Indications & formulation #
Schizophrenic disorders in adults. This reference covers the selected formulation; other indications and products need their own evidence.
Dose reference #
Adult educational reference · Oral tablet; UK SmPC · United Kingdom. The clinician selects treatment after assessment; this page does not calculate or change a prescription.
Acute positive symptoms: 400–800 mg/day; maximum 1200 mg/day. Predominant negative symptoms: 50–300 mg/day. Divide doses above 400 mg/day.
Contraindications & important cautions #
Contraindications include prolactin-dependent tumors, phaeochromocytoma and levodopa. Review QT, prolactin and neuroleptic malignant syndrome.
Selected important cautions; consult the full product information for all contraindications and warnings.
Adverse effects #
Prolactin elevation, movement symptoms and QT prolongation.
Interactions #
Levodopa is contraindicated; review QT-prolonging combinations.
Monitoring #
Monitor renal function, movements, prolactin symptoms and cardiac risk.
Special populations #
CrCl 30–60: half dose; 10–30: one-third dose. Below 10, evidence is insufficient. Older adults need particular caution.
Adult scope. Pregnancy, breastfeeding and pediatric use require the exact product’s population-specific guidance and individual assessment.
Discontinuation, restarting & counseling #
Withdraw gradually. This oral reference does not derive from the US intravenous antiemetic product.
Brands & products #
Historical catalogue observations. Prices and catalogue presence do not establish current availability or Indian approval.
Reference coverage #
Structured summary of selected adult uses, not an exhaustive monograph. Indian product authorization and local prescribing requirements have not been reconciled.
References · 1
- Amisulpride oral tablets — UK SmPC · United Kingdom · Checked 2026-10-27 · Selected formulation: Oral tablet; UK SmPC · Supports indications, dose, cautions, adverse effects, interactions, monitoring, special populations and stopping. Source sections: 4.1–4.6 Clinical particulars
