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Dysport® (Clostridium botulinum type A toxin-haemagglutinin complex)
Dysport<sup>®</sup> (<em>Clostridium botulinum</em> type A toxin-haemagglutinin complex)

Dysport® (Clostridium botulinum type A toxin-haemagglutinin complex) therapeutic indications

Dysport® is indicated for symptomatic treatment of focal spasticity including:

  • Adult upper limbs
  • Adult ankle joint due to stroke or traumatic brain injury (TBI).
  • Please visit the PI link at the top of this page for the full list of indications.
Adult focal spasticity

Adult focal spasticity

Spasticity is a motor disorder characterised by a velocity-dependent increase in muscle tone.1 It is a disabling condition that, if left untreated, can lead to a host of serious locoregional complications and health-related quality of life issues.2–4

There are three main disabling features of adult spasticity: muscle overactivity (reduced ability to relax), soft tissue contracture (muscle shortening and joint retraction) and paresis (reduced voluntary recruitment of skeletal motor units).5

Muscle overactivity
i.e. reduced ability to relax muscle

Soft tissue contracture
In particular, muscle shortening and joint retraction

Paresis
i.e. reduced voluntary recruitment of skeletal motor units

Adult spasticity has a wide-ranging and variable impact on the lives of patients.3 A multidisciplinary approach is required to manage symptoms, improve function and posture, and reduce the burden on the patient and carer.6,7 As each patient experience is different, it is important to formulate and agree personal treatment goals that are clear and achievable and reflect the patient and carer needs.6,7

Figure adapted from Royal College of Physicians. National guidelines. 2018;6 Turner-Stokes L, et al. 2018.7

Local intramuscular injection of Dysport® is an established and well-tolerated pharmacological treatment recommended for the management of focal spasticity.6,8 It is used, in conjunction with physical therapy and other pharmacological treatments, to prevent contractures and achieve the patient’s individual treatment goals.6 The dose of Dysport® can be titrated to the individual’s requirements.8 Clinical improvement may be expected 1 week after injection and may last up to or slightly beyond 12 weeks, depending on the individual patient.8

References:

  1. Guo X, et al. J Neuroeng Rehabil. 2022;19(1):138.
  2. Kheder A, et al. Pract Neurol. 2012;12:289–298.
  3. Barnes M, et al. Disabil Rehabil. 2017;39:1428–1434.
  4. Bhimani R, et al. Rehabil Res Pract. 2014:2014:279175.
  5. Gracies JM, et al. Muscle Nerve. 2005;31:535–551.
  6. Royal College of Physicians. Spasticity in adults: management using botulinum toxin. National guidelines. 2018. Available at: Spasticity in adults: management using botulinum toxin | RCP London (Accessed: September 2025).
  7. Turner-stokes L, et al. Eur J Phys Rehabil Med. 2018;54(4):605–617.
  8. Dysport® Summary of Product Characteristics.

Abbreviations:

BoNT-A, botulinum toxin type A; FES, functional electrical stimulation.

For further information, please refer to the Prescribing Information or the Summary of Product Characteristics.

To access relevant information about Adult Spasticity, please choose one of the following options:

Adverse events should be reported.
Reporting forms and information can be found at www.hpra.ie or e-mail medsafety@hpra.ie.
The HPRA can also be contacted on +353 16764971. Adverse events should also be reported to Ipsen via email at pharmacovigilance.uk-ie@ipsen.com or phone on +353 1 8098256.

Reporting of side effects:
If you get any side effects, talk to your doctor, pharmacist or nurse. This includes any possible side effects not listed in the package leaflet. You can also report side effects directly to the HPRA. Reporting forms and information can be found at www.hpra.ie or email medsafety@hpra.ie. Adverse events should also be reported to Ipsen via email at pharmacovigilance.uk-ie@ipsen.com or phone on +353 1 8098256. By reporting side effects, you can help provide more information on the safety of this medicine.