[Toxicity associated to efavirenz in HIV-infected persons enrolled in an expanded access program]

Med Clin (Barc). 2000 Sep 23;115(9):337-8. doi: 10.1016/s0025-7753(00)71549-1.
[Article in Spanish]

Abstract

Background: Efavirenz (EFV) is one of the latest antiretroviral compounds appeared in the market. Its toxicity profile is not well known.

Patients and methods: The rate of adverse events was examined in 250 subjects enrolled in the expanded access program in a single institution located in Madrid, Spain.

Results: Adverse events grade >= 2 (WHO) were recorded in 33 (13.2%) persons. The most common were neuropsychiatric disorders (8.4%), cutaneous lesions (3.2%), and gastrointestinal problems (0.8%). The drug needed to be discontinued in 17 (6.8%) patients.

Conclusion: The rate of adverse events grade moderate-to-severe in patients receiving EFV is relatively low (13. 4%), without evidence of cross-toxicity (i.e., rash by nevirapine). Neuropsychiatric and dermatological conditions are the most common, and ten to resolve spontaneously in two

MeSH terms

  • Alkynes
  • Anti-HIV Agents / adverse effects*
  • Benzoxazines
  • Cyclopropanes
  • Female
  • HIV Infections / drug therapy*
  • Humans
  • Male
  • Oxazines / adverse effects*

Substances

  • Alkynes
  • Anti-HIV Agents
  • Benzoxazines
  • Cyclopropanes
  • Oxazines
  • efavirenz