Public recall detail

Risk of anaphylactic reaction associated with glatiramer acetate, used to treat multiple sclerosis

2025-08-21

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Recall Safety notice
Quick summary

Quick summary: Risk of anaphylactic reaction associated with glatiramer acetate, used to treat multiple sclerosis. Date: 2025-08-21.

Recommended action

Recommended action: compare your product with the official notice and follow the instructions published by the official source.

Recall details

Quick summary: Risk of anaphylactic reaction associated with glatiramer acetate, used to treat multiple sclerosis. Date: 2025-08-21.

Official details

Affected product details

Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.

Brand
ProductGlatiramer acetate
IssueHealth products - Product safety Health products - New safety information
IdentificationRA-77939

Affected products

ProductProduct
ProductCopaxone (glatiramer acetate)
ProductCopaxone (glatiramer acetate)
ProductCopaxone (glatiramer acetate)
ProductGlatect (glatiramer acetate)
ProductMylan glatiramer acetate injection

Issue

Health Canada is warning patients that they may experience anaphylactic reactions after receiving glatiramer acetate, which is used to treat relapsing-remitting multiple sclerosis. These anaphylactic reactions can be fatal and may occur at any point during treatment, from as soon as the first dose to months or even years after starting therapy. Anaphylactic reaction symptoms generally appear within one hour of injection and may include: Sudden shortness of breath, wheezing, or difficulty breathing Swelling of the eyelids, face, lips, mouth, tongue, or throat Uncontrolled shaking Fainting or dizziness Trouble swallowing or speaking Widespread rash, hives Collapse Health Canada confirmed this new safety risk following a review of all available data, including 11 Canadian cases of anaphylactic reactions from Copaxone and three additional cases from other glatiramer acetate products. While there have been no fatal cases reported in Canada, some cases required treatment with epinephrine and other appropriate medical interventions. There have been fatal cases reported internationally. Health Canada has informed healthcare professionals, including neurologists, emergency room physicians and staff, nurses, and pharmacists about this new safety risk. The manufacturer for Copaxone has updated its Canadian product labelling to include this risk, and Health Canada is working with the manufacturers of other glatiramer acetate products — including Glatect and Mylan glatiramer acetate injection — to update their respective labelling.

What you should do

  • If you experience anaphylactic reaction symptoms, stop taking glatiramer acetate and seek immediate medical help by calling 9-1-1.
  • Do not restart taking glatiramer acetate if you have experienced anaphylaxis unless your healthcare provider has identified another clear cause for the anaphylaxis.
  • Report any health product-related side effects to Health Canada.
  • Inform patients and/or caregivers of the signs and symptoms of anaphylactic reactions, which may overlap with those of an immediate post-injection reaction.
  • Instruct patients to seek immediate emergency medical care in the event of an anaphylactic reaction.
  • Instruct patients to discontinue treatment with glatiramer acetate if they have an anaphylactic reaction.
  • Do not restart the medicine unless there is another clear reason the patient experienced an anaphylactic reaction.
Additional official information
AudienceIdentification number RA-77939
CategoryHealth products - Drugs
CompaniesPublished by Health Canada
Published byHealth Canada
Alert / recall typePublic advisory
Identification numberRA-77939
Background{}
CompaniesPublished by Health Canada
AudiencesIdentification number RA-77939
Source updated2025-08-21

Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.

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