FDA Issues Safety Warning for Xarelto®
Xarelto® was approved by the US Food and Drug Administration (FDA) in 2011. A Xarelto® lawsuit has been filed against Bayer AG and Janssen, the manufacturers of of this drug, alleging that the side effects include and increased in risk of internal bleeding and strokes. The Plaintiff is the lawsuit claims that the manufacturers of Xarelto did not adequately warn about the associated risks.
If you experienced complications after using Xarelto®, you may be entitled to compensation.
Injuries alleged to be associated with Xarelto® include:
- Retinal Hemorrhages
- Epidural Hematoma
- Intracranial Hemorrhages
- Pulmonary Embolism
- Hemoglobin decrease
- Gastrointestinal Hemorrhages
- Deep Vein Thrombosis (DVT)
- Adrenal Bleeding
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