Explanatory Note Epinephrine
(This note is not part of the Order.)
The Interim Order Respecting Epinephrine Auto-injectors (the Interim Order) made by the Minister of Health on August 27, 2018 permits the immediate importation and sale of epinephrine auto-injectors, sold under the brand name AUVI-Q® (0.15 mg and 0.3 mg doses) and authorized by the United States Food and Drug Administration for use in the emergency treatment of life-threatening allergic reactions.
The objective of the Interim Order is to address the significant risk to the health of Canadians as a result of a shortage of epinephrine auto-injectors. This Interim Order represents one of a number of actions to help address a critical shortage of a life-saving drug.
Epinephrine auto-injectors are life-saving drug delivery products used in the treatment of life-threatening allergic reactions in adults and children. The Canadian market for epinephrine auto-injectors is currently supplied by Pfizer Canada’s products EpiPen (0.3 mg dose) and EpiPen Jr (0.15 mg dose for children weighing between 33-66 pounds), manufactured by Meridian in the United States.
Supplies of EpiPens have been in shortage globally for several months due to manufacturing issues and it is unclear when the situation will be resolved. These issues have resulted in limited importation of supplies into Canada. Health Canada communicated publicly advising Canadians of the shortage in January and April 2018. On July 30, 2018, Health Canada further advised Canadians of the limited supply and likely depletion of the supply of EpiPens in the 0.3 mg format at pharmacies across Canada. Supplies of EpiPen Jr are also limited. The beginning of the school year has historically been a time of peak demand for the 0.15 mg dose. Moreover, the monthly demand for both doses is anticipated to increase significantly once product becomes available as people have been coping with limited supply for several months.
Health Canada has identified an alternative supplier, Kaléo Inc., whose epinephrine auto-injector product, AUVI-Q®, is authorized for sale in the United States. This product is comparable to another product by the same company that has been authorized by Health Canada previously, but that is not currently marketed in Canada. The most significant difference is that the U.S. product does not include French labelling and instructions. Health Canada will address this difference by requiring that instructions in English and French be provided to all consumers.
The Interim Order permits shipments of AUVI-Q® (0.15 mg and 0.3 mg doses) to be imported from the United States and sold in Canada.
In order to be sold to consumers in Canada, AUVI-Q® will need to be accompanied by the U.S. approved patient information, available in French and English on Health Canada’s website.
Most provisions in Part C of the Food and Drug Regulations will not apply to the importation or sale of AUVI-Q®. However, requirements relating to the reporting of serious adverse drug reactions, recall by the manufacturer, and the ministerial power to order a test or study will continue to apply. In addition, AUVI-Q® will be required to be imported by an importer holding an establishment licence issued by Health Canada.
Representatives of provinces and territories and pharmacists have been made aware of the Minister’s intent to take action to address the shortage of epinephrine auto-injectors. They have indicated their support for the Interim Order as a mechanism to facilitate an improved supply of life-saving products for Canadians.
Director, Policy and Regulatory Strategies Directorate
Regulatory Operations and Regions Branch
Health Canada / Government of Canada
Address Locator: 1907A
200 Eglantine Driveway
Jeanne Mance Building
7th Floor, Room 705A
Ottawa, Ontario K1A 0K9
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