Yes, Difelikefalin is FDA approved. The U.S. Food and Drug Administration (FDA) approved Difelikefalin on August 23, 2021, for the treatment of moderate-to-severe pruritus (itching) associated with chronic kidney disease in adults undergoing hemodialysis (HD).
Difelikefalin is specifically used in adults who are on dialysis to manage itching associated with chronic kidney disease. This condition, known as pruritus, can significantly impact the quality of life for dialysis patients. Difelikefalin works as a peripheral opioid receptor agonist, helping to alleviate the discomfort caused by severe itching.
Difelikefalin is administered as follows:
A healthcare provider administers Difelikefalin by IV bolus injection into the venous line of the dialysis circuit at the end of each HD treatment. The dose is determined by the patient's target dry body weight.
Common side effects of Difelikefalin may include:
Serious side effects that require immediate medical attention include signs of an allergic reaction such as hives, difficulty breathing, and swelling of the face, lips, tongue, or throat.
Patients should report any side effects to their doctor and can also report them to the FDA at 1-800-FDA-1088.
Before starting treatment with Difelikefalin, patients should consider the following precautions:
Difelikefalin provides a significant treatment option for adults undergoing hemodialysis who suffer from moderate to severe pruritus associated with chronic kidney disease. It is crucial to follow the prescribed administration guidelines, take necessary precautions, and consult healthcare providers for personalized medical advice and treatment plans.
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