DOSING &
LAB MONITORING
ONE PILL. ONCE-DAILY.
IR=intolerance or inadequate response;
TNFi=tumor necrosis factor inhibitor
US-MULT-240253
IR=intolerance or inadequate response;
TNFi=tumor necrosis factor inhibitor
One strength for induction and two strengths for maintenance
The recommended induction dose of RINVOQ is 45 mg QD for 8 weeks.
The recommended dose of RINVOQ for maintenance treatment is 15 mg once daily.
A dose of 30 mg once daily may be considered for patients with refractory, severe or extensive disease.
Discontinue if an adequate therapeutic response is not achieved with the 30 mg dose.
Use the lowest effective dose needed to maintain response.
Limitations of Use: RINVOQ is not recommended for use in combination with other JAK inhibitors, biological therapies for ulcerative colitis, or with other potent immunosuppressants such as azathioprine and cyclosporine.
Administration1
Perform lab testing for:
INTERRUPT IF PATIENT DEVELOPS A SERIOUS OR OPPORTUNISTIC INFECTION.
*Treatment can be initiated or restarted after levels return above specified values, drug-induced liver injury diagnosis is excluded, or infection is controlled.1
See RINVOQ’s safety data across clinical trials
RINVOQ is indicated for the treatment of adults with moderately to severely active ulcerative colitis who have had an inadequate response or intolerance to one or more TNF blockers.
Limitations of Use: RINVOQ is not recommended for use in combination with other JAK inhibitors, biological therapies for ulcerative colitis, or with other potent immunosuppressants such as azathioprine and cyclosporine.
REFERENCE