section name header

Pronunciation

fos-TEM-sa-vir

Classifications

Therapeutic Classification: antiretrovirals

Pharmacologic Classification: gp120 attachment inhibitors

Indications

REMS


Action

  • Fostemsavir is a prodrug that is hydrolyzed to the active form, temsavir. Temsavir binds directly to the gp120 subunit within the HIV-1 envelope glycoprotein gp160 and selectively prevents attachment of the virus to the CD4 receptors on cells.
Therapeutic effects:
  • Reduction in viral load.

Pharmacokinetics

Absorption: 27% of temsavir absorbed following oral administration; absorption with high-fat meal.

Distribution: Moderately distributed to extravascular tissues.

Metabolism/Excretion: Fostemsavir is a prodrug that is hydrolyzed to the active form, temsavir. Temsavir undergoes metabolism to inactive metabolites through the liver via hydrolysis and oxidation (via the CYP3A4 isoenzyme). Primarily excreted in urine (51%, <2% as unchanged drug), with 33% excreted in feces (1% as unchanged drug).

Half-Life: 11 hr.

Time/Action Profile

(plasma concentrations)

ROUTEONSETPEAKDURATION
PORapid2 hr12 hr



Contraind./Precautions

Contraindicated in:

Use Cautiously in:

Adv. Reactions/Side Effects

CV: QT interval prolongation

Derm: rash

Endo: Graves' disease, hyperglycemia

GI: nausea, lipase, liver enzymes, abdominal pain, autoimmune hepatitis, diarrhea, dyspepsia, hyperbilirubinemia, vomiting

GU: serum creatinine

Hemat: anemia, neutropenia

Metab: hypercholesterolemia, hyperuricemia

MS: creatine kinase, polymyositis

Neuro: Guillain-Barré syndrome, headache, insomnia, sedation

Misc: fatigue, immune reconstitution syndrome

Interactions

Drug-drug:

Drug-Natural Products:

Route/Dosage

Availability

Assessment

Lab Test Considerations:

Implementation

Patient/Family Teaching

Evaluation/Desired Outcomes

US Brand Names

Rukobia