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ONTARIO regulation 173/01

made under the

Drug interchangeability and
dispensing fee Act

Made: May 16, 2001
Filed: May 17, 2001
Printed in The Ontario Gazette: June 2, 2001

Amending Reg. 935 of R.R.O. 1990

(General)

Note: Since the end of 2000, Regulation 935 has been amended by Ontario Regulation 15/01.  Previous amendments are listed in the Table of Regulations published in The Ontario Gazette dated January 20, 2001.

1. (1) The definition of “Formulary” in subsection 1 (1) of Regulation 935 of the Revised Regulations of Ontario, 1990 is revoked and the following substituted:

“Formulary” means the Ministry of Health publication titled “Drug Benefit Formulary/Comparative Drug Index” (No. 37) dated March 7, 2001, including the amendments to the publication dated June 7, 2001;

(2) Section 1 of the Regulation is amended by adding the following subsection:

(2) For the purposes of this Regulation, items 255 and 256 of Part III of the Formulary are deemed to read as follows:

255

5mg Tab

 

 

4.5900

 

02232043

Aricept

PFI

4.5900

 

256

 

10mg Tab

 

 

 

4.5900

 

02232044

Aricept

PFI

4.5900

 

 

 

Reason for

Use Code

 

 

Clinical criteria

 

 

 

347

For the initial trial for patients with mild to moderate Alzheimer’s disease (Mini-Mental State Exam [MMSE] 10-26), patients will be reimbursed for a period of up to three months after which continued treatment must be reassessed.

 

 

348

For continuation of therapy, further reimbursement will be made available to those patients whose disease has not progressed or deteriorated while on this drug. Patients must continue to have a MMSE score of 10-26.

 

2. (1) Subsection 1 (1) comes into force on June 7, 2001.

(2) Subsection 1 (2) comes into force on June 1, 2001.