Compliance

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Adverse Event Reporting

Please contact us if you experience an Adverse Event associated with the use of a iON Pharma USA product. An Adverse Event (or ADE) is any undesirable experience associated with the use of a medical product in a human patient, whether or not considered drug-related.

If you are currently experiencing a life threatening event, please immediately call 9-1-1.

To Report an Adverse Event (or Adverse Experience) related to a iON Pharma USA product:
Contact the iON’s Drug Safety Team at (833) 711-8833 or at [email protected]

You are encouraged to report negative side effects of prescription drugs to the FDA. Visit www.fda.gov/medwatch, or call (800) FDA-1088.

Product Complaints

Please contact us if you have concerns regarding the identity, efficacy, purity, safety, or quality of a iON Pharma USA product or its immediate container.

If you are currently experiencing a life-threatening event, please immediately call 9-1-1.

For complaints about a iON product:

Contact the iON Pharma USA’s Drug Safety Team at (833) 711-8833 or at [email protected]

You are encouraged to report negative side effects of prescription drugs to the FDA. Visit www.fda.gov/medwatch, or call (800) FDA-1088.