Urovant Sciences, Inc.
5281 California Ave, Suite #100
Irvine, CA 92617 United States
Urovant Sciences GmbH
Basel 4052 Switzerland
At Urovant Sciences we are committed to high standards of product safety, efficacy and regulatory compliance, including post-market requirements for reporting adverse events, product complaints and other reportable events.
An adverse event or adverse drug experience is an unexpected medical problem that occurs during treatment with a drug or other therapy in a patient, whether or not it is considered to be related to use of the therapy.
A product complaint is any perceived product defect. A product complaint may include information relating to product deficiencies (identity, quality, strength, or durability), including the drug product itself and/or all components distributed with the product, such as packaging, container-closure systems, delivery systems, labelling, and package inserts.