ARTICLE
7 November 2024

Understanding The Legal Implications Of Failure To Warn Of Medical Risks In Ontario

This process, known as informed consent, is important under Ontario law. Failing to warn patients of possible risks undermines the patient's ability to make informed decisions about their health.
Canada Ontario Food, Drugs, Healthcare, Life Sciences

When patients undergo medical treatments or procedures, they have the right to be informed about the potential risks of those treatments and procedures.

This process, known as informed consent, is important under Ontario law. Failing to warn patients of possible risks undermines the patient's ability to make informed decisions about their health. This blog post explores what constitutes a failure to warn, its implications for patient safety, and the legal recourse available to patients.

What is Informed Consent?

Healthcare providers are expected to inform patients about the known risks of the medical interventions they are recommending to their patient. This allows patients to make informed decisions about their health.

The Importance of Informed Consent

Informed consent is a fundamental patient right and a legal obligation that requires doctors to disclose significant medical information to patients. This information should include:

  • Nature of the Procedure: A clear description of the treatment or procedure they are recommending to the patient.
  • Risks and Benefits: An explanation of the potential risks and benefits of the procedure.
  • Alternatives: Information about alternative treatments, including those that might be non-surgical or involve different risks.
  • Consequences of Non-Treatment: Insight into what might happen if the patient declines treatment.

Common Scenarios of Failure to Warn

  • Complex Surgeries: Not disclosing potential complications such as infection, loss of function, or even death.
  • Prescription Medications: Failing to inform about possible side effects or adverse reactions, especially with drugs that have severe known risks.
  • Routine Procedures: Underestimating the necessity to inform about risks because a procedure is typically considered safe.

Implications for Patients

The failure to adequately warn patients can lead to:

  • Unanticipated Medical Complications: Patients may suffer from severe side effects or complications that they could have chosen to avoid.
  • Psychological Impact: The shock and stress of unexpected outcomes can lead to significant emotional distress.
  • Loss of Trust: Patients may lose trust in the medical profession, affecting their willingness to seek future care.

The content of this article is intended to provide a general guide to the subject matter. Specialist advice should be sought about your specific circumstances.

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