Emerging Kayexalate Litigation
Kayexalate, made by Concordia Pharmaceuticals, Inc. was first approved by the FDA subsequent to New Drug Application 011287.
September 2017 : FDA is recommending that patients avoid taking the potassium-lowering drug sodium polystyrene sulfonate (Kayexalate) at the same time as other medicines taken by mouth. A study found that sodium polystyrene sulfonate binds to many commonly prescribed oral medicines, decreasing the absorption and therefore effectiveness of those oral medicines.
A study was conducted in the laboratory, called an in vitro study, to evaluate the binding potential for certain administered medicines commonly taken together with sodium polystyrene sulfonate. These medicines included certain:
Blood pressure medicines
Blood Thinner Medication
By reducing or eliminating the effectiveness of other drugs, patients may be more likely to suffer adverse events intended to be controlled by the effected drugs.
Prior to the September 2017 FDA action, the Kayexalate label included warnings related to the concomitant use of several drugs however, these warnings did not include a significant number of drugs now found to be potentially harmful when used in combination with Kayexalate.
To Learn More About the Emerging Kayexalate Litigation:
The emerging Kayexalate Litigation will be used as a case study in the May 18th to 21st 2018 Mass Tort Nexus, “Four Days to Mass Tort Success Course” To register for the May Course, contact Jenny Levine at email@example.com or call (954) 520-4494.
For information on the class and to enroll, use this link-“Enroll Here To Attend “Four Days to Mass Tort Success”
Course attendees will receive the benefit of a step by step analysis of the emerging Kayexalate Litigaton, using these primary metrics:
Some of the top mass tort trial lawyers in the country have endorsed the Mass Tort Nexus Immersion Course, including Michael Brady Lynch>
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