Table 1:

Mechanisms of pharmacokinetic drug interactions between antiretrovirals and medications commonly used in older adults

MechanismRelevant antiretroviralsCoadministered agentsPossible management strategy
Absorption
Gastric acidity
  • Atazanavir

  • Rilpivirine

AntacidsSeparate administration times by at least 2 h26,27
H2-receptor antagonists
  • Alter timing of administration and limit dose of H2-receptor antagonist

  • Consider increasing atazanavir dose to 400 mg (along with 100 mg ritonavir)

Proton pump inhibitorsAvoid concomitant use
Chelation
  • Dolutegravir

  • Elvitegravir

  • Raltegravir

AntacidsSeparate administration times by at least 2 h2830
Metabolism
CYP450 3A4
  • Protease inhibitors, cobicistat

  • NNRTIs

  • Fentanyl, oxycodone

  • Anticonvulsants (e.g., carbamazepine, phenytoin)

  • Antiplatelet agents

  • Anticoagulants

  • Calcium-channel blockers (e.g., amlodipine, diltiazem, nifedipine, verapamil)

  • Corticosteroids (e.g., inhaled fluticasone–budesonide, triamcinolone by injection)

  • Phosphodiesterase inhibitors

  • Psychotropics (e.g., aripiprazole, quetiapine, ziprasidone)

  • Statins (e.g., lovastatin, simvastatin)

  • Concentrations of coadministered agents may be increased or decreased

  • Consider agents less likely to interact

  • Monitor patient’s response and adjust dose of coadministered agent accordingly

Other CYP450 isoenzymes (e.g., CYP2D6, CYP2B6, CYP2C9, CYP2C19)
  • Protease inhibitors, cobicistat

  • NNRTIs

  • Antidepressants

  • Oral hypoglycemic agents (e.g., repaglinide, nateglinide, rosiglitazone)

  • Warfarin

  • Concentrations of coadministered agents may be increased or decreased

  • Consider agents less likely to interact

  • Monitor patient’s response and adjust dose of coadministered agent

  • Note: CYP450 = cytochrome P450, NNRTI = non-nucleoside reverse transcriptase inhibitor.