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Reporting Adverse Reactions

This online form is intended for the voluntary reporting of suspected adverse reactions by health professionals and consumers involving pharmaceuticals (prescription and non-prescription), biologics (including fractionated blood products, as well as therapeutic and diagnostic vaccines), natural health products, and radiopharmaceuticals.

Reactions involving preventative vaccines, e.g. flu or travel vaccines should be reported to the Public Health Agency of Canada New window

http://www.phac-aspc.gc.ca/im/aefi-form_e.html .

Reactions involving medical devices should be reported to the Health Products and Food Branch Inspectorate New window

http://www.hc-sc.gc.ca/dhp-mps/compli-conform/prob-report-rapport/rep_md_prob-rap_inc_im_tc-tm_e.html .

To report reactions involving products not listed above, please visit the following link New window

http://www.hc-sc.gc.ca/ahc-asc/media/reaction/index_e.html .

This online form is not intended for use by market authorization holders who are to continue to mail or fax their reports to the Canadian Adverse Drug Reaction Monitoring Program (CADRMP).


Last Update: 2006-06-28	Important Notices