Medical Adverse Events Canada

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Adverse Reaction Database - Canada.ca

https://www.canada.ca/en/health-canada/services/drugs-health-products/medeffect-canada/adverse-reaction-database.html

The Canada Vigilance Adverse Reaction Online Database contains information about suspected adverse reactions (also known as side effects) to health products. Adverse reaction reports are submitted by: consumers and health professionals, who submit …

Adverse reactions, medical device incidents and health …

https://www.canada.ca/en/health-canada/services/drugs-health-products/reports-publications/medeffect-canada/adverse-reactions-incidents-recalls-2019-summary.html

Canada Vigilance Program - Canada.ca

https://www.canada.ca/en/health-canada/services/drugs-health-products/medeffect-canada/canada-vigilance-program.html

Canada Vigilance Program Health Products Surveillance and Epidemiology Bureau Marketed Health Products Directorate Health Products and Food Branch Health Canada …

Incident reporting for medical devices: …

https://www.canada.ca/en/health-canada/services/drugs-health-products/reports-publications/medeffect-canada/incident-reporting-medical-devices-guidance-2021.html

Reportable incidents involving a medical device that affected one or more patients, users or other persons, on the same, or different, dates are to be reported to Health Canada as separate …

Canadian Adverse Events Following Immunization …

https://www.canada.ca/en/public-health/services/immunization/canadian-adverse-events-following-immunization-surveillance-system-caefiss.html

Health Canada (HC) and the Public Health Agency of Canada (PHAC) share the monitoring of the safety of vaccines in Canada. Market authorization holders are required to report …

The Canadian Adverse Events Study: the …

https://www.cmaj.ca/content/170/11/1678

Background: Research into adverse events (AEs) has highlighted the need to improve patient safety. AEs are unintended injuries or complications resulting in death, disability or prolonged …

Mandatory reporting of serious adverse …

https://www.canada.ca/en/health-canada/services/drugs-health-products/medeffect-canada/adverse-reaction-reporting/mandatory-hospital-reporting/drugs-devices/guidance.html

Medical device incident contributing factors: the hospital must submit any contributing factors to the medical device incident, including any medical condition of the patient that directly relates …

Mandatory Medical Device Problem Reporting Form for …

https://www.canada.ca/en/health-canada/services/drugs-health-products/medeffect-canada/adverse-reaction-reporting/mandatory-medical-device-problem-reporting-form-industry-adverse-reaction-reporting.html

This section contains information about the reporter, who is submitting the report to Canada Vigilance - Medical Devices Problem Reporting Program (CV-MD) to fulfil their …

Adverse events and patient safety in Canadian health care

https://bcmj.org/articles/adverse-events-and-patient-safety-canadian-health-care

Adverse events and patient safety in Canadian health care | British Columbia Medical Journal About The Journal Classifieds CME Calendar Submit Content Advertise About …

TTISS assesses risk of adverse transfusion events after …

https://www.canada.ca/en/public-health/services/publications/drugs-health-products/transfusion-transmitted-injuries-surveillance-system-2018-2019-infographic.html

TTISS project. The Transfusion Transmitted Injuries Surveillance System (TTISS) captures data on adverse transfusion events (ATEs) during blood transfusions in all Canadian …

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