If you would like to report an adverse event or product quality issue, please complete the Adverse Events Form linked below. The form asks for details about what happened, the product involved, and the person affected, along with contact information for the person submitting the report. It also includes space for relevant test results, medical history, allergies, and other products or medications being used.

Please provide as much detail as possible when completing the form. The document notes that submission of a report does not constitute an admission that medical personnel or the product caused or contributed to the event.

If available, keep the product in case further evaluation is needed, but do not send the product unless you are contacted directly. The completed form should be emailed to the contact address listed on the document: adverse.events@regulatorymatters.com.au