PFIZER®
Failed to warn doctors and patients about the risks behind Xeljanz® and deadly side effects such as blood clots and pulmonary embolisms
The Risks Behind Xeljanz®
The active ingrediants in Xeljanz® are designed to oppress a patient's immune system, which can lead to multiple side effects. Recently, the FDA released a safety alert stating that consuming Xeljanz® at certain levels can increase the change of blood clots. Patients were never informed of these deadly risks.
Follow-up studies have also found that Xeljanz® may also lead patients to suffer from multiple cancers, heart-related issues, and more. Those impacted are encouraged to come forward and receive a 100% free legal case review.
FDA issues warning about xeljanz® and blood clots
(2017)
European Union Rejects Xeljanz® for RA Treatment
(2013)
Xeljanz® is approved for use in the United States
(2012)
First-ever clinical trails of Xeljanz®
(2002)
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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