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Victims Who’ve Used Xeljanz® And Then Suffered From Serious Heart-Related Conditions May Be Able To Seek Both Justice And Compensation

Victims Who’ve Used Xeljanz® And Then Suffered From Serious Heart-Related Conditions May Be Able To Seek Both Justice And Compensation

Victims who have taken Xeljanz® and have reported one of the following serious conditions are encouraged to get a free, private case evaluation: 

  • Cancer
  • Blood clots
  • Heart-related events 
  • Death

Limited Time To File A Claim. Check Eligibility Today.


While using the drug did you or loved one experience any of the following? Please check all that apply(Required)

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How Xeljanz® (Sold Generically As Tofacitinib) May Lead To Serious Complications


Xeljanz®, a drug made by Pfizer, is commonly prescribed to treat ulcerative colitis or arthritis in older adults.

Xeljanz® works to suppress the patient’s immune system in order to treat arthritis inflammation, but in such a way that may lead to a variety of dangerous side effects that are clearly displayed on the drug’s label.

However, one set of side effects not specifically warned about on Xeljanz® labels is a variety of heart-related events, such as cancer, blood clots, and even death.

The FDA issued 3 safety warnings to patients who take Xeljanz® that, taken in certain doses, can potentially cause an increased risk of heart-related events in the lungs, up to and even including death

The history of FDA approval for certain ailments Xeljanz® includes:

  • In 2020, the FDA approved Xeljanz® for polyarticular juvenile idiopathic arthritis
  • In 2018, the FDA approved Xeljanz® for ulcerative colitis
  • In 2017, the FDA approved Xeljanz® and Xeljanz XR® for psoriatic arthritis
  • In 2012, the FDA approved Xeljanz® for rheumatoid arthritis

How Xeljanz® (Sold Generically As Tofacitinib) May Lead To Serious Complications


Just because the FDA approves a medication safe for use doesn’t mean that it’s completely safe to take–which is a truth that millions of patients are finding out the hard-way.

In February 2019, an ongoing FDA Xeljanz® safety trial found an increased risk of blood clots in the lungs that may cause death.

Also in July 2019, the FDA issued new warnings about thrombosis–when blood clots block a vein or artery–potentially leading to death in patients treated with a 10 mg twice-daily dose of Xeljanz®.

In fact, the following qualifications may potentially make for a strong case and compensation:

  • Patients treated for arthritis with Xeljanz® or Xeljanz® XR; and
  • Patients taking a 10 mg twice daily dose of Xeljanz® or Xeljanz® XR; and
  • Patients suffering a Pulmonary embolism (“PE”), Pulmonary thrombosis (“PT”), Deep vein thrombosis (“DVT”), stroke, or similar blood clot injury.

Xeljanz® victims and their families should be able to address big pharma and their prescribing doctors about the failure to warn and to get the compensation and justice they deserve. 

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Please seek the advice of a medical professional before making health care decisions. This advertisement is not associated with Pfizer®, Xeljanz®, Xeljanz XR®, or any government agency.

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