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Neuromuscular Blocking Agent (Botulinum Toxin)

Botulinum Toxin Type A (ENT)

Brand names: Botox, Dysport, Xeomin

Botulinum toxin type A is given by targeted local injection for several ENT indications, including spasmodic (laryngeal) dysphonia, troublesome sialorrhoea and certain cricopharyngeal and salivary-gland disorders.

Dosing — not shown for this use

The product information we hold does not support a dose for this page's specific use, route or population, so none is shown. Follow your local or national guideline, and confirm against the product SmPC.

The licensed dosing — for the medicine's licensed uses, which may differ from this page's — is on Botulinum Toxin Type A.

Clinical monograph

How it works

It blocks presynaptic release of acetylcholine at the neuromuscular junction and cholinergic autonomic terminals, producing temporary, dose-dependent weakening of injected muscle or reduction of glandular secretion.

Prescribing in practice

  • Different botulinum toxin products are not interchangeable in units and dosing errors can cause toxin spread with serious effects such as dysphagia, aspiration or breathing difficulty, so the specific product and indication must be confirmed and injection performed by appropriately trained clinicians.
  • Effects are temporary, developing over days and lasting some months, so repeat treatment is generally needed.
  • Use cautiously in patients with neuromuscular disorders (such as myasthenia gravis) or pre-existing swallowing problems, who are more prone to adverse effects.

Monitoring

Assess the targeted clinical effect and watch for local spread effects such as new or worsening swallowing or voice difficulty after each treatment.

Counselling the patient

  • The effect is temporary and usually needs repeating after a few months.
  • Seek urgent help for difficulty swallowing, breathing or speaking after injection.
  • Voice or swallowing may change for a short period after laryngeal injection.

Evidence & guidelines

Local botulinum toxin injection is the established treatment for adductor spasmodic dysphonia and an option for refractory sialorrhoea.

Reference: MHRA Botulinum Toxin Guidance 2012; NICE TA107 (chronic sialorrhoea); Borodic et al. Laryngoscope 1992 (spasmodic dysphonia); BAO-HNS Frey's Syndrome Guideline; Drug verified in RxNorm (NLM); confirm dosing against the manufacturer SPC (eMC). Verify against your local formulary and current prescribing references before prescribing. Monograph status: clinician-reviewed (2026-07-04).

Related

Curated clinical cross-links plus same-class fallbacks.