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Indications

REMS


Contraind./Precautions

Contraindicated in:

Use Cautiously in:

Adv. Reactions/Side Effects

Interactions

Drug-drug:

Availability

Route/Dosage

US Brand Names

Evrysdi

Action

  • Acts as a survival of motor neuron 2 (SMN2) splicing modifier, which facilitates production of full-length SMN in patients with spinal muscular atrophy caused by genetic mutations leading to SMN protein deficiency.
Therapeutic effects:
  • Improvement in ability to sit without support and improvement in survival without requiring permanent ventilation in infantile-onset spinal muscular atrophy.
  • Improved motor function in later-onset spinal muscular atrophy.

Classifications

Therapeutic Classification: none assigned

Pharmacologic Classification: survival of motor neuron 2 splicing modifiers

Pharmacokinetics

Absorption: Well absorbed following oral administration.

Distribution: Extensively distributed to extravascular tissues.

Metabolism/Excretion: Primarily metabolized by flavin monooxygenase 1 and 3 as well as the CYP1A1, CYP2J2, CYP3A4, and CYP3A7 isoenzymes. Primarily excreted in feces (53%; 14% as unchanged drug), with 28% excreted in urine (8% as unchanged drug).

Half-Life: 50 hr.

Time/Action Profile

(plasma concentrations)

ROUTEONSETPEAKDURATION
POunknown1–4 hrunknown

Patient/Family Teaching

Pronunciation

ris-DIPlam

Code

NDC Code