence
  • Xerostomia
  • Dizziness
  • Orthostatic hypotension
  • Increased BP (peds patients)
  • Tachycardia
  • Hypotension
  • Constipation
  • Weight gain
  • Diarrhea (peds patients)
  • Increased appetite
  • Dyspepsia
  • Tremor
  • Dysarthria
  • Dysphagia
  • Extrapyramidal symptoms
  • Blurred vision
  • Anemia
  • Rash
  • Transiently elevated ALT/AST
  • Abdominal pain
  • Back pain
  • Hyperprolactinemia
  • Increased cholesterol
  • Hypertriglyceridemia
  • Asthenia
  • Headache
  • Fatigue
  • Insomnia
  • Irritability
  • Nausea
  • Vomiting
  • Peripheral edema
  • Fever
  • URI symptoms
  • Impaired body temperature regulation
  • Anticholinergic effects
  • Hypersensitivity to components
  • Uncorrected electrolyte abnormalities
  • Hypokalemia
  • Hypomagnesemia
  • Congenital long QT syndrome
  • Arrhythmia history
  • Bradycardia
  • QT prolongation
  • Abrupt withdrawal

WARNING

  • May cause tardive dyskinesia (often irreversible)
  • Not approved for dementia-related psychosis, there is an increased mortality risk in elderly dementia patients on conventional or atypical antipsychotics
  • Increased suicidality risk in children, adolescents and young adults with major depressive or other psychiatric disorders
  • Lurasidone
  • Lefamulin
  • Pimozide
  • Thioridazine

                          Drug Status

Availability Prescription only
Pregnancy Category C
Breastfeeding Weigh risk vs benefit
Schedule Controlled
BRAND NAME STRENGTH FORMULATION PACK SIZE MANUFACTURER DISTRIBUTOR
Quti 200mg Tablet 30’s Lords Healthcare Lords Healthcare
Quti 150mg Tablet 30’s Lords Healthcare Lords Healthcare
Quti 50mg Tablet 30’s Lords Healthcare Lords Healthcare
Qutipin 50mg Tablet 30’s Sun Pharma Sun Pharma
Qutipin 100mg Tablet 30’s Sun Pharma Sun Pharma
Qutipin 200mg Tablet 30’s Sun Pharma Sun Pharma
Qutipin 300mg Tablet 30’s Sun Pharma Sun Pharma