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Adverse Event Report
Please complete this form to report any unexpected side effects or adverse events associated with our products. Your health and safety are our priority.
Adverse Events & Product Complaints
Learn how to report adverse events, product complaints, and access our safety resources.
Adverse Events & Product Complaints
What Is an Adverse Event?
An adverse event (also known as an adverse experience) is any undesirable, unintended, or unexpected medical occurrence that happens after the use of a pharmaceutical product, whether or not it is believed to be caused by the product.
Medical Emergencies
If you are experiencing a medical emergency or a life-threatening reaction, call 9-1-1 or seek immediate medical attention before submitting an adverse event report.
Report an Adverse Event or Product Complaint
At AmVerza, patient safety is our highest priority. We are committed to monitoring, evaluating, and responding to reports of adverse events and product quality concerns associated with our products.
If you experience an adverse event, side effect, or product complaint related to the use of an Amverza product, we encourage you to report it to us promptly so it can be reviewed by our Drug Safety team.
To report an adverse event, side effect, medication error, or product quality issue related to an Amverza product, please contact our Drug Safety team:
Phone: 1-855-AMVERZA
Email: drugsafety@amverza.com
When reporting an event, please provide as much information as possible, including:
Product name
Description of the event or concern
Date the event occurred
Patient age and gender (if available)
Contact information for follow-up
Providing complete and accurate information helps us evaluate and process reports more efficiently.
Report to the FDA
Patients and healthcare professionals may also report adverse events and side effects directly to the U.S. Food and Drug Administration (FDA).
Website: https://www.fda.gov/medwatch
Phone: 1-800-FDA-1088
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