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      Low Discontinuation Rates

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PREZISTA® /r: Tolerability Proven Over Time
  • Important Safety Information
  • Low Discontinuation Rates
  • Proven Lipid Profile
  • Low Rates of Drug-Related ADRs

Low discontinuation due to ADRs* with Once-Daily PREZISTA®/r in the first 90 days and through 192 weeks1, 2

Low discontinuation due to ADRs* with Once-Daily PREZISTA®/r in the first 90 days and through 192 weeks


* Excluding laboratory abnormalities as ADRs.

ADRs=adverse drug reactions; TDF/FTC=tenofovir disoproxil fumarate/emtricitabine.

Kaletra (lopinavir/ritonavir) is a registered trademark of AbbVie Inc.


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  • Lipids in Experienced Adults
  • GI ADRs in Experienced Adults
  • GI ADRs in Naïve Adults
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