Crohn's Disease in
the Clinical Setting
About CIMZIA®
Dosing and
Administration
Clinical Trials Overview
Patient Support
Safety Information
Resources
For Patients & Caregivers
Prescribing Information


This site is intended for
US residents.

Adverse Events

Most common adverse reactions (≥5% of CIMZIA-treated patients and with a higher incidence compared to placebo) in controlled Crohn's clinical studies1

Incidence of serious adverse events in CIMZIA clinical trials
(per 100 patient-years)1

In completed and ongoing clinical studies1*: CIMZIA, n=5118

  • Tuberculosis: CIMZIA, 0.61 vs placebo, 0

In all clinical trials1*: CIMZIA, n=4650; placebo, n=1319

  • Malignancies: CIMZIA, 0.5 (0.4, 0.7) vs placebo, 0.6 (0.1, 1.7)

In CIMZIA RA clinical trials1*: CIMZIA, n=2367

  • A total of 3 cases of lymphoma were observed1

*Including other investigational uses.
Numbers in parentheses represent a 95% confidence interval.

Reference:

  1. CIMZIA [prescribing information]. Smyrna, GA: UCB, Inc.; 2009.

CIMZIA is indicated for reducing signs and symptoms of Crohn's disease and maintaining clinical response in adult patients with moderately to severely active disease who have had an inadequate response to conventional therapy.
For more information 1.866.4.CIMZIA
CIMZIA