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Aptivus (tipranavir) capsules

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  • About Aptivus
    • About APTIVUS
    • Consider APTIVUS/ritonavir For
  • Clinical Data
    • The RESIST Trials
      • Treatment Response
      • Where Undetectable Is Possible
      • Greater Outcomes
      • Treatment Response by Number of PI Mutations
    • Phenotype & Genotype Testing
  • Resistance Data
    • Susceptibility
    • Treatment-Emergent Mutations & Cross Resistance
  • Dosing and Administration
    • Dosing
    • Indications and Usage
    • Drug Interactions
  • Adverse Events
    • Adverse Effects
    • Laboratories Abnormalities & Cholesterol
    • Hepatic Impairment and Intracranial Hemorrhage
  • Important Safety Information
  • Full Prescribing Information

Open a World of Possibilities

Laboratory Abnormalities in RESIST Trials

Incidence of laboratory abnormalities

Treatment-Emergent Laboratory Abnormalities Reported in ≥2% of Adult Patients (48-Week Analysis)

ALT and/or AST, cholesterol, and triglyceride levels

  • Significantly greater elevations in ALT and/or AST, cholesterol, and triglyceride levels were observed in patients treated with APTIVUS/r vs CPI/r
  • In controlled clinical trials extending up to 96 weeks, the proportion of patients who developed Grade 2-4 ALT and/or AST elevations increased from 26% at week 48 to 32.1% at week 96 with APTIVUS/r
  • The risk of developing transaminases elevations is greater during the first year of therapy

Please consult the Full Prescribing Information ,including boxed WARNINGS, and Important Safety Information for APTIVUS, as well as information on the RESIST Trials.

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