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Indications

REMS


Contraind./Precautions

Contraindicated in:

Use Cautiously in:

Adv. Reactions/Side Effects

CV: bradycardia, heart block, hypertension

Derm: BASAL/SQUAMOUS CELL CARCINOMA, MELANOMA

EENT: macular edema, vision abnormalities

GI: liver enzymes, nausea

GU: urinary tract infection

Hemat: lymphopenia

Metab: hypercholesterolemia

MS: arthralgia

Neuro: posterior reversible encephalopathy syndrome (pres), dizziness, headache, PML

Resp: pulmonary function

Misc: infection (including bacterial and viral), IMMUNE RECONSTITUTION INFLAMMATORY SYNDROME, MALIGNANCY

Interactions

Drug-drug:

Availability

Route/Dosage

US Brand Names

Velsipity

Action

  • Acts as a sphingosine 1-phosphate (S1P) receptor modulator that binds to SIP receptors 1, 4, and 5, resulting in migration of lymphocytes from lymph nodes into the intestines.
Therapeutic effects:
  • Achievement of clinical remission.

Classifications

Therapeutic Classification: gastrointestinal anti-inflammatories

Pharmacologic Classification: receptor modulators

Pharmacokinetics

Absorption: Unknown.

Distribution: Well distributed to extravascular tissues.

Protein Binding: 97.9%.

Metabolism/Excretion: Primarily metabolized in the liver via the CYP2C8, CYP2C9, and CYP3A4 isoenzymes, with some metabolism by the CYP2C19 and CYP2J2 isoenzymes. Primarily excreted in the feces (82%; 11% as unchanged drug), with 5% excreted in the urine.

Half-Life: 30 hr.

Time/Action Profile

(plasma concentrations)

ROUTEONSETPEAKDURATION
POunknown4 hr24 hr



Patient/Family Teaching

Pronunciation

e-TRAS-i-mod