Benztropine (Cogentin)

Class

Anticholinergic agent with antihistaminic properties

Mechanism

Blocks central cholinergic receptors to restore dopaminergic-cholinergic balance in extrapyramidal symptoms

FDA-Approved Use

Adjunctive treatment of parkinsonism and control of extrapyramidal symptoms (excluding tardive dyskinesia) induced by antipsychotics

Off-Label Use

Management of focal dystonias, prophylaxis of dystonia in high-risk individuals, and drug-induced parkinsonism

Formulation

Oral tablets and injectable forms

Titration

Usually starts at 0.5 mg p.o. daily, titrated based on symptom control

Dose Range

0.5–2 mg/day, given once or twice daily

Kinetics

Well absorbed orally with peak plasma levels in 1–3 hours; metabolized hepatically and excreted renally

Common AEs

Dry mouth, constipation, urinary retention, blurred vision, confusion, and tachycardia

Serious/Rare AEs

Cognitive impairment risk increases with age and higher doses

Monitoring

Monitor cognitive function and urinary symptoms, especially in elderly patients; assess for anticholinergic burden

Black Box Warning

None

Considerations

Benztropine should be used with caution in patients with cognitive impairment, and regular reassessment, including trials of discontinuation, should be considered to minimize the risk of cognitive adverse effects and to ensure that ongoing therapy remains appropriate. It may be cautiously used in younger patients with extrapyramidal symptoms or as needed for acute dystonic reactions.