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FDA Approves PREZISTA®/ritonavir Once-Daily Dosing for HIV-1 Treatment-Experienced Adults With No Darunavir Resistance-Associated Mutations
Date:12/13/2010

moderate intensity (greater than or equal to Grade 2) in the PREZISTA/ritonavir arm through 96 weeks were diarrhea (8%), headache (6%), abdominal pain (5%), and rash (5%)
  • In treatment-experienced adult patients, the most common adverse drug reactions (greater than or equal to 5%) reported of at least moderate intensity (greater than or equal to Grade 2) in the PREZISTA/ritonavir arm through 96 weeks were diarrhea (14%), nausea (7%), rash (7%), abdominal pain (6%), and vomiting (5%)
  • This is not a complete list of all adverse drug reactions reported with the use of PREZISTA/ritonavir.Please see accompanying full Prescribing Information for more details. Full prescribing information is also available at www.PREZISTA.com.You are encouraged to report negative side effects of prescription drugs to the FDA.  Visit www.fda.gov/medwatch, or call 1-800-FDA-1088.

    About Tibotec PharmaceuticalsTibotec Pharmaceuticals, based in Cork, Ireland, is a pharmaceutical research and development company. The Company's main research and development facilities are in Beerse, Belgium, with offices in Titusville, NJ, USA. Tibotec is dedicated to the discovery and development of innovative HIV-1/AIDS drugs and anti-infectives for diseases of high unmet medical need.

    About Tibotec TherapeuticsTibotec Therapeutics, a division of Centocor Ortho Biotech Products, L.P., headquartered in Titusville, NJ, is dedicated to delivering innovative virology therapeutics that help healthcare professionals address serious unmet needs in people living with HIV-1.

    (1) Resistance-associated mutations are also referred to as resistance-associated substitutions.Media Contact:  Pamela Van Houten, 609-730-7902 (office)908-295-7367 (mobile)Investor Contacts:  Louise Mehrotra, 732-524-6491 Stan Panasewicz, 732-524-2524
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    SOURCE Tibotec Therapeutics
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