Patient Safety

Report a Side Effect or Product Quality Complaint

To keep patients safe, it is vital that the highest possible quality is maintained with our products. If you have experienced an unwanted effect or quality issue, please let us know.

drug.safety@mydawa.com

What to Report

Definitions of reportable events

AE

A side effect or adverse event is any unwanted medical occurrence in a patient who has been given a pharmaceutical product that may have been caused by treatment with the product.

PQ

Product quality complaints relate to a physical issue with a pharmaceutical product or a device and/or its packaging — for example, a broken seal, unusual appearance, or suspected contamination.

Information to Include in Your Report

Provide as much detail as possible to help our pharmacovigilance team

  • Contact information (name, phone number or email)
  • Age of the patient who experienced the effect
  • Product name and dosing information
  • Batch / Lot number (found on the packaging)
  • Date you experienced the side effect or quality concern
  • Detailed description of the side effect or quality concern
The list above is not exhaustive. Include any additional information you believe is relevant to the report — more detail helps us investigate more thoroughly.

Submit Your Report

Write to our dedicated drug safety team with the information above. We review every report and take patient safety very seriously.

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