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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.
Dosing and administration

Dosing and administration

Dysport® is a flexible treatment option for patients with cervical dystonia.1

Initial recommended dose: 500 U per patient

Given as a divided dose and administered into the two or three most active neck muscles.

Initial dose equivalent to:
1 x 500 U vial

Subsequent dose: Up to 1000 U and no lower than 250 U*

On subsequent administration, the doses may be adjusted according to the clinical response and side effects observed.

Titration of dose to a
maximum of:
2 x 500 U vial

 

 

Figure adapted from Dysport® Summary of Product Characteristics.1

Cervical dystonia dilution table2

In the treatment of cervical dystonia, Dysport® is reconstituted with sodium chloride injection B.P. (0.9% w/v) to yield a solution containing 500 units per ml of Dysport®.2

Volume Injected (ml) Volume of injectable NaCl solution (0.9%) used to reconstitute a vial of Dysport® 500 U
1ml
Dysport® units delivered
0.1 50
0.2 100
0.3 150
0.4 200
0.5 250
0.6 300
0.7 350
0.8 400
0.9 450
1.0 500

The dosing recommendations in the Dysport® SmPC should always be followed.1 Dysport® should only be administered by an appropriately qualified healthcare professional.1 The relief of cervical dystonia symptoms may be expected within a week of the injection. Injections may be repeated approximately every 16 weeks, or as required to maintain a response, but not more frequently than every 12 weeks.1

*Higher doses may be accompanied by an increase in side effects, particularly dysphagia.1

References:

  1. Dysport® Summary of Product Characteristics.
  2. Dysport® dosing and administration guide.

 

Abbreviations:

SmPC, Summary of Product Characteristics; U, units.

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.