Hepatotoxicity of nevirapine in virologically suppressed patients according to gender and CD4 cell counts

Author:

De Lazzari E,León A,Arnaiz JA,Martinez E,Knobel H,Negredo E,Clotet B,Montaner J,Storfer S,Asenjo MA,Mallolas J,Miró JM,Gatell JM

Publisher

Wiley

Subject

Pharmacology (medical),Infectious Diseases,Health Policy

Reference22 articles.

1. 1 US Food and Drug Administration Center for Drug Evaluation and Research. FDA public health advisory for nevirapine (Viramunetm) (19 January 2005). Efficacy and safety concerns regarding the coadministration of tenofovir disoproxil fumarate (TDF, Viread) and didanosine (ddI, Videx). EMEA Public Statement (EMEA/6231/2005). Available at: http://www.fda.gov/cder/drug/advisory/nevirapine.htm

2. 2 EMEA. No. II/0049, 16 March 2005.

3. A Comprehensive Hepatic Safety Analysis of Nevirapine in Different Populations of HIV Infected Patients*

4. The effect of baseline CD4 cell count and HIV-1 viral load on the efficacy and safety of nevirapine or efavirenz-based first-line HAART

5. 5 S Storfer, J Leith, P Robinson, P Piliero, and D. Hall Analysis of hepatic events within the 2NN study: controlling for geographic region and CD4+ cell count at initiation of nevirapine therapy.45th Interscience Conference on Antimicrobial Agents and Chemotherapy. Washington, DC, December 2005 [LB-13].

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