Casirivimab (casirivimab) and imdevimab (imdevimab)

Product description

Brand name
Casirivimab and imdevimab
Company name
Hoffmann-La Roche Limited
Ingredient
casirivimab / imdevimab
Date of approval

Resources

Click on a resource to visit a page with more information. You may be taken away from this page to a different Government of Canada website.

Updated Date Resources for Resources Description Date
Consumers, Health Care Professionals

Information about the product including what the product is used for, dosage, warnings, proper use and side effects.  This summary will not tell you everything about the product. Contact your healthcare professional if you have any questions about the product.

Health Care Professionals, Researchers

The Product Monograph is a scientific document that describes the properties, claims, indications and conditions of use of the product and contains any other information that may be required for optimal, safe and effective use.

The Product Monograph includes three sections:

  • Part I: Health Professional Information;
  • Part II: Scientific Information; and
  • Patient Medication Information
Health Care Professionals

The Canadian reference labels for the vial and carton labels. These labels provide information specific to Canada in both French and English and can be used as reference until the manufacturer implements them on the Canadian-specific product vial and carton.

Health Care Professionals

Vial and carton labels for product with English-only labeling.

Consumers

The Summary Basis of Decision explains why the product was approved for sale in Canada. The document includes regulatory, safety, effectiveness and quality (in terms of chemistry and manufacturing) considerations.

Health Care Professionals, Researchers

The Summary Basis of Decision explains why the product was approved for sale in Canada. The document includes regulatory, safety, effectiveness and quality (in terms of chemistry and manufacturing) considerations.

Health Care Professionals, Researchers

The Post Authorization Activity Table includes brief summaries of the activities that occur after the approval of the product. It is updated on a monthly basis.

Researchers

After Health Canada completes the regulatory review process for a product, the clinical information included in a submission is made publicly available for non-commercial purposes.

Health Care Professionals, Researchers

For COVID-19 authorizations, Health Canada can impose terms and conditions on the authorization. This allows Health Canada to continue to gather information on the safety, effectiveness and/or quality of the product. The status of the terms and conditions will be updated on a regular basis.

Consumers, Health Care Professionals, Researchers

Advisories are published when Health Canada has important updates or other information to share about the product, such as information on new approvals, shortages, labelling updates, or risks.

Clicking the link will retrieve any advisories  that Health Canada has issued about the product from November 2021 onward.  If no advisories have been issued, no results will be returned.

Various
Consumers, Health Care Professionals, Researchers

Advisories are published when Health Canada has important updates or other information to share about the product, such as information on new approvals, shortages, labelling updates, or risks.

Clicking the link will retrieve any advisories and risk communications that Health Canada has issued about the product prior to November 2021.  If no advisories have been issued, no results will be returned.

Various