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The Pharmaceutical Journal Vol 267 No 7171 p585-589
27 October 2001

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Antiretroviral monitoring needed

Yearly surveys of people on antiretroviral therapy could help to identify changes in prevalence of specific toxic side effects, say Swiss researchers.

Adverse drug reactions are recorded anecdotally and in trials but there is little information about their prevalence and severity in routine clinical practice, say Dr Jacques Fellay, division of infectious diseases, University of Lausanne, and colleagues. Therefore, they conducted an observational study in 1,160 patients to describe clinical and laboratory abnormalities potentially associated with antiretroviral therapy. Clinical adverse events probably or definitely linked to antiretroviral therapy occurred in 47 per cent of patients with a further 23 per cent having events possibly linked to therapy. The figures for laboratory abnormalities were 27 per cent and 51 per cent, respectively.

The researchers identified specific adverse events for each antiretroviral drug. Some of the less expected results include thrombocytopenia with saquinavir, mood disorders with lamivudine and unconjugated hyperbilirubinaemia with ritonavir.

The researchers conclude that various antiretroviral treatments have comparable efficacy so toxic effects are one of the important factors that will drive choice of treatment (Lancet 2001;358:1322).

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