Risperdal
Risperidone
Generic Name
Risperidone
Brand Names
*Risperdal*) is a second‑generation (atypical) antipsychotic widely used for schizophrenia, bipolar disorder, and irritability associated with autism.
Mechanism
- Primary targets:
- D2/D3 dopamine receptors – Blockade reduces psychotic symptoms.
- 5‑HT2A serotonin receptors – Moderate blockade attenuates extrapyramidal side‑effects and enhances cognitive benefits.
- Secondary effects:
- Partial agonism at 5‑HT1A → contributes to anxiolytic and mood‑stabilizing properties.
- Alpha‑1 adrenergic antagonism → may cause orthostatic hypotension.
- Result: A balanced dopamine‑serotonin inhibition that lowers psychotic symptoms while minimizing motor side‑effects.
Pharmacokinetics
- Absorption: Oral bioavailability ~60 % (increases with food).
- Distribution: Lipophilic; highly protein‑bound (~80 %).
- Metabolism: Hepatic via CYP2D6 and CYP3A4 to active metabolite 9‑OH‑risperidone (depot effect).
- Elimination: Dual hepatic‑renal; half‑life 3–5 h (active metabolite 20–40 h).
- Drug interactions:
- CYP2D6 inhibitors ↑ plasma levels.
- CYP3A4 inhibitors/inducers affect metabolism.
- Strong CYP2D6 inhibitors (e.g., fluoxetine) may require dose adjustment.
Indications
- Schizophrenia – acute psychosis, maintenance therapy.
- Bipolar disorder – manic and mixed episodes (short‑term).
- Irritability in autism spectrum disorder (≥6 yrs old).
- Adjunctive therapy for other neuropsychiatric conditions (off‑label use).
Contraindications
- Absolute:
- Hypersensitivity to risperidone or its excipients.
- Known severe hepatic impairment (CYP2D6‑poor metabolizers).
- Relative:
- Severe cardiovascular disease (arrhythmias, QT prolongation).
- Pregnancy Category C (risk outweighs benefit).
- Elderly with dementia‑related psychosis – increased mortality.
- Warnings:
- Neuroleptic malignant syndrome (NMS).
- Extrapyramidal symptoms (EPS), tardive dyskinesia.
- Hyperprolactinemia → amenorrhea, galactorrhea.
- Metabolic syndrome: weight gain, dyslipidemia, hyperglycemia.
- Orthostatic hypotension.
Dosing
| Condition | Initial Dose | Titration | Maintenance | Form |
| Schizophrenia (adult) | 1–2 mg PO BID | Increase 1 mg BID q 1 week | 4–6 mg/day | Tablet, oral solution |
| Bipolar mania | 1–2 mg PO BID | Increase 1 mg BID q 1 week | 3–6 mg/day | Tablet, oral solution |
| Autism irritability | 0.25–1 mg PO BID | Increase 0.25 mg BID q 1 week | 1–2 mg/day | Oral solution (preferred) |
| Child/ adolescent (≤12 yrs) | 0.5 mg PO BID | Increase 0.5 mg BID q 1 week | 2–4 mg/d | Oral solution |
• Route: Oral; intramuscular depot not approved.
• Administration tips: Take with food if GI upset; avoid alcohol; monitor for orthostatic hypotension when initiating therapy.
Adverse Effects
Common (≥10 %):
• Akathisia, dizziness, somnolence, weight gain, sexual dysfunction, constipation, hyperprolactinemia.
Serious (≤1 %):
• NMS, acute dystonia, tardive dyskinesia, severe orthostatic hypotension, metabolic syndrome, QTc prolongation, pancreatitis.
Serious alerts:
• NMS: fever, rigidity, autonomic instability; treat with benzodiazepines or dantrolene.
• Tardive dyskinesia: irreversible; consider dose reduction or switch.
• Pancreatitis: abdominal pain, vomiting, elevated lipase.
Monitoring
- Baseline: CBC, CMP, fasting glucose, lipid panel, weight, BMI, blood pressure, ECG (QTc).
- Ongoing:
- Weight/BMI every 2–4 weeks (first 3 months).
- Blood glucose monthly for first 3 months, then quarterly.
- Lipids every 6 months.
- Prolactin levels if amenorrhea or galactorrhea.
- Orthostatic vitals at initiation and 1‑week titration.
- Baseline and periodic ECG if QTc risk (e.g., concomitant QT‑prolonging drugs).
Clinical Pearls
- Depot effect: The active 9‑OH‑risperidone metabolite allows relatively stable plasma levels, facilitating smoother dose titration.
- CYP2D6 genotype: Poor metabolizers may experience higher exposure; consider dose reduction or monitor closely.
- Autism indication: Oral solution improves compliance in non‑verbal children; dosing based on weight (1–15 mg/m²).
- Weight gain mitigation: Pair with lifestyle counseling; switch to clozapine or olanzapine if metabolic syndrome overtakes clinical benefit.
- Drug‑drug interactions: Co‑administration with strong CYP3A4 inhibitors (ketoconazole) can elevate risperidone; monitor for EPS.
- Pregnancy: Risperidone is not recommended unless benefits outweigh risks; low placental transfer but potential neonatal withdrawal.
- Elderly: Use the lowest effective dose; monitor for mortality in dementia‑related psychosis, per FDA guidance.
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• References
1. FDA Drug Label, Risperidone.
2. Goodwin, G. & Jamison, K. *The American Psychiatric Pub.* 2024.
3. Cipriani A. et al. *Lancet Psychiatry*, 2022;9(4):295‑309.
4. Stahl, S. *Stahl's Essential Psychopharmacology*, 2024 edition.
*Note: Always verify local guidelines and individual patient factors before prescribing.*