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Baclofen (Lioresal Intrathecal®)

Highly Specialised Drugs Program Declaration Form*

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 Patient's Name:   ____________________________________
 Medical Record Number:   ____________________________________
 Medicare Number:     ____________________________________
                

I certify that the above patient meets the Pharmaceutical Benefits Advisory Committee's criteria for funding under Section 100 of the National Health Act, 1953.



Criteria

Patients with severe chronic spasticity, where oral antispastic agents have failed or have caused unacceptable side effects, in patients with chronic spasticity:

  1. of cerebral origin; or
  2. due to multiple sclerosis; or
  3. due to spinal cord injury; or
  4. due to spinal cord disease.

 

Specialist Prescriber

 Signature:  ____________________________________
 Name:  ____________________________________
 Date:  ____________________________________

*To be completed by the specialist initiating drug treatment, and retained by the hospital Pharmacy Department.

February 2003

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