"The US Food and Drug Administration (FDA) has approved tofacitinib citrate extended-release (Xeljanz XR, Pfizer Inc) 11-mg tablets for once-daily treatment of moderate to severe rheumatoid arthritis (RA) in patients who have not responde"...
Hypersensitivity to any component of this product.
Severe toxicity resulting from previous exposure to gold or other heavy metals.
Systemic lupus erythematosus.This monograph has been modified to include the generic and brand name in many instances.
Last reviewed on RxList: 11/25/2008
Additional Myochrysine Information
Report Problems to the Food and Drug Administration
You are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.
Get the latest treatment options