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Thalidomide (Thalomid®)

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.


CAUTION: Thalidomide is a category X drug and must not be given to pregnant women. Pregnancy in female patients or in the partners of male patients must be avoided during treatment and for 1 month after cessation of treatment.

Criteria

Multiple myeloma.

NOTE: Patients receiving thalidomide under the PBS listing must be registered in the i-access® risk management program.

Specialist Prescriber

 Signature:  ____________________________________
 Name:  ____________________________________
 Date:  ____________________________________

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

August 2010

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This web page is managed and authorised by Pharmaceutical Services of Centre for Health Protection of the NSW Department of Health. Last updated: 13 August, 2010