Finished product reference
Biperiden Lactate
Injection · Parenteral · 5 mg/1mL
- List code
- 165
- Pharmacologic class
- Antimuscarinic antiparkinsonian agent
What it is and how it works
Biperiden is a centrally acting muscarinic receptor antagonist that reduces the relative cholinergic excess in the striatum resulting from dopamine deficiency or dopamine-receptor blockade.
Indications
Parkinsonism, particularly for tremor; drug-induced extrapyramidal symptoms (excluding tardive dyskinesia), including acute dystonic reactions caused by antipsychotics.
Dosage and administration (summary)
Oral: initially 1 mg twice daily, increased gradually to a usual maintenance of 3–12 mg daily in divided doses. Acute drug-induced reactions: 2.5–5 mg by intramuscular or slow intravenous injection, repeated if necessary (maximum about 20 mg in 24 hours).
Contraindications
Angle-closure glaucoma, gastrointestinal obstruction, megacolon, untreated urinary retention, and hypersensitivity to biperiden.
Warnings and precautions
Antimuscarinic effects include dry mouth, blurred vision, constipation, urinary retention and tachycardia; confusion, memory impairment and hallucinations are more likely in the elderly. It does not improve and may worsen tardive dyskinesia; potential for misuse due to euphoriant effects. Avoid abrupt withdrawal; may impair ability to drive.
Pregnancy
Use in pregnancy only if clearly necessary.
Storage and supply
Store below 25 °C, protected from light.
Source: reference summary prepared from the EU SmPC/EPAR, BNF and WHO Model Formulary. The approved product information in Iran governs.
Other presentations of the same active ingredient
Reference information for professional sourcing and registration enquiries, not medical advice or a promotion. Drug information is condensed from US FDA prescribing information (public domain, via openFDA and DailyMed) and does not replace the product’s approved labelling in Iran. Availability, origin and documentation are confirmed per enquiry.
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