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Letters to the Editor

Letter to the Editor: Comparison of Lopinavir Level Between the Two Formulations (Soft-Gel Capsule and Tablet) in HIV-Infected Pregnant Women

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Pages 254-255 | Published online: 06 Jan 2015

REFERENCES

  • French HIV therapy guidelines, 2006. Available at: http://www.sante.gouv.fr/htm/actu/yeni_sida/rapport_experts_2006.pdf. Accessed March 21,2007.
  • Stek A, Mirochnick M, Capparelli E, et al. Reduced lopina-vir exposure during pregnancy: preliminary pharmacoki-netic results from PACTG 1026. In: Program and abstracts of the XVth International AIDS Conference; July 11–16, 2004; Bangkok, Thailand. Abstract LbOrB08.
  • Manavi K, McDonald A, Al-Sharqui A. Plasma lopinavir trough levels in a group of pregnant women on lopinavir, ritonavir, zidovudine, and lamivudine. AIDS. 2007;21: 643–647.
  • Mirochnik M, Stek A, Capparelli E, et al. Adequate lopinavir exposure achieved with higher dose during the third tri-mester of pregnancy. In: Program and abstracts of the 13th Conference on Retroviruses and Opportunistic Infections; February 5–8, 2006; Denver, Colorado. Abstract 710.
  • Klein CE, Chiu YL, Awni W, et al. The tablet formulation of lopinavir/ritonavir provides similar bioavailibility to the soft-gelatin capsule formulation with less pharmacokinetic variability and diminushed food effect. J Acquir Immune Defic Syndr 2007;44:401–410.

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