Keveyis (dichlorphenamide tablets - Xeris, generic) — Cigna
Hypokalemic Periodic Paralysis (HypoPP) and Related Variants
Initial criteria
- Patient has a confirmed diagnosis of primary hypokalemic periodic paralysis by meeting at least ONE of the following (serum potassium concentration < 3.5 mEq/L during a paralytic attack; OR family history of the condition; OR genetically confirmed skeletal muscle calcium or sodium channel mutation); AND
- The prescriber has excluded other reasons for acquired hypokalemia (e.g., renal, adrenal, or thyroid dysfunction; renal tubular acidosis; diuretic or laxative abuse); AND
- Patient has had improvements in paralysis attack symptoms with potassium intake; AND
- Patient has tried oral acetazolamide therapy; AND
- According to the prescriber, acetazolamide therapy did not worsen the paralytic attack frequency or severity; AND
- The medication is prescribed by or in consultation with a neurologist or a physician who specializes in the care of patients with primary periodic paralysis (e.g., muscle disease specialist, physiatrist)
Reauthorization criteria
- Patient is currently receiving dichlorphenamide and has responded to dichlorphenamide (e.g., decrease in the frequency or severity of paralytic attacks) as determined by the prescriber
Approval duration
initial 2 months; renewal 1 year