Treataware

Darunavir and the risk of hepatitis

A warning has been issued by Tibotec, the manufacturers of Prezista (darunavir) regarding the risk of developing drug-induced hepatitis while taking the treatment. Apparently, 0.5% of clinical trial participants who took a combination including darunavir (boosted with ritonavir) developed severe hepatotoxicity. Anyone with a history of liver-related complications such as hepatitis B or C are particularly susceptible, so appropriate tests prior to starting darunavir and regular monitoring while on the drug are vital to avoid developing any hepatotoxic reaction. http://www.ashm.org.au

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This information was retrieved from the Treataware website (www.treataware.info) on 19 Nov 2008. For further information, please consult the website or call the NAPWA office on 02 8568 0300.