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Indications ⬇

REMS


Contraind./Precautions ⬆ ⬇

Contraindicated in:

Use Cautiously in:

Adv. Reactions/Side Effects ⬆ ⬇

Derm: pruritus

GI: HEPATOTOXICITY (↑ WITH HEPATITIS B OR C)

GU: renal impairment

MS: myositis

Neuro: headache, insomnia, fatigue

Misc: hypersensitivity reactions (including rash, constitutional symptoms, and liver injury), immune reconstitution syndrome

Interactions ⬆ ⬇

Drug-drug:

Drug-Natural Products:

Availability ⬆ ⬇

(Generic available)

Route/Dosage ⬆ ⬇

Tablets (Tivicay) and tablets for oral suspension (Tivicay PD) are not interchangeable.

US Brand Names ⬆ ⬇

Tivicay, Tivicay PD

Action ⬆ ⬇

  • Inhibits HIV-1 integrase, which is required for viral replication.
Therapeutic effects:
  • Evidence of decreased viral replication and reduced viral load with slowed progression of HIV and its sequelae.

Classifications ⬆ ⬇

Therapeutic Classification: antiretrovirals

Pharmacologic Classification: integrase strand transfer inhibitors (INSTI)

Pharmacokinetics ⬆ ⬇

Absorption: Bioavailability is unknown.

Distribution: Enters CSF.

Protein Binding: >98.9%.

Metabolism/Excretion: Metabolized primarily by the UGT1A1 enzyme system with some metabolism by the CYP3A4 isoenzyme. 53% excreted unchanged in feces. Metabolites are renally excreted; minimal renal elimination of unchanged drug. Poor UGT1A1 metabolizers have ↑ dolutegravir concentrations and an ↑ risk of adverse effects.

Half-Life: 14 hr

Time/Action Profile ⬆ ⬇

( plasma concentrations)

ROUTEONSETPEAKDURATION
POunknown2–3 hr12–24 hr‡

‡Depends on concurrent use of metabolic inducers.

Patient/Family Teaching ⬆ ⬇

Pronunciation ⬆ ⬇

doe-loo-TEG-ra-vir

Code ⬆

NDC Code