Abstract
Tolerability of the combination of zidovudine-lamivudine and lopinavir-ritonavir as postexposure prophylaxis (PEP) for human immunodeficiency virus infection was prospectively assessed. A total of 121 patients were enrolled in the study; 23 patients discontinued PEP prematurely for reasons other than adverse events. Of the other 98 patients, 58 (59%) experienced adverse effects, which led to premature PEP discontinuation in 20 cases (20%).
Publication types
-
Clinical Trial
-
Research Support, Non-U.S. Gov't
MeSH terms
-
Adult
-
Anti-HIV Agents / adverse effects*
-
Anti-HIV Agents / pharmacology
-
Anti-HIV Agents / therapeutic use
-
CD4 Lymphocyte Count
-
Drug Combinations
-
Female
-
HIV Infections / prevention & control*
-
Humans
-
Lamivudine / adverse effects
-
Lamivudine / pharmacology
-
Lamivudine / therapeutic use
-
Lopinavir
-
Male
-
Pyrimidinones / adverse effects
-
Pyrimidinones / pharmacology
-
Pyrimidinones / therapeutic use
-
Ritonavir / adverse effects
-
Ritonavir / pharmacology
-
Ritonavir / therapeutic use
-
Viral Load
-
Zidovudine / adverse effects
-
Zidovudine / pharmacology
-
Zidovudine / therapeutic use
Substances
-
Anti-HIV Agents
-
Drug Combinations
-
Pyrimidinones
-
lamivudine, zidovudine drug combination
-
Lopinavir
-
Lamivudine
-
Zidovudine
-
Ritonavir