Please report any side effect, adverse event, or product quality complaint related to the use of Imbruvica by calling +1 (877) 877-3536. An operator is available 24 hours/day, 7 days/week.
Alternatively, this information may be reported to the FDA MedWatch Adverse Event Reporting program online (https://www.fda.gov/safety/medwatch-fda-safety-information-and-adverse-event-reporting-program) or by telephone at +1 (800) 332-1088.