Trihexyphenidyl Oral: Dosing and Safety
Trihexyphenidyl guidance for second-line treatment of antipsychotic-induced extrapyramidal reactions, with anticholinergic precautions.
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Source reviewed
source date listed on the source page
Guide category
Oral drugs
Safety boundary
Prescription medicine information for clinician-guided use.
Kenza Health Hub presents this medicine page as structured health education. Check dose, route, interactions, pregnancy or breast-feeding considerations, and local protocol with a qualified clinician or pharmacist. Read our medical editorial policy.
Therapeutic action
Anticholinergic antiparkinson drug.
Indications
Second-line treatment of extrapyramidal reactions induced by antipsychotics.
Forms and strengths
- 2 mg tablet.
Dose
- Adult: 2 mg once daily, then increase if necessary up to 2 mg 2 or 3 times daily, maximum 12 mg daily.
- Administer the lowest effective dose in elderly patients and do not exceed 10 mg daily.
Duration
As long as antipsychotic treatment lasts.
Contra-indications, adverse effects, precautions
- Do not administer to patients with closed-angle glaucoma, prostate disorders, gastrointestinal obstruction, or atony.
- Administer with caution and carefully monitor use in elderly patients because of the risk of mental confusion and hallucinations.
- May cause anticholinergic effects, confusion, hallucinations, and memory loss.
- Avoid or monitor combination with other anticholinergic drugs such as atropine, amitriptyline, chlorpromazine, and promethazine.
- Pregnancy: re-evaluate whether the antipsychotic treatment is still necessary. If treatment is continued, administer trihexyphenidyl at the lowest effective dose and observe the neonate if exposure occurred in the third trimester.
- Breast-feeding: if treatment is necessary, administer at the lowest effective dose and observe the child for anticholinergic effects.
- Take with meals.
Source
MSF Essential drugs practical guidelines (January 2026)
This page combines source-derived medicine reference sections with Kenza editorial context, while leaving out the Storage and Remarks sections from the source batch.
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