ACTEMRA (tocilizumab)

Product description

Brand name
ACTEMRA
Company name
Hoffmann-La Roche Limited
Ingredient
tocilizumab
Date of approval

Resources

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Updated Date Resources for Resources Description Date
Consumers

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

he 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
Consumers

The Regulatory Decision Summary explains Health Canada’s decision for the product seeking market authorization. The RDS includes the purpose of the submission and the reason for the decision.

Consumers, Health Care Professionals, Researchers

Public Advisories and Health Product Risk Communications are two ways that Health Canada communicates safety issues. They are published when Health Canada has important updates or other information to share about the product, such as new approvals, information on shortages, or risks.

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

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