Interactive Drug Benefit List
DIN/NPN/PIN 02244148 PROTOPIC 0.1 % TOPICAL OINTMENT TACROLIMUS
840000 SKIN AND MUCOUS MEMBRANE AGENTS
849200 MISCELLANEOUS SKIN AND MUCOUS MEMBRANE AGENTS
Date Listed/Coverage Update: 01-Jul-2002
Unit Price: 2.6177
LCA Price: N/A
MAC Price:

N/A

Unit of Issue: Gram
Manufacturer: LEO PHARMA INC. (LEO)
ATC: D11AX14
1
Interchangeable Products: No

Coverage Status: SPECIAL AUTHORIZATION
Applies to Clients of: Non-Group Coverage (Group 1)
Coverage for Seniors (Group 66)
Palliative Coverage (Group 20514, Please note your client may have Group 1 or Group 66 coverage)
Child and Family Services (Group 20403)
Alberta Child Health Benefit (Group 20400)
Children and Youth Services (Group 19824)
Income Support (Group 19823)
Alberta Human Services (AISH) (Group 19823)
Alberta Adult Health Benefit (AAHB) (Group 23609)

Special Authorization Request Form:

Tacrolimus Topical Ointment Special Authorization Request Form (ABC 60047)

SPECIAL AUTHORIZATION


"For use in patients 16 years of age and older with atopic dermatitis affecting face and flexures who are unable to tolerate or have failed topical steroid therapy."

"For use in patients 16 years of age and older with atopic dermatitis who require ongoing use of potent (Class 3 or higher) topical steroids over greater than 30 % of body surface area."

"Special authorization for all criteria may be granted for 6 months."

Information is required regarding the patient's diagnosis, previous medications utilized (including specific topical steroids) and the patient's response to therapy. In order to comply with the first criterion, information is also required regarding the area(s) affected. In order to comply with the second criterion, information is also required regarding the percentage body surface area affected.

The following product(s) are eligible for auto-renewal.

All requests for tacrolimus topical ointment must be completed using the Tacrolimus Topical Ointment Special Authorization Request Form (ABC 60047).

Review Status / Past Decisions

Indication Reviewing
Body
Submission
Completion
Date
CDR
Recommendation
Date
Expert Committee
Recommendation
Date
ADBL
Effective
Date
CDR
Recommendation
Review
Status
N/A Expert Committee 2001/10/02 2009/07/01 Special Authorization Criteria Change
Indication N/A
Reviewing
Body
Expert Committee
Submission
Completion
Date
2001/10/02
CDR
Recommendation
Date
Expert Committee
Recommendation
Date
ADBL
Effective
Date
2009/07/01
CDR
Recommendation
Review
Status
Special Authorization Criteria Change
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