Pfizer’s Xeljanz (tofacitinib) has been on the market since 2012. First approved to treat rheumatoid arthritis, Xeljanz has since received FDA approval for the treatment of other types of arthritis as well as ulcerative colitis.

In just the last two years, however, the FDA has warned that Xeljanz can be associated with heart problems, blood clots, and even cancer. But the question remains: why didn’t Pfizer warn consumers about these potential risks sooner?

Xeljanz lawsuits claim that Pfizer failed to give adequate warning about the drug’s side effects, which caused preventable harm to patients who suffered blood clots in the lungs, heart attacks, strokes, breast and colon cancer, and other severe health problems. We are accepting these cases on a contingency-fee basis. That means our clients don’t pay unless we win. If you need to discuss a Xeljanz lawsuit with a lawyer, free of charge, please contact us.

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