How to Report an Adverse Event to Delta Medical

At Delta Medical, patient safety is our top priority. If you are a healthcare professional or consumer and suspect that one of our pharmaceutical products or medical devices may have caused an adverse event, we encourage you to report it to us promptly. 

Adverse events may include:

  • Unexpected side effects
  • Adverse reactions
  • Product quality issues
  • Medication errors
  • Lack of effect

Reporting Adverse Events

To report a suspected adverse event related to a Delta Medical product, please contact us through one of the following methods:

  1. Fill out our online Adverse Event Reporting Form on our website. Provide as much detail as possible, including:
    • Patient information (age, gender, medical history)
    • Product name, dose, and lot number if available
    • Description of the adverse event and any treatment provided
    • Contact information
  2. Attach any relevant documents or photographs

What Happens Next

Our pharmacovigilance team will carefully review the adverse event report. We may contact you for additional information if needed. Suspected adverse events are reported to the appropriate regulatory agencies as required.

By reporting adverse events, you can help Delta Medical monitor the safety of our products and contribute to public health. We appreciate you taking the time to inform us of any suspected adverse events. Your partnership helps us ensure we are providing the safest and most effective therapies to patients.

Thank you for assisting us in our mission to improve patient safety.


    Accepted file types: doc, docx, rtf, txt, odt, pdf, pptx, Max. file size: 24 MB.