
Halopid5 mg
Incepta Pharmaceuticals Ltd.
Haloperidol is a first-generation (typical) antipsychotic of the butyrophenone class.
Haloperidol is a first-generation (typical) antipsychotic of the butyrophenone class. Its evidence-based indications are classified below by strength of evidence.
Haloperidol is not FDA-approved for treatment of dementia-related psychosis or behavioural disturbances in elderly patients with dementia (see Precautions and Warnings).
Dosing of Haloperidol is individualised to the indication, severity of symptoms, formulation, and patient response, using the lowest effective dose.
| Indication | Typical Adult Dosing |
|---|---|
| Schizophrenia/psychosis - moderate symptoms | 0.5-2 mg orally 2-3 times daily; titrate as needed |
| Schizophrenia/psychosis - severe symptoms or chronic/resistant cases | 3-5 mg orally 2-3 times daily; some patients may require higher doses under close specialist supervision, up to a generally accepted maximum of about 20 mg/day (higher doses used rarely and only under specialist care) |
| Acute agitation/acute psychosis | 2-5 mg by deep IM injection; may repeat every 4-8 hours as clinically needed (immediate-release injection is for short-term use) |
| Maintenance therapy (long-acting depot) | Haloperidol decanoate, typically 10-20 times the previous stabilised daily oral dose, given by deep IM injection every 4 weeks, after oral stabilisation |
| Tourette's disorder | 0.5-5 mg orally 2-3 times daily, individualised to response |
No formal renal dose-adjustment schedule is established; caution and lower starting doses are advised in renal impairment. In hepatic impairment, since Haloperidol is extensively hepatically metabolised, lower doses and slower titration with close monitoring are recommended.
Haloperidol is contraindicated in:
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