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Contact: Marketed Health Products Directorate (MHPD)
The Health Products and Food Branch (HPFB) posts on the Health Canada web site safety alerts, public health advisories, press releases and other notices as a service to health professionals, consumers, and other interested parties. These advisories may be prepared with Directorates in the HPFB which includes pre-market and post-market areas as well as market authorization holders and other stakeholders. Although the HPFB grants market authorizations or licenses for therapeutic products, we do not endorse either the product or the company. Any questions regarding product information should be discussed with your health professional.
This is duplicated text of a letter from Wyeth, a Pfizer Company.
Contact the company for a copy of any references, attachments or enclosures.
Public Communication
Health Canada Endorsed Important Safety Information on Rapamune (sirolimus)
November 26, 2009
Subject: Sirolimus Blood Level Measurement Changes
Wyeth (a Pfizer company)* in collaboration with Health Canada would like to inform patients that different ways to measure Rapamune in the blood produce results that cannot be substituted one for the other.
Rapamune belongs to a group of medicines called immunosuppressants. It is used to prevent rejection of transplanted kidneys and is often used in combination with other immunosuppressants and corticosteroids.
Health Care Professionals will inform patients taking Rapamune exactly what dose of Rapamune to take and how often to take it. They will also monitor the quantity of the drug in patients' blood.1
Patients taking Rapamune should always take their medicine exactly as prescribed. Rapamune should not be stopped unless advised by a physician. Rapamune doses are adjusted based on age, other medications, and medical conditions.
Rapamune should be taken once a day at about the same time each day either with or without food. Rapamune should not be taken with grapefruit or grapefruit juice. Rapamune tablets should not be crushed, chewed, or split. Patients should inform their Doctor if they have difficulty taking the tablet.1
Wyeth Canada, in collaboration with Health Canada, issued a letter to Health Care Professionals informing them of important changes in monitoring the quantity of Rapamune in the blood. A copy of that letter is available on the Health Canada web site.
Managing marketed health product-related adverse reactions depends on health care professionals and consumers reporting them. Reporting rates determined on the basis of spontaneously reported post-marketing adverse reactions are generally presumed to underestimate the risks associated with health product treatments. Any case of serious or unexpected adverse reactions in patients receiving Rapamune should be reported to Wyeth Canada or Health Canada at the following addresses:
Any suspected adverse reaction can also be reported to:
Canada Vigilance Program
Marketed Health Products Directorate
Health Canada
Address Locator: 0701D
Ottawa, Ontario, K1A 0K9
Telephone: 613-957-0337 or Fax: 613-957-0335
To report an Adverse Reaction, consumers and health professionals may call toll free:
Telephone: 1-866-234-2345
Fax: 1-866-678-6789
CanadaVigilance@hc-sc.gc.ca
The Adverse Reaction Reporting Form and the Adverse Reaction Guidelines can be found on the Health Canada Web site or in The Canadian Compendium of Pharmaceuticals and Specialties.
For other inquiries related to this communication, please contact Health Canada at:Rapamune Consumer Information and a full Product Monograph can be accessed at the
Wyeth web site or on the Health Canada web site. Please contact Wyeth Canada Medical Information at 1-800-461-8844 with any additional questions or concerns about Rapamune.
original signed by
Dr. Neil Maresky, M.B., B.Ch.
Vice-President
Scientific Affairs
1. Rapamune® - Product Monograph dated Oct. 9, 2009, Wyeth Canada.
* Wyeth is now a part of Pfizer Inc. The merger of local Wyeth and Pfizer entities may be pending in various jurisdictions and is subject to completion of various local legal and regulatory obligations.