Report an Adverse Event

Last updated 20 August 2026

If you experience a side effect or unexpected reaction to a treatment prescribed through CLARIA, tell us. Reports are reviewed by a clinician.

If it is an emergency

Do not use this page. Call 911 or go to the nearest emergency room. Signs needing emergency care include difficulty breathing, swelling of the face, lips or throat, chest pain, sudden severe headache, weakness on one side, fainting, or pain and swelling in one leg.

How to report

Email __PLACEHOLDER_SUPPORT_EMAIL__ with the subject line ADVERSE EVENT, or call __PLACEHOLDER_SUPPORT_PHONE__. Tell us the medication, the dose, when it started, what you experienced, and how you are now.

What we do with it

• A clinician reviews every report, and urgent reports are triaged the same business day.
• Your clinician is notified and will contact you about whether to stop, change or continue treatment.
• The event is recorded in your medical record and in our adverse event log.
• Where required we report the event to the FDA through MedWatch and notify the dispensing pharmacy and, where applicable, the manufacturer.

Reporting directly to the FDA

You may also report directly to the FDA MedWatch program at fda.gov/medwatch or by calling 1-800-FDA-1088. You do not need our permission.

Contact

__PLACEHOLDER_LEGAL_ENTITY__, __PLACEHOLDER_PHYSICAL_ADDRESS__. Email __PLACEHOLDER_SUPPORT_EMAIL__. Phone __PLACEHOLDER_SUPPORT_PHONE__.