Report an Adverse Event or Product Complaint
Any untoward medical occurrence in a patient or clinical investigation subject administered a pharmaceutical product and which may or may not have a causal relationship with this treatment.
Additional safety information includes (but is not limited to) the following report types:
- Unapproved or off-label use
- Use during pregnancy
- Exposure to a drug during breastfeeding/lactation
- Overdose (whether intentional, accidental, or prescribed)
- Drug abuse or misuse
- Medication errors
- Drug-drug interactions
- Drug-food interactions
- Lack of therapeutic effect
To report a suspected adverse event or product complaint, please complete our online web form.
Submit a Medical Inquiry
Ask us a product-related question and someone from our ucbCARES® or Medical Information team will provide a response via email, phone, fax, or mail.
Connect With an MSL
Request a meeting with your local Medical Science Liaison.
Or speak with a ucbCARES® Associate
1-844-599-CARE (2273) or email email
US Corporate Headquarters
1950 Lake Park Drive
Smyrna, GA 30080
Website Technical Support
If you’re interested in contacting UCB about clinical trial opportunities,
visit the Opportunities for Investigators page