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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 in adults for:

  • Spasmodic torticollis
  • Blepharospasm
  • Hemifacial spasm
  • Persistent severe primary axillary hyperhidrosis (interfering with daily living and resistant to topical treatment)
  • Please visit the PI link at the top of this page for the full list of indications.
Efficacy information

Efficacy information

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Dysport® injections may be repeated approximately every 16 weeks, or as required to maintain a response, but not more frequently than every 12 weeks.1

In an open-label extension study, the mean time to retreatment was 15–17 weeks over repeat cycles.2

Mean time to retreatment over repeated cycles (n=108)

15(±5.6)-17(±8.0) WEEKS OVER THREE OPEN-LABEL CYCLES

82% of patients did not require reinjection at week 12, with more than 40% not requiring reinjection at week 16.3

Dysport® may allow your patients to find lasting symptom relief between injections.2,3

Figure adapted from Esquenazi A, et al. 2020.3

In an open-label prospective study, Dysport® improved quality of life and pain intensity.4

Dysport® is the only BoNT-A with a Level A recommendation (the highest quality of evidence for efficacy) for cervical dystonia by the AAN5,6

Indication Level of recommendation      
  Level A Level B Level C Level U
Cervical dystonia Dysport® OnabotulinumtoxinA
IncobotulinumtoxinA
   

Table adapted from AAN Guidelines.6

*Statistically significant (P<0.001) vs baseline.

Statistically significant (P<0.001) vs baseline change from baseline score was worse at weeks 12 to 4.

Level A: established as effective, or useful; should be offered.6 Level B: probably effective, or probably useful; should be considered.6 Level C: possibly effective, or possibly useful; may be considered.6 Level U: data inadequate or conflicting; insufficient to support or refute a benefit.6

References:

  1. Dysport® Summary of Product Characteristics.
  2. Truong D, et al. Parkinsonism Relat Disord. 2010;16:316–323.
  3. Esquenazi A, et al. Front Neurol. 2020;11:576117.
  4. Hefter H, et al. BMJ Open. 2013;3(4):e001853.
  5. Simpson DM, et al. Neurology. 2016;86(19):1818–1826.
  6. Practice Guideline Update: Botulinum Neurotoxin for the Treatment of Blepharospasm, Cervical Dystonia, Adult Spasticity, and Headache. Available at: https://www.aan.com/Guidelines/home/GetGuidelineContent/738 (Accessed: September 2025).

 

Abbreviations:

AAN, American Academy of Neurology; BoNT-A, BoNT-A, botulinum toxin type A; CD, cervical dystonia; CDQ-24, Craniocervical Dystonia Questionnaire; QoL, quality of life; VAS, visual analogue scale.

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

To access relevant information about Cervical Dystonia, 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.