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U.S. Food and Drug Administration (FDA) placed a Boxed Warning for added risk of mortality with gout medication Uloric (febuxostat)

U.S. Food and Drug Administration (FDA) placed a Boxed Warning for added risk of mortality with gout medication Uloric (febuxostat)

conduct uloric stroke . The trial was conducted in over 6,000 patients with gout treated with either Uloric or allopurinol. The primary outcome was a combination of heart-related death, non-deadly heart attack, non-deadly stroke, and an issue of inadequate blood supply to the heart requiring intervention, called unstable angina.

 

Does Your Case Qualify for an Action Against the Manufacturers of Uloric? According to the new Black Box warnings mandated by the FDA, use of Uloric can increase the risk of experiencing one of the following side-effects:

 

Death

 

Heart Attack

 

Stroke

 

Pulmonary Embolism (PE)

 

Deep Vein Thrombosis (DVT)

 

If you or a loved one has experienced any of the above while taking Uloric for the condition of gout, you might be entitled to a settlement from Takeda Pharmaceuticals, as well as for expenses, emotional distress, and inconveniences you have experienced as a result of your medical treatment.

 

The attorneys at The Meneo Law Group not only have the skill, experience, and knowledge to manage your Uloric lawsuit, but a proven history of success in representing people, like you, who have been injured by dangerous drugs and products.

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Domenica, Ottobre 20, 2019

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