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Table 13. Antiretroviral Therapy-Associated Common and/or Severe Adverse Effects

 (See Appendix B for additional information listed by drug.)  (Page 2 of 4)




 Adverse Effects  NRTIs  NNRTIs          PIs                        INSTI            EI


 Diabetes mellitus  ZDV, d4T, and ddI  • Reported for some PIs (IDV, LPV/r), but
 (DM)/insulin         not all PIs studied
 resistance
                     • ATV +/- RTV not found to alter insulin
                      sensitivity of HIV-uninfected individuals in
                      short-term studies.

 Dyslipidemia  d4T > ZDV > ABC:  EFV   LDL,  TG,  HDL: all RTV-boosted PIs
 •  LDL and TG  •  TG
 •  LDL              TG:
                     LPV/r = FPV/r and LPV/r > DRV/r and ATV/r
 •  HDL

 Gastrointestinal  Nausea and vomiting:  GI intolerance (diarrhea, nausea, vomiting)
 (GI) effects  ddI and ZDV > other NRTIs
                     Diarrhea:
 Pancreatitis: ddI   common with NFV. LPV/r > DRV/r and ATV/r

 Hepatic effects  Reported for most NRTIs  NVP > other NNRTIs  All PIs: Drug-induced hepatitis and hepatic  MVC:
 NVP:                decompensation (and rare cases of fatalities)             Hepatotoxicity
 ddI: Prolonged exposure linked to
                     have been reported with all PIs to varying                with or without
 noncirrhotic portal hypertension,  • Severe hepatic toxicity with NVP is often associated  degrees. The frequency of hepatic events is  rash or HSRs
 some cases with esophageal  with skin rash or symptoms of hypersensitivity.  higher with TPV/r than with other PIs.  reported
 varicees
 • For ARV-naive patients, risk is greater for women  IDV, ATV: Jaundice due to indirect
       3
 Steatosis: Most commonly seen  with pre-NVP CD4 count >250 cells/mm and men
       3             hyperbilirubinemia
 with ZDV, d4T, or ddI  with pre-NVP CD4 count >400 cells/mm . Overall
 risk is higher for women than men.  TPV/r: Contraindicated in patients with
 Flares: HIV/HBV-coinfected  moderate to severe hepatic insufficiency
 patients may develop severe  • Risk is greatest in the first few months of treatment.   (Child-Pugh classification B or C)
 hepatic flare when TDF, 3TC, and
 • 2-week dose escalation of NVP reduces risk of rash
 FTC are withdrawn or when HBV
 resistance develops.  and possibly hepatotoxicity if related to
 hypersensitivity.

 • NVP is contraindicated in patients with Child-Pugh
 classification B or C.

 • Liver failure observed in HIV-uninfected individuals
 receiving NVP for post-exposure prophylaxis. NVP
 should never be used for this indication.







 Guidelines for the Use of Antiretroviral Agents in HIV-1-Infected Adults and Adolescents                                                                                                                K-9
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