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Adverse Event Reporting

Adverse Event Reporting

Please contact us if you experience an Adverse Event associated with the use of a SOLA Pharmaceuticals 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 SOLA product:
Contact the SOLA Drug Safety Team at (866) 747-7365, Ext.4 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.